Tag Archives: Dr. Robert O. Young

“As I Lay Dying..” LA Times Writer’s Last Words Will Make You Question Entire Breast Cancer Industry

 A former Los Angeles Times staff writer, Laurie Becklund, battled breast cancer since 1996. Earlier this year she knew her time was limited, and as she greeted her last few months, she wrote an opinion piece “As I Lay Dying” about her story. Becklund died Feb. 8 this year. This is what she wanted you to know about breast cancer.

Early detection does not cure cancer with mammograms DOES NOT SAVE LIVES!

Becklund: “I had more than 20 mammograms, and none of them caught my disease. In fact, we now have significant studies showing that routine mammogram screening, which may result in misdiagnoses, unnecessary treatment and radiation overexposure, can harm more people than it helps.”

To detect a cancer early in many cases means to catch it before it produces symptoms. That is a problem, because not every precancerous condition will actually become cancer or not the type of cancer that can affect a person’s life, but every case is treated as if it was the same type of cancer. Mammogram screening is responsible for about 25% of overdiagnosis in breast cancer, according to an article published in Oxford Journals. The overdiagnosis may harm patients and lead to “overuse of anticancer therapies” such as chemotherapy.

31% over diagnosed

Another article by The New England Journal of Medicine estimated that in 2008, 70,000 U.S. women were overdiagnosed with breast cancer, which is a shocking 31% of all breast cancer diagnoses.

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The first time Becklund discovered a lump in her breast in 1996 during a self-exam, she was treated by a lumpectomy and radiation. She had the most “curable” type of breast cancer. Five years after the treatment her doctor told her she had minimal chance of it ever coming back.

Yet in 2009 she received a diagnosis of stage IV breast cancer that spread to her bones, liver, lungs and brain.

Metastatic breast cancer (MBC) is the only kind of breast cancer that kills

Metastatic cancer is “cancer that has spread from the place where it first started to another place in the body,” states Cancer.org. According to a non-profit patient advocacy group Metastatic Breast Cancer Network (MBCN) breast cancer itself does not kill, instead breast cancer patients die from cancer cells travelling to other vital organs.

Breast cancer most commonly spreads to bone, brain, liver and lung. And in Becklund’s case it spread to all four places. When she went to an MBCN conference other attendees were shocked that she was even alive. Almost everyone else had cancer spread to only one organ. When later a group of people she was in was asked to stand if they survived 2 years after diagnosis, most sat down. As far as she could see Becklund was the only one standing for 7 years of survival.

The medical establishment fails their patients

An estimated 40,000 MBC patients die annually. Another 250,000 are waiting for their death.

“I say ‘estimated because no one is required to report a metastatic diagnosis. Death certificates normally report symptoms such as “respiratory failure,” not the actual disease. We are literally uncounted,” Becklund wrote.

Lauire Becklund speaks to an audience. PHOTO: Stanford Medical X/Flickr

Lauire Becklund speaks to an audience. PHOTO: Stanford Medical X/Flickr

While the Surveillance, Epidemiology and End Results (SEER) Program is the main source for cancer statistics, it does not take into account metastatic breast cancer, according to MBCN. It is however estimated up to 30% of all cases are metastatic, and yet they are not counted. Moreover, only 2% of all breast cancer research has been estimated to go towards finding a solution for preventing or treating metastatic breast cancer, according to METAvivor, a non-profit MBC patients’ advocacy organization.

There is no one “cure”

“We are each, in effect, one-person clinical trials. Yet the knowledge generated from those trials will die with us because there is no comprehensive database of metastatic breast cancer patients…” Becklund wrote.

While there is a belief that if a person lives 5 years after the diagnosis they are a cancer survivor, for patients with MBC that means almost nothing. Though there is a treatment, MBC is incurable, according to Fred Hutchinson Cancer Research Center.

Early detection does not help MBC patients either. Another type of breast cancer that was once labeled “cured” by doctors, often comes back years later as stage IV metastatic. And one type of treatment does not work for all MBC patients.

Right now, while new therapies are just starting to emerge, there is still little hope for survival for MBC, and natural and holistic therapies that have shown promise are routinely ignored.

Susan G. Komen’s mission is not helping anyone

list-428312_1280 2“Promise that you’ll never wear a pink ribbon in my name or drop a dollar into a bucket that goes to breast cancer ‘awareness’ for ‘early detection for a cure,’ the mantra of fund-raising juggernaut Susan G. Komen, which has propagated a distorted message about breast cancer and how to ‘cure’ it,” Becklund wrote.

I would be surprised if I could find one literate person who is not aware that breast cancer exists and that it is life-threatening for many patients. We are fully aware of that fact. Now what?

Susan G. Komen’s income was $287,409,269 in 2014 and allegedly 79% went into its programs for education, research and support, yet besides being aware, the money spent for over 30 years ($2.6 billion worth) did little for the survival rates of the breast cancer that actually kills – MBC.

“Pink is pretty, but it does not disguise the fact that metastatic breast cancer kills,” reads METAvivor take-action page.

For thousands of women and men who are dying from MBC right now, that is a more believable and honest public-awareness campaign.  It is called The pH Miracle for Cancer – http://www.phoreveryoung.com

Scientific Breakthrough! The Most Powerful Selective Anti-Oxidant, Alkalizer, Energizer and Cell Hydrator

The Incredible Power of Molecular Reduced Magnesium ... Bringing Cutting Edge Nutritional Science To You Now!
Dr. Robert Young

Naturopathic Practitioner – The pH Miracle Ti Sana Detox Medical Spa

The Incredible Power of Molecular Reduced Magnesium … Bringing Cutting Edge Nutritional Science To You Now!

Nov 11, 2015

Scientific Breakthrough!

The Most Powerful Selective Anti-Oxidant, Alkalizer, Energizer and Cell Hydrator in the World!

With An Instant Impact on Alkalinity, Blood Quality and Energy!

My mission is to make optimal health as easy and as cost effective as possible. I am  constantly researching to find the most effective and natural ways to achieve and maintain optimal health, fitness and vitality for myself, my family, my friends and my clients. So I am extremely excited to share with you mu latest and greatest breakthrough research in nutritional science!

My 30 years of research has shown that nearly every health condition and chronic dis-ease have three factors often associated with them:

  • Excess metabolic and dietary acidity in the interstitial body fluids
  • That excess interstitial acidity triggers tissue inflammation
  • This tissue inflammation activates cell signaling  to release anti-oxidants or acid buffers to protect the tissues, glands and organs.

Medical Science has been looking at a way of tackling these three issues for quite some time now. 

I have recently discovered that molecular activated and reduced magnesium (MgOH-) that is potentiated with lithium ions tackles all of these problems! It acts as a super anti-oxidant or a super anti-acid, a super anti-inflammatory, a super neutralizer of excess metabolic, dietary, respiratory and environmental acids, acting alone as its own cell signaling molecule!

In our body’s, activated and reduced magnesium that carries an extra electron (MgOH-) acts as a very powerful and selective anti-oxidant helping to prevent cellular damage from acid caused inflammationprotecting DNA and combating out of control metabolic and dietary acids that are the primary cause of cellular degeneration.

According to my recent research published in the medical journal, “The International Journal of Complimentary and Alternation Medicine”, entitled, “Alkalizing Nutritional Therapy in the Prevention and Reversal of Any Cancerous Condition!”, I suggest:

As deficiencies are corrected in the intracellular and interstitial fluids with key alkalizing nutritional treatments, patients see the difference  in the improved interstitial pH and chemistry counts through follow-up tests using quantitative non-invasive 3-D FBBES.  They also feel the difference physiologically and functionally with increased energy and vitality.

This is how I know proper alkalizing nutritional support in any cancerous condition is important in the prevention and treatment of cancer, the metastasis of cancer, and the shrinking of a cancerous cyst or mass without chemotherapy and-or radiation. The best part about these alkalizing nutritional treatments is they are helpful in most, if not in all cancerous conditions.”  (To read the full article go to: https://www.linkedin.com/pulse/alkalizing-nutritional-therapy-prevention-reversal-any-young-6057087895716507648?trk=mp-reader-card)

There are now well over 1000 studies from peer reviewed medical journals discussing the countless health benefits from elemental magnesium.

Activated and reduced magnesium (MgOH-) has been shown to reduce inflammation and joint discomfortincrease stamina and energy.

Activated and reduced magnesium (MgOH-) has shown promise to be cardio protectiveneuro protective, offer intestinal protectionskin rejuvenation and many more conditions caused by metabolic and dietary acids that are not properly eliminated via the four channels of elimination – skin, lungs, bowels and kidneys.

Activated and reduced magnesium (MgOH-) also acts as a powerful cell signalling molecule to maintain our cellular communications system. The interference in this through excess metabolic and dietary acidity is the cause of many health and fitness problems in the body.

The Benefits of Activated and Reduced Magnesium

The health benefits of activated and reduced magnesium are new to the world.

This was because, until NOW, the delivery was only attainable through:

  • Electron-enriched ionized water (inefficiently delivered from water current electrical ionization)
  • Electrons release through hydroxyl Gas from a metallic cylinder under high pressure

The problem with these delivery systems is that electrons disappear very quickly and therefore are not very accessible to our cells to buffer or neutralize metabolic and/or dietary acids.

Basic chemistry has demonstrated that in the stomach, the generation of electrons carried by sodium bicarbonate is more complete and faster than any other means.

I took it upon myself to find some way of getting a highly accessible form of elections stabilized by magnesium that was  easy to use and highly bioavailable to the body.

I discovered the first reduced form of magnesium potentiated by lithium that would deliver a concentration of free-electron for buffering the dietary, respiratory, environmental and metabolic acids that cause ALL sickness and disease.

I have found that this is the most efficient and easiest way of getting the benefits of activated and reduced magnesium loaded with electron energy.

Benefits Include:

  • FAST RED BLOOD CELL TRANSFORMATION: Immediate improved difference which is viewable using phase contrast microscopy in just five minutes.
  • ALKALIZING EFFECTs: Pure Energy(TM) is a potent alkalizer serving to effectively neutralise all types of metabolic and dietary acids in our body including lactic acid.
  • NEGATIVE-CHARGED ORP EFFECT: Pure Energy(TM) has a high Negative-Charged Oxidative Reduction Potential.  My electron tests show an ORP of up to -1000mV!  In this case the negative-charge is good, not bad and represents a concentration of free electron energy! As we age, we oxidize or ferment, like an old car that rusts. Things that oxidize have a positive ORP or positive-charge. Therefore if we want to slow down the aging (rusting or fermenting) process, then it’s a good to ingest foods, liquids or supplements that carry a negative-charged ORP. This was only available before with an expensive water ionizers – but is now available in supplement form to all through my latest invention called Pure Energy(TM)
  • BIO-AVAILABLE:  Pure Energy(TM) is activated and reduced magnesium potentiated with lithium and is 100% bio-available, so it will act on ALL of the body’s fluids, tissues, glands and organs.
  • ANTI-INFLAMMATORY: Pure Energy(TM) acts as a powerful anti-inflammatory in the body because it neutralizes the metabolic, respiratory, dietary and environmental acids that cause inflammation.
  • ENHANCED CELLULAR HYDRATION: Pure Energy(TM) has been shown to increase cellular hydration by enhancing the ability to move alkalizing extracellular water into the cell.
  • ENERGY PRODUCTION: Pure Energy(TM) when added to distilled or purified water will activate and reduce and potentiated with lithium as it releases electron-energy which becomes available to the mitochondria in our cells.  Activated and reduced magnesium potentiated with lithium also increases electron stores in the liver and may improve functioning of all organs in the body by increasing stores of available electron energy.
  • ANTI-AGING: Aging is created by the body being broken down by metabolic and dietary acids. By having a continual supply of electrons released from activated and reduced magnesium potentiated with lithium, the body can use the increased electrons to neutralize the acids that cause aging and slow down the aging process.
  • SPORTS RECOVERY & LEGAL PERFORMANCE ENHANCER: By increasing alkalizing cellular hydration, reducing the acids that cause inflammation and most importantly reducing the lactic acid by up to 18% that causes inflammation that leads to pain, Pure Energy(TM) is a powerful (and fully permittedsports performance and recovery enhancer.
  • POWERFUL ANTIOXIDANT: Due to its extremely small size (0.24 Trillionth of a Meter), it can spread throughout the body in seconds and penetrate all tissue, cells, and cell components providing rapid protection from metabolic and dietary acids.
  • SELECTIVE ANTIOXIDANT: Activated and reduced magnesium has special SELECTIVE properties that allow the abundant release of electrons to deal with the “bad” acid but leave the “good” alkalizing buffers, such as sodium bicarbonate and hydrogen peroxide to do their tissue protective jobs.
  • HOLISTIC ANTIOXIDANT: Due to its molecular size, Pure Energy(TM) can provide protection to the inside and outside of body cellsexternal surface of the cell membrane (lipid-bi-layer), the extra-cellular matrixplasmainterstitial fluids and all external surfaces of cells, organs, and all tissue.
  • PURE ENERGY(TM) ENABLES THE PRODUCTION OF YOUR BODY’S OWN ANTIOXIDANTS: Acts as a natural Nrf2 transcription factor activator that allows the body to make its own antioxidant compounds (e.g., superoxide dismutase (SOD), catalase, and glutathione peroxidase).
  • CELL SIGNALLING: Cell signalling is a way the body can send a message to different parts of the body to supply it with required red blood cells. The released hydroxyl ions or OH- that releases an extra electron has recently been found to act as a cell signalling molecule.  The release of this electron from reduced and activated magnesium acts as a powerful antioxidant and anti-inflammatory.
  • NATURAL & SAFEPure Energy(TM) contains natural mineral ingredients and tested to be 100% safe, even at high doses. There are no known negative direct or side-effects.
  • Pure Energy(TM) can ONLY be obtained by calling this special phone number: 760-484-3797 or you can order on line at: http://store.phoreveryoung.com/products/pure-energy?variant=10089006916, or email us at: phmiraclelife@gmail.com
  • www.phoreveryoung.com and www.phoreveryoung.wordpress.com

How To Prepare the Pure Energy(TM) Magnesium for Activation and Reduction:

1) Take a 12 ounce surgical stainless steel bottle and fill the bottle to the top with distilled or purified water.  Make sure there is no air at the top of the bottle where electrons might escape.

2) Drop one Pure Energy(TM) magnesium tablet in the water and immediately seal the bottle with the screw on top in order to trap all the electrons inside.

3) Let the distilled or purified water sit for 2 hours while the magnesium activates and reduces.

4) When you are ready to drink the Pure Energy(TM) activated and reduced magnesium water you can take off the lid or you can flip up the straw to drink.  Drink the whole 12 ounces once opened.

Please note that the Pure Energy(R) activated reduced magnesium water is stable and drinkable for up to 1 year as long as the cap or the lid has not been opened.

Recommendations:

Drink one 12 ounce Pure Energy(TM) activated reduced magnesium water in the morning and one 12 ounce Pure Energy(TM) activated reduced magnesium water in the afternoon.

To order your Pure Energy(TM) go to: http://store.phoreveryoung.com/products/pure-energy?variant=10089006916

You will receive with your Pure Energy(TM) order, free shipping, Dr. Robert O. Young’s “Alkalizing Nutritional Therapy” book, a special container for your Pure Energy(TM) tablets and two stainless steel 12 ounce bottles, with each order of one month supply or a minimum of 60 tablets of Pure Energy(TM).

Alkalizing Fruit, Vegetables, Nuts, Seeds and Sprouts May Prevent or Reverse Depression!

Alkalizing Fruit, Vegetables, Nuts, Seeds and Sprouts May Prevent or Reverse Depression!
Dr. Robert Young

 M.Sc., D.Sc., Ph.D., N.D.

Naturopathic Physician at the pH Miracle Ti Sana Medical Spa, Arlate, Italy

Alkalizing Fruit, Vegetables, Nuts, Seeds and Sprouts May Prevent or Reverse Depression!

Eating a plant-based alkaline diet comprising of fruit, vegetables, sprouts, legumes, and healthy polyunsaturated oils is associated with preventing the onset of depression, according to research published in the open access journal BMC Medicine. A large study of 15,093 people suggests depression could be linked with nutrient deficits.

Following extensive research into diet and its effect on our physical health, researchers are now exploring the link between nutrition and mental health. This is the first time that several healthy dietary patterns and their association with the risk of depression have been analyzed together.

The researchers compared three diets; the Mediterranean diet, the Pro-vegetarian Dietary Pattern and Alternative Healthy Eating Index-2010. Participants used a scoring system to measure their adherence to the selected diet, i.e. the higher the dietary score indicated that the participant was eating a healthier diet.

Food items such as meat and sweets (sources of animal fats: saturated and trans fatty acids) were negatively scored, while nuts, fruit and vegetables (sources of omega-3 fatty acids, vitamins and minerals respectively) were positively scored.
Lead researcher, Almudena Sanchez-Villegas, University of Las Palmas de Gran Canaria, says “We wanted to understand what role nutrition plays in mental health, as we believe certain dietary patterns could protect our minds. These diets are all associated with physical health benefits and now we find that they could have a positive effect on our mental health.”

“The protective role is ascribed to their nutritional properties, where nuts, legumes, fruit and vegetables (sources of omega-3 fatty acids, vitamins and minerals) could reduce the risk of depression.”

The study included 15,093 participants free of depression at the beginning of the study. They are former students of the University of Navarra, Spain, registered professionals from some Spanish provinces and other university graduates. All are part of the SUN (Seguimiento Universidad de Navarra) Project, a cohort study started on 21st December 1999. The cohort has been used to identify dietary and lifestyle determinants of various conditions, including diabetes, obesity and depression.

Questionnaires to assess dietary intake were completed at the start of the project and again after 10 years. A total of 1,550 participants reported a clinical diagnosis of depression or had used antidepressant drugs after a median follow-up of 8.5 years.

The Alternative Healthy Eating Index-2010 was associated with the greatest reduction of risk of depression but most of the effect could be explained by its similarity with the Mediterranean Diet. Thus, common nutrients and food items such as omega-3 fatty acids, vegetables, fruits, legumes, nuts and moderate alcohol intake present in both patterns (Alternative Healthy Eating Index-2010 and Mediterranean diet) could be responsible for the observed reduced risk in depression associated with a good adherence to the Alternative Healthy Eating Index-2010.
Almudena Sanchez-Villegas says, “A threshold effect may exist. The noticeable difference occurs when participants start to follow a healthier diet. Even a moderate adherence to these healthy dietary patterns was associated with an important reduction in the risk of developing depression. However, we saw no extra benefit when participants showed high or very high adherence to the diets.
So, once the threshold is achieved, the reduced risk plateaus even if participants were stricter with their diets and eating more healthily. This dose-response pattern is compatible with the hypothesis that suboptimal intake of some nutrients (mainly located in low adherence levels) may represent a risk factor for future depression.”

A limitation of this study was that the results are based on self-reported dietary intake and a self-reported clinical diagnosis of depression. More research is needed to predict the role of nutrient intake for neurophysiological requirements and identify whether it is minerals and vitamins or proteins and carbohydrates that cause depression.

Read more: https://phoreveryoung.wordpress.com
Follow us: @drrobertyoung on twitter and The pH Miracle Fan Club on Facebook

The Cure for Cancer? That’s an easy question to answer! The Cure for Cancer is Found in its Prevention NOT in its Treatment! – Dr. Robert O. Young
Do you know what rotten apples, grapefruit or bananas look like? If you do then you know what cancer cells look like. Cancer cells are nothing more that healthy cells that are spoiling because of a compromised environment! Look at the picture below and you will see colorized cancerous body cells rotting in their toxic acidic environment.

What compromises the internal environment of a human body that causes body cells to begin spoiling and rotting? The answer is simple! The body’s build-up of acidic metabolic and dietary waste that has not been properly eliminated through the four channels of elimination – urination, defecation, respiration and perspiration!

Cancer is not a noun but an adjective that describes what is happening to body cells in an acidic environment due to an acidic lifestyle and diet. http://www.phoreveryoung.com

To learn more about Dr. Robert O. Young go to: https://www.linkedin.com/in/drrobertoyoung
To read more of Dr. Young’s articles go to: http://www.phoreveryoung.wordpress.com
To join Dr. Young on Twitter go to: @drrobertyoung
To watch more videos on YouTube go to: https://www.youtube.com/user/pHMiracleCenter
Join Dr. Young on Facebook at: The PH Miracle Medical Association or The pH Miracle
To purchase Dr. Young’s books or nutritional productts go to: http://www.phoreveryoung.com or http://www.phmiracle.com

From Beer to Greens

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Aquí las consecuencias de una Dieta Alcalina, de seguir a la naturaleza, de actuar de acuerdo a tu biología, de dedicarse tiempo, de levantarse más temprano, de limpiar el extractor, de aguantar el “bullying”, de manejar el stress, de soltar, de enfocarse, de amarse……

Cambio de insumos = cambio de resultados, la ciencia (naturaleza) es tan simple que solo con seguir sus pasos podemos sanar y vivir mejor!!

Aplausos y admiración para Noel, su esfuerzo y disciplina, por tomar el toro por los cuernos, por poner su salud en sus propias manos, y claro para sus super coaches VIP, Sofia ReyesOfelia Reyes y Sofía De la Rosa

Sus resultados son un motivo más para seguir trabajando de “salmones” nadando contracorriente, pero seguimos avanzando.

Read morehttp://phoreveryoung.wordpress.com
Follow us: @drrobertyoung on twitter and The pH Miracle Fan Club on Facebook

The Cure for Cancer? That’s an easy question to answer! The Cure for Cancer is Found in its Prevention NOT in its Treatment! – Dr. Robert O. Young

Do you know what rotten apples, grapefruit or bananas look like? If you do then you know what cancer cells look like. Cancer cells are nothing more that healthy cells that are spoiling because of a compromised environment! Look at the picture below and you will see colorized cancerous body cells rotting in their toxic acidic environment.

What compromises the internal environment of a human body that causes body cells to begin spoiling and rotting? The answer is simple! The body’s build-up of acidic metabolic and dietary waste that has not been properly eliminated through the four channels of elimination – urination, defecation, respiration and perspiration!

Cancer is not a noun but an adjective that describes what is happening to body cells in an acidic environment due to an acidic lifestyle and diet. www.phoreveryoung.com or http://www.phmiracle.com

To learn more about Dr. Robert O. Young go to: https://www.linkedin.com/in/drrobertoyoung

To read more of Dr. Young’s articles go to: www.phoreveryoung.wordpress.com and http://www.articlesofhealth.blogspot.com

To join Dr. Young on Twitter go to: @drrobertyoung

To watch more videos on YouTube go to: https://www.youtube.com/user/pHMiracleCenter

To Join Dr. Robert O. Young on Facebook go to:

1) The pH Miracle Fan Club: https://www.facebook.com/groups/50864627953/

2) Dr. Robert O. Young Fan Club: https://business.facebook.com/Dr.Robert.O.Young?business_id=10152751050143317

3) The pH Miracle Center: https://business.facebook.com/ThepHMiracle?business_id=10152751050143317

4) The pH Miracle Medical Association: https://www.facebook.com/pHMiracleMedicalAssociation?fref=ts
To purchase Dr. Young’s books or nutritional productts go to: www.phoreveryoung.com for wholesale or www.phmiracle.com for retailTo become a pH Miracle Coach or Microscopist go to: http://www.phoreveryoung.com or http://www.phmiracle.com or call: 760-751-8321 or 760-484-1075

To become a distributor for Dr. Robert O. Young’s nutritional and water products call: 760-751-8321 or 760-484-1075

To purchase a water purification system and ionizer go to: http://www.phoreveryoung.com or call: 760-751-8321 or 760-484-1075

The 4 Best Natural Organic Oils For Beautiful Wrinkle-Free Skin!

The 4 Best Natural Oils For Beautiful Wrinkle-Free Skin!

Dr. Robert Young

 MSc., DSc., PhD., N.D.

Naturopathic Physician at the pH Miracle Ti Sana Medical Spa, Arlate, Italy

The 4 Best Natural Oils For Beautiful Wrinkle-Free Skin!

Putting oils on your face sounds very unusual and people usually turn to oil-free products thinking that oil will make the skin greasy and blemished. However, it has NOW been proven that using natural oil based skincare products is basically the best thing you can do when it comes to beautiful skin. The natural cole-pressed oil has the ability to soothe and nourish the skin, allowing the active ingredients in the skincare to penetrate deeper into the skin, boosting their beneficial properties.

There are various amazing cold-pressed organic oils out there, but the following are the best ones due to their proven skin-loving benefits:

Extra Virgin Cold-Pressed Avocado Oil

This oil is best for dry and dehydrated skin. It serves as a great moisturizer thanks to its vitamin A, vitamin E, and fatty acids content. It resembles the oils naturally produced by our skin, allowing it to be easily absorbing. This characteristic contributes to boosting the skin`s elasticity. The antioxidant in this oil, lutein may even prevent skin cancer. It can be applied prior taking a shower or be added to luscious bath. The warm water contributes to better absorption of moisture from the oil, and the towel dries off the excess. You will be surprised with the amazing unit-aging and anti-wrinkle benefits after 4 weeks of use!  To purchase USA grown organic raw cold-pressed avocado oil from Dr. Young’s Rancho del Sol go to: www.phoreveryoung.com or www.phmiracle.com

Rosehip Oil

The rosehip oil is best oil for acne-prone skin, fine lines, anti-aging, and uneven scars. It is capable of deep penetration into the skin, which in turn helps in the regeneration of the cells and increase of collagen production. It is high in omega-3 fatty acids, omega-6 fatty acids, and vitamin C, known to reduce inflammation and heal scar tissue. It also contains retinoic acid, the main ingredient in retinol products, which helps in the reduction of fine lines and wrinkles. It offers a whole range of anti-aging properties.

Besides its ability to prevent signs of premature aging, it can help repair acne-probe skin with mild scares and blemishes and it can also prevent more breakouts. This is due to the linoleic acid it contains, which when combined with avocado oil it becomes an amazing remedy. Hello clear, radiant skin!

Sesame Oil

This oil is ideal for wound-prone skin as well as for sun lovers. Apart from being one of the most commonly used cooking oils; the sesame oil has a significant part in the skincare world. As a matter of fact, this golden toned oil is a skin`s secret weapon. It resembles the sunscreens we normally use, as it protects the skin from sun damage, resisting up to 30 percent of UV rays. Moreover, it can help you a lot in case you`ve cut yourself. Just apply some sesame oil on cuts or wounds, and thanks to its anti-acid properties, it can help them heal faster. It is beneficial for skin conditions, such as eczema and psoriasis as well, because it provides anti-inflammatory or anti-acid properties, it nourishes the skin, and it gives the necessary moisture. It is rich in potent antioxidants, sesamol, and vitamin E. This content allows the oil to buffer excess metabolic and dietary acids as well as to repair and nourish acid-damaged skin cells, thanks to its high viscosity.

Extra Virgin Cold-Pressed Coconut Oil

It is best for eczema, normal, sensitive and/or dry skin. However, it is perfect for extra sensitive skin. It provides anti-acid, anti-inflammatory, and anti-mycotoxin properties. It also contains a small molecular structure, allowing easier absorption and giving the skin a smooth and soft texture. What contributes to its ability to treat skin conditions like eczema is the medium chain fatty acids which helps to retain the moisture content of the skin. This oil can be used all year round because it replenishes moisture after a direct sun exposure and it soothes the skin in the cold, windy months. Finally, it contains lauric acid which protects the skin`s surface and it serves as an amazing remedy for rough and dry skin.

Read more: https://phoreveryoung.wordpress.com
Follow us: @drrobertyoung on twitter and The pH Miracle Fan Club on Facebook

The Cure for Cancer? That’s an easy question to answer! The Cure for Cancer is Found in its Prevention NOT in its Treatment! – Dr. Robert O. Young
Do you know what rotten apples, grapefruit or bananas look like? If you do then you know what cancer cells look like. Cancer cells are nothing more that healthy cells that are spoiling because of a compromised environment! Look at the picture below and you will see colorized cancerous body cells rotting in their toxic acidic environment.

What compromises the internal environment of a human body that causes body cells to begin spoiling and rotting? The answer is simple! The body’s build-up of acidic metabolic and dietary waste that has not been properly eliminated through the four channels of elimination – urination, defecation, respiration and perspiration!

Cancer is not a noun but an adjective that describes what is happening to body cells in an acidic environment due to an acidic lifestyle and diet.

http://www.phoreveryoung.com

To learn more about Dr. Robert O. Young go to: https://www.linkedin.com/in/drrobertoyoung
To read more of Dr. Young’s articles go to: http://www.phoreveryoung.wordpress.com
To join Dr. Young on Twitter go to: @drrobertyoung
To watch more videos on YouTube go to: https://www.youtube.com/user/pHMiracleCenter
Join Dr. Young on Facebook at: The PH Miracle Medical Association or The pH Miracle
To purchase Dr. Young’s books or nutritional productts go to: http://www.phoreveryoung.com or http://www.phmiracle.com

The Future for Cancer Prevention and Treatment Here Today – The pH Miracle for Cancer!

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Cancer Metastasis Rev. 2014 Dec;33(4):1095-108. doi: 10.1007/s10555-014-9531-3.

Microenvironmental acidosis in carcinogenesis and metastases: new strategies in prevention and therapy.

Fais S 1, Venturi GGatenby B.

Author information:

  • 1Department of Therapeutic Research and Medicines Evaluation, Unit of Antitumor Drugs, Istituto Superiore di Sanità, Viale Regina Elena 299, Rome, Italy, stefano.fais@iss.it.

Abstract

Much effort is currently devoted to developing patient-specific cancer therapy based on molecular characterization of tumors. In particular, this approach seeks to identify driver mutations that can be blocked through small molecular inhibitors. However, this approach is limited by extensive intratumoral genetic heterogeneity, and, not surprisingly, even dramatic initial responses are typically of limited duration as resistant tumor clones rapidly emerge and proliferate. We propose an alternative approach based on observations that while tumor evolution produces genetic divergence, it is also associated with striking phenotypic convergence that loosely correspond to the well-known cancer “hallmarks”. These convergent properties can be described as driver phenotypes and may be more consistently and robustly expressed than genetic targets. To this purpose, it is necessary to identify strategies that are critical for cancer progression and metastases, and it is likely that these driver phenotypes will be closely related to cancer “hallmarks”. It appears that an antiacidic approach, by targetting a driver phenotype in tumors, may be thought as a future strategy against tumors in either preventing the occurrence of cancer or treating tumor patients with multiple aims, including the improvement of efficacy of existing therapies, possibly reducing their systemic side effects, and controlling tumor growth, progression, and metastasis. This may be achieved with existing molecules such as proton pump inhibitors (PPIs) and buffers such as sodium bicarbonate, citrate, or TRIS.

To learn more about the prevention and non-invasive treatment for Cancer  read the following introduction to the pH Miracle for Cancer  by Dr. Robert O. Young:

 The pH Miracle for Cancer is coming out next week. I thought you might enjoy a preview by reading the introduction – I am very, very grateful to be able to share with you my cancer research I call the New Biology(R). I also refer to my research as the pH Miracle – a new way of living, a new way of eating, a new way of thinking. Some of the questions I will be covering in the pH Miracle for Cancer include:

What is Cancer?
What is the cause of all cancers? (Is cancer a mutant cell, a virus, a mold? Or is cancer an acidic liquid?) Is cancer a noun or is it actually an adjective that explains what’s happening to the body cells? Are tumors bad or good? What role does the lymphatic system play in preventing and reversing a cancerous condition? The focus for preventing and reversing cancer must be on the alkaline pH of the body fluids as a systemic acidic condition. The key to preventing and/or reversing cancer is to obtain the necessary sustainable energy for optimal body function and the elimination of toxic acidic waste products from diet, metabolism, respiration and the environment that all contribute to the cause of a cancerous condition.

Most of the last 30 years of my cancer research has been focused on what is happening to the cells as it pertains specifically to the environment around those cells. I love this quote by Ralph Waldo Emerson: “What lies behind us and what lies before us are tiny matters compared to what lies within us.” The focus of my cancer research has been specifically on what lies within us and, more specifically, how the internal fluids of the body affect the health, energy, and vitality of the human cell, tissues, organs and glands. Dr Benjamin Rush, eminent physician and signer of the Declaration of Independence, said: “Unless we put medical freedom into the Constitution, the time will come when medicine will organize into an underground dictatorship. To restrict the art of healing to one class of men and deny equal privileges to others will constitute the Bastille of medical science. All such laws are un-American and despotic.”

As I think about my vision, the relative purpose of medicine I believe medicine must include not just the treatment but also the prevention of illness and the promotion of health and fitness, rather than just focusing all of our attention on a specific diagnosis or even the treatment of the disease. Because disease is an illusion! In reality, disease is the body trying to prevent over-acidification or fermentation or breakdown of the body cells, tissues, organs or glands.

Disease is the body in preservation mode trying to maintain the homeostasis of the internal fluids of the body, which are all alkaline.

I believe that the ultimate purpose of medicine is to help people discover something fundamental within themselves. And that is an awareness of the true source of wellbeing, the true source of joy, the true source of contentment that we all seek which lies in one’s mind and in one’s heart – which are the emotions and the spirit. And this is important so that you and I can all begin to be free from the process of grasping for happiness in a physical world.
To support this approach, this theory, I believe we must begin to embrace a more spiritual vision of ourselves and of humanity as a whole, while at the right time providing great love, care, and attention to the physical body. Then, and only then, will medicine (or the treatments that medicine is current performing) help people discover this non-physical, spiritual dimension of themselves. And when this happens I believe that we can live and work with less fear.

Rather than working in fear you can work in its opposite – you can work in faith. You are going to have less stress grasping to preserve the physical body at all costs, then I believe you can truly be happy, energetic, and free from ALL sickness and disease, especially cancer.

Several years ago Shelley and I had the opportunity to have a wonderful experience with Dr. Lawrence Carter who is the caretaker of the estate of Martin Luther King, at Morehouse College and also the protégé of M. L. King, and there he honored. The most important thing that I learned about Dr. Carter was his openness to not just thinking outside the box, because we talk a lot about thinking outside the box, but making our box of knowledge bigger. I would like to suggest rather than thinking outside the box as you contemplate my theories on the prevention and treatment of cancer but making your box bigger to include all truth. I would also suggest as you read this book that you do not have to think outside the box, you just need to make your box of knowledge bigger to allow for new technology, new biology, and new protocols that are effectively making the difference, specifically in the prevention and treatment of cancer.

I truly believe in the words of Gandhi when he said, “you must be the change you want to see.”

If you are looking for the cure for cancer, I believe you must be change you want to see. You’ll have to look at cancer differently, not outside the box but inside the box making it bigger. Expanding your views and your perspective as it relates to prevention and the true cause of cancer.

Now, before you start exploring the pH Miracle for Cancer, I must start by defining a ‘pH miracle’. I would suggest that a ‘pH miracle’ is a natural phenomenon, that is not currently understood by medical researchers, specifically in the cause and effect relationship. What is the cause? Is cancer a cause for disease? I say NO! Cancer is the body perfectly attempting to maintain alkaline homeostasis. Cancer is the body in perfect preservation mode trying to maintain its natural healthy alkaline design. So first, you must understand that cancer is unequivocally not a disease, but a symptom or better yet an effect of gastrointestinal, respiratory, environmental and metabolic acids that build up in the blood and then thrown off into the tissues poisoning and suppressing our immune system making it increasingly difficult to maintain the alkaline pH of the internal fluids of the body. Metabolic, respiratory, environmental and dietary acids also destroy the white cells’ ability to remove toxins and the cells which they spoil or degenerate.

What I’m simply suggesting is that cancer is not a cell, but an acidic toxic liquid that spoils and degenerated the body cells that make up our tissues, organs and glands. This happens when toxic acidic waste products are not properly eliminated through the four channels of elimination, which are urination, perspiration, respiration and defecation.

Let’s now look at the current medical definition of cancer. What is it? Cancer is a group of diseases characterized by uncontrolled growth and spread of abnormal body cells. If the spread is not controlled it can result in death. Cancer is caused by both external factors, some of which are known and are common in our society such as tobacco, chemicals, radiation (from our cellular phones) and internal factors: hormone imbalances, immune deficiency and gene mutations – which is what they’re suggesting. These factors may act together in a sequence to promote what is called carcinogenesis. This is the classical definition of cancer, taken directly from the American Cancer Society.

What is being suggested by current medical science is that the cancer is some mutating cell – a transmutation of the genes – triggered by internal or external factors. This is true but what is not understood is these internal or external factors are the acidic waste products of diet, metabolism, respiration and the environment. When you are dealing with any symptom or an effect, you need to look at the cause. Whether externally or internally, the focus traditionally has been to look at the matter or cells that make up your tissues, organs and glands rather than looking at the internal environment around the matter. And, to understand the cause of cancer is very simple just like the treatment. The New Biology® explains the cause and effect of all sickness and disease and specifically cancer as well as how to improve the quality and quantity of life without chemical therapy, radiation or surgery. The pH Miracle for Cancer is a drug-free protocol to a cure for cancer!

Let me give you an example. Enervation (ie, lack of energy), muscle weakness, you’ve probably seen the commercials on television, it’s a new disease they call restless legs syndrome (RLS) for which there are drugs that supposedly treat the syndrome. Current medical researchers want to put everything in a disease modality – a nice little box – that has a specific treatment. Yet restless legs syndrome is weakness or loss of electrical power to the muscles. It’s not a disease. But, by causing a flagging of the toxic elimination from the tissue, the blood becomes charged with these metabolic toxic acids and when it’s charged with these metabolic toxic acids the blood has to purify itself by throwing these metabolic toxic acids into the tissues to maintain its delicate pH balance of 7.365. This is what I call the body in preservation mode, which leads to what I refer to as latent tissue acidosis or acid build-up in the connective and fatty tissues. Acid is poison in the blood, and if that poison is not eliminated through urination, defecation, respiration or perspiration the body has to purify itself so it eliminates this acidic poison into the connective and fatty tissues. This is the disease, or is it? Not even skin challenges when the acids accumulate beyond the toleration point, a crisis takes place, which means that the acidic poison is being eliminated through the pores of the skin.

Looking at the 2012 statistics for cancer, this coming year in America we’re looking at 1,400,000 new cases of cancer. By the way, this statistic doesn’t even include skin cancer, which is actually bigger than lung cancer, breast cancer or prostate cancer combined. And, prostate cancer is known to be the leading cause of death in men while lung cancer being the leading cause of death in women. And yet when we look at cancer, the new incidents of cancer and the new diagnoses are skin cancers because the skin is the third kidney – the largest acid elimination organ for removing acidic toxic waste products. And if acids are not properly eliminated through normal elimination channels, then those acids are thrown out into the tissues and this is what’s not currently recognized or understood by medical science.

This is the way the blood maintains its delicate alkaline pH and purity by either eliminating acid through urination or defecation or throwing it into the connective or fatty tissues which leads to this crisis, this poisoning, this elimination through the pores of the skin, again the third kidney! And this is not a disease! The only disease is systemic, because acids flow out through your whole body. They are the waste products of metabolism, diet, respiration and the external toxic environment.

Your body is like a car. You are constantly on 24/7 and you require energy and when energy is being used, a waste product like carbon dioxide or carbon monoxide or lactic acid or uric acid is being created. So acid is constantly being created by the body cells, which has to be eliminated or it will cause cancer!
When energy is being used to think, to move, to breathe, at the same time an acidic waste product is being created and this acidic waste product needs to be eliminated. If the acid is not eliminated, it is pushed out into the connective tissue. It is your connective tissue that becomes the ‘acid catcher’ in order to maintain the purity and alkalinity of the blood. The blood has to maintain its purity and alkalinity and this is why the blood has a constant pH of 7.365. If it varies even just one-tenth of one point you can have ill effects. The proper healthy pH balance of the blood is 7.365. If the blood pH starts dropping or if it starts going up, the body will do whatever it can to maintain its delicate pH. This is very significant in order to understand the cause and treatment of cancer and why it’s not a cell but the spoiling of the cells by dietary and/or metabolic acids, which have not been properly eliminated through normal elimination. When you are enervated or fatigued you do not have the energy to move the acidic waste products out of the body to maintain the purity of the blood. When this happens the blood pushes these acidic waste products out into the connective and fatty tissues.

For example, when acidic waste elimination takes place through the mucus membrane of the nose, it is called a cold – catarrh of the nose. And when this crisis is repeated for years the mucus membrane thickens and ulcerates, and the bones enlarge, closing the passages. At this stage hay fever, then asthma develops. When the tonsils or any other respiratory passages become the seat of the crisis of acidity (because the acids were not properly eliminated through urination or defecation or respiration or perspiration) then we have tonsillitis, laryngitis, bronchitis, asthma, pneumonia, and finally cancer. You see, it’s progressive. It’s the same disease at different levels of acidity. All of these symptoms are happening in different progressions from the same thing – just different levels of states of acidosis.

When acid is located in the cranial cavity we have dementia, Alzheimer’s, Parkinson’s, muddle thinking, and/or forgetfulness. If the acids accumulate in the digestive area, we end up with irritable bowel syndrome, gastro intestinal problems, stenosis, and colitis. And, when the acids locate in the pelvic tissue, or in the breasts, we end up with micro-calcifications and finally cancerous breast and reproductive organs. When the body is in the preservation mode, it is using alkaline buffers such as calcium, potassium, magnesium and sodium to neutralize or solidify the acidic liquid waste.

This is why I first see, using Ultrasound imaging, micro-calcifications in the pelvic area and in the breast tissue prior to the cancerous breast condition. The buffering of toxic acidic waste, forming micro-calcifications always precedes the cancerous condition of the tissue, organ or gland. Even in prostate cancer.

Hence all cancerous conditions are the expulsion of acids from the blood and then the tissues, organs and glands at different points and are essentially the same character evolving from the same cause, namely systemic acidosis – a crisis of toxemia. The description can be extended to every organ of the body: the lung, the liver, the pancreas, the bowels, the brain, including the largest organs which have the highest incidents, the skin. Any organ that is enervated or fatigued below the average standard (from stress of habit, from overstressed at work, from worry, anxiety, fear, injury, etc.) may become the location of the crisis of systemic latent tissue acidosis. The symptoms are presented differently depending upon which organ is being affected. Which is what makes it appear as if every symptom complex is a separate and distinct disease. You need to begin thinking inside the box and make your box bigger.

I give thanks to this new light and knowledge shed upon nomen culture naming disease by the philosophy of The New Biology(R), every symptom complex goes back to the one and only cause of all so-called cancers, namely systemic latent tissue acidosis. To find the cause of all symptomologies – lung cancer, breast cancer, brain cancer, bowel cancer, pancreatic cancer, thyroid cancer, and prostate cancer – you start with colds and catarrh, and watch the pathology as is it travels from irritation to catarrh to inflammation to induration to ulceration and finally to degeneration or cancer – Nothing more than rotting degenerating tissues, organs or glands. And what is causing this transformation or the degeneration of the cell(s), including the gene transmutation? It is simply the spoiling of the cell(s) due to the build-up of dietary, respiratory, environmental and/or metabolic acids, which have not been properly eliminated through urination, defecation, respiration or perspiration!

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Have you ever opened a refrigerator and smelt the spoiling of food at the back? What you are smelling is the acidic wastes from spoiling food! It’s not some germ, it’s not some virus, it’s not some mold that’s breaking the food down, it’s the acidic waste products that are breaking the tissue down and giving rise to the symptomatology. Mold is like a smoking gun, the bullet being the acid. And yet it’s not the bullet or the acid that kills, and surely not the smoke or some gene mutation, or some bacteria or virus, but it is the person himself or herself that is pulling the acidic lifestyle and dietary trigger which then releases the acids that then tenderizes or spoils or rots the cells that make up your tissues, organs and glands. And, a cancerous condition always expresses itself first in the weakest parts of the body.

Nature’s order is interfered with by innovating acidic lifestyle and dietary habits until acidosis is established.

A vaccination as evidenced by the Spanish flu epidemic or an infection, in truth is literally an out-fection from the same source causing the most vulnerable organ, specifically the bowels, to take on organic or anatomical changes. The organ however has nothing to do with the cause, and directing treatment to the organ is actually compounding the problem. You cannot treat disease when in reality disease is the body in preservation mode trying to re-establish alkaline homeostasis when in a state of systemic acidosis that is affecting the weakest parts of the body, first!

When you realize that breast cancer is the second leading cause of death in women and these fatty tissues (breast areas) are being used by the body to bind or collect acidic waste products in order to protect the organs that sustain life. And, by the way, when one does a mammogram and sees these micro-calcification in the breast tissue, this is an indication of a state of tissue acidosis – the body’s defensive mechanism to relieve or remove or neutralize and solidify acidity that has not been properly eliminated though urination, defecation, respiration or perspiration.

If you are dealing with a cancerous prostate, you are dealing with localized acidity. If you are dealing with lung cancer, you are dealing with localized acidity that has been caused by external or internal forces even though a cancerous condition begins from within. As you take in tobacco smoke, there are acids or toxins or poisons – one being sugar which breaks down to acetaldehyde, which tenderizes and rots the lung tissues. Tobacco smoking is not an addiction of nicotine alone. It is an addiction of sugar, which causes excess acidity in the lung causing lung cancer. The cause is always constant, ever-present, always the same, only the effects change. To illustrate, a catarrh of the stomach presents first irritation, then inflammation, then ulceration, induration and finally degeneration or a cancerous stomach. Cancer is not at the first, it’s the culmination of deteriorating or broken tissue spoiled by an over-acidic stomach from an over-acidic lifestyle and diet.

Most people in the world are challenged with the symptomatology of indigestion, which can include acid reflux, bloating, heartburn, burping, diarrhea, or even constipation. The proper way to study a disease is to study health in every aspect. Disease is perverted health. Cancer is perverted health – any influence that lowers energy becomes disease-producing.

There’s an important question now to answer. Why do I crave sugar? It’s interesting when doing an MRI or a CAT scan. What is used but radioactive sugar that is taken up by the acidic cancerous cells – not cancer cells because we don’t have cancer cells, we have acidic cells or cancerous cells – cells that have been spoiled by the environment in which they live. So sugar cravings are the body’s need for sustainable energy. And energy can only be transported through a matrix of salt. Therefore sugar cravings are the body’s needs for salt, not sugar. I would suggest that sugar is an acid of cellular transformation – a waste product – not a product of energy, but a by-product of what the body truly uses which is electrical potential in the form of electrons.

The body doesn’t use carbohydrates, the body uses electrons to run. The body is electrical. And sugar is nothing more than an acidic waste product of cellular breakdown and transformation. Isn’t that what happens to the banana? As the banana moves from irritation to inflammation to induration and then to cancer, going from green to yellow to brown, getting its “liver spots” the same way you get liver spots, through excess fermentation and rotting. You do not say the banana has cancer, you say the banana is spoiling. In the same way you shouldn’t say that the lung has cancer but rather that the lung is spoiling – it is cancerous. Cancer is not a noun but an adjective expressing the process of cellular transformation. Again, sugar is the waste product. In fact, that’s why a banana gets sweeter and sweeter as it ferments. Consistently in my cancer research I see that we have a release of sugar from the breakdown of tissues, organs or glands. And to overcome sugar cravings you don’t have to eat sugar, you need to eat more salt. The secondary metabolites of this primary acid or sugar are acetaldehyde and ethanol alcohol. So sugar cravings are the body’s signal that the body needs more sustainable energy. You need energy to remove the acids of diet and metabolism – the body utilizing electrons for energy purposes. Food, water, sun, minerals, vitamins, drugs… are common choices made by us to achieve sustainable energy, but yet what you are looking for are the electrons from these sources. And your choices will determine whether or not your cravings will lead to true sustainable energy which maintains the alkaline integrity of the fluids of body and therefore the integrity of the tissues, organs and glands, or gives you false energy which creates this over-acidic state that leads to latent tissue acidosis which begins the process of spoiling of the tissues, organs and glands and finally a degenerative or cancerous condition.

Sugar stimulates and gives the body a deceptive quick-fix – it’s illusionary – whereas salt provides the matrix of life and gives your body the rise in sustainable energy, over a longer period of time, without the high and extreme lows that come from eating an acid – whether it be sugar or any other acidic foods or drinks.

It is the skin that suffers most, because if the body can’t eliminate the acids that are created through energy use, it throws the acidic wastes out into the connective and fatty tissues and into the lymphatic system. This is why the lymphatic system is so critical in the prevention of cancer and in the treatment of cancer, because it is the lymphatic system that is the vacuum cleaner of the acids that are in the interstitial fluids of the body, pulling these poisonous acids out in order to maintain the integrity of the tissue through diaphramic breathing and perspiration (that is if you are perspiring, which is one of the most important things you need to do on a daily basis to remove cancer causing acids). If you cannot eliminate your acidic wastes completely through urination, respiration or defecation then your body urinates through the skin – which is why there is over a million cases of skin cancer a year in the United States alone. It’s not talked about. Why? Because the etiology of skin cancer is not understood. It is unknown. Scientists don’t know what causes basal cell carcinoma, melanoma, they do not understand it because they don’t understand latent tissue acidosis and the importance of the lymphatic system as the vacuum cleaner to remove poisonous acidic wastes out via the kidneys and through perspiration. But people are not exercising, and this is why obesity and a lack of exercise have been associated with cancer. Yet when you are moving your body you are moving the acidic wastes out of the connective and fatty tissues, organs and glands. The lymphatic system, unlike the circulatory system, does not have a pump (the heart), it actually flows through movement. It is the diaphragm muscle that acts as a pump for the lymphatic system that moves acidic wastes through the system – out through perspiration or back into general circulation to be eliminated through urination.

And if you have a cancerous condition you have to pee your way to health. Because cancer is not a cell, but a poisonous acidic liquid. A cancer cell is a cell that has been spoiled or poisoned by the metabolic, respiratory, environmental and/or gastrointestinal acids that are produced internally, or may be taken in via the lungs or skin. That’s when the body will go into the preservation mode by forming fibrous materials, which cross-link to encapsulate the spoiled cancerous cells and thus forming the protective tumor. Hence, the tumor is the body’s protective mechanism to encapsulate spoiled or poisoned acidic cells from excess acidic wastes which have not been properly eliminated through urination, defecation, respiration and/or perspiration. The tumor is the body’s solution to protect healthy cells that make up tissues, organs and glands of the body. So, the tumor is not the problem. Let the tumor go. Let it do its job. The focus must be placed not on the tumor but on the internal environment around the tumor, which is full of acidic cells. One of the common acids which is in higher concentration around all tumors is lactic acid. Lactic acid is a by-product of metabolism when you are in a state of oxygen deprivation. Think of any cancerous condition as a systemic acidic condition that affects first the weakest parts of the body, not a local problem that metastasizes. You see metastasis is localized acids that spoil other cells much like a rotten apple placed in the center of a bushel of healthy apples will spoil the whole bushel. I call this the ‘domino effect’ where one acidic cell spoils another healthy cell causing a chain reaction. The body stops the ‘domino effect’ by forming the tumor around the cancerous or acidic body cells.

Therefore, there is no such thing as a cancer cell. A cancer cell in reality is a cancerous cell. Cancer is an adjective expressing the spoiling body cells that are rotting in an over-acidic environment. A cancerous cell was once a healthy cell that has been spoiled from an over-acidic lifestyle and diet and the body’s inability to remove these acids through the proper channels of elimination.
The only solution to the acidic toxic liquids that poison our body cells causing the effect that medical doctors call cancer, is to change the environment. It has to be a contextual approach. You must restore and maintain the alkaline design of the human body if you want to prevent or reverse a cancerous condition. This has been my great discovery of the 21st century – that the human organism is alkaline by design and acidic by function. Every part of the body that makes up every anatomical element, that makes up your genetic material, that makes up your body cells, every single part has to be bathed in an alkaline fluid which needs to be purified every 24 hours to remain healthy.

Early in the 19th century, beginning on January 17, 1912, a famous French physiologist of the Rockefeller Institute and Nobel Prize winner, Dr. Alexis Carrel, removed a very small piece of heart muscle from an un-hatched chicken embryo—still warm and living—and placed it in fresh nutrient solution in a glass flask of his own design. He transferred the tissue every forty-eight hours, during which time it doubled in size and had to be trimmed before being moved to its new flask. Every time he moved the heart he would put it into an alkaline saline solution with the appropriate alkalizing minerals. Twenty years later the heart tissue was still growing. Keep in mind that the average chicken lives for 5 – 7 years. So, after getting bored of singing “Happy Birthday” to the chicken heart for over twenty years he decided to pull the plug and not change the fluids every 48 hours and the heart finally died.

This is a very important discovery, which very few people know about. Why? Because it answers the question about why cells live and why cells die. You see, the life expectancy of the human cell is infinite. The body cells become compromised by their environment. Once you understand that matter cannot be created nor can it be destroyed it can only change its form or function, then you will realize that the environment is everything, the terrain is everything, and the cell is subservient to that.

The secret to Dr. Carrel’s chicken heart surviving for twenty years lies in this knowledge, this New Biology, this new way of living and thinking as we expand the box rather than thinking outside the box, that the cell is only as healthy as the alkaline fluids it is bathed in. The heart is only as healthy as the cells and the fluids they are bathed in. If you have any cancerous condition, this cancerous condition is the expression of your internal environment. The human cell will only breakdown in an acidic environment and become cancerous.

Carrel’s experiment brought me to the modern New Biology, the new understanding, the new expansion, the new medicine and the new definition of cancer – that the composition of our body fluids that bath the outside of our cells must be controlled very carefully from moment to moment and day-to-day with no single important constituent varying more than a one percent. This condition of health can be controlled and you can do it yourself!

In 1932 Otto Warburg received his Nobel Prize in medicine for discovering the cause of cancer. He described it as a cell changing its mode of respiration, its mode of metabolism – from respiration to fermentation. He suggested that cancer was the result of acidic environment, a state of oxygen deprivation. Warburg also wrote a paper entitled, “The Prime Cause and Prevention of Cancer.” He states: “There is no disease whose prime cause is better known – over acidity.”

When you understand this you realize that all conditions of cancer potentially can be reversed if the treatments are focused on the fluids and not the cells of the body. Therefore it doesn’t matter what the cancerous condition is, because cancer is not the cause but the effect of an over-acidic lifestyle and diet which is the cause of cancer. It’s you pulling the acidic lifestyle and dietary trigger that causes cancer. You do NOT get CANCER – You DO CANCER with your daily lifestyle and dietary choices!

After 30 years of doing blood research, after looking at thousands and thousands of cancerous patients, I’ve never seen healthy blood or an alkaline internal environment – whether testing the pH of the saliva, or the urine, or the blood, or the sweat, or the tears – they are all acidic in an over-acidic internal environment. I have come to understand that the human organism is alkaline by design and acidic by function, and if you maintain this alkaline design of your body through an alkaline lifestyle and diet you WiLL prevent all cancerous conditions. For the cure of cancer is not found in its treatment, because a cancerous condition is the body in preservation mode trying to restore its alkalinity. The cure for a cancerous condition will not be found in its treatment of the tissues but in maintaining the alkaline design of the body fluids.

As Thomas Edison said: “The doctor of the future will give no medicine, but will involve the patient in the proper use of food, fresh air and exercise.

The future is here and NOW and is found in the following chapters of pH Miracle for Cancer.

My hope is The pH Miracle for Cancer will expand your box of truth and knowledge to protect you from the acidic condition medical science calls Cancer.

To pre-order The pH Miracle for Cancer go to: http://www.phoreveryoung.com

The digital version of The pH Miracle for Cancer is NOW Available just order on line at: http://www.phoreveryoung.com

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110. Yeo M, Kim DK, Kim YB, Oh TY, Lee JE, Cho SW, Kim HC, Hahm KB. Selective induction of apoptosis with proton pump inhibitor in gastric cancer cells. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research. 2004;10(24):8687–8696.  [PubMed]

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113. Bellone M, Calcinotto A, Filipazzi P, De Milito A, Fais S, Rivoltini L. The acidity of the tumor microenvironment is a mechanism of immune escape that can be overcome by proton pump inhibitors. Oncoimmunology. 2013;2(1):e22058. [PMC free article]  [PubMed]

114. Calcinotto A, Filipazzi P, Grioni M, Iero M, De Milito A, Ricupito A, Cova A, Canese R, Jachetti E, Rossetti M, Huber V, Parmiani G, Generoso L, Santinami M, Borghi M, Fais S, Bellone M, Rivoltini L. Modulation of microenvironment acidity reverses anergy in human and murine tumor-infiltrating T lymphocytes. Cancer Research. 2012;72(11):2746–2756.  [PubMed]

115. Vishvakarma NK, Singh SM. Immunopotentiating effect of proton pump inhibitor pantoprazole in a lymphoma-bearing murine host: Implication in antitumor activation of tumor-associated macrophages. Immunology Letters. 2010;134(1):83–92.  [PubMed]

116. Singh, S., Garg, S.K., Singh, P.P., Iyer, P.G. & El-Serag, H.B. (2013). Acid-suppressive medications and risk of oesophageal adenocarcinoma in patients with Barrett’s oesophagus: a systematic review and meta-analysis. Gut. [PMC free article]  [PubMed]

117. Kastelein F, Spaander MC, Steyerberg EW, Biermann K, Valkhoff VE, Kuipers EJ, Bruno MJ, ProBar Study Group Proton pump inhibitors reduce the risk of neoplastic progression in patients with Barrett’s esophagus. Clinical Gastroenterology and Hepatology: The Official Clinical Practice Journal of the American Gastroenterological Association. 2013;11(4):382–388.  [PubMed]

118. Harley W, Floyd C, Dunn T, Zhang XD, Chen TY, Hegde M, Palandoken H, Nantz MH, Leon L, Carraway KL, 3rd, Lyeth B, Gorin FA. Dual inhibition of sodium-mediated proton and calcium efflux triggers non-apoptotic cell death in malignant gliomas. Brain Research. 2010;1363:159–169.[PMC free article]  [PubMed]

119. Yang X, Wang D, Dong W, Song Z, Dou K. Inhibition of Na(+)/H(+) exchanger 1 by 5-(N-ethyl-N-isopropyl) amiloride reduces hypoxia-induced hepatocellular carcinoma invasion and motility. Cancer Letters. 2010;295(2):198–204.  [PubMed]

120. Wong P, Kleemann HW, Tannock IF. Cytostatic potential of novel agents that inhibit the regulation of intracellular pH. British Journal of Cancer. 2002;87(2):238–245. [PMC free article]  [PubMed]

121. Chang WH, Liu TC, Yang WK, Lee CC, Lin YH, Chen TY, Chang JG. Amiloride modulates alternative splicing in leukemic cells and resensitizes Bcr-AblT315I mutant cells to imatinib. Cancer Research. 2011;71(2):383–392.  [PubMed]

122. Miraglia E, Viarisio D, Riganti C, Costamagna C, Ghigo D, Bosia A. Na+/H+ exchanger activity is increased in doxorubicin-resistant human colon cancer cells and its modulation modifies the sensitivity of the cells to doxorubicin. International Journal of Cancer. Journal International Du Cancer. 2005;115(6):924–929.  [PubMed]

123. Lauritzen G, Jensen MB, Boedtkjer E, Dybboe R, Aalkjaer C, Nylandsted J, Pedersen SF. NBCn1 and NHE1 expression and activity in DeltaNErbB2 receptor-expressing MCF-7 breast cancer cells: contributions to pHi regulation and chemotherapy resistance. Experimental Cell Research. 2010;316(15):2538–2553.  [PubMed]

124. Kellen JA, Mirakian A, Kolin A. Antimetastatic effect of amiloride in an animal tumour model. Anticancer Research. 1988;8(6):1373–1376.  [PubMed]

125. Matthews H, Ranson M, Kelso MJ. Anti-tumour/metastasis effects of the potassium-sparing diuretic amiloride: an orally active anti-cancer drug waiting for its call-of-duty? International Journal of Cancer. Journal International Du Cancer. 2011;129(9):2051–2061.  [PubMed]

126. Reshkin SJ, Bellizzi A, Cardone RA, Tommasino M, Casavola V, Paradiso A. Paclitaxel induces apoptosis via protein kinase A- and p38 mitogen-activated protein-dependent inhibition of the Na+/H+ exchanger (NHE) NHE isoform 1 in human breast cancer cells. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research. 2003;9(6):2366–2373.  [PubMed]

127. Pacchiano F, Carta F, McDonald PC, Lou Y, Vullo D, Scozzafava A, Dedhar S, Supuran CT. Ureido-substituted benzenesulfonamides potently inhibit carbonic anhydrase IX and show antimetastatic activity in a model of breast cancer metastasis. Journal of Medicinal Chemistry. 2011;54(6):1896–1902.  [PubMed]

128. Touisni N, Maresca A, McDonald PC, Lou Y, Scozzafava A, Dedhar S, Winum JY, Supuran CT. Glycosyl coumarin carbonic anhydrase IX and XII inhibitors strongly attenuate the growth of primary breast tumors. Journal of Medicinal Chemistry. 2011;54(24):8271–8277.  [PubMed]

129. Lou Y, McDonald PC, Oloumi A, Chia S, Ostlund C, Ahmadi A, Kyle A, Auf dem Keller U, Leung S, Huntsman D, Clarke B, Sutherland BW, Waterhouse D, Bally M, Roskelley C, Overall CM, Minchinton A, Pacchiano F, Carta F, Scozzafava A, Touisni N, Winum JY, Supuran CT, Dedhar S. Targeting tumor hypoxia: suppression of breast tumor growth and metastasis by novel carbonic anhydrase IX inhibitors. Cancer Research. 2011;71(9):3364–3376.  [PubMed]

130. Dubois L, Peeters S, Lieuwes NG, Geusens N, Thiry A, Wigfield S, Carta F, McIntyre A, Scozzafava A, Dogne JM, Supuran CT, Harris AL, Masereel B, Lambin P. Specific inhibition of carbonic anhydrase IX activity enhances the in vivo therapeutic effect of tumor irradiation. Radiotherapy and Oncology: Journal of the European Society for Therapeutic Radiology and Oncology. 2011;99(3):424–431.  [PubMed]

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133. Matsubara T, Kusuzaki K, Matsumine A, Shintani K, Satonaka H, Uchida A. Acridine orange used for photodynamic therapy accumulates in malignant musculoskeletal tumors depending on pH gradient. Anticancer Research. 2006;26(1A):187–193.  [PubMed]

134. Hashiguchi S, Kusuzaki K, Murata H, Takeshita H, Hashiba M, Nishimura T, Ashihara T, Hirasawa Y. Acridine orange excited by low-dose radiation has a strong cytocidal effect on mouse osteosarcoma. Oncology. 2002;62(1):85–93.  [PubMed]

135. Kusuzaki K, Aomori K, Suginoshita T, Minami G, Takeshita H, Murata H, Hashiguchi S, Ashihara T, Hirasawa Y. Total tumor cell elimination with minimum damage to normal tissues in musculoskeletal sarcomas following photodynamic therapy with acridine orange. Oncology. 2000;59(2):174–180.[PubMed]

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Summary of Double Blind Research Study on the Negative Effects of Everyday Lifestyle Stressors on the Human Cell and the QLink Device to Buffer Stress1

Live and Dried Blod Analysis - Copyright ROY

Introduction

A double blind study was conducted by Robert Young2, PhD, DSc, microbiologist, to investigate and validate the potential of the Clarus QLink Pendant as a device for buffering everyday stress and maintaining the integrity of the human cell.

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Materials and Methods

Human blood cells are examined for cellular organization and disorganization in which live and dried blood samples are tested before and after wearing QLink pendants.

In this study, two blood microscopy tests are used to examine the organization of matter in the human blood. These tests are the “Unchanged Blood Test” , also referred to as the live blood test and the “Mycotoxic Oxidative Stress Test” 3, also referred to as the dried blood test. (See page 2, Figures 1 & 2)

The Live Blood Test examines the unstained blood. Blood is drawn from the test subject and placed on a microscope slide for examination. From the live blood micrographs, the organization and disorganization of matter present in the blood plasma such as red blood cells, white blood cells, bacteria, yeast, mold and acid crystals can be seen and characterized.

Live Blod Analysis - Crystals .Copyright ROY

The Dried Blood Test examines the coagulation of blood. Blood is drawn from the fingertip and allowed to dry and clot in a normal manner. Dr Young states that the states of imbalance are reflected by changes in blood composition and clotting ability4. When blood is allowed to clot, the pattern seen in normal healthy subjects is essentially the same. This pattern is characterized by a dense mass of red areas interconnected by dark, irregular lines, completely filling the area of the drop. (figure 2) However, blood containing abnormal artifacts will distort the normal pattern. The blood of a subject under mycotoxic oxidative stress will exhibit a variety of characteristic patterns that deviate from the normal pattern. One common characteristic observed in these abnormal patterns is the presence of “clear” or white areas seen in the dried blood. These clear areas indicate the absence of the fibrin net or red blood cell conglomerate typically found in the normal healthy blood.5 These areas are the result of cellular disorganization from factors such as EMF exposure, poor diet, etc.

Live and Dried Blod Analysis - Copyright - ROY

References:

1 Young, Robert, Ph.D., D.Sc., Research Study for Everyday Lifestyle Stressors and the QLink Pendant, January 2001.

2 Founder of Robert O. Young Research Center, Salt Lake City, Utah

3 Young, Robert, Ph.D., D. Sc., Sick and Tired, Pathological Blood Coagulation, Woodland Publishing, January 2000.

4 The medical term disseminated intravascular coagulation is characterized by the abnormal presence of fibrin monomer in the blood.

5 These white areas are referred to as polymerized protein puddles and are the result of cellular disorganization from disturbing factors like low EMF. These polymerized protein puddles will appear in various areas of the red blood cell conglomerate based upon their molecular weight, indicating cellular disorganization in specific areas of the body.

Figure 1. Live Blood Test Micrograph Figure 2. Dried Blood Test Micrograph

To micrographs go to: http://www.qlinkproducts.com/pdf/young.pdf

A total of 16 adult volunteer subjects were tested. Personal history interviews were conducted for each individual case study prior to testing. The 16 subjects were divided into two groups, A & B. Subjects were given an inactive QLink (Group A) or real QLink (Group B) to wear continuously for 72 hours. Neither the test subjects nor the microbiologists conducting the blood tests knew which were wearing the dummy or the real QLink pendants.

Results and Conclusions

Live and dried blood samples are examined for cellular integrity and organization. Baseline micrographs were taken for each subject prior to wearing the real QLink or the dummy. After approximately 72 hours of wearing the QLink or dummy, each test subject was retested. The Baseline micrographs were compared against the micrographs taken 72 hours later. Significant differences or changes seen between the two conditions are highlighted in the micrographs taken. (Typical micrographs are shown in Appendix A).

To micrographs go to: http://www.qlinkproducts.com/pdf/young.pdf

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Based upon microscopic examination of the blood, the blood micrographs (see Example Micrographs in Appendix A) taken and comments from each individual test subject, Dr Young6 made the following conclusions.

Group A (Dummy QLink):

To micrographs go to: http://www.qlinkproducts.com/pdf/young.pdf

“In all 8 subjects, there was little or no impact on the morphology of the red and white blood cells and the red blood cell conglomerate while wearing QLink A. In addition, all 8 reported little or no notable improvement in increased energy and/or health experiences. No perceived beneficial effects were reported while wearing QLink A.”

6 Individual case study comments and conclusions are detailed in the original report by Robert Young, Research Study for Everyday Lifestyle Stressors and the QLink Pendant, January 2001.

2  Group B (Real QLink):

To micrographs go to: http://www.qlinkproducts.com/pdf/young.pdf

“In all 8 subjects, there was a significant impact on the morphology of the red and white blood cells and the red blood cell conglomerate while wearing QLink B. After 72 hours the red blood cells appeared to be more round and symmetrical which is the normal healthy profile. The major white blood cells (neutrophils) were healthy, active and streaming, collecting and removing morbid matter. There appears to be a reduction in the presence of bacteria, yeast, acid crystals and colloid symplasts in the blood plasma. The red blood cell conglomerate appeared hyper-coagulated which represents the health normal profile rather than hypo-coagulated, an abnormal profile in which clear or white areas of protein mass are present in the conglomerate.”

A notable improvement in the morphology of the live and dried blood was seen in all 8 subjects in Group B as viewed in the micrographs. This improvement is hypothesized to be a direct result of the QLink pendant mediating disturbing lifestyle stressors. The QLink achieves this by maintaining the integrity of the energy fields that surround each individual blood cell. In addition, all 8 test subjects reported experiences of increased energy and/or health.

3  Appendix A

To micrographs go to: http://www.qlinkproducts.com/pdf/young.pdf

Example Blood Micrographs from Test Subject in Group A – Dummy QLink

Without QLink A – Baseline Live Blood Test

Without QLink A – Baseline Live Blood Test

With QLink A ~72 Hours Later Live Blood Test

With QLink A – ~72 Hours Later Live Blood Test

Dr Young reports little or no visible changes in the live or dried blood tests between the baseline micrographs and the micrographs taken after wearing QLink A.

4  Appendix A

To micrographs go to: http://www.qlinkproducts.com/pdf/young.pdf

Example Blood Micrographs from Test Subject in Group B – Real QLink

Without QLink B – Baseline With QLink B ~72 Hours Later Live Blood Test Live Blood Test

In the examples above, Dr Young reports significant visible changes between the Baseline and With QLink micrographs. The baseline micrographs show irregular shaped red blood cell organization with a “stacking” condition while the With QLink micrograph indicates more symmetrical, round shaped red blood cells. The cells also appear separate and free flowing, which is necessary in delivering oxygen and the removal of cellular waste.

Without QLink B – Baseline With QLink B ~ 72 Hours Later Dried Blood Test Dried Blood Test

To micrographs go to: http://www.qlinkproducts.com/pdf/young.pdf

In the above micrographs, Dr Young reports significant changes between the Baseline and With QLink Dried Blood Test. Evidence of several “clear” or white areas through the center of the red blood cell conglomerate is seen in the Baseline micrograph. Dr Young suggests that this indicates an abnormal blood clot or hypo-coagulation condition associated with lack of exercise, diet, adrenal and psychological stress. The With QLink micrograph indicates hyper-coagulation of the dried blood, which is a normal profile. Note that the large white protein mass in the center has filled in.

What Causes Kidney Stones and How To Remove Them Naturally?

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The kidneys are one of the most important organs in the human body. The kidneys help to detox and filter impurities from the blood, as well as waste products from your urine.
A kidney stone, also known as a renal calculus is a solid concretion or crystal aggregation formed in the kidneys from dietary minerals and acid salts.

Urinary stones are typically classified by their location in the kidney (nephrolithiasis), ureter (ureterolithiasis) or bladder (cystolithiasis) or by their chemical composition (calcium-containing, struvite, uric acid, or other compounds). Kidney stones vary in size. A small stone may pass on its own, causing little or no pain. A larger stone may get stuck along the urinary tract and can block the flow of urine, causing severe pain or bleeding.
Men are affected more often than women. Overweight and obese people are more likely to get a kidney stone than people of normal weight. People who do not drink enough water may be at higher risk, as their urine is more concentrated.

The urinary tract is the body’s drainage system for removing wastes and extra water. The urinary tract includes two kidneys, two ureters, a bladder and a urethra. The kidneys are two bean-shaped organs, each about the size of a fist. They are located near the middle of the back, just below the rib cage, one on each side of the spine. Every day kidneys process about 200 quarts of blood to produce about 1 to 2 quarts of urine, composed of wastes and extra water. The urine flows from the kidneys to the bladder through tubes called ureters. The bladder stores urine until releasing it through urination. When the bladder empties, urine flows out of the body through a tube called the urethra at the bottom of the bladder.

Kidney stones typically leave the body by passage in the urine stream, and many stones are formed and passed without causing symptoms. If stones grow to sufficient size (usually at least 3 millimeters (0.12 in)) they can cause obstruction of the ureter. Ureteral obstruction causes hydronephrosis (distension and dilation of the renal pelvis and calyces). This leads to pain, most commonly felt in the flank (the area between the ribs and hip), lower abdomen, and groin (a condition called renal colic). Renal colic can be associated with nausea, vomiting, fever, blood in the urine, pus in the urine, and painful urination. The diagnosis of kidney stones is made on the basis of information obtained from the history, physical examination, urinalysis. The best visual Diagnostic test without radiation is Ultrasound examination which may detect the size and position of the stone.

People who are at increased risk of kidney stones are those with:
– hypercalciuria, a condition that runs in families in which urine contains unusually large amounts of calcium; this is the most common condition found in those who form calcium stones
– cystic kidney diseases, which are disorders that cause fluid-filled sacs to form on the kidneys
– hyperparathyroidism, a condition in which the parathyroid glands, which are four pea-sized glands located in the neck, release too much hormone, causing extra calcium in the blood
– renal tubular acidosis, a disease that occurs when the kidneys fail to excrete acids into the urine, which causes a person’s blood to remain too acidic
– cystinuria, a condition in which urine contains high levels of the amino acid cystine
– hyperoxaluria, a condition in which urine contains unusually large amounts of oxalate
– Chronic diseases such as diabetes and high blood pressure (hypertension) are also associated with an increased risk of developing kidney stones.
– hyperuricosuria, a disorder of uric acid metabolism
– gout, a disorder that causes painful swelling of the joints
– blockage of the urinary tract
– chronic inflammation of the bowel
– a history of gastrointestinal (GI) tract surgery
– diuretics—medications that help the kidneys remove fluid from the body
– calcium-based antacids
– the anti-seizure medication topiramate (Topamax)

People can help prevent kidney stones by making changes in their fluid intake. Depending on the type of kidney stone a person has, changes in the amounts of sodium, animal protein, calcium, and oxalate consumed can also help. Drinking enough fluids each day is the best way to help prevent most types of kidney stones.

Natural Remedies for Kidney Stones

– Change in Diet

Unhealthy food intake is a primary cause of kidney stones. Highly acidic diets tend to create an environment which encourages kidney stones, while more alkaline diets help prevent these kind of deposits. Soft drinks, alcohol, products containing corn syrup and most forms of animal protein have an acidic effect on the body.
Some fruits and vegetables have a more alkaline effect, while others are more acidic.
Drinking plenty of pure water also helps discourage the formation of mineral deposits in the kidneys. Holding the bladder rather than urinating when nature calls can also contribute to stone formation.
For optimal health its recommended to do a colon cleanse, liver and gallbladder cleanse, kidney cleanse, chemical and heavy metal cleanse at least 1-2 times a year.

– Lemon Juice, Olive Oil

olive-oil-and-lemon-juice

Kidney Stones are among the most painful conditions you can have. About 80% of kidney stones are the type known as calcium stones. Normal calcium in the body when combined with oxalate, phosphate, or carbonate can form a stone.

According to John Milner, a urology expert from the Loyola University Chicago Stritch School of Medicine, lemons and other citrus fruits contain chemicals that can help prevent against the development of kidney stones. Lemons have the highest concentration of citrate of any citrus fruit which can naturally inhibit kidney stone formation.
Lemons can raise the citrate levels in urine which helps to protect you against calcium stones. The olive oil provides lubrication for easier passage through the urinary tract.

Ingredients

2 ounces of organic Olive Oil

2 ounces of organic Lemon Juice

2 Drops of Lemon Essential Oil

Mix everything together and drink. Make sure to follow it with 12 ounces of 9.5 alkaline water, and then drink plenty of alkaline water throughout the day. Take this mixture up to 3 times a day. . Wait 30 minutes and repeat every hour until symptoms improve.

– Uva Ursi

Uva Ursi is a common folk remedy for kidney stones. Not only will it help fight off infection in the kidneys, but it may also help reduce pain and cleanse the urinary tract. 500mg three times a day is recommended for kidney stones.

– Dandelion Root

Organic dandelion root is a great kidney tonic and cleanser. Taking up to 500 mg twice a day may be beneficial.

– Kidney Beans

The shape of this bean may be indicative of its healing potential. Try removing the beans from inside the pods, and then boil the pods in purified hot water for six hours. This liquid can be strained through cheese cloth, cooled and taken throughout the day for one day to ease kidney stone pain.
.
– Horsetail
.
A diuretic, horsetail tea is an effective natural remedy for kidney stones. Drink up to 3-4 cups of horsetail tea daily or 2 grams of the herb in capsule form daily.

– Pomegranate Juice

Eat organic pomegranates and drinking freshly-squeezed pomegranate juice.

– Cranberry Juice

Unsweetened Cranberry juice is a very beneficial for urinary tract health.

– Magnesium

Studies show that people with recurrent kidney stones who took magnesium supplements had a 92.3 percent improvement rate in reduction of kidney stones.

– Organic Celery

Celery in vegetable form and celery seed are great diuretics and kidney tonics. Regular use of celery seed, as a spice or as a tea, may prevent kidney stone formation.

– Basil

A kidney tonifier, basil tea can be taken throughout the day for overall kidney health. If you have kidney stones, try taking one teaspoon each of basil juice daily for up to six months. It’s believed that folk remedies with pure basil juice can help induce stone expulsion from the urinary tract.

Ultrasound Trumps CT Scan for Diagnosing Kidney Stones in Study

(HealthDay News) — When diagnosing kidney stones, using ultrasound instead of CT scans reduces costs as well as patients’ exposure to radiation, according to new research.
A separate study also found that people with type 2 diabetes who maintain tight blood sugar control can lower their risk for developing kidney stones — small, solid deposits that form in the kidneys.

“Enhancing patient safety and lowering incidence of disease in higher-risk patients are major priorities within the medical community,” said Dr. Margaret Pearle, professor of urology at the University of Texas Southwestern Medical Center in Dallas. “Understanding how to prevent kidney stones combined with further evaluation of the methods used to detect and treat them can only increase the quality of care we strive to deliver patients every day,” she said in an American Urological Association news release.

When kidney stones are suspected during an emergency room visit, patients usually undergo imaging to rule out other conditions and confirm the diagnosis. Although use of CT scans has risen, data compiled from 15 U.S. medical centers revealed that when it comes to patient results, CT scans are no better than ultrasound, the researchers found.

The study involved nearly 2,700 patients, ranging in age from 18 to 75 years. The patients who had symptoms of kidney stones were randomly assigned to receive either an ultrasound or a CT scan as their first diagnostic test. The researchers also examined the number of serious negative events that occurred within 30 days and the number of patients who returned to the emergency room or were hospitalized.

No significant differences emerged in terms of adverse events. Of the patients examined, about 11 percent who had a CT scan experienced a serious negative event, compared to about 12 percent who received an ultrasound from an emergency room doctor. Negative events also affected nearly 11 percent of the patients who had an ultrasound performed by a radiologist.

The researchers also compared patients’ overall radiation exposure and the costs of imaging tests over a six-month period.

The study found that CT scans exposed patients to much more radiation than ultrasound, potentially raising cancer risk. CT scans were also more expensive.

The study was presented at the annual meeting of the American Urological Association, which concluded Wednesday in Orlando, Fla.

Meanwhile, a separate study conducted by researchers at the Cleveland Clinic in Ohio found that people with type 2 diabetes who maintained normal blood sugar levels were at lower risk for developing kidney stones than those who did not keep their blood sugar levels in check.

In conducting the retrospective study, researchers examined information on 1,831 patients with type 2 diabetes who also had kidney stones. Factors they considered included participants’ age, gender, medications, and whether or not they used insulin.

Based on their medication, the participants were divided into two groups: the insulin group and the diabetes pill group. The study found that insulin injection therapy — which is needed in more severe cases of diabetes — is linked with higher levels of acid in the urine than diabetes medications. Therefore, the researchers said, managing diabetes and keeping blood sugar levels within normal levels can lower the risk for kidney stones.

Studies presented at meetings are typically considered preliminary until published in a peer-reviewed medical journal.

SOURCE: American Urological Association, news release, May 17, 2014

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The Cure for Cancer? That’s an easy question to answer! The Cure for Cancer is Found in its Prevention NOT in its Treatment! – Dr. Robert O. Young
Do you know what rotten apples, grapefruit or bananas look like? If you do then you know what cancer cells look like. Cancer cells are nothing more that healthy cells that are spoiling because of a compromised environment! Look at the picture below and you will see colorized cancerous body cells rotting in their toxic acidic environment.

What compromises the internal environment of a human body that causes body cells to begin spoiling and rotting? The answer is simple! The body’s build-up of acidic metabolic and dietary waste that has not been properly eliminated through the four channels of elimination – urination, defecation, respiration and perspiration!

Cancer is not a noun but an adjective that describes what is happening to body cells in an acidic environment due to an acidic lifestyle and diet.

http://www.phoreveryoung.com

To learn more about Dr. Robert O. Young go to: https://www.linkedin.com/in/drrobertoyoung
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EVERY MASS SHOOTING OVER LAST 20 YEARS HAS TWO THINGS IN COMMON… AND ONE OF THEM IS NOT GUNS!

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The Santa Barbara shooter Elliott Rodger, The Sandy Hook Elementary shooter, Adam Lanza, the Aurora movie theater shooter, James Holmes, the Columbine killer, Eric Harris, the Charleston shooter Dylann Storm Roof, and a host of other mass murdering young children, students, employees or total strangers were all on some type of psychotropic drugs when they committed their crimes.

In addition, all of them including Christopher Harper Mercer on, age 26, who killed 9 people and injured 7 people in Roseburg, Oregon this last week, were all mentally ill.  I would also suggest that ALL of these crimes were committed by children and young adults who had highly acidic lifestyles and diets while on Big Pharma psychotropic drugs.

About 3,000 people died in 9/11. Tens of thousands have died fighting in Iraq and Afghanistan, but at least 750,000 people die every year inside the United States from cancer, a totally preventable disease that the FDA, the CDC, and the Biotech Agricultural Industry of the United States perpetuates with GMO and Junk food.

Junk food has NO nutritional value and often high in fat, sugar, salt, and calories. Foods commonly considered junk foods include salted snack foods, gum, candy, sweet desserts, fried fast food, and sugary carbonated beverages. The more highly processed items usually falling under the junk food category.

A study by Paul Johnson and Paul Kenny at the Scripps Research Institute in 2008 suggested that junk food consumption alters brain activity in a manner similar to addictive drugs like cocaine or heroin. After many weeks with unlimited access to junk food, the pleasure centers of rat brains became desensitized, requiring more food for pleasure. After the junk food was taken away and replaced with a healthy diet, the rats starved for two weeks instead of eating nutritious fare.

So here is your real weapon of mass destruction that needs to be taken off the street! This weapon of mass destruction of the minds of our children and young adults coupled with Big Pharma psychotropic drugs  are playing a major role in the mental illness of our children and young adults.

Acidic Foods and Drinks Combined With BIG PHARMA Mind-Altering Drugs!

According to a study published in the journal PLoS One and based on the FDA’s Adverse Event Reporting System, the following mind-altering drugs are most frequently linked to violence.  

Here are eleven brain-killers of our children and young adults:

11.  Suboxone contains a combination of buprenorphine and naloxone. Buprenorphine is an opioid medication. An opioid is sometimes called a narcotic.  Suboxone is a habit-forming drug that has been connected with sudden outbursts of aggressive and violent behaviors.

10.  Naloxone is an special narcotic drug that reverses the effects of other narcotic medicines. Desvenlafaxine (Pristiq) is an antidepressant associated with 7.9 times more violence than many other drugs.

9.  Venlafaxine (Effexor) is related to Pristiq and is an antidepressant also used in treating those with anxiety disorders. Effexor is 8.3 times more associated with violent behavior than other drugs.

8. Fluvoxamine (Luvox) is an antidepressant that affects serotonin (SSRI), and is 8.4 times more likely to be linked to violence than other medications

7.  Triazolam (Halcion) can be addictive and is a benzodiazepine that supposedly treats insomnia. It’s 8.7 times more likely to be associated with violence than other medications.

6.  Atomoxetine (Strattera) is often prescribed to treat ADHD and is 9 times more likely to be associated with violence.

5.  Mefoquine (Lariam) treats malaria and sometimes produces bizarre behavior, and is 9.5 times more likely to be linked to violence.

4.  Amphetamines come in many forms and are often used to treat ADHD (even to children not diagnosed with ADHD). They are 9.6 times more likely to be linked to violence.

3.  Paroxetine (Paxil) is an SSRI (selective serotonin reuptake inhibitor) antidepressant. Many users experience severe withdrawal symptoms and are more likely to produce children with birth defects as well as 10.3 times more likely to be linked to violence than other medications.

2.  Fluoxetine (Prozac) is a household name for a powerful SSRI antidepressant linked with 10.9 times more violence than other drugs.

1.  Varenicline (Chantix) is administered to smokers to supposedly help curb cigarette cravings, but it’s a whopping 18 times more likely to be linked to violent behavior than other drugs.

The Food and Drug Administration, which approves these drugs, recognizes that more 100,000 adverse drug reaction (ADR) deaths occur each year. ADR’s are the fourth leading cause of death, ahead of pulmonary disease, diabetes, AIDS, pneumonia, accidents and automobile deaths.

Drug companies market to doctors to prescribe their medications and use fake studies to sell their efficacy. The drug company GlaxoSmithKline was recently fined a mere $93,000 in Argentina for killing 14 babies during illegal lab vaccine trials in which the company falsified parental authorizations so that the babies could participate without legitimate parental permission. According to one pediatrician working at the public hospital when GSK began recruiting babies for their illegal human trials, not only did GSK force illiterate parents into handing over their children, but they also “recruited” several doctors working at the hospital into their cause. The actual number of children affected may run in the thousands.

According to a study published in Human and Experimental Toxicology, the more vaccinated a baby, the more likely he or she will die or suffer from a serious reaction.

Yet lawful gun owners may become the scapegoat for the mess Big Pharma is creating and more draconian, liberty stealing laws will likely result from the shooting.

Congress Funds Psychological Tests for Kids

archive.newsmax.com/archives/articles/2004/11/22/215244.shtml- Similar to Congress Funds Psychological Tests for Kids – Nov 23, 2004 … Congress Funds Psychological Tests for Kids … to implement mandatory psychological testing programs for all students in the school system.

Mandatory:  Bush Seeking Psychological Testing for all School Kids Without …

mydd.com/users/descrates/posts/bush-seeking-psychological-testing-for-all-s…    DON’T  LEAVE  ANY CHILD  unMEDICATED !      Sell  more drugs for more $ profits?    Too many young children are medicated with powerful drugswww.kevinmd.com/blog/2010/08/young-children-medicated-powerful-…- Similar to Too many young children are medicated with powerful drugs

Aug 28, 2010 … Too many young children are medicated with powerful drugs

Yes: its’ not the drugs and not the guns! here: Want to stop the violence?   THAN ADD TO THIS, ACIDIC DIET, POOR PARENTING or the  LACK OF PARENTING or ONE MEMBER PARENTING, etc., etc., etc. 

EVERY MASS SHOOTING OVER LAST 20 YEARS HAS TWO THINGS IN COMMON… AND ONE OF THEM IS NOT GUNS!

Here are 44 answers to the potential cause of mass murdering children and young adults:

1)  Eric Harris age 17 (first on Zoloft then Luvox) and Dylan Klebold aged 18 (Colombine school shooting in Littleton, Colorado), killed 12 students and 1 teacher, and wounded 23 others, before killing themselves. Klebold’s medical records have never been made available to the public.

2)  Jeff Weise, age 16, had been prescribed 60 mg/day of Prozac (three times the average starting dose for adults!) when he shot his grandfather, his grandfather’s girlfriend and many fellow students at Red Lake, Minnesota. He then shot himself. 10 dead, 12 wounded.

3)  Cory Baadsgaard, age 16, Wahluke (Washington state) High School, was on Paxil (which caused him to have hallucinations) when he took a rifle to his high school and held 23 classmates hostage. He has no memory of the event.

4)  Chris Fetters, age 13, killed his favorite aunt while taking Prozac.

5)  Christopher Pittman, age 12, murdered both his grandparents while taking Zoloft.

6)  Mathew Miller, age 13, hung himself in his bedroom closet after taking Zoloft for 6 days.

7)  Kip Kinkel, age 15, (on Prozac and Ritalin) shot his parents while they slept then went to school and opened fire killing 2 classmates and injuring 22 shortly after beginning Prozac treatment.

8)  Luke Woodham, age 16 (Prozac) killed his mother and then killed two students, wounding six others.

9)  A boy in Pocatello, ID (Zoloft) in 1998 had a Zoloft-induced seizure that caused an armed stand off at his school.

10)  Michael Carneal (Ritalin), age 14, opened fire on students at a high school prayer meeting in West Paducah, Kentucky. Three teenagers were killed, five others were wounded..

11)  A young man in Huntsville, Alabama (Ritalin) went psychotic chopping up his parents with an ax and also killing one sibling and almost murdering another.

12)  Andrew Golden, age 11, (Ritalin) and Mitchell Johnson, aged 14, (Ritalin) shot 15 people, killing four students, one teacher, and wounding 10 others.

13)  TJ Solomon, age 15, (Ritalin) high school student in Conyers, Georgia opened fire on and wounded six of his class mates.

14)  Rod Mathews, age 14, (Ritalin) beat a classmate to death with a bat.

15)  James Wilson, age 19, (various psychiatric drugs) from Breenwood, South Carolina, took a .22 caliber revolver into an elementary school killing two young girls, and wounding seven other children and two teachers.

16)  Elizabeth Bush, age 13, (Paxil) was responsible for a school shooting in Pennsylvania

17)  Jason Hoffman (Effexor and Celexa) – school shooting in El Cajon, California

18)  Jarred Viktor, age 15, (Paxil), after five days on Paxil he stabbed his grandmother 61 times.

19)  Chris Shanahan, age 15 (Paxil) in Rigby, ID who out of the blue killed a woman.

20)  Jeff Franklin (Prozac and Ritalin), Huntsville, AL, killed his parents as they came home from work using a sledge hammer, hatchet, butcher knife and mechanic’s file, then attacked his younger brothers and sister.

21)  Neal Furrow (Prozac) in LA Jewish school shooting reported to have been court-ordered to be on Prozac along with several other medications.

22)  Kevin Rider, age 14, was withdrawing from Prozac when he died from a gunshot wound to his head. Initially it was ruled a suicide, but two years later, the investigation into his death was opened as a possible homicide. The prime suspect, also age 14, had been taking Zoloft and other SSRI antidepressants.

23)  Alex Kim, age 13, hung himself shortly after his Lexapro prescription had been doubled.

24) Diane Routhier was prescribed Welbutrin for gall stone problems. Six days later, after suffering many adverse effects of the drug, she shot herself.

25)  Billy Willkomm, an accomplished wrestler and a University of Florida student, was prescribed Prozac at the age of 17. His family found him dead of suicide – hanging from a tall ladder at the family’s Gulf Shore Boulevard home in July 2002.

26)  Kara Jaye Anne Fuller-Otter, age 12, was on Paxil when she hung herself from a hook in her closet. Kara’s parents said “…. the damn doctor wouldn’t take her off it and I asked him to when we went in on the second visit. I told him I thought she was having some sort of reaction to Paxil…”)

27)  Gareth Christian, Vancouver, age 18, was on Paxil when he committed suicide in 2002,
(Gareth’s father could not accept his son’s death and killed himself.)

28)  Julie Woodward, age 17, was on Zoloft when she hung herself in her family’s detached garage.

29)  Matthew Miller was 13 when he saw a psychiatrist because he was having difficulty at school. The psychiatrist gave him samples of Zoloft. Seven days later his mother found him dead, hanging by a belt from a laundry hook in his closet.

30)  Kurt Danysh, age 18, and on Prozac, killed his father with a shotgun. He is now behind prison bars, and writes letters, trying to warn the world that SSRI drugs can kill.

31)  Woody ____, age 37, committed suicide while in his 5th week of taking Zoloft. Shortly before his death his physician suggested doubling the dose of the drug. He had seen his physician only for insomnia. He had never been depressed, nor did he have any history of any mental illness symptoms.

32)  A boy from Houston, age 10, shot and killed his father after his Prozac dosage was increased.

33)  Hammad Memon, age 15, shot and killed a fellow middle school student. He had been diagnosed with ADHD and depression and was taking Zoloft and “other drugs for the conditions.”

34)  Matti Saari, a 22-year-old culinary student, shot and killed 9 students and a teacher, and wounded another student, before killing himself. Saari was taking an SSRI and a benzodiazapine.

35)  Steven Kazmierczak, age 27, shot and killed five people and wounded 21 others before killing himself in a Northern Illinois University auditorium. According to his girlfriend, he had recently been taking Prozac, Xanax and Ambien. Toxicology results showed that he still had trace amounts of Xanax in his system.

36)  Finnish gunman Pekka-Eric Auvinen, age 18, had been taking antidepressants before he killed eight people and wounded a dozen more at Jokela High School – then he committed suicide.

37)  Asa Coon from Cleveland, age 14, shot and wounded four before taking his own life. Court records show Coon was on Trazodone.

38)  Jon Romano, age 16, on medication for depression, fired a shotgun at a teacher in his New York high school.

39) The Charleston shooter Dylann Storm Roof was reportedly taking a drug, Suboxone, a narcotic that is used to treat opiate addiction. that has been linked with sudden outbursts of violence, fitting the pattern of innumerable other mass shooters who were on or had recently come off pharmaceutical drugs linked to aggression behaviors.

Missing from list… known to have taken these same meds….

40)  What drugs was Jared Lee Loughner on, age 21…… killed 6 people and injuring 14 others in Tuscon, Az?

41)  What drugs was James Eagan Holmes on, age 24….. killed 12 people and injuring 59 others in Aurora Colorado?

42)  What drugs was Jacob Tyler Roberts on, age 22, killed 2 injured 1, Clackamas Or?

43)  What drugs was Adam Peter Lanza on, age 20, Killed 27 of which 14 were children and wounded 2 in Newtown Ct?

And NOW the Latest Tragedy in Roseburg, Oregon!

44)  What drugs was Christopher Harper Mercer on, age 26, Killed 9 people and injured 7 people in Roseburg, Oregon was mentally ill and was on psychotropic drugs?

Those focusing on further firearms bans or magazine restrictions are clearly focusing on the wrong issue and asking the wrong questions, either as a deliberate attempt to hide these links, or out of complete and utter ignorance.

Perhaps rather than gun-control, we should be looking closer to instituting Big pharma-control?

Chris Christie Urges Focus on Mental Health After Oregon Mass Shooting

New Jersey Governor and 2016 presidential candidate Chris Christie weighed in on the recent mass shooting in Roseburg, Oregon, saying that America should get “tougher” on mental health issues.

“I’m very concerned about the mental health side of this,” Christie told ABC’s George Stephanopoulos Sunday on “This Week.” Christie advocates making involuntary commitment easier for doctors to enforce if they fear a mentally ill patient could become violent.

“We don’t want to involuntarily commit them, to put them away,” he said. “We want to protect others and get them the help they need.”

Christie, a former prosecutor, also supports stricter enforcement of gun laws. “There’s lawlessness out there,” he said, pointing to Chicago, a city with tough gun laws and high violent crime rates. “We are not enforcing the law in as aggressive way as we should.”

As governor of New Jersey, which has some of the strictest gun laws and lowest murder rates in the country, Christie has vetoed a gun control bill that would have limited the size of munitions magazines.

“I think it’s about the mental health issue,” Christie said. “I don’t think we’re as aggressive as we should be.”

Learn more:

http://abcnews.go.com/Politics/chris-christie-urges-focus-mental-health-oregon-mass/story?id=34237689

http://www.naturalnews.com/039752_mass_shootings_psychiatric_drugs_antidepressants.html#ixzz3dgN3cbU8

Prevention is the Cure That Will Save Our Children from Physical and Mental Dis-Ease NOT GUN CONTOL or more BiG PHARMA DRUGS!

In my own research, I have yet to find one single child who is depressed or psychotic to be alkaline in his/her urine or saliva.  In fact, I have found that children with emotional and mental challenges are highly acidic in their saliva and urine and are constipated from the over-acidification of animal proteins, dairy products, grains, sugar and processed foods.   These children with so-called emotional or mental problems who are taking anti-depressant or antipsychotic drugs are constipated in their primary brain – the small and large intestines.  When a child eliminates ALL acidic foods and drinks and follows an alkaline lifestyle and diet then the bowels clear and their cranial brain clears.  This in turn eliminates the need for any mind-altering drugs.
Most people do not know that they have more brain cells in their gut than in their head.  When the gut is healed and the child is having 3 to 5 bowel movements a day the brain heals and clears and then there is no more need for drugs.

Conclusion

Here are a few of my suggestions for returning a child back to physical and mental health: 

1)  Eliminate all animal proteins, including beef, chicken, turkey, pork, fish and eggs from the diet.
2)  Eliminate all grains from the diet including rice,
3)  Eliminate all dairy products – especially cheese.
4)  Eliminate all sugar whether natural or artificial.
5)  Eliminate all fermented foods, including vinegar and soy sauce.
6)  Eliminate all nuts except for nut milks such as almond milk.
7)  Eliminate mushrooms.
8)  Eat liberal amounts of alkalizing green fruit and vegetables such as cucumber, avocado, broccoli, spinach, celery, parsley, lemon, lime, tomato, just to name a few.
9)  Drink only clean alkaline water at a pH of 9.5.  Drink at least 1 liter per 30 pounds of weight.
10)  Increase your mineral salts daily.
11)  Drink at least 250ml of chlorophyll a day.
12)  Drink at 50ml of Omega 3 oil per day.
13)  Take a lower bowel cleanser like pH Miracle pHlush to remove undigested animal protein and mucous from the small and large bowel.
14)  Have daily alkalizing colonics.
15)  Keep the urine and saliva pH above 7.2 daily.
16)  Daily 1 hour exercising, which can include rebounding, swimming, walking, jogging, etc.
17)  Daily breathing and stretching exercises.
18)  Daily meditation and prayer.
19) Take them off ALL psychotropic drugs – PERIOD!

When a child starts feeling better from an alkaline lifestyle and diet, a child will start thinking better and when a child starts thinking better than a child will immediately start doing better.  

REMEMBER THAT EVERY MASS SHOOTING OVER LAST 20 YEARS HAS TWO THINGS IN COMMON… AND ONE OF THEM IS NOT GUNS!

To learn more about alkalizing and for alkalizing recipes read The pH Miracle revised and updated.

Read more: https://phoreveryoung.wordpress.com
Follow us: @drrobertyoung on twitter and The pH Miracle Fan Club on Facebook

The Cure for Mental Illness? That’s an easy question to answer! The Cure for Mental Illness is Found in its Prevention NOT in its Treatment! – Dr. Robert O. Young

To learn more about Dr. Robert O. Young go to: https://www.linkedin.com/in/drrobertoyoung

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To watch more videos on YouTube go to: https://www.youtube.com/user/pHMiracleCenter

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To purchase Dr. Young’s books or nutritional productts go to: www.phoreveryoung.com for wholesale or www.phmiracle.com for retailTo become a pH Miracle Coach or Microscopist go to: http://www.phoreveryoung.com or http://www.phmiracle.com or call: 760-751-8321 or 760-484-1075

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GcMAF INVESTIGATION: Three days before Dr. Bradstreet was found dead in a river, U.S. govt. agents raided his research facility to seize a breakthrough cancer treatment called GcMAF

GcMAF

INVESTIGATION: Three days before Dr. Bradstreet was found dead in a river, U.S. govt. agents raided his research facility to seize a breakthrough cancer treatment called GcMAF

(NaturalNews) The history of the suppression of medical science in America is a long one, filled with true accounts of pioneering doctors and clinicians being threatened, intimidated and even assassinated in order to bury emerging cures and keep the “sick care” industry in control. (The American Medical Association, for example, has been found guilty by the U.S. federal courts of a conspiracy to destroy the chiropractic industry, by the way.)

Over the last few days, we’ve learned that before being found shot in the chest and floating in the river, pioneering medical researcher Dr. Bradstreet was working with a little-known molecule that occurs naturally in the human body. Called, “GcMAF”, this molecule has the potential to be a universal cancer cure for many people. It has also been shown to reverse signs of autism in the vast majority of patients receiving the treatment.

While GcMAF is perfectly legal as a treatment in dozens of advanced nations around the world, the U.S. Food and Drug Administration has outlawed it, calling it an “unapproved drug.” It is with this designation — an effort to suppress the forward progress of medical science — that the U.S. government conducted a raid on Dr. Bradstreet’s clinic, specifically seeking to confiscate GcMAF in order to shut down his research and halt his treatment of patients. Meanwhile, Big Pharma gets special permission to unleash untested, experimental drugs on the public as long as those drugs earn sufficient profits (http://www.naturalnews.com/044197_FDA-approved_drugs_Big_Pharma_scientific_evidence.html).

In this article, I summarize the videos, articles and documents covering GcMAF and the mysterious death of Dr. Bradstreet. An exhaustive investigation needs to be pursued on this matter, possibly involving private investigators. The timing and manner of Dr. Bradstreet’s death seems highly suspicious, especially in light of the many other holistic doctors who have recently been found dead under mysterious circumstances. (Dr. Nicholas Gonzalez died just days ago…)

Motive to murder medical researchers and suppress a promising cancer treatment breakthrough

Is there a motive for the murder of pioneering cancer researchers working on a possible universal cancer cure? Of course there is… it’s the most common motive in the world: MONEY.

A universal cancer cure would destroy the profitability of the highly lucrative cancer industry and collapse the American Cancer Society, hospitals, oncology clinics and pharmaceutical companies that depend on chemotherapy revenues to stay profitable. Key to their profitability is the inescapable fact that conventional cancer treatments simply don’t work most of the time (http://www.naturalnews.com/033847_chemotherapy_cancer_treatments.html), creating a reliable profit stream of repeat business from patients who are never cured (by design).

Would the cancer industry murder doctors to protect its profits? Of course it would. The industry kills patients as a routine part of its business operations! For example, an oncologist named Farid Fata was recently sentenced to 56 years in prison for falsely diagnosing patients with cancer so that he could sell them chemotherapy treatments they didn’t need. See the article Cancer doctors ‘fess up to making false diagnoses just to make more money.

Click here to search for “cancer false diagnosis” at GoodGopher.com, the search engine for truth seekers.

INVESTIGATION: Here’s what we know so far

Multiple hat tips to all the outstanding citizen journalists, video creators and bloggers who have created the items cited below:

U.S. govt. search warrant document served against Dr. Jeffrey Bradstreet to confiscate GcMAF from his research facility (http://www.naturalnews.com/files/GCMAF-Bradstreet-Search-Warrant.pdf).

Video that connects the dots between Dr. Bradstreet, GcMAF, cancer cures and the suppression of medical science by the U.S. government.

Video detailing the Dr. Bradstreet search warrant, served June 30 (https://www.youtube.com/watch?v=0v3IA2Hj1TA), during which the U.S. government seized GcMAF from Dr. Bradstreet’s research clinic:

HealthNutNews story that covers the apparent series of murders of holistic doctors, many of whom are working on advanced treatment protocols that render high-profit sectors of conventional medicine OBSOLETE:

Yet another doctor was just found murdered inside his home here on the East Coast of Florida. This makes six doctors to be found dead in the last month just from this region of the country alone. Four out of the six were found dead here in Florida. We lost the holistic Dr. Teresa Sievers, MD, who was found murdered in her Florida home just weeks ago. We’ve also lost the alternative Dr. Jeff Bradstreet, MD, who was found in a river with a gunshot to his chest. He’d recently moved to Georgia from Florida. We’ve also lost the Osteopath. Dr. Riley, who was found in Georgia at her home; just a few hours from the Florida border. She was found with a gunshot wound to her head.

Now we’ve lost Dr. Schwartz MD, who was found murdered in his home, on Sunday, July 19th, 2015. This was four weeks to the day after the death of the first physician: (Dr. Bradstreet MD) who I broke the story on a month ago. His family is still seeking answers as to what happened to him and they’re some of the kindest people I know. The latest MD, Dr. Schwartz, in the picture above, lived just north of the fit, healthy, holistic Dr. Hedendal; who was the second doctor to be found dead this past Father’s Day, in Boca Raton. This was the same day that Dr. Holt died at the age of 33. Both were fathers; and again, both men died here in Florida on June 21st, 2015.

SCIENCE.NaturalNews.com entry describing the extraordinary benefits of GcMAF in a published study (http://science.naturalnews.com/2008/4030259_Immunotherapy_of_metastatic_breast_cancer_patients_with_vitamin_D_binding.html):

Stepwise incubation of purified Gc protein with immobilized beta-galactosidase and sialidase generated probably the most potent macrophage activating factor (termed GcMAF) ever discovered, which produces no adverse effect in humans…

After about 16-22 administrations (approximately 3.5-5 months) of GcMAF, these patients had insignificantly low serum enzyme levels equivalent to healthy control enzyme levels, ranging from 0.38 to 0.63 nmole/min/mg protein, indicating eradication of the tumors. This therapeutic procedure resulted in no recurrence for more than 4 years.

In other words, the administration of GcMAF eradicated tumors and left patients cancer-free for 4+ years with no additional treatment!

Both U.S. and UK governments desperately seizing all supply, shutting down clinics, even as millions die from cancer every decade…

UK govt. admission that GcMAF was on track to being commercialized as a pioneering cancer treatment (http://www.gov.uk/government/news/regulator-warns-against-gcmaf-made-in-unlicensed-facility-in-cambridgeshire), so they had to confiscate it!

GcMAF (Globulin component Macrophage Activating Factor), a blood product, claims to treat a range of conditions including cancer, HIV and autism…

More than 10,000 vials were seized at this site and production of this unlicensed medicine has now ceased. These products were sold through various European websites and UK patients may have bought it from one of these websites. We are working with colleagues in other countries to alert them to the potential risks. Our investigations are ongoing and we have received no reports to date of side effects caused by this product.

That same page lists some of the websites where GcMAF had been available for purchase:

www.GcMAF.eu
www.immunobiotech.eu
www.immunocentre.eu
www.petgcmaf.com
www.firstimmune.fr
www.firstimmune.de
www.firstimmune.it
www.gcmaf.gr
www.gcmaf.se
www.gcmaf.es
www.gcmaf.ru
www.gcmaf.pl

GcMAF is readily available as a medical treatment in Japan (http://www.saisei-mirai.or.jp/gan/index_eng.html). This site explains:

GcMAF (Gc Protein derived Macrophage Activating Factor) – Gc MAF treatment is a highly effective macrophage activating therapy, used to stimulate the immune system and activate macrophages so that they can destroy cancer cells and other abnormal cells in the body.

From the FAQ page of the treatment clinic (http://www.saisei-mirai.or.jp/gan/macrophage_gcmaf_faq_eng.html):

What exactly is Second Generation GcMAF?
High Dose Second Generation Gc-MAF is produced using our new Patent Pending process which was developed here in Japan by Saisei Mirai in collaboration with Dr Hitoshi Hori and Dr Yoshihiro Uto at the University of Tokushima who have been studying GcMAF for over 20 years. Studies on GcMAF began at the University of Tokushima in 1992, after they were introduced to Dr Nobuto Yamamoto’s work and a collaboration began…

Second Generation GcMAF is made using a new and improved 2nd generation method of Gc-MAF production which is 10-20 times more concentrated and is more active and stable than other GcMAF that is currently available. Importantly, this much higher concentration GcMAF has been clinically demonstrated to be largely free of any side effects in the great majority of patients and is much more stable because it is resistant to oxidation.

That same site describes Oral GcMAF as follows: “Oral GcMAF is a form of GcMAF produced from bovine colostrum by Saisei Mirai which was developed in collaboration with Tokushima University.”

It also lists the following health conditions as being treatable with GcMAF, potentially a “universal cancer cure” substance:

Gc-MAF and/or oral Colostrum MAF macrophage activation therapy is indicated in the treatment of any diseases where there is immune dysfunction or where the immune system is compromised, such as:

Cancer
Autoimmune diseases
Epstein-Barr Virus (EBV)
Hepatitis B virus (HBV)
Herpes Simplex virus (HSV)
Cystitis
Hepatitis C virus (HCV)
Multiple sclerosis (MS)
Urinary tract infection (UTI)
Autism Spectrum Disorders (ASD)
Rheumatoid arthritis (RA)
Endometriosis
Chronic Fatigue Syndrome (CFS)
Lyme disease (Lyme borreliosis)
IgA deficiency disorder
Myalgic Encephalomyelitis (ME)
Mycobacteria infections
Parkinson’s disease
Tuberculosis
Fibromyalgia
Human papillomavirus (HPV)
Lupus (Systemic lupus erythematosus, SLE)
HIV AIDS
Dengue fever
Pneumonia infection
Warts caused by viral infection
Norovirus
Malaria Influenza virus (flu)
Herpes simplex virus (HSV)
Q fever (Coxiella burnetii)
Polycystic ovary syndrome (PCOS)
Chicken pox (varicella zoster virus)
Psoriasis
Respiratory tract infections
Ulcerative colitis, Crohn’s disease
Type 1 diabetes (T1DM), insulin-dependent diabetes (IDDM)
Type 1.5 diabetes, Latent autoimmune diabetes of adults (LADA)

Do you see yet why the medical establishment must SUPPRESS GcMAF and destroy all knowledge of its clinical applications? This one substance holds the potential to render numerous vaccines and pharmaceuticals utterly obsolete.

GcMAF protein described at NaturalHealth365.com:

Researchers and practitioners have demonstrated that GcMAF can reverse diseases that attack the immune system such as: chronic inflammation, bacterial and viral infections, chronic herpes, chronic acne, Lyme disease, fibromyalgia osteoporosis, Hodgkin’s, Lupus, MS, Parkinson’s and remarkably – autism.

A clinical study out of Italy on 94 children with autism showed that 83 of them made considerable progress while on GcMAF. The most common reported improvements involve:

• Cognitive abilities including attention and focus, learning and understanding, receptiveness and awareness of the environment and both receptive and expressive language gains.

• Social Skills including willingness to interact and communicate with peers.

• Behavior including less hyperactivity, less stereotypical behaviors and improved cooperation and compliance.

In another study of 1500 children with autism, 85% had high levels of viruses and a compromised immune system. All 1500 received weekly GcMAF injections and 70% of the children responded to the treatment with reduced symptoms and another 15% made full recoveries. The other 15% did not respond.

It was stated that the reduction of autistic symptoms is permanent provided that GcMAF has been taken long enough for the body to produce its own GcMAF which typically takes 24 weeks.

The systematic suppression of medical science to protect the lucrative cancer treatment industry (chemotherapy, oncology, radiotherapy, etc.)

ANH-EUROPE.org covers the systematic suppression of advanced cancer treatments and cures (http://anh-europe.org/news/how-maverick-cancer-treatments-are-suppressed-by-the-mainstream):

Back in 1993, Nobuto Yamamoto, then working at Temple University School of Medicine in Philadelphia, PA, USA, first described a remarkable molecule. His paper reported the conversion of vitamin D3 binding protein (DBP, known in humans as Gc) into a potent macrophage-activating factor (MAF), known as Gc-MAF. Macrophages are a key part of the human immune system with two roles: to engulf and destroy pathogens and cellular debris, and to recruit other immune cells to respond to the pathogen.

Gc-MAF hasn’t had the benefit of a single patent owner – as a natural molecule, it cannot be patented without being modified – with the will and resources to push it under the noses of the public and health authorities. Dr Yamamoto has run small human trials in breast, prostate and colorectal cancers, with promising results.

David Noakes might just be the person to bring Gc-MAF into the mainstream. He’s the CEO of Immuno Biotech Ltd. and spokesperson for First Immune Gc-MAF, a project he describes as, “PhD and BSc biochemists and biomedical scientists… with external doctors, oncologists and scientists who kindly provide advice, committed to bringing some of the increasing number of published but relatively unused medical cures to as many people as we can.” At the moment, Noakes and his colleagues are supplying Gc-MAF to 30 countries where it is legal, via a network of “around 300” doctors. Their Gc-MAF is made to extremely high standards, and is being used in ongoing clinical research by Noakes’ collaborators and others. Their ultimate goal is to, “Build the case that GcMAF is effective for various illnesses, which will help to make it available to the public”.

GcMAF suppliers fighting for survival against a global medical monopoly that profits from disease

MUST-SEE website: http://gcmaf.se/

From the site:

The medical laws have been changed over the last 40 years so that all the brilliant breakthroughs in cancer are denied to the British public. Lord Maurice Saatchi had to watch his wife die, while his doctor told him the only thing he was allowed to prescribe her was chemotherapy, which would shorten her life. He hopes to bring the Medical Innovation Bill to Parliament, so instead of obeying a destructive government law, a doctor will be able to prescribe whatever treatment is best for the patient…

Bad law kills, and Britain has the worst medical laws in Europe. The 1939 Cancer Act makes it illegal to discuss the possibility cancer can be cured, which is partly why 160,000 people die unnecessarily of cancer in Britain every year. Science and treatments are decades ahead of where the medical industry is today. The MHRA’s job is to get life saving treatments like GcMAF out to people as quickly as possible. Instead they block them to protect billion dollar Big Pharma monopolies, who also fund the MHRA. Over a hundred thousand lives could be saved every year if the 1939 Cancer Act were repealed, and the MHRA were closed down.

There are 142 eminent scientists who have published GcMAF research papers on the US National Library of Medicine alone.

From the how GcMAF works page(https://gcmaf.se/gcmaf-science/how-gcmaf-works/):

Your GcMAF empowers your body to cure itself. In a healthy person your own GcMAF has 11 actions discovered so far, including two on cells, three excellent effects on the brain, and 6 on cancer. Amongst these it acts as a “director” of your immune system. But viruses and malignant cells like cancer send out an enzyme called Nagalase that prevents production of your GcMAF: that stops its 11 beneficial effects, and neutralises your immune system. So diseases become chronic, and cancer cells grow unchecked.

Minutes after a receiving a dose, 10 of the body’s actions restart. In three weeks of two GcMAF 0.25ml doses a week, your immune system is rebuilt to above normal strength. You need two doses a week for typically 24 weeks for many diseases and early cancers, up to seven one ml doses a week and a year for stage 4 cancers. Your body then takes the disease down without side effects, and successfully in 80% of cases -depending upon how well you follow the protocol under “Treatment Protocol” on this website.

What is GcMAF?
It is a human protein. One week’s GcMAF looks like a small raindrop. If properly produced it is perfectly sterile, and a most ethical course for doctors.

GcMAF is therefore a replacement therapy for those who can’t make their own. Taking GcMAF replaces the missing part of the immune system, and also acts as the body’s own internal medicine.

GcMAF is extracted and isolated; its a 24 step process, and at the end it must have tests to prove its sterility and activity. (If it does not come with published tests, its probably not GcMAF.) One GcMAF has been tested in universities, laboratories and clinics, where, as a result of the testing, consistent activity and sterility have always been found, and been the subject of 40 scientific research papers.

What does GcMAF do?
The GcMAF Conference 2013 showed GcMAF is a far more powerful molecule than thought, both in terms of the science, and doctors’ results. In stage 4 cancer, some doctors who use the full protocol, listed on “Treatment Strategies,” are saving every patient (if they have not had chemotherapy.) Success can be achieved with all tumour cancers including breast, lung, prostate, pancreatic and melanoma.

GcMAF can eradicate chronic inflammation and viral infections. It is better than antibiotics in many areas, and 25% successful with Autism, 50% or more with Chronic Herpes, Chronic Acne, Chronic cirrhosis of the liver, Chronic kidney disease, Chronic depression, Colitis, Crohn’s, Fibromyalgia, Hepatitis, Herpes, LMBBS, ME/CFS, Osteoporosis, Periodontal disease, Psoriasis and various types of Immune dysfunction including allergies. Research shows GcMAF can halt deterioration in Parkinsons, multiple sclerosis (MS), dementia and ALS, and in its role of immune system regulator, can reverse diseases that attack the immune system like Lupus and Arthritis. And is effective with wound healing. Its successful with tumour cancers, and some others.

In addition to rebuilding a depressed immune system, GcMAF:
Inhibits angiogenesis – stops blood supply to tumours
Activates macrophages – phagocytosis and destruction of cancer cells
Apoptosis – suicide of cancer cells
Reverts the cancer cell phenotype to normal (Turns cancer cells into healthy cells)
Reduces the metastatic potential of human cancer cells in culture.
Increases energy production at the mitochondrial level – ME/CFS
Improves human neuronal metabolic activity through cAMP signaling – autism, ME/CFS, MS, ALS
Counters toxic effects including cadmium – ME/CFS

It abolishes neuropathic pain due to neuro-oxidative stress (stress due to the anti-cancer drug oxaliplatin) in the lab. (neurodegenerative diseases and autism that have oxidative stress as a pathogenetic mechanism)
It increases neuronal connectivity by promoting differentiation and the formation of dendrites and neuritis (autism and ME/CFS, where there is a lack of connectivity between neurons).

See the 31 research papers published, particularly Brescia, and the 60 published by others listed under “The science”.

80% of terminal stage four tumour cancers cases can be saved (40% if they’ve had chemo), but usually when they are closely monitored, which is why residential Treatment Centres are being run in Switzerland. If they have three months to live and have not had chemo, almost no one needs to be lost.

The 180 scientists who have published papers on trials of GcMAF selected those in the early stages of cancer and HIV, and reported nearly 100 percent success, with no recurrence after many years. They did not attempt trials on people with large tumours.

Our trials are quite different: many people are over 50, some over 80, with advanced or terminal cancers, with significant tumour mass. Most come to us when their doctors tell them they can do no more.

The life of GcMAF is only six days – you have to keep taking it until your disease has gone (ie your nagalase is under 0.65 nmol/min/mg) then a further 8 weeks, or the immune system gets shut down again.

How long should you take GcMAF for?
8 weeks for chronic herpes/acne, fibromyalgia, inflammation.
Allow 24 weeks plus of GcMAF for: Autism (85% improve, 25% eradication), CFS (70% eradication), HIV, Lyme (8% respond, most appear to have the VDR gene blocked and the viruses conceal themselves with biofilms) and stage 1 to 2 cancer, (80% respond).
Late stage cancer, if you follow “Treatment Protocol” again has 80% responders, but it takes a year to 18 months to become cancer free.
Cirrhosis of the liver: 16 months

Remember everyone responds differently. We can’t say how you will respond.

The more minor the disease, the easier it is for GcMAF to eradicate. GcMAF needs normal levels of vitamin D to function strongly (take 10,000iu a day). in low responders, larger doses are required.

We have probably proved GcMAF can work for people up to age 90, and can destroy large tumour mass. See “Participants experiences”.

If you have your blood taken for monocyte counts, relevant markers and vitamin D levels, and again for a nagalase test at the beginning, you should see on your next test after three weeks that your immune system is back to full strength, and after 8 weeks significantly falling nagalase will indicate the disease is losing its grip. Don’t stop the GcMAF until your nagalase gets below 0.65 nmol/min/mg, when it loses the ability to prevent your body producing your own GcMAF, and then you no longer need ours. Even better, get scans.

Autism children can improve at five weeks with substantial improvements at 8 weeks. See “Participants experiences.” But everyone is different.

The beauty of using your own immune system to attack disease or cancer is that it remembers how to defeat it for the rest of your life: it doesn’t come back. And unlike chemotherapy, the side effects are trivial.

The only way you can tell if GcMAF is genuine and active is to test with living cells in a laboratory. See “Quality and Tests of our GcMAF.” To recap:

We put live macrophages cells and MCF7 breast cancer cells together; nothing happens. Then we add GcMAF; in 72 hours the macrophages eat all the MCF7 cancer cells. We then put only GcMAF and MCF7 together, and the GcMAF turns the cancer cells back into healthy cells.

We have GcMAF available for preclinical trials. See “Buy GcMAF”.

You must read at least all of “Buy GcMAF” and “Treatment strategies” on the left if you want to take this further. And you must be prepared to give us feedback.

Patent document on GcMAF

See the Yamamoto patent involving GcMAF (http://www.google.com/patents/US5620846):

Cancerous cells and HIV-infected cells secrete -N-acetylgalactosaminidase into the blood stream, resulting in deglycosylation of serum Gc protein. This inactivates the MAF precursor activity of Gc protein, leading to immunosuppression… When peripheral blood monocytes/macrophages of 175 cancer patients bearing various types of cancer were treated in vitro with 100 pg GcMAF/ml, monocytes/macrophages (phagocytes) of all cancer patients were activated for phagocytic and superoxide generating capacity. This observation indicates that patient phagocytes are capable of being activated… 

Also see BetterHealthGuy.com coverage on GcMAF:

first heard about GcMAF almost a year ago. At the same time, I had first learned about “nagalase”, a blood test that is used to in part determine whether or not one might be a candidate for GcMAF therapy. Nagalase is an enzyme that prevents Vitamin D receptors (VDR) from being activated on the surface of the macrophage. As a result, macrophages are not “activated” and our immune systems are not able to properly respond to invaders.

Here are some points that I have learned thus far on GcMAF:

– GcMAF has reportedly been tested more for safety, purity, etc. than other human blood products.
– Macrophages are cultured, destroyed, and the GcMAF receptors are purified.
– Treatment is via injection 1x/week for 8-20 weeks. Dose is titrated initially to avoid exacerbation or Herx responses as much as possible.
– A commonly used dose is .25ml once weekly (a 2.2 ml vial should last 8 injections).
– The primary test used in looking at whether or not GcMAF may be a reasonable intervention is nagalase.
– Nagalase inactivates macrophages.
– I personally would NEVER consider this option without having a baseline nagalase test. Normal is < 0.95. Mine was 2.9.

The practitioner I worked with suggested that 2.9 was in the range of someone with HIV or cancer in terms of the impact on the immune system. I’d like to hear from others in the Lyme community as you get test results as well to see if there is a pattern of elevated nagalase in those with Lyme disease. Whether or not Lyme itself has anything to do with nagalase elevation is something I have not been able to find anything on. We certainly all have underlying viral co-factors that are likely in play as well, but I suspect that Borrelia may also play a role in nagalase elevation.

– In healthy college students, a nagalase 0.4 is not uncommon (the lower the better).

– At 2.9, my practitioner was surprised that I did not have more cognitive deficits such as memory loss and other cognitive issues.

– It has been suggested that ongoing antimicrobial therapy without a working immune system is like leaving the house with the door wide open inviting burglars in. By using GcMAF to activate macrophages, nagalase drops, and one may regain a functional immune system. The door is then closed to further invaders and we may no longer serve as a microbe hotel.

– Maintenance therapy should not be needed once the immune system is once again properly functioning.

– Activated macrophages only remain active for 7 days so any negative responses are generally short-lived. That said, some people do have strong inflammatory responses that are not believed to be typical die-off reactions.

– It has been indicated that in some cases, other medications may be needed in order to manage the inflammatory response. This is another reason that one needs to be working closely with a knowledgeable practitioner before considering GcMAF in my opinion. In the CFS and GcMAF world, this more severe form of a die-off reaction is called IRIS.

– VDR genetics do not seem to play a role in predicting response as earlier thought according to one practitioner that I have spoken with. That said, Vitamin D levels do correlate with the positive response rate of GcMAF. Thus, Vitamin D supplementation may be required in order to optimize outcome.

– Other than die-off reactions or activation of symptoms (inflammation), no other side effects are generally expected.

– Nagalase should be monitored every 1-2 months while on treatment to determine the required duration of the therapy. Target nagalase after treatment would be 0.4 to 0.6.

– Elevated nagalase has a profound detrimental effect on the immune system. Elevated nagalase is often presumed to be related to microbes of viral origin or cancer. Viruses that are nagalase producers open the door to chronic infections.

– Hemagglutinin contains nagalase and is also found in flagella of some bacteria so it could also be the case that some bacteria may produce nagalase.

– Parents with ASD children also often have elevated nagalase.

– A practitioner I spoke with likened Lyme disease to a “peat moss fire” burning below the surface. Activating macrophages should help to deal with the fire.

– GcMAF should be helpful in dealing with other infections that are not of viral origin; for example, Borrelia, Bartonella, and other infections commonly associated with Tick-Borne Infections (TBIs). GcMAF is active against many cancers and many different kinds of microbes.

– Neopterin is another test that is sometimes used as an indicator of immune suppression. As macrophages become activated, neopterin may rise and later fall. If one is in the normal range for neopterin and has an immune-related illness, this could be an indication that the immune system is suppressed and not responding appropriately.

– People with autoimmune conditions can generally use GcMAF. However, GcMAF may be contraindicated in people with Multiple Sclerosis.

– Reduction in nagalase is generally seen early in the course of treatment; within the first 3-6 weeks. In some studies, nagalase dropped by over 50% in less than six weeks.

– Cancer patients may initially feel as bad on GcMAF as they do on chemotherapy, but often feel much better after the first month.

– Anti-inflammatories may limited the effect of GcMAF.

– Enzymes and biofilm-reducing supplements may have a negative impact on GcMAF therapy and may be best avoided. It is still too early to know what the impact may be, but one practitioner I spoke with feels that it is best to avoid these.

– One should not be on any immune-suppressing agents while on GcMAF as the immune system must be partially functional in order to respond appropriately to the treatment.

– A common pattern is to see elevated lymphocytes, high nagalase, and low NK cells. Once nagalase drops, it may be the case that NK cell function could be positively impacted. CD57 is a type of NK cell. It is too early to know if this proves to be true, but it is one of the things I’m quite interested in.

Watch this video presentation on GcMAF therapy to learn more.

http://cfspatientadvocate.blogspot.com/2011/11/mt-sinai-mecfs-conference-de-meirleir.html

Read about GcMAF from Alternative-Health-Group.org.
http://cfspatientadvocate.blogspot.com/2011/11/mt-sinai-mecfs-conference-de-meirleir.html

Read The GcMAF Book at this link.
http://gcmaf.timsmithmd.com/book/chapter/44/

Open the “Stop Fighting Cancer” PDF document (http://www.stopfightingcancer.com/stop-fighting-cancer.pdf) and search it for “GcMAF” to read some intriguing passages:

Researchers testing GcMAF stated it, “works 100% of the time to eradicate cancer completely, and cancer does not recur even years later.” (This was stated based on the tested group of patients -nothing works 100% for everyone) The weekly injection GcMAF, a harmless glyco-protein activates the human immune system which then can kill the growing cancer. Studies among breast cancer and colon cancer patients produced complete remissions lasting 4 and 7 years respectively. This glyco-protein ‘cure’ is totally without side effect but currently goes unused and completely ignored by cancer doctors. Why? Maybe it is because there is little money to be made in selling it. For less than $2000USD a cancer patient can obtain an adequate amount of GcMAC.

See the National Library of Medicine page Immunotherapy for Prostate Cancer with Gc Protein-Derived Macrophage-Activating Factor, GcMAF (http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2510818/):

When human macrophages were treated in vitro with 100 pg GcMAF/ml for 3 hours and a prostate cancer cell line LNCaP was added with an effector/target ratio of 1.5, approximately 51% and 82% of LNCaP cells were killed by 4 and 18 hours of incubation, respectively [14,15]. This in vitro tumoricidal capacity of macrophages activated by GcMAF led us to investigate the therapeutic efficacy of GcMAF for prostate cancer. GcMAF therapy as a single remedy modality can eradicate metastatic breast and colorectal cancers most effectively

Click here to search for “GcMAF” on GoodGopher.com, the new search engine for truth seekers.

Read this article from The Telegraph on how scientists are being assassinated because of what they know.

http://www.telegraph.co.uk/news/earth/environment/globalwarming/11762680/Three-scientists-investigating-melting-Arctic-ice-may-have-been-assassinated-professor-claims.html
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