Category Archives: Cancer

Lectures From Around The World

Galina MIgalko MSc, MD, NMD and Robert O Young CPT, MSc, DSc, PhD, Naturopathic Practitioner
Galina MIgalko MSc, MD, NMD and Robert O Young CPT, MSc, DSc, PhD, Naturopathic Practitioner 

Come listen and learn from Key Note Speakers, Robert O Young CPT, MSc, DSc, PhD, Naturopathic Practitioner and Galina Migalko MSc, MD, NMD, in four different countries around the World as they lecture on non-invasive medical diagnostics, the interstitium, pH, nutrition and their break-through research on prevention and non-invasive treatments for cancer, diabetes, heart disease, arthritis, osteoporosis, lupus, multiple sclerosis, infections, and many more acidic-caused diseases.

To pre-register for one or more World Conferences please email phmiraclelife@gmail.com and receive an additional 10 to 20 percent discount on the listed early-bird pricing. You can also register by phone by calling 760 484 1075.

When you enroll in one of our Conferences you will receive a credit for a live and dried blood cell analysis, valued at 1200 euros.

Please check out the Countries, Cities, Dates and Pricing below!

Is There a Cure for Brain Cancer?

Is There Any Cure for a Brain Tumor?

Robert Young

Robert Young

Research Scientist at the pH Miracle Center

This was a question asked by Sahar Sahar (a face book friend) and here is my answer:

My own young and beautiful daughter Ashley, at the age of 21 followed the pH Miracle Alkaline Lifestyle and Diet with great success. She has now been in remission from brain cancer for over 15 years. She elected not to have brain surgery, radiation or chemotherapy.

 

Ashley was married and pregnant with her first child and in her 3rd trimester when she had a shocking seizure while at the movie theater. She was rushed to the hospital and after brain scans was found to have a large complex mass in her brain.

She was told that she needed emergency surgery and that since she was pregnant the Doctors recommended the termination of her pregnancy by C-section so they could begin treating her cancer.

With the help of her husband Matthew and Ashley’s strong faith and courage she decided no surgery and no taking the baby prematurely. She rested at home for several weeks until it was time to give birth.

She gave birth to a healthy boy (who is now 16 pictured below loving his sisters) and was told by the Doctors that she would not be able to have any more children because of her brain condition.

 

Ashley did not believe what she was hearing and had faith in God and the truth she had learned from her parents. She now has 4 beautiful healthy children – 1 boy and 3 girls. The newest addition came to their family just one year ago.

 

Her decision to follow the pH Miracle alkaline lifestyle and diet was her own decision and was supported by her loving husband and her parents.

 

As her Father who loves his daughter is so happy she is alive, healthy and able to attend to all her family needs. She is a wonderful example of Motherhood, a wonderful wife and has a strong abiding faith in God. I am so proud of Ashley and her bravery, courage and especially her faith to make such a bold decision at the young age of 21.

With love I share this very personal story that has a happy ending with many tears and trails knowing Ashley is healthy and alive today because she followed her heart with the knowledge that healing comes from within and is our personal responsibility.

Each person must decide for themselves (not the government) the path they will choose to go. It is all about free-agency to choose YOUR own healing path. Ashley listened to her parents, to her husband and especially to that still-small voice that speaks to our minds and through prayer and the support of family members made a wise choice. That choice is why she is alive today!

You might remember in the story of Alice in Wonderland when Alice came to a crossroads on her path and encountered the Cheshire Cat. As the story goes Alice asked the Cheshire Cat which road she should choose to go. The Cheshire Cat answered wisely, “If you do not know where you want to go any road will do.”

 

May God bless all of you who are at the crossroads of life with the depth of perception and the faith to choose YOUR own road wisely. Listen to that still-small voice that will speak to your mind and tell YOU the path YOU should choose. This voice will never deceive YOU or lead you astray!

Believe in Miracle even pH Miracles!

With sincere gratitude, love and healing light,

Robert O Young (Ashley’s Father)

To learn more about Ashley’s choice and the pH Miracle alkaline lifestyle and diet go to: www.drrobertyoung.com and www.phmiracleretreat.com

PS I believe that the road Ashley chose was the road that gave her a cancer cure and a healthy life, including the protection and love of her family, friends and a living and loving Father in Heaven!

PSS Ashley’s husband Mathew operates the pHmlife.com that sells the pH Miracle alkaline nutritional products.

From Terminal Cancer to Courage and a Self-Cure

Inger Hartelius with her Daughter Tea Hartelius
Inger Hartelius with her daughter Tea Hartelius
In 2011, I had the unique pleasure of meeting Inger Hartelius at the Rancho del Sol/pH Miracle Center in Valley Center, California, and had the chance to follow her journey from diagnosis to recovery from terminal cancer to courage to her self-cure. It is an honor for me to pass along her story and personal journey. We all have a choice, a personal choice in terms of health, wellness, energy and fitness. Please take the time and read Inger’s enriching and empowering story that I believe will make you wiser and possibly change your life or even save your life –  If not your life maybe the life of a friend or a loved one!

This is how I regained my future from terminal metastatic lung cancer:

By Inger Hartelius,

This article was initially published in the magazine ”Tidslerne”, (Danish Cancer Association Tidslerne) in January 2018.

 

I was diagnosed with pulmonary adenocarcinoma lung cancer in one of my lungs and lymph nodes near the esophagus in July, 2011. I chose to say NO to chemo and NO to radiation and today – six and a half years later after a life threatening terminal diagnosis. Today, I have no evidence of cancer in anywhere in my body.

In a small dark office, without windows, at the Pulmonary Department in Roskilde Hospital, my husband and I were informed that on the basis of tests from a PET-CT scanning, they had found lung adenocarcinoma, stage 2, R7 og 4L, T1bN3MO, a diagnosis so severe that the doctors in an interdisciplinary conference had booked me for chemotherapy and radiation at Herlev Hospital already the following week.

As written in my medical record, I was “appropriately in tears”, while saying no thank you to the offer and later also to an orientation on the treatment possibilities, side effects and potential consequences of the hospitals offer. An offer which, according to the doctor, could prolong life – not cure. And, it was a matter of a short extension of lifespan, which was also confirmed by the statistical evidence I asked for. Potentially it was a matter of just a few months.

Six and a half years without any signs or symptoms of cancer

Even before I got the final diagnosis, I wasn’t considering chemotherapy or radiation. Between the scan and the results I researched into alternative treatments.

Today I have no evidence and no symptoms of metastatic lung cancer. A CAT scanning in April, 2016 confirmed my belief of being cured of terminal metastatic pulmonary adenocarcinoma lung cancer. (No one has ever been cured of metastatic pulmonary adenocarcinoma lung cancer)  In many ways I feel better than before I was diagnosed. I am 64 years old – and I believe that I have many more healthy years ahead of me.

Did they give the correct diagnosis? The doctor who gave me the results of the scan in April, 2016 asked himself this out loud while reading my medical journal. Am I just one of the lucky ones who indescribably doesn’t follow the statistics (approx. 1 year lifespan post diagnosis and with treatment), or is what I chose to do instead of chemo and radiation the reason why I am still alive, health and cancer free? Who knows?

Extreme bravery to say yes to chemotherapy

Though it is difficult to know for sure why I have survived cancer it is important for me to tell the world that some of us actually survive cancer without the conventional treatments and also therefore avoid the medical side effects, one of which is death – and gaining many positive results, which we choose instead.

Many have asked me: How did you dare? This question actually surprises me because this wasn’t how I was thinking. Many tell me they think I am brave.

Before the diagnosis I thought that the people who chose the conventional treatments were extremely brave. How can they let their bodies be filled with chemo with all its horrible side effects, which often result in injuries both inside and outside the body, including death? To entirely trust the doctor’s hasty decisions on standardized cancer treatment programes, without being able to see what is happening and take control over one’s own life.

“Put your life in the hands of your doctor”

If I only had a few months to live I definitely didn’t want to spend it in a hospital. On top of that I had first hand experience seeing how chemotherapy didn’t only treat, but resulted in days and weeks of deathly side effects – potentially lasting the rest of life – sometimes with death as a consequence; maybe the treatments would also shorten my lifespan.

I couldn’t do it, as a calming nurse suggested after a consultation with the doctor: “Put your life in the hands of your doctor”. I would rather not!

I am very thankful for the nurse saying this to me. It was at a moment where I was consumed by the confusion of the diagnosis and thoughts of never getting to experience having grandkids, that something inside me became connected. I got myself together, dried my eyes, stood up straight and took my final decision. Either I would die from cancer or I would find another way to be cured!

A long, conventional treatment program wasn’t something I, nor my family, would let myself go through, instead I would look for other possibilities. I left the hospital in shock, but with a decision to go to an alternative way of treating my cancer.

”Tidslerne” (Danish Cancer Association) took time to listen

Already, when I was told I needed to have a biopsy taken from the area in my lungs and the swollen lymph nodes, I got in touch with a volunteer at the Cancer Association ”Tidslerne”. I had Googled the risks of taking the biopsy, and was aware that there was a 25% risk that the cancer would spread afterwards.

No-one at the hospital had informed me of this. That is why I needed to talk to others. Simultaneously, the conversations strengthened me in my belief of following my gut feeling and pursuing alternative treatment methods for my cancer. Many others had done this before me with great results.

Starting to find a solution

I read the book: Andreas Moritz: “Cancer is not a disease. It is a survival mechanism”. Some other possibilities were META-medicine, healing and Dr. Robert Young [i], who is known for having a highly effective approach to treating cancer. (over 80% success with terminal metastatic cancer and over 90% success with Stage 1, 2 and 3 cancers)

In Denmark I found advice and guidance by Dr. Claus Hancke, MD in Lyngby, who suggested high dose of Vitamin C intravenously as well as supplements of vitamins and minerals. I also consulted Frede Damgaard’s clinic of complementary treatment in Aarhus. Their key focus is on nutritional guidance supplemented with natural medicine/herbs, vitamins and minerals. His recommendations were built on extensive analysis of my body’s resources and weaknesses.

With my family in California 

Descriptions of Dr. Robert Young’s live and dry blood tests combined with focus on the body’s resources and regulation of the body’s pH-levels is what spoke to me. I wrote an email to him and was later encouraged to call him. In the following conversation with one of Dr. Young’s assistants, I was encouraged to bring my husband and kids with me and come to California. I was lucky. There was a house available for us if we could come within a couple of days. They believed that with the serious diagnosis I had, I would have a greater chance of survival if i invested in a retreat at Dr. Young’s pH Miracle Center, in Valley Center, California.

 

It was a miracle: Being with my husband, kids and my son’s girlfriend was fantastic. Being in an avocado and grapefruit plantation in California and living in a house feeling like I was in the middle of a great dream during my life’s biggest nightmare. While we were there I asked myself many times: Am I dreaming?

Because a couple of days ago I was getting my head around the concept that I was going to die. Instead I was now in paradise, being inspired to change my mindset of why people get cancer. At the same time we were informed daily on how to live according to Dr. Young’s recommendations, to prevent cancer and get rid of it by building up the body’s resources, so that it will not accumulate cancer cells.

Live and dried blood tests

 

Dr. Young’s blood tests showed that I should not fear dying from that cancer which the doctors had discovered in my body. I had many resources I could activate and through a whole body cleanse I could rid my body of this cancerous condition.

The blood test took place in a large teaching room where there was plenty of space for all five of us and one of Dr. Young’s assistants. We were surrounded by posters and other interesting teaching materials. A small prick in the finger was enough to make a live blood test, and the seven drops of blood dried on a glass plate. I sat by Dr. Young and his computer and followed along. The others saw the tests on the wall. He placed the blood from my finger on the glass plates and placed them under a microscope connected to a computer and a projector.

It was fantastic getting to see the tests instantly with my own eyes. There was no waiting time and Dr. Young let me in on how he interpreted the tests. It was personal and caring; “Try to see the many regular round blood cells floating freely around each other surrounded by clear liquid. The more of these there are and the clearer the liquid, the better the blood’s ability is to clean and transport oxygen to your body. The liquid between the cells shows no sign that the current cancer is a serious threat to your body. Here some of the cells are aggregating, which is a sign of dehydration. And the shape of the cells here shows that you need more nutritional oils.”

 

In the dries blood tests Dr. Young was focused on the patterns in which the blood coagulated. Experience shows that patterns can tell a lot about a person’s health and current challenges and resources. In my tests it was clear that I had to focus on my immune system and my digestion. On top of that there was a sign that I had had a lot of heavy metals in my blood – maybe because of the long period in my life where I ate a lot of fish.

Alkaline plan against terminal cancer 

Along with the blood tests I tested the pH levels of my saliva and my urine every morning and night. There was space for improvement. The pH levels of my saliva and urine were between 5 and 6. It should in both cases be a minimum of 7.4, a little higher than the pH levels of the blood.

From the blood tests and the pH levels Dr. Young made a protocol, which I followed, telling me which special supplements I should take with my alkaline meals[ii] as well as which activities I should carry out.

First and foremost I had to drink approximately 4 liters of liquid every day as well as a glass of salt water every morning and night. The liquid should consist of juice from vegetables and water with high pH levels, preferably with freeze dried vegetable powder and liquid chlorophyll. [iii]. I also had to stay physically active on a daily basis and partake in various therapeutic treatments.

 

It was very in depth and I have to admit it was a little hard to grasp it all. Luckily my son was good at helping me stay on top of it all so I could go in depth with it all one step at a time.

After the blood test we moved our focus from the cancer in my body to building up healthier and a more well functioning body. An exciting journey into the pH Miracle lifestyle. We focused on how we could keep our blood alive and healthy while strengthening the body’s ability to maintain a high pH level. It was all about what we eat. what we drink, what we breath, what we think, as well as how we challenged ourselves both physically and mentally.

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The days were full of exciting activities: Younga Yoga in the morning followed by Dr. Young’s workshop, breakfast with delicious avocado-smoothies, juice from vegetables and almond milk, food demonstrations, time in an infrared sauna, salt baths and activities on the center’s many training machines as well as hiking and running trips in the area.

A life affirming place

In Dr. Young’s plan there was a therapeutic colonic hydrotherapy with 20 liters of liquid consisting of water with high pH-levels, powder of freeze dried alkaline vegetables, salt and chlorophyll. I got a minimum of one hour’s massage focused on activating my lymphatic system.

At home we started preparing alkaline food and I started training to run 5 kilometers. In the beginning it was just a small run where I live. I was exhausted. Later it was longer trips along the beach.

To make it easier to prepare the food we invested in an effective blender and a juicer. We also got an infrared sauna, a bathtub (for salt baths), a rebounder (to jump on), a colonic board (to frequently clean my colon with 20 liters of water) as well as a pH Miracle water ionizing machine. The cleansing ionized water played an especially big role in the change I could see in the pH levels of my saliva and urine – both in the morning and the evening. The pH levels rose steadily and landed somewhere between 9 and 10 in the urine and 7 and 8 in my saliva. The values are still at this level.

 

I had consultations with Dr. Pernille Knudtzon, MD, a psychologist and reflexologist. Dr. John Arnved, MD at the Lung- and Allergy clinic in Copenhagen followed me and tested my lungs frequently as well as my allergy reaction to mold. My own doctor followed my progress with blood tests to keep an eye on the mineral and vitamin levels in my body.

I was busy and sometimes completely overwhelmed with all the changes in my body and the doubt: Was it the right thing, I had started? Why was I still losing weight? Would I be cured? Just think… I didn’t trust my body completely; maybe the cancer was growing despite my hard work to get rid of it. The support of family, friends and the people whom I contacted for help was very important to me.

Frequent follow up meetings

After three months I had two medical thermography scans with a month’s time between each. The results were quite shocking. The American doctors analysed the pictures and recommended that I start conventional treatment as the pictures showed that the cancer may have spread.

I decided to go to Spain to see Dr. Pernille Knudtzon, MD, who would supplement what I could do myself to be cured, with a week of intensive cleansing and building up of the body and soul. The experiences of the week with Pernille Knudtzon gave me new tools to tackle my thoughts and feelings so they weren’t in the way of my work on getting healthy. After a week in Spain with my sister I returned home with renewed courage. [ii]

In April, 2012 Dr. Young had a retreat in Como, Italy (pH Miracle protocol is now available at Forte Village, Sardegna, Italy) where I had the chance to regain inspiration and support to intensify my healing process. My husband and daughter went with me and we had a fantastic week. My blood tests again showed a big improvement, so Dr. Young recommended that I continue my process to take care of myself and my health.

In September of the same year Dr. Young invited me to another retreat in Como, Italy to give me another chance to be thermographically scanned and get an ultrasound by his partner, Dr. Galina Migalko (MD, NMD, RDMS).[iii] Neither test methods are harmful to the body. The tests showed, to everyone’s pleasure, that I had built up my immune system. It was now a year since I received the diagnosis and none of the tests showed any trace of cancer in my body. I had no symptoms either and had more energy and was starting to gain weight again.

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”10 Steps to Perfect Health 2012”

When I came home, I decided that I wanted to share my journey. I needed to share my experiences with others to confirm to myself that it was a success. It could motivate me to continue living an alkaline lifestyle as taught by Dr. Young.

 

To stand in front of a large group of people and talk about how the lifestyle I had chosen had played a role in me being healthy, compelled me to continue. I knew now that ensuring the daily maintenance of my health was the best way for me to prevent the cancer from returning to my body. See the YouTube video: ”10 Steps to Perfect Health 2012”, a film about the workshop I had at the National Museum in Copenhagen with Paulo Fernandes, one of Dr. Young’s students.

In the summer of 2012 my son and sister took part in a course in California where Dr. Young was teaching his experiences and theories behind his way of analyzing living and dried blood tests. They both brought a microscope with them home so that they could connect to their laptops. I could now sit with them and see my own blood. They got very good at analyzing it, which gave us all the possibility to frequently keep an eye on how our bodies reacted to different challenges and changes in our lives.

All that fear for no reason!

When I saw my blood tests after an appendicitis which ended in a burst appendix, it was clear that I now had to invest in my cleansing activities. In this period I started coughing, losing weight and sweating again. The fear of the intensive operation meant that again there would be cancer in my lungs. Cancer with renewed power. I felt weak and powerless.

The family was again there to help me get back on track. My blood tests showed progression. An ultrasound scan at the Scanning clinic in Herlev showed that my inner organs were healthy and in good shape. At the same time the test that I had done at the Allergy and Lung clinic in Copenhagen showed that my lungs were not seriously affected by the cough. Dr. John Arnved, MD, dared to say that such positive results wouldn’t be there if the cancer was growing in my lungs again. So he encouraged me to start up my runs by the beach again so I could cough up what was irritating my lungs. Fantastic advice – I ran again for my life and coughed a lot by the beach for a couple of days. After a week’s time I discovered that I wasn’t coughing anymore! Wow! All this fear for no reason.

The fear of dying died down

As previously said I renounced contact with the hospital. I knew from what I had read that it was very hard for the body to be scanned. I was also very aware of the psychological challenges. Both the experience of being in the scanner, the waiting time between the scan and the results as well as the thick atmosphere I experienced with the results coming in. It is not easy to have hope for life in such a universe. In the big picture though I managed with help from all those who believed in my decision. The time periods in the beginning where I had mistrust and ideas about how it would be to die from lung cancer died out, so in 2016 I built up the courage to be CT scanned. I wanted to know if such a test also confirmed that I was cured from metastatic pulmonary adenocarcinoma lung cancer..

CT-scan 5 years later

The CT scan in 2016 showed that the area which was compressed in my lung was still the same size, and there were also no more swollen lymph nodes. According to the doctors there were scars from the original cancer in the lung.

There was also a little compression of 8 millimeters further down the lungs. They wanted to follow the little spot, so I had some more tests done a couple of months later. The next test showed that there was still no change, not even in the small 8mm compression.

After this I again said no thank you to the hospital’s offer for further investigations. When the compression hadn’t changed in over five years and there were no signs of enlarged lymph nodes or signs of cancer in any other parts of my body, I didn’t wish to provoke my body with more physically and psychologically stressful investigations.

My doctor, Thomas Børresen, MD, wrote this, which I look at when I am in doubt:

“The patient sought help from Dr. Robert Young, Valley Center, CA, who started a program, which didn’t only give complete remission but continuous remission of the patients cancer, which is remarkable and unique and can only be related  to the program. Normal expected survival rate with conventional medical treatment and radiation is 0%.”

I no longer have life threatening metastatic cancer in my body – and I now also have documentation from conventional sources saying it was the right thing to do to follow Dr. Young’s pH Miracle Protocol.

Alkaline as healing and a lifestyle

I still want to continue living an alkaline lifestyle, not because I need to, but because I experience that it is life affirming on many levels. It gives me a special energy and courage, which I in no way wish to lose.

It is fantastic and strengthens my belief that I still have many more healthy years ahead of me. I get a lot of time to be there for those whom I love and those I can share an active work life with. I also have the belief that there will be many years, where I can be the grandmother of my grandchildren when they come one day.

I have regained my future and will enjoy every day of it.

Inger Hartelius

References

[1] Robert Oldham Young CPT, MSc, DSc, PhD, ND, is a naturopathic practitioner and not a medical doctor. The titles after his name represent different doctoral graduations he has obtained in the USA where he has, among other things, studied nutrition, hematology, microbiology and chemistry. As a practitioner he has worked as an American Naturopath. He is also the author of 75 books published in 29 different languages, 20 peer-reviewed published articles, over 3000 blog published articles and hundreds of youtube videos concerning alkaline nutrition, lifestyle, detoxification, human pH research and chemistry of the blood and interstitium. www.drrobertyoung.comhttps://www.youtube.com/user/pHMiracleCenter, https://www.amazon.com/Robert-O.-Young/e/B001ILKCSU/ref=sr_tc_2_0?qid=1526157267&sr=8-2-ent

 

He is now practicing in Marbella, Spain and Sardegna, Italy, and produces delicious, organic, alkaline products in Italy and the USA: www.iJuicenow.comwww.phoreveryoung.comwww.phmiraclestore.comwww.alkalinecare.com, and www.phmlife.com.

You can contact Dr. Young at the following email addresses: phmiraclelife@gmail.com and universalmedicalimaging@yahoo.com

Meals containing food which produce as little acid as possible and as much alkaline as possible in the body when they are digested.

Chlorophyll is the green pigment found in plants. It can be extracted from green plants and algae. It contains magnesium and antioxidants. The material in its basic structure is similar to the molecules of our blood. It can help increase the production of red blood cells, cleanse the body from poison and waste products hence raising our energy levels. www,ijuicenow.com

[ii] Pernille Knudtzon is one of Europe’s most groundbreaking doctors. She is a traveller in the field of health and says: “Health is a choice – you can make a difference”. Residing in Spain, she hosts consultations, lectures, workshops and retreats – helping thousands of people overcome serious illnesses – also in Denmark. Read more on http://www.vitafakta.es. At Pernille Knudtzon’s clinic you can, among other things get support to cleanse and rebuild your body on several levels. You can receive live and dried blood tests, medical thermographic scans and deep insight into yourself and your healing potentials.

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[iii] Galina Migalko MD, MND, RDMS, is a medical doctor with a speciality in non-invasive medical imaging, diagnostics and naturopathic medicine. http://www.universalmedicalimaging.com and universalmedicalimaging@yahoo.com

What Happens to ALL the Disappearing Can

12311128_1639530499647197_8412997691509003664_nWhat Happens to ALL the Disappearing Cancer Patients?

It’s been almost 20 years since I met my first disappearing patient — a nurse in her early 40s, let’s call her Kate. Kate was diagnosed with breast cancer. As a nurse, she had seen the results of breast cancer treatments. She was terrified, and determined. She was not heading for surgery, nor chemotherapy, nor radiation.

But Kate worked in a hospital. She worked with the doctors who diagnosed her cancer, and she worked with the surgeon, who wanted to schedule her into surgery “as soon as possible.”

The first thing Kate did was slow down. She did some research. It didn’t take her long to remind herself that in Canada, and in the USA, the treatments for cancer are akin to law. No hospital would dare deviate from the deadly three (cut, poison, burn).

Kate’s cancer was not large. She had been tested for cancer last year and no cancer was found. She knew it took many years for cancers to develop. At first, she was furious, “If it is here today, it must have been here last year. Why didn’t you find it last year?” It had not metastasized. It was not growing rapidly and was not affecting her health in any way. In theory, she had lots of time. So, she took some time.

But Kate didn’t look for magic cures. She didn’t search for the latest “cancer medicine.” She wasn’t interested in curing herself. She knew she was a nurse, not a doctor. She searched instead for the “cured” – patients who were diagnosed with cancer, and no longer had cancer. She knew from her work in the hospital, from conversations with patients, and with some staff, that these people existed — but from the perspective of the medical establishment, they seemed to disappear.

It didn’t take her long to find some patients who claimed they were cured. They hadn’t disappeared from life. They were eating, drinking, loving, and living full healthy and prosperous lives. But according to the medical records, they didn’t exist. They were “never cured.”

The medical system treated their cures as “anecdotal.” It ignored them. There was no attempt by any doctors to understand what happened to these cancer patients. They were no longer sick. The medical system looks after sick patients, treats sick patients. These patients were not sick.

Kate looked and listened. Her interest was not clinical science vs. anecdotal evidence. Her interest was personal. She talked, listened, compared stories. From several, she learned about a clinic that did not claim to cure cancer. It did not use medicines to treat cancers. But patients were cured, somehow. This clinic was not in Canada. It was not in the USA. She would have to go to Mexico to learn more.

There are lots of alternative treatment clinics in Mexico. Are some of them valid, using important techniques to cure cancers? Are some of them scams, wanting to take money from desperate clients? Do some of them have a cure that works sometimes, but might not work for her? Kate didn’t know. She did more research. She called the clinic.

The staff did not claim to cure cancer. Claiming to cure cancer is dangerous, even for a clinic outside of North America. They suggested Kate visit the clinic and see what happens there, no charge for a visit, but she would need to pay for her travel to Mexico. Kate had done her research. She had met and talked to patients whose cancers had disappeared.

Kate made her decision. She was familiar with cancer diagnosis techniques in Canada. She had undergone a physical examination, a mammogram, that detected a lump in her breast. Then she had a biopsy, where tissue was taken from the lump and was sent to a lab for analysis. The lab technician tested and examined the sample and issued a diagnosis “cancer” or “not cancer.” Once the diagnosis is issued, everybody swings into action. Kate knew that the mammogram had a high false positive rate and a false negative rate. Many people who are diagnosed with a “possible cancer” by a mammogram do not actually have cancer. She was also aware that cancer biopsies have a false positive rate and a false negative rate, as well. Her work in the hospital, with real patients, had made this very clear.

She didn’t really know for certain if she had cancer. Her surgeon, on the other hand, was still pressing her to schedule treatment.

Kate knew one thing. She had time. She cashed out some savings and booked a “holiday” in Mexico.

At the clinic, Kate was surprised that there was no “cancer diagnosis.” They did check the presence and size of the lump on her breast. But they didn’t repeat the biopsy. The clinic read her diagnostic reports, but did not investigate them further. There was instead a very thorough analysis completed by a suite of doctors. It took two full days of tests and interviews, if I remember correctly.

Kate was asked about her family’s medical histories. She gave blood samples. She was questioned extensively about her diet, about what she eats on a regular basis. What foods does she like and eat often. What foods does she not like and never eat. Doctors examined her lungs, her heart, liver, and other bodily organs with various tests. Her immune system was tested. Extensive interviews about her life, her work, her relationships, and more.

At the time I talked to Kate, I didn’t realize that she was not getting a “medical analysis,” she was actually getting a “healthicine analysis.” Her tests and questions fit perfectly to the hierarchy of healthicine: genetics, nutrition, cells, tissues, organs, bodily systems, body, mind, spirit, and community.

Kate’s genetics were analyzed through family history. There may have been further genetic analysis, I don’t remember all of the details. Her nutritional status was analyzed, not just by analyzing what she ate, and what she preferred to eat, but also by studying what she didn’t like to eat, what she deliberately never ate, what foods she believed she was allergic to. Her cells and tissues were analyzed directly, through blood samples and physical examination, and indirectly through medical history and other tests. Many of her organs were tested for healthiness. Her bodily systems, immune system, circulatory system, respiratory system, hormonal systems and more were analyzed and assessed. Her physical body was measured, weighed, and examined. Her mental health was assessed, as well as her spiritual healthiness. She was in good spirits, even in light of a potentially life threatening illness. Her community health was analyzed as well. Her family, her relationships with her children, her spouse, her parents, her work community, and more.

After a few days, Kate met with a group of doctors to discuss her health, not her illness, her healthiness. Diagnosing illness is difficult. Analyzing healthiness is more complex. It took several doctors and several hours for Kate to learn and understand what they had learned about her healthinesses and her unhealthinesses.

They then “prescribed” two weeks, if I remember correctly, of healthiness training, tailored to Kate’s specific situation. She spent the next two weeks at the clinic, learning to be healthier, not learning how to be “healthier in principle,” rather – learning what Kate needed to do to make her diet, her body, her mind, her spirits, and even her relationships with her communities healthier. She could not change her work community. But she could change how she reacted to and interacted with it – to improve her own health. After two weeks of learning at the clinic, her breast lump had started to shrink.

Kate went back to Canada, to put her learning into action. The lump disappeared. Her diagnosis was still there on paper. But her “cancer” had disappeared. She was retested at her hospital and no cancer was found.

Then Kate began to disappear.

When the surgeon asked again, she explained that she was not going to surgery. The surgeon looked away. He refused to look her in the eye after that.

But Kate didn’t disappear from her family. She went back to her family. She didn’t disappear from her job. She went back to her job. She disappeared from the cancer system. Her cancer disappeared, so, as a cancer patient, she disappeared.

Was she cured? We don’t know. There is no useful definition of a cancer cure. No medical or scientific test that can prove a patient has been cured of cancer. Our cancer treatment statistics have no count for people who are cured of cancer. Patients that are cured, whether they are cured with medicines or not, are not counted. No breast cancer patients are officially cured by medicine. If their cancer goes away without treatment, they disappear from statistics. If their cancer is killed by radiation, chemotherapy or surgery, they are not cured, they are a “survivor.” Everyone knows that cancer survivors are always waiting for the cancer to reappear. Their symptoms are in remission, but their cancer is not cured. They are not cured. With no proof of a cure, it might just be hidden.

Kate no longer has cancer. She paid, from her own pocket, for her trip to a clinic in Mexico. After the trip, her cancer disappeared. She had medical insurance. But her insurance wouldn’t pay for her trip. Insurance pays for treatments, not for cures. It pays for treatments, even if they fail. But it does not pay for success. Success disappears.

There are two ways for a cancer patient to disappear. You might be cured by health. Or you might be cured by a medicine that is not approved. In both cases, the medical system will ignore the cure, and ignore the patient.

In healthicine, there are no incurable diseases. If it is not curable – it is not a disease, it is a handicap, a disability, a deficiency, or simply an attribute of the person. All diseases can be cured by definition.

I have since met several cancer patients who have disappeared, and not just cancer patients. Maybe you have too? I’ve met more by internet, email, etc. There is no way for me to determine if a disappeared patient actually had cancer, if their treatment cured their cancer, if their body cured their cancer or if they still have cancer. We can only tell if there is another cancer diagnosis. Nothing can be told from the absence of a diagnosis.

There is no way for any doctor to tell either. There are no tests for a cancer cure. There is no way to recognize, much less document a cancer cure. There are no statistics for cancers cured.

Many cured patients don’t disappear quietly. They speak out. They write books and newspaper articles. They blog. But it doesn’t matter. They still don’t count. Once cured, they disappear. The medical system does not study their cases, does not study their diagnosis, does not study their cures. For chronic diseases, like cancer, arthritis, diabetes, heart disease, even obesity, and many more, there are no techniques to document “cured patients.” As a result, there are no statistics for “cured patients” of any chronic illness.

Once they are cured, they disappear. Health doesn’t cure illness, it disappears illness. And medicine doesn’t count people who have disappeared.

To your health

Alkalizing Nutritional Therapy For Any Cancerous Condition: How It Works

51978-william170

 Abstract

Due to the evident ineffectiveness of conventional cancer treatments (e.g. chemotherapy and radiation), more efficient alternatives are needed.  The potential of Alkaline Nutritional Infusion (ANI) as a legitimate alternative to chemotherapy and radiation is examined.  While largely ignored in conventional oncology, the pH of the interstitial fluids is suggested as paramount in identifying a pre-cancerous and cancerous condition. It is further suggested that cancer is an over-acidic condition of the body that can be reversed and prevented with alkalizing treatments such as ANI.  Full Body Bio-Electro Scan (FBBES), Full Body Thermography (FBT) and Full Body Ultrasound (FBU) is presented as a noninvasive and nonradioactive means to examine body pH and the presence of pre-cancerous or cancerous condition.  In contrast to the acidosis caused by conventional cancer treatments, ANI methods such as Intravenous Nutritional Infusion (INI) and Rectal Nutritional Infusion (RNI) provide an alkalizing approach to cancer prevention and treatment.Introduction

While largely ignored in conventional oncology for decades, intravenous  and rectal nutritional infusion therapy plays a major key in recovering from and reversing any metabolic, environmental, or dietary caused dis-ease. But when you visit your conventional doctor for any condition or dis-ease, he or she will never address the patient’s lifestyle or diet, besides sometimes shrugging and saying, “Eat better and get more exercise.”  This is generally stated to the patient without giving any specific recommendations of what to eat, what to drink or how to exercise.

This general mindset stems from medical schools where a physician may receive only a few hours of nutritional, dietary or physical training in their nutritional, biochemistry or physiology courses on the importance of nutrition, diet and exercise. Then all training, including residency and fellowship is completely pharmaceutical-drug focused. Only a select few take the time to be trained and mentored by traditional, integrative or naturopathic physicians that specialize in the prevention and treatment of cancer or other dis-ease conditions.

Powerful Insights to Non-Invasive Cancer Treatment

Alkalizing nutrition, diet and exercise is key in prevention, treatment and recovery, especially with a cancerous condition, because chemotherapy and radiation treatments deplete the nutrients and electron energy right out of the body. This is why patients undergoing chemo lose their hair, lose weight and look so gaunt or ill – their bodies are literally starving for electron-rich alkalizing nutrition, food and water while simultaneously loading-up with an acid-rich and toxic diet combined with their associated metabolic waste, such as lactic, uric or acetic acid.  In addition, it is important to understand when dietary and metabolic acids are NOT eliminated through the four channels of elimination via urination, defecation, perspiration and respiration, these toxins will eventually buildup in the connective tissues leading to inflammation and ultimately degenerative disease, namely cancer. [1,2,3,4]

Every person has unique dietary and metabolic needs, meaning that telling a patient to open wide and then administer some minerals and vitamins orally will not always do the trick. Some people need more sodium or potassium and some may need extra vitamin A or E in their diet, while others may need less. Some patients need more magnesium and others have iron deficiencies due to the poor health in the crypts of the small intestines where stem cells are made for differentiation into new and healthy red blood cells.[5]

Even though oncology as a whole has ignored intravenous and/or rectal alkalizing nutritional infusions, fearing that alkalizing nutrients will adversely impact chemotherapy or radiation, they really detour patients from these kinds of supportive and non-invasive treatments. This is in spite of 280 peer-reviewed studies, including 50 human studies involving 8,521 patients that have emerged since the 1970’s. 5081 subjects that were give nutrients have shown that supplementing  nutrients do not interfere with conventional therapeutic modalities for cancer. [6]

So what are we left with? The fact is, every cancer patient needs a complete, personalized physiological, anatomical, functional, hematological and nutritional profile if he or she really wants the edge in preventing and removing the acids that cause the inflammation that leads to a cancerous condition. [1,2,3,4] Let’s explore what this all means and how it can make the difference in a patients survival and improving the quality and quantity of  life.

In The Beginning . . .

Life on earth depends on appropriate pH levels in and around living organisms and cells. Human life requires a tightly controlled pH level in the serum of about 7.365 (a slightly alkaline range of 7.35 to 7.45) to survive [7].

As a comparison, in the past 100 years with increasing industrialization, the pH or acid/base balance of the ocean has dropped from 8.2 to 8.1 because of increasing CO2 or carbon monoxide deposition. This has a negative impact on life in the ocean [8, 9] and may lead to the collapse of the coral reefs.  Why”  Because the ocean is using the calcium in the coral to maintain its alkalinity much like the body uses the calcium from the bones to maintain the alkalinity of the intracellular fluids, interstitial fluids and blood fluids. [7]. Even the pH of the soil in which plants are grown can have considerable influence on the mineral content of the food we eat (as minerals are used as buffers to maintain pH). The ideal pH of soil for the best overall availability of essential nutrients is between 6 and 7. Acidic soils below pH of 6 may have reduced calcium and magnesium, and soil above pH 7 may result in chemically unavailable iron, manganese, copper and zinc. Adding dolomite and manure are ways of raising pH in an acidic soil environment when the pH is below 6. [10]

When it comes to the pH and net acid load in the human diet, there has been considerable change from the hunter gather civilization to the present. [11]  With the agricultural revolution (last 10,000 years) and even more recently with industrialization (last 200 years), there has been an decrease in potassium (K) compared to sodium (Na) and an increase in chloride compared to bicarbonate found in the diet. [12]  The ratio of potassium to sodium has reversed, K/Na previously was 10 to 1 whereas the modern diet has a ratio of 1 to 3. [13] It is generally accepted that agricultural humans today have a diet poor in magnesium and potassium as well as fiber and rich in saturated fat, simple sugars, processed sodium containing aluminum, and processed chloride as compared to the preagricultural period. [14]  This results in a diet that may induces dietary acidosis which is mismatched to the genetically determined alkaline nutritional requirements. [15]  With aging, there is a gradual loss of renal acid-base regulatory function and a resultant increase in diet-induced metabolic acidosis while ingesting the modern or Standard American Diet. [16]

A low-carbohydrate high-protein diet with its increased acid or proton/hydrogen load results in very little change in blood chemistry, and pH, but results in many changes in interstitial and urinary pH chemistry. Urinary and interstitial fluid sodium and magnesium levels, urinary citrate and pH are decreased, urinary calcium,  potassium, undissociated uric acid, and phosphates are increased. All of these result in an increased risk for metabolic tissue acidosis, bone loss and an increase in blood, breast, brain, liver, gallbladder, pancreas, prostate, uterus and kidney stones. [16]  The reason for the increase in stones throughout the body is to buffer the increase of dietary and metabolic acids found throughout the fluids of the body.  The increase of stones is the direct result of an increase of the dietary and/or metabolic acid-load which if not corrected will lead to a cancerous condition in those specific areas. [16]

Alkalinity and Chemotherapy in the Treatment of Cancer

The effectiveness of chemotherapeutic agents is markedly influenced by the pH or the acid/base chemistry of the body.  Numerous agents such as epirubicin and adriamycin require an alkaline media to be more effective. Others, such as cisplatin, mitomycin C, and thiotepa, are more cytotoxic in an acid media [17]. Cell death correlates with acidosis and intracellular pH shifts higher (more alkaline) after chemotherapy may reflect response to chemotherapy [18]. I have noted with many of my patients that inducing metabolic alkalosis may be useful in enhancing some treatment regimes by using alkalizing intravenous or rectal mineral and vitamin infusion therapy of sodium bicarbonate, carbicab, and furosemide [19]. In addition, extracellular alkalinization by using mineral salts such as sodium and potassium bicarbonate may result in improvements in the effectiveness of chemotherapy. [20]

Alkalizing Nutrition, the Immune System and How Together They Fight Cancer

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Briefly, let’s review: cancer is an adjective not a noun.  Cancer is what happens to cells in a toxic acidic environment.  Simply put cancer is an acidic metabolic or dietary waste that spoils healthy cells. Healthy cells are affected by their environment which can activate protective genes. [21]  If the acidic internal environment of the body is not returned to its alkaline design this will cause mutations or fermentation of the cell and the acids from these spoiling cells will spoil other cells, just like one domino tipping-over another domino leading to a cancerous condition. [61, 62]

The reason the body can have such trouble fighting cancer varies – in part, it has do with protecting the alkaline design of the body fluids, the health of the white blood cells and the body’s ability to neutralize metabolic and/or dietary acidic waste that has NOT been properly removed via the four channels of elimination – urination, defection, perspiration and respiration.

Poor circulation, elimination and alkaline nutrition leads to a build-up of acidic waste and poor immune defense (the janitors of the blood and interstitial fluids), which can increase the number of cancerous cells, as one spoiled or rotting cell spoils another, much like one rotten apple will spoil a bushel of healthy apples creating an acidic microenvironment that creates more and more rotten apples or cancerous cells  that would be resistant to any conventional acidic treatment.

Now, the most commonly accepted forms of cancer treatment are chemotherapy and radiation therapy. These acidic drugs and ionizing radiation will systemically destroy already acidic cancerous cells, but they will also turn healthy blood and body cells into cancerous cells.  This will create an immediate response from the body to produce and release alkaline compounds, such as sodium bicarbonate to buffer the increased amounts of acidic waste draining the body of essential nutrients and critically paralyzing the white blood cells making them inactive and ineffective in buffering and removing cellular waste. During these acidic conventional treatments, the immune system is essentially obliterated, which can lead to metastasis while not even affecting the original cancerous condition.  According to a medical researcher, Steve Gullans, Ph.D, only 30% of  ALL people respond to chemotherapy or radiation, leaving 70% unresponsive. [22]  In addition, the data is clear that after initial chemotherapy fails, as many as 95% of cancer patients will not respond to the next suggested chemotherapy drug recommended by conventional methods.[23 ]  It is also important to understand that conventional treatments for cancer are NOT a cure for cancer.[24]

Truly, the alkaline buffering system (the stomach is the main alkalizing organ and responsible to maintain alkalinity of the blood, tissues and organs by producing sodium bicarbonate) which releases antioxidants to buffer increased acidic toxic waste build-up is the first and last defense against a cancerous condition. [25] If poor alkalizing nutrition is ignored, as it has been by conventional oncology for decades, how can a full recovery or at least a satisfactory quality of life be expected? In my clinical experience it’s difficult. Some oncology groups have improved by offering in house nutritionists, but oral supplementation is nowhere near sufficient in reversing a cancerous condition.

The best analogy is that it’s like trying to take out a forest fire with a squirt gun.  Or another analogy would be treating a fish in a polluted pond without changing or cleaning the water.  In other words if the fish is sick what would you do?  Treat the fish or change the water? (63,64)  Unfortunately, most groups that advertise integrative, alternative or naturopathic medicine for reversing a cancerous condition lack proper testing, a targeted method of administration or proper combination with personalized alkalizing treatments. That’s the difference that lengthens the quality and quantity of life, in my 30 plus years of clinical research experience.

Nutritional Deficiencies and Their Negative Health Effects

Below are some common alkalizing nutrients, their purpose and symptoms, as well as how frequent these deficiencies are seen in the general public in pre-cancerous and cancerous conditions.

Sodium (extremely common)

Purpose: Maintains alkalinity of the blood, interstitial and intracellular fluids, and provides the matrix for the transport of electrons for the energy of body cells.

Common Sources: Sea salt, celery, green fruit and vegetables, sprouted seeds and grasses.

Symptoms of Deficit: Low sodium bicarbonate levels, acid reflux,  excess stomach acid, headache, nausea, compensated, decompensated and latent tissue acidosis, low energy, low interstitial and intracellular pH, hypertension, heart disease, diabetes, all cancers and death. [26]

Potassium (extremely common)

Purpose: Low potassium bicarbonate, maintains alkalinity of the blood, interstitial and intracellular fluids. Major alkalizing element in the body to maintain the alkaline design of all body fluids.  The major alkaline buffer in neutralizing metabolic, dietary, respiratory and environmental acids.

Common Sources: Avocado, almond, green fruit and vegetables, sprouted seeds. nuts and grasses.

Symptoms of Deficit: Compensated, decompensated and latent tissue acidosis, low energy, low interstitial and intracellular pH, hypertension, heart disease, diabetes, and all cancers. [27]

Calcium (extremely common)

Purpose: Builds bones, teeth, assists the heart, nerves and muscles.

Common Sources: Green fruit and vegetables, sprouted seeds, nuts and grains, brazil nuts, broccoli, cabbage, dark leafy greens, hazelnuts, and salmon.

Symptoms of Deficit: Osteoporosis, osteomalacia, osteoarthritis, muscle cramps, irritability, acute anxiety and increased colon cancer risk.[28]

Magnesium (very common)

Purpose: More than 300 biochemical reactions, including muscle and nerve function, heart rhythm, immune system, strong bones, regulates calcium, copper, zinc, potassium, vitamin D.

Common Sources: Green fruit and vegetables, sprouted beans, peas, nuts, seeds, whole unprocessed alkalizing grains.

Symptoms of Deficit: Appetite, nausea, vomiting, fatigue cramps, numbness, tingling, seizures, heart spasms, personality changes, heart rhythm and colon cancer. [29]

Zinc (extremely common)

Purpose: Supports alkalizing, immune system, wound healing, taste and smell, DNA synthesis, normal growth and development during pregnancy, childhood and adolescence.

Common Sources: Found in green fruit and vegetables, sprouted seeds, grains and beans, nuts, whole grains.

Symptoms of Deficit: Growth retardation, hair loss, diarrhea, impotence, eye and skin lesions, loss of appetite, taste, weight loss, mental lethargy. [30]

Vitamin E (very common)

Purpose: This antioxidant regulates oxidation reactions, stabilizes cell membranes, immune function, protects against cardiovascular disease, cataracts and macular degeneration. [31]

Common Sources: Found in  green fruit and vegetables, sprouted seeds and grains, wheat germ, nuts, seeds, dark leafy greens, avocados, asparagus and certain cold-pressed vegetable oils, like hemp oil. [32]

Symptoms of Deficit: Anemia, rupturing of red blood cells, bruising, PMS, hot flashes, eczema, psoriasis, cataracts, wound healing, muscle weakness, sterility. [31,32,33]

Vitamin B1 (very common)

Purpose: Carbohydrate conversion, breaks down fats and protein, assists digestion, the nervous system, skin, hair, eyes, mouth, liver, immune system.

Common Sources: Green fruit and vegetables, sprouted seeds and grains, brown rice, wheat germ, and bran.

Symptoms of Deficit: Age-related cognitive decline, heart problems, Alzheimer’s and fatigue. [34]

Vitamin B2 (very common)

Purpose: Like Vitamin B1, works in carbohydrate conversion, breaks down fats and proteins, assists digestion, the nervous system, skin, hair, eyes, mouth, liver and also metabolism.

Common Sources: Green fruit and vegetables, almonds, sprouted seeds and grains, wheat germ, sprouts of all kinds, including soy sprouts.

Symptoms of Deficit: Anemia, decreased free radical protection, cataracts, poor thyroid function, B6 deficiency, fatigue, elevated homocysteine. [35, 36, 37, 38, 39, 40]

Vitamin B3 (less common)

Purpose: Helps with energy, digestion, nervous system, skin, hair, eyes, liver, eliminates harmful toxins, assists sex and stress hormones and improves circulation.

Common Sources: Green fruit and vegetables, beets, sprouted seeds, nuts and grains.

Symptoms of Deficit: Cracking, scaling skin, digestive problems, confusion, anxiety, fatigue. [41]

Vitamin B6 (common)

Purpose: Assists with buffering metabolic acids, protein metabolism, RBC production, reduces homocysteine, helps nerve and muscle cells, DNA/RNA, B12 absorption, and immune function.

Common Sources: Green fruit and vegetables, especially avocado, and sprouted seeds, nuts and grains.

Symptoms of Deficit: Depression, sleep and skin problems, confusion, anxiety and fatigue. [42, 43]

Vitamin C (common)

Purpose: Aids in alkaline buffering activation, second messenger roles (transmitting hormonal information), blood clotting, cell and cell organelle membrane function, nerve impulse transmission and muscular contraction, tone and irritability. (Not to be confused with High Dose Vitamin C that acts as an oxidative therapy)

Common Sources: Supplements, broccoli, Brussels sprouts, avocado, and all green fruit and vegetables.

Symptoms of Deficit: Muscular and nervous irritability, muscle spasms, muscle cramps and tetany, tooth decay, periodontal disease, depression and possibly hypertension. [44, 45, 46]

Vitamin D (very common)

Purpose: Calcium and phosphorus levels, calcium absorption, bone mineralization.

Common Sources: Sunlight, green fruit and vegetables, sprouted seeds, nuts and beans and fish.

Symptoms of Deficit: Osteoporosis, calcium absorption and thyroid issues, cardiovascular risks and 15 cancer risks.[47]

Folate (very common)

Purpose: Mental health, infant DNA and RNA, adolescence and pregnancy, works with vitamin B12 to regulate red blood cell production, iron function and reduce homocysteine.

Common Sources: Supplements, sprouted grains, tomato, green vegetables and fruit, avocado, black-eyed peas, sported lentils and beans.

Symptoms of Deficit: Anemia, poor immune function, fatigue, insomnia, loss of hair, high homocysteine, colon cancer, and cardiovascular disease.[48]

N-aetyl-Cysteine (very common)

Purpose: Powerful antioxidant or anti-acid, normalizes the alkaline interstitial fluid pH, urinary tract infections, neutralizes metabolic and dietary alcohol poisoning, protects lungs against toxins from air pollution and tobacco smoke.

Common Sources: Supplements, sprouted grains, sulfur-rich vegetables such as garlic, onions, parsley and cruciferous vegetables are particularly helpful in addition to avocados, squash and tomatoes.

Symptoms of Deficit: Anemia, poor immune function, fatigue, insomnia, loss of hair, high homocysteine, urinary tract infections,  lung cancer, gastric cancers, colon cancer, ovarian cancer. .[49, 50, 51, 52, 53, 54, 55, 56, 57, 58]

Glutathione (very common)

Purpose: Potent antioxidant or anti-acid, protects endothelium from dietary and metabolic acids, protects against chemotherapy toxicity, inhibits platelets formation, buffers aflatoxins, infections of the lung, used in cases of Malaria and AIDS, supports immune system, as an alkaline effect on the body fluids.

Common Sources: Supplements, sprouted grains, sulfur-rich vegetables such as garlic, onions, parsley and cruciferous vegetables are particularly helpful in addition to avocados, squash and tomatoes.

Symptoms of Deficit: Anemia, poor immune function, fatigue, insomnia, loss of hair, infections, high homocysteine, lung congestion and cancer, gastric cancer, colon cancer, reproductive cancers in men and women, neurological and cardiovascular disease. [59, 60, 61, 62]

Consider that, if these shortages are found in a healthy population, what I see in patients with a cancerous condition is far worse, due to their high acidity and metabolic demands. Though an alkaline lifestyle and diet is important, it’s the amount and quality of care received at therapeutic intravenous, oral, rectal and respiratory levels that is vital.

Alkalizing Non-Invasive Rectal Nutrient Infusions

One important point concerning the infusion of alkalizing nutrients!  For those who do not want an invasive intravenous infusion of alkaline minerals, salts, vitamins, chlorophyll, antioxidants such as glutathione, and/or long-chain polyunsaturated oils you can elect a non-invasive rectal infusion or nebulize your nutrients, which I believe is just as effective.  When these supportive nutrients are infused via the anus into the rectum, the hemorrdoidal vein absorbs these alkalizing nutrients into the blood.  The blood has a very narrow pH range so these highly alkalizing nutrients are pushed-out into the interstitial fluids to the body cells.  This becomes a very important therapy in reducing the metabolic acids that surround the cell and cause the fermentation and break-down of cell leading to a cancerous condition.

How Supplementation Can Kick-Start Your Recovery from a Cancerous Condition

As you can see, nutritional deficiencies can lead to a serious amount of health issues. These problems can become exponential in a patient with a cancerous condition because of the severe strain placed on the patient, especially when chemotherapy and/or ionizing radiation is involved.

To make matters worse, absorption of salts, minerals, and vitamins is impaired. This means, eating a alkaline diet and swallowing a few minerals and vitamins is not sufficient to support the nutritional needs of the patient. These changes are essential for long-term health, but in the wake of a cancerous condition, it’s hardly enough.

What needs to be done is intravenous and/or rectal nutritional infusion therapy. When nutrients are channeled directly into the bloodstream and then to the interstitial fluids, the results are immediate, targeted and dramatic. Keep in mind, this methodology isn’t a treatment in-and-of itself. Intravenous and rectal nutritional therapy must be combined with other forms of treatment to be truly effective. But once it is combined with the correct, personalized alkalizing therapy, alkalizing diet, exercise, and proper alkalizing water, then a revolutionary pH Miracle can begin. [63, 64]

Using 3-D Bio-Electro Functionality Scanning to Determine the Best Possible Strategy for Preventing and/or Reversing Any Cancerous Condition [65]

In modern day oncology, surgeons biopsy the lymph nodes to determine how cancer is spreading or provide staging. Lymphocytes, a type of white blood cell that is found in these lymph nodes which are catch-basins for acidic waste and cancerous cells are responsible for breaking-down and removing cellular acidic waste and cancerous cells. Impaired lymphocytes and/or congested lymph nodes are at least one major factor in the many areas I test for functionality.

The lymphatic system, the lymph nodes and the lymphocytes themselves must be functional in preventing and reversing any cancerous condition.

Using electrodes attached to the head, hands and feet I am able to test the functionality of the lymphatic system, circulatory system, muscular system, skeletal system, endocrine system, neurological system, reproductive system, vascular system, digestive system,  and respiratory system.  interstitial chemistry, interstitial pH for metabolic acidosis and the electro-conductivity of the cells to determine the state of health of ALL organs, glands and tissues in the prevention and reversal of any cancerous condition.[65]

3-D

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I also test for nutritional deficiencies and metabolic alkalosis or acidosis by measuring the  interstitial chemistry, interstitial pH and the electro-conductivity.  Measuring the pH of the interstitial fluids is more revealing of a cancerous condition since the blood is always trying to maintain its delicate alkaline pH of 7.365 and does not vary much.  Based upon my theory that cancer is a compromised acidic environment of the interstitial fluids which then negatively affects the state of health of ALL body cells which make up the organs, glands and tissues.  It is significantly more important to measure interstitial and intracellular fluids than blood fluids in order to obtain a correct chemistry and pH when making nutritional recommendations in the prevention and treatment of a cancerous condition. [63, 64, 65,66,67]

The following are quantitative measurements in healthy patients, without cancer, comparing Blood fluids with Intracellular and Interstitial fluids of the body compartments as a benchmark which I use to determine deficiencies in alkalizing minerals, protein and whether or not the patient is in metabolic acidosis or a pre-cancerous or cancerous condition (Note: all cancer patients are in interstitial metabolic acidosis, low in interstitial sodium and high in interstitial calcium and potassium): [66,67]

1) Sodium: Na+ mEq/l

Venous blood: 130, Arterial blood: 137, Capillary blood: 135, Intracellular fluid: 10 and Interstitial fluid: 135

2) Potassium: K+ mEq/l

Venous blood: 3.2, Arterial blood: 3.5, Capillary blood: 4, Intracellular fluid: 140 and Interstitial fluid: 3.17

3) Calcium: Ca++ mEq/l

Venous blood: 2.5, Arterial blood: 2.2, Capillary blood: 2.3, Intracellular fluid: 0.0001 and Interstitial fluid: 1.55

4) Magnesium: Mg mEq/l

Venous blood: 0.64, Arterial blood: 0.62, Capillary blood: 0.60, Intracellular fluid: 58 and Interstitial fluid: 0.50

5) Chloride: Cl- mEq/l

Venous blood: 104, Arterial blood: 101, Capillary blood: 103, Intracellular fluid: 4 and Interstitial fluid: 106

6) Bicarbonate: HCO3 mEq/l

Venous blood: 22, Arterial blood: 24, Capillary blood: 23, Intracellular fluid: 10 and Interstitial fluid: 24

7) Phosphorus: P mE/l

Venous blood: 2.5, Arterial blood: 2.3, Capillary blood: 2, Intracellular fluid: 75 and Interstitial fluid: 0.70

8) Sulfate: SO4 mEq/l

Venous blood: 0.8, Arterial blood: 0.6, Capillary blood: 0.5, Intracellular fluid: 2 and Interstitial fluid: 0

9) Glycemia mg/dl

Venous blood: 1, Arterial blood: 1, Capillary blood: 1.01, Intracellular fluid: 0.20 and Interstitial fluid: 0.90

10) Cholesterol mg/dl

Venous blood: 0.66, Arterial blood: 0.630, Capillary blood: 0.676, Intracellular fluid: 0.2 and Interstitial fluid: 0.188

11) Partial Pressure of Oxygen or PO2 mmHg

Venous blood: 80, Arterial blood: 90, Capillary blood: 89, Intracellular fluid: 20 and Interstitial fluid: 87.2

12) Carbon Dioxide Or PCO2

Venous blood: 46, Arterial blood: 40, Capillary blood: 42, Intracellular fluid: 50 and Interstitial fluid: 46

13) pH or potential of hydrogen

Venous blood: 7.36, Arterial blood: 7.4, Capillary blood: 7.38, Intracellular fluid: 7.2 and Interstitial fluid: 7.36

14) Protein g/dl

Venous blood: 72, Arterial blood: 74, Capillary blood: 73.7, Intracellular fluid: 68 and Interstitial fluid: 20.6

As I correct the deficiencies in the intracellular and interstitial fluids targeted with key alkalizing nutritional treatments, patients see the difference through follow-up tests using quantitative non-invasive 3-D Full Body Bio-Electro scanning.  They also feel the difference physiologically and functionally.[65,66,67]

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.[61, 64,65]

The following case study with one of my patients was diagnosed by biopsy with inflammatory ductal cell carcinoma who reversed her cancerous condition without chemotherapy, radiotherapy, and surgery.[65]

Using breast thermography and tumor location and size measured by breast ultrasound you can see the week by week reduction of a 14.2cm tumor in the left breast reduce to less than 2cm in 7 weeks of treatment using an alkaline lifestyle and dietary protocol as outlined in Chapter 11 of the pH Miracle revised and updated book. (63,64,65)

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Summary

The safest, painless, non-invasive, affordable full body screening tests are a combination of a Medical Diagnostic Ultrasound and Thermography, which may give the Physician about 95% accuracy in detecting breast cancer.[65]

Thermography is a physiological, non-invasive screening procedure that detects and records infrared heat emissions from the pre-cancerous or cancerous area, which can aid in the early detection of abnormal changes in body tissues, organs and glands. Thermography offers information that no other procedure can provide. The procedure is based on the principle that chemical and blood vessel activity in both pre-cancerous or cancerous tissue and the area surrounding a developing cancer is almost always higher in temperature than in the normal tissue.

Since pre-cancerous and cancerous masses are highly metabolic tissues, they need an abundant supply of nutrients to maintain their growth. The cells release substances that stimulate the formation of new blood vessels (neoangiogenesis). This process results in an increase in surface temperatures of the affected tissue, organ or gland.

The most promising aspect of medical diagnostic thermography is its ability to spot abnormalities years before the tumor is seen on any anatomical test. Since thermal imaging detects changes at the cellular level, this test can detect activity 8 to 10 years before any other test. This makes it unique in that it affords the physician the opportunity to view changes before the actual formation of the cancerous tumor.

Studies have shown that by the time a tumor has grown to sufficient size to be detectable by physical examination or mammography, it has in fact been growing for about seven years achieving more than 25 doublings of the malignant cell colony. At 90 days there are two cells, at one year there are 16 cells, and at five years there are 1,048,576 cells–an amount that is still undetectable by a mammogram. Thermography has the ability to provide the patient with future risk assessment. If discovered, certain thermographic risk markers can warn the patient that she/he needs to work closely with their physician with regular checkups to monitor her  health.


Full-Body Ultrasound [FBU} is an anatomical non-invasive, painless screening test without ionized radiation. Ultrasound, also known as sonography, uses sound waves to outline a part of the body. For this test, a small instrument called a transducer is placed on the skin (which is often first lubricated with ultrasound gel) and emits sound waves off body tissues. The echoes are converted by a computer into an image that is displayed on a computer screen.

Full Body Ultrasound imaging is “real-time,” meaning that it can show exactly what’s happening in the tissue, organ or gland at that moment, help to distinguish between cysts (fluid-filled sacs) and solid masses, detect increased vascularity around or within the mass, see the shape, exact size and location of the mass, cyst, calcification or dilated mammary ducts.

These safe medical diagnostic tests can be done on early bases for a regular check up, or more often if the problem was detected, to monitor a noninvasive alkalizing nutritional treatment progress.

Early detection, which includes self examination and safe, painless, non-invasive medical diagnostic Full Body Bio-electro Scan(FBBES) Full Body Thermography (FBT) and Full Body Ultrasound (FBU) screenings with no ionizing radiation coupled with a supportive alkalizing nutritional diet and ANI whether or not the patient is receiving chemotherapy and/or radiation, I have found that this approach a precancerous or cancerous condition will saves lives!

If you have questions concerning any specific acidic cancerous condition or to learn more about ANI and a alkalizing nutritional dietary and lifestyle protocol in the prevention and reversal of any precancerous or cancerous condition, please read The pH Miracle revised and update, Reverse Cancer NOW and The pH Miracle for Cancer. [63, 64] http://www.phoreveryoung.com  You can also email: phmiraclelife@gmail.com

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References

[1] Immunity, Inflammation, and Cancer http://www.sciencedirect.com/science/article/pii/S0092867410000607

[2] Inflammation: Gearing the journey to cancer –http://www.uccs.edu/Documents/rmelamed/kundu_surh_2008_18485806.pdf

[3] Researchers examine how BRD4 contributes to sustained presence of NF-kappa B in cancer cells – http://www.news-medical.net/news/20130520/Researchers-examine-how-BRD4-contributes-to-sustained-presence-of-NF-kappa-B-in-cancer-cells.aspx

[4] The Epidermal Growth Factor Receptor: A Link Between Inflammation and Liver Cancer – http://ebm.sagepub.com/content/234/7/713.abstract#target-1 – See more at: http://envita.com/cancer/chronic-inflammation#sthash.1KCydZeZ.dpuf

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[23]  Holly G. Prigerson, PhD1,2; Yuhua Bao, PhD3; Manish A. Shah, MD4; M. Elizabeth Paulk, MD6; Thomas W. LeBlanc, MD, MA5; Bryan J. Schneider, MD7; Melissa M. Garrido, PhD8,9; M. Carrington Reid, MD, PhD2; David A. Berlin, MD10; Kerin B. Adelson, MD13; Alfred I. Neugut, MD, PhD11,12; Paul K. Maciejewski, PhD1,14[+] Author Affiliations, “Chemotherapy Use, Performance Status, and Quality of Life at the End of Life.” JAMA Oncol. 2015;1(6):778-784. doi:10.1001/jamaoncol.2015.2378.

[24] Cancer Treatment & Survivorship, Facts & Figures, Estimated Numbers of Cancer Survivors by State as of January 1, 2014.

http://www.cancer.org/acs/groups/content/@research/documents/document/acspc-042801.pdf

American Cancer Society Inc. 250 Williams Street, NW, Atlanta, GA 30303-1002, 404-320-3333

[25] Scand J Gastroenterol. 1992 Oct;27(10):829-36, “Measurement of gastric bicarbonate secretion in the human stomach: different methods produce discordant results.” Odes HS1, Hogan DLSteinbach JHBallesteros MAKoss MAIsenberg JI

[26] Campling BG, Sarda IR, Baer KA, Pang SC, Baker HM, Lofters WS, Flynn TG. Secretion of atrial natriuretic peptide and vasopressin by small cell lung cancer. Cancer. 1995;75:2442-51

[27] Rethinking Cancer – http://www.rethinkingcancer.org/resources/magazine-articles/18_7-8/potassium.php

[28] “Calcium supplementation may attenuate the hyprproliferation and hyperplasia induced in the mouse colon by a Western-stye diet.”

Click here to read the entire abstract

Pubmed Data : Carcinogenesis. 1995 Nov;16(11):2685-9. PMID: 7586187Article Published Date : Nov 01, 1995Study Type : Animal Study

Additional Links

Substances : Calcium : CK(232) : AC(35)Diseases : Colon Cancer : CK(895) : AC(233)Western-Style Diet Induced Toxicity : CK(6) : AC(3)Pharmacological Actions : Antiproliferative : CK(1061) : AC(775)

[29] “Magnesium intake and colorectal tumor risk: a case-control study and meta-analysis.” Petra A WarkRosa LauTeresa Norat, and Ellen KampmanThe American Journal of Clinical Nutrition September 2012

[30]  L C Costello1, P Feng1, B Milon1, M Tan2 and R B Franklin1Prostate Cancer and Prostatic Diseases (2004) 7, 111–117. doi:10.1038/sj.pcan.4500712, “Role of zinc in the pathogenesis and treatment of prostate cancer: critical issues to resolve.”

  1. 1Department of Biomedical Sciences, Dental School, University of Maryland, Baltimore, Maryland, USA
  2. 2Division of Biostatistics, Greenebaum Cancer Center, University of Maryland, Baltimore, Maryland, USA

Correspondence: LC Costello, Department of Biomedical Sciences, Dental School/University of Maryland, 666 West Baltimore Street, Baltimore, MD 21201, USA. E-mail: lcc@dental.umaryland.edu

Received 17 December 2003; Revised 22 January 2004; Accepted 2 February 2004.

[31] Bjelakovic G, Nikolova D, Gluud LL, et al. Antioxidant supplements for prevention of mortality in healthy participants and patients with various diseases. Cochrane.Database.Syst.Rev. 2012;3:CD007176. – See more at: http://ww5.komen.org/BreastCancer/VitaminE.html#sthash.cTdPRkTA.dpuf

[32] Chalasani N, Younossi Z, Lavine JE, et al. The diagnosis and management of non-alcoholic fatty liver disease: Practice guideline by the American Association for the Study of Liver Diseases, American College of Gastroenterology, and the American Gastroenterological Association. Am.J.Gastroenterol. 2012;107(6):811-826. – See more at: http://ww5.komen.org/BreastCancer/VitaminE.html#sthash.cTdPRkTA.dpuf

[33] Cortes-Jofre M, Rueda JR, Corsini-Munoz G, et al. Drugs for preventing lung cancer in healthy people. Cochrane.Database.Syst.Rev. 2012;10:CD002141. – See more at: http://ww5.komen.org/BreastCancer/VitaminE.html#sthash.cTdPRkTA.dpuf

[34] Cancer Chemother Pharmacol. 2014 Mar;73(3):585-94. doi: 10.1007/s00280-014-2386-z. Epub 2014 Jan 23., “High-dose vitamin B1 reduces proliferation in cancer cell lines analogous to dichloroacetate.” Hanberry BS1, Berger RZastre JA.

[35]  Bareford L M, Avaritt B R, Ghandehari H, Nan A, Swaan P W (2013), “Riboflavin-targeted polymer conjugates for breast tumor delivery.” Pharm Res, 30, 1799-812.

[36] Ainiwaer J, Tuerhong A, Hasim A, et al (2013), “Association of the plasma riboflavin levels and riboflavin transporter (C20orf54) gene statuses in Kazak esophageal squamous cell carcinoma patients.” Mol Biol Rep 40, 3769-75.

[37] Bassett J K, Severi G, Hodge A M, et al (2013), “Dietary intake of B vitamins and methionine and colorectal cancer risk.” Nutr Cancer, 65, 659-67.

[38] Powers HJ (2003). Riboflavin (vitamin B-2) and health. Am J Clin Nutr, 77, 1352-60

[39] Chaves Neto A H, Pelizzaro-Rocha K J, Fernandes M N, Ferreira- Halder C V (2014). Antitumor activity of irradiated riboflavin on human renal carcinoma cell line 786-O. Tumour Biol.

[40] Powers HJ (2005). Interaction among folate riboflavin genotype and cancer with reference to colorectal and cervical cancer. J Nutr, 135, 2960-66

[41] Nutr Cancer. 2003;46(2):110-8, “Niacin and carcinogenesis.” Kirkland JB1.

[42]  Zhang SM, Moore SC, Lin J, et al (2006), “Folate vitamin B6 multivitamin supplements and colorectal cancer risk in women.” Am J Epidemiol, 163, 108-115

[43] Ma E, Iwasaki M, Kobayashi M, et al (2009), “Dietary intake of folate vitamin B2 vitamin B6 vitamin B12 genetic polymorphism of related enzymes and risk of breast cancer: a case-control study in Japan.” Nutr Cancer, 61, 447-456.

[44] Nutr Cancer. 2003;46(2):110-8, “Niacin and carcinogenesis.” Kirkland JB1.

[45) Cameron E, Pauling L (October 1976). “Supplemental ascorbate in the supportive treatment of cancer: Prolongation of survival times in terminal human cancer”PNAS 73 (10): 3685–3689. Bibcode:1976PNAS…73.3685Cdoi:10.1073/pnas.73.10.3685PMC 431183PMID 1068480.

[46] Cabanillas, F (2010). “Vitamin C and cancer: what can we conclude–1,609 patients and 33 years later?”. Puerto Rico health sciences journal 29 (3): 215–7. PMID 20799507edit

[47] Review: there is a consistently strong inverse correlations with solar UVB for 15 types of cancers, Anticancer Res. 2012 Jan ;32(1):223-36. PMID: 22213311Substances : Vitamin D : CK(1682) : AC(238)Diseases : Bladder Cancer : CK(186) : AC(60)Breast Cancer : CK(2372) : AC(660)Cervical Cancer : CK(378) : AC(69)Colon Cancer : CK(895) : AC(233)Colorectal Cancer : CK(877) : AC(321),Endometrial Cancer : CK(269) : AC(45)Esophageal Cancer : CK(328) : AC(55)Hodgkin Lymphoma : CK(53) : AC(7)Lung Cancer : CK(496) : AC(198)Non-Hodgkin Lymphoma : CK(525) : AC(67),Ovarian Cancer : CK(154) : AC(58)Pancreatic Cancer : CK(530) : AC(168)Renal Cancer : CK(25) : AC(4)Vulvar Cancer : CK(52) : AC(4)Therapeutic Actions : Sunlight exposure : CK(432) : AC(39)Pharmacological Actions : Chemopreventive : CK(1528) : AC(382)

[48] “High dose folic acid supplementation is associated with a significant reduction in the recurrence of colon cancers” World J Gastroenterol. 2008 Jul 28;14(28):4492-8. PMID: 18680228

[49} Guan D, Xu Y, Yang M, Wang H, Wang X, Shen Z. N-acetyl cysteine and penicillamine induce apoptosis via the ER stress response-signaling pathway. Mol Carcinog. 2010 Jan;49(1):68-74.

[59] Li J, Tu HJ, Dai G, et al. N-acetyl cysteine inhibits human signet ring cell gastric cancer cell line (SJ-89) cell growth by inducing apoptosis and DNA synthesis arrest. Eur J Gastroenterol Hepatol. 2007 Sep;19(9):769-74.

[51] Yang J, Su Y, Richmond A. Antioxidants tiron and N-acetyl-L-cysteine differentially mediate apoptosis in melanoma cells via a reactive oxygen species-independent NF-kappaB pathway. Free Radic Biol Med. 2007 May 1;42(9):1369-80.

[52] Krasnowska EK, Pittaluga E, Brunati AM, et al. N-acetyl-l-cysteine fosters inactivation and transfer to endolysosomes of c-Src. Free Radic Biol Med. 2008 Dec 1;45(11):1566-72.

[53] Reliene R, Pollard JM, Sobol Z, Trouiller B, Gatti RA, Schiestl RH. N-acetyl cysteine protects against ionizing radiation-induced DNA damage but not against cell killing in yeast and mammals. Mutat Res. 2009 Jun 1;665(1-2):37-43.

[54] Balansky R, Ganchev G, Iltcheva M, Steele VE, De Flora S. Prevention of cigarette smoke-induced lung tumors in mice by budesonide, phenethyl isothiocyanate, and N-acetyl cysteine. Int J Cancer. 2010 Mar 1;126(5):1047-54.

[55] Nishikawa-Ogawa M, Wanibuchi H, Morimura K, et al. N-acetyl cysteine and S-methylcysteine inhibit MeIQx rat hepatocarcinogenesis in the post-initiation stage. Carcinogenesis. 2006 May;27(5):982-8.

[56] Van Schooten FJ, Besaratinia A, De Flora S, et al. Effects of oral administration of N-acetyl-L-cysteine: a multi-biomarker study in smokers. Cancer Epidemiol Biomarkers Prev. 2002 Feb;11(2):167-75.

[57] Ponz de Leon M, Roncucci L. Chemoprevention of colorectal tumors: role of lactulose and of other agents. Scand J Gastroenterol Suppl. 1997;222:72-5.

[58] Estensen RD, Levy M, Klopp SJ, et al. N-acetyl cysteine suppression of the proliferative index in the colon of patients with previous adenomatous colonic polyps. Cancer Lett. 1999 Dec 1;147(1-2):109-14.

[59] Cascinu S, Cordella L, Del Ferro E, et al., “Neuroprotective effect of reduced glutathione on cisplatin-based chemotherapy in advanced gastric cancer: a randomized double-blind placebo-controlled study.” J Clin Oncol. 1995; 13:26-32.

[60] Hercbergs A, Brok-Simoni F, Holtzman F, et al., “Erythrocyte glutathione and tumor response to chemotherapy.”  Lancet. 1992; 339:1074-1076.

[61] Schmidinger M, Budinsky AC, Wenzel C, et al., “Glutathione in the prevention of cisplatin induced toxicities. A prospectively randomized
pilot trial in patients with head and neck cancer and non small cell lung cancer.” Wien Klin Wochenschr. 2000; 112:617-623.

[62] Smyth JF, Bowman A, Perren T, et al., “Glutathione reduces the toxicity and improves quality of life of women diagnosed with ovarian cancer treated with cisplatin: results of a double-blind, randomized trial.” Ann Oncol. 1997; 8:569-573.

[63] (Robert O. Young, Ph.D., D.Sc., ND and Shelley Redford Young, LMT) “The pH Miracle revised and updated,”Hachett Publishing, Boston, USA, June, 2010.

[64] Robert O. Young, Ph.D., D.Sc., ND and Shelley Redford Young, LMT, The pH Miracle for Cancer,” Hikari Omni Publishing, Valley Center, California, September, 2015.

[65] Galina Migalko, MD, ND, Universal Medical Imaging Group, Valley Village, California, http://www.universalmedicalimaging,com

[66] Reference Studies: Niels Fough-Anderson, Burton M, Attura, BElla T. Attura, Ole Siggard-Andersen, Clinical Chemistry, 41/10, 1522-1525, (1995)

[67] Gilariyi M., Bcriyi C., Fekete J, Ikreriyi K., Kovach AGB, “Ion Concentration in Subcutaneous Interstitial Fluid Measured versus Expected Values.” AMJ of Physiololgy 1988.

– See more at: www.phoreveryoung.com

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
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
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: www.phoreveryoung.com or www.phmiracle.com

Drinking Coffee Causes Heart Disease, Cancer and Many Other Serious Dis-Ease Conditions!

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The United States buys nearly one-half of the world’s supply of coffee beans. It is said that a food service operation can stand or fall on its reputation of the coffee it serves. Every mid-morning and mid-afternoon working day millions of office and factory workers abandon jobs for an employer-paid “coffee break.”

Over 15 million Americans are coffee addicts, and most of them don’t even know it, so insidious is its addictive onslaught. The child or adult may unknowingly ingest several hundred milligrams of caffeine daily.

Like narcotics, alcohol, or cigarettes, coffee and caffeinated beverages are addictive, destructive drugs that each year predispose millions of Americans to crippling illnesses and sometimes fatal diseases.

Coffee and black tea are the two most popular beverages in America. Coffee is America’s number one addictive drug problem leading to hypertension, hypercholesterolemia, and other heart dis-ease problems.

Caffeine Withdrawal

Caffeine withdrawal can occur from missing just one cup of coffee in the morning. Symptoms of caffeine withdrawal are headaches, irritability, inability to work effectively, nervousness, restlessness, and lethargy. A steady user of caffeine may, at times, experience tight headaches in the back of the neck area and be quick to anger or irritation.

Caffeine Acts as a Stimulant

Caffeine is a toxic acidic stimulant. This is not natural for the body. It activates the “fight or flight” response.

It’s important to remember that the caffeine in coffee is a powerful substance. It can stimulate the central nervous system, increase heartbeat and metabolic rate, increase the secretion of stomach sodium bicarbonate, and step up kidney and bladder action. It’s also well known for its annoying ability to affect sleep.i

At higher doses, caffeine can cause “coffee nerves”—a wide assortment of symptoms including anxiety, irritability, headaches, light-headedness, nausea, and diarrhea.

Coffee can cause a temporary increase in blood sugar, but it is quickly followed by a decrease, and stimulates the release of adrenaline, which causes body tissues to be broken down into sugar giving rise to high blood sugar associated with diabetes. Too much insulin is produced, and the blood sugar falls to a low level.

Caffeine is an Acidic Poison

Caffeine, which is the main chemical in coffee, is a powerful poison! A drop of caffeine injected into the skin of an animal will produce death within a few minutes. An infinitely small amount injected into the brain will cause convulsions. The amount of caffeine in a cup of coffee is quite small, yet people drink coffee because of the effect of the caffeine, just as people  smoke because of the effect of the nicotine. Both are drugs, and both are habit-forming.  Both are poisons.  And both will eventually kill you by causing heart failure or a cancerous conditions.

Coffee Drinking and Stomach Ulcers

The general public usually associates ulcers and heart trouble with coffee drinking. J.A. Roth and A.C. Ivy, whose experiments on coffee are famous, state this:

“Caffeine produces gastro-duodenal ulcers in animals to whom the drug is given in a beeswax container so that their stomachs are absorbing caffeine continually. Also, caffeine produces very definite changes in the blood vessels of animals, which are similar to changes produced by prolonged resentment hostility and anxiety.”

Coffee Linked to Hip Fractures

“People who drink more than two cups of coffee or four cups of black or green tea a day could be increasing their risk of hip fracture in old age, according to a new study.”  The study, published in the October issue of the American Journal of Epidemiology, is the first to link caffeine consumption with hip fractures that occur in older people whose bones have weakened. A hip fracture often marks an elderly person’s final decline into dependency or death.

Brown University’s Dr. Douglas P. Kiel and his colleagues looked at how much coffee or tea 3170 people reported drinking over 14 years. They then looked to see which ones fractured their hips, a sign that bones had become brittle. They found that heavy caffeine drinkers were 53% more likely to suffer hip fractures.

Infertility

Trying to become pregnant? Stop drinking caffeinated drinks. Among 104 women, those who drank just one cup of caffeinated coffee a day were half as likely to become pregnant during any given menstrual cycle as those who drank less, according to a 1988 study by Allen Wilcox of the National Institute of Environmental Health Sciences.

Most of the studies conducted since then have also found that caffeine impairs fertility, but usually only at three or more cups of regular coffee a day.

But the research is only as good or bad as the women’s memories. For example, scientists at John Hopkins University found that among 2500 women who were trying to become pregnant, consuming more than 300 mg of caffeine a day reduced their chances of succeeding in any given month by 17%. But those results were based on the amount of coffee and soft drinks the women could remember having consumed as many as ten years earlier.

Even so, “it’s probably prudent for women who are trying to become pregnant, and especially for those having trouble, to cut back on caffeine,” says Mark Klebanoff of the National Institute of Child Health and Human Development in Bethesda, Maryland.

Does Coffee Cause Heart Disease and  Cancer?

There is mounting evidence suggesting that if you want to avoid certain heart and cancerous conditions, you are well-advised to kick the coffee habit. Consider these examples:

One study revealed that not only was coffee drinking associated with increased risk of bladder cancer, but the drinking of non-diet cola drinks also was linked to this problem.

Coffee drinking increases the risk of birth defects.

Coffee drinking increases blood pressure, increasing the risk of heart disease.

It is commonly thought that the drinking of coffee, soft drinks, and other caffeinated drinks is a minor matter as far as our health is concerned. But is it?  We cannot estimate its effect on mind and emotions, discrimination, and judgment.  And then there are the harmful effects of the stimulation on the heart and other vital organs.

Coffee and other caffeinated beverages are poor substitutes for water. The body needs alkaline fluids, but not stimulating drugs. Giving up the coffee and tea habit is relatively easy to do for most folks—once a commitment has been made. Since caffeine is a less toxic drug than alcohol or street drugs, the majority of coffee and tea drinkers can give up the habit without the sort of difficulties that alcoholics and drug addicts typically experience.

When giving up caffeine, eat and drink only what contributes in some way to good alkaline nutrition for the body. Any food or drink that does not contain alkalizing chlorophyll, oil, water, salts, vitamins, or minerals, should automatically be crossed off the list. While breaking the coffee, tea, cola, energy drink habit, be sure to drink plenty of fresh alkaline green juices and alkaline water at a pH of at least 9.5.

Just how widespread is coffee, tea, soda drinking? The average American drinks over twenty-six gallons of coffee, tea and cola drinks per year, but perhaps more germane to the discussion is caffeine itself.  Coffee has over three hundred chemicals; caffeine is only one of them.

23  Reasons to NEVER Drink Coffee Again!

1. Methyl parathion

This is the most toxic pesticide of all. It is  is highly toxic to humans, birds, fish, and mammals. It’s used to fight leaf miner infestations. Leaf miners are insects that eat at leaves of plants.  Despite how dangerous it is, it’s still (mis)used in some countries.

2. Endosulfan

This pesticide is used against coffee cherry borer, a common coffee consuming bug. It’s doesn’t dissolve easily and takes ages to break down in soil and is toxic to most animals. It affects the central nervous system, reproductive organs, kidneys, and liver, and is considered to be worse than the pest itself; it’s even been responsible for human death!

3. Chlorpyrifos

This is also used against common coffee pests and has been banned in the US for household use because it has caused human death and birth defects. Needless to say, it’s quite detrimental to delicate ecosystems.

4. Triadimefon

Copper-based fungicide used to against coffee rust. Only slightly toxic to birds, little is known about its effect on humans, but it is suspected that there is potential for reproductive problems with chronic exposure.  (Like people who drink coffee every day.) It has been found to induce hyperactivity in rats. The major concern is that long-term use of this and other copper-based fungicides is copper accumulation in soils, such as that found in coffee farms in Kenya and in Costa Rica.  Copper toxicity has been found in other crops grown in these soils, and copper impacts other biochemical and biological processes in soil which will poison people eating these crops not to mention the people who drink coffee.

5. Caffeine

One 8-ounce cup of coffee has 95 milligrams of caffeine and a 1-ounce single shot of espresso has 64 milligrams. Consuming too much caffeine can make you restless, anxious, irratable and then dead.  Caffeine is an acid or oxidant poison with a pH of 5.5 and an oxidative reduction pH of over +250 mV. When you drink a cup of coffee the body reacts to the poisons in the coffee and you feel it as adrenalin rush as the body starts releasing alkaline buffers to neutralize the poison or the caffeine acid.  It only takes 3 cups of coffee or acid to go into potential caffeine intoxication or 300mg which can cause a cardiac arrest.  One drop of pue caffeine or 2 grams of caffeine powder will kill you instantly.

6. pH

Coffee has a perfect pH for cancerous cells 5.5. Research at the Brigham Young University showed that you can keep cancer cells alive indefinitely in a cup of coffee.

7. Oxidative Reduction Potential or ORP

Coffee is NOT an antioxicant but an oxidant which acitivates the alkaline buffering system and depletes your body of alkalizing minerals such as sodium bicaronatea and potassium bicaronate.

8.  Stomach

Because coffee an acid beverage it causes the stomach to produce sodium bicarbonate which increases the hydrochloric acid in the stomach leading to acid reflux, GERD, ulcers and stomach cancer.

9.  Damages Cover Cells of the Stomach

Coffee is a hot beverage and any hot beverage will damage the cover cells of the stomach which cells produce sodium bicarbonate for maintaining the alkaline design of all the body fluids.

10.  Stimulate

Coffee is saturated with hydrogen ions or protons and thus steals energy from your body making you more tired after the stimulating effects wear-off.  This creates the addiction for more coffee in order to achieve an energy increase or buzz.  Continued use of coffee leads to enervation then irritation, then inflammation, then ulceration and finally degeneration or cancer.

11.  Cafestol

Coffee increases the level of cholesterol. Why? Because coffee contains an acid substance called cafestol which triggers the rise of cholesterol levels. The cafestol blocks a receptor in an intestinal pathway crucial for cholesterol regulation, and is the most potent food chemical to do this.   Increased amounts of this acid will increase cholesterol for the purpose of buffering and maintaining the alkaline design of the body.

12.  Intestinal Villi Damage

Coffee compromises the alkalinity of the small intestine at a pH of 8.4.  This causes the intestinal villi to lie down preventing the biological transformation of food or chyme into stem cells which takes place in the crypts of the intestinal villi.   This leads to lowered blood counts, improper blood cell formation and symptoms anemia, pernicious anemia, and hemolytic anemia.  Coffee also damages the intestinal villi leading to more serious conditions such as proper bone, muscle and organ regeneration.

13. Cancer

Coffee contains over 1000 chemicals of which only 22 have been studied leaving 978 left to study.  All of the chemicals studied to date have been found to be carcinogentic.  So next time to pick up that cup of coffee think of it as your cup of cancer.

14.  Sugar and Cream

Add the sugar and cream and you just created one toxic and addictive acidic/poisonous beverage.

15. Heart Disease –

There is controversial scientific evidence linking coffee consumption to heart diseases. Some studies even state that “consumption is associated with significantly increased risk of cardiovascular disease.” These same studies have shown a cholesterol-raising effect in some of the chemical compounds of coffee, such as determines, cafestol, kahweol and plasma homocysteine. This may be of-set by some of the antioxidants, but the overall agreement is that coffee may adversely effect the heart.

16. Blood Vessels

Coffee disturbs the functioning of blood vessels, both in turgidity and tone.

17. Cardiovascular System

Coffee affects our nervous system, heart rhythms and has been consistently linked to irregular heartbeats. It may also adversely affect blood pressure.

18. Osteoporosis

Coffee drinking should be heavily avoided by people at risk, or who have Osteoporosis. Studies show a link between drinking coffee and urinary calcium excretion.

19.  Heartburn

Many people report that coffee increases heartburn.

20.  Sleep Disturbance

Coffee, particularly in the evening or at night, can lead to sleep disturbance.

21. Dehydration 

Drinking coffee depletes water reserves in the body.

22. Addiction 

While the FDA recognizes caffeine as “safe,” it is still a drug, as it significantly alters the nervous system, leading to addiction

over time.

23. Extreme Withdrawal Symptoms

You may experience withdrawal symptoms when you try to give up coffee. This can lead to headaches, irritability, body aches, and other more extreme symptoms.

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Coffee beans are green and alkaline on the tree until they are fermented and spoiled rotten to a brownish black acidic,  heart dis-ease causing color.

For more information, check out these references:

Charles F. Wetherall, Kicking The Coffee Habit, Wetherall Publ. Co. MN.

Andrew Weil, MD & Winifred Rosen, Chocolate To Morphine, Houghton Mifflin Co., Boston, Mass.

Mervyn G. Hardinge, MD, A Philosophy of Health, Loma Linda University, CA.


1. Executive Fitness Newsletter (October 13, 1984).

2. Gastroenterology (November, 1948).

3. Providence Journal (October 1, 1990).

4. Carol Simontacchi, The Crazy Makers (New York: Tarcher, 2001).

Ten Acidic Signs That Your Liver is Toxic and Sick!

liver-disease-s1a-did-you-knowLiver disease is any disturbance of liver function that causes illness. The liver is responsible for many critical functions within the body and should it become dis-eased or injured, the loss of those functions can cause significant damage to the body.  Liver dis-ease is also referred to as hepatic dis-ease.

Liver dis-ease is a broad term that covers all the potential problems that cause the liver to fail to perform its designated functions. Usually, more than 75% or three-quarters of liver tissue needs to be affected before a decrease in function occurs.

The liver is the largest solid organ in the body; and is also considered a gland because among its many functions, it makes and secretes an alkaline substance called bile. The liver is located in the upper right portion of the abdomen protected by the rib cage. It has two main lobes that are made up of tiny lobules. The liver cells have two different sources of blood supply. The hepatic artery supplies oxygen rich blood that is pumped from the heart, while the portal vein supplies alkalizing minerals from the large intestine and the spleen.

Normally, veins return blood from the body to the heart, but the portal vein allows alkaline minerals from the large intestines to enter the liver for “detoxification” and filtering prior to entering the general circulation. The portal vein also efficiently delivers minerals and fats that liver cells need to produce the proteins, cholesterol, and electrons required for normal body activities.

There are several early signs of  an acidic liver to understand in order to protect the liver and its many functions from sickness and dis-ease.
Without a fully functioning liver,  your health and wellbeing will be compromised.  Fortunately your liver is capable of repairing and renewing itself every six weeks.  Understanding the following acidic liver conditions and spotting them early,  will help to prevent and/or reverse a serious life-threatening degenerative live dis-ease.

livertoxicity

Warning Sign # 1 – Skin discoloration – Jaundice

One of the early signs of excess liver acidity and the beginning of liver dis-ease is the liver’s inability to filter out all of the dietary and/or metabolic toxins from the blood.  With a build-up of toxins this may also lead to a build-up of Bilirubin which is a breakdown product of the blood.  The breakdown of the blood which increases bilirubin is caused by an acidic lifestyle, diet, congested liver and gallbladder and constipation of the elimination organs,  The body and specifically the gallbladder uses bile  to help alkalize the food ingested coming out of the stomach.  When the body cannot evacuate Bilirubin from the liver/gallbladder and blood via the bowels, it will accumulate in the bloodstream and results in the skin taking on a yellowish hue.  This yellowing can also affect the fingernails, the tips of the fingers, and especially the eyes. This acidic condition caused by an acidic lifestyle and diet is known as Jaundice.  Read, share and like more:

Continue reading Ten Acidic Signs That Your Liver is Toxic and Sick!

Research Study Suggests that Radiation and Chemotherapy Can Make Cancers 30x More Malignant

RadiationTherapy

Following on the heels of recent revelations that x-ray mammography may be contributing to an epidemic of future radiation-induced breast cancers, in a new article titled, “Radiation Treatment Generates Therapy Resistant Cancer Stem Cells From Aggressive Breast Cancer Cells,” published in the journal Cancer July 1st, 2012, researchers from the Department of Radiation Oncology at the UCLA Jonsson Comprehensive Cancer Center report that radiation treatment actually drives breast cancer cells into greater malignancy.

Continue reading Research Study Suggests that Radiation and Chemotherapy Can Make Cancers 30x More Malignant

A Self-Care to a Self-Cure for Terminal Metastatic Breast, Lung, Liver, Lymphatic, Lymph and Bone Cancer!

Watch the following YOUTUBE Video of Catherine Livingston sharing her incredible life-changing and life-saving Metastatic Cancer Reversal story!

Catherine Livingstone was diagnosed with breast cancer in 2011 that metastasized to her lungs, liver, lymphatic system. lymph nodes and bone. She was given only 2 months to live in 2012. She started the pH Miracle Lifestyle and Diet!  It is now June, 2015 and she is in complete remission with NO CANCER in the lungs (over 25 tumors), NO CANCER in the liver (the liver was full of tumors with to many to count), NO CANCER in the lymph nodes, NO CANCER in the bones and in fact NO CANCER anywhere in her body. Catherine is healthy, happy and NOW CANCER FREE living the pH Miracle Lifestyle and Diet!

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In her own words, “I intend to live a long and healthy life free from cancer thanks to the pH Miracle lifestyle.”

To learn more read The pH Miracle book 1, The pH Miracle revised and updated book 2, Reverse Cancer NOW!, The pH Miracle for Cancer, and Sick and Tired by Dr. Robert O. Young – www.phoreveryoung.com, www.phmiracle.com, www.amazon.com and www.barnesandnoble.com

Support Dr. Robert O. Young and his fight for Health Freedom to choose your health care, your own doctor and your own treatment whether it be conventional, traditional or integrated!

http://www.phmiracleliving.com/t-Innerlight-Foundation.aspx

Share Dr. Robert O. Young and his revolutionary life-changing and life-saving research with all those who you love and care about at:

www.phoreveryoung.comwww.phoreveryoung.wordpress.comwww.linkedin.com/in/drrobertoyounghttps://www.facebook.com/groups/50864627953/https://business.facebook.com/Dr.Robert.O.Young…, https://business.facebook.com/ThepHMiracle…, https://business.facebook.com/ThepHMiracle…, https://twitter.com/drrobertyoungwww.youtube.com/watch?v=phmiraclecenterwww.pinterest.com/drrobertyounghttps://plus.google.com/+RobertYoung555http://www.myspace.com/drrobertoyoungwww.phmiracle.comwww.phmiracleliving.com
www.phoreveryoung.com and www.phoreveryoung.wordpress.com

The Research Validating That The Ingredients in Vaccines Cause Cancer!

SV40, an ingredient found in vaccines is Associated with Causing Different Cancerous Conditions! 

Senior Medical - Vaccination

Below are types of human cancers in which SV40 has been found. By clicking on the name, you will link to some study abstracts that provides additional details. Please note that this is not a comprehensive list of all SV40-associated cancers or all medical/scientific articles written about the detection of SV40 in cancer.

Brain Cancers
Bone Cancers
Chest Cancers
Lymphomas
Thyroid Cancers

Astrocytomas

Huang H., et al. Identification in human brain tumors of DNA sequences specific SV40 large T antigen. Brain Pathol 1999 Jan;9(1):33-42.

Zhen H.N., et al. Expression of the simian virus 40 large tumor antigen (Tag) and formation of Tag-p53 and Tag-pRb complexes in human brain tumors. Cancer 1999 15;86(10):2124-32.

Martini, F., et al. Simian Virus 40 Footprints in Normal Human Tissues, Brain and Bone Tumours of Different Histotypes; 1997. Brown F, Lewis AM (eds): Simian Virus 40 (SV40): A Possible Human Polyomavirus. Dev Biol Stand. Basel, Karger, 1998, vol 94, pp 55-66.

Krieg, P., et al. Episomal simian virus 40 genomes in human brain tumors Proc Natl Acad sci USA 1981 Oct;78(10):6446-50.

Anaplastic Astrocytoma

Huang H., et al. Identification in human brain tumors of DNA sequences specific SV40 large T antigen. Brain Pathol 1999 Jan;9(1):33-42.

Choroid Plexus Papilloma

Huang H., et al. Identification in human brain tumors of DNA sequences specific SV40 large T antigen. Brain Pathol 1999 Jan;9(1):33-42.

Zhen H.N., et al. Expression of the simian virus 40 large tumor antigen (Tag) and formation of Tag-p53 and Tag-pRb complexes in human brain tumors. Cancer 1999 15;86(10):2124-32.

Martini, F., et al. Simian Virus 40 Footprints in Normal Human Tissues, Brain and Bone Tumours of Different Histotypes; 1997. Brown F, Lewis AM (eds): Simian Virus 40 (SV40): A Possible Human Polyomavirus. Dev Biol Stand. Basel, Karger, 1998, vol 94, pp 55-66.

Wang, J and Garcea R.L., et al, Simian virus 40 DNA sequences in human brain and bone tumours. Brown F, Lewis AM (eds): Simian Virus 40 (SV40): A Possible Human Polyomavirus. Dev Biol Stand. Basel, Karger, 1998, vol 94, pp 13-21.

14 of 17 pediatric brain tumors (13 choroid plexus tumors, 3 ependymomas and 1 ganglioneuroma) were positive for SV40 regulatory region sequences. Butel, J.S., et al. Detection of authentic SV40 DNA sequences in human brain and bone tumors Brown F, Lewis AM (eds): Simian Virus 40 (SV40): A Possible Human Polyomavirus. Dev Biol Stand. Basel, Karger, 1998, vol 94, pp 23-32.

Lednicky, et al., Natural simian virus 40 strains are present in human choroid plexus and ependymoma Virology. 1995 Oct 1;212(2):710-7. tumors.

Ependymoma

Huang H., et al. Identification in human brain tumors of DNA sequences specific SV40 large T antigen. Brain Pathol 1999 Jan;9(1):33-42.

Zhen H.N., et al. Expression of the simian virus 40 large tumor antigen (Tag) and formation of Tag-p53 and Tag-pRb complexes in human brain tumors. Cancer 1999 15;86(10):2124-32.

Martini, F., et al. Simian Virus 40 Footprints in Normal Human Tissues, Brain and Bone Tumours of Different Histotypes; 1997. Brown F, Lewis AM (eds): Simian Virus 40 (SV40): A Possible Human Polyomavirus. Dev Biol Stand. Basel, Karger, 1998, vol 94, pp 55-66.

Wang, J and Garcea R.L., et al, Simian virus 40 DNA sequences in human brain and bone tumours. Brown F, Lewis AM (eds): Simian Virus 40 (SV40): A Possible Human Polyomavirus. Dev Biol Stand. Basel, Karger, 1998, vol 94, pp 13-21.

14 of 17 pediatric brain tumors (13 choroid plexus tumors, 3 ependymomas and 1 ganglioneuroma) were positive for SV40 regulatory region sequences. Butel, J.S., et al. Detection of authentic SV40 DNA sequences in human brain and bone tumors Brown F, Lewis AM (eds): Simian Virus 40 (SV40): A Possible Human Polyomavirus. Dev Biol Stand. Basel, Karger, 1998, vol 94, pp 23-32.

Lednicky, et al., Natural simian virus 40 strains are present in human choroid plexus and ependymoma Virology. 1995 Oct 1;212(2):710-7. tumors.

Gemistocytic Astrocytoma

Huang H., et al. Identification in human brain tumors of DNA sequences specific SV40 large T antigen. Brain Pathol 1999 Jan;9(1):33-42.

Glioblastoma

Huang H., et al. Identification in human brain tumors of DNA sequences specific SV40 large T antigen. Brain Pathol 1999 Jan;9(1):33-42.

Zhen H.N., et al. Expression of the simian virus 40 large tumor antigen (Tag) and formation of Tag-p53 and Tag-pRb complexes in human brain tumors. Cancer 1999 15;86(10):2124-32.

Martini, F., et al. Simian Virus 40 Footprints in Normal Human Tissues, Brain and Bone Tumours of Different Histotypes; 1997. Brown F, Lewis AM (eds): Simian Virus 40 (SV40): A Possible Human Polyomavirus. Dev Biol Stand. Basel, Karger, 1998, vol 94, pp 55-66.

Krieg, P., et al. Episomal simian virus 40 genomes in human brain tumors Proc Natl Acad sci USA 1981 Oct;78(10):6446-50.

Gliosarcoma

Huang H., et al. Identification in human brain tumors of DNA sequences specific SV40 large T antigen. Brain Pathol 1999 Jan;9(1):33-42.

Medulloblastoma

Huang H., et al. Identification in human brain tumors of DNA sequences specific SV40 large T antigen. Brain Pathol 1999 Jan;9(1):33-42.

Zhen H.N., et al. Expression of the simian virus 40 large tumor antigen (Tag) and formation of Tag-p53 and Tag-pRb complexes in human brain tumors. Cancer 1999 15;86(10):2124-32.

Krieg, P., et al. Episomal simian virus 40 genomes in human brain tumors Proc Natl Acad sci USA 1981 Oct;78(10):6446-50.

Meningioma

Zhen H.N., et al. Expression of the simian virus 40 large tumor antigen (Tag) and formation of Tag-p53 and Tag-pRb complexes in human brain tumors. Cancer 1999 15;86(10):2124-32.

Krieg, P., et al. Episomal simian virus 40 genomes in human brain tumors Proc Natl Acad sci USA 1981 Oct;78(10):6446-50.

Weiss A.F., et al. Simian virus 40-related antigens in three human meningiomas defined chromosome loss Proc Natl Acad Sci USA 1975 Feb;72(2):609-13.

Oligodendroglioma

Huang H., et al. Identification in human brain tumors of DNA sequences specific SV40 large T antigen. Brain Pathol 1999 Jan;9(1):33-42.

Krieg, P., et al. Episomal simian virus 40 genomes in human brain tumors Proc Natl Acad sci USA 1981 Oct;78(10):6446-50.

Pituitary Adenoma

Zhen H.N., et al. Expression of the simian virus 40 large tumor antigen (Tag) and formation of Tag-p53 and Tag-pRb complexes in human brain tumors. Cancer 1999 15;86(10):2124-32.

Osteosarcoma

Martini, F., et al. Simian Virus 40 Footprints in Normal Human Tissues, Brain and Bone Tumours of Different Histotypes; 1997. Brown F, Lewis AM (eds): Simian Virus 40 (SV40): A Possible Human Polyomavirus. Dev Biol Stand. Basel, Karger, 1998, vol 94, pp 55-66.

Wang, J and Garcea R.L., et al, Simian virus 40 DNA sequences in human brain and bone tumours. Brown F, Lewis AM (eds): Simian Virus 40 (SV40): A Possible Human Polyomavirus. Dev Biol Stand. Basel, Karger, 1998, vol 94, pp 13-21.

Ewing’s Tumors

Martini, F., et al. Simian Virus 40 Footprints in Normal Human Tissues, Brain and Bone Tumours of Different Histotypes; 1997. Brown F, Lewis AM (eds): Simian Virus 40 (SV40): A Possible Human Polyomavirus. Dev Biol Stand. Basel, Karger, 1998, vol 94, pp 55-66.

Mesothelioma

Cristaudo A, et al., SV40 enhances the risk of malignant mesothelioma among people exposed to asbestos: a molecular epidemiologic case-control study. Cancer Res. 2005 Apr 15;65(8):3049-52.

Pass HI, et al., Evidence of an important role for SV40 in mesothelioma. Thorac Surg Clin. 2004 Nov;14(4):489-95.

Carbone M, et al., New developments about the association of SV40 with human mesothelioma. Oncogene. 2003 Aug 11;22(33):5173-80.

Non-Hodgkins Lymphoma

Vilchez RA, et al., Simian virus 40 tumor antigen expression and immunophenotypic profile of AIDS-related non-Hodgkin’s lymphoma. Virology. 2005 Nov 10;342(1):38-46.

Butel JS, et al., Association between SV40 and non-Hodgkin’s lymphoma. Leuk Lymphoma. 2003;44 Suppl 3:S33-9.

Papillary Thyroid Carcinomas

Vivaldi, et al., Simian virus 40-like sequences from early and late regions in human thyroid tumors of different histotypes. J Clin Endocrinol Metab. 2003 Feb;88(2):892-9.

Anaplastic Thyroid Carcinomas (ATC)

Vivaldi, et al., Simian virus 40-like sequences from early and late regions in human thyroid tumors of different histotypes. J Clin Endocrinol Metab. 2003 Feb;88(2):892-9.

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