The Phenomena of Male Microchimerism in Women and Homosexual Men!

DID YOU KNOW?

Women (or homosexual men) absorb and carry living DNA and cells from every male they have ever had sexual intercourse with. In fact, anyone who has consumed male spermatozoa into their bodily system has the living anatomical elements and genetic energetic imprint/signature of each individual whose sperm they have consumed or received IN ANY WAY.

This phenomena is called “Male Microchimerism”
Microchimerism is the harboring of a small number of cells that have originated in a genetically different animal or human.

When scientists autopsied the brains of women who had never  been pregnant researchers  found male DNA prevalent in the female brain.

CONCLUSIONS:

Male microchimerism was not infrequent in women without sons. Besides known pregnancies, other possible sources of male microchimerism include unrecognized spontaneous abortion, vanished male twin, an older brother transferred by the maternal circulation, or SEXUAL INTERCOURSE. Male microchimerism was significantly more frequent and levels were higher in women with induced abortion than in women with other pregnancy histories. Further studies are needed to determine specific origins of male microchimerism in women and homosexual men.

The current research has very important ramifications for women and homosexual men. Especially promiscuous women or homosexual men who practice unprotected sexual intercourse. Every male you have sexual relations you will absorb spermatazoa and that spermatozoa will become a living part of your FOR LIFE. The women autopsied in the following study were elderly. Some had carried the living male DNA for well over 50 years!

Spermatazoa contains living anatomical elements. When it is impregnated into the human body it swims, attaches and burrows into  tissues, organs and glands. If its in your mouth it swims and climbs into your nasal passages, inner ear, and behind your eyes. Then digs in. It enters your blood-stream and collects in your brain and spine.

The male DNA can also pass into and becomes part of a fetus from an entirely different male. So if your girlfriend or spouse has a long track record with other men, then it is highly probable your kids will carry the DNA from her past relationships.

Is this why the ancient Prophets specifically said it was forbidden to have premarital sex? Is this why they also forbid homosexuality?

We have only begun to understand the power and ramifications of male microchimersim in women and homosexual men.

To read and learn more about male microchimerism go to the following links:

Male microchimerism in women without sons: quantitative assessment and correlation with pregnancy history
http://www.ncbi.nlm.nih.gov/m/pubmed/16084184/

Male microchimerism was not infrequent in women without sons. Besides known pregnancies, other possible sources of male microchimerism include unrecognized spontaneous abortion, vanished male twin, an older brother transferred by the maternal circulation, or sexual intercourse. Male microchimerism was significantly more frequent and levels were higher in women with induced abortion than in women with other pregnancy histories. Further studies are needed to determine specific origins of male microchimerism in women.

Women absorb and carry living DNA and cells from every male they have sexual intercouse with
http://www.godlikeproductions.com/forum1/message2299543/pg1

Male Microchimerism in the Human Female Brain
” In conclusion, male microchimerism is frequent and widely distributed in the human female brain.”
http://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0045592#pone.0045592-Lambert1

In humans, naturally acquired microchimerism has been observed in many tissues and organs. Fetal microchimerism, however, has not been investigated in the human brain. Microchimerism of fetal as well as maternal origin has recently been reported in the mouse brain. In this study, we quantified male DNA in the human female brain as a marker for microchimerism of fetal origin (i.e. acquisition of male DNA by a woman while bearing a male fetus). Targeting the Y-chromosome-specific DYS14 gene, we performed real-time quantitative PCR in autopsied brain from women without clinical or pathologic evidence of neurologic disease (n = 26), or women who had Alzheimer’s disease (n = 33). We report that 63% of the females (37 of 59) tested harbored male microchimerism in the brain. Male microchimerism was present in multiple brain regions. Results also suggested lower prevalence (p = 0.03) and concentration (p = 0.06) of male microchimerism in the brains of women with Alzheimer’s disease than the brains of women without neurologic disease.

In conclusion, male microchimerism is frequent and widely distributed in the human female brain.