Fetal micro-chimerism: the Forever Connection between our Lord & our Immaculate Mother Mary

Introduction. In pregnancy, fetal and maternal circulation systems are not separate. Normally, there is 2-way cell traffic through the placenta. This inter-person highway is called the transplacental passage. Moreover, mothers store living fetal cells from every biological child. Even after her death, a mother's circulation contains fetal cells. Proof exists in both human and animal-model, post-mortem exams. This phenomenon is known as fetal micro-chimerism or FMc.

The purpose of this article is to explore FMc, advantages and complications. What are implications in the post-abortive mother? What are implications with foreign DNA i.e. surrogacy, in vitro fertilization (IVF) or rent-a-womb programs? What are implications with foreign RNA, i.e. inoculations? Please see box for DNA and RNA differences. Most important, what are Divine implications in Mother Mary from the bearing of Our Lord Jesus Christ?

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How does DNA and RNA differ?

At the risk of oversimplification, below are 4 major contrasts.

Bases: DNA uses thymine while RNA uses uracil.
Sugars: DNA uses deoxyribose while RNA uses ribose.
Structure: DNA is double-stranded, usually, while RNA is single-stranded.
Function: DNA stores genetic blueprints while RNA transmits instructions for building.
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Definition. Chimerism is defined as one human or mammal possessing 2 sets of DNA. Fetal micro-chimerism is where a mother stores micro-amounts of fetal stem cells from each biological offspring. Each child leaves behind small amounts of fetal cells in their mother. Storage may occur in any tissue, hollow or solid organ. This normal phenomenon occurs in every pregnancy to include miscarriages and abortions. However, complications arise with rent-a-womb, surrogacy or IVF programs. These introduce non-related DNA; sometimes more than 2 sets. Exposure to multiple foreign DNA is interpreted by the body as a threat. Similarly with mRNA inoculations, exposure to the foreign RNA may be interpreted by the body as a threat. This explains why Transfusion and Transplantation Medicine--organ and bone marrow--match donor and recipients' histology with painstaking accuracy. It also explains why mismatch recipients take anti-rejection medications for life.

Advantages. The many FMc advantages may explain why women live longer. In both human and animal data, FMc cells will repair their mom's tissue damage especially upon injury. Fetal stem cells offer extra immunity, since half of paternal DNA is buried within fetal stem cells. Fetal stem cells carry anti-cancer properties. Overall, FMc plays an essential role in maternal pathophysiology. In His brilliance, God's reasons are veiled but someday all will be revealed. Even after abortions, God uses fetal cells to heal and support their Mama until her death. How is that for God's love?

Disadvantages. Problems occur with DNA overexposures and breaches. For example, what if you are transfused with the wrong blood type? This could be an existential threat. Without immediate intervention, signs of shock will appear. Mixing some ABO blood types, not all, and Rh factors are incompatible with life. If the blood donor is a woman who has been pregnant, there may be other incompatible, fetal cell-specific properties. To show their respect for God's handiwork, Jehovah's witnesses refuse blood transfusions. Blueprints and building instructions are unique. If respected. God can work His magic in our bodies.

After tissue breaches and overexposure, foreign cells reside wherever they land, all body parts, even the brain. This may explain how autoimmune diseases develop. Auto means self. Auto-immune diseases are when the immune system attacks the self. Examples of auto-immune diseases are lupus, rheumatoid arthritis, certain diabetes types, pancreatitis, etc. In auto-immune diseases, no one knows why the attacks occur. Often viruses are blamed. Perhaps, an established deposit of someone's DNA or RNA is housed in the targeted organ? The good news is that chimerism is studied closely today. Transplant medicine studies tissue mismatches, to fine-tune doses of anti-rejection medicines, which are needed for the daily survival of their patients.

Rent-a-womb, surrogacy and IVF programs may expose both mom and baby to multi-sourced DNA, hence all have risks. With exposures and breaches, we can theorize that these souls will face higher rates of miscarriage, histological incompatibilities and auto-immune diseases. Who is counting the number of DNA sets used in each case?

Immaculate Mary & our Lord Jesus Christ. God and sin are incompatible. To be chosen, Mother Mary needed to be free from original or any other sin. This supports why Jesus had no siblings. No one with original sin, could share the same womb where Divine DNA is left behind. It explains why demons flee from Mother Mary; she is peppered with Jesus' FMc cells. It also supports her Assumption. Why would Mother Mary's remains be left behind to decompose if she harbors living God cells?

Conclusion. DNA and RNA are unique to every individual. Mixing multiple blueprints or building instructions would compromise a construction project. In our bodies, so too; cells are confused when >2 sets of blueprints or instructions are in play. Despite our best intentions, foreign blueprints or building instructions may target healthy cells, tissues, organs or processes.

Mothers who birthed priests will always have pieces of their favorite priest within them. Similarly, there is good news for miscarriage and abortion-regretting parents. Babies remain alive in FMc cells to help their beloved Mama throughout her life.

If our bodies are temples of the Holy Spirit; every effort should be made to preserve God's masterpiece, our uniqueness. If we follow all the science, God uses DNA to facilitate forever connections. Mother Mary is forever connected to her Son, through the fetal stem cells He left behind. When we honor her, we honor Jesus. Mother Mary's womb is a sacred space in which His cells reside forever. She is still His tabernacle.

Sources

Fetal Microchimerism: self and non-self, who are we? | PubMed

Fetal microchimerism: benevolence or malevolence for the mother? - PubMed