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Dr. Lynn Fynn-derella🐭

@Fynnderella1224,640 subscribers

Accurate about origin,low virulence, tx since Feb 2020 and public health for decades. BANNED until 1/15/2023! 🩺 Treat Early! Posts are my opinion. 🩸

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Good morning all. I’m exhausted. Got zero sleep. Who knew raccoons played such pranks? 😡

Good morning all. I’m exhausted. Got zero sleep. Who knew raccoons played such pranks? 😡

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Don’t miss tomorrow’s Senate Hearing with Senator Ron Johnson and testimony from many including Dr Aseem Malhotra Covered by Broken Truth

Don’t miss tomorrow’s Senate Hearing with Senator Ron Johnson and testimony from many including Dr Aseem Malhotra Covered by Broken Truth

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Dear South Carolina: #lindabell Careful with semantics - this is perjury. They state fetal cells have nothing to do with MMR, so they are trying to remove all exemptions on South Carolina- This fact has been consistently distorted by institutions eager to downplay ethically relevant and biologically significant facts. The reality: Yes, the MMR (measles, mumps, rubella) vaccine does involve fetal-derived cells, specifically, human diploid cell lines that originated from electively aborted fetuses in the 1960s. However, it’s crucial to understand where and how these cells are involved. Specific cell lines used WI‑38 (Wistar Institute 38): Female fetal lung fibroblasts. Derived in 1962 (Sweden/Philadelphia). Used notably for the rubella component of the original MMR. MRC‑5 (Medical Research Council‑5): Male fetal lung fibroblasts. Derived in 1966 (UK). Used in various live viral vaccines, sometimes substituting for WI‑38. These cell lines were created from lung tissue taken from two separate aborted fetuses, not from a continuous series of abortions — but the fact remains: aborted fetal cells were the original source material. How they’re used: In the MMR vaccine (particularly the rubella component): The rubella virus (RA27/3 strain) was first isolated and attenuated in WI‑38 cells. Once the vaccine strain was developed, production continued using human diploid fibroblasts as a cell substrate (the “factory” in which the virus is grown). The virus is later harvested, purified, and stabilized. So, while no intact fetal cells are in the final vaccine, residual human DNA fragments and cellular debris are, because the viral culture medium derives from these diploid cell lines. Small amounts of human DNA (~10–20 nanograms per dose) remain after filtration. Ingredient label explanation The ingredient list won’t explicitly say “fetal cells,” but look for terms like: “WI‑38 human diploid lung fibroblasts” “MRC‑5 human diploid fibroblasts” Or in some documentation: “cell culture media derived from human diploid lung cells” Those descriptors mean fetal-derived cells were used in propagation. Ethical & scientific considerations Bioethical dimension: Many people object on moral or religious grounds to products developed from fetal tissue, even if no new abortions occur today. The lack of transparency on insert labeling prevents fully informed consent. Scientific concern: independent researchers have long debated whether residual human DNA could integrate or trigger unintended immune or epigenetic effects, particularly in developing brains — a matter regulators have been reluctant to examine openly. To summarize: COMPONENTCELL LINE SOURCEFETAL ORIGINSTILL PRESENT IN FINAL PRODUCT? MeaslesChicken embryo cellsNoNo MumpsChicken embryo cellsNoNo RubellaWI‑38 (human diploid fetal lung)YesResidual DNA fragments remain So the truthful answer is: The rubella component of the MMR vaccine is cultured in human fetal cell lines (WI‑38 or MRC‑5), meaning fetal-derived material was essential to its production, and trace human DNA fragments remain in each dose. Sen. Josh Kimbrell where did it come from? Scientific fact that your epidemiologist buddy giving testimony is either not qualified to discern, or she’s just not being honest under oath.

Dr. Lynn Fynn-derella

32,914 views • 3 months ago

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