I firmly believe the 3 MMR shots that I had to receive as an adult triggered my Hashimotos.
2000: Indiana required the MMR prior to issuing a marriage license 🙄 I was young and didn’t question. So I got it.
2005: Now trying to conceive. Bloodwork from the OB office shows I do not have immunity to rubella. So they recommend. I get the shot again.
2007: Still trying to conceive we see a fertility specialist. Again bloodwork reveals no immunity to rubella and they recommend the MMR again. I take it because I’m still trusting doctors at this point.
Dec 2007 we get pregnant. Jan 2008 diagnosed with Hashimotos. Pregnancy triggered.
I took natural childbirth classes and THATS what made me question the whole medical industry.
From my own research I believe that there are ingredients in that shot that mimic the thyroid and that’s what caused mine.
Hashimoto's thyroiditis is primarily listed in VAERS under "autoimmune thyroiditis" - COVID19 - 770 reports, HEP - 46, HPV4 - 76, HPV9 - 26, MMR - 21. This appears as a signal to investigate for MMR that is 3 to 4-times higher than FLU3 - 6 and FLU4 - 5. Next steps: data normalization and comparisons with expected background frequency.
Thanks for this article. That endotoxins cause autoimmunity is no longer theory, LPS as a promoter has been tagged for years in the celiac and non-celiac, MS, Lupus and other communities. Those pesky graham negative bacteria overcrowding commensals, causing a slew of extra exhaust particles that eventually get into the bloodstream. These small, sticky particles can cause havoc anywhere in the body, and dangerously, much like spike protein, can also cross the BBB. From years of myriad repeated shots, society now has over 100 named, possibly more, autoimmune conditions on the rise. Just imagine doctors telling their people with autoimmunity (BTW, mostly women), to take the shots as these will protect them? Ha, an INVERSION OF TRUST of the highest order, as many whose conditions were in remission found their conditions returned, worse than ever before!! "Keeping us safe" actually means runaway like hell from standard doctors. Represents inadequate medical training, yet another form of ignorant evil.
In case one misses the numbers, in the US we had, pre-plandemic, approx 50million people, mostly women, with at least one autoimmune condition, less than 2x the number of folks with cancers, about 4x the number of people with heart conditions. Adding these together, more people have autoimmunity than combined number of people with cancers and heart disease. Please look at the skyrocketing Parkinson's diagnosis after these modRNA shots, you will see this issue more blatantly presenting itself.
Recent Nobel Prize winner Dr. Drew Weisman recognized in 2018 the safety issues of mRNA vaccines sand the need to identify individuals susceptible to autoimmune reactions prior to injection.
mRNA vaccines — a new era in vaccinology
"Safety
The requirement for safety in modern prophylactic vaccines is extremely stringent because the vaccines are administered to healthy individuals. Because the manufacturing process for mRNA does not require toxic chemicals or cell cultures that could be contaminated with adventitious viruses, mRNA production avoids the common risks associated with other vaccine platforms, including live virus, viral vectors, inactivated virus and subunit protein vaccines. Furthermore, the short manufacturing time for mRNA presents few opportunities to introduce contaminating microorganisms. In vaccinated people, the theoretical risks of infection or integration of the vector into host cell DNA are not a concern for mRNA. For the above reasons, mRNA vaccines have been considered a relatively safe vaccine format.
Several different mRNA vaccines have now been tested from phase I to IIb clinical studies and have been shown to be safe and reasonably well tolerated (Tables 2, 3). However, recent human trials have demonstrated moderate and in rare cases severe injection site or systemic reactions for different mRNA platforms22,91. Potential safety concerns that are likely to be evaluated in future preclinical and clinical studies include local and systemic inflammation, the biodistribution and persistence of expressed immunogen, stimulation of auto-reactive antibodies and potential toxic effects of any non-native nucleotides and delivery system components. A possible concern could be that some mRNA-based vaccine platforms54,166 induce potent type I interferon responses, which have been associated not only with inflammation but also potentially with autoimmunity167,168. Thus, identification of individuals at an increased risk of autoimmune reactions before mRNA vaccination may allow reasonable precautions to be taken. Another potential safety issue could derive from the presence of extracellular RNA during mRNA vaccination. Extracellular naked RNA has been shown to increase the permeability of tightly packed endothelial cells and may thus contribute to oedema169. Another study showed that extracellular RNA promoted blood coagulation and pathological thrombus formation170. Safety will therefore need continued evaluation as different mRNA modalities and delivery systems are utilized for the first time in humans and are tested in larger patient populations."
I firmly believe the 3 MMR shots that I had to receive as an adult triggered my Hashimotos.
2000: Indiana required the MMR prior to issuing a marriage license 🙄 I was young and didn’t question. So I got it.
2005: Now trying to conceive. Bloodwork from the OB office shows I do not have immunity to rubella. So they recommend. I get the shot again.
2007: Still trying to conceive we see a fertility specialist. Again bloodwork reveals no immunity to rubella and they recommend the MMR again. I take it because I’m still trusting doctors at this point.
Dec 2007 we get pregnant. Jan 2008 diagnosed with Hashimotos. Pregnancy triggered.
I took natural childbirth classes and THATS what made me question the whole medical industry.
From my own research I believe that there are ingredients in that shot that mimic the thyroid and that’s what caused mine.
Any thoughts Dr Ricke?
Hashimoto's thyroiditis is primarily listed in VAERS under "autoimmune thyroiditis" - COVID19 - 770 reports, HEP - 46, HPV4 - 76, HPV9 - 26, MMR - 21. This appears as a signal to investigate for MMR that is 3 to 4-times higher than FLU3 - 6 and FLU4 - 5. Next steps: data normalization and comparisons with expected background frequency.
You might like Endotoxin in HPV causing Harms
https://geoffpain.substack.com/p/cervarix-hpv-jab-deaths-and-injuries
Thanks for this article. That endotoxins cause autoimmunity is no longer theory, LPS as a promoter has been tagged for years in the celiac and non-celiac, MS, Lupus and other communities. Those pesky graham negative bacteria overcrowding commensals, causing a slew of extra exhaust particles that eventually get into the bloodstream. These small, sticky particles can cause havoc anywhere in the body, and dangerously, much like spike protein, can also cross the BBB. From years of myriad repeated shots, society now has over 100 named, possibly more, autoimmune conditions on the rise. Just imagine doctors telling their people with autoimmunity (BTW, mostly women), to take the shots as these will protect them? Ha, an INVERSION OF TRUST of the highest order, as many whose conditions were in remission found their conditions returned, worse than ever before!! "Keeping us safe" actually means runaway like hell from standard doctors. Represents inadequate medical training, yet another form of ignorant evil.
In case one misses the numbers, in the US we had, pre-plandemic, approx 50million people, mostly women, with at least one autoimmune condition, less than 2x the number of folks with cancers, about 4x the number of people with heart conditions. Adding these together, more people have autoimmunity than combined number of people with cancers and heart disease. Please look at the skyrocketing Parkinson's diagnosis after these modRNA shots, you will see this issue more blatantly presenting itself.
Recent Nobel Prize winner Dr. Drew Weisman recognized in 2018 the safety issues of mRNA vaccines sand the need to identify individuals susceptible to autoimmune reactions prior to injection.
mRNA vaccines — a new era in vaccinology
"Safety
The requirement for safety in modern prophylactic vaccines is extremely stringent because the vaccines are administered to healthy individuals. Because the manufacturing process for mRNA does not require toxic chemicals or cell cultures that could be contaminated with adventitious viruses, mRNA production avoids the common risks associated with other vaccine platforms, including live virus, viral vectors, inactivated virus and subunit protein vaccines. Furthermore, the short manufacturing time for mRNA presents few opportunities to introduce contaminating microorganisms. In vaccinated people, the theoretical risks of infection or integration of the vector into host cell DNA are not a concern for mRNA. For the above reasons, mRNA vaccines have been considered a relatively safe vaccine format.
Several different mRNA vaccines have now been tested from phase I to IIb clinical studies and have been shown to be safe and reasonably well tolerated (Tables 2, 3). However, recent human trials have demonstrated moderate and in rare cases severe injection site or systemic reactions for different mRNA platforms22,91. Potential safety concerns that are likely to be evaluated in future preclinical and clinical studies include local and systemic inflammation, the biodistribution and persistence of expressed immunogen, stimulation of auto-reactive antibodies and potential toxic effects of any non-native nucleotides and delivery system components. A possible concern could be that some mRNA-based vaccine platforms54,166 induce potent type I interferon responses, which have been associated not only with inflammation but also potentially with autoimmunity167,168. Thus, identification of individuals at an increased risk of autoimmune reactions before mRNA vaccination may allow reasonable precautions to be taken. Another potential safety issue could derive from the presence of extracellular RNA during mRNA vaccination. Extracellular naked RNA has been shown to increase the permeability of tightly packed endothelial cells and may thus contribute to oedema169. Another study showed that extracellular RNA promoted blood coagulation and pathological thrombus formation170. Safety will therefore need continued evaluation as different mRNA modalities and delivery systems are utilized for the first time in humans and are tested in larger patient populations."
https://www.nature.com/articles/nrd.2017.243