Clotting Risk and MTHFR Gene Mutations

Dr. Been one thing that is super important and they need to update the messaging for pregnancy. Folate! needs to be supplemented rather than folic acid. It will not do what it needs to do (and I believe builds up) unless it is actual folate rather than the synthetic folic acid.

I just found out I have the double heterozygous mutation which is a bummer. I also had a very bad reaction to the Pfizer Covid vaccine - neurological, elevated liver enzymes, pain in lower legs and feet and I think maybe vasculitis. This could certainly be linked. However, I had Covid as well and did not suffer any adverse symptoms, only with the vaccine. I would love another video with more insight into the various health issues that could arise. I did read that people w the mutations also have trouble removing toxins from the body and as a results that causes issues. There is a list of drugs to avoid beachside they are harder for people with the mutations to clear. I would love to know more about that too. Thank you for your wonderful lectures. ❤🙏🏻

Funny you don't hear nothing on TV about mutations no more

Please check as synthetic folic acid blocks the methylation pathway for those with the mthfr gene, ref, Dr Ben Lynch.

I have the mutations in these genes and found out that I needed 65% more folate. It was suggested that I use "Methylated' B group vitamins when supplementing. Some of the doses are extremely high in supplements We only need 1-2 mg's per day so only take them when I feel haven't had enough leafy greens or folate laden foods. Didn't take the vaccine. So far no problems. For those here in Australia - noticed that Aldi had Methylated' B vitamins ( lower milligrams) for a reasonable price. Some companies name their B group vitamins "activated" B group. Remember, Food is the best source!! Stay active. Thank you Dr Been for this wonderful explanation!

Thanks for another important talk, this is a great resource for us post v/lc Aussies! 💚

This would explain why the 💉 is so dangerous for some people. They should have screened people before mass Rollout.

I'm being treated by Dr.Jordan Vaughn in Alabama for Long Covid.... he checked me for a MTHFR mutation and I do have one along with PAI-1 4g/4g gene....

My daughter never took the C-shot. The MTHFR gene mutation has caused her to barely be able function. The number of western doctors she has been to for help - numerous - the help she has received - none. She has found one, more holistic, that at least ordered the test she has been asking for. She can barely eat -only one or two things now. She finally got a continuous glucose monitor ordered from this latest doctor. The critical low alarm goes off about 9 times a night. About the only thing she can eat now, without severe repercussions, is meat. She’s always been thin, but now it is scary how little she can tolerate. She has insurance, but western medicine will not, or cannot, be bothered with any complications outside requiring pills(which she cannot take of course). I’m extremely concerned. I hope to find some answers for her. It was funny that she had done so much research and arrived at some answers on her own, then when she shared all the symptoms with Chat GPT, it came back with what she had figured out so far! Thank you Dr Been for any help with this MTHFR mutation issue. It’s very complicated.

So we can see by your drawing that Homocysteine can increase when not methylating properly.