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MTHFR and the Methylation Cycle

This is what I am finally learning about. I have known for over 10 years that I had 2 MTHFR variants (C667T and A1298C variants). Also called Compound Heterozygous. I knew that this made the methylation cycle(whatever that was) not work well. I thought I could just take the supplements and not worry about it, but after a while, I kinda started thinking I didn't need to take the supplements or to worry about the MTHFR. So, I started taking them only when I felt bad. 😔

It is a little rare to have both variants.

"Understanding the Variants
C677T Variant: This variant is more prevalent, affecting around 30-40% of certain populations, especially among those of Hispanic descent.

A1298C Variant: This variant is less common, found in about 7-12% of individuals in North America and Europe.

Having both the C667T and A1298C variants of the MTHFR gene is relatively uncommon. Estimates suggest that this combination occurs in approximately 10-20% of the population. Having both the C667T and A1298C variants of the MTHFR gene is relatively more common among European populations."
GPT-4o mini


I recently started having very mild memory problems, and I felt it pressed on me to start taking all my supplements again and to learn more about the methylation cycle. It is a little harder to figure this all out now that I am having some brain issues. It would have been easier to figure out last year, but I will get this figured out. I am now taking a gazillion supplements, and I do think it is helping. 👍

From what I am now learning, the Methylation Cycle is very very important, and I should have taken it seriously years ago. Live and learn,I guess.
🤦‍♀


https://www.casi.org/node/1924

https://lowerdementiarisk.com/understanding-mthfr-and-its-impact-on-brain-health/

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Gosh, id never heard of this condition until now.

Its crazy that your doctor didn't explain it to you better...
....but when do they ever?
HappyHobbiest · 56-60, F
@OogieBoogie I got my results from my DNA testing through Ancestry, and then by using Promethease I found all my variants and mutations.
https://promethease.com/

Then I took the results to my family practitioner here in Wyoming, and although he had heard of the MTHFR variants, he really didn't know much. I knew I had to do the research, and I did, but I didn't yet feel really bad, so I didn't take it seriously enough. I'm afraid the blame for my mistake is on me.

Thank you so very much for your kind comment. I really do appreciate it. 🙂