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who has the MTHFR gene mutation?

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Posted 2/8/2013 11:53 PM (GMT 0)
Hi all,

I know there are some members here that have this mutation. My daughter has  c667 and a1298 (one of each). I am still waiting on my results, but seeing how methyl b12 injections have helped me so much, I am pretty certain she got them from not. Not to mention, I can't detox ammonia well.

My question is, have you began proper therapy? What did you do? Have you gotten better? What symptoms have gone away? Has anything gotten worse?

Any and all info would be greatly appreciated. I can see from what I have read that there are going to have to be some lifestyle changes, but treating this properly can be completely beneficial.

Thanks all,

Samantha

Posted 2/9/2013 3:33 AM (GMT 0)
I just found out I have this gene mutation, at least the c667 one. I am about to start taking NeeVo DHA. Curious to see what it'll do.
Posted 2/9/2013 3:38 AM (GMT 0)
Are you or will you also be treating with Methyl b12 and b6 or other b vitamins? Please let me know how much you take and if you begin to herx or detox. Please keep me informed. My daughter and I will be beginning therapy soon too.
Posted 2/9/2013 11:01 AM (GMT 0)
I don't know if I have the mutation as I have not been tested, but I suspect that I do based on the fact that I don't respond typically to treatment and methylcobalamin shots help me tremendously (mainly for psychological symptoms).

I take 1mg/ml every day via IM injection. I haven't started 5-mthf yet but am considering it for the next time I put in my vitamin order. I don't herx from B12, but I get a rapid decrease in depression and anxiety. It works on a daily basis. Meaning that when I skip a dose for some reason (like trouble with my hands/motor skills) the psychological symptoms return very quickly. I also take extra b6 because I'm on Flagyl. I take 100mg per day orally.
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