hey again, impossible. I read through your message again and have 2 questions. I’m going to call that doctor tomorrow to see when I get get in with him
1. How do my mutations compare to yours and/or others you’ve seen? More significant? Similar? Less drastic? I’m just wondering. I only had a couple homozygous but several heterozygous, so I was just wondering if this really does seem like it could be “it” for me as to why I’m not improving. I’m thinking it has definitely potential, but just wondering on your take.
2. Do you think I could safely start on some supplements before I get in with that doctor? I have the feeling it’ll be a while until he can see me, though who knows. I know SHMT and ACAT should be addressed first since I’m hetero…as such, would it be dangerous for me to try that Folinic Acid and other supplements that go along with that? I think you mentioned methlyfolate (but no good for me — rather mb12??), 5 formyl THF (actifolate), adenosyl b12, other b12, etc. Does that seem like a good plan? If so, maybe just focus on the Folinic, mb12 and 5 formyl THF? What do you think?
Thanks so much again!