mthfr, tmg, dmg, and folate

[Guest guest]

Hello! I've been looking through the archives and not seeing what I wanted to

know. My son was recently diagnosed as heterozygous on 677 of the mthfr alleles.

I already started Folapro (thank you Toni) on a hunch that he had this mutation.

He was doing well on 800 mcg. He has already been getting MB12 shots. I added

TMG after I read that it was helpful, and initially he showed good progress, but

then the progress slowed. I couldn't go past a half-dose BTW due to sleep

issues. THEN...I read Dr. Neubrander's article that stated TMG blocks the

effects of B12 in the brain and should not be used, but DMG seems to be ok. So

now we are weaning off of TMG and considering DMG instead. I also need to try

P5P.

My questions are: what else do I need to do for MTHFR heterozygous? Should I

test my 2 yo daughter? Should my husband and I get tested? Should we all take

Folapro just in case?

I'm really at a loss here since there is next to nothing on the internet besides

the usual unhelpful mainstream medicine info.

Also...my son has a very high folate level in his blood. I called Dr.

Neubrander's office and they said this is very common in the kids they treat,

but of course I couldn't get any more info because I'm not a client there.

Anyone have any comments about high serum folate?

Thanks!