Hi there,
I'm new to the forums but not ME/CFS (since 2001). A year ago I did the 23andMe test for my son and I. I am having a hard time finding a practitioner to help me in New Zealand this science is still so new. I have been quite ill again since surgery under GA in 2012. This is what made me think there was a strong chemical/metabolic component to my issues.
I've read the b12 protocols pinned here, however I did very poorly with Seeking Health's multi and methylb12/methyl folate. Once I got my SNPs I realised it was a lot more complicated than that.
I'd so appreciate some input into where to safely start. I can post my main polymorphisms relevant here if that helps.
I have ME/CFS, PCOS, MCS, histamine intolerance, leaky gut & food intolerances, sensitivity to sulphur & I think excess ammonia, insomnia and a stubborn chronic parasitic infection.
I think maybe I need to start with P5P and hydroxyb12 but unsure...
Tia
I'm new to the forums but not ME/CFS (since 2001). A year ago I did the 23andMe test for my son and I. I am having a hard time finding a practitioner to help me in New Zealand this science is still so new. I have been quite ill again since surgery under GA in 2012. This is what made me think there was a strong chemical/metabolic component to my issues.
I've read the b12 protocols pinned here, however I did very poorly with Seeking Health's multi and methylb12/methyl folate. Once I got my SNPs I realised it was a lot more complicated than that.
I'd so appreciate some input into where to safely start. I can post my main polymorphisms relevant here if that helps.
I have ME/CFS, PCOS, MCS, histamine intolerance, leaky gut & food intolerances, sensitivity to sulphur & I think excess ammonia, insomnia and a stubborn chronic parasitic infection.
I think maybe I need to start with P5P and hydroxyb12 but unsure...
Tia