[QUOTE=aneczka;1118719]Just received preliminary results of my genetic screening. My methylation profile shows some mutations, actually a lot of them. Two homozygous, which are supposed to be more serious, and a lot of heterozygous. Can anyone help with analysing them? The information I received is a bit overwhelming, since it is all new to me. A quick, superficial read suggests I may have issues with vitamines D3, B12 and methylfolate.

Hi aneczka
How were you able to get genetic screening? Is that the same as getting a genetic blood work-up? Did your health Ins help pay for it?
Does your Doctor think these mutation problems could be responsible for your neuropathy?

Hi Marie33, I paid myself to 23andme (look it up online), it was not too expensive. My new neuro didn't seem too interested, but he will test for one specific gene which seems to be very relevant in neurology, SMN1, I think to confirm my diagnosis and to exclude something.