Guest guest Posted December 30, 2006 Report Share Posted December 30, 2006 Hello Everyone! I am hoping that someone can help answer a few questions for me about Yasko Testing. First, Should ALL Genetic Dr's be able to help with this protocol after learning from Amy's website?? My son goes to his genetics Dr. for a re-check & he hasn't seen her in 2 yrs. He just turned 5 & was sent to her from his neurologist to check for mitochondrial problems, due to him showing autistic tendencies, but something not being right (extemely affectionate w/ people,good eye contact, but stimming (w/ hands, vocally & visually) covering his ears, and non-verbal. (AND STILL IS NON-VERBAL!!). His 2 MRI's both came back showing low myelin in the brain but not deteriorating, just low/normal. Nothing came back from the blood work showing mitochondrial issues at all. We haven't seen either his neurologist or Genetics since learning about ALL of this (DAN!, GF/CF/SF, Supps, Hbot,YEAST, Metals (he being mercury,lead,arsenic,aluminum & antimony)etc,etc) in MARCH of THIS yr.The earlies his gentics Dr. can work him in is April 2nd. DOES ANYONE KNOW OF A GENETICS DR. AROUND MY AREA THAT EXCEPTS NC MEDICAID, WHO " KNOWS " THIS PROTOCOL?? We live between Asheville, NC & Spartanburg/Greenville SC. I have read several times that after getting this test results, that there were kids that couldn't tolerate the B-12. My son had practically NO cobalt on his hair test, & he getting shots now, just curious if there is a way to KNOW they can't tolerate it, before getting the tests.... Is there ANYTHING else anyone would like to share about this?? We are waiting on a french urine test so we can do this next. Thanks so much for any help anyone can give me!!! Michele Quote Link to comment Share on other sites More sharing options...
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