I've considered getting some testing done through 23andme. I think it's only like $100 too, huh? Oh, and while I'm on the topic, I heard that they changed the way they present their results, making it more geared toward the "ancestry" side of things, instead of things like, yes, genetic mutations a person might have. Is that true? If so, guessing it's because of outside pressure from healthcare people, upset that people are using their services to diagnose themselves?
I feel like it's true, 'cause I usually see people basically saying "help me decipher my test results." Though, could just be because they're unintentionally confusing, that's just their nature.
Also, I seem to remember hearing that people with the MTHFR mutation have trouble sweating. Is that correct, or have I been mislead? Maybe it was just the one person who had trouble.. and she also had the MTHFR, the two being unconnected.
Hm, could be hypo, though I cannot gain weight, like you - might just be my poor diet. Yeah, I had both my thyroid and adrenals tested, a couple months ago. Though, it was done through a GP, so I'm certain it was the crappiest of the tests. She said everything looked normal. Most of the people I've heard from that have gotten their levels checked, and received helpful results, they mentioned getting tested through an LLMD, independent labs, etc.
That'll cost me money. How much?
Regardless, more possible causes to add to the list, more testing, more treatment, supplementation. It's all too much. Ha. Can't even begin.
edit: many thanks.
Post Edited (NotQuiteAntonio) : 9/21/2015 6:26:54 PM (GMT-6)