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Re: Still going.. just. (posted Dying from ME/CFS a year ago)
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Published: 6 years ago
This is a reply to # 2,079,970

Re: Still going.. just. (posted Dying from ME/CFS a year ago)

My physician ordered the MTHFR gene mutation lab test for me... I've also seen people get it from 23andMe:

This website also says you can ask your physician or order from the online website:

If you have the MTHFR mutation the B12 injections with hydroco are probably not a huge help. You would need methylcobalamin instead.

For about 15 months I've done a combination of approaches to detox copper. I did "Nutritional Balancing" hair analysis testing (well except for the fact that I didn't take the recommended copper supplements and the calcium they recommended was way too much for me).

I also followed the advice from the book by Ann Louise Gittleman about detoxing copper. And most recently I started doing three days on ALA (Cutler protocol - every three hours) and then a week off.

I can't even tell you how much better I feel - even though I'm not a 100%... I don't feel like I'm dying anymore (which is AWESOME)!

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