Re: Still going.. just. (posted Dying from ME/CFS a year ago) (Liver Flush Support Forum) 7/1/2013 2080096

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

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

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I agree the MTHFR test would be a waste of money, especially if you had to pay for it out of pocket. My insurance covered the test so I didn't really have to pay for anything aside from the doctor visit. I guess if you were really curious about whether you had the gene mutation or not, it might be worth it to get the test.

Regardless - I was just answering the question.

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

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