New era for ME/CFS research as top cytokine study attracts media headlines
The immune systems of patients who have recently developed ME/CFS look markedly different from those who have been ill for much longer, according to a major new study from Drs. Ian Lipkin and Mady Hornig at Columbia University. This shift in immune function hadn’t been seen before.
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23 and me results

Discussion in 'Genetic Testing and SNPs' started by Red04, Jul 28, 2013.

  1. Red04

    Red04 Senior Member

    My mom got the following 23 and me results. She has MCS and a bunch of other sleep and thyroid issues. She tried Freddds protocol for a while and didn't have and significant reactions. Maybe some slight improvements. I haven't started to read up on the specific mutations she has just yet. Any advice would be appreciated.

    Attached Files:

  2. Valentijn

    Valentijn Activity Level: 3

    Amersfoort, Netherlands
    Nothing I see there really sticks out as being particularly problematic. Maybe mild problems with folate or B12.

    Something else you can do is upload her 23andMe results to (after changing the file name so it doesn't have her real name in it, and making an account also without real names). Then another site will download those results and email you a list of her rare alleles - something useful might pop up there.

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