1. Patients launch $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
    Check out the website, Facebook and Twitter. Join in donate and spread the word!
Join the National PR Campaign for ME: Power to the Patient (P2tP)
Have you had enough of all the neglect and abuse of ME/CFS patients? Gabby Klein says now is the time for a National PR Campaign for ME/CFS to impress a change. Join the Patient Revolution to restore power to ME patients ...
Discuss the article on the Forums.

23 and me results

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

  1. Red04

    Red04 Senior Member

    Messages:
    178
    Likes:
    77
    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

    Messages:
    6,692
    Likes:
    10,146
    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 http://opensnp.org/ (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.
     

See more popular forum discussions.

Share This Page