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Found 3 results

  1. Here is the AP story http://news.yahoo.com/fda-tells-23andme-halt-sales-genetic-test-173620516--finance.html and here is the FDA letter to 23&me http://www.fda.gov/ICECI/EnforcementActions/WarningLetters/2013/ucm376296.htm Hopefully this will all be sorted out soon as many people have found tremendous benefit from this testiing!
  2. Guest

    23&me

    Who knows how to decipher this stuff, medically speaking? Just wondering if I could see someone local though I've studied it and don't really see much of anything. There were a few sensitive to this medication and 23% risk for gallstones but nothing of much value. Also said risk of obesity which I find hard to believe as my entire family is too thin actually. Bizarre. Not good to hear when you've had anorexia and bulimia. Anyways, still trying to find a local PCP but none accept medicaid. There is one NP, female, who treats lyme and CFS and lupus supposedly but not sure if she'd be a
  3. For those who have had genetic testing on their children, has anyone found a gene mutation for PNKD? This gene causes a form of dyskinesia. If your child is positive for this mutation, are you doing anything to address this concern? Do you find that it relates to their behavior during a PANDAS / PANS flare? What are the behaviors your child displays during a PANDAS / PANS flare? Looking for similarities since I know PANDAS / PANS presents differently in different children. Thanks for any input!!!
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