Jump to content
ACN Latitudes Forums

Search the Community

Showing results for tags 'genetic testing'.



More search options

  • Search By Tags

    Type tags separated by commas.
  • Search By Author

Content Type


Forums

  • Welcome to our Forums
  • ACN Services
  • Advanced, Complementary, and Alternative Approaches
    • Attention Deficit Disorders
    • Autism Spectrum Disorders
    • Obsessive Compulsive Disorder
    • PANS / PANDAS (Lyme included)
    • Tourette Syndrome and Tics
  • Prevention and Integrative Therapies
    • Cognitive Behavior Therapy (New)
    • Diet and Gastrointestinal Issues (New)
    • Environmental Factors (New)
    • Nutrition and Supplements (New)
  • School and Home Related
    • Academic Challenges
    • Behavioral Issues and Behavior Charts (New)
    • Educational Plans (New)
  • General

Blogs

  • ACN Latitudes Blog
  • sarama37's Blog
  • kptrsn's Blog
  • lulu648's Blog

Product Groups

  • Advertisements
  • Test Category

Calendars

There are no results to display.


Find results in...

Find results that contain...


Date Created

  • Start

    End


Last Updated

  • Start

    End


Filter by number of...

Joined

  • Start

    End


Group


AIM


MSN


Website URL


ICQ


Yahoo


Jabber


Skype


Location


Interests

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 able to review it or not. Thanks.
  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!!!
×
×
  • Create New...