23andMe

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I saw the information presented on 23andme yesterday on the media. This is so sad. 23andme was told to pull their product not because the results were not valid but because Americans cannot understand risk. 23andme now has to find a way of communicating risk. This is exactly the problem with women not understanding chemo will only give them a 1 or 2 in 100 decreased risk. Good grief how sad.

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  • Englishmummy
    Englishmummy Member Posts: 337
    edited October 2015

    This is an interesting article too, poses another train of thought/perspective...

    http://www.scientificamerican.com/article/23andme-...

  • coraleliz
    coraleliz Member Posts: 1,523
    edited October 2015

    UInfortunately it's true about people not understanding what the percentages/risk actually mean. I sent my saliva in before the FDA intervened. They have boards where members can post. Per 23 & me, I have a rather high risk of getting macular degeneration(49.7%), normal risk 7%. My mom had this. So I asked my opthamologist if my elevated risk could be explained by family history alone. He said no. His only advice was to eat lots of green leafy veggies & hope to stay in the 50% without it. There were people on the 23&me board who were "freaking out" & others who were trying to talk them down. There were people posting research articles about how "eye vitamins" aren't helpful, etc. I still think this kind of information should be available to us, even though some people can't handle it. They probably can't handle many other things in life either.

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