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Thread: I'm new and concerned about vCJD

  1. #1

    I'm new and concerned about vCJD

    Hi,
    I am new on here and read a post by someone who was very worried about vCJD, I can recommend a website that is very informative www.justiceforandy.com I have worries about my sister who had a blood transfusion which was not screened for vCJD, the Department of Health & NHS do not recognise that they have responsibilities to inform & support anyone who has had a blood transfusion in the UK. There is a culture of secrecy over vCJD and many symptons can be confused with illnesses such as dimentia and MS.

    Greekgirl
    Last edited by GreekGirl; 20-06-10 at 11:31. Reason: upset member

  2. #2
    Join Date
    Apr 2003
    Location
    , , United Kingdom.
    Posts
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    Hi GreekGirl

    A huge warm welcome to nmp.

    You'll get loads of advice and support here and make some lovely friends along the way.

    Best wishes
    __________________
    Nicola

    “Don't be afraid of death; be afraid of an unlived life. You don't have to live forever, you just have to live.” - Natalie Babbitt

    Please help keep NMP running and donate to the running costs: http://www.nomorepanic.co.uk/donate




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