GreekGirl
17-06-10, 15:42
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 (http://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
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 (http://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