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Old 10-13-2003, 04:26 AM   #1
Join Date: Dec 2002
Posts: 433
Sampy123 HB User
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I read your post in the MS forum. I too, having been trying to get the word out about antiphospholipid antibody syndrome and how easily one can be misdiagnosed. I know I have systemic lupus and APS, but they're testing me extensively for MS. Just trying to spread the word as well.

Last edited by Administrator; 08-09-2014 at 01:29 PM.

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Old 10-13-2003, 09:26 AM   #2
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Join Date: Jan 2003
Posts: 663
AngelicBrat HB UserAngelicBrat HB UserAngelicBrat HB UserAngelicBrat HB UserAngelicBrat HB UserAngelicBrat HB User

Hi Sampy!

I too agree that we have to get the word out about APS. Where I live, no doctor really knows much about it and that is why I went to England to see Dr. Hughes. It is so important for people to be diagnosed properly, because if not then there can be such devistating results!! I am so glad that you are getting the word out too ~Angelic

Last edited by Administrator; 08-09-2014 at 01:28 PM.

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