AngelicBrat,
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.

[This message has been edited by moderator1 (edited 10-15-2003).]

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 http://www.healthboards.com/ubb/smile.gif ~Angelic

[This message has been edited by moderator1 (edited 10-15-2003).]