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.
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.