Living with RSDThis section is a place to share stories about Living with RSD Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation. You may also Help others by sharing your story. To quickly access health information from your website's browser, download My story Seven years ago i was diagnosed with a very rare type of a rare blood disorder called TTP. During that time i had 2 what i call strokes. They said they were TIA’s but to this day still cant grip with right hand..it was a stroke I also had to have plasmapharesis to take the bad red blood cells out of my body, this went on for 9 days. When I was on the machine i had to be given calcium by injection. One day they decided they were just gonna try giving me Tums and no injection since i was holding up so well, it didnt work, i crashed. That was the day i got RSD and i have been begging for help since 2001. People thought i was depressed, im not depressed i am sick, and in the most horrible pain in my whole body that you could possibly imagine. And I am lucky because i live close to the doctor who specializes in it….but, I can not see this man for a whole year.. u heard right, a whole year. I could be dead by then. I hope i live long enough for them to tell me i wasnt crazy and that what i have really is a disease.. I feel bad for anyone who has even the smallest amount of RSD I have it systemically now and i think about how am i spose to live my life like this….i really do need help. As i am sure all of us do. Comments
November 2007
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