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 Living with RSD I have had RSD for the past 15 years. It happened after I fractured my right shoulder (scapula). While the shoulder was healing I fell down a flight of stairs and tore the main nerve that runs down my right arm. This has caused me to have extreme pain in my right hand. The worst part is that I am right handed and a computer programmer. Fifteen years ago, RSD was not common and I went through several doctors that told me it was all in my head before I was referred to an anesthesiologist who then gave me nerve blocks once a month for two years along with prescribing pain meds. I was tired of the blocks and we researched another alternative which was a sympathectomy, which resulted in 1 year of recovery and the RSD pain didn’t go away and since has become worse. I have since learned through research that surgery is not the answer. By having the sympathectomy, nerve blocks are no longer an option. The only option that I have been given is pain meds. Currently I am out of work with no insurance and my doctor will no longer prescribe any meds to help. Therefore, I am dealing not only with looking for a job but trying to get through each day as best I can with the pain. Using over the counter meds, like Tylenol, Advil, Aleve or any of the other pain relievers doesn’t even touch the pain. I do know that for me that stress makes the condition worse and there is nothing more stressful than looking for a job right now the way the economy is. If anyone knows of any over the counter meds that might help, I would appreciate the information. After living with RSD for as long as I have, I feel for anyone that has to live with it. RSD is not a pleasant condition and finding doctors that understand what it means to have RSD still isn’t easy to find. Comments
March 2009
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