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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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Senior Member
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Another good website is rsdrx.com Dr. Hooshmand researched RSD 40 years in Florida. Under his website is called puzzles list. It is 146 questions and his answers. He is retired now. but has an associate taking his patients. My Dr. is a neurologist, psychiatrist and a pharmacologist. Does trial studies, teaches, just built two clinics here in Scottsdale, AZ with HBOT, which I am going to try. I have full body and internal RSD plus trigeminal neuralgia, fibromyalgia, PTSD, and now having lung issues-possibly sleep apnea-am waiting to get tested. The ketamine trials were done about 10 years ago at the Mayo Clinic-Scottsdale. On Neurotalk on March 7th there is a question regarding lung involvement and the 2nd post has a website mentioned I found very informative. RSD reacts differently to many of us as well as meds. Please research before doing anything. Some have gotten spread from a procedure that is supposed to arrest this disorder. I was misdiagnosed and wasn't correctly diagnosed for 4 years. I flew a couple states away to a well known sports injury orthopedic group, he knew in one minute followed up with nuclear med test. Our bones deteriorate. It is a very complicated disorder. Most of us are on a combination of meds. There are meds that help with nerve pain, that aren't opiods.Raised blood pressure is a common symptom, immune system deterioration, and body temperature control. I go from ice cold to red hot steaming. This is a serious disorder and extremely important to get treatment asap. I found physical therapy, massage therapy, and pool 86degree water therapy good for me. ![]() Please ask away, we are 'here for you' and want to provide support and comfort. One of your new friends, loretta ![]() |
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