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I have a growing number of friends with Reflex Sympathetic Dystrophy. Yesterday my new Internist suggested that I may have RSD, myself. I will be looking for more informational sites to list here for both of us.
The Reflex Sympathetic Dystrophy Coalition is an international organization focused in providing medical, social, and therapeutic information on Reflex Sympathetic Dystrophy.
Reflex Sympathetic Dystrophy Syndrome Association of America. - RSDS's home page with lot of helpful information about this multi-symptom, multi-system, syndrome.
RSD Support From Ones Who Care. - An online support group to ensure that people who endure the pain and agony of RSD or related illnesses do not suffer needlessly because they do not have anyone that validates and understands their pain. Provides an avenue of support to these individuals and their families and caregivers.
Pain Pal's RSD and Medical Links. Maine's RSDHope, an International RSDS Group, offers useful information on everything from Medical aspects of RSD to support information for patients and loved ones. RSD Information. RSD information for patients and others. The Reflex Sympathetic Dystrophy Syndrome Association of California. A statewide
non-profit corporation comprised of individuals dedicated to promoting education in the medical condition known as Reflex Sympathetic Dystrophy Syndrome (RSD), to render assistance to those people who suffer from RSD, and to assist groups or research facilities in an attempt to develop effective diagnosis, treatment and cure for
Reflex Sympathetic Dystrophy and all Complex Regional Pain Syndromes.