This site exists to spread
awareness of Reflex Sympathetic Dystrophy and to encourage those who
already have RSD.
Pass the word on.
RSD related websites and
Support Groups
RSD patients and carers now
have many places to find help as concerned people have created
support groups, campaigns and websites to raise awareness and
provide help. Here is a selection of websites where you can find
information, advice and contact with people who understand. If
you know of sites we ought to be listing here, please click the
Contact button and write to one of the RSD Alert team.
Both run by Anthony Tobin
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RSD World News gives daily updates on sites, medicines,procedures
and papers on RSD/CRPS.
Quickbase is a vast resource of links to RSD websites
and on-line articles, stories and news.
This UK based site is designed
for anyone who has pain of any kind. Pain Support
promotes a multi-disciplinary approach, where
conventional medicine and complementary therapies
work side by side.
USA based Support Group
for parents of children with RSD. RSDParents was
born out of a need for a place for parents of
children with RSD to reach out to other parents
in the same situation for support, information,
and friendship. They welcome parents or guardians
of these children, no matter how young or old
the child. They want you to be able to speak freely
about the issues you are dealing with. RSDParents
don't want you to feel alone any longer.
Search for specialists
or GP etc in any area of Australia. Create a personal
health record online and keep articles of interest,
a record of your medication, your doctor's contact
details and more.
