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People who join RSDSA are not content to be victims of this
devastating disorder, but take an active role in achieving
our goals of education, awareness, and research.
Our members are patients, family and friends, healthcare professionals,
attorneys, and businesspeople who understand the devastating
effects of CRPS, and are dedicated to helping people like
you live more functioning lives. We invite
you to join a community dedicated to working for you and
your future.
Your RSDSA membership is important. There is power in numbers,
and we would like to see our membership, currently over 7000,
grow to encompass all those who are afflicted with the syndrome
so that when we speak to the legislature, the pharmaceutical
companies, and medical associations, our voice is strong and
our message is clear.
As
a member, you have a forum to communicate your concerns, share
your experiences, and learn about the most recent advances
in CRPS treatment and research. Join RSDSA online now or fill out an application.
Member Benefits:
- RSDSA Review, our quarterly newsletter, provides
up-to-date information on treatment, research, legislation
and legal issues. Sample
Issue
- RSDSA Review Digest, a compendium of research
and treatment articles from 2002 to 2005
- Pen Pal Service, a patient support program exclusively for
RSDSA members
- Referral Service to physicians and other services
- Special mailings announcing timely news about Discounts
on RSDSA literature and Conferences
Dues:
- $20 per year in the US.
- $25 per year outside the US, payable in US Funds
At the end of one year membership, renewal cards are mailed. RSDSA does not provide membership cards. If you are unable to pay dues, please fill out the application with a note to that effect. You will be put on the membership list.
RSDSA
99 Cherry Street
PO Box 502
Milford, CT 06460
203.877.3790
Toll Free: 877.662.7737 |
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