|
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 now - fill out an application.
Click here for more Ways to Give
Member Benefits:
- RSDSA Review, our quarterly newsletter, provides up-to-date information on treatment, research, legislation and legal issues. Sample Issue (PDF)
- RSDSA Review Digest, a compendium of research and treatment articles from 2006 to 2008
- 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
Join RSDSA online:
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
|
