Welcome from RSDSA Patient Representative Mary Beth Kenny Ludington

Here’s a look from last year’s Achilles Walk for
Hope & Possibility TEAM RSDSA 2011

Quick Flicks:
Mary Beth Kenny Ludington, Patient Representative and Vice President, and Jim Broatch, Executive Director, share some quick thoughts with you.

We Have Excellent Information and Resources
RSDSA and FaceBook Communities
What is CRPS (RSD)?
RSDSA's Mission
Join RSDSA Today

RSDSA VIDEOS

You can now download and view all of the presentations from the October workshop on Imaging Neuroinflammation and Neuropathic Pain. The link will take you to the RSDSA YouTube channel.

CRPS Therapies: Clinicians Share Their Expertise

Call 877-662-7737 to order your copy. Copies are available for people with CRPS for a good-will donation and for $15 for a health care professional.

RSDSA publications can help you explain CRPS
I Have CRPS.pdf Download the 2-page pdf or call the RSDSA office (toll free: 877-662-7737) for a free laminated card.

Emergency Department Protocol for Patients with CRPS.pdf

New Brochure: Helping Children With CRPS Succeed in School

New! TSA Launches Toll Free Helpline for Travelers With Disabilities, Medical Needs

Summary of Glial Conference

RSDSA to Fund a New Opportunity in Clinical Research for CRPS Care

Help us Work for Your Better Future!
Enroll today in RSDSA's Study on the Natural History and Long-Term Health Effects of CRPS

If you are in crisis, please call 1-800-SUICIDE (800-784-2433) Click here or Contact The National Suicide Prevention Lifeline 800-273-TALK (8255)
(888-628-9454 en Español)

State-By-State Opiod Prescribing Policies
Prescribing controlled substances involves adherence to federal regulations in addition to stricter requirements imposed by individual states.

Resources for Veterans with CRPS

With a $1,000 donation you can be a Friend of RSDSA. You will be listed in the RSDSA Review and on our website for one year (if you choose) and will be invited to participate in a future teleconference call with one of our scientific advisors to discuss emerging research of interest to the CRPS community.
Your generous donation helps support RSDSA’s operating budget and allows staff and volunteers to concentrate on accomplishing our vital mission of promoting greater awareness and earlier recognition of CRPS, funding critical research, and providing support to people with CRPS and their loved ones.

 To learn more about this opportunity, please call Jim Broatch at 877-662-7737 or send an e-mail to jwbroatch@rsds.org.

The Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) was founded in 1984 to promote public and professional awareness of Complex Regional Pain Syndrome (CRPS), also known as Reflex Sympathetic Dystrophy (RSD).

Our website is designed to give patients, family members, and healthcare professionals the most up-to-date information on treatment, legislation, support groups, research, fundraising, and patient stories. RSDSA does not accept advertising for this website. Our website is funded by RSDSA membership revenue.

The website is not intended to provide advice on personal medical matters or to substitute for consultation with a physician.