"Dedicated To Helping RSD/CRPS Patients Worldwide"
We hope to assist patients, as well as family, and friends of those who suffer from Reflex Sympathetic Dystrophy (RSD) or more recently known as Complex Regional Pain Syndrome (CRPS). This organization was formed in July 1990; and since then, has sent information regarding RSD/CRPS to hundreds of thousands patients and professionals worldwide. The free information we offer will help educate and inform you, your family, friends as well as your physician regarding the signs, symptoms, diagnosis and the latest methods of treatment for RSD/CRPS.
RSD Article # 6
The following article RSDS-Reflex Sympathetic DystrophySyndromewas published in the medical journal Clinical Management. Vol 9, No.1.
This article was authored by Ellen G. Wattay, Ph.D., PT.
Below is an abstract from the article RSDS-Reflex Sympathetic DystrophySyndrome.
Please click on the link below to view the full text of this article in PDF-format.
RSDS Reflex Sympathetic Dystrophy Syndrome By: Ellen G. Wattay, Ph.D., PT
Physicians are becoming more familiar with the symptoms of reflex sympathetic dystrophy syndrome (RSDS), but there are still many health care professionals who, when they see no objective signs of tissue injury or believe that a patient has had adequate medical and therapeutic intervention but still complains of pain, tell the patient that nothing further can be done. If a patient reports one or a variety of seemingly bizarre symptoms of swelling, temperature changes in the involved region, burning pain, muscle pain, or spasm limiting motor function, atrophy, and skin changes in the area concerned, he or she too often is dismissed as having a psychological problem. The patient is told to see a psychiatrist or that “you must learn to live with it” but is not told how.
Ellen G. Wattay, PhD, P.T. RSDS-Reflex Sympathetic Dystrophy Syndrome, Clinical Management, Vol. 9: (1) 28-29.