Living With RSDS, Inc. is a non profit organization. Our mission is to offer education, support and advocacy to those afflicted with CRPS/RSDS, their family, caregivers, friends, communities and medical professionals. We currently provide two free virtual meetings per month via Zoom.
Living with RSDS, Inc. is a non-profit 501(c)3 organization founded in 1997 to offer education, support and advocacy for those whose lives have been affected by Complex Regional Pain Syndrome (CRPS) also known as Reflex Sympathetic Dystrophy Syndrome (RSDS). CRPS/RSDS is a rare chronic neuro-inflammatory disorder. This extremely painful and often disabling syndrome is caused by a malfunction of the nervous system and immune system in response to a trauma. The nerves msifire causing constant pain signals being sent to the brain. There is no single diagnostic tool and CRPS/RSDS remains without a cure.