I swam seven hours in a ten hour period on the 27th of November, marking seven years of living with CRPS/RSDS.
1. Raise funds to promote education, awareness and hope for people diagnosed with this condition through the donation of funds, products and services to RSDSA
2. Encourage healthcare providers, insurance providers, researchers and employers to support (and pay for) alternative therapies, such as aqua therapy, for CRPS and other chronic pain conditions
3. Raise funds to support Reflex Sympathetic Dystrophy Syndrome Association (RSDSA).
RSDSA is a national non-profit organization driven to provide education,
support and hope to all those affected by CRPS/RSD while driving research for better treatments and a cure. All donation and products/service donations are tax-deductible.
CRPS/RSD is a neuroinflammatory syndrome characterized by intense chronic pain, swelling, tropic changes, vascular changes, and functional impairment of the limb or affected area. CRPS is considered the most painful of all medical problems – pain that is rated on the McGill Pain Index as worse than cancer, amputation and childbirth. CRPS/RSD is often called the “suicide disease” and is so painful that many people cannot tolerate being touched, hugged or even wearing normal clothes or shoes. There is no cure for CRPS.
Outside funding is crucial to creating awareness of CPRS and providing assistance, education, guidance, advocacy and support for people diagnosed with this condition. In addition to funding research for better treatments and a possible cure, RSDSA also provides emergency financial assistance to support people with medical expenses due to disability and loss of careers from CRPS.