Search the RSDSA Website Search Blog Instagram Links January 1, 2015 Read the latest from the RSDSA Blog Telltale Signs and Symptoms of CRPS/RSD Register: Advancing Rare Disease Therapies Through an FDA Rare Disease Innovation Hub – October 16, 2024 Donate… Blog Support for People with CRPS January 8, 2020 Written by Phyliss Shanken, MA I wrote an article about my personal experience with CRPS that appeared in ADVANCE for Physical Therapists and for Occupational Therapists in 1993. In response to that article,… Blog How To Lose Your Case In 12 Easy Steps April 15, 2023 Written by R. Steven Shisler, Esq. for the RSDSA blog. Frequently, I receive telephone calls from potential clients who have, frankly, severely damaged their ongoing claims or lawsuits. When you pursue legal… Blog Supporting Role: CRPS Support Group Leader Awarded Hero of Hope By Stefani Kronk November 10, 2010 The Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) held its 12th Annual Bounty of Hope to Benefit RSDSA on November 3, 2010 in New York City. In addition to fundraising and promoting disease… Blog My Life’s Journey With RSD September 20, 2020 Written by Louise Plaster for the RSDSA blog. February 17, 1992 started out like any other day. I got up and got ready for work, got my daughter ready for… Pages: 1234567891011121314151617181920212223242526272829303132333435363738394041424344454647484950515253545556575859606162636465666768697071727374757677787980818283848586878889909192939495
