Advocacy
Advocacy is easier than you may think, as it is simply public support for a particular cause – your cause! Everyone has a story to tell, and you can use yours to raise awareness and advocate for our community.
When you speak with your medical providers, pharmacists, colleagues, family and friends about CRPS, you are using your advocacy skills. As an advocate, you can also be an important part of the legislative and policy making process.
You can make your voice heard by writing or calling your Senators and Representatives.
- Take a moment to write to your Congressmen and Congresswomen using our template. Be sure to include your unique story and touches to your letter so it will stand out when their offices receive it via email or mail.
- If you need help finding your representatives, visit house.gov and enter your ZIP code.
If you are interested, we suggest checking out the Rare Disease Legislative Advocate (RDLA) website. RDLA is a part of EveryLife Foundation for Rare Diseases and they have a wealth of information on how to speak up for CRPS in the rare disease community. Included are advocacy tools and tip sheets, along with information on how to foster a relationship with your Member of Congress, how to schedule a meeting with your legislator, and how to lobby for rare disease nonprofit organizations.
You can make a difference!
Our Mission
- Equip, enable, and empower for self-advocacy
- Develop, recommend, and promote state and federal legislation
- Promote awareness, equal treatment, and fair coverage
RSDSA Advocacy Committee
Contact us by emailing [email protected]
Read Lisa Van Allen’s latest posts on the RSDSA blog:
Advocacy Update on S.2922/H.R.7164, The Advancing Research for Chronic Pain Act