Your voice is incredibly important! Help us advocate for patients by selecting one of our pre-written emails to customize and send to your lawmaker.
You can help us advocate for better rheumatic disease care by answering a short survey.
The Rheumatology Research Foundation funds research to improve the lives of people with rheumatic diseases and awards and grants to recruit and train rheumatologists.
A national survey revealed what it’s like to live with a rheumatic disease. Find out the results and consider sharing them with others.
We have social media graphics and posts to help you spread the word about Rheumatic Disease Awareness Month. You can also view (and share) this year’s public service announcement (PSA) to learn how Venus got back on top of her game after being diagnosed with Sjogren’s Syndrome. Be sure to check out some of the latest Rheum4You blog posts as well.
By: Venus Williams, RDAM 2019 spokesperson, tennis champion and CEO of EleVen and V Starr Interiors My journey to diagnosis was not an easy one. It [...]
Exciting things are happening here in Washington, D.C.! Not only is September Rheumatic Disease Awareness Month, but also Advocates for Arthritis will bring patient advocates [...]
Whether you just learned that you have a rheumatic disease or have been living with one for a while, you should ask questions regularly throughout [...]