Solving Problems By Listening to Patient Voices

We are you. Led by persons living with AiArthritis diseases, our organization understands exactly what resources are needed to improve lives. For example, our program RANT! was created because often we have a lot to say but may not want to voice our opinions, perspectives, or experiences publicly. So RANT was created so you could express yourself anonymously (optional). But your RANTS also help us identify needs for resources and programs. 

Check Out These Patient-Inspired Resources


  • AiArthritis Voices 360 Talk Show. Over 100 episodes covering all the topics we focus on at AiArthritis, led by a dozen patient voice co-hosts from around the world. Pull up a seat at the table, it's your turn to add your comments, options, perspectives, and experiences to the conversation!
  • RANT! Created by patients who said, "We are always venting to one another in social groups. Why not have a place to 1) do it privately if we don't want others to say, just vent to people who understand and 2) capture some of the most pressing issues that are truly bothering us." Submit with your name or not. Feel better, vent away!
  • "Go With Us!" to Scientific (research) Conferences. Every year leaders from AiArthritis (people living with AiArthritis diseases) attend the American College of Rheumatology (ACR) and European Alliance of Associations for Rheumatology (EULAR) and we bring the world of patients along with us (virtually; some committed volunteers in person). Be part of it and learn more about your disease than ever imagined! It's a truly unique and interactive experience.
  • Biosimilars Education. Biosimilars are here - what do you want to know?
  • COVID-19 Related Resources. Links to guidance and a vaccination hotline.




  • COVID-19 Related Resources

    Trusted resources, vaccination hotline.

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    • Check Out These Patient-Inspired Tools

    • Clinical Trials. Complete our aid if you are thinking about being part of a clinical trial - and then let us help you talk about it with your doctor.
    • Support Tool. Start your own Support Tool to uncover your needs as a patient AND the needs of those in your support network - because they are going through some stuff, too. Use as a communication tool to build understanding, acceptance, and relationships.
    • Disease Education. "What does it feel like?" Top downloaded resource to help others understand what it feels like to have an AiArthritis disease.
    • Still's Disease Brochures and Awareness Posters.* Patient-led disease brochures, medical information folding card, and awareness posters to help others understand.

    *In 2017, the International Still's Disease Foundation dissolved into AiArthritis. Our promise to the founders, who have now passed on, was to finish the work they started, which included disease brochures , awareness materials, and hosting Still's Disease Awareness Day every September.

    The Mystery Patient - For Those Still Searching to Be Heard

    For those not yet diagnosed, but looking for answers, we really do understand. Most of us have been exactly where you are. Soon we will be publishing advice like what questions to ask, what to do if you are told 'nothing is wrong with you', and other tips. In the meanwhile, what do you need to know?

    FOR THOSE NOT YET DIAGNOSED

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