We rely on the voices of those affected by these diseases to guide our education and awareness initiatives to prevent misunderstandings, accelerate diagnosis, improve disease management, and advance global awareness.
Experienced Advocates. Several people leading our organization has served on advisory panels, participated in focus groups, and presented at conferences - all to help the public and other stakeholders understand the awareness and education needs of our community.
Peer-to-Peer Communications. We do not represent the patient voice, we are the patient voice. Whether we are hosting discussions to explore issues of unmet need or to help our community understand complex topics, we are trusted peers and appreciated leaders.
Cross Category Initiatives. While we focus on improving education, advocacy, and research, our work often overlaps these pillars, as one often influences the other.
* In 2017, the International Still's Disease Foundation (ISDF) dissolved into AiArthritis. As a result, we honored a commitment to continue their work to provide resources and educational materials that can help expedite diagnosis and maintain quality of life to those impacted by Still's Disease. We plan to develop similar patient-led educational materials for other disease groups we cover over the next several years.
Based on our new "patient journey" designed website, and in conjunction with our blog and existing programs, we will publish 100's of resources to help patients from pre-diagnosis through comorbidities and remission.
Through a variety of programs we aim to help the public and "first line" health practitioners identify our diseases and expedite diagnosis and therapeutic intervention. Focus on diverse demographics, "mystery patients", the undiagnosed, and those most at risk.
Although biosimilars have been proven to be as safe and effective as the brand drug ("originator"), complex patients and some physicians worry about non-active ingredients or changing methods of administration (shot, injection, pill). AiArthritis hopes we can help patients make the transition and talk to their doctor if they have any concerns.
Help patients by designing peer-led guidance and tools so they feel empowered to participate in discussions with healthcare professionals. These tools can help to improve disease management.
As the hosts of World AUTOimmune & AUTOinflammatory Arthritis Day every May 20th, we strive to DRIVE global awareness of all AiArthritis diseases and the issues we face individually and as a community.
International Foundation for AiArthritis
6605 Nottingham Ave.
St. Louis, MO 63109-2661
Tax ID: 27-1214308
Copyright 2024. All rights reserved. Information on this site is intended for informational purposes only Our foundation does not engage in the practice of medicine. Please consult a physician to obtain personal healthcare and treatment options. 501(c) 3 Nonprofit Tax ID: 27-1214308.