Overview
Mentions in press and media 11
| Date | Title | Description |
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| Sep 21, 2026 | The Myositis Association recognizes leaders in rare disease advocacy, science and care with Heroes in the Fight awards | Father Stuart Long, inspiration for the Mark Wahlberg film Father Stu, will be posthumously honored at MyoCon 2026 ST. LOUIS, MO, UNITED STATES, September 21, 2026 /EINPresswire.com/ -- The Myositis Association (TMA) is proud to honor inspi... |
| Sep 21, 2026 | In a big year for rare disease, experts examine key developments in myositis research at MyoCon 2026 | From AI-assisted research and emerging cell therapies to a new drug approval, The Myositis Association's global conference takes stock of the latest science It’s an exciting time for myositis research, with new therapies advancing through c... |
| May 1, 2026 | May Is Myositis Awareness Month | The Myositis Association Leads Nationwide Effort to Raise Awareness, Advance Research, and Support Patients Each interview by these Emmy-award winning journalists brings to life the challenges of a myositis diagnosis. Thank you to the 11Ali... |
| Mar 31, 2026 | The Myositis Association Selected for NIH NOURISH Autoimmunity Challenge | TMA’s innovative, nutrition-focused research proposal is one of 15 projects selected in crowd-sourced search for ideas to reduce autoimmune disease burden. The proposal was created through extensive engagement with TMA’s patient and medical... |
| Sep 30, 2025 | The Myositis Association Announces Inaugural Recipient of Meredith C. Thomas Memorial Fellowship | Angeles Galindo Feria, MD, PhD The Myositis Association announces recipient of Meredith Thomas Fellowship grant to support research in antisynthetase syndrome and interstitial lung disease. This fellowship is a transformative opportunity to... |
| Sep 17, 2025 | From Sand to Spotlight: Volleyball Star Bourne Turns Battle with Rare Disease into National Honor for Myositis Awareness | Tri Bourne Tri Bourne, TMA Patient Ambassador Award Olympian and beach volleyball champion Tri Bourne is celebrated for resilience and powerful advocacy on behalf of people living with rare autoimmune diseases. I’m honored to receive this a... |
| Jan 22, 2025 | Myositis research awards bring hope to those with rare diseases | Projects exploring inclusion body myositis and juvenile myositis awarded The importance of independent funding for rare diseases like myositis cannot be overstated. Projects increase understanding and gather preliminary data to support appl... |
| Sep 4, 2024 | The Myositis Association Announces 2024 International Annual Patient Conference | COLUMBIA, MARYLAND, UNITED STATES, September 4, 2024 /EINPresswire.com/ -- The Myositis Association (TMA) is excited to announce its 2024 International Annual Patient Conference: Celebrating Our Connection, set to take place from September ... |
| Sep 3, 2024 | Supermodel Karen Alexander Honored as Patient Ambassador Awardee by The Myositis Association | Supermodel Karen Alexander It is a great honor to receive TMA’s Heroes in the Fight Patient Ambassador Award. Together I believe that we women of color can help to change the face of this disease.” — Karen Alexander COLUMBIA, MARYLAND, UNIT... |
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FAQ about The Myositis Association
When was The Myositis Association founded?
The Myositis Association was founded in 1993.
What has the press written about The Myositis Association?
Parsers VC has collected 11 articles mentioning The Myositis Association, among them “The Myositis Association recognizes leaders in rare disease advocacy, science and care with Heroes in the Fight awards” (Sep 21, 2026) and “In a big year for rare disease, experts examine key developments in myositis research at MyoCon 2026” (Sep 21, 2026).
Is The Myositis Association still active?
Yes, The Myositis Association is active; its latest activity on Parsers VC dates from Sep 21, 2026.