In a victory for patients, a federal judge recently struck down a policy that allowed health insurance plans to use copay accumulator and maximizer programs, thereby charging patients more for essential prescription medications. This is good news for those who live with myositis and want to use a manufacturer’s assistance coupon to help them afford…
Continue ReadingPeter Frampton leads the fight against myositis from front stage
When an individual goes above and beyond, representing, raising awareness, and contributing financially to the work of The Myositis Association (TMA), it is more than fitting to present them with the Patient Ambassador Award. TMA is excited to announce that the 2023 Patent Ambassador Award is being presented to composer, musician, and beloved American icon,…
Continue ReadingHow I moved from paralysis to hiking the Alps
Fiona Ratkoff is grateful to The Myositis Association for enabling her to get back on skis again after being paralyzed with dermatomyositis.
Continue ReadingBreaking news: Medicare coverage for power wheelchairs
TMA is excited to share the news about Medicare coverage for seat elevation for Medicare beneficiaries using power wheelchairs. The Centers for Medicare & Medicaid Services (CMS) has made a significant expansion to its coverage policies for individuals relying on power wheelchairs. Effective immediately, Medicare will now cover seat elevation in power wheelchairs for Medicare…
Continue ReadingThe Myositis Association announces myositis research awards
COLUMBIA, MD, May 9, 2023 – The Myositis Association announces the awarding of two new research grants to fund basic and applied investigations in myositis diseases. Since 2002, TMA’s annual research funding program has awarded nearly $8.2 million in research support. They are pleased to announce the following research projects selected by TMA’s Board of…
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