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TMA Flying Solo Affinity Group Meeting
Join TMA’s Flying Solo Affinity Group: Support for Those Living with Myositis Without a Live-In Care Partner
The TMA Flying Solo Affinity Group is a dedicated space for individuals diagnosed with myositis who do not have a live-in care partner. Whether you live alone, are married but your spouse is unable to provide care, or even find yourself as the caregiver for your spouse, this group is here to offer understanding and support.
Living with myositis can be particularly challenging without a live-in care partner, but Flying Solo offers a community where you can connect with others who truly understand your unique circumstances. Share experiences, find helpful resources, and gain insights on managing daily life with myositis while navigating the complexities of independence and self-care.
When?
First Wednesday of each month at:
8:00 PM ET | 7:00 PM CT | 6:00 PM MT | 5:00 PM PT
Join us for this monthly meeting to connect, find strength, and support each other in our myositis journeys. You are not alone – come share and learn with others who “fly solo” like you!
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About the Leader | Rhonda Rogers
Rhonda Rogers, diagnosed with Inclusion Body Myositis (IBM), is a passionate myositis advocate, also known as “Myositis Warrior”, who brings connection, humor, and heart to everything she does. She co-leads TMA’s Southern California Support Group and facilitates the TMA Flying Solo Affinity Group for people living with myositis who do not have a live-in care partner. Rhonda also administers the popular Myositis Warrior Facebook public group, known for its upbeat, candid, and often humorous take on the unbelievable realities of life with myositis. Whether leading community groups or raising awareness in her signature Myositis Warrior cape at events like Comic-Con, Rhonda inspires others to meet life with resilience and a smile.
In recognition of her outstanding leadership and support for the myositis community, Rhonda will receive the Marianne Moyer Myositis Leader Award at MyoCon 2025, along with her TMA Southern California co-leader, Nancy Harber. This award honors TMA volunteers who lead the way by helping others and making a lasting impact.
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Access Myositis Education Here
Interested in learning more about myositis? Virtually all TMA webinars are available to watch anytime on our YouTube channel! Whether you missed a live session or want to revisit important information, you’ll find a wide range of educational and support-focused webinars. Explore our many curated playlists—including by diagnosis subtype—for easy access to the content that matters most to you. Subscribe and start watching today!
