• CartoonGems Myositis Awareness Month Fundraiser

    Virtual Event
    Commemorative

    Honey Dee - May is "Myositis Awareness" Month and I am here to help get the word out for all of those affected by this rare disease. Watch for merchandise available in the CartoonGems online store to show your support for those affected. During the month of May ALL proceeds from "Myositis Awareness" merchandise will...

  • TMA Southwest Florida Myositis Meeting (HYBRID)

    HealthFit 5880 Rand Blvd, Sarasota, FL, United States
    Hybrid Event
    Support or Affinity Group Meeting

    This group welcomes all Florida residents (and snowbirds) with myositis and their care partners to attend. This group meets four times a year in hybrid format (in-person and on zoom) every three months on the first Saturday from 11 AM-3 PM ET. Register Here TMA support groups are a place to connect, be understood, and...

  • TMA Care Partner Affinity Group Meeting

    TMA Care Partner Affinity Group Meeting
    Virtual Event
    Support or Affinity Group Meeting

    Please note there will be no July meeting to allow our volunteers to celebrate the holiday with their families. Join the TMA Care Partner Affinity Group: A Space Just for You Being a care partner to someone with myositis can be emotionally and physically challenging. Whether it’s dealing with stress, anxiety, or the weight of...

  • TMA Worldwide Myositis Support by Diagnosis

    TMA Worldwide Myositis Support by Diagnosis
    Virtual Event
    Support or Affinity Group Meeting

    TMA’s Worldwide Myositis Support by Diagnosis Group is open to all, especially those without an active support group in their local area. Formally known as Nationwide, this group has hosted international members since its inception in 2022. The meeting divides into breakout rooms by diagnosis, and the TMA Care Partner Affinity Group meets in its own...

  • TMA Arizona & Nevada Myositis Support Group Meeting

    Virtual Event
    Support or Affinity Group Meeting

    Register here. Join us for connection, support, and shared experiences with others living with myositis in Arizona and Nevada. This welcoming group meets quarterly—on the first Saturday of February, May, August, and November—via Zoom. Whether you're newly diagnosed or have been living with myositis for years, you’re invited to be part of a caring community...

  • Research Briefing from the Global Conference on Myositis (GCOM)

    Virtual Event
    Webinar

    What’s next in myositis treatment—and what are the latest clinical trials revealing? To kick off Myositis Awareness Month, The Myositis Association (TMA) and the Myositis Clinical Trials Consortium (MCTC) are partnering together to present this special webinar called Research Briefing from the Global Conference on Myositis (GCOM). This leading scientific conference, held every two years,...

  • TMA New Jersey Support Group Meeting

    TMA New Jersey Support Group Meeting
    Virtual Event
    Support or Affinity Group Meeting

    This group for all myositis diagnoses meets every other month on the first Monday at 6:30 PM ET | 5:30 PM CT | 4:30 PM MT | 3:30 PM PT. Register here. TMA support groups are a place to connect, be understood, and feel less alone — whether you’re seeking support, offering encouragement, or somewhere...

  • Diagnosis Day: Ask the Expert Immune-Mediated Necrotizing Myopathy (IMNM)

    Virtual Event
    Commemorative

    In recognition of Myositis Awareness Month and IMNM Diagnosis Day, The Myositis Association (TMA) invites you to a special Ask the Expert webinar focused on Immune-Mediated Necrotizing Myopathy (IMNM). This program will feature Dr. Andy Mammen, Chief of the Muscle Disease Unit at the National Institutes of Health (NIH), who will share expert insights on...

  • Diagnosis Day: Cafe Chat Immune-mediated Necrotizing Myopathy (IMNM) Edition

    Virtual Event

    In honor of Diagnosis Days during Myositis Awareness Month this May, join us for a special Café Chat focused on immune-mediated necrotizing myopathy (IMNM). This relaxed, informal gathering is a space to connect with others who truly understand the IMNM journey. We’ll be sharing stories of the day we were diagnosed—the moments, emotions, and experiences...