TMA volunteer Holly Jones caught up with the amazing Linda Sabatino on the Red Carpet at the 2024 Heroes in the Fight Award Celebration! Don't miss this exclusive sneak peek, and head over to our YouTube channel for the full interview with all the inspiring moments. Watch now! https://lnkd.in/efW78Byq #Myositis #MyositisWarrior #MyositisAwareness #TheMyositisAssociation #MyositisSupport #RareDisease #MYOMovement #MyositisLife #MyTMA #PatientAdvocacy #TheMyositisAgenda
About us
The Myositis Association (TMA) is a non-profit, voluntary health agency dedicated to improving the lives of people affected by myositis. Founded in 1993, TMA has grown from 16 patients, who helped form the organization, to more than 6,000 members who have been served by TMA. TMA is governed by a volunteer Board of Directors that includes patients, family members and interested professionals, bringing diverse strengths and perspectives to the organization. Through member newsletters, publications, support groups, research and advocacy, TMA helps those who have myositis today and works to prevent any others from having to experience myositis in the future.
- Website
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http://myositis.org
External link for The Myositis Association
- Industry
- Non-profit Organizations
- Company size
- 2-10 employees
- Headquarters
- Columbia, Maryland
- Type
- Nonprofit
- Founded
- 1993
Locations
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Primary
6950 Columbia Gateway Dr
Suite 370
Columbia, Maryland 21046, US
Employees at The Myositis Association
Updates
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Pre-order the 2024 International Annual Patient Conference recordings now! You'll get access to over 30 sessions, including keynotes and the Heroes in the Fight Awards, for just $149. Conference attendees get automatic access. Don't miss out—download available soon! https://lnkd.in/eCgtzfGC #Myositis #MyositisWarrior #MyositisAwareness #TheMyositisAssociation #MyositisSupport #RareDisease #MYOMovement #MyositisLife #MyTMA #PatientAdvocacy #TheMyositisAgenda #MyTMA #MyoNews #TMAIAPC24 #myositisIAPC2024 #TheMyositisAgenda #TMA2024IAPC
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Tee off for a cause! ⛳️ Join us on October 25th at Coyote Creek Golf Course for Nori's Fight: Drive for MDA5 Golf Tournament in Morgan Hills, CA. Enjoy a fun day of golf, contests, and a luncheon—all while supporting awareness for myositis ILD. Don't miss out on this amazing event! Register today to make a difference. 💙 📅 Date: October 25, 2024 📍 Location: Coyote Creek Golf Course 🕒 Time: 7:30 AM - 5:00 PM Register today! https://lnkd.in/enHt8kje #GolfForACause #NorisFight #Myositis #MyositisWarrior #MyositisAwareness #TheMyositisAssociation #MyositisSupport #RareDisease #MYOMovement #MyositisLife #MyTMA #PatientAdvocacy #TheMyositisAgenda
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⏳️LAST CALL - Tickets are on sale through MIDNIGHT tonight! ! If you're in the greater Chicago area there is still time to register for the 1st Annual Meredith C. Thomas Trivia Night Fundraiser on November 1, 2024, at 6 pm at the Butterfield Country Club, Oak Brook. It will be an unforgettable evening of trivia, a buffet dinner, with plenty of ways to support the Meredith C. Thomas Myositis Research Fellowship. Celebrate Meredith's passion for learning and community spirit by registering today! 💜 https://lnkd.in/eyQuC5jq #Myositis #MyositisWarrior #MyositisAwareness #TheMyositisAssociation #MyositisSupport #RareDisease #MYOMovement #MyositisLife #MyTMA #PatientAdvocacy #TheMyositisAgenda
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Join us on October 24 at 4 PM ET for a live webinar on managing Dermatomyositis with IVIg therapy, led by Dr. Christina Charles-Schoeman. Learn how this treatment works and its impact on patient outcomes. https://lnkd.in/e3fSF3Ff #Myositis #MyositisWarrior #MyositisAwareness #TheMyositisAssociation #MyositisSupport #RareDisease #MYOMovement #MyositisLife #MyTMA #PatientAdvocacy #TheMyositisAgenda
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The COVAD group is conducting a survey to explore holistic care for autoimmune conditions. The survey is open to anyone over 18, whether healthy or living with an autoimmune disease. Please take a moment to complete this survey today! Survey Link: https://lnkd.in/gtyZ-SeN #Myositis #MyositisWarrior #MyositisAwareness #TheMyositisAssociation #MyositisSupport #RareDisease #MYOMovement #MyositisLife #MyTMA #PatientAdvocacy #TheMyositisAgenda
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Are you in the greater Chicago area? Join in on celebrating the incredible life of Meredith Claire Thomas at the 1st Annual Meredith C. Thomas Trivia Night Fundraiser on November 1st! Come together for a night of trivia, fun, and community—all while supporting the Meredith C. Thomas Myositis Research Fellowship. Form your team or join one and enjoy an exciting evening in Oak Brook, IL! 📅 When: Friday, November 1, 2024, 6 PM – 10 PM 📍 Where: Butterfield Country Club, Oak Brook, IL RSVP Today! https://lnkd.in/eyQuC5jq #Myositis #MyositisWarrior #MyositisAwareness #TheMyositisAssociation #MyositisSupport #RareDisease #MYOMovement #MyositisLife #MyTMA #PatientAdvocacy #TheMyositisAgenda
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Living with myositis is hard, but you don't have to walk this journey alone. TMA's Virtual Support and Affinity Groups are here to support you. Our weekly virtual groups offer a secure and compassionate space for individuals living with myositis to connect with others who share similar experiences. With groups like TMA Adelante! Un grupo de apoyo sobre miositis para hispanohablantes and TMA's Flying Solo Affinity Group, there is a group for everyone to feel seen, heard and supported. Check out our events calendar on the TMA website to find a group that fits you and join us! We can't wait to meet you. https://lnkd.in/eN2N7HMd #Myositis #MyositisWarrior #MyositisAwareness #TheMyositisAssociation #MyositisSupport #RareDisease #MYOMovement #MyositisLife #MyTMA #PatientAdvocacy #TheMyositisAgenda
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Throw Back Thursday to our red carpet event during the 2024 Heroes in the Fight Award Celebration. Stay tuned as we share clips from interviews with our awardees and guests over the coming days. #Myositis #MyositisWarrior #MyositisAwareness #TheMyositisAssociation #MyositisSupport #RareDisease #MYOMovement #MyositisLife #MyTMA #PatientAdvocacy #TheMyositisAgenda
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In honor of Meredith Claire Thomas, we are showcasing the Meredith C. Thomas Myositis Research Fellowship. This fellowship will fund researchers studying myositis, antisynthetase syndrome, and interstitial lung disease. Help us celebrate Meredith's legacy by making a donation today to support the future of myositis research! "We know Meredith's hope was that someday, there will be an effective treatment for all of these diseases. This fellowship will help bring about a world without myositis." -The Thomas Family https://lnkd.in/eHGv3M-5 #Myositis #MyositisWarrior #MyositisAwareness #TheMyositisAssociation #MyositisSupport #RareDisease #MYOMovement #MyositisLife #MyTMA #PatientAdvocacy #TheMyositisAgenda