MDA USA

@MDAnews

MDA is leading the fight to free individuals—and the families who love them—from the harm of muscular dystrophy, ALS and related muscle-debilitating diseases.

Nationwide and HQ in Chicago
mda.org
Bergabung Juni 2009
902 Foto dan video Foto dan video

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  1. me-Retweet
    8 jam yang lalu

    Leading patient groups urge Congress to abandon proposed 'skinny repeal' and instead work in a bipartisan manner on health care reform

    4 retweet 6 suka
  2. 14 jam yang lalu

    Jared King is climing Mt. Kilimanjaro to raise money for MDA and ALS Awareness

    2 retweet 8 suka
  3. 27 Jul

    Living with ? Help find the causes of ALS. Complete the Nat’l ALS Registry’s risk factor surveys at .

    2 retweet 4 suka
  4. me-Retweet
    26 Jul

    health care 'repeal only' effort fails to gain necessary votes in Senate to pass. See how your Senator voted here

    5 retweet 8 suka
  5. me-Retweet
    25 Jul

    On July 26th, 1990 President George H. W. Bush signed the Americans with Disabilities Act. It's been 27 years, let's celebrate!

    12 balasan 222 retweet 264 suka
  6. 26 Jul

    Ryan Karlin, who lives w DMD, is thriving thx to the care he receives at MDA Care Center

    2 retweet 6 suka
  7. 25 Jul

    Let us help u & ur family be prepared for anything with MDA's emergency resources guide.

    7 retweet 5 suka
  8. 25 Jul

    Tip: share relevant content created by others - it's authentic, engaging & is cheap. RoundTeam makes it easy to do:

    1 retweet 1 suka
  9. me-Retweet
    25 Jul

    MDA & leading patient groups urge Congress not to repeal the ACA w/o replacement legislation & to take bipartisan approach

    29 retweet 25 suka
  10. 24 Jul

    Meet the members of Henry's Heroes an who run for Henry, living with CMD

    2 retweet 4 suka
  11. 23 Jul

    Who exactly is ? Meet these spirited athletes and learn what inspires them to keep pounding the pavement.

    6 retweet 13 suka
  12. 22 Jul

    Carla who lives with an NMD shares what it's like living w a disability in a world designed for able - bodied people

    1 retweet 4 suka
  13. 21 Jul

    Meet Pat Sawhill, who runs w for his son Finley, who lives with nemaline myopathy

    4 retweet 7 suka
  14. 20 Jul

    Should u check out this summer? Accessible travel blogger shares the scoop

    4 retweet 3 suka
  15. 20 Jul

    Did u miss the DMD Treatment Update: Emflaza webinar? Find the full webinar and key highlights here:

    1 retweet 1 suka
  16. 19 Jul

    Stay up to date on clinical trial opportunities that you may be eligible for.

    3 retweet 2 suka
  17. 18 Jul

    Johanna Hamel shares insight into her work in comparative studies of RNA toxicity in myotonic dystrophy (DM).

    4 retweet 7 suka
  18. 18 Jul

    Incredible work 😀Looks like the event was a major success!

    Our Beach Party raised over $7,000 for ! Thanks to everyone who chipped in! See you next year!
    2 retweet 5 suka
  19. 17 Jul

    . in his first blog about MDA-sponsored research shares updates about glucocorticoid steroids

  20. 17 Jul

    When you know is right around the corner!

    2 retweet 7 suka

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