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
Gått med juni 2009
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  1. Retweetade
    för 8 timmar sedan

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

    4 retweets 6 gillanden
  2. för 14 timmar sedan

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

    2 retweets 8 gillanden
  3. 27 juli

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

    2 retweets 4 gillanden
  4. Retweetade
    26 juli

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

    5 retweets 8 gillanden
  5. Retweetade
    25 juli

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

    12 svar 222 retweets 264 gillanden
  6. 26 juli

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

    2 retweets 6 gillanden
  7. 25 juli

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

    7 retweets 5 gillanden
  8. 25 juli

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

    1 retweet 1 gillande
  9. Retweetade
    25 juli

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

    29 retweets 25 gillanden
  10. 24 juli

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

    2 retweets 4 gillanden
  11. 23 juli

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

    6 retweets 13 gillanden
  12. 22 juli

    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 gillanden
  13. 21 juli

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

    4 retweets 7 gillanden
  14. 20 juli

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

    4 retweets 3 gillanden
  15. 20 juli

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

    1 retweet 1 gillande
  16. 19 juli

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

    3 retweets 2 gillanden
  17. 18 juli

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

    4 retweets 7 gillanden
  18. 18 juli

    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 retweets 5 gillanden
  19. 17 juli

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

  20. 17 juli

    When you know is right around the corner!

    2 retweets 7 gillanden

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