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
Iscritto a giugno 2009
902 foto e video Foto e video

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  1. ha ritwittato
    8 ore fa

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

    4 Retweet 6 Mi piace
  2. 14 ore fa

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

    2 Retweet 8 Mi piace
  3. 27 lug

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

    2 Retweet 4 Mi piace
  4. ha ritwittato
    26 lug

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

    5 Retweet 8 Mi piace
  5. ha ritwittato
    25 lug

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

    12 risposte 222 Retweet 264 Mi piace
  6. 26 lug

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

    2 Retweet 6 Mi piace
  7. 25 lug

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

    7 Retweet 5 Mi piace
  8. 25 lug

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

    1 Retweet 1 Mi piace
  9. ha ritwittato
    25 lug

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

    29 Retweet 25 Mi piace
  10. 24 lug

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

    2 Retweet 4 Mi piace
  11. 23 lug

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

    6 Retweet 13 Mi piace
  12. 22 lug

    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 Mi piace
  13. 21 lug

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

    4 Retweet 7 Mi piace
  14. 20 lug

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

    4 Retweet 3 Mi piace
  15. 20 lug

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

    1 Retweet 1 Mi piace
  16. 19 lug

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

    3 Retweet 2 Mi piace
  17. 18 lug

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

    4 Retweet 7 Mi piace
  18. 18 lug

    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 Mi piace
  19. 17 lug

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

  20. 17 lug

    When you know is right around the corner!

    2 Retweet 7 Mi piace

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