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
Đã tham gia tháng 6 năm 2009
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  1. đã Tweet lại
    8 giờ trước

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

    4 tweet lại 6 thích
  2. 14 giờ trước

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

    2 tweet lại 8 thích
  3. 27 thg 7

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

    2 tweet lại 4 thích
  4. đã Tweet lại
    26 thg 7

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

    5 tweet lại 8 thích
  5. đã Tweet lại
    25 thg 7

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

    12 replies 222 tweet lại 264 thích
  6. 26 thg 7

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

    2 tweet lại 6 thích
  7. 25 thg 7

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

    7 tweet lại 5 thích
  8. 25 thg 7

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

    1 tweet lại 1 thích
  9. đã Tweet lại
    25 thg 7

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

    29 tweet lại 25 thích
  10. 24 thg 7

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

    2 tweet lại 4 thích
  11. 23 thg 7

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

    6 tweet lại 13 thích
  12. 22 thg 7

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

    1 tweet lại 4 thích
  13. 21 thg 7

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

    4 tweet lại 7 thích
  14. 20 thg 7

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

    4 tweet lại 3 thích
  15. 20 thg 7

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

    1 tweet lại 1 thích
  16. 19 thg 7

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

    3 tweet lại 2 thích
  17. 18 thg 7

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

    4 tweet lại 7 thích
  18. 18 thg 7

    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 tweet lại 5 thích
  19. 17 thg 7

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

  20. 17 thg 7

    When you know is right around the corner!

    2 tweet lại 7 thích

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