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
S-a alăturat în iunie 2009
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  1. a redistribuit
    acum 8 ore

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

    4 redistribuiri 6 aprecieri
  2. acum 14 ore

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

    2 redistribuiri 8 aprecieri
  3. 27 iul.

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

    2 redistribuiri 4 aprecieri
  4. a redistribuit
    26 iul.

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

    5 redistribuiri 8 aprecieri
  5. a redistribuit
    25 iul.

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

    222 de redistribuiri 264 de aprecieri
  6. 26 iul.

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

    2 redistribuiri 6 aprecieri
  7. 25 iul.

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

    7 redistribuiri 5 aprecieri
  8. 25 iul.

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

    1 redistribuire 1 apreciere
  9. a redistribuit
    25 iul.

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

    29 de redistribuiri 25 de aprecieri
  10. 24 iul.

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

    2 redistribuiri 4 aprecieri
  11. 23 iul.

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

    6 redistribuiri 13 aprecieri
  12. 22 iul.

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

    1 redistribuire 4 aprecieri
  13. 21 iul.

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

    4 redistribuiri 7 aprecieri
  14. 20 iul.

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

    4 redistribuiri 3 aprecieri
  15. 20 iul.

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

    1 redistribuire 1 apreciere
  16. 19 iul.

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

    3 redistribuiri 2 aprecieri
  17. 18 iul.

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

    4 redistribuiri 7 aprecieri
  18. 18 iul.

    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 redistribuiri 5 aprecieri
  19. 17 iul.

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

  20. 17 iul.

    When you know is right around the corner!

    2 redistribuiri 7 aprecieri

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