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
Uniuse en xuño 2009
902 Fotos ou vídeos Fotos e vídeos

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  1. rechouchiou
    Hai 8 horas

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

    4 rechouchíos 6 gústames
  2. Hai 14 horas

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

    2 rechouchíos 8 gústames
  3. 27 xul

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

    2 rechouchíos 4 gústames
  4. rechouchiou
    26 xul

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

    5 rechouchíos 8 gústames
  5. rechouchiou
    25 xul

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

    12 respostas 222 rechouchíos 264 gústames
  6. 26 xul

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

    2 rechouchíos 6 gústames
  7. 25 xul

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

    7 rechouchíos 5 gústames
  8. 25 xul

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

    1 rechouchío 1 gústame
  9. rechouchiou
    25 xul

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

    29 rechouchíos 25 gústames
  10. 24 xul

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

    2 rechouchíos 4 gústames
  11. 23 xul

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

    6 rechouchíos 13 gústames
  12. 22 xul

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

    1 rechouchío 4 gústames
  13. 21 xul

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

    4 rechouchíos 7 gústames
  14. 20 xul

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

    4 rechouchíos 3 gústames
  15. 20 xul

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

    1 rechouchío 1 gústame
  16. 19 xul

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

    3 rechouchíos 2 gústames
  17. 18 xul

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

    4 rechouchíos 7 gústames
  18. 18 xul

    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 rechouchíos 5 gústames
  19. 17 xul

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

  20. 17 xul

    When you know is right around the corner!

    2 rechouchíos 7 gústames

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