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
Haziran 2009 tarihinde katıldı
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Tweetler

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  1. Retweetledi
    8 saat önce

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

    4 retweet 6 beğenme
  2. 14 saat önce

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

    2 retweet 8 beğenme
  3. 27 Tem

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

    2 retweet 4 beğenme
  4. Retweetledi
    26 Tem

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

    5 retweet 8 beğenme
  5. Retweetledi
    25 Tem

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

    12 yanıt 222 retweet 264 beğenme
  6. 26 Tem

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

    2 retweet 6 beğenme
  7. 25 Tem

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

    7 retweet 5 beğenme
  8. 25 Tem

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

    1 beğenme
  9. Retweetledi
    25 Tem

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

    29 retweet 25 beğenme
  10. 24 Tem

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

    2 retweet 4 beğenme
  11. 23 Tem

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

    6 retweet 13 beğenme
  12. 22 Tem

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

    4 beğenme
  13. 21 Tem

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

    4 retweet 7 beğenme
  14. 20 Tem

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

    4 retweet 3 beğenme
  15. 20 Tem

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

    1 beğenme
  16. 19 Tem

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

    3 retweet 2 beğenme
  17. 18 Tem

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

    4 retweet 7 beğenme
  18. 18 Tem

    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 beğenme
  19. 17 Tem

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

  20. 17 Tem

    When you know is right around the corner!

    2 retweet 7 beğenme

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