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
Joined June 2009
902 Photos and videos Photos and videos

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  1. Retweeted
    8h

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

    4 retweets 6 likes
  2. 14h

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

    2 retweets 8 likes
  3. Jul 26

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

    2 retweets 4 likes
  4. Retweeted
    Jul 26

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

    5 retweets 8 likes
  5. Retweeted
    Jul 25

    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 retweets 264 likes
  6. Jul 26

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

    2 retweets 6 likes
  7. Jul 25

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

    7 retweets 5 likes
  8. Jul 25

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

    1 retweet 1 like
  9. Retweeted
    Jul 25

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

    29 retweets 25 likes
  10. Jul 24

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

    2 retweets 4 likes
  11. Jul 23

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

    6 retweets 13 likes
  12. Jul 22

    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 likes
  13. Jul 21

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

    4 retweets 7 likes
  14. Jul 20

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

    4 retweets 3 likes
  15. Jul 20

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

    1 retweet 1 like
  16. Jul 19

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

    3 retweets 2 likes
  17. Jul 18

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

    4 retweets 7 likes
  18. Jul 18

    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 retweets 5 likes
  19. Jul 17

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

  20. Jul 17

    When you know is right around the corner!

    2 retweets 7 likes

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