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
Clárú: Meitheamh 2009
902 Pictiúr nó físeán Pictiúir agus físeáin

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  1. Rinne Atweetáil
    8 n-uaire an chloig ó shin

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

    4 atweetáil 6 chroí
  2. 14 uair an chloig ó shin

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

    2 atweetáil 8 gcroí
  3. 27 Iúil

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

    2 atweetáil 4 chroí
  4. Rinne Atweetáil
    26 Iúil

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

    5 atweetáil 8 gcroí
  5. Rinne Atweetáil
    25 Iúil

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

    12 freagra 222 d’atweetálacha 264 croí
  6. 26 Iúil

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

    2 atweetáil 6 chroí
  7. 25 Iúil

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

    7 n-atweetáil 5 chroí
  8. 25 Iúil

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

    1 atweetáil amháin 1 chroí
  9. Rinne Atweetáil
    25 Iúil

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

    29 d’atweetálacha 25 croí
  10. 24 Iúil

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

    2 atweetáil 4 chroí
  11. 23 Iúil

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

    6 atweetáil 13 croí
  12. 22 Iúil

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

    1 atweetáil amháin 4 chroí
  13. 21 Iúil

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

    4 atweetáil 7 gcroí
  14. 20 Iúil

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

    4 atweetáil 3 chroí
  15. 20 Iúil

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

    1 atweetáil amháin 1 chroí
  16. 19 Iúil

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

    3 atweetáil 2 chroí
  17. 18 Iúil

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

    4 atweetáil 7 gcroí
  18. 18 Iúil

    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 atweetáil 5 chroí
  19. 17 Iúil

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

  20. 17 Iúil

    When you know is right around the corner!

    2 atweetáil 7 gcroí

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