La Muscular Dystrophy Association è una
associazione privata che si basa sulla collaborazione fra
scienziati e cittadini che sono intenzionati a sconfiggere
la malattie neuromuscolari che affliggono più di un milione
di americani.
La MDA combatte le malattie neuromuscolari per mezzo di
ampi programmi di ricerca, compresi servizi medici e
comunitari, ed una diffusa educazione sanitaria pubblica e
professionale.
Il Rapporto
Ross Read about the
latest in MDA’s programs and progress from the perspective of Robert Ross,
MDA’s President & CEO
(5/4/06).
E' tornato il
carnevale MDA It's Cool to Care!
Visit the MDA Carnival
Web site for ideas on how to host a carnival.
Ricordando
Mattie Read about Mattie
Stepanek's remarkable life and
spirit.
Billy
Gilman Meet teen singing
sensation and MDA National Youth Chairman Billy
Gilman.
Campo estivo della MDA It’s the best week
of the year! Just ask any child who’s been to MDA summer
camp. Find out how you can help send “Jerry’s kids” to camp.
And if you're over 16 years of age you may be interested in volunteering
at your local MDA camp.
Divisione ALS della
MDA The ALS
Division leads the world in research and services to defeat
ALS.
Augie e Lynne
Nieto The Nietos are
co-chairpersons of MDA’s ALS Division. Find out how this
all-American family copes with the devastating effects of Lou
Gehrig’s disease.
MDA en
Español MDA
habla español. Click here to learn about all of MDA’s programs –
in
Spanish.
