lauracrocbateman (December 31, 1969 at 4:59 pm)

i have a freind with this disease and it upsets me knowing that hes going 2 die cos of it

afslayer (December 31, 1969 at 4:59 pm)

Im 18 and also have this disease, thanks for producing this film, every thing that raises awareness helps. Thanks again. Matt...

DemmiV (December 31, 1969 at 4:59 pm)

My cousin had muscular dystrophy, and its such a difficult disability. Unlike most he wasnt lucky to live any longer and died at age 20 (estimated age he was given from a young age). That illness personally took away the one person i loved in my life. Best of luck to those who are battling with the illness. Bless you :)

JacksonVHT (December 31, 1969 at 4:59 pm)

Holy shit, those Harleys are awesome.

danlydiate123 (December 31, 1969 at 4:59 pm)

ive god MD. im 15 an ive got that duchhenes. but luckily for me i had a blood test and the blood was sent to london. my bloods getting tested as we speak. and there trying to fix the defect in my cells. if they repair one of the cells, all they have to do is inject the cell back into my body. and all the MD cells will die. and normal cells wil replace them. im very excited but cautious aswell.

Gifts41GiftsFor4All (December 31, 1969 at 4:59 pm)

Great video.

brittny92 (December 31, 1969 at 4:59 pm)

i have CMT and my camp changed the age from 6-21 to 6-17 and next year is my last year and im sooo nervous about going out in the world on my own and such i only have leg braces so i know i don't have it bad but still...

msmooniepie (December 31, 1969 at 4:59 pm)

I'm a 32 yr old with CMT type 3 Muscular Dyatrophy. MDA does alot for children but what about us adults that still need help? We can no longer attend camp, which is sad!! Most of my friend are long deceased but I still need support.

thaatxboss (December 31, 1969 at 4:59 pm)

Very informative, thank you for this video.