2006 Muscular Dystrophy Documentary

[DefyingDystrophy]

Breakthrough Muscular Dystrophy Treatment has been found!!!! Visit my channel to see the featured video of my 6 month progress! I am 22 years old with BMD & am showing more hope than anyone could have possibly imagined!

[WheelchairThailand]

The specialist in holidays for disabled in seaside resort Hua Hin, Thailand with wheelchair accessible beaches. Adapted holiday homes for handicapped people with free use of beach wheelchair and other aids / medical equipment.

[robmayben]

I am a high school teacher who works with students with all types of abilities. Over the past several years I have worked to develop a device to help my students stay independent in my classroom. Last month Fox News in California did a story about David, who has Duchenne Muscular Dystrophy and my device the desktop desk. The story is on YouTube, desktop desk and David.

[Devilsnevercry6]

I have ulreches. Honestly it was random since my family had no historey or signs of the gene yet I got it. It was just bad luck.

[keenandwhat009]

What is ( ulreches) are you sure your spelling it right, because theres no such thing, i tryed to look it up and theres nothing. '' Devilsnervercry6''

[Devilsnevercry6]

@keenandwhat009

Try Ulrich.

[keenandwhat009]

@Devilsnevercry6 again! NO such word. Now thats really weird... your weird

[Devilsnevercry6]

@keenandwhat009

Thats funny I can find results for Ulrich Muscular Dystrophy.

[juditkarajko]

DEAR DANLYDIATE123,could you please write down for me the address of that London Hospital,where your blood is tested and under cure.I have a relative who has the desease,and they asked me to help finding a good clinique.I happen to live in England,so I could get into contact with them maybe.I preshiate every help,and dear all of you,I wish you to be cured very very soon.Luv ya lots!

[masterofoverkill2]

i got congenital. it means i won't die at YOUNG AGE BUT I GET WEAKER FASTER

[lauracrocbateman]

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

[afslayer]

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

Thanks again.

Matt...

[DemmiV]

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]

Holy shit, those Harleys are awesome.

[danlydiate123]

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.

[Devilsnevercry6]

Can you send me the adress. I live in Hong Kong but knowing that there might be some hope to get rid of the dicease I would try and do it

[aidanne07]

I'm glad to hear that you maybe able to get some help. But keep opened minded. Good luck.

[Gifts41GiftsFor4All]

Great video.

[brittny92]

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]

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]

Very informative, thank you for this video.