Wow, what a touching video, we too are trying our hardest to help rare disease researchers find cures for DMD and many other rare diseases. In conjunction with the Children's Rare Disease Network we are giving away a $50,000 rare disease research system to the winner of a video contest and the organization of their choice. You should enter your video. For more info, visit RemedyMD's website and click on the "About" section then look under "Press Releases".
my son is 2 and was just diagnosed with this heartwrenching disease in my family we have lost soo many young men to dmd .my brother also had dmd we lost him when i was very young but he taught my family so much these boys are truly angels .i am so sad for my angel my heart hurts thank u and your brother for posting this video .it helps to know we are not alone ..
Damn I know it feels beecause i have muscular dystrophy since i was 3years old and stopped walking at age 10 but they still don't know what kind i have. I just hope they find a cure SOON<3(:
wonderful video. very inspiring. your brother is in my prayers. 1 of my best friends has DMD. He is 24. thanks for making this video. I believe a cure will be found.
I can inform you, that everyone can help finding a cure for
Muscular Dystrophy. Please write BOINC or worldcommunitygrid into the search field of Youtube or any search engine for further info
Running the Programm BOINC on your homecomputer you donate unused computer capacity to researchers. One of their projects is about
Muscular Dystrophy. Please note that this is fundametal research. So, a cure cannot be expected too soon, unfortunately. BOINC is safe and has been working several years now.
This was very touching I'm sure they'll find a cure in time. One of the teachers at my school's sons both have DMD and a student made a video called run for our sons Elliot and Henry
This is a really moving video Hayley and very well done :) You should send it to the charity and see if they will publish it on the website? Very well done.
Wow, what a touching video, we too are trying our hardest to help rare disease researchers find cures for DMD and many other rare diseases. In conjunction with the Children's Rare Disease Network we are giving away a $50,000 rare disease research system to the winner of a video contest and the organization of their choice. You should enter your video. For more info, visit RemedyMD's website and click on the "About" section then look under "Press Releases".
RemedyMD 11 months ago
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angelsabout 1 year ago
Comment removed
angelsabout 1 year ago
my son is 2 and was just diagnosed with this heartwrenching disease in my family we have lost soo many young men to dmd .my brother also had dmd we lost him when i was very young but he taught my family so much these boys are truly angels .i am so sad for my angel my heart hurts thank u and your brother for posting this video .it helps to know we are not alone ..
angelsabout 1 year ago
Damn I know it feels beecause i have muscular dystrophy since i was 3years old and stopped walking at age 10 but they still don't know what kind i have. I just hope they find a cure SOON<3(:
14sadgirl 1 year ago
a very lucky boy with faithfully eyes. God bless !!!!
SabSisHameln 1 year ago
wonderful video. very inspiring. your brother is in my prayers. 1 of my best friends has DMD. He is 24. thanks for making this video. I believe a cure will be found.
coolokiechick91 2 years ago
This has been flagged as spam show
I can inform you, that everyone can help finding a cure for
Muscular Dystrophy. Please write BOINC or worldcommunitygrid into the search field of Youtube or any search engine for further info
Running the Programm BOINC on your homecomputer you donate unused computer capacity to researchers. One of their projects is about
Muscular Dystrophy. Please note that this is fundametal research. So, a cure cannot be expected too soon, unfortunately. BOINC is safe and has been working several years now.
Adamus70 2 years ago
This Videoo is really touching i have two older brothers with the same condition one is 21 and the other is 18. So thanks for this video .:D
shelly24294 2 years ago
This was very touching I'm sure they'll find a cure in time. One of the teachers at my school's sons both have DMD and a student made a video called run for our sons Elliot and Henry
kikudog6 2 years ago
thats so moving, nice video hayley :) x
jimothie1 2 years ago
my brother has dmd as well..hes 10...ive made a video too if you want to watch it
he is also my inspiration in life, everyday. i love him so much and i can tell you love your brother too
clicker009 2 years ago
my brother jus passed from DMD. he was 18.. its very sad.. my brother was a good kid and went thru alot. Get back to me
tiffany
dreamz123181 2 years ago
I'm really sorry to hear that - my brother's 14 and it's getting tough now. But we are getting through it one day at a time.
Hayley
moviemakingbanter 2 years ago
Awesome work! :D
BonkersVideos 2 years ago
This is a really moving video Hayley and very well done :) You should send it to the charity and see if they will publish it on the website? Very well done.
DirectorClairey 2 years ago