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Fight Spinal Muscular Atrophy

Mixed Martial Arts Video Collection
Mixed Martial Arts Video Collection Mixed Martial Arts Video Collection
Mixed Martial Arts Video Collection

From Fight SMA ( http://www.fightsma.org ), a powerful and gut-wrenching video made by a brave family about their young son Billy's fight against spinal muscular atrophy (SMA), the leading genetic killer of children under two.

Channel: Nonprofits & Activism
Uploaded: November 30, 1999 at 12:00 am
Author: stevemullen

Length: 03:06
Rating: 4.85
Views: 38509

Tags: atrophy  billy  families  health  medical  muscular  parenting  sma  spinal  

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Video Comments

jaymie9000 (November 30, 1999 at 12:00 am)
he is absolutely gorgous.. xx
kaerlvin (November 30, 1999 at 12:00 am)
WE NEED TO KILL OFF MYOSTATIN TO SAVE THESE CHILDREN!The mentioned chemical inhibits muscular development, removing it would allow proper skeletal muscle function.
ohitisjustme (November 30, 1999 at 12:00 am)
Do more in the fight against spinal muscular atrophy by signing the petition: petitiontocuresma. com
ShaylovesCarter (November 30, 1999 at 12:00 am)
My son has Sma Type 1 also, he iseight months old and we fight to help find acure everyday. Your son is sobeatiful and I just want you to know that you are ot alone. Contact me if you would like. Our prayersare with your family among many. Love Shaylyn and Carter
pi8370 (November 30, 1999 at 12:00 am)
My dear Katy.....what a beautiful and absolutely incredible and marvellous way to love your beautiful angel!!!!!! I will pass this video allover Spain.....All my love always to my Biscones!!!!!!!SILVIA
1992peter (November 30, 1999 at 12:00 am)
Hello.My name is Peter John Foster, I'm visually impared, and have several health problems. I'm 16. I am determined to finda cure for ur little son. I'm sad to see children dying from Tay-Sachs, and SMA, and other disorders Linked Genetically. I'm determined to find the cure for him. I'll give my own life to FIND THE CURE IF I HAVE TO. I WILL DO ALL IN MYPOWER. I WILL.
adhira77 (November 30, 1999 at 12:00 am)
I never knew this condition existed either. Your son touched my heart in a way I can't even begin to express. I will pass this on to others in hopes that they too will contribute to the organization that will find a cure for your little miracle. You are in my thoughts and prayers.
kf12bono (November 30, 1999 at 12:00 am)
I had no idea this disorder existed. I have a 15mo old son and this information strikes me at my core. Your son is beautiful and amazing. I will donate to your cause and encourage as many others to do so as well. I can not beleive, after visiting the fight sma site, that this disorder is not discussed between doctors and potential parents. The stats speak for themselves. I hope a cure is on the horizon for your son.
mszdiimndx3 (November 30, 1999 at 12:00 am)
aw=[

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