He's My Son - For Philip
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Uploaded by sjmolitor on Jun 2, 2007
Video for my son, Philip, who has Duchenne Muscular Dystrophy
37 videosYouTube Mix for Mark Schultz- 7:59
Cure Duchenne: Experts on Duchenne Muscular Dystrophyby CureDuchenne15,951 views
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In the First Light - GLADby KJoRodDogMan31,332 views
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Out of Eden-More Than you Know (with Lyrics)by TruSouljah712102,190 views
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Duchenne Muscular Dystrophy 2swim4lifeby AnnetteRush7,224 views
- 1:09
Justusby yoaxello17,317 views
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Celebration of Life - He's My Son - Leukemiaby KANIKY0420,508 views
- 4:17
Before the Throne of God Aboveby katiekatew78,517 views
- 8:04
CIRM "Spotlight On Cerebral Palsy" - August 8, 2007by BenKaplan142,997 views
- 4:43
Kathy Troccoli's Draw Me Closeby fireflame0621112,417 views
- 2:41
Potential Stem Cell treatment of Duchenne Muscular Dystrophyby Gibholio14,730 views
- 1:35
Ten Angry Reporters Meltingdown & Blowing Up(Compilation)by somethingstupid1232,808,109 views
I hope Philip will get better soon.Doctors said the cure will be out in 10 years or less.They already test it on a group of children.He is an amazing,beautiful kid.Philip,I hope one day I will have such a nice son,as you are.Best luck,Judit
juditkarajko 3 years ago
what happned to your son?
videolver2 3 years ago
Im from Germany and Im only 14 so I dont know if you understand what I write.
I think kids are little wonders
Kids are our future and they make the world a little bit better and happier
When we look in their eyes we want to smile or we want to cry.
So I want to pray for you and your family because my brother is dead since Im 13 and noone prayed for him. But I want to make it better
BigBrotherBella1994 3 years ago
I'm praying for you.
God bless.
emilydemily8 3 years ago
ím no speak inglish,i hope you understand my words. i´m from México, Los cabos Baja California Sur. i have two child in my school with DMD. Im teacher and i like help the family of two child. i know no cure, but i like have more information and how can help this people.
eldagperalta 3 years ago
God bless you and your family. Even with his disease he still smiles in most of the pictures. I doubt he could ask for a better family than yours.
amandawilson81 3 years ago
i have 4 boys we have challanges to god bless you love helps my sons are everything to me
doublemoms 3 years ago
This little boy in the video has quite a resemblance to my little brother, though my brother doesn't have DMD. He just looks like him in the face and this video touches my heart because if my little brother was faced with this or even my own son I don't know if I could be as strong as you. I'd want to hug that child and never let go to do anything ever again. I'd be so pathetic. :) I want to find a cure for it too. good luck and may he have a beautiful life.
futuremrsgerber 3 years ago
this video sparked my interest in the disease. I am in school for massage therapy and my paper is going to be about this particular disease. I can see how my chosen profession would be benificial for victims and I want to work with babies and children.
futuremrsgerber 3 years ago
aww keep up the good work and never give in!!! make sure he goes to summer camp its the best place ever!!! (i have CMT)
brittny92 3 years ago