We are on earth for a reason, I think Nicks was to touch peoples Hearts.. And see no matter what happens in life not to dwell on it. But Embrace it and Love Life.
i came a cross your video as i was studying for a genetics exam, one of the topics being DMD. one of my professors dedicates all his research funding into researching duchenne. I hope they find a cure soon, your son looks like a wonderful person with great parents
This is very moving video of your son, Nicks amazing life! Thank you so very much for producing and sharing on YouTube! Our grandson, Beau who is 8 was diagnosed this past spring with Duchenne Muscular Dystrophy. We pray for a cure each and every day so our children can live.
I hate diseases
rgz1985 8 months ago
We are on earth for a reason, I think Nicks was to touch peoples Hearts.. And see no matter what happens in life not to dwell on it. But Embrace it and Love Life.
Thanks Nick. You touched Mine:)
1958louief 1 year ago
lovely pics..iam from Germany and my son has Duchenne too he is 18years old he is such a sweet and handsome young man like Nick .
Whitebabe1 1 year ago
i came a cross your video as i was studying for a genetics exam, one of the topics being DMD. one of my professors dedicates all his research funding into researching duchenne. I hope they find a cure soon, your son looks like a wonderful person with great parents
aswad877 2 years ago
This is very moving video of your son, Nicks amazing life! Thank you so very much for producing and sharing on YouTube! Our grandson, Beau who is 8 was diagnosed this past spring with Duchenne Muscular Dystrophy. We pray for a cure each and every day so our children can live.
hdiho 3 years ago