End Duchenne: Time is Ticking

Duchenne is a fatal genetic disorder that slowly robs young men of their muscle strength. PPMD will not rest until every young man has a treatment to end Duchenne. Help support our efforts: EndDuchenne.org
Video Production: Catherine Collins, Eugene Faba, and Mark Trottenberg

[@JuanGarcia-jr3ij]

2021 born 2006 he still here. Thank you.

[@gracewill7494]

My younger cousin has Duchenne, and though much money has been raised for research, it is still very likely that he will die when he gets to be a young adult. This is a terrible disease and I pray for anyone that has it or knows/loves someone else that does.

[@Gornodd]

I am learning for my final exam in medical science in munich and stumbled over this video. Ill have too chose a topic for my doctors degree in research. Im highly interested in genetical deseases and frankly im so moved by this video that I so very much want to help.

[@ShakSterTV]

We need to share this with the world!

[@meldyl96]

My son was named Dylan too. Praying for your family and the cure.

[@shesakillerqueenxx]

Thank you for providing this video - I am a graduate nursing student studying for my boards and wanted to learn a bit more about this diagnosis. You have helped me to better understand the struggles a family with a child that has muscular dystrophy has to face. I hope to use this knowledge in my practice as a nurse. God Bless both of your families...never stop working towards a cure.

[@UmabrasileiranaAmerica]

I learned about this video in my Anatomy and Physiology class, what a touching subject! As a healthcare worker and going towards my nursing degree, all I can say is that I emphasize with you all, and may God bless each one of you.

[@jakemcl07]

I have this and my life is amazing

[@HighTen_Melanie]

Remembering my friend James Inch who had DMD he passed away at just 22.

[@sharonc8138]

I’m glad I found your channel. I was diagnosed with Myotonic Muscular Dystrophy Type 1. All my siblings have it and sadly before we were diagnosed my sister passed on to her two children and I’m positive my daughter was the one of my kids that received the unstable gene.

[@AnnetteMurphyger]

Good short and very positive documentary!

[@finley9045]

My brother has Duchenne I know how you feel it's heartbreaking

[@uberhaxornovagentwo]

man like im 15 i cant walk but i can still move freely no assistance yet except walking

[@HanifKhan-ui7ht]

My grandson is 10 years old he have DmD he cannot walk please pray for him 🙏

[@lissa4922]

I wonder where they are now, and hope everyone in the comments is fairing okay especially during this pandemic and having DMD

[@youtuubechannell]

My brother had DMD and died at 20, wanna know what's the possibility of this disease to be carried in next generations. Please help 🙏

[@vedantg.4794]

my friend in california gets treatment in a stanford study

[@UnsuccessfulINSAAN]

🙂🙂i want to Ask god...why we get this disease 😔

[@user-ok6br6wx2m]

مرحبا ابني مصاب بمرض الحثل العضلي نمط دوشين ويحتاج الى مساعدة وعلاج قبل ان يتدهور الحالة

[@evansdolyna7]

I heard something about light therapy that heal cells and dna...is this true?