Documentary: Stem Cell Therapy for Muscular Dystrophy - Ryan Benton's Story
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Uploader Comments (cellmedicine)
All Comments (9)
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And people still try to oppose stem cell research. Insane.
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whats to dislike about this video...i am so happy to hear this :)
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hello, ryan. how are you? believe it, or not, my name is ryon benton, too, and i have muscular dystrophy as well. although, you can see i spell my name with an 'o' hehehe ... i live in watkinsville, georgia. i have an account here. i go by the name, LUNG SUNG HERO. you can check out my songs, but im not very good. i just ran across your story by chance. i was trying to see if i could get to my songs by searching my name, ryon benton. well, i found ryan benton, but it was you lol
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What a wonderful inspiring young man. It sickens me that the US with all its resources is not pushing the research forward. Many best wishes to the Ryan and his family.
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I'm so glad people are getting to finally see this! I need a "love" button, the "like" button just doesn't cut it!
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God Bless'm!
BTW, 1 voter needs a stem cell transplant to his brain
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U did such an amazing job with this video! Thanks for helping spread the word.
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I'm very happy to cure Ryan , I have the MD, I contact many times to cellmedicine com but I didn't get any answer to my Emails plzzz anyone can help me how can reach this hospital ,I ready to go any hospital give the same result they gave it to ryan
my Email :bassaam158 AT yahoo.com
bassam5000 8 months ago
@bassam5000 - Please understand that Ryan is not "cured" of muscular dystrophy and the Stem Cell Institute is not claiming that this treatment is a cure for MD. Your email address was passed to our staff who should have contacted you by now. Please let us know if that has not happened yet. Thank you.
cellmedicine 6 months ago