Give as a gift
This film is available to viewers everywhere
A portion of the proceeds from this screening will be donated to the non-profit organization Coming Together for a Cure, a 501c3 on a mission to advance stem cell therapy for people battling Duchenne Muscular Dystrophy and millions fighting other rare diseases.
Ryan Benton is a young musician afflicted with the muscle-wasting disease, Duchenne Muscular Dystrophy, which carries an average life expectancy of 16 to early 20s. He was the first human with MD to be treated with Mesenchymal Stem Cells. This treatment has worked on MD and many other untreatable rare diseases with no negative side effects! However, large pharmaceutical companies in the United States and the E.U. work hard to block this remedy since they stand to lose hundreds of billions in revenue if legalized. The film is a sobering snapshot of an uncured rare disease and an uplifting portrait of an artist who dreams big against all odds.
This film is available to viewers everywhere
A portion of the proceeds from this screening will be donated to the non-profit organization Coming Together for a Cure, a 501c3 on a mission to advance stem cell therapy for people battling Duchenne Muscular Dystrophy and millions fighting other rare diseases.
Ryan Benton is a young musician afflicted with the muscle-wasting disease, Duchenne Muscular Dystrophy, which carries an average life expectancy of 16 to early 20s. He was the first human with MD to be treated with Mesenchymal Stem Cells. This treatment has worked on MD and many other untreatable rare diseases with no negative side effects! However, large pharmaceutical companies in the United States and the E.U. work hard to block this remedy since they stand to lose hundreds of billions in revenue if legalized. The film is a sobering snapshot of an uncured rare disease and an uplifting portrait of an artist who dreams big against all odds.
