Potential medicines, especially for rare genetic diseases, take years to develop and test. Patients with Duchenne muscular dystrophy -- who rarely live past 25 years -- dont have that time. Dr. Benjy Seckler took action, creating a foundation that raises money for a cure to save not only his son's life, but the lives of all children affected by DMD.
Videos that have been watched and reviewed by peers and found to meet the standards of this site are labeled "Magnified."
Anyone can upload or link to a video for this channel. From here, videos are reviewed by site peers, and videos that meet site standards are labeled "Magnified" and become searchable and visible for all site visitors.