We were given an amazing opportunity to share our story of living with Duchenne Muscular Dystrophy (DMD), with a room full of Doctors, Pediatricians, and OBGYNs. We discuss the importance of prenatal screening, genetic testing, DMD resources, and the impact of DMD on a family's life. Learn about the challenges and triumphs we've faced and how they're advocating for a brighter future for those affected by this rare disease.
This is the life of a DMD Family.
Disclaimer: This is not medical advice. We are just a normal family, with extraordinary kids, just like you. Please consult with your doctors before making any significant medical decisions. Most importantly- do your own research.
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