Fighting for Sons with Duchenne

As a new mother and young college student, Jennifer McNary noticed that her first son, Austin, wasn’t meeting his developmental milestones, but it wasn’t until he was 3 years old that Austin was diagnosed with Duchenne Muscular Dystrophy. The same diagnosis would follow for his younger brother, Max. Today, Jenn is the mother of four children as well as an advocate, public speaker and consultant in the rare disease space. Story Reference Points: What is Duchenne Muscular Dystrophy? @ 1:05 Austin’s diagnosis with Duchenne @ 3:10 Raising sons with Duchenne @ 7:32 Spotlight on Duchenne advocacy organizations @ 13:57 Jenn’s work as a consultant in the rare disease space @ 25:53 Links and Resources Jenn on Twitter Jenn on LinkedIn Beauhawks Foundation Little Hercules Foundation Parent Project Muscular Dystrophy Check out other Patient Stories podcast episodes. Read other Patient Stories on the Grey Genetics Patient Stories Page Do you want to support Patient Stories? You can now make a donation online! Want to support Patient Stories in a non-monetary way? Leave us a review on iTunes, or share your favorite episodes on Social Media. Patient Stories on Twitter: @GreyGeneticsPod Patient Stories on Instagram: @patientstoriespodcast Are you looking for genetic counseling? Patient Stories is sponsored by Grey Genetics, an independent telehealth genetic counseling and consulting company. Book an appointment with a genetic counselor specialized in your area of concern. Choose from our growing Network of Genetic Counselors. All genetic counseling appointments take place over secure, HIPAA-compliant video-conferencing or by phone.