DCM Foundation
Heartfelt Thanks
to our Sponsors

Patient Stories and Videos

Medical Disclaimer: All DCM patients are different. Information presented on the DCM Foundation website is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Please consult your physician, cardiologist, or other qualified health providers with any questions you may have regarding a medical condition and/or before doing any activity.

Patient Stories & Videos

Call for Genetic Cardiomyopathy Patient Videos

Interested in sharing your story of genetic cardiomyopathy to help others? The DCM Foundation and the Genetic Cardiomyopathy Awareness Consortium (“GCAC”) are looking for short patient videos or written stories about genetic cardiomyopathy to share in our awareness campaign. Please submit a short video or written piece that tells your genetic cardiomyopathy story using the

Read More… from Call for Genetic Cardiomyopathy Patient Videos

Stephanie Fallon’s Story – Living Well with DCM Since Age 15

We’re honored to be able to share the story of Stephanie Fallon, a patient advocate and friend of the Foundation. Her story reflects the advancement of DCM awareness and treatment since her diagnosis. Her life is a testament to our ability to adapt and persevere.  Stephanie was born with DCM but wasn’t diagnosed until she

Read More… from Stephanie Fallon’s Story – Living Well with DCM Since Age 15

Connect with us!
Facebook Instagram Twitter YouTube

Contact Us

1-833-DCM-HOPE
(1-833-326-4673)

7826 Kate Brown Drive
Dublin, Ohio 43017

Info@DCMFoundation.org