2021 The Latest in DCM Genetics Research \u0026 Therapies in Development

(59:41)

DCM Foundation: Progress to Date and Hope for the Future

(49:11)

DCM Foundation's Strategic Pillars Unveiled - What this Means for You

(59:28)

Global Heart Hub Partnership with DCM Foundation for the Genetic Cardiomyopathy Campaign Launch

(2:15)

DCM Foundation: The Journey from Diagnosis to Advocacy Group

(37:50)

Stephanie's video promoting genetic cardiomyopathy awareness \u0026 the March 8th DCM Foundation webinar

(46)

Insights and Hope When Living with a Device - with guest Doug Rachac

(58:27)

The latest in DCM therapies in development - with Tenaya

(10:45)

DCM Foundation's \

(58:56)

2021.06 Hope for MYH7 \u0026 TTN DCM Patients

(5:41)

DCM Patient and Family Conference - Session #1: Dilated Cardiomyopathy Education

(1:45:22)

Defying a 5-Year Prognosis: Stephanie Thrives with Genetic Cardiomyopathy Decades Later

(1:48)

Visiting Vignette with Greg Ruf from the DCM Foundation

(26:)

The Science Behind DCM Gene Therapies (and Tenaya's quest to make it affordable for all)

(59:20)

British Heart Foundation - Living with Cardiomyopathy, Deborah Coleman

(1:25)

DCM Patient and Family Conference: Session #2 The Latest in DCM Research and Therapies

(1:48:41)

Supporting Women with Cardiomyopathy – with WomenHeart \u0026 DCM Foundation

(1:1:4)

Greg Ruf Talks About Being Undiagnosed and Misdiagnosed for Dilated Cardiomyopathy

(1:32)