Please click on this link or the image above to view a recording of this webinar and learn about: Cardiomyopathy, Genetics, and YOU Getting Better Care: How to find the best doctor(s) for your care and why this is so important Getting More Involved: Learn how patients can get more involved in the Genetic Cardiomyopathy
Recorded Webinars
Myths and Truths About Clinical Trials
Please click on this link or the image above to view a recording of this webinar and learn about: Myths and Truths About Clinical Trials Industry experts discuss the Myths and Truths of Clinical Trials on a panel discussion Learn about the phases and average timeline for clinical trials Hear about the measures taken to ensure
“Healthy Together” Wellness Webinar
Please click here or on the image above to view a recording of this webinar and learn about: Tips to improve the quality of your health and life today Learn how to develop a hope-filled mindset and how to create lasting change Simple nutritional tips to improve your diet Reduce stress and learn several mindfulness skills
Cardiomyopathy & Genetics Webinar / Launch of “GCAC” – Get the Facts & Save Lives
Learn about the important role of GENETICS in cardiomyopathy and celebrate the LAUNCH of the Genetic Cardiomyopathy Awareness Consortium (“GCAC”). Getting more people genetically tested can save lives and advance therapies! In this webinar, hear from other cardiomyopathy patients and learn about: The role genetics plays in cardiomyopathy How easy and affordable it is to
Read More… from Cardiomyopathy & Genetics Webinar / Launch of “GCAC” – Get the Facts & Save Lives
Support for Your DCM Journey – DCMF Programs, Services, and Helpful Advice
Learn helpful health and emotional wellness advice from a DCM patient and a clinical expert. Then, hear about the expanding patient resources the DCM Foundation is working on to support DCM patients in 2023 and beyond.
Read More… from Support for Your DCM Journey – DCMF Programs, Services, and Helpful Advice
Insights and Hope When Living with a Heart Device
Doug Rachac talks about living with a pacemaker, ICD, or CRTD device. Special guest speakers include Dr. Savona, electrophysiologist, and Julie Mease, NP, from The Ohio State University’s Ross Heart Hospital.
Read More… from Insights and Hope When Living with a Heart Device
DCM Patient and Family Conference: Session #3 Patient-to-Patient Panel Discussions
Two DCM Patient Panels discuss: Successfully Living with DCM- Fitness & Nutrition, Heart Transplant – Hope for the Future: Maintaining a Healthy, Productive Life; Panel 2: Self-Advocacy – When to Seek a Second Opinion, Talking with Health Practitioners, Finances and Insurance
Read More… from DCM Patient and Family Conference: Session #3 Patient-to-Patient Panel Discussions
DCM Patient and Family Conference: Session #2 The Latest in DCM Research and Therapies
Potential New Therapies for Dilated Cardiomyopathy – Presentations by Industry Leaders; Industry Panel Discussion: Positive Research and Hope for the Future, Potential Roadblocks, Patient Involvement.
DCM Patient and Family Conference – Session #1: Dilated Cardiomyopathy Education
Dilated Cardiomyopathy Basics (Presenter: Dr. Kathy Crispell) – What is DCM – Diagnosis & Causes – Genetics & DCM; Successfully Navigating a DCM Diagnosis (Presenter: Barbara McKenna-Amos)
Read More… from DCM Patient and Family Conference – Session #1: Dilated Cardiomyopathy Education
What You Should Know About Cardiomyopathy & SILENT Sleep Apnea
Dr. Robin Germany explains Central Sleep Apnea and its connection to dilated cardiomyopathy.
Read More… from What You Should Know About Cardiomyopathy & SILENT Sleep Apnea