felt Thanks
We hope you can JOIN US for our second annual DCM Patient & Family Conference, taking place online Wednesday, October 18th from 6:00-7:30 PM ET. Click HERE to register. This year’s conference features information to help guide you on your DCM journey and three special guest speakers – all DCM patients who are living well
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Please click on this link or the image above to view a recording of this webinar and learn about: Heart Transplant Overview A New Heart Transport Technology Stories from Heart Transplant Patients Live Panel Q&A Additional Heart Transplant Resources & Information: Click here to view a more detailed webinar called “The Heart Transplant Journey – What You
The DCM Foundation Is Teaming up with the Children’s Cardiomyopathy Foundation to Call Attention to a Deadly Heart Disease The DCM Foundation is proud to partner with the Children’s Cardiomyopathy Foundation (CCF) to promote Children’s Cardiomyopathy Awareness Month throughout the month of September. The awareness month calls attention to the signs, symptoms, and risk factors for
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“My story is the hardcore battle.” Jim Hogan has been fighting that battle since he was diagnosed with non-ischemic DCM in December 2021. The six months after his diagnosis were hard because he thought he only had a year to live. He got his affairs in order and started to disappear: he lost weight, sold
Please click on this link or the image above to view a recording of this webinar and learn about: Causes of DCM Symptoms of DCM and How is DCM Diagnosed Stages of Heart Failure Common Treatments for DCM Q&A Session with a Cardiologist Additional Resources & Information: Treatments for DCM: https://dcmfoundation.org/living-with-dcm/treatments-for-dcm All DCMF Recorded Webinars: https://dcmfoundation.org/webinars-news/recorded-webinars Genetics and
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Good news! Researchers at the University of Maryland School of Medicine identified a new cause of infantile DCM and reversed the effects of the mutation. “In an effort to determine the cause behind a rare condition that causes heart failure in children, University of Maryland School of Medicine (UMSOM) researchers have identified new gene mutations responsible
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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
Genetic Cardiomyopathy Awareness Consortium (GCAC) is Proud to Support Global Heart Hub in Their Second Annual Cardiomyopathy Awareness Week Columbus, Ohio, 26 June, 2023 – The Genetic Cardiomyopathy Awareness Consortium (“GCAC”) is excited to partner with Global Heart Hub to support the second annual Cardiomyopathy Awareness Week, taking place June 26 – July 2, 2023. This
The Global Heart Hub held a webinar earlier this spring entitled: “Why Genetics Matter.” The recording of this webinar is now available to view – please click here to watch the webinar. Additional details are below. Speakers: Prof James Ware – an expert in the field of genetics at Imperial College London Ellie Quinn –
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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
