felt Thanks
As we reflect on 2024, we are filled with gratitude for the incredible generosity of our supporters. Your contributions have been instrumental in advancing the mission of the DCM Foundation and the Genetic Cardiomyopathy Awareness Consortium (GCAC). Together, we’ve achieved impactful milestones, bringing hope and tangible benefits to patients and families affected by dilated cardiomyopathy (DCM)
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Fred, a successful entrepreneur and philanthropist, recently shared his inspiring story of immigrating to the United States, overcoming personal challenges, and advocating for those affected by dilated cardiomyopathy (DCM). Born and raised in Argentina, Fred immigrated to Miami at the age of 14. Fred found himself homeless at the age of 18, but he embraced
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June 4, 2024 – News from the Global Heart Hub Global Heart Hub (GHH), the international alliance of heart patient organisations, today launches its 2024 Cardiomyopathy Awareness Campaign, along with cardiomyopathy patient organisations across the globe. Cardiomyopathy is a disease of the heart muscle that can occur at any age and can be passed down
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FOR IMMEDIATE RELEASE DCM Foundation Announces Launch of Spanish Website Dublin, OH (February 7, 2024) – The DCM Foundation is thrilled to announce the launch of its website in Spanish, expanding its reach and resources to the Spanish-speaking community of Dilated Cardiomyopathy (DCM) patients and families. This landmark initiative was made possible by a generous
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It is critical that cardiomyopathy patients receive treatment from a medical center that specializes in cardiomyopathy or heart failure. It is important to note that not all cardiologists are specially trained in these two areas. When seeking expert care for your cardiomyopathy or heart failure, do not look only for a single doctor to manage your
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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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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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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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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