felt Thanks
Celebrating a Win for the Cardiomyopathy Community The DCM Foundation joins the Children’s Cardiomyopathy Foundation (CCF) in celebrating the signing of the Cardiomyopathy Health Education, Awareness, And Research and AED Training in Schools (HEARTS) Act into law by President Biden. This landmark legislation marks a significant step forward in the fight against cardiomyopathy. CCF’s Journey
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Cardiomyopathy is a serious heart condition, and many people are battling it every day. The Genetic Cardiomyopathy Awareness Consortium (GCAC) is fighting back! Our mission is to raise awareness and encourage genetic testing for cardiomyopathy patients and their families. This will not only save lives but also accelerate research for better treatments. Become a Hero: Spread
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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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Please click on this link or the image above to view a recording of this webinar and learn about: DCM Basics Overview The Future of DCM Therapies Support for Your DCM Journey Living with DCM – Panel Discussion with 3 Patients Live Q&A
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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“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
We’re excited to have Julie Wilde from Transform with Wellness as the guest speaker at this month’s webinar: “DCM Foundation’s Healthy Together Wellness Program.” During this April 19th live event, Julie will share practical tips and ideas for healthy living – from diet and exercise to mindfulness, sleep and stress management. Julie is a certified
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The DCM Foundation website has been reorganized to provide you with faster and easier access to the information you need. This website provides the most current information and resources available to DCM patients and their families. The redesigned homepage gives you links to access important information about DCM including Symptoms, Stages, Arrhythmias, Causes, and Genetics
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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.
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We heard you! Many DCM patients and family members have expressed a need for local DCM support groups where they can discuss their shared experiences with dilated cardiomyopathy. As a result of your input, we are excited to announce the DCM Foundation is beginning discussions with a number of DCM hospitals and research centers around
