felt Thanks
Please click on this link or the image above to view a recording of this webinar and learn about: Gene Therapy Clinical Trials for Genetic Cardiomyopathies What is a gene therapy clinical trial and how does it differ from other trials Phases of gene therapy trials in the US Potential considerations and support How to identify
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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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Please click on this link or the image above to view a recording of this webinar and learn about: DCM Foundation: Progress to Date and Hope for the Future History and growth of DCMF Why we created the Genetic Cardiomyopathy Awareness Consortium (“GCAC”) Progress to date with DCMF and “GCAC” What must still be accomplished to
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We’re honored to share the story of Stephanie Fallon, a patient advocate and friend of the Foundation. Her story reflects the advancement of DCM awareness and treatment since her diagnosis. Her life is a testament to our ability to adapt, persevere, and live life to the fullest each and every day. Stephanie was born with
Read More… from Stephanie Fallon’s Story – Living Well with DCM Since Age 15
COLUMBUS, OHIO, UNITED STATES, April 11, 2024 /EINPresswire.com/ — FOR IMMEDIATE RELEASE DUBLIN, OH. April 11, 2024. – The Genetic Cardiomyopathy Awareness Consortium (GCAC), launched by the DCM Foundation, has embarked on an aggressive campaign to increase awareness of cardiomyopathy and encourage more people to get genetically tested. During a recent webinar, GCAC representatives introduced the new
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Greg Ruf, Founder and Executive Director of the DCM Foundation, was recently interviewed by WVA Living Magazine to share his life’s journey with DCM and increase awareness about cardiomyopathy. Read the full story HERE. Greg continues his work to forward the mission and goals of the DCM Foundation and the Genetic Cardiomyopathy Awareness Consortium
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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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Please click on this link or the image above to view a recording of this webinar. Learn how you can become part of the GCAC Advocacy Army to help spread the word about genetic cardiomyopathy. Help us SAVE LIVES! Please click HERE to join us in this fight!
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 Dilated Cardiomyopathy from a noted DCM cardiologist and a genetic counselor as well as hear from patients on living well with this disease. Topics Include: DCM Overview The Link Between DCM & Genetics Hear Two DCM Patient
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