felt Thanks
Are you affected by cardiomyopathy? Please CLICK HERE to access a 5-10 minute survey. Learn more below. CureHeart is developing genetic therapies to treat inherited cardiomyopathy. https://cureheart.org/patients The CureHeart project brings together researchers across the UK, US and Asia, and commercial as well as patient advocacy partners, to develop effective genetic therapies for cardiomyopathies. The
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Please click on this link or the image above to view a recording of this webinar and learn about genetics and the future of genetic therapies for cardiomyopathy: Topics Include: Genetics 101 Gene Therapy Basics Clinical Trials for Gene Therapy Tenaya and Gene Therapy Advancement Live Q&A
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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
Clinical Trial Now Enrolling for Patients with Dilated Cardiomyopathy (DCM) due to Genetic Mutations or Unknown Causes Bristol Myers Squibb is conducting a clinical trial in patients with DCM due to genetic mutations or unknown causes. Details of the study and eligibility requirements are listed below and participating in such research can help advance therapies
“COLUMBUS, Ohio – A new study led by researchers at The Ohio State University Wexner Medical Center and College of Medicine shows the benefit of having patients with advanced disease from dilated cardiomyopathy (DCM) undergo genetic testing to help identify the inherited heart muscle disease in family members. Researchers found that DCM patients with advanced heart disease, defined as
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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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
