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Hope for People with Dilated Cardiomyopathy. If you need support, contact info@dcmfoundation.org or visit our website. The DCM Foundation provides hope and support to DCM patients and their loved ones. We offer informational resources, support groups, free webinars, inspiring stories and more. Visit dcmfoundation.org for more information. Formed in 2017 by a DCM Patient and a noted Heart Failure Cardiologist and DCM Genetic Researcher, the DCM Foundation’s mission is to provide HOPE and support to DCM Patients and Families with Dilated Cardiomyopathy through education, research and advocacy.
Our mission is being executed through three foundational pillars:
Information and Education
Patient and Family Support
Understanding the Need for Genetic Testing
823562019
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Dublin, OH 43017 USA
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dcmfoundation.org
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DCM_Foundation
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DilatedCardiomyopathyFoundation
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News

Signs and symptoms of cardiomyopathy can vary widely. In its earliest stages cardiomyopathy may not have symptoms and some individuals may not notice symptoms that are mild. #ThinkCardiomyopathy https://t.co/XU2YbK1gYM (tw)

It’s time to take notice of cardiomyopathy. You or a loved one could unknowingly be at risk. #ThinkCardiomyopathy https://t.co/nhzJKMHjB1 (tw)

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About the organization
- 740, T22 -
What is Dilated Cardiomyopathy DCM. DCM is a heart condition that has many causes. It can affect entire families if the cause is genetic. There are specific areas that are common to DCM despite the cause.
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