DCM Foundation

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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

ICO

823562019

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1651

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236

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Dublin

Address: 7826 Kate Brown Dr, DublinWeb: Sign in to see organisation websiteFacebook: DilatedCardiomyopathyFoundationX (Twitter): DCM_FoundationICO: 823562019

DCM Foundation - Home 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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Sarah

2. What role can genetic research play in the future of treatment and support for families dealing with DCM?

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Anna

I’m so grateful for the DCM Foundation’s work in promoting awareness and education about Dilated Cardiomyopathy. Together, we can bring hope and light to those who need it most! 🌟💙

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Victor

1. How can we better leverage patient stories to raise awareness and support for those affected by Dilated Cardiomyopathy?

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Evelyn

Just wanted to say a huge thank you to the DCM Foundation for all the incredible support and resources you provide to those affected by Dilated Cardiomyopathy. You’re making a real difference in the lives of patients and families! ❤️🙏

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