The Cardiomyopathy Association exists to help sufferers and medical professionals find ways to deal with a life threatening heart disease which can be monitored and, if required, managed with medication.

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Membership information is discussed as well as in-depth discussion on this disorder. Some topics are, how common it is, symptoms, diagnosing, cures and research.

Krizinne Cross : Needs a Heart Transplant: Krizinne's Story : I want to tell you about 24 year-old Krizinne Cross from the town of Dubois, Wyoming. Krizinne is a survivor of

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Dilated cardiomyopathy and child heart disease advocacy is explained by the Children s Cardiomyopathy Foundation, a non-profit organization.

The Hypertrophic Cardiomyopathy Center at Stanford is specialized in the care of patients and families with hypertrophic and other forms of familial cardiomyopathy. From the latest

The Cardiomyopathy Association of Australia is a voluntary, non-profit organisation that supports people with Cardiomyopathy and their families.

Scottish Support Group for patients and families affected by cardiomyopathy Welcome to the Cardiomyopathy Scottish Support Group . Are you or someone you know affected by

The Pediatric Cardiomyopathy Registry was established to describe the epidemiologic features and clinical course of selected cardiomyopathies in patients aged 18 years or