CARDIOMYOPATHY is a disease of the heart muscle — “cardio” means heart, “myo” means muscle, and “pathy” means disease.

What is Cardiomyopathy

Learn more about cardiomyopathy – the types, symptoms, and treatments

Support and Resources

Discover how cardiomyopathy may affect you or your loved one

Research
and trials

Find out about current cardiomyopathy research opportunities

Cardiomyopathy isn’t one condition, but a group of conditions that change the structure of the heart and affect how well it pumps blood around the body. It is estimated that up to 1 in 250 people have cardiomyopathy. It can affect people of any age.

Cardiomyopathy Australia New Zealand (CMANZ) is the only not-for-profit solely focused on supporting and advocating for individuals impacted by cardiomyopathy in Australia and New Zealand.

The aims of CMANZ are to

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By helping and supporting each other, people with cardiomyopathy can live a good and fulfilling life

Community Voices

Jodie’s Hypertrophic Cardiomyopathy (HCM) story

My Hypertrophic Cardiomyopathy Story Hi, my name is Jodie. I am 35 years old. I am a Disability Support Worker and qualified Teachers Aide. I love my family, volunteering with

Dino’s Dilated Cardiomyopathy (DCM) story

My Journey with Dilated Cardiomyopathy Hi, my name is Dino, and I’m from Adelaide. I’m 51 years old, and was diagnosed with Idiopathic Dilated Cardiomyopathy in 2024. This is my

Leo’s Amyloid Cardiomyopathy (ATTR-CM) story

Leo’s Story – Living with ATTR Wild-Type Amyloidosis Hi, my name is Leo and I am living with ATTR wild-type amyloidosis. It is a rare disease where abnormal proteins called

Jessie’s Hypertrophic Cardiomyopathy (HCM) story

Hello! My name is Jessie and I have hypertrophic cardiomyopathy. What led to your diagnosis? What has happened since then? Growing up, I was very active and played a lot

Cardiomyopathy can affect children, adults and older people

Cardiomyopathy can affect people of all ages, including children, working-age adults and older people, depending on the underlying type and cause.

Many people with cardiomyopathy have no symptoms in the early stages

Many people with cardiomyopathy have few or no symptoms in the early stages, and the condition may be detected through imaging, routine tests, or family screening.

Genetics plays a role in many cardiomyopathies

Many cardiomyopathies have a genetic component, and inherited forms are common in conditions such as hypertrophic, dilated and arrhythmogenic cardiomyopathy.

Many people with cardiomyopathy live full and active lives

With appropriate diagnosis, monitoring and treatment, many people with cardiomyopathy are able to live full and active lives.

Early diagnosis and regular follow-up can improve quality of life

Early diagnosis, risk assessment and regular follow-up are central to cardiomyopathy care and can help improve quality of life and long-term outcomes.

News & Events

Macquarie Uni seeks the views of those with lived experience of heart failure via interview

Dr. Kathryn Waddell-Smith Discusses Cardiomyopathy Genetics: Watch the recording

Summer 2025 Newsletter Released

Amyloid Cardiomyopathy Webinar: Meet the Experts, with A/Prof Elizabeth Paratz and A/Prof Nikki Bart

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