The Cardiomyopathy Association operates a policy of not charging people for the information resources we provide. Our view is that this would result in some people not being able to access the information they need. We are a national UK charity that receives no funding from government and need your support to help us continue our provision of information and services to help people and families affected by cardiomyopathy.
If you find these information resources helpful please help us by
Joining the CMA and/or Making a Donation
CMA members receive a quartlerly newsletter, 'CMA News', which contains many varied and interesting articles.
What you need to know about swine flu
Exercise and dilated cardiomyopathy
Exercise and hypertrophic cardiomyopathy
Sexual health and cardiomyopathies
Working together at relationships
Disability Living Allowance - can you claim?
The genetics of the cardiomyopathies
Knowledge of inheritance grows
The importance of family screening
Why survival rates have improved markedly in dilated cardomyopathy
Gene testing will help future treatment
Know your rights to information
Sleep apnoea and its links to cardiomyopathy
Biventricular pacemakers can improve heart timing
Implantable defibrillators (ICDs)
Taking control helps patients cope
Planning for pregnancy and birth
Causes of chest pain in cardiomyopathy
What's new in heart support devices
Reducing patient stress and worry
Why no more antibiotics before dental treatment
Fighting Cardiomyopathy
Dedicated to Damian McLoughlin, who died age 20 of cardiomyopathy. This site is supported by Damian's family and friends.
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