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People affected by cardiomyopathy face a bewildering situation as they come to terms with their situation and seek to learn more about the condition. The Cardiomyopathy Association is there to help them. Our services respond to the feelings of anxiety, isolation and confusion which people commonly feel when affected by cardiomyopathy. We work to assist and empower people by helping them to understand cardiomyopathy, allaying their fears and promoting independence. We provide information booklets, a help line, a website and regional information meetings. We also support clinical care by funding specialist nurses posts in different parts of the UK and provide free educational opportunities doctors through our academic conference programme. The Cardiomyopathy Association is the only UK charity dedicated to providing support and information to families affected by cardiomyopathy is supported solely by public donation. For more information about the charity and what it does, download our leaflet (by clicking on the leaflet top left) or ask for a copy by emailing Sarah Dennis. We understand and we sympathise but mostly we take action to help. |

Carolyn Biro

Information booklets

Nurse specialists

Information days

Helpline

Key contacts

Medical conferences

Annual reports
The CMA is run by a small dedicated team:
Chief Executive - Robert Hall
Finance Officer - Pam Lacey
Membership Secretary - Anne Foster
Information Manager - Sarah Dennis
Fundraising Development Manager - Celia Blakeway-Phillips
Office Assistant - Daniel Jackson
Trustees
Mr Peter McBride (Chair of Trustees)
Ms Amy Williams (Trustees Secretary)
Mr Bob McConnachie
Mrs Tina Amiss
Mr Peter Davies
Mrs Gillian McFarlane
Mr Mark Hayden
Mr Chris Horwood