DarlingtonCardio

Darlington Cardiomyopathy Self Support Group

FOR THE BIG HEARTED

DarlingtonCardio

Affiliated to:

Promoting better understanding, diagnosis, treatment and quality of life for individuals with cardiac arrhythmia

About Us

WHAT DO WE OFFER?

ACCESS TO:

  • Booklets on all forms of Cardiomyopathy
  • Video Dilated Cardiomyopathy
  • Video Hypertrophic Cardiomyopathy
  • CD-ROM Dilated Cardiomyopathy
  • CD-ROM Hypertrophic Cardiomyopathy
  • CD-ROM Dilated/Hypertrophic Cariomyopathy
  • Useful tips on how to manage your condition, such as keeping a diary and a list of your medication.
  • List of useful contact numbers
  • Information on how to join the Cariomyopathy Association, an organisation dedicated to our particular form of heart disease
  • Patient Booklet “A Personal Experience” - a simple and easy to use information pack to help you learn how to manage your condition more quickly.

MISSION STATEMENT

  1. To offer help and support to all Cardiomyopathy patients in the Northeast of England
  2. To raise greater awareness of CMO and other Arrhythmia related illnesses.
  3. To work closely with medical professionals and parent bodies.

    These Include:
    Cardiomyopathy Association
    Caridac Rehabilitation Personnel
    Darlington Primary Care Trust
    Doctor J J Murphy (Consultant cardiologist)
    Darlington Coronary Support Group (winners of 2007 Queen’s Award)
    British Heart Foundation
    Arrhythmia Alliance
  4. We aim to support patients at monthly meetings, provide up-to-date and accurate information provided by the aforementioned bodies
  5. We understand that patients do not have support groups in all areas of the UK and to this end we welcome all contacts (E-Mail, in person, by telephone or letter)
  6. We aim to provide vital links between patients and the above mentioned professional and parent bodies
  7. To Campaign, whenever and wherever possible; to increase greater Awareness in G.P. Practices, Hospitals and local Primary Care Trusts
  8. To have a representative, when possible, at patient conferences which are linked to our condition
  9. To consult regularly with members to enable us to understand what they want from a support group.
  10. To provide theses services free, if possible, to all members.