Arrhythmia Alliance was launched in 2004 at the start of the first Arrhythmia Awareness Week in Westminster to raise awareness and highlight the deficiencies in the treatment and care of arrhythmia sufferers. A-A has established a respected relationship with government, and the result is a significant and vital change in government policy. The charity was fundamental in pushing through one of the most essential policy issues to affect cardiology and cardiac patients, resulting in the inclusion of a new Chapter on Arrhythmias and Sudden Cardiac Death in the National Service Framework (NSF). Before lobbying began, the word ‘arrhythmia’ was mentioned only once in the NSF for Coronary Heart Disease; there were no guidelines dictating diagnosis, treatment or care for those with heart rhythm disorders relating to the ‘electrics’ of the heart. A-A is now influencing government with lobbying efforts to make pulse checks a standard procedure for all doctor appointment visits in the UK.
A-A continues to strive for access to early diagnosis, appropriate treatment, ongoing patient support and improved quality of life for those affected by cardiac arrhythmias. The unique coalition of charities, organisation, patients, carers, patient groups, medical and health groups and allied professionals provides an integral information and support network for those affected by arrhythmias and it is a springboard for medical discussion and health service improvement.
Specialties
Cardiac arrhythmia awareness, Patient support, Cardiac care policy in the UK, Improving cardiology patient care outcomes
