ABOUT US
Lymphwatch North Devon is one of many lymphoedema support groups established around the country. Advice for
lymphoedema support groups is provided by the only patient-led lymphoedema charity in the UK, the Lymphoedema
Support Network (LSN) based in Chelsea in London. The LSN has been working since 1991 for the benefit of
lymphoedema patients; it campaigns for the better recognition and treatment of lymphoedema and provides a helpline
and leaflet information.
Lymphwatch North Devon is an independent patient-led support group which started in 2005 in response to a
growing need for help and advice for people in North Devon living with lymphoedema.
The two organisers:
Ann is a Vodder-trained Lymphoedema Specialist Practitioner with clinics in South Molton and Barnstaple and is also
a visiting therapist in Somerset and Dorset.
Madeleine is a patient with long-standing primary leg lymphoedema. Her knowledge of the condition and how
to manage the symptoms is extensive. She contributed a chapter on ‘The Patient’s Perspective’ in the first edition
of ‘Lymphoedema’ a book published in 2000, written by leaders in the lymphoedema field and aimed at doctors,
specialists and physiotherapists. She is a former chairman of The Lymphoedema Support Network (LSN), the
national UK charity.
The group is fortunate also to have a retired physiotherapist. Chris was with the NHS for many years and
she offers help and advice on exercise and breathing techniques specific to lymphoedema.
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