Who Are we?

Lymphoedema Ireland (formerly Irish Lymphoedema Support Network) was founded in 1995. Our volunteer patient-led national network offers support, help and information to anyone in Ireland affected with lymphoedema.

Membership

Membership is open to anyone who suffers from Lymphoedema, their family and friends and those with an interest in furthering the aims of the network. All members will be circulated regarding the activities of the group.

Aims and Objectives

To campaign for improved services and standards of care in Ireland for people with lymphoedema.
To publicise the lack of diagnosis, services, treatment and support for people with lymphoedema.
To provide support and information to such persons and their families.
To promote a high standard of information and promote self-help.
To advance the education of the public on the subject of Lymphoedema.
To maintain contact with healthcare professionals working in Lymphoedema management.
To promote better awareness of lymphoedema as a major health condition to local health authorities, healthcare professionals and politicians.

What Lymphoedema Ireland offers to members:

Twice yearly public meeting for members and their families.
Opportunities to meet others having or involved with lymphoedema, locally where possible.
Distribution of information, posters, etc., aimed at increasing public awareness of Lymphoedema.
Telephone Help Line.