The mission of the Alberta Lymphedema Association is to optimize health for lymphedema patients through education and support, and increase awareness of lymphedema within the medical community and the general public of Alberta.
About ALBERTA LYMPHEDEMA ASSOCIATION
The Alberta Lymphedema Association (ALA) is a not for profit charitable organization founded in 2003 by a team of people who recognized the need to help people living with, or at risk of, lymphedema. A learning association committed to ongoing education of its stakeholders, ALA works to make a difference and empower affected individuals and their families to help manage this condition. ALA works from the patient standpoint.