Who Are We?

The Lymphedema Association of Saskatchewan Inc. (LAS) is a non- profit organization founded in 2004 by a group of people who recognized the need to help those who have or are at risk of developing lymphedema and related lymphatic disorders. We strive to be a learning association, committed to ongoing education. LAS works to empower affected individuals and their families to successfully manage these conditions.

Large Mixed Age, Multiethnic Crowd of Men and Women

LAS Goals

  • To promote health by providing an annual symposium on lymphedema management for health professionals and patients;
  • To promote health by providing workshops and educational materials for health professionals and patients on matters relating to diagnosing and treating lymphedema;
  • To promote support for those affected by lymphedema by offering education and counselling and by establishing mutual support groups; and
  • To undertake activities incidental and ancillary to the attainment of the above charitable purpose(s).

Are You an LAS Member?

Please consider becoming one. For just $30/year you receive the following:

  • Four very informative issues of Pathways, a magazine published by the Canadian Lymphedema Framework
  • Updates on LAS through the provincial association’s inserts in the Pathways magazine
  • Updates on the latest projects, events and happenings of LAS
  • Lymphedema events and updates of each provincial association across Canada
  • Direction and support for lymphedema patients and families

To become a member Click on LAS and Membership, then on membership. We ask that you also fill out the application form on the LAS Printable Brochure Payment can be made by mail or electronically. We look forward to your support. LAS Executive

group of people around a table

March 6th- Lymphedema Awareness Day.
This day is dedicated to those who have been an inspiration to the lymphedema community and to honour lymphedema patients, caregivers, therapists and advocates alike.