LAS Lymphedema Patient's Survey

  • This survey is for SK patients only
  • All information will be strictly confidential
  • Due date is Oct. 20, 2014
  • Please complete yours today.

Aqua Lymphatic Therapy Certication: The Tidhar Method

January 3, 2015 in Saskatoon. View the poster.


LAS is hosting a Regal On Line Party - October 1, 2014 to November 30, 2014. View the poster.

2014 LAS Lymphedema Symposium Presentations

Noreen Campbell is a retired Clinical Specialist for wound care and has developed the Wound Management course - level 1 and 2 for continuing education at the University of Victoria and continues to work with the University.

Lymphedema and Lipedema Wound Management

Dr. Anna Towers is a physician who runs the Lymphedema Clinic in Monteal and is qualified in Lymphedema therapy. She is also involved with the Canadian Lymphedema Framework.

Symposium Brings Attention to Chronic Edema - Prince Albert Daily Herald, May 11, 2014

Canadian Lymphedema Conference

The conference took place over a two-day period and provided up-to date information through two plenary sessions, concurrent information sessions for health professionals, patients and caregivers, a trade show of exhibitors and poster presentations. Read More.

Very Exciting News for SK

Extended Health Benefits Information Bulletin October 1, 2013: COMPRESSION GARMENT PROGRAM CHANGES

Charitable #: 844468074RR0001

$20.00 donations or more will receive a charitable donation receipt. (LAS will mail the receipt to you.)

Free Lymphedema Alert Bracelets
These bracelets which are for arm and/or leg say:

ALERT: LYMPHEDEMA No Blood Tests, Blood Pressure, No I.V or Injections into this Arm or Leg. For free bracelet please contact: Peninsula Medical, Inc. ReidSleeve ® 1-800-29-EDEMA

Lymphedema Awareness Day

March 6 has been proclaimed Lymphedema Awareness Day in SK again this year!!.

View the proclamation.

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.

LAS Goals


Crystal BallThis group is through Facebook, meet people from all around the world with lymphedema! Share your story, read others stories, get and give advice, learn tips and connect with others who are struggling with lymphedema. Extremely supportive and loving group!!!

If you are interested in joining this group please add Angela Connell-Furi to your friends list on Facebook and leave a message that you want to be added to the group! Please note that this group is private for lymphedema patients and their caregivers and can not be seen by others who are not in the group. Hope to see you in the group soon!


We now have a Facebook group for the Association and all members and potential members are welcome.

Association events will be posted on there. Join and meet other members, ask questions, etc.


Lymphedema Working Group

The Lymphedema Working Group was formed to review the policies and practices regarding lymphedema in the province of Saskatchewan. Working group members from LAS strove to educate and inform the Ministry of Health about patients' needs, the cost of lymphedema treatment to patients, and needed changes to policies and practices. On May 1, the working group met with then health minister Don McMorris to present the report to him in person and to answer questions he had about the report.

View the report.

Ombudsman Saskatchewan

Ombudsman Saskatchewan promotes and protects fairness in the design and delivery of government services, including health services. If you have a concern about government services you've received:

  • Step 1: Talk with your service provider.
  • Step 2: If you are still concerned, contact Ombudsman Saskatchewan.