Registration for the 2018 LAS Lymphedena and Lipedema Symposium

Poster and Registration

Registration for the 2018 LAS Lymphedena and Lipedema Symposium on September 6th and 7th in Regina,SK will begin June 11th!

View the poster which includes a registration form. (The poster and registration form are printable from your browser.)

For further assistancer email

Facebook Interview LinkWatch this interview on Global Regina on our Facebook page.

2018 Symposium Volunteers Needed

Volunteers are always appreciated! If you are interested in volunteering at this event please email Tracy Gardikiotis at

Pizza Fundraiser Results

Photo of our brochures

You can help bring lymphedema awareness and education in SK!

SK Residents, Please help LAS distribute lymphedema brochures and posters to your doctor's offices. Also please ask them if they would be willing to receive a mailed copy of the Pathways magazine for their office free of charge (four issues yearly). LAS must order a minimum of 150 Pathways issues and we would like to use the extra copies towards education.

Please contact us if you would like to help (

Photo of our poster boardThank You Tracy Gardikiotis and our Graphic Designer, Lori Varishagen-Mazzei for working on the LAS Poster Board to help raise lymphedema awareness & education! The poster board will be used for Education events, trade shows and LAS Symposiums. If you have an event in your area please contact LAS.

An Introduction To LYMPHEDEMA
For People With or At Risk of Developing Lymphedema

Telehealth educational sessions are offered to clients with or at risk of lymphedema. Family members/caregivers and health care professionals are also welcome to attend. Please feel free to circulate to anyone else you feel should be aware of this.

Above message from: Senior Physical Therapist at RUH Outpatient and Acute Orthopedic Physical Therapy

Presented by the Certified Lymphedema Health Care Professionals Working for the Health Regions of Saskatchewan Via Telehealth

Spring 2018 Dates/Time
Monday, February 12, 2018 – 1:00 – 2:00 pm
Monday, May 14, 2018 – 1:00 – 2:00 pm

Saskatoon: Contact (306)655-2431 for location and to RSVP
Rural Saskatoon Health Region and all other SK Health Regions: Contact (306) 655-1573 to get local contact number, then call the number they provide you for your location and to RSVP

2017 National CLF Conference Report-by Kelly Lloyd

The 2017 National Canadian Lymphedema Conference was held in Montreal on October 27th and 28th at the Hotel Omni Mont-Royal in Montreal. The conference began with business meetings where provincial representatives networked and shared ideas. more...

2017 LAS Education Day Overview


John Mulligan's Presentation

Julie Jensen's Presentation

LAS Members may view the AGM Reports when logged in

2017 National Lymphedema Conference:

October 27 & 28

BSN Educational Webinars

Please note that this site is more for health professional like physicians, nurses, therapists, etc.

You will need to create a profile and you will have access to information such as recorded webinars and upcoming events. You will also be able to register for future webinars.

March 6 is Lymphedema Awareness Day

Your Journey- A guide for Women Diagnosed with Breast Cancer

A new breast cancer patient education resource booklet and video, Your Journey, developed by the Lymphedema Working Group is now available on the Ministry of Health website at . A written resource and video will be soon be distributed to all newly diagnosed breast cancer patients across Saskatchewan.

SK Lymphedema Patient's Coverage from SAIL

Compression Garments and Bandaging Supplies

Patients diagnosed with lymphedema in Saskatchewan receive the following (100%) coverage under the SAIL program (Saskatchewan Aids to Independent Living Program) Compression Garment Policy:

  • 2 day-time compression garments every six months
  • 1 night-time compression garment once per two years.
  • Garments include socks (calf), hose (thigh/pantyhose), arm sleeves, gloves and non-elastic garments (ie. Circa-Aid).
  • Bandaging supplies (foam/artiflex, short-stretch bandages), swell spots and scar pads.
  • Accessories/supplies such as gel sheets, adhesives, stocking applicators, ulcer liners, and rubber gloves when used in conjunction with a compression garment.
  • Patients must have the garment requisitioned by an Occupational Therapist (OT), Physical Therapist (PT), Public or Private CDT Therapist (CDT), Enterostomal Therapy Nurse (ET), Diabetes Nurse (DNS) or Wound Care Nurse (IIWCC).

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

Busting With Energy is Saskatchewan's only breast cancer survivors dragon boat team. 

2017 LAS Appreciation Award

New in 2017 LAS decided to award an outstanding member. Gail Swain has won this year as she is so generous in making and donating quilts to help LAS raise funds for education through raffle sales. Her generosity is greatly appreciated, congratulations Gail!

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


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.

Congratulations past and present LAS Volunteers

Congratulations past and present LAS Volunteers!

Disclaimer — The purpose of the health information on the web site of the Lymphedema Association of SK Inc. (LAS) is to inform and educate. This information does not replace the knowledge expertise, skill, and judgement of health care providers. It is not meant to be used as diagnosis or treatment. If you have medical questions or concern for your own health, please consult a qualified health care provider. LAS makes every effort to ensure that the information on this web site is correct and up-to-date, but cannot guarantee that it is error- free or complete. Links to our website are presented for informational purposes only and any mention of a product, form of therapy, or therapist does not constitute a recommendation.