Meet Our Conference Speakers

New ILA diagnostic recommendations for lipedema

Dr. Towers will present Working Group recommendations, supported by the Board of the International Lipoedema Association, on how to diagnose Lipedema.

Anna Towers, MD is Director, Lymphedema Program, Supportive and Palliative Care Services, McGill University Health Centre, and Associate Professor in the Department of Oncology, McGill University, Montréal. Her main academic interest is in the development of lymphedema services for cancer patients, an area in which she is recognized as a national and international leader. Dr. Towers is a founding member and former Co-Chair of the Canadian Lymphedema Framework.

Learn more about Dr. Towers and her session here.

Discoveries in genetics and primary lymphedema 

Dr. McCuaig will explore which genetic mutation is responsible for lymphedema, and how these findings may lead to preventative measures.

Catherine McCuaig, MD is a pediatric dermatologist working at the Sainte-Justine University Hospital Center Sainte-Justine, and clinical professor at the University of Montreal, Quebec. Her special interests include neonates, vascular anomalies (Hemangioma Investigator Group and the International Society for the Study of Vascular Anomalies), lymphedema, epidermolysis bullosa, laser and teaching. Dr. McCuaig is co-chair of the Canadian Lymphedema Framework.

Learn more about Dr. McCuaig and her session here.

Meet Our Industry Sponsored Speakers

Moving Forward Together: IPC and Self-Management

It is recognized worldwide that lymphedema and lipedema are underdiagnosed and undertreated diseases. Not only are there physical symptoms of these conditions, there is a massive psychosocial restriction. An essential part of this therapy concept is the direct involvement of the patients in the sense of self-management.

Learn more about Dr. Küppers

and Bauerfeind's industry sponsored

session here.

Lymphedema Is Challenging, Let’s Make Choosing the Right Juzo Compression Garment Easy

This session will explore the K.E.Y (Knowledge Empowers You) to selecting the correct Juzo Garments for various stages of lymphedema that a patient may present. Juzo offers high-quality medical compression garments for treatment during both decongestive and maintenance phases of Lymphedema. Come join us to learn about the K.E.Y to your success.

Learn more about Kim Gladman and Juzo's industry sponsored session here.

2023 National Lymphedema Conference Program

Our conference program is in development and we are thrilled to share with you all of the exciting presentations, breakout sessions, workshops, and abstracts that will be featured this year. You will hear from the top surgeons, doctors, therapists, researchers, industry partners, and treatment providers within the lymphedema and lymphatics community.

See the latest updates and current program.

We can't wait to see you there!

Are you a subscriber?

Pathways is the official publication of the Canadian Lymphedema Framework. The magazine is dedicated to lymphedema and aimed at both health professionals and patients.

Pathways is published four times per year in both a print and digital edition. Print subscriptions to Canada and all digital subscriptions are just $30 CAD.

Our 2023 Fall Pathways issue will be released in September, so don't wait any longer and subscribe now. You won't want to miss it!

Lymphedema & Chronic Edema Management Online Course

U of A Online Microcredential Course for Healthcare Professionals

This medical introduction to lymphedema and chronic edema management is geared toward medical and related industry professionals. The course is delivered online by the University of Alberta on their eClass platform and consists of 4 modules, self-paced over 6 weeks. A certificate of 35 educational hours is given on completion.

Click below to learn more about the lecturers and topics covered and to enroll for the next course which begins on October 16. Course Fee: $350 CAD.

Stay tuned for winter course dates!

The Canadian Lymphedema Framework would like to acknowledge the financial support of the Government of Canada through the Department of Canadian Heritage.

As a non-profit organization, we rely on grants, government funding, donations, and events to support our mission work to improve the management of lymphedema and related disorders in Canada. Thank you for your continued support for our cause.

To learn more on how you can contribute to the Canadian Lymphedema Framework, please check out current opportunities on our "Work With Us" web page or donate now.

Meet Our Sponsors

The Canadian Lymphedema Framework gratefully acknowledges the participation of these companies whose support makes our 2023 National Lymphedema Conference possible.

You will have the chance to thank them in person and learn about their products and services by visiting with them in the Exhibit Hall during the conference.

(c) 2023 Canadian Lymphedema Framework | Website