Canadian Lymphedema Framework

Canadian Lymphedema Framework Canada’s national voice for advancing lymphedema care through collaboration, education, research, and advocacy.

🎗️ Gynecologic Cancer Awareness Month: Let’s talk about lymphedemaGynecologic cancers include cancers of the cervix, ova...
09/11/2026

🎗️ Gynecologic Cancer Awareness Month: Let’s talk about lymphedema

Gynecologic cancers include cancers of the cervix, ovaries, uterus, va**na, and v***a. Lymphedema is a recognized potential effect of some gynecologic cancer treatments, particularly in the lower limbs. Reported rates vary depending on the type of cancer, treatment received, and how lymphedema is identified and measured.

Cancer treatments such as lymph node removal and radiation therapy can affect the lymphatic system, impairing the body's ability to move lymph fluid, increasing the risk of chronic swelling and related complications. Lymphedema can develop during or soon after treatment, but it can also appear months or even years later.

Learning about lymphedema risk after cancer treatment and the signs to watch for can support earlier recognition and conversations with your health care team.

To learn more about lymphedema in gynecological cancer, explore our Lymphedema Learning Library: Cancer-related lymphedema: https://tinyurl.com/Cancer-related-lymphedema

You can also find free educational resources on lymphedema on our website at: www.canadalymph.ca/education-materials/

Did you know that 1.25 million Canadians are affected by lymphedema? That’s approximately 1 in every 33 people. 💙While i...
09/11/2026

Did you know that 1.25 million Canadians are affected by lymphedema? That’s approximately 1 in every 33 people. 💙

While it is often associated with cancer treatment, lymphedema can also develop as a result of surgery, radiation therapy, infection, trauma, congenital conditions, obesity, or chronic venous disease.

At the Canadian Lymphedema Framework (CLF), we’re working to improve lymphedema care across Canada by bringing people together, advancing education, supporting research, and amplifying the voices of patients and clinicians.

Our goal is simple: to help ensure that every person in Canada living with lymphedema has timely access to knowledgeable care, reliable information, and supportive resources.

Whether you’re a health professional, researcher, advocate, caregiver, or living with lymphedema, the CLF is here for you.

Visit our website to explore:

💙 Free, downloadable educational resources for patients and health professionals
💙 Information about provincial associations and local resources and supports
💙 Pathways magazine, including digital access and subscription information
💙 The latest lymphedema prevalence data in Canada
💙 Information about the CLF and how you can get involved

Together, we can raise awareness, strengthen lymphedema care, and make a meaningful difference in the lives of those affected.

To learn more about lymphedema, our organization, and how you can help make a difference in the lives of those affected, please visit www.canadalymph.ca

🍂 Pathways Fall Issue is out! 🍂Are you a subscriber? Check your email for an early access code to view our digital editi...
09/04/2026

🍂 Pathways Fall Issue is out! 🍂

Are you a subscriber? Check your email for an early access code to view our digital edition while you wait for the printed issue in the mail.

Do you want to subscribe? Subscribe now at: https://www.canadalymph.ca/subscriptions/ or visit the link in our bio.

Did you know that September is Childhood Cancer Awareness Month? For children and families navigating cancer, there can ...
09/03/2026

Did you know that September is Childhood Cancer Awareness Month?

For children and families navigating cancer, there can be many unexpected challenges along the way. Lymphedema is one possible side effect of certain cancers and cancer treatments.

Secondary lymphedema can develop when the lymphatic system is affected by factors such as infection, cancer or cancer-related treatment, or surgery.

While not every child will develop lymphedema, understanding signs and symptoms, risk reduction, and knowing where to find support can make a difference.

If you are a parent or primary caregiver of a child with cancer and would like to learn more about lymphedema, we invite you to visit our website at www.canadalymph.ca/education-materials/ to explore our digital and downloadable educational and support resources.


As we begin to return to our regular updates and announcements, we want to thank our community for the kindness, support...
08/31/2026

As we begin to return to our regular updates and announcements, we want to thank our community for the kindness, support, and heartfelt messages shared with us over the past week following the sudden passing of our Past Chair and Founding Member, Dr. David H. Keast.

The many stories, reflections, and expressions of gratitude we’ve received are a powerful reminder of the impact David had on the lymphedema community in Canada and beyond.

As we move forward, we will carry his legacy with us in the work that continues – bringing people together, advancing education and research, strengthening the voice of the lymphedema community, and continuing to work toward better lymphedema care across Canada.

David gave so much to this organization and this community, and we will honour that contribution by continuing the work he cared so deeply about – together.

We are deeply saddened to share the news of the passing of Dr. David H. Keast.David was a founding member of the Canadia...
08/25/2026

We are deeply saddened to share the news of the passing of Dr. David H. Keast.

David was a founding member of the Canadian Lymphedema Framework and one of the organization’s most important and enduring leaders. He served first as Co-Chair, then as Chair and Treasurer, and most recently as Past Chair.

His contributions to the CLF were extraordinary. He supported our work with deep knowledge, experience, care, and compassion; served on our Editorial Board and Scientific Committee; helped shape our conferences; contributed to Pathways; and provided trusted guidance on educational materials, consensus statements, and national initiatives.

David’s influence extended across wound care and lymphedema communities in Canada and internationally. For the CLF, his loss is profound.

We extend our deepest condolences to David’s family, friends, colleagues, patients, and all those whose lives and work were touched by him.

A fuller tribute will be published in the Winter issue of Pathways.

To read the full announcement visit: https://conta.cc/4bYMsQm

🌟Sponsored Advertisement: Bauerfeind Canada🌟Heavy, tired, or swollen legs? 🦵 They could be early signs your veins need a...
08/18/2026

🌟Sponsored Advertisement: Bauerfeind Canada🌟

Heavy, tired, or swollen legs? 🦵

They could be early signs your veins need attention. Swipe to learn more.
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Jambes lourdes, fatiguées ou enflées?🦵

Ces symptômes peuvent être les premiers signes d'un problème veineux. Faites défiler pour en savoir plus. 👣

Our mission is to improve lymphedema care in Canada by fostering collaboration among interest-holders, advancing educati...
08/17/2026

Our mission is to improve lymphedema care in Canada by fostering collaboration among interest-holders, advancing education, supporting research, and amplifying the voices of patients and clinicians.

Thank you to our board of directors, education working group, editorial board, staff, community, supporters, and volunteers for making this possible. Together, we're making a difference!

To learn more about our organization, visit our website canadalymph.ca and check out our 2025-2026 Impact Report at https://tinyurl.com/25-26CLFImpactReport 💙

Our colleagues at the Lymphedema Association of Quebec (LAQ) are currently gathering input through a short survey on exp...
08/15/2026

Our colleagues at the Lymphedema Association of Quebec (LAQ) are currently gathering input through a short survey on experiences with cellulitis. We’re pleased to share this opportunity with our community in support of their work, and to help ensure Canadian perspectives are well represented.

Cellulitis is a significant concern for many people living with lymphedema, and improved understanding can help inform education, prevention, and care.

If you are interested in participating in the survey, or learning more, please visit: https://bit.ly/LAQ_Cellulitis_Survey or visit the link in our bio!

Movement plays an important role in supporting the lymphatic system. When our muscles contract, they help move lymph flu...
08/14/2026

Movement plays an important role in supporting the lymphatic system. When our muscles contract, they help move lymph fluid through the lymphatic vessels — often referred to as the “muscle pump” effect.

However, the benefits of movement go beyond the lymphatic system. Regular physical activity can support cardiovascular health, strength and mobility, while also helping to reduce stress, improve sleep and support our overall mental well-being.

Exercise snacking is exactly what it sounds like: short bursts of physical activity sprinkled throughout your day. These might be as simple as a few minutes of walking, some gentle movements, a few repetitions of an exercise, or taking an active break from sitting.

Not sure where to begin?

✨ Choose a goal that matters to you, such as improving cardiovascular fitness, mobility or strength.
✨ Start with movements you can do comfortably and safely.
✨ Look for opportunities to move more often throughout your day.
✨ If you’re starting a new exercise routine, we recommend that you talk with your health care team or lymphedema therapist about what's right for you.

To learn more, read Margie McNeely's article on "Exercise snacking: An alternative to boost your overall health" in our Lymphedema Learning Library feature: Exercising with Lymphedema: https://tinyurl.com/ExercisingWithLymphedema

Whether you’re already active or just getting started, this resource offers encouraging, practical guidance to help you move in ways that feel safe and manageable for you.

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Saint Catharines, ON
L2P0C5

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