August 2026 eCommunication | | |
Living with lymphedema can add an ongoing layer to everyday life – physically, practically, and emotionally. Everyone’s experience is different, and the things that help people feel informed, supported, and connected can look different too.
Wellness can take many forms. It may include learning more about movement and physical well-being, giving ourselves some compassion when things feel difficult, and connecting with people, information, and resources that make the journey feel a little less isolating.
This Wellness Month, we’re exploring three aspects of wellness through movement, self-compassion, and community. We’re sharing CLF resources that offer practical information, thoughtful perspectives, and opportunities for connection – with the hope that you’ll find something useful for you.
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Movement can support cardiovascular health, strength, mobility, and overall well-being, while also helping with stress and sleep.
Whether you’re already active or just getting started, explore our Lymphedema Learning Library: Exercising with Lymphedema for downloadable Pathways articles featuring expert guidance, practical advice and helpful tips.
Not sure where to start? Talk with your lymphedema therapist and/or health care team to help determine which forms of movement are right for you.
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You don’t have to navigate life with lymphedema alone. Connection and community can be an important part of wellness, providing support, encouragement, and a sense of belonging.
Whether you’re looking for practical support, a listening ear or guidance in managing lymphedema, asking for help is an important part of caring for yourself.
Visit our Provincial Lymphedema Associations webpage to find an association serving your province or region and explore available support, resources, and community connections.
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SPECIAL ANNOUNCEMENT
New Canadian Comprehensive Network of Excellence
| | The CLF congratulates the Dianne and Irving Kipnes Health Research Institute: Lymphedema Education and Research Pillar at the University of Alberta and its province-wide network of partners – including the CLF and ALA – on designation as a LE&RN Comprehensive Network of Excellence in Lymphatic Diseases. A wonderful milestone for lymphedema research, education, and care in Alberta and across Canada. | | |
What if the future of lymphedema care in Canada wasn't decided for us—but shaped by all of us?
Join us in Halifax from May 13-15 for the Canadian Lymphedema Framework Assembly 2027: Canada Connects – a national, three-day Assembly built around a fresh, innovative format designed for connection and collaboration.
We’ve expanded the CLFA2027 website with new information about Lymphedema LEAD Day, the Open Space Forum, travel and accommodations, frequently asked questions, and more.
| | The CLF believes in strengthening connections across the lymphatic care community. In addition to CLF news, we are pleased to share important stories and noteworthy news, research updates, academic opportunities, and events shaping the lymphatic care landscape. Our emphasis is on Canadian initiatives, but we also feature items with international impact and relevance for our community. | | | | |
Lymphedema Association of Nova Scotia: Lymphedema Education and Resource Day
A Special Invitation for Atlantic Canada
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The #BLS2026 Lymphoedema Conference
When: October 5-7, 2026
Where: Chester Racecourse, Chester, United Kingdom
Learn More and Register: theblsconference.com/
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2026 Wounds Canada National Hybrid Conference
When: October 22-24, 2026
Where: Niagara Falls, Ontario, Canada
Learn More and Register: woundscanada.ca/health-care-professional/education-health-care-professional/2026-national-conference
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13th International Lymphoedema Framework Conference
Lymphoedema and Lipedema: What future lies ahead, between lights and shadows
When: October 28-31, 2026
Where: Rome, Italy
Learn More and Register: ilfworldcongress-rome2026.org/
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Canadian Lymphedema Framework Assembly 2027:
Canada Connects
When: May 13-15, 2027
Where: Dalhousie University Campus, Halifax, Nova Scotia
Registration Opens: October 1, 2026
Learn More: CLFA2027.ca
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Continuing Education Opportunities | | |
Australasian Lymphology Association:
Management of Cellulitis in Lymphoedema/Chronic Oedema
This document has been developed and endorsed by the Australasian Lymphology Association to provide an Australasian perspective and consistent, evidence-informed principles on the management of cellulitis in people with lymphoedema/chronic oedema.
The paper was developed on behalf of the ALA by Dr Robyn Sierla, Dr Blake Nield, Dr Elizabeth Webb, Professor Warwick Britton, Associate Professor Helen Mackie, Janette Jacka, Dr Debbie Geyer, and Professor Elizabeth Dylke.
Learn More: lymphoedema.org.au/education-&-resources/cellulitis-position-paper/
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Lymphedema Association of Quebec (LAQ):
Pan-Canadian Survey on Cellulitis Episodes
and Lymphedema
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This survey aims to collect information about:
- the frequency of cellulitis episodes,
- the symptoms experienced,
- the treatments received,
- related hospitalizations,
- the impact on lymphedema management and the financial burden for patients.
The insights gathered will play a vital role in informing efforts to strengthen lymphedema screening, improve access to timely and appropriate care, and advance the prevention of complications. Your participation is an opportunity to contribute to meaningful change and help shape a more responsive and supportive system for the lymphedema community across Canada.
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LE&RN Patient Survey:
Your Experience with Lymphatic Disease Care
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LE&RN invites patients, caregivers, and families to complete a brief survey designed by patients, for patients.
Your feedback will directly inform discussions at LE&RN's inaugural Centers of Excellence Global Summit this October, where clinicians, researchers, and healthcare leaders from around the world will explore ways to strengthen research, diagnosis, treatment, and access to high-quality care.
| | Thank You to Our Industry Partners | | The Canadian Lymphedema Framework gratefully acknowledges the support of our industry partners. Their contributions help make our work possible and support education, awareness, and connection across the lymphedema community. We invite you to visit them online to learn more about their lymphedema products and services. Click any logo below to go directly to their website. | | ©2026 Canadian Lymphedema Framework | Website | | | | |
