Canadian Lymphedema Framework

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Canadian Lymphedema Framework

Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from Canadian Lymphedema Framework, Medical and health, PO Box 35062 RPO Hartzel, Saint Catharines, ON.

The Canadian Lymphedema Framework (CLF) is an academic and patient stakeholder collaboration, which is part of an international initiative to promote research, best practices and lymphedema clinical development worldwide.

06/01/2026

The Canadian Lymphedema Framework is proud to present a sponsored webinar by our Diamond Partner, Bauerfeind Canada!

📢 Lipedema, Lymphedema, and Obesity… Putting an End to the Confusion
🎤 Presented by: Marie-Eve Letellier
🗓️ June 10, 2026 | 7:00PM EDT
📍 Virtual | FREE - Registration Required

Learning Objectives: Following this presentation, participants will be able to:

👉 Distinguish the key characteristics of the three conditions
👉 Understand their similarities and differences
👉 Clarify the diagnostic challenges
👉 Review the therapeutic approaches suited to each condition
👉 Explore the role of compression in management, including a presentation of Curaflow compression garments and the Lympha-mat compression device

Register today: www.tinyurl.com/Bauerfeind-Webinar-26

05/30/2026

Foot health is connected to whole-body wellbeing. For people living with lymphedema, especially when the feet, ankles, or legs are affected, foot care becomes even more important. Whether you are managing lymphedema yourself, supporting someone who is, or simply looking for practical prevention-focused information, small daily habits can make a meaningful difference.

Watch to learn more about our simple steps to support your foot health:

👉 Inspect your feet daily
👉Keep your skin clean and moisturized
👉Wear supportive footwear
👉Stay active
👉Protect your feet
👉Seek professional support

05/29/2026

Join our friends at the International Lymphoedema Framework in Rome for the 13th ILF Conference & 10th ITALF Conference. Early bird registration is available until May 31, 2026!

📍 Rome, Italy
🗓 28–31 October 2026

🔗 To learn more, visit: ilfworldcongress-rome2026.org

05/27/2026

80,000 Canadians are currently living with a bladder cancer diagnosis. Some of them will go on to develop lymphedema. If you, or someone you love has been diagnosed with bladder cancer, or are in treatment, we invite you to visit our website at www.canadalymph.ca to understand the risks, signs and symptoms of lymphedema.

05/25/2026

Applications are now open for the Canadian Rare Disease Network (CRDN) RAREvolution Scholarship, supporting students aged 17 to 29 living with a diagnosed or suspected rare disease as they pursue post-secondary education in Canada.

The scholarship exists to recognize resilience, leadership, and lived experience within the rare disease community.

Although recent prevalence data show that secondary lymphedema is not rare, primary lymphedema continues to be recognized as a rare condition.

👉 If you are interested in learning more, CRDN will be hosting a live information webinar May 27, 2026 at 12:00PM MT

Learn more and apply before June 12: https://canadianrdn.ca/scholarship/

05/22/2026

Foot health matters for everyone. Our feet support mobility, balance, independence, and overall quality of life — yet they are often overlooked until pain, injury, swelling, or other concerns arise.

For people living with lymphedema, especially when the feet, ankles, or legs are affected, foot care becomes even more important. Swelling, skin changes, reduced mobility, and difficulty finding properly fitting footwear can increase the risk of discomfort, injury, infection, and complications such as cellulitis.

At the same time, foot health is connected to whole-body wellbeing. Whether you are managing lymphedema yourself, supporting someone who is, or simply looking for practical prevention-focused information, small daily habits can make a meaningful difference.

Explore our Learning Library collection, “Lower Extremity Lymphedema,” featuring trusted articles on foot care, skin care, mobility, and managing lower-limb lymphedema: www.tinyurl.com/LowerExtremityFoot (or visit the link in our bio)

Whether you are living with lymphedema, supporting someone who is, or caring for patients in your practice, this collection offers practical information to support awareness, prevention, and better day-to-day care.

05/21/2026

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

On behalf of the CLF, we encourage you to explore our Lymphedema Learning Library collection, “Lymphedema and Cellulitis,” featuring articles that cover what cellulitis is, along with guidance on skin care, effective management strategies, and risk reduction.

👉 Read Now: www.tinyURL.com/Lymphedema-Cellulitis

Whether you’re a patient, caregiver, or health professional, we invite you to explore this resource and share it widely. Together, we can promote earlier recognition, better care, and stronger support for those affected.

05/19/2026

With summer around the corner, these skin care tips are an important reminder of simple steps you can take to help protect your skin.

These tips are especially important for people living with lymphedema. The combination of heat, humidity, and environmental exposure places vulnerable skin at greater risk for developing irritation or serious complications, like cellulitis.

• Use broad-spectrum sunscreen (SPF 30 or higher) daily and reapply every 2 hours
• Wear protective clothing, hats, and sunglasses outdoors to help protect your skin from sunburn
• Avoid peak sun hours (11 a.m. – 3 p.m.) and stay in air-conditioned or shaded areas when possible
• Check your skin regularly for early signs of redness, warmth, tightness, or itching as these can be early indicators of infection or inflammation, so seek medical care promptly
• Keep skin clean and dry, especially in areas prone to sweating or friction.
• Drink extra water to prevent dehydration and to help maintain skin integrity

Healthy skin plays an important role in reducing irritation, lowering infection risk, and supporting long-term skin health. Small daily habits can make a meaningful difference.

05/18/2026

Happy Victoria Day! Wishing everyone a wonderful long weekend with family and friends!

05/17/2026

Movement matters — for your heart health and your lymphatic health. 💙

This World Hypertension Day, it’s a great reminder that regular physical activity can help support healthy blood pressure, improve circulation, and encourage lymphatic flow.

For individuals living with lymphedema, gentle and consistent movement can play an important role in managing symptoms and supporting overall wellness. Whether it’s walking, stretching, strength exercises, or range-of-motion activities, every movement counts.

Looking for guidance? Our Exercising and Lymphedema Issuu stack from our Lymphedema Learning Library includes helpful resources and exercises for both upper and lower extremities to help you move safely and confidently.

👉 To read now, visit: https://tinyurl.com/ExercisingWithLymphedema

If you are starting a new exercise program, be sure to consult your healthcare team to determine what activities are most appropriate for your individual needs.

Address

PO Box 35062 RPO Hartzel
Saint Catharines, ON
L2P0C5

Telephone

+16476931083

Website

http://www.canadalymph.ca/

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