May 2026 eCommunication

 

This week, we’re inviting our community to contribute to two important survey initiatives, while also sharing additional educational resources on cellulitis.


In partnership with the Lymphedema Association of Quebec (LAQ), we are supporting the distribution of a survey on experiences with cellulitis in lymphedema.


We’re also pleased to share a second survey led by Dr. Shelley DiCecco (PCOM Georgia), in collaboration with Lymphoedema Wales, exploring experiences during pregnancy and post-partum for those living with lymphedema and/or lipedema.


Your input can help inform future care, education, and support.

If you’re interested in participating in or learning more about additional research opportunities, please visit our website:

www.canadalymph.ca/getinvolved/research-opportunities/

 

Lymphedema and Episodes of Cellulitis

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.

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.

Cellulitis is a sudden, non-contagious, bacterial infection of the tissues under the skin. Infection can enter the body through a break in the skin, fungal infections (under nails), or an existing wound or skin inflammation.


Keeping the skin clean, well-moisturized, and intact reduces the risk of these entry points forming. Good skin care practices—like gentle cleansing, daily moisturizing, prompt treatment of cuts or fungal infections, and protecting the skin from injury—help maintain the skin’s barrier function. This is especially important because recurrent cellulitis can worsen lymphedema over time, creating a cycle of swelling and infection.



Signs and symptoms of cellulitis include:


  • Rapid onset of skin redness, swelling or pain
  • Skin that feels hot or painful to the touch or tingling
  • Skin that is red or with a reddish rash or red streaks or swollen
  • A feeling of tiredness or heaviness
  • If cellulitis worsens, you may feel flu-like symptoms, feelings of nausea, fever or chills



IMPORTANT: If you notice any of these symptoms, seek medical help without delay. Cellulitis can spread quickly and requires antibiotic treatment.


People with lymphedema are at risk for cellulitis because their lymphatic system is less able to fight infection. By prioritizing skin care, individuals with lymphedema can significantly lower their risk of cellulitis and support more stable, long-term management of their condition.

Lymphedema Learning Library:

Lymphedema and Cellulitis

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.


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.

 
 

Your voice is also needed in another important area of research.


We’re pleased to share a second survey exploring experiences with pregnancy and post-partum for individuals living with lymphedema and/or lipedema.

 

🌟Paid Promotion🌟


This research opportunity is being shared as a paid promotion through the CLF to support broader dissemination to our community.

 

Are You Interested in Sharing Your Experience Living with Lymphedema or Lipedema During Pregnancy and Post-Partum?

Progress is being made in the prevention and treatment of lymphedema and lipedema, but the relationship between these conditions and pregnancy is still not well understood! Please consider taking part in a short international survey to help us gain insight into your experience with lymphedema/lipedema and pregnancy! The survey is available in 10 languages. The hope is that the information gained from this study will help shape the understanding and treatment guidelines for lymphedema/lipedema during pregnancy! Please share this with others who may be interested in participating.

 

Our 2026/2027 Sponsors

The Canadian Lymphedema Framework gratefully acknowledges the contributions of these industry partners whose support helps to make our important work possible. Please visit them online to learn about their lymphedema products and services. Simply click on their logo, below, to be taken directly to their website.

 
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