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This December and January, your gift for lymphedema goes twice as far, thanks to the incredible support of our partners.
A heartfelt thank you to Essity, Bauerfeind, Juzo, and Medi for matching your donations.
The MUHC Lymphedema Clinic is threatened with closure.
Thousands of patients are at risk of being abandoned in the coming months due to lack of funding. Sign and share the petition!
We offer support, resources, and information to help people living with lymphedema, an incurable but manageable chronic disease.
Lymphedema is a global health problem affecting more than 250 million people worldwide, women, men, and children of all ages...
Lymphedema is a chronic, incurable swelling that can affect children, adults, and seniors in the arms, legs, torso, head, mouth, and even genitals. With the right tools, lymphedema can be controlled.
Be part of the solution: show your support for the LAQ. The LAQ is Québec’s only support and education organization for people living with lymphedema. More broadly, we raise awareness among healthcare professionals and the general public. We encourage scientific research to find more effective and sustainable solutions.
As a member of the LAQ, you benefit from the support of people who are determined to keep lymphedema under control and live life to the fullest. You’re not alone! The community is there to support you and provide you with all the information you need.
Provides help and resources to people diagnosed with lymphedema when they feel overwhelmed by their condition.
Informs and empowers healthcare professionals about lymphedema and how to treat it.
Demonstrates to the public that the lymphedema cause is important and that the people affected need help.
Enables lymphedema sufferers to become part of a community with which they can identify.
Your generosity enables the LAQ to support those affected by the disease.
The LAQ is grateful to the RAMQ for administering the Compression Garment Program.
The LAQ is your source for information on lymphedema whether of primary or secondary origin. Have a question? Would you like to verify some information? Feel free to turn to the LAQ and its team of professionals for clear, well-founded answers.
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Lymphedema is swelling that develops in one or more parts of the body where the lymphatic system is deficient due to malformation or trauma. A poorly functioning lymphatic system abnormally engulfs skin tissue with protein-rich fluid, causing swelling and inflammation.
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Don’t ignore these symptoms. Consult your doctor. Prompt intervention will limit swelling and help prevent complications.
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NO. More than half of suspected lymphedema cases in Canada are secondary to chronic venous insufficiency and severe obesity (body mass index over 50), which is why it’s so important to treat venous insufficiency and obesity promptly and appropriately. While only 31% of lymphedema cases can be linked to cancers (sarcoma, gynecological, breast, melanoma, genitourinary, and others), cancer survivors will pay special attention to preventing and managing obesity and venous disease.
Lymphedema is still a little-known disease, and the number of sufferers is growing.
Help the LAQ, an association that transforms people’s lives!
The Lymphedema Association of Québec provides support, education, and awareness to people living with lymphedema, as well as their families, friends, and healthcare professionals. We provide information and educate about lymphedema and its causes, risk reduction, and treatments for this chronic disease, and encourage scientific research leading to a cure.
Lymphedema Association of Québec
Therapeutic Support Program
1 866 979-2463
514 979-2463
Mailing address
CP 152, Bureau Chef Branch,
Saint-Hyacinthe,
QC, J2S 7B4
Telephone
1 866 979-2463 / 514 979-2463
Email
aql@infolympho.ca
Website
www.infolympho.ca
© 2023 Lymphedema Association of Québec. All rights reserved. | Credits