Thanks to your enthusiasm and the generosity of people who are sensitive to your cause, you’ll prove that together, lymphedema is less of a burden! Whatever the size of your fundraising campaign, every gesture counts in supporting people suffering from this underdiagnosed, under-treated and under-researched disease. Get involved by making your fundraising a reality!
To find out more, call us at 514 979-2463 / 1 866 979-2463
Thank you so much for helping us with an event in your community!
Thanks to our affiliation with the Grand défoulement à ma façon movement, you can raise funds specifically for lymphedema.
Choose your activity and follow the organizer’s guide!
Ready to get started on your lymphedema fundraising project?
We invite you to fill out the online form on the Quebéc Cancer Foundation’s Grand défoulement à ma façon portal.
BE SURE TO SPECIFY THAT YOUR CAMPAIGN BENEFITS THE LAQ.
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 (LAQ) provides support, education, and awareness to individuals living with lymphedema, lipedema, or lipo-lymphedema, as well as to their families, loved ones, and healthcare professionals.
We inform and educate about these chronic conditions – their causes, risks of progression (including how lipedema can develop into lipo-lymphedema), and the available conservative and postoperative treatment options, such as decongestive therapy and compression.
We also actively support scientific research aimed at improving care and advancing knowledge toward a cure.
Lymphedema Association of Québec
Therapeutic Support Program
1 866 979-2463
514 979-2463
Mailing address
648 Lajeunesse Street,
Laval, Quebec, H7X 3K5CP
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