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Are you a company looking to maximize your visibility within Québec’s lymphedema, lipedema, and chronic edema community?
With the LAQ, the opportunities are endless!
See your logo, advertisements, or business information featured in:
To learn more, consult the 2026–2027 Sponsorship Package or contact the Executive Director at 514-979-2463.
The Lymphedema Association of Québec (LAQ) respects your privacy and does not rent, sell or trade its mailing lists. Any information you provide is used solely for the purpose of providing services, processing and acknowledging donations, and keeping you informed of LAQ activities, including programs and services, special events, annual general meetings, fundraising needs, volunteer opportunities, and other periodic contacts. Please allow 30 days for our records to be updated.
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
514 979-2463
Mailing address
648 Lajeunesse Street,
Laval, Quebec, H7X 3K5CP
Telephone
514 979-2463
Email
aql@infolympho.ca
Website
www.infolympho.ca
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