Are you a company looking to support the cause of lymphedema and lipedema while gaining visibility within the chronic edema community in Québec? With the LAQ as your partner, the possibilities are endless!
See your logo, advertisement or contact information in:
* LAQ sponsors and corporate members are invited to add the LAQ logo with an active link to their website(material provided upon registration/sponsorship).
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.
Consult our complete corporate chart for full details on each of the partnership levels offered.
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
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