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Your membership is confirmed, and we thank you.
We will mail you a receipt for the transaction, your membership card and various general information documents on lymphedema. You will also receive emails from the LAQ, including our newsletters and messages about our free support groups.
Stay tuned to take full advantage of your membership. Also visit our website, a veritable encyclopedia on lymphedema at www.infolympho.ca.
And at any time, receive answers to your questions by leaving us a message at 1 866 979-2463 (514 979-2463).
Welcome among us and thank you for your support!
The LAQ team
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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