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An estimated 274,000 Quebecers suffer from lymphedema or chronic edema. For lipedema, the prevalence is estimated at 90,000 individuals. Due to limited resources, only a fraction of this population is diagnosed and treated.
ProLymph has established itself as a resource center for professionals, to better meet the network’s needs in the field of lymphedema/chronic edema/lipedema.
*Any member of a professional order or association
A simple email registration gives you access to:
ProLymph supports healthcare professionals in the screening, diagnosis, and management of lymphedema, chronic edema, and lipedema by providing rapid access to clinical expertise and reliable resources.
Join ProLymph today to support your clinical decisions.
Free registration by email at: aql@infolympho.ca
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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