An estimated 271,000 Quebecers suffer from lymphedema/chronic edema. 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.
*All members of a professional order or association
1-800 line – For information and peer consultation on complex cases
Discussion forum – Ask questions, share answers, discuss clinical cases, learn about lymphedema clinical practices
Reference library – Documents to download from recognized organizations
Lymphedema calendar – Training courses and events offered in Canada, the U.S. and Europe
Free with registration by e-mail to aql@infolympho.ca
Welcome to the ProLymph Resource Center!
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