Coping with a lymphedema diagnosis and persevering with self-management over time present different challenges. Marie-Eve Letellier, certified lymphedema therapist, discusses the main challenges you’ll face in the short, medium and long term.
ZOOM presentation in French. Bilingual Q&A session. This free event organized by the LAQ will take place on THURSDAY, September 26, 2024 at 7pm. Free registration MANDATORY.
We look forward to seeing you there!
To receive a priority invitation to our next education and support group, become an LAQ member.
This lymphedema event is made possible by the dedication of volunteer therapists and the Lymphedema Association of Québec. The LAQ’s mission is to support people at risk and those affected, while raising awareness of lymphedema as a chronic disease among the community of healthcare professionals.
The Lymphedema Association of Québec provides support, education, and awareness to people living with lymphedema, as well as their families, friends, and healthcare professionals. We provide information and educate about lymphedema and its causes, risk reduction, and treatments for this chronic disease, and encourage scientific research leading to a cure.
Lymphedema Association of Québec
Therapeutic Support Program
1 866 979-2463
514 979-2463
Mailing address
CP 152, Bureau Chef Branch,
Saint-Hyacinthe,
QC, J2S 7B4
Telephone
1 866 979-2463 / 514 979-2463
Email
aql@infolympho.ca
Website
www.infolympho.ca
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