About

About

Support for those affected with or at risk of primary or secondary lymphedema

The Lymphedema Association of Manitoba (LAM) is a patient focused, non-profit organization founded in 2011.

Lymphedema Association of Manitoba is an organization in the pursuit of resources, information, education and awareness, and support for those affected with or at risk of primary or secondary lymphedema; their families, health care professionals and the general public.

We are committed to improving the lives of people living with or who are at risk of developing lymphedema. There is much work to be done!

See our online brochure.

Mission statement

The LAM will work to ensure all who are impacted by lymphedema have equal access to appropriate resources.

Description

Our organization is providing education and awareness of lymphedema to the general public and the medical community.