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                                           Lymphedema Association of Manitoba Annual Symposium
                                                          
Friday & Saturday, March 9 &10, 2018
                                                                Deer Lodge Learning Centre

                  Join us and be part of the call to action to improve the lives of Manitobans living with lymphedema. 

We welcome Dr. Marc Hamel who will speak on distress and resilience. Dayna Mascitelli and Claudette ZinkoInjury will be talking about prevention and ergonomics. Click here for more information.    

Please print and fill out this registration form or contact us at lymphmanitoba@gmail.com

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Consider joining our organization! 

The Board would welcome all community-minded individuals interested in joining LAM’s efforts but would particularly invite those with communications, media, website or fundraising interest or experience. 

Please consider joining us by contacting through emailWe are interested in broadening the involvement of skilled, engaged individuals to join us as we work together to improve the lives of those living with lymphedema.   

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March 6th in each year

Bill 209, Lymphedema Awareness Day Act proclaims March 6th as Lymphedema Awareness Day in Manitoba!

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Join www.CanadaHelps.org as they make it easy to donate and support the LAM. Once on their site, search for us with key word 'lymphedema' and then scroll to the bottom of the page to find our organization.  
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Hilary Druxman Design (Winnipeg) has designed a unique pendant we call JourneyOrder the necklace and 100% of the net proceeds sold supports the LAM in our mission to raise lymphedema awareness. 

"Symbolic of the challenges on every journey
as we move forward,
one step at a time, discovering hope, strength and joy."

It is a journey of ups and downs; it is hard and good all at the same time

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Lymphedema Association of Manitioba is an organization in the pursuit of resourcesinformation, 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.

Available online and easy to print is our LAM 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.

2018 Board of Directors

Left to right: David Van Hellemond, Claire Ann Deighton-Lamy, Cherida Olson, Susan Tole, Susan Stratford

Missing: Cara Hutchison and Rupal Purohit


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