We are committed to finding a cure for WM.

Message from WMFC

A Message from the President of the WMFC

The Waldenstrom’s Macroglobulinemia Foundation of Canada was founded in 2003. Our goal is to reach out to those living with Waldenstrom’s Macroglobulinemia. With our dedicated volunteers we aim to provide a forum for support and to meet with others living with this rare disease. You are not alone.

We encourage all of you who have been diagnosed with WM to register with the WMFC so that together we can stand up and be counted to promote the much needed research to find the cause and ultimately a cure.

WMFC thanks all our Canadian members for their continued support to our membership and research funds. With your gift we are able to continue our quest in promoting new research and education.

Become a member; make a difference not only in your life but to so many others. Click here to join via the donations form,

“As you grow older, you will find that the only things you regret

             are the things you did not do”  Zachary Scott

Arlene Hinchcliffe

President, WMFC

The WMFC has In Memory and In Honour donation cards which can be obtained by contacting Arlene Hinchcliffe at ahinchcliffe@wmfc.ca or 905-337-2450. Donation forms for membership, In Memory, and In Honour can be accessed at this website under the heading  donations.