Make a Difference
You can make a difference in many ways; whether living with or supporting someone with WM.
As an orphan disease we count on you to do what you can to spread the word. We need volunteers to be part of this rare disease movement and make a difference.
*Build awareness or hold an event in your community.
*Bring the issues that rare disease patients face to the attention of the general public, policy makers and researchers.
*Stimulate much needed WM research through fundraisers.
*Become involved with the WMFC and be part of the many volunteers working on behalf of all WMers and their families.
*Become a support group leader in your community, bringing those living with WM together to share the challenges of life after diagnosis.
*Join the Waldenstrom’s Macroglobulinemia Foundation of Canada whose focus is to offer hope, give support, inform you on the current treatment options available, and to stimulate research for WM
We need each and every one of you to stand up and be counted to “Make a Difference”. Click here to find local support.