WM Information for the Newly Diagnosed

Waldenstrom’s Macroglobulinemia Foundation of Canada (WMFC)

WMFC is the only Canadian Charitable organization dedicated solely to the Support, Education and Research for a Cure of WM.

Support Groups

A diagnosis of WM, a rare type of cancer may cause fear, anxiety or uncertainty. Having a rare cancer may make you feel like you’re all alone. But you’re not!

Find a Support Group

Welcome, fellow WMer! We hope the information collected below is useful to you in your journey with WM.

But first, we suggest you take a few minutes to view these four videos. They contain much that you need to know in the first days after your diagnosis.

About WM

Learn More

About WM

Newly diagnosed
What is WM?
Symptoms & Diagnosis
Preparing for your Appointment
Treatment
Booklets, Fact Sheets, Treatment Option Guides
WM quarterly Magazine, the “Torch”
Common Canadian Questions Answered

Support

Learn More

Support

Support Groups
Canadian LifeLine
Online Discussion
Living With WM
Stories of Inspiration
Support for Caregivers

Education

Learn More

Education

Booklets, Fact sheets & Treatment Option Guides
Torch Magazine
Education Forums
WMFC Publications and Newsletters
WM in Canada
Video & Webcast Library
Articles
Covid-19 Resources
Archive
One-liner archive
WMFC Partners

Donate

Learn More

Donate

Make a Donation

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