WM Information for the Newly Diagnosed

Welcome, fellow WMer!  We hope the information collected below is useful to you as you undertake  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.

And these three booklets are part of a global initiative to educate both patients and doctors on the current knowledge of WM.

You can download and print your own copy of “Essential Information: A Patient’s Guide“, “Essential Information: A Physician’s Guide“, and “WM: Frequently Asked Questions“.

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!

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.

Join the WMFC and stay in the loop!

Get the latest news, events and membership information via email.