We are committed to finding a cure for WM.

Article: The Rarity of WM Challenging

Treatment options are limited for patients with Waldenstrom’s macroglobulinemia (WM), says Morie A. Gertz, MD. Combination therapies offer a potential solution, but the rarity of the disease is an obstacle. The disease occurs in roughly 4 patients per million, per… Continue reading

Health Canada Approves IMBRUVICA

IMBRUVICA® is an oral, once-daily, single-agent therapy associated with a durable response in patients with this rare B-cell lymphoma

TORONTOMay 12, 2016 /CNW/ – Janssen Inc. announced today that Health Canada has issued… Continue reading

A father’s day gift for WM

Shelby Bell Knowlton is undertaking a Tough Mudder competition on June 18th in Whistler, BC. She will be donating 100% of donations to the WMFC. We are so very appreciative of this courageous father/daughter team and invite you to support… Continue reading

2016 IWMF Ed Forum

waterplace2_nicholas-millard2016 IWMF Educational Forum

Providence, RI

June 10-12, 2016

Omni Providence Hotel

The IWMF Educational Forum has something for everyone. From presentations addressing symptoms and complications, treatments, new therapies in the works and research findings by specialists of Waldenstrom’s Macroglobulinemia… Continue reading