I am a 67 year old WM patient living in Calgary, Alberta, Canada. My wife, Nancy, and I lead an active lifestyle, especially since retiring about 5 years ago. We are avid downhill skiers… Continue reading
Click here “WMFC in the Torch!” to read a review of the 2016 WMFC Educational Forum in the Torch by Halifax Support Group Leader Ron Ternoway!
Contributing Member – Ron Ternoway
Ron Ternoway has shared his experience with WM in “Trials of a Wally”. We thought we would share with the WMFC community!
Meletios Dimopoulos, MD
Improved understanding of Waldenström’s macroglobulinemia (WM) and expanded treatment options have made individualized treatment based on clinical indications a feasible strategy, Meletios Dimopoulos, MD, said at the 2016 Society of Hematologic Oncology annual… Continue reading
Michael Knowlton has found a new way of embracing life while living with WM. This video is about his journey and story of inspiration.
WMFC Member was featured in the QEII Time – The Chronicle. The article discusses the support he has received from the QEII Hematology Clinic.
The Waldenstrom’s Macroglobulinemia Foundation of Canada would like to extend a sincere thank you to Bert Visheau, a Board of Director member since 2003, for his dedication and support to the WMFC. Bert has stepped down after… Continue reading
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