Many of you may already recognize Shirley, as she has served for several years as the support group leader in the Seattle, Washington area, and most recently...
Getting a diagnosis of WM can feel overwhelming. You have questions, we have answers! Tap in to our comprehensive resources about this rare disease.
We are here to support you throughout your journey living with Waldenstrom macroglobulinemia. Remember, with the IWMF, you are never alone.
When you join the IWMF, you become a member of an international community of people affected by Waldenstrom macroglobulinemia.
Day(s)
:
Hour(s)
:
Minute(s)
:
Second(s)
Many of you may already recognize Shirley, as she has served for several years as the support group leader in the Seattle, Washington area, and most recently...
Investigators aim to present important WM Quality of Life data at International Conference – YOUR HELP IS NEEDED! A huge congratulations and thank you to the...
Ryan’s story was first published in the in the IWMF Torch, January 2015, page 21. This is an update to that story. I was diagnosed with WM in 2010 when I was...