Pete DeNardis Waldenstrom’s Macroglobulinemia Story
Pete DeNardis, IWMF Board Chair, shares his WM journey with The Patient Story.
HOW CAN THE IWMF HELP?
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.