Since WM is a rare disease, many community oncologists seldom see a WM patient. Increasing awareness and knowledge about WM among community oncologists has...
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.
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Since WM is a rare disease, many community oncologists seldom see a WM patient. Increasing awareness and knowledge about WM among community oncologists has...
The National Organization for Rare Diseases (NORD) has a financial assistance program that is currently open with funds available to help caregivers (spouse,...
Recently, Dr. Robert Kyle, Mayo Clinic, informed the IWMF of his decision to retire from the IWMF Board of Trustees. Dr. Kyle has been an active board member...