f you’ve recently been diagnosed with WM and need help, but can’t seem to find information in your preferred language, the IWMF website can help you. Once...
View rebroadcasts from the October 6th 2021 Ed Forum WM Basics Workshop and NEW Q&A with our presenters! Please note that you will need to register to view the live and on demand webcasts.
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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f you’ve recently been diagnosed with WM and need help, but can’t seem to find information in your preferred language, the IWMF website can help you. Once...
Regarding the Amyloidosis in WM Request for Proposals (RFP), IWMF President Carl Harrington said, “This RFP represents an extension of our search to improve...
Triage Cancer is a nonprofit organization that provides cancer survivorship information to patients, survivors, caregivers, and health care professionals,...