In these uncertain times, there is one thing that we know for sure: With the IWMF, we are never alone. That unifying truth is even more important and...
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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In these uncertain times, there is one thing that we know for sure: With the IWMF, we are never alone. That unifying truth is even more important and...
In the summer of 2014, I became slightly short of breath during a hike up a granite dome mountain called “The Thumb” at Sequoia National Park. This was highly...
Due to the coronavirus global health pandemic we are all facing now, and out of concern for the health and safety of the worldwide community of WM patients,...