International Waldenstrom’s Macroglobulinemia Foundation



This is the second in a series of three videos recently produced for the IWMF.

In this video, Bob Rupert, a WM patient, discusses how WM has affected his life and his family, and how he approaches living with the disease.

His story and his message reinforce the reality that, given the options available to us today, WM is a disease that can be “lived with”, rather than “died from”. He emphasizes the importance of utilizing the IWMF resources that are available to assist all patients and caregivers, and the importance of being able to continue to live life with passion and purpose.

The video can be found here.


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