Eileen's Walking WITH and FOR Waldenströms Page

Dear Friends,

I hope this message finds you well. A cancer diagnosis changes everything. When that diagnosis is Waldenstrom’s macroglobulinemia (WM)—a rare and incurable cancer—it becomes even more overwhelming. This is where the International Waldenstrom’s Macroglobulinemia Foundation (IWMF) becomes vital.

I was diagnosed with WM in 1995 and began treatment 8 years later...and recently have become a volunteer for the IWMF. When I meet folks who are newly diagnosed, I am happy to be able to say that I've had WM for 29 years and "I'm still here!" thanks to the support of family, friends and a great medical team.

The IWMF has been a lifeline for WM patients, caregivers, and families, investing millions in research since 2000. Their mission is to support and educate those affected by WM while advancing the search for a cure, providing crucial resources and community. I'm happy to serve as a volunteer Support Group Leader, Board member and Zoom support for several international WM specialty support groups.

Thank you so much! Any contribution is welcome...