The IWMF raised more than five million dollars for WM medical research
The IWMF raised more than 60 support groups in North America and nearly 20 others world-wide
The IWMF has a current worldwide membership of nearly 4,000
IWMF-TALK is a wonderful place to share information and learn from other survivors
Each year 1,500 new cases of Waldenstrom's macroglobulinemia are diagnosed in the USA
Volunteers at the IWMF Telephone Lifeline are waiting to share their experiences with you
You can order DVD recordings of past WM Educational Forums online or by mail
All IWMF programs and services are funded by WM survivors, caregivers, friends, and family
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Find Support and More
We are always working to reach out to both the newly diagnosed and veteran patients with WM in order to provide them with educational materials developed for them to understand their disease. We will also inform them about support groups for WM patients, our annual Educational Forum for patients, and IWMF-Talk–an e-mail discussion list where patients can share their experiences with WM.
It would be most helpful if you would give your WM patients one of our brochures that explains what we do and gives our contact and website information. We are happy to send you as many brochures as you might like.
Last Updated: 1/16/2015