Did you know?

The IWMF raised more than five million dollars for WM medical research

Did you know?

The IWMF raised more than 60 support groups in North America and nearly 20 others world-wide

Did you know?

The IWMF has a current worldwide membership of nearly 4,000

Did you know?

IWMF-TALK is a wonderful place to share information and learn from other survivors

Did you know?

Each year 1,500 new cases of Waldenstrom's macroglobulinemia are diagnosed in the USA

Did you know?

Volunteers at the IWMF Telephone Lifeline are waiting to share their experiences with you

Did you know?

You can order DVD recordings of past WM Educational Forums online or by mail

Did you know?

All IWMF programs and services are funded by WM survivors, caregivers, friends, and family

Referring your Patients to the IWMF

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.