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

Frequently Asked Questions

Welcome to the "Frequently Asked Questions" section of the IWMF website.  Here you will find answers to many of the questions you may have regarding Waldenstrom's macroglobulinemia, how to live with the disease, and how to treat it.

 

Just click here to go to the page that lists all the "most popular" questions and answers that we've collected over the years from patients and caregivers and medical professionals.

 

Should you find that we haven't addressed a specific question you may have, or if you have any other suggestions, please feel free to email the IWMF Website manager at .