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

IWMF Website

The IWMF website (www.iwmf.com) is often the first point of contact that newly diagnosed patients have with the IWMF. From that initial contact they go on to discover the wealth of information and support that the IWMF provides. Most find that the website is the premier resource for valid and up-to-date information regarding Waldenstrom’s macroglobulinemia (WM). However, the website is not engaged in providing medical advice or other professional medical services and is not meant to serve as a substitute for dialogue between WM patients and their physicians regarding important topics such as treatment decisions.

 

Our IWMF website administrator is Pete DeNardis at .