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

Grant Opportunities

The International Waldenstrom’s Macroglobulinemia Foundation (IWMF) is a nonprofit organization which offers support for basic scientific research that will further knowledge of the cause, diagnosis, treatment and cure for the disease Waldenstrom’s macroglobulinemia. Research proposals may be submitted at any time. Each proposal will receive consideration from the IWMF Research Committee, the Scientific Advisory Committee, and the IWMF Board of Trustees. Scientific researchers interested in applying for a grant may receive an application packet by contacting:

 

Tom Myers
IWMF Vice President of Research
117 Pinnacle Dr.
Swanton, MD 21561
Fax: 301-387-9162
Tel: 301-616-9200
Email: