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 Facebook Page

International Waldenstrom's Macroglobulinemia Foundation

Promote Your Page Too

The IWMF now has an official presence on Facebook, which can be found at:

http://www.facebook.com/waldenstroms.support

 

The Facebook page serves as an additional mechanism where people can gain information about the IWMF and WM in general. More specifically, it is intended to be:

  • a source of support for patients and caregivers
  • an additional source of information for family, friends, and acquaintances of patients and caregivers (we want to spread the word about our rare disease and how special our patients, caregivers, researchers, and health professionals truly are!)
  • an additional source of information about upcoming WM-related events
  • a place for Facebook friends (members of the page) to "virtually" socialize with each other, share information, and provide comfort and support for each other

 

Please bear in mind that this website, the IWMF publications (and especially the Torch) and the IWMF-TALK discussion list will still be the primary mechanisms for information sharing with the WM community.