If you have been diagnosed with Waldenstrom's macroglobulinemia, or care about someone who has, welcome to the IWMF family of WM patients, caregivers, friends and relatives.

The purpose of the Foundation is to provide information, resources, a communications network, and experience on how to live with WM, plus encouragement to those affected by this rare and incurable blood cancer.

After diagnosis with WM, we often feel alone and afraid. By joining our focused interest, commitment and energy together, we can make a dramatic difference in each other's daily lives. We can help each other learn more about this disease by sharing our symptoms and treatment results. We can learn how to take control of our treatment decisions. We can seek recognition and attention from government agencies, and more importantly, we can sponsor research towards an ultimate cure.

This site is much more than informational, it is a call to action; an extended hand in a time of need; an invitation to join us, to work together in mutual support in a determined search for a solution. We need your help.

The IWMF is a non-profit, all-volunteer organization, developed and financed solely by patients and their friends and families. What we can accomplish is determined by how much we are willing to contribute of our time, energy, talents and resources. If you find this place and our information helpful, please give back by joining the Foundation, and helping us to make a difference and find a cure. Welcome.

CONTACT:
Sara McKinnie
IWMF Business Office
3932D Swift Road, Sarasota, FL 34231
Tel: (941) 927-4963 • FAX: (941) 927-4467 • Email: info@iwmf.com