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 .