We are always working to reach out to both the newly diagnosed and veteran patients with WM in order to provide them with educational materials developed for them to understand their disease. We will also inform them about support groups for WM patients, our annual Educational Forum for patients, and IWMF-Talk–an e-mail discussion list where patients can share their experiences with WM.

It would be most helpful if you would give your WM patients one of our brochures that explains what we do and gives our contact and website information. We are happy to send you as many brochures as you might like.