With the IWMF, You are Never Alone
Getting a diagnosis of WM can feel overwhelming. Tap in to our comprehensive resources about this rare disease and find the information you need to get your questions answered.
IWMF Resources
IWMF Brochure
Learn more about the organization by downloading our comprehensive brochure, About the IWMF. Share it with your friends, family, and healthcare team.
Download NowFAQs
Find answers to your most pressing questions about WM. Download our Frequently Asked Questions booklet, written in a Q&A format for easy reading.
Download NowMedical Tests
To better understand the purpose and results of medical tests used to diagnose and monitor WM, consult our reference booklet, Medical Tests.
Download NowInfo Pak
Get our comprehensive packet of information, which includes the most current, easy-to-understand information, designed specifically for the newly diagnosed.
Learn MoreEducational Resources
Access a variety of educational resources to learn more about your disease: webinars; the IWMF Torch, our quarterly magazine; and our annual Educational Forum.
Learn MoreGet Support
Find all the support you need with our global support groups, physician directory, our online forum, and our telephone support LIFELINE, and more.
Learn MoreGet Involved with the IWMF
Join
The IWMF exists to support you! Join the IWMF community and become part of an international group of people affected by Waldenstrom’s macroglobulinrmia.
Donate
Your gift to the IWMF funds information, education, and support programs, and advances research to find more effective treatments and ultimately a cure for WM.
Volunteer
Put your unique talents and strengths to work toward helping us fulfill our mission by volunteering at the International Waldenstrom’s Macroglobulinemia Foundation.
