Support When You Need It the Most
IWMF provides comprehensive resources to meet the needs of patients, caregivers, and families affected by Waldenstrom’s macroglobulinemia (WM). Through our community programs, you can connect with others dealing with the disease, learn about the latest treatments, find physician experts, and access information to help you every step of the way in your journey living with WM. With IWMF, you are never alone! Learn more about how we support our WM community.
Directory of WM Physicians
Find physicians worldwide who specialize in the treatment of people with Waldenstrom’s macroglobulinemia.
Peer Support Groups Worldwide
Participate in a support group to share experiences, discuss concerns and exchange information.
Stories of Hope
Get inspired reading about other people’s trials and tribulations living with Waldenstrom’s macroglobulinemia.
Global Partners
If you live outside the US, check out our list of global partners in other countries.
Patient Advocacy Partners
Learn about the organizations we partner with to help you better meet your needs.
IWMF Connect
Join the conversation about Waldenstrom macroglobulinemia with our online discussion group.
LIFELINE
Connect one-on-one with an experienced WM patient volunteer via telephone or email.
Financial Assistance
Find resources to help you manage medical expenses and associated costs of living with WM.
Caregiver Support
Get helpful tips, information, and resources to support you in your role as caregiver.
Get Involved with IWMF
Join
The IWMF exists to support you! Join the IWMF community 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 IWMF.