IWMF Media Toolkit

With the IWMF You Are Never Alone

Our Vision

A World without WM (Waldenstrom’s macroglobulinemia).

Our Mission

Support and educate everyone affected by Waldenstrom’s macroglobulinemia (WM) to improve patient outcomes while advancing the search for a cure.

About the IWMF

The International Waldenstrom’s Macroglobulinemia Foundation (IWMF) is a patient-founded and patient-driven, nonprofit organization that is dedicated to a simple but compelling vision and mission.

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Waldenstrom Macroglobulinemia Facts

Waldenstrom macroglobulinemia (WM) is a rare, slow-growing cancer of the lymphatic system. Cancers of the lymphatic system are called lymphomas. WM is a type of lymphoma called non-Hodgkin lymphoma.

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Learn More About the IWMF

IWMF Annual Report

Our History
Our Officers and Board of Trustees

IWMF Contacts

Newton Guerin
IWMF President & CEO
[email protected]

Alix Redmonde
Director of Development and Communications
[email protected]

Sara McKinnie
IWMF Meetings & Partner Engagement Manager
[email protected]

Maureen Baeck
Digital & Creative Services Manager
[email protected]

Michelle Postek, MSW
Manager, Information & Support
[email protected]

IWMF Websites

IWMF Website: https://iwmf.com
IWMF Walk for Waldenstroms: https://www.mightycause.com/event/Iwmfwalk2022
Donate to the IWMF: https://interland3.donorperfect.net/weblink/weblink.aspx?name=E189844&id=6
IWMF Research Strategy: https://iwmf.com/research-strategy/
Current Research Recipients: https://iwmf.com/current-research-recipients/

IWMF Boilerplate Copy

About the International Waldenstrom’s Macroglobulinemia
We are a non-profit organization supports everyone affected by Waldenstrom’s macroglobulinemia while advancing the search for a cure. Since 1999, the IWMF has funded more than $18 million in global WM research. We are a patient-founded and patient-driven, nonprofit organization that is dedicated to a simple but compelling vision and mission.

Our Vision
A World without WM (Waldenstrom’s macroglobulinemia).

Our Mission
Supporting and educate everyone affected by Waldenstrom’s macroglobulinemia (WM) while advancing the search for a cure.

Learn more about the IWMF at iwmf.com. Reach out to the IWMF office: 941-927-4963 or email [email protected] with any questions you might have.

IWMF Social Media

There are plenty of ways to connect with the International Waldenstrom’s Macroglobulinemia Foundation on social media:


Facebook	Twitter	Instagram	LinkedIn	YouTube

IWMF Walk for Waldenstrom's

Walk for Waldenstrom's 2022

What is the Walk for Waldenstrom’s?

The Walk for Waldenstrom’s is a virtual 5k run/walk which will take place on October 29th 2021. There is no registration fee or cost to attend. Leading up to the Walk for Waldenstrom’s, you will create your very own fundraising page, and reach out to your friends and family for support. If you already created a Walk for Waldenstrom’s fundraising page this year, it is still active, and you can continue to use it. The funds raised during the Walk for Waldenstrom’s will make a very real difference to WM community members around the globe – these funds will support vital research into WM, the creation of IWMF publications and literature, and they will help the IWMF continue to offer free resources and materials to all those affected by WM.

Sign-up for the Walk for Waldenstrom’s