Latest Bing Center News
Welcome to the WM Digest: a place where you can find vital information and education about Waldenstrom macroglobulinemia (WM), hear the latest WM research updates, meet WM community members who share their stories, and get diverse support for managing WM. This issue includes news about IWWM-13, scheduled for October 13-17 in Palm Springs!
The Waldenstrom Digest from the International Waldenstrom Macroglobulinemia Foundation (IWMF) provides a comprehensive update on medical advancements and community support for those affected by this rare blood cancer. This issue highlights the upcoming IWWM-13 conference in Palm Springs, which will feature the first-ever session dedicated to translating complex scientific research into practical patient takeaways.
Welcome to the WM Digest: a place where you can find vital information and education about Waldenstrom macroglobulinemia (WM), hear the latest WM research updates, meet WM community members who share their stories, and get diverse support for managing WM.
Welcome to the WM Digest: a place where you can find vital information and education about Waldenstrom macroglobulinemia (WM), hear the latest WM research updates, meet WM community members who share their stories, and get diverse support for managing WM.
Peter Bing, MD, was a nationally- renowned philanthropist and public health expert. Dr. Bing served as executive director of the National Advisory Commission on Health Manpower during the Johnson Administration and made significant contributions to the Dana-Farber Cancer Institute in Boston (DFCI) to support research on Waldenström’s Macroglobulinemia (WM), a rare and chronic type of slow-growing, non-Hodgkin’s lymphoma.
Founded in 1999, the WM program at DFCI was officially designated as the Bing Center for Waldenström’s Macroglubulinemia in 2005 in honor of Dr. Bing. Led by Dr. Steven Treon, the Bing Center aims to advance understanding of the cause of WM and pursue novel therapies.
Welcome to the WM Weekly: a place where you can find vital information and education about Waldenstrom macroglobulinemia (WM), hear the latest WM research updates, meet WM community members who share their stories, and get diverse support for managing WM.
Welcome to the WM Weekly: a place where you can find vital information and education about Waldenstrom macroglobulinemia (WM), hear the latest WM research updates, meet WM community members who share their stories, and get diverse support for managing WM.
Watch as Susanne Öhrn of WM Scandinavia accepts her IWMF 2026 Judith May Volunteer of the Year Impact Award, embodying the very best of volunteerism—grace, generosity, and heart. "I'm not a doctor, I'm not a researcher. I'm just a patient among others. And maybe that is exactly why this community exists. Because sometimes, what we need most is someone who truly understands, who can say 'I've been there. You are not alone.'
Welcome to the WM Weekly: a place where you can find vital information and education about Waldenstrom macroglobulinemia (WM), hear the latest WM research updates, meet WM community members who share their stories, and get diverse support for managing WM.
Celebrate 5 years of IWMF Wellness! The International Waldenstrom Macroglobulinemia Foundation (IWMF) publishes a monthly newsletter titled "Living Well with WM," which details their Integrative Wellness Program for patients and caregivers. (Read it here: https://conta.cc/4mwIOAY). This May 2026 edition celebrates the program's fifth anniversary, highlighting its evolution from a single yoga class to a comprehensive curriculum featuring meditation, fitness, and music therapy. The document includes a recap of the U.S. Educational Forum, personal testimonials regarding the positive impact of community support, and a calendar of upcoming virtual sessions. Additionally, the newsletter features a moving tribute to Shawna Lattimore, a beloved community member, and provides links to educational recordings and donation opportunities. Ultimately, the source serves as a guide for those seeking to enhance their quality of life through holistic practices alongside traditional medical treatment for this rare blood cancer.