MM Fighters exists so you know that you are not alone. We represent the strength, resilience, and shared wisdom of living with multiple myeloma. Whether you’re newly diagnosed, in remission, or facing relapse, there’s always something new to learn and something valuable to share.
We are a volunteer, peer-led organization based in Seattle, created by and for patients and caregivers. We serve members throughout the Pacific Northwest. Our mission is to support people living with multiple myeloma through trusted information, practical education, and encouragement rooted in hope. To accomplish this, we provide a discussion group with lots of time for questions and answers.
MM Fighters was founded in 1998 as an independent support group by Ray Larsen. Soon after, Tom Blakney took on the role of facilitator. From 2018 to 2025, Chris Beebe continued the work with great dedication. In 2025, Mary Rose stepped into the facilitator role, supported by steering committee members Donna Loken and Jonathan Jantzen, along with several other members who contribute in essential ways. Today, MM Fighters includes over 400 families across the Pacific Northwest.
To join our group, or if you have questions, please click here.
For information on other regional MM support groups, click here.
Meetings
The group offers three meetings per month, January through November.
The MM Fighters primary group is open to all members and meets via Zoom or in a hybrid format on the fourth Saturday of each month. We start with an informal “chat” time from 9:30 to 10:00 a.m. Pacific for members who want to join early to visit with one another. At 10:00 a.m., the featured speaker begins a presentation on a topic relevant to our community. These expert speakers include oncologists discussing the latest treatment options, specialists addressing relapses and side effects, physical therapists, financial aid advisors, social workers, and more. There is always time included for Q&A.
After a short break, we have a group roundtable check-in and discussion. We welcome new members and share updates from those already in the group. It’s an inspiring opportunity to witness myeloma progress being made in the treatment of multiple myeloma, and the strength of our community in action.