THE MICHIGAN LUPUS FOUNDATION APPOINTS ERIC SPENCER TO THE BOARD OF DIRECTORS
(Michigan – September 24, 2026) – The Michigan Lupus Foundation is pleased to announce Eric Spencer of Belmont, MI has been appointed to the Board of Directors. Spencer will help the foundation serve its mission to improve the quality of life for those living with lupus through support, education and research with the goal of finding a cure.
“We are proud to welcome Eric to our Board of Directors, bringing valuable representation from the Grand Rapids area,” said Michael Lang, Board Chair. “Eric brings an impressive combination of technology and operations expertise, strong connections throughout West Michigan and the perspective of someone who understands firsthand what it means to receive a lupus diagnosis. His professional experience and personal commitment to our mission will be tremendous assets as we continue to strengthen the foundation and expand our reach across Michigan.”
About Eric Spencer
Spencer is Vice President of Architecture at Springthrough, a Grand Rapids-based technology consulting firm, where he has spent more than 20 years helping organizations improve their technology systems, digital operations and processes. A Central Michigan University graduate and Belmont resident, he brings extensive experience in technology, operations and strategic planning, as well as a strong professional network throughout West Michigan. Spencer was diagnosed with lupus in December 2025. His experience navigating a new lupus diagnosis inspired him to become more involved in supporting others affected by the disease.
As a member of the Michigan Lupus Foundation Board of Directors, Spencer hopes to use both his professional expertise and personal perspective to strengthen the foundation’s operations, expand its reach and help ensure newly diagnosed patients have access to reliable information, resources and support.
About Lupus
Lupus is a chronic autoimmune disease that causes the body’s immune system to attack its own healthy tissues and organs. It can affect any part of the body causing widespread pain and inflammation. Common symptoms include debilitating fatigue, fever and joint pain. Lupus affects each person differently and may go into periods of flares and remissions.
More people are living with lupus than cerebral palsy, multiple sclerosis, sickle cell disease and cystic fibrosis combined. It is estimated that more than 20,000 Michiganders have been diagnosed with lupus and up to 1 million people nationwide. Lupus primarily affects women of childbearing age and occurs more frequently among African American, Hispanic/Latina, Asian American, Native American and Pacific Islander women. There is currently no cure for lupus.
About the Michigan Lupus Foundation
The Michigan Lupus Foundation is a 501(c)3 nonprofit organization that exists to improve the quality of life for those living with lupus through support, education and research with the goal of finding a cure. The foundation provides financial and informational resources for patients, caregivers and healthcare providers including support groups, counseling services, educational opportunities, state and nationwide research efforts, advocating with lawmakers at the state and federal level to amplify the patient voice, as well as hosting awareness events across the entire state of Michigan. The Michigan Lupus Foundation has been continually serving Michigan since 1974 and is working to build a brighter future for all lupus patients and their families. For more information, visit milupus.org.
For volunteers interested in joining the Board of Directors, visit https://www.milupus.org/board-application.
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