Peter DeNardis
Board Member, International Waldenstrom’s Macroglobulinemia Foundation
When Peter DeNardis was diagnosed with Waldenstrom's macroglobulinema in 2003 at the age of 43, he found support through the International Waldenstrom’s Macroglobulinemia Foundation (IWMF), a nonprofit providing information, support and resources to patients with WM. While working full time in financial systems, and dealing with intermittent periods of remission and relapse, he also has been very active as a volunteer with the IWMF over the years and is currently a board member and trustee. He lives in Hopewell Township, Pennsylvania, with his wife, Terri, and their three adult children and their partners live nearby.
