I am Lori Carver, the President/Founder of the Foundation. I started this foundation after being diagnosed myself with ZES in April of 2017. After researching and learning about the disease, I felt led to start this Foundation due to limited support and help for those of us with this disease and lack of awareness, so on June 8th, 2018, the Zollinger Ellison Syndrome (ZES) Foundation came into existence.
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