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BK 23 |
The Ben Kelhoffer Foundation |
| Ben's Life |
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Ben Kelhoffer was
diagnosed with Chronic Myelogenous Leukemia four days after his 18th birthday in October of 1997. This
type of leukemia is characterized by an overabundance of white blood cells
(Ben’s white blood cell count was 480,000 when diagnosed – a normal
count is between 3,000 and 5,000). Ben would need a bone marrow transplant
as treatment for the disease. In
June of 1998, Ben and his family went to the Fred
Showing signs of improvement, Ben was able to leave the hospital. Unfortunately, two days later, he was readmitted with graft-vs.-host disease (an immune attack on the recipient by cells from a donor). Ben and the family
returned to Throughout
his illness, and through his rounds with Chemotherapy and radiation, Ben
never once complained or felt sorry for himself. He fought a courageous
fight, shielding his pain from his family and friends.
Thankfully, Ben was able to discuss his fears with his spiritual advisor,
confidant, and friend, Fr. Chuck Mentrup. To learn more about Fr. Chuck's
impact on Ben's life and the Foundation, please visit our
special tribute to Fr. Chuck.
Ben will always be remembered as a free-spirited person who enjoyed life. He had a unique sense of humor, a distinct laugh, and a great smile. His mom, Barb, would describe him as very “ornery,” and a jokester who loved to laugh. But just as he loved to laugh, Ben loved spending time with family and friends. Ben’s life, and his courageous fight against leukemia, continues to be an inspiration to many. The work of the Ben Kelhoffer Foundation aims to remember and celebrate Ben’s life. Currently, the memorial golf outing is the major annual event put on by the foundation. Click here for information about this year’s outing. |
Ben with mom, Barb, and dad, Lawrence in the fall of 1997 |