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Our story…

John Vittrup Callahan would be turning 30 this November and we are remembering his 30th by creating a team in his memory! John was diagnosed with ALD in the fall of 1997. Within 60 days of diagnosis, John received his bone marrow from a non-relative donor outside of the United States. In the 22 years since John's passing Franci, Christy and I are very happy to see that many states are now testing newborns for the possible existence of this genetic disease. We also see advantages to new, innovative ALD treatments. First, the patient's own cells are employed. Thus, there is no need to find a matching bone marrow donor. Second is the safety factor (no introduction of a stranger's bone marrow into a child). Third, gene therapy is potentially a permanent lifetime cure because a boy's broken gene is replaced with a perfect replacement gene. We believe that raising funds for continued ALD research is a very worthy cause.

Help us raise money for participating in Run for ALD, Cure the Boys

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