In preparation for World Rare Disease 2021, February 28, 2021, founder of BPAN Warriors, Sarah Chisholm put together a brief video of her daughter Eva "Magoo", who was diagnosed with BPAN in 2017. Eva has and continues to serve as Sarah's inspiration for the work that she continues to do daily on behalf of BPAN Warriors.
top of page
BPAN WARRIORS TERMS & CONDITIONS OF USE
Last Updated: January 7, 2020
(414) 909-BPAN
bottom of page