Shortly after birth, Angie & Travis’ son Jackson was diagnosed with a Peroxisomal Disorder, a fatal rare congenital affliction caused by the absence of cell components. In June 2007, at three months old, Jackson underwent two weeks of testing at Children’s Healthcare of Atlanta at Scottish Rite. It wasn’t until August that the Jinrights received the diagnosis. There is no cure, and there are few options for significant treatment.

It is with great sadness that we share the passing of Jackson Jinright.
Thank you to all that helped to make his wish trip to Disney come true in March, 2012 – something that his parents never thought would be possible with Jackson.
Please keep his entire family in your prayers, especially his wonderful parents Angie and Travis, during this difficult time.