Our son, Ethan, was diagnosed with peroxisomal biogenesis disorder - zellweger spectrum disorder (PBD-ZSD), a very rare genetic disease, when he was just four weeks old. There is no cure for PBD-ZSD and treatment is symptomatic. This is our PBD-ZSD journey.
Prayers for the Castaneda family from Texas and the Clarke family from the UK
This week two more little ones have left the arms of their parents for the arms of Jesus. These two very special little girls had PBD, just like our Ethan. Please pray for comfort and strength for the Castaneda and Clarke families.
Gabriela Faith Castaneda - October 19, 2009 - January 15, 2012
Emilia Grace Clarke - April 13, 2011 - January 2012