Judah's Cranial Journey
Donation protected
I am Judah's grandmother. Judah and his parents Justin and Lacey Hoffman live in Cook, Ne. At birth, my grandson Judah Hoffman was born with a rare condition called Metopic Craniosynostosis. This condition causes the soft spot on the front of his skull to close early, requiring surgery in infancy to reopen the soft spot and allow his brain to grow properly. Because of how rare the condition is, Justin and Lacey will be traveling to San Antonio in October to have it done. This page is set up to help with the additional medical and travel expenses required for our sweet grandson. We so appreciate all of the support and love they have received and are continuing to believe in God’s faithfulness.
Organizer and beneficiary
Lisa Burianek
Organizer
Fairbury, NE
Lacey Hoffman
Beneficiary