Juliana Wetmore is continuing to undergo extensive, complex and risky cranio-facial surgery in an attempt to rebuild her face.
The Jacksonville community have been a huge support for the Wetmore family with regular fund-raising events for Juliana’s charity.
A rare genetic craniofacial disorder known as Treacher Collins Syndrome has left Juliana Wetmore badly disfigured and in need of much surgery.
Juliana will need continuous surgery for many years to complete the rebuilding of her face.
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