Project Pixie Dust was founded in 2012, by Tina and Matt Daniels. |
The goal behind the project, is to bring some extra magic, or "pixie dust" to families and individuals affected by hydrocephalus, spreading awareness of the condition while doing so.
Project Pixie Dust is looking for Walt Disney World Cast Members, cosplayers, Party Princesses, and character performers who are willing to donate their time.
We're collecting short, inspiring 'in character' videos, directed towards children 13 and under. Hydrocephalus, while the most common reason for pediatric brain surgery, is surprisingly not well known. As a result, kids can feel 'different' or lonely when their friends at school, or their teachers don't know about their condition.
We hope that by making these videos, and showing them that not only do Peter Pan, Cinderella, or Batman know about their medical condition, but that they care enough to film a short message for them,we can make kids feel a little more at ease with themselves, and the condition.
Email us with any questions you may have: firstname.lastname@example.org