Peyton's Place
$100 raised
10% of $1k goal
3 contributors
5 Years running
~Peyton was born March 21 2005, Even though it was a normal pregnacy. Once she was born we new at first she was special. Peyton was born with Bilateral Club Feet.

~After 3 months of castings Peyton had her first of many surguries a heel cord ...
~Peyton was born March 21 2005, Even though it was a normal pregnacy. Once she was born we new at first she was special. Peyton was born with Bilateral Club Feet. ~After 3 months of castings Peyton had her first of many surguries a heel cord lengthing. After she was all healed we started Physical therpay on her feet. That is when Her therapyst realized she had Torticullos(one neck muscle was really tight). This prohibited her from moving her neck to left. Which in turn created a flat spot on the back of her skull. Which at this point a corrective helmut was made to restructure the shape of her head ~Since she had her first surgery she has had 8 more on her right foot and 5 on her left with numerous cast changes and braces to try to correct her feet. With no avail her right foot has been the most trouble. she will have more surgey with in time but for now Her Drs at Shriners want to hold off untill she is done growing(after every surgery her right foot regresses back to where it was) ~In 2010 we discovered that Peyton has Soclliosis. This has been a challange for Peyton because it is only getting worse. She started off only having to wear a night time brace but now must wear a daytime brace too. So she has a brace on 23 hours out of the day. ~Also in 2011 we finally got test results back that pinpointed why she was developly delayed and non verbal. Peyton has a rare gentic disorder called Deletion in Chromosone 12p Syndrome ~Peyton will have to travel from Northwestern Pa to Philladelphia numerous times over nthe next year to correct her feet without having to do surgery
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