This is Cadence and she suffers from a rare condition called FoxG1 Syndrome. She is actually 1 in 375 in the world to have this disorder! The characteristics of this condition is epilepsy, microcephaly,Non-Verbal, Non-Ambulatory and a feeding tube. As Cadence grows her hips are starting to separate and her scoliosis is getting worse. Doctors say if we don’t do intensive physical therapy Cadence will need double hip and spine correction surgery ! Unfortunately this type of therapy is not covered under insurance. This therapy is very costly!
Family and friends of Cadence McGoldrick are raising money for the nonprofit Help Hope Live to fund uninsured medical expenses associated with Catastrophic Illness.
Photo Galleries (2)
Guestbook
November 24, 2018
Sorry we couldn't make it today but Brooke and I wanted to donate a little something ..every little bit helps they say
Loretto Pierson
November 20, 2018
God bless Cadence ❤️
Chris / Vikki Weiss
November 19, 2018
Dear Mr. & Mrs. McGoldrick & the Lovely Miss Cadence,
I pray that you raise the support you seek; have faith & you will. Cadence, I believe that God put special children like you in the world to show us all what real strength, perseverance, & compassion really look like. You have impacted more people than you can imagine. You express more joy in a single beautiful smile & that is a remarkable gift. You have a very important purpose in this life: that is to inspire the masses with faith, hope, compassion, empathy, kindness and most importantly love. Words aren’t required to do so. May God bless you all the days of your blessed life. Love to you & your family, Gina Christina
Gina Christina
