HUNTER SYNDROME WARRIOR
REMEMBERING BABY GATLIN AND HELPING HIS BROTHER AXILE!
Axile Needs Your Help!
My name is Axile, I am 4 years old and I have Hunter Syndrome, a rare disease that affects all of my organs and tissues. Unfortunately, there is no cure. In April 2024, I lost my little brother, Gatlin, to this same disorder.
I'm uncertain how much longer I have with my family, and while Make-A-Wish is incredibly generous, they can't cover the costs for all of us. I need your help!
Please consider sponsoring this once-in-a-lifetime trip. As a sponsor of $100 or more, your name will be included on the shirts my family will wear both at Disney and around town at home. Every dollar truly makes a difference!
Axile'S Medical trips and expenses
https://gofund.me/61ab2e0c
LIVING WITH HUNTERS SYNDROME
THE BRAVEST, TOUGHEST KID I KNOW...
TRYING TO LIVE HIS
BEST LIFE
UNDERSTANDING HUNTERS SYNDROME
Mucopolysarcharidosis type II (MPS II) is a rare, inherited disorder. MPS II is also known as Hunter syndrome. Children with this condition have an abnormal accumulation of complex sugars in their cells, which affects many systems in their bodies. Hunter syndrome primarily occurs in boys, and there is no cure.
Remembering Gatlin...
ON APRIL 22, 2024 at just 2 years old THIS SWEET LITTLE ANGEL'S HEART WAS TIRED AND HE WENT TO HIS FOREVER HOME WITH OUR HEAVENLY FATHER..
Gatin Ion Moretz will be remembered for his contagious smile, his spunky little attitude and his endless lovins.
Gatlin was a little fireball and always on the go, if you blinked you would miss him. This little boy bless his heart was sick almost everyday of his short little life, but he never let his disease stop him. He is dearly missed here with us, and will forever leave an empty space in our hearts, but we know we would be selfish to want him back. Now he is happy and healthy and living his eternal BEST life and we know in our hearts he is here with us everyday and we will see him again.
Until then though we are determined to do whatever we can as a family and asking our community to help us, help Axile his 4 Year old brother suffering from the same disease he needs your help, with medical expenses, his once in a lifetime trip with his family to Disney and to bring awarness to this rare horrible disease, that robs these sweet babies of the life they deserve.
