In October 2015, Kaden (My prince) received his wish through The Children’s Wish Foundation and travelled with his mother, father, and big sister to Disney World. It was a trip of a lifetime and one they will treasure forever!
As you can probably imagine, this has been very difficult news to process in such a short period of time. Not only is it hard to come to terms with all of this, but his family has had had to sell their home to purchase a wheelchair accessible home, they have had to purchase his wheelchair, a chair lift, and other specialized equipment. Kaden has also had to change schools to accommodate his needs.
He is now at a point where he requires more assistance to make life a little better. He is in need of many things, such as a wheelchair accessible van, a lift for home, a hospital bed, and an accessible bathroom. I am hoping you will find it in your heart to give. Even if it is only a little, it will be greatly appreciated.
My family doesn’t usually reach out, but we are in a time of need and will require lots of prayer and love to make it through.
If you would like to know more about Kaden’s condition please visit: http://www.muscle.ca/about-muscular-dystrophy/types-of-neuromuscular-disorders/duchenne-muscular-dystrophy/
FYI - I am located in New Brunswick, but Kaden resides in Newfoundland
- Wanda Jane
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