Freedom for kristin!

This is kristin, my miracle...I was told when she was 8 months old that she had a type of Muscular Dystrophy, and that she Would not live to be 2 years old..guess what? ?..shes 27..she has been at home on life support for 24 of those years,.and she is amazing! All of her life support equipment is built into a special wheelchair, and myself and our family have tried to help her experience as much of life as possible, and to love and be loved, and to learn and share, she by her example has taught so many , how can anyone ignore the simple gifts we are blessed with every day? If this child can smile , how can we let the daily grind steal or joy? As I have said she is amazing! ! However,  we are very limited, by transportation, . Our town is fairly small so walking to the park or a movie, or trick or treating have been easy, but she needs more, she deserves more, ..I dream of taking her to the zoo, or to see fireworks, or driving her around to see the amazing fall colors, mabey find a pumpkin patch and pick one out, or as we live 20 minutes from it, taking her to see lake Michigan, mabey showing her all of the beautiful Christmas lights in December, there are so many things.. most of us take for granted, so many things I want to share with her, but I can't afford a van with a lift, its one thing to except that your child wont ever walk or jump in a mudd pudle ,go to a sleep over, or get married..have children,  this disease is something I have had to except.,but I do not except that her world must be small, so I am asking for help, to purchess a van with a lift for kristin, help me open her world...thankyou so very much