Juniper's Ride to Life

This is our sweet Juniper! She was born with an ultra rare genetic mutation called RHOBTB2. We soon learned that Juniper is one of about 30 documented children with very little research on her mutation. She has global developmental delays, cannot sit or walk, is non-verbal, cannot eat solid food, has epilepsy and a movement disorder. She has made great strides over the past two years, and continues to work in occupational and physical therapies.

Now that Juniper is getting bigger it is difficult for us to carry her around as she cannot walk. We are asking for help in purchasing a handicap accessible vehicle for our family. Juniper can be wheeled in and out the car with ease and safety on the ramp. She received her pediatric wheelchair which can be strapped into a mobility vehicle.

Thank you so much for helping Juniper explore the world with her family!