Why should I donate to DEAP?
Here is one example of how your donation could help an individual.
Paxton was referred to DEAP at birth as a result of a cleft palate. Soon after he was born he was also diagnosed with Smith-Lemli-Opitz 
syndrome, which is a developmental disorder that affects many parts of the body. This condition is characterized by distinctive facial features, small head size, intellectual disability or learning problems, and behavioral problems. Paxton does not walk or talk and needs a feeding tube to have his nutritional needs met. Paxton has had two surgeries on his cleft palate and is doing very well. He has also had several hospitalizations as a result of his medical fragility.
Despite all of the obstacles in his way, Paxton is doing very well. He is getting stronger and healthier, opening him up to the desire to learn new things and reach for independence. While he is not yet walking he has developed his own little “skootch” on his bottom to get where he wants to be. And just recently he was fitted with braces and got his very own walker. It is only a matter of time before he is running out the door to play the sport he loves - basketball! He would give Shaq a run for his money, shooting baskets all day long on his indoor hoop.
Paxton is also developing great communication skills while learning sign language. The first sign he learned was “ball”, of course! But he is constantly learning different signs and loves learning all new skills.
He does have some spoken language, saying “mama” and “hi”, but his favorite word to say is the Cheyenne word for Grandma, who lives in the house with him, playing a big part in his life. Paxton is a very blessed little boy with an amazingly supportive family who all work together to give him the things he needs to succeed.
We accept donations by: