Customer Stories

Tessa is a twin who loves baby dolls, animals and music. She and her brother were born at 24 weeks and had a long stay in the NICU. Tessa had three brain surgeries because of a brain bleed which resulted in her official diagnosis of cerebral palsy around eighteen months old.

Katelynne is happiest when she is outside breathing in the salty air from the Cape. She has a service dog named Jones who helps her to live independently.

With the help of his mobility technology, he has been able to attend sporting events and concerts but his most recent accomplishment is graduating from college. Seth is a recent graduate from Lipscomb University in Nashville, Tennessee with a major in Theology and Bible Studies.

Meet Mckenna, a fifteen-year-old junior in high school who has a passion for soccer and loves spending time with her friends. One year ago she was injured in a jet-ski accident where she broke her neck. Her story and courage inspired so many people not only in her area but around the country and she was named the 2019 SheBelieves Hero by the US Women’s Soccer team.

Hattie loves music and her dogs. She is two years old and has overcome obstacles already. Hattie received a stander and activity chair from Numotion.

Parker is an energetic five-year-old from Palmyra, PA diagnosed with spastic cerebral palsy. When Parker started preschool, it became clear that he would need new equipment that would fulfill his and his parents’ needs. Numotion helped Parker’s family find the perfect fit and he received what he calls his “Blue Racer” manual wheelchair in the summer of 2018.

Paralyzed in a high school hockey game, the moment Matt crashed headfirst into the boards his life changed in a huge way. But his confidence never wavered. Matt’s “Never Quit” attitude allowed him to finish high school, graduate from college, become a well respected motivational speaker and now, his most recent achievement, author of a book.

Heidi is a congenital quadrilateral amputee meaning she was born without the lower part of her arms or legs. But that has never stopped her from excelling at anything she sets her mind to accomplish.

Lillie is a lover of water and bubbles. She was diagnosed with a rare genetic condition called DDX3X Syndrome.

Vance has made it his life’s mission to advocate for those with disabilities and has helped change the way governmental organizations around the world respond to individuals with access and functional needs before, during and after crisis situations.

Hayden is a sweet five-year-old who is smart and very caring to others. She is currently in kindergarten and loves to play t-ball and spend time with her family, especially at the beach or pool. According to her mom, Hanna, “Hayden has a few things that make her extra special – one is Beckwith-Wiedemann Syndrome (BWS).”

Life for Adam, a political science major at Sacramento State University, has completely changed since receiving his new Permobil standing power wheelchair.

Jamie is a 53 year-old-man with SMA. He has a lot of interests in life and is driven to learn and build things. He especially loves computers because they allow him to do the same things as everyone else.

Ian is a lover of the outdoors. He likes to spend as much time outside as possible enjoying nature, bird watching and experiencing the seasons change all around him. Ian’s life drastically changed in 2008 when he was in a bicycle crash that resulted in a spinal cord injury. At 26, Ian found himself paralyzed from the neck down and completely lost.

The Evans family has eight children, four with special needs. The parents, Melanie and Mike, have adopted three of their eight children.