Customer Stories

Avery Joy is 4 years old and from Mangham, Louisiana. She was diagnosed with Adenlysuccinate Lyase Deficiency, a metabolic, genetic disorder when she was 8 months old. She developed epilepsy at 3 months old and continues to have almost daily seizures.

Sean and his Numotion team worked very hard to obtain this life-changing equipment, the Jaco Robotic Arm. The Jaco Robotic Arm resembles a full human arm that corresponds to the shoulder, elbow, and wrist. The Jaco Robotic Arm trial was a huge success. Sean quickly learned how to operate this complex device through his wheelchair joystick. He was immediately able to pick up a fork and simulate feeding himself, grasp a bottle of water from the counter and get himself a drink. Sean can do a variety of things independently with the assistance from his Jaco Robotic Arm like: drinking, eating, scratching an itch,  holding his phone, playing chess and reaching things. 

Kyann was born and raised in Bellingham, Washington. She was diagnosed with Charcot Marie Tooth (CMT) when she was eight years old. She then received a second diagnosis of Heredity Spastic Paraplegia at age twenty-four. Kyann is Director of Accessibility for Wandke Consulting and a passionate advocate for the disability community. As a disabled woman, she strives to educate society on how social barriers like ignorance and stereotypes, limit the disability community. Kyann loves to travel, write, and drink coffee.

Lexi is an 18-year-old from Charlotte NC, who is a writer avid reader. She loves world history, mythology, anything Star Wars or Marvel universe and enjoys swimming and adaptive horseback riding.

Meet Nakia, she is a 33-year-old woman who loves spending time with her seven nephews and one beautiful niece. She loves eating, shopping, and watching movies. In high school, Nakia was active with cheerleading and volleyball. In 2007 Nakia was involved in a motor vehicle accident that broke her neck, bones in the left side of her face cracked her skull, and a ruptured her spleen. The doctors didn’t think she would make it through the night, and she was in a coma for a month. Nakia woke up with a T4 spinal cord injury.

Rebecca is 31 years old and lives in Southeast Michigan. She was born with Escobar Syndrome. This is a genetic condition that affects all of her joints and muscles. She can’t straighten out her fingers, elbows, knees, and hips and has severe scoliosis which affects her breathing and wears hearing aids in both ears and has glasses due to being low vision. However, since receiving her new Quantum Stretto wheelchair she said she has found more independence and mobility with its many features.

Paul has been a Numotion customer since 2015, living a happy and thriving life. Paul tributes his custom wheelchair for allowing him to become a member of the broadcast media. “I have been able to cover different events and conventions and interview some pretty amazing folks,” said Paul. “I wouldn’t have been able to achieve many career accomplishments like becoming an Accessibility consultant for the gaming community and working with major video game developers if I didn’t have mobility help from my wheelchair.”

Caleb was born with Trisomy 21 (Down syndrome) and at 14, developed catatonia. Catatonia is the loss of different skills, including the ability to communicate meaningfully. In 2017 Caleb received a speech device. It took him a while to figure it out, but he has worked hard at it and it’s getting easier.

Levi is a happy 2-year-old boy with translocation (14,21) Down Syndrome (one of the rarest types). He lives with his mom and dad in Denham Springs, LA right outside of Baton Rouge. He loves anything that involves water, so bath time is super fun at their house. He also really loves to eat! His favorite shows are Puppy Dog Pals and PJ Masks. He is hard of hearing but he can hear when those songs play on the TV. His parents also believe he has an imaginary friend with whom he laughs and babbles ALL DAY LONG.

James considers himself a Professional Hobbyist. He is not sure that is a legitimate title but it is the best way to describe his lifetime of learning. James has gained some proficiency in Martial Arts, mountain biking, and paintball while dabbling in 3D design & printing, screen-printing, line skating, bicycle polo, Radio Controlled car racing, and a couple of other hobbies he has forgotten. Fueled by a seemingly unlimited supply of duct tape and cardboard as a child, James has always been a maker.  

Analiese was born with Spina Bifida which impacts the amount of sensation and movement she has in her legs. When she was younger, she walked with a walker but that became more difficult as she got older. “I found more independence in my wheelchair because I was able to fully take in every experience, rather than that using all of my energy getting to my destination and being tired when I got there.”

Numotion Brand Ambassador Karen Roy, introduces us to Numotion customer and Ms. Wheelchair Louisiana 2019, Tamara.

Joe is a twenty-three-year-old senior in college who is hoping to work in film and television production. He enjoys movies, sports, and long walks with his dog Winifred.

Andre is a happy, smart, and joyful eight-year-old twin boy that developed hydrocephalus and cerebral palsy with spastic triplegia as a result of a brain bleed at birth. He loves Pete the Cat, slides, swings, and bubbles.

Danielle is the proud mother of a very special toddler named Kai. She lovingly refers to him as her “sour patch kid,” and it’s an apt reference to their story, one filled with the highest of highs and lowest of lows. Kai was diagnosed with a rare medical condition called Beta-propeller protein-associated neurodegeneration disorder (BPAN), a progressive disease that damages the nervous system, and there is no cure. First it’s sour, then it’s sweet. A sour patch kid story, for sure.