We know your mobility and independence are critical to you. For those of you with open orders, please know that we continue to do everything we can in working with our suppliers to ensure timely delivery of your mobility equipment or parts needed for a repair. We may occasionally need to adjust a previously communicated delivery date as component delays continue. Thank you for using Numotion and for your patience as we all work through these highly challenging global supply chain issues. 

Numotion's COVID-19 
Response: What you Need to Know

Filter Stories

Amaya

Amaya’s Story

Amaya is fourteen years old from Slidell, Louisiana. Amaya loves music and dancing; she is a part of a special needs dance therapy group and performs in recitals every year and attends a weekly dance class. At two years old, Amaya was diagnosed with cerebral palsy and this past year was diagnosed with Lennox Gastaut syndrome, a type of epilepsy.

Analiese

Analiese’s Story

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."

Elizabeth

Elizabeth’s Story

Elizabeth is from Cincinnati, Ohio. She is a mom to a one-year-old little boy. She loves to travel, hike, hula hoop, and practice adaptive yoga. In August of 2015, she was on her way home when her driver’s side tire blew out and caused her car to veer off the road. Her car flipped multiple times down a hill and eventually wrapped itself around a concrete manhole resulting in her spine being severed in half.

Evelyn

Evelyn’s Story

Evelyn is three and a half years old and loves Sesame Street, swimming, sledding in the snow, and will become a big sister this summer. Evelyn was diagnosed with Rett Syndrome which affects the way the brain develops, causing a progressive loss of motor skills and speech.

Andre

Andre’s Story

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.

Adam

Adam’s Story

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

Avery Joy

Avery Joy’s Story

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.

Caleb

Caleb’s Story

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.

Chris

Chris’s Story

Chris became the only licensed quadriplegic performance stage rally racer in the U.S., with his desire to race to come after his injury. Finding enjoyment in physical work and construction, Chris’s hobbies include building and racing my rally car, fishing, kayaking and just building anything I needed it wished to.

Christine

Christine’s Story

Christine worked closely with Numotion for a few months to evaluate and trial different mobility devices – over time a trusting relationship was formed. Numotion was not a contracted provider with her insurance plan, but continued to work with both Christine and the health plan in order to help get Christine her much needed customized power wheelchair.

Customer Advisory Board

Customer Advisory Board’s Story

Numotion’s Customer Advisory Board is comprised of diverse individuals who share direct customer insights with Numotion regarding experiences and perspectives, as well as provide ideas and guidance resulting in lasting positive change at Numotion and the CRT industry as a whole.

Cyndi

Cyndi’s Story

Cyndi had polio at age two before the vaccine. A high percentage of people who had polio now have what’s called, Post Polio Syndrome (PPS). PPS causes new-onset weakness of your nerves and muscles. Symptoms usually start between 20 and 40 years after the original polio illness. Cyndi was born and raised in central Illinois but now lives in Tennessee. She proudly holds the title of Ms. Wheelchair Tennessee 2019 and 3rd Runner Up to Ms. Wheelchair America 2020.