Intensive PT with Cerebral Palsy: Nick's Story
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- Опубликовано: 22 ноя 2017
- Young adults, like Nick, with cerebral palsy and other neuro-muscular disorders, seek out Euro-Peds National Center for Intensive Therapies to learn new skills, improve mobility, increase self-esteem and independence.
Located in Pontiac, Michigan, Euro-Peds opened as North America’s first intensive pediatric physical therapy center in 1999 for for seeking a specialized therapies, including the use of the Universal Exercise Unit and patented suit therapy, to optimize motor training and significantly improve motor skills. Specialized programs feature intensive bouts of individualized, one-on-one physical therapy with appointments ranging from 1.5 - 4 hours for up to 5 days per week over several weeks. Local patients often visit 2 - 3 times per week over several months.
Thousands of patients with cerebral palsy, traumatic brain injuries, spina bifida and a variety of other gross motor disorders throughout the U.S. and beyond are part of the Euro-Peds community. Each patient benefits from a team of PTs, PTAs and aides to keep sessions fun. Follow-up home exercise programs with photos, video and directions also are part of each session. For more information about Euro-Pēds’ individualized PT and speech programs, visit www.EuroPeds.org or call (248) 857-6776.
Euro-Peds accepts many insurances. For families who may have large insurance deductibles, large co-pays or no coverage, the Euro-Peds Foundation may be a resource.
Visit www.europedsfoundation.org to learn more about treatment and travel grants then complete a no cost, no commitment program application at www.europeds.org. It's the first step towards securing a grant. Call 248-857-6776 with any questions.
SUPPORT KIDS LIKE NICK!
Help change the lives of children with gross motor disorders. When you give to the Euro-Peds Foundation, you empower children and young adults to develop the strength, confidence and independence they need. Visit www.europedfoundation.org to donate and more information or follow us on Facebook at @theeuropedsfoundation.org. 
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Oh my goodness. What a tribute to Nick, Euro-Peds and yourself! Great job guys. Bet this will help a lot of people! --leslie
He is an amazing young adult!
Awesome dude. Cheers!
You remind me so much of my husband, very similar CP. I’d love to know how you go about passive stretching every day? We have struggled for so long now due to his muscles being so spastic since covid closed gyms and affected support services.
3
Great
How is Nick doing now is he in college?
What type of cp he have
Troy