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My Child Is Different: What I Learned About Neurodiversity at TeletonUSA

When Logan’s parents first heard the diagnosis, they couldn’t even pronounce it.

“Pelizaeus-Merzbacher.”

All they knew was that their child’s development wasn’t going as expected. And while there was fear and uncertainty, there was also love, curiosity, and hope.

Like thousands of families who come to TeletonUSA, they learned a word that changed how they see the world: neurodiversity. TeletonUSA is a non-profit organization that provides comprehensive support and resources for neurodivergent children and their families.

What is neurodiversity?

Neurodiversity isn’t an illness. It’s a different way of processing the world.

It’s a term that includes conditions like autism, ADHD, dyslexia, cerebral palsy, brain injuries, and many others. Some children are born this way; others develop these conditions through illness or accidents. But they all have one thing in common: their brains work differently.

And while that can present challenges, it also brings forth unique talents, unexpected strengths, and beautiful ways of seeing life, inspiring hope and a sense of wonder.

1 in 6 children in the U.S. lives with a condition like these.

Why does it matter?

Because neurodivergent children don’t learn at the same pace or in the same way as others, some may speak later, struggle to play with peers, or feel overwhelmed by certain sounds or textures.

But that doesn’t mean they can’t grow and thrive.

At the CRIT, for example, Logan has learned to hold toys, take steps with support, and communicate more clearly, all thanks to therapies designed for his unique learning style.

What can you do if your child is neurodivergent?

  1. Find professional support. TeletonUSA’s therapists are trained to guide neurodivergent children with empathy and respect.
  2. Keep going at home. Therapy doesn’t stop in the treatment room. Your daily support is part of their progress.
  3. Understand their senses. Some children feel “too much,” others “too little.” Learning how they experience the world helps you care for them better.
  4. Celebrate what they can do—every small step matters. What counts isn’t when the progress happens—it’s that it happens.

At TeletonUSA, we celebrate difference.

Every time a child says their first word or takes a step no one thought possible, we celebrate.

Because with support, love, and patience, neurodivergent children can do incredible things.

And the best part is they don’t have to do it alone.

Do you know someone who needs to hear this message? Share it with them.

Want to help more children like Logan receive personalized therapy?

Make your donation today at teletonusa.org/donate

Thanks to You, Reyna Keeps Going 

Meet Reyna, our Star of the Month — a bright and curious 4-year-old from San Antonio, TX!  

Reyna has spastic quadriplegic cerebral palsy caused by a devastating brain injury she experienced after birth. This condition affects her ability to move and communicate freely. Everyday tasks can be more challenging for her and her family. But Reyna meets these challenges with determination and heart. 

Reyna began her journey at CRIT in March 2024, starting with Speech Therapy. At the time, she was working on basic communication skills like looking at toys, focusing her attention, and responding to her environment. With the support of her family and therapists, she has made huge strides in using her eyes and head to interact with the world around her. One big win? Reyna now uses adaptive switches with her head to activate lights and sounds, allowing her to explore, play, and express herself. 

Her success didn’t stop there. Soon after, she began Occupational Therapy to work on moving her body more intentionally. She practices rolling over, holding herself up in different positions, and turning her head to follow toys and people. These small movements are significant milestones for Reyna and are helping her build the foundation for future independence. 

Most recently, Reyna added Physical Therapy to her weekly routine. She’s learning to sit with better balance and even stand with support—things that once seemed out of reach. Every session helps her strengthen her body and build her skills to engage more fully with the world. 

What makes Reyna’s story so special isn’t just how far she’s come—it’s also the joy and determination she brings to each session. Her team describes her as “vibrant,” and her progress reflects her spirit and the unwavering support of her family. 

Reyna’s primary goals are to keep building her strength, improve her communication, and gain more independence in daily activities. She still has challenges ahead, but her CRIT team is confident that she’ll keep moving forward with her attitude and the proper support. 

Reyna’s journey is a powerful reminder of what’s possible when families and therapists come together with hope and dedication.  

We are proud to celebrate her as our Star of the Month!