Your life transformed the moment you received a diagnosis. In that instant, your plans, priorities, and sense of peace shifted.
You have faced tough days—times when exhaustion feels heavy and the future is uncertain. Yet, there have also been days filled with love, determination, and meaningful victories.
Every step your child takes, every word spoken, and every bit of progress showcases your unwavering effort and strength.
At CRIT, we acknowledge and honor your incredible journey. You are not alone; we walk this path together. Your battles matter, and your dreams inspire us all.
Thank you for being a powerful example of resilience, for always showing up, for rising again and again, and for your endless love.
With respect and admiration,
Your CRIT Family
Happy Mother’s Day!
My Child Is Different: What I Learned About Neurodiversity at TeletonUSA
By: 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?
Find professional support. TeletonUSA’s therapists are trained to guide neurodivergent children with empathy and respect.
Keep going at home. Therapy doesn’t stop in the treatment room. Your daily support is part of their progress.
Understand their senses. Some children feel “too much,” others “too little.” Learning how they experience the world helps you care for them better.
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
By: TELETONUSA /
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!
March Star of the Month: Logan Quiroz
By: TELETONUSA /
Meet Logan, our March Star of the Month! At just 4 years and 5 months old, Logan is already showing the world what strength, perseverance, and joy look like.
Logan was born with a rare genetic condition called Pelizaeus-Merzbacher Disease, which affects his muscle control, movement, and ability to speak. Everyday tasks—like sitting up, grasping toys, or trying new foods—are more challenging for him. But Logan doesn’t let that stop him.
Since starting therapy at CRIT, Logan has made amazing progress. He receives occupational, physical, and speech therapy—and his team is in awe of how far he’s come.
In Occupational Therapy, Logan is now able to follow toys with his eyes while turning his head, showing better control and focus. He’s also working on using his hands, and can now grasp and let go of toys on purpose—something that used to be very difficult. These skills help him explore his environment and play more independently.
In Physical Therapy, Logan is gaining strength in his legs and improving how he moves his body. He can now lift his hips to help with dressing and is showing better head control while sitting and standing with support. One of his biggest victories? Taking steps in supported standing using an assistive device—an exciting sign of what’s possible for his future mobility.
In Speech Therapy, Logan is exploring new tastes and textures and becoming more comfortable trying different foods. He’s also working on his voice, using a special device called a Passy Muir Speaking Valve to help with vocal sounds. His favorite part? Recording videos for his personal YouTube channel! This fun hobby helps motivate him to keep practicing—and brings out his creative side.
Logan is a curious, motivated, and energetic little boy who loves learning and being part of the action. His big goal right now is to continue improving his strength, communication, and independence. He still faces challenges, but his positive spirit—and the support of his family and therapy team—keep him moving forward.
Every milestone Logan reaches is a reminder of what’s possible when a child receives the care, tools, and encouragement they need to thrive.
Thank you for supporting children like Logan. Your generosity makes stories like his possible—stories filled with hope, courage, and the power of progress.
We have officially been certified as a Great Place to Work!
By: TELETONUSA /
This milestone reflects our commitment to well-being, inclusion, and excellence.
Today, we proudly share that the Children’s Rehabilitation Institute TeletonUSA (CRIT) has received the Great Place to Work certification. This recognition highlights our ongoing effort to create a workplace where every team member can grow and feel valued.
Why is this achievement so exceptional?
At CRIT, we aim not only to change the lives of children with disabilities, but also to ensure that we care for those who make our mission possible. This recognition is a testament of our team member’s trust, collaboration, and shared commitment.
More than a workplace: a place of hope
Every day at CRIT is an opportunity to transform lives. From therapists to administrative staff, we all share the same vision: to provide the best care for the children and families who depend on us.
“This is more than just a job—it’s a purpose. Every achievement of our patients is a shared accomplishment. Working in a place where your efforts truly change lives is priceless.”
— Cristina Prieto, Corporate Sponsorship Officer
This certification inspires us to continue strengthening a culture rooted in respect, inclusion, and teamwork. We understand that caring for those around us positively impacts our care for every child.
Our gratitude
Thank you to all of our team members. This accomplishment is yours. Your dedication, energy, and love for our mission make today’s celebration possible.
What’s next?
Now more than ever, we continue our commitment to improving our work environment and transforming lives.
🔗 Visit our website to learn more about our work and how you can join this mission.
An act of love: make helping children with disabilities your purpose in 2025.
By: TELETONUSA /
A new year brings us the opportunity to reflect and make positive changes in our lives—and in the lives of others. This 2025, why not embrace a purpose that transcends? Make supporting children with disabilities your selfless act of love.
At the Children’s Rehabilitation Institute TeletonUSA (CRIT), we witness how small acts of solidarity can have an extraordinary impact on the lives of our patients and their families. Here’s how you can make a difference and why this purpose can transform multiple lives.
Why supporting a cause is a transformative purpose.
When you support a cause, you’re not just helping those in need but nurturing values like empathy, generosity, and gratitude. You’re also building a more inclusive world filled with hope for children with disabilities.
Regardless of size, every donation to CRIT becomes a powerful tool to provide therapies, treatments, and moments of joy to children and families facing immense challenges every day.
How to turn this purpose into action
Making this purpose a reality is easier than you think. Here are a few ways to get started:
Make a monthly donation:
Commit to a recurring donation to become a TeletonUSA Dream Maker. Your contribution will fund anything from therapies to specialized equipment.
Get involved in activities:
Join our volunteer events, such as food banks or family activities. Every moment of your time makes a difference.
Invite others to join:
Share CRIT’s mission with friends and family. You never know who might want to join this movement of change.
Be a Hero for CRIT:
Create your digital fundraising page to rally your community. Together, you can allow a child to take steps toward a better quality of life.
Because helping is the greatest act of love.
Including the Children’s Rehabilitation Institute TeletonUSA in your resolutions won’t just transform other lives—you’ll transform your own. Witnessing the impact of your support will remind you of the power of a simple act of kindness and how, together, we can build a future full of possibilities.
This 2025, make your purpose one of giving. Give hope, give opportunities, give love. Visit our website, critusa.org, to learn how you can start this journey with us.
Let’s make this year count—for someone else.
Meet Jameson: Our First Star of the Month for 2025!
By: TELETONUSA /
Jameson is a bright and determined 7-year-old boy with a rare neurological condition called Landau-Kleffner Syndrome. At CRIT, he receives a variety of therapy services, and his team couldn’t be prouder of his incredible progress and unwavering dedication! Jameson’s therapy journey began in early 2024 with Recreational Therapy. Together with his therapist, he has worked tirelessly to improve key skills, including attention to tasks, turn-taking, social and communication skills with peers and therapists, transitioning between activities, and emotional regulation. Week after week, Jameson tackles new challenges with a big smile, showing resilience and enthusiasm every step of the way. Soon after, Jameson started Speech Therapy to enhance his communication skills and speech clarity (how well he speaks and is understood). He’s made steady progress, focusing on improving his breath support and awareness to communicate more effectively. Most recently, Jameson began Physical Therapy, where he’s working to strengthen his balance and coordination. His creative spirit shines through as he turns exercises into fun games and activities. Jameson is a fun-loving, imaginative child with a passion for Super Mario Brothers, playing board games like Don’t Break the Ice, and memory or flash card games. He loves singing silly songs, blowing bubbles, and popping them just as quickly! Since starting his journey at CRIT, Jameson has made remarkable strides, and 2025 promises even greater growth for this inspiring young star. This and other success stories are made possible thanks to the support of thousands of generous individuals—just like you! Your kindness and commitment help children like Jameson achieve their dreams and reach their full potential.
How to support NICU parents: 5 Practical Ways to Help
By: TELETONUSA /
World Prematurity Day on November 17th is a time to raise awareness and support families with babies born too soon. Premature births can be emotionally and physically challenging, especially when babies need to stay in the Neonatal Intensive Care Unit (NICU) for an extended period. If you have a loved one with a newborn in the NICU, here are a few meaningful ways to provide support and comfort during this challenging journey.
What is the NICU?
The Neonatal Intensive Care Unit (NICU) is a specialized hospital area where premature or critically ill newborns receive intensive medical care. It is staffed by neonatologists, nurses, and other medical professionals who monitor and treat babies around the clock. Although the NICU is a place of healing and hope, it can also be a very overwhelming environment for parents. They are often separated from their baby for long periods and may feel a mix of joy, anxiety, and fear during their baby’s stay.
1. Celebrate the Small Victories
Parents of NICU babies often miss out on the traditional newborn moments, like dressing their baby in a cute outfit or holding them right after birth. Instead, they are focused on their baby’s health and well-being. This can be an incredibly stressful time, and celebrating their baby’s small victories can be a powerful way to lift their spirits.
Small milestones like weaning off oxygen, gaining weight, or transitioning to bottle feeding are huge achievements in the NICU. Congratulating the family and celebrating these victories reminds them that their baby’s journey is just as special as any other. Your encouragement can help them feel less isolated during this challenging time.
2. Be Mindful with Your Words
A common question that parents often hear is, “When will the baby come home?” While this question comes from a place of care, it can be deeply painful. Parents of NICU babies desperately want to bring their baby home, and every day spent in the NICU can feel long and exhausting. Instead, ask, “How are you and the baby doing today?” This shows your concern and opens up the opportunity to celebrate any of the baby’s progress—big or small.
3. Avoid Comparisons
Every baby is unique, and every journey in the NICU is different. While you may feel inclined to share your own parenting experiences or your child’s developmental milestones, it’s important to remember that NICU babies often have different timelines and medical needs. What worked for a full-term baby may not apply to a premature baby, so avoid offering advice unless specifically asked. NICU parents are already navigating recommendations from doctors, nurses, and therapists, so it’s important not to add to their overwhelm.
4. Respect Health Boundaries
Premature babies often have weakened immune systems and are more vulnerable to infections, particularly during their first two cold/flu/RSV seasons. Families may set strict health boundaries to protect their baby, such as requesting visitors to wear masks, wash hands thoroughly, or even limit physical contact with their baby. Respect these requests without hesitation. Avoid kissing the baby and follow any other precautions the parents ask for—this is essential to keeping their baby safe.
5. Offer Practical Support
Families with a baby in the NICU often face logistical challenges, from managing their time at the hospital to caring for siblings at home. Offering practical support can be a huge relief. Here are a few ideas:
Prayers and encouraging words: Sometimes, knowing that others are rooting for their baby’s health and their well-being can be incredibly uplifting.
Visits: If the family is comfortable with visitors, offer to visit them in the NICU or provide company during the long waiting hours.
Help at home: Offer to babysit siblings so parents can spend time at the hospital. Hiring a cleaning service to prepare the house before the baby comes home can also be a thoughtful gesture.
Gift cards: Gas and meal gift cards can help ease the financial burden of traveling back and forth to the hospital or grabbing a quick bite.
Books: Reading to a baby in the NICU is a wonderful bonding experience for parents. Consider gifting books and writing a personalized message inside the cover for the baby and family to treasure—a thoughtful “time capsule” to look back on.
Conclusion: Why Your Support Matters
Supporting a family in the NICU can make a world of difference during a difficult time. By offering empathy, respect, and practical help, you can be part of their healing journey and celebrate every step of their baby’s progress. Share this post to join us in spreading awareness this World Prematurity Day. Let’s honor the strength of these incredible families!
5 Inclusive Costume Ideas for Children with Disabilities
By: TELETONUSA /
Halloween is one of the most anticipated times of the year for children, filled with magic, creativity, and loads of fun. For families of children with disabilities, the excitement of choosing a costume can come with some challenges. However, with a bit of imagination, it’s possible to create costumes that are not only fun but also inclusive and comfortable for everyone.
Here are some costume ideas that can adapt to different needs while celebrating each child’s uniqueness.
1. Superheroes on Wheels
If your child uses a wheelchair, why not turn it into a superhero vehicle? You can transform it into the Batmobile or the DeLorean from Back to the Future. You can even create simple options at home, such as a firetruck or a rocket ship using recyclable materials.
2. Soft-Textured Animals
Choose costumes made from soft, tag-free fabrics for children with tactile sensitivities. Plush animal costumes, like bears or bunnies, can be a comfortable and fun option.
3. Movement-Friendly Monsters
If your child has limited mobility and uses crutches or a walker, incorporate those into the costume! Costumes that integrate these elements can be very creative and help integrate them in a funnier way. A long-legged monster, a robot, or a scarecrow can be easy and comfortable costumes to make at home.
4. Capes and Accessories
Children with sensory needs often feel more comfortable in simple costumes, such as capes or hats. Make sure the materials are soft and non-restrictive. Capes can recreate their favorite superhero and include a hidden pocket to store a treat so you can add a surprise element.
5. Accessible Fairy Tales
If your child uses a walker or other assistive device, you can transform it into Cinderella’s carriage or Peter Pan’s pirate ship. Your child will be the star of their very own fairy tale!
Extra Tips for Enjoying This Halloween:
Plan Ahead: Make sure the costumes are comfy and easy to move in.
Map an Accessible Route: If you’re going trick-or-treating, plan a friendly and accessible route.
Inclusive Parties: Consider hosting a party at home with adapted games for all children to enjoy.
At Children’s Rehabilitation Institute TeletonUSA, we believe every child deserves to experience the magic of Halloween. We invite you to explore more costume ideas this season and share them with us.
Explore our website to find inspiring life stories and discover different ways to support our mission of creating a more inclusive world for all children.
