Enzo’s Miracle Van

July 22, 2025

Enzo is a vibrant 6-year-old with a contagious love for life. He’s happiest when he’s surrounded by his family, watching his brother and sister race around him, laughing and shouting “FASTER!” as they push his wheelchair. He adores dinosaurs, Mickey Mouse, swimming, and music—something that’s played a big role in his journey since the NICU, where music therapy helped stimulate his brain development. Today, Enzo continues to sing and memorize songs, often bursting into tune at any moment. He attends school in the Wilson School District, where his teacher, Mrs. P, has had a lasting impact on his growth and happiness.


Enzo was born with special needs, and his journey has reshaped his family’s outlook on life. His parents, especially his mom, speak openly about the challenges and beauty that come with raising a child with disabilities. They’ve learned to let go of societal expectations and focus on what truly matters—love, patience, and celebrating every small victory. Through Enzo, they’ve found strength, resilience, and a deeper sense of compassion not only for him but for others walking similar paths.


Before receiving help from Maddie’s Miracles, daily tasks like transportation were physically and emotionally exhausting. Enzo had outgrown his car seat, and lifting him and his wheelchair into their old van was a heavy, tiring process. His mom often found herself canceling outings simply because it became too difficult to get Enzo in and out of the car. That changed when Maddie’s Miracles stepped in and provided a wheelchair-accessible van, nominated by a colleague from the occupational therapy clinic where Enzo’s mom works. Since receiving the van, life has become significantly easier—allowing Enzo to travel more comfortably and giving the whole family a sense of freedom and relief. His siblings even help secure his wheelchair, turning car rides into moments of connection and teamwork.


Beyond practical support, the family leans heavily on their faith and the special needs community for strength. Enzo’s mom finds hope and healing in her belief that God has a plan for their family, often reflecting on the ways her faith carried them through their darkest moments. She finds inspiration in stories like the paralyzed man lowered through the roof to meet Jesus—believing, like that story, that there is always a place for Enzo in this world and beyond. She also cherishes the deep bond she shares with other moms in the special needs community, celebrating milestones together and lifting each other up.


To parents just beginning their special needs journey, Enzo’s mom offers this advice: don’t be afraid of the diagnosis—it’s the first step toward getting the right help. Let go of expectations and trust that you were chosen for a reason. With love, support, and the right resources, your child can thrive.

Enzo’s story is a beautiful reminder of the power of perseverance, the importance of accessibility, and the joy that shines through even the toughest challenges. Maddie’s Miracles is proud to have played a small part in helping Enzo and his incredible family continue their journey with hope and strength.

Family stands beside a gray accessible van with a ramp. One child is in a wheelchair. Forest background.

Group of people standing by a blue car on a snowy street, smiling.
July 21, 2025
Alesia is 12 years old and has had Cerebral Palsy since birth it has been an extreme challenge simply managing the day-to-day tasks and activities. Alesia has no control or support of her lower body. She does have an adaptive car seat. However, it causes her extreme discomfort. The task of simply transporting her to the numerous appointments she has throughout the week can be heart-aching to watch. We have had to cancel appointments and cancel on family gatherings simply because Alesia is too uncomfortable to leave the house without her chair. The vehicle will help us tremendously, not only in transporting her to and from her appointments, but will also allow us to bring Alesia’s wheelchair along in hopes she will be eager to head out and do more.  Cerebral palsy (CP) is a group of neurological disorders that affect movement, muscle tone, and posture. It is caused by damage to the developing brain, often before or during birth, or in early infancy. The condition can vary in severity, with some individuals experiencing mild coordination issues, while others may have significant physical and intellectual challenges. Symptoms can include difficulty with walking, speaking, and fine motor skills. Although there is no cure for cerebral palsy, treatments such as physical therapy, medication, and assistive devices can help improve quality of life and independence.
Family poses in living room; daughter in wheelchair, parents smile, neutral colors, sunny.
January 16, 2025
Niya is a happy girly girl who loves pink and spending time with her family. She has a large family of eight brothers and sisters who always make her smile and laugh. She loves funny noises, listening to The Boxcar children’s books, and loves being outside. Niya faces lots of challenges with her mental and physical disabilities. She was born prematurely at 29 weeks with peri ventricular leukomalacia. This is damage to the brain that resulted in spastic quadriplegic cerebral palsy and cortical visual impairment. She currently uses a manual wheelchair, a stander; to help her stand and bear weight, a gait trainer; to help her take steps, an activity chair; for feeding and participating in family time, a handicap accessible vehicle for transportation, and a medical grade hi low bed for assisting with transfers and safe sleeping. She uses all this equipment daily. Niya’s family reached out to Maddie’s Miracles for assistance with a ceiling lift to help transport her to her handicap accessible bathroom. The family needed the lift as Niya is getting older and will continue to grow. Transferring her in and out of the bed and shower chair was getting more difficult and would continue to worsen as she got older and bigger. The safest and less strenuous option was a ceiling lift. The lift was denied several times by the family’s insurance company. A ceiling lift is quoted to cost anywhere from $7,000 to $12,000 which is not affordable so that is when the family decided to seek help elsewhere. Once Maddie’s Miracles read their submission we decided to meet the family. Within two minutes of meeting Niya and her beautiful smile and spunky personality we knew she her family needed the lift and decided on providing it for her and her family as our next miracle. The ceiling lift was installed by Laurel Medical on September 24th, 2024. It took less than two days to have the lift fully installed and ready for use. The family told us immediately after it was installed how much Niya loved it and how it has helped them tremendously. It has allowed them to provide a safe mode of transfer to and from her bathroom. Niya always enjoys taking her zipline and always has a huge smile on her face when she’s in it.
Two women and a child are posing for a picture on a couch.
December 13, 2024
Declan is diagnosed with TARP Syndrome, which is a rare genetic condition that mainly affects boys and is caused by changes in the RBM10 gene on the X chromosome. The syndrome itself is a spectrum, varying in how it presents itself in each case. It is marked by several health problems, including clubfoot (a twisting of the foot), heart defects, issues with jaw and palate development (like a small lower jaw and cleft palate), and abnormal blood vessels. These issues can cause breathing and heart problems, making the condition very serious, especially in infants. Early diagnosis and care from a team of doctors can help manage the challenges caused by this condition. As Declan gets older, his family has adjusted to how they care for him in day-to-day activities. Maddie’s Miracles saw the opportunity to help by providing this family with essential pieces of medical equipment to make Declan and both his parents lives a bit easier. Maddie’s Miracles was able to provide Declan with a shower chair, as well as an adaptive chair called the Go To Firefly Seat, which is a lightweight, portable, postural support seat designed for kids with disabilities. Stefany, one of Declan’s parents told us: “These pieces of equipment have aided in Declan’s day-to-day activities in so many ways. We are able to have him be a part of the dinner table when we go out to eat, as it provides him with the amount of support he needs to sit at the table. With bathing each day, the shower chair has given a whole new outlook and has put the fun back in bath time! Life before these pieces of equipment was not easy, nor were we able to have Declan be an active member of the family when out and about. He is now able to swing at parks with other kids his age, and his is able to comfortably have a bath with the support he needs. We are forever grateful for Maddie’s Miracles and cannot say enough how wonderful the entire process was to get Declan the equipment he needed. Thank you so much for the generosity!” Maddie’s Miracles continues to seek out families of children with severe disabilities who could use assistance to make their daily lives easier. If you, or someone you know could benefit from our mission, please visit our nomination page and submit an application for us to review. We will be in contact with you shortly!