Children Supported
At Family First Children’s Foundation, every donation directly impacts the lives of children and their families. With your support, we’ve been able to provide therapy services, adaptive equipment, and resources that make everyday life more accessible and full of possibilities.
This section is dedicated to sharing stories of the children we’ve helped—because behind every donation is a child gaining independence, confidence, and new opportunities.
Meet Some of the Children Your Donations Support:
Jace
Jace has cerebral palsy and has worked hard to achieve independent sitting on the floor, but was not quite ready to sit at a table. Having outgrown traditional baby seating options, he needed a chair that could properly support his posture while allowing him to continue developing strength and independence.
Through the generosity of our donors at our 2025 Silent Auction, a specialized Testa Seat was purchased for Jace, giving him the support he needs to participate more fully in daily activities, build functional sitting skills, and continue moving forward in his journey.
Vinny
Vinny has cerebral palsy and is still learning to sit independently. He needed more support than standard baby floor seats could provide, along with positioning to help stretch his tight legs safely.
Through the generosity of our donors at our 2025 Silent Auction, a specialized Testa Seat was purchased for Vinny. Giving him a safe place to sit on the floor, stretch, and participate in everyday moments while continuing to build strength and independence.
Jace
Jace has CRELD1, an extremely rare genetic condition that causes intractable epilepsy. Due to weakness and dystonic movements, he is unable to sit independently and requires support.
Through the generosity of our donors at our 2025 Silent Auction, a specialized Testa Seat was purchased for Jace. This supportive and portable seating option has been life-changing for his family allowing his parents to safely sit him on the floor to play with his toys and bring him along to restaurants and community outings. As he continues to grow, this portable support will remain essential for his safety, comfort, and participation in everyday life.
Alistair , 2 years old
Diagnosed with SMA Type 1, Alistar bravely received gene therapy, making him an ideal candidate for our two-week intensive strength-building program. Research shows that the first two to three years after gene therapy are the most critical for building strength and motor skills, which made this an important time to focus on therapy.
During his intensive, Alistar worked hard to build muscle strength, coordination, and confidence. Each session was designed to help him make the most of this crucial period of growth. We are so proud of his determination and honored to support him on his journey toward greater independence.
Jonah, 4 years old
Jonah is full of life and always gives his best in therapy. He’s been making amazing progress in his weekly sessions and was especially excited for his upcoming intensive to work toward independent walking.
Unfortunately, just a week before, his family learned he wouldn’t be receiving the funding they expected and had to cancel. That’s when Family First Children’s Foundation stepped in covering the expenses.
Ava, 5 years old
Ava was provided with 20 speech therapy sessions to address a severe phonological disorder that significantly impacted her ability to communicate clearly. Through therapy, Ava worked on improving speech production and motor planning using specialized techniques, visual and verbal cues, and individualized support. We are proud to help give Ava the tools and therapy she needs to find her voice and communicate with greater confidence.
Jace, 2 years old
Jace has cerebral palsy secondary to a stroke, which impacts his strength, coordination, and ability to move independently. Family First Children’s Foundation provided funding for a DMI therapy intensive designed to help him build strength, improve motor control, and work toward greater independence. During his intensive, Jace began taking steps in his gait trainer! We are honored to support Jace as he continues working toward increased mobility and independence.
Everly, 2 years old
Everly lives with lissencephaly and hemiplegia, which significantly impact her strength, coordination, and ability to move independently. Family First Children’s Foundation provided funding for a DMI therapy intensive focused on building strength, improving motor skills, and supporting her progression toward standing and walking. During her intensive, Everly worked hard toward these important milestones and made meaningful progress toward standing and taking steps in her gait trainer. We are proud to be part of her journey toward greater independence.
Liam, 2 years old
Liam has a genetic condition that impacts his strength, balance, and coordination, resulting in gross motor delays. Family First Children’s Foundation provided funding for a DMI therapy intensive focused on strengthening his body, improving coordination, and developing the motor skills needed for mobility. During this intensive, Liam achieved an incredible milestone he took his first independent steps! We are so proud of his hard work and grateful to help provide the therapy that allowed him to keep reaching for what comes next.
Evelyn, 2 years old
Evelyn’s journey has been impacted by medulloblastoma, which has significantly affected her gross motor development and ability to move independently. Family First Children’s Foundation provided funding for a DMI therapy intensive to help her build strength, improve motor control, and regain important developmental skills. During her intensive, Evelyn reached an exciting milestone and began pulling herself to stand. We are honored to support her continued progress and help her work toward greater independence.
Matthias, 5 years
Matthias has Down syndrome and sustained brain bleed at birth resulting in secondary cerebral palsy, which significantly impacts his upper-extremity function and ability to communicate through traditional methods. Matthias needed a specialized AAC communication device that he could control using his eyes, giving him a way to communicate more independently. Although insurance helped cover the device, his family was left with a $2,500 deductible before he could receive this essential equipment. Family First Children’s Foundation stepped in to cover the cost, helping ensure that Matthias had access to a voice of his own.
Milo, 6 years old
Milo was diagnosed with a complex visual condition that significantly impacted his ability to use his vision effectively, including challenges affecting learning and participation in school. His doctor recommended an intensive program of binocular vision therapy twice a week, which left his family facing significant out-of-pocket costs. Family First Children’s Foundation stepped in to help cover the cost of his vision therapy, easing the financial burden on his family while helping ensure he could access the treatment he needed.
Why These Stories Matter
Every piece of equipment purchased, every therapy session funded, and every milestone reached is made possible through your generosity. These stories are just a glimpse of the difference you are making in the lives of local children.
Together, we are building a future where no child is left without the tools they need to thrive.
