A Journey Fueled by Hope: The 2nd Annual Teddy Morse’s Ride for Kids
Every mile tells a story. When you start your engine for the 2nd Annual Teddy Morse’s Ride for Kids, you aren't just joining a procession of motorcycles; you are becoming a vital part of a legacy of compassion. For decades, this community has shown up with unmatched heart to support the mission of Camp Boggy Creek, ensuring that children facing serious medical challenges have a place to rediscover the simple, transformative joy of childhood.
More Than a Destination
Imagine a place where "serious illness" takes a backseat. That place is Camp Boggy Creek—a 232-acre haven designed specifically to be medically safe, yet overflowing with laughter. It is a sanctuary where every child belongs, where their resilience is celebrated, and where the weight of their daily battles is lifted, if only for a while.
The funds raised from the 2nd Annual Teddy Morse's Ride for Kids directly cover the costs for things like medical staff, specialized activities, and adaptive equipment—creating unforgettable memories for our campers.
You are not just joining a ride – you are giving children with serious illnesses a sense of belonging, empowerment and joy.
Meet the incredible Camp Champions who ride with you in spirit — each representing thousands of courageous kids whose lives are brighter because of you.
Meet the 2026 Ride for Kids Camp Champions
Noah, K. , Cancer
“We’re so thankful for Camp Boggy Creek, because it helps families walking through childhood serious illnesses that they are not alone.” ~ Gabrielle, Noah’s Mom
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Noah was only 3 years old when a hard lump on his jaw, high fevers, pain, and exhaustion led to more than two months of appointments, ultrasounds, bloodwork, ER visits, and eventually the earth-shattering news that he had stage 4 Anaplastic Large Cell Lymphoma, a rare form of Non-Hodgkin’s Lymphoma.
Noah endured scans, a bone marrow biopsy, a spinal tap, multiple port placements, inpatient and outpatient chemotherapy, and more than any little boy should ever have to face.
This journey reaffirmed what his family already knew: life is precious, and no moment should be taken for granted.
For Noah’s family, Camp Boggy Creek gave them the gift of fun, joy, and connection during one of the darkest seasons of their lives.
“We’re so thankful for Camp Boggy Creek, because it helps families walking through childhood serious illnesses that they are not alone.” ~ Gabrielle, Noah’s Mom.
Josie, O. , Craniofacial
“She has taught us about resilience and strength and we are better because of her. We love how Camp Boggy Creek supports families like ours and makes our Josie feel like a normal kid.” ~ Anna, Josie’s Mom
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At just three days old, Josie was diagnosed with Antley Bixler Syndrome, a rare genetic disorder that primarily impacts her musculoskeletal system, and according to Josie’s family, has impacted every aspect of their lives.
Josie has continued to defy expectations since the day she was born, undergoing multiple surgeries, constant doctors’ visits, and ongoing physical therapy to support her needs. Through the encouragement of their unwavering support system, Josie and her family have faced every challenge head on.
Today, Josie is your typical 6 year-old. She’s bubbly and happy - making friends at school, going on adventures with her siblings, and developing her own sense of independence and confidence as she achieves milestones that many thought were once unattainable.
Josie’s mom Anna attributes part of the development of Josie’s sense of independence to their time at Camp Boggy Creek, “ She has taught us about resilience and strength and we are better because of her. We love how Camp Boggy Creek supports families like ours and makes our Josie feel like a normal kid.”
Logan, F. , Epilepsy
“For the first time, he was surrounded by other children living with epilepsy; witnessing his realization that he was not alone was a truly powerful moment.” ~ Amy, Logan’s Grandmother
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Since his epilepsy diagnosis at the age of two and a half, Logan has demonstrated remarkable resilience. Despite the numerous therapies, medical tests, and hospitalizations he has faced, he continues to be a joyful and compassionate person.
A significant milestone occurred this past February when Logan was matched with Rowan, his service dog. This partnership has provided him with a new sense of independence and a profound connection.
Rowan, along with Logan’s "village" of friends and family members, provide constant support, love, and care, helping him continue to face the struggles of his diagnosis every day.
A huge milestone in Logan’s journey with epilepsy was coming to Camp Boggy Creek. According to Logan’s grandmother Amy: “Logan's experience at a Camp Boggy Creek family retreat last year was transformative. For the first time, he was surrounded by other children living with epilepsy; witnessing his realization that he was not alone was a truly powerful moment. We remain deeply grateful to Camp Boggy Creek for offering programs that empower Logan to see his condition as a strength.”
Ariana, F. , Heart
“We’re so grateful to Camp Boggy Creek for creating a place where Ari belongs, where her diagnosis doesn’t define her and she can just be a kid.” ~ Nateisha, Ariana’s Mom
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From the moment Ari entered this world, she began fighting for her life.
Ari was born with a rare congenital heart disease so uncommon that only 1 in 5 people in the world had ever been diagnosed with it. Before most babies even leave the hospital, she had already endured three major heart surgeries by just 3 weeks old.
During those early days, she survived a stroke and a pulmonary embolism. But even then, she showed what true strength looked like.
For a while, life felt almost normal. Ari laughed, played, and grew into a happy little girl. Her family cherished every milestone, every smile, and every ordinary moment that once felt impossible.
Then, at 4 years old Ari went into heart failure and required a heart transplant.
For 8 long months, Ari lived as an inpatient—fighting every single day. In January 2023, Ari received her new heart.
Her journey has been filled with fear, tears, surgeries, and hospital stays. But it has also been filled with unwavering faith, hope, resilience, and miracles.
Today, Ari is a thriving 8-year-old who loves trying every sport, enjoys anything involving water, and has a smile that lights up every room she walks into. Though her journey with congenital heart disease will always make Ari unique, Ari’s mother Nateisha says that Ari is just like any other kid:
“Congenital heart disease may always be a part of Ari’s story, but it will never define who she is. She is brave. She is joyful. She is resilient. She is loved beyond words. We’re so grateful to Camp Boggy Creek for creating a place where Ari belongs, where her diagnosis doesn’t define her and she can just be a kid.”
Mason, L. , Cerebral Palsy
“Camp Boggy Creek gave our son something every child deserves: the chance to be seen, included, and to discover what is possible. And it gave our family something we will carry forever: hope.” ~ Sara, Mason’s Mom
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Mason was born at just 27 weeks old, weighing only 2 pounds. He was later diagnosed with athetoid cerebral palsy. Since then, his life has been filled with determination – countless hours of physical, speech, and occupational therapy that have helped him grow into the happy, strong 12-year-old he is today.
From the very first time we arrived at Camp Boggy Creek, Mason was welcomed into a place where he could simply be a kid. He started approaching others on his own and joining activities without hesitation. For the first time, we saw him fully step into a sense of confidence and belonging.
Mason’s mom, Sara, says Camp Boggy Creek has given Mason and her family more than she could have asked for: “Camp Boggy Creek gave our son something every child deserves: the chance to be seen, included, and to discover what is possible. And it gave our family something we will carry forever: hope.”
Guenivere, F. , Asthma
“Camp Boggy Creek means so much to our family. It gives my daughter a place where her asthma does not define her, a place where she feels safe, understood, and free to simply be a kid. Seeing her return home with greater confidence, wonderful memories, and new friendships is a gift our family will always cherish.” ~ Heather, Guenivere’s Mom
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From the moment Gwen was born she struggled to breathe on her own. As a baby and then a toddler she would sound like a pug when she slept. As she got older, she would wake up in the middle of the night coughing so hard it would make her sick. Concerned she wasn't getting enough oxygen we went to a pulmonologist, and they told us that she had Asthma. From there we did a sleep study and found that she wasn't getting enough oxygen and began treatment with two inhalers, antihistamine, and two nasal sprays.
Gwen is doing better now that she's got a treatment plan, and some days are better than others. She has so much energy and love for life and people. She excels in school and is always eager to learn something new and share that information with everyone.
Camp Boggy Creek means so much to our family. It gives my daughter a place where her asthma does not define her, a place where she feels safe, understood, and free to simply be a kid. Seeing her return home with greater confidence, wonderful memories, and new friendships is a gift our family will always cherish.