


This September, put a child's name on a race car.
Through the IMSA Resilient Racers program, IMSA pairs kids from its charity partners — the Austin Hatcher Foundation and Camp Boggy Creek — with teams competing in the TireRack.com Battle on the Bricks at Indianapolis Motor Speedway on September 20. Each child's name goes above the doors, alongside the pros, for every fan in the stands to see.
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Meet Our Resilient Racers
Real Kids. Real Strength. Unstoppable Drive.

Abby C.
#57 - Winward Racing
Read My Story
Abby was diagnosed with B-cell Acute Lymphoblastic Leukemia (ALL) with CNS involvement in August 2022 at just 2 years old. In an instant, our lives changed from worrying about typical toddler milestones to navigating chemotherapy, countless hospital stays, procedures, and long days at the oncology clinic. Through it all, Abby has amazed us with her resilience. She has faced every challenge with a smile that somehow shines even on the hardest days. We have learned to celebrate every victory, whether it is a good lab report, a treatment milestone, or simply watching her laugh, play, and be a little girl. Cancer has forever changed our family’s perspective. It has taught us to slow down, cherish the ordinary moments, and find joy even in the middle of uncertainty. We are newly joining the Austin Hatcher Foundation and are so thankful for the opportunity to connect with other families who truly understand this journey. Having Abby’s name represented in this special way is incredibly meaningful to us. It is a reminder that she is not defined by cancer, but by her courage, kindness, joyful spirit, and the hope she continues to inspire in everyone she meets.

Abby Y.
#10 - Cadillac Wayne Taylor Racing
Read My Story
In the fall of 2022, we noticed that Abby had more limited use of her right arm, hand and, eventually, her leg as well. After pursuing other treatments that did not resolve the issue, her doctors ordered an MRI and we were shocked to find she had a large brain tumor. She was flown to Nationwide Children's Hospital in Columbus, OH for a biopsy and to start treatment. She went through six rounds of chemotherapy, three bone marrow transplants, and six weeks of proton radiation. She rang the bell in September 2023 to signal the end of her inpatient and radiation treatment. She continued on oral chemotherapy until July 2024 and, after completing that regimen, was declared in cancer free, in remission with no evidence of disease. What a joyous day!! Such a long road for our family but absolutely worth every step. We found the Austin Hatcher Foundation early in our journey and they have walked by our side every step of the way. They have supported our entire family completely with occupational therapy, mental health and educational support. With so many unknowns that come with this diagnosis, it is such a comfort to know that we have them to help us and guide us, whatever comes our way. We are honored that we have been asked to have Abby's name on a car in this race. The Austin Hatcher Foundation has been such a blessing for our family and we are thrilled to be able to use this very painful experience in a positive way to let others know about this incredible organization.

Ariana F.
#40 - Cadillac Wayne Taylor Racing
Read My Story
From the moment Ari entered this world, she began fighting for her life. Ari was born with a rare congenital heart disease. 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—complications that could have taken her from us. But even then, she showed us what true strength looked like. For a while, life felt almost normal. Ari laughed, played, and grew into a happy little girl. We cherished every milestone, every smile, and every ordinary moment that once felt impossible.Then, at 4 years old, our world changed again. Ari went into heart failure. She was airlifted to UF Health in Gainesville in critical condition. Sitting in that hospital, hearing the words that our daughter would need a heart transplant, was one of the most terrifying moments of our lives. For 8 long months, Ari lived as an inpatient—fighting every single day while waiting for the gift that could save her life. And then, on January 6, 2023, our miracle arrived. Ari received her new heart.There are no words that can fully express the gratitude we carry for her donor and the family who made the most selfless decision imaginable. In the midst of their greatest heartbreak, they gave our daughter the greatest gift—the chance to live. Because of them, Ari is here today. 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.Her journey has been filled with fear, tears, surgeries, hospital stays, and moments when we didn’t know what tomorrow would bring. But it has also been filled with unwavering faith, hope, resilience, and miracles. Ari is our warrior. Our miracle. Our living proof that even the smallest heart can carry the greatest strength. 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. And every heartbeat she has today is a reminder that miracles are real.

Brayden R.
#93 - Acura Myer Shank
Read My Story
Brayden’s complex health journey first began in 2018 when he received his initial diagnosis of Lyme disease. Over the years, his path has unfolded through major milestones as he was diagnosed with Autism Spectrum Disorder in 2022, Hypermobility in 2024, and ultimately Marfan Syndrome in 2026. These conditions make everyday things we take for granted incredibly difficult for Brayden, from the simple physical task of opening a water bottle or chip bag, to the frustration of getting easily winded when trying to run a field or ride a bike.
Fortunately, Camp Boggy Creek has provided a vital sanctuary of hope, boosting his spirits and showing him he truly belongs by introducing him to wonderful kids who share similar struggles. Having Brayden’s name proudly represented on a race car symbolizes his incredible resilience, giving our family a powerful moment of celebration and recognition for everything he continues to overcome.

Caelan A.
#8 - Tower Motorsports
Read My Story
Caelan was struggling to breathe around his second birthday. We initially thought is was croup, but when he didn’t improve we ended up at Knoxville children’s where they found a mass in his trachea. He was flighted to Cincinnati to have it removed and was able to return home to Chattanooga for chemotherapy. The Austin Hatcher Foundation was there from our first stay and helped us with some behavioral issues after treatment using Child Parent interaction therapy. They continue to be a constant positive presence in our lives and have embraced our whole family. Caelan has thrived in survivorship playing multiple sports and getting top marks in school.

Cam M.
#12 - Vasser Sullivan Racing
Read My Story
Cam's journey began shortly into her 5th Grade year. She was feeling unwell and not getting any better. After a weekend on medications, we took her to our local hospital and were rushed via ambulance an hour south to Joe Dimaggio Children's Hospital. Within 24 hours of arrival, she had surgery to remove the massive tumor and began to fill some relief before starting her treatment journey. There were many meaningful moments along the way, we feel most fortunate to be treated at JDCH their staff always went above and beyond for Cameron and our family. Throughout Cameron's treatments certain opportunities became available like going to sleepaway camp. It was our child life specialist who told us about Camp Boggy Creek, a special place for kids who have battled the unthinkable. The opportunity to attend this camp, at no cost to us, couldn't have come at a better time. Having missed so much her last year in elementary school, a summer to remember was exactly what she needed. To be surrounded by peers living the same journey, with the safety of medical professionals to administer needed medications was a great comfort to us. Cameron has overcome so many things, always with a smile on her face, as many would remark. To be represented in this way, would be a true testament to her bravery and perseverance through a time that most people find unfathomable.

Chanel M.
#1 - Paul Miller Racing
Read My Story
My daughter's childhood cancer journey began on December 1, 2024, when she was diagnosed with B-cell Acute Lymphoblastic Leukemia. In an instant, life as we knew it changed. One day I was raising a happy, energetic little girl, and the next I was learning about chemotherapy, hospital admissions, spinal taps, and a treatment plan that would span years. Today, I am incredibly grateful to share that she is in remission and is currently in the maintenance phase of her treatment. While we still have a road ahead of us, reaching this milestone has given us hope and allowed her to return to many of the things she loves while continuing her fight with remarkable courage. Through every phase of treatment, my daughter has amazed me with her strength. She has endured chemotherapy, countless clinic visits, procedures, and days when she simply didn't feel like herself, yet she continues to smile, laugh, and find joy in being a kid. Some of my most cherished moments have been celebrating each milestone along the way, hearing the word "remission," watching her regain her energy, seeing her return to school, and witnessing the resilience she shows every single day. This experience has changed both of us in ways I never could have imagined. It has taught me to appreciate the little moments, celebrate every victory, and find hope even on the hardest days. My daughter has shown me what true courage looks like. She has faced challenges that most adults would struggle to endure, yet she continues to inspire everyone around her with her strength, resilience, and joyful spirit. The Austin Hatcher Foundation has been an incredible source of support for me. The counseling services gave me a safe place to process the fear, grief, and uncertainty that come with having a child diagnosed with cancer. Having that support reminded me that caring for myself emotionally was also an important part of caring for my daughter and being the mother she needed throughout this journey. Having my daughter's name represented on this race car is an honor that represents her courage, resilience, and everything she has overcome. It is a celebration of how far she has come and a reminder that she is so much more than her diagnosis. Seeing her name displayed in this way fills me with immense pride and gratitude. I hope it also brings awareness to childhood cancer and honors every child and family walking this difficult path. We are deeply thankful for everyone who has supported us and for this meaningful tribute to my incredible little girl.

Cynthia L.
#99 - AO Racing
Read My Story
Cynthia was diagnosed with leukemia twice, first at 3 years old and again at 6 years old. She has undergone significant treatments including chemotherapy, total body radiation, and a life-saving stem cell transplant from her sister Emily. During treatment, Cynthia and Emily lost their father to suicide. Cynthia's transplant recovery was hard, but she fought all the way through it. She has been cancer-free for 2 years! Her cognitive ability was impacted and she has some neurological and occupational differences. Austin Hatcher has helped us navigate Cynthia's survivorship since she came into our custody shortly after treatment. They support our entire family in ways that we never would have imagined. Cynthia will be thrilled to see her name on a race car and have her story shared with others.

Dyran H.
#96 - Turner Motorsport
Read My Story
Dyran was diagnosed with high-risk neuroblastoma in April 2023, when he was just 4 years old. His treatment was long and hard but he smiled every day. Today, Dyran is 2 years cancer free. We don’t know what the future holds for him but we refuse to live our lives in fear of what may or may not happen. Today is a good day. The Austin Hatcher Foundation has been very helpful holding our hand through everything that we did not see coming after cancer. Dyran is doing very well but he suffers side effects both physically and emotionally. It is very important for us to tell our story and raise awareness for funding. Childhood cancer is not rare!

Ethan H.
#60 - Acura Myer Shank
Read My Story
When Ethan was just 2.5 years old, our world changed forever with his leukemia diagnosis. Life instantly became filled with fear, hospital stays, and uncertainty. Along this journey we discovered Ethan’s incredible strength. With endless compassion from organizations like the Austin Hatcher Foundation, we were never alone. They gave our family therapies we all needed, and many events where we could laugh, have fun and simply be together when we needed it most. They are amazing with including siblings (like Ethan’s brother Mason). Today, we honor how far Ethan has come and carry hope for every family still fighting this battle. By supporting childhood cancer nonprofits, you’re giving families like ours comfort, community, and the courage to keep believing in brighter days.

Fernanda
#3 - Corvette Racing by Pratt Miller Motorsports
Read My Story
Fernanda is an extraordinary girl whose courage has carried her through a rare liver cancer called HEMNOS since age six, beginning with emergency surgery in Venezuela and continuing at Nicklaus Children's Hospital in Miami starting in 2022. Despite chemotherapy and tumor removals in 2023, the cancer spread and returned, culminating in a new large tumor found in July 2025. Her medical team performed a nine-hour surgery to remove it, followed by an innovative therapy that opened a new door just as options seemed to be running out. Today, a year later, Fernanda remains cancer-free, with every clean check-up a victory for her family and all who've walked this path with her. Fernanda's story shows that love, science, perseverance, and faith can light the way even in the darkest moments—thank you for joining us on this journey of hope.

Fynn W.
#6 - Porsche Penske Motorsport
Read My Story
Fynn was diagnosed with leukemia, and like most families who receive that news, our world stopped. Nothing prepares you for hearing those words about your child but from that moment, Fynn showed us what strength really looks like. There are so many moments etched into our hearts from this journey, but nothing compares to the day Fynn rang the coast guard bell to mark the end of his treatment. That sound meant everything every hard day, every hospital visit, every prayer all leading to that one moment. We will never forget it. This journey has changed the way our family sees everything. We don’t take ordinary days for granted anymore. Fynn has taught us more about resilience and joy than we ever expected and watching him fight has shaped who we all are. The Austin Hatcher Foundation gave Fynn and our whole family something medicine alone couldn’t: connection, joy, and the feeling that we weren’t doing this alone. Having Fynn’s name represented in this way means the world to us. It’s a reminder that his story matters, his fight was real, and the love surrounding him has always been bigger than the diagnosis.

Gabe D.
#4 - Crowdstrike Racing by APR
Read My Story
Our journey began at the end of third grade with a germinoma brain tumor diagnosis, launching our family into an intense, "all gas, no brakes" season of inpatient chemotherapy and exhausting daily trips to Knoxville for radiation. We received the incredible news that Gabe was finally cancer-free on a day he was attending a Parent's Day Out program at the Austin Hatcher Foundation! When Gabe transitioned back to fourth grade, the Austin Hatcher Foundation stepped in to provide vital neurocognitive testing for his academic ISP, and they have remained an invaluable continuum of support ever since through summer camps, teen programs, and the Teen Ambassador Program. While the late effects of treatment are a very real reality, this path has shaped Gabe into a resilient rising senior at Chattanooga Christian School. He is a varsity cross-country runner, a dedicated employee at two summer jobs, and a natural "people connector" who loves life and serves his community through his church and YoungLife group. Having Gabe’s name represented through Resilient Racers is a deeply meaningful honor that celebrates his incredible grit and ensures his lasting legacy of thoughtfulness and strength inspires other families walking this non-linear path.

Hayden M.
#66 - Gradient Racing
Read My Story
Hayden's journey began when she was diagnosed with Stage 4 ependymoma at just 2 years old. After surgery to remove a tumor attached to her brain stem, she lost all motor function from the neck down and faced the enormous challenge of learning to walk again during radiation treatment. Watching her fight through therapy and regain her independence has shown our family what true courage and determination look like. The Austin Hatcher Foundation has been an incredible source of support, providing counseling and educational services that have helped Hayden build confidence and thrive. Having Hayden's name represented on this race car is a powerful reminder of how far she has come and a celebration of the strength, resilience, and hope that carried her through her cancer journey.

Hudson A.
#70 - Inception Racing
Read My Story
Our family's cancer journey began unexpectedly in September 2022 when Hudson woke up one morning with pain in his right side. Less than 24 hours later, we found ourselves at Vanderbilt Children's Hospital, where he was diagnosed with a Wilm's tumor on his right kidney. Just three days later, Hudson underwent surgery to remove his right kidney one week before his ninth birthday. After his nephrectomy, he began a five-month course of chemotherapy. In February 2023, he completed treatment and received the wonderful news that he was cancer-free. Today, Hudson is a healthy, active 12-year-old who loves riding bikes, playing guitar, and playing baseball. We continue to travel to Vanderbilt twice a year for scans and follow-up appointments, and next year we'll celebrate his five-year cancer-free milestone as he transitions to the survivorship clinic. Throughout this journey, we were surrounded by an incredible community of family, friends, and supporters who prayed for us, encouraged us, and walked alongside us every step of the way. We are deeply grateful for every act of kindness, every prayer, and every person who helped carry us through one of the most challenging seasons of our lives.

Jack Jack C.
#22 - United Autosports USA
Read My Story
Jack Jack was moonwalking across the living room and tripped over a little orange bouncy ball. We thought he had a broken leg and ended up in Urgent Care, where we discovered his intense leg pain was the result of cancer. His X-ray revealed a cluster of leukemia cells. We started the hardest fight we had ever imagined, and on December 28, 2022, Jack took his last chemo pill! Jack has been in remission for 7 years and off of treatment for 3 and a half years!! #TeamJackJack1120

Jackson B.
#4 - Corvette Racing by Pratt Miller Motorsports
Read My Story
Jackson was diagnosed with T-cell Lymphoblastic Lymphoma in September 2025 at 6 years old. He had a 15 cm mediastinal mass that wrapped around his heart lungs and airway. He just finished aggressive frontline chemo and will be receiving maintenance chemo for the next 1.5 years. Jackson has been a brave inspiration to many and he keeps a good attitude while battling blood cancer. We are grateful for the Austin Hatcher Foundation and thankful for this opportunity.

Jackson W.
#34- Conquest Racing
Read My Story
Jackson’s journey began at my 17-week pregnancy appointment. During a routine examination, a specialist noticed that his heart did not sound “normal.” From that moment on, we underwent countless tests, including ultrasounds, amniocentesis, and extensive blood work. Despite years of evaluations, doctors could only tell us that Jackson had three heart abnormalities, but they were unable to provide a definitive diagnosis. As a first-time parent, it was terrifying, but I was grateful for the information and support we received along the way. On October 27, 2014, Jackson entered the world via C-section, surrounded by an incredible team of healthcare professionals. His arrival was supported by obstetricians, radiologists, specialized pediatricians, nurses, nurse practitioners, anesthesiologists, and, of course, his outstanding pediatric cardiology team from UF Shands. Little did we know, this was only the beginning of Jackson’s remarkable journey through the healthcare system. Now, at eleven years old, Jackson has undergone three open-heart surgeries and numerous other specialized procedures. He has experienced more hospital admissions than we can count, many of them due to infections unrelated to his heart condition. Through it all, Jackson has remained incredibly resilient. Most importantly, he is the sweetest child. His frequent hospital stays have given him a unique ability to empathize with and show kindness to others. As his parent, it is truly inspiring to watch him bring joy, comfort, and hope to so many people. Despite every challenge he has faced, Jackson continues to shine with strength, compassion, and an unwavering spirit.

Janan C.
#16 - Myers Riley Motorsports
Read My Story
My wife went to China to bring our son Janan home. We were told he would most likely not survive the flight. Upon descent to Orlando airport Janan's nose started to bleed and his lips and extremities were blue. We left the airport heading straight to the hospital. Many tests were run, and we were informed that they would try to give Janan meds and send us home for him to be made comfortable. They did not think he was going to live long or was a candidate for surgery. After several days in the hospital and regular nutrition, Janan started showing some improvement. They asked if we would like to attempt surgery making sure we knew that there was a strong chance Janan wouldn't survive the surgery. We said yes. Janan's surgery was a success! After 3 months in the hospital we came home with Janan. He was 3 1/2. Janan is now 13. Janan loves life, people, and Jesus. He never met a stranger, and everyone he meets becomes his friend in his eyes. He has attended Camp Boggy Creek for several years now. Without hesitation I can say that camp is the highlight of his year. The friendships he has made and the impact of camp is indescribable. We've experienced first hand the care they have for each camper and family, as well as the attention to their medical needs. We would not have been able to afford a camp like this for Janan. Janan is a light to so many. His early life as an orphan and his continued fight of being a congenital heart warrior has not dimmed his light. His name being represented this way would be one more way he could see that he is valuable and seen, and that his life matters.

Jireh V.
#52 - Bryan Herta Autosport with PR1/Mathiesen
Read My Story
Our journey began after yet another sick visit to our pediatrician, where a simple finger-prick blood test changed our lives forever. We were told to immediately go to our local hospital, and in the early hours of the morning, while in the ER, we received the likely diagnosis of infant B-cell acute lymphoblastic leukemia. Over the course of Jireh's two-year treatment journey, we spent 164 days inpatient, where he even learned to take his first steps. On February 11, 2026, he proudly rang the bell, marking the end of treatment. This experience has forever changed our family's perspective. We have learned to cherish the everyday, ordinary moments because life can change in an instant, and tomorrow is never promised. We are incredibly grateful to be where we are today and never take our health or time together for granted. I discovered the Austin Hatcher Foundation through an online support community and was overjoyed to find an organization that offered counseling services. As a single mom, I couldn't afford therapy on my own, and having access to counseling gave me the opportunity to begin processing the trauma of our journey and move beyond simply surviving. Having our son's name represented in this way means more than words can express. It reminds us that organizations like the Austin Hatcher Foundation and Camp Boggy Creek are committed to supporting families like ours while raising awareness for pediatric cancer.

Jo'bri C.
#37 - Intersport Racing
Read My Story
In 2018, Jo’bri was diagnosed with stage 1 Wilms Tumor. At the age of 3 and a half, Jo’bri was treated at the Children’s Hospital in Erlanger and later received her second diagnosis in May 2019. She received treatment again – with her second relapse she had to get an auto bone marrow transplant. Thanks to the Austin Hatcher Foundation we not only had activities to attend, but they played a huge part of our support system and have given us family therapy throughout the years, even after Jo’bri finished her treatment. Thanks to the Austin Hatcher Foundation we have been apart of many events and we will forever be grateful. Jo’bri has been now in remission since 2020. All Glory to God.

Josie O.
#2 - United Autosports USA
Read My Story
Josie was born with a rare genetic disorder at three days old, and it has impacted every aspect of our lives. 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.

Kasey L.
#27 - Heart of Racing Team
Read My Story
Kasey was diagnosed with acute lymphoblastic leukemia in 2018 when she was two years old after having weeks of unexplained fevers. She went through two and a half years of treatment and is now considered cured. Being a part of the Camp Boggy Creek family has meant the world to us- it gave us a place to connect as a family without worrying about appointments and treatments. Kasey still enjoys going to camp and loves to reunite with old friends as well as make new ones each year. We are so fortunate to have organizations that support families during really tough times.

Kensley C.
#14 - Vasser Sullivan Racing
Read My Story
Kensley was diagnosed right before her first birthday, at a local children’s emergency room. We went in for abnormal breathing. An x-ray was ordered, and we then discovered a tumor closing her airway. Kensley had almost all her big milestones throughout treatment. Before, she couldn’t walk or even really stand. Once the tumor was removed, those milestones came fast and easy. Her first birthday was spent receiving chemo, and we hadn’t been home in weeks. Kensley’s diagnosis completely flipped our world upside down, but it has brought us closer in faith and taught us to be thankful and soak up every single precious memory because you truly never know when it can change. The Austin Hatcher Foundation lifted us up when we were getting used to being out of treatment and offered an amazing experience we really enjoyed. It means the world to us to have such a big recognition on not only Kensley’s diagnosis, but childhood cancer all together. It truly is a blessing to be able to shine a light and offer support, and fun experiences for all of the kids.

Kylie T
#13 - 13 Autosport
Read My Story
Kylie was born seven weeks early with a traumatic brain injury due to lack of oxygen during her birth. The doctors didn’t give much hope for her future.She is unable to walk or talk or take care of the most basic needs. She is nonverbal but she has learned to communicate with us in her own unique ways. She has the biggest smile and an infectious laugh, and she lights up every room she enters, bringing joy to everyone in her life. Kylie loves going to school and socializing with her classmates. She goes to CECO which is a school with a specialized program for kids and adults like Kylie. Kylie has showed our family how important it is to always be kind to everyone we come in contact with because you never know what kind of challenges they might be facing. We are so proud to have Kylie’s name be represented. There are so many things that she is unable to participate in and the attention that this brings gives her such joy.

Landon M.
#23 - Aston Martin THOR Team
Read My Story
In July 2021, Landon was being treated (along with his sister) for what we thought was strep throat. When he was nine days into his antibiotic, his neck was twice its normal size - we went to the pediatrician's office, then to the emergency room. Later that night, we were escorted to the Oncology/Hematology floor. Landon contracted covid on a hospital stay in January of 2022 and suffered a stroke at the age of 14. He's still in therapy to this day working to regain use of his right ankle, foot, arm, and hand. Landon is the truest and purest person you'll ever meet. He went through every bit of treatment with a smile on his face for anybody he meets! Austin Hatcher has supported Landon in therapeutic ways as well as his three sisters. They offer outings, classroom (hands-on) learning of life skills, and a community where those that are alike can find solace. To have our son represented in this way through Resilient Racers is so amazing! He is a ROCKSTAR and we are so thankful this helps him feel that way!

Landon R.
#73 - Pratt Miller Motorsports
Read My Story
Landon was diagnosed with bilateral retinoblastoma at 11 months old and our world quickly turned upside down. Although the unthinkable happened, she was very resilient and impressed everyone around her with her strength and unwavering spirit. We are so grateful for the Austin Hatcher Foundation. It has given us a second home where our entire family receives specialized programming including counseling, grief support, camps, entertainment outings and more. Thank you to Resilient Racers for spreading awareness of pediatric cancer and recognizing the cancer fighters in our lives.

Landry G.
#59 - RLL Team McLaren
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On November 1, 2014, our son Landry was diagnosed with ALL leukemia before he was even two years old. Throughout his 3½ years of treatment, he faced every challenge with an incredible smile and positive spirit. One of our most memorable moments was watching his resilience and joy despite the difficult journey. The love and support of family, friends, and medical staff helped carry us through the toughest days. Landry’s journey taught us the true value of health, gratitude, and finding strength in the face of adversity.

Logan F.
#45 - Wayne Taylor Racing
Read My Story
t is a privilege to share Logan's story and extend our heartfelt appreciation for the support he has received. Since his epilepsy diagnosis at the age of two and a half, Logan has demonstrated remarkable resilience. In spite of 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. We are also incredibly thankful for the "village" of friends and family members who consistently stand by him. 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 the IMSA Resilient Racer Program and Camp Boggy Creek for offering programs that empower Logan to see his condition as a strength. Seeing Logan represented on a race car would celebrate his unique spirit and offer a message of love and encouragement to other children facing similar journeys.

Maddie K.
#77 - AO Racing
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Our daughter, Maddie, began her journey when she was born a day shy of 23 weeks gestation, weighing less than most people can imagine and spending her first 84 days in the NICU. When she finally came home, she relied on oxygen, a heart monitor, and a pulse oximeter, and later received a G-tube due to severe reflux and feeding difficulties. Through years of medical appointments and developmental follow-up care, she was diagnosed with cerebral palsy at nearly two years old. Maddie uses a wheelchair for mobility and works hard every week in physical, occupational, and speech therapies, but she has continued to show us that a diagnosis does not define a child’s potential, personality, or joy. Along the way, she has inspired our family with her resilience, determination, and ability to find happiness in every accomplishment, while also helping others see beyond disabilities and recognize the incredible strengths each child possesses. Camp Boggy Creek gave our family a place where Maddie could simply be a kid—fishing, horseback riding, creating art, and making memories alongside other families who understand our journey. Having Maddie’s name represented during the IMSA Battle on the Bricks is especially meaningful because Maddie absolutely loves cars—they are her favorite toys and one of her greatest joys. Seeing her name on a race car is a tremendous honor that celebrates how far she has come while helping raise awareness for children with disabilities whose courage, achievements, and dreams deserve to be seen and celebrated.

Marlowe D.
#43 - Inter Europol Competition
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Five years ago, Marlowe was diagnosed with JDM after developing significant rashes and muscle degeneration. Since then, she has endured medications, MRIs, countless lab draws, and 59 IVIG infusions, while continuing to meet each challenge with remarkable strength and resilience. Camp Boggy Creek has given her a place to feel understood, build confidence, make lasting memories, and simply enjoy being a kid. This summer, she completed her final IVIG infusion and is now officially in remission and off all medication, while continuing regular monitoring with her care team. Having her name represented on an IMSA race car would be an incredible celebration of how far she has come and a meaningful way to help more children experience the joy and community of Camp Boggy Creek.

Noah C.
#31 - Cadillac Whelen
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Noah has never known a life without challenges, but he has also never known a day without choosing courage. Living with severe Hemophilia B and Von Willebrand disease has taught him responsibility and resilience from a very young age, yet it has never taken away his passion for sports, adventure, or simply being a kid. Instead, these challenges have given him a remarkable sense of empathy and compassion. Noah is always looking out for others because he understands that everyone is fighting battles we cannot always see. Camp Boggy Creek has given Noah something truly special. It’s a place where he feels accepted for who he is, not for his diagnosis. It has helped him build confidence and create memories that remind him he is never alone in this. Having Noah’s name represented through the IMSA Resilient Racers program means more than words can express. It is a beautiful recognition of his courage, kindness, and unwavering spirit. We are so proud of the compassionate young boy he is becoming, and we hope his story reminds others that resilience isn’t just about overcoming challenges. It’s about choosing joy, lifting up those around you, and never letting a diagnosis define who you are.

Noah K.
#64 - Ford Racing
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Noah was only 3 years old when a hard lump on his jaw, high fevers, pain, and exhaustion led us through 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 our family already knew: life is precious, and no moment should be taken for granted. Camp Boggy Creek gave our family the gift of fun, joy, and connection during one of the darkest seasons of our lives. Having Noah’s name represented in this way means so much to us because it honors what he survived, reminds us of God’s faithfulness, and shows other families walking through childhood cancer that they are not alone.

Owen M.
#9 - Pfaff Motorsports
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Our journey began the moment Owen took his first breath, when he suddenly turned blue and panic filled the delivery room as we learned he was born with transposition of the great arteries, a life-threatening congenital heart defect we never knew existed. From that day forward, our family has walked through surgeries, uncertainty, and countless medical appointments, but Owen has faced every challenge with incredible strength and resilience. Now 13 years old, he is thriving—he loves basketball, sports cars, racing, and proudly collects Lamborghini Hot Wheels across his bedroom wall, reminding us daily that he is so much more than his diagnosis. Camp Boggy Creek has been an incredible gift to our family because it gives Owen a place where he feels understood, accepted, and free to simply be a kid among others with stories and scars like his. Having Owen’s name represented in this way means honoring not only how far he has come, but also the courage, hope, and perspective this journey has brought to our entire family.

Piper W.
#65 - Ford Racing
Read My Story
Piper has had a difficult start to life, being born with a complex congenital heart defect, combined immune deficiency, suffering a stroke at 2 days old, etc - a list that is much too long for such a young child. Piper was diagnosed with B-cell acute lymphoblastic leukemia (B-ALL) through a bone marrow biopsy after months of random fevers and hospitalizations with no clear cause. This diagnosis was devastating, but it brought out a side of Piper that we never knew was there. She has grown so much and has become this confident, outgoing, bright light that touches so many people everywhere she goes, never letting her setbacks dull her outlook and shine. We have been so blessed to be connected to with so many organizations, families, and events in our pediatric cancer community and have truly been held up and carried through this journey when the weight was too much for us to carry alone. Being connected to the Austin Hatcher Foundation has been incredible. The way the Austin Hatcher Foundation heals the WHOLE family is much needed. The journey is difficult for the patient and caregivers, but the siblings are impacted just as strongly and need so much help and attention to navigate the diagnosis, too. Having Piper, her story, and her presence represented in this way is an honor for us to help bring a spotlight to the pediatric cancer community. This attention helps to continue further funding for research and provide comfort for families going through this so they know that they are not alone during this unimaginable time.

Porter P.
#25 - BMW M Team WRT
Read My Story
Porter was diagnosed with rhabdomyosarcoma in January 2026. He underwent surgery to have his tumor removed and and is now receiving 24 weeks of chemotherapy. We have felt such support from the Austin Hatcher Foundation providing our family with therapy and opportunities for camp, allowing Porter to interact with other peers affected by pediatric cancer. Porter has a five-year-old brother named Keller and a 10-year-old sister named Amelia. This journey has made us realize the importance of community and giving ourselves grace as a family. To appreciate the important things and slow down. To have his name represented would be an enormous highlight as we wrap up our journey with cancer this coming July.

Quinn W.
#120 - Wright Motorsports
Read My Story
On April 20, 2020, our lives changed in an instant. As we headed out for a family walk during the shutdown, Quinn suddenly collapsed and suffered a terrifying tonic-clonic seizure that lasted more than 30 minutes. Thankfully, our neighbors--both nurses--rushed to help and urged us to call 911. More than six years later, after multiple procedures, dozens of medication trials, surgery, and a specialized diet, Quinn still faces near-daily seizures. Epilepsy is far more than seizures alone--it impacts learning, development, and emotional and mental well-being, leaving lasting effects with every episode. We are deeply grateful for the family weekends at Camp Boggy Creek, where we found a community that truly understands this journey. There, Quinn met friends who share similar challenges and discovered that he is not alone in this fight. Just as race cars zoom lap after lap around the track, we hope Camp Boggy Creek keeps its engine running for generations to come--speeding into the future, giving kids and their families a safe and welcoming pitstop, filled with belonging, community, and joy! If Quinn could share a message with others, it would be this: You are stronger than you know. Inspired by his role model, Lily Hevesh of Hevesh5, he lives by these words, "Whatever life throws your way, KEEP ON BUILDING!"

Remi R.
#81 - DragonSpeed
Read My Story
In 2021 we were on vacation in Minnesota when Remi suddenly stopped walking. This is our 3rd year cancer free and every year is a big milestone! This has showed us how many children are impacted by cancer. Camp Boggy Creek has given the opportunity to spend time as a family one week per year and allow my kids to spend a week away to have some quality time and make new memories with kids and families that understand this journey! It means victory and awareness for us!

Ryder R.
#24 - BMW M Team WRT
Read My Story
Ryder started having leg pain and things progressivly got worse. We took him to a pediatrician, who ordered bloodwork and x-rays. He then saw an orthopedic surgeon. The next day they did an MRI, and I knew it wasn't good news when 8-10 doctors walked in. Over the next few days, Ryder got extra fluid drained from his brain and had a 7-hour-long brain and spine surgery to get a shunt put in and remove a small piece of the cancer out of his spine to biopsy.
We spent Christmas at the hospital that year. In January, Ryder started 18 months of chemo. He was 5 years old.
He is now 10 years old. He attended Camp Boggy Creek this year for the first time and had a blast and met kids that he has stuff in common with.

Summer D.
#11 - TDS Racing
Read My Story
Summer’s journey began in the summer of 2025, when a sudden fracture in her left leg led to the devastating diagnosis of osteosarcoma at just seven years old. Since then, she has faced nine months of chemotherapy, an above the knee amputation, two lung surgeries, blood clots, and countless hospital visits with extraordinary courage, strength, and determination. All while being over 800 miles from the rest of her family and anyone she knew. Through every difficult moment, Summer has taught our family to appreciate the smallest victories, live more fully in the present, and never take an ordinary day together for granted. Camp Boggy Creek helped remind Summer, and our entire family, that we are not alone by providing understanding, encouragement, connection, and opportunities to experience joy beyond cancer! She was also able to connect with another girl amputee cancer survivor and have since become great friends. Having Summer’s name represented in this way is a beautiful celebration of everything she has overcome and a lasting reminder of the bravery, hope, and light she continues to bring into the lives of everyone around her.

Taylor C.
#7 - Porsche Penske Motorsport
Read My Story
Taylor was 8 when she had her first seizure. She has endured hospital stays, testing, countless doctors visits but finally has found a treatment that has her epilepsy better controlled. Taylor is a warrior, and is a role model for how you can overcome fear a seizures to return to activities such as swimming. Camp Boggy Creek was an important milestone for her, giving her a safe and encouraging environment to enjoy summer camp and many new activities like riding a horse.
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Donate to honor a child by placing their name on a race car!
All proceeds from the Resilient Racers campaign will be split between IMSA's official non-profit partners: the Austin Hatcher Foundation for Pediatric Cancer and Camp Boggy Creek.
Your donation celebrates a child's strength and courage and supports essential services for children facing serious illnesses. Let's make an impact together.
To learn more about the non-profits' missions please visit the links below:
Your donation celebrates a child's strength and courage and supports essential services for children facing serious illnesses. Let's make an impact together.
To learn more about the non-profits' missions please visit the links below:


