Where kids are #1!
At Dayton Children's, our patients are what make us who we are. Every single child that walks through our doors is special and deserves to be treated as if they were #1.
Whether they visit us with a broken bone or for chemotherapy, each of their stories are unique and important. They are stories of hope and determination. Stories of love and care. We invite you to take the time and read about some of our patients and how we make them #1. Or visit our Youtube channel to see their videos. We can guarantee you will be inspired and encouraged by their stories.
To say that the Minor family are frequent flyers of Dayton Children’s is an understatement. Their two children Jay and Joy are regulars at Dayton Children's being treated in over eight clinics throughout the hospital
Battle against a brain tumor
At only five years old, Carson Bailey was diagnosed with medulloblastoma, a brain cancer that had the ability to spread to other areas of the central nervouse system, including the spinal cord. Carson quickly underwent surgery to have the brain tumor removed and then received 31 doses of radiation and nine cycles of chemotherapy. Now two years into remission, Carson has returned to the Optimus Prime loving, chicken joke sharing kid he was before.
Breathing a sigh of relief: First airway reconstruction a success
Born prematurely, and weighing only two pounds, Lainey Perry spent the first seven months of her life in the NICU at Miami Valley and then at Dayton Children's due to breathing difficulities. Doctors attempted to dialate Lainey's airways several times, but each time resulted in a collapse. So at just seven pounds, Lainey became Dayton Children's very first airway reconstruction patient.
The road to healthy
When you first meet Emily you know you are meeting someone special. This sassy red head can brighten up any room with her big smile and laugh. But Emily is not your normal 10 year old. Diagnosed at 17-months with Type 1 diabetes, a life of insulin injections and counting her carbs is the only life that Emily knows. Recently Emily made big strides in her journey with diabetes by opening up and sharing with her classmates about her condition. Emily is also benefiting from new health care technology as she wears an insulin pod instead of a pump which gives her more flexibility and control. Also, free of wires, it allows her to do one of her favorite activities – hula dance, complete with a grass skirt.
Holding tight to happiness
Andray Simmons has a permanent smile on his face. You can’t help but smile back when talking to him. You would never know that he lives every day fighting the pain that comes along with sickle cell disease. Even though it can be very painful, Andray refuses to miss school due to his condition and never lets it bring him down. As a frequent flyer of Dayton Children’s, Andray also serves on the Kids’ Advisory Board providing input into the design of the new patient tower. Through this role and as an ambassador, Andray uses his experience with sickle cell to teach others and encourage patients along their journey.
Together we fight
There’s a saying that lightning doesn’t strike twice, but Caulin’s family would say differently. Caulin was diagnosed with Acute Lymphoblastic Leukemia with T-cell when he was in the third grade. After a difficult treatment journey, including a bone marrow transplant, Caulin was then diagnosed with a second cancer, lymphoma. Thanks to the care provided to Caulin in children’s hospitals, Caulin is currently in remission and is an active young man who enjoys playing soccer, golf and helping other families in need. Along with close family friends who also beat childhood cancer, Caulin and his family started a family-based charity, “Together We Fight,” designed to support future families who hear the words, “Your child has cancer.”
A mother's hero
Gabby is a star soccer player and can run a six-minute mile. But unlike many other kids her age, Gabby hasn’t gone through the normal training to get to this point. At the age of 6 doctors discovered that Gabby’s airway was the size of an infant’s, making it very difficult for Gabby to breathe. Gabby underwent an emergency surgery and was placed in a medically-induced coma. After recovery, Gabby began seeing the pulmonary specialists. She also began intense physical training with her mom to improve her breathing and ultimately save her life! As Gabby grows her airway continues to grow, and today Gabby is an active and engaged teenager ready to take on the world!
Living with an invisible illness
In his four short years of life Trevor has already been hospitalized 16 times due to living with celiac disease. But this boisterous 4-year-old hasn't let it slow him down! Learn more about Trevor's journey including diagnosis and how his family manages his disease.
Surviving monsters inside you
Although Ethan Conley is described as “fearless with faith,” faith took on a new meaning after Ethan survived Dayton Children’s only diagnosed case of viral myositis with rhabdomyolysis. This extremely rare virus caused his muscles to break down, leading to multiple organ failure and 7 days on advanced life support.
200 seizures a day to zero
Low-carb diets have been in and out of the news for years as a way to lose weight, but in the case of 6-year-old Chloe Busch, this unique type of diet helped her reduce seizures from up to 200 a day to zero.
Hope lives at Dayton Children's
Two decades after Matthew Birdsall was a patient at Dayton Children's, his daughter Sophia was pronounced dead – twice – from hypoxia, or lack of oxygen to the brain during birth at a local hospital. Thanks to the hope his wife Melissa, him and the NICU staff held onto, Sophia left with her family after 22 days in the NICU at Dayton Children’s.
Our Very Best
You may not expect us there, and you may not even realize how close we’ve grown to you. But in the end, we find ourselves right where we want to be – part of your family. Dayton Children’s is now Magnet recognized for nursing excellence.
Up and Running
Michael Albert, MD, director of sports medicine and orthopaedics at Dayton Children’s, along with the company that developed Grace Norman's cheetah foot, have kept her up and running with the goal of making the 2016 Paralympic team.
Dorian and Derek Lowen from Springboro are your typical brothers. They pick on each other but at the end of the day love spending time together. What makes Dorian and Derek a-typical is the fact that they are living life together both with a genetic blood disorder. The Lowen brothers have hemophilia severe factor 9. They were both diagnosed as infants and have grown up learning how to manage this lifelong condition together
Seeing cancer as an opportunity
In March 2013 Mariah was diagnosed with anaplastic large cell lymphoma. Mariah immediately began treatment and spent most of her spring and summer at Dayton Children’s. Mariah is no longer in treatment and has come out of this experience with an extremely positive attitude seeing cancer as not a burden but rather an opportunity to look at her life in a new light!
Breathing strong on and off the field
Nick Thomas plays everything from baseball to basketball to wrestling and soccer. Watching him, you would never know that Nick lives every day with cystic fibrosis. Diagnosed at 5 months old, Nick has spent his life in and out of Dayton Children’s seeing pulmonary specialist Gary Mueller, MD. Even though Nick is extremely active, he still has to spend every day giving himself treatments to help him breathe. However, Nick keeps a positive attitude and is thankful that Dayton Children’s is close to home to help care for him.
Getting her seizures under control
Parker McCalip began having seizures when she was in second grade. Since being referred to the neurology department at Dayton Children's she has learned how to keep her seizures under control. Parker is a 2014/2015 Dayton Children's ambassador
Cancer care close to home
Gabe Duplechian was diagnosed with acute lymphoblastic leukemia at age 7. He is seen by the hematology/oncology specialists at Dayton Children's Hospital.
The newest, non-surgical technique corrects a common deformity
When Liam Back was born just nine months ago, he was born with a very common deformity. His ears were “floppy.” Infant ear deformities occur at a rate of between 20 percent and 35 percent of all births, making it one of the most common abnormalities.
Landon's Lust for Life
Riding a horse for the first time is a magical moment for most children, a milestone that speaks of the essence of childhood. Growing up in Jackson Center, Ohio, Landon Reese has been around horses since he was 6 months old.
However, in June 2012, the animal that Landon loved so much brought him close to death, placing him on a path that now has far different milestones than other children.
Back to baseball after brain surgery
Cameron Caldwell is 11 years old. His idol is Starlin Castro who plays short stop for the Chicago Cubs. His secret weapon in baseball is his slow pitching style. His favorite subject is math. He has a little brother named Caleb. To anyone who meets him, he seems like any other kid his age: smart, talkative, in love with baseball. What most people don’t know about Cameron is the sport he loves so much almost killed him.
The patient experience expert
Kelsey Colins, 16, from Bellbrook was diagnosed with type 1 diabetes at age four.Since her diagnosis Kelsey has worked with physicians at Dayton Children’s to help manage her diabetes by controlling her insulin intake and her dietary needs. Recently Kelsey was also diagnosed with hyperthyroidism as well as Addison’s disease.
Meghan Mays, 17, from Centerville was diagnosed with scoliosis at age six and began seeing Mike Albert, MD, orthopaedic surgeon at Dayton Children’s. After nine years of wearing different back braces to try to fix the problem it was decided that Meghan would need surgery. Her back had gone from a 20 degree curve to 54 degrees. Dr. Albert performed spinal surgery on Meghan in December 2011 and placed two rods and 16 screws in her back to straighten her spine. Today Meghan is standing a little taller and is extremely active in cross country and working at multiple part-time jobs. Meghan wants to be a nurse when she grows up because of the amazing care the nurses at Dayton Children’s gave her while she was here.
A true inspiration
Kristopher Rodgers, 13, from Springfield has been living with a diagnosis of cystic fibrosis (CF) since he was 6-months-old.Since then he has been seen in the pulmonary clinic at Dayton Children’s in order to manage this lifelong condition. As a young child Kristopher spent many days as an inpatient at Dayton Children’s but today has gone seven years without having to be admitted. Kristopher has matured quickly and has learned how to manage and perform treatments for his CF on his own. Even though CF often makes it difficult for Kristopher to breathe sometimes he has not let this stand in his way. Kristopher recently began taking karate lessons and is already on his way to his purple belt!
A young philanthropist
Kayleigh Crabtree, 11, from Beavercreek was diagnosed with Acute Lymphoblastic Leukemia on August 20, 2010. Kayleigh underwent five rounds of chemotherapy under the care of Mukund Dole, MD at Dayton Children’s. Kayleigh is a true philanthropist at heart and has helped to raise tens of thousands of dollars for pediatric cancer research during her battle with the disease. Kayleigh completed her last round of chemo in fall 2012 and is excited to be an ambassador so that she can help other kids at Dayton Children’s!
Katie Hollingsworth, a senior at National Trail High School in New Paris, is one of
the top students in her class and survived multiple organ failure due to cancer. A child life specialist at Dayton Children’s helped Katie set up an online blog to stay in touch with her friends during the 264 days she spent at Dayton Children’s. These excerpts are her story of courage, hope and survival.
Meet the cast of “The World of Hope”
How children deal with chronic illnesses, such as cancer, is completely different than adults. To shine a light on how children fight the battle of cancer, Dayton Children’s created “The World of Hope,” a video that showcases how children use their vivid imaginations in a world of make believe to cope with living in a world of chemotherapy, radiation and staying for weeks in a hospital.
Basketball player slam-dunks sports-induced asthma
Kristen Stryker never thought she had asthma, she
just assumed she was tired during basketball, until she
collapsed one day during practice. Kristen, a sophomore at
Franklin Monroe High School, is a starter for junior varsity
basketball and is also a pitcher for varsity softball. But two
years ago, she noticed she was short of breath during practice.
Every breath you take
One little boy fights a lifelong battle to breathe as a result of 22q deletion syndrome.
Recovering by leaps and bounds
Rachael Hayes, a seventh grader, is still on the road to her dreams of becoming a professional dancer, even after major knee surgery.
The World of Hope
In their World of Hope, the kids aren’t fighting cancer - they imagine themselves as a cowboy fighting bandits and a knight slaying the dragon. They aren’t taking chemotherapy or having an MRI - they are a princess with a magic potion and an astronaut going into the healing space. Take a moment to visit the World of Hope where you will meet four young heroes from our community who are battling cancer.
Saving Baby Bailey
Meet the Stager family from Troy, Ohio, whose 15-month-old daughter Bailey was saved at Dayton Children's after she came down with a life-threatening virus.
31 days to a miracle
Ethan came to Dayton Children’s in January 2010 and was diagnosed with an extremely rare virus called viral myositis with rhabdomyolysis. Ethan spent 31 days at Dayton Children’s. During this time he was unable to walk and had to be placed on dialysis. He spent 19 of those days in the pediatric intensive care unit fighting for his life. Read more about Ethan's story to see what happened.
A long and winding road to remission
At age 14 Katie was diagnosed with acute myelocytic leukemia (AML). AML is a form of leukemia that is not very common in children and has only 40 percent survival odds. Katie began seeing Dr. Broxson and underwent five rounds of chemotherapy. She faced a number of other complications throughout her treatments which required her to stay in the pediatric intensive care unit at Dayton Children’s. Today Katie is in remission from her cancer and is a happy and energetic teenager.
Taking control of a chronic disease
Awo was born with sickle cell anemia. Sickle cell disease is an inherited disorder in which red blood cells (which are normally round and flexible), are sticky, hard and shaped like crescent moons. Due to her sickle cell, Awo often experiences a lot of pain in her joints and bones. Awo sees Dr. Dole in the hematology and oncology clinic at Dayton Children’s. Despite her illness, Awo has a very positive outlook on life and doesn’t let her sickle cell slow her down.
Never slowing down
Justin was born with spina bifida, a birth defect that involves the incomplete development of the spinal cord or its coverings. Since birth Justin has had over thirty surgeries and has seen 14 different specialties at Dayton Children’s. Even though his condition has required him to be on crutches or in a wheelchair, Justin is still extremely active. He has tried almost every sport that he could including soccer and baseball, but his real love is basketball. He also plays the French horn in his school’s band.
The right specialists all the time
Sara and Todd Cutter of Liberty Township were typical of first-time parents until the unexpected happened. Two days after Amelia was born, doctors discovered the baby had a rapid heartbeat and needed specialized care. Amelia was transported to Dayton Children's Regional Level III B Newborn Intensive Care Unit (NICU).
Make the right choice when choosing a NICU
Crystal and Chris Crane of New Lebanon are researchers--not as professionals, but as parents. And when Crystal found out they were expecting twins, both wanted to be as prepared as possible. They knew there was a chance their twins would come early, so Chris researched area hospitals to determine which were best prepared to care for premature babies if that care was needed.
A world full of sounds- 20 years later
In 1991, Ashley Sorensen was one of the first patients to ever receive the cochlear implant allowing her to go from a world of silence to a world full of new sounds. Over 20 years later, Ashley is still benefiting from her implants. Her successful surgery at Dayton Children's has inspired her to go on to school to become a hearing aid specialist.
Family taking care of family
When her 7-year-old daughter Paige started feeling poorly in May 2008, Jill Lord didn’t think too much about it. But when the flu-like symptoms persisted for a few more weeks, she was worried. Paige was diagnosed with acute lymphoblastic leukemia (ALL), a cancer affecting the white blood cells and began treatment at Dayton Children's.
Never underestimate a fall
Erin Bruner, 14, never thought that one basketball game would change the whole course of her eighth grade year. However after suffering from a concussion during one of her games, Erin would go on to have a severe headache for nearly six months.
Avenego and Emma Hernandez do not speak a word of English. However, thanks to interpreters, this has never prevented them from getting first-class medical care for their son, Benjamin, 4, right here in Dayton, Ohio.
When the unexpected happens - Newborn Intensive Care Unit
Kelly Watts had a completely normal pregnancy. On March 2, 2011 she gave birth at Miami Valley Hospital to a beautiful 10-pound baby girl, Ryleigh. She never expected that two weeks later her precious newborn would be in the Regional Level III Newborn Intensive Care Unit (NICU) at Dayton Children’s.
A Special Day Takes a Traumatic Turn
A surprise Memorial Day 2011 trail ride at Englewood Reserve quickly turns tragic for Olivia Fowler. Fortunately, the Soin Pediatric Trauma and Emergency Center was just moments away.
Changing Habits Out of Love
In April 2009, 8-year-old Ghiman McKinney’s pediatrician was concerned because he was gaining more than ten pounds each year and already weighed 105 pounds.
Small in Size, BIG in Personality and Heart
Kaitlyn Dove, 12, has had more medical complications in her life than most people could even imagine having. Even with multiple heart and lung conditions as well as a variety of other complications, Kaitlyn continues to have a positive outlook on life and always wants to help others.
Never Asks "Why Me?" - A Spinal Cord Surgery Success Story
Patrick Bleser, 16, has spent his whole life in and out of Dayton Children’s for vast medical issues and has been through eight surgeries, but you wouldn’t know it talking to him. Patrick doesn't let his medical problems dictate his life but rather goes into each day with a positive attitude and his stellar smile!
Seeing Life Differently - Dayton Children's Cancer Center
At the age of 5 months, Colin Beach was diagnosed with a rare malignant tumor in the retina of his eye. Despite the severity of his disease and the number of surgeries he has needed – his parents stopped counting after 30 – Colin, now 10 years old, has learned to accept it as part of his life.
A Fighting Spirit
Hanna Katherine Ying Lebamoff has been amazing her mother and the care team at Dayton Children's since she was adopted by Mary Chellis Lebamoff in 2006.
Happy-Go-Lucky Little Miracle
The mother of Gabrielle Smelko, now seven years old, was told her newborn daughter had a slim-to-none chance at living. Gabrielle was diagnosed with a diaphragmatic hernia which also included the need for a tracheal tube and a Gtube. She is a happy little girl, but without the help of Medicaid her mother says it would not have been possible.
Not So Sweet Summer
Ken Luke, an 18-year-old from Beavercreek, has taken charge of his diabetes.
What We Never Expected - Pediatric Cancer
At just two years old, Donovan Trentham's routine evaluation appointment turned out to be a visit that no parent or child would want to experience; he was diagnosed with stage three neuroblastoma. With immediate treatment and care, Donovan is now cancer free two years later.
An Accidental Summer Burn
Owen Sanford, ten-years-old, suffered from a serious in home burn that took place on their treadmill. After his parents arrived home to discover his devastating burns, they rushed him to Dayton Children's where treatment was addressed quickly.
Scoliosis Surgery to Senior
In 2009, Shirray Burnside had been diagnosed with scoliosis and was quickly scheduled a surgery date to correct her spinal curve. After a summer long recovery, Shirray now enjoys a typical and active senior year.
Seen and Heard
What families are saying about the care they receive at Dayton Children's.
Comfort Alleviated the Uncontrollable
Nine month old, Selah Knopp was rushed to the hospital when her father Joe found her suffering from a spiked fever and uncontrollable chills. Selah’s parents were greeted with calming spirits and control while she was treated immediately at the hospital.
The miracle of a premature
Mandie Yannitti's routine pregnancy visit turned into a Cesarean section birth of her son Carmine, at just 26 weeks. With a 15 percent survival at birth, three and a half months later, Carmine was allowed to go home where he now weighs a happy and healthy baby. Carmine has also been recognized as the smallest baby ever cared for at Dayton Children's NICU.
Strived for strength, thriving at life
On Christmas Day 2008, Immanuel Vaughn was born at just 26 weeks. Through continuous care and difficult decisions, Immanuel was considered a “Miracle in Progress” during his stay at the hospital. Now, Immanuel is an energetic toddler keeping his parents busy.
Teen Hurdles Through Her Disease
At an early age, Taylor Bush was diagnosed with a moderate stage of cystic fibrosis. Dealing with the daily struggles has become part of her routine and regardless of her condition she is active in track, onstage productions, and gaining a love for animals.
Poster Children for Awareness
Sydney and Antonio Copher have been selected to share the title of Ohio Sickle Cell and Health Association for 2009-2011 as their Ohio Poster Children. These two siblings represent the sickle cell community and gain on-going opportunities through promoting awareness for their disease.
Cancer Remission Drives His Inspiration
Since 1997, Michael Dosedel has been in remission from a stage four, rare muscle cancer which was found in 1996. Being in remission has inspired Michael to start a non-profit organization and to one day become an orthopedic surgeon or diagnostician.
A Tumor to Live and Grow With
After finding a tumor on Emily Staggs pituitary gland, doctors soon determined during surgery that the tumor was fortunately benign, however inoperable. Emily undergoes several routine treatments and check-ups, but happily continues to live an active, 13-year-old life.
From Sickle Cell to Spotlight
Shayla Ellington was diagnosed with sickle cell anemia at an early age, but has left her with no excuses as to making astonishing accomplishments in her life. Along with consistently receiving top grades, Shayla also enjoys being the center of attention and has high hopes of becoming an R&B singer one day.
Guardian Angel to the Rescue
A fall from the monkey bars and a CT scan later, Abigail Kurdin learned that she had a rare malformation, probably present since birth, at the base of her brain. Since the surgery, Abigail has a positive outlook on life and places a special value on showing off her scar left by the surgery.
Not your Typical Teenager
At just 13-years old, Kyle Crawford was diagnosed with Type I diabetes. After a visit with their family doctor, he was quickly admitted to Dayton Children's to treat and learn the process of managing his diabetes. Now, at 15-years old, he knows how to control his illness and has achieved living an active teenage life.
Tough Times Calls for Strength and Spirit
As a newborn, Chardanai White was diagnosed with sickle cell disease and as anyone would be her parents were shocked to found out the news. A few years later Chardanai was also diagnosed with von Willebrand disease and a blood disorder called Beta Thalassemia. Despite her illness, Chardanai manages her diseases and tries to live a community active childhood.
It's Cool to Tell My Story!
Bailey Allen is an active girl involved in dance, soccer, softball, and basketball; concealing that fact that she even had cancer. At just six weeks old, Bailey was diagnosed with a cancer called congenital fibrosarcoma, which left her parents devastated as her right leg may have had to be amputated.
Grew Four Inches in One Day - A Spinal Surgery Success Story
In 2008, Burr Simpson underwent a six and a half surgery to correct a curvature in his spine due to kyfosis and scoliosis. A week after his surgery, Burr left the hospital standing tall, proud and a success as being the first patient in the country to have underwent this procedure.
Fighting the Bad Guys
Continuous complaints of leg pain, and the return of the Ormsby’s 2006 family vacation changed their lives as Nathan Ormsby was diagnosed with Neuroblastoma, a common childhood cancer. Now, three years later he continues his tough treatment, but has also continued to show a positive attitude towards life.
A Family Deals, Three at a Time
Non-stop crying and struggling to eat, Adrianna Scott was diagnosed with cystic fibrosis at just six months old; then at just two years old, Adrianna’s twin sisters were also diagnosed. Despite their challenges as a family, Adrianna especially has learned to not let cystic fibrosis prevent her from accomplishing her goals.
A Walking Miracle
When Mitchell Franzer was diagnosed with spina bifida at birth, his family was told he would never walk. With constant training and a positive attitude, Mitchell proved them wrong.
Small but Mighty
Layla Musgrove was born prematurely at 1 lb. 2 oz. with fluid in her brain, and needing heart and eye surgeries. Despite a scary beginning for Layla’s family, together they fought through for a happy ending.
Nothing will keep him from college
Justin Ferrene was born 11 weeks early and diagnosed with cerebral palsy at 10 months. Despite many obstacles, Justin is determined to graduate from college and follow his dream to be a teacher.
Beating Brain Cancer Every Step of the Way
When 11-year-old Casey Mowen was diagnosed with brain cancer, he was more concerned with making the grade and playing soccer than losing his hair. But with a brave attitude, Casey came out on top- both in the classroom and in life.