Say HELLO to
OAAT Campaign Kids!
Leah Faith Soner
Leah is a 4-year-old girl from KY who was diagnosed with x2 Relapsed High-Risk B-cell infantile Acute Lymphoblastic Leukemia s/p BMT in November of 2019.
She has faced unimaginable challenges in her young life. She cherishes her family and has a special bond with her aunts, uncles, and grandparents.
Leah, once a healthy baby, faced a drastic turn in her health at seven months old, leading to a diagnosis of High-Risk B-cell infantile Acute Lymphoblastic Leukemia. This sudden and agonizing news transformed her from a happy, healthy child to a fragile one. Her treatment journey included numerous chemotherapy rounds, a bone marrow transplant, dual CarT therapy trials, and a stem cell transplant across different hospitals. She endured multiple relapses, PICU stays, and various medical procedures, experiencing severe complications like swollen organs, severe anemia, and critically low hemoglobin levels.
Leah Faith had infantile ALL, a more challenging and intense form of the disease. Her mom faced a tough journey alongside her.
That's why we're on a mission to raise $5000 to fund a dream trip for Leah and her family, offering an exclusive opportunity to experience Disney and Give Kids the World. This unique journey will enable them to create new, joyful moments in a different setting, providing a break from their current hardships!
Kyleigh Beasley
Kyleigh is a 7-year-old girl from North Dinwiddie, VA, who was diagnosed with Rhabdomyosarcoma in June of 2022.
Kyleigh, a vibrant and adventurous individual, enjoyed various activities like going to the park, shopping, trampoline fun and being a cheerleader before her diagnosis. She had to stop cheerleading due to treatment. Her interests now include riding horses, trying hip-hop dance, and soccer.
The discovery of a lump on her left forearm, accompanied by unexplained fevers, led to the diagnosis of Rhabdomyosarcoma, a rare type of cancer. Finding suitable treatment and doctors familiar with this cancer was difficult, significantly impacting the family's lifestyle. This resulted in a change where a parent left their job to care for Kyleigh and their other children, switching to homeschooling.
Since the diagnosis of stage 3 Rhabdomyosarcoma in June 2022, Kyleigh began chemotherapy in July, lasting for nine months, along with 33 radiation sessions and surgery to remove the tumor from her arm. Currently, she's undergoing a 6-month maintenance chemotherapy phase, with upcoming scans in November.
That is why we are on a mission to raise $1,000 to provide Kyleigh with a joyful experience of a Disney-themed birthday party as she approaches her 9th birthday in December. This celebration aims to create precious moments for Kyleigh, offering a temporary escape from her challenges and filling her heart with warmth and hope!
Abigail Alvey
Abby is an 8-year-old girl from Richmond, VA, who was diagnosed with Niemann Pick Type C in March 2019.
Abby's journey to diagnosis was challenging due to the rarity of her disease. She was born healthy with no initial red flags but started showing symptoms of gallbladder and liver issues, leading to an initial misdiagnosis that persisted for several years. It was only after seeking a second opinion at CHOP and later consulting a metabolic specialist that Abby was finally diagnosed with Niemann Pick Type C (NPC). The diagnosis revealed that her entire family carried the genetic disorder.
To manage her condition, Abby entered a trial medication program at the National Children's Hospital, involving spinal infusions every two weeks. She also attends numerous appointments in various locations, including Chicago, Maryland, and D.C., and undergoes regular therapy. Abby requires assistance with walking and understanding her needs.
Abby's diagnostic journey underscores the importance of finding the right doctor at the right hospital to fully understand her symptoms and provide her with the correct diagnosis and challenging prognosis.
Her family holds onto the hope that the medication received through a spinal infusion every other week, 2 hours from her home, will keep her disease progressing slowly. NPC has no cure, so they take each day as it comes.
Her dad said, “She would just be happy with nearly anything. She always talks about going to Disney World. She dreams of being a YouTube star, too. She loves to talk about traveling to another country to see a castle.”
Our goal is to gather $5,000 to send Abby and her family on a magical journey to Disney World and Give Kids the World. This incredible experience will let them cherish moments of joy in a place where their current challenges can momentarily fade away, filling their hearts with warmth and hope!
Leah Faith Soner
Leah is a 4-year-old girl from KY who was diagnosed with x2 Relapsed High-Risk B-cell infantile Acute Lymphoblastic Leukemia s/p BMT in November of 2019.
She has faced unimaginable challenges in her young life. She cherishes her family and has a special bond with her aunts, uncles, and grandparents.
Leah, once a healthy baby, faced a drastic turn in her health at seven months old, leading to a diagnosis of High-Risk B-cell infantile Acute Lymphoblastic Leukemia. This sudden and agonizing news transformed her from a happy, healthy child to a fragile one. Her treatment journey included numerous chemotherapy rounds, a bone marrow transplant, dual CarT therapy trials, and a stem cell transplant across different hospitals. She endured multiple relapses, PICU stays, and various medical procedures, experiencing severe complications like swollen organs, severe anemia, and critically low hemoglobin levels.
Leah Faith had infantile ALL, a more challenging and intense form of the disease. Her mom faced a tough journey alongside her.
That's why we're on a mission to raise $5000 to fund a dream trip for Leah and her family, offering an exclusive opportunity to experience Disney and Give Kids the World. This unique journey will enable them to create new, joyful moments in a different setting, providing a break from their current hardships!
Isaac Wicklund
Isaac is a 15-year-old boy from Ramsey, MN, who was diagnosed with Myasthenia Gravis and cryopyrin-associated periodic syndrome in September 2018.
Before diagnosis, he was very caring and thoughtful. He's also really funny with a quirky sense of humor. He enjoys making funny videos with friends, cracking jokes and especially loves sharing dad jokes.
Isaac has faced ongoing challenges with his immune system, coping with a difficult CAPS diagnosis that caused various childhood symptoms. Over time, he developed muscle weakness, affecting his daily life. In 2022, he was diagnosed with Myasthenia Gravis, impacting muscle control and leading to multiple instances of respiratory failure, necessitating ICU admissions and extended ventilator use. Isaac not only has Myasthenia Gravis but also significant hearing loss in one ear and profound loss in the other. Moreover, he deals with gastroparesis, affecting his food digestion. To manage this, he travels from Minnesota to California every 6-8 weeks for a sedated procedure, essential for nutrient absorption. His health conditions have led to complications.
His mom said, “I explain it to people sometimes like it feels like there's, you know, sometimes when you get a tornado that's big enough, it'll spin up these side tornadoes, kind of, that's how it feels that we have this big tornado.” Isaac should be driving by now, but his health condition prevents it. The family has had to cancel many vacations and miss important events like holidays due to medical commitments. Last year, during his older sister's wedding, Isaac was in the PICU on a ventilator, highlighting the unfortunate timing of his hospitalizations. This emphasizes how frequently he is hospitalized.
That is why we’re on a mission to raise $10,000 to fund a special trip for Isaac and his family to Hawaii. This journey will offer them a chance to make happy memories in a different setting, providing a break from their current challenges!
Cye Zamora
Cye is a 4-year-old boy from Albuquerque, New Mexico, diagnosed with High-Risk Acute Lymphoblastic Leukemia in May 2023.
Before his diagnosis, Cye enjoyed outdoor activities, dancing, singing, family vacations, swimming, playing with toys, and spending time with his siblings and friends. He was energetic, cheerful, funny, and talkative and had an impressive knowledge of dinosaurs.
However, when he started experiencing symptoms like knee pain, fatigue, a low appetite, sudden bruises, refusal to walk, pale skin, and swollen lymph nodes behind his head, his mom took him to the Emergency Room. His mom initially thought he had a cold but felt something was wrong. After a second opinion at urgent care, they rushed to the main hospital, where he was diagnosed with High-Risk Acute Lymphoblastic Leukemia
Since being diagnosed, Cye has had difficulty walking and developed neuropathy. He deals with fatigue, nausea, weight fluctuations, and changes in appetite. He also experiences sporadic physical pain and emotional ups and downs, missing his family and friends and the ability to enjoy outings.
Cye has a strong passion for dinosaurs and superheroes, using their courage as inspiration when facing fears. He often says, "I'll be strong like Hulk!" and "I'm tough like a T-Rex."
Cye has undergone extensive medical treatments, including chemotherapy, transfusions, and procedures, leading to isolation, hospital stays, and side effects requiring medication adjustments.
His mom said, “This dream would be a chance to experience joy and give him a light amid what he has to endure. It would allow us to let go of our current stresses, anxieties, and fears and enjoy the smiles on each other's faces.”
That is why we are on a mission to raise $5,000 to send Cye and his family on a unique journey to Disney World and Give Kids the World. This trip will allow them to make joyful memories in a different, stress-free place!
Herbert James Taylor
Herbie is a 6-year-old boy from Bartlett, IL, diagnosed with Medulloblastoma in September 2021.
Before his diagnosis, Herbie was vibrant, full of energy, loved to play soccer, and ran around outside whenever he had the chance. Several months before his diagnosis, he began experiencing occasional headaches, which were essentially his only symptom. Still, his mom had a strong feeling that something was wrong. They had to see multiple doctors before they decided to request an MRI. Their lives changed as quickly as an MRI captured brain images. The doctor urgently instructed them to take Herbie to Lurie Children's Hospital because they had discovered a large brain mass.
He should have been starting his first day of kindergarten but Instead was lying in a hospital bed. He underwent 30 rounds of proton radiation, daily sedation for six weeks, a year of chemotherapy, two surgeries, numerous MRIs, and extensive blood work.
His mom said, “Our lives completely were turned upside down. None of us are the same person, nor will ever be. The child we knew at four years old is no longer the same child. We grieve the child we lost at four but embrace the beautiful new child we have at six years old now. Every day is. Gift, and we know that.”
This dream would mean the world to their family. It's been three years since they had a proper vacation, and Disney World has always been Herbie's dream destination. It's on his vision board.
We aim to raise $5,000 to send Herbie and his family on a unique journey to Disney World and Give Kids the World. This trip will give them the opportunity to create joyful memories in a new environment, away from their current difficulties!
Eliana Barrera
Eliana is an 8-year-old girl from Long Island, NY, who was diagnosed with Leukemia in December 2020, just a few months after turning six years old.
Before her diagnosis, she loved sports, especially soccer, and wanted to learn to play the violin. She enjoyed making new friends.
Eliana experienced ongoing discomfort in her wrist and leg, which they initially thought was a sprain. However, after a visit to the doctor and some blood tests, she was diagnosed with acute lymphoblastic leukemia.
During her treatment, she faced both physical pain and emotional struggles. Her illness made it impossible to pursue soccer and the violin due to her weakened state. She also struggled with her self-esteem, fearing that her bald appearance might lead to bullying.
Despite these challenges, Eliana remained positive and brave, ultimately entering remission. Her battle with cancer has made her even stronger and more fearless. She's now able to learn soccer and will soon begin violin lessons.
In a few weeks, she'll be nine and hopes to celebrate her birthday at Disney World. It would mean so much to her to meet Mickey Mouse, Goofy, Donald, and the princesses at the happiest place on Earth. She wants to enjoy all the rides with her brothers and have an amazing time!
We aim to raise $5,000 to send Eliana and her family on a special trip to Disney World and Give Kids the World. This trip will allow them to make happy memories together in a different place, away from their current challenges.
Alexus Campbell
Alexus, a 17-year-old girl from Chickasha, Oklahoma, was diagnosed with Stage 3 kidney cancer in May 2021.
Before her diagnosis, Alexus was very active. She loved to swim, be outdoors, jump on the trampoline, and she loved to ride bikes with her siblings.
When the doctor told them about Alexus having cancer, her mom recalls, “I felt like a pain hit my stomach & I was extremely upset & mad at the same time. I felt like it was unfair for her to have to go through this. I felt like I wanted to take it for her. She was quiet. After the doctors left, she cried and said why did this happen to me?”
This diagnosis has had a profound impact on her life, stealing away important teenage experiences and physical abilities. She faces feelings of not fitting in and has encountered numerous challenges that no child should have to go through.
The family's quality time together has been greatly diminished, and they are also struggling financially due to the costs of her medical treatment. Alexus has faced a series of hardships that no child should have to endure, including fighting cancer, enduring harsh treatments, dealing with hair loss, feeling isolated at school, and coping with physical issues like neuropathy.
Due to her mother's inability to work due to the situation, the family's financial condition has worsened, adding more strain. Additionally, Alexus's siblings have experienced prolonged separations from her. When they do manage to spend time together, her appearance is troubling, leading to worries about her overall health and condition.
We believe that this dream trip will be the way for Alexus and her siblings to smile, laugh, and be free from fear and struggles. This is their chance for their much-needed moments of pure happiness.
Our goal is to raise $5,000 to send Alexus and her family on a special trip to Disney World and Give Kids the World. This amazing adventure will provide them with an opportunity to escape their daily routine and create new wonderful memories together as a family!
Evelena Chee-Metternick
Evelena is a 9-year-old Fort Knox, KY local who was initially diagnosed with B Cell Acute Lymphoblastic Leukemia in August of 2018 and relapsed just recently in May of this year.
Before her diagnosis, Evelena was a remarkably affectionate, gentle, and compassionate young girl with a passion for exploring the world through travel. She had exciting trips planned to Hawaii, Canada, and Florida, which unfortunately had to be put on hold due to her illness. Evelena faced her diagnosis with incredible bravery, and cancer did not diminish her strength or spirit. She remains the same resilient and courageous young girl she has always been.
In the face of relapse, every day can feel like a battle. But it's important to celebrate the small victories along the way. Whether it's a day with minimal pain, a successful treatment, or even a moment of laughter amidst the tears, these moments remind them that there is still joy to be found in their family's journey.
Having the opportunity to do this DREAM Trip as a family promises an adventure and a chance for their family to build lasting bonds and make new beautiful memories together!
That's why we are on a mission to raise $5,000 to fund a DREAM trip for Evelena and her Family to Give Kids The World and Disney World, where they can make awesome moments together and step away from the clutches of cancer.
Zayden DePina
Zayden is a 15-year-old boy from Bakersfield, California who was diagnosed with B cell acute lymphoblastic leukemia (Philadelphia +) in October 2022.
Before his diagnosis, Zayden was excited to start high school and had plans to attend a new school where his grandma taught. He enjoyed skateboarding with friends, attended music concerts with his mom and grandpa, and had just started boxing classes. Zayden also loved music, collected records, enjoyed computer work and gaming, and had a strong interest in history.
However, Zayden's life took a turn when he experienced weight loss, stomach pain, and nausea. Numerous visits to urgent care, and the pediatrician didn't provide answers. During a trip to Colorado, severe stomach pain led to an emergency department visit, revealing lab results that indicated leukemia. He was then transferred to Valley Children’s in Madera, where further tests confirmed pre-B cell acute lymphoblastic leukemia (Philadelphia +).
His treatment has been challenging, marked by many ups and downs. He began chemotherapy and faced various complications, including infections, pneumonia, liver failure, heart issues, and malnutrition, which necessitated extended hospital stays. His treatment plan frequently changed to meet his specific needs.
Zayden's cancer diagnosis had a profound impact on their single-parent family. They received support from friends and grandparents. Zayden's older brother, Andy, took emergency leave from the military to be with him, while his younger brother, Graham, stayed with his grandparents and his father. Zayden's mom took medical leave during hospital stays, and the hospital's distance prevented him from spending time with his friends.
A dream trip would bring immense joy to Zayden and provide a welcome distraction from his illness. It represents a positive focus for him, offering the opportunity to experience the world outside a hospital room and helping him feel "normal" again. It's also a special chance for their family to create cherished memories together.
That is why we are on a mission to raise $5,000 to fund a special trip for Zayden and his family to Disney World and Give Kids the World. This journey will provide them with the opportunity to build happy new memories in a different environment, away from the challenges they've been facing!
Mia Irvine
Mia is an 8-year-old Oceanside, CA, local who was diagnosed with Acute lymphoblastic leukemia (ALL) in February of 2021.
Prior to her diagnosis, Mia was a bubble-active little girl who loved riding her bike with other kids, going on walks with her brother Logan, and playing at the beach.
Her mom said, "Getting the news was a shock to all of us. Mia was only 6, so didn't really understand what was happening."
Dealing with the diagnosis has been extremely difficult and heartbreaking for Mia. She went from running around freely to needing to be pushed in a stroller. And from having a beautiful head of wavy hair that went almost to her butt to losing it all the way about 6-7 weeks into treatment.
Our mission is to raise $5,000 to fund a trip for Mia and her Family to Give Kids The World and Disney World. This special journey will allow them to experience the joys of life beyond their challenges. We invite you to join us in supporting them to create wonderful new memories. Together, we can turn this dream into a reality!
Treyvon Allen Robinson
Treyvon is a local of North Kingstown, Rhode Island who was identified with Complex Congenital Heart Defects shortly after birth, followed by a diagnosis of Non Verbal Autism and Pica when he turned 2 years old.
The experiences that this little boy had undergone were beyond anyone's ability to imagine. He went through his initial open-heart operation when he was just seven days old, his second procedure at four months old, and his third open-heart surgery took place when he was two.
As his Mom said, "Having your child you brought home for only two days diagnosed with a life-threatening illness is an emotional roller coaster. We thank God every day that he is here with us thriving. But the worry of what ifs haunts you every day. We are always worried about what the future holds for Treyvon. Unfortunately, there is no cure for CHD, and Treyvon will live left with half a functioning heart."
Having the opportunity to do this DREAM Trip as a family promises not just a breathtaking adventure but a cherished opportunity for our family to forge lasting bonds and craft beautiful memories together.
Our mission is to raise $5,000 to fund a DREAM trip for Treyvon and his Family to Give Kids The World and Disney World. This extraordinary journey will give them a chance to break away from their daily routine and create new beautiful memories together as a family!
Kayla Nelson
Kayla is a 4-year-old little girl from Menifee, California, who was diagnosed with Acute Lymphoblastic Leukemia (ALL) in July of 2021.
Despite her tender age, she had already encountered hardship. Her biological mother's inability to provide proper care led Child Welfare Services to place her in foster care.
Through the adoption of her elder sister Anajade, the family became acquainted with Kayla's existence. Anajade asked if she could have a relationship with her new baby sister, who was 2 only weeks old, so The family arranged for them to meet. Instantly, the family developed a strong affection for Kayla then Anjade asked if they could keep her. And that is the beginning of their beautiful family.
As the youngest member, she received constant affection and attention. Kayla has been the princess in their family. As she grew older, she made their lives livelier.
The most dreadful day for the family was when they discovered Kayla's diagnosis. Her Mom said, "I kept praying on my hands and knees in the ER for God to take it away and give it to me. I started bargaining with God."
Kayla being a warrior, has gone through numerous hospital stays, lumbar punctures, clinical visits, surgeries, blood transfusions, oral chemos, and so on.
This trip would mean the world to their whole family, especially Kayla. Her wish is to meet the princesses and ride the rides!
Our mission is to raise $5,000 to fund a trip for Kayla and her Family to Give Kids The World and Disney World. This unique adventure will allow them to experience the joys of life beyond their challenges. We invite you to join us in supporting them to create new beautiful memories together as a family!
Paxton Idell
Paxton is a 7-year-old boy from San Antonio, Texas, who was first diagnosed with Medulloblastoma back in April of 2021 and relapsed this year in April of 2023 with Leptomeningeal spread to the lining of his brain.
Prior to being diagnosed, Paxton was known for his adventurous spirit. However, this illness has altered his willingness to engage in new activities. He missed the ability to have real play dates as he couldn’t keep up with other kids despite how hard he tried.
Within three weeks, he underwent multiple brain surgeries, received proton radiation targeted at both his brain and spine, endured intense chemotherapy sessions, and underwent blood and platelet transfusions.
As his mom recalls, “he has already watched many of his friends pass away with this cancer and is scared he is going to die also.”
Paxton is in Hospice right now but still never fails to light up the room with his presence and the funny faces he makes. He is fighting this battle with all he's got.
Our goal is to raise $5,000 to send Paxton and his family on a special trip to Disney World and Give Kids The World. This trip will give them the chance to create new joyful memories together in a different setting, away from all these struggles!
Natalie Dorsey
Natalie is a 3-year-old baby girl from Taneytown, Maryland, who's been fighting for her life even before she was born.
She's diagnosed with Strokes, Hydrocephalus, Cerebral Palsy, CVI, Esotropia, Hemiplegia, and Epilepsy.
Her Mom was being examined at the doctor's office for a late-term sonogram when they discovered excess fluid on Natalie’s brain in utero. She never got to experience a normal life.
This 3-year-old girl has been through upwards of 700- 1000 appointments and therapies, 3 brain surgeries to date, 60-70 images, 5 medivac rides, 6 ambulance rides, upwards of 10 hospital stays, several bowel blockages, 40 vomiting events, countless seizure events, several NG tube placements, daily orthotic and seizure monitoring fit-ups, daily falls, mobility impairment, medical trauma, and panic events. What this family has gone through is way beyond her diagnosis.
Going on this Dream Trip could mean so much more than just being there and having fun. This will help them disconnect from all these difficulties.
We are on a mission to raise $5,000 to send Natalie and her Family to Disney World and Give Kids The World to experience the beauty of life again! Let us help them make new wonderful memories outside of the hospital!
Isabella Melgarejo
Isabella is a 3-year-old little girl from Phoenix, Arizona, who was diagnosed with Embryonal rhabdomyosarcoma just this year, in February.
She was a healthy normal 3-year-old before her diagnosis. She had long black flowy hair that everyone loved. She was always doing fashion shows up and down the hallways at home. She would play dress up in kid heels and Disney princess dresses.
The day her family got the news about her diagnosis was the worst day of their lives. Her Mom said, "I'll never forget feeling like I was drowning, and I couldn't breathe my eyes swelled shut from crying so hard. I even told the doctors they had the wrong room and asked how this could be happening.."
It's been devastating how this whole experience caused Isabella to have major anxiety, which must be treated with medication. Every time they go to an appointment, she cries and begs why they need to do it. She thinks she did something wrong she makes promises that she will be a good girl and promises not to be sick anymore it breaks everyone's heart every single time.
Isabella's DREAM Trip to Give Kids the World and Disney World is a present that would mean everything to her and her family.
We are on a mission to raise $5,000 to send Isabella and her family to Disney World and Give Kids The World to experience life beyond these difficulties. Let us help them make new wonderful memories together outside of the hospital!
David Santiesteban Parga
David is a 6-year-old boy from Riverview, Florida, diagnosed with relapse pulmonary stage III cancer earlier this year in March.
He was initially diagnosed with Wilms tumor abdominal stage III cancer and finished his treatments in August of 2021, then December of 2021, on his birthday, he was diagnosed again with a relapse Wilms tumor on his lungs; he finished his treatments on July 2022 then relapsed again March this year, pulmonary stage III cancer.
What David has gone through was unimaginable. This precious little boy has been fighting for his life over and over, and this battle is still on as he continues with this journey.
"You know how God gives his hardest battles to his strongest warriors? Well, my son is the definition of a warrior. He is brave; he is light, hope, love."
We are on a mission to raise $5,000 to send David and his Family to Give Kids The World and Disney World to experience life beyond these difficulties. Join us in helping them forge incredible new memories together outside the confines of the hospital!
Tenzin Tanaka
Tenzin is a 9-year-old boy from Port Jefferson Station, NY, who was diagnosed with Acute Lymphoblastic Leukemia (ALL) in June of last year, 2022.
He was a happy-go-lucky 8-year-old before diagnosis. He enjoyed karate and had just earned his junior black belt. He loved running and being outdoors. He had just received a trampoline for his birthday that he was constantly jumping on.
According to his Mom, "The news of diagnosis felt unreal. All I heard was "Leukemia blah blah blah chemo blah blah blah" I was instantly fearful for how Tenzin would handle the news and how his brother would cope."
Tenzin has gone through so much since then. He had lengthy hospital stays, treatments, antibiotics, blood and platelet transfusions, and chemo sessions. He even had an NG tube placement due to malnutrition from frequent vomiting. Sadly, Tenzin developed some anxiety from the diagnosis that has been worked through with therapy and medication.
This dream would be such a milestone for Tenzin and his family. It would allow them to step away from the world of cancer.
We are on a mission to raise $5,000 to send Tenzin and his Family to Disney World and Give Kids the world to experience life beyond these struggles. Let us help them make new wonderful memories outside of the hospital!
Kathryn Lewis
Kathryn is a 6-year-old little girl from Newton, Texas, who was diagnosed with Acute Lymphoblastic Leukemia (ALL) in October of 2021.
Before diagnosis, Kathryn was your typical 4-year-old, happy all the time second child. She was in public pre-k and having a blast! She has always been the kiddo with no fear. She enjoyed her baby dolls, barbies, and LOLs. Her family and friends have always been a huge part of who she is.
When they received the news, they were ready for battle! The diagnosis has changed Kathryn and their entire community. While it has not been fun, it had to be their new normal, they have accepted it is what it is now, and they needed to just keep going. They counted down the treatments; her family is still doing their best to look at the brighter side for Kathryn. Whatever ups and downs this journey may lead them to, they are grateful that this road has made their family stronger.
This DREAM TRIP would be such an amazing way to celebrate all the crazy from the last few years for this family. Kathryn said, "It would be so fun to ride a roller coaster with her sister!".
We are on a mission to raise $5,000 to send Kathryn and her family on a DREAM TRIP to Disney World and Give Kids The World where they can create new beautiful memories as a FAMILY!