Born at just 23 weeks, Ezra entered the world too soon, facing unimaginable battles from his first breath. Seventeen months in the NICU, countless surgeries, and a lifetime of challenges, but through it all, he’s fought with resilience and joy.

Now, we have a chance to change the narrative—to give Ezra a world beyond survival, where joy replaces hardship, even just for a moment.

We’re raising $5,000 to send Ezra and his family on a dream trip to Disney World and Give Kids The World. Let’s make this happen!

This is Mateo, a brave 3-year-old from Wyoming, Michigan, whose life was changed overnight. What seemed like a simple cold turned into a nightmare when doctors diagnosed him with B-cell Acute Lymphoblastic Leukemia. Suddenly, Mateo’s world was filled with IV drips, blood infusions, chemotherapy, and endless hospital visits—things no child should ever endure.

Despite the everyday pain, Mateo’s spirit remains strong. Even on his hardest days, he smiles and comforts his family, reminding them about his medications, showing a strength beyond his years. But Mateo is just a little boy who deserves laughter, play, and a life beyond hospital walls.

His family has sacrificed everything to support him, and they deserve a break—a chance to find the peace and happiness they’ve longed for, and for Mateo, this is his chance to feel like any other normal little boy.

We need your help to raise $5,000 to send Mateo and his family on a special trip to Disney World and Give Kids The World, where they can experience life from a different perspective—one filled with happiness every family deserves. Let’s make this DREAM COME TRUE!

Adrian is a 16-year-old boy from Santa Rosa, CA who was diagnosed with Chronic lung disease cerebral palsy, uncontrollable seizures, nonverbal, and non-ambulatory in June of 2008.

Adrian was born healthy and happy but suffered severe injuries due to shaken baby syndrome inflicted by his biological father. Hospitalized for over 35 days, Adrian's mother had to learn to care for him as he developed CVI, a G-tube placement, and controllable seizures.

He experienced cerebral bleeds, forgetting basic functions like swallowing and eating. He had retinal detachment, bleeding behind the eyes, and bleeding in the brain, leading to life-threatening seizures. His mother, alongside him for the entire hospitalization and rehabilitation, faced immense challenges adjusting to caring for a changed Adrian.

Meanwhile, his mom was diagnosed with cancer two years ago, adding to the family's hardships. Adrian's brothers struggled with their mental health due to the uncertainty of losing Adrian and their mother. Adrian requires full-time care indefinitely, and his family lives cautiously to ensure his safety and well-being.

That is why we are on a mission to raise $5000 to fund a DREAM trip for Adrian and his family to Disneyland—providing them with the chance to craft cherished moments in a serene and special atmosphere, filled with warmth and love!

Aria, a brave 9-year-old from Yorba Linda, CA, faces a daunting battle with Acute Lymphoblastic Leukemia. Her journey began with a childhood accident in 2022, leading to unexplained pains. Despite countless doctor visits and trips to the emergency room, Aria's condition remained a mystery, deeply affecting her school life and her family's well-being.

As a mother and nurse, watching her daughter suffer without answers was excruciating. Aria's innocent question "Am I going to die?" to this day, this is and will always be the hardest thing her Mom could ever hear, and it still breaks her Mom’s heart to this day when this memory randomly pops up.

Finally, after a long wait, a rheumatologist diagnosed Aria with Acute Lymphoblastic Leukemia, changing their lives forever.

Since then, Aria has been through endless battles and endured treatments with a courage that pierces the heart. She has become the cornerstone of her family, their rock amid turmoil, She has become her family's hero.

A magical dream adventure to Disney World and Give Kids The World would be an absolute lifeline for this family, especially for Aria. It's an opportunity for her to glimpse life beyond her struggles — a chance she wholeheartedly deserves.

Our mission is to raise $5,000 to make this dream a reality. Help us make this happen for Aria!

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!

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 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!

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!

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 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.