We’re not certain you can look at Everly without smiling! This sweetheart is a Mississippi girl who’s treated at Masonic Children’s for a rare genetic condition called Hurler’s Syndrome. In June 2023, three-year-old Everly received a life-changing Bone Marrow Transplant and we’re happy to report that it was a success! In order to celebrate one-year […]
Gabrielle was born in August, the youngest of six children to Patrick & Dorsey. She was absolutely adored by her large family. This little fighter was born at just three pounds and in addition, she battled Edwards Syndrome. After two months in the hospital, she was able to go home and enjoy family time surrounded
No one thinks about starting a New Year in response to a diagnosis of cancer. But in January of 2024, that was what Kyah faced by receiving treatment for Hodgkin’s Lymphoma at Masonic Children’s Hospital. Just like many other teens, she loves playing sports, going shopping, reading, writing, & watching movies; however, her most favorite thing is
Guests at the 2025 Winter Ball had the pleasure of meeting Deacon, our extremely social and charming redhead. He let all of our guests know that he wanted to meet his superhero friends at Universal Studios. He was on stage with his sister, Elizabeth, who received a wish 5 years ago and everyone enjoyed their surprise in
Our Memorial program is more than just sending a check, it’s an opportunity for parents to share words about their precious child. It’s our pleasure to share these words even further than our office walls. “Even though Kelsey passed away, we will always use present tense talking about her because she is always in our
Rosielys is a friendly and joyful toddler who loves music & dancing, princesses & Mickey Mouse, and splashing in the water. As you can see, this three-year-old also has the BIGGEST smiles we’ve ever seen! Ely’s mom shared that she is very independent and likes to do things on her own and loves to be
17-year-old Augustine’s condition has taken away his ability to communicate with words, but this fun-loving and friendly teen makes sure his feelings are known through happy noises and grunts. He joins his family in loving all things Disney and Augustine has the biggest smile whenever he sees Mickey Mouse! A wish trip to Disney World
Jonas has been living with a brain tumor for several years now. This brave young man has a chasm optic nerve glioma, but he still loves to use his brain. In fact, he is described as a bookworm, and the stories he reads inspire his imagination & desire to travel the world. Jonas wished to visit Hawaii and his family left
Cooper’s parents and his three older brothers eagerly awaited his birth. Although he had a prenatal diagnosis of a heart defect, they had faith that he would be okay and they showered him with love on his arrival. He was only two days old when he endured his first delicate surgery on his walnut-sized heart.
At two months old, Chandler underwent his first open heart surgery and after complications, more procedures and lots of hospital time, he finally went home in July. When we met with his family, they shared how much they love spending time outdoors together. Whether it’s going on walks, playing on their playset, hiking, or camping,
Meet Orlan! This charming 4-year-old would love to climb, swing and play all day! Unfortunately, he’s been cooped up for the last year receiving treatments for Langerhan’s Cell Histiocytosis (a rare form of cancer), but then he met Wishes & More! His adoring parents agreed that a jungle gym bedroom would be a perfect wish and with
Nine-year-old Beau was a total outdoors kid. He especially loved fishing, baseball, and hockey. He also loved to learn new things and write stories. He would do many things in his free time, including help work outside with horses, ride around in the skid steer, work on vehicles, plow snow, and play video games. One
Hope was born with a rare genetic condition and a need for a heart transplant. Initially, doctors reported that Hope was making progress and plans were underway for her to transfer to a Chicago hospital for the delicate procedure. Unfortunately, Hope’s condition declined with the discovery of additional complex medical issues including a cancerous tumor. Her parents and her medical team
In 2011, four-year-old Nathaly struggled with a rare condition called Histiocytosis. Her wish, similar to many of our other young wish kids, was to visit Disney World to meet the princesses! Her whole family traveled to Florida in August and returned just in time for Nathaly to start Kindergarten. Fast forward to 2024 and we
Last Fall, 5-year-old Ella was diagnosed with a growth hormone deficiency resulting in terrible migraines. After weeks of testing, an MRI was scheduled and the diagnosis couldn’t have been worse: a brain tumor. Although there is currently no cure to shrink or stabilize the tumor other than removal or radiation, which would both cause some
Thirteen-year-old Lucy has a congenital condition that causes dangerous episodes of iron overloads. She is reliant upon frequent transfusions to maintain her health; consequently, she knows her way around the hospital. However, she is also engaged in quite an impressive number of extracurricular activities and interests: french horn, piano, basketball, and theater. This exceptional young
Jack was not only diagnosed with brain cancer, he also contracted meningitis after surgery. Because of this serious infection, he became dependent in every aspect, from needing assistance with eating and drinking to re-learning how to walk and talk – in his words it was, “demoralizing and humiliating.” Jack graduated high school in 2023 and
Last year, 18-year-old Broten’s summer fun was hampered by frequent colds, minor illnesses and fatigue. He was just starting his senior year in high school and his parents sent him in for a physical to see what might be slowing him down. Some of the blood work was off which started him on a path
Karsen, aka “Kasey,” is a 17-year-old from Clearwater who was diagnosed with Hodgkin’s lymphoma during the last month of her sophomore year of HS. After months of treatments and the difficult loss of this pretty teen’s hair, she spent her junior year struggling with online classes. Today she is thrilled to be back for her
With gently rolling upland, large swamps, and a scenic steep stream valley, Nemadji State Forest is known for its trail system that draws outdoor enthusiasts throughout the year. Landon’s family loves being out on the trails and the entire family was enjoying an ATV adventure in July of 2023 when the unthinkable happened. His four-wheeler tipped
Frederick, or Freddy as his loving parents called him, had just made it to three months when he tragically passed away. This little angel loved being the little brother to his siblings Stella, Wallace and Edith; his favorite spot was in the arms of his Mommy; and he warmed his Daddy’s heart with his smile.
At just one-year-old, Kinsley suffered from a traumatic episode of septic shock. She spent 12 weeks in the hospital, fighting for her life from this dangerous blood infection. Her dad shared, “Kinsley’s journey, especially the first half, was filled with much more than one lifetime’s worth of pain.” This girl has a fighting spirit, though,
We had the pleasure of following Emmett’s medical journey from nearly the very beginning until the very end. This sweet boy came to Wishes & More about a year ago when he was waiting for a bone marrow transplant at Mayo. He had been diagnosed with a rare disease called XLP2, and his doctors expected
Fourteen-year-old Conner has struggled with serious neurological and other medical complications since birth. He has chronic kidney disease and is recovering from a recent hip surgery. Additionally, he is challenged with Spastic Quadriplegic Cerebral Palsy that causes all four of his limbs, his face, and his torso to be spastic and stiff. You can imagine how difficult all
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