This four-year-old’s diagnosis of B-Cell Acute Lymphoblastic Leukemia was shocking and frightening for her whole family but now that she has completed treatments, her wish will provide her with endless joy and imaginative play, right in her own backyard. Grace’s wish was for a custom-designed playhouse perfectly decorated for a princess. Wishes & More provided […]
With sparkling blue eyes and brilliant red hair, this little guy captures the heart of everyone. And it’s heartbreaking to share that after 18-months of battling intractable epilepsy and a critical neurodevelopmental disorder, sweet Oliver passed away in March. In his short life, he faced many difficulties which he fought with the loving support from his
Cazen is a precocious young teen from Austin, MN who loves everything from hunting for fossils, metal detecting and panning for gold – to playing video games and having Nerf wars. Cazen has B-cell Acute Lymphoblastic Leukemia and throughout his treatment, he was able to put a lot of thought into his wish. He carefully
16-year-old Ashley, known for her playful sense of humor and love of dancing, was dealt a huge blow when she was diagnosed with a Diffuse Midline Glioma, an aggressive brain tumor. Her family – a particularly close knit set of five siblings and two remarkable parents – were shocked with the diagnosis and a daunting
Adeline was a brave little heart warrior with a big personality. She was diagnosed with a congenital heart defect and fought every day like a brave heart warrior does. Sadly, she passed away before she could turn five. Adeline’s family will remember her as their princess that adored spending time with her sister and playing
Samy is incredibly strong, but it isn’t the kind of strength that comes from the gym. It’s a strength from within. He also has an abundance of grit and resilience from a battlefield that was a result of remarkably serious birth defects. This 19-year-old has endured more than we can imagine as a result of
Three-year-old Finn has Acute Lymphoblastic Leukemia and, unfortunately, he has suffered damage to his liver as a side effect from his treatments. He has spent 1/3 of his life enduring chemo treatments and has had a hard time battling this illness. His parents informed our team that after spending so much time in the hospital, the entire
Little Ivy was born with a host of serious health complications and spent only two of her 13 months of life in her family home. Wishes & More was not able to grant a wish for this little angel; however, our Memorial funds were given to the family immediately after her passing. We share the
“Our” Maddie prides herself on her honest opinions, quick wit, and tasteful sass. We first met her a few years ago when she was diagnosed with leukemia in her junior year of high school. We call her “our Maddie” because she has been in the process of her wish since that time as she struggled
Attendees of the 2022 Winter Gala enjoyed Braxton on stage and were captivated by watching him and hearing about his love of superheroes, especially Ironman. Braxton is an absolute joy of a kid and we were incredibly thrilled to surprise him with the opportunity to meet Ironman, receive some special gifts from him – including a
Ava was born with a heart defect and she was only 3-months old when her loving parents waited in a surgical lounge while their precious little girl endured her first heart surgery. Ava also faced the challenges of having Down Syndrome but neither one stopped her from bringing joy and having her life filled with
Juniper is a 4-year-old from La Porte, MN who suffers from a brain dysfunction called Hypoxic Ischemic Encephalopathy. Her three siblings are very active and love playing outdoors on their acreage. Sadly, due to her condition and physical limitations, Juniper was often left behind and in the house. Her parents talked about their wish for
Alyssa was born with a serious genetic disorder called Angelman Syndrome. Alyssa’s two brothers absolutely adore her, and her favorite moments are when they are all together…or when she is snuggling with mom. Alyssa enjoys spending time in the water and we hear that she pouts when it’s time to dry off. She also loves the
Pierce is an eighteen-year-old struggling with myotonic dystrophy, a genetic condition that causes his muscles and organs to weaken seriously and progressively- especially his heart. His condition has depressed his energy-levels and health so much that he missed out on a full semester of his senior year of high school. However, he graduated in January and
Parker’s life was changed after a series of doctor’s visits trying to figure out the source of his high fever. Eventually, he was diagnosed with Acute Myeloid Leukemia (AML) and endured nine months of chemo treatments. After enduring the fight of his life, Parker sadly passed away at the age of four from the cancer
Haley is a pretty typical teenage girl – she loves going to the theater, Nick Jonas & singing along to John Legend and Christmas tunes! This sweet lady was born with Down syndrome – but her true battle began recently when she was diagnosed with Acute Myeloid Leukemia. This diagnosis has forced Haley to endure
Pie is a seven-year-old from Becker who is the youngest child of five kids. As you can see from their photo, she is obviously adored by her older siblings and her parents. Battling T-Lymphoblastic Lymphoma, her blood counts have been a concern and have even pushed back some of her treatments. Wishes & More volunteers
Remember Alex? In June of 2020 we granted his wish for a car allowance to buy a 1994 Toyota MR2 GT. A true car fanatic, the search for his perfect car was a great distraction during his cancer treatments for ALL. We recently checked in with this ambitious teen and learned that the car is in
Cameron was rushed to the NICU at birth and his first 100 days of life was spent in the hospital due to a serious esophageal birth defect. He endured surgery after surgery with setback after setback in the attempt to repair his leaking esophagus before he could go home to his own nursery. We met him
Sixteen-year-old Austin had complained of knee pain for a couple months before he and his parents decided to have a doctor check it out. As an intense varsity soccer player, they did not think much of it, assuming the pain was a byproduct of the sport. After several scans, an MRI, and a biopsy, it
Meet Harrison! This little sweetheart has had quite the journey in just two short years. He was born in January of 2020 under high risk circumstances, three weeks early with fluid in his lungs. Doctors struggled to determine the correct diagnosis for Harrison because of the rarity of this cancer, infantile spindle cell rhabdomyosarcoma. He endured two
Tatum was diagnosed with Neuroblastoma when he was 6-months-old, and has fought through multiple rounds of chemo and 15 surgeries. After his initial diagnosis, he immediately underwent emergency surgery to remove a mass and in recovery, his heart and breathing stopped. This little fighter came through it all and is now four-years-old and declared cancer-free.
Reuven is a teenager from New Hope who came to us in 2018 after receiving a diagnosis of a Brain Tumor. This young man is very spiritual and his Jewish heritage is held very closely to his identity and heart. He attends a Jewish boarding school to fully immerse in his studies and, consequently, told
Three-year-old Xenia may be little, but her personality is big! This precious little girl could not wait until Halloween this year because that was the day that she was leaving for her Disney World Wish to come true! Xenia is the middle child of a young family of five and she struggles with a brain malformation
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