At three-months-old, Sawyer’s parents received the heartbreaking news that their perfect baby boy had a very rare neurological and degenerative disorder. His adoring Mom stayed home to be with him each and every day and gave him the best childhood she could! He loved the outdoors, hiking and spending time at a Park Reserve just […]
Valens is a curious and active 8-year-old who has battled a rare and very serious hormonal condition all his life resulting in extended periods of hospitalization. In fact, he’s so familiar with being an inpatient that he shared his favorite memories as “getting x-rays” and he would like to grow up to be a heart
This handsome young man has been a Wishes & More “Kid” since 2006 when he received his wish for a hot tub! He was battling Stage 4 Neuroblastoma when we met him and water therapy was incorporated into his treatment. This hot tub is still a part of his daily life and he mentioned in
Recently, Wishes & More provided memorial funds to the parents of a precious 6-month-old. This little angel was the youngest of four sisters and brought an incredible amount of joy to her household from day one. Just days after enjoying her first Christmas, Ivanna took her final breath. Her heart wrenching obituary read, “Her wide
Mateo is an active, playful 3-year-old from Brooklyn Park battling Acute Lymphoblastic Leukemia. He is the middle child of three and this little cutie loves playing with cars & balls, and has a fascination with bugs. Our Wish Wizards spoke with Mateo’s parents with the help of a fantastic Spanish-speaking interpreter. They learned of his love
Bragging is typically something moms and grandparents do, but we are so proud of our former Wish Kid Linae, that we can’t help but do a big shout out about what she’s accomplished and where she is now! You may remember Linae’s wish from 2019 – she visited Washington DC and we included a special
John’s critical condition requires water therapy 4-5 days per week; however, his family let us know that the therapy location isn’t nearby or convenient and, with five other kids, they are unable to make the drive as much as is needed. The other option of him receiving warm water therapy in the bathtub also became
Everybody loves “small world” connections that weave through our lives. Like those people you meet on vacation in Florida, who knew your best friend when they were kids. Or in this case, the two little girls diagnosed with a very similar cancer who live in small towns just 20 miles from each other – who BOTH received
Hazley is a fun and spunky Halloween baby who turned four this year! This young family was having dinner one night when her dad lifted her up and felt something abnormal in her stomach. By the next week, Hazley was in surgery to remove a tumor and started treatment immediately afterwards. For 7-1/2 months, this
Three-year-old Lola is a HUGE fan of Minnie Mouse. Throughout her little life, Lola has used Minnie as a coping and comfort tool. Unfortunately, this blue eyed sweetheart, with bouncing curls, visits doctors quite often as a result of her extremely rare genetic condition. Mom relayed, “Minnie goes everywhere with us. Minnie keeps us brave when at appointments. And
Brody is an outdoorsy 10-year-old who suffers from a rare bone disease. His diagnosis has meant surgery and months of chemotherapy, but the family stayed strong and so did Brody! When our volunteers talked with this adventuresome kid, he had many things to say! He talked about wanting to be a cowboy and pretending to ride bulls. Then he
Will was born with congenital heart disease and doctors told his parents that he would require on-going treatment and quite a few surgeries as he grew. Now at the age of 12, he’s become more aware of the gravity of his condition and, not surprising, he has suffered ongoing anxiety and fear surrounding his checkups
You’ll be hard-pressed to find a more inquisitive mind than Kingston’s, especially when it comes to outer space! This twelve-year-old from White Bear Lake can often be found with his gaze turned upward. Kingston came to Wishes & More because he has a rare, life-threatening blood disorder that causes the formation of blood clots in
Matthew’s mom served 20 years in the Army Reserve including a year’s deployment in Iraq when he was just three-years-old. But her greatest challenge came more recently in 2021 when, as a single mom, her 17-year-old son, Matthew, was diagnosed with Ewing’s Sarcoma – a rare cancer of the bone or soft tissue. His diagnosis
Elias struggles with a genetic condition that has adverse effects on his whole body, including his ability to eat or speak. He’s battled this severe condition every day for the past 18 years and requires round the clock care, shared by two nurses, but he’s also enjoyed many happy moments with his loving family. As a single
Meet Emma! She’s a happy 11-year-old from North Branch who loves nothing more than swimming! In fact, she had her mind made up on a pool wish even before we met with her. She’s a little fish in the water and her medical team shared that it is great therapy for her and fulfills her need for
Thirteen-year-old Addie began experiencing pain in her right leg that came from nowhere and wasn’t going away. This led to numerous scans and testing and no one in her family will forget September of 2021 when they determined the source – B-Cell Lymphoma. Mom describes her as “humble, kind, strong, brave, and a very driven
Wishes & More had the pleasure of surprising one of our wish kids with his Wish Reveal at our Fall Beer & Wine Sampling Event. Thirteen-year-old Max reluctantly agreed to be introduced as a “Wish Kid” in front of our 120+ attendees. He’s a very shy young man – unless he is on a baseball, football or
Asiya is a sweet 9-year-old from Roseville who’s challenged by cerebral palsy and is also battling heart disease. Despite these difficulties, she is an incredibly sweet and smiley little lady with a family who simply adores her. Her therapist has set a goal to get Asiya outside more and her family thought that a trip would inspire
High school commencement is a date to look forward to and remember, but not in the way it will be remembered by Ryla. Due to a genetic condition, this strong-willed young lady has dealt with benign tumors along her nerve lines all of her life. And for the last 11 years she has dealt with
The first thing people notice about nine-year-old Nevaeh is her infectious, bright, and beautiful smile. It rarely leaves her face, despite her daily struggles with a congenital brain malformation and severe seizure disorder. Nevaeh is nonverbal, uses a wheelchair, functions developmentally at a two-year-old level, and is surrounded by love! Nevaeh, and her 11 siblings, all have
Four years ago, Edward was diagnosed with Acute Lymphoblastic Leukemia at age 5. This diagnosis shrunk his world, which soon revolved around constant doctor visits and medical procedures. Throughout the pandemic, he and his family had to be very, very careful due to the lack of his immune system, so even leaving the house made
Layla was a senior in high school when she was brought to the ICU having experienced a seizure, partial paralysis and loss of speech. It took two agonizing months for doctors to ultimately confirm that she has a high-grade malignant glioma – brain cancer. She immediately underwent radiation and chemo while keeping up her schoolwork and
All things are not created equal for siblings and that goes for triplets as well. Victor, a triplet from Columbia Heights, was born with a rare syndrome called Polymicrogyria that, among other things, causes epileptic episodes. This sweet 10-year-old shares many things with his brothers, but fortunately they don’t share this diagnosis. As Victor has gotten
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