Wishesandmore

Cole's ATV wish

Cole

According to Wish Kid Cole, his wish day was his “Best. Day. Ever!”  It was Summer 2023 when he complained to his parents of a persistent headache and started acting a bit off, then his face started to droop on the left side and his parents became alarmed. A CT scan revealed a brain mass and

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Withrow Car & Tractor Show

16th Annual Show! Withrow is a family-friendly outdoor event with a wish presentations mid-day! Event venue is along the main road in Withrow from Sal’s Angus Grill (12010 Keystone Ave N, Stillwater, MN 55082) to The Withrow Ballroom (12169 Keystone Ave N #9100, Hugo, MN 55038).

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Dannon by his playset with bubbles

Dannon

Dannon “Yogurt” is a delightful 3-year-old with an endearing smile who has battled Acute Myeloid Leukemia. Because kiddos with Down Syndrome have a higher chance of developing this cancer, he had been receiving regular blood draws since birth to track his counts. Everything looked great for two years until his doctor found that he had a

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Cydney

Cydney

Shopping is a favorite activity for a teenage girl; however, when Wishes & More grants a shopping wish we do it up big! Please meet, Cydney.  She just graduated from high school and plans to head to the University of Texas – Austin in the Fall… an amazing feat considering what she has gone through in

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Kellen

Enjoy an update on Kellen’s journey “After the Wish!” Kellen’s parents reached out to Wishes & More in 2018 as he was enduring a hard-fought battle with a brain tumor, meningitis, a stroke and all of the terrible side effects of these unimaginable diagnoses.  This six-year-old’s wish was very simple – he wanted to golf. 

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Van

Van

Van is described as “a little man of action” who is happiest when he’s on the go. This four-year-old from Dayton has Rhabdomyosarcoma of the right leg and among other treatments, he’s had to endure the complex surgery of removing the upper portion of his right leg. Coupling this drastic surgery, he suffers with low core strength,

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Laney

Laney

A heartfelt thank you note is never expected, but it is so rewarding to receive. A recent message we received was a beautiful reminder that our charity is an important and impactful part of our family’s lives during very emotional and difficult days.  We hope you enjoy Laney’s Mom’s words:  “Your team made the whole

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Abbie engaged scholarship

Abbie

Enjoy an update on Abbie’s journey “After the Wish!” You may remember Abbie from 2020 when she received her wish for a Sleep Number bed as she was seeking a comfortable space while going through treatments for Hodgkin’s Lymphoma. She had just started college at UW Eau Claire when she was diagnosed with this devastating

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Jonas

Jonas

Jonas is a little guy born with a big diagnosis. His heart disease affected his heart’s ability to pump blood efficiently through his little body and contributed to multiple surgeries in Jonas’s short life. Ultimately, it also contributed to his death. Mom wrote, “Our sweet Jonas loved being held and loved singing and talking with us. 

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Gunnar

Gunnar

One year ago, Gunnar, an athletic and outdoorsy kid from Prior Lake was diagnosed with metastasized testicular cancer. Sadly, instead of enjoying his Summer months with his family at their cabin, fishing and enjoying time outside, he had to undergo chemo and many weeks in the confines of the hospital walls.  For a kid who’s used

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Aubrey

Aubrey

An intense headache and blurry vision alarmed Aubrey’s parents and initiated a trip to the ER. The scans were alarming – a golf ball size malignant tumor as well as hydrocephalus! An intense treatment plan began immediately; and so did many days of not being able to keep food down, dizziness, emergency shunt drains, extreme

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Kelly after a successful hunt

Kelly – After the Wish!

We’re excited to periodically take a look back at past wishes and we’d like to take the opportunity to share Kelly’s journey “After the Wish!”  You may remember Kelly from her on-stage debut at the Winter Ball in 2014 when she found out that her wish to go deer hunting with her favorite television huntress,

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Quentin's wish

Quentin

We met Quetin as he was going through treatment for Leukemia and dealing with on-going issues in and out of the hospital.  He was a sophomore in high school in the Stillwater school district, but with his health struggles, he decided to take a year of home learning to try to keep up with his

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Lolita

Lolita

One day shy of her six-month birthday Lolita’s parents had to say goodbye to their beautiful, blue-eyed baby girl.  Lolita endured open heart surgery and a number of debilitating complications stemming from RSV.  In the Memorial application, her parents poignantly wrote, “Lolita let her light shine brighter than the sun since the day she was born.

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Abigail

Abigail

Abigail is a delightful sixteen-year-old with a creative mind, love for Harry Styles, and enjoyment of fantasy novels. She not only uses her brain power, she also enjoys staying physically active, particularly through basketball, volleyball, and track & field. This is even more impressive when you consider that she has a critical and unresolved congenital heart

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Regina

Picture a ten-year-old who loves to be active, but lives with a dependence on regular blood transfusions to stay alive.  That’s the life of our Regina.  She has a dangerous genetic condition that requires constant monitoring due to episodes of extremely low oxygen that may lead to organ failure – you can imagine the stress this puts on

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Rhys

Rhys

Rhys is a total outdoorsman! When we met this 16-year-old from Brainerd, we found out that he is not only battling cystic fibrosis, he’s also enduring Class IV heart failure. During his wish interview, he couldn’t stop talking about how much he loves being outdoors – boating, fishing, and snowmobiling. He even stopped the Zoom interview

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Sawyer

Sawyer

The Memorial program at Wishes & More is a financial grant to parents who lose a child.  But it is more than a gift of money, it is a gift that comes from the heart of a community who cares and is symbolic of that community.  We recently gave that support to the family of Sawyer,

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Sara

Sara

Little Sara was diagnosed with Acute Lymphoblastic Leukemia in November of 2004, about a month after celebrating her 3rd birthday. Sara was born with Down Syndrome and the extra chromosome endeared her to all who knew her. She radiated love and charm and her diagnosis was a huge blow to the entire family. As Sara

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Kenedi

Kenedi

Twin sisters, Kendal & Kenedi, were both diagnosed with AML at just three-months-old. After both girls made it into remission, it was a devastating blow when Kendal relapsed almost two years later, and her parents reached out to Wishes & More. We rushed into action to support a trip to Disney for her and a

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