Helena unexpectedly experienced nausea and vomiting, accompanied by a tremor in her left arm, and was rushed by ambulance to the nearest hospital. Immediately, a CAT scan was performed, which revealed a large tumor in the middle of her brain. After she was stable, they life-flighted her to St. Paul Children’s Hospital. While in flight, […]
At just three-years old Raphael took his last breaths in the arms of his parents. He suffered an extensive brain injury during his birth that was not identified until 24 hours later. The doctors rushed him to surgery but did not cure the damage the brain injury had caused – resulting in poor vision, breathing
AD was seventeen years old when he was diagnosed with Osteosarcoma. This shocking discovery was followed by an entire year of intense and difficult treatments before he came to Wishes & More and we learned of his desire to get a car allowance to help him pay for the car of his dreams! As AD
Alexa is a strong-willed young lady who suffered a stroke and brain bleed, resulting in many months in the hospital fighting for her life. When we first connected with Alexa’s parents, she was still in critical condition and they were hopeful that she would survive to experience a wish, but her future was very uncertain.
Four-year old Leo suffers from numerous conditions – epilepsy, chronic lung issues, and blindness. Additionally, he is nonverbal and Gtube dependent. Leo absolutely loves music and even though he is nonverbal, he will hum to himself while the music plays. Sensory items bring him joy along with hanging out with friends, his brothers, his dog,
Six-year-old Kellen was thought to simply have a lazy eye, but when an eyepatch didn’t solve the issue, his parents sought a second opinion. They were blind-sided by the news that Kellen had a brain tumor the size of a tangerine. Soon after the diagnosis, Kellen had a successful surgery to remove the tumor but
Anna was sixteen years old when she went into kidney failure. For months, Anna experience symptoms of a common cold such as coughing fits, feeling weak, and simply under the weather. Finally, after the lingering cold symptoms lasted far too long, Anna and Mom decided to go to the hospital. Tests revealed that her body
Jamie was a sweet and loving toddler who suffered from chronic respiratory failure along with a variety of other conditions. Jamie was fully dependent on his BiPAP machine and assortment of medications; however, he loved to be around his family and in the middle of the action. He also enjoyed playing at the park and
Linae struggles daily with a serious and incurable condition caused by damage to her mitochondria. The condition restricts her to a wheelchair, but certainly doesn’t slow her down! Recently, through her own focus and hard work, this very intelligent young lady has found a love for astrophysics and quantum mechanics and her wish revolved around
Vincent is an active little guy who is the light of his parent’s lives, and they were completely devastated when they heard his diagnosis of Neuroblastoma. Little Vinny continued to shine brightly and surpass some major milestones – including completing his cancer treatments with clear scans after 8 rounds of chemo and a surgery to
Fifteen-year-old Julie is an outgoing, but quiet, young lady who suffers from a serious genetic disorder resulting in fragile & brittle bones; it also confines her to a wheelchair. Julie is a “family” girl and her condition also restricts her from participating in activities that are an important part of her family’s culture. Every weekend
After doctors found cancer in his lymph nodes, spleen and lungs, eighteen-year-old, Finn, immediately started treatments and spent many, many days confined to a hospital or resting at home. Before the diagnosis, he was a very active kid who loved backpacking and the outdoors – so you can imagine how this news rocked his world.
The 20’s Roar Again on Saturday, February 1st at the Marriott City Center! Wise Guys and Glamorous Dolls, join us as we celebrate a time of “anything goes”. Don your dinner jackets and fedoras – or slip into dresses with feathers and fringe and gather at the greatest Speakeasy to roar in a century. We’ll
2020 Winter Ball – The 20s Roar Again! Read More »
This event is SOLD OUT! Please note that there are no additional reservations available at this time; however, if you would like to be added to the waiting list in case of a last minute cancellation, please call the office 763-502-1500. Thank you! Santa Claus is coming to Acapulco Mexican Restaurant in New Brighton on Saturday,
Breakfast with Santa – December 21st Read More »
Join Wishes & More on Wednesday, October 2nd from 6-8:30pm at Tom Reid’s Pub in St. Paul for our Fall Craft Beer & Wine Tasting! You’ll enjoy a variety of great craft beer samples and wine tasting along with tasty appetizers from Tom Reid’s Hockey City Pub. All guests will also receive a souvenir take-home glass. This is a very social affair
Craft Beer & Wine Tasting Read More »
Hailey is a gentle five-year-old who loves to play outside with her brother, taking care of her dolls, Mickey Mouse, and watching Peppa Pig! She was diagnosed with Neurodegenerative Langerhans Cell Histiocytosis and is undergoing chemo, but that hasn’t stopped her from smiling and caring for others. Hailey loves Disney princesses, especially Ana and Elsa
Join us at Lucky’s 13 in Roseville for our Spring Sips & Samples Tasting Fundraiser! Guests will enjoy a variety of great boozy sips along with tasty food samples from Lucky’s + all guests will receive a souvenir take-home glass. This is a very social affair with plenty of opportunities to mingle and bid on
Sips & Samples Tasting Event Read More »
Zoe was born to loving parents with a diagnosis of Down’s syndrome and a condition known as Transient Myeloproliferative Disorder causing her lungs to enlarge two times the normal size. Brave Zoe encountered multiple rounds of low dose chemotherapy causing her challenges in breathing, trips to the operating room, and requiring intubation. Doctors found that
Morgan was born on March 21st, 2017. She was a strong and feisty girl that kept her parents on their toes throughout many ultrasounds. Through unfair circumstances, this beautiful girl was born with a severe brain dysfunction which reduced the amount of oxygen flow to her brain. With grief, Morgan passed in the arms of
Immediately after birth, Hazel was put on a ventilator and closely monitored. Hazel was born with a diaphragmatic hernia. This scary congenital defect caused Hazel’s stomach and intestines to be moved into her chest, shifting her heart to the right, leaving little room for her lungs to develop fully. After a valiant fight, on her
6-month-old Owen sadly passed away in April due to his condition called CHARGE Syndrome which resulted in extensive medical and physical difficulties. Owen peacefully passed away in his mother’s arms after his health took a turn for the worse. His mother wrote: “Brad and I decided it was best for Owen to pass in a
Grant is a sixteen-year old, struggling with a Mitochondrial Disease, who has a passion for projects and putting things together. He enjoys spending hours following directions and creating something “really cool.” He’s a LEGO pro and he hates to stop construction once he gets started and the bigger the better; consequently, his wish could not
Hayley is a 16-year-old from Bloomington who had been experiencing unexplainable symptoms for months before a diagnosis of ALS. She had already lost her ability to speak when doctors were finally able to diagnose this terrifying condition. This teen’s focus and drive is amazing and the dignity and strength she displays in handling this devastating
Miah is six years old with a rare genetic disorder called CDKL-5. This causes her to have seizures; and the inability to walk, talk, or feed herself due to the severe neurological impairments. Miah loves being active and outdoors but was restricted due to her wheelchair. Miah and her family wished for a deck so
* Office: 763.502.1500 | Fax: 763.502.4707
