Wishesandmore

Ava

Ava

Little Ava was born with multiple developmental delays that left her with a defective heart and minor hearing difficulties. Ava is still an active and joyful four-year-old who loves to sing and dance, play with her older brother, and has a strong passion for the movie Frozen. Ava’s number one wish was for a chance […]

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Anthony

Anthony

18-year-old Tony loves listening to and playing music. He suffers from a rare form of Acute Lymphoblastic Leukemia, called T-Cell Lymphoma, and spends much of his time in Texas in order to receive treatment. Music has been such an inspiration for Tony, especially that of Andrew McMahon who also lives with T-Cell Lymphoma. Tony’s number

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Afton

Afton

Little Afton, at only two-years-old, was diagnosed with an extremely rare condition called Total Intestinal Aganglionosis. Wishes & More® was honored to aid in granting this sweet girl’s wish of a special one-level, backyard activity playground that is easy for her to use. Sweet Afton was able to enjoy her special playground with her loved

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Abby

Abby

14-year-old Abby suffers from a unique heart condition called Univentricular Heart pulmonary valve atresia, meaning she has valves that obstruct the outflow of blood from the heart to the lungs. Abby’s interest include shopping, sports, animals, and her favorite color is green. Her old room was small and didn’t have much space for her to

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Aimee Jo

Aimee Jo

Aimee Jo is 17-years-old and a member of the Totino Grace High School Show Choir. She was diligently preparing for the competition season when she began to feel ill, and by January she was diagnosed with Ovarian Cancer and was immediately brought into surgery. During her recovery she began chemo treatments and lost her hair,

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Jordan

Jordan

Jordan is a sweet young girl living with the challenging condition of Cystic Fibrosis. Jordan is as brave as it comes and never lets her smile fade even as she endures her daily routine of 20 -25 pills; two nebulizers with 3 medications; and two vest treatments taking a total of two hours. Jordan loves

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hannah

Hannah

Hannah, a sweet, brown-eyed girl “with more spunk than a firecracker,” was diagnosed two years ago with Steven Johnson Syndrome, which progressed into Toxic Epidermal Necrolysis, a shockingly painful disease.  She has endured blisters covering her body, both internally and externally, loss of her vision and inability to eat. Whether showing her fabulous sense of

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Matthew

Matthew

In the beginning of August 2011, Matthew began feeling overly tired and ill, so he went in for what he thought was mono. Unexpectedly, it was cancer – Acute Lymphoblastic Leukemia. From that point, Matthew had to return to Children’s hospital on a weekly basis for chemotherapy. Matthew showed his strength and determination and completed

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mason

Mason

Mason has been carefully and extensively shopping for a used car that will take him to NDSU next January. He excitedly visited the Wishes & More® office when he found the one – a used Infinity! When Mason stopped by to pick up his allowance check, we also gave him a few supplies to keep

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Jax

Jax

In October of 2014, sweet little Jax lost his battle to brain cancer at just four months old. An only child, his smile filled his home. We weren’t able to fulfill a wish for this little guy so Wishes & More® immediately wrote a memorial check to his grieving parents. When speaking with his mother

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Ahmed

Ahmed

Ahmed is an adorable 2-year-old boy who loves the character Elmo and playing with balloons and musical toys. Unfortunately, Ahmed suffers from Undiagnosed Neurodegenerative Disease. When Wishes & More spoke with Ahmed’s family, they wished for items to make Ahmed a safe and comfortable home nursery. Wishes & More was able to grant this wish

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Derrick

Derrick

Derrick was a cheerful, athletic teen ready to head to Southwest Minnesota State University in the fall to play baseball when he started feeling tired and weak. In August 2011, Derrick was diagnosed with Leukemia which marked the beginning of his struggle with chemotherapy and numerous hospital visits. Derrick’s wish was to receive all of

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Eddie

Eddie

Eddie, nicknamed “Eddie Bear” by his devoted family, faced many struggles during his too short lifetime, including Stage 5 kidney failure. Despite the challenges Eddie faced, he was an incredibly sweet, loving child who touched the lives of everyone he met. He enjoyed music, listening to his sisters as they played joyfully in his presence

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Emily

Emily

Seven-year-old Emily began having unexplained seizures at birth. They vary in length and severity, and she often has hundreds a day. A multitude of medications has caused severe sleep and digestive disturbances, intense pain, infections and visual and motor coordination impairments. Emily undergoes numerous therapeutic treatments weekly and had a device implanted in her brain

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Haley

Haley

At age 15, Haley noticed small dots and bruises on her body. Suddenly her life changed forever when she learned that she had acute lymphoblastic leukemia. She endured grueling treatments resulting in fatigue, pain, nausea and hair loss. At one point, Haley developed a clot in her brain causing terrifying speech and mobility difficulties. Wishes

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Isabella

Isabella

Isabella, a loving and bubbly baby, had a big heart, literally and figuratively. Due to her enlarged heart (caused by Ebstein’s Anomaly), and Pulmonary Artesia, Isabella braved three open-heart surgeries, throughout which she never stopped expressing her love through smiles and cuddles. She proved that it is not the size of a heart that counts,

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Michael

Michael

Mike is a bright 8th grader who loves to visit the science museum, play on the computer and build model rockets. In April, he began to develop headaches. Then one evening his mom noticed he was walking funny and the next morning the left side of his tongue went numb. They soon discovered Mike had

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Natalie

Natalie

Friends & family, exploring Uptown, keeping up on shows of Grey’s Anatomy and playing with the iTouch are all things a regular, healthy, 18-year-old girl has on her mind, and Natalie was no exception. That is until she was diagnosed with Ewings Sarcoma and her life was forced to change a little bit. All the

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Noah

Noah

Since birth, Noah has suffered from development delays and a disorder causing chronic seizures requiring brain surgery and a cocktail of medications. Debilitating side effects have included chronic pneumonia, which sometimes necessitates a ventilator and feeding tube. Despite this, Noah is a “sweet, funny guy” who enjoys reading and going to school. His favorite pastime,

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Riley

Riley

Riley was just four-years-old when he was diagnosed with Leukemia. After many hospital stays and on-going treatments, Wishes & More sent Riley, his sister MaCayla and his parents to Disney World. Riley’s favorite part was the Jedi training but they all had a blast at the parks, meeting the characters and getting the behind the

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Shelby

Shelby

Shelby is a 16-year-old girl who lives in Bay City, Wisconsin. She recently completed treatment for Hodgkin’s Lymphoma and she is working at getting back into being an active teenage girl. She loves the Green Bay Packers, her horses and country music. Her favorite country singer is Dierks Bentley and she has all of his

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Riley

Riley

Six-year-old Riley was born with a very rare disease called Aicardi Syndrome (a neurological syndrome). This disease is so rare that there are only approximately 500 cases worldwide. After developing complications from pneumonia, Riley passed away before she could experience the joy of a wish from Wishes & More. After Riley passed, Mom wrote: “This

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Sophia

Sophia

Little Sophia’s battle with seizures can take it’s toll on a daily basis.  But when she talked about visiting Disney World – her eyes lit up with joy at the thought of visiting all the parks and meeting her favorite characters.  Sophia’s wish came true in March when they jetted off to FL leaving the

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Christina

Christina

Tina is a teenager with a lot of hobbies and interests. She enjoys listening to music on her iPod and playing Just Dance on her Wii. She also likes the Minnesota Wild, Italian and Chinese food, and hopes to visit Norway one day. Tina was diagnosed with Mitochondrial disease, making it hard for her to

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