Danielle and Jareth were thrilled with the anticipation of the birth of their baby girl. The excitement turned to fear when she arrived extremely early, at only 22 weeks, and weighing a mere 14.5oz. Right away, their precious Kenley was given a very poor prognosis…but her doctors obviously didn’t know this tiny girl was such […]
A wonderful reminder of our “why”! Enjoy reading this thoughtful note from Mom! “Our daughter, Cary Lynn, qualified for a wish from Wishes & More due to her having several life limiting medical conditions. Cary Lynn is complex and doesn’t get to go out much or travel due to a compromised immune system. COVID shrunk
Milo was a very happy baby, but as he grew, he started exhibiting problems with movement of his limbs, especially his right arm. At 6-months-old, his parents knew something serious was wrong. After a whirlwind roller coaster of procedures and testing, his doctors confirmed that Milo has cerebral palsy caused by a congenital brain malformation.
Meet our warrior wish baby – Brandyn! This little guy just had a big milestone and Wishes & More was incredibly happy to be a part of the big celebration! Brandyn was born at 28 weeks with Down Syndrome and a critical heart condition. His frightened mother found out that before he would ever be
Thirteen-year-old, Makena, is a delightful young lady who struggles daily with a very rare chromosomal syndrome resulting in developmental delays and a hole in her heart. Makena’s communication is very limited, but Dad knows exactly when she likes something because of her sweet smile and contagious giggle! She loves participating in lots of activities –
Meet Bowdenn! He is a typical, active one-year-old who loves to be outside swinging and playing . This little guy is an only child, and his diagnosis of Neuroblastoma rocked his family’s world. Cancer isn’t something that anyone wants to hear, and for first-time parents, Allie & Austin, their baby’s diagnosis was terrifying, and the
This past Easter, shortly after her 17th birthday, Paige came down with a severely high fever accompanied by a sore throat, stiff neck, and upset stomach. Oh no – COVID-19! No, that test came up negative. Mono? Strep? – also negative. Doctors continued testing, and to everyone’s surprise and dismay, cancer was the official diagnosis.
Just short of his first birthday, this adorable little boy was diagnosed with a Wilms Tumor – resulting in large growths on each of his kidneys. Asher immediately got started on a chemo protocol and his tumors responded well; however, he then developed Nephrotic syndrome. This condition damaged his kidneys to the extent that both
In May of 2012, little Ethan was born with a host of health care issues that would forever affect him physically, emotionally, and developmentally. He was put up for adoption in Florida and in December of 2012 he was adopted into a loving family in Minnesota. Knowing that he would need a high level of
Blake’s parents experienced the unimaginable in the delivery room when their son was born and unable to breathe on his own. He was immediately transferred to Children’s Hospital where they discovered a lump on his neck and, just two days later, Blake underwent surgery for a biopsy and bone marrow test. The results were Neuroblastoma
It was right before Christmas in 2017 when Ara & Ailey decided to make their premature arrival. Unfortunately, their early delivery came with a host of complications due to their underdeveloped organs and these first-time parents made the hospital their second home. They lived every minute under the strain of watching their two tiny babies
At only 6-weeks-old in December 2018, Whitney was diagnosed with a large brain tumor. She immediately underwent three surgeries within a month’s time to remove 95% of the tumor. As you can imagine, her parents were extremely frightened by everything their daughter was enduring but were grateful when Whitney was able to be home for
Little Livi’s parents wanted to convert their backyard into an outdoor play area that was safe and fun for her to enjoy with her two older brothers. A costly, but critical component, was a privacy fence and that’s what they shared with Wishes & More as a wish on her behalf. We were happy to
Jeremy was born with a very serious and debilitating condition where large portions of his spine were missing. These deformities have led to other serious difficulties with eating, breathing, fluid on the brain, among others. He has never been too far from a hospital stay and his wish was to spend more time outdoors. Sounds
This beautiful and bright young woman was born with a severe heart problem and had three open heart surgeries before the age of seven. We met Abby when she was 14 and we granted her wish for a full bedroom makeover because she wanted to enter high school with an updated space where she could
17-month-old Carter was born with very serious lung function issues and just one-hour post-birth, he was intubated and his life-long struggle to breathe began. His medical team was running out of local options and he was air transported to lung specialists in Texas. At three months old, he was placed on a lung transplant wait
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,
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
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
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
Sweet little Rockii was born extremely premature and continued to battle serious medical issues that kept the tough fighter in the hospital for thirteen months. When mom finally heard she could take her precious, little guy home she realized that she didn’t even have a crib because he hasn’t been home since birth. Rockii’s mama
4-year-old Ryan suffers from Transverse Myelitis, an inflammation of the spinal cord that has him anchored to a wheelchair. However, in his heart and his mind he is still “all boy” and he desperately wants to play sports and be outside “running” around with his siblings. Uneven and unlevel ground are additional barriers and
Olivia, from Glenwood City, WI is an adorable little girl with a very rare condition which gradually shrinks her brain. As you can imagine, this is incredibly difficult for her family to deal with and to understand especially for big brothers, Brandan and Charlie, who love and adore their baby sister. Olivia’s parents recognize the
Rosie is a 18-year-old with a rare genetic disease called Tuberous Sclerosis which causes benign tumors to grow in many parts of her body. She is developmentally at the age of a three year old and is unable to verbally communicate so she expresses herself with hand gestures. But she doesn’t need to speak when
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