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 […]
Carter’s mom describes her fifteen-year-old son as, “….the most delightful and loving boy.” More than anything, Carter loved spending time with his family and friends. Carter’s smile would light up his world and his favorite spot was the patio in his backyard where he could bask in the sun, hear the cardinals, and see the
Thanksgiving wasn’t the same for many people this year; for Karson, it was VERY different as he spent it in anticipation of his Wish Day on FRIDAY! This six-year-old struggles with spina bifida, hydrocephalus, chiari malformation, and neurogenic bowel & bladder (inability to control,) and yet this bundle of energy doesn’t let any of these difficulties slow
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 Emmalee! She is currently in her Senior Year at Sebeka High School and just like many other teens, COVID has taken away a lot of the fun activities of her final year of HS – but so has her diagnosis of kidney disease. Her condition has continued to worsen throughout her life to the
Ana’s Mom endured a long, intense labor, battling infection and ending with an emergency c-section. After her traumatic birth, Ana was immediately put on oxygen and whisked from her mother’s arms. Scans indicated that her brain and spine were underdeveloped and over the following days, she had constant seizures that were so severe that they
Cash spent over half of his eight months of life in the hospital, undergoing countless procedures and multiple open heart surgeries. He was born in April 2019 with down syndrome and a serious heart condition that ultimately took his life. Cash wasn’t with his family for long, but he was adored by his parents, sister,
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
Seven-year-old, Lilah has struggled all her life with an extremely rare genetic disorder that is destroying nerve cells in her brain and spinal cord. She is one of only 10 people in the US with this disease – but she has beaten the odds by her will to stay alive and and has outlived her
Last September, Chris & Christine became concerned about their 9-month old son, Brice, because he had become irritable and appeared to be in pain. A trip to their pediatrician resulted in a diagnosis of an ear infection and, yet, a couple weeks later, he still wasn’t the healthy, happy baby they knew. Back to the
Marques was born with congenital heart disease and had his first open heart surgery at just 12 days old. With continued monitoring, he was able to live a relatively normal life for the next 14 years and then things began to change. He started to have issues with breathing, chest pain, high blood pressure and,
Eliana’s parents knew they would adopt a child someday and after the birth of their 4th biological child they knew the time had come. These incredible parents traveled halfway around the world to the see the little girl they knew had special needs. But when they arrived at the Philippines orphanage, they discovered that the
Meet Willow! This outgoing, creative girl loves being in front of a crowd – whether she is singing, dancing or acting in a play, she is the life of the party. Despite her daily struggles with a gamut of spinal and bladder issues and constant monitoring for recurring infections, Mom describes her as “brave, happy
Remember Samson, the sweet and happy boy who has spent his life in and out of treatments because of his serious congenital condition? You may remember this little cutie from the video we posted of him receiving his official Wish Approval Letter (https://tinyurl.com/vop7jme). We’re happy to report that after all of the anticipation, Samson’s Disney
Nolan is a firecracker of a kid! He is always moving and loves anything that is big or loud! Monster trucks and trains are “the best” and he sleeps in a car bed, so you can guess that he loves cars as well! Nolan was born with a rare genetic mutation and severe muscular dystrophy.
Meet Jake… and Josh! If you weren’t told, you would never know that these athletic 16-year-old twins have struggled all their lives with significant, genetic heart conditions. These great guys are athletes and are a dynamic duo who are always at each other’s side – even on the baseball field! Jake and Josh play on
Eighteen-year-old Abigail had just started college at UWEC for Athletic Training when she received the diagnosis of Hodgkins Lymphoma. She has had to put her long-awaited college dream on hold and focus instead on resting and allowing her intense treatments to take effect. These treatments have taken a toll on Abbie both emotionally and physically
Meet Rory! This artsy, creative teen recently endured a reconstructive surgery on her mouth, just one of the major health issues that she deals with due to her condition – Ehlers-Danlos Syndrome. When Rory was six-years-old, she was diagnosed with this rare genetic condition and it has caused numerous issues for this kind young lady,
Like many teenagers, Rikki needed to have her wisdom teeth removed; however, when she went in for this routine surgery, she didn’t expect to hear that her jaw bone was deteriorating. The oral surgeon immediately took a biopsy, and when the results came back – Rikki learned that she had Ewing Sarcoma. Rikki’s life soon
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 –
Tia was a fighter from day one. She and her twin were born at 24 weeks gestation and both overcame many obstacles in their first year. Mom shared that Tia fought especially hard for every ounce of freedom that she could get and through it all, she had a smile on her face. She also
Caleb has spent the last year in and out of the hospital after being diagnosed with a brain tumor. He has endured 33 rounds of radiation and year-long chemotherapy treatments. His tumor is intertwined with much of his brain, and only a small portion could be removed so, unfortunately, the remaining mass is inoperable. However,
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.
