There is an adage about music being a universal language: “With music, you can communicate across boundaries in ways that you can’t with ordinary languages.” Shane, at eight years old, is non-verbal with numerous disabilities, but it is very evident that he hears or feels the music. Weighing 1pound,13 ounces at his very premature birth, Shane had bleeding on the brain, requiring a permanent shunt that has since been replaced twice. He does not sit or stand without support, with a Cerebal Palsy diagnosis, and is very developmentally delayed. Shane also lives with Visual Impairment-Optic Nerve Atrophy and Generalized Hypotonia, commonly recognized as decreased muscle tone.

Shane’s parents were able to move their family, which also includes his little sister, to a ranch style home to better accommodate his wheelchair. Home is a bustling place where Shane’s sister is a very active child. She is quite protective of Shane, and dad likes to say she talks enough for the two of them. The family also includes Shane’s grandparents, who immigrated from India to help with his care. The financial burden of Shane’s care has kept the family from being able to add an accessible bathroom, so they must lift Shane’s 60 pounds (and growing) frame and carry him from outside the bathroom to the tub. Giving a bath has become an overwhelming physical and emotional task after days filled with physical therapy, occupational therapy, feeding therapy, vision, aquatic, and speech therapy.

Shane may not be able to carry on an interactive conversation but imagine a less stressful end to a busy day; a safe bath and then his enjoying some music with his family in the safe harbor of a colorful and accommodating bedroom.

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Most soccer moms agree that driving teenage boys home from practice and games can make for a pungent experience and that a shower is first on the agenda at home. If only it were that easy for Alejandro, who plays for the Atlanta Sting power soccer team. Having been diagnosed with Duchenne Muscular Dystrophy when he was six years old, he has been able to overcome many challenges. Alejandro has participated in numerous sports, including soccer, basketball, baseball, swimming, and even competed in a special needs triathlon. Unfortunately, whereas most boys go home and jump in the shower after sporting events, Alejandro’s bathroom is not adapted; his wheelchair doesn’t fit. Transferring from the chair to the shower and back is difficult, frightening, and risky as his bones are brittle. Recently a fracture in his legs caused a fat embolism that led to respiratory failure and resulted in a one week stay in the intensive care unit. This experience has caused Alejandro to fear the transfer and exemplifies the need for an accessible bathroom.

There is no more deserving teen than Alejandro. He approaches all challenges with great effort and courage. Alejandro has been very cooperative with all of his treatments since day one as well as participating in various research and clinical trials to help the scientific community find treatments and better care for boys with Duchenne Muscular Dystrophy. At home, Alejandro likes to play video games with his brother and friends and loves movie nights with his family. Like most teens, he enjoys relaxing in his room, listening to music. He plans on going to college and getting a degree in Endangered Species Biology.

A “Dream Bedroom” and an accessible bathroom will provide Alejandro with the independence teens crave and keep him motivated as he works toward his dream of becoming a scientist.

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Light shows can be quite mesmerizing, and at the end of the day, ten-year-old Caitlin loves to go to her room where various lights provide her own nightly “light show.” Caitlin is severely developmentally delayed, non-verbal, unable to walk, requires around the clock care, and is at risk due to her yet to be determined mitochondrial disease/disorder. From her first seizure at four months old to now, Caitlin’s ten short years have been a whirlwind of medical procedures and surgeries. As Caitlin grows older, the impact of her conditions will cause further delays and her system will begin to deteriorate.

Although she is non-verbal, Caitlin has no trouble letting people know how she feels or what she wants by giving a cute, little yell! She loves to be on the move, both in her wheelchair and the car. Caitlin’s family feels fortunate to have been able to move into a one-story home where everything is on one level, and she is blessed with wonderful grandparents, friends, and neighbors who love and adore her.

Caitlin stays home with her mother and participates in the hospital homebound school program as well as therapy programs. Caitlin requires round the clock care. As she continues to defy the odds, her growing size has made bathing difficult for her parents, and an accessible bathroom will make bath time safer and even fun. An adapted bathroom and “Dream Bedroom” will help Caitlin end her day with her mesmerizing light show and she will continue to shine as the light of her parents’ lives.

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This handsome fella with dazzling eyes and an incredibly bright smile is Pablo. He is the lucky recipient of the next dream make over from Sunshine on a Ranney Day!

Twelve years ago, the family was excited to welcome Pablo into the world after a joyous pregnancy. When he finally arrived, he endured a traumatic birth with his umbilical cord wrapped around his neck. During this time, adequate oxygen was not being delivered to his brain and tremendously affected his ability to thrive. At birth, he was diagnosed with cerebral palsy, diplegia, spasticity and asthma. Although devastated by this trauma, his family was determined to ensure that he had a brilliant future in which he’d achieve all of his goals. That is exactly what he is doing.

This self-determined preteen is diligently working toward great achievements and does so with a happy spirit. He enjoys hippotherapy at MacKenna Farms where he has grown to love riding horses. He wears AFOs on his legs to help with tone and gait, as well as uses a wheelchair to get around on his own. He requires assistance with his activities of daily living including toileting and taking a shower. His home currently only has one bathroom and it is not wheelchair accessible. This makes his daily routine challenging and has become a barrier to developing further independence. Sunshine On A Ranney Day will be remodeling his bathroom to be fully accessible and will provide him an unforgettable designer bedroom. We can’t wait to see him beaming with glee when he sees it!

Pablo is fond of many things including dogs, classic cars, the color blue and Bruno Mars. Like most teens, he loves to chat about the things he loves most and those who know him best say he is quite the chatterbox. Despite the obstacles he faces, he continues to reach for the stars.

We hope that his newly decorated room inspires him to soar even further. We’d love to have your support in completing this project and hope that you will join us for the big reveal.

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We are proud to introduce you to Lainey. This beautiful princess is thirteen years old and is a devoted daddy’s girl. Her biggest fans are her two big brothers and her dog Buddy. She recently became aware that Sunshine on A Ranney Day will be renovating her home and she is absolutely thrilled! Sunshine on A Ranney Day is planning a spectacular dream make over for her and is looking forward to breaking ground on this project.

Lainey is the baby of the family and was born with Spina Bifida. She resided in the NICU at Children’s Hospital of Atlanta at Scottish Rite for 27 days. While there, she endured multiple medical procedures and three distinct surgeries. Since that time, the number of surgeries she has undergone has risen to twenty-seven. Despite the fact that surgery is a major event and most people never endure more than one, Lainey withstands them like a champ. She is exceptionally brave and extraordinarily cheerful. In addition to a vast number of surgeries, she also has a VP shunt, a spinal shunt, a neurogenic bladder, scoliosis, and is wheelchair dependent. She relies on others to meet all of her needs throughout the day.

Currently, Lainey has growing rods, also known as Harrington Rods, that were surgically implanted along her spinal column to correct scoliosis and they are lengthened every six months. This procedure is excruciatingly painful, but she faces these procedures with positivity and poise.

Lainey is a 7th grader at McClure Middle School and wholeheartedly loves her teachers, friends and the school community. She has an amazing memory and is obsessed with learning people’s names and the names of their dogs and children. She participates in aquatic therapy at Kool Kidz as well as occupational therapy and at McKenna Farms. For fun, she likes playing on her iPad, swimming and the beach. Lainey loves all things Disney and princesses. She is using her experience to inspire others and make a difference in the world by serving as a miracle child for UGA Miracle and loves raising funds for Children’s Hospital of Atlanta.