Tag: Dream Bedroom

Jacob

Written by Garrett Nantz on June 26, 2021. Posted in Meet the Kids.

18 Years Old
Down Syndrome, Leukemia

We’d like to introduce you to Jacob. This handsome and ambitious young man will be getting a spectacular bedroom makeover from Sunshine on a Ranney Day. Although Jacob has endured many challenges in his short nineteen years, he hasn’t let them thwart his energetic and loving spirit! Despite having Down Syndrome, undergoing over 100 surgical procedures and surviving Acute Lymphoblastic Leukemia, he has accomplished a plethora of high honors in advocacy for children’s healthcare, educational reform and in several sports through the Special Olympics. He has won three gold medals; one for the 50 M Dash, one in Softball and one for the 50 M walk! With his mom by his side, Jacob has been involved in media awareness events with CBS, CNN, Fox and The Associate Press. He is also involved in many organizations including Rally Foundation for Childhood Cancer Research, the National Down Syndrome Congress, the Down Syndrome Association of Atlanta, North Metro Miracle League, Georgia Autism Society, Autism Speaks, Sibley Heart Center, Make-a-Wish Foundation and Camp Sunshine. The list goes on as he has dedicated his life to reaching his ultimate dream: that society will see him for his abilities and not his disabilities. This is his dream, not only for himself, but for all children. He does not let disability, illness, chemotherapy or anything else get in the way. Although he completed 3.5 years of chemotherapy, he has 4.5 more years of monitoring before he can be considered cured from cancer.

Despite having Down Syndrome, undergoing over 100 surgical procedures and surviving Acute Lymphoblastic Leukemia, he has accomplished a plethora of high honors in advocacy for children’s healthcare, educational reform and in several sports through the Special Olympics.

It will not stop him from achieving his goals and working hard to make a difference. Jacob is adventurous and spirited, enjoying the wonders of teenage living including listening to music, going on roller coasters, attending sporting events and attending Prom at Night to Shine. He loves reading, playing the bells and xylophone, hanging out with his friends, dancing in his tuxedo and playing baseball. We love his smile and warm heart. Nothing will give us greater pleasure than spreading a little sunshine through a dream makeover especially for him!

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Photography by Nicole Photography

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Preston

Written by Garrett Nantz on June 26, 2021. Posted in Meet the Kids.

17 Years Old
Tranverse Myelitis

Preston is a 14 year old boy who loves Spider Man, learning about the customs of foreign countries and building blanket forts. He is non-verbal, hearing impaired, medically fragile and suffers from Cerebral Palsy. Preston lives with his 4 siblings in an active household. He shares a room with his 6 year old brother, Asher. Preston cannot walk for long distances and uses a wheelchair when venturing out of the house. Preston must be supervised 100% of the time and is home schooled during the winter months. Before he was born, Preston was diagnosed with Polymicroygria, a genetic disorder, causing seizures, delayed speech and muscle weakness. Preston is a private child who loves to spend time in his room. Sunshine on a Ranney Day is excited to partner with sponsor, Kids R Kids, to build Preston a Dream Bedroom which will give him an escape from his bustling household and his 3 year old twin sisters!

Before he was born, Preston was diagnosed with Polymicroygria, a genetic disorder, causing seizures, delayed speech and muscle weakness.

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Photography by Pear Tree Photography

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Sophia

Written by Garrett Nantz on June 26, 2021. Posted in Meet the Kids.

16 Years Old
Cystic Fibrosis

We are beaming with excitement to announce that Sunshine on a Ranney Day will be giving Sophia a dazzling dream bedroom makeover! This smart, beautiful and wildly spunky sixteen year old is proof that mighty power can come from within a tiny package. From the beginning, she was a ball of spit and fire. Her unwavering perseverance has served her well. Diagnosed with Cystic Fibrosis at the age of four, she has faced her trials with the strength and courage of a superhero. She has endured daily airway treatments, multiple lengthy hospitalizations and fought off the most dangerous bacterial infection, Burkholderia Cepacia. Despite these aggressive ailments, she exudes confidence, fierce passion and a desire to change the world for the better. Sophia loves music and singing. She has been playing the drums soulfully for over four years and learned to play the ukulele during her last hospital stay. She is a gifted writer, putting this talent to good use by writing songs that her music teacher is helping her produce. She is also writing a compelling novel that is centered around a character who lives with Cystic Fibrosis. This is just one of many opportunities she takes to educate others about CF. Sophia has been actively engaged in her treatment with medical professionals since she was old enough to ask and answer questions. Admirably, she has also chosen to participate in research studies to help further scientific advancements in CF care. We can’t wait to surprise her with the makeover of her dreams! We hope that you will support our efforts and join us at the unveiling of this completed project.

Diagnosed with Cystic Fibrosis at the age of four, she has faced her trials with the strength and courage of a superhero.

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Photography by Niki Murphy Photography

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Christian B

Written by Garrett Nantz on June 26, 2021. Posted in Meet the Kids.

17 Years Old
Lennox-Gastaut Syndrome

This dapper seventeen-year old young man with an ear to ear smile is Christian. His infectious grin can melt your heart and comfort your soul. He touches the hearts of everyone he meets and inspires others to make a difference. Christian is seventeen years old and attends Dacula High School. He lives with his Mom, Dad and two younger sisters (Cathryn 15 and Ashlyn 13). Christian was born healthy and developed as an infant should, meeting milestones as expected. He was a quiet little guy and didn’t have much to say in terms of babbling or words as he was approaching two years old. He was a late walker, as he started walking around 18 months. That was also about when he started having frequent involuntary breath holding spells. His lips and fingers went blue and he would go limp for 30 seconds or so. This was incredibly concerning and it was happening involuntarily. Christian began having grand mal seizures, drop seizures and breath holding spells on a daily basis. It was a challenge to get these seizures under control, as well as obtaining a true diagnosis. He and his family spent most of their time with neurologists or in the hospital. They were desperately looking for answers and sought the help of a geneticist. Christian was in status epilepticus meaning that his seizures were constant and wouldn’t stop. Doctors had to put Christian in a drug induced coma and he was in the PICU for almost 2 weeks. He was only 3 years old. He was in the hospital for a month and they still needed a way to manage his seizures. They tried multiple medications and a Ketogenic diet. Neither worked. He also had reflux and difficulty swallowing, so it was decided that he needed a G-Tube and a Fundoplication to help with the reflux.

Christian began having grand mal seizures, drop seizures and breath holding spells on a daily basis. It was a challenge to get these seizures under control, as well as obtaining a true diagnosis.

Christian was also diagnosed with Spastic Cerebral Palsy due to his disordered muscle tone and contractures. He endured another significant episode of epilepticus and was hospitalized in November 2013. He spent Thanksgiving in the hospital and wasn’t released until Christmas. After that, he was assessed by a new neurologist, who diagnosed him with Lennox-Gastaut Syndrome (LGS). LGS is a severe form of epilepsy that typically becomes apparent during infancy or early childhood and is most often diagnosed between 3-5 years of age although it took longer to determine that this was another syndrome Christian had. Since then Christian has been on a regimen of six medications and daily supplements which have minimized his seizures. He is essentially nonverbal, but can vocalize some sounds and words including Momma, Dadda, PopPop, Nana and Papa. He also uses sign language with a few consistent signs that he uses to communicate basic want and needs. He requires full assistance when walking and wears AFO braces to help support his feet and legs. He can take a few steps on his own when he’s highly motivated. If he does walk, he tires very easily and can only walk short distances. His home is currently not wheelchair accessible. When he needs help with mobility, his family carries him from room to room. He uses a wheelchair for mobility outside of the home. Christian is such a laid back kid and just goes with the flow. He can be quite the jokester. He loves to be silly and get a reaction out of you. He enjoys looking at pictures of family members and friends. He has a special memory book of photos that he looks through every day. He also loves going on family vacations to the beach and Disney World. He enjoys watching his favorite shows when he’s relaxing. Christian’s favorite place to unwind and be free is his bedroom. That is why Sunshine on a Ranney Day is thrilled to be able to give him a dream room makeover and renovate his bathroom to be accessible. This project will soon be under way and we hope that you will get a kick out of seeing the finished product. This will be a labor of love and we invite you to join us in support of this venture.

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Photography by Dinah Sutton Photography

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Photography by Sweet Life Photography by Kim

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Joseph

Written by Garrett Nantz on June 25, 2021. Posted in Meet the Kids.

19 Years Old
Spina Bifida

We’d like to announce that this handsome man, Joseph, will be the lucky recipient of a dream room makeover and bathroom renovation from Sunshine on a Ranney Day. He is not only charming, but also a victorious warrior who has won many battles throughout his lifetime. During pregnancy, Joseph’s parents were given the news that Joseph was going to be born with Spina Bifida as well as a Chiari malformation, which is s structural defect in the brain, and hydrocephalus. Joseph was born three weeks early and was immediately rushed over to Children’s Hospital for surgery. He spent the first several months in and out of the hospital and has endured seventeen surgeries over his nineteen years of life.

During pregnancy, Joseph’s parents were given the news that Joseph was going to be born with Spina Bifida as well as a Chiari malformation, which is s structural defect in the brain, and hydrocephalus.

His disabilities do not define who he is and he never lets them slow him down. Joseph always has a smile on his face, loves to laugh and make jokes. He has a deep love for sports and has played Baseball, Wheelchair Basketball and Wheelchair Football. His incredible passion for sports is unwavering and he loves not only to play, but also to watch or help coaching younger teams. He currently helps manage his old 8th grade Middle School team at Vickery Creek Middle. Joseph aspires to work for a professional sports team one day. He is always willing to try new adventures and works diligently to reach his goals. He is encouraged to dream big and he will surely succeed as he never gives up. Sunshine on a Ranney Day is overjoyed to be working on a special renovation project designed especially for Joseph. This project will not only provide him with a fabulous new room, but also an accessible bathroom. Join us in spreading cheer throughout his home so he can enjoy his bright future in style.

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Photography by Dinah Sutton Photography

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Photography by Dinah Sutton Photography

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Devon

Written by Garrett Nantz on June 25, 2021. Posted in Meet the Kids, The Wall Nut.

20 Years Old
Spinal Injury

You may have heard the story. You may think you understand the challenges Devon Gales and his family have faced over the last 2 years since Devon suffered a traumatic spinal injury during a football game between the University of Georgia and Southern University. There’s always more to the story, however, and for Devon and the Gales family, there’s a lot more life to live. Starting the next chapter is where we can help. If you do a Google search for “Devon Gales”, chances are you’ll find pictures of a smiling young man, probably wearing a cross around his neck, and possibly with his Mom, Tish, close by his side. Those are just a couple of the things that have helped Devon through many of the adversities he’s faced in his life. Devon has been dealing with challenges since the day he was born. He was born with a birth defect and almost didn’t make it through his first few days. He persevered from the outset, however, and the world has gained a shining, happy smile, with a spirit to match, as a result. Through the adversity in his life, Devon’s parents, Tish and Donny, have always pointed to God’s plan. It’s been through this profound faith instilled in the entire Gales family that they have pressed forward, confident that God has a plan and a place for us all. Perhaps the biggest challenge to that long-instilled faith was first realized on September 26th, 2015. Devon had only received a few chances to play in the first half of the game. He was committed to do his part on a kickoff return at the beginning of the 2nd half. He saw that opportunity present itself as Georgia’s kicker, Marshall Morgan, charged down the field. Devon put his all into a block, trying to slow Marshall down and, moments later, he was lying on his back, staring at the clear blue September sky, unable to move his legs.

Devon put his all into a block, trying to slow Marshall down and, moments later, he was lying on his back, staring at the clear blue September sky, unable to move his legs.

Tish and Donny had been unable to make the trip to Athens for the game. As they watched from the family’s home in Baton Rouge, The report was that a “Southern player was down on the field.” Tish’s motherly instinct kicked in and she knew Devon was hurt. Getting information about Devon’s status was difficult at first. When a nurse from Athens Regional Hospital finally called, Tish’s only question was “Do I need to be on the next flight to Georgia?” The nurse’s quick response was “Yes, I think so.” As the Gales have continued down this path which God has placed them on, adversities have continued, as well. Their home in Baton Rouge was in an area which flooded only a few months ago. They had previously been struggling with the idea of moving the family to Atlanta. Moving to Georgia would put Devon closer to the care of The Shepherd Spinal Center and the expert care there. The flood, they decided, was another way of God telling them “it was time.” The time has come and this family is being blessed. The community has pulled together to build Devon and his family a new home. Currahee Homes, Paran Homes, WSB Radio took the lead on making this happen. There are some amazing people working on this project. Go over to to learn more about these amazing people. Sunshine on a Ranney Day, along with our designers at Crosby Design Group, are doing the interior design of Devon’s new home and completing his wheelchair accessible bathroom, bedroom, and in-home therapy room. We are blessed to be just a small part of this very large and heart-felt project!

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Photography by Nicole Photography

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Noah

Written by Garrett Nantz on June 25, 2021. Posted in Meet the Kids.

19 Years Old
Spinal Injury

This handsome and adventurous young man is Noah. Exploration of the great outdoors and exhilarating activities fuel Noah’s passion. He lives for adventure and spending almost every waking moment outdoors. While some teens enjoy playing video games for hours on end, Noah prefers to keep his eyes on the sky and feet off the ground. As a young teenager, he spent most of his time pedaling his bike over mountain trails, flipping off boulders into a lake, diving, snowboarding or wakeboarding. He and his friends shared many escapades at skate parks and trampoline parks where he excelled at skilled tricks and flips. His favorite organized sport is baseball and he played in several levels throughout the years, including recreational ball, All-Stars and Travel ball. He even achieved his ultimate goal: playing at Dreams Park in Cooperstown, NY. On July 26 of 2017, everything changed within a split second. Noah was in an accident that altered his future tremendously. He had gone with two of his friends to their favorite trampoline park. They were jumping for most of the afternoon, doing their usual flips and tricks. Noah was working on perfecting a flip when he under-rotated and landed on his neck. This harsh landing ended up compressing his spinal cord and fracturing three vertebrae. Instantly, he lost all feeling from his chest down. His arms and hands went limp and he felt the sensation of being outside of his body. He was rushed to the hospital via ambulance and endured a significant live saving surgery. In this invasive procedure, two rods were inserted to re-align his spinal cord and eleven screws attached the vertebrae to those rods.

Upon his homecoming, Noah faced a new set of challenges as his home was not adequately designed for living with a wheelchair.

Fortunately, the spinal cord was not severed, but he sustained spinal cord injury that left him a quadriplegic. He spent two weeks in ICU and then transferred to an intensive inpatient therapy program for nine weeks. He worked diligently in physical therapy several hours per day to regain motor skills and relearn how to do everyday tasks that previously happened automatically. After inpatient rehab, he spent six weeks in a specialized outpatient therapy program where they continued to target skills that seem so simple. The skills we all take for granted, like rolling over. Through determination and hard work, Noah found himself becoming stronger, regaining sensation and learning how to live life after his injury. He and his therapists worked on getting dressed, bathing and completing school work. He also learned to mobilize via a wheelchair. This was quite different than what he was used to. Upon his homecoming, Noah faced a new set of challenges as his home was not adequately designed for living with a wheelchair. The home’s floor plan included narrow doorways and neither a bathroom nor a bedroom on the ground floor. He only had access to two rooms in the house and the formal living room had to become his bedroom. In addition, he was forced to take showers at the local YMCA since there was an accessible shower there. After four months of the day program with outpatient therapy, it was time for Noah to return to school. Since Noah was injured right before his senior year of high school, he missed the entire first semester while he was working to recover. In order to graduate with the rest of his classmates, he doubled up on work and completed the entire year’s curriculum in one semester. To top that off, he graduated with all A’s and B’s. Noah’s hard work and never give-up attitude has paid dividends in academics and rehabilitation. He has regained so much movement that as he has regained substantial movement and feeling below the point of injury that his condition is no longer classified as a complete injury. Noah continues today to work toward reaching his goals. This year, Noah’s sights are set on college. His ambition is to study audio and video technology. Although he previously biked down mountains, he is currently learning to maneuver his wheelchair on the rugby court as a member of the Shepherd Smash team at Shepherd Rehabilitation Center. Noah is determined to enjoy many more adventures despite his injury and refuses to allow the challenges he faces to get in the way of his dreams. He faces life with gratefulness and a reverence for those who have shown him an outpouring of love. He is especially thankful that Sunshine on a Ranney Day will be renovating his bathroom and bedroom to allow his greater independence and mobility. Please join us in bringing a little sunshine to Noah’s life by supporting this project and coming to the great reveal party!

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Photography by Nicole Photography

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Bristol

Written by Garrett Nantz on June 19, 2021. Posted in Meet the Kids.

5 Years Old
Leukemia

Howdy! This is Bristol, a steadfast warrior who has earned the title, “Bristol the Pistol” due to his perpetual triumphs and incessant desire to live life to the fullest no matter what obstacles come his way! His battle began in 2015 as a rambunctious toddler who began to experience vague symptoms that made his pediatrician suspicious. After a few rounds of testing, his parents were given the news that no parent ever dreams of hearing. Bristol had cancer. B Cell Acute Lymphoblastic Leukemia (ALL) to be exact. This rare type of cancer that was once not thought of, has become a common term in Bristol’s home. Aggressive treatment began immediately and he had the love and support of friends and family with him from the start. He has now endured 38 months of treacherous treatment that is never easy for a child to endure. Chemotherapy, blood work, spinal taps and never-ending physician visits. However, Bristol takes on every challenge with a can-do attitude and that positivity and vigor is what has kept him overcoming. During this process, Bristol was also given the diagnosis of Muscular Dystrophy. The addition of this diagnosis has not slowed him down. His spunky personality is what gets his through and gives others the desire to help him heal. Bristol is a true fighter who has proven that a country boy can survive. He loves riding horses, John Deere tractors and enjoying all that the great outdoors have to offer including fishing, hunting and camping. A hat and cowboy boots have always been part of his favorite attire. A spectacular dream bedroom makeover is just what the doctor ordered to keep him smiling ear to ear!

He has now endured 38 months of treacherous treatment that is never easy for a child to endure. Chemotherapy, blood work, spinal taps and never-ending physician visits.

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Photography by Laurie Christine Photography

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Photography by Birchfield Photography

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Gabrielle

Written by Garrett Nantz on June 16, 2021. Posted in Meet the Kids.

14 Years Old
Muscular Spasticity

Gabrielle is a beautiful young teenager that is resilient, brave, determined, vibrant, feisty, and loving. She is full of personality and is a social butterfly. She keeps people laughing. Her contagious smile symbolizes her victories over many challenges in her life. Gabrielle means “God is my strength.” Her name exemplifies how, with God’s power and resources, she has triumphed over surgeries, academic demands, physical opposition, and personal challenges. Her parents were told by doctors that she may never walk, talk or do anything. She certainly proved them wrong. Gabrielle’s story began with her being diagnosed with Schizencephaly at six months old. She has Muscular Spasticity in her arms, hands, legs and feet. Her left side, arm and leg have minimal movement.

She is unable to walk and utilizes her power wheelchair for mobility and requires assistance in transitioning activities.

She is unable to walk and utilizes her power wheelchair for mobility and requires assistance in transitioning activities. Her right side is more flexible and allows her the ability to move for feeding herself and other activities such as writing or typing on the computer. Gabrielle’s story continues with highlights of her growing from glory to glory. She is experiencing the teenage years just as she should, having fun and reaching for great goals. Gabrielle enjoys computers, editing YouTube videos and basketball. She wants to become a video editor. She loves music, dancing and playing with her best friend and cousin, William. Her favorite PS4 games are Fortnite and NBA19. Sunshine on a Ranney Day was so excited to be able to give Gabrielle a life changing wheelchair accessible bathroom and dream bedroom makeover! This will not only help Gabrielle, but will majorly help her parents so they don’t have to lift her as much! We love our job!

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Photography by Niki Murphy Photography

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Photography by Niki Murphy Photography

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Caliyah

Written by Garrett Nantz on June 15, 2021. Posted in Meet the Kids.

4 Years Old
Grease Fire Burn Victim

This radiant beauty is Caliyah. She received the bedroom makeover of her dreams. Caliyah a is spirited and poised four-year old. She loves the splendor of glitz and glamour. He favorite things to do include dressing up, doing her make-up, watching You Tube tutorials for applying make-up and of course, magical unicorns with sparkling horns. In her spare time, she enjoys producing videos of her own and she is quite the star. She certainly shines bright and loves to inspire others. Her sweet nature and perseverance are moving indeed. This year, Caliyah experienced a horrific tragedy that changed her life forever. She was severely burned in a grease fire that started in the kitchen. She suffered third degree burns on her face and arms. The pain she suffered was so tremendous that doctors put her into a medically induced coma. She spent a month receiving intensive care in the hospital followed by rigorous physical therapy.

Sunshine on a Ranney Day gave her the glamorous bedroom makeover of her dreams! It promises to be as beautiful as she is!

She missed her preschool graduation ceremony since she was hospitalized, but the school and hospital joined forces to bring a special graduation ceremony of her own right to her room. Being able to enjoy the rite of passage of graduating preschool really lifted her spirits. Although Caliyah is making great progress, she has a long road of recovery ahead of her. Her scars are still healing and she is not able to go in direct sunlight. Sunshine on a Ranney Day gave her the glamorous bedroom makeover of her dreams! It promises to be as beautiful as she is!