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Oakley

  • 9 Years Old

  • Spina Bifida & Hydrocephalus

Oakley was born in China in March of 2014. She was found in a baby box, and taken to the orphanage. Oakley has Spina bifida, and this is likely the reason her biological parents were unable to care for her as best as she needed. Her medical file looked really complex and scary, but the moment her family saw her picture, none of it mattered, whatever it looked like. They began the process to adopt Oakley when she was about a year and a half old, and finalized the process just before she turned two. 

Because of her Spina bifida, Oakley is paralyzed mid thigh down. She was also born with hydrocephalus and tethered cord syndrome that required surgery on her spine. Oakley uses a wheelchair but when she is at home, she likes to be out of her chair more than when she is at other places, so she will scoot around using her arms. She has some seriously strong arms! She can show you how to do a pull up or two under the table! And there is really nothing she can’t figure out a way to make work where she needs to. 

Oakley is the happiest, most joyful, hilarious child you will ever meet. She has no cognitive delays, and her sense of humor is on point. She is sharp. So smart. Her family likes to say she is 8 going on 22. She seriously runs the ship. She keeps everyone in the house in order, and I am pretty sure she does the same at school. She is a social butterfly, and every kid loves her. You would never know in her tiny little life that she had ever dealt with anything. She’s the one who reminds her family to be grateful, to not forget what they have, and to find the joy even where it seems it shouldn’t be. 

“You would never know in her tiny little life that she had ever dealt with anything.”

For her, a wheelchair accessible bathroom or a ramp will mean the world. Currently, they carry her in and out of the house to and from the van when they leave and come home. A new bathroom ahead of beginning her new bowel management process will be such a sweet step towards making her more independent and giving her somewhere private that she would actually enjoy being in during this process every night. She is also starting to get heavier as she is getting older, so this makeover will make the bathroom process much easier for her family, as well. But she finds such joy in such little things, this would truly make her world. She longs to be independent, but never complains about not feeling completely so. She is truly sunshine on a rainy day. She radiates joy like no other child. Her laughter is infectious. Her knock knock jokes are no joke. They’re the real deal. She is peace, and love. The no nonsense, no fuss attitude she has is contagious, and it changes everybody else’s environment. Her family is so much better because she is here.

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Photography by Hales Photo

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Amanda, Caleb & Isaac

  • 19, 10 & 10 Years Old

  • Amanda: Spina Bifida

    Caleb: Autism, congenital CMV, hearing & vision loss, sensory issues

    Isaac: Pallister Killian Syndrome 

Amanda, Caleb & Isaac come from a family of eight! Sunshine on a Ranney Day’s plans to create an accessible bathroom and therapy room for them will impact all three in different and wonderful ways.

Amanda is 19 years old and was born in China. She was born with spina bifida which causes her to be paralyzed from the waist down. She has been with her family since she was 13 years old and is such a joy! She uses a wheelchair and other medical equipment and has had many major surgeries since she’s been home. Amanda loves reading, anime, art and is very talented with drawing. She is also very excited to start her first job soon. A handicap accessible bathroom will be such a blessing to her!

Sunshine on a Ranney Day’s plans to create an accessible bathroom and therapy room for them will impact all three in different and wonderful ways.

Caleb is 10 years old and was born with congenital CMV and calcifications on his brain. He was adopted at 4 weeks old and he is such a cutie pie. He has severe autism and loves to quote books, movies and especially nursery rhymes. Singing, swinging and swimming are his very favorite activities. Everyone who meets Caleb falls in love with him. He is funny, sweet and silly. He will enjoy a new playroom/therapy room so very much.

Isaac is 10 and was born with Pallister Killian Syndrome which is a rare genetic disorder that affects the 12th chromosome. He was adopted at 5 months old when he was discharged from the NICU. He is blind, deaf and intellectually he is still their baby. He is an absolute JOY to his family. Isaac’s smile can melt a heart of stone! His laughter echoes through their home reminding his family that there is joy all around us if we just open the eyes of our hearts to see it! He loves swinging, lights, vibrating toys, and being held and tickled. He also utilizes a wheelchair and because of his size, an accessible shower is going to be the most amazing gift to him and to his parents. He will also love and enjoy the new therapy room! 

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Photography by Shana Darnell

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The Drake House

Founded in 2006

The Drake House provides housing and education programs for single mothers and their children who are experiencing homelessness in North Metro Atlanta. It is a community where every family has the opportunity to recover quickly and with dignity from their homeless situation.

Each year Sunshine on a Ranney Day completes a special community project that helps a large number of children & families. Sunshine on a Ranney Day is excited to announce that we will be helping The Drake House by renovating their main headquarters. This makeover includes redesigning and renovating multiple rooms that serve as classrooms for kids studying, learning life skills, arts and crafts, and safe spaces for them to lounge. The rooms also serve to help moms with relationship building, parenting, health and wellness, and money management.

“Over 40% of Atlanta’s homeless population are women and children.”

The goal of the makeover is to create flexible use spaces that allow the children to feel at home in a learning/activity environment. The spaces also help keep the community of kids engaged with each other, creating an extended ‘family’ feel. The central community space in the basement is the food serving spaces. These spaces are currently extremely cramped and do not have a natural flow, inhibiting the ability to smoothly and efficiently cater to each family that is participating in the buffet line. We will be creating this natural flow through relocation of structural walls and the addition of a large island space. There is not currently a dedicated space for older children to teens to be able to gather for free time and engage with The Drake House volunteers for tutoring. We will be converting the upstairs executive offices into that space, providing a leisure space as well as a learning/meeting space.

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Reid

  • 7 Years Old

  • Recessive Dystrophic Epidermolysis Bullosa

Reid is a somewhat shy seven-year-old boy who was born with Recessive Dystrophic Epidermolysis Bullosa; an extremely painful and debilitating genetic skin disease. At birth, Reid was missing large pieces of skin on his back, legs, hands and arms. Kids born with RDEB lack a critical protein that binds our layers of skin together like velcro. Without this protein, Collagen VII, Reid’s skin blisters and tears all over his body, mouth, esophagus, and eyes. What he and others with this severe form of the disease go through is beyond anyone’s comprehension. Reid endures extremely painful daily bandage changes. The severe wounds all over his body must be carefully cleaned and his mother must puncture any blisters to prevent them from spreading. Without the Collagen VII protein, blisters develop from the slightest friction (clothes seams, car seats, daily life) and can get larger because the velcro is not there to stop the spreading. 

“We are so pleased that Sunshine on a Ranney Day has offered to transform our bonus room into a dream bedroom for Reid.”

Despite living with this debilitating condition, Reid enjoys building with Lincoln Logs and riding his plasma bike. He also enjoys the company of his two older siblings, Avery and Barret. Although Reid has a feeding tube, he loves food! Even though eating can be painful, he enjoys small bites of cheese pizza and hotdogs when he doesn’t have any blisters in his mouth or throat. He is homeschooled and loves listening to Christian Hip Hop or watching The Spy Ninjas on YouTube.

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Photography by Pear Tree Photography

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Carson

  • 9 Years Old

  • Autism, Sensory Processing Disorder

As a fan of SpongeBob, sea creatures, aquatic life, Shark Week, and his multiple pets, Carson is like most nine-year-old boys. His favorite things to do are swinging, jumping, and climbing. Carson also likes small places, like a tent or under the bed, to hide if he’s having a bad day. Like all mothers and as a single mother of two, Carson’s mother is concerned with balancing activity and safety.  Having been diagnosed with sensory processing disorder, SPD at age three, and recently diagnosed with Autism, Carson is a sensory seeker who likes to move all of the time. He has received occupational therapy for SPD and worked on fine motor skills. They also worked with the vestibular system for some motor functions of the head and posture, and the proprioceptive senses to help combine sensory information from the inner ear to receptors in the muscles and the joint-supporting ligaments for stance.

Having been diagnosed with sensory processing disorder, SPD at age three, and recently diagnosed with Autism, Carson is a sensory seeker who likes to move all of the time.

As Carson gets older, it will be even more important to have a safe space of his own, including appropriate sensory stimulation.  A custom sensory room from Sunshine on a Ranney Day will give Carson what he needs to be and grow happier and healthier. Together with his family, he will better enjoy their three cats, bearded dragon, and beta fish and will have spent some energy so he can sit down and watch Shark Week like other kids his age.

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Photography by Pear Tree Photography

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Devon

  • 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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