pixel

Tag: Accessible Bathroom

MarQuis

  • 18 Years Old

  • Mitochondrial Encephalopathy

MarQuis and his twin brother were born without any complications.  When MarQuis was around 10 months old, he was sick with a typical virus and woke up the next day a completely different child.  The initial thought was that MarQuis had a seizure until he had another episode.  MarQuis and his family traveled to multiple cities for an official diagnosis and finally at the age of 2 after a muscle biopsy MarQuis was diagnosed with mitochondrial disorder.  In 2005 MarQuis had an episode that the doctors did not think he would survive but God had other plans.  Fortunately, that was the final episode. 

MarQuis has a love for life and speaks his own language to communicate his needs.

MarQuis is permanently disabled and needs assistance with all daily needs.  MarQuis has a love for life and speaks his own language to communicate his needs.  His house is currently not accessible which is very challenging for his family and caregivers.  MarQuis and his family are so excited for MarQuis to have a space that is truly his own and reflective of his personality!

  • marquis_2022_family_00004

  • marquis_2022_family_00005

  • marquis_2022_family_00006

  • marquis_2022_family_00003

  • marquis_2022_family_00002

  • marquis_2022_family_00001

Photography by Jennifer Boxley Photography

meet_the_kids_makeover_in_progress

  • logo_the_voila_foundation

  • logo_kids_r_kids

  • logo_jackson_healthcare

  • logo_randall_paulson

  • logo_randall_brothers

  • logo_real_floors_commercial

  • logo_tko_plumbing

  • logo_asv_productions

  • logo_rooms_to_go

  • logo_cambria

  • logo_cr_construction_v2

  • logo_mohawk

  • logo_delta_faucet

  • logo_pulley&associates

  • logo_devore_&_johnson

  • logo_top_knobs

  • logo_bin_there_dump_that

  • logo_jennifer_boxley_photography

  • logo_nothing_bundt_cakes

Continue reading

Mariah

  • 17 Years Old

  • Brain Tumor

In 2013 when Mariah was nine years old, she had a headache that would not go away.  After several visits to various doctors, Mariah went to the emergency room at Children’s Healthcare of Atlanta.  The emergency room doctor initially thought Mariah had a viral infection but ran a CT scan for confirmation.  The CT scan showed a mass in Mariah’s brain which required a follow-up with a neurosurgeon.  Mariah underwent brain surgery and had the tumor removed and the prognosis was positive, Mariah was expected to recover and unlikely to have any more issues. 

Unfortunately, less than one year later Mariah had a regrowth of the tumor which required another surgery for removal.  After the second surgery, the doctors learned that the tumor was extremely aggressive. The type of tumor is called ATRT and the chances of survival are about 50/50. The doctors explained that Mariah would be extremely sick and spend the majority of the next year in the hospital. Mariah was sick at the beginning of treatment but later in the year she was doing so well that the doctors were baffled at how well she tolerated her therapies and medications. Towards the end of Mariah‘s treatment, she had difficulty walking and increased weakness in her legs.  An MRI revealed that she had extreme swelling building in her brain and it was affecting all of her motor movements. Mariah’s condition continued to worsen, she eventually lost all of her ability to move and was very close to not being able to breathe on her own. Around 2016 Mariah was using a machine to rattle her lungs so that she would not get pneumonia.  She also needed help with all of her needs including going to the bathroom, getting dressed, and turning over in the night. Mariah was almost like a zombie.

“Life has recently become more challenging for our family as Mariah is growing more everyday.”

Since 2016, Mariah’s family has been on a path to help Mariah get better. The treatments that she received for her brain swelling left her with bone integrity issues as well as post-menopausal.  She also needed double hip replacements and hormone replacement. She has had one hip replacement.  Mariah has lived with a lot of pain and sadness as to why this has happened to her. However, God has truly used Mariah to grow her parent’s faith and to touch many lives around her in the community. Mariah continues to show signs of improvement to this day. She has not regained the ability to walk or use of her hands but she is much more alert and spunkier! Currently, Mariah attends therapies twice a week and is active in the church.  She is also involved in a special-needs organization called, Extra Special People. These outlets have provided an abundance of joy for Mariah.  Mariah and her parents are so thankful for their family and community.  They are eager to see what the future holds for Mariah and do not think God is finished healing Mariah. 

  • mariah_2023_family_00006

  • mariah_2023_family_00002

  • mariah_2023_family_00003

  • mariah_2023_family_00005

Photography by Jennifer Boxley Photography

  • logo_reliable_heating&air

  • logo_randall_brothers

  • logo_cambria

  • logo_cr_construction_v2

  • logo_echols

  • logo_real_floors_commercial

  • logo_delta_faucet

  • logo_pulley&associates

  • logo_devore_&_johnson

  • logo_bin_there_dump_that

  • logo_jennifer_boxley_photography

  • logo_nothing_bundt_cakes

Continue reading

John & Joseph

  • 10 & 9 Years Old

  • MECP2 Duplication Syndrome

John and Joseph are brothers born 16 months apart with MECP2 Duplication Syndrome or M2DS. This rare genetic condition causes many issues such as severe intellectual disabilities, impaired motor function, epilepsy, spasticity, speech, as well as gastrointestinal and respiratory issues.

When John was in his toddler and pre-school years, he worked hard to make developmental strides that most people take for granted.  Crawling and walking were milestones that, with therapy and determination, John achieved by the age of 4.  After enjoying his success for only a few short years, John began to experience seizures at the age of 6.  The onset of epilepsy caused John to lose skills that he had once gained such as walking, eating, and even turning pages in his books.  John now gets all of his nutrition through a G-Tube and uses a wheelchair for mobility.  John has also required frequent and lengthy hospital stays at Scottish Rite for respiratory infections and seizures. 

Despite the tremendous setbacks that John has experienced, he is an absolute joy to encounter! He embodies the phrase, “Sunshine on a Ranney Day” because even when things seem like they couldn’t get much worse to those who love him, John’s will, determination, strength and love shine through the darkness to declare that brighter days are ahead!

John and Joseph are overcomers who know that life is not a race where the finish line is at the end but rather, it is a celebration of what one has achieved at the end of each day!

Joseph’s primary struggles with M2DS are developmental.  Joseph began walking just a few weeks shy of his 2nd birthday and has been on the go ever since!  Fine motor skills, such as eating and writing with utensils, have been challenging for Joseph.  He communicates non-verbally and is learning to use a picture exchange binder with the hopes of getting a communication device in the near future.  

Both John and Joseph bring so much joy to their family, friends and everyone who has the pleasure of meeting them.  Their older sister, A.J., is their favorite person in the world and their favorite activities include taking walks to the lake and riding in the golf cart.  John and Joseph are overcomers who know that life is not a race where the finish line is at the end but rather, it is a celebration of what one has achieved at the end of each day!

  • burgess_2022_family_00003

  • burgess_2022_family_00007

  • burgess_2022_family_00006

  • burgess_2022_family_00008

  • burgess_2022_family_00005

  • burgess_2022_family_00004

  • burgess_2022_family_00001

Photography by Nicole Wood Photography

meet_the_kids_makeover_in_progress

  • logo_helen_jimmy_Carlos

  • logo_beruna_restoration

  • logo_reliable_heating&air

  • logo_interceramic

  • logo_randall_brothers

  • logo_cambria

  • logo_cr_construction_v2

  • logo_echols

  • logo_real_floors_commercial

  • logo_delta_faucet

  • logo_pulley&associates

  • logo_devore_&_johnson

  • logo_bin_there_dump_that

  • logo_nicole_photography

  • logo_nothing_bundt_cakes

Continue reading

Celia

  • 13 Years Old

  • Leigh’s Disease

Celia and her twin sister were adopted from China at the age of 26 months. Celia and her twin are currently thirteen years old and the youngest of six kids.  During adoption, it was thought that Celia had cerebral palsy (CP) but after extensive testing, Celia likely has a mitochondrial disorder, which is neuro-degenerative, called Leigh’s disease or a Leigh-like syndrome. 

“She even has a superpower; Celia can use her toes to type and play games on her iPad!”

Celia cannot walk unassisted, use her hands purposefully, or eat by mouth.  Celia has endured many surgeries and hospitalizations and unfortunately had a setback in 2020 during a procedure that was supposed to help improve her dystonia (painful involuntary muscle contractures).  Celia lost the ability to speak, process information, sleep, and most devastatingly her sweet spunky personality.  In 2021 the procedure was reversed and hopefully with the love and support of Celia’s family, their faith in God, and extensive therapies she can regain what was lost.

Celia’s family wishes everyone had a Celia in their lives.  She’s joyful, happy, has an amazing smile, and loves her family.  She even has a superpower; Celia can use her toes to type and play games on her iPad!  Celia has good days and bad days, she struggles with strength, stamina, communication, and mental cognition but through it all, she is the brightest of lights and a gift to all that know her.  Celia truly is God’s precious blessing!

  • celia_2022_family_00002

  • celia_2022_family_00003

  • celia_2022_family_00006

  • celia_2022_family_00004

  • celia_2022_family_00005

  • celia_2022_family_00007

Photography by Nicole W Photography

Celia_2022_reveal_00002

  • Celia_2022_reveal_00003

  • Celia_2022_reveal_00004

  • Celia_2022_reveal_00005

  • Celia_2022_reveal_00006

  • Celia_2022_reveal_00007

  • Celia_2022_reveal_00008

  • Celia_2022_reveal_00010

  • Celia_2022_reveal_00012

  • Celia_2022_reveal_00009

  • logo_real_floors_commercial

  • logo_ranney_blair

  • logo_reliable_heating&air

  • logo_randall_brothers

  • logo_cambria

  • logo_cr_construction_v2

  • logo_echols

  • logo_schluter_systems

  • logo_asv_productions

  • logo_interceramic

  • logo_tko_plumbing

  • logo_delta_faucet

  • logo_pulley&associates

  • logo_devore_&_johnson

  • logo_bin_there_dump_that

  • logo_nicole_photography

  • logo_nothing_bundt_cakes

Continue reading

Brylee

  • 9 Years Old

  • Nemaline Rod Myopathy

Brylee was born with a rare disease, Nemaline Rod Myopathy.  She spent time in the NICU at Children’s Healthcare of Atlanta.  Brylee had a tracheotomy procedure in order to keep her alive.  It was also explained to Brylee’s family that kids with severe Nemaline, like Brylee, typically live 18 months and can only use their eyelids since the disease affects the muscles.  Brylee has defied the odds, she can move her arms with help, kick her legs, and talks nonstop.

“Brylee loves animals and wants to be a veterinarian when she grows up.”

Brylee is now 10 years old and has had multiple surgeries and visits to the hospital. Brylee is a fighter!  Brylee can drive her wheelchair around the house.  She loves playing with her cousins and friends along with trips to the playground.  Brylee loves animals and wants to be a veterinarian when she grows up.  Brylee and her family are so excited about her accessible bathroom!

  • brylee_2022_family_00001

  • brylee_2022_family_00002

  • brylee_2022_family_00003

  • brylee_2022_family_00004

Photography by Kristi Weaver Photography

brylee_2022_reveal_00001

  • brylee_2022_reveal_00005

  • brylee_2022_reveal_00004

  • brylee_2022_reveal_00003

  • brylee_2022_reveal_00002

  • brylee_2022_reveal_00006

  • brylee_2022_reveal_00007

  • logo_studio_wellington

  • logo_interceramic

  • logo_randall_brothers

  • logo_reliable_heating&air

  • logo_builders_cabinet_company

  • logo_cambria

  • logo_cr_construction_v2

  • logo_echols

  • logo_real_floors_commercial

  • logo_delta_faucet

  • logo_pulley&associates

  • logo_devore_&_johnson

  • logo_bin_there_dump_that

  • logo_Matouk

  • logo_schumacher

  • logo_kristi_weaver_photography

  • logo_nothing_bundt_cakes

Continue reading

Braxton

  • 12 Years Old

  • Spina Bifida Lipomyelomeningocele

Braxton is 13 years old and the oldest of 3, he’s a big brother to Wyatt and Landry.  On most days, you can find him playing basketball in the driveway, gaming on the Xbox, or begging his mom to take him to the Lego store.  Braxton was born with Spina Bifida/Lipomyelomeningocele and has endured over 14 surgeries to date at Children’s Healthcare of Atlanta.  Braxton attends Veritas Classical Schools which is a home school hybrid.  This allows Braxton’s schedule to be more flexible when medical appointments, therapies, and surgeries arise.  Although ambulatory, Braxton’s mobility has lessened over the years and he’s relying more on his wheelchair and other assistive devices to accomplish daily activities. 

“He is very creative and has an 8-foot table housing a giant city that he has designed and continuously recreates all himself.”

Braxton sometimes struggles physically since he is unable to run and walk like most kids his age but that has not slowed him down!  Braxton is the athlete of his family, playing both wheelchair basketball and competing in adaptive track and field for BlazeSports.  He would actually like to participate in ALL adaptive sports, but he would need his own chauffer.  On the basketball court, #5 plays with his whole heart and fierce determination!  Braxton recently made the Prep All-Tournament Team at the NWBA Nationals in 2022.  He hopes to play wheelchair basketball at the collegiate level as well as dreams to make Team USA one day.   On the track, he is a lover of field events and broke the national record for shotput in 2019.  Braxton is also an avid member of Scouts in Troop 1459 and is on track to earn his Eagle Scout Ranking in the future. He recently went on a 4-day adventure to Cumberland Island where he was able to hike over 20 miles with his troop in his Grit Freedom Chair.   Braxton is also a LEGO MANIAC and has thousands and thousands in his room!  He is very creative and has an 8-foot table housing a giant city that he has designed and continuously recreates all himself. He is an amazing artist as well and loves to veg out and play video games with his brother and friends. Braxton is active in his church youth group at North Point Community Church and is surrounded by amazing leaders and friends.  

Braxton’s family calls him Braxton the Brave as he inspires his family everyday through the path that God has laid out before him.  Braxton and his family are so excited about his bedroom and bathroom accessible makeover.  Gaining that extra independence will be a game changer as well as make each day brighter!

  • Braxton_2022_family_00001

  • Braxton_2022_family_00002

  • Braxton_2022_family_00003

  • Braxton_2022_family_00005

  • Braxton_2022_family_00004

Photography by Niki Murphy Photography

meet_the_kids_makeover_in_progress

  • logo_jackson_healthcare

  • logo_kids_r_kids

  • logo_means_and_carney

  • logo_real_floors_commercial

  • logo_mohawk

  • logo_interceramic

  • logo_randall_brothers

  • logo_builders_cabinet_company

  • logo_asv_productions

  • logo_cambria

  • logo_cr_construction_v2

  • logo_echols

  • logo_delta_faucet

  • logo_pulley&associates

  • logo_devore_&_johnson

  • logo_bin_there_dump_that

  • logo_niki_murphy_photography

  • logo_nothing_bundt_cakes

Continue reading

Joseph

  • 5 Years Old

  • Spina Bifida Myelomeningocele

Joseph has always been a little Superman. Even after receiving the prenatal diagnosis of spina bifida, we couldn’t have been prepared for the challenges we were about to face. Joseph was born prematurely with a large, open hole in his spine and bravely began his life with 77 days in the NICU. He underwent ten surgeries, countless medical scans and tests, revolving doctor appointments, and multiple hospital stays, which are the routine for so many special needs children. This can be scary for a young child, but Joseph is brave beyond his years.  

Like many children with spina bifida, Joseph developed hydrocephalus, a condition that allows fluid to accumulate in the brain. This can cause brain damage from the buildup of pressure. Joseph had a shunt surgically placed in his skull as a newborn to protect his brain. The tiny tubing and valve keep the fluid that cushions the brain freely flowing. Despite the effects of hydrocephalus and an underdeveloped cerebellum, Joseph grew into a smart, funny little five-year-old boy.

For the first year and a half of his life, Joseph required 24-hour oxygen and a feeding tube for all his nutrition. By 18 months, he received his first tiny wheelchair as he is paralyzed from the waist down. He was non-verbal and used a voice-producing device until the was three and half years old. Then one day he recited the entire alphabet and hasn’t stopped talking since! Today, he only requires supplemental oxygen at night and eats by mouth on his own. He loves showing off his wheelchair “tricks,” meeting new people and learning their names. Although he has some developmental delays you will notice when you meet him, what outshines those is how earnestly he wants to be your friend. He has a strong memory for stories and loves to repeat (and repeat!)  the adventures of historical heroes he has learned about.  

“He loves showing off his wheelchair “tricks,” meeting new people, and learning their names.”

Joseph’s determination through each health challenge is growing into a resolution to be independent. His family and amazing team of therapists is doing everything they can to help him accomplish this. Unfortunately, even something as simple as a narrow doorway can thwart his efforts. That obstacle, along with a flight of stairs, means he must be carried to his bedroom. And this is just the beginning of how Joseph becomes like an infant all over again. He must be lifted to a changing station for diaper changes and all his grooming and bathing needs are fulfilled by mom and dad in a bathroom designed for those who can walk independently. 

Generous friends of the Smith family sent Joseph’s story to Sunshine on a Ranney Day and soon Joseph will have the independence and dignity he desires. The makeover of a downstairs bedroom and the transformation of a bathroom that is not accessible will provide him with the physical means to begin an independence that will stay with him his entire life. We are incredibly excited and grateful to everyone involved with this phenomenal gift.  

Just like Superman, underneath his sweet smile and friendly conversation, Joseph has strength and bravery that has kept this little guy soaring through everything life presents. Thank you to Sunshine on a Ranney Day for breaking down walls to help Joseph not just roll, but fly!

  • joseph_2022_family_00001

  • joseph_2022_family_00002

  • Joseph_2022_featured_photo

  • joseph_2022_family_00005

  • joseph_2022_family_00004

  • joseph_2022_family_00003

Photography by Vicki Alsup Photography

joseph_2022_reveal_00009

  • joseph_2022_reveal_00001

  • joseph_2022_reveal_00004

  • joseph_2022_reveal_00011

  • joseph_2022_reveal_00003

  • joseph_2022_reveal_00010

  • joseph_2022_reveal_00008

  • joseph_2022_reveal_00007

  • joseph_2022_reveal_00006

  • joseph_2022_reveal_00005

  • logo_beazer_homes

  • logo_kids_r_kids

  • logo_crosby_design_group

  • logo_real_floors_commercial

  • logo_mohawk

  • logo_interceramic

  • logo_randall_brothers

  • logo_american_signature_furniture

  • logo_echols

  • logo_builders_cabinet_company

  • logo_asv_productions

  • logo_cambria

  • logo_cr_construction

  • logo_pulley&associates

  • logo_delta_faucet

  • logo_devore_&_johnson

  • logo_top_knobs

  • logo_vicki_alsup_photography2

  • logo_nothing_bundt_cakes

Continue reading

Brianna

  •  18 Years Old

  • Cerebral Palsy, Brain Damage, Epilepsy

Brianna “Breezy” was born on June 4, 2004.  During birth, Breezy experienced complications causing brain damage and she received a later diagnosis of cerebral palsy and epilepsy.  Breezy continues to defy odds; the doctors did not expect Breezy to live to see her first Christmas and now she is 17 years old!  Breezy has a love for music and being outdoors. She comes from a musically talented family and attends a church that has many different types of instruments.  Breezy enjoys attention and interaction with people from reading a book to simply holding hands. 

“Breezy lights up a room with her beautiful blue eyes and contagious smile.”

Breezy is nonverbal and wheelchair dependent.  Breezy has faced so many challenges throughout her 17 years of life and proves what love, prayer, and faith can do.  Breezy lights up a room with her beautiful blue eyes and contagious smile.  She continues to amaze and capture the hearts of her family, friends, church family, and community.  

Breezy is fully dependent on her family to take care of her everyday needs and an accessible bathroom and bedroom renovation will make life easier for the whole family.

  • brianna_2022_family_00001

  • brianna_2022_family_00002

  • brianna_2022_family_00003

  • brianna_2022_family_00004

  • brianna_2022_family_00005

Photography by Niki Murphy Photography

brianna_2022_reveal_00003

  • brianna_2022_reveal_00009

  • brianna_2022_reveal_00008

  • brianna_2022_reveal_00011

  • brianna_2022_reveal_00011

  • brianna_2022_reveal_00012

  • brianna_2022_reveal_00007

  • brianna_2022_reveal_00006

  • brianna_2022_reveal_00001

  • brianna_2022_reveal_00002

  • brianna_2022_reveal_00003

  • brianna_2022_reveal_00004

  • brianna_2022_reveal_00005

  • logo_jc_foundation

  • logo_artisan_design_studio

  • logo_interceramic

  • logo_reliable_heating&air

  • logo_randall_brothers

  • logo_echols

  • logo_cambria

  • logo_cr_construction

  • logo_real_floors_commercial

  • logo_all_purpose_construction

  • logo_rooms_to_go

  • logo_bin_there_dump_that

  • logo_chases_jiffy_johns

  • logo_pulley&associates

  • logo_delta_faucet

  • logo_builders_cabinet_company

  • logo_devore_&_johnson

  • logo_niki_murphy_photography

  • logo_boheme_winter_photography

  • logo_nothing_bundt_cakes

  • logo_iframe_media

Continue reading

Kaitlyn

  •  12 Years Old

  • Cerebral Palsy, Epilepsy

Kaitlyn is a happy and fun-loving 10-year-old girl.  She, unfortunately, lost oxygen during her birth process and experienced seizures shortly after birth.  She had a 16 day NICU stay after birth and experiences many health and gross and fine motor challenges due to her brain injury.  She was diagnosed with Cerebral Palsy at just 8 months old and has been in weekly speech, physical and occupational therapy since just 6 months old.  She also participates in ABA therapy and intensive robotic therapy.   She is unable to use her physical voice but uses a communication device to communicate.  Kaitlyn uses a power wheelchair in the school and community settings and can walk with the support of a gait trainer in her home. 

“Kaitlyn works so hard to overcome her challenges and puts forth so much effort each and every day”

Despite this multitude of challenges, Kaitlyn lives a happy and fulfilling life.  She loves doing yoga, playing Mario Kart with an adaptive controller, and baking with her family.  She runs races with her Dad in an adaptive jogging stroller and has already completed 2 half marathons.  She loves our family beach trips to Hilton Head Island and she even does yoga on the beach!  What fun!  She is active in her church and participates in church worship and dances up a storm each week.  Kaitlyn works so hard to overcome her challenges and puts forth so much effort each and every day.  

We’re so excited for Kaitlyn to have an accessible space to give her independence and a calm place to relax after those sometimes really tough and overstimulating and overtiring days.  She is already starting to ask about makeup and becoming more interested in fashion so it will be so neat to have a space where she can learn to become more independent as she heads into her teen years soon. 

  • kaitlyn_2022_family_00002

  • kaitlyn_2022_family_00005

  • kaitlyn_2022_family_00003

  • kaitlyn_2022_family_00004

  • kaitlyn_2022_family_00001

Photography by Pear Tree Photography

kaitlyn_2022_reveal_00001

  • kaitlyn_2022_reveal_00002

  • kaitlyn_2022_reveal_00003

  • kaitlyn_2022_reveal_00004

  • kaitlyn_2022_reveal_00006

  • kaitlyn_2022_reveal_00011

  • kaitlyn_2022_reveal_00007

  • kaitlyn_2022_reveal_00008

  • kaitlyn_2022_reveal_00009

  • kaitlyn_2022_reveal_00010

  • kaitlyn_2022_reveal_00005

  • kaitlyn_2022_reveal_00012

  • logo_pga_superstore

  • logo_vickers_design_group

  • logo_kids_r_kids

  • logo_interceramic

  • logo_reliable_heating&air

  • logo_randall_brothers

  • logo_builders_cabinet_company

  • logo_mohawk

  • logo_asv_productions

  • logo_cambria

  • logo_cr_construction

  • logo_real_floors_commercial

  • logo_pulley&associates

  • logo_delta_faucet

  • logo_devore_&_johnson

  • logo_pear_tree_photography

  • logo_nothing_bundt_cakes

Continue reading

Ethan

  • 17 Years Old

  • Mecp2 Duplication Syndrome

Ethan spent the first seven years of his life without an official diagnosis other than a general diagnosis of mentally disabled.  That changed when Ethan was seven and experienced a seizure where he ultimately ended up at Children’s Healthcare of Atlanta (CHOA).  Fortunately for Ethan, the neurologist at CHOA specialized in what would eventually become Ethan’s diagnosis, Mecp2 Duplication Syndrome or M2DS.  M2DS is a rare genetic condition causing many issues such as severe intellectual disabilities, impaired motor function, spasticity, speech, gastrointestinal, and respiratory issues.

Ethan is able to enjoy life in general; he is still mobile and eats soft foods by mouth.  He has had setbacks over the years but he continuously proves how strong he is time and time again.  Ethan’s mobility has declined over the past few years due to severe seizures.  Ethan’s Sunshine makeover includes a wheelchair-accessible bathroom and wheelchair ramp going into his house to make daily life a little easier for everyone.

  • ethan_2022_family_00001

  • ethan_2022_family_00008

  • ethan_2022_family_00002

  • ethan_2022_family_000020

  • ethan_2022_family_000014

Photography by Marcelino Aguilar Photography

Ethan_2022_reveal_00001

  • Ethan_2022_reveal_00002

  • Ethan_2022_reveal_00003

  • Ethan_2022_reveal_00a0 4-min

  • Ethan_2022_reveal_00007

  • Ethan_2022_reveal_00005

  • Ethan_2022_reveal_00006-min

  • logo_kids_r_kids

  • logo_preston

  • logo_interceramic

  • logo_reliable_heating&air

  • logo_randall_brothers

  • logo_us_cabinetworks

  • logo_echols

  • logo_a1a_environmental

  • logo_cambria

  • logo_cr_construction

  • logo_pulley&associates

  • logo_bin_there_dump_that

  • logo_delta_faucet

  • logo_top_knobs

  • logo_devore_&_johnson

  • logo_pls_carpentry

  • logo_marcelino_aquilar_photography

  • logo_nothing_bundt_cakes

  • logo_iframe_media

Continue reading

Follow Us

42-C Oak Street, Roswell GA 30075
770.990.2434 | info@soardcharity.com

Privacy Policy | Terms

© 2021 | 42-C Oak Street, Roswell GA 30075 | Sunshine on a Ranney Day is a 501 (c)(3). EIN: 45-4773997