Tag: Dream Bedroom

Logan

Written by Clareece Cunningham on June 30, 2023. Posted in Bin There Dump That Atlanta, Cambria, Construction Resources, Meet the Kids, Mohawk, Pulley and Associates, Randall Brothers, Ranney Blair Weidmann, Real Floors Commercial, ServiceWise Electric, TKO Plumbing Services.

13 Years Old
Transverse Myelitis, paraplegia and autonomic dysreflexia

Logan is an active 13 year old that does not let his wheelchair or crutches cramp his style. He loves to be independent and show the world he can! Most of the time he is in his wheelchair, but uses crutches periodically to get up and down steps or to transfer. Logan acquired transverse myelitis in his spine at 5 months of age, which left him with incomplete paraplegia.

He is an athlete! He excels at everything he tries. He has been on a competition swim team, Challenger baseball (where his picture is hanging in the Little League Baseball Hall of Fame in Williamsport, PA), and currently plays on the Jr. Hawks prep basketball team with Blaze Sports. He loves his coaches and teammates and plans on hopefully getting a college scholarship in the future.

“Logan is an active 13 year old that does not let his wheelchair or crutches cramp his style.”

Logan’s other interests include the guitar, books, e-sports, content creating on social media platforms and chorus in school. He also thinks he’s funny – he will tell you jokes 24/7 if you let him. Some are funny, some are dumb dad jokes, but he always thinks he’s a pro. He will tell you that when he grows up, his parent’s want him to go to college and maybe become a computer programmer or something in that field, but he wants to become a “sit down comedian.” Sunshine on a Ranney Day can’t wait to give spunky Logan an accessible dream bedroom and bathroom!

Logan_2023_family_0002
Logan_2023_family_0004
Logan_2023_family_0006
Logan_2023_family_0003
Logan_2023_family_0010
Logan_2023_family_0011
Logan_2023_family_0009

Photography by Your Agent Catelyn

Logan_2023_reveal_0007

Logan_2023_reveal_0022
Logan_2023_reveal_0011
Logan_2023_reveal_0008
Logan_2023_reveal_0010
Logan_2023_reveal_0009
Logan_2023_reveal_0014
Logan_2023_reveal_0017
Logan_2023_reveal_0001
Logan_2023_reveal_0006
Logan_2023_reveal_0005
Logan_2023_reveal_0004
Logan_2023_reveal_0003
Logan_2023_reveal_0002
Logan_2023_reveal_0018
Logan_2023_reveal_0021
Logan_2023_reveal_0020
Logan_2023_reveal_0012

logo_jackson_healthcare
logo_Sunshine_on_a_Ranney_Fairway
logo_ranney_blair
logo_your_agent_catelyn
logo_randall_brothers
logo_delta_faucet
logo_pulley&associates
logo_traditions_in_tile
logo_schluter_systems
logo_cambria
logo_cr_construction_v2
logo_builders_cabinet_company
logo_cowan_supply
logo_top_knobs
logo_mohawk
logo_real_floors_commercial
logo_echols
logo_american_signature_furniture
logo_Southern Exposure ATL
logo_bin_there_dump_that
logo_nothing_bundt_cakes
logo_iframe_media

Lyra

Written by Clareece Cunningham on June 30, 2023. Posted in Bin There Dump That Atlanta, Means & Carney Interiors, Meet the Kids, Mohawk, Randall Brothers, Real Floors Commercial, ServiceWise Electric, TKO Plumbing Services.

7 Years Old
Autism spectrum, sensory processing and speech disorders, global developmental delay

Lyra is an incredible 7 year old kid. She has never met a stranger because everyone is a friend and she cares deeply for them. She loves all things glitter, unicorn, and pink. She is a kind, inclusive, and thoughtful kiddo that brightens the world of everyone she knows. She loves to craft and make things like cards, bracelets, pictures, and trinkets for all of her friends. Lyra lives to help especially in the kitchen and caring for the chickens. Her family adores her and she is her little brother’s hero.

“She has never met a stranger because everyone is a friend…”

Her family learned that Lyra is autistic when she was two and a half years old at the Marcus center and she has grown so much since then. She receives support from services at McKenna farms and Focus on Function. On top of that, she gets to learn at her own pace and in her preferred learning styles at home. Sunshine on a Ranney Day is excited at the opportunity to transform her basement room into a safe learning/therapy room! Her favorite place to be is outside – swings, picking flowers, riding her scooter, horseback riding at McKenna, and anything with water!

Lyra_2023_family_0002
Lyra_2023_family_0004
Lyra_2023_family_0005
Lyra_2023_family_0006
Lyra_2023_family_0007
Lyra_2023_family_0008

Photography by Niki Murphy

Lyra Reveal_30

Lyra Reveal_33
Lyra Reveal_35
Lyra Reveal_36
Lyra Reveal_32
Lyra Reveal_38
Lyra Reveal_51
Lyra Reveal_59
Lyra Reveal_65
Lyra Reveal_1
Lyra Reveal_3
Lyra Reveal_16
Lyra Reveal_18
Lyra Reveal_6
Lyra Reveal_12
Lyra Reveal_10
Lyra Reveal_20
Lyra Reveal_5
Lyra Reveal_14
Lyra Reveal_9
Lyra Reveal_69
Lyra Reveal_75
Lyra Reveal_71
Lyra Reveal_47
Lyra Reveal_78
Lyra Reveal_25

logo_KFC_Foundation
logo_leadcoverage
logo_hargrove
logo_means_and_carney
logo_randall_brothers
logo_american_signature_furniture
logo_servicewise_electric
logo_mohawk
logo_real_floors_commercial
logo_top_knobs
logo_schumacher
logo_comfort_research
logo_fun_&_function
logo_sherwin_williams
logo_dependable_paint
logo_nothing_bundt_cakes
logo_bin_there_dump_that
logo_iframe_media

Peyton

Written by Clareece Cunningham on December 8, 2022. Posted in Artisan Design Studio, Bin There Dump That Atlanta, Cambria, Construction Resources, Meet the Kids, Pulley and Associates, Randall Brothers, ServiceWise Electric, TKO Plumbing Services.

7 Years Old
Cerebral Palsy, Hydrocephalus, Epilepsy

In 2015, Crystal gave birth to twins Peyton and Taylor at 26 weeks. Both only weighed a little over a pound a piece! Taylor had a brain bleed and Peyton suffered bilateral brain bleeds grade 3 and 4. After both came down with hydrocephalus, the girls got a VP shunt to help drain extra cerebrospinal fluid from the brain. All of this resulted in 3 months in the NICU! For the first year of their lives afterward, all seemed normal until they noticed Peyton was ignoring her right hand. They soon began early interventions and before long Peyton was diagnosed with cerebral palsy, affecting the right side of her body. She worked super hard in therapies and was able to take her first steps at 3 years old! Since then, Peyton began having seizures and now has the diagnosis of focal epilepsy as well.

“Despite everything she has gone through, she is the sweetest, happiest girl!“

Despite everything she has gone through, she is the sweetest, happiest girl! In June of 2022 she underwent a surgery called selective dorsal rhizotomy at Children’s Healthcare of Atlanta. This surgery was intended to relieve some of her symptoms of cerebral palsy and hopefully help her stay mobile and gain more skills. Peyton spent 30 days in the rehab facility at the hospital, working through intensive physical therapy. Even though this surgery requires a lot out of Peyton for the first year post-op, she has stayed so joyful and determined! Her hard work of relearning how to walk again paid off when she took her first independent steps again a week before Halloween. She attends intensive physical therapy 5 days a week and is making great strides towards a full recovery! “She is truly my hero,” – Peyton’s mom, Crystal.

Peyton_2023_family_0008
Peyton_2023_family_0003
Peyton_2023_family_0010
Peyton_2023_family_0007
Peyton_2023_family_0004
Peyton_2023_family_0002

Photography by Carrie Birchfield

Peyton_2023_reveal_00028

Peyton_2023_reveal_00026
Peyton_2023_reveal_00025
Peyton_2023_reveal_00027
Peyton_2023_reveal_0017
Peyton_2023_reveal_00024
Peyton_2023_reveal_00022
Peyton_2023_reveal_00029
Peyton_2023_reveal_0005
Peyton_2023_reveal_0009
Peyton_2023_reveal_0013
Peyton_2023_reveal_0016
Peyton_2023_reveal_0008
Peyton_2023_reveal_00023
Peyton_2023_reveal_00030
Peyton_2023_reveal_0015
Peyton_2023_reveal_0018
Peyton_2023_reveal_0012
Peyton_2023_reveal_0019

Caitlin_In Loving Memory
logo_cobb_emc_foundation
logo_Sunshine_on_a_Ranney_Fairway
logo_artisan_design_studio
logo_randall_brothers
logo_cambria
logo_cr_construction_v2
logo_builders_cabinet_company
logo_delta_faucet
logo_pulley&associates
logo_american_signature_furniture
logo_traditions_in_tile
logo_schluter_systems
logo_cowan_supply
logo_tko_plumbing
logo_servicewise_electric
logo_bin_there_dump_that
logo_birchfield_photography
logo_nothing_bundt_cakes

Ciaran & Geordan

Written by Clareece Cunningham on December 8, 2022. Posted in Bin There Dump That Atlanta, Meet the Kids, Mohawk, Randall Brothers, Real Floors Commercial, ServiceWise Electric.

19 & 16 Years Old
Lebers Congenital Amaurosos, Severely Autistic, Immune System Disorder, Tic Disorder

Ciaran and Geordan were both born with major disabilities. 19 year old Ciaran is totally blind and significantly autistic. On top of that, he has a tic disorder (tourette syndrome) and an immune system disorder. He has no sense of safety and will wake up throughout the night and bang on walls, doors, windows, and even his bed – waking up his brother.

Geordan is 16 and was also born blind. He was also diagnosed with pretty severe non-verbal autism. Geordan also has no concept of safety, making the level of care required for the two boys quite extensive. With their mom’s recent cancer diagnosis, both parents work tirelessly to care for the boys and give them the fullest life they can.

“They are both passionate about music and have an acute sense of hearing for pitch and tone due to their blindness.“

Ciaran and Geordan are highly anxious and noise sensitive, so therapy items like swings, trampolines and instruments are very calming to them. They are both passionate about music and have an acute sense of hearing for pitch and tone due to their blindness. Both boys are unique and talented in their own ways, something that is so evident in their passions and skills! The space that Sunshine on a Ranney Day is providing for them will be life-changing in regards to their independence and individual needs.

ciaran&geordan_2023_family_00010
ciaran&geordan_2023_family_00008
ciaran&geordan_2023_family_00003
ciaran&geordan_2023_family_00002
ciaran&geordan_2023_family_00004
ciaran&geordan_2023_family_00009
ciaran&geordan_2023_family_00007
ciaran&geordan_2023_family_00005

Photography by Niki Murphy Photography

Ciaran&Geordan_2023_reveal_00020

Ciaran&Geordan_2023_reveal_00010
Ciaran&Geordan_2023_reveal_00012
Ciaran&Geordan_2023_reveal_00013
Ciaran&Geordan_2023_reveal_00011
Ciaran&Geordan_2023_reveal_00014
Ciaran&Geordan_2023_reveal_00015
Ciaran&Geordan_2023_reveal_00016
Ciaran&Geordan_2023_reveal_00009
Ciaran&Geordan_2023_reveal_00006
Ciaran&Geordan_2023_reveal_00004
Ciaran&Geordan_2023_reveal_00017
Ciaran&Geordan_2023_reveal_00007
Ciaran&Geordan_2023_reveal_00005
Ciaran&Geordan_2023_reveal_00018
Ciaran&Geordan_2023_reveal_00008
Ciaran&Geordan_2023_reveal_00003
Ciaran&Geordan_2023_reveal_00019
Ciaran&Geordan_2023_reveal_00021

logo_cobb_emc_foundation
logo_preston
logo_real_floors_commercial
logo_mohawk
logo_randall_brothers
logo_american_signature_furniture
logo_servicewise_electric
logo_bin_there_dump_that
logo_niki_murphy_photography
logo_nothing_bundt_cakes
logo_iframe_media

Bryce

Written by Clareece Cunningham on December 8, 2022. Posted in Bin There Dump That Atlanta, Cambria, Construction Resources, Meet the Kids, Mohawk, Pulley and Associates, Randall Brothers, Real Floors Commercial, ServiceWise Electric, TKO Plumbing Services.

5 Years Old
Cerebral Palsy

Bryce is a vibrant and remarkable 5 year old boy who lights up the room. Bryce was born at 27 weeks and spent 2 months in the NICU . As an infant, he was diagnosed with Cerebral Palsy. Most of the time, he utilizes a walker and crutches to get around but recently received a wheelchair for long distances. His diagnosis does not deter him from his eagerness to explore and become independent. He was destined to stand out in the most amazing way while warming the hearts of everyone who crosses his path. His great sense of humor and clever personality is loved and embraced by so many.

“Bryce is the nucleus of their village that keeps everyone connected and in high spirits.”

He attends kindergarten at Still Elementary with his 10 year old sister, London. His family feels so fortunate to have such a strong network of individuals who genuinely care about his mental and physical well-being. Bryce is the nucleus of their village that keeps everyone connected and in high spirits.

Bryce enjoys drawing and telling elaborate stories with fantasy and supernatural themes. He can spend hours creating intricate designs with magnetic blocks and participates in the Horizon Baseball League for children with special needs. We have no doubt that Bryce’s compassionate spirit, inquisitive mind and strong determination will go a long way!

Bryce_2023_family_00010
Bryce_2023_family_00001
Bryce_2023_family_00009
Bryce_2023_family_00005
Bryce_2023_family_00004
Bryce_2023_family_00006

Photography by Nicole Wood Photography

Bryce_2023_reveal_00021

Bryce_2023_reveal_00020
Bryce_2023_reveal_00019
Bryce_2023_reveal_00018
Bryce_2023_reveal_00017
Bryce_2023_reveal_00016
Bryce_2023_reveal_00015
Bryce_2023_reveal_00014
Bryce_2023_reveal_00013
Bryce_2023_reveal_00012
Bryce_2023_reveal_00011
Bryce_2023_reveal_00010
Bryce_2023_reveal_00009
Bryce_2023_reveal_00008
Bryce_2023_reveal_00007
Bryce_2023_reveal_00005
Bryce_2023_reveal_00004
Bryce_2023_reveal_00003
Bryce_2023_reveal_00002
Bryce_2023_reveal_00001

logo_cobb_emc_foundation
logo_roswell_womens_club
logo_nicole_west_interiors
logo_real_floors_commercial
logo_randall_brothers
logo_builders_cabinet_company
logo_rooms_to_go
logo_mohawk
logo_comfort_research
logo_cr_construction_v2
logo_cambria
logo_echols
logo_traditions_in_tile
logo_schluter_systems
logo_asv_productions
logo_delta_faucet
logo_pulley&associates
logo_devore_&_johnson
logo_TKO_Plumbing_2023
logo_bin_there_dump_that
logo_nicole_photography
logo_niki_murphy_photography
logo_servicewise_electric
logo_nothing_bundt_cakes

Ellie

Written by Clareece Cunningham on December 8, 2022. Posted in Cambria, Construction Resources, Meet the Kids, Mohawk, Pulley and Associates, Real Floors Commercial.

4 Years Old
Pontocerebellar Hypoplasia

Ellie was a perfectly healthy baby during prenatal check ups and Jenn (Ellie’s momma) had a wonderful pregnancy. However, the last two minutes of labor changed everything. She swallowed Meconium, got stuck in the birth canal, and had the umbilical cord wrapped around her neck. She was blue and limp when she arrived. It took two minutes to revive her and just in that amount of time, she lost oxygen to her brain causing injury to her cerebellum, which controls fine motor skills and balance. Since Ellie’s birth, her family has been learning and handling challenge after challenge.

“It’s hard to believe the first year of her life they tried just about everything to make her smile or laugh but now it’s effortless!“

Due to her developmental delay and strange movement disorder (later diagnosed as dystonia) her Neurologist conducted a genetic test for Pontocerebellar Hypoplasia type 2A. Soon after her first birthday in April 2019, they received the positive results. This means both parents passed the gene to Ellie causing her cerebellum and half of her brain stem to stop growing in the womb. So now, on top of her birth injury, she also has this genetic mutation. It’s such a rare disease that doctors really don’t know a prognosis and only about 100 people have been documented having this gene. Some children pass away during childhood years, however, some have lived well into her twenties.

What we DO know is Ellie is the happiest baby in the world! It’s hard to believe the first year of her life they tried just about everything to make her smile or laugh but now it’s effortless! She is the silliest girl and keeps everyone laughing. She loves any and all music, including the jams on Cocomelon and when her Daddy plays guitar for her! Even though she is technically “non-verbal” she definitely communicates in her own little language and is such a social butterfly. Water is at the top of her favorites because it gives her freedom and some independence. When in her special float, she is able to move freely by herself and is not dependent on help.

Ellie_2023_family_0002
Ellie_2023_family_0001
Ellie_2023_family_0003
Ellie_2023_family_0004
Ellie_2023_family_0005
Ellie_2023_family_0006

Photography by Christina Elmore Photography

Ellie_2023_reveal_0003

Ellie_2023_reveal_0007
Ellie_2023_reveal_0004
Ellie_2023_reveal_0008
Ellie_2023_reveal_0005
Ellie_2023_reveal_0006
Ellie_2023_reveal_0009
Ellie_2023_reveal_0023
Ellie_2023_reveal_0022
Ellie_2023_reveal_0018
Ellie_2023_reveal_0019
Ellie_2023_reveal_0011
Ellie_2023_reveal_0010
Ellie_2023_reveal_0014
Ellie_2023_reveal_0015
Ellie_2023_reveal_0012
Ellie_2023_reveal_0013
Ellie_2023_reveal_0021
Ellie_2023_reveal_0020
Ellie_2023_reveal_0001
Ellie_2023_reveal_0002
Ellie_2023_reveal_0016
Ellie_2023_reveal_0017
Ellie_2023_reveal_0024

logo_Sunshine_on_a_Ranney_Fairway
logo_kids_r_kids
logo_cobb_emc_foundation
logo_jackson_healthcare
logo_deep_south_construction
logo_christina_elmore
logo_SEAS_interiors
logo_101_mobility
logo_fodac
logo_mohawk
logo_builders_cabinet_company
logo_american_signature_furniture
logo_cambria
logo_cr_construction_v2
logo_schluter_systems
logo_traditions_in_tile
logo_cowan_supply
logo_delta_faucet
logo_pulley&associates
logo_top_knobs
logo_nothing_bundt_cakes

Noah

11 Years Old
Rasmussen Encephalitis

Noah was born at 32 weeks with no complications. He was a healthy active kid until 6 yrs old when he had his first seizure episode in the summer of 2018. Doctors couldn’t figure out why Noah was having seizures 10 times a day until an amazing doctor at Children’s Healthcare of Atlanta figured out what was wrong with him. In the spring of 2019, Noah was diagnosed with Rasmussen Encephalitis. In late fall of 2019, he had his first brain surgery (Right Hemispherectomy) and his last seizure.

“Noah has always had an open mind with the outcome of his surgery.”

Today, Noah is now physically disabled on the left side of his body and needs help with day-to-day needs. Noah has always had an open mind with the outcome of his surgery. He remains strong and motivated to regain some of his independence while playing sports with Gwinnett Heat in Gwinnett County. He has physical/occupational therapy 2 times a week, Botox every 4-6 months, and is doing amazing with his long recovery. Noah is super excited to have a space he can call his own where he can move around freely and independently.

SOARD Noah-11
SOARD Noah-20
SOARD Noah-5
SOARD Noah-19
SOARD Noah-27

Photography by Niki Murphy Photography

Noah_2023_reveal_00002

Noah_2023_reveal_00007
Noah_2023_reveal_00003
Noah_2023_reveal_00004
Noah_2023_reveal_00024
Noah_2023_reveal_00006
Noah_2023_reveal_00026
Noah_2023_reveal_00008
Noah_2023_reveal_00009
Noah_2023_reveal_00027
Noah_2023_reveal_00012
Noah_2023_reveal_00028
Noah_2023_reveal_00010
Noah_2023_reveal_00011
Noah_2023_reveal_00013
Noah_2023_reveal_00014
Noah_2023_reveal_00022
Noah_2023_reveal_00016
Noah_2023_reveal_00017
Noah_2023_reveal_00029
Noah_2023_reveal_00018
Noah_2023_reveal_00019
Noah_2023_reveal_00020
Noah_2023_reveal_00021
Noah_2023_reveal_00031

logo_jc_foundation
logo_cobb_emc_foundation
logo_color_fresh_home_designs
logo_randall_brothers
logo_real_floors_commercial
logo_mohawk
logo_cambria
logo_cr_construction_v2
logo_echols
logo_servicewise_electric
logo_builders_cabinet_company
logo_top_knobs
logo_traditions_in_tile
logo_schluter_systems
logo_rooms_to_go
logo_comfort_research
logo_asv_productions
logo_delta_faucet
logo_pulley&associates
logo_TKO_Plumbing_2023
logo_cowan_supply
logo_bin_there_dump_that
logo_niki_murphy_photography
logo_nothing_bundt_cakes

Jason

Written by Clareece Cunningham on December 8, 2022. Posted in Bin There Dump That Atlanta, Cambria, Construction Resources, Meet the Kids, Mohawk, Pulley and Associates, Randall Brothers, Randall Paulson Architects, Real Floors Commercial, ServiceWise Electric, TKO Plumbing Services.

19 Years Old
Cerebral Palsy & Dystonia

Jason recently completed his freshman year at University of West Georgia! He was born a preemie weighing 2lb 9oz, spent 86 days in the NICU and by age one he was diagnosed with Cerebral Palsy and Dystonia. Today, Jason is wheelchair bound and uses a power wheelchair like a boss! He is completely dependent on someone to assist him with everyday life. Since he is not able to use his arms, he must be fed, but can clearly tell you that the food is too hot, salty or disgusting. So from the neck up Jason is a “typical” 17-year-old!

“…from the neck up Jason is a ‘typical’ 17-year-old!”

For Jason to take a shower, his family needs to undress him in his room and carry him through most of the house to reach the bathroom. Once in the bathroom, he uses a tub chair to shower. However, when Jason goes to camp and respite, he has a lot more independence and ability to do normal things like showering and using the restroom because of the accessibility of the bathrooms there. Because of this, he loves when he goes to camp – so we can’t wait to help him have the same feeling about his own space in his house!

Aside from going to camp, Jason loves going to the movies with friends and family to watch Marvel movies – of which he is an avid fan! He also loves anything Anime and frequently reads Fan Fiction Anime. His favorite places to visit are New Orleans and DC, but he has dreams of going to New York City! At home, Jason’s younger sister, Junia, frequently keeps him entertained with all kinds of shenanigans.

Jason_2023_family_0009
Jason_2023_family_0004
Jason_2023_family_0010
Jason_2023_family_0012
Jason_2023_family_0008
Jason_2023_family_0003
Jason_2023_family_0001

Photography by Niki Murphy Photography

Jason_2023_reveal_0004

Jason_2023_reveal_0001
Jason_2023_reveal_0002
Jason_2023_reveal_0003
Jason_2023_reveal_0005
Jason_2023_reveal_0006
Jason_2023_reveal_0007
Jason_2023_reveal_0008
Jason_2023_reveal_0016
Jason_2023_reveal_0009
Jason_2023_reveal_0010
Jason_2023_reveal_0011
Jason_2023_reveal_0012
Jason_2023_reveal_0013
Jason_2023_reveal_0014
Jason_2023_reveal_0015
Jason_2023_reveal_0021
Jason_2023_reveal_0018
Jason_2023_reveal_0020

logo_helen_jimmy_Carlos
logo_Sunshine_on_a_Ranney_Fairway
logo_jackson_healthcare
logo_kids_r_kids
logo_cobb_emc_foundation
logo_randall_paulson
logo_real_floors_commercial
logo_mohawk
logo_randall_brothers
logo_pls_carpentry
logo_servicewise_electric
logo_american_signature_furniture
logo_comfort_research
logo_cambria
logo_cr_construction_v2
logo_echols
logo_traditions_in_tile
logo_schluter_systems
logo_top_knobs
logo_builders_cabinet_company
logo_delta_faucet
logo_pulley&associates
logo_TKO_Plumbing_2023
logo_bin_there_dump_that
logo_niki_murphy_photography
logo_iframe_media
logo_nothing_bundt_cakes

Cade

Written by Joe Lane on November 28, 2022. Posted in Bin There Dump That Atlanta, Cambria, Construction Resources, Meet the Kids, Pulley and Associates, Randall Brothers, Real Floors Commercial, ServiceWise Electric, TKO Plumbing Services.

20 Years Old
Spinal Injury C4 Incomplete

Cade graduated highschool in May of 2020. In January of 2021, he was a passenger during a motor vehicle accident and was ejected from the vehicle. Miraculously, he survived. He spent 5 days in a local ICU and was transferred to Shepherds Spinal Center in Atlanta where he spent one week in ICU followed by 9 weeks of inpatient rehab for a spinal cord injury. He was given the diagnosis of C4 incomplete (when damage is dealt about mid-way down the cervical spinal cord), spent 6 weeks on a vent, and is now in a power wheelchair to get around day to day.

“Miraculously, he survived.”

Cade is making progress towards being functional, but right now still requires around the clock care for someone to bathe him, feed him, etc.. even scratch his “itches”! His parents were able to remodel their bathroom so that he can shower there, but his current room is tough for him to get around in and he can’t get in his bathroom. He plans on going to college online at Georgia Highlands for the fall of 2022. While there, he will be studying Psychology and Computer Animation, perfectly in line with his interests of Anime, Star Wars and cars. The world is blessed to still have Cade in it and we are so excited to help make modifications that will allow him to be more independent!

Cade_2023_family_00008
Cade_2023_family_00009
Cade_2023_family_00005
Cade_2023_family_00004
Cade_2023_family_00003
Cade_2023_family_00002

Photography by Carrie Birchfield Photography

Cade_2023_reveal_00005

Cade_2023_reveal_00014
Cade_2023_reveal_00015
Cade_2023_reveal_00013
Cade_2023_reveal_00006
Cade_2023_reveal_00007
Cade_2023_reveal_00008
Cade_2023_reveal_00002
Cade_2023_reveal_00012
Cade_2023_reveal_00003
Cade_2023_reveal_00001
Cade_2023_reveal_00004
Cade_2023_reveal_00009
Cade_2023_reveal_00011
Cade_2023_reveal_00010

logo_cobb_emc_foundation
logo_b_interiors
logo_urostat_healthcare
logo_birchfield_photography
logo_real_floors_commercial
logo_randall_brothers
logo_cambria
logo_cr_construction_v2
logo_echols
logo_traditions_in_tile
logo_schluter_systems
logo_pls_carpentry
logo_servicewise_electric
logo_cowan_supply
logo_TKO_Plumbing_2023
logo_3lp_engineering
logo_delta_faucet
logo_pulley&associates
logo_rooms_to_go
logo_iframe_media
logo_bin_there_dump_that
logo_nothing_bundt_cakes

MarQuis

Written by Joe Lane on May 31, 2022. Posted in Bin There Dump That Atlanta, Cambria, Construction Resources, Meet the Kids, Mohawk, Pulley and Associates, Randall Brothers, Randall Paulson Architects, Real Floors Commercial, ServiceWise Electric, TKO Plumbing Services.

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!