Matt

Boy, Age: 6
Country Code: LA-2
Spina bifida, paraplegia; Hydrocephalus (shunt placed); Club foot (left and right) (surgically corrected)
Listed: Nov 2022
$25.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Matt, who agency staff met in October of 2022, has a bright smile that is infectious! Matt recognizes animal sounds. He can wash his hands and face by himself. Matt interacts well with his environment, peers, and adults. He adapts well to changes in routines and plays well with his peers. He can play by himself for short time periods. He can focus his attention on different stimuli. Matt has advanced considerably since entering the care of his current care center. He can move his hands spontaneously and hold a pencil correctly. He can move himself with the use of his wheelchair. Matt is right-handed. His speech is well developed, and he can express himself well.

We hope his forever family sees him while he is still so young! Contact the agency to learn more about Matt and his special needs!

VIDEO:
https://vimeo.com/maaspecialkids/maa-matt
Password: Adoptmaa

Julianna

Girl, Age: 12
Country Code: EE-2
Primary Diagnosis: Spina bifida
Shunt,
Listed: Sep 2022
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
The girl has a congenital defect of the nervous system in the form of a meningeal hernia at the lumbosacral level, a bifurcation of the thoracic spine with hydrocephalus and paralysis of the lower limbs. The girl has a valve in her head that regulates the blood flow in the head and prevents the increase in intracranial pressure. She also has a neurogenic bladder – she needs to drink fluids regularly and change the catheter every 3 hours. She has a visual impairment, wears glasses: ER: +3.5, EL: +4. and uses a wheelchair.

Despite her disabilities, the girl is very active. She is very happy to work during rehabilitation, thanks to which she is willing to participate in social life and has accepted her disabilities. She is attending wheelchair dance classes. The girl functions very well on a daily basis and is independent.  She likes to play with younger children and often organizes games for them.

Hennes #

Boy, Age: 5
Primary Diagnosis: Spina bifida
Arnold-Chiari type II, spina bifida at level L5
Listed: Aug 2022
$1,060.20
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Hennes has Arnold-Chiari type II with spina bifida at level L5.

Hennes is described as a very social and happy child. He communicates well with others. He can ask and answer questions and make general conversation. When he has difficulty with a task, he says, “It doesn’t work” in order to get help. A member of the agency’s team visited Hennes and said that he is “very easy to talk to and very smart”. Videos from July 2022 show him talking, answering questions and interacting with the adults. Hennes moves from place to place by crawling and using his upper body strength. He can pull to a stand and hold onto a support. He likes to play with all kind of toys, like balls, cubes, cars, puzzles and etc. He eats independently. He told the team member that he loves apples and orange juice.

Julee

Girl, Age: 4
Country Code: Asia.2
Region: Asia
Listed: May 2022
$1,162.50
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Julee likes to live a relaxed and easy lifestyle. She laughs around familiar caregivers and takes initiative to ask for hugs. Her caregivers report that she has a persistent personality and clear preferences. We have videos of Julee playing with toys, feeding herself with a spoon, walking with a baby walker, and more. We can see in the videos that she maintains good eye contact and are told that she is able to walk for 20-30 minutes if pushing a baby walker. She of course will take pauses to rest, but typically doesn’t sit down. Julee likes to watch T.V. and play with toys that make sounds. She has been diagnosed with spinal bifida and hydrocephalus and has delayed speech when compared with children her age. However, she has been receiving early interventions on weekly basis and she practices walking 3 to 4 times daily. Julee has received leg splints to support walking and improve muscle tone, and with great success, she is now able to stand up on her own! Could your family be the one Julee needs to support her as she reaches more developmental milestones?

Zeek #

Boy, Age: 4
Primary Diagnosis: Hydrocephalus, Spina bifida
Spina Bifida; shunt placed for hydrocephalus
Listed: Sep 2021
$1,000.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Zeek is being taught to use a wheelchair. He can currently turn, but has not yet mastered going forward and backwards. He is also learning to pull his torso up and move around when in his bed or on the floor. He can physically handle toys. He picks them up, transfers them between hands, looks for them and retrieves them if he drops them. He can push buttons and activate sensory toys. He follows simple directions such as “give me”. He plays peek-a-boo. He enjoys interacting with the staff. He will hold out his hand for a hand shake, make kissing noises, and reaches to be held. He uses his hands to show how big he will grow up to be when asked by an adult. He is pronouncing sounds and syllables.

Updated May 2022: Zeek was recently moved from a large orphanage to a small group home, where he’s now receiving more interaction and attention. His language skills have started developing. He can now say several words. He enjoys interacting with staff and responds when he receives attention. He enjoys music.

Danny #

Boy, Age: 4
Primary Diagnosis: Hydrocephalus, Spina bifida
Spina Bifida, hydrocephalus-shunt placed
Listed: Nov 2020
$1,535.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Danny loves being in the playroom at the orphanage. He plays with toys and gets very excited when adults interact with him. He enjoys listening to music. He participates in therapy each day to work on learning new skills.

UPDATE August 2022: He pulls to a stand in his crib. He crawls using his arms to drag his lower body (“army crawl”). He has a lot of upper body strength. He participates in group activities. He plays with toys. He pushes the buttons on toys, “dials” a toy phone, etc. He follows simple directions. He says a few simple words. He responds to his name. He enjoys listening to music. He eats from a spoon and drinks from an open cup. He tries very hard to be more mobile, despite his lower paralysis. As a result, he has broken a bone in one of his legs. The staff tries to keep him sitting in a chair where he can see everything going on in the room and participate in activities, without risking further injury to his leg. He interacts with other children sitting around him.

Penn

Boy, Age: 12
Primary Diagnosis: Spina bifida
Spina bifida (congenital malformation of the central nervous system, spina bifida of lower thoracic spine and upper lumbar spine) lower paraplegia, pelvic organs dysfunction, hydrocephalus
Listed: Jan 2013
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

Linda

Girl, Age: 13
Primary Diagnosis: Spina bifida
Spina bifida; hydrocephalus
Listed: Nov 2015
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Smart girl, she can talk, very affectionate Updated picture in stroller from March 2018.

Lanora

Girl, Age: 13
Primary Diagnosis: Spina bifida
Congenital malformation of the central nervous system, myeloradiculomeningocele with rachischisis of lumbar spine; internal hydrocephalus, low paraplegia
Listed: Oct 2012
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Lovely Lanora needs a mama to let her beautiful hair grow out!

Eric

Boy, Age: 14
Eric has arthrogryposis and compensated hydrocephalus. He has had a surgical repair of spina bifada.
Listed: Jan 2012
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Eric is a smiley little fellow who likes to feel his caretaker’s heartbeat or pulse, because it comforts him. He would be a wonderful little brother in a household of older children.

Overall, he is healthy and would do well in a family without smaller children. His upper body is quite strong and he has full use of his hands, fingers and arms, but he has little control or movement in his lower limbs and they are significantly smaller than his upper body. He can squeeze very tightly with his hands, and reach a full arm’s length with no problems even though his resting position is the one you see in the pictures. He does not talk, according to the caretakers but does make sounds to communicate. Cognitively, he has significant delays due to his history of spina bifida and hydrocephalus. He is very much still an infant in many ways.

He may have a sister a few years older in a different region who possibly could also be available for adoption or he could be adopted separately. She also has special needs.

Brodan

Boy, Age: 10
Primary Diagnosis: Spina bifida
lumbar spina bifida with hydrocephalus; Unspecified personality and behavioral disorder due to known physiological condition; Esotropia; Other acquired deformities of limbs; Flaccid paraplegia; Vasomotor rhinitis; Hypertrophy of adenoids
Listed: May 2018
$1,089.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
sweet smile!

Scotty #

Boy, Age: 8
Primary Diagnosis: Spina bifida
Lumbar spina bifida (surgically corrected), grand mal seizures, spastic cerebral palsy, hydrocephalus
Listed: Mar 2017
$27.90
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Scotty has little support from his legs. His head control has improved and he can turn from his back to his belly. He sits independently by holding on to the bars of his crib and also makes attempts to stand up. Scotty can hold toys in his hands and tries to clap! He maintains eye contact and recognizes the faces of his caregivers. Scotty expresses appropriate emotions to happiness and agitation and will laugh out loud when teases. He imitates and pronounces combinations of sounds and syllables. Scotty interacts with all children and caregivers. He likes music and toys. Scotty is fed by a spoon and receives additional nutrition from a bottle.

Julian #

Boy, Age: 8
Primary Diagnosis: Spina bifida
Spina Bifida; Hydrocephalus: shunt placed: Slight paraplegia of lower limbs; Left kidney agenesis; Vesicostomy.
Listed: Dec 2018
$1,057.50
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Julian enjoys playing with toys. He is well attached to his caregivers and responds to them when they talk to him. When he is happy, he responds by making noises and clapping his hands. His report indicates that when held by the hands, he will take steps.

Update Jan 2020:

Julian sits on his own while supporting his weight on his hands. He uses his hands to change his posture and move his body. He stands in the walker. He actively grabs and manipulates toys and objects, tries to use them as intended – shakes to produce sound, pulls the string of a musical toy. Visual-motor coordination is slightly impaired.

Delaney #

Girl, Age: 10
Primary Diagnosis: Spina bifida
Hydrocephalus internal – ventriculoperitoneal shunt, Spina bifida, congenital anomalies of the urinary system, ventral hernia.
Listed: Apr 2016
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Update Jan 2017: Delaney is a beautiful, sweet, calm girl. She likes to be hugged and held. She likes it when someone takes care of her and to be outside, with her stroller and recognizes the people that take care of her. She feels most comfortable in her bed and during her walks with the stroller in the garden. She eats and sleeps well.

Delaney expresses her preferences to people and objects to which she is more attached. She has three favorite toys that are colorful and soft. She also enjoys listening to music especially children’s songs. She doesn’t like lying on her back and sudden and quick movements. She is able to sit independently and grab and hold objects she has very strong hands she uses well. She feels comfortable when around her there are people with who she is familiar with.

Delaney is able to express her opinion and preference with gestures. Delaney is very calm child with big potential for improvement with the needed care, attention and the feeling of the real family environment.

Ryan

Boy, Age: 12
Region: Asia
Primary Diagnosis: Spina bifida
meningocele (post-op), hydrocephalus (shunt placed)
Listed: Aug 2015
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Ryan is a sweet, shy little boy. He was abandoned outside a hospital when he was about 12 months old. Shortly after coming into orphanage care, he had surgery for a meningocele and also had a shunt placed to decrease the pressure in his head caused by hydrocephalus. The procedures were successful and he has recovered well. Ryan has good bowel and bladder control and his latest medical report says he’s healthy now.

We visited Ryan in his orphanage in late June and were taken in by his shy smile. He enjoyed playing with our iPad. Ryan demonstrated his excellent walking and running, and sang us a song. His video will melt your heart.

Ryan lives with a foster family. He sleeps with his foster mother and is very attached to her. Ryan is described as introverted and not very talkative. His motor and speech development are a bit delayed.

Could Ryan be the son you’ve been searching for?

Rory

Boy, Age: 11
Region: Asia
Primary Diagnosis: Spina bifida
meningocele (post surgery) / hydrocephalus (post surgery)
Listed: Nov 2015
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Rory is a handsome, engaging, and active boy who is 3 years old. He came to the orphanage at around 6 months old, and they discovered he had already received surgery for a meningocele, and had a shunt placed for his hydrocephalus. Rory was able to sit unassisted, and before long was crawling. He is having casting procedures to correct his club foot, so he is temporarily using a wheelchair. You can see in his video that being sidelined from the action is almost more than he can stand! Rory has undescended testicles, which need to be corrected as soon as possible. His shunt has been trouble-free. Rory (without the cast) is able to stand with assistance, but is unable to walk at this time. He is incontinent. Rory has no cognitive delays, is a bright and social boy. Before his recent cast, he would get around by crawling and moving with his knees in a kneeling position. Physical therapy would be so beneficial for Rory! He needs a family! Video is available from the agency.

Riley

Boy, Age: 10
Region: Asia
Primary Diagnosis: Spina bifida
tethered cord release (post surgery) / cystostomy
Listed: Dec 2015
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Riley is an active, and incredibly adorable, little boy who is 3 years old! He came into care when he was about 8 months old. He was already crawling, and standing with support. Riley received surgery for a tethered cord in May of 2013. After his successful surgery,when they removed his catheter, they found there was an apparent urethral injury. They performed a cystostomy (a surgically created connection between the urinary bladder and the skin which is used to drain urine from the bladder in individuals with obstruction of normal urinary flow). Riley recovered well, and was returned to his foster family. He is a smart little guy who is very social. His fine motor skills and speech are on target. Riley is attached to his foster dad, and loves to play with the other children in the foster home. Riley needs a family of his own!

OCTOBER 2017 UPDATE: Percy is a very bright and cheerful boy. He has an adventurous personality, is eager to try new things, and has an open disposition that is friendly, but not inappropriately so. He is not afraid of foreigners from overseas and was immediately interested in learning English with American volunteers in school and was one of the first to master the alphabet song. He has a good ear for language and has soaked up everything he can learn in English and he retains it (colors, shapes, animals, clothing, parts of the body, etc.). He has a great sense of humor, loves to laugh, and gives a loud “Good Morning!” and hard high five whenever he sees his English teachers. He has learned to read some characters in his native language, knows his numbers, has started basic math and knows many songs and dances from school. Percy lives with an attentive foster family who would love to see him adopted as they know that he needs medical treatment from pediatric specialists. He interacts appropriately with peers, is silly and fun with his little friends, but not unkind.

Magnolia Mae

Girl, Age: 9
Region: Asia
Primary Diagnosis: Hydrocephalus, Spina bifida
Spina Bifida, Hydrocephalus
Listed: Nov 2019
$33.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Magnolia is a precious little girl, who is described as being extroverted and sweet tempered. She is fairly active, talkative, and has quick reaction time. Magnolia enjoys singing and listening to music. She gets along well with others and likes playing outdoors with her friends and with toy cars. Magnolia lives with a foster family and though she likes to be cuddled by her foster grandfather, she is closest with her foster grandmother. She is a good sleeper and sleeps in her own bed. She is not a picky eater, though she has been spoiled by her foster grandparents who tend to hand-feed her and let her use a bottle to drink her drinks from. Magnolia’s favorite foods are meat, dumplings, noodles, vegetables, and fruits. Magnolia can walk independently. She was able to imitate words and say simple things like, “What is this?” Her intelligence was said to be delayed compared to her peers, but her orphanage also seems to say this about many children in their care.

In January of 2014, Magnolia received surgery for lumbar spinal meningocele and hydrocephalus. She had good recovery after the surgery, though she is not toilet trained. We are unsure if that is a result of her meningocele surgery or because she just hadn’t been trained yet, but a family should be prepared for her to be incontinent. An update from August (you can read the full update below) mentions that Magnolia has had a handful of seizures over the years. Magnolia has the sweetest little face with the cutest little voice.

Magnolia has a $2,500 agency grant for her adoption with a specific adoption agency. You have to watch her sweet videos! The agency has several.

London

Girl, Age: 10
Region: Asia
Primary Diagnosis: Spina bifida
Spina Bifida, Clubbed feet
Listed: Nov 2020
$27.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
London is a kind, smart, beautiful, shy, and determined girl, born in November of 2012, who interacts positively with her caregivers and the other children. London enjoys watching cartoons, listening to music, and playing with other children. Her favorite activities include singing and playing with dolls and stuffed animals. She likes to be near her caregivers and prefers they hold her hand when they go outside. London has normal cognitive and language development. She speaks in clear and complete sentences and can sing children’s songs. London was born with spina bifida and clubbed feet. She had surgery for her spina bifida, but has not had anything done with her feet/ankles. London is able to crawl, stand with assistance, and sit independently. Her report indicates she has good fine motor skills as she is able to pick-up small objects, play with toys, hold a pen to draw, and turn the pages of a book. This adorable little girl is going to such a blessing to a very lucky family!

Kyle Cole

Boy, Age: 11
Region: Asia
Primary Diagnosis: Hydrocephalus, Spina bifida
Spina bifida, hydrocephalus
Listed: Aug 2015
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Kyle has an adorable smile! Kyle was abandoned when he was only one month old. He had surgery for a meningocele and had a shunt placed for hydrocephalus when he was only 7 months old, but is now doing well although he does not yet have bowel or bladder control. Kyle is described as an active little boy who is walking and talking and has age-appropriate mental development. He likes to play with toy cars and to dance along to music! Could Kyle be your son?

Joe

Boy, Age: 12
Region: Asia
Primary Diagnosis: Spina bifida
postoperative meningocele on lumbosacral area; postoperative prolapse of rectum; strephenopodia of both feet.
Listed: Mar 2014
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Joe has a ready smile, he watches what his caregivers are doing and gets their attention by shaking his head and wiggle his upper body. Perhaps because of his body, he prefers to have motion of upper body, shake head, wiggle body and roll over to one side etc. At 10 months old, he could sit alone, say ba and ma, liked colorful toys; he liked to be close to others. He communicates with others with his eyes and has sweet smiles.

Halden

Boy, Age: 15
Region: Asia
Primary Diagnosis: Spina bifida
Congenital meningocele
Listed: Nov 2014
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Halden really loves car toys that make sounds. Every time he picks out a toy, he will first take a big car, run wildly all around the room, and laugh happily! He is able to speak a lot and his ability to take care of himself is very strong. Before he goes to bed, he will take his clothes and neatly fold them in a pile. He will share his toys and food with other children. He is very sensible. When other children feel wronged, he will take the initiative to run to the other children, comfort them and say: “No problem, don’t be afraid!”

In his early education classes, he has completed many craft projects. He can paste simple pictures and color in animal coloring books. After class, he will tidy up his own learning materials. He is also very intelligent and can recite “student rules, three character words” etc., as well as children’s songs.

Aaron

Boy, Age: 12
Region: Asia
Primary Diagnosis: Spina bifida
Spina Bifida- Mylomeningocele in sacrococcygeal region. He has not received any treatment for this condition at this time.
Listed: Feb 2013
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Aaron is a shy little boy who always has a ready smile. He gets along well with others and is very energetic. Aaron loves playing with his toys especially if they are stuffed and fluffy toys. He is closest to his caretakers and enjoys playing with others. Aaron’s mental development is good and he knows to cooperate when putting on clothes. Aaron can crawl and can respond when speaking to him.

Yanni

Boy, Age: 13
Region: Asia
Primary Diagnosis: Spina bifida
meningocele and tethered spinal cord (post-surgery), Achilles tendon surgery corrected
Listed: Aug 2015
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Yanni was born with a meningocele and tethered spinal cord and was abandoned when he was just two days old. Two weeks later, he had surgery to correct his meningocele and spinal cord and is doing well. Yanni also had surgery on his Achilles tendon. He now walks and runs, and even marched like a soldier when we visited his orphanage in late June. Yanni is potty trained but sometimes needs reminders when he’s tired. He counts to ten, knows his colors, and plays well with his foster mom’s grandson. Can he be your son?

Kohen

Boy, Age: 4
Primary Diagnosis: Spina bifida
$6,009.80
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Kohen has had surgery for his spina bifida.  His mental development is normal.