Samson #

Boy, Age: 1

Non-occlusive internal hydrocephalus- shunt placed after birth; Agenesis of corpus callosum; cleft upper lip

Listed: Jan 2023

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Samson currently lives in a group home. He loves being held and cuddled by staff members. He will smile and coo and “blow raspberries” in response to being talked to. He enjoys musical toys.

Barron

Boy, Age: 5

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

Congenital megaureter bilaterally and delays in development

Listed: Jan 2023

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Barron responds to his name with a smile, to sounds and noise. He keeps an eye on the movement of people and objects in the room. He is described as a calm and pleasant child. He is well attached to his caregivers and responds well to them. When given attention, he reacts positively and with a smile. Most of the time, the child is energetic and physically active. It is difficult for him to stay in one place, constantly moving and exploring.

The child expresses his joy by erratically clapping his hands and by making noises. When held by the hand he makes several steps.

Thomas #

Boy, Age: 10

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy, Congenital Heart Defect

Infantile Cerebral Palsy; Functional heart murmur; Hemangioma on the right chest ; cognitive delays

Listed: Nov 2017

**** 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 ***

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Thomas lived in an orphanage for the first 4 years of his life. He was then moved to a group home with 10 other children with disabilities, where he lived for another 4 years. He made developmental progress while in the group home, but was still not receiving the 1:1 care and attention that he needed. He was moved into foster care at age 8 and has made significant gains in all aspects of his development since then.

Thomas can communicate verbally with words and short phrases. He also uses gestures and pointing to objects, in order to communicate his wants and needs to his foster family.
He is a sociable child who enjoys the company of other children, particularly his friends with whom he loves to play. He is so full of energy, enjoying running, climbing, and riding his bike (which is fitted with stabilizers). He particularly likes to kick a ball around in the garden with his friend and play with balloons. On outings to the park and the zoo, he takes great interest in everything he sees but loves most of all anything with wheels.

His motor skills have improved recently and he is able to do more complex activities without being told how. For example, when his jacket sleeves are inside out he turns them the right way round before dressing himself. He takes great interest in many different kinds of toys. He loves the rides in the school bus every day. He is in a small class group. He is independent with self-help skills such as dressing, undressing, toileting, eating and drinking.

Marcko #

Boy, Age: 3

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy, Hydrocephalus

Hydrocephalus-shunt placed; Cerebral Palsy;

Listed: Dec 2022

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Marcko had a shunt placed shortly after birth due to hydrocephalus. In February 2022, the shunt failed. Marcko experienced several seizures during the shunt failure. A new shunt was installed and he has not had any additional seizures.

Marcko can walk, go up/down steps, kick and throw a ball and stack objects. He will play with toys. He knows a few of his body parts and other very basic skills. He’s learning to feed himself. He can say a few words, but is not yet speaking in sentences.

Gordon #

Boy, Age: 1

Region: Eastern Europe

Primary Diagnosis: Congenital Heart Defect, Global developmental delays, Hydrocephalus

Listed: Nov 2022

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

He can pull to stand with a stable support and can “cruise” around. He crawls and walks when held by the hand, but is not yet walking independently. He purposefully grabs objects. He uses his palm to grab, globally with the palm and the three last fingers. He is capable of purposefully grabbing larger objects placed in front of him. He manipulates with the toy and places it in his mouth. Dropping the toys is on purpose. He can move the objects from one hand to the other. By imitation, he hits two blocks in each other. The child is calm and smiles to a familiar adult. He seeks individualized attention. When placed in the crib he would cry and is upset for a long time. His cry is a way of communication. When the adult comes back to him he expresses his happiness. His impressive and expressive speech is not developed. He clearly expresses his need to communicate by differentiating the intonation and the tone of the voice.

Karmen, Kevin & Kendel #

Sibling Group

Ages: 8, 8, 7

Region: Eastern Europe

Primary Diagnosis: Global developmental delays, Muscular Dystrophy

Listed: Nov 2022

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***

Available to Large Families, Available to Older Parents, Available to Single Mothers

Karmen and Kevin are twins and Kendel is their little sister.
Both girls are physically healthy and developmentally on target for their age.

Kevin has been diagnosed with Duchenne spinal muscular dystrophy and has developmental delays.

Elon #

Boy, Age: 8

Region: Eastern Europe

Primary Diagnosis: Arthrogryposis

Arthrogryposis, delays in development

Listed: Oct 2022

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Elon walks independently. He feeds himself and cleans up after his meals. He does not talk at this time, but understands what is said to him and follows simple instructions. He responds to his name. He interacts appropriately with adults and with other children. He attends to tasks and works well 1:1 and in a small group.

Raydor #

Boy, Age: 7

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

Possible Autism, Premature

Listed: Sep 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Raydor was previously listed on Reece’s Rainbow as Randy.

Raydor’s birth mother was addicted to Heroin and took Methadone during pregnancy. Raydor was born premature and spent the first 5 months of his life in the hospital. Raydor knows his alphabet, numbers and colors in both his native language and English. He can do simple addition problems (single digit plus single digit and single digit plus double digit). He speaks in 2 word sentences and memorizes poems. He loves to build houses and other things with Legos and will stay focused on this task for long periods of time. He plays independently and with other children. He enjoys music and often tries to imitate melodies. Raydor has some behaviors that are commonly seen in children on the Autism spectrum. He has not had any type of formal evaluation for Autism.

Katrina #

Girl, Age: 9

Region: Eastern Europe

Primary Diagnosis: Global developmental delays

Listed: Sep 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Mothers

Katrina’s physical development and gross motor skills are age appropriate. She talks, but has some difficulty with articulation. Her fine motor skills are developed, but slightly delayed. She is diagnosed with mental delays. She knows and names the colors. She knows the letters of the alphabet and she has started reading. She already counts up to 30 and she writes some numbers. She knows the days of the week, seasons, left vs right, body parts, and can follow directions using instructions such as over/under, front/back, etc. She plays well with other children and enjoys attention from adults. She likes to work on a magnetic board, kinetic sand and active cards. She already colors in a contour and she is very diligent when connecting lines. She can cut and glue ready elements. She can read and the fact that she is being praised for that makes her very happy.

She follows the directions of an adult in relation to the hygiene and household activities. She can dress and undress her. She washes her hands and feeds herself independently, she makes attempts for self-serving. She takes care her belongings. She keeps her materials from school in a certain place.

Cattleya #

Girl, Age: 4

Region: Eastern Europe

Primary Diagnosis: Craniofacial disorder, Hydrocephalus

Shunt due to hydrocephalus

Listed: Aug 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Mothers

Cattleya crawls, pulls to a stand, cruises around furniture and takes steps while holding two hands. She’s not yet walking independently, but she’s trying! She explores her environment and interacts with people and with toys. She babbles, but is not yet speaking any words. She is happy and enjoys interactions. She enjoys musical toys. Medically speaking, while her official diagnosis is “malformative syndrome”, she has signs of craniosynostosis.

Hennes #

Boy, Age: 5

Region: Eastern Europe

Primary Diagnosis: Spina bifida

Arnold-Chiari type II, spina bifida at level L5

Listed: Aug 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers

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.

Rose #

Girl, Age: 11

Region: Eastern Europe

Primary Diagnosis: Other Special Needs, Speech Delay

Mild Mental delays and speech delays

Listed: Jul 2022

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***

Available to Large Families, Available to Older Parents, Available to Single Mothers

Rose was removed from an abusive home at 9 years old and could not even speak the language of her birth country at that time. She now speaks in sentences, understands everything that is said to her and has made rapid developmental progress. During the visit with our team member, she was talking about the Mom and Dad that she’s waiting for and having a fun time posing for all the photos (see below). She currently lives with an older foster couple, who she calls grandma and grandpa. They have worked with her to teach her many self-help skills. She’s now in school and doing well working with a resource teacher.

Michey #

Boy, Age: 10

Region: Eastern Europe

Primary Diagnosis: Congenital Heart Defect, Craniofacial disorder, Down syndrome

Internal hydrocephalus – post Ventriculoperitoneal shunt condition. heart condition – complete AVSD with partially closed chambers. Cleft palate -surgically corrected. Post bacterial meningitis condition – unspecified and acute pyelonephritis. Delays in all aspects of development.

Listed: Jun 2022

*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Michey walks while holding one hand of an adult. He can take 2-3 steps independently, but is not yet walking independently. He can pull up and cruise along furniture and objects, and also crawls and scoots on his bottom very quickly to get where he wants to go. He has a very short attention span. He lived in an orphanage for the first 7+ years of his life and received very little intervention or opportunities to learn skills. He’s now living in a group home, where he’s receiving therapy and instruction in basic skills. He enjoys listening to music and playing outside on the swing.

Brad #

Boy, Age: 3

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

Glanzmann thrombasthenia; delays in development

Listed: May 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Brad walks independently. He plays with toys. He will fill a container with small toys and “pour” or “dump” into another container and continue the game back and forth. He can nest cups by putting them in the correct size order. He goes to other children, smiles to them and takes them by the hands. He smiles and observes with interest the faces of adults when gently talked to or sung to. He understands object permanency. He demonstrates pretend play skills related to kitchen/cooking (putting a spoon in a bowl and stirring, etc) and also bathing a baby. He shows good development in social play skills.

Sadie #

Girl, Age: 3

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

Progressive ossifying fibrodysplasia

Listed: May 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Mothers

Sadie has limited movement in her neck, back and hands/arms (due to limited movement of the shoulders). She has more range of motion in her left arm vs her right. She compensates for her limited mobility. She stands on her toes to reach objects (when she cannot extend her arms) and holds on to a support to bend down or she seeks assistance from an adult. She walks, plays with toys, and interacts with her environment. She can put together wooden puzzles, stack rings and perform other basic tasks. She can take the cap off a pen and tries to draw shapes. She interacts with familiar people. She initiates games such as peek-a-boo. She will point to things she wants to communicate her wants/needs. She dances along to music. She can say some simple single syllable words such as ma-ma, but mostly communicates with gestures. She lived in a home with a younger child for a while and did well with the younger child. The foster family limits her interactions with other people, because they are afraid she will get hurt, due to her physical limitations. She plays well with other people, when she is around them. She does not go to preschool due to the fear her foster family has that she will be injured. She shows a preference to certain objects and TV shows (Peppa Pig and Masha the Bear).

Videos from May 2022 show Sadie walking, playing with toys, putting a puzzle together and interacting with adults. The videos show Sadie’s physical limitations.

Bronner #

Boy, Age: 4

Region: Eastern Europe

Primary Diagnosis: Craniofacial disorder

Congenital maxillofacial anomaly – haylognoplatosis. Condition after cheiloplasty. Protein energy malnutrition, developmental delays

Listed: May 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Bronner has recently started walking. He eats from a spoon. He explores toys, but often throws them. He remembers the activities of his daily routine and follows his daily schedule well. He explores his environment and interacts with other people.

Trey #

Boy, Age: 4

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy

Cerebral palsy with paraparesis of the lower limbs, mixed form.

Listed: May 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Trey had a rough birth with vacuum extraction; he received treatment in the intensive care unit. He has been lagging behind in his neuro-psychic development since his early childhood. He started walking without aid late in his life. He follows simple instructions and plays with musical toys; with assistance he nests rings. He often imposes his will. He is restless when sleeping. Trey often cries without a reason. He does not play with other children and prefers contacts with adults. At times he exhibits auto-aggression and stops after distraction.

Presently, the child does not show interest towards his environment and is not interested in the surrounding world. He looks at his toys and touches them but is not interested in them. He takes a toy but quickly throws it away. He does not react to his name but now he makes a difference between known people and strangers. When asked, he does not seek objects with his eyes. He reacts to sounds and likes it when people talk to him tenderly. He responds with joy to simple jesting. His speech is not developed; he produces guttural sounds and listens to them. He reacts positively when hearing human voices.

Trey has regular consultations with a psychologist and a speech therapist, as well as with a pediatric psychiatrist and a neurologist. His delay in his neuro-psychic development was confirmed. The child has undergone a surgery for his strabismus.

Alexei #

Boy, Age: 5

Region: Eastern Europe

Primary Diagnosis: Epilepsy/ seizure disorder, Hydrocephalus

hypoxic ischemic encephalopathy; multicystic encephalopathy; nonobstructive internal and external hydrocephalus; epilepsy; cavernous hemangioma; umbilical hernia; specific developmental disorder of the motor function.

Listed: May 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

This is the case of a male child born with extremely low weight (grade III immaturity) and heavy early neonatal period (intubation in the first minutes after his birth; seizures). Later he had disorder of the central nervous system, i.e. hypoxic ischemic encephalopathy, multicystic encephalopathy, internal and external hydrocephalus. The child is in an impaired general state of health; he takes opisthotonos position; he has spastic quadriparesis and repeated day and night tonic seizures against the background of anticonvulsant therapy; myorelaxant medication is applied. He is not subject to surgical treatment and insertion of a VP shunt.
The child needs special care and supervision by medical specialists.

He depends completely on the staff taking care of him and often has respiratory infections. He takes food from a bottle and hardly takes in the quantity of food determined for him, and throws out from time to time. The boy reacts to speech and when being touched.

Alexei exhibits no interest to contact other children. He easily makes tactile contacts with adults with no resistance, including with strangers.

The child depends on the staff of the institution. Diapers are used; he does not communicate his physiological needs by crying. Sleeping routine: he naps in the day and sleeps at night; he easily falls asleep and easily wakes up. He has a routine in receiving proper food and liquids distributed over time.

Dean #

Boy, Age: 4

Region: Eastern Europe

Primary Diagnosis: Blind / VI, Hydrocephalus

Congenital cytomegalovirus infection. Internal hydrocephaly: state post implantation of a VP shunt. Quadriparetic syndrome. Cortical blindness. Cataract. Rickets. Protein energy malnutrition.

Listed: May 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

This is the case of a male child born from a pathological pregnancy with very low weight and indications of congenital cytomegalovirus infection. In the early neonatal period posthemorrhagic internal hydrocephaly was found and at the age of 2 months a VP shunt was implanted. Due to malfunctioning of the shunt, it was replaced when the child was 9 months old.

Dean is in a stationed impaired general state of health with a severe quadriparetic syndrome, pseudobulbar paresis and cortical blindness. Also, total cataract of both eyes has been found which cannot be treated surgically due to the severely damaged state of health of the child. He is fed via a nasogastric tube. He is severely delayed in his physical and neuro-psychic development. His condition is being monitored by medical professionals.

Nevan #

Boy, Age: 4

Region: Eastern Europe

Primary Diagnosis: Congenital Heart Defect, Hydrocephalus

State after intraventricular hemorrhage. Internal hydrocephaly: VPA inserted. Cortical blindness. Congenital heart abnormality: type 2 atrial septal defect (persisting foramen ovale). Hypospadias. Bilateral cryptorchidism. Delayed physical development and severely delayed psychomotor development.

Listed: May 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Nevan was born prematurely, to a young mother. He had a difficult neonatal period, with use of mechanical ventilation.
The child has a severe impairment of the central nervous system: posthemorrhagic internal hydrocephaly; a VPA shut was inserted in April 2018; later it was twice revised. The child is in a stationed impaired state of health. ECG: Persisting foramen ovale with positive natural evolution; no therapy needed.

Nevan will need observation by a neurosurgeon, pediatric cardiologist; he needs specialized care, physical therapy and kinesiotherapy.

The child turns his head towards sounds. When placed on his side by adults and with help, he can turn the lower part of his body and flip from back to front and vice versa. When awake he is placed in a baby chair. Coefficient of development: 8.
The boy laughs loudly when teased; he is happy when hearing the voice of a known to him adult that he likes. He reacts to the tone of the voice of the person speaking to him. He grasps a toy but does not manipulate with it. He falls easily asleep and sleeps well. He is fed with a bottle. He is calm when being changed and when being bathed.

Augustus #

Boy, Age: 4

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy, Hydrocephalus

Internal hydrocephalus: state after implantation of a VP-shunt; epilepsy; spastic quadriparesis; cortical blindness; delay in the neuro-psychic development

Listed: May 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Augustus was born full term, and was found that he has internal hydrocephalus; at the age of 4 months a liquid drainage valve system was implanted. The child lies in bed; he has spasticity in his limbs and his active and passive movements are limited. He depends completely on the care provided by adults. He receives kinesiotherapy. The child is subject to observation by a neurologist and by a neuro-surgeon.

The child’s lower and upper limbs are highly spastic and are with diffuse muscle hypotonia. His fine motor skills are not developed. He does not grasp a toy given to him. Atanas holds his hands bent in fists. He is seriously delayed in his psychomotor development. The boy reacts to tactile stimulation by adults. When teased, he does not smile. He is unable to interact with the other children. Atanas depends completely on the care provided by adults. He is fed by a bottle. From time to time he cries when given a shower. He sleeps well.

Orion #

Boy, Age: 3

Region: Eastern Europe

Primary Diagnosis: Congenital Heart Defect, Hydrocephalus

Premature, Congenital Heart Defect, strabismus, hydrocephalus, general delays

Listed: May 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Special needs: Prematurity III stage Bronchopulmonary dysplasia; persistent foramen ovale; peripheral pulmonary stenosis; moderate communicating hydrocephalus; retinopathy of a prematurely born child; convergent strabismus.

This is the case of a male child, born prematurely III degree (1180 g), with a complicated perinatal history and pathological neonatal period. Subsequently he developed moderate communicating hydrocephalus and is delayed in his motor and mental development; there are changes in his tone and reflexes.

The child was diagnosed with a congenital heart malformation (persisting foramen ovale and PAC), which required therapy for a certain period of time. His cardiac status has improved. Given the severe prematurity, he has retinopathy of a prematurely born child and strabismus. The ophthalmic status is being monitored. The boy needs to be followed up by a pediatric cardiologist, a neurologist and an ophthalmologist. A systematic motor rehabilitation is conducted.

The child can flip from back to front, he is unable to sit, he is unable to rise on his feet on his own. The boy reaches out and grabs with his hands and can hold toys for a short time. He follows with his eyes and turns his head after moving toys and people; he smiles when they talk to him gently; he winces and listens to a loud sounds and reacts briskly when familiar adults are talking to him. The boy pronounces sounds and random sound combinations. The child is completely dependent on the care of adults. Diapers are used.

Bodie #

Boy, Age: 5

Region: Eastern Europe

Primary Diagnosis: Endocrine disorder, Global developmental delays

Listed: Apr 2022

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Bodie has a diagnosis of moderately impaired general condition which requires constant adult attention and supervision. He was born prematurely. He has congenital hydronephrosis grade 3 of both kidneys with congenital mega-ureters and is underdeveloped in his neurological and mental development. He does not make eye contact and does not have developed speech — although he does not use words, he hums and shouts to express himself. He is interested in toys but without creative play. He began sitting independently at 2 years 9 months. He stands but cannot walk independently, and uses diapers day and night due to kidney condition, and requires constant adult supervision for his daily needs. Additional photos and a brief video are available upon request.

Ethan Adrian #

Boy, Age: 7

Primary Diagnosis: Cerebral palsy, Deaf / HoH, Hydrocephalus

Bilateral neuro-sensory hearing loss; hydrocephalus (controlled without a shunt); developmental delays; reflux; premature; Cerebral palsy, spastic form – moderate degree. Bronchopulmonary dysplasia /BPD/. Delayed physical and psychomotor development.

Listed: Mar 2022

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Ethan is well developed for his age. He is a warm and curious little boy. His best toy is a ball. He laughs and shouts every time he got his ball. Ethan is a cheerful and peaceful child. He likes the other children. Observes and manipulates with toys. He knows how to charm his caregivers and receives lots of attention.

With a familiar adult, Ethan has a good emotional tone – he enjoys a hide and seek game and sometimes gives his hand for “hello”.

He cannot walk yet, but he sits, crawls and staying straight caught for fixed support, showing progress in his motor skill development. The child has flat feet with valgus deviation of both feet – it was recommended to wear orthopedic shoes. Ethan stands up on his own until he is caught on a fixed support, stands on tiptoe, does not step aside, placed in a walker, moves short distances; pronounces long sound combinations.

Wayne #

Boy, Age: 5

Region: Eastern Europe

Primary Diagnosis: Craniofacial disorder, Deaf / HoH

Congenital cleft of the hard and soft palate with a one-sided cleft of the upper lip on the left. Moderate mental retardation. Bilateral conductive hearing loss.

Listed: Feb 2022

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Wayne has had surgery to repair the cleft lip and palate. He will be having orthodontic treatment and possible surgery on his nose in the future. His hearing was tested in June 2021 and it was determined that he has mild hearing loss of 10/15 decibels bilaterally.

His physical development is on track for his age. He walks, runs, kicks a ball, climbs, etc. His fine motor skills and speech are delayed. He has delays in his intellectual development and has difficulty with focus and attention. He attempts to communicate using non-verbal gestures and sounds or emotions. He is not aggressive and does not have any behavioral concerns. He was recently moved from a large orphanage into foster care, where he is learning new skills. He is completely toilet trained.

Update September 2022: Wayne continues to make developmental progress.
He follows verbal instructions. His speech is still delayed, but he does well identifying colors, objects and answering simple questions with pointing and gestures. He can make some animal sounds and attempts to mimic other sounds. He appears to understand everything said to him. He does have a documented mild hearing loss and a repaired cleft lip and palate. Wayne feeds himself with a spoon, can dress and undress himself independently and is independent with toileting. He can arrange objects by color, shape and size. His developmental skills continue to improve.

Videos from September 2022 show him identifying objects, answering questions (with pointing and making noises), following simple instructions, playing appropriately on playground equipment and with toys and interacting with the adults on the playground.

Izak

Boy, Age: 6

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: Congenital Heart Defect, HIV or Hep

possible HIV infection or contact with smb. HIV positive
encephalopathy of unspecified aetiology
CHD: atrial septal defect, ventricular septal defect

Listed: Mar 2019

Available to Large Families, Available to Older Parents, Siblings

Sizable Grants $2,500+

Izak has two older siblings, same region but far away; they must be adopted together!

Vann #

Boy, Age: 3

Region: Eastern Europe

Primary Diagnosis: Craniofacial disorder, Hydrocephalus

bilateral cleft of the upper lip with a cleft of the hard and soft palate; cheiloplasty; hydrocephalus; cognitive delays

Listed: Oct 2021

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Vann smiles and reacts when caregivers interact with him. He can roll around in his crib and is often placed in a walker. He picks up toys, shakes them and tries to manipulate them.

Update Jan 2022: He’s now independently sitting, standing up in his crib holding on to the rails and taking steps when holding the hands of an adult. He’s receiving daily physical therapy to get stronger and the therapist believes he will soon learn to walk. He maintains eye contact and enjoys interacting with other adults and children Vann has undergone the second stage of cleft surgeries. He’s now eating soft foods from a spoon. He’s currently living in a group home with children who are more significantly delayed. His social worker believes this will prevent him from developing appropriate communication and social skills, so she is actively looking for a therapeutic foster family for Vann, so that he can continue to reach developmental milestones.

Alivia

Girl, Age: 7

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: Epilepsy/ seizure disorder, Fetal Alcohol Syndrome

Listed: Oct 2021

Available to Large Families, Available to Older Parents

She has FAS and epilepsy and resides at the orphanage in Eastern Europe. Alivia is an affectionate girl who loves to hug and kiss the staff. She is soft spoken and initially with new people she will observe quietly but then she is not shy and initiates conversation with people she knows. She loves singing, acting, and dancing. She also loves to draw and listen stories. Alivia’s psychological evaluation report indicates that she has developmental delays. She can be easily distracted but is easily redirected with reminders.

.3

Sage

Girl, Age: 4

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: Global developmental delays

Speech disorder, developmental delay, Candidiasis, Neurogenic arthritis, Eustachian tube disorder

Listed: Oct 2021

Available to Large Families, Available to Older Parents

.3

Edwin

Boy, Age: 7

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: HIV or Hep

Toxic liver disease with chronic hepatitis, HIV disease associated with another conditions

Listed: Oct 2021

Available to Large Families, Available to Older Parents

.3

Draco

Boy, Age: 4

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: HIV or Hep

Paraplegia, brain disorder, HIV disease associated with another conditions.

Listed: Oct 2021

Available to Large Families, Available to Older Parents

.3

Vicky

Girl, Age: 4

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: Global developmental delays

Brain disorder, developmental delay, speech disorder

Listed: Oct 2021

Available to Large Families, Available to Older Parents

.3

Nova

Girl, Age: 6

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: Global developmental delays, HIV or Hep

HIV, Umbilical hernia, speech disorder, developmental delay, ptosis of eyelid, flaccid hemiplegia

Listed: Oct 2021

Available to Large Families, Available to Older Parents

.3

Brody #

Boy, Age: 7

Region: Eastern Europe

Primary Diagnosis: Deaf / HoH

bilateral deafness-choclear implant on the ride side; Moderate mental delay with autistic characteristics; Strabismus

Listed: Sep 2021

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Brody walks independently. He is able to navigate stairs and playground equipment at the park. Most of Brody’s delays seem to be related to being unable to hear and communicate his wants/needs. For example, the foster family reports that he is not aggressive, but he does demonstrate frustration at being unable to communicate with them to express his thoughts and what he wants. He uses some gestures to communicate, such as opening the refrigerator to express that he is hungry. He is supposed to be under the care of a specialist to work with him now that he has the cochlear implant (and to continue to develop his communication skills), but this has not been consistent due to COVID restrictions and the fact that the family must travel to another town for Brody to see the specialist. The foster family does report that Brody seems to be able to hear now that he has the implant and they have seen improvements with the implant in place. Brody does attend a day program for children with disabilities and has recently become more interested in the other children.

Emma #

Girl, Age: 6

Region: Eastern Europe

Primary Diagnosis: Global developmental delays, Hydrocephalus, Other Special Needs

Condition after herpes-viral encephalitis. Hepatitis caused by CMV. Hypotrophy. Hydrocephaly – of mild degree. Congenital dyserythropoietic anemia. Delayed neuro-psychological development.

Listed: Sep 2021

Available to Large Families, Available to Older Parents, Available to Single Mothers

Emma was recently transferred to a group home where she can receive more specialized care to help her continue to develop and receive appropriate medical care. She is receiving monthly blood transfusions at this time for her anemia. She had surgery to correct clubbed feet in 2020. She can sit unassisted, stand next to a stable support, walk around fixed supports and walk while holding the hand of an adult. Videos from May 2021 show Emma playing with an electronic toy. She is pushing the button to get the toy to make a sound. Her fine motor skills are not well-developed at this time, due to her spasticity. Emma responds positively to adults and other children. She smiles and laughs when adults interact with her.

Zeek #

Boy, Age: 4

Region: Eastern Europe

Primary Diagnosis: Hydrocephalus, Spina bifida

Spina Bifida; shunt placed for hydrocephalus

Listed: Sep 2021

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

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.

Kai

Boy, Age: 6

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

Congenital tracheomalacia

Listed: Oct 2020

Available to Large Families, Available to Older Parents

Sizable Grants $2,500+

At age of 2 months old he survived a surgery for heart defect

Mitchell #

Boy, Age: 6

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy

cerebral palsy – an ataxic form

Listed: Jul 2021

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Mitchell walks independently with an ataxic gait. He talk using simple words and simple sentences. He plays with toys. He shows interest in his environment and everything happening around him. He seeks contact with familiar adults.

Photos and videos are available through the agency.

Ian #

Boy, Age: 6

Region: Eastern Europe

Primary Diagnosis: Global developmental delays

premature birth, delays in all aspects of development

Listed: Jul 2021

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Ian walks with support and can take some independent steps. He’s easily comforted with hugs and affection. He loves music and will smile and dance when he hears it. He also loves cars and trains. His expressive and receptive speech are delayed. He is not yet speaking and the difficulty with communication (his foster mother not understanding what he wants) leads to crying and “meltdowns”. He foster mother reports that he likes to do things his way and he has learned that when he’s told “no”, he can have a “meltdown” and get his way. He has recently started speech therapy to assist with his language delays, but is living in a small town that has limited resources to provide the therapies and support he needs.

Photos and videos are available through the agency.

Blaine

Boy, Age: 14

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy, Epilepsy/ seizure disorder

Malnutrition, Epilepsy, Vision issues, tightened limbs/joints (exact cause/condition unknown); possible cerebral palsy

Listed: Jul 2021

Available to Large Families, Available to Older Parents

.2

Sierra

Girl, Age: 8

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy, Congenital Heart Defect, Epilepsy/ seizure disorder

spastic diplegia, Sequelae of subarachnoid haemorrhage, Epilepsy, Congenital malformation of optic disc, Hypoplasia and dysplasia of lung, Cardiomyopathy

Listed: Feb 2018

Available to Large Families, Available to Older Parents

Sizable Grants $2,500+

Joanna

Girl, Age: 11

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: Hydrocephalus

Hydrocephalus

Listed: Oct 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 ***

Available to Large Families, Available to Older Parents

New pictures, April 2017

Anna

Girl, Age: 14

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: Hydrocephalus

Internal hydrocephalus (operated), spastic tetraparesis with movement disorders, open oval window, development delays

Listed: Oct 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 ***

Available to Large Families, Available to Older Parents

This little girl is wonderful! I have never met a child with so much personality and spunk. She absolutely loves people and she is so desperate for attention. I held her for most of our visitation time one day. If I tried to put her down she demanded that I pick her up again and then she would kiss all over me. She just wanted someone to be near her. Everyday when my husband would walk through the playground gates she would get a stern look on her face and point at him and then motion for him to come to her… NOW. She would smile from ear to ear when he acknowledged her. You can not help but laugh when you are with her. Even the cold and distant nannies couldn’t keep a solemn expression on their faces when we interacted with her.

She is in need of urgent dental care! I have never seen such decayed teeth before. I am not sure why her mouth is so much worse than all the other children but her mouth is really concerning. She can stand on her own but struggles to lift and bend her legs when she is bearing weight on them. She has a little walker that she does wonderful with. She can walk along a bench by holding on to it but we never saw her walk independently. From what I could tell she does not have any limitations of her upper body.

We never witnessed her show any aggression towards any of the children. When I would sit on the bench holding my daughter she would try to climb in my lap as well, but she never tried to harm my daughter or push her out of the way. She is very hungry for attention and for the love of a family. She would make a wonderful daughter and I am sure she would provide you with a life time of laughter.

This child has significant facial features of FAS (fetal alcohol syndrome). This is a cautionary disclosure only. Families should research the varying impacts of this condition.

Tyson #

Boy, Age: 5

Primary Diagnosis: Cerebral palsy, Deaf / HoH, Hydrocephalus

Listed: Apr 2021

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Bilateral sensorineural hearing loss (with hearing aid); shunt due to internal hydrocephalus; spastic cerebral palsy

Tyson was born premature and had several complications after birth. He can sit on his own with good balanced reactions. He crawls following the correct motor model. He stands up and walks sideways vertically. He can walk when one of his hands is held and has more control when it’s his right hand being held. He can stand up straight without falling for 2-3 seconds. When walking with a walker, he begins to bend his knees. He purposefully grabs a toy that is handed to him and can switch it from hand to hand. He shows an interest in musical toys and enjoys them. He has started making sounds and simply syllables such as “ma-ma”. He enjoys having someone sing to him and likes to receive hugs. He eats from a spoon. His overall development is delayed.

Photos and videos from August 2020 are available through the agency.

Lacey

Girl, Age: 8

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: Craniofacial disorder

Cleft palate

Listed: Mar 2021

Available to Large Families, Available to Older Parents

Sizable Grants $2,500+

This child shows significant facial features of FAS (fetal alcohol syndrome). This is not a diagnosis, but a cautionary disclosure.

.2

Nadine

Girl, Age: 13

Country Code: EE-1: Adoptions are not currently being processed in this country. Further information can be given by an adoption agency.

Region: Eastern Europe

Primary Diagnosis: Global developmental delays

Moderate mental delay; congenital brain malformation; ventriculomegalia; crossed eyes

Listed: Apr 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 ***

Available to Large Families, Available to Older Parents

Nadine was recently relisted (March 2021)

Danny #

Boy, Age: 4

Region: Eastern Europe

Primary Diagnosis: Hydrocephalus, Spina bifida

Spina Bifida, hydrocephalus-shunt placed

Listed: Nov 2020

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

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.

Brett #

Boy, Age: 8

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

Mental delays

Listed: Jul 2020

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Brett lived with a foster family from birth to age 4. He did not attend preschool or receive any interventions during that time. The family was not experienced in how to work with him. He was placed in a small group home at 4 years old. He has thrived in this setting. He has learned many new skills and continues to make improvements in all aspects of his development. He communicates using words and simple sentences. He understands everything said to him and can answer basic questions. He takes care of all his personal hygiene independently (brushes his own teeth, hair, dresses/undresses himself, is toilet trained, etc). He can count to 10, recognize colors and shapes, work puzzles, say his name and age, and also say the names of the other children living in the home. The staff at the group home believe that his mental delays are mild and state that this is because he made such rapid progress once he was placed in the group home and began receiving instruction. The foster family had reported behavior issues, mainly an inability to concentrate. The staff reports no behavior problems and stated that he just needed attention and appropriate instruction. They describe him as very affectionate.

Jax #

Boy, Age: 11

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

hyperkinetic conduct disorder and a mild mental delay

Listed: May 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 ***

Available to Large Families, Available to Older Parents, Available to Single Mothers

He has been living with a foster family since 2013.

He has a systolic murmur along the precordium; hyperkinetic conduct disorder and a mild mental delay. The child started walking on time, but his speech is underdeveloped. The child cannot stay focused for a long time while playing. He understands and follows simple instructions.

The agency has current medical reports available for serious inquiries.

UPDATE March 2017: previous Diagnosis of Atypical autism that was changed to hyperkinetic disorder, very interested in motor activities. Responds to positive interactions and praise from familiar adults, but can become anxious in new situations or if a familiar caregiver is not around. He seeks comfort from familiar adults and can become sad if one leaves.

Jesse #

Boy, Age: 9

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy, Hydrocephalus

Jesse has Moderate external hydrocephalus; Arachnoid cyst – cortical atrophy; Infantile cerebral palsy – spastic quadric paresis; Hypotrophy; Delays in the neuro-psychological development; Severe mental delay.

Listed: Jun 2015

2022 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Sizable Grants $2,500+

Update November 2015: He demonstrates interest in musical and mechanical toys. He will play for a short time – studies a toy, puts it in the mouth, transfers it from one hand to the other. He likes activities involving music. He recognizes familiar areas of the orphanage and understands his daily routine related to familiar tasks such as eating. He is very happy when interacting with familiar adults.

Update 2018: Jesse attention span is short-lived and unstable in relation to objects and people. There is some sharing with a close adult. Jesse responds when called by name. His memory and speech are poorly developed. When happy, he laughs loud and when anxious, he cries. Sometimes he pronounces unspecified sounds and separate syllables. He is sensitive and emotional and tends to be nervous around strangers. When given a toy he reaches out and takes it. He is working on the pinch grip. He hasn’t mastered fully the ability to move a toy from one hand to the other. Jesse is fed with a spoon and sleeps calmly through the night. He cannot control his physiological needs. Jesse is entirely cared for by the team in his orphanage.

(Jesse was also previously listed as Andy)

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