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.

Sally and Cory

Sibling Group

Ages: 6, 5

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy, Congenital Heart Defect

Listed: Dec 2022

Cory was born premature. He has cerebral palsy, paresis of the limbs, with a predominance of the lower limbs. He moves in a wheelchair, has a vision defect, convergent strabismus, amblyopia, cryptorchidism. Cory moves on his fours or in a wheelchair. The boy tries to be independent – he feeds himself, uses the toilet, gets dressed. He has therapies every day and can walk with adult’s help. The caregiver shared with the agency representative that there is a huge potential that he can walk independently.

Sally was probably born prematurely as well. Not much data about her history as well. She has never been hospitalized. The girl is under the supervision of a cardiologist due to a heart murmur. She is also under the care of an allergist – rhinitis. She has a strong character and could be a leader. She is a very protective of her brother and they have a very strong bond.

They are sweet and cheerful children who curious about the world around them.

Klair

Girl, Age: 2

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Fetal Alcohol Syndrome

Listed: Dec 2022

FAS, defect of the atrial septum, kidney agenesis, impaired and delayed psychomotor development, hypoplasia of the corpus callosum. The girl is making progress, but her development is now estimated at 12-15 months of age. She is curious about her surroundings and active in movement. She walks alone (still with her legs wide apart) and climbs the stairs holding her caregiver’s hand. Klair manipulates objects by shaking them or tapping them against herself. She can put items into box and take them out and build the tower. She does not know how to use a crayon yet and she can’t trace. She seeks contact with adults. She likes to be carried, tickled and hugged. The girl is making progress, but her development is estimated at 12-15 months of age.

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.

Hanelle #

Girl, Age: 5

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy

Strabismus

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 ***

Hanelle was admitted to the Group home in March 2021. The director of the home reported that since then the child has improved significantly – she has become stronger, she has started to eat better; she can now turn her self from the back to the abdomen. There is no support for the legs – when they put her on her feet. If she is put to sit, leaning on pillows, she stays in this position stably. She does not receive any therapies. She has better head control, now.

The child has adapted to the new environment. At first, she didn’t want to eat. She is eating well now. She likes to be paid attention to, held in her arms and rocked, she likes to be massaged. She seeks attention and tries to attract attention to herself by making sounds. She smiles, even laughs out loud at the teasing of adults. She reacts when they talk to her and when she hears her name.

She started eating better. She eats pureed common food with both a pacifier and a spoon. They feed her. She prefers to eat sweet things. Hanelle loves mashed fruits and vegetables. They give her adapted and vitamin-enriched milk with biscuits. Drinks water from a pacifier; can’t drink from a glass.

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.

Julianna

Girl, Age: 12

Country Code: EE-2

Region: Eastern Europe

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.

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.

Justice and Marley

Sibling Group

Ages: 13, 10

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

vision impairment, allergies, scoliosis

Listed: Aug 2022

2022 MACC

Sizable Grants $2,500+

They have lived in the orphanage since December 2018. Justice is a sweet, social, independent and kind girl. She is very bonded with her sister, Marley. She is a good student and her life is busy with school activities, trips and competitions. Marley is shy and her sister Justice is a role model for her. She likes to play with other children.

The girls want to be adopted and dream about their future family and new life.

Ernest

Boy, Age: 10

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Autism, Blind / VI, Global developmental delays

Listed: Aug 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 ***

This boy wants to be adopted very much, he writes letters for his future family and asks them to come and visit him soon. He is very sensitive and caring child who longs for love and tenderness but sometimes he gets angry and disrespectful… His grades in school are very good but he doesn’t remember about his homework sometimes. He needs a lot of support and supervision from his teacher along with love and support from his future family.

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.

Pattie and Paul

Sibling Group

Ages: 7, 11

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Fetal Alcohol Syndrome, Global developmental delays, Speech Delay

Listed: Jul 2022

2022 MACC

Pattie has FAS, hypothyroidism and mental delay.

She completed 3rd grade and needs help with her classes. Her caregivers describe her as kind and nice girl who smiles a lot. She has a positive attitude with her peers and adults. She is very close with her brother.

Paul graduated from kindergarten this year. His health is good, but he has a speech impairment and minor developmental delay. He likes to play outside and enjoys soccer and biking. He loves art and is making progress with learning.

They are nice children who are dreaming of having parents and will do well in a family.

Wynonna

Girl, Age: 15

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

Mental Health

Listed: Jul 2022

2022 MACC

Wynonna has suffered from mental health issues associated with the grief and loss around the death of her mother. She has made improvements in the orphanage and needs a family who can support her through the process of grief. She lives in the institution since 2021. She is an average student. She is a medically healthy and active young girl waiting for the loving family she deserves.

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.

Geno

Boy, Age: 5

Country Code: EE-6

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

Multiple congenital anomalies, primarily of the urinary system, and developmental delay

Listed: Jun 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 Single Mothers

Davit

Boy, Age: 10

Country Code: EE-6

Region: Eastern Europe

Primary Diagnosis: Epilepsy/ seizure disorder

Symptomatic epilepsy; Developmental delay

Listed: Jun 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 Single Mothers

Georgi

Boy, Age: 9

Country Code: EE-6

Region: Eastern Europe

Primary Diagnosis: Hydrocephalus, Spina bifida

Spina bifida; hydrocephalus

Listed: Jun 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 Single Mothers

Darla

Girl, Age: 9

Country Code: EE-6

Region: Eastern Europe

Primary Diagnosis: Craniofacial disorder, Genetic Condition (non-DS)

Crouzon Syndrome; Delayed development

Listed: Jun 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 Single Mothers

Buddy

Boy, Age: 11

Country Code: EE-6

Region: Eastern Europe

Primary Diagnosis: Epilepsy/ seizure disorder

Symptomatic epilepsy; Delayed development.

Listed: Jun 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 Single Mothers

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: 5

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.

Adrien

Boy, Age: 6

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

Hernia, Arnold Chiari II syndrome, orthopedic foot defect (clubfoot)

Listed: Apr 2022

Available to Single Mothers

Adrien is a charming and smiley boy. His behavior is very good, he respects the rules in the orphanage. He is interested in learning new things and willingly participate in games and activities. His skills are importing in all spheres. He is willing to play all games proper to his age.

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.

Wayne #

Boy, Age: 6

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.

Mariah

Girl, Age: 8

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Congenital Heart Defect, Fetal Alcohol Syndrome

FAS, premature birth, heart defect, anemia, lordosis, short lower and upper limbs, microcephaly, respiratory failure

Listed: Jan 2022

According to her caregiver, Mariah is a sweet girl, she is such a little “doll”, she likes dresses, shoes, likes to dance and she has an amazing personal charm. But she also has a strong character, pursues a goal, and is very curious about the world. She wants to be independent – she eats her meals alone, uses the toilet herself (and has a good appetite!) – and she also is willing to help.

Mariah has good motor activity, she is physically active, willing to dance and sing. Mariah has a lot of energy, is enduring, does not get tired quickly, and often changes body positions. She tries to be independent. She does not react with anger to her failures. She is persistent in carrying out instructions and tries to finish what has been started. The girl eats her meals alone, uses the toilet herself, and has a good appetite.

The agency’s representative in country met her in December 2021 and they have videos and photos to share with an interested family. At the end of the visit while saying goodbye, she quietly asked the representative to find a mother for her.

The agency offers a discount to a special family for this beautiful and brave girl.

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!

Alan

Boy, Age: 12

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

Listed: Dec 2021

Alan is amazing 10 years old boy who had a rough start with an unstable and unhealthy environment. He is the victim of parental physical abuse and suffers from post-traumatic past

He connects well with both peers and adults. He is calm, helpful and kind. The boy eagerly learns about nature, sings songs, makes interesting art works, uses computer programs well.

He needs a forever home to support him as he continues to overcome negative experiences of his past and shower him with the love every child deserves.

He has a lot of potentials and wants to be adopted. He is highly recommended by his caregivers. The family with an involved, hands-on father will be ideal for this boy. He would do really well as the youngest or only child (or in a family where the other children are grown). He needs an experienced adoptive family who can give him a lot of one-on-one attention and help build his trust in humanity back.

Tristan

Boy, Age: 12

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

Listed: May 2021

2022 MACC, Available to Single Mothers

He lives at the orphanage since 2016. Normal weight and height parameters. Psychomotor development is normal. He is the victim of parental physical abuse and suffers from post-traumatic past. He is under the care of psychiatrist and take medication. No medical diagnoses in his chart, but trauma. You could tell that he is emotionally somewhat fragile.

He is communicative, talkative and charming boy. Positive relationship with peers and adults. His teachers describe him as very good, active and independent student. The computer class, math and English are his favorite subjects. He loves to play soccer, card games and chess. He has a lot of potentials and wants to be adopted. He is highly recommended by his caregivers. The family with an involved, hands-on father will be ideal for this boy. He would do really well as the youngest or only child (or in a family where the other children are grown). He needs an experienced adoptive family who can give him a lot of one-on-one attention and help build his trust in humanity back.

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.

Leo & Kyle (Twins)

Sibling Group

Ages: 10, 10

Country Code: EE-7

Region: Eastern Europe

Primary Diagnosis: Blind / VI, Other Special Needs

Listed: Oct 2021

Leo is very agile and curious. He likes to read and play sports and is talented in music. He has many friends, has completed 3rd grade and is eager to learn at school. He is helpful and quick to understand. He is describe as curious, calm, friendly and smart. He forms his own opinions and quickly absorbs new information. He is very interested in creative play and books. He is talented in music and likes to sing, dance and play instruments. When conflict occurs, he tends to feel hurt and then he checks for others feelings. He tries to provoke other children when he gets angry. He communicates well and has strong social skills. He enjoys playing with other children. He is diagnosed with Hypermetropia.

K is active, strong and is very close with his brother. He enjoys music and is in the 2nd grade. He is independent, curious and likes to think. He is talented in music and enjoys tasks where fine motor skills are required. He has congenital glaucoma and can’t see with his left eye. He is self conscious of his eye, has low self esteem and visits a psychologist to help him learn how to manage his anger and express his emotions. He likes to be alone or in a quiet environment and enjoys watching TV. He has difficulty making friends but wants to communicate with other children and staff members. He has a speech disorder and difficulty with attention, concentration and self regulation. He takes medication to lower his anxiety. He is diagnosed with mixed disorder of scholastic skills, congenital cataract and congenital glaucoma.

Jayson

Boy, Age: 14

Country Code: EE-7

Region: Eastern Europe

Primary Diagnosis: Other Special Needs

He has been diagnosed with disturbance of activity and attention and mixed disorder of scholastic skills. He received medication which helps him concentrate and do better on daily tasks and school work.

Listed: Oct 2021

Jayson is described as brave, happy, active and loves all sports. He is independent and is able to take care of himself. He takes care of his room and tries to help with food preparation. He likes to be helpful and knows how to repair and construct bikes. He is friendly and tends to take a leadership role by organizing different activities. He is sensitive and impulsively reacts negative to criticism. He loves to be outside and to participate in all kinds of sports. He likes basketball, bike riding, jumping on a trampoline and likes to work “with his hands”. He enjoys art, construction, repair, drawing and listening to music.

Sebastian

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: HIV or Hep, Limb differences

HIV, Speech disorder, atopic dermatitis, clubbed foot

Listed: Oct 2021

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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.

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