Liamo

Boy, Age: 4
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Blind / VI, Cerebral palsy, Epilepsy/ seizure disorder
spastic cerebral palsy, microcephaly, overall developmental delay, epilepsy, gastrostomy, and blindness.
Listed: Jul 2024
$20.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Single Fathers, Available to Single Mothers
Info is from January 2023; the agency can get updated information when there is a serious inquiry.

Liamo was placed into protective care upon discharge from the hospital when he was born. At the time of his birth, he suffered severe asphyxia. His mother’s pregnancy was unplanned and she had not received any prenatal care. His parents were unable to grasp his medical diagnosis and condition, they were not in the position to care for his medical needs. No one in the biological family was able to care for him either.

Liamo is a child who needs constant supervision. His oxygen levels needed to be always monitored; however, oxygen support has been removed and he seems to have a better mood. He has not had any seizures but does have some spasms during the day. He cannot stay in a seated position. Despite his diagnosis, Liamo loves to receive affection. He communicates through babbling and other sounds. He needs support to fulfill all daily activities. He wakes up very early in the morning and is still not able to sleep throughout the night. Liamo wears diapers all day.

Liamo can kick his legs and with the help of external support equipment he can stay in a seated position for a period of time. His neck control is getting better, as he now can hold his head up for 40 to 50 seconds. He can grab objects with his hands without applying pressure. Liamo goes to occupational, physical, and speech therapy. He gets easily uncomfortable when he needs to wear more clothes, he prefers to wear very light clothes. He turns his head when he hears a strong noise. He takes daily medication. Liamo likes to change positions constantly and likes to participate in activities where there are sounds involved.

Sani

Boy, Age: 11
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Blind / VI, Trauma History
Vision loss, trauma history
Listed: Jul 2024
$34.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Single Fathers, Available to Single Mothers
Intelligent, extroverted, spontaneous, resilient, loyal, a dreamer, creative, affectionate, loving, self-efficient, autonomous, astute, brave, perseverant, with a restless mind to learn new things and face new challenges, and with great capabilities. Despite extreme difficulties in life, this is how Sani is described even though being a victim of severe child abuse of various types—including abuse that led to vision loss —could have led him to be otherwise described. Sani came into protective care in 2022 at the age of 7 years old. He is now 9 years old.

Sani is currently enrolled in the 4th grade. According to his teacher´s report, the child is loved by his classmates. He uses his cane to walk around and there are no major concerns regarding his motor, language, cognitive and social development taking into consideration his diagnoses of secondary vision loss and severe child abuse syndrome. He has great communication skills and can verbally expresses his feelings and emotions with people he is very familiar with. Sani recognizes authority figures, but many times has trouble being respectful and obedient, especially if he does not agree with an instruction given by them. Sani can easily make new friends and has leadership skills among his peers.

Sani goes to psychological therapy. He is still learning to take full responsibility for his consequences, and sometimes he lies to avoid any kind of discipline. Sani is learning to manage his impulses and frustration. If there is a situation that he cannot handle emotionally, he will start yelling or behaving in a hostile way with his peers. Whenever he throws a tantrum, he sometimes experiences psychomotor agitation and uses bad language. Whenever there are situations that make him feel anxious, he bites his sleeves, has sweaty hands or has motor restlessness. He gets upset when he needs to continue pushing to do his best in order to fully know the Braille system. He is afraid of being in a dark room alone. Because of his severe history of child abuse, it is recommended that Sani be the youngest child in the family though this may be negotiable depending on a family’s experience with children from abuse. Sani has expressed that he would like a family with two heterosexual parents and he would like to have siblings.

Sani likes to play soccer and enjoys building with Legos and also engaging in conversations with adults. He likes to listen to music in English or Portuguese since he has expressed his desire of learning new languages. Sani favorite colors are blue, white, black and orange. He loves to practice soccer, swimming, martial arts such as capoeira and riding his bicycle. He even likes to breakdance as evidence in a video sent with his profile. Sani is good at playing musical instruments. He would like to become a scientist, learn about biology and astronomy and also speak different languages.

Jean-Luc #

Boy, Age: 8
Region: Eastern Europe
Primary Diagnosis: Epilepsy/ seizure disorder
Pyruvate dehydrogenase deficiency – homozygote for mutation p.R446 (disorder of pyruvate metabolism and gluconeogenesis). Microcephaly. Epilepsy
Diagnosis: Pyruvate dehydrogenase deficiency – homozygous for mutation p.R446 (disorder in the metabolism of pyruvic and gluconeogenesis). Microcephaly. Epilepsy.

A male child, born 2460 g., with a congenital genetic metabolic disease (pyruvate dehydrogenase deficiency), leading to a disorder in the absorption of sugars and carbohydrates. The child is on a strictly individual ketogenic diet (rich in fat and completely excluding carbohydrates). He is fed with special diet milk – Ketocal.

When conducting electroencephalography, epileptic activity was registered, which is why constant anticonvulsant therapy with Trileptal is being carried out. No epi-seizures have been observed after its initiation.

The child lags behind in physical, neuropsychiatric development and motor skills. He needs follow-up by a pediatric endocrinologist and dietician and a pediatric neurologist.

The boy has pronounced axial muscle hypotonia, hypertonia of the limbs. He sits up independently, but still does not stand up in the crib. He is placed in a walker and permanent rehabilitation is carried out. He is calm, does not isolate himself in the children’s group. He shows discontent when he does not like something, but quickly calms down. The child’s sleep is peaceful.

According to a Psychologist’s last Individual Characteristic from November 2024: “ …Over the past months, progress has been reported in the child’s general and fine motor skills. He stands up on his own on a stationary support and steps to the sides, holding on to the stationary support. The child moves by crawling. He can sit alone without support. He spends his waking hours with the other children in the group and he likes it very much, calm and smiling.

Jean-Luc is smiling, radiant, calm. He stands next to the children and does not isolate himself. There is no joint play yet. He cannot initiate contact with the children by himself. He shows dissatisfaction when he does not like something. He enjoys teasing from a familiar adult. During activities, he is involved, but is not active and shows little interest.

Listed: Jul 2024
$45.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Diagnosis: Pyruvate dehydrogenase deficiency – homozygous for mutation p.R446 (disorder in the metabolism of pyruvic and gluconeogenesis). Microcephaly. Epilepsy.
A male child, born 2460 g., with a congenital genetic metabolic disease (pyruvate dehydrogenase deficiency), leading to a disorder in the absorption of sugars and carbohydrates. The child is on a strictly individual ketogenic diet (rich in fat and completely excluding carbohydrates). He is fed with special diet milk – Ketocal.
When conducting electroencephalography, epileptic activity was registered, which is why constant anticonvulsant therapy with Trileptal is being carried out. No epi-seizures have been observed after its initiation.
The child lags behind in physical, neuropsychiatric development and motor skills. He needs follow-up by a pediatric endocrinologist and dietician and a pediatric neurologist.
The boy has pronounced axial muscle hypotonia, hypertonia of the limbs. He sits up independently, but still does not stand up in the crib. He is placed in a walker and permanent rehabilitation is carried out. He is calm, does not isolate himself in the children’s group. He shows discontent when he does not like something, but quickly calms down. The child’s sleep is peaceful.
According to a Psychologist’s last Individual Characteristic from November 2024: “ …Over the past months, progress has been reported in the child’s general and fine motor skills. He stands up on his own on a stationary support and steps to the sides, holding on to the stationary support. The child moves by crawling. He can sit alone without support. He spends his waking hours with the other children in the group and he likes it very much, calm and smiling.
Jean Luc is smiling, radiant, calm. He stands next to the children and does not isolate himself. There is no joint play yet. He cannot initiate contact with the children by himself. He shows dissatisfaction when he does not like something. He enjoys teasing from a familiar adult. During activities, he is involved, but is not active and shows little interest.

Gene

Boy, Age: 14
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Behavior, Learning Disability, Speech Delay
Listed: Jul 2024
**** 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 Single Fathers, Available to Single Mothers

Gene’s information is from a report in June 2024 — the agency does have older reports as well.  Gene was 7 years old when he entered care due to neglect. He spent most of his days on the streets and there were behavioral issues within his family of origin. His father was in jail and his mother was involved in criminal activities as well as drug usage. While she said she was going to make changes in her life to regain her son’s custody, she did not follow through. Gene is now 12 years old.

Gene is in the 4th grade. He struggles academically. It is difficult for him to understand new concepts and therefore is unmotivated to do his best. He still has trouble pronouncing properly many words. In 2020 he was diagnosed with mild cognitive developmental delay, but this diagnosis was overruled though an IQ test is pending. He can get easily distracted if he does not like a specific activity. There are no concerns regarding his motor development. His language development is behind, it is difficult for him to comprehend a reading assignment; and he mispronounces some words. In the middle of the night, it is necessary to wake him up to go to the bathroom so that he will not have any accidents. Gene has been learning to manage his frustrations and impulses in a better way. Gene interacts in a positive way with his peers. Gene recognizes authority figures; he is respectful and obedient towards them. It has been observed that Gene interacts positively with adults, kids his age, younger children, and animals.

Currently, Gene goes to therapy, and he has been diagnosed with unspecified mixed behavioral issues for which he takes daily medication. He gets anxious whenever he is not permitted to do something he wants or whenever he does not fully understand a task. He gets upset when he feels he is being attacked, but he has not become aggressive. Gene is afraid of being alone, getting lost and being in the dark. Whenever he feels sad it is because he longs to have a family.

Gene loves to participate in any recreational activity, including sports. Some of Gene’s favorite activities are playing soccer, going to the park, playing cops and robbers, making bracelets and painting. When he grows up, he would like to be a professional soccer player or a chef.

Mia

Girl, Age: 9
Country Code: Asia.4
Region: Asia
Primary Diagnosis: Autism, Global developmental delays, Other Special Needs
Listed: Jul 2024
$45.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Single Fathers, Available to Single Mothers

Mia is a cheerful and smiley girl. She has been diagnosed with spastic diplegia, severe mental grade intellectual disability and Autism Spectrum Disorder (ASD) with no current medication needed. She is currently taking sleeping and vitamin supplements. Mia has divergent squint, hypertropia and astigmatism. She is recommended to wear glasses but she shows resistance as she does not like anything to be put on her face or head. Nevertheless, her vision seems not to be affected significantly during classes. Mia was assessed to have severe gross motor delay with dystonia but her walking was commented to become more stable.

Mia is currently attending a special school children with severe intellectual disability and multiple disabilities. She has made steady progress in her development and shown an interest in interacting with adults and peers. She is well loved by her school teachers and caregivers and is one of the brightest students in her special school. She enjoys listening  to children’s songs, playing with spinning and musical toys, watching cartoons, playing with the swing during leisure time. Regarding her self-care skills, Mia needs assistance in teeth brushing and washing up and she does not like these tasks. She wears diapers all day long. She receives regular potty training and can urinate on the potty occasionally. She needs assistance in dressing but is able to take off her clothes, shoes and AFOs. She is also learning to put on her shirt when being prompted.  She sits in a chair with a safety belt when her caregiver helps her to take a shower.

Liam

Boy, Age: 14
Country Code: Asia.4
Region: Asia
Primary Diagnosis: Global developmental delays, Older Child, Other Special Needs
Listed: Jul 2024
**** 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 Single Fathers, Available to Single Mothers

Liam was born December 2011. He was found to have multiple health and development issues, including a history of Infantile Spasm, left temporal arachnoid cyst, severe low vision, and moderate to severe grade mental retardation. He received training from different therapists and maintained steady improvement all along. Although he has a history of Infantile Spasm, he has a stable health condition with no records of any epileptic attacks since his admission to the present school. Due to his parents’ inability to take care of him, he was placed in a orphanage at the age of 3.

Liam is observed to be a lovely, easygoing, and well-behaved child, who is well loved by his teachers and caregivers. He is described as a happy child with stable emotions, and expresses enjoyment through his lovely smile which is heart-melting. He enjoys one-on-one interaction with his main caregiver.

Esta, Sophie and Luke

Sibling Group
Ages: 13, 8, 6
Country Code: LA-7
Region: Latin America
Primary Diagnosis: Craniofacial disorder, Trauma History
Listed: Jun 2024
$808.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Single Fathers, Available to Single Mothers, Siblings
Esta, Sophie and Luke are waiting for a family in Latin America.

Esta is an affectionate child who loves dance, judo, art and making bracelets. She has a strong bond with her siblings and relates well with her caregivers and peers. She is clinically healthy with good physical and motor development.

Sophie shows leadership skills even at her young age when playing with others. She also participates in judo, ballet and other workshops. She also likes to participate in tours to exhibits, the cinema and theater. he also exhibits a strong bond with her siblings and is well-adapted at the institution she lives in.

Luke is an active little boy who loves to play ball. He is bonded with his siblings and interacts well with those at the institution.

The children have experienced trauma in their past and will need to continue to receive counseling to help through the transition to an adoptive family and to continue to work through their past. They are doing well though as they receive services in country. Esta received corrective surgery for a cleft palate and Luke has myopia and strabismus for which he receives care. Aside from her trauma care, Sara has no known needs. All of the children follow the Christian faith.

Ricky

Boy, Age: 5
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Global developmental delays, Other Special Needs
Listed: May 2024
$100.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Single Fathers
Three-year-old Ricky has special needs primarily due to his diagnosis of agenesis of the corpus callosum. While his birth family tried to care for him, he entered into care in November 2022 and was (then) also diagnosed with global neurodevelopmental delay, cryptorchidism, dysmorphic syndrome, and failure to thrive. His current diagnoses are neurodevelopmental delay, dysmorphic syndrome under follow-up, history of intrauterine growth retardation, agenesis of the corpus Callosum and repeated Broncho obstructive Syndrome. The orphanage does report that since coming into care, Ricky has made progress with various types of therapy toward reaching his personal potential.

Ricky’s listing agency also has video available!

Brooklyn and Bailey #

Sibling Group
Ages: 10, 11
Region: Eastern Europe
Primary Diagnosis: Muscular Dystrophy
Listed: May 2024
$9,049.80
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Sizable Grants $7,500+
Brooklyn and Bailey are brothers, they reside in a foster family.

Brooklyn has muscular dystrophy and a speech disorder. He has normal mental development. In 2020 he experienced burns over a large portion of his body and had right-sided bronchopneumonia. Therapy: Operative excisional cleaning of the wounds, sterile dressings; intensive treatment of thermal shock; antibiotic therapy. Brooklyn receives additional support in the form of resource teaching. With him a team of specialist work –speech therapist, psychologist, and resource teacher within the limits of the pre-school. The child is for a second year in a row in the same preschool class, because he was delayed from starting first grade because of medical reasons. He likes artistic activities and playing with his peers. He understands and strongly desires to be adopted, even if he does not talk much, his short dialogs are for his future surrounded by his loved ones.

Bailey is a healthy child with age-appropriate physical and neuropsychological development. He has good communication skills, has leadership qualities which sometimes turn bossy, and has a group of friends. He is curious, social and actively interacts with the people around him of different ages. Bailey has the attitude and the mindset for the adoption process with the needed positivity towards providing good living
conditions, including satisfying of the physiological needs, the needs for security, love and belonging, respect and self-affirmation. He understands and strongly desires to be adopted, he often talks about his future, surrounded by his loved ones. The adoption process is so desired and awaited by Bailey. The child is prepared and
ready to have his family, his adoptive parents.

Zander

Boy, Age: 13
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Limb differences, Other Special Needs
Cognitive delay, anxiety, depression, macrodactyly and gigantism, hand deformity
Listed: Apr 2024
**** 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 ***
25 for 2025, Available to Large Families, Available to Single Fathers, Available to Single Mothers
Zander entered care in 2018 at the age of 5 or 6. He is in school and is currently attending the 4th grade for the second time. He is in a special education program due to multiple diagnoses. Zander took an IQ test in September 2022 and the results showed a mild cognitive delay. He has also been diagnosed with mixed anxiety and depressive disorders, for which he takes medication. According to the child´s medical history, he also has a diagnosis of macrodactyly and gigantism, in addition to congenital hand deformity. However, this does not affect Zander’s state of health. There are no concerns regarding his overall motor development. Zander has proper language, but sometimes his tone of voice and vocalization make it hard to fully understand what he is trying to say. It is hard for him to concentrate on one specific task.

While Zander enjoys school and has a good relationship with peers, he often experiences a lack of motivation regarding school. When faced when academic challenges he often gives up. Zander experiences sudden changes in his behavior, and his mood and disposition towards activities can vary from one moment to another. When he is in a good mood, he follows instructions and is respectful and obedient. Zander likes it when people invite him to participate in an activity. He is still learning to manage his impulses and frustration. Many times, when he does not get what he wants, he reacts inappropriately without measuring the consequences of his actions. Zander is not disrespectful towards authority figures, but it is hard for him to follow instructions and directions.

When interacting with other kids, at first he is shy due to the condition of his right hand, but once he feels comfortable he starts to interact with others. Sometimes he cannot get along well with peers due to comments he says that might be hurtful to others or because of bad behaviors to call for attention. Zander gets anxious when he wants to interact with a peer he likes. Playing with peers, watching TV, or playing on the computer makes him happy. He experiences sadness when people do not pay attention to what he is doing. He is scared of horror movies.

Zander enjoys sports such as swimming, basketball, and soccer. He also enjoys artistic activities such as dancing and singing. He is good at drawing and painting. Zander says he likes birds and dogs.

Brent #

Boy, Age: 9
Region: Eastern Europe
Primary Diagnosis: Other Special Needs
moderate mental delay due to premature birth as well as an enlarged ureter on one side
Listed: Apr 2024
$54.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Meet this cute fellow, Brent. Agency in-country staff met him in April of 2024 and made the following report:

Brent lives in a family environment. He eats pureed food and can drink from a cup. He can crawl very fast on his hands and knees although he does not walk without support. He can pull himself to standing when he desires to do so. He is frightened easily by loud sounds. He does not have a specific activity that he enjoys.

There are no manifestations of aggression, but there are manifestations of auto-aggression, most often expressed as hitting his head against the wall, the bed frame, but not with his hands. Brent loves to go outside and he is taken in a wheelchair to do so.

The in-country staff member made the following personal observations:

Brent is cared for at a basic level. Unfortunately, I don’t get the impression that the child is being worked with systematically and purposefully. There is no connection and exchange of information and guidelines between the Day Care Center and the Family-type Accommodation Center for children with disabilities. Brent needs a loving and caring family environment. He needs a family that would be willing to pay attention to him, play with him, and patiently and purposefully help and teach him.

Ivan #

Boy, Age: 9
Region: Eastern Europe
Primary Diagnosis: Behavior, Deaf / HoH
Hearing loss, scoliosis
Listed: Mar 2024
$90.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
25 for 2025, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Someone who met Ivan recently said he is an “extremely active, agile and very cute boy who loves attention as well as cuddles.” Ivan seems very happy and smiles a lot. He is said to have age-appropriate physical development.

Ivan has a moderate mental delay with hearing loss in one ear. He also has scoliosis of the spine. He can walk, run, climb and descend stairs alone. Ivan does not speak however he enjoys watching children’s movies. He prefers to play alone. He can feed himself and drinks from a cup. The staff is working on potty training with him.

The agency has a video of Ivan, from Feb 2024.

Update 8/2024

Ivan was born in 2016 and resides in a family-type accommodation center for children. He is a child of Roma origin. The parents consented to full adoption, due to the
inability to care for him. Diagnoses include moderate mental retardation, behavioral disorder, expressive speech disorder with hearing impairment – unilateral conductive hearing loss in one ear. Normal hearing with the other. Scoliosis. He has normal physical development for his age and is in good health. He walks independently, with an unsteady gait, goes up and down stairs alone, runs. Fine motor skills are poorly developed – knows how to match elements, string figures on a rope with help. He feeds himself, holds a pencil with his whole palm and scribbles on the paper, does not know how to draw, does not know how to color, does not know colors, does not know how to cut with a knife, does not arrange a constructor and a puzzle.

He rarely responds to his name. Positive emotion is expressed through a smile. When he is cheerful, he laughs loudly. He shows stubbornness and impatience but does not show
aggression or auto-aggression. He has no developed speech. He understands what is being said to him, recognizes the tone. Feelings are expressed through whining, crying, laughing. No expression of interest in anything specific is observed. He watches children’s movies. He loves attention from an adult. Does not play with peers. Eye contact is not complete. He likes to be hugged. He likes strollers, tries to play with them, prefers to hold them in his hand. Chase and kick a ball. Loves light up toys. He likes to spend time outdoors. During the academic year 2024-2025, he will be in 1st grade with an independent form of education.

He has a peaceful sleep. He knows how to feed himself; he knows how to drink from a cup, he does not know how to dress and undress himself, put on and take off his shoes by himself, but he must be asked. He does his physiological needs in the toilet or potty after prompting, he does not use a diaper.

George & Miles #

Sibling Group
Ages: 13, 14
Region: Eastern Europe
Primary Diagnosis: Limb differences
Listed: Mar 2024
$1,080.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers, Siblings
Please meet George & Miles! These brothers must be adopted together, and both are said to want to be adopted together.

George was born in 2013 and is said to have well developed general and fine motor skills. George is emotionally stable and has good social contact with other children in the school. He does need resource help in school. He has friends and shows respect for adults. He has established habits for independence in dressing, eating and sleeping.

Miles was born in 2012. Miles is diagnosed with deformed feet. He also has some contracture of the fingers in both hands. He has congenital syphilis however he has no clinical symptoms and is not contagious. Miles moves independently but walks on his toes. He also has contractures of his upper and lower limbs. He feels pain with prolonged loading of the musculoskeletal system. However he continues to be energetic and happily runs, jumps and plays with other children. Miles shows affection to adults. He is curious and shows interest an interest in everything. He does need resource help in school. He enjoys being involved in outdoor games with other children.

The adoption agency has very recent videos available of the boys.

Vincent #

Boy, Age: 5
Region: Eastern Europe
Primary Diagnosis: Blind / VI, Genetic Condition (non-DS)
Listed: Mar 2024
$1,325.90
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Single Fathers, Available to Single Mothers
His diagnoses is Edwards Syndrome including congenital cardiac malformation with large intracardiac defect, cortical blindness, and severe delay in the neuro-psychological development. The August report says the following:

Vincent was extremely calm during the whole visit. He sleeps in a small room, together with three other children with disabilities. He sleeps in a crib. He spends most of his time in his bed, being periodically put in a chaise lounge or in a car basket. He cannot sit upright, either independently, as well as with support. His position in the lounger/car seat is semi-recumbent.

Vincent predominantly uses his right hand and his body is almost constantly turned slightly to the right. He can turn from his back to one side and vice versa, he cannot turn on his stomach. When placed on his stomach, he cannot raise his head. Vincent is basically blind, according to the diagnosis and by a specialist, although the staff has doubts because the child often reacts to light. During my visit, when displaying and attempting to stimulate a reaction with a ball of light, no such reaction was observed.

Vincent showed interest in the new toys and especially in the noisy book which he grabbed with his right hand, held for a while and even waved it with his hand. As the teacher shared, he grabs like a crab, with pincers. The ball turned out to be too big for him to hold in one hand. Although the book was kind of prickly, Vincent did not react in any way, not even by pulling away.

A sharp noise does not startle Vincent, this was also evident from the sharp squealing from the side of the ball. He listens when there is music, and can show a slight liveliness/activity. He does not react to his name. He likes to be paid attention to, to be spoken to gently and to be hugged. He does not mind being touched … even from a stranger. Vincent’s entire care must be provided for by an adult.  He is fed with a tube, being on 5 feedings per day. He doesn’t get angry or protest when changing or bathing. His sleep is peaceful.

From what I saw Vincent would be much better in a family environment. In the “home”,  he mostly spends his time in his bed doing nothing and getting no attention.  Every child deserves attention and love and stimulation. I really hope that this sweet boy will find his forever family soon!

Eddie #

Boy, Age: 4
Region: Eastern Europe
Primary Diagnosis: Congenital Heart Defect, Global developmental delays
Listed: Mar 2024
$2,118.85
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
2025 MACC, Available to Large Families, Available to Single Fathers, Available to Single Mothers
Meet Eddie! This sweet little man just turned two years old. He likes to transfer a toy from one hand to the other and will look for a dropped toy. He is able to push buttons on electronic toys, and he reacts positively when adults try to engage him. He is able to roll from side to side and can sit with some assistance. Because of his medical diagnoses, Eddie receives all of his nutrition via a g-tube. He sleeps well and protests at bath time. His diagnoses include Congenital malformation of the digestive system – atresia of the esophagus with tracheoesophageal fistula. Condition following surgical intervention; implanted percutaneous g-tube. Congenital heart malformation – small intraventricular defect. Protein-energy malnutrition. Delayed psychomotor development. He will almost certainly need  more surgeries in the future in order to eat by mouth, and any family considering Eddie should be sure they are prepared to meet his medical needs.

Malcolm

Boy, Age: 11
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Autism, Down syndrome
Down syndrome, autism
Listed: Feb 2024
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
Available to Large Families, Available to Single Fathers, Available to Single Mothers
Malcom is described as a cheerful boy who can give affection exclusively to those whom he has a strong affective bond. He likes to listen to music and swing back and forth on a swing. He also likes to play with his toys. Malcom feels best with repetitive daily routines.

VIDEOS:
https://vimeo.com/maaspecialkids/maa-malcom
https://vimeo.com/maaspecialkids/maa-malcom2
https://vimeo.com/maaspecialkids/maa-malcom3
Password: Adoptmaa

There is a $1,500 agency fee reduction for Malcom’s adoption. Additional agency fee reductions may be available for Malcom’s adoption based on the adoptive family’s circumstances.

Vance #

Boy, Age: 5
Region: Eastern Europe
Primary Diagnosis: Cerebral palsy, Epilepsy/ seizure disorder, Global developmental delays, Hydrocephalus
Communicating internal hydrocephalus, implantation of ventriculoperitoneal shunt. Spastic cerebral palsy. Localized epilepsy. Atrophy of the optic nerve. Plagiocephaly. Delayed neuropsychological development.
Listed: Feb 2024
$2,095.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Single Fathers, Available to Single Mothers
Meet Vance! This three-year-old boy needs a family who has easy access to the many specialists he will need to thrive, as, in addition to regular medical assessments, he will benefit from ongoing physical and occupational therapies. Vance is able to roll from back to front. He reacts to sounds, and is able to be calmed by familiar adults when he is upset. He can be coaxed to give a smile, and while he does not purposefully play with toys, he does have a favorite teddy bear. He is able to eat from a spoon, though this picky eater cannot feed himself. 

Vance was also previously listed as Vinnie.

Stefi #

Boy, Age: 11
Region: Eastern Europe
Primary Diagnosis: Cerebral palsy, Global developmental delays
Spastic cerebral palsy; moderate mental delays; Congenital deformities of the foot.
Listed: Feb 2024
**** 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
Stefi uses a wheelchair for mobility. He can propel the wheelchair by himself. He tries to talk by making vocalizations to approximate words. He responds positively to attention and seeks out interactions with staff and the other children in his home. He enjoys playing with stuffed animals. He will push other children if they are playing with a toy he wants. He is completely dependent on an adult for all care tasks (feeding, toileting, dressing, etc).

Jolene #

Girl, Age: 16
Region: Eastern Europe
Primary Diagnosis: Global developmental delays
Delays in all aspects of development
Listed: Feb 2024
*** 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 Fathers
Jolene has lived with a foster family since 2014. She is very attached to them.

Her fine motor skills are delayed. She has difficulty with writing, cutting and grasping objects. She speaks using single words and short phrases. She mispronounces sounds. She has difficulty making choices and decisions and relies on her foster parents for assistance with tasks. She has difficulty with social boundaries and often tries to hug strangers. She shows interest in other children and observes them, but has difficulty with following instructions or following rules with interacting with other children. She requires assistance with dressing. She can feed herself, but has to be monitored to ensure she doesn’t overeat. She is eager to help with household tasks, but struggles to complete them independently. She assists with cleaning the table, sweeping, and similar tasks.

Sven #

Boy, Age: 8
Region: Eastern Europe
Primary Diagnosis: Congenital Heart Defect
Diagnosis: Muscular hypotension. Cerebellar hypoplasia. congenital heart failure  – benign venous anomaly
Listed: Feb 2024
$90.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Sven walks independently with a slow gait. His fine motor skills are developed. He plays with toys, but not with their intended purpose. He does not initiate contact with other children and does not participate in cooperative play. He responds positively to familiar adults. He does not have any verbal communication and does not follow verbal directions. He is currently fed with a bottle. He cannot chew and will not accept the staff’s efforts to teach him to eat with a spoon. He requires full assistance for all care tasks.

Bowen #

Boy, Age: 7
Region: Eastern Europe
Primary Diagnosis: Cerebral palsy
Congenital CMV infection. Central coordination disorder
$1,635.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Bowens’s muscles are very tight. When placed in a sitting position, he can sit “rigid”, with his legs outstretched in front of him. When he moves, he can not control his body (bend at the waist, catch himself, etc) and falls over. His movements are uncontrolled. The amount of vision he has is unknown. He does not follow light with his eyes.
Bowen lags behind in all aspects of his development. He makes sounds, but does not have any functional communication. He does not appear to understand what is said to him. He does respond positively to touch at times. His report indicates that he has difficulty accepting any type of change in his environment.

Izaiah #

Boy, Age: 4
Region: Eastern Europe
Primary Diagnosis: Blind / VI, Global developmental delays, Hydrocephalus
CCFDN syndrome, which includes: congenital bilateral cataracts, facial dimorphism, psychomotor developmental delay, decreased muscle tone and peripheral neuropathy, internal hydrocephalus which does not require neurosurgical treatment at this stage.
Listed: Jan 2024
$1,717.50
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Izaiah is now living in a foster family and is receiving physical therapy at a rehabilitation center three days a week. The foster family reports that they are seeing major improvements in his motor skills now that he is receiving support and intervention services. His foster mother reports that he can pull himself up to a standing position using support (example: laying down in the crib and pulls to stand by holding on to the side of the crib). His physical therapist stated that he is making “visible progress” and should soon be independently walking. Izaiah has had surgeries for cataracts in both eyes (2 on the right and one on the left). It is believed he has limited vision from his left eye. He has a diagnosis of internal hydrocephalus, however, his foster mother reports that he was recently seen again by neurology and the diagnosis was dropped. Izaiah understands what is said to him. He smiles and makes eye contact. He says a few single words and also uses gestures and facial expressions to communicate. When asked how old he is he shows two fingers. He is beginning to indicate when he needs to use the restroom, but is still wearing diaper. He holds items in his hands and explores them. He plays with toys and participates in games. He shows an interest in other children.

Marco

Boy, Age: 13
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Cerebral palsy
Cerebral Palsy
Listed: Dec 2023
Available to Large Families, Available to Single Fathers, Available to Single Mothers
Marco has a beautiful smile that lights up his face. Marco was born with cerebral palsy. He is trying so hard to walk. Be sure to watch his videos to see him moving. Marco loves to look at books. The listing agency has more information about Marco and his special needs!

VIDEOS:
https://vimeo.com/maaspecialkids/maa-marco1
https://vimeo.com/maaspecialkids/maa-marco2
Password: Adoptmaa

There is a $500 agency fee reduction for Marco’s adoption via the listing agency. Additional agency fee reductions may be available based on the adoptive family’s circumstances.

Maci, Marcel, and Milan

Sibling Group
Ages: 17, 13, 12
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Trauma History
Maci: Physical abuse, sexual harassment, and negligence by bio family; Mild depressive episode

Marcel: Physical abuse and negligence by bio family

Milan: None listed

Listed: Dec 2023
**** 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 Single Fathers, Available to Single Mothers, Siblings
Maci, Milan, and Marcel are a beautiful sibling group waiting for a loving forever family of their own! These siblings participated in a summer 2023 hosting program and still wait. The in-country team still talks to their host family regularly and knows these kids VERY well!

Additional information & pictures available from the listing agency.

Maci, born in March of 2009, is feminine and gets along very well with girls. She is described as smiley, friendly, a good friend, and empathetic. She is always ready and eager to help others. Maci needs to make everything suitable for everyone. She very much loves her siblings and has a great capacity to give love and care. She can search for help to resolve difficult situations. She loves to look good and likes using make-up and doing her hair. Sometimes learning is challenging for Maci, but her motivation allows her to overcome obstacles and persevere. She always wants to belong to something.

Milan, born in April of 2014, loves animals. She really likes taking care of them and pampering them. Milan is characterized by being playful, tender, empathetic, and loving. She is very close to her siblings and enjoys spending time with them. Her favorite activities are going to the farm, playing in the pool, and coloring. Sometimes it is difficult for her to make decisions. She must be motivated to learn to recognize those things that she likes and that make her feel good. You will always find her joking. To make her laugh, you need to tickle her a little.

Marcel, born in July of 2012, is a sweet, loving, disciplined child, eager to explore his environment and learn something new daily. One of the activities he most enjoys is building new objects and assembling Legos. He really likes learning new languages and about other cultures. Marcel is a very healthy boy. His favorite foods are fruits and salads. It is easy for him to relate and interact with others. He is expressive and friendly and knows how to recognize and express his needs.

There is a $2,000 agency fee reduction for Maci, Milan, and Marcel’s adoption with the listing adoption agency. Additional agency fee reductions may be available with the agency based on the adoptive family’s circumstances.

Maci, Milan, and Marcel have an additional $5,500 grant through Children Need Families; The adoption agency will allocate this grant. Maci, Milan, and Marcel also qualify for a RODS Heroes grant (RODS Applications are based on financial need)

Dallas

Boy, Age: 14
Country Code: LA-2
Region: Latin America
Mild cognitive delay- learning delays
Listed: Dec 2023
**** 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 Single Fathers, Available to Single Mothers
We are so happy to have permission to share Dallas’s pictures!  There are also several videos of him available with the agency, as well!

Dallas enjoys going to the park and eating ice cream. He lives with a foster family. Dallas likes to spend time with his foster family. He likes affection from people who are close to him.  Dallas has been part of the summer hosting program- don’t miss all his videos!

JULY 2023 Hosting Update: Dallas is a calm, lovely, and talkative boy. He loves to learn new things and talk about different topics. His favorite activities are talking, playing board games, and playing soccer. Although sometimes it is difficult to keep his attention, he perseveres to achieve his goals and learn. He has a leisurely soul and a more incredible spirit. He also is cautious about trying new things that involve risk. In him is a big desire to find a family forever. He is very respectful and helpful in the household chores. He cares about the well-being of the people he loves.  The adoption agency program director said he is AWESOME and she’d bring him home herself if she had the room! Contact us to learn more about Dallas and his listed non-medical need!

There is a $4500 agency fee reduction for Dallas’ adoption with the listing adoption agency. Additional agency fee reductions may be available based on the adoptive family’s circumstances.

Dallas now has an additional $2,500 grant through Children Need Families; the listing adoption agency will allocate this grant.

Vernon #

Boy, Age: 6
Region: Eastern Europe
Primary Diagnosis: Global developmental delays, Hydrocephalus, Spina bifida
Spina bifida; hydrocephalus- shunt; delays in all aspects of development
Listed: Dec 2023
$2,018.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Vernon crawls using his upper body. He plays with toys and interacts with familiar adults. He responds to his name by turning toward the person calling him.

 

Update 10/24

He has several special needs including congenital internal hydrocephalus and spina bifida aperta (thoraco-lumbar). Vernon is undergoing daily rehabilitation. His condition is monitored by a pediatric neurologist, a neurosurgeon and a pediatrician.

Vernon can turn independently from his back to his stomach and vice versa. He has good head control. He can purposefully grab a toy and hold it.  He enjoys personal attention from an adult, laughs loudly at teasing and reacts with displeasure when left unattended. He is mostly calm. No aggressive behavior was recorded. When he is called by name, he turns toward the direction of the sound.  He reacts to a noise stimulus. He speaks syllables and long sound combinations.

Liam #

Boy, Age: 5
Region: Eastern Europe
Primary Diagnosis: Arthrogryposis
congenital multiplex arthrogryposis
Listed: Oct 2023
$948.50
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
25 for 2025, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Liam works with a physical therapist every day. The PT also acts as a primary caregiver most days and is the adult that Liam is the most familiar with in the orphanage. Liam has recently gained head control and can now lift and hold up his head when on his stomach. He reaches for toys and other desired objects. He attends to toys and electronics (will focus on a video on a phone). He rolls to try to get to toys on a mat. He is very attentive to his environment. He drinks from a bottle and eats pureed foods from a spoon. He prefers fruit puree and other sweeter flavored foods. A team member who visited him said, “He is a lovable little guy who shows lots of potential and ability for emotional attachment.”

Rosita

Girl, Age: 7
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Cerebral palsy, Deaf / HoH, Epilepsy/ seizure disorder
Epilepsy, Cerebral Palsy-delayed motor skills; Cognitive delay; Language delay; Psychomotor delays; Neurodevelopmental disorder; Hearing loss on the right side; Umbilical hernia; Urinary incontinence
Listed: Oct 2023
$1,025.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Single Fathers, Available to Single Mothers
Rosita is a sweet young girl waiting for a family of her own. We hope Rosita’s forever family sees her while she’s still so young! Contact the agency to learn more about Rosita and her listed medical needs!

VIDEOS:

https://vimeo.com/maaspecialkids/maa-rosita
https://vimeo.com/maaspecialkids/maa-rosita1
https://vimeo.com/maaspecialkids/maa-rosita02
Password: Adoptmaa

Agency fee reductions may be available based on the adoptive family’s circumstances.

Channing

Boy, Age: 14
Country Code: LA-2
Region: Latin America
Primary Diagnosis: ADHD, Trauma History
History of abuse; ADHD; History of oppositional defiant disorder
Listed: Oct 2023
**** 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 Single Fathers, Available to Single Mothers
Channing is a talented boy, born in December of 2011, with many interests. He likes to play with Legos, create Origami, and play soccer. He is a waiting child hoping for the love and stability of a family of his own. Contact the agency to learn more about Channing and his listed needs!

NEWER VIDEOS:

https://vimeo.com/maaspecialkids/maa-channingupdate
https://vimeo.com/maaspecialkids/maa-channingupdate

The agency has several older videos available, too.
Password: Adoptmaa

There is a $2000 agency fee reduction for Channing’s adoption. Additional agency fee reductions may be available based on the adoptive family’s circumstances.

Alfie

Boy, Age: 7
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Deaf / HoH, Epilepsy/ seizure disorder, Other Special Needs
Secondary ventilatory failure: bacterial pulmonary co-infection-bronchopneumonia, severe persistent broncho obstructive syndrome exacerbated secondary to: aspirative neuropathy (gastroesophageal reflux disease and swallowing disorder) sequelae of bronchopulmonary dysplasia, sequelae of bronchiolitis, small ductus arteriosus without hemodynamic repercussion, mild pulmonary hypertension, symptomatic focal epilepsy, global developmental delay with hearing loss
Listed: Oct 2023
$592.50
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Single Fathers, Available to Single Mothers
Alfie is a young boy boy who shows interest in sounds and stimulation with mechanical objects. He is responsive and turns and looks towards the person who is talking to him. He engages in vocal exchanges emitting cooing. He responds with a smile when his name is called. He acquires strength through painting workshops for motor stimulation. Contact the agency to learn more about Alfie and his medical needs!

https://vimeo.com/maaspecialkids/maa-alfie
Password: Adoptmaa

Agency fee reductions may be available based on the adoptive family’s circumstances.

Irio and Hamilton #

Sibling Group
Ages: 17, 15
Region: Eastern Europe
Primary Diagnosis: Older Child
Listed: Sep 2023
**** I am eligible for a $500 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
There is a grant of 7800 euros toward foreign fees (with the agency) and this specific adoption agency will assist with applying for more.

The brothers have been in foster care for many years now and they are such great kids. They want to have a family and to be together as brothers. Next year, because the older one will become 14 in the summer, they will have to move to another town because of his school. There are no options for foster families there and they will have to go to an institution. The social worker is very hopeful this won’t need to happen and that they will be adopted instead.

IRIO – He is social and communicative. He easily makes new friends. In most cases his relationships with the children and the adults are good. According to the foster parents, he communicates well with the children and the adults. They describe him as a well-mannered child, who can assess different situations and adjust his behavior with them. He is aware that there are many social roles in society, which warrant a certain behavior. He participates adequately in the games of his peers. He can follow the instructions and the rules. He prefers games with physical activity, but he can participate in some role plays, too, and symbolic games (he gets into the role of a policeman or a criminal). He seeks the attention of the other children. He enjoys drawing, riding his bicycle, and games with a ball and other sport games. He only likes to be alone if he is using the computer. He fits in well among his peers.

HAMILTON – The boy is calm, observant, and curious about the surrounding world. He is attached to his brother, who is placed in the same foster family. Together they take care of each other, communicate, and play. He talks about his biological family calmly and talks about how they used to live. He did not like the conditions in his home then. He is attached to the foster family, their children, and their grandchild. It is hard for him to accept the pain of others and is always ready to help. When in conflict situations he defends his opinion, he is stubborn. He follows the rules at home and at school. He sometimes presents himself with stubbornness, but he does not argue and is not aggressive. He has an idea of good and bad, and for punishment and justice. He shares his experiences with the foster family and respects them. In his free time, he enjoys watching movies, listening to music, and dancing.

Axel #

Boy, Age: 13
Region: Eastern Europe
Primary Diagnosis: Autism
Autism, mental delays
Listed: Sep 2023
$25.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Axel has been assessed to have atypical autism against the background of a mild degree initial mental disability. Satisfactory general state of health. Ali understands and follows simple instructions. He imitates speech. He communicates non-verbally by pointing at things. He enjoys in his own way activities such as making things from playdough or clay. He does not get involved in the play and activities of the children in the group. Ali seeks contact with adults and peers in his own way by slapping or by caressing their heads. His play doesn’t match his age. Ali shows no interest in toys or blocks. He prefers to look at pictures and to watch educational videogames with animals. He prefers to do something alone. He likes being alone and does not seek attention. In the 2021/2022 school year Axel studied in the first grade at the elementary school in the town. He has a resource teacher as additional support. He studies under an individual plan for his education. His self-service skills are partially formed. He can eat on his own and prefers to eat with his hands. He needs support and care.

Bless #

Girl, Age: 7
Region: Eastern Europe
Primary Diagnosis: Global developmental delays
Listed: Aug 2023
$2,253.90
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Bless was born in June 2019. She resides in a Home for Medical and Social Care.
Bless was born from a pathological pregnancy, 3rd degree premature, experienced fetal asphyxia and congenital measles infection with subsequent spasticity of the 4 limbs, oral automatisms, severe retardation in neuro-psychic development, blindness as a result of retinopathy of prematurity.

She does not respond to sound signals. She does not blink. She often suffers from respiratory diseases. Bless turns from her back to her stomach and vice versa but prefers to remain in a supine position. From a supine position, she pushes herself up with her legs and shoulders and moves into space. She obliges herself in a passive sitting position in a walker. She has control over her head. She steps on her toes, but there is no support for her legs. The child holds a toy placed by the adult in her hand, puts it in her mouth, but for a short time. Undeveloped impressive and expressive vocabulary. Increased sound sensitivity. Spontaneously utters vocals and guttural sounds. She does not pay attention to her surroundings. The child is fed by an adult. She falls asleep on her own. She is completely dependent on the adult.

Archibald #

Boy, Age: 7
Region: Eastern Europe
Primary Diagnosis: Hydrocephalus
Listed: Aug 2023
$1,022.50
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Diagnoses include severe prematurity, including damage to the central nervous system –
hydrocephalus; a ventriculoperitoneal shunt was implanted. There is a lag in physical and
neuropsychological development.

Archibald cannot walk independently. He moves by pushing when placed in a walker. Stands up on his own and stands on his feet when in his crib. He can get out of bed by himself. He can go around the whole game room. He can sit for about 15-20 minutes. In terms of fine motor skills, he can pick up a toy himself if it is nearby; he plays for a long time and prefers to manipulate with his left hand. If the toy is at a distance, he tries to reach it. He likes musical toys. He recognizes adults. He has a good emotional tone, he enjoys contact with adults he knows; he loves when they praise him. He gets angry if his toy is taken away and tries to keep it in his possession. Archibald cannot speak but he makes long sounds. In interpersonal relationships he shows preferences for certain adults and initiates contact with them. He plays with toys. The child doesn’t have independent household hygiene habits. He is calm when changing and bathing, as well as in his sleep. Archibald does not take an afternoon nap, he eats everything. He is very stubborn and when he decides that he wants to pick up an object, no matter how heavy and large, he does his best. He still uses a diaper, potty several times a day. His sleep at night is
peaceful. He has daily kinesitherapy and sessions with a teacher. He is followed by a
neurosurgeon.

Sage

Girl, Age: 8
Country Code: EE-4
Region: Eastern Europe
Primary Diagnosis: Congenital Heart Defect, Down syndrome
Down syndrome, Congenital heart defect: full atrioventricular conduction, (post-op); premature newborn child
Listed: May 2023
*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***
Available to Single Fathers, Available to Single Mothers
This country only provides limited information upfront on waiting children.

Narek

Boy, Age: 8
Country Code: EE-4
Region: Eastern Europe
Primary Diagnosis: Down syndrome
Down syndrome, Type II respiratory failure, CNS injury, mature newborn child, Intrauterine pneumonia
Listed: May 2023
*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***
Available to Single Fathers, Available to Single Mothers
This country only provides limited information upfront on waiting children.

Quinn

Boy, Age: 8
Country Code: EE-4
Region: Eastern Europe
Primary Diagnosis: Congenital Heart Defect, Down syndrome
Down syndrome; Intrauterine infection, pneumonia, premature newborn child of 35-36 weeks of gestation, respiratory disorders; CHD: PFO
Listed: May 2023
*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***
Available to Single Fathers, Available to Single Mothers
This country only provides limited information upfront on waiting children.

Kacee

Girl, Age: 8
Country Code: EE-4
Region: Eastern Europe
Primary Diagnosis: Down syndrome
Down syndrome; premature child at 30 weeks; Syndrome of respiratory disorders, Hypoxic CNS injury, Depression Syndrome, Anemia of prematurity, Retinopathy of prematurity,
Listed: May 2023
*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***
Available to Single Fathers, Available to Single Mothers
This country only provides limited information upfront on waiting children.

Kohar

Girl, Age: 7
Country Code: EE-4
Region: Eastern Europe
Primary Diagnosis: Congenital Heart Defect, Down syndrome
Down syndrome; Premature newborn child of 36 weeks; Congenital heart defect – VSD, PFO, Tricuspid valve regurgitation
Listed: May 2023
*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***
Available to Single Fathers, Available to Single Mothers
This country only provides limited information upfront on waiting children.

Sam

Boy, Age: 7
Country Code: EE-4
Region: Eastern Europe
Primary Diagnosis: Congenital Heart Defect, Down syndrome
Down syndrome; Hypoxic-ischemic injury of the central nervous system, Muscular distal syndrome, Congenital hypothyroidism, Congenital heart defect: PFO, additional trabecula in the left ventricle.
Listed: May 2023
*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***
Available to Single Fathers, Available to Single Mothers
This country only provides limited information upfront on waiting children.

Rylee

Boy, Age: 7
Country Code: EE-4
Region: Eastern Europe
Primary Diagnosis: Down syndrome
Down syndrome; Perinatal growth delays, right side cryptorchidism. Congenital hypothyroidism; concurrent conditions: Microcephaly, developmental delays
Listed: May 2023
*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***
Available to Single Fathers, Available to Single Mothers
This country only provides limited information upfront on waiting children.
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