Tio

Boy, Age: 1
Country Code: LA-2
Primary Diagnosis: Congenital Heart Defect
Listed: Apr 2026
$0.00
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!
Trust me, I’m cute under this sticker they put on my face! 

Here is what is said about me:

Tio was born 4 weeks prematurely with a complex congenital heart condition, including pulmonary atresia and Tetralogy of Fallot. He has undergone multiple cardiac surgeries, including right ventricle-to-pulmonary artery conduit placement and angioplasty with stent placement. He has experienced postoperative complications, including surgical site infection and respiratory infections, all of which were medically managed. He currently requires continuous oxygen support via nasal cannula (1 liter per minute) and takes cardiac medications including furosemide, spironolactone, and low-dose aspirin. He remains under close pediatric and cardiology follow-up, with additional evaluations pending in genetics and general pediatrics.

Despite his significant medical history, Tio is described as a calm, affectionate, and resilient child. He responds warmly to caregivers, makes eye contact, smiles socially, and enjoys music, light-up toys, and physical closeness. He demonstrates curiosity about his environment and enjoys sensory exploration.

Developmentally, Tio presents global developmental delay secondary to his complex medical condition and prolonged hospitalizations. He can sit independently, roll, assume a crawling position, and manipulate objects with his hands. His fine motor skills are emerging, though slightly below expectations. Expressively, he babbles and produces repetitive syllables, though language development is delayed for his age. He receives ongoing interdisciplinary services including physical therapy, speech therapy, and psychological support. With continued therapeutic intervention and a stable family environment, he is expected to continue progressing.

Nutritionally, Tio is stable and well nourished, with adequate weight and height for age. His vaccination schedule is up to date. He tolerates solid foods well and maintains appropriate daily intake. Emotionally and socially, Tio forms attachments and responds positively to consistent caregiving. He expresses joy through smiles and gestures, communicates needs through crying and vocalization, and is receptive to affection. He has shown increasing emotional security and regulation within the structured environment of his current placement.

Tio would benefit from an adoptive family that is emotionally sensitive, patient, and well-prepared to manage complex medical needs. His family should be committed to ongoing cardiology care, therapeutic follow-up, and providing structured routines with nurturing support. A family with strong advocacy skills and access to pediatric cardiology services will be essential to meet his ongoing medical needs. Most importantly, he needs a loving, stable home that will encourage his development at his own pace and celebrate his resilience and strengths.

Tio is a gentle, sweet, and determined child whose smile reflects his strong will to live and connect. With proper medical care and the unconditional love of a permanent family, he has significant potential to thrive.

Mike

Boy, Age: 4
Country Code: EE-11
Listed: Mar 2026
$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!
Mike was born via cesarean section at 32 weeks. At birth, he required resuscitation and spent much of his early life in hospitals.

Mike has polymalformative syndrome, complex congenital heart disease, agenesis of the left radius and thumb, agenesis of the right kidney, psychomotor developmental delay, intestinal malrotation, and asplenia, for which he receives prophylactic treatment. He has undergone several cardiac interventions, including pulmonary venous return, Glen surgery, and two catheterizations, and he is expected to undergo another catheterization and heart surgery (Fontan procedure) in the future.

He also has gastroesophageal reflux disease, treated with Nissen fundoplication, and a gastrostomy. Mike receives multidisciplinary care across pediatrics, nutrition, ENT, orthopedics, plastic surgery, child psychiatry, and gastroenterology, with upcoming appointments in genetics and developmental pediatrics. He takes medications including captopril, cetirizine, mometasone nasal spray, amoxicillin, vitamin D, and acetylsalicylic acid.

Mike is a courageous and resilient little boy, making progress every day with dedicated medical care and support.

Ethan and Zariah

Sibling Group
Ages: 9, 11
Country Code: Central.Asia.1
Region: Asia
Listed: Feb 2026
**** 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 ***
Ethan is 9 years old. He’s a quiet child, obedient and helpful.

Special needs: pulmonary artery stenosis, tetralogy of fallot, developmental disorder, speech delay, acute malnutrition.

Zariah is 11 years old. She is a quiet and kind-hearted girl. She plays well with other children. She is developmentally delayed and will need help to reach her potential. She wants to be adopted.

Special needs: developmental disorder, speech delay.

Isabella

Girl, Age: 4
Country Code: EE-2
SN: Ventricular septal defect (VSD), atrial septal defect (ASDII), pulmonary stenosis (PS), FAS, Low birth weight, Moderate bilateral hearing loss
Listed: Feb 2026
$36.00
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!
Isabella shows a delayed psychomotor development. Her concentration is short but good. She shows a great interest in her surroundings, follows objects with her eyes. She grabs toys with her hands and puts them in her mouth. She can grab two objects and rotate them with her hands.
She recognizes the familiar people from strangers, and she reacts to her name. Her active speech is delayed – she doesn’t speak full sentences yet but she can say a simple words.  She actively participates in the group activities and also can initiate games by choosing some toys.  Motor skills are delayed – lack of age-appropriate skills, but she is learning every day.  She is very active and her behavior is described as high hyperactivity with anxiety. She is able to understand and follow the instructions; she is doing with in a group with other children. She is learning to put on shoes independently. She can eat some food without help if it is sliced to small pieces.

Recent visit Feb.2026: Isabella is a very promising child. She has undergone cardiac surgery. It was not possible to test her hearing, but she functions normally. Despite her heart problems, she never had blue lips or excessive fatigue.

Her currently weight is 12 kg. She communicates verbally very well and is able to express her needs and emotions. She still uses diapers but she is in the potty training. She is a very active child, but not hyperactive. She functions well one-on-one. She has two favorite friends at the orphanage. She likes to play with other children and does not exhibit any aggressive behavior.
She is a picky eater, but she likes to try new flavors (she recently enjoyed olives). She sleeps throughout the night. She sometimes takes naps during the day. She likes to do puzzles (30 pieces) and “read” the books. She is a girl who likes to dress nicely and has a pretty hairstyle.

Axton #

Boy, Age: 2
Special needs: prematurity (2nd degree); low birth weight (1,560 g); microcephaly; congenital bilateral cleft lip and cleft palate (status post plastic surgery); congenital duodenal atresia (status post surgical correction); delayed neuropsychological development.
Listed: Feb 2026
$0.00
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!
Meet adorable Axton!  Axton has never lived with his biological family and has spent his entire life in hospitals and children’s institutions. His special needs are primarily medical, and his congenital malformations have been successfully treated surgically. Although his neuropsychological and motor development are delayed, Axton is making steady progress.

Axton moves around using a walker and is very active. He sits independently without support. His speech is in the process of development; he pronounces individual sounds and produces a variety of vocalizations.

Axton is cheerful and smiles often. He actively seeks the attention of adults and laughs out loud during playful interactions. He shows good adaptation to new environments and daily routines. Axton is calm and does not display self-aggressive behavior. He independently reaches for toys placed around him, taps them, and explores them with curiosity.

Axton is fed with a spoon by an adult while seated in a high chair. Efforts are being made to teach him to drink liquids from a cup. He falls asleep in a crib, and his sleep is calm.

Kenny

Boy, Age: 2
Country Code: LA-2
Down syndrome, surgically corrected congenital heart disease , generalized hypotonia, glycion disorder with gastrostomy management, congenital hypothyroidism, malnutrition in correction, and global developmental delay with impairment in the motor, cognitive, language and social areas
Listed: Jan 2026
*** I am eligible for an additional $2,500 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome under the age of 6 are eligible for this grant. ***
$215.00
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!
Kenny enjoys spending time in his children’s jumper which comes with various sensory stimulation accessories, as well as his crib. He is happy with physical contact, having movements made in his legs, and being lifted up. He has physical, occupational, and speech therapies 3 time a week. Kenny has achieved a notable improvement in his nutritional status. He needs an adoptive family with high emotional, affective, and physical availability, who has a solid support network and preferably experience in the care of children with special needs. It is essential that this family is committed to the active management of the health, therapeutic, and educational services that Kenny requires.

NEW VIDEOS:
https://vimeo.com/manage/videos/1151669660
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Password: Adoptmaa

There is a $1,000 agency fee reduction for Kenny’s adoption via a specific agency.

Yoshi

Boy, Age: 4
Country Code: LA-2
Neurodevelopmental delay, macrocephaly, muscular hypotrophy, growth concerns, expressive language disorder, and cardiac concerns
Listed: Dec 2025
$35.00
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!
Information is from June 2025:

Yoshi was removed from his family at a young age, due to their lack of ability to provide adequate care. Yoshi presents with a complex medical profile requiring ongoing attention and care. His primary diagnoses include: Neurodevelopmental delay: affecting various areas of growth; Macrocephaly: disproportion of the skull/face and minor facial dysmorphisms; Muscular Hypotrophy: specifically noted in the lower extremities, though they are symmetrical; Growth Concerns: short stature and low weight, previously hospitalized for protein-calorie malnutrition; Expressive Language Disorder: significant difficulties in verbal communication; Cardiac Concerns: possible pulmonary valve insufficiency and mild tricuspid insufficiency (syndrome under study). He has a history of hospitalization for respiratory infections (pneumonia) and malnutrition but has stabilized under current care. He has no known allergies. His current medical regimen includes nutritional support. His vaccination schedule is up to date for his age.

Yoshi faces several developmental challenges. He exhibits a significant delay in verbal expression. His vocabulary is limited, and he struggles with pronunciation, articulation, and structuring sentences. He primarily uses gestures and short words to communicate. While he has shown improved mobility, he experiences difficulties with gross motor skills such as running, jumping, and climbing stairs. He exhibits generalized hypotonia and issues with balance and coordination. He has cognitive difficulties understanding complex instructions. He is currently working on sphincter control and still requires diapers. However, he is showing progress in independence, such as using a spoon during meals.

Despite his challenges, Yoshi possesses a warm and engaging personality. He is described as an active, affectionate, and receptive child. He shows a genuine interest in social interaction and engaging with the world around him. Yoshi has an adequate capacity to form bonds with significant adults and is progressively learning to interact with peers. He enjoys group play and is capable of sharing toys. He tends to express his emotions clearly through facial expressions and gestures. He thrives in environments where he feels emotionally secure.

Yoshi is a child with distinct likes and dislikes that help define his daily life: He has a strong preference for symbolic and construction games. He enjoys recreational activities, particularly playing ball, searching for elements, and visiting parks or rivers. He enjoys fruits such as bananas, watermelon, tangerines, and oranges. He dislikes pineapple and chopped papaya (though he accepts papaya in juice form). He benefits from a structured sleep routine, sleeping easily and restfully, which contributes positively to his mood and willingness to participate in daily activities.

Yoshi requires a parenting style that combines deep affection with structure. His ideal home will prioritize his medical and therapeutic needs—including ongoing nutritional support and developmental therapies—while providing an emotionally safe and orderly environment.

Taliyah

Girl, born 2027
Country Code: EE-7
Listed: Oct 2025

This precious child is calm, responds to being spoken to, smiles often and is interested in everything. She knows how to clap her hands, likes different musical toys, dolls, blocks, animation and radio. She is rolling in her bed and can sit up by herself. She has a gastrostomy but can eat mashed food from a spoon and drink liquids from a bottle. She sleeps soundly. The institution has medical staff working with her:  nurses, nurses’ assistants, occupational therapist, physiotherapist and she gets massages.

Diagnosed with subarterial ventricular septal defect, multiple congenital malformations, not elsewhere classified, oter secondary pulmonary hypertension, atrioventricular block, complete, supraventricular tachycardia, congestive heart failure, mild to moderate intrathoracic asphyxia, neonatal cardiac arrhythmia, other neonatal feeding disturbances, cerebellar reduction abnormalities, secondary atrial septal defect, patent ductus arteriosus, congenital absence of umbilical artery, oesophageal atresia with tracheoesophageal fistula, unilateral renal agenesis, cardiac appliance, and specific motor development disorder. It should be noted that prospective adoptive parents should have the knowledge and skills to be able to provide the necessary assistance, as the girl needs nursing and care.

Eleanor

Girl, Age: 11
Country Code: EE-11
heterozygous variant in the KAT6A gene. Heart issues, global developmental delay, severe language delay
Listed: Sep 2024
$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!
Eleanor is a beautiful young girl who needs a family.

Brandon #

Boy, Age: 6
Microcephaly. Hydrocephalus. Agenesis of the left hemisphere, persistent foramen ovale, Interatrial defect and Schizencephaly.
Listed: Sep 2024
$2,048.40
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!

Please meet Brandon; he has multiple special needs. Sadly Brandon relies totally on the care of others.  He sleeps in a room with four other children.  The caretaker says he seems to like music and likes the bath.  He can make some sounds for speech.  He has difficulty feeding and swallowing.

The agency staff member that met Brandon said the following:  “According to the caretaker, there is a slight regression, especially in terms of feeding. Unfortunately, I have not been given an opportunity to speak to any of the specialists engaged with the boy and possibly what exactly they are working on. Brandon could have some potential, but it’s very hard to tell.  In any case, he needs a lot of love, a lot of attention and a lot of activities.”  Could you be the family for Brandon?

Nick

Boy, Age: 11
Country Code: LA-2
Listed: May 2024
$35.00
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!

 Nick is a very affectionate child who has bilateral hearing loss. While he has multiple diagnoses, he is able to attend school regularly and is in the second grade. Nick has adjusted well to school, his classmates, and teachers. Sometimes he gets easily distracted. He has constant support to improve his learning skills, especially his language development. Nick has trouble expressing his ideas, as his vocabulary needs to expand more and his reading comprehension is weak.

Nick is described as “so sweet and empathic that it is easy for him to interact with adults, peers, younger children, and animals.” He interacts positively with peers, makes eye contact, and loves to participate in games and activities with them. He is always willing to meet new people. Nick recognizes authority figures, and he is respectful and obedient towards them. There are no major concerns regarding his motor development, but it is important to mention that due to his medical diagnoses sometimes he can be perceived as clumsy. In the past 4 years, it has been noted that Nick gets anxious when he is not near his foster mother; however, he still is able to do all the things he is supposed to do.

As mentioned above, Nick has bilateral hearing loss, but is not deaf. He mainly communicates through facial gestures and guttural sounds. He can say and pronounce some words. He goes to special education sessions in order to improve his cognitive abilities. Sometimes Nick gets sad when his peers do not include him in an activity due to his language limitations. He is afraid of sudden loud noises and does not like when vehicles such as motorcycles are very loud. Nick has also been diagnosed with Localized Adenomegaly, Epilepsy, and related symptomatic epileptic syndromes with combined focal localization, Mitral Valve Insufficiency, moderate mental delay, and has an IQ of 40. He takes daily medication.

It makes Nick happy to be able to play with his foster siblings and to spend time with his foster mother. He also enjoys taking care of the household pets. Nick likes to sing, draw and paint. He is good at crafts and loves to play soccer in the park.

His listing agency has additional information and precious pictures of this child from when he was 3 years old! They will be happy to share this information with interested families!

Eddie #

Boy, Age: 4
Listed: Mar 2024
$2,100.85
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!
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.

Sven #

Boy, Age: 7
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!
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.

Waylon

Boy, Age: 14
Country Code: EE-7
Listed: Nov 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 ***
Waylon is in 5th grade with average academic achievements. He excels in mathematics and is particularly diligent in art and technology. He is inquisitive during educational trips and is an active participant in physical play. Waylon’s reading skills are good, he is able to narrate and read a text, answer questions, observe, and analyze. He attends wrestling, science, drama and sports clubs. In his free time, he plays basketball, and football, cycles, draws, does needlework, plays computer games, and watches TikTok or films. He has several friends with whom he spends his free time.

Waylon tries to follow rules but has difficulty following rules during lessons and concentrating on tasks. He sometimes
struggles to control his behavior and emotions. When angry, he behaves impulsively and uses verbal aggression. Seeks
leadership positions sometimes overestimating his own strength. He can become angry when he loses an activity and then
refuses to continue.

At first contact, the impression is that he is shy and withdrawn. After familiarizing himself with his
surroundings in a group of other children, he becomes bold and eager to make an impression. Waylon is able to make friends with other children, but is not always able to maintain them for long periods of time. Relationships with staff are generally warm, friendly and respectful. He is willing to interact, spontaneously develops a conversation and initiates conversations on topics of interest to him. Can distinguish, understand and relate emotions (sadness, anger, happiness, joy) to personal experience, although more often suppresses them and then acts them out on impulse. He lacks emotional self-regulation skills and sometimes has complex emotional experiences (loneliness, insecurity, anger, hopes and dreams about family life). Waylon is helpful, inquisitive, polite, generous, loves animals and likes to joke. He has age-appropriate decision-making skills, problem-solving skills. He has some signs of inappropriate behavior (swearing, insulting other children, not always responding to comments, etc.) due to being around older children. Waylon has been receiving psychological counselling since 2019. His caregivers say that it is likely that his mental health will improve significantly if he is provided with a safe, affectionate family environment.

Galen

Boy, Age: 11
Country Code: EE-2
VSD,ASD, epilepsy, optic nerve hypoplasia, hyperopic astigmatism in both eyes.
$43.00
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!

Galen is an eight year old boy with Fetal Alcohol Syndrome, which has left him with some dysmorphic facial features and difficulties with problem solving. In difficult situations he resorts to verbal and physical aggression. He enjoys helping out with household activities, specifically in the kitchen. He is visually impaired and has mild intellectual disability. He has been receiving preschool education since last September. He works with a psychologist, speech therapist, and physiotherapist on a daily basis.

Galen enjoys participating in group activities, but he works better when one-on-one with a therapist. He is capable of focusing for long periods of time on a single activity. When something doesn’t go his way, he can get upset, but with the right motivation he can easily return to his activity. Galen can’t read, but he can distinguish single letters of the alphabet, and can even copy letters. He can count to twenty. In the future, more focus will be put toward improving his knowledge of the alphabet and helping him manage his emotions.

Sage

Girl, Age: 8
Country Code: EE-4
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! ***
This country only provides limited information upfront on waiting children.

Quinn

Boy, Age: 8
Country Code: EE-4
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! ***
This country only provides limited information upfront on waiting children.

Kohar

Girl, Age: 7
Country Code: EE-4
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! ***
This country only provides limited information upfront on waiting children.

Sam

Boy, Age: 7
Country Code: EE-4
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! ***
This country only provides limited information upfront on waiting children.

Dalita

Girl, Age: 6
Country Code: EE-4
Down syndrome; Congenital heart defect: VSD, PFO, Pulmonary artery stenosis; discoid dermatitis
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! ***
This country only provides limited information upfront on waiting children.

Kerry

Girl, Age: 4
Country Code: EE-4
Down syndrome; Congenital heart defect (ASD, PDA)

Listed: Apr 2023
*** 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 country only provides limited information upfront on waiting children.

Thomas #

Boy, Age: 13
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 ***
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.

Cale

Boy, Age: 5
Country Code: LA-2
Global developmental delay; Severe perinatal asphyxia, hypoxic-ischemic encephalopathy, epileptic events under management and controlled, modulated and overcome cardiogenic shock, secondary ventilatory failure, suspected early sepsis, late sepsis due to treated Klebsiella pneumoniae, resolved hypocalcemia, resolved hyponatremia, hyperphosphatemia, child of a consuming mother of psychoactive substances and high neurological and psychosocial risk.
Listed: Nov 2022
$25.20
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Cale loves to be cuddled and held. Cale likes to listen to music and feel different textures. Agency staff met Cale in October of 2022. Contact them to learn more about Cale and his listed medical needs!

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

Jeremy

Boy, Age: 6
Country Code: LA-2
Development delay, Epilepsy, Cerebral Palsy, Microcephaly, & gastrostomy
Listed: Oct 2022
$821.10
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!
Jeremy was met by agency staff in July of 2022. He has a beautiful smile that lights up the room. Jeremy is affectionate with his foster mother and loves to listen to her sing. He really enjoys music! Jeremy will need a family who can provide dedicated care and one who can continue to help him develop and grow. We can’t wait to see who his family will be.

The agency has additional medical information and videos available.

Paula

Girl, Age: 13
Country Code: EE-2
Primary Diagnosis: Congenital Heart Defect
speech delay, kidney and heart defects, ADHD
Listed: Sep 2021
$159.40
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!

She has multiple special needs including mild intellectual disability, speech delay, ADHD, heart and kidneys defects.

She is a sensitive and cuddly girl who is friendly with other children and likes playing together. She is working on new skills every day and making a great progress! She willingly participates in all activities and has no problems with behavior.  She likes to help with making sandwiches for lunch and always eager to help. Her self-serving skills are good.

 

 

Teddy #

Boy, Age: 11
Primary Diagnosis: Congenital Heart Defect
congenital heart malformation: ASD, VSD; infantile cerebral palsy – ataxic form; moderate mental delay; autistic manifestations in behavior
Listed: Jul 2019
$50.00
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!
Despite his diagnosis of infantile cerebral palsy Teddy walks independently. He climbs on and gets off the bed independently. Teddy examines objects with hands, eyes and mouth. He is able to transfer objects from one hand to another. He is able to hold two toys in his hands and knock them in one another.

When the foster mother leaves the room Teddy would start crying and looking for her.

He likes playing with musical toys and shows excitement when they make sounds. He also looks at and likes some of the TV commercials.

The foster mother feeds Teddy with a spoon and some improvement has been reported, as he is now eating solid food. Teddy loves bananas, biscuits with milk, homemade soups and sops.

Pablo

Boy, Age: 15
Country Code: LA-5
Primary Diagnosis: Congenital Heart Defect
Mental delays, speech developmental disorder, congenital cardiopathy – Ebstein anomaly or Horner syndrome (heart murmur)
Listed: Jan 2015
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
An echo-cardiogram and electrocardiogram performed showed ebstein anomaly (Horner Syndrome), moderated apical interventricular communication. He doesn’t require surgical treatment based on electrocardiogram results; he requires biannual follow up with both echo-cardiogram and electrocardiogram. It is possible that as an adult he will probably require tricuspid valve replacement.  Pablo doesn’t show signs of recent or past of physical abuse.
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