Ezekiel

Boy, Age: 2

Country Code: LA-2

Primary Diagnosis: Genetic Condition (non-DS), Global developmental delays

Listed: Apr 2026

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

Ezekiel was born to a teenage mother whose family faced socioeconomic struggles including overcrowding, poor housing conditions, and a lack of access to basic needs. While his biological mother and grandmother tried to care for him, they lacked the resources and knowledge to meet his specific needs. When Ezekiel was just two months old, health workers noticed he was receiving improper nutrition, such as being fed gelatin from a bottle, and he was taken into care.

Ezekiel primary diagnoses include a genetic condition called Mosaic 1q21.1q22 duplication syndrome, microcephaly, and congenital hypotonia. He also has vision conditions, including optic atrophy and right convergent strabismus (a turned eye). A significant part of Ezekiel’s daily care revolves around his feeding. He has an infantile feeding and swallowing disorder. Because he cannot safely tolerate solid foods, he requires a specialized liquid and purée diet. He needs to eat while sitting at a 90-degree angle, offering thick textures and liquids from a spoon to protect his airway. Despite these challenges, his nutritional status is currently stable. He maintains a healthy weight for his height. He takes a daily iron supplement and actively participates in physical, occupational, and speech therapies. He will need ongoing care from a team of specialists, including genetics, gastroenterology, neuropediatrics, and ophthalmology.

Because of his genetic condition and low muscle tone, Ezekiel experiences significant global developmental delays. Although he is 18 months old chronologically, his developmental milestones currently align with those of a 5- to 6-month-old infant. He requires constant supervision and full support for all daily activities. His motor skills are slowly progressing with the help of his physical therapies, but his hypotonia affects his ability to move independently. His communication is primarily non-verbal, relying on expressions and sounds to connect with his caregivers. With consistent therapy and a structured environment, Ezekiel continues to show steady, beautiful progress at his own pace.

Ezekiel has a remarkably calm, happy, and gentle temperament. In his current foster home, he has formed strong, secure emotional bonds. He finds true refuge, acceptance, and security in the presence of the people who care for him. He manages his emotions well when he feels safe. Ezekiel thrives on physical affection and gentle reassurance. He shows a wonderful sense of confidence and relaxation when his trusted caregivers are nearby. He is an exploratory and willing child who embraces the world around him as long as he feels emotionally supported.

Ezekiel is a delightful little boy who finds joy in the simple things. He loves discovering his own body and spends time happily playing with his hands and feet. He enjoys it when adults and other children play with him, and he loves hearing the familiar voices of his foster family. He is a big fan of animal sounds and enjoys watching colorful shows like Paw Patrol, La Granja de Zenón, and La Vaca Lola. He also loves listening to children’s music. Mornings are a special time for Ezekiel because he absolutely loves taking baths, followed by relaxing gentle massages. He also enjoys going out, looking through car windows, and visiting cool, air-conditioned places like the grocery store.

When it comes to his special diet, Ezekiel has a great appetite! His absolute favorite meals are smooth purées made from beans, spinach, or arracacha mixed with chicken. For a sweet treat, he loves natural fruit compotes made from mango, banana, and apple.

Ezekiel needs a family that can embrace his medical routine while celebrating his beautiful spirit.

Kevin

Boy, Age: 3

Country Code: EE-11

Region: Eastern Europe

Primary Diagnosis: Genetic Condition (non-DS), Global developmental delays, Microcephaly, Other Special Needs

Listed: Mar 2026

Kevin is 3 years old and he is in his first year of preschool at a public school. His integration into the school system has gone smoothly. He is a cheerful, calm, affectionate, and happy child.

Kevin has a global developmental delay; Prenatal microcephaly (cranial magnetic resonance imaging performed in September 2023);
Strabismus and decreased visual acuity – uses ocular prostheses and alternating occlusion

Genetic testing was performed. The results indicate that the child is heterozygous for the identified variants. This does not confirm, but also does not exclude, a possible diagnosis. Analysis of copy number variation (CNV) coverage data did not detect any large deletions or duplications that could explain the patient’s phenotype. A genetic consultation has been requested and is pending.

Dolly

Girl, born 2026

Country Code: EE-11

Region: Eastern Europe

Primary Diagnosis: Endocrine disorder, Genetic Condition (non-DS), Other Special Needs, Speech Delay

Dolly has Bardet-Biedl Syndrome, along with several other medical conditions, including: Bronchiolitis obliterans, Kidney disease, Tubulopathy with pseudohypoaldosteronism, Hyperparathyroidism and hyponatremia, Risk of developing diabetes; Strabismus, nystagmus, and myopia (corrected with glasses, which she wears); Moderate to severe AGDPM (non-verbal), with a functional level of approximately 12 to 15 months (GS-II); Global delay in psychomotor development; Bilateral post-axial polydactyly of the feet (six toes on each foot); Stage I arterial hypertension due to renovascular causes

Listed: Feb 2026

Available to Single Mothers

Dolly is a sweet and friendly girl. She enjoys spending time with her peers and especially likes one-on-one interactions with adults. She is usually in a good mood, and both the children and caregivers are very fond of her.

During the 2024/2025 school year, Dolly attended the 2nd grade. She is well integrated into the school environment and enjoys going to school. She receives support from special education teachers and also benefits from Speech Therapy, Occupational Therapy, and Physiotherapy.

She also has chewing difficulties and is non-verbal. However, she shows some understanding of simple messages, such as recognizing when someone is calling her or playing with her. She makes sounds and vocalizes when engaged or entertained.

Tiana

Girl, Age: 2

Country Code: EE-11

Region: Eastern Europe

Primary Diagnosis: Genetic Condition (non-DS)

Chromosome 22 Duplication Syndrome

Listed: Feb 2026

Available to Single Fathers, Available to Single Mothers

Tiana is a social, affectionate toddler who enjoys interacting with adults and responds well to familiar caregivers. While she is not yet using words to communicate, she understands simple directions such as “give” and “walk,” and communicates through gestures, pointing during play, and imitation.

A recent and exciting milestone is that Tiana has begun walking, showing growing independence, stability, and confidence. Motor development—especially locomotion—is one of her strongest areas and has allowed her to explore her environment and increase interaction with caregivers.

Tiana has a global developmental delay. At 19 months, her developmental skills were assessed at approximately a 13-month level. She shows progress across areas, with particular gains in mobility. She has a short attention span and prefers sensory-based play, especially activities involving sound and movement. She can be sensitive to noise and visual stimuli but is gradually becoming more tolerant of touch and motion.

She demonstrates oral sensory-seeking behaviors and has a high-arched palate, which may contribute to mouth breathing. Her eye-hand coordination is improving, and she can track and grasp objects, though her exploration remains limited.

Angelina

Girl, Age: 5

Region: Eastern Europe

Primary Diagnosis: Genetic Condition (non-DS)

Listed: Feb 2026

Available to Large Families, Available to Single Mothers

She has been diagnosed with a rare syndrome characterized by tall stature and congenital facial differences. While these differences may be noticeable, they do not define who she is.

Since being placed in a loving foster family, her story has already begun to change. She has shown accelerated growth, improved neuropsychological development, and her physical development is age-appropriate. She is in good general health and does not require ongoing medical treatment at this time, aside from her speech delay, related to her congenital anomalies.

But here’s the part that matters most: she is making real progress. She forms 3-word sentences, asks questions, uses polite expressions, initiates communication, and loves role-play and interaction. With consistent speech therapy, her potential continues to grow.

Brianna #

Girl, Age: 4

Region: Eastern Europe

Primary Diagnosis: Genetic Condition (non-DS), Global developmental delays

arthrogryposis multiplex congenita (AMC); polymalformative syndrome; congenital hip luxation; atopic dermatitis; significant delays in neuropsychological and physical development

Listed: Oct 2025

2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Mothers

Darling Brianna sometimes turns herself to a side position. She grabs toys with both hands and handles them. A smile is observed when interacting with an adult. She looks at herself in the mirror. She pronounces vowel sounds. She enjoys individual attention, and she gets upset if she is not paid attention to or if she is left alone in the crib after she has been paid attention to. She tries to initiate contact with her eyes and facial expressions, and she responds to her name.

The position of Brianna’s legs doesn’t allow her to sit and she doesn’t straighten her head, but sometimes she rotates her torso laterally to some extent. She reaches and grabs a toy handed to her by an adult or placed in her immediate environment and handles it briefly. She follows moving objects and people with a glance and a turn of the head.

Brianna is described as “absolutely adorable, easy to communicate with, and curious about new people and new toys.” Her caregiving staff says she is a calm and gentle child and is “everyone’s favorite in the house where she lives!” Please help us find Brianna’s family!

Rexx

Girl, Age: 15

Country Code: EE-11

Region: Eastern Europe

Primary Diagnosis: Epilepsy/ seizure disorder, Genetic Condition (non-DS)

Angelman syndrome, cortical dysplasia, microcephaly, epilepsy

Listed: Jan 2025

**** 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

Melissa

Girl, Age: 13

Country Code: LA-3

Region: Latin America

Primary Diagnosis: Genetic Condition (non-DS)

Cornelia de lange syndrome

Listed: Jul 2019

**** 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 Mothers

Sizable Grants $2,500+

Melissa is an extremely loving girl! She enjoys playing with her dolls. Although she likes all food, she loves chicken and rice.

Melissa has a diagnosis of Cornelia de Lange syndrome, which causes developmental delays. She continues to make progress with therapy.

Melissa was previously listed on Reece’s Rainbow as “Lucia.”

Dezi

Boy, Age: 7

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Epilepsy/ seizure disorder, Genetic Condition (non-DS)

severe mental delay, significant behavioral disorders, overall developmental delay, overall developmental disorder, epilepsy, Soto Syndrome

Listed: Oct 2024

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

Information in this report is from July 2024:

Dezi lived with his biological parents and older sibling until he was almost four years old. While his parents tried to take care of him, money was always lacking and ultimately, his parents knew they could not meet Dezi’s healthcare needs. In order for him to get all the help he needs and to have a better life, his parents relinquished him to protective care services in July 2022.

Due to the child´s medical diagnosis, he is not enrolled in school. There were two times were Dezi attended a special school, but his needs were much greater than what the teachers could manage. Dezi´s adjustment to a foster home was challenging but his current foster mother has done a great job with him. He has developed a strong bond with his foster mother and regulates his emotions in accordance with what she is doing or how close she is to him. He is now able to give and receive affection, which is a great achievement, and he even sometimes gets jealous when his foster mother pays attention to the other children. Dezi’s language is almost nonexistent, but he says a few words such as “ma.” He communicates mostly through facial gestures and by pointing at things he wants to grab or do. When Dezi gets upset, he cries and has “tantrums,” throws objects, and lays himself on the floor. Dezi is not comfortable being around people he is not familiar with. If he likes somebody, he will usually pull that person by the arm to start a game. Dezi likes to play with other children for short periods, and he is not aggressive towards them. He gets anxious when he is not familiar with an environment. He gets upset when he is not allowed to do something or eat at different moments throughout the day.

Dezi is very active, he changes from one activity to another in short periods, it is very hard for him to focus his attention on one specific thing. There are no concerns regarding his gross motor development, he is still working on his fine motor skills. He needs guidance and support to fulfill his daily routines though there are some activities that he can do on his own, such as eating with no help and dressing up. He sleeps throughout the night without any inconvenience. Dezi does not wear diapers during the day as he can go to the bathroom alone but needs help to clean himself up; he wears diapers during the night. He does not like animals.

Dezi’s favorite show is Paw Patrol. He gets happy when he gets new toys, especially cars even though toys do not usually last a long time because he plays roughly with them. He likes to wear clothes with Superman logos or drawings. Dezi has a good appetite and eats every kind of food. He likes to play with water.

Jana

Girl, Age: 8

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Cerebral palsy, Epilepsy/ seizure disorder, Genetic Condition (non-DS)

Edwards Syndrome (Trisomy 18 by translocation) and pulmonary dysplasia, fully dependent on oxygen. Epilepsy, gastroesophageal reflux without esophagitis, nausea and vomiting, urinary tract infection, gastrostomy, congenital malformation syndromes associated mainly with short stature, hypothyroidism, and spastic cerebral palsy.

Listed: Oct 2024

Available to Large Families, Available to Single Mothers

Information in this report is from March 2023 when Jana was 5. The adoption agency has medical records and pictures for Jana dating back to 2019.

Jana entered care at one year of age due to abandonment and negligence. Within her foster home, it is evident that Jana likes to interact with others. In her own special way, Jana is able to share and receive affection. She communicates with others through body language and eye movements. The foster mother has learned to read her body movements to identify if something is bothering her. Jana responds to stimuli generated through loud voices. Due to her medical diagnoses, she needs constant supervision and guidance to fulfill all her daily routines. Jana´s gross and fine motor development is delayed. Her cognitive development is severely damaged due to her medical diagnoses. She wears diapers all day. Jana spends her days seated in her wheelchair or laying down in her bed when she sleeps. She receives therapy and medication through her gastrostomy.

According to the foster mother, Jana loves to receive massages. She likes when people speak to her in a soft voice. Jana enjoys going outside for short periods.

Eleanor

Girl, Age: 11

Country Code: EE-11

Primary Diagnosis: Congenital Heart Defect, Genetic Condition (non-DS), Global developmental delays

heterozygous variant in the KAT6A gene. Heart issues, global developmental delay, severe language delay

Listed: Sep 2024

Available to Single Fathers, Available to Single Mothers

Eleanor is a beautiful young girl who needs a family.

Bianca #

Girl, Age: 4

Region: Eastern Europe

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

Syndrome of congenital anomalies with predominantly facial. Microphthalmi Abnormalities of the thoracic vertebrae. She is missing her left eye ball and right ear.

Listed: Jul 2024

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

Bianca was recently transferred from a large orphanage to a small group home. She’s been making developmental progress in her new home. She can pull to a stand in her crib and cruise along the rail. She will take steps when holding the hands of a caregiver. She reaches for toys and will hold and explore them.

Ben

Boy, Age: 7

Country Code: Asia.4

Region: Asia

Primary Diagnosis: Genetic Condition (non-DS)

Chromosome 2q deletion with developmental epileptic encephalopathy, and global developmental delay

Listed: Jun 2024

Available to Single Mothers

Ben is a determined and easy-going child despite his significant medical and developmental needs. He is described as having a gentle temperament and finds contentment in simple pleasures like listening to children’s songs, sleeping peacefully and engaging with his caregivers.

Ben has been diagnosed with Chromosome 2q deletion with developmental epileptic encephalopathy, and global developmental delay. His developmental age is estimated to be under 3 months. Ben also experiences visual impairment due to right eye congenital ptosis. While these conditions necessitate using a manual wheelchair and a gastrostomy feeding tube, they do not diminish his indomitable spirit. is a courageous fighter who has persistently strived for survival and shown constant improvement in his health. As of December 2023, he has successfully been weaned off oxygen therapy. Furthermore, the ward nurses report that Ben exhibits consistent progress in his motor development under the guidance of therapists. This highlights Ben’s progress in his development through appropriate stimulation. It is believed Ben will gain more opportunities to explore and develop his potential once he starts attending school. To learn more about Chromosome 2q deletion, here is one of many articles available online: GARD Rare Disease Information – Chromosome 2q deletion – National Organization for Rare Disorders (rarediseases.org)

With a loving, committed family who is open to acquiring the necessary medical knowledge, his care staff believes that Ben will receive the support he needs to continue flourishing. Ben’s gentle nature, resilience, and evident potential make him a truly special child deserving of a forever home filled with unconditional love. While some development is expected, Ben will need lifelong care from his loved ones.

A family with a home study for any country can submit for consideration of this child. If matched, the family would need to update their home study to this specific country.

Vincent #

Boy, Age: 5

Region: Eastern Europe

Primary Diagnosis: Blind / VI, Genetic Condition (non-DS)

Listed: Mar 2024

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!

Andy

Boy, Age: 13

Country Code: EE-11

Primary Diagnosis: Genetic Condition (non-DS)

Fragile X

Listed: Mar 2024

Available to Single Fathers, Available to Single Mothers

Andy was born with Fragile X Syndrome,and his needs were complex from the start. He was placed in residential care as a newborn.

He has been making progress in his current placement. He enjoys going to school and participating in music class. He may need assistance to focus during school.

Phineas

Boy, Age: 4

Country Code: EE-11

Primary Diagnosis: Craniofacial disorder, Deaf / HoH, Epilepsy/ seizure disorder, Genetic Condition (non-DS), Hydrocephalus

Polymalformative syndrome, with craniofacial dysmorphia; suspicion of Goldenhar Syndrome; Hydrocephaly; upper airway malformation with tracheostomy since 10/4/2021. Currently with cannula. Epilepsy. Gastrostomy. Sensory-neuro deafness – uses hearing aids.

Listed: Mar 2024

Available to Single Fathers, Available to Single Mothers

Phineas was previously listed as Phil — he is a sweet boy who was born with a polymalformative syndrome. His condition comes with needs that set him apart, and he was placed in care early on.

Phineas uses a wheelchair in his daily life. He also spends time in a standing frame. He enjoys smiling at people and laughing. Phineas enjoys sensory experiences with tactile or auditory input. He enjoys listening to a maraca or touching a soft stuffed animal.

Elise #

Girl, Age: 7

Region: Eastern Europe

Primary Diagnosis: Genetic Condition (non-DS)

Cornelia de Lange syndrome,

Listed: Feb 2024

2025 MACC, Available to Large Families, Available to Single Mothers

Elise arrived with a unique constellation of traits known as Cornelia de Lange syndrome, primarily affecting her facial features. She’s a delicate soul with a sweet disposition, and her gentle nature is simply heartwarming.

This precious little one thrives on affection — she has an incredible capacity for love and blossoms with nurturing care that includes endless cuddles, tender personal interaction, and thoughtful understanding. She merits a patient touch and activities tailored just for her, which will provide not only pleasure but also enriching experiences.

During our time together, Elise remained serene and composed, displaying a quiet passivity. My playful attempts to tickle and engage her elicited limited response initially, but as patience persevered, her awareness and interaction gradually emerged.

Elise’s life would be beautifully complimented by a loving family atmosphere, filled with unwavering support and encouragement. A home that teems with warmth and offers plentiful one-on-one interaction, a trove of stimulating activities, and specialist involvement, would cultivate her growth and happiness.

To the kind-hearted families contemplating the rewarding path of adoption: envision a life with Elise, where every day is an opportunity to nourish and celebrate a precious child’s potential, and where love knows no bounds.

Nolan

Boy, Age: 9

Country Code: SE.Asia.Pac

Region: Asia

Primary Diagnosis: Deaf / HoH, Genetic Condition (non-DS)

mild hearing loss in left ear; moderate hearing loss in right ear; Global developmental delays- fed with PEG tube; Multiple congenital anomalies- Kleefstra syndrome is to be considered

Listed: Jun 2023

Available to Single Mothers

SEPTEMBER 2023 UPDATE:

Nolan can walk by himself. He enjoys walking around the center, engaging everyone, or just checking out what is happening around him. He enjoys morning and afternoon walks with his caregivers. He loves to look at himself in front of the mirror. He dances when he wants what he is watching while on the sofa. His caregivers assist and let him practice going up and down the stairs. There are times he prefers to be carried and hugged. He enjoys closeness and physical touch. He is sociable and plays on the trampoline with other children. Nolan pays attention to social stimulation and imitates some actions. He is currently attending occupational and speech therapies, which has greatly helped him improve his skills. He can now hold toys and put blocks on top of one another. Nolan likes everyone in the center and loves it when visitors come around. He does not display stranger anxiety. He still does not use words, but shows his excitement by laughing and shouting “ha ha ha” in a loud exaggerated voice similar to how Santa would say “Ho ho ho.” Nolan eats solid foods such as rice, meat, and vegetables that are cut into small pieces. He likes biscuits, yakult, plain bread, and yogurt as snacks. Nolan is becoming better at expressing what he wants. He points out stuff and says, “ah ah ah” when he wants to hold something. He is cooperative with his houseparents and caregivers during his morning and evening care routine when taking a bath and getting dressed. Nolan is loved by everyone at the child caring agency, but they are praying that he will be placed in a permanent family. He has a lot of unique needs that will require special attention, financial resources, good medical specialists, and commitment of parents. He might have delays in development, but having the presence of a loving family will be of great benefit to him in reaching his full potential. He shows signs of being able to learn and improve with dedicated staff taking one-on-one time with him each day. Nolan’s agency believes that he will bring so much joy to a family and he will teach them how to love deeply.

—————————————————————————

Nolan was found to have multiple congenital anomalies. Kleefstra Syndrome is to be considered. He was diagnosed as having global developmental delays and has mild hearing loss of the left ear and moderate hearing loss of the right ear. Nolan is being fed through a Percutaneous Endoscopic Gastrostomy (PEG) tube. However, his caregiver sometimes tries to feed him orally with infant cereal or yogurt, which he enjoys. Nolan is undergoing physical therapy and can pull himself up by holding the rails of his crib. He can sit by himself in his crib for a maximum of 30 minutes. He can stand with support and can move his legs freely. Nolan can walk approximately 100 steps with assistance. He can stretch his arms and hands to reach toys or any object near his crib. He loves playing with toys, such as rattles, that produce sound. Nolan responds when his name is called, and he can convey his needs through different tones when he cries or babbles. Nolan smiles, laughs, and babbles when talked to. He loves to be cuddled and played with! Despite his medical needs, Nolan is not demanding and is easy to care for.

A traveling family that met Nolan said, “We’ve met this child and he is the BEST cuddler! He hardly ever cries and loves to walk while holding your hands. He laughs hard when you talk loudly into his ear, and he loves cartoons that sing! We were with him for a whole summer and would be happy to share more info and pictures!”

We hope just the right family comes forward for Nolan!

Miriam

Girl, Age: 7

Country Code: SE.Asia.Pac

Region: Asia

Primary Diagnosis: Genetic Condition (non-DS), Global developmental delays

Moderate to severe global developmental delay; Noonan Syndrome

Listed: Mar 2023

Available to Single Mothers

Miriam came into care at six months of age. She was very small and had poor sucking reflex. At the age of 16 months, her skills were at about the 11-month mark. She is listed as having global developmental delay in the moderate to severe range. In April of 2022, Miriam walked without any assistance from anyone for the first time. Everyone was thrilled! Despite her delays, Miriam shows remarkable improvements daily. She is becoming active and physically strong. She is emotionally attached to the staff and relates well to all the house parents and caregivers. Miriam plays and interacts with some of the children. She is sweet and lovely. Her smile makes her even more adorable. The whole team is very fond of her. Miriam needs a family that would wholeheartedly accept her condition and one who is willing to walk her through the struggles and challenges of Noonan Syndrome. The family must be willing to seek the professional help she will need as she grows. Contact the agency to learn more about Miriam!

Mina

Girl, Age: 9

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Arthrogryposis, Genetic Condition (non-DS)

Developmental delays/malnutrition; Arthrogryposis; Osteogenesis Imperfecta; Bilateral club feet; Congenital Glaucoma

Listed: Mar 2023

24 for 2024, Available to Large Families, Available to Single Mothers

Sizable Grants $2,500+

Mina is a beautiful little girl who likes to paint and play “sleepover” with her friends. Mina likes to go to the park and put together puzzles. She also loves to sing and listen to music of all genres, especially tango. Mina enjoys children’s stories and watching her favorite cartoons, which include Masha and the Bear, Puss in Boots, and Blue Shortcuts. Contact the agency to learn more about Mina and her listed medical needs!

The agency staff met lovely Mina in August 2024. She was very talkative and outgoing. She doesn’t allow her special needs to limit her. Mina, born in November of 2016, knows how to start and maintain a conversation. She is very observant and knows how to ask questions and engage in it and the context. She uses very sophisticated words for a seven year old – it was impressive!! She knows how to count in English from one to ten, knows some colors in English, and knows the colors in Spanish. She has a great memory and can remember facts. Mina can easily express her thoughts and ideas.

Mina likes to paint and play “sleepovers” with her friends. Mina likes to go to the park, put together puzzles. She also loves to sing, listen to music of all genres, especially tango. Mina enjoys children’s stories and watching her favorite cartoons (Masha and the Bear, Puss in Boots, Blue Shortcuts).

VIDEOS:
https://vimeo.com/maaspecialkids/maa-mina
https://vimeo.com/maaspecialkids/maa-mina2
https://vimeo.com/maaspecialkids/maa-mina3
https://vimeo.com/maaspecialkids/maa-mina4
https://vimeo.com/maaspecialkids/maa-mina5
https://vimeo.com/maaspecialkids/maa-mina6
https://vimeo.com/maaspecialkids/maa-mina7
https://vimeo.com/maaspecialkids/maa-mina8
https://vimeo.com/maaspecialkids/maa-mina9
Password: Adoptmaa

Mina also has a $500 agency fee reduction, with a specific adoption agency.

Darla

Girl, Age: 12

Country Code: EE-6

Region: Eastern Europe

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

Crouzon Syndrome; Delayed development

Listed: Jun 2022

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

Available to Single Mothers

Clifton #

Boy, Age: 14

Region: Eastern Europe

Primary Diagnosis: Genetic Condition (non-DS), Other Special Needs

Born with positive Wassermann test result; he underwent treatment with Penicillin; ectopic left kidney; convergent concomitant strabismus; hypermetropia (long-sightedness); dolichocephaly; Arnold-Chiari syndrome, type I; irritable bowel syndrome without diarrhea; secondary lactase deficiency; food allergy – slight intolerance to foods containing gluten, dairy products and eggs;delayed physical development; generalized developmental disorder; moderate mental delay

specific disorders of motor function development, Moderate mental delay, ectopic left kidney, strabismus

Listed: Mar 2017

**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

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

Clifton lives with a foster family. He loves to listen to music and dance and is always looking for a dancing partner! His foster family is working on him walking longer distances independently. He is learning how to play with toys and interact appropriately with other children. He has few words and does not follow verbal directions. Clifton is receiving therapy multiple times a week.

Clifton’s gross motor skills are well-developed – he moves around independently, even at long distances, and he has no difficulties walking on different surfaces. He can now run (since the beginning of January 2017). The deficits noted previously in Clifton’s fine motor skills have been compensated to a great extent. He can transfer small elements with a spoon from one bowl into another with an adult’s assistance, he plays with certain materials and toys, he clips and unclips clothes pegs, he looks for an object hidden in the sand and he takes it out with great interest. He holds a pencil and leaves pale traces with it on a sheet of paper. He does great eating with a spoon. Clifton accepts the toothbrush and allows for his teeth to be brushed.

It happens more and more rarely for Clifton to demonstrate anxiety in response to being introduced to unfamiliar places and people. The stereotypic movements he demonstrates when someone initiates interactions with him have decreased significantly. He imitates actions he has observed more often and more successfully than before. Clifton becomes lively and starts dancing whenever someone is singing or plays music.

Clifton is calm in his new foster family, he often smiles and he laughs aloud while playing with an adult (or with the girls in the foster family). He is especially attached to the foster father and the younger daughter in the family. Clifton has become a lot more sociable in the last 6 months: he seeks children’s attention, initiates interactions, accepts unfamiliar people a lot easier, maintains a smaller distance between himself and others and makes eye contact.

Although Clifton has poor passive vocabulary, he follows simple instructions provided that those are accompanied by nonverbal means of communication. His speech development is at the level of producing chains of syllables. He uses “No” appropriately so as to express his disagreement, he sometimes uses “Yes” and “Give me”. Clifton initiates physical and emotional contact with his foster parents and their children as well as with the specialists working with him. He is especially attached to the foster father and the youngest daughter in the foster family. His interactions with other children have changed significantly – he plays with them for a long time and he is making attempts to cooperate with them.

More photos/file are available from his agency

Connor #

Boy, Age: 14

Region: Eastern Europe

Primary Diagnosis: Genetic Condition (non-DS)

Listed: Sep 2015

**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

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

Severely impaired condition, polymalformative syndrome: Dandy-Walker syndrome, epilepsy, congenital hydrocephalus-ventriculoperitoneal shunt installed, dysfunction of the valve with a neuroinfection and a surgical treatment and revision of the valve system in the spring of 2015; anal atresia, sigmostoma and sagittal proctoplasty; mylticystic right kidney, kidney dysplasia, pyelectasis and hypertrophy of the left kidney, severe mental delay.

Connor is being raised in one of the biggest orphanages in Bulgaria where children often suffer from severe malnutrition, muscle hypotrophy and have severe delays in the neuropsychological development. He has a polymalformative syndrome, but one could see a dramatic change in his appearance in just two pictures- the first one taken in the end of November 2014 and the second one in June 2015.

He grabs a toy that is handed to him, holds it for a while and manipulates with it. He has started to more and more often reach with his hands and manipulate with hanging toys independently.

While involved in active interactions with adults, he would make his emotional responses known with his nonverbal behavior. He seeks contact with familiar adults by reaching out his hand, grabbing an adult’s hand and he would even sometimes direct an adult’s hand towards his face so as to be caressed.

He falls asleep easily and his sleep is calm. He is fed with a bottle. He gets anxious while his clothes are changed and while bathed.

Ozzie #

Boy, Age: 12

Region: Eastern Europe

Primary Diagnosis: Genetic Condition (non-DS)

Coffin-Lowry Syndrome

Listed: Mar 2021

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

Ozzie has decreased muscle tone. He can’t walk, but has recently started standing up in his crib with support. He smiles and has positive emotions when interacting with adults and when he is with the other children. He pronounces combinations of sounds. He laughs when playing peek-a-boo.

*There is an older child that is believed to be Ozzie’s older brother. However, they are NOT listed as needing to be adopted together. The other child is listed as Ollie.

Ollie #

Boy, Age: 14

Region: Eastern Europe

Primary Diagnosis: Genetic Condition (non-DS)

Coffin-Lowry Syndrome

Listed: Dec 2018

**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

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

Ollie is now living in foster care. He is physically well developed. He has good coordination of his hands and feet. He walks without falling, and can run as well. Climbs up and goes down by the stairs when holding an adult or the railing. He can play with cubes by putting them and taking them out of a cup, but has some problems manipulating with smaller objects. He cannot eat and dress by himself yet, but does make attempts. He understood almost everything and fulfils small tasks. He likes playing hide and seek. He hides behind the door and when he is found, he laughs and stomps his feet. He is interested in musical cartoons and copies the movements of the actors.

*There is a younger child that is believed to be Ollie’s younger brother. However, they are NOT listed as needing to be adopted together. The other child is listed as Ozzie.

Molly May #

Girl, Age: 10

Region: Eastern Europe

Primary Diagnosis: Genetic Condition (non-DS)

Trisomy 7; cleft lip & palate; Cerebral Palsy

Listed: May 2019

2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Mothers

Sizable Grants $5,000+

Molly May has made progress in her development during recent months. She is able to sit unassisted, get up on her knees and has begun to start trying to move around in a walker. She is becoming more physically active. She makes eye contact, looks around for families adults and smiles when someone looks at her. She will laugh out loud when an adult plays with her. She watches children’s cartoons and movies on the TV and will get excited and point to the screen when the TV is turned on. She picks up toys and attempts to play with them. She still needs instructions in how to appropriately play with toys. She makes vocalizations in an effort to communicate. She eats soft foods from a spoon.

Molly May has undergone multiple surgeries to repair her cleft lip & palate. She is under the continued care of the doctor who is performing these procedures. She is also under the regular care of a neurologist, who diagnosed her with CP in 2018. She had suffered from “constant shaking” resulting in uncontrollable movements up until a few months ago. The social worker reports that this has greatly improved and that Molly May’s movement are now more calm and she also sleeps calmly too. Videos taken in April 2019 show her interacting with toys.

Photos and videos are available through the agency.

Josiah #

Boy, Age: 10

Region: Eastern Europe

Primary Diagnosis: Genetic Condition (non-DS)

genetic metabolic disease – pyruvate-kinase deficiency – homozygote mutation p-R 446; mild to moderate core and periventricular lesions; generalized muscle hypotonia; severely delayed physical and neuro-psychological development;

Listed: Oct 2018

2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

Josiah moves in space by turning from back to belly and vice versa. He has started forming some of the perceptions about objects from his constant surroundings and everyday life. He connects some objects from his surroundings with the actions performed with them.

When awake, Josiah is mostly calm. He would laugh out loud when jested. During active interactions with adults Josiah pronounces various sounds and random syllables. Josiah follows a specific dietary regime and has food individually prepared for him. He is fed with a spoon by an adult and has a picky appetite. He is calm during dressing and bathing. Josiah’s sleep is calm.

Ezekiel

Kevin

Dolly

Tiana

Angelina

Brianna #

Rexx

Melissa

Dezi

Jana

Eleanor

Bianca #

Ben

Vincent #

Andy

Phineas

Elise #

Nolan

Miriam

Mina

Darla

Clifton #

Connor #

Ozzie #

Ollie #

Molly May #

Josiah #

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