Anna

Girl, Age: 12
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Autism, Speech Delay
autism, language and speech developmental delay, moderate mental developmental delay, expressive language disorder.
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 Mothers
Anna, now 10 years old, entered the Protection Services for the first time when she was a newborn baby as her mother used drugs while pregnant. She lived with her grandmother for a while, but reentered care at 13 months old.

Anna is known for being a happy girl. Anna is not enrolled in school as it has been difficult to find an Institution that can work with her diagnosis and special needs. However, when she was enrolled in school, it was noted that she behaved positively and recognized authority figures. Anna loves to give and receive affection, and she does not get jealous when her foster mother pays attention to other children. Her closest bond is with the 12-year-old daughter of her foster mother. She needs support and supervision to fulfill her daily routines. Anna has a good sleep and eating patterns; however, she very occasionally wets the bed. Anna sometimes throws objects to the floor when she feels frustrated. She can follow simple instructions. Due to her diagnosis, it is hard for her to stay focused on one specific task.

Anna can keep her balance and walk, and she tries to jump but is not fully able to do it. She can run slowly and up the stairs if an adult holds her hand. Her fine motor skills are still developing. Anna is not able to hold scissors, but she can grab pencils and color. She needs help with dressing and hygiene. For the most part, Anna communicates through signs and very short words; it is not hard to understand what she wants. She goes to speech therapy. Anna recognizes familiar faces, and she does not get shy when meeting new people. She can play with younger children or with peers, but she gets upset when other children take her belongings. She recognizes her foster mother as an authority figure. She likes dogs as long as they are away from her, and she gets nervous when pets are near her.

Being told she looks pretty or that she is beautiful makes Anna happy. She loves to have her hair done in pretty styles and enjoys wearing new clothes. She likes to watch children’s movies and videos of people doing exercises. She is very good at swimming. Anna´s favorite foods are spaghetti and chicken with rice. She loves to listen to music and do puzzles.

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.

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
$769.00
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 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.

Dawn and Donna #

Sibling Group
Ages: 6, 6
Region: Eastern Europe
Primary Diagnosis: Blind / VI, Cerebral palsy, Global developmental delays, Hydrocephalus
Listed: Jul 2024
$1,642.00
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 Mothers
Dawn & Donna are  twin girls who were born in Ukraine at 29 weeks gestation. They lived in an orphanage in Ukraine until they were 1.5 years old, at which time they were moved to an orphanage in Bulgaria. They were then moved to a different placement in Bulgaria at age 3, where they still reside.

 

Donna’s medical diagnosis includes: Retinopathy of prematurity (ROP) stage 5, post vitrectomy condition bilaterally; secondary glaucoma. Left eye ROP stage4 Nystagmus. Delayed neuro-psychic development. Condition after low birth weight. Self-aggression. Spastic quadriparesis. Iron deficiency anaemia

 

Dawn was born first. Her medical diagnosis includes: cerebral palsy – spastic quadriparesis. Spastic quadriparesis. Suspected hydrocephalus with normal pressure and hypoplasia of corpus callosum. Grade 1 hypotrophy. Convergent strabismus; hypermetropia. Condition following very low birth weight.

 

Update July 2024: After their placement into the foster home on May 14, 2024, the girls have adjusted well and made noticeable developmental progress. They show an attachment to the foster mom and follow her instructions. One of the girls can now walk independently and is well oriented in the foster home. The other girl sits with little support. The girls now eat mashed food from a fork or spoon and chew well. They have learned to speak their first meaningful words and are also observed to repeat syllables. While there’s some jealousy between the sisters when it comes to receiving attention, they are emotionally close and hug/hold hands. Videos from July 2024 show one girl as tenacious in exploring her environment and the other as joyful when playing on the floor. The girls attend therapy twice a week and their foster mom is proactive in seeking additional services for them. They like music and singing and enjoy massage from the foster mom. They are thrilled to be playing in the inflatable pool in the backyard. Their foster mom describes them as positive children who will continue to make progress with the right interventions and lots of love.

From a family who met them in 2023

I met these twins when I visited my daughter for trip one in 10/2023. One twin was active and was able to stand holding on and cruise around her crib. She was able to climb right out of her floor crib and back in herself. It was an activity for her and she did it with great ease. She wasn’t trying to escape at any point and would just flip In and out over and over again. She seemed like what you would expect for a toddler. She stopped what she was doing when someone called her name and turned in the direction of their voice. The other sweet twin was always laying down when I saw her. Sometimes in a crib, sometimes in a seat. My daughter asked for “baby” all the time and they would put this twin in her crib with her to lay together. They said she was more “severe”. She definitely seemed more infantile. They were in a really great place where they got plenty of food and were carried around a lot by the staff there. There were 8 kids on that floor in four rooms. The twins shared a room. I believe they are now in a foster situation. They def were pretty easygoing. They had a lot of musical toys which they seemed to like. The active twin kept herself busy a lot but the quiet twin seemed to love cuddling and other kids being around her. I think some of the delays they have may be related to vision impairments. I would imagine they would do well with siblings.

Esta, Sophie and Luke

Sibling Group
Ages: 13, 7, 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.

Tiana and Tenaya

Sibling Group
Ages: 11, 15
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Other Special Needs
Tenaya: Leukemia Lymphoid Acute- diagnosed at the age of 4 years
Listed: Jun 2024
Available to Large Families, Available to Single Mothers, Siblings

Tiana and Tenaya are loving sisters who look forward to a permanent and loving home of their own, with parents who will support them. Tenaya, born October of 2010, is a lovely girl who enjoys spending time with her sister and friends. She is affectionate with those people she feels close to and loves. She tends to be more introverted. Tenaya shows respect to her caretakers and peers. Tiana’s favorite activities include jumping, dancing, singing, and playing with her sister and her friends. She also likes to go for walks and listen to music. She adheres to change without difficulty and accepts the home rules. Tiana, born October 2014, is described as a cheerful and quiet girl. She has good social skills, which allow her to interact with adults and her peers. She likes to participate in active games, especially those that include running. She also likes to play board, such as dominoes, at the local park.

VIDEOS:

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

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

Password: Adoptmaa

There is a $500 agency fee reduction for Tiana and Tenaya’s adoption, with a specific grant agency. Additional agency fee reductions may be available based on the adoptive family’s circumstances.

Ben

Boy, Age: 8
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
$27.00
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 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.

Hailey

Girl, Age: 15
Country Code: Asia.4
Region: Asia
Primary Diagnosis: Older Child
Listed: Jun 2024
**** 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 Single Mothers
Hailey is a 13 year old girl in Asia. She is reported to have good overall development with normal physical and motor development. While her vision has been listed as normal as of July 2022, she had some prior surgeries for visual issues and it is suggested she wear glasses due to myopia. 

Hailey is able to communicate easily and freely. She is described as outgoing, expressive and a frank teenager with a kind heart. She loves to share her thoughts and feelings to those around her. She seems to be a sensitive soul as her emotions are quite easy to read on her face and admonishing her in public, she becomes defensive or cries, but when spoken to in private she responds much more positively to constructive criticism. 

In December 2023, Hailey allegedly had a suicide attempt after breaking up with her boyfriend. She was hospitalized for a few days, but was not prescribed any medication. She also was reported to be smoking, which she admitted to as a way of calming her mood, but she has responded very positively to the staff’s positive reinforcement means of handling this situation. 

As with most teenagers these days, Hailey enjoys dancing, making dance videos with classmates, and watching videos on YouTube or  TikTok. She is on the basketball team at school and also enjoys playing volleyball. She expresses admiration of her geography, computer and Chinese history teachers.  Her social worker says “her smiles and laughter are contagious and powerful.” She enjoys the Korean Pop Culture music. 

Due to the process in her country and her age, a family wishing to adopt her will need to work quickly to complete paperwork if the foreign agency in charge of their adoption chooses the family for the child.

Nick

Boy, Age: 11
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Congenital Heart Defect, Deaf / HoH, Epilepsy/ seizure disorder, Other Special Needs
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!
Inquire About This Child
Available to Large Families, Available to Single Mothers

 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!

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.

Alice #

Girl, Age: 15
Region: Eastern Europe
Primary Diagnosis: Cerebral palsy
Listed: May 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 Mothers
She resides with a foster family. She has ataxic cerebral palsy. She walks with slight unsteadiness. She attends a regular school with special education support services. She needs monitoring by a child neurologist and psychiatrist, motor rehabilitation, sessions with a psychologist and speech therapist, as well as special care and supervision by an adult in all social situations. She is friendly and initiates communication and contact with peers and adults, but often misunderstands intent or meaning and takes offense. She can easily be distracted, becoming fixated on an idea or object. Her emotional and social immaturity can put her at risk in social settings. She needs a predictable, safe and secure environment.

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.

Nany #

Girl, Age: 4
Region: Eastern Europe
Primary Diagnosis: Blind / VI, Cerebral palsy
Nany has retinopathy of her left eye, cerebral leukomalacia with manifestation of spastic quadriparesis, bronchopulmonary dysplasia and asthma.
Listed: Apr 2024
$2,432.20
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!
Inquire About This Child
2025 MACC, 25 for 2025, Available to Large Families, Available to Older Parents, Available to Single Mothers
Nany was born with an extremely low weight and a complicated neonatal period. She has retinopathy of her left eye, cerebral leukomalacia with manifestation of spastic quadriparesis, bronchopulmonary dysplasia and asthma. This sweetie needs a very special family.

The agency staff member who met her during March of 2024, says the following: Nany likes music, and it seems to settle her down. She also likes being in the swing. At times she turned to various sounds. She can lift her head slightly while lying on her stomach. Nany is an extremely fragile, sweet and lovable little girl who needs lots of love, attention, understanding, support and lots of cuddles. Given the serious diagnoses, working with additional specialists definitely would ease and help the child’s condition. Nany is in need of a very prepared and supportive family.

Nany’s current adoption agency has grant funding is available for qualifying families.

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.

Elise #

Girl, Age: 7
Region: Eastern Europe
Primary Diagnosis: Genetic Condition (non-DS)
Cornelia de Lange syndrome,
Listed: Feb 2024
$1,027.00
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 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.

Daniel & Alexis

Sibling Group
Ages: 13, 11
Country Code: LA-5
Region: Latin America
Primary Diagnosis: ADHD, Skin Condition
$40.50
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 Single Mothers, Siblings
Daniel is described as fun and easy physically and mentally. He enjoys activities such as reading, drawing, making crafts and anything related to movies or horror characters. He was diagnosed with ADHD in 2021 and is being treated with medication. Daniel is a calm child who behaves with kindness when situations turn out the way he wants. He can be irritable when they don’t. He is 4th grade and shows good social skills with his classmates. He requires adult support to understand the importance of following rules since his ADHD diagnosis can make it difficult to manage impulsivity and anticipation of consequences of their actions.

Alexis is a happy, playful girl with a lot of charisma. She quickly gains the affection of those around her. She likes to make jokes and her energy level can lead to difficulty regulating her emotions. Alexis is bold, outgoing and social. She likes to give and receive affection such as hugs and kisses and demands attention of adults. She has managed to adapt socially and behaviorally to school and demonstrates autonomy, security and enthusiasm when participating in routines and activities. She is in 3rd grade and is kind to peers and adults. She is being treated for atopic dermatitis and asthma.

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).

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.

Natasha

Girl, Age: 6
Country Code: LA-4: Due to the in-country crisis, government offices and courts that process adoptions may be closed or delayed.
Region: Latin America
Primary Diagnosis: Cerebral palsy, Epilepsy/ seizure disorder
Cerebral Palsy, Epilepsy
Listed: Jan 2024
$4,277.00
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
24 for 2024, Available to Single Mothers
Sizable Grants $2,500+
Natasha is a pretty little girl, with very calm with big eyes and beautiful white teeth. She is very special. She doesn’t smile at everyone. She must first know you, and trust you, but her smile is fascinating. She loves to drink juice and she likes to eat sweets. She really likes music. She likes to be pampered by her foster family and only cries if she needs a little attention.

In therapy, she works on ways to improve her functional mobility, and increase the functional use of her arms. At school, she does a lot of sensory activities to work on ways to respond and communicate better and fixate her eyes on objects to learn.

Serene

Girl, Age: 12
Country Code: SE.Asia.Pac
Region: Asia
Primary Diagnosis: Cerebral palsy, Global developmental delays
Cerebral Palsy (spastic quadriplegic type) with scoliosis, wasting, and profound Intellectual Disorder.

She has regular evaluation with a developmental pediatrician and regular check-ups with pediatric neurologist, ped gastro enterologist and nutrition specialist. She regularly attends physical and occupational therapy once a week and homebased therapy is continuously being provided by the houseparent as per instruction from the therapist.

Listed: Jan 2024
$1,047.00
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 Mothers
Serene is a beautiful girl with a contagious smile, born in June of 2014 with cerebral palsy (spastic quadriplegic) and scoliosis. She is listed as having cognitive delays as well. Serene has regular evaluations with a developmental pediatrician and regular check-ups with her pediatric neurologist, gastro enterologist, and nutrition specialist. She regularly attends physical and occupational therapy once a week and receives continuous home-based therapy by her houseparent, as per instruction from the therapist. Serene smiles when somebody plays or talks with her. She laughs while watching other children play. She cries when wet, in an uncomfortable position, and when she hears thunder. Serene enjoys watching cartoon shows and listening to nursery rhymes. Serene is fully dependent on the care of her houseparent since her development is limited. She can put her head up, but she is unable to sustain it for longer period of time. She can sit up straight but tends to tilt forward. Serene cannot pull herself to sitting. She reaches her hand out to get the block or object, but she might swipe the block off the table. She can hold objects or blocks using her right hand. Serene can open her hands, but her left wrist is flexed. She can raise both hands slowly. She can hold biscuits and slowly puts it in her mouth. Serene can place both feet on the floor and make steps while the houseparent or therapist holds her body, though her legs are crossed. Serene’s care center hopes for her to be placed in a family who will unconditionally love her, despite of her health condition, and one who has enough resources to sustain her therapy and medical needs.

There is a $500 agency fee reduction for Serene’s adoption with the listing adoption agency. Additional agency fees may be available with that agency, based on the adoptive family’s circumstances.

Serene needs a family with an approved home study to be able to adopt her.

Goliath

Boy, Age: 7
Country Code: LA-4: Due to the in-country crisis, government offices and courts that process adoptions may be closed or delayed.
Region: Latin America
Primary Diagnosis: Blind / VI, Cerebral palsy, Epilepsy/ seizure disorder
Microcephaly, CP, epilepsy, blind
Listed: Dec 2023
$5,086.14
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 Single Mothers
Sizable Grants $5,000+
Goliath is the cutest, most chill baby ever! He loves cuddles, being bounced on the trampoline, swimming, going for bike rides, being held, and chocolate. He would do great either in a big family with lots of siblings or being the only one to soak up all the attention!

He is a great eater with either blended or soft foods, but not great at drinking liquids. He has a lot of small seizures throughout the day, but is on the max amount of seizure medication that can be found consistently in his country.

In school and therapy he does a lot of sensory activities and is working on using his arms for purposeful movement. He has a stander that he likes to use while playing his toy piano. He doesn’t have an advanced way to communicate yet as he is blind and doesn’t have much purposeful movement but he does let us know when he is happy, mad, or would like something. He mostly only gets fussy sometimes at night time when he wants to be rocked to sleep, when he has to take baths, or when he thinks his food is too spicy.

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)

Mariah

Girl, Age: 13
Country Code: LA-2
Region: Latin America
Primary Diagnosis: ADHD, Other Special Needs, Sensitive Special Need
Cognitive delay; Bipolar disorder; ADHD
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 Mothers
Mariah enjoys activities such as drawing, coloring, and painting. Her favorite activity is to make cards for her caretakers. At the time of her referral, she was learning to write. Mariah is a social, affectionate, and talkative girl who loves playing with her friends. They like to play dolls, hair, and play with dresses. Mariah likes stuffed animals, dolls, mermaids, unicorns, and dinosaurs. Her favorite colors are pink and green. She likes animals, especially chickens, dogs, cats, horses, cockroaches, and mice. She likes clothes, such as dresses and cute shoes. She loves running, dancing, drawing, swimming, acting, and watching SpongeBob. Mariah loves princesses, especially Ana and Elsa from Frozen. She is afraid of snakes, thunder, and darkness. When she grows up, Mariah would like to be a cook. We hope a loving family will see Mariah and all her potential. The adoption agency has additional information about her history to share.

VIDEO: https://vimeo.com/maaspecialkids/maa-mariah1
Password: Adoptmaa

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

Mariah needs a family with an approved home study to be able to move forward with adopting her.

Mae

Girl, Age: 4
Country Code: LA-2
Region: Latin America
Primary Diagnosis: Cerebral palsy
Cerebral Palsy; Significant neurodevelopmental delay, but showing significant progress; Recurrent broncho-obstructive symptoms; Fed by gastrostomy; Receiving comprehensive therapies
Listed: Dec 2023
$1,270.00
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 Mothers
Mae is a precious little girl, born in September of 2021.  Agency staff met Mae in August of 2023. She is an adorable little girl! We’ve been told she is doing well in her current care center since our staff visited her. Mae is described as a sweet, affectionate, and cheerful young girl. She is always smiling! Mae has managed to adapt to the routines around her required special care. She has made great progress since entering her care center, and she learns quickly through repetition She is a girl who likes to move forward and shows interest in learning new things. It is evident that she manages to bond with her caregivers. Contact us to learn more about Mae and her listed medical needs from her placing agency!

NEW VIDEO:

https://vimeo.com/maaspecialkids/maa-mae20

 

Update: 10/24

Mae is a precious little girl, born in September of 2021.  Our staff met Mae in August of 2023 and again in October of 2024. She is an adorable little girl!  We’ve been told she is doing well in her current care center since our staff visited her. Mae is described as a sweet, affectionate, and cheerful young girl. She is always smiling! Mae has managed to adapt to the routines around her required special care. She has made great progress since entering her care center, and she learns quickly through repetition She is a girl who likes to move forward and shows interest in learning new things. It is evident that she manages to bond with her caregivers. Contact us to learn more about Mae and her listed medical needs!
NEW VIDEOS:

https://vimeo.com/maaspecialkids/maa-mae21

https://vimeo.com/maaspecialkids/maa-mae22

https://vimeo.com/maaspecialkids/maa-mae23

https://vimeo.com/maaspecialkids/maa-mae24

https://vimeo.com/maaspecialkids/maa-mae25

https://vimeo.com/maaspecialkids/maa-mae026

Password:  Adoptmaa

Password: Adoptmaa

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.

Gustav

Boy, Age: 10
Country Code: EE-4
Region: Eastern Europe
Primary Diagnosis: Limb differences
congenital malformation, lumbar spinal disc herniation, ventriculoperitoneal shunting; dysfunction of the pelvic organs; deformity of the left leg 
Listed: Dec 2023
$630.00
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 Mothers
Gustav is in need of an surgery on his legs that will allow him to walk independently. His mental and speech development is almost age-appropriate and he loves playing with toys and other children.

Anne #

Girl, Age: 4
Region: Eastern Europe
Primary Diagnosis: Global developmental delays, Spina bifida
Spina Bifida, hydrocephalus-shunt placed
Listed: Dec 2023
$2,984.50
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, 24 for 2024, Available to Large Families, Available to Older Parents, Available to Single Mothers
Sizable Grants $2,500+
Anne is delayed in all aspects of her development. She recently began eating from a spoon, and the NG tube was able to be removed. She enjoys attention from staff. She smiles when caregivers speak to her. She reaches and grabs objects, but is not yet playing with toys.

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.

Atticus, Natalie, and Ross #

Sibling Group
Ages: 15, 11, 12
Region: Eastern Europe
Primary Diagnosis: ADHD, Behavior, Limb differences
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 ***
Available to Large Families, Available to Older Parents, Available to Single Mothers, Siblings
Meet “A, N & R” – three siblings who are longing for a family where they can grow up loved and together. A is a 12-year-old boy who does well in school and gets along with others. He has vision loss in one eye, but that has not seemed to slow him down! His sister, N, just turned nine years old. She has diagnoses of a mild intellectual delay and minor behavioral issues. N is described as mobile and energetic. She enjoys playing with her classmates and while she may learn more slowly than her peers, she is making continual progress. Their brother, R, just turned ten years old. R likes to color, watch TV, and ride on scooters and bicycles. He has diagnoses of a mild intellectual delay and ADHD as well as a congenital foot deformity for which he has undergone some treatment.

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.

Christopher

Boy, Age: 9
Country Code: LA-3
Region: Latin America
Primary Diagnosis: Autism, Speech Delay
Language delay; Autism
Listed: Oct 2023
$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!
Inquire About This Child
Available to Single Mothers
Christopher is a precious little boy waiting for a family of his own. Contact the agency to learn more about Christopher and his listed needs.

 

Christopher now has a $500 agency fee reduction for his adoption;  Additional agency fee reductions may be available based on the adoptive family’ circumstances!

Reece's Rainbow 20th Anniversary