Libby

Girl, Age: 2
Country Code: EE-7
Listed: Oct 2025

This sweet girl loves music, animation, musical toys, taking baths, being outdoors and riding in the stroller. She often plays in the playpen and ball pool. She likes to sit and play alone. She can sit, roll, clap her hands, tries to stand up on her own in the crib, struggles, but stands up holding onto the crib rails. She is spoon-fed and likes a variety of mashed food. She drinks well from a bottle and from a baby bottle. She takes a variety of toys in her hands and holds and plays with them. She likes dolls and has a favourite doll which she plays with nicely. She has attended rehabilitation services and physiotherapy and occupational therapy specialists work with her. She responds to being spoken to by her name and observes and makes eye contact.

Diagnosed with mixed specific developmental disorders, disorder of normal physiological development, congenital hypotonia (reduced muscle tone); bilateral unstable hip joint; specific motor development disorder, hypermetropia (farsightedness).

Taliyah

Girl, Age: 1
Country Code: EE-7
Listed: Oct 2025

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

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

Nelson & Nellie

Sibling Group
Ages: 6, 6
Country Code: LA-2
Primary Diagnosis: Autism, Other Special Needs
Listed: Sep 2025
$0.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Information in this report is from May 2025

Twins Nelson and Nellie are six years old. They were born to a teenaged mother who was in protective care herself. Given specific familial concerns that will need to be discussed with interested families, the children were placed into foster care together and eventually were deemed in need of an adoptive family. There is no history of abuse with these children.

Nelson is overall healthy and does not have any medical diagnoses nor does he take any medication. However, while his motor development is age-appropriate, he has a mild language delay. Nelson is able to pay attention and communicate with others, but he has an impairment in his ability to pronounce words and complete sentences with difficulty pronouncing “l” sounds especially. He is receiving speech therapy. His profile indicates a learning delay “considering the developmental scale he is currently in” and recommends stimulation, but there is not a specific diagnosis given. He does not show any difficulty processing sensory information. He is receiving occupational therapy and psychiatric follow-up for a “diagnostic impression of Unspecific Conduct Disorder” but he does not have an official diagnosis. He does not react well when given limits and sometimes throws tantrums when he is not able to do something he wants to do. He does not have any social development concerns, though there are time he prefers to play alone while other times he plays and interacts with his peers.

Nelson is an affectionate child who is able express his emotions to others. He is attached to his foster parents and appropriate seeks their attention and approval when completing tasks. He tends to allow his sister to lead him and to be the dominant sibling in the relationship. It saddens him when he cannot play with her or is separated from her (normal daily temporary reasons, not separated with regard to where they live).

Nelson enjoys playing with cars, dinosaurs and balls. He loves going to the park, playing sports—especially soccer—with his classmates, and he is noted to be a skilled painter.

While Nellie also does not currently have any physical/medical diagnoses, she is being evaluated for Autism Spectrum Disorder. A psychiatric evaluation appointment is pending due to testing showing sufficient criteria for a diagnosis of Autism Spectrum Disorder, but a thorough evaluation is needed to determine a diagnosis. Symptoms noted including persistent language development delay, attention lability, motor restlessness, stereotyped behavior, limited eye contact, and difficulty in understanding directions. A pedagogy evaluation appointment is also scheduled. Nellie displays behavioral concerns, especially with regard to her schoolwork. She is resistant to doing schoolwork (though she is capable to do the work) and to obeying the rules and limits of the classroom. At home, she has resisted doing homework and even has scribbled on her notebooks and thrown them on the floor. At her previous early childhood educational program, she also showed behavioral difficulties and difficulties recognizing authority figures, trouble staying involved in activities and a preference for more open areas of the institution. She cries when she is not allowed to do something she wants to do. However, she is able to play alone or focus on tasks she wants to do such as playing with dolls or dancing.

Nellie’s motor development is age-appropriate. She does not have any difficulty processing sensory information. Like her brother, she is able to communicate but has difficulty with word pronunciation—especially in pronouncing the “l” sound. Socially, she is able to establish relationships with other children and plays with others. Despite her behavioral concerns, she is noted to usually have a good disposition, be cheerful and integrated with her foster family. Her foster family has been given instruction on how to help improve her behavior and there has been progress made.

Nellie is strongly attached to her foster parents and her brother. She is able to give and receive affection with them and sometimes exhibits jealousy when the foster mother shows affection toward other children in the home. She seeks approval from her foster parents and from others with whom she has an emotional bond. Nellie is the more dominant sibling and takes the initiative to ask for things for both herself and her brother.

Nellie finds joy in playing with her dolls and receiving affection from those she is close to. She is an expressive child who engages in caregiving role-play. She likes wearing dresses and having bows in her hair. She enjoys and is good at dancing and singing, and also likes playing with toys, going to the park and watching television.

Holly

Girl, Age: 5
Country Code: Asia.4
Region: Asia
Listed: Sep 2025
$0.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!

Holly is a cheerful, lovely, friendly and cheeky 5-year-old girl who lights up her surroundings as a true superstar. She loves people and her medical staff adores her, often gifting her beautiful clothes. She treasures relationships as she can easily remember faces after just two meetings. Holly is learning to use alternative and augmentative communication (AAC) with the help of a tablet, where she can tap to select people she wants to see (picture available). During the social worker’s child visit, she even used gestures to request adding the worker’s face to her tablet even though it was her first-time meeting her. Despite her many medical needs, this child has shown the ability to learn and engage with her with a variety of engagement types. She is a funny girl who makes people smile with her bright personality. A picture is available of her making funny faces when the social worker was taking her pictures for the child study.

Holly is diagnosed with incomplete DiGeorge syndrome, bilateral vocal cord palsy, oropharyngeal dysphagia, gastroesophageal reflux disease (GERD), Methicillin-resistant Staphylococcus aureus (MRSA), scoliosis, global developmental delay and exotropia. She is on tracheostomy and percutaneous endoscopic gastrostomy (PEG) feeding. She has remained hospitalized since birth for her medical needs even though she is medically stable now. To learn more about DiGeorge Syndrome, visit the Mayo Clinic’s syndrome page here: DiGeorge syndrome (22q11.2 deletion syndrome) – Symptoms and causes – Mayo Clinic

As mentioned, despite Holly’s significant medical needs, she has made remarkable progress in her development over the past year. She can follow simple instructions, point to familiar objects, and use tools after observing her teacher’s demonstrations. Holly shows interest and joy while learning various play skills and can imitate appropriate play behaviors with prompting and encouragement. She consistently communicates her needs using gestures and she also has great eye contact. Additionally, she can sit independently, take a few steps without assistance, self-propel her wheelchair for short distances, and manage tasks like eating and dressing on her own. She enjoys watching cartoons and listening to music.

Despite having a tracheostomy, Holly does not require ventilator support. However, in the event of tracheostomy dislodgement, there is a risk of hypoxia and immediate tracheostomy reinsertion is necessary. She needs to be accompanied by a trained caregiver at all times. Holly has been assessed as medically fit for home care. The doctor has recommended that Holly requires a well-trained and attentive caregiver who can provide vigilant around-the-clock care, and the caregiver would need to be proficient in special care skills, including managing tracheostomy emergencies.

Holly has made great strides in the past half year and we strongly believe she will continue to make great progress in reaching her potential within a loving and fun family.

Due to the country’s matching process, families with an approved home study for any country are able to request consideration to be Holly’s parents. If matched, the family would then need to quickly update their home study and gather the dossier for the country.

Amelia & Scarlett

Sibling Group
Ages: 6, 6
Region: Africa
Primary Diagnosis: Other Special Needs
Sickle Cell Disease
Listed: Sep 2025
$0.00
has been donated towards the cost of my adoption, including $0.00 from MACC donations!

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!
These 6-year-old twin sisters from western Africa are ready to bring double the joy to their forever family! While they might greet you with a touch of initial shyness, don’t let that fool you. Beneath their gentle exteriors lie curious minds and warm hearts that blossom quickly. Their caregivers consistently remark on their intelligence and enthusiastic approach to learning. Amelia, the more contemplative of the pair, loves playing with her dolls, watching Disney films, and creating colorful masterpieces with her drawing. Scarlett, with her inquisitive nature, is full of thoughtful questions and energy. She has a passion for dance and loves playing with Barbies. Imagine the joy of witnessing these two smart young girls explore the world around them. If you’re looking to open your heart and home to not one, but two little girls ready to learn, grow, and share their unique personalities, perhaps Amelia and Scarlett are the perfect fit for your family.

Amelia and Scarlett have been diagnosed with Sickle Cell Disease, which is currently managed with daily medication.

Arlen

Boy, Age: 10
Country Code: LA-2
Listed: Jul 2025
$25.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!

Arlen and his four siblings came into care in 2022 due to being victims of multiple types of abuse in their family. Their parents were known to be drug users with emotional instability and aggressive behaviors between them. They were also verbally abusive toward the police and other authorities. Arlen is being placed for adoption as a single child.

As Arlen was never enrolled in school until he was taken into protective custody, he is in the first grade. He is familiar with some letters and numbers but cannot read or do simple arithmetic problems. He truly enjoys art class since he has great skills for doing crafts. He seeks adult validation in every activity he participates in. However, while he recognizes authority figures, he is defiant toward them and only obeys with some difficulty. Arlen usually gets along well with peers and adults; however, when he gets mad or frustrated, he begins to behave in a bad and aggressive way. He lies whenever he wants to avoid his responsibilities. He gets upset when he cannot do what he wants. His cognitive development is affected. Arlen has been diagnosed with ADHD, mild cognitive developmental delay, focalized epilepsy, and oppositional defiant disorder. He goes to occupational and psychiatric therapy, and also takes daily medication. There are no concerns regarding his motor and language development.

As mentioned, Arlen and his siblings were subjected to multiple types of abuse. It has been reported by his teachers that in addition to being aggressive toward other children in the class. Though Arlen can verbally express his feelings and emotions, he has a hard time managing them. He gets easily frustrated and has trouble finishing any given task. He is afraid of the dark and of being alone. Arlen gets anxious when he consumes sugary foods, and he also gets anxious when an outing is going to happen soon. He goes to bed around 8 pm but takes a long time to fall asleep.

Even though Arlen has been known to be aggressive toward others, his child study also reports he usually gets along with adults, peers, younger children and animals. Arlen is not shy when meeting people; it is easy for him to take the initiative to start a conversation with anybody. He likes to take the lead in any game. Arlen can be affectionate toward those he knows and is comfortable with. He likes to maintain good hygiene habits and takes care of his personal belongings.

Arlen is very active during the day. He loves to go to the park and to play soccer with friends. Arlen is interested in any outdoor recreational activity; he loves to do physical exercise. He has stated that he is good at swimming. Arlen has stated that he would love to get married and have kids. He does not want to go to college but would like to work handling heavy machines. He is open to being adopted by any type of family.

Sophie

Girl, Age: 9
Country Code: Asia.4
Region: Asia
Listed: Dec 2024
$40.00
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!
Sophie is a gentle, cheerful, and agreeable 8-year-old girl. She loves listening to music and is attracted to various sensory toys and materials. When her caregivers and teachers play music, she becomes attentive and smiles. Sophie has been diagnosed with cerebral palsy with multiple medical conditions. She requires daily medications and intensive medical follow-up in various specialties. She needs support and assistance with mobility and daily living activities. In the face of her challenges, Sophie works hard to participate in different training sessions and therapies including physiotherapy and occupational therapy.

Sophie loves people. She can be easily comforted by hugging, gentle stroke, and comforting words. Sophie expresses herself nonverbally. She nods or smiles when she likes something, and pouts or frowns when she does not. She joyously participates in the activities the caregivers and teachers give her such as sunbathing outside and sensory activities. Her caregivers and teachers report that she is easy to care for and manage because of her calm nature and generally stable health condition. She also adjusts to changes quickly and easily.

It is believed Sophie will continue to make progress in reaching her potential within a loving and caring family. Due to the unique child/family matching system in her country, a family with a current home study for any country can submit to be considered to become her family.

Katy

Girl, Age: 5
Country Code: LA-3
Primary Diagnosis: Other Special Needs
Mucopolysaccharidosis syndrome type IV, and mild cognitive scoliosis
Listed: Nov 2024
$25.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Katy is a very intelligent and curious girl.  She loves going to the pool on sunny days.  Her favorite foods are soup and smoothies.

Valeria

Girl, Age: 14
Country Code: LA-3
microcephaly, epilepsy
Listed: Nov 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 ***
Valeria is a very protective girl.  She loves drawing and doing art projects.  Valeria currently has a feeding tube.

Update in 2025 states that she no longer has a feeding tube, and is doing really well!

Valeria was previously listed on Reece’s Rainbow as Marisol.

Cheyenne

Girl, Age: 13
Country Code: LA-2
Mild cognitive delay
Listed: Nov 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 ***

Information in this report is from March 2024

Cheyenne, 12, came into care in 2020 when her mother left her with a woman and it became clear that she was not returning. In the child investigation, it was discovered that Cheyenne had been the victim of abuse by both a non-family member when she was young and a minor relative though there is not much information regarding the later situation. Due to being moved around so much and the chaotic environment of the biological family, Cheyenne was not consistently enrolled in school which has affected her cognitive development.  Cheyenne is now enrolled in school, and she is in 4th grade where she is respectful, responsible, and motivated at school. In 2023, she was given an IQ test and scored 63, which led to a diagnosis of mild cognitive delay.  At the age of 11 when the test was performed, it was estimated that she had the cognitive development and maturation of a 7-year-old.  She goes to cognitive therapy to overcome her diagnosis of mild cognitive delay due to the family environment she grew up in.

Cheyenne has adjusted well to her foster family and being in a positive family environment. For example, while she likely did not attend religious services in the past, she enthusiastically attends Catholic services with her foster family and participates in spiritual activities such as praying the rosary with the family. Her foster family has helped her work on her social development, interaction with others, taking responsibility for her actions in a positive way, etc. It is noted that Cheyenne had a habit of lying to avoid negative consequences; however, great improvements were made in this area. While she still gets anxious when confronted about any inappropriate behaviors, Cheyenne is no longer afraid to accept the consequences of her actions. It is upsetting to her when someone lies about her. She is cooperative and strives to be obedient, and she is getting better at managing her emotions, impulses, and frustrations. She gets sad when others positively talk about their biological families, and she just wants to find her forever family. She is afraid of feeling alone.

Cheyenne is very affectionate and sweet. She is friendly and has wonderful skills to be a leader inside and outside her foster home. Cheyenne interacts positively with adults, peers, younger children, and animals. Cheyenne is quiet and feels good when she finishes the tasks assigned to her. She is independent and fulfills her daily routines on her own.

Cheyenne enjoys participating in recreational or playful activities with her peers. She especially likes riding her bicycle and playing soccer. She also likes to draw and dance. Cheyenne loves to eat spaghetti, rice with chicken, and oatmeal, but she does not like to eat broccoli. Cheyenne has stated that she would love to become a Chef to express her love through food.

Nia

Girl, Age: 8
Country Code: EE-2
Listed: Sep 2024

SN: FAS, motor aphasia, celiac disease, hyperopia

 

This girl is much loved by her caregiver and peers! She lived with her biological family for 2 years and was neglected. After a few years in the foster family, she was placed to the orphanage where she adjusted well.  She established a positive relationship with others. She likes to cuddle and is seeking the contact with adults. She is a little bit behind for her age, but she is a smart girl with a lot of potential. She is attending a regular school and her teachers like her.

Jonathan

Boy, Age: 5
Country Code: Asia.2
Region: Asia
Listed: Jul 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!

This is Jonathan!  Jonathan is almost 4 years old, and we had the absolute pleasure of meeting him on our last visit to Taiwan.  He is an active toddler who loves cars, balls, steering wheels, and toys that make sound and light up.  He also adores toys that spin!  While Jonathan is interested in meeting new people, he still maintains caution and will distinguish between familiar and unfamiliar people and surroundings.  At this time, Jonathan prefers to play on his own, but will occasionally engage with peers when a friend is playing with a toy that Jonathan wants.

Jonathan attends school regularly, and positively interacts with his teachers.  He follows instructions and participates in activities. Jonathan has made significant progress over the past eight months, with increased verbal expressions and connection with others.  While he does primarily use non-word vocalizations to express himself, more recently he has correctly pronounced several words.  Jonathan can accurately identify objects, and follow direction such as ‘go get your school bag.’

Jonathan has made great progress over the past year, and we know his progress would be even stronger with the love and support of a forever family!

Mia

Girl, Age: 8
Country Code: Asia.4
Region: Asia
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!

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: 13
Country Code: Asia.4
Region: Asia
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 ***

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.

Tiana and Tenaya

Sibling Group
Ages: 11, 15
Country Code: LA-2
Primary Diagnosis: Other Special Needs
Tenaya: Leukemia Lymphoid Acute- diagnosed at the age of 4 years
Listed: Jun 2024

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.

Ricky

Boy, Age: 4
Country Code: LA-2
Listed: May 2024
$100.00
has been donated towards the cost of my adoption!

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

Ricky’s listing agency also has video available!

Seth

Boy, Age: 5
Country Code: Asia.2
Region: Asia
Listed: May 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!
This little guy is a big fan of cuddle time and giggles in delight when his nanny calls his name! At the age of two he was diagnosed with pediatric lymphoma and was responsive to chemotherapy. Seth is currently 4-years old and has lots of energy! He enjoys taking walks with his nanny, listening to music and playing with toys that light up and make sound. Seth receives comprehensive development services in Taiwan for significant global delays. A family interested in adopting Seth will need to be available for therapies, medical care, and life-long care. Seth is not timid and he enjoys interacting with people so we expect him to have a life full of accomplishments! Seth needs a family to celebrate each milestone he meets!

The adoption agency has additional photos and videos available.

 

Nick

Boy, Age: 11
Country Code: LA-2
Listed: May 2024
$35.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!

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

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

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

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

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

Zander

Boy, Age: 12
Country Code: LA-2
Cognitive delay, anxiety, depression, macrodactyly and gigantism, hand deformity
Listed: Apr 2024
$1,667.50
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!
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: 8
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!
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.

Ames

Boy, Age: 10
Country Code: E-11
Region: Europe
Developmental challenges such as intellectual limitations, learning difficulties, linguistic delays, and special behaviors; maternal mental health issues
Listed: Feb 2024
$25.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Ames is a joyful youngster who displays notable independence for his age, showing advancement in managing personal responsibilities in spite of his cognitive development in areas such as language mastery, social dynamics, and self-regulation. Ames is progressing, revealing a promising trajectory.

His interests are as varied as they are engaging, ranging from the energetic spinning of beyblades to the strategic play of table football, and the creative assembly of Legos. A fondness for stories also defines him—he delights in listening, reading, and sharing tales with others.

Understanding and following rules come naturally to Ames when they are communicated clearly and applied consistently. He flourishes under positive reinforcement and thrives on routine, which helps him navigate his day with confidence. When faced with choices, he benefits from being offered two options to help enhance his decision-making skills.

Adaptable and responsive, Ames shows a commendable capacity for assessing situations; however, he does rely on adult guidance to navigate safely through his environment. Previously having not experienced a traditional family setting, he formed emotional attachments with his caregivers. Ames longs for what many take for granted—a loving family to call his own.

At his current developmental stage, it’s essential to tailor Ames’s transition towards adoption, ensuring the introduction to a potential family is mindful and gradual. Psychotherapeutic support has been assisting Ames in processing his hopes and feelings about family life, laying groundwork for his future relationships.

Mariah

Girl, Age: 13
Country Code: LA-2
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 ***
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.

Alfie

Boy, Age: 6
Country Code: LA-2
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
$567.50
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!
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.

Mahleah

Girl, Age: 16
Country Code: SE.Asia.2
Region: South Asia
Primary Diagnosis: Older Child, Other Special Needs
$3,270.56
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!
Maleah is a medically healthy, active, tall and athletic beautiful teen girl!  More than anything she wants to be part of a family, and is open to both a two parent family as well as a single Mom.  Maleah has overcome much hardship and adversity in her past and needs a strong, committed family who is well-versed in trauma.  Maleah adores younger children and would benefit greatly from cousins or younger friends in the community!  Agency staff has met and spent time with Maleah and were immediately struck with the incredible potential this young woman has, if only given the opportunity!  Maleah will turn 16 in October 2025, making her ineligible for international adoption to the US at the time.  Her family must be ready and willing to race to her in time!

Eric

Boy, Age: 6
Region: Africa
Primary Diagnosis: Other Special Needs
Sicke Cell Anemia
Listed: Feb 2023
$455.50
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!
Eric was previously listed as Freeman. His social worker reports that he has good behavior and plays well with other children. He attends preschool and does not currently have any developmental concerns.

Photos are available through the agency for qualified families.

Zoey

Girl, Age: 7
Country Code: Africa-1
Region: Africa
Developmental Delay, Post-stroke
Listed: Jan 2023
$3,632.50
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!
Zoey is one of the most beautiful little girls you’ll ever meet. She was born with some developmental delays, but then experienced a stroke when she was two and a half. This greatly set back her abilities. However, since then she’s been in a foster family where she’s relearned how to sit, roll, and grasp toys. She is working on self-feeding and becoming verbal again. Although Zoey had a seizure with her stroke she hasn’t had one since, and rarely requires medical care now. However, she may benefit from a better neurologist to understand her brain’s unique functions and abilities. Zoey is not short of opinions and will let you know exactly how she is feeling with tears or laughter! She loves to play and her giggle is absolutely infectious. She loves playing with water, musical instruments, and anything that makes noise. Zoey also loves to eat and isn’t picky at all! She is a social girl who has loved having two foster brothers. Zoey will bring an abundance of joy to any family who chooses to love her forever!

Angelo

Boy, Age: 8
Country Code: LA-2
Primary Diagnosis: Other Special Needs
osteogenesis imperfecta and a unspecified conduct disorder
Listed: Oct 2022
$579.50
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!
Update from June 2025: Over the past 3 months, Angelo has made great progress walking. He is doing better and is more confident in himself! He has also come a long way with his communication, making himself understood through signing. He is precious and tender and will continue to blossom!

———————————————————–

So excited we have permission to share Angelo’s pictures!

Angelo likes playing with bubbles and painting with tempera. He enjoys crafts and exploring the different materials and textures. Angelo also likes building towers and playing in water. He is described as social and showing great interest in everything that happens around him. He is a great observer.

Angelo is able to kick a ball forward with help, throw a ball over his shoulder and catch a ball with rebound most of the time. He is able to pedal a tricycle and climb the stairs with help. He is able to undress. His motor coordination is good, which makes it easier for him to string objects. Angelo has a good understanding of orders and knows and recognizes language. Contact the agency to learn more about Angelo and his medical needs!

 

NEW VIDEO:
https://vimeo.com/maaspecialkids/maa-angelo2

NEW VIDEOS: 10/2024

https://vimeo.com/maaspecialkids/maa-angelo3

https://vimeo.com/maaspecialkids/maa-angelo04

https://vimeo.com/maaspecialkids/maa-angelo5

https://vimeo.com/maaspecialkids/maa-angelo06

Password:  Adoptmaa

 

Raydor #

Boy, Age: 12
Primary Diagnosis: Other Special Needs
Possible Autism, Premature
Listed: Sep 2022
$1,067.50
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!
Raydor was previously listed on Reece’s Rainbow as Randy.

Raydor’s birth mother was addicted to Heroin and took Methadone during pregnancy. Raydor was born premature and spent the first 5 months of his life in the hospital. Raydor knows his alphabet, numbers and colors in both his native language and English. He can do simple addition problems (single digit plus single digit and single digit plus double digit). He speaks in 2 word sentences and memorizes poems. He loves to build houses and other things with Legos and will stay focused on this task for long periods of time. He plays independently and with other children. He enjoys music and often tries to imitate melodies. Raydor has some behaviors that are commonly seen in children on the Autism spectrum. He has not had any type of formal evaluation for Autism. 

Rose #

Girl, Age: 14
Primary Diagnosis: Other Special Needs, Speech Delay
Mild Mental delays and speech delays
Listed: Jul 2022
*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***
Rose was removed from an abusive home at 9 years old and could not even speak the language of her birth country at that time. She now speaks in sentences, understands everything that is said to her and has made rapid developmental progress. During the visit with our team member, she was talking about the Mom and Dad that she’s waiting for and having a fun time posing for all the photos (see below). She currently lives with an older foster couple, who she calls grandma and grandpa. They have worked with her to teach her many self-help skills. She’s now in school and doing well working with a resource teacher.

Sadie #

Girl, Age: 6
Primary Diagnosis: Other Special Needs
Progressive ossifying fibrodysplasia
Listed: May 2022
$2,777.00
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!
Sadie has limited movement in her neck, back and hands/arms (due to limited movement of the shoulders). She has more range of motion in her left arm vs her right. She compensates for her limited mobility. She stands on her toes to reach objects (when she cannot extend her arms) and holds on to a support to bend down or she seeks assistance from an adult. She walks, plays with toys, and interacts with her environment. She can put together wooden puzzles, stack rings and perform other basic tasks. She can take the cap off a pen and tries to draw shapes. She interacts with familiar people. She initiates games such as peek-a-boo. She will point to things she wants to communicate her wants/needs. She dances along to music. She can say some simple single syllable words such as ma-ma, but mostly communicates with gestures. She lived in a home with a younger child for a while and did well with the younger child. The foster family limits her interactions with other people, because they are afraid she will get hurt, due to her physical limitations. She plays well with other people, when she is around them. She does not go to preschool due to the fear her foster family has that she will be injured. She shows a preference to certain objects and TV shows (Peppa Pig and Masha the Bear).

Videos from May 2022 show Sadie walking, playing with toys, putting a puzzle together and interacting with adults. The videos show Sadie’s physical limitations.

Adrien

Boy, Age: 9
Country Code: EE-2
Primary Diagnosis: Other Special Needs
Hernia, Arnold Chiari II syndrome, orthopedic foot defect (clubfoot)

Listed: Apr 2022
$2,468.02
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!
Adrien is a charming and smiley boy. His behavior is very good, he respects the rules in the orphanage. He is interested in learning new things and willingly participate in games and activities. His skills are importing in all spheres. He is willing to play all games proper to his age.

Alan

Boy, Age: 14
Country Code: EE-2
Primary Diagnosis: Other Special Needs
Listed: Dec 2021
$667.00
has been donated towards the cost of my adoption, including $0.00 from MACC donations!

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!

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

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

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

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

Tristan

Boy, Age: 14
Country Code: EE-2
Primary Diagnosis: Other Special Needs
Listed: May 2021
$2,822.34
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!
He lives at the orphanage since 2016. Normal weight and height parameters. Psychomotor development is normal. He is the victim of parental physical abuse and suffers from post-traumatic past. He is under the care of psychiatrist and take medication. No medical diagnoses in his chart, but trauma. You could tell that he is emotionally somewhat fragile.

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

Emma #

Girl, Age: 9
Condition after herpes-viral encephalitis. Hepatitis caused by CMV. Hypotrophy. Hydrocephaly – of mild degree. Congenital dyserythropoietic anemia. Delayed neuro-psychological development.

Listed: Sep 2021
$2,190.50
has been donated towards the cost of my adoption, including $0.00 from MACC donations!

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!
Emma was recently transferred to a group home where she can receive more specialized care to help her continue to develop and receive appropriate medical care. She is receiving monthly blood transfusions at this time for her anemia. She had surgery to correct clubbed feet in 2020. She can sit unassisted, stand next to a stable support, walk around fixed supports and walk while holding the hand of an adult. Videos from May 2021 show Emma playing with an electronic toy. She is pushing the button to get the toy to make a sound. Her fine motor skills are not well-developed at this time, due to her spasticity. Emma responds positively to adults and other children. She smiles and laughs when adults interact with her.

 

The agency staff member who visited her during March of 2024, says the following:

Emma is a sweet little girl who needs a loving and supportive family environment. During my brief visit, the child was constantly on the move except for the brief moments when she played with a particular toy or during her brief moments of protest. At the present time, the child’s needs are met at a basic level, with particular attention paid to her medical needs. The lack of systematic and in-depth work of specialists (such as a rehabilitator, occupational therapist, special pedagogue, speech therapist and others) is felt, which the institution currently does not have the opportunity to provide. By falling into a suitable loving family, receiving more attention and adequate care and activities, Emma could show her potential to a greater extent.

Update 8/2024

Special needs: low birth weight – 1800 gr; condition after herpes viral encephalitis; condition after hepatitis caused by CMV; congenital dyserythropoietic anemia; hydrocephalus – mild degree; infantile cerebral palsy – spastic quadriparesis; symptomatic epilepsy; delayed neuropsychological development
Therapy: Convulex 4+4+4 ml., Clonarex 2 x ¼ tablet, Repitend 4 ml – 0,4 ml. Carsil – 2 x ½ capsule daily, EXJADE – 1 tablet daily, Urinal x 5 ml daily, Vitamin D3 x 2
Emma makes steps but always and only with the help of a support. She does not control her physiological needs and wears diapers. She listens to children’s songs and fairy tales and claps with her hands. She holds a toy she has been offered but she would most often put it in her mouth without playing with it.
Emma needs monthly blood transfusions and regular consultations with a neurologist and hematologist.

Silvio

Boy, Age: 8
Country Code: EE-2
Primary Diagnosis: Other Special Needs
Extremely premature, tracheotomy
Listed: May 2021
$1,128.65
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!
Silvio is a Roma boy who was born extremely premature (22 weeks), with a very low birth weight. He spends 6 months at the hospital and fought for his life! He had a tracheotomy procedure and eye Lasik surgery in October 2017.

Last update 2020: Delayed psychomotor development. Visible improvement after rehabilitation. Feeding the by the bottle, playing with toys, rolls out of the back on the stomach and vice versa. He tries to crawl. A very active child who initiates contact. He makes eye contact, focuses his attention on the human face, and smiles back. Video is available from the adoption agency.

Trina

Girl, Age: 16
Country Code: LA-6
Primary Diagnosis: Other Special Needs
Sickle Cell Anemia
Listed: Mar 2021
$604.50
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!
Trina just glows with positivity! She likes to participate in the activities carried out in the institution, mainly those related to the creative arts such as painting and dancing, she likes to play with her peers and sometimes acts as a leader in social groups. In the psychological report, they describe the girl as responsible, obedient, dedicated, organized and friendly. Trina has a tendency to withdrawal and mild depression, due to the presence of feelings of insecurity, low self-worth and low self-esteem.

Trina also projects a strong need for belonging, parental protection and a strong desire for firm support, these aspects are explained by her life history and have been worked from different approaches by psychology, overall a calm state of mind is reported.

We know that an adoptive family can greatly help Trina feel valued and loved, and will help her improve in these areas with love, security, acceptance and healing.

Photo available from agency!

Trina has Sickle cell anemia, and she was medicated with folic acid. Sickle cell anemia is one of a group of disorders known as sickle cell disease. Sickle cell anemia is an inherited red blood cell disorder in which there aren’t enough healthy red blood cells to carry oxygen throughout your body. While there’s no cure for most people with sickle cell anemia, treatments can relieve pain and help prevent complications associated with the disease. Many people with this condition live very normal lives. Learn more about the illness and living with Sickle Cell by visiting Sickle Cell Speaks.

High altitude risk: The air at high altitudes, such as in an unpressurized airplane or in the mountains at altitudes greater than 5,000 ft (1,524 m), has less oxygen than at sea level. The lack of oxygen can cause cells to sickle which is painful and dangerous for a carrier. For that reason, it is not advisable to place a child for adoption with a family living at higher altitude / mountains.

AJ

Boy, Age: 8
Country Code: LA-6
Primary Diagnosis: Other Special Needs
Grade I Osteogenesis imperfecta, controlled asthma, controlled atopic dermatitis, right cryptorchidism (undescended testicle)
Listed: Mar 2021
$590.00
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!
AJ is a calm, loving, shy boy who came into the care when he was about a year old; he was found abandoned. He has favorably adapted to the institution where he is being cared for and he has made significant progress in his motor process.  The boy moves his upper and lower extremities, he can take his feet to his mouth, he crawls, and tries to stay standing with support. The report also states that AJ is a boy who explores the environment, he maintains attention and interacts with people, appropriately responding to the sensory stimuli that are presented to him. AJ likes children’s songs and dances imitating his peers, he likes colorful musical instrument toys.

Photo available from agency!

When the medical report was first performed when he was about one year old, AJ was not walking and a level of delay is reported in the cognitive, language and motor areas that are related to the state of severe malnutrition with which he was found as an infant.

His Grade I Osteogenesis Imperfecta is the mildest form of the condition. Osteogenesis imperfecta (OI) is a genetic disorder characterized by bones that break easily. OI is highly variable. Its signs and symptoms range from mild to severe. In addition to fractures (broken bones), people with OI sometimes have muscle weakness, loose joints (joint laxity), curvature of the spine (scoliosis), brittle teeth (dentinogenesis imperfecta), and hearing loss. A classification system dividing OI into several types is commonly used to help describe how severely a person is affected. Type I is the mildest and most common form of OI.

Brett #

Boy, Age: 11
Primary Diagnosis: Other Special Needs
Mental delays
Listed: Jul 2020
$751.50
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!
Brett lived with a foster family from birth to age 4. He did not attend preschool or receive any interventions during that time. The family was not experienced in how to work with him. He was placed in a small group home at 4 years old. He has thrived in this setting. He has learned many new skills and continues to make improvements in all aspects of his development. He communicates using words and simple sentences. He understands everything said to him and can answer basic questions. He takes care of all his personal hygiene independently (brushes his own teeth, hair, dresses/undresses himself, is toilet trained, etc). He can count to 10, recognize colors and shapes, work puzzles, say his name and age, and also say the names of the other children living in the home. The staff at the group home believe that his mental delays are mild and state that this is because he made such rapid progress once he was placed in the group home and began receiving instruction. The foster family had reported behavior issues, mainly an inability to concentrate. The staff reports no behavior problems and stated that he just needed attention and appropriate instruction. They describe him as very affectionate.

Jax #

Boy, Age: 14
Primary Diagnosis: Other Special Needs
hyperkinetic conduct disorder and a mild mental delay
Listed: May 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 ***
He has been living with a foster family since 2013.

He has a systolic murmur along the precordium; hyperkinetic conduct disorder and a mild mental delay. The child started walking on time, but his speech is underdeveloped. The child cannot stay focused for a long time while playing. He understands and follows simple instructions.

The agency has current medical reports available for serious inquiries.

UPDATE March 2017:   previous Diagnosis of Atypical autism that was changed to hyperkinetic disorder, very interested in motor activities. Responds to positive interactions and praise from familiar adults, but can become anxious in new situations or if a familiar caregiver is not around. He seeks comfort from familiar adults and can become sad if one leaves.

Norton #

Boy, Age: 13
Primary Diagnosis: Other Special Needs
hyperactive disorder, mild mental disability and a speech delay
Listed: Nov 2017
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Norton is a boy who lives with a foster family in Eastern Europe. He loves to play with other children and particularly likes to play with musical toys and cars. He also likes to paint using watercolor paints. He manages to play games for a long time, and he likes to help around the household.

Norton is in good health and is stronger than typical of his age. He can independently move larger items, including furniture. He loves to run and jump, and he knows how to roll over forward and squeeze in narrower spaces. Like many little boys, Norton brushes his teeth twice a day. He can tell others when he needs to go to the restroom, and he eats with great appetite. He naps for two hours in the afternoon and sleeps peacefully at night.

His short-term and long-term memories function at a good level, and Noah can easily remember things related to the lifestyle, as well as past events related to pleasant or unpleasant memories.

Although he has been diagnosed with hyperactive disorder, mild mental disability and a speech delay, Norton has shown progress in his development. He understands everything that is required of him, executing commands correctly. He is persistent in his demands, but he understands when he has violated rules, and he does not oppose correction.

Norton chatters a lot, but he is incomprehensible. He repeats syllables he hears, and he uses gestures to help him communicate with others and make them clearly understand what he wants or wants to do. Norton is working with therapists to improve his speech abilities.

Clifton #

Boy, Age: 13
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 ***
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

Jonas #

Boy, Age: 14
2nd-degree prematurity; epilepsy; convergent strabismus; esotropia of the left eye; hypermetropia (long-sightedness); mild mental delay; delayed speech development; other pervasive developmental disorders;
Listed: May 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 ***
Jonas is on several medications.  Jonas’s motor activity completely corresponds to the expected developmental level for his calendar age.  Although his fine motor skills need to improve further, Jonas is able to hold a pencil properly. He can inlay elements with some guidance. He puts cubes one on top of the other. He threads colored rings on a fixed stand, but not yet in accordance with their size.

There are some difficulties in attracting and keeping his attention focused. Jonas plays for a longer period of time whenever he is interested in the respective activity. Jonas orientates well in a familiar environment. He distinguishes between day and night based on his everyday routines – sleeping, meal times, rest. He recognizes the neighborhood around the foster family’s home.

Jonas is reported to have achieved noticeable progress in terms of expressing his emotions and feelings, which are becoming more diverse. He reacts appropriately to smiles and angry faces and also to the tone of voice one talks to him with. He demonstrates his love, attachment and attention for others. He greatly enjoys it when others play with him. Jonas has attached to all members of the foster family.

Rocky #

Boy, Age: 14
Primary Diagnosis: Other Special Needs
Listed: Nov 2017
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Rocky is a calm, pleasant  boy who lives in a group home in Eastern Europe. He is attached to his caregivers and responds well to them.

Although Rocky was born premature and with low birth weight; cerebral palsy; and speech, motor and cognitive delays, he is making good progress in his physical therapy and other supports. He can walk with minimal support, and his fine motor skills are also improving.

Sally #

Girl, Age: 9
Primary Diagnosis: Other Special Needs
congenital anomaly of the central nervous system; dysmorphic stigmas(dysmorphic facies, four-finger groove of left hand, six fingers on right leg, longer right foot with a larger surface area); generalized hypotonia and forming hemiparesis on the left.
Listed: Jan 2019
$942.70
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!
Sally had one seizure at age one. She’s been on seizure medication since that time and has not had any additional seizures. She touches and grabs with her right hand and moves her right foot. The left hand is almost clenched in a fist. Her muscles are very tight, but she can sit up when placed in that position. She will reach and grab toys with her right hand. She tracks objects that are moving in front of her face. She laughs when adults interact with her. She makes sounds and produces syllabes when imitating someone. She enjoys musical toys and will scoot to get to a toy that is near her when on the floor. She is fed by an adult and can eat from a spoon.

Robby #

Boy, Age: 10
Primary Diagnosis: Other Special Needs
nonspecific reactive hepatitis. Hepatosplenomegalia. Heart malformation foramen ovale, initial lung hypertonia. Condition after hypoxic ischemic encephalopathy 2-3 degree. Hemoragia. Intraventricular bleeding 2 degree. bilateral otomastoidit – mastoidectomy in the right. Retention testicle in the left. Delay in the neuro-psychical development.
Listed: Jul 2018
$1,600.00
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!
Robby is delayed in all aspects of his development, but has begun to make small gains in learning . He will interact with caregivers and other children if an activity is interesting to him. His attention span when working on tasks has begun to increase. He enjoys playing in the sensory room. He learns best with multiple repetitions of a task.

His current agency has videos and pictures that can be shared with interested families

Malory #

Girl, Age: 15
Primary Diagnosis: Other Special Needs
Microcephalous; Moderate mental delays; Speech delay; Behavioral Issues
Listed: Jan 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 ***
Malory is a beautiful, giggly girl who lives with a foster family in Eastern Europe. With a contagious smile and laughter, Malory runs, climbs and could be described as an active child. She enjoys the extra attention she receives from her foster parents. She is physically healthy, and she eats well. Her weight and height are catching up with the standards for her age.

Malory has some developmental delays that her caregivers attribute to early neglect and lack of stimulation. She has difficulty pronouncing some words, and her learning is below the norm for her age. Malory understands everything her elders say. She cannot talk yet, but she can pronounce separate words and sounds. She knows her name and the people’s names living around her. She plays with the other kids from the group, and she prefers more dynamic games.

Malory gets one-on-one instruction in each subject, participating in different programs – therapeutic, musical and rehabilitation. She is much calmer then she was before, and she respects the authority of the foster family.

Additional videos are available from her agency.

Gabi #

Girl, Age: 15
Primary Diagnosis: Other Special Needs
moderate mental delay- significant impairment of behavior requiring attention or treatment; microcephaly; hyperactive behavior
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 ***
Gabi is physically healthy with normal physical development. She is radiant and very active.

Gabi responds adequately to praise and punishment. Gabi establishes and maintains eye contact. She seeks the attention of the people around and she seeks familiar people and their closeness purposefully.

Gabi understands the meaning of words that are often used in her surroundings. She expresses her needs and wishes through vocalization.

In her spare time Gabi likes watching TV, playing on a phone, listening to music and going out for walks.

Drako #

Boy, Age: 10
Primary Diagnosis: Other Special Needs
Cognitive delays; repaired cleft lip & palate with additional surgeries needed
Listed: Apr 2019
$817.12
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!
Drako has undergone surgeries to repair a cleft lip and palate. He is under continues care by medical professionals and will need future orthodontic surgery and other possible surgeries as well related to his cleft issues. Developmentally, his speech, motor skills, and cognitive processing are all delayed. He can crawl, pull to a stand, cruise around furniture/objects, and walk while holding an adult’s hand. He will interact with toys that play music or light up. He babbles, but is not yet saying any words.

Photos and videos are available.