
Jandron



This 10-year-old girl from Asia may be little, but she has made mighty strides in her life! Wendy was born prematurely, but she has shown the doctors and therapists who’s boss in her life–over the years she has caught up in motor skills and has even improved from being declared mentally retarded when she was small to upgrading her cognitive functioning diagnosis twice to now having borderline intellectual functioning and deficiencies in adaptive functioning. Don’t let this diagnosis mislead you though–she has satisfactory self-care abilities, she performs well AND at a higher ability than her peers at her special school, and this girl has a wonderful ability to draw and dance!
The agency has additional information available for inquiring families!

Mike has polymalformative syndrome, complex congenital heart disease, agenesis of the left radius and thumb, agenesis of the right kidney, psychomotor developmental delay, intestinal malrotation, and asplenia, for which he receives prophylactic treatment. He has undergone several cardiac interventions, including pulmonary venous return, Glen surgery, and two catheterizations, and he is expected to undergo another catheterization and heart surgery (Fontan procedure) in the future.
He also has gastroesophageal reflux disease, treated with Nissen fundoplication, and a gastrostomy. Mike receives multidisciplinary care across pediatrics, nutrition, ENT, orthopedics, plastic surgery, child psychiatry, and gastroenterology, with upcoming appointments in genetics and developmental pediatrics. He takes medications including captopril, cetirizine, mometasone nasal spray, amoxicillin, vitamin D, and acetylsalicylic acid.
Mike is a courageous and resilient little boy, making progress every day with dedicated medical care and support.

Kevin has a global developmental delay; Prenatal microcephaly (cranial magnetic resonance imaging performed in September 2023);
Strabismus and decreased visual acuity – uses ocular prostheses and alternating occlusion
Genetic testing was performed. The results indicate that the child is heterozygous for the identified variants. This does not confirm, but also does not exclude, a possible diagnosis. Analysis of copy number variation (CNV) coverage data did not detect any large deletions or duplications that could explain the patient’s phenotype. A genetic consultation has been requested and is pending.

About Josh:
Josh is a sociable, playful 4th grader who loves hugs, laughter, and outdoor adventures. He enjoys football, walks, and beach outings, and is independent with eating and personal care. Josh has ADHD and receives support for focus and learning, showing great progress in language and social skills.
About Vance:
Vance is a calm, sweet little boy who enjoys quiet play, cartoons, cars, and short walks. He has a gentle personality and is well-adapted to his preschool environment. Vance is healthy overall and continues routine medical follow-ups.
Their bond:
These brothers have been through a lot together and provide each other comfort and companionship. They would thrive in a loving, patient home where their sibling relationship can remain strong.
Josh and Vance are looking for a family that can offer stability, warmth, and support, giving them the chance to grow, play, and flourish together. If your family might be a fit for Josh and Vance, please reach out — the agency would love to share more about these special brothers!

He is physically fit and eagerly participates in all activities: bike trips, swimming, and bowling. He is a very bright boy and has no behavioral issues. He has a very good manners and rich vocabulary. He is a student of the 4th grade this year. He made a good progress at school and his motivation just visibly increased. The boy attended remedial classes at the clinic, made great progress in education, and his motivation to learn at school has visibly increased. He is good with writing, can solve the math problem and has difficulties with memorization. He feels good of being an “expert”, then he can be very involved and eager to act. He is polite and helpful at the place he lives, he treats the staff with respect, and he has an empathy toward young kids. He has many friends who appreciate his sensitivity and empathy, as well as his sense of humor.
Robin’s joy and carefree nature are sometimes overshadowed by a longing for someone close to him, for whom he would be important and special. He hides his emotions behind a tough exterior, but inside he is fragile and delicate. He lacks love and affection, which he compensates by hugging his teachers when he greets them.
Dakota: FAS suspected, microcephaly, facial dysmorphia, low weight, history of trauma and neglect
Dakota is a healthy, charming and cheerful girl. She is open and kind and eager to play with her peers. She is in the first grade this year. She has a vision impairment and wears glasses: -0.75 in both eyes. According to her teachers, she can be forgetful, has problem with concentration and needs to be motivated. However, she is eager to learn, work fast, she and is active in class. She is very artistic, likes to sing and dance. Often, she will come up with ideas of choreography, grab the microphone, and sing.
Dakota has an age-appropriate knowledge about the world around her, but her cognitive development is below average. She also struggles with math, and her results are lower than normal. She was tested for FAS and according to her pediatrician, she doesn’t meet the criteria for FASD. She is underweight, has microcephaly, and moderate facial dysmorphia.
For some time, the siblings were placed in two different institutions but since January 2026 they have lived at the same place. They are very close and Robin cares about his sister a lot. Since this year, they have been in the same institution. They are very close. Robin is a caring brother to Dakota.
The caregiver describes them as a very good and unique children. The brother is very mature for his age. They are both eager for being adopted. The boy has a plan in his head of what he wants to do with his new family, and his sister is dreaming of a good family who will love her. They want to be adopted together.

Sienna has a speech delay, although she has recently been eagerly repeating and saying words on her own. Some words are difficult to understand, but progress in speech development is evident. The girl also has difficulty understanding speech, but here too, progress is visible. She understands simple words, especially when they are supported by gestures. The girl can be engaged in a simple form of “dialogue” through play such as sharing toys. She is learning how to draw and eat independently using the spoon. She is able to pick up food cut into smaller pieces and put it in her mouth, although she does so slowly and uncertainly. She has difficulty biting off solid food and chewing it.
Sienna is a very cheerful and smiling child. She is speaking more and more – she can use many basic words, such as “give,” “more,” “come,” “yes,” “no,” “auntie,” and “hello.” She uses them in appropriate situations to express her needs and emotions. She recognizes various animals and can imitate most of their sounds.
Sienna to cuddle and read books. She participates enthusiastically in the group activities and enjoys walks. She responds to smiles, touch, and the voice of her caregivers. The girl has recently made significant progress in her emotional and social development. She is also able to initiate contact – she waves her hands in greeting, says “hello” in her own way, or responds with simple vocalizations. She is able to express her dissatisfaction, joy, or excitement and her progress is getting better and better in many areas.

Annie’s medical history includes a neurological condition with early-onset epilepsy (seizures are currently well controlled with medication), a syndrome of congenital anomalies with predominantly facial involvement, microcephaly, strabismus, and global developmental delays (neurological and psychological). She can stand with support but does not yet walk independently and has limited coordination. She loves interacting with caregivers and is a very sweet little girl.

Jay’s psychological assessment shows above-average intelligence. However, he tends to become easily frustrated and distracted, and benefits greatly from positive reinforcement to complete tasks and support his self-esteem. Jay has been diagnosed with ADHD.
Martin is 7, he interacts well with both peers and adults. He is described as friendly, affectionate, and somewhat stubborn, displaying occasional oppositional behavior. He benefits from an assertive and consistent approach from adults and requires positive reinforcement to complete tasks and boost self-esteem. His psychological evaluation shows average cognitive functioning.
Martin has a history of sleep disturbances and oppositional behavior. He currently takes melatonin and risperidone, which have improved his sleep and behavior stability. Medically, Martin underwent adenoidectomy and bilateral myringotomy in November 2023 and continues ENT follow-up due to a ventilation tube in his right ear. He wears glasses for astigmatism and is followed in Ophthalmology. He also attends speech therapy.
Martin is described as emotionally immature, showing attention-seeking behaviors likely linked to early emotional neglect. While initially reserved, he eventually engages warmly and responds well to structured interaction.
Ian is nearly 6 years old. He is a cheerful, affectionate, and communicative child. He attends kindergarten, where he engages positively with adults and peers. Like his brothers, he seeks attention and affection, and shows signs of emotional immaturity—likely the result of early emotional abandonment.
His developmental assessment showed results within the expected range for his age. Ian is described as enthusiastic and motivated, both in structured tasks and in everyday interactions. He responds warmly to attention and maintains appropriate eye contact and spontaneous speech for his age.
Ian was referred to Neurosurgery for dolichocephaly, but surgery was not recommended as the condition does not affect cognitive development. The team attempted to obtain a second opinion, but there has been no follow-up from the consulting doctor. He was also discharged from ENT in March 2024 after an adenoidectomy, and continues to be followed in Ophthalmology for astigmatism, wearing glasses since December 2022. He currently attends speech therapy.
Jay, Martin, and Ian have not had the opportunity to form attachments to parental figures. Instead, their primary psychological and emotional bonds are with each other. As such, joint adoption is strongly recommended to preserve their emotional security and sibling connection.
All three boys have been informed about their adoption plan and have welcomed the idea. They no longer reference their biological family and are beginning to show anxiety and anticipation about the arrival of their new family. During their first meeting with the adoption team, the strong bond among the siblings was evident.

Kody: prematurity; attachment disorder – disinhibited type, in a child with low stimulation

During the 2024/2025 school year, Dolly attended the 2nd grade. She is well integrated into the school environment and enjoys going to school. She receives support from special education teachers and also benefits from Speech Therapy, Occupational Therapy, and Physiotherapy.
She also has chewing difficulties and is non-verbal. However, she shows some understanding of simple messages, such as recognizing when someone is calling her or playing with her. She makes sounds and vocalizes when engaged or entertained.

Yoshi was removed from his family at a young age, due to their lack of ability to provide adequate care. Yoshi presents with a complex medical profile requiring ongoing attention and care. His primary diagnoses include: Neurodevelopmental delay: affecting various areas of growth; Macrocephaly: disproportion of the skull/face and minor facial dysmorphisms; Muscular Hypotrophy: specifically noted in the lower extremities, though they are symmetrical; Growth Concerns: short stature and low weight, previously hospitalized for protein-calorie malnutrition; Expressive Language Disorder: significant difficulties in verbal communication; Cardiac Concerns: possible pulmonary valve insufficiency and mild tricuspid insufficiency (syndrome under study). He has a history of hospitalization for respiratory infections (pneumonia) and malnutrition but has stabilized under current care. He has no known allergies. His current medical regimen includes nutritional support. His vaccination schedule is up to date for his age.
Yoshi faces several developmental challenges. He exhibits a significant delay in verbal expression. His vocabulary is limited, and he struggles with pronunciation, articulation, and structuring sentences. He primarily uses gestures and short words to communicate. While he has shown improved mobility, he experiences difficulties with gross motor skills such as running, jumping, and climbing stairs. He exhibits generalized hypotonia and issues with balance and coordination. He has cognitive difficulties understanding complex instructions. He is currently working on sphincter control and still requires diapers. However, he is showing progress in independence, such as using a spoon during meals.
Despite his challenges, Yoshi possesses a warm and engaging personality. He is described as an active, affectionate, and receptive child. He shows a genuine interest in social interaction and engaging with the world around him. Yoshi has an adequate capacity to form bonds with significant adults and is progressively learning to interact with peers. He enjoys group play and is capable of sharing toys. He tends to express his emotions clearly through facial expressions and gestures. He thrives in environments where he feels emotionally secure.
Yoshi is a child with distinct likes and dislikes that help define his daily life: He has a strong preference for symbolic and construction games. He enjoys recreational activities, particularly playing ball, searching for elements, and visiting parks or rivers. He enjoys fruits such as bananas, watermelon, tangerines, and oranges. He dislikes pineapple and chopped papaya (though he accepts papaya in juice form). He benefits from a structured sleep routine, sleeping easily and restfully, which contributes positively to his mood and willingness to participate in daily activities.
Yoshi requires a parenting style that combines deep affection with structure. His ideal home will prioritize his medical and therapeutic needs—including ongoing nutritional support and developmental therapies—while providing an emotionally safe and orderly environment.

She successfully manipulates toys, grabs and pulls objects, and looks at them. Her orientation is preserved. The child moves her gaze from object to object, looks for the source of sound, and follows the movement of people and objects. She focuses on illustrations in children’s books. She looks for objects that disappear from view.
Her communication skills continue to progress. The girl actively vocalizes and syllabifies, using her own speech more and more clearly. She does not speak, but understands repeated words, mainly those with emotional connotations. She displays appropriate social behavior. She responds to smiles and voices with smiles and vocalizations. She is responsive to changes in facial expressions. She listens to what is said and responds to her name. She willingly cuddles with her caregiver, initiates contact with adults she knows, and maintains an appropriate distance from strangers, as is appropriate for her age.
She does not use pointing gestures, but she does use gestures to express emotions and imitates clapping. She is interested in her reflection in the mirror and laughs. She is reactive to the presence of others. The girl actively seeks attention and initiates interaction with people around her. She plays with her peers. She maintains a daily rhythm and has a normal appetite. She drinks from a cup, is fed with a spoon, and tries to eat solid foods on her own.
Update November 6, 2025: Little Ember started walking today!

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).

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.

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

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 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.

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.

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.

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.

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 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 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 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’s listing agency also has video available!

The adoption agency has additional photos and videos available.

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!

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 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.

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.

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.

https://vimeo.com/maaspecialkids/maa-alfie
Password: Adoptmaa
Agency fee reductions may be available based on the adoptive family’s circumstances.

Photos are available through the agency for qualified families.


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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/
https://vimeo.com/
https://vimeo.com/
https://vimeo.com/
Password: Adoptmaa

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.



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.


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.

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.

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

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 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.

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.
