Malachi #

Boy, Age: 2
Primary Diagnosis: Hydrocephalus
Posthemorrhagic extreme internal hydrocephalus; implantation of a ventriculoperitoneal shunt (VPS). Bronchopulmonary dysplasia. Retinopathy of prematurity
Listed: Feb 2025
$90.00
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!
He lives in a home for medical and social childcare. He was born to a minor mother who had epilepsy and took anti-epileptic medications during pregnancy. There was a complicated pregnancy and birth, resulting in extreme posthemorrhagic hydrocephalus. A shunt was implanted but failed. A new one was inserted. Malachi is on permanent antiepileptic monotherapy, without convulsive manifestations.

Due to the extreme hydrocephalus, Malachi is in impaired general condition, with significant lag in psychomotor development – no head control, does not turn around, does not sit or stand. He needs specialized care, monitoring by medical specialists, and daily medical rehabilitation. He is usually in a positive emotional state. He coos frequently and continuously. He reacts animatedly to the speech of an adult. He initiates a desire for physical contact by smiling. The boy is completely dependent on the care of an adult. His sleep is peaceful. He takes food with a pacifier. The agency has videos of him.

Owyn #

Boy, Age: 4
Primary Diagnosis: Hydrocephalus
Listed: Jan 2025
$25.00
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!
Precious Owyn is looking for a special family.

He is diagnosed with hydrocephalus and has some other medical issues that require in-depth care. The adoption agency has a lot more photos and more information about his needs and video footage.  A specific adoption agency also has grant funding in the amount of $2500 available.

Morty #

Boy, Age: 9
Primary Diagnosis: Epilepsy/ seizure disorder
grand mal seizures
Listed: Jan 2025
$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!
Morty is looking for a very loving family who has time to spend helping with his needs. He has been diagnosed with grand mal seizures and takes medication for this. He has other delays in all aspects of his development.  The agency has video available, for inquiring families.

Melanie #

Girl, Age: 5
Primary Diagnosis: Hydrocephalus, Spina bifida
spina bifida, hydrocephalus, psychomotor developmental delay, urinary incontinence
Listed: Jan 2025
$112.50
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!

Meet smiling Melly.   She had surgical treatment for correction of a meningocele.  A ventriculoperitoneal shunt was also implanted to treat hydrocephalus. Unfortunately after surgery Melly’s lower limbs are paralyzed.

Melly moves independently in a wheelchair. She can pull herself up with her hands She enjoys contact with children and adults.  She plays with toys, handles them, and can throw them.  Melly pronounces various sounds and syllables although she points to make her needs known. She can maintain interest in an activity for 15-20 minutes.

Hans

Boy, Age: 6
Country Code: LA-2
Hydrocephalus; Epilepsy; Cerebral palsy; Macrocephaly, hip dislocation; gastrostomy
Listed: Nov 2024
$41.20
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Information in this report is from November 2024

Hans was born to a young teenage girl who, tragically, had already given birth to a child at a very young age. Due to her chronological age and emotional immaturity the mother was not able to fully understand her responsibility, and despite the support of her family, the bond between Hans and his mother was not positive. After Protection Services became involved, it was evident that the biological mother and her family were not able to take care of the child due to his special needs, economic struggles and already caring for Hans’s older sibling. He, therefore, came into care at the age of 3 years old. There is no information about the biological father.

Hans is not enrolled in school due to his medical diagnoses. Hans loves to receive affection, and he responds through smiles. He is totally dependent on others to fulfill his daily routines. He communicates through guttural sounds, screams or by crying. Hans cries whenever his diaper is dirty. Hans´s gross and fine motor skills are not developed. The child cannot hold his head up, and he cannot crawl or walk. He has some body movements, and the foster mother has received training on how to stimulate his motor development. He does not like to be held and prefers when people change his body position without holding him for too long. Due to Hans’s medical diagnosis, he has a severe cognitive delay and is not able to interact with other children. Hans receives occupational, physical and speech therapy. Hans takes daily medication.

Hans likes to listen to soft music. He needs a family who can always take care of him due to the severity of his condition.

Elsa

Girl, Age: 12
Country Code: E-11
Region: Europe
Primary Diagnosis: ADHD, Learning Disability
attention deficit/Academic school disorder
Listed: Nov 2024
$2,191.00
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 lovely older girl has an ADHD/ learning disability diagnosis.  She could do great with a family to help her with her schoolwork!

Eloise

Girl, Age: 2
Congenital right clubfoot, Spina Bifida, Hydrocephalus- ventriculoperitoneal shunt, Congenital bilateral hip dislocation – hip reduction plus harness
Listed: Nov 2024
$135.00
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!
Eloise is a joyful, affectionate, and calm child, who enjoys the simple pleasures of life such as music, dancing, and storytelling. Her sunny disposition radiates through her interactions, whether she’s playing freely in the park, lying peacefully on the grass, or engaging with her peers. Despite any initial nervousness around new people, her warm and gentle demeanor quickly puts others at ease, leading to the formation of close emotional bonds, particularly with her foster mother.

Eloise’s ability to communicate her needs and emotions through gestures and sounds demonstrates her keen self-awareness, and her empathetic nature is evident when she comforts her loved ones. Though faced with medical challenges, Eloise has proven to be remarkably resilient.

VIDEOS:
https://vimeo.com/maaspecialkids/maa-eloise01
https://vimeo.com/maaspecialkids/maa-eloise02
https://vimeo.com/maaspecialkids/maa-eloise03
https://vimeo.com/maaspecialkids/maa-eloise04
https://vimeo.com/maaspecialkids/maa-eloise05
https://vimeo.com/maaspecialkids/maa-eloise06

Password:  Adoptmaa

Agency fee reductions may be available based on the adoptive family’s circumstances.

Mell

Boy, Age: 4
Country Code: LA-2
Primary Diagnosis: Hydrocephalus, Spina bifida
bilateral hip dysplasia with congenital hip dislocation, congenital hydrocephalus, lumbosacral meningocele corrected, congenital malformation of the corpus callosum, hypermetropy (far-sightedness), and malnutrition.
Listed: Oct 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!
Info from March 2024:

When Mell was born, his biological parents tried to take care of him even with his special needs, but they lived in a small town far away from cities and hospitals. At his one month check-up, he was diagnosed with congenital malformation of the spinal cord, hydrocephalus, low weight, fetal growth delay, and respiratory syndrome. At one of his following check-ups, the doctor sent Mell to the hospital due to a high fever and inflammation of the brain. Sadly, though they had tried, his parents recognized that they did not have the means of caring for him in the ways he needed, both due to finances and distance from necessary medical care, and they asked Protective Services to care for him. No other family members were able to provide the care he needed as well. Mell was placed in a foster home and is doing well.

Mell has been receiving various types of therapies which have been valuable in his development. When meeting adults for the first time, he becomes shy, but he recognizes familiar people and loves to interact with them. Mell identifies the emotions on people´s faces and interacts accordingly. He is a very expressive child who shows affection in various ways, and sometimes gets jealous when his foster mother gives affection to the other children. According to the professionals who care for him, Mell has the language development of a 12-month toddler. He communicates through crying and screaming and can say some short words such as “mama” and “papa.” He also imitates animal sounds, such as those of a dog or cat. He responds to simple instructions such “Take this” and “Give me that.” Mell identifies different body parts, plays with Play-Dough, and performs other activities that strengthen his fine motor skills. His movements are spontaneous despite the limitations he has in his lower limbs.  Due to his chronological age, Mell requires support, supervision, and guidance to fulfill his daily routines. Mell takes two naps during the day and sleeps throughout the night. He wears diapers all day.

Mell likes to interact with peers or adults and loves to spend time outside. He gets excited when he hears a motorcycle engine as he immediately thinks he is going to go out and gets anxious. He gets upset when his diaper is dirty and when he is not allowed to go out. Mell gets happy with simple things, and he likes to laugh a lot. Mell loves to drink sweet juices. Due to his medical condition, he does not wear shoes but wears very soft socks. He enjoys it when adults help him to kick the ball to play soccer. Mell also likes to play with cars and airplanes.

Nate

Boy, Age: 5
Country Code: LA-7
Primary Diagnosis: Cerebral palsy
Premature birth, Cerebral palsy
Listed: Sep 2024
$32.50
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!
Information in this report is from Summer 2024:

Nate was born prematurely at 27 weeks gestation and was hospitalized for two months. After living with his mother for two months, he came into protective care at 4 months old after his mother abandoned him in the care of a neighbor. Initially she visited him occasionally, but the last visit was in 2022. Nate lives with a foster family.

Nate has unidentified cerebral palsy, but it doesn’t hold him down! While at 8- months-old he showed significant delays in neuro-psychomotor development, today he has shown significant development. He is being monitored a team of specialists including a neuro-pediatrician, orthopedist, physiotherapist, psychologist, speech therapist and nutritionist, in addition to receiving specialized educational care. Nate can now move around with some independence and is in the process of adapting to the use of an orthotic equipment, which may help his locomotion. According to the physiotherapist’s report, Natey crawls, sits in a W position with balance, stands with support and walks sideways. He has the potential to use a walker for home distances and a wheelchair for community distances.

Socially, Nate is an extroverted child who loves to participate in activities and communicate. He can focus on activities. He understands what is asked of him and responds coherently within his ability. He demonstrates caring and affection with other children and adults. He is observant to what is going on around him. Nate lives in a house where there are children younger than him and this fact limits his social interactions, which has significantly compromised his progress.

It is believed that Nate has great potential for development, as long as there is proper stimulation. The possibility of starting family life through adoption at this time is considered extremely important for the progress of the child’s physical, social and cognitive development.

Bowie #

Boy, Age: 8
Vision issues, cerebral palsy, seizures
Listed: Sep 2024
$31.50
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!

Please meet this cute boy named Bowie.  He was diagnosed with congenital cataracts in both eyes.   However he underwent surgical treatment with implantation of intraocular lenses. There is suspected Glaucoma.  He is also diagnosed with Children’s cerebral palsy – Quadri pyramidal syndrome. Grand mal seizures with or without petit mal seizures.

Bowie can sit up independently from a lying position. He can stand up by holding on to various objects. He walks independently but it is uncoordinated. The child lags in neuropsychological development. He accepts bodily closeness with pleasure.  It is pleasant for him to be held by an adult. The presence of children in his immediate space does not bother him, but he does not show interest in them and does not initiate interaction. He is soothed by riding in a pram or listening to favorite children’s songs.  He prefers the environment to be quiet.  He becomes nervous and anxious around loud noise.  He is entirely dependent on the care of an adult.

Bella #

Girl, Age: 9
Primary Diagnosis: Cerebral palsy
Her multiple special needs include Cerebral Palsy and severe quadriparesis.  She is also severely delayed mentally.
Listed: Sep 2024
$1,043.50
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!

Look at the sweet smile on Bella!  Bella spends the majority of the time in her bed or in the special stroller that she can be pushed in.  She is often fed in the stroller as well.  She is fed with a bottle.

Agency staff member said the following:  Given the fact that only a rehabilitator is currently working with the child and the staff at the Home only have time to cover her basic needs, it is definitely very difficult to say to what extent the little girl has developmental potential. In my opinion, Bella liked it when she received personal attention such as being spoken to gently, being teased by me or by my showing her different toys. She had been working on a smile during that time.  Most of the time, both her arms and legs were in motion, and she even managed to roll over in bed. She needs a lot of love and attention and systematic and purposeful activities with specialists.

Samson #

Boy, Age: 3
hydrocephalus, spina bifida in the lumbosacral area –condition following implantation of a VP shunt and closing of the spinal defect; lower flaccid paraplegia; pelvic reservoir incontinence; delayed psychomotor development; delayed psychological development.
Listed: Aug 2024
$1,015.00
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!

Update Nov 2024:  Samson was recently moved from a large orphanage to a small group home for children with disabilities. He  loves attention and responds with joy with staff interacts with him. He is described as a calm and radiant child.

Samson sits independently and can stay in this position for extended period of time. He reaches for distant toys by directing his hands and turning his torso towards the desired direction and after that he pulls the toy. He prefers toys with buttons, which make sounds, light or melody, as well as toys with movable elements, which he can spin. He initiates interactions with adults, whom he likes and with children. Samson enjoys being praised and reacts with discontent when something is being denied or forbidden to him. He is fed via baby bottle and spoon.

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.

Nany #

Girl, Age: 3
Primary Diagnosis: Blind / VI, Cerebral palsy
Nany has retinopathy of her left eye, cerebral leukomalacia with manifestation of spastic quadriparesis, bronchopulmonary dysplasia and asthma.
Listed: Apr 2024
$1,356.70
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!
Nany was born with an extremely low weight and a complicated neonatal period. She has retinopathy of her left eye, cerebral leukomalacia with manifestation of spastic quadriparesis, bronchopulmonary dysplasia and asthma. This sweetie needs a very special family.

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

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

Ivan #

Boy, Age: 8
Primary Diagnosis: Behavior, Deaf / HoH
Hearing loss, scoliosis
Listed: Mar 2024
$90.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Someone who met Ivan recently said he is an “extremely active, agile and very cute boy who loves attention as well as cuddles.” Ivan seems very happy and smiles a lot. He is said to have age-appropriate physical development.

Ivan has a moderate mental delay with hearing loss in one ear. He also has scoliosis of the spine. He can walk, run, climb and descend stairs alone. Ivan does not speak however he enjoys watching children’s movies. He prefers to play alone. He can feed himself and drinks from a cup. The staff is working on potty training with him.

The agency has a video of Ivan, from Feb 2024.

Update 8/2024

Ivan was born in 2016 and resides in a family-type accommodation center for children. He is a child of Roma origin. The parents consented to full adoption, due to the
inability to care for him. Diagnoses include moderate mental retardation, behavioral disorder, expressive speech disorder with hearing impairment – unilateral conductive hearing loss in one ear. Normal hearing with the other. Scoliosis. He has normal physical development for his age and is in good health. He walks independently, with an unsteady gait, goes up and down stairs alone, runs. Fine motor skills are poorly developed – knows how to match elements, string figures on a rope with help. He feeds himself, holds a pencil with his whole palm and scribbles on the paper, does not know how to draw, does not know how to color, does not know colors, does not know how to cut with a knife, does not arrange a constructor and a puzzle.

He rarely responds to his name. Positive emotion is expressed through a smile. When he is cheerful, he laughs loudly. He shows stubbornness and impatience but does not show
aggression or auto-aggression. He has no developed speech. He understands what is being said to him, recognizes the tone. Feelings are expressed through whining, crying, laughing. No expression of interest in anything specific is observed. He watches children’s movies. He loves attention from an adult. Does not play with peers. Eye contact is not complete. He likes to be hugged. He likes strollers, tries to play with them, prefers to hold them in his hand. Chase and kick a ball. Loves light up toys. He likes to spend time outdoors. During the academic year 2024-2025, he will be in 1st grade with an independent form of education.

He has a peaceful sleep. He knows how to feed himself; he knows how to drink from a cup, he does not know how to dress and undress himself, put on and take off his shoes by himself, but he must be asked. He does his physiological needs in the toilet or potty after prompting, he does not use a diaper.

Philip

Boy, Age: 11
Country Code: E-11
Region: Europe
Primary Diagnosis: Down syndrome
Listed: Feb 2024
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
Philip is a charming and inquisitive young boy with a tender heart and a keen interest in the world around him. Although language poses a challenge for him, with difficulties in speech and vocabulary, he is able to understand simple directions and express himself with basic sentences. His abilities in non-verbal communication are a strength, helping to support and enhance his spoken words. While written language and abstract concepts such as time and money are challenging for him, his non-verbal skills greatly aid his interactions.

Despite facing motor skill limitations typical of his condition, which affect balance and coordination, Philip is remarkably independent in day-to-day activities. He can manage personal care routines such as eating and hygiene with minimal supervision and dresses without assistance, though may require guidance in selecting suitable clothing based on weather conditions. Philip sleeps well and follows a regular routine but benefits from support in other daily tasks.

Among Philip’s favorite activities, he relishes the simple pleasures of walking, drawing, and engaging with the world of letters and words in his own unique way—he enjoys “writing.” Although the marks he makes may not form recognizable words, he delights in having adults “read” his creations. He has a passion for football and admires players like Cristiano Ronaldo and Lionel Messi.

His social interactions are an area where Philip truly shines. He is strong in building relationships with those around him—proactive and animated with peers, demonstrating a particular fondness for younger children. When it comes to adults, Philip is affectionate and seeks connection and warmth, establishing bonds with preferred caregivers and understanding the importance of rules and boundaries.

Philip is ready to embrace a loving family who will understand and respond to his emotional needs. His new family should be prepared to provide the unique care required in cases of Trisomy 21, which includes attention to his medical needs like heart conditions and vision care, as well as understanding his background and history. This family will receive in Philip a child who offers boundless warmth and the potential for rewarding growth and connection.

Marcy

Girl, Age: 6
Country Code: EE-2
Primary Diagnosis: Craniofacial disorder, Deaf / HoH
Listed: Nov 2023
$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!
Marcy is a 4 year old girl with frontal craniostenosis and tuberous sclerosis. Marcy was diagnosed with conductive and sensorineural deafness. Non-orbidity of both eyes. The girl currently does not use corrective glasses, as recommended by ophthalmologists. She is generally cheerful, and is able to imitate gestures and independently eat meals. She struggles with dressing herself and identifying some shapes and colors. Marcy is able to respond to simple commands and messages. She enjoys playing with toys and demonstrates improvement in her coordination. She is very patient and kind. It is recommended for her to wear glasses. Her speech development is delayed, but she can still communicate, and she has demonstrated improvement. Above all she is a nice girl with very many good qualities.

Liam #

Boy, Age: 5
Primary Diagnosis: Arthrogryposis
congenital multiplex arthrogryposis
Listed: Oct 2023
$948.50
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Liam works with a physical therapist every day. The PT also acts as a primary caregiver most days and is the adult that Liam is the most familiar with in the orphanage. Liam has recently gained head control and can now lift and hold up his head when on his stomach. He reaches for toys and other desired objects. He attends to toys and electronics (will focus on a video on a phone). He rolls to try to get to toys on a mat. He is very attentive to his environment. He drinks from a bottle and eats pureed foods from a spoon. He prefers fruit puree and other sweeter flavored foods. A team member who visited him said, “He is a lovable little guy who shows lots of potential and ability for emotional attachment.”

Maeve

Girl, Age: 8
Country Code: EE-2
Listed: Sep 2023
$500.00
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!

SN:  Moderate intellectual disability, Asperger’s syndrome, sensory hypersensitivity

Maeve is a six year old girl with moderate intellectual disability and Asperger’s syndrome. She attends a kindergarten where she receives therapy for movement, speech, and autism. She had disorders in speech, balance, and coordination. She gets anxious when on unstable ground. She has been making tremendous improvement lately. Maeve struggles with sensory hypersensitivity. She is capable of building relationships with her peers and caregivers.

Despite being able to communicate verbally, her speech used to be unclear, but lately it has improved tremendously. Recently, she has become more and more independent. Maeve stands out from the rest of the children at the orphanage.

Nilo #

Girl, Age: 13
Primary Diagnosis: Limb differences
Cognitive Delays
Listed: Aug 2023
$1,092.50
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!
Nilo resides in a professional foster family. She has a congenital absence of her right forearm. Nilo is educated according to the Individual Study Plans of Students with a lower degree of complexity than the educational minimum for the calendar age, tailored to her individual needs. At a moderate pace, with individual help and guidance from the
teacher, she acquires knowledge, skills and competences foreseen in the individual curriculum for each subject of the individual curriculum. The girl distinguishes between the categories of good and bad, she knows generally accepted rules of behavior in social communication. She defines and expresses own desires and needs in words.

Nilo has diverse interests.

Nilo experiences attachment to children and therapists. She is sad when separated from someone. She seeks contact with adults, classmates and older students and engages in joint activities with them, she participates in role-playing games. She has mastered the social role of a student and classmate. Nilo helps her classmates when she sees that they are having a hard time. The comfort zone is the classroom and Montessori room.

The child communicates verbally, expresses wishes, and is often persistent about them, especially about things that spark her interest. When asked a question, she needs time to think about it and reproduce an answer; she constantly asks questions and seeks approval. The answer is not always adequate to the situation. She doesn’t always
understand the meaning of what was said and the execution of a relevant instruction.

Nilo likes a variety of toys, and she possesses different ones. She can play with other children and is cooperative, she shares her belongings. Nilo has developed self-service skills and readiness for academic work. She has established hygiene habits. She eats independently; dresses and undresses; unfastens and fastens; puts on and takes off shoes; she knows the parts of clothing. She can’t tie shoelaces.

She can say that she is in a foster family and that the foster mother raised her. The girl partially understands that foster care is temporary. She listens and accepts information related to the possibility of being adopted and meets potential adoptive parents, but still, she cannot imagine living in a different place.

Ariana

Girl, Age: 8
Country Code: LA-3
Primary Diagnosis: Epilepsy/ seizure disorder
epilepsy; congenital hypothyroidism without goiter, and mild cognitive delay
Listed: Jun 2023
$1,015.00
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!
Ariana is a young girl waiting for a loving family of her own.

NEW VIDEO

OLDER VIDEO

Password: Adoptmaa

There is a $500 agency fee reduction for Ariana’s adoption. Additional agency fee reductions may be available based on the adoptive family’s circumstances.  If you are interested in reviewing Ariana’s file or in adopting Ariana, please contact the agency for additional information.

Elon #

Boy, Age: 10
Primary Diagnosis: Arthrogryposis
Arthrogryposis, delays in development
Listed: Oct 2022
$1,402.26
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!
Elon walks independently. He feeds himself and cleans up after his meals. He does not talk at this time, but understands what is said to him and follows simple instructions. He responds to his name. He interacts appropriately with adults and with other children. He attends to tasks and works well 1:1 and in a small group.

Lena

Girl, Age: 10
Country Code: EE-7
Primary Diagnosis: Down syndrome
Listed: Oct 2020
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
$2,697.24
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 girl with Down syndrome is described as brave, loving and interested in activities. She adapts well to a new environment and enjoys coloring, painting, musical activities, singing and playing with toys and dolls. She is developmentally delayed and needs a loving family to help her reach her full potential.