Jana

Girl, Age: 8
Country Code: LA-2
Edwards Syndrome (Trisomy 18 by translocation) and pulmonary dysplasia, fully dependent on oxygen. Epilepsy, gastroesophageal reflux without esophagitis, nausea and vomiting, urinary tract infection, gastrostomy, congenital malformation syndromes associated mainly with short stature, hypothyroidism, and spastic cerebral palsy.
Listed: Oct 2024
$610.00
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 March 2023 when Jana was 5. The adoption agency has medical records and pictures for Jana dating back to 2019.

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

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

Declan

Boy, Age: 8
Country Code: LA-2
Primary Diagnosis: Down syndrome
Down syndrome
Listed: Oct 2024
*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***
$841.50
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!
Our sweet Delcan, was born in May of 2017 with Down Syndrome. We are so excited to share his referral with interested families.

There is a $1,000 agency fee reduction for Declan’s adoption with a specific agency. Additional agency fee reductions may be available based on the adoptive family’s circumstances.

VIDEOS:
https://vimeo.com/maaspecialkids/maa-declan10
https://vimeo.com/maaspecialkids/maa-declan11

Password: Adoptmaa

Rose and Sawyer #

Sibling Group
Ages: 17, 16
Listed: Sep 2024
**** I am eligible for a $500 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount. To inquire about this child, email childinquiry@reecesrainbow.org ***
Rose
Diagnosis: school skills disorder
SAWYER
Diagnosis: school skills disorder. Other mixed behavioral and emotional disorders

Kevin #

Boy, Age: 4
Primary Diagnosis: Hydrocephalus, Spina bifida
Congenital anomaly of the nervous system: internal hydrocephaly; condition after ventriculo-peritoneal anastomosis implantation. Holoprosencephaly. Lumbosacral spina bifida aperta; condition after plastic surgery. Lower flaccid paraplegia. Pelvic-reservoir incontinence. Delayed neuro-psychic development
Listed: Sep 2024
$1,614.00
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!
Kevin can sit on his own. He plays with toys. He interacts positively with caregivers. He makes some sounds, but is not yet saying any words.

Nate

Boy, Age: 6
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.

Eleanor

Girl, Age: 11
Country Code: EE-11
heterozygous variant in the KAT6A gene. Heart issues, global developmental delay, severe language delay
Listed: Sep 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!
Eleanor is a beautiful young girl who needs a family.

Bowie #

Boy, Age: 8
Vision issues, cerebral palsy, seizures
Listed: Sep 2024
$51.50
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.

Mira #

Girl, Age: 11
Primary Diagnosis: Trauma History
Listed: Sep 2024
Mira is physically healthy. She lived in a neglected environment for the first 7 years of her life. She has delays in her speech, but she understands everything said to her and speaks in short sentences. She is in 2nd grade in school (in her country, children start school at age 7). She can read and write. She plays the piano and enjoys the lessons. She says when she grows up, she wants to a police woman and a piano player. She has good self-help skills and no behavior concerns.

Brandon #

Boy, Age: 6
Microcephaly. Hydrocephalus. Agenesis of the left hemisphere, persistent foramen ovale, Interatrial defect and Schizencephaly.
Listed: Sep 2024
$2,053.40
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 Brandon; he has multiple special needs. Sadly Brandon relies totally on the care of others.  He sleeps in a room with four other children.  The caretaker says he seems to like music and likes the bath.  He can make some sounds for speech.  He has difficulty feeding and swallowing.

The agency staff member that met Brandon said the following:  “According to the caretaker, there is a slight regression, especially in terms of feeding. Unfortunately, I have not been given an opportunity to speak to any of the specialists engaged with the boy and possibly what exactly they are working on. Brandon could have some potential, but it’s very hard to tell.  In any case, he needs a lot of love, a lot of attention and a lot of activities.”  Could you be the family for Brandon?

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
$2,043.50
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!

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.

Pah

Boy, Age: 5
Country Code: Asia.4
Region: Asia
Listed: Sep 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!

Pah is a lovely little 4-year-old boy in need of a permanent home. He has been with his foster family since he a little baby. He is bonded to his foster family as well as another foster child in the home who is 3 months younger than him.

Pah currently is in good normal health. However, when Pah was 22 days old he showed peripheral pulmonary artery stenosis, small patent foramen ovale (PFO), and secundum atrial septic defect 1.5 mm. On the follow-up echocardiogram in April 2022, the results showed normal heart anatomy and function. As of his August 2024 child checkup, his hearing and vision were reported to be normal. While Pah’s physical health remains good, he has been diagnosed with Autism Spectrum Disorder (ASD) in August 2023, for which he attends Child and Adolescent Psychiatry therapy. During the same evaluation, he was assessed to have a mild delay in gross motor skills as well as a mild delay in oral language. He had been previously diagnosed in 2022 with Borderline Developmental Delay. As observed, he can speak clearly, except that he may mispronounce some words.  He is able to hold conversations with adults and express his needs and feelings in sentences.  He can also follow instructions. Pah receives speech therapy about 2 times per month, and physiotherapy and occupational therapy 3-4 times per year at school. Pah can walk and run confidently.  He can jump forward 12inches with both feet, stand on one leg, walk upstairs and downstairs with alternative feet by holding onto the handrail, throw and catch a ball, and kick a ball forward 5 feet away. He can also climb up the rope net.  In terms of fine motor skills, Pah can build a tower of 9 blocks, remove bottle caps, hold a pen to draw, turn pages one by one, and thread beads.

Pah is described as a happy, outgoing but also stubborn child who has shown improvements in his emotional expression. He has become more accepting of reasoning as he gets older. Due to his ASD features, Pah has a set way of doing things. He also tends to cry easily over trivial things such as when he cannot find a toy or complete a task on his own. Pah shares a normal relationship with the other foster child in the home. They have typical sibling-like rivalries and will sometimes fight over toys. He shares a close relationship with the foster mother and accepts her guidance and follows her instructions. Overall, Pah is generally an easy child to take care of. He is well-behaved and manageable most of the time except that he tends to cry easily and can also be quite stubborn at times.

Pah performs well in his self-care tasks. Being able to drink from a cup and a straw, he can feed himself with spoon and a fork. He can wash and dry his hands with a towel; put on and take off his clothes, shoes and socks; brush his teeth and wash his face. He has finished toilet training and does not need to wear diapers. He can go to the toilet by himself. He only needs assistance in bathing, washing his hair and cleaning after a bowel movement.

Pah is attending pre-kindergarten at a nursery school.  As described by the teacher, Pah has some close friends at school and enjoys a satisfactory relationship with his teachers. He can follow school rules and routines.  Being attentive in class, he enjoys participating indifferent activities.  As described, Pah is sometimes sensitive to the teacher’s reminders and sometimes is emotional about this. Pah knows lots of colors, shapes, fruits, animals, food and body parts. He also knows some concepts such as “big-small,” “up-down,” etc. He can recite the numbers from 1 to 50 and recognize some letters and numbers. He can tell others his name and age.

Families with a home study prepared for any international country can submit for consideration of Pah. The agency program specialist can explain the child/family matching process in his country.

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
$5,188.00
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!

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.

Salazar #

Boy, Age: 10
Mild to moderate mental delay. Delay in expressive speech. Hyperopia. Astigmatism.
Intermittent heterotropy. Low birth weight, moderate mental delays
Listed: Aug 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!
Salvador has resided with a foster family since July 2018.

He was born with low weight and with pathological neonatal period. The child has a
physical development within the lower limit of the norm and mental delay in mild to moderate degree (IQ-41). Phrase speech is not developed, he utters single words; lags behind in the development of habits, skills, emotional and social development.
Uses optical correction due to intermittent heterotropy and astigmatism of the eyes.

The child walks stably and independently. There is delay in the development of the fine motor skills. The emotional status of the child is mostly positive – he is calm and curious. He does not show aggression, he is adaptive. He understands phrasal speech, utters single words, but does not speak. The child is able to play by himself, but he also is looking for the company of other children. Participates in the game process. He feeds himself, his personal hygiene is well-maintained. He controls physiological needs.

Roman

Boy, Age: 13
Country Code: LA-2
anxiety disorder; unspecified emotional and behavioral disorder
Listed: Aug 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 ***

Report is from August 2024 — Roman, 12, lived with his biological and an older brother until he was 7 years old. At that time, the place where his mother worked burned and she had to leave his brother with that child’s father, and she moved to a different town with Roman. Unfortunately, she could not find a stable job or place to live and she sought assistance from Protective Services. Roman was previously hosted by a family, but that family opted not to adopt him. More information is available.

Roman is in the 4th grade. It has been observed that Roman has great leadership skills, especially at school. Most of his teachers have stated that Roman has a lot of potential but his lack of motivation hinders his progress and development. However, Roman has great skills in math. He recognizes authority figures; he is respectful and obedient towards them. He can follow simple and complex instructions. There are no concerns regarding his motor, language, cognitive and social development.

Roman is an affectionate child after he has built a positive relationship with an adult. He can verbally express his feelings and emotions; however, when there are situations of high emotional demand, he limits the externalization of what he is feeling. Roman is still learning to manage his frustration and impulses, but good improvements have been observed. Roman is shy when meeting people but can easily overcome this behavior once he feels the adult is trustworthy. He interacts in a positive way with adults, peers, younger children, and animals. Roman gets anxious when he does not get what he wants immediately or when something he was expecting does not end up happening. Roman is sad when remembering his biological family, and this connection is part of why the hosting family did not choose to adopt him. Roman is afraid of dark, thunder, rain, and heights. In order to fall asleep, he needs some light or a stuffed animal.

Roman loves it when he gets to go to amusement parks, the movies or the pool. Roman likes to ride his bike, listen to music, and watch TV. He has stated that he would like to improve his drawing skills.

Sal & Monty

Sibling Group
Ages: 11, 9
Country Code: LA-5
Primary Diagnosis: Trauma History
Listed: Aug 2024
$788.00
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!

Sal and Monty are eager to go to a family as soon as possible! These brothers from Latin America are currently 8 and 7 years old.

Sal and Monty came into care in late 2020 after their teacher reported noticing repeated physical injuries with one of the children. At that time, protective services investigated and found that the children living with their mother who had previously lost custody of them due to abuse when Sal was only a year old.

Sal

Sal is currently 8 years old. He is predominantly affectionate, sociable, and respectful. He likes to play and interact a lot, and he is very interested in learning new things and being accepted by his peers. He shows autonomy and confidence to perform routine activities by himself, and he only asks for help for the things he cannot manage. He is well bonded with his younger brother. He expresses affection toward Monty, plays with him, and is attentive to his well-being. Sal is currently enrolled in a Montessori school and is in the 3rd grade. He continues to work on following the rules and order within the environment. Sal has a tendency to downplay incidents where other children have been aggressive or abusive toward him, and he often does not report such incidents to adults. He tends to normalize these types of negative rough or violent interactions and does not remove himself from the situation. However, the caregivers have been working with him on this situation and he is improving as well as learning measures on how to protect himself from any abusive situation.

Sal has been diagnosed with attention deficit hyperactivity disorder for which he is taking medication. He suffers from atopic dermatitis, has dry skin on his cheeks, currently treated with symptomatic management with the use of moisturizing creams. The child has compound hypermetropic astigmatism and currently wears glasses.  He also has a low weight and height for his age.

Monty

Monty is 7 years old little boy who is described as kind, giggly, and playful. Monty is also enrolled in the Montessori school with his brother and he is in the 2nd grade. At school, he is polite and cordial as he is at home, establishing effective bonds with his classmates and guides. He has a stable mood and is affectionate with his caregivers and most people at the foundation where he lives. He is also able to communicate things that bother him and stand up for himself. He has a good relationship with his older brother Sal, trusts him, and likes to be taken care of by him. His favorite activities are playing soccer with his brother, drawing, and playing video games. His favorite characters are Hulk and Spiderman.

Monty was evaluated by neurology after presenting motor coordination with lag and decreased strength in his lower limbs. A decrease in the strength of both legs with frequent falls was identified, with no apparent alterations in sensitivity. Sensory and motor neuro conduction velocity studies and electromyography of bilateral tibial and peroneal nerves were performed, resulting in a diagnosis of severe sensory-motor polyneuropathy for which he requires follow-up by neurology and rehabilitation (to read about this condition, visit this site:  Sensorimotor polyneuropathy: MedlinePlus Medical Encyclopedia. He has also been diagnosed with mixed astigmatism and low weight/height for his age.

Hope

Girl, Age: 12
Country Code: Asia.4
Region: Asia
Primary Diagnosis: ADHD
Listed: Aug 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 ***

Hope is a bright, assertive, and courageous girl with many endearing qualities and undiscovered traits. She is highly active and enjoys a range of sports activities, including running, swimming, and hiking. In her spare time, she loves engaging in craft work like origami. Her recent obsession with Sudoku has highlighted her strong logical thinking skills.

Despite facing challenges such as eczema, ADHD, and ODD, Hope is managing with her prescribed care routine. She thrives better with individual attention and consistent, firm, yet gentle care. She has shown significant improvement since being moved from an orphanage to her current foster home where she is adhering to rules and routines, and slowly learning how to live in a family atmosphere.

Hope was previously approved for adoption overseas. However, due to concerns the family had regarding her psychological/mental health once in-country, they withdrew their petition to adopt. A further report about Hope’s emotional development and readiness for adoption after the previous withdrawal will be ready by September.

Now, Hope is seeking a loving family who can provide the consistent, gentle care she needs to flourish. Hope’s institutional upbringing has shaped her attachment and emotional needs, but with the right support, she has the potential to thrive in a family environment. Given that adoptions from her country take approximately two years to complete, while Hope is entering her pre-teen years now it is important to realize she will be a teenager when adopted.  Interested families need to be willing to learn and be well aware of the challenges of adopting an older child so her family will have the capacity to support her emotional and behavioral needs. It is also recommended that the family be well-equipped with trauma-informed care and understand issues related to delayed adolescence and the impact of long-term institutionalization. This includes understanding family roles, including those of a father and mother, and sibling relationships.

CHI has given this child the pseudo name Hope because we and her social service staff in HK believe that with the right family who understands her past and can provide her with and affection with proper rules and routines, Hope can overcome her difficult past and achieve great things. We look forward to finding a family that can offer her the stability and care she deserves. CHI has past child studies to provide to seriously interested families.

 

Jaxon

Boy, Age: 8
Country Code: LA-2
Primary Diagnosis: Deaf / HoH, Down syndrome
Down syndrome; Bilateral sensorineural hearing loss; Language delays- communicates through sounds, signs, and screams; Von villebrand disease; Other specific leukocyte disorders, Gastrostomy; Hypothyroidism; Other specified disorders of the kidney and ureter; Other types of infantile paralysis
Listed: Aug 2024
*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***
$2,036.50
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!
Jaxon has a warm smile and readily shares it with anyone around him. He is also affectionate. He does not like to feel limited or subject to restraints. Jaxon likes to explore and laugh a lot with the people he recognizes as close.

VIDEOS:

https://vimeo.com/maaspecialkids/maa-jaxon01

https://vimeo.com/maaspecialkids/maa-jaxon02

https://vimeo.com/maaspecialkids/maa-jaxon003

https://vimeo.com/maaspecialkids/maa-jaxon004

Password: Adoptmaa

There is a $1,000 agency fee reduction for Jaxon’s adoption, with a specific adoption agency. Additional agency fee reductions may be available based on the adoptive family’s circumstances.

Wyatt

Boy, Age: 9
Congenital Zika, Cerebral Palsy, Epilepsy
Listed: Aug 2024
$3,080.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Wyatt is a child with a lot of energy. He is very handsome with long hair and a beautiful smile. He loves music and anything that makes noise around him. He thoroughly enjoys interacting with people who talk to him and will make noise in response to them. He loves many activities including the trampoline, swings, going for a walk, and playing with other children.

A therapist works with him weekly. He presents with many neuromuscular deficits that impact his ability to move his arms. He is able to move his left arm a little to touch objects; however, he does not pick up and hold objects yet. Movement is also limited in both legs, with his right leg having less mobility. He is unable to sit, stand or walk. He is able to hold his head up for short periods of time; however, he is making great progress with this. Wyatt is extremely motived during his therapy sessions.

Cognitively, he is extremely aware and currently does very well in school. He knows shapes, colors, some letters and numbers. He can identify them and answer questions using eye gaze with 2 choices. He loves to laugh at kids when they are running around. Sensory materials and adapted activities are helpful in school to further develop his academic abilities.

Liamo

Boy, Age: 4
Country Code: LA-2
spastic cerebral palsy, microcephaly, overall developmental delay, epilepsy, gastrostomy, and blindness.
Listed: Jul 2024
$20.00
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 is from January 2023; the agency can get updated information when there is a serious inquiry.

Liamo was placed into protective care upon discharge from the hospital when he was born. At the time of his birth, he suffered severe asphyxia. His mother’s pregnancy was unplanned and she had not received any prenatal care. His parents were unable to grasp his medical diagnosis and condition, they were not in the position to care for his medical needs. No one in the biological family was able to care for him either.

Liamo is a child who needs constant supervision. His oxygen levels needed to be always monitored; however, oxygen support has been removed and he seems to have a better mood. He has not had any seizures but does have some spasms during the day. He cannot stay in a seated position. Despite his diagnosis, Liamo loves to receive affection. He communicates through babbling and other sounds. He needs support to fulfill all daily activities. He wakes up very early in the morning and is still not able to sleep throughout the night. Liamo wears diapers all day.

Liamo can kick his legs and with the help of external support equipment he can stay in a seated position for a period of time. His neck control is getting better, as he now can hold his head up for 40 to 50 seconds. He can grab objects with his hands without applying pressure. Liamo goes to occupational, physical, and speech therapy. He gets easily uncomfortable when he needs to wear more clothes, he prefers to wear very light clothes. He turns his head when he hears a strong noise. He takes daily medication. Liamo likes to change positions constantly and likes to participate in activities where there are sounds involved.

Ally

Girl, Age: 16
Country Code: LA-2
Primary Diagnosis: Older Child, Trauma History
Listed: Jul 2024
**** I am eligible for a $500 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount. To inquire about this child, email childinquiry@reecesrainbow.org ***
Ally, now 14, lived with her mother and stepfather in their indigenous community until her parents separated. At that time she went to live with her grandparents who used physical punishment with her. Her mother started a new relationship with a man and they were negligent and abuse toward Ally. At that time, Ally suffered from enuresis (bedwetting), and whenever she would hear the word punishment she would wet herself. She entered into protective care at the age of 7 and her biological mother showed no interest in fulfilling the requirements to regain custody. Ally is now said to be clinically healthy, but as with all children in care, she has suffered trauma from her abusive and difficult past.

Ally is enrolled in school; she is in 8th grade. Her academic performance is good, and her main interest is art—she loves to draw and paint. Her least favorite subject is math. She has a positive relationship with her teachers and classmates. Ally does not get jealous when her caregivers pay attention to other kids, and she is able to give and receive affection. She is an independent girl who fulfills all her daily routines without help. Ally has good sleep and eating habits. She manages her frustration and impulses in accordance with her chronological age. She stays focused and does her best to complete every activity even if it is challenging.

There are no concerns regarding her motor, language, cognitive and social development. She used to go to psychological therapy, but every goal was achieved and she no longer needs this type of support. It is still difficult for Ally to fully express her feelings and emotions verbally, but a great improvement has been shown. At the moment there are no specific triggers that will cause her to feel anxious. In the past, the thought of being reintegrated with her biological family was a cause of anxiousness.

Ally does not get shy when meeting new people but might wait for others to take the initiative to start a conversation. She recognizes authority figures and is respectful and obedient towards them. She interacts positively with adults, peers, younger children, and animals. Ally has great hygiene habits and takes good care of her belongings.

Ally loves playing sports like basketball, and she is part of her school team. She likes to walk outdoors and is very interested in learning English. Ally is currently clinically healthy and does not take any medication. Ally is very aware of fashion and likes to wear clothes that are aesthetically correct. She likes to listen to K-pop.

Ally will need a family who is motivated to get paperwork done quickly as she is 14.5 years old and in danger of aging out of being able to immigrate to the U.S. While we do not anticipate any problems (we can never guarantee), a family must be committed to completing a home study and dossier in a efficient manner so the process can have time to complete.

Sani

Boy, Age: 11
Country Code: LA-2
Primary Diagnosis: Blind / VI, Trauma History
Vision loss, trauma history
Listed: Jul 2024
$34.00
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!
Intelligent, extroverted, spontaneous, resilient, loyal, a dreamer, creative, affectionate, loving, self-efficient, autonomous, astute, brave, perseverant, with a restless mind to learn new things and face new challenges, and with great capabilities. Despite extreme difficulties in life, this is how Sani is described even though being a victim of severe child abuse of various types—including abuse that led to vision loss —could have led him to be otherwise described. Sani came into protective care in 2022 at the age of 7 years old. He is now 9 years old.

Sani is currently enrolled in the 4th grade. According to his teacher´s report, the child is loved by his classmates. He uses his cane to walk around and there are no major concerns regarding his motor, language, cognitive and social development taking into consideration his diagnoses of secondary vision loss and severe child abuse syndrome. He has great communication skills and can verbally expresses his feelings and emotions with people he is very familiar with. Sani recognizes authority figures, but many times has trouble being respectful and obedient, especially if he does not agree with an instruction given by them. Sani can easily make new friends and has leadership skills among his peers.

Sani goes to psychological therapy. He is still learning to take full responsibility for his consequences, and sometimes he lies to avoid any kind of discipline. Sani is learning to manage his impulses and frustration. If there is a situation that he cannot handle emotionally, he will start yelling or behaving in a hostile way with his peers. Whenever he throws a tantrum, he sometimes experiences psychomotor agitation and uses bad language. Whenever there are situations that make him feel anxious, he bites his sleeves, has sweaty hands or has motor restlessness. He gets upset when he needs to continue pushing to do his best in order to fully know the Braille system. He is afraid of being in a dark room alone. Because of his severe history of child abuse, it is recommended that Sani be the youngest child in the family though this may be negotiable depending on a family’s experience with children from abuse. Sani has expressed that he would like a family with two heterosexual parents and he would like to have siblings.

Sani likes to play soccer and enjoys building with Legos and also engaging in conversations with adults. He likes to listen to music in English or Portuguese since he has expressed his desire of learning new languages. Sani favorite colors are blue, white, black and orange. He loves to practice soccer, swimming, martial arts such as capoeira and riding his bicycle. He even likes to breakdance as evidence in a video sent with his profile. Sani is good at playing musical instruments. He would like to become a scientist, learn about biology and astronomy and also speak different languages.

Anna

Girl, Age: 12
Country Code: LA-2
Primary Diagnosis: Autism, Speech Delay
autism, language and speech developmental delay, moderate mental developmental delay, expressive language disorder.
Listed: Jul 2024
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Anna, now 10 years old, entered the Protection Services for the first time when she was a newborn baby as her mother used drugs while pregnant. She lived with her grandmother for a while, but reentered care at 13 months old.

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

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

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

Jean-Luc #

Boy, Age: 8
Primary Diagnosis: Epilepsy/ seizure disorder
Pyruvate dehydrogenase deficiency – homozygote for mutation p.R446 (disorder of pyruvate metabolism and gluconeogenesis). Microcephaly. Epilepsy
Diagnosis: Pyruvate dehydrogenase deficiency – homozygous for mutation p.R446 (disorder in the metabolism of pyruvic and gluconeogenesis). Microcephaly. Epilepsy.

A male child, born 2460 g., with a congenital genetic metabolic disease (pyruvate dehydrogenase deficiency), leading to a disorder in the absorption of sugars and carbohydrates. The child is on a strictly individual ketogenic diet (rich in fat and completely excluding carbohydrates). He is fed with special diet milk – Ketocal.

When conducting electroencephalography, epileptic activity was registered, which is why constant anticonvulsant therapy with Trileptal is being carried out. No epi-seizures have been observed after its initiation.

The child lags behind in physical, neuropsychiatric development and motor skills. He needs follow-up by a pediatric endocrinologist and dietician and a pediatric neurologist.

The boy has pronounced axial muscle hypotonia, hypertonia of the limbs. He sits up independently, but still does not stand up in the crib. He is placed in a walker and permanent rehabilitation is carried out. He is calm, does not isolate himself in the children’s group. He shows discontent when he does not like something, but quickly calms down. The child’s sleep is peaceful.

According to a Psychologist’s last Individual Characteristic from November 2024: “ …Over the past months, progress has been reported in the child’s general and fine motor skills. He stands up on his own on a stationary support and steps to the sides, holding on to the stationary support. The child moves by crawling. He can sit alone without support. He spends his waking hours with the other children in the group and he likes it very much, calm and smiling.

Jean-Luc is smiling, radiant, calm. He stands next to the children and does not isolate himself. There is no joint play yet. He cannot initiate contact with the children by himself. He shows dissatisfaction when he does not like something. He enjoys teasing from a familiar adult. During activities, he is involved, but is not active and shows little interest.

Listed: Jul 2024
$45.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Diagnosis: Pyruvate dehydrogenase deficiency – homozygous for mutation p.R446 (disorder in the metabolism of pyruvic and gluconeogenesis). Microcephaly. Epilepsy.
A male child, born 2460 g., with a congenital genetic metabolic disease (pyruvate dehydrogenase deficiency), leading to a disorder in the absorption of sugars and carbohydrates. The child is on a strictly individual ketogenic diet (rich in fat and completely excluding carbohydrates). He is fed with special diet milk – Ketocal.
When conducting electroencephalography, epileptic activity was registered, which is why constant anticonvulsant therapy with Trileptal is being carried out. No epi-seizures have been observed after its initiation.
The child lags behind in physical, neuropsychiatric development and motor skills. He needs follow-up by a pediatric endocrinologist and dietician and a pediatric neurologist.
The boy has pronounced axial muscle hypotonia, hypertonia of the limbs. He sits up independently, but still does not stand up in the crib. He is placed in a walker and permanent rehabilitation is carried out. He is calm, does not isolate himself in the children’s group. He shows discontent when he does not like something, but quickly calms down. The child’s sleep is peaceful.
According to a Psychologist’s last Individual Characteristic from November 2024: “ …Over the past months, progress has been reported in the child’s general and fine motor skills. He stands up on his own on a stationary support and steps to the sides, holding on to the stationary support. The child moves by crawling. He can sit alone without support. He spends his waking hours with the other children in the group and he likes it very much, calm and smiling.
Jean Luc is smiling, radiant, calm. He stands next to the children and does not isolate himself. There is no joint play yet. He cannot initiate contact with the children by himself. He shows dissatisfaction when he does not like something. He enjoys teasing from a familiar adult. During activities, he is involved, but is not active and shows little interest.

Gene

Boy, Age: 14
Country Code: LA-2
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 ***

Gene’s information is from a report in June 2024 — the agency does have older reports as well.  Gene was 7 years old when he entered care due to neglect. He spent most of his days on the streets and there were behavioral issues within his family of origin. His father was in jail and his mother was involved in criminal activities as well as drug usage. While she said she was going to make changes in her life to regain her son’s custody, she did not follow through. Gene is now 12 years old.

Gene is in the 4th grade. He struggles academically. It is difficult for him to understand new concepts and therefore is unmotivated to do his best. He still has trouble pronouncing properly many words. In 2020 he was diagnosed with mild cognitive developmental delay, but this diagnosis was overruled though an IQ test is pending. He can get easily distracted if he does not like a specific activity. There are no concerns regarding his motor development. His language development is behind, it is difficult for him to comprehend a reading assignment; and he mispronounces some words. In the middle of the night, it is necessary to wake him up to go to the bathroom so that he will not have any accidents. Gene has been learning to manage his frustrations and impulses in a better way. Gene interacts in a positive way with his peers. Gene recognizes authority figures; he is respectful and obedient towards them. It has been observed that Gene interacts positively with adults, kids his age, younger children, and animals.

Currently, Gene goes to therapy, and he has been diagnosed with unspecified mixed behavioral issues for which he takes daily medication. He gets anxious whenever he is not permitted to do something he wants or whenever he does not fully understand a task. He gets upset when he feels he is being attacked, but he has not become aggressive. Gene is afraid of being alone, getting lost and being in the dark. Whenever he feels sad it is because he longs to have a family.

Gene loves to participate in any recreational activity, including sports. Some of Gene’s favorite activities are playing soccer, going to the park, playing cops and robbers, making bracelets and painting. When he grows up, he would like to be a professional soccer player or a chef.

Mia

Girl, Age: 9
Country Code: Asia.4
Region: Asia
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: 14
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.

Bianca #

Girl, Age: 4
Syndrome of congenital anomalies with predominantly facial. Microphthalmi Abnormalities of the thoracic vertebrae. She is missing her left eye ball and right ear.
Listed: Jul 2024
$769.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Bianca was recently transferred from a large orphanage to a small group home. She’s been making developmental progress in her new home. She can pull to a stand in her crib and cruise along the rail. She will take steps when holding the hands of a caregiver. She reaches for toys and will hold and explore them.

Dawn and Donna #

Sibling Group
Ages: 6, 6
Listed: Jul 2024
$1,642.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Dawn & Donna are  twin girls who were born in Ukraine at 29 weeks gestation. They lived in an orphanage in Ukraine until they were 1.5 years old, at which time they were moved to an orphanage in Bulgaria. They were then moved to a different placement in Bulgaria at age 3, where they still reside.

 

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

 

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

 

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

From a family who met them in 2023

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

Esta, Sophie and Luke

Sibling Group
Ages: 13, 7, 6
Country Code: LA-7
Listed: Jun 2024
$808.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Esta, Sophie and Luke are waiting for a family in Latin America.

Esta is an affectionate child who loves dance, judo, art and making bracelets. She has a strong bond with her siblings and relates well with her caregivers and peers. She is clinically healthy with good physical and motor development.

Sophie shows leadership skills even at her young age when playing with others. She also participates in judo, ballet and other workshops. She also likes to participate in tours to exhibits, the cinema and theater. he also exhibits a strong bond with her siblings and is well-adapted at the institution she lives in.

Luke is an active little boy who loves to play ball. He is bonded with his siblings and interacts well with those at the institution.

The children have experienced trauma in their past and will need to continue to receive counseling to help through the transition to an adoptive family and to continue to work through their past. They are doing well though as they receive services in country. Esta received corrective surgery for a cleft palate and Luke has myopia and strabismus for which he receives care. Aside from her trauma care, Sara has no known needs. All of the children follow the Christian faith.

Tiana and Tenaya

Sibling Group
Ages: 11, 15
Country Code: LA-2
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.

Ben

Boy, Age: 7
Country Code: Asia.4
Region: Asia
Primary Diagnosis: Genetic Condition (non-DS)
Chromosome 2q deletion with developmental epileptic encephalopathy, and global developmental delay
Listed: Jun 2024
$27.00
has been donated towards the cost of my adoption!

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

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

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

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

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

Hailey

Girl, Age: 15
Country Code: Asia.4
Region: Asia
Primary Diagnosis: Older Child
Listed: Jun 2024
**** I am eligible for a $500 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount. To inquire about this child, email childinquiry@reecesrainbow.org ***
Hailey is a 13 year old girl in Asia. She is reported to have good overall development with normal physical and motor development. While her vision has been listed as normal as of July 2022, she had some prior surgeries for visual issues and it is suggested she wear glasses due to myopia. 

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

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

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

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

Alina

Girl, Age: 13
Country Code: LA-2
Primary Diagnosis: Down syndrome
Down syndrome, muscular hypotonia, cognitive developmental delay, moderate mental delay and behavioral disorder.
Listed: Jun 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 ***
Alina’s file was updated in Feb 2024.

At the age of 21 months old, Alina was admitted to the hospital with leukemia. Fortunately, her treatments worked and her leukemia was cured. However, Alina also has Down Syndrome and her mother could not care for her.  She is currently not taking any medication. She drinks a lot of water during the day, which led to a medical evaluation as to why she drinks so much, but nothing was found.

As is the case with many children with Down Syndrome, Alina loves to give and receive affection. She is enrolled in an inclusive academic program where she attends sixth grade. She interacts in a positive way with her peers and participates in class. Alina cannot say the days of the week, but she knows what she is supposed to do daily. Even though Alina needs to be told what to do she somehow finds out the way to solve problems on her own.

Alina is able to use the restroom and she has been walking since the age of 3. She has been diagnosed with muscular hypotonia, for which she goes to physical, occupational, speech, and psychological therapies. Her fine motor skills are continuing to develop, and Alina cannot fully write or read yet. A special academic curriculum has been designed for her for some subjects. Alina said her first words when she was 4 years old. She has a cyst in her brain and is monitored periodically. The foster mother stated that the child was able to talk and most of her words were correctly pronounced but after having surgery on her tonsils in 2018, there has been a setback on her language skills. However, her language comprehension is the same.

Alina loves to play games on a cell phone, and she is a great helper around the house. She is a very talkative girl who loves to wear dresses. She also likes to color and draw. She easily makes friends and loves to interact with peers. It has been observed that many times, Alina has great leadership skills when it comes to organizing games among her peers. She can verbally express (in a limited way) her feelings and emotions. She interacts in a positive way with adults, peers, younger children, and animals. Alina has learned to be independent in many ways.

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!

Brooklyn and Bailey #

Sibling Group
Ages: 9, 11
Primary Diagnosis: Muscular Dystrophy
Listed: May 2024
$8,329.80
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Brooklyn and Bailey are brothers, they reside in a foster family.

Brooklyn has muscular dystrophy and a speech disorder. He has normal mental development. In 2020 he experienced burns over a large portion of his body and had right-sided bronchopneumonia. Therapy: Operative excisional cleaning of the wounds, sterile dressings; intensive treatment of thermal shock; antibiotic therapy. Brooklyn receives additional support in the form of resource teaching. With him a team of specialist work –speech therapist, psychologist, and resource teacher within the limits of the pre-school. The child is for a second year in a row in the same preschool class, because he was delayed from starting first grade because of medical reasons. He likes artistic activities and playing with his peers. He understands and strongly desires to be adopted, even if he does not talk much, his short dialogs are for his future surrounded by his loved ones.

Bailey is a healthy child with age-appropriate physical and neuropsychological development. He has good communication skills, has leadership qualities which sometimes turn bossy, and has a group of friends. He is curious, social and actively interacts with the people around him of different ages. Bailey has the attitude and the mindset for the adoption process with the needed positivity towards providing good living
conditions, including satisfying of the physiological needs, the needs for security, love and belonging, respect and self-affirmation. He understands and strongly desires to be adopted, he often talks about his future, surrounded by his loved ones. The adoption process is so desired and awaited by Bailey. The child is prepared and
ready to have his family, his adoptive parents.

Alice #

Girl, Age: 15
Primary Diagnosis: Cerebral palsy
Listed: May 2024
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
She resides with a foster family. She has ataxic cerebral palsy. She walks with slight unsteadiness. She attends a regular school with special education support services. She needs monitoring by a child neurologist and psychiatrist, motor rehabilitation, sessions with a psychologist and speech therapist, as well as special care and supervision by an adult in all social situations. She is friendly and initiates communication and contact with peers and adults, but often misunderstands intent or meaning and takes offense. She can easily be distracted, becoming fixated on an idea or object. Her emotional and social immaturity can put her at risk in social settings. She needs a predictable, safe and secure environment.

Zander

Boy, Age: 13
Country Code: LA-2
Cognitive delay, anxiety, depression, macrodactyly and gigantism, hand deformity
Listed: Apr 2024
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
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.

Nany #

Girl, Age: 4
Primary Diagnosis: Blind / VI, Cerebral palsy
Nany has retinopathy of her left eye, cerebral leukomalacia with manifestation of spastic quadriparesis, bronchopulmonary dysplasia and asthma.
Listed: Apr 2024
$2,432.20
has been donated towards the cost of my adoption!

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

Carl

Boy, Age: 14
Country Code: EE-11
Primary Diagnosis: Fetal Alcohol Syndrome
Fetal Alcohol Syndrome
Listed: Mar 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 ***
Carl was born prematurely in a home environment lacking the basic necessities; he was moved into residential care homes. He has been diagnosed with fetal alcohol syndrome (FAS), which has impacted his development.

In his current residence, Carl has blossomed into a kind-hearted and friendly child, creating bonds with his caretakers and peers. He partakes in meals with growing independence, embraces dressing routines and self-care; Carl sleeps soundly.

Carl carries a history of medical complexities. Despite an unsupervised pregnancy and a birth weight of less than a kilogram, Carl continues to receive dedicated medical attention across a spectrum of specialties to bolster his growth.

His therapeutic services include speech therapy, psychomotricity, and psychology, extended under the nurturing folds of his supportive abode. Carl delights in equine therapy and the companionship of dogs. Carl is a good student, benefiting from customized learning supports. He also enjoys music, tablets and computers.

Ivan #

Boy, Age: 9
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.

George & Miles #

Sibling Group
Ages: 12, 14
Primary Diagnosis: Limb differences
Listed: Mar 2024
$1,080.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Please meet George & Miles! These brothers must be adopted together, and both are said to want to be adopted together.

George was born in 2013 and is said to have well developed general and fine motor skills. George is emotionally stable and has good social contact with other children in the school. He does need resource help in school. He has friends and shows respect for adults. He has established habits for independence in dressing, eating and sleeping.

Miles was born in 2012. Miles is diagnosed with deformed feet. He also has some contracture of the fingers in both hands. He has congenital syphilis however he has no clinical symptoms and is not contagious. Miles moves independently but walks on his toes. He also has contractures of his upper and lower limbs. He feels pain with prolonged loading of the musculoskeletal system. However he continues to be energetic and happily runs, jumps and plays with other children. Miles shows affection to adults. He is curious and shows interest an interest in everything. He does need resource help in school. He enjoys being involved in outdoor games with other children.

The adoption agency has very recent videos available of the boys.

Vincent #

Boy, Age: 5
Listed: Mar 2024
$1,325.90
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
His diagnoses is Edwards Syndrome including congenital cardiac malformation with large intracardiac defect, cortical blindness, and severe delay in the neuro-psychological development. The August report says the following:

Vincent was extremely calm during the whole visit. He sleeps in a small room, together with three other children with disabilities. He sleeps in a crib. He spends most of his time in his bed, being periodically put in a chaise lounge or in a car basket. He cannot sit upright, either independently, as well as with support. His position in the lounger/car seat is semi-recumbent.

Vincent predominantly uses his right hand and his body is almost constantly turned slightly to the right. He can turn from his back to one side and vice versa, he cannot turn on his stomach. When placed on his stomach, he cannot raise his head. Vincent is basically blind, according to the diagnosis and by a specialist, although the staff has doubts because the child often reacts to light. During my visit, when displaying and attempting to stimulate a reaction with a ball of light, no such reaction was observed.

Vincent showed interest in the new toys and especially in the noisy book which he grabbed with his right hand, held for a while and even waved it with his hand. As the teacher shared, he grabs like a crab, with pincers. The ball turned out to be too big for him to hold in one hand. Although the book was kind of prickly, Vincent did not react in any way, not even by pulling away.

A sharp noise does not startle Vincent, this was also evident from the sharp squealing from the side of the ball. He listens when there is music, and can show a slight liveliness/activity. He does not react to his name. He likes to be paid attention to, to be spoken to gently and to be hugged. He does not mind being touched … even from a stranger. Vincent’s entire care must be provided for by an adult.  He is fed with a tube, being on 5 feedings per day. He doesn’t get angry or protest when changing or bathing. His sleep is peaceful.

From what I saw Vincent would be much better in a family environment. In the “home”,  he mostly spends his time in his bed doing nothing and getting no attention.  Every child deserves attention and love and stimulation. I really hope that this sweet boy will find his forever family soon!

Eddie #

Boy, Age: 4
Listed: Mar 2024
$2,100.85
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Meet Eddie! This sweet little man just turned two years old. He likes to transfer a toy from one hand to the other and will look for a dropped toy. He is able to push buttons on electronic toys, and he reacts positively when adults try to engage him. He is able to roll from side to side and can sit with some assistance. Because of his medical diagnoses, Eddie receives all of his nutrition via a g-tube. He sleeps well and protests at bath time. His diagnoses include Congenital malformation of the digestive system – atresia of the esophagus with tracheoesophageal fistula. Condition following surgical intervention; implanted percutaneous g-tube. Congenital heart malformation – small intraventricular defect. Protein-energy malnutrition. Delayed psychomotor development. He will almost certainly need  more surgeries in the future in order to eat by mouth, and any family considering Eddie should be sure they are prepared to meet his medical needs.

Ariel & Gabe

Sibling Group
Ages: 13, 9
Country Code: EE-11
Primary Diagnosis: ADHD, Skin Condition
Listed: Mar 2024
$1,088.10
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!
Siblings Ariel and Gabe, lived with their mother and older brother until they were placed in residential care over five years ago.

The siblings go to school and enjoy time with their friends. They follow routines for eating sleeping and personal care with minimal support. Their vaccinations are up-to-date and they have routine health checks. Ariel has managed psoriasis with the support of medication and therapies, while also enjoying the gifts of dance, music, and social activities. Gabe has had a minor surgical procedure, that he now manages with medications. He has medications and therapy for behavior support.

Academically, Ariel is in her fourth year and Gabe his second year.
Gabe enjoys watching tv, playing games, painting, and caring for animals. He attends a catechism class and church services. He may have behavior outbursts.

Both children are working through the child preparation plan for adoption.

Anne Marie

Girl, Age: 13
Country Code: EE-11
Primary Diagnosis: Older Child
Listed: Mar 2024
**** I am eligible for a $500 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount. To inquire about this child, email childinquiry@reecesrainbow.org ***
Anne Marie’s life has been marked by many transitions. Anne Marie lived in a family home previously, and then was placed in care of the government due to neglect. Even when the initial transition towards an adoptive family was unsuccessful, Anne Marie returned familiar surroundings with ease.

Anne Marie has a box of keepsakes that is important to her. Her diet is well-balanced, and she manages a minor visual impairment with glasses.

She is a typical teen in many ways — enjoying TikTok, beach outings, cycling adventures, and shared laughter with peers. Her active engagement in Sunday school further enhances her communal ties.

 

Andy

Boy, Age: 13
Country Code: EE-11
Primary Diagnosis: Genetic Condition (non-DS)
Fragile X
Listed: Mar 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!
Andy was born with Fragile X Syndrome,and his needs were complex from the start. He was placed in residential care as a newborn.

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

Phineas

Boy, Age: 4
Country Code: EE-11
Polymalformative syndrome, with craniofacial dysmorphia; suspicion of Goldenhar Syndrome; Hydrocephaly; upper airway malformation with tracheostomy since 10/4/2021. Currently with cannula. Epilepsy. Gastrostomy. Sensory-neuro deafness – uses hearing aids.
Listed: Mar 2024
$1,025.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Phineas was previously listed as Phil — he is a sweet boy who was born with a polymalformative syndrome. His condition comes with needs that set him apart, and he was placed in care early on.

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

Malcolm

Boy, Age: 11
Country Code: LA-2
Primary Diagnosis: Autism, Down syndrome
Down syndrome, autism
Listed: Feb 2024
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
Malcom is described as a cheerful boy who can give affection exclusively to those whom he has a strong affective bond. He likes to listen to music and swing back and forth on a swing. He also likes to play with his toys. Malcom feels best with repetitive daily routines.

VIDEOS:
https://vimeo.com/maaspecialkids/maa-malcom
https://vimeo.com/maaspecialkids/maa-malcom2
https://vimeo.com/maaspecialkids/maa-malcom3
Password: Adoptmaa

There is a $1,500 agency fee reduction for Malcom’s adoption. Additional agency fee reductions may be available for Malcom’s adoption based on the adoptive family’s circumstances.

Vance #

Boy, Age: 5
Communicating internal hydrocephalus, implantation of ventriculoperitoneal shunt. Spastic cerebral palsy. Localized epilepsy. Atrophy of the optic nerve. Plagiocephaly. Delayed neuropsychological development.
Listed: Feb 2024
$2,095.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Meet Vance! This three-year-old boy needs a family who has easy access to the many specialists he will need to thrive, as, in addition to regular medical assessments, he will benefit from ongoing physical and occupational therapies. Vance is able to roll from back to front. He reacts to sounds, and is able to be calmed by familiar adults when he is upset. He can be coaxed to give a smile, and while he does not purposefully play with toys, he does have a favorite teddy bear. He is able to eat from a spoon, though this picky eater cannot feed himself. 

Vance was also previously listed as Vinnie.

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