Arlen

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

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

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

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

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

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

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

Margo and Gabi #

Girl, Age: 3
Listed: Jan 2025
$125.00
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!
Margo
Polymalformative syndrome: Congenital internal hydrocephalus and brain malformation with atrophy of the cerebral lobes and cerebellum; Implantation of the VPS. Hydronephrosis IIIst. on the right with renal calculus; pyeloplasty. Persistent foramen ovale and arterial duct. Symptomatic epilepsy Grand mal seizures. Spastic quadriparesis. Microcephaly. Severe neuropsychiatric development delay

Gabi
Short bowel syndrome. Abnormalities of absorption after surgery. Small bowel insufficiency. Condition after necrotizing enterocolitis. Condition after surgical intervention – termino-lateral ileo-colic anastomosis. Allergy to cow’s milk protein. Cavernous hemangioma on the right side of the face. Condition after: Prematurity IV degree. Neonatal respiratory distress syndrome. Retinopathy of prematurity. Bronchopulmonary dysplasia. Retention in the neuropsychological development. Hypotrophy II degree

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.

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.

Valeria

Girl, Age: 14
Country Code: LA-3
microcephaly, epilepsy
Listed: Nov 2024
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Valeria is a very protective girl.  She loves drawing and doing art projects.  Valeria currently has a feeding tube.

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

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

Dezi

Boy, Age: 7
Country Code: LA-2
severe mental delay, significant behavioral disorders, overall developmental delay, overall developmental disorder, epilepsy, Soto Syndrome
Listed: Oct 2024
$125.00
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 July 2024:

Dezi lived with his biological parents and older sibling until he was almost four years old. While his parents tried to take care of him, money was always lacking and ultimately, his parents knew they could not meet Dezi’s healthcare needs. In order for him to get all the help he needs and to have a better life, his parents relinquished him to protective care services in July 2022.

Due to the child´s medical diagnosis, he is not enrolled in school. There were two times were Dezi attended a special school, but his needs were much greater than what the teachers could manage. Dezi´s adjustment to a foster home was challenging but his current foster mother has done a great job with him. He has developed a strong bond with his foster mother and regulates his emotions in accordance with what she is doing or how close she is to him. He is now able to give and receive affection, which is a great achievement, and he even sometimes gets jealous when his foster mother pays attention to the other children. Dezi’s language is almost nonexistent, but he says a few words such as “ma.” He communicates mostly through facial gestures and by pointing at things he wants to grab or do. When Dezi gets upset, he cries and has “tantrums,” throws objects, and lays himself on the floor. Dezi is not comfortable being around people he is not familiar with. If he likes somebody, he will usually pull that person by the arm to start a game. Dezi likes to play with other children for short periods, and he is not aggressive towards them. He gets anxious when he is not familiar with an environment. He gets upset when he is not allowed to do something or eat at different moments throughout the day.

Dezi is very active, he changes from one activity to another in short periods, it is very hard for him to focus his attention on one specific thing. There are no concerns regarding his gross motor development, he is still working on his fine motor skills. He needs guidance and support to fulfill his daily routines though there are some activities that he can do on his own, such as eating with no help and dressing up. He sleeps throughout the night without any inconvenience. Dezi does not wear diapers during the day as he can go to the bathroom alone but needs help to clean himself up; he wears diapers during the night. He does not like animals.

Dezi’s favorite show is Paw Patrol. He gets happy when he gets new toys, especially cars even though toys do not usually last a long time because he plays roughly with them. He likes to wear clothes with Superman logos or drawings. Dezi has a good appetite and eats every kind of food. He likes to play with water.

Lilian and Sonny

Sibling Group
Ages: 10, 7
Country Code: LA-7
Sonny is a quadriplegic child with cerebral palsy and epilepsy.
Listed: Oct 2024
$520.00
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!

Lilian is described as happy and communicative girl who is very creative. She interacts positively with adults and other children. She is currently in the fifth grade where she is known to be a good student.

Sonny is a quiet boy though he smiles and babbles to communicate with others. He is a quadriplegic child with cerebral palsy and epilepsy.

The agency can attempt to obtain additional information for interested families.

Jana

Girl, Age: 7
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.

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.

Wyatt

Boy, Age: 9
Congenital Zika, Cerebral Palsy, Epilepsy
Listed: Aug 2024
$1,252.00
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!
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.

Jean-Luc #

Boy, Age: 7
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.

Dane

Boy, Age: 15
Country Code: E-11
Region: Europe
Prematurity, post-hemorrhagic hydrocephalus, carrier of a short circuit ventricle-peritoneal shunt, cerebral palsy, spastic tetraparesis, psychomotor retardation, epilepsy, myopia and astigmatism. Frequent respiratory infections.
**** 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 ***

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!

Phineas

Boy, Age: 4
Country Code: E-11
Region: Europe
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.

Maria, Brenda, Marcely, Jose & Vanessa

Sibling Group
Ages: 7, 8, 9, 11, 13
Country Code: LA-5
Primary Diagnosis: ADHD, Epilepsy/ seizure disorder
Listed: Mar 2024
$9,000.00
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!
Maria (6) is very sociable girl and likes to start conversations with adults. She asks them questions, seeks attention and affection. She has the most skills expected for her age in the areas of language, motor skills, sociability and learning. Maintains a close affective and communication bond with her siblings. Maria was diagnosed in 2020 with local epilepsy of which she is currently under follow-up and treatment with magnesium valproate. She has not presented convulsive events to date. She also presents a diagnosis of intolerance to lactose. She is in the 3rd year of preschool.

Brenda (7) is known for her intelligence and autonomy. She learns easily and despite her young age, has great confidence in her abilities to perform any activity assigned to her. She seeks academic challenges and enjoys increasing her skills and knowledge. She is more selective with others although she is affectionate with her siblings. She likes to play individual games, loves to play to babies, draw, video games and coloring. Her favorite activity is playing soccer with her brother. She reflects a healthy emotional state. Brenda has a suitable academic performance and is in the first grade at a Montessori school. She presents a good state of health and is diagnosed with a history of trauma cranioencephalic without clinical repercussions with a history of violence family (Assessed by neurology with CT and EEG reporting normal).

Marcely (8) is described as in good health. She has favorable development in all areas. She is tender and collaborative with adults, she is also very active, and likes to keep moving, climbing, running, skating or cycling. She loves playing with dolls and coloring. Once her confidence is gained, she enjoys giving lots of hugs. She has built a healthy bond with her siblings which contributes to her self-esteem and feeling of protection. She is in the second grade and has an interest in learning and collaborating with adults. She has improved in her impulsivity control and emotional responses.

Jose (10) is intelligent, kind, friendly and bold and affectionate with adults and their colleagues. He has a protective attitude towards his sisters, shows them affection, but also seeks his own friends and does his activities independently. He has a leadership role with colleagues. He is competitive but also sensitive to needs and emotions of others. Jose shows emotional stability, establishes close and healthy social and emotional ties with peers and adults. His development is corresponding to his chronological age. He presents a state of good health and has a diagnosis of myopia and asthmatic which is being treated. He is in the 4th grade and interacts appropriately with his colleagues and guides.

Vanessa (11) has a calm temperament and has developed self-confidence and loving attitude towards her caregivers and siblings. She is very independent in her routine activities, helps younger children and assumes a role of caregiver. She enjoy activities like reading, coloring, making bracelets and playing with dolls. Vanessa is diagnosed with developmental delay psychomotor and speech disorders, ADHD, learning disorder, disorder secondary cognitive development, disorder specific pronunciation, delay expected physiological development for age and seasonal allergic rhinitis. Despite this, she maintains good health and doesn’t take medicine. She is in 5th grade and has established important emotional ties with her colleagues and friends.

Vance #

Boy, Age: 4
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.

Natasha

Girl, Age: 6
Cerebral Palsy, Epilepsy
Listed: Jan 2024
$4,268.00
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!
Natasha is a pretty little girl, with very calm with big eyes and beautiful white teeth. She is very special. She doesn’t smile at everyone. She must first know you, and trust you, but her smile is fascinating. She loves to drink juice and she likes to eat sweets. She really likes music. She likes to be pampered by her foster family and only cries if she needs a little attention.

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

Goliath

Boy, Age: 6
Microcephaly, CP, epilepsy, blind
Listed: Dec 2023
$2,786.14
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!
Goliath is the cutest, most chill baby ever! He loves cuddles, being bounced on the trampoline, swimming, going for bike rides, being held, and chocolate. He would do great either in a big family with lots of siblings or being the only one to soak up all the attention!

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

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

Christian

Boy, Age: 6
Cerebral Palsy, history of Epilepsy, possible visual impairment
Listed: Dec 2023
$2,648.00
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!
Christian is a handsome boy, calm and very adorable with his beautiful smile. He often falls asleep. He is sensitive to noise. He jumps and cries when he is picked up to change position. Nevertheless, he likes to listen to music, he likes to be rocked and he likes when people communicate with him.

At school, he progresses slowly with his sensory exercises which he likes and are helping him to stay awake longer than before. In therapy, he works on functional mobility, which helps him raise his hand to touch an object. He has consistently shown slight improvement in engagement with increased stimuli. He is responding more to toys and people by raising his head, laughing, smiling, and keeping his eyes open.

Rosita

Girl, Age: 7
Country Code: LA-2
Epilepsy, Cerebral Palsy-delayed motor skills; Cognitive delay; Language delay; Psychomotor delays; Neurodevelopmental disorder; Hearing loss on the right side; Umbilical hernia; Urinary incontinence
Listed: Oct 2023
$1,025.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Rosita is a sweet young girl waiting for a family of her own. We hope Rosita’s forever family sees her while she’s still so young! Contact the agency to learn more about Rosita and her listed medical needs!

VIDEOS:

https://vimeo.com/maaspecialkids/maa-rosita
https://vimeo.com/maaspecialkids/maa-rosita1
https://vimeo.com/maaspecialkids/maa-rosita02
Password: Adoptmaa

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

Alfie

Boy, Age: 6
Country Code: LA-2
Secondary ventilatory failure: bacterial pulmonary co-infection-bronchopneumonia, severe persistent broncho obstructive syndrome exacerbated secondary to: aspirative neuropathy (gastroesophageal reflux disease and swallowing disorder) sequelae of bronchopulmonary dysplasia, sequelae of bronchiolitis, small ductus arteriosus without hemodynamic repercussion, mild pulmonary hypertension, symptomatic focal epilepsy, global developmental delay with hearing loss
Listed: Oct 2023
$567.50
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Alfie is a young boy boy who shows interest in sounds and stimulation with mechanical objects. He is responsive and turns and looks towards the person who is talking to him. He engages in vocal exchanges emitting cooing. He responds with a smile when his name is called. He acquires strength through painting workshops for motor stimulation. Contact the agency to learn more about Alfie and his medical needs!

https://vimeo.com/maaspecialkids/maa-alfie
Password: Adoptmaa

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

Galen

Boy, Age: 10
Country Code: EE-2
VSD,ASD, epilepsy, optic nerve hypoplasia, hyperopic astigmatism in both eyes.
$43.00
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!

Galen is an eight year old boy with Fetal Alcohol Syndrome, which has left him with some dysmorphic facial features and difficulties with problem solving. In difficult situations he resorts to verbal and physical aggression. He enjoys helping out with household activities, specifically in the kitchen. He is visually impaired and has mild intellectual disability. He has been receiving preschool education since last September. He works with a psychologist, speech therapist, and physiotherapist on a daily basis.

Galen enjoys participating in group activities, but he works better when one-on-one with a therapist. He is capable of focusing for long periods of time on a single activity. When something doesn’t go his way, he can get upset, but with the right motivation he can easily return to his activity. Galen can’t read, but he can distinguish single letters of the alphabet, and can even copy letters. He can count to twenty. In the future, more focus will be put toward improving his knowledge of the alphabet and helping him manage his emotions.

Jemma

Girl, Age: 14
Country Code: Asia.2
Region: Asia
**** 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 ***
Jemma is outgoing, enjoys meeting new people and exploring new environments. Some of her favorite activities include, putting together jigsaw puzzles, listening to music while singing and dancing, riding her kick scooter, and riding her bicycle. When she is not engaged in physical activities, she enjoys watching cartoons, with Pippa Pig and Doraemon being her favorites! 

Jemma has a diagnosis of epilepsy, hypotension, cataracts, and has moderate developmental delays. Jemma attends special education classes and has a good relationship with her teacher. She can recognize several Chinese characters and can write her own name. She enjoys helping her teacher and receiving praise for her work. During the summer of 2021, Jemma participated in a 3 day camp.  Her favorite activities were baking, sewing and physical games. By the end of her experience, she was able to share her feelings with a few words.

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.

Jesslyn

Girl, Age: 3
Country Code: Asia.2
Region: Asia
Listed: May 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!
Jesslyn is a snuggly baby that likes to be cuddled and hugged by her caregivers. When tired or upset she is able to relax when she hears music or soothing sounds. Although Jesslyn is not able to say words yet, she is able to vocalize through babbling.

Jesslyn needs parents who are comfortable with the many unknowns that are presented by her significant special needs. Jesslyn has epilepsy, hydrocephalus, global developmental delays, and vision concerns.

June

Girl, Age: 6
Country Code: Africa-1
Region: Africa
Cerebral Palsy, Visual Impairment, Epilepsy
Listed: Jan 2023
$1,298.50
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!
June is a little girl, but she can make a lot of noise! You can often hear her in every room of the children’s home. Just when you start reading a story or giving directions June will start up, blowing raspberries or just experimenting with how high she can yell. When she’s feeling less feisty June loves to cuddle. She enjoys spending time in someone’s arms or a carrier, and will often fall asleep there. June cannot see well so she prefers toys that make lots of noise- she’s especially good at using her legs to kick the piano mat or crinkle wrapping paper. She also enjoys being tickled or gently bounced on a lap. June is working very hard at sitting up on her own- she has fantastic head control, can flip herself onto her stomach, and is also improving at grasping toys independently. June would benefit from good medical care to better control her epilepsy. She will bring lots of noise and fun, as well as an abundance of love to any family that chooses to bring her home.

Jay

Boy, Age: 12
Country Code: LA-2
Primary Diagnosis: Epilepsy/ seizure disorder
Lennox syndrome, epilepsy, cognitive delays, and developmental delays
Listed: Dec 2022
$1,642.20
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!
Agency staff met Jay in October of 2022. They said they love his smile! Contact the agency to learn more about Jay and his listed medical needs!

There is a $500 agency fee reduction for Jay’s adoption with a specific adoption agency; additional agency fee reductions may be available based on the adoptive family’s circumstances.

Joyce

Girl, Age: 10
Country Code: Asia.2
Region: Asia
Listed: Dec 2022
$1,047.00
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!
Joyce LOVES to sing and dance!  Her favorite sing along songs are “Baby Shark”, “Cagabrie Island” and “Jasmine”. Joyce also enjoys riding on a motor scooter because she enjoys looking around at the sights and feeling the wind in her hair!

Those who know Joyce say she has a gentle personality. She likes to act cute and will become lively around familiar people. Joyce has a good relationship with her foster parents and gets excited when their 7 year old grandson visits on the weekend. They get along well and play with each other for hours.

Joyce presents with global delays and has Epilepsy and Thalassemia.  It is suspected she has ADHD.  Joyce attends OT and PT sessions. Joyce attends special education classes at elementary school and an afterschool class. She is making progress with her language skills and can respond to questions with single words.

Are you a family that can support Joyce with growing her language skills? Enjoy singing along to nursery rhymes with her?

Cale

Boy, Age: 4
Country Code: LA-2
Global developmental delay; Severe perinatal asphyxia, hypoxic-ischemic encephalopathy, epileptic events under management and controlled, modulated and overcome cardiogenic shock, secondary ventilatory failure, suspected early sepsis, late sepsis due to treated Klebsiella pneumoniae, resolved hypocalcemia, resolved hyponatremia, hyperphosphatemia, child of a consuming mother of psychoactive substances and high neurological and psychosocial risk.
Listed: Nov 2022
$25.20
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!
Cale loves to be cuddled and held. Cale likes to listen to music and feel different textures. Agency staff met Cale in October of 2022. Contact them to learn more about Cale and his listed medical needs!

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

Bailey

Girl, Age: 12
Country Code: LA-2
spastic quadriplegia; generalized hyperreflexia; epilepsy; global developmental delays
Listed: Oct 2022
$67.50
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!
Bailey accepts physical and verbal contact from others. Bailey likes toys that make noise, and she sometimes smiles at the stimulation of an adult. Bailey will need a family who is able to care for her special needs and provide for her daily care. Agency staff met Bailey in July of 2022. We hope her family sees her soon! Contact the agency to learn more about Bailey and her listed medical needs.

VIDEOS:
https://vimeo.com/maaspecialkids/maa-bailey001
https://vimeo.com/maaspecialkids/maa-bailey002
https://vimeo.com/maaspecialkids/maa-bailey003
https://vimeo.com/maaspecialkids/maa-bailey004
Password: Adoptmaa

Rowan

Boy, Age: 10
Country Code: LA-2
Primary Diagnosis: Epilepsy/ seizure disorder
developmental delays and epilepsy
Listed: Oct 2022
$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!
Rowan is smiley, and loves to clap and listen to what is going on around him. Agency staff met Rowan in July of 2022! Contact them to learn more about Rowan and his medical needs!

VIDEO:
https://vimeo.com/maaspecialkids/maa-rowan01
Password: Adoptmaa

Brock

Boy, Age: 11
Country Code: LA-2
Listed: Oct 2022
$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!
Brock is a very social boy, who likes to kick a ball. Brock has continued to develop and grow. Agency staff met Brock in July of 2022! We hope his forever family will see him soon! The agency has additional information available for inquiring families.

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

Jeremy

Boy, Age: 6
Country Code: LA-2
Development delay, Epilepsy, Cerebral Palsy, Microcephaly, & gastrostomy
Listed: Oct 2022
$821.10
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!
Jeremy was met by agency staff in July of 2022. He has a beautiful smile that lights up the room. Jeremy is affectionate with his foster mother and loves to listen to her sing. He really enjoys music! Jeremy will need a family who can provide dedicated care and one who can continue to help him develop and grow. We can’t wait to see who his family will be.

The agency has additional medical information and videos available.

Owen #

Boy, Age: 9
Primary Diagnosis: Epilepsy/ seizure disorder
Cognitive delays; epilepsy; Carrier of the thalassemia trait. Astigmatism. Hypermetropia. Cryptorchidism.
Listed: Jun 2022
$1,093.50
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!
Owen has established self-care skills: He can dress/undress himself, feed himself and is toilet trained. He talks in sentences using 3 or more words. His gross motor skills are well-developed. He can walk, run, go up and down stairs and climb. He participates in conversations, understands everything said to him, and answers questions. He has issues with articulation. He attends a day program where he is receiving academic instruction and therapies. He is interested in everything happening around him. He enjoys Montessori toys. He can string beads, nest items, sort by color, and manipulate items of different sizes. His memory skills are developed. He can recall and reproduce information.

Natala

Girl, Age: 6
Country Code: Asia.2
Region: Asia
Listed: May 2022
$28.00
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!
Introducing….Natala! Natala likes crawling, rolling around, and making sounds like she is talking. Sometimes, when she is unhappy, she lets you know by crying and fussing but will calm down quickly once attended to. Natala has good adaptability for a young child and is not shy with strangers. Currently, Natala takes 2 short naps each day, once in mid-morning and once in the early afternoon. Her nap schedule is flexible. She can flip herself over while lying down, stay seated for up to 20 minutes with support, and has recently started crawling! Because she has high muscle tension, her legs sometimes stay lifted slightly in the air while crawling. Among many other capabilities, Natala is able to grasp objects in each hand and pass them from one hand to the other. Although Natala has delayed speech, she has shown progress between her most two recent visits in March and August of 2021. She currently understands a couple of simple words including ‘goodbye’ and ‘kiss’, in her language of course, and has normal hearing. Doctors are monitoring mild vision damage and plan to continue to assess her vision as she develops. Natala has also been diagnosed with epilepsy however since beginning medication, no tremors or twitching have been observed. Natala is currently being cared for by a foster family and has formed appropriate attachment to her foster mother. Young Natala needs a forever family that can support her, love her, and celebrate along with her as she continues to reach milestones. Could you be that family?

Update 2022:

Natala participated in our February 2022 Virtual Superkids trip.  She was 2 1/2 years old during the visit. Natala is a special girl who will require lifelong care by her adoptive parents.

Natala expresses her joy through smiling and laughing.  She enjoys toys that make sounds and lights up when playing with dolls.  She expresses sadness through crying.  Natala has global delays in development and non-verbal.  She is most comforted and connected to her foster mother.

Lena

Girl, Age: 11
Country Code: LA-2
Listed: Apr 2022
$1,326.35
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!
Lena has a diagnosis of Turner Syndrome with associated delays and epilepsy.

Jolie

Girl, Age: 7
Country Code: Asia.2
Region: Asia
Epilepsy, Cerebral Palsy, Hearing loss, low vision, Global Delays
Listed: Apr 2022
$795.00
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 JolieJolie enjoys walks with her caregiver.  Her favorite part of their walk is when her caregiver speeds up pushing her stroller, and Jolie giggles with joy!  Jolie loves being embraced by her caregivers and communicates with them through giggles and cooing.  

 Jolie has a diagnosis of epilepsy, cerebral palsy, hearing loss, low vision, and overall global delays. Jolie continues to make progress in physical therapy, occupational therapy and speech therapy, which she attends once a week.  Jolie recently accomplished being able to turn her body over from her back to her side! 

 Jolie needs a loving, patient, and caring family who will be able to provide lifelong care and help her develop to her full potential.

Emma #

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

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

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Emma was recently transferred to a group home where she can receive more specialized care to help her continue to develop and receive appropriate medical care. She is receiving monthly blood transfusions at this time for her anemia. She had surgery to correct clubbed feet in 2020. She can sit unassisted, stand next to a stable support, walk around fixed supports and walk while holding the hand of an adult. Videos from May 2021 show Emma playing with an electronic toy. She is pushing the button to get the toy to make a sound. Her fine motor skills are not well-developed at this time, due to her spasticity. Emma responds positively to adults and other children. She smiles and laughs when adults interact with her.

 

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

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

Update 8/2024

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

Jonas #

Boy, Age: 14
2nd-degree prematurity; epilepsy; convergent strabismus; esotropia of the left eye; hypermetropia (long-sightedness); mild mental delay; delayed speech development; other pervasive developmental disorders;
Listed: May 2017
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Jonas is on several medications.  Jonas’s motor activity completely corresponds to the expected developmental level for his calendar age.  Although his fine motor skills need to improve further, Jonas is able to hold a pencil properly. He can inlay elements with some guidance. He puts cubes one on top of the other. He threads colored rings on a fixed stand, but not yet in accordance with their size.

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

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

Shay #

Girl, Age: 12
Primary Diagnosis: Epilepsy/ seizure disorder
Seizure disorder-currently on seizure meds; delays in development; ataxic cerebral palsy; ADHD
Listed: Jan 2019
*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***
Shay lives in a foster home. She was hospitalized to look for a cause for her seizures and was diagnosed with ataxic cerebral palsy. She is currently taking medication for seizures, but still has 1-2 seizures each month. She is able to walk and has good gross motor skills. Her fine motor skills are delayed. Her speech is delayed. She uses single words or short phrases to communicate. She has difficulty focusing, which makes it difficult for her to learn new skills. She is very active and needs constant supervision.

 

Update 9/2024

Shay lives in a foster family and is very close to her foster mom.  She says a lot of words and sentences, but they are in Turkish.  She is extremely mobile and can run, climb on fitness equipment, go up and down stairs and can jump on one leg.  She enjoys playing with dolls and pretending to cook.  She likes nice clothes and likes to look good.  She does not manifest any aggression and in fact is very loving and sweet.  She is also very curious.   A resource teacher works with Shay at school, and she also visits with a psychologist at the Community Support Center. Unfortunately she lives in a very small town with very few other resources.  She really needs the love, attention and resources that only a family can give.

Brogan #

Boy, Age: 15
Primary Diagnosis: Epilepsy/ seizure disorder
Intercranial trauma (surgery done at 11 months for it), mild-moderate delays, seizures
Listed: Jun 2017
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Updated 2022:  When he was 11 months old, Brogan was abused and suffered a traumatic brain injury. He has weakness on the left side of his body as a result. His gross and fine motor skills are slightly uncoordinated. He walks, runs, and navigates stairs independently. He’s worked extensively on fine motor skills and can now write and draw more purposefully. He can talk, though he has some expressive language delays, particularly with articulation. He can answer basic questions. He will use pointing and gestures as needed to communicate. He is becoming more confident with his speech and expressing his thoughts and opinions verbally.  He is very empathetic and helps care for younger children. He has a great desire to learn and will ask a lot of questions in order to gather information on a topic of interest. He tries very hard to learn new skills, but is aware of his delays. As a result, he prefers to play and interact with younger children. He has numerous self-help skills and is learning to perform all the household activities and tasks in the foster home where he currently lives.

Original posting from 2017:  Brogan is amiable, friendly, at times is too enthusiastic. He cooperates with others; participates in group activities; He shows that he is proud with his achievements; often searches for the approval of the adults and insist to make things independently. He likes role games and pretend games. Brogan easily memorizes and reproduces what he learned and his attention is more sustainable and focused. Because of that he is secure in his expressions and does undertake initiative in the learning process. He likes to impose his opinion in the game and to be a leading figure, but agrees with the opinion of the others as well. He willingly communicates with the others, without too much physical closeness, and seeks approval of his foster parent. His understanding corresponds to his age and environment. He is able to lead a dialogue with others and is empathetic towards others. When communicating with others he uses non-verbal methods as gestures and mimics for better communication. He has some vocabulary is working on that. He knows his first name and his age. He understands and uses the specifications for emotional states, features of the character, for himself and others as well. He loves to listen to tales or stories, expresses interest towards the pictures in the books. He can tell overall if he likes certain story or not. He has established perception of his body structure. He has developed feeling of good and evil. He has developed a sense of justice. He is more patient. He has vast desire to explore the world around him and is constantly asking questions until he receives a satisfactory answer. He demonstrates care for the others and his foster parent.

He loves to play with car toys, constructors, to listen to music and dance. He enjoys independent and group games with peers. He had surgery at 11 months old for inter-cranial trauma. He shows mild to moderate delays and occasional seizures if ill or upset.

Anders #

Boy, Age: 11
Primary Diagnosis: Epilepsy/ seizure disorder
Seizures
Listed: Aug 2019
$1,774.50
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!
Anders currently lives in a small Eastern European country. He is happiest listening to soft music or playing with toys that make sound! Anders is described as a happy, calm child. Tests show that Anders has learning and motor delays, as well as occasional seizures.

Leonard

Boy, Age: 14
Country Code: Africa-1
Region: Africa
Primary Diagnosis: Epilepsy/ seizure disorder
Autism and Epilepsy
Listed: Jul 2020
**** 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 ***
This update and new photos were added in October 2022.

Leonard is one of the most clever boys you could ever meet. Although he’s non-verbal in conversations he often sings his favorite songs out loud for everyone to hear. His favorite toys include tennis shoes, books, and anything that spins! He also loves any sort of sensory experience, such as playing in the dirt looking at moving lights, and swinging. Leonard is not difficult to please. He finds joy in all the small moments in life. His favorite days are water days. He could truly sit in the kiddie pools for hours! He loves splashing and experimenting with how the water moves. Leonard is so much fun to play with and be around.

Leonard is gaining more independence everyday. He can eat, walk, and use the bathroom on his own. He has many ways of communicating what he wants using gestures, verbal sounds, and expressions or body language. Leonard is almost never sad or unhappy. His laugh can be heard even in another room, his joy is truly contagious. When he gets to know you Leonard can be very affectionate. He loves to hold hands or lay in your lap. He might also take your hand to show you he wants his head or back rubbed. He knows how to seek out his favorite people, forming clear attachments to those he loves. Leonard would absolutely thrive with the consistency of a forever family who can love him fully and keep him safe always.