Molly May #

Girl, Age: 10
Primary Diagnosis: Genetic Condition (non-DS)
Trisomy 7; cleft lip & palate; Cerebral Palsy
Listed: May 2019
$4,195.10
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!
Molly May has made progress in her development during recent months. She is able to sit unassisted, get up on her knees and has begun to start trying to move around in a walker. She is becoming more physically active. She makes eye contact, looks around for families adults and smiles when someone looks at her. She will laugh out loud when an adult plays with her. She watches children’s cartoons and movies on the TV and will get excited and point to the screen when the TV is turned on. She picks up toys and attempts to play with them. She still needs instructions in how to appropriately play with toys. She makes vocalizations in an effort to communicate. She eats soft foods from a spoon.

Molly May has undergone multiple surgeries to repair her cleft lip & palate. She is under the continued care of the doctor who is performing these procedures. She is also under the regular care of a neurologist, who diagnosed her with CP in 2018. She had suffered from “constant shaking” resulting in uncontrollable movements up until a few months ago. The social worker reports that this has greatly improved and that Molly May’s movement are now more calm and she also sleeps calmly too. Videos taken in April 2019 show her interacting with toys.

Photos and videos are available through the agency.

Mila #

Girl, Age: 9
Hydrocephaly; Strabismus; G-tube feeding; delays in development
Listed: Jul 2018
*** 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 ***
$853.00
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!
Mila turns her head towards sound and looks at people and objects of interest. She recognizes the faces of the staff. She can roll over, but still has difficulty with head control. She enjoys musical toys that spin and will focus on those for short periods of time.

Update 8/2024

Special needs: low birth weight (2410 gr.); congenital anomaly of the central nervous system: moderate ventriculomegaly; cyst of the cave of septum pellucidum and cave Vergae; rejected prior diagnosis of hydrocephalus; brain atrophy; infantile cerebral palsy; syndrome of congenital anomalies mainly affecting the facial area; convergent strabismus; nystagmus; occipital alopecia areata;  severely delayed physical and neuropsychological development; severe mental delay
                                                                                                                        
Family history: born from a high-risk pregnancy by a mother with positive serology for hepatitis B and epilepsy (on three medications for epilepsy).
Molly turns independently in bed. Although she is unable to sit independently, Molly maintains a sitting position for a more continuous period at the presence of additional support. She has no stable support in the legs.Molly selectively responds with an appropriate emotional reaction to different situations and objects. She is able to express discontent from internal discomfort through crying. She smiles as a response to a smile, speech and closeness from the caregiver, she positively reacts to positive stimulation. Molly easily handles being moved from one space to another, she is calm and sometimes demonstrates interest. She has formed emotional preferences to certain significant members of the staff, mostly the rehabilitator who works with her, as well as the teacher from the group at the Center for Special Educational Support. Molly laughs at specific sounds coming from a musical toy. She shows preferences for specific children’s songs while she does not react to others.
Molly wears diapers, easily goes to sleep and easily wakes up. She eats food from a spoon

Malory #

Girl, Age: 15
Primary Diagnosis: Other Special Needs
Microcephalous; Moderate mental delays; Speech delay; Behavioral Issues
Listed: Jan 2018
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Malory is a beautiful, giggly girl who lives with a foster family in Eastern Europe. With a contagious smile and laughter, Malory runs, climbs and could be described as an active child. She enjoys the extra attention she receives from her foster parents. She is physically healthy, and she eats well. Her weight and height are catching up with the standards for her age.

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

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

Additional videos are available from her agency.

Kaylyn #

Girl, Age: 11
Primary Diagnosis: Cerebral palsy
symptomatic epilepsy-partial seizures with secondary generalization; spastic cerebral palsy; hypoxic-ischemic encephalopathy of 2nd degree; profound mental delay;
Listed: Feb 2018
$2,004.50
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!
Kaylyn is in severely impaired condition and her development is delayed in all areas. She is completely dependent on adults’ care. Her sleep is calm and rhythmical. She is fed with a spoon by an adult.

Julian #

Boy, Age: 10
Primary Diagnosis: Spina bifida
Spina Bifida; Hydrocephalus: shunt placed: Slight paraplegia of lower limbs; Left kidney agenesis; Vesicostomy.
Listed: Dec 2018
$1,057.50
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!
Julian enjoys playing with toys. He is well attached to his caregivers and responds to them when they talk to him. When he is happy, he responds by making noises and clapping his hands. His report indicates that when held by the hands, he will take steps.

Update Jan 2020:

Julian sits on his own while supporting his weight on his hands. He uses his hands to change his posture and move his body. He stands in the walker. He actively grabs and manipulates toys and objects, tries to use them as intended – shakes to produce sound, pulls the string of a musical toy. Visual-motor coordination is slightly impaired.

Josiah #

Boy, Age: 9
Primary Diagnosis: Genetic Condition (non-DS)
genetic metabolic disease – pyruvate-kinase deficiency – homozygote mutation p-R 446; mild to moderate core and periventricular lesions; generalized muscle hypotonia; severely delayed physical and neuro-psychological development;
Listed: Oct 2018
$1,000.10
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!
Josiah moves in space by turning from back to belly and vice versa. He has started forming some of the perceptions about objects from his constant surroundings and everyday life. He connects some objects from his surroundings with the actions performed with them.

When awake, Josiah is mostly calm. He would laugh out loud when jested. During active interactions with adults Josiah pronounces various sounds and random syllables. Josiah follows a specific dietary regime and has food individually prepared for him. He is fed with a spoon by an adult and has a picky appetite. He is calm during dressing and bathing. Josiah’s sleep is calm.

Isaac #

Boy, Age: 12
Primary Diagnosis: Cerebral palsy
Craniosynostosis with microcephalus; Infantile cerebral palsy – spastic quadric paresis; Suspected atrophy of the visual nerve on both eyes; Delay in the physical and neuro-psychical
Listed: Jun 2015
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Isaac is a sweet little boy living in an Eastern Europe orphanage. He cannot sit without support or turn between his stomach and back. There is little support in the legs. Isaac doesn’t have an attention span and doesn’t focus on his surroundings. He reacts to touch but doesn’t when verbally addressed. He doesn’t understand speech but sometimes makes sounds. Isaac is mostly calm and smiles. He doesn’t interact with the children and adults around him.

There is little reaction with toys and no playing when in his possession. Isaac is completely dependent on the help of the staff.

Condition after a brain hemorrhage. Cyst in the left cerebral hemisphere. Microcephaly. Spastic quadriparesis. Cryptorchidism. Anemic syndrome. Behind in his neuro-psychical development. When put on his belly or held, he keeps his head up. He slightly turns to one side but doesn’t turn independently from back to stomach and vice versa. He doesn’t try to sit up and doesn’t get up to a standing position. He doesn’t have good support in his legs. He starts after loud sound but doesn’t turn his head to the direction of the sound. He listens to the speech of adults. He doesn’t look at an adult leaning over him. He doesn’t follow with a look moving objects or people. He reacts to touch. He is calm and doesn’t cry without reason. He reacts positively to interactions and laughs loud. Photos and videos from June 2015 are available through the agency.

Gary #

Boy, Age: 15
Primary Diagnosis: Cerebral palsy
Listed: Oct 2018
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Gary is currently living in a group home for children with special needs. He can move around the group home in a gait trainer. Due to his low tone, he can not sit or stand independently. He can roll from back to stomach. He can hold a toy and will manipulate it, though he does not always understand the purpose of the toy. He enjoys interacting with adults and will smile and demonstrate appropriate emotions when engaged in activities.

Gabi #

Girl, Age: 15
Primary Diagnosis: Other Special Needs
moderate mental delay- significant impairment of behavior requiring attention or treatment; microcephaly; hyperactive behavior
Listed: Jul 2019
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Gabi is physically healthy with normal physical development. She is radiant and very active.

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

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

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

Evelyn #

Girl, Age: 11
Primary Diagnosis: Craniofacial disorder
Congenital abnormality of skull and face bones; cerebral palsy. Spastic cerebral palsy; Partial epilepsy-takes medication
Listed: Oct 2019
$1,490.00
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!
Evelyn crawls in order to get where she wants to go. She can stand with support and take steps to the side while holding on to something. She has spastic muscle tone. She picks up objects and transfers them from hand to hand. She does not talk. She responds positively to attention from adults.

Emeric #

Boy, Age: 7
Primary Diagnosis: Cerebral palsy
Listed: Jul 2020
$1,050.00
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!
Emeric can sit up in a special chair with support. He has poor support for his legs. He can hold a rattle with his left hand and shake it. He turns his head in the direction of sound. He has recently started tracking objects with his eyes. He enjoys listening to music. When music plays, he will get very still and listen to it with interest. He laughs and smiles in the presence of familiar adults. He eats blended food from a bottle.

Drako #

Boy, Age: 10
Primary Diagnosis: Other Special Needs
Cognitive delays; repaired cleft lip & palate with additional surgeries needed
Listed: Apr 2019
$817.12
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Drako has undergone surgeries to repair a cleft lip and palate. He is under continues care by medical professionals and will need future orthodontic surgery and other possible surgeries as well related to his cleft issues. Developmentally, his speech, motor skills, and cognitive processing are all delayed. He can crawl, pull to a stand, cruise around furniture/objects, and walk while holding an adult’s hand. He will interact with toys that play music or light up. He babbles, but is not yet saying any words.

Photos and videos are available.

Delaney #

Girl, Age: 13
Primary Diagnosis: Spina bifida
Hydrocephalus internal – ventriculoperitoneal shunt, Spina bifida, congenital anomalies of the urinary system, ventral hernia.
Listed: Apr 2016
**** 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 ***
Update Jan 2017: Delaney is a beautiful, sweet, calm girl. She likes to be hugged and held. She likes it when someone takes care of her and to be outside, with her stroller and recognizes the people that take care of her. She feels most comfortable in her bed and during her walks with the stroller in the garden. She eats and sleeps well.

Delaney expresses her preferences to people and objects to which she is more attached. She has three favorite toys that are colorful and soft. She also enjoys listening to music especially children’s songs. She doesn’t like lying on her back and sudden and quick movements. She is able to sit independently and grab and hold objects she has very strong hands she uses well. She feels comfortable when around her there are people with who she is familiar with.

Delaney is able to express her opinion and preference with gestures. Delaney is very calm child with big potential for improvement with the needed care, attention and the feeling of the real family environment.

David #

Boy, Age: 9
Primary Diagnosis: Cerebral palsy
cerebral palsy; quadriparesis ; epilepsy; Bronchial asthma; delays in all aspects of development
Listed: Feb 2020
$2,857.50
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!
David was declared clinically dead at birth and resuscitated. He currently lives in a group home. He reaches for hanging objects and can hold a toy for brief periods of time. He is very responsive to caregivers. He smiles and shows pleasure when spoken to. He tracts objects and tries to focus on people who are talking to him and objects being presented to him. He rolls from his back to stomach in his bed.

Caryn #

Girl, Age: 13
Primary Diagnosis: Cerebral palsy
Listed: Dec 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 ***
Most of the time, Caryn is calm, especially when she is in the playroom. When somebody pays attention to her, she laughs loudly. Caryn totally depends on the care of others. She sleeps peacefully and stays calm when getting dressed and bathing. She has cerebral palsy and needs specific care, though she has no severe deficit in terms of physical activity.

From a teacher who works with her: This little blind girl is progressing so well, but she is so scared. Can you imagine to be in a world where at any given moment you could get pinched, pushed over, knocked down, hair pulled, eyes poked. I don’t blame her, especially when there are so many other special needs children around her and so few staff and no family love and care. But inspite of all of this she is a fighter and a giggler.

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.

Brendan #

Boy, Age: 12
Primary Diagnosis: Blind / VI
background retinopathy; retinopathy of prematurity; a condition after 2-degree intracranial hemorrhage (he is blind); Specific developmental disorder of motor function; hypotrophy; delayed neuropsychological development. Prematurely born second degree, with low birth weight. Microcephalus; Delay in the neuro-psychical development.
Listed: Jun 2015
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
The child is calm and rarely cries when he’s upset or protests. Single demonstrations of stereotypical shaking of the head right-left have been observed. He reacts with cheer and liveliness to the presence of familiar adults and accepts their presence and contact; he smiles to tender speech and laughs loud to teases. He likes close physical contact. He is distanced with strangers and is distrustful with them not showing activity in play interactions. His attention is difficult to attract and keep. He has support in his legs. His motor development is at the level turning from back to stomach and vice versa and moving by crawling. He is steady in the walker and makes attempts to move around in it. His grip is palmar and he manipulates for long time with toys put in proximity, with alternation of the hands. He picks up a toy put in proximity, makes attempts to evoke sounds from it or puts it in his mouth. Currently, he plays with toys manipulating with them for a long time. He rarely pronounces syllables or other combinations of sounds.

He readily enters into play interactions with adults. He spontaneously pronounces syllables and other combinations of sounds. He eats well, with appetite. While bathed, he’s calm. His sleep is calm and long. He sucks his thumb while sleeping. He eats blended food from a spoon.

Brian #

Boy, Age: 10
Primary Diagnosis: Craniofacial disorder
Congenital malformation syndromes predominantly affecting facial appearance. Foramen ovale persistens. Transient pulmonary hypertension. Pes equinovarus bilateralis. Severe delay in neuro-psychical development
Listed: Jul 2018
$2,116.62
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!
Brian recognizes familiar adults and has formed an attachment to his favorite caregiver. He is uncomfortable around strangers. He is working with a physical therapist and a teacher on fine and gross motor skills. He can pick up toys and transfer them from hand to hand. His teacher reports that he understands what is being said to him and has recently begun responding to simple directions such as “give me”. He is able to sit unassisted and moves around in a baby walker.

Photos and videos are available through the agency.

Ashford #

Boy, Age: 10
Primary Diagnosis: Craniofacial disorder
Microcephaly
Listed: Sep 2017
$1,610.00
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!
Ashford enjoys the presence of adults and emotionally expresses himself with laughter, crying and sounds. He laughs when tickled and smiles when he sees familiar faces. Ashford is unable to sit, stand, nor does he have head control. He prefers to be on his stomach. He does not have coordinated movement of his arms or legs and has little ability to hold a toy. Ashford’s diagnosis is Microcephaly. He was born prematurely and received intervention at the hospital at birth. Some history of convulsions, controlled with medication. Suspicion of left nasal atresia.

Archer #

Boy, Age: 13
Primary Diagnosis: Other Special Needs
Atypical Autism; Chronic suppurative otitis media; Chronic rhinitis; Reduction of hearing;
Delays in psychomotor skills development.
Listed: Jan 2018
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Archer is living in an Eastern European baby home. Short, smiling and calm, Archer’s main diagnosis is atypical childhood autism. He does not speak, but he pronounces sounds and syllables, and he performs stereotypical movements. Archer loves to be alone, and her prefers angles, areas near the window, mirror or door.

Physically well-developed, Archer’s height and weight are normal for his age. He walks by himself, improving his balance. He also climbs, going up and down stairs held by a hand. He can easily open doors.

Archer eats with a spoon, drinks from a cup and goes to sleep by himself. He is not potty trained. Archer makes short-term contacts with the children he knows by touching them with a hand or pulling their clothes gently. He prefers to play with music toys that have buttons, which he pushes to release the music by himself.

Anthony #

Boy, Age: 10
Primary Diagnosis: Hydrocephalus
Neonatal, cerebral schemia; hydrocephalus; ventriculoperitoneal shunt
Listed: Mar 2017
$2,348.00
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!
Anthony is an adorable, sweet boy! Anthony has a lack of development physically and neurologically. In late 2015, a ventriculoperiteneal shunt was placed and he has been free of seizures since then. He cannot sit upright by himself and does not talk, but responds to sound. Anthony is tube fed due to lack of suck reflex. He does not react well to teasing or tactile stimulation by smiling but by irritation and crying.

Andy #

Boy, Age: 15
Primary Diagnosis: Other Special Needs
Listed: Oct 2019
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Update: Jan 2023:  Agency reported the boy is will waiting on the list as available for adoption, but neither of his sisters are.   The agency assumption is that she has been adopted.

Update Sept 2022: Agency reported the oldest girl was no longer listed as available for adoption. The younger girl & the boy are still on their country’s list, and listed as available for adoption together or separately.

Original listing for “Andy, Izzy & Kayla”:
Currently, Andy & Kayla are being raised together in a foster home, while Izzy is being raised in a different foster home in the same town. The children see each other often and want to be adopted together so that they can all live in the same home. The foster families do not speak the country’s native language in the home, so the children speak one language while at home and a 2nd language at school.

Andy tested at age appropriate levels on all psychological and emotional testing. He does well in school and does not have any behavioral concerns. He has age appropriate friendships, social skills, communication skills, and self-help skills. He likes to play football and eat French fries. When he grows up, he wants to be a policeman.

Izzy tested at age appropriate levels on all psychological and emotional testing. She does well in school and does not have any behavioral concerns. She has age appropriate friendships, social skills, communication skills, and self-help skills. She enjoys playing outside with her friends. When she grows up, she wants to be a teacher.

Kayla has speech delays that make it difficult to understand what she is saying. She is working with a speech therapist and learning to make the correct sounds so that her words are more easily understood. She is very active and takes medication to control impulsive behaviors and to help her attention span. Her foster mother reports that her behaviors have greatly improved with the addition of medication. She is attending kindergarten and responds well to play based learning.

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.

Abner #

Boy, Age: 14
Primary Diagnosis: Other Special Needs
hyperkinetic conduct disorder, congenital cardiac malformation – in a condition after surgical correction, atypical autism*
Listed: Sep 2018
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
*Abner’s social worker reported that according to the specialists, supervising Abner’s condition and development, the diagnosis of atypical autism is no longer valid and it will be deleted from Abner’s formal paperwork that is to be updated in the following months

Abner likes to keep himself busy exploring! His favorite activities are the ones that include movement, such as going for a walk. He very much likes to spend time looking through books. He also likes all musical instruments and toys that play melodies and sounds. His favorite toy is a children’s laptop that plays songs. When he hears a melody he tries to dance.

There has been a progress in Abner’s speech development as he has started using a lot of words. He now forms sentences containing 3-4 words, albeit dyslexia is observed.

Adeline #

Girl, Age: 13
Primary Diagnosis: Other Special Needs
cognitive delays
Listed: Jan 2021
**** 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 ***
Adeline is communicative with children and adults. She answers questions. Her expressive and impressive speech is developing. She follows verbal directions. She demonstrates a desire for emotional closeness. She willingly interacts with children and adults. She has established friendly relationships with her classmates. She loves listening music and dancing, as well as, drawing and coloring. She has delays in academics and receives support from a resource teacher at school.

Emery #

Girl, Age: 13
Primary Diagnosis: Hydrocephalus
hydrocephalus-shunt placed; delays in development
Listed: Jan 2021
**** 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 ***
Emery can move using a walker and can make a few steps with support, too. Specialists are working with her to continue to strengthen her legs and are hopeful that she’ll become more independently mobile. Emery likes listening to music and is able to reproduce some of them. She can say a few words and makes short sentences as well. She receives support and intervention from specialists in the local community. She likes to receive an individual attention. She has emotional bonds with adults. She eats by herself and her sleep is calm.