Hunter

Boy, Age: 10
Country Code: Asia.4
Region: Asia
Primary Diagnosis: Coffin-Lowry Syndrome, Deaf / HoH
Listed: Oct 2025
**** 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 ***

Hunter is a cheerful 10-year-old boy in need of a loving home capable of supporting him and his long-term needs. In 2018, Hunter was diagnosed with Coffin-Lowry Syndrome, a genetic disorder, with dysmorphic features including hypertelorism, depressed nasal bridge, thick lips, wide mouth, and broad tapering fingers. He also has developmental delay, profound sensorineural hearing loss, scoliosis, hyperopia and astigmatism, asthma, beta thalassemia trait, and short stature. He received a cochlear implant in his left ear in April 2020 and continues to use a hearing aid in his right ear. He is required to attend medical appointments at different specialties, including the Endocrine Clinic, Eye Clinic, Asthma Clinic, ENT, Prosthetic & Orthotic, Neurology Clinic, General Pediatrics, Hearing Aid Prescription and Spinal and Brace Clinic. His asthma has become stable in recent years and is prescribed medication if needed.  He also has history of seizure but has been stable as well.  Despite all of his long-term conditions, his health is generally stable and he does not take any regular medications.

Hunter is an active, pleasant, friendly and outgoing boy who always shows his smiles. He is an affectionate child who enjoys holding hands, cuddles and hugs from his familiar caregivers. Hunter currently does not have any speech; however, he can express himself by producing some vocal sounds, such as “er” or “ar” or through some simple gestures, such as pointing to things he is interested in or wants or through pictures and Quick Talker. He has received sign language training and learned to use body gestures to express himself. He can wave his hand to greet or to show refusal occasionally. Even with his limitations, Hunter shares a good relationship with the other children. He is generally calm, though he can get upset when he doesn’t get what he wants, but he is easily diverted and his frustration will resolve.

Though Hunter is slightly weaker in trunk control, shoulder stability, upper limb control, muscle tone, bilateral coordination, and motor planning, he can keep his balance while standing and walking. He can also walk up and down stairs by holding someone’s hand, run, and climb up and down as shared. In terms of fine motor skills, he has poor to fair finger strength, finger dexterity and bilateral coordination of both upper limbs. He has a fair to poor tripod and pincer grip in picking up small objects, and fair to poor performance in handwriting and manipulating scissors to cut a straight line. Being curious, Hunter likes exploring his environment and new things.  He likes playing with building blocks, coloring, and watching TV and YouTube videos. He enjoys participating in activities at the orphanage.

Hunter needs a family who can help him continue in his development and who will be dedicated to his life-long needs.

Lexi

Girl, Age: 4
Country Code: LA-6
Primary Diagnosis: Deaf / HoH
Listed: Sep 2025
$0.00
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!
Lexi is a bright-eyed 4-year-old girl with bilateral hearing loss and developmental delays, but these do not diminish her joyful spirit. Lexi communicates in her own unique ways and is curious about the world around her. Lexi will thrive in an environment where she receives consistent, patient attention and where her efforts to communicate are celebrated. She’s looking for a family who will provide a nurturing and stimulating home, eager to support her continued development and help her reach new milestones. With love and encouragement, Lexi has the potential to blossom and bring immense joy to her adoptive family.

Theodore #

Boy, Age: 8
Listed: Jan 2025
$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!
Internal obstructive hydrocephalus – VPA. Spastic cerebral palsy. Umbilical hernia. Convergent strabismus. Hemangioma pedis dextra. ROP in regress. Bilateral sensorineural hearing loss – hearing aid. Mixed specific disorders of psychological development. Severe mental delays.

Jaxon

Boy, Age: 8
Country Code: LA-2
Primary Diagnosis: Deaf / HoH, Down syndrome
Down syndrome; Bilateral sensorineural hearing loss; Language delays- communicates through sounds, signs, and screams; Von villebrand disease; Other specific leukocyte disorders, Gastrostomy; Hypothyroidism; Other specified disorders of the kidney and ureter; Other types of infantile paralysis
Listed: Aug 2024
*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2025, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***
$1,036.50
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!
Jaxon has a warm smile and readily shares it with anyone around him. He is also affectionate. He does not like to feel limited or subject to restraints. Jaxon likes to explore and laugh a lot with the people he recognizes as close.

VIDEOS:

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

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

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

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

Password: Adoptmaa

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

Deacon

Boy, Age: 8
Country Code: LA-6
Primary Diagnosis: Deaf / HoH, Limb differences
Club foot, hearing impaired, general delays, scoliosis
Listed: Jul 2024
$618.00
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!
Deacon, born January 2017, is a cheerful and loving little boy, who is often smiling! He interacts well with both children and adults and likes to give and receive hugs and kisses. He enjoys all kinds of play, especially musical activities, and his favorite toys include balls, cars, and blocks. Due to the pandemic he is receiving educational instruction at the orphanage. When he was found at one month old, Deacon was admitted to the hospital immediately due to sepsis. While there he was diagnosed with left club foot, malformative syndrome, and possible spina bifida occulta due to a pit on his sacrum. He began weekly casting for his club foot, then received a tenotomy in April 2017, and wore a harness to keep his feet in correct position. However, he needed casting again in 2020, and then began AFO therapy. Later he was diagnosed with dorsolumbar scoliosis and moderate bilateral hearing loss. Deacon is reported to be moderately delayed for his age, but at four years old has achieved many milestones! He can kick a ball, and go up and down stairs while supervised by an adult. He is able to build with blocks, scribble, shape play-dough, and hold a glass and a spoon to feed himself. He can communicate basic needs through short phrase such as “give me water” and “let’s go” and is reported to speak well. When presented with a picture he can identify elements by name, and recognizes several body parts and animals.

Deacon has seen many specialists, but has not received a conclusive diagnosis tying together his needs yet; they feel the most likely diagnosis is Klippel-Feil syndrome or Jarcho-Levin syndrome, but have also considered arthrogryposis and mucopolysaccharidosis. He needs a family open to his orthopedic needs who will get him the care and treatment he needs as he continues to grow!

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!

Ivan #

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

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

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

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

Update 8/2024

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

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

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

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.

Marcy

Girl, Age: 6
Country Code: EE-2
Primary Diagnosis: Craniofacial disorder, Deaf / HoH
Listed: Nov 2023
$45.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Marcy is a 4 year old girl with frontal craniostenosis and tuberous sclerosis. Marcy was diagnosed with conductive and sensorineural deafness. Non-orbidity of both eyes. The girl currently does not use corrective glasses, as recommended by ophthalmologists. She is generally cheerful, and is able to imitate gestures and independently eat meals. She struggles with dressing herself and identifying some shapes and colors. Marcy is able to respond to simple commands and messages. She enjoys playing with toys and demonstrates improvement in her coordination. She is very patient and kind. It is recommended for her to wear glasses. Her speech development is delayed, but she can still communicate, and she has demonstrated improvement. Above all she is a nice girl with very many good qualities.

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.

Nolan

Boy, Age: 9
Country Code: SE.Asia.Pac
Region: South Asia
mild hearing loss in left ear; moderate hearing loss in right ear; Global developmental delays- fed with PEG tube; Multiple congenital anomalies- Kleefstra syndrome is to be considered
Listed: Jun 2023
$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!

SEPTEMBER 2023 UPDATE:

Nolan can walk by himself. He enjoys walking around the center, engaging everyone, or just checking out what is happening around him. He enjoys morning and afternoon walks with his caregivers. He loves to look at himself in front of the mirror. He dances when he wants what he is watching while on the sofa. His caregivers assist and let him practice going up and down the stairs. There are times he prefers to be carried and hugged. He enjoys closeness and physical touch. He is sociable and plays on the trampoline with other children.  Nolan pays attention to social stimulation and imitates some actions. He is currently attending occupational and speech therapies, which has greatly helped him improve his skills. He can now hold toys and put blocks on top of one another.  Nolan likes everyone in the center and loves it when visitors come around. He does not display stranger anxiety. He still does not use words, but shows his excitement by laughing and shouting “ha ha ha” in a loud exaggerated voice similar to how Santa would say “Ho ho ho.”   Nolan eats solid foods such as rice, meat, and vegetables that are cut into small pieces. He likes biscuits, yakult, plain bread, and yogurt as snacks. Nolan is becoming better at expressing what he wants. He points out stuff and says, “ah ah ah” when he wants to hold something. He is cooperative with his houseparents and caregivers during his morning and evening care routine when taking a bath and getting dressed. Nolan is loved by everyone at the child caring agency, but they are praying that he will be placed in a permanent family. He has a lot of unique needs that will require special attention, financial resources, good medical specialists, and commitment of parents. He might have delays in development, but having the presence of a loving family will be of great benefit to him in reaching his full potential. He shows signs of being able to learn and improve with dedicated staff taking one-on-one time with him each day. Nolan’s agency believes that he will bring so much joy to a family and he will teach them how to love deeply.

—————————————————————————

Nolan was found to have multiple congenital anomalies. Kleefstra Syndrome is to be considered. He was diagnosed as having global developmental delays and has mild hearing loss of the left ear and moderate hearing loss of the right ear. Nolan is being fed through a Percutaneous Endoscopic Gastrostomy (PEG) tube. However, his caregiver sometimes tries to feed him orally with infant cereal or yogurt, which he enjoys. Nolan is undergoing physical therapy and can pull himself up by holding the rails of his crib. He can sit by himself in his crib for a maximum of 30 minutes. He can stand with support and can move his legs freely. Nolan can walk approximately 100 steps with assistance. He can stretch his arms and hands to reach toys or any object near his crib. He loves playing with toys, such as rattles, that produce sound. Nolan responds when his name is called, and he can convey his needs through different tones when he cries or babbles. Nolan smiles, laughs, and babbles when talked to. He loves to be cuddled and played with! Despite his medical needs, Nolan is not demanding and is easy to care for.

A traveling family that met Nolan said, “We’ve met this child and he is the BEST cuddler! He hardly ever cries and loves to walk while holding your hands. He laughs hard when you talk loudly into his ear, and he loves cartoons that sing! We were with him for a whole summer and would be happy to share more info and pictures!”

We hope just the right family comes forward for Nolan!

Jordan

Boy, Age: 6
Country Code: LA-2
Primary Diagnosis: Cerebral palsy, Deaf / HoH
Cerebral palsy; developmental delays; malnutrition; bone growth disorder; hearing loss
Listed: Jan 2023
$1,454.30
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!
Jordan is an affectionate little guy with a beautiful smile and bright eyes. He loves attention. Jordan also likes to spend time in his walker and being massaged.

Contact the adoption agency to learn more about Jordan and his special needs! We sure hope someone brings this cutie pie home while he’s still so little!

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

Jack

Boy, Age: 13
Country Code: LA-2
Primary Diagnosis: Cerebral palsy, Deaf / HoH
Cerebral palsy; Hearing impairment; Developmental delays
Listed: Dec 2022
**** 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 ***
Jack is a smiley boy who enjoys hot cocoa. Agency staff met sweet Jack in October of 2022. Contact the agency to learn more about Jack and his listed medical needs!

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

Ethan Adrian #

Boy, Age: 10
Bilateral neuro-sensory hearing loss; hydrocephalus (controlled without a shunt); developmental delays; reflux; premature; Cerebral palsy, spastic form – moderate degree. Bronchopulmonary dysplasia /BPD/. Delayed physical and psychomotor development.
Listed: Mar 2022
$1,896.00
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!
Ethan is well developed for his age. He is a warm and curious little boy. His best toy is a ball. He laughs and shouts every time he got his ball. Ethan is a cheerful and peaceful child. He likes the other children. Observes and manipulates with toys. He knows how to charm his caregivers and receives lots of attention.

With a familiar adult, Ethan has a good emotional tone – he enjoys a hide and seek game and sometimes gives his hand for “hello”.

He cannot walk yet, but he sits, crawls and staying straight caught for fixed support, showing progress in his motor skill development. The child has flat feet with valgus deviation of both feet – it was recommended to wear orthopedic shoes. Ethan stands up on his own until he is caught on a fixed support, stands on tiptoe, does not step aside, placed in a walker, moves short distances; pronounces long sound combinations.

A family met Ethan in late 2024 & would be willing to share their experiences with another inquiring family.

Brody #

Boy, Age: 10
Primary Diagnosis: Deaf / HoH
bilateral deafness-choclear implant on the ride side; Moderate mental delay with autistic characteristics; Strabismus
Listed: Sep 2021
$1,050.00
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!
Brody walks independently. He is able to navigate stairs and playground equipment at the park. Most of Brody’s delays seem to be related to being unable to hear and communicate his wants/needs. For example, the foster family reports that he is not aggressive, but he does demonstrate frustration at being unable to communicate with them to express his thoughts and what he wants. He uses some gestures to communicate, such as opening the refrigerator to express that he is hungry. He is supposed to be under the care of a specialist to work with him now that he has the cochlear implant (and to continue to develop his communication skills), but this has not been consistent due to COVID restrictions and the fact that the family must travel to another town for Brody to see the specialist. The foster family does report that Brody seems to be able to hear now that he has the implant and they have seen improvements with the implant in place. Brody does attend a day program for children with disabilities and has recently become more interested in the other children.

Update 2024

Brody was born in  2015 and resides with a foster family. He is a smiley child. He is clinically and medically healthy. Brody has a cochlear implant but despite this, there is no clear evidence of hearing recovery. He vocalizes individual sounds without any meaning or meaning. He uses non-verbal means of communication to satisfy basic needs. He does not have a developed active and passive vocabulary for his age. Lacks developed speech. After the placement of the hearing implant, different-sounding sounds are heard more often, but it cannot be determined whether there is a connection with this. He has been assessed with moderate mental retardation with atypical autism, bilateral hearing
loss, a disorder in receptive and expressive speech, atypical communicative development, and delay in developmental stages.

He looks carefully at those around him. When stimulated, the child reacts, hugs and seeks contact with the foster parent. He smiles when teased, as well as gets angry when a toy he is interested in is taken away. According to information from the foster parent, there are no depressive and aggressive occurrences. He reacts to the absence of the foster parent and looks for her. According to information from the foster parent, the child is active in contacts with significant adults – both close and surrounding. Affectionate and seeking tenderness and attention from them. He takes a man by the hand to show him something he wants. No anxiety is observed when meeting a stranger but does not want to be left with strangers and reacts with grumbling and crying. He likes to be taken care of, smiles at caress and attention from adults. When observed, the boy moves steadily, independently and without assistance. Squats, stands, stretches and contracts arms. Climbing stairs with legs one after another. Handles objects equally with both hands. It is noticed that he walks on his toes. Climbs on chairs and sofas. His movements are chaotic – there is no real judgment of danger

Fine motor skills for the age are not well developed. No stacking of cubes is observed. Holds objects for a short time and throws them. The child does not have skills related to making coordinated movements with his fingers. Tries to play with constructor set but fails to assemble items. Under direct observation, he holds a pencil in his hand but shows no interest in the white sheet. It leaves no traces. With support, he manages to pull a zipper to fasten it. Unsustainable attention and concentration. Difficulty sharing attention. Orients himself in the space of the room, opens the door and wants to go outside. Does not recognize, does not name, does not show parts of his body. It has an orientation to the position of its body in space. Deal with obstacles by removing or bypassing them.

Brody does not use the toys as intended. Interest in the environment is chaotic. During the examination, chaotic play, grasping and scratching of the toys on the ground were observed. Plays with a given toy, but for a short time. According to information, when visiting a children’s corner or park, he prefers the same activities. He does not seek contact with peers, he is more interested in their toys. During observations in an outdoor environment / in a park / the boy walks and runs chaotically, no play activity is observed. Prefers to walk and walk holding hands.

In September 2022, the child was enrolled in the first grade at school, with classes taking place at the Center for Special Educational Support. There were a total of 7 children with different degrees of disability in the class. He was not able to adapt there and for this reason he was admitted to another specialized institution for the child to visit. At the time of preparation of his description to visit the center daily from 9:00 a.m. to 3:30 p.m. There he adapted very well to the new environment. A speech therapist, a psychologist, a rehabilitator and a resource teacher work with the child. Brandon feels very good at the center, interacting with the specialists. Physical therapy – passive and active – was carried out in the center. He did exercises for general strengthening of the body, improvement of independence and improvement of general motor patterns. Work was done on maintaining attention, stimulating fine motor skills and orientation in space, but it was not possible to carry out any educational activity, because of the lack of interest in the educational process. From the information received, he did not communicate with other children in the group, but accepted attention and proximity from the staff there.

Brody lacks developed self-care skills. From the information received from the caregiver, the child does not feed independently but uses a spoon with the support of an adult. He is on a general diet. The child is reported to have a good appetite. Differentiates the taste of food. Shows preferences for certain foods. He likes to eat sweet things. Constant salivation is observed. He is dependent on an adult for dressing and undressing, but according to the caregiver, he is involved and helps with dressing more than before. He undresses himself for sleep and when he needs to go to the bathroom. Brody is reported to be a restful sleeper, sleeping soundly at night and not waking up. The child uses a diaper all day. He cannot control and does not report when a physiological need arises.

Tyson #

Boy, Age: 8
Listed: Apr 2021
$1,854.00
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!
Bilateral sensorineural hearing loss (with hearing aid); shunt due to internal hydrocephalus; spastic cerebral palsy

Tyson was born premature and had several complications after birth. He can sit on his own with good balanced reactions. He crawls following the correct motor model. He stands up and walks sideways vertically. He can walk when one of his hands is held and has more control when it’s his right hand being held. He can stand up straight without falling for 2-3 seconds. When walking with a walker, he begins to bend his knees. He purposefully grabs a toy that is handed to him and can switch it from hand to hand. He shows an interest in musical toys and enjoys them. He has started making sounds and simply syllables such as “ma-ma”. He enjoys having someone sing to him and likes to receive hugs. He eats from a spoon. His overall development is delayed.

Photos and videos from August 2020 are available through the agency.