Nolan

Boy, Age: 7
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.

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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: 4
Country Code: LA-2
Primary Diagnosis: Cerebral palsy, Deaf / HoH
Cerebral palsy; developmental delays; malnutrition; bone growth disorder; hearing loss
Listed: Jan 2023
$64.80
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
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: 11
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: 8
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
$1,046.57
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.

Brody #

Boy, Age: 8
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.

Tyson #

Boy, Age: 6
Listed: Apr 2021
$54.00
has been donated towards the cost of my adoption!

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

Penelope

Girl, Age: 15
Region: Asia
Primary Diagnosis: Deaf / HoH
Listed: Nov 2012
**** 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 ***
Penelope has been diagnosed as deaf. She is also post-operative for a PDA heart condition and has received treatment for cataracts, which do limit her vision. Penelope can visually perceive light and people moving around her.

Penelope came into care when she was about a year and a half old. She has good development of fine motor skills in that she could do the motions of grasping, holding, picking and putting things down as well as feeding herself. She has a strong sense of curiosity and experiences the world primarily by touch. We hope she can be adopted by a family who can provide her with the special education and care she needs.

Frannie

Girl, Age: 15
Region: Asia
Primary Diagnosis: Deaf / HoH
congenital deafness; CHD- mild pulmonary stenosis and mild patent foramen ovale (PFO)
Listed: Oct 2014
**** 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 ***
From reading 6.5 year old Frannie’s file, it is clear that this girl will do very well in a forever family! And speaking of files, hers is full of information! Frannie likes to play with other children. She also likes to play with dolls, games, and do puzzles. Her favorite foods are apples and eggs and she like to drink milk. She also loves snacks.

At the age of 6, Frannie began going to a special school. She quickly became a favorite. Frannie quickly learned to follow the teachers and learned some sign language. She is learning more gestures, such as one for her name, the numbers 1-10, and a sign for toilet. She has learned to write many numbers and some words. She is an active student in school and she enjoys games and crafts. Frannie won two awards at school- one for “good child prize”, and one for “small pacesetter who helps others prize.” The awards made her very happy and proud. Her overall performance is excellent! Even when she loses a game, she will smile. Frannie needs some help when it comes to fine motor skills, but she is fond of learning and can imitate quite well. She seems to be very interested in gymnastics and can do many tricks. She is flexible and has talent in dancing. Frannie is enthusiastic, outgoing, and fond of learning. All the caretakers in the orphanage love her very much! It is clear that with the love of a forever family and some guidance, this child will make huge gains and will soar!

Connor

Boy, Age: 13
Region: Asia
Primary Diagnosis: Deaf / HoH
Hearing loss
Listed: Feb 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 ***
Conner is a handsome boy who will be 5 years old in February. He came into care when he was about 1 year old, and was found to have mild hearing loss (30dB) Conner’s file was done when he was 2 years 7 months old. At that time, Conner’s motor skills were on target, and he was imitating words. Conner is active, engaging, and lovable. He enjoys listening to music, and can swing all by himself (at 2 years 7 months old). As often happens, a child with hearing loss can be misdiagnosed as having an intellectual delay. Conner’s medical reflects this misconception. Conner appears to be a typical little guy who happens to have some hearing loss. We do not know if this could be improved with treatment, or hearing aids (if necessary), but he will certainly not receive the help he needs until he comes home! Conner is ready for a family!

Sasha

Girl, Age: 12
Country Code: LA-4
Primary Diagnosis: Deaf / HoH
Developmental delays, deaf, VSD, history of seizures
Listed: Mar 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 October 2022:  Sasha is the cutest, most mischievous 11 yr old! She is deaf, has a hole in her heart, and a global development delay. She understands a lot of things and pays very close attention to so many things but has not learned to sign yet in school. She is very curious and is always wanting to explore (or put in her mouth!) everything around her. She makes our whole house laugh all day long with all the random things she does while playing! She is curious about other kids occasionally but mostly likes to play by herself or wander around by herself. Her favorite thing to do is jump on the trampoline. She is very cuddly and will come up to you and lay her head on your shoulder, climb in your lap, ask for kisses by pressing her forehead repeatedly on your mouth or even give you a kiss! She loves to make silly faces at you and we are trying to get her to copy our silly faces we make back. In school she is working on following simple gesture commands and using the sign “more”, sorting things, and attention to task activities. She loves the sensory activities we do the most! At home she eats (very messily) by herself and is learning to sit on a special toilet seat with a buckle after she eats. She likes to put hats and shoes on by herself but still is learning to do the rest without help. She brings so much joy and laughter into our lives and would thrive in a family! Videos on request!

2021:  Sasha is a spunky, free spirited girl. She has developmental delays, but is very curious about her surroundings. She is constantly walking around and picking things up to examine them, play with them, or chew on them. She loves to interact when you mimic the things she does as well as being tickled. She laughs and has a fun sparkle in her eye. She also loves watching and interacting with herself in the mirror.

Communication with her is limited since she is deaf and has yet to learn sign language. She understands some signs such as “sit” and “no”, but has yet to repeat signs back to us such as “more” and “food.” Sasha continues to work on those both in her foster home and with her teacher at school, but it has been very slow progress. She also has a VSD (hole in her heart), but her body has learned to live with it well. She has been taken off all her heart medicine, and seems to be doing well so far. She has seen doctors about surgery, but none has been needed so far. She is also on medication for seizures, but under the current combination of seizure medication, she has not a had a seizure.