There is a very special joy that boys bring to life. Unfortunately, they are often the last ones to be chosen for adoption. We so hope you will find YOUR new son right here at the end of Reece’s Rainbow.

PLEASE HELP US raise grant funds and awareness for these precious, waiting angels. You really can save a life, with even the smallest gift!
You are also invited to send a check (no Paypal fees) to
Reece’s Rainbow, PO Box 146, Combined Locks, WI  54113

“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!

FOR MORE INFORMATION ABOUT THE PROCESS AND/OR ANY OF THE WAITING CHILDREN ON THIS PAGE, PLEASE INQUIRE.

Marcko #

Boy, Age: 3
Primary Diagnosis: Cerebral palsy, Hydrocephalus
Hydrocephalus-shunt placed; Cerebral Palsy;
Listed: Dec 2022
$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!
Marcko had a shunt placed shortly after birth due to hydrocephalus. In February 2022, the shunt failed. Marcko experienced several seizures during the shunt failure. A new shunt was installed and he has not had any additional seizures.

Marcko can walk, go up/down steps, kick and throw a ball and stack objects. He will play with toys. He knows a few of his body parts and other very basic skills. He’s learning to feed himself. He can say a few words, but is not yet speaking in sentences.

Mason #

Boy, Age: 1
Primary Diagnosis: Craniofacial disorder
Craniofrontonasal syndrome
Listed: Dec 2022
$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!
Mason has undergone extensive genetic testing to determine if he has any type of syndrome or genetic condition. Currently, all testing has come back negative. Mason has recently learned to walk independently. He engages with caregivers and other adults. He explores his environment and interacts appropriately. He is interested in toys, picks them up and explores them. When shown how to play with a toy, he mimics the actions of the adult. He smiles, laughs and responds to verbal directions. He cries at appropriate times (hungry, needs a diaper change, etc). His speech is in the beginning stages of development. He eats transitional food and sleeps well at night.

Ashton

Boy, Age: 4
Country Code: LA-2
Primary Diagnosis: Hydrocephalus
Hydrocephalus and Developmental delays
Listed: Nov 2022
$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!
Ashton is an adorable little boy who is described as a social child who loves to be around others who give him affection. He shares with the people around him. He loves to hear music and pleasant sounds. He likes painting and watching animated shows. Contact the agency to learn more about Ashton and his special needs!

NEW VIDEOS:
https://vimeo.com/maaspecialkids/maa-ashton3
https://vimeo.com/maaspecialkids/maa-ashton4
https://vimeo.com/maaspecialkids/maa-ashton05
Password: Adoptmaa

OLDER VIDEOS:
https://vimeo.com/maaspecialkids/maa-ashton1
https://vimeo.com/maaspecialkids/maa-ashton2
Password: Adoptmaa

Matt

Boy, Age: 5
Country Code: LA-2
Spina bifida, paraplegia; Hydrocephalus (shunt placed); Club foot (left and right) (surgically corrected)
Listed: Nov 2022
$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!
Matt, who agency staff met in October of 2022, has a bright smile that is infectious! Matt recognizes animal sounds. He can wash his hands and face by himself. Matt interacts well with his environment, peers, and adults. He adapts well to changes in routines and plays well with his peers. He can play by himself for short time periods. He can focus his attention on different stimuli. Matt has advanced considerably since entering the care of his current care center. He can move his hands spontaneously and hold a pencil correctly. He can move himself with the use of his wheelchair. Matt is right-handed. His speech is well developed, and he can express himself well.

We hope his forever family sees him while he is still so young! Contact the agency to learn more about Matt and his special needs!

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

Cale

Boy, Age: 2
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
$18.00
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!
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

Gordon #

Boy, Age: 1
Listed: Nov 2022
He can pull to stand with a stable support and can “cruise” around. He crawls and walks when held by the hand, but is not yet walking independently. He purposefully grabs objects. He uses his palm to grab, globally with the palm and the three last fingers. He is capable of purposefully grabbing larger objects placed in front of him. He manipulates with the toy and places it in his mouth. Dropping the toys is on purpose. He can move the objects from one hand to the other. By imitation, he hits two blocks in each other. The child is calm and smiles to a familiar adult. He seeks individualized attention. When placed in the crib he would cry and is upset for a long time. His cry is a way of communication. When the adult comes back to him he expresses his happiness. His impressive and expressive speech is not developed. He clearly expresses his need to communicate by differentiating the intonation and the tone of the voice.

Noland

Boy, Age: 3
Country Code: Asia.2
Region: Asia
Motor Delay
Listed: Nov 2022

Noland loves to sing and dance! He also enjoys playing with toy cars with his foster brother. Those who know Noland describe him as curious. When around new people and introduced to new environments, he likes to observe before joining in to play.

Noland has a good relationship with his foster family and gets along well with his 6 year old foster brother. When he needs comforting, he will actively seek hugs from his foster mother. Noland has one older brother and 2 younger brothers who currently reside in Taiwan.

Noland has overall global delays. He receives OT, PT and speech therapies weekly. Noland has made improvements with his speech and fine motor skills through early interventions.

There is a potential Noland may not able to live independently and will need supportive care throughout his life. He needs a loving, patient, and caring family. Are you a family that can provide Noland with support to develop to his full potential?

Zeek #

Boy, Age: 4
Primary Diagnosis: Hydrocephalus, Spina bifida
Spina Bifida; shunt placed for hydrocephalus
Listed: Sep 2021
$1,000.00
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!
Zeek is being taught to use a wheelchair. He can currently turn, but has not yet mastered going forward and backwards. He is also learning to pull his torso up and move around when in his bed or on the floor. He can physically handle toys. He picks them up, transfers them between hands, looks for them and retrieves them if he drops them. He can push buttons and activate sensory toys. He follows simple directions such as “give me”. He plays peek-a-boo. He enjoys interacting with the staff. He will hold out his hand for a hand shake, make kissing noises, and reaches to be held. He uses his hands to show how big he will grow up to be when asked by an adult. He is pronouncing sounds and syllables.

Updated May 2022: Zeek was recently moved from a large orphanage to a small group home, where he’s now receiving more interaction and attention. His language skills have started developing. He can now say several words. He enjoys interacting with staff and responds when he receives attention. He enjoys music.

Wayne #

Boy, Age: 5
Primary Diagnosis: Craniofacial disorder, Deaf / HoH
Congenital cleft of the hard and soft palate with a one-sided cleft of the upper lip on the left. Moderate mental retardation. Bilateral conductive hearing loss.
Listed: Feb 2022
$27.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Wayne has had surgery to repair the cleft lip and palate. He will be having orthodontic treatment and possible surgery on his nose in the future. His hearing was tested in June 2021 and it was determined that he has mild hearing loss of 10/15 decibels bilaterally.

His physical development is on track for his age. He walks, runs, kicks a ball, climbs, etc. His fine motor skills and speech are delayed. He has delays in his intellectual development and has difficulty with focus and attention. He attempts to communicate using non-verbal gestures and sounds or emotions. He is not aggressive and does not have any behavioral concerns. He was recently moved from a large orphanage into foster care, where he is learning new skills. He is completely toilet trained.

Update September 2022: Wayne continues to make developmental progress.
He follows verbal instructions. His speech is still delayed, but he does well identifying colors, objects and answering simple questions with pointing and gestures. He can make some animal sounds and attempts to mimic other sounds. He appears to understand everything said to him. He does have a documented mild hearing loss and a repaired cleft lip and palate. Wayne feeds himself with a spoon, can dress and undress himself independently and is independent with toileting. He can arrange objects by color, shape and size. His developmental skills continue to improve.

Videos from September 2022 show him identifying objects, answering questions (with pointing and making noises), following simple instructions, playing appropriately on playground equipment and with toys and interacting with the adults on the playground.

Silvio

Boy, Age: 5
Country Code: EE-2
Primary Diagnosis: Other Special Needs
Extremely premature, tracheotomy
Listed: May 2021
$1,128.65
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!
Silvio is a Roma boy who was born extremely premature (22 weeks), with a very low birth weight. He spends 6 months at the hospital and fought for his life! He had a tracheotomy procedure and eye Lasik surgery in October 2017.

Last update 2020: Delayed psychomotor development. Visible improvement after rehabilitation. Feeding the by the bottle, playing with toys, rolls out of the back on the stomach and vice versa. He tries to crawl. A very active child who initiates contact. He makes eye contact, focuses his attention on the human face, and smiles back. Video is available from the adoption agency.

Emeric #

Boy, Age: 5
Primary Diagnosis: Cerebral palsy
Listed: Jul 2020
$50.00
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!
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.

Dorie, Nathan, Iggie

Sibling Group
Ages: 9, 7, 5
Country Code: EE-2
Primary Diagnosis: Fetal Alcohol Syndrome
FAS, Abuse, Neglect
Listed: Sep 2021
$209.00
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!

Dorie

The girl has a poor vocabulary, and therefore difficulties with understanding. She is active in words, conducts a dialogue, makes a simple description, but her statements are simplified and not always logical. Speech defect (interdental). She is an active child, shows great curiosity and wants to attract attention. She is willing to play and imitate but is less fond of organized games and has difficulty concentrating, as well as controlling and planning his activities.  She shows a bond with her siblings, especially her brother Nathan.

Nathan

Strong motor skills – correct for age. Walks, runs, overcomes obstacles. He participates in games, wants to attract attention and is upper active.

Perception and hand-eye coordination – within the normal range for age. The boy notices details, differentiates shapes and colors. Recognizes pictures, selects pairs. He connects the pictures. He places the blocks in the holes of the puzzle. Builds block structures – simple and complex at the age level. Slight speech delay. Social behavior and emotional zone – age appropriate. There is a great need for a relationship, attention and contact. Sometimes he is too impulsive and reacts hypersensitive.

Iggie

Low birth weight,  FAS

Strong motor skills – the boy walks independently, runs, overcomes obstacles with a slightly lower fluency. He imitates simple, single body movements, claps his hands, raises his hands up, stomps his feet, enjoys simple games with adults, keeps up with the group. He puts circles on the pyramid, builds a tower from blocks, creates a row (“trains”). He scribbles with a crayon without imitating the direction and shapes, but he likes to draw with adults.

Speech shaping – reacts to sounds from the environment, looks for the source of the sound, reacts to musical sounds. Active speech at the word stage – repeats many one and two-syllable words on command. Points to parts of the face, says the correct words (ear, eye, etc.).

Social behavior and the emotional sphere – visible improvement of contact and relationships, establishing contact without difficulty. He is cheerful, establishes basic relations with children, reacts positively to games, and imitates. Develops the basics of independence in everyday activities. Eat by himself.

 

The children experienced neglect and abuse before coming to the orphanage.

Bodie #

Boy, Age: 5
Listed: Apr 2022
$51.00
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!
Bodie has a diagnosis of moderately impaired general condition which requires constant adult attention and supervision. He was born prematurely. He has congenital hydronephrosis grade 3 of both kidneys with congenital mega-ureters and is underdeveloped in his neurological and mental development.  He does not make eye contact and does not have developed speech — although he does not use words, he hums and shouts to express himself. He is interested in toys but without creative play. He began sitting independently at 2 years 9 months. He stands but cannot walk independently, and uses diapers day and night due to kidney condition, and requires constant adult supervision for his daily needs.   Additional photos and a brief video are available upon request.

Aleks

Boy, Age: 5
Country Code: S.Asia.1
Region: South Asia
Listed: Feb 2021
$659.50
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!
Aleks is a sweet boy who has cerebral palsy and epilepsy. He receives physical therapy and is working on bearing weight and sitting independently. He is active and alert and smiles whenever anyone interacts with him. He loves playing with all the kids and gives big laughs. He enjoys music class and shakes the bells. He dances by kicking his legs and making his chair rock.

AJ

Boy, Age: 5
Country Code: LA-6
Primary Diagnosis: Other Special Needs
Grade I Osteogenesis imperfecta, controlled asthma, controlled atopic dermatitis, right cryptorchidism (undescended testicle)
Listed: Mar 2021
$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!
AJ is a calm, loving, shy boy who came into the care when he was about a year old; he was found abandoned. He has favorably adapted to the institution where he is being cared for and he has made significant progress in his motor process.  The boy moves his upper and lower extremities, he can take his feet to his mouth, he crawls, and tries to stay standing with support. The report also states that AJ is a boy who explores the environment, he maintains attention and interacts with people, appropriately responding to the sensory stimuli that are presented to him. AJ likes children’s songs and dances imitating his peers, he likes colorful musical instrument toys.

Photo available from agency!

When the medical report was first performed when he was about one year old, AJ was not walking and a level of delay is reported in the cognitive, language and motor areas that are related to the state of severe malnutrition with which he was found as an infant.

His Grade I Osteogenesis Imperfecta is the mildest form of the condition. Osteogenesis imperfecta (OI) is a genetic disorder characterized by bones that break easily. OI is highly variable. Its signs and symptoms range from mild to severe. In addition to fractures (broken bones), people with OI sometimes have muscle weakness, loose joints (joint laxity), curvature of the spine (scoliosis), brittle teeth (dentinogenesis imperfecta), and hearing loss. A classification system dividing OI into several types is commonly used to help describe how severely a person is affected. Type I is the mildest and most common form of OI.

Angelo

Boy, Age: 5
Country Code: LA-2
Primary Diagnosis: Other Special Needs
osteogenesis imperfecta and a unspecified conduct disorder
Listed: Oct 2022
$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!
Angelo likes playing with bubbles and painting with tempera. He enjoys crafts and exploring the different materials and textures. Angelo also likes building towers and playing in water. He is described as social and showing great interest in everything that happens around him. He is a great observer.

Angelo is able to kick a ball forward with help, throw a ball over his shoulder and catch a ball with rebound most of the time. He is able to pedal a tricycle and climb the stairs with help. He is able to undress. His motor coordination is good, which makes it easier for him to string objects. Angelo has a good understanding of orders and knows and recognizes language. Contact the agency to learn more about Angelo and his medical needs!

Stanley #

Boy, Age: 3
Primary Diagnosis: Global developmental delays
Delays in all aspects of development
Listed: Oct 2022
$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!
Stanley was recently moved into a group at the orphanage with older children. The staff reports that they believe this change will be good for him. He walks and can climb on/off of furniture. He is not saying any words or word approximations at this time. His teacher reports that in the past couple of weeks, he has started saying one or two syllables when he hears music. He has recently begun responding to his name and some simple directions. He examines and explores objects, but does not use them for their intended purpose. He will flip through the pages of a book. He enjoys opening/closing doors. He is interested in people and shows awareness of familiar adults vs unfamiliar adults. He smiles and reacts positively to interactions from adults. Due to the delays in his communication skills and development, he will undergo a comprehensive evaluation for Autism in November.

Jasper #

Boy, Age: 5
Primary Diagnosis: Other Special Needs
Cerebral leukomalacia, feed via NG tube
Listed: Aug 2019
$295.00
has been donated towards the cost of my adoption, including $260.00 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!
Jasper is a bright little boy, smiling all the time. He holds toys and tries to play with them. He is currently fed with a NG tube. He does have a sucking reflex, but has difficulty with swallowing.

He can turn without help from his stomach to his back and backwards again. He can hold his head up and control it. He has a weak leg support and cannot stay upright, yet, but can kick with his legs and if put into a walker, can even move to a short distance. He plays with hanging toys when he’s laying on his back. He babbles and makes sounds. He cries at appropriate times, like when he rolls over into the side of the crib and needs help to be moved.

Nevan #

Boy, Age: 4
State after intraventricular hemorrhage. Internal hydrocephaly: VPA inserted. Cortical blindness. Congenital heart abnormality: type 2 atrial septal defect (persisting foramen ovale). Hypospadias. Bilateral cryptorchidism. Delayed physical development and severely delayed psychomotor development.
Listed: May 2022
$165.00
has been donated towards the cost of my adoption, including $140.00 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!
Nevan was born prematurely, to a young mother. He had a difficult neonatal period, with use of mechanical ventilation.
The child has a severe impairment of the central nervous system: posthemorrhagic internal hydrocephaly; a VPA shut was inserted in April 2018; later it was twice revised. The child is in a stationed impaired state of health. ECG: Persisting foramen ovale with positive natural evolution; no therapy needed.

Nevan will need observation by a neurosurgeon, pediatric cardiologist; he needs specialized care, physical therapy and kinesiotherapy.

The child turns his head towards sounds. When placed on his side by adults and with help, he can turn the lower part of his body and flip from back to front and vice versa. When awake he is placed in a baby chair. Coefficient of development: 8.
The boy laughs loudly when teased; he is happy when hearing the voice of a known to him adult that he likes. He reacts to the tone of the voice of the person speaking to him. He grasps a toy but does not manipulate with it. He falls easily asleep and sleeps well. He is fed with a bottle. He is calm when being changed and when being bathed.

Mitchell #

Boy, Age: 5
Primary Diagnosis: Cerebral palsy
cerebral palsy – an ataxic form
Listed: Jul 2021
$260.00
has been donated towards the cost of my adoption, including $260.00 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!

Mitchell walks independently with an ataxic gait. He talk using simple words and simple sentences. He plays with toys. He shows interest in his environment and everything happening around him. He seeks contact with familiar adults.

Photos and videos are available through the agency.

Danny #

Boy, Age: 4
Primary Diagnosis: Hydrocephalus, Spina bifida
Spina Bifida, hydrocephalus-shunt placed
Listed: Nov 2020
$535.00
has been donated towards the cost of my adoption, including $535.00 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!
Danny loves being in the playroom at the orphanage. He plays with toys and gets very excited when adults interact with him. He enjoys listening to music. He participates in therapy each day to work on learning new skills.

UPDATE August 2022: He pulls to a stand in his crib. He crawls using his arms to drag his lower body (“army crawl”). He has a lot of upper body strength. He participates in group activities. He plays with toys. He pushes the buttons on toys, “dials” a toy phone, etc. He follows simple directions. He says a few simple words. He responds to his name. He enjoys listening to music. He eats from a spoon and drinks from an open cup. He tries very hard to be more mobile, despite his lower paralysis. As a result, he has broken a bone in one of his legs. The staff tries to keep him sitting in a chair where he can see everything going on in the room and participate in activities, without risking further injury to his leg. He interacts with other children sitting around him.

Brad #

Boy, Age: 3
Primary Diagnosis: Other Special Needs
Glanzmann thrombasthenia; delays in development
Listed: May 2022
$325.00
has been donated towards the cost of my adoption, including $300.00 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!
Brad walks independently. He plays with toys. He will fill a container with small toys and “pour” or “dump” into another container and continue the game back and forth. He can nest cups by putting them in the correct size order. He goes to other children, smiles to them and takes them by the hands. He smiles and observes with interest the faces of adults when gently talked to or sung to. He understands object permanency. He demonstrates pretend play skills related to kitchen/cooking (putting a spoon in a bowl and stirring, etc) and also bathing a baby. He shows good development in social play skills.

James

Boy, Age: 4
Country Code: Asia.2
Region: Asia
Primary Diagnosis: Global developmental delays
premature (34 wks), suspected neonatal abstinence syndrome, developmental delays (motor, cognitive), cerebal palsy, microcephaly, esotropia, undescended testicles; BM may have used drugs while pregnant, moderate intellectual disability
Listed: Sep 2021
$459.00
has been donated towards the cost of my adoption, including $200.00 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!
James is 3 years old and has the cutest smile and the sweetest little giggle! His relations with others are close and he is not afraid of strangers.

James has a stable mood and strong curiosity. He can also play attentively for more than 30 minutes! We hear that he has a good appetite and is not a picky eater. His favorite food is corn although he also really enjoys pudding! James can fall asleep on his own and sleeps well throughout the night. He primarily crawls around on his belly and forearms to get around. He has attended daycare since September 2020 and receives physical and occupational therapies once a week and speech therapy once every two weeks.

James was born prematurely and has been diagnosed with cognitive and motor delays, as well as cerebral palsy and microcephaly. That being said, James is able to say some words such as ‘okay’ and ‘yes’, can sit up properly in a chair to feed himself, and is able to express ‘bye-bye’ and blow a kiss!

Hennes #

Boy, Age: 5
Primary Diagnosis: Spina bifida
Arnold-Chiari type II, spina bifida at level L5
Listed: Aug 2022
$285.20
has been donated towards the cost of my adoption, including $260.00 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!
Hennes has Arnold-Chiari type II with spina bifida at level L5.

Hennes is described as a very social and happy child. He communicates well with others. He can ask and answer questions and make general conversation. When he has difficulty with a task, he says, “It doesn’t work” in order to get help. A member of the agency’s team visited Hennes and said that he is “very easy to talk to and very smart”. Videos from July 2022 show him talking, answering questions and interacting with the adults. Hennes moves from place to place by crawling and using his upper body strength. He can pull to a stand and hold onto a support. He likes to play with all kind of toys, like balls, cubes, cars, puzzles and etc. He eats independently. He told the team member that he loves apples and orange juice.

Ned #

Boy, Age: 3
Ataxic Cerebral Palsy; obstructive hydrocephalus; delays in mental development

Listed: Aug 2022
$1,020.00
has been donated towards the cost of my adoption, including $750.00 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!
He runs, climbs stairs with help, rides a scooter, plays with cubes and figures which he can nest. Ned recognizes animals and knows their places when arranging a puzzle. He plays with other children, preferring the older ones and copying their actions. He loves music and musical toys, and sometimes dances. He responds to his name, follows directions, is well-intentioned, does not get angry and is not aggressive at all. Ned pronounces various sounds and syllables such as “ma-ma”, “ba-ba”(gandma), “ka-ka”(older sister), “hop”(ups), “meow”(what the cat says), “bau” (what the dog says), “da”(yes), “liu-liu”(swing), “ku -ku”(what the cuckoo says) etc. However, the main communication is related to taking the hand of a familiar adult and bringing her to the object the child wants. He arranges things in his room, chooses his clothes, can put on and take off his shoes, washes his hands by himself, likes to bathe by playing with balls and watering himself with a jug. He’s learning to feed himself independently with a spoon, but still needs pureed foods.

Ned lived in an orphanage for the first 2.5 years of his life. When he entered foster care, he could not sit, stand, make any sounds or have any form of communication. He has made a large amount of progress in just one year, with the help of multiple specialists and his foster family.

Salvador

Boy, Age: 3
Country Code: LA-2
Primary Diagnosis: Blind / VI
Norrie’s disease; neurodevelopmental delays; blind
Listed: Jul 2022
$135.00
has been donated towards the cost of my adoption, including $110.00 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!
Agency staff met sweet Salvador in July of 2022. Salvador receives physical, occupational, and language therapy weekly. He is doing well with advances in development. He walks, jumps, and climbs the stands. He combines words, counts numbers from 1 to 20, and says about 25 words. Salvador can feed himself with help. Contact the adoption agency to learn more about this sweet boy!

VIDEOS:

https://vimeo.com/maaspecialkids/maa-salvador1
https://vimeo.com/maaspecialkids/maa-salvador2
https://vimeo.com/maaspecialkids/maa-salvador3
https://vimeo.com/maaspecialkids/maa-salvador4
https://vimeo.com/maaspecialkids/maa-salvador5
https://vimeo.com/maaspecialkids/maa-salvador6
https://vimeo.com/maaspecialkids/maa-salvador7
https://vimeo.com/maaspecialkids/maa-salvador8
https://vimeo.com/maaspecialkids/maa-salvador9

Password: Adoptmaa

Trey #

Boy, Age: 4
Primary Diagnosis: Cerebral palsy
Cerebral palsy with paraparesis of the lower limbs, mixed form.
Listed: May 2022
$120.00
has been donated towards the cost of my adoption, including $110.00 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!
Trey had a rough birth with vacuum extraction; he received treatment in the intensive care unit. He has been lagging behind in his neuro-psychic development since his early childhood. He started walking without aid late in his life.  He follows simple instructions and plays with musical toys; with assistance he nests rings. He often imposes his will. He is restless when sleeping. Trey often cries without a reason. He does not play with other children and prefers contacts with adults. At times he exhibits auto-aggression and stops after distraction.

Presently, the child does not show interest towards his environment and is not interested in the surrounding world. He looks at his toys and touches them but is not interested in them. He takes a toy but quickly throws it away. He does not react to his name but now he makes a difference between known people and strangers. When asked, he does not seek objects with his eyes. He reacts to sounds and likes it when people talk to him tenderly. He responds with joy to simple jesting. His speech is not developed; he produces guttural sounds and listens to them. He reacts positively when hearing human voices.

Trey has regular consultations with a psychologist and a speech therapist, as well as with a pediatric psychiatrist and a neurologist. His delay in his neuro-psychic development was confirmed. The child has undergone a surgery for his strabismus.

Bronner #

Boy, Age: 4
Primary Diagnosis: Craniofacial disorder
Congenital maxillofacial anomaly – haylognoplatosis. Condition after cheiloplasty. Protein energy malnutrition, developmental delays
Listed: May 2022
$145.70
has been donated towards the cost of my adoption, including $120.00 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!
Bronner has recently started walking. He eats from a spoon. He explores toys, but often throws them. He remembers the activities of his daily routine and follows his daily schedule well. He explores his environment and interacts with other people.

Jonah and Jonas

Sibling Group
Ages: 10, 3
Country Code: Asia.2
Region: Asia
Primary Diagnosis: ADHD, Speech Delay
Listed: May 2022
$175.00
has been donated towards the cost of my adoption, including $130.00 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!

Jonah is described as a “clever” child who likes to explore new places!  Jonah enjoys hand crafts, such as origami and building blocks.  Jonah can be shy towards strangers and he takes time to warm up and feel comfortable around new people. Jonah has a close relationship to his foster family, especially his foster mother.  He is able to express thoughts about his day openly with her and express himself.

Jonah has a diagnosis of ADHD and is currently on medication to help with his concentration. Jonah is in 3rd grade and participates in his elementary school’s afterschool program.  He has an excellent academic performance and positive relationships with his peers!

Jonas is fond of music and LOVES to sway to the beat of the music! Jonas enjoys playing on riding toys and playing with toy cars.  He has a good bond with his foster family and acts affectionately towards them.

Jonas is receiving occupational therapy for fine motor delays and speech therapy for his language delays. Speech therapy has assisted him to build onto his vocabulary and he is now able to say two-three word phrases, such as “shui-shui” (water), “mama”, “fan-fan” (rice/food), and “wo-yao-chi” (I want to eat it.)! Jonas attends preschool where he has more learning stimulation and is able to work on his interpersonal interactions.

While Jonah and Jonas do not live in the same foster family, they have been able to connect on multiple occasions and had an overnight sleepover at Jonah’s foster home. Jonah enjoys taking walks with Jonas, and he is excited to help his brother when he can!

Alexei #

Boy, Age: 5
hypoxic ischemic encephalopathy; multicystic encephalopathy; nonobstructive internal and external hydrocephalus; epilepsy; cavernous hemangioma; umbilical hernia; specific developmental disorder of the motor function.
Listed: May 2022
$216.10
has been donated towards the cost of my adoption, including $145.00 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!
This is the case of a male child born with extremely low weight (grade III immaturity) and heavy early neonatal period (intubation in the first minutes after his birth; seizures). Later he had disorder of the central nervous system, i.e. hypoxic ischemic encephalopathy, multicystic encephalopathy, internal and external hydrocephalus. The child is in an impaired general state of health; he takes opisthotonos position; he has spastic quadriparesis and repeated day and night tonic seizures against the background of anticonvulsant therapy; myorelaxant medication is applied. He is not subject to surgical treatment and insertion of a VP shunt.
The child needs special care and supervision by medical specialists.

He depends completely on the staff taking care of him and often has respiratory infections. He takes food from a bottle and hardly takes in the quantity of food determined for him, and throws out from time to time. The boy reacts to speech and when being touched.

Alexei exhibits no interest to contact other children. He easily makes tactile contacts with adults with no resistance, including with strangers.

The child depends on the staff of the institution. Diapers are used; he does not communicate his physiological needs by crying. Sleeping routine: he naps in the day and sleeps at night; he easily falls asleep and easily wakes up. He has a routine in receiving proper food and liquids distributed over time.

Dean #

Boy, Age: 4
Primary Diagnosis: Blind / VI, Hydrocephalus
Congenital cytomegalovirus infection. Internal hydrocephaly: state post implantation of a VP shunt. Quadriparetic syndrome. Cortical blindness. Cataract. Rickets. Protein energy malnutrition.
Listed: May 2022
$227.00
has been donated towards the cost of my adoption, including $200.00 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!
This is the case of a male child born from a pathological pregnancy with very low weight and indications of congenital cytomegalovirus infection. In the early neonatal period posthemorrhagic internal hydrocephaly was found and at the age of 2 months a VP shunt was implanted. Due to malfunctioning of the shunt, it was replaced when the child was 9 months old.

Dean is in a stationed impaired general state of health with a severe quadriparetic syndrome, pseudobulbar paresis and cortical blindness. Also, total cataract of both eyes has been found which cannot be treated surgically due to the severely damaged state of health of the child. He is fed via a nasogastric tube. He is severely delayed in his physical and neuro-psychic development. His condition is being monitored by medical professionals.

Augustus #

Boy, Age: 4
Primary Diagnosis: Cerebral palsy, Hydrocephalus
Internal hydrocephalus: state after implantation of a VP-shunt; epilepsy; spastic quadriparesis; cortical blindness; delay in the neuro-psychic development
Listed: May 2022
$139.00
has been donated towards the cost of my adoption, including $112.00 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!
Augustus was born full term, and was found that he has internal hydrocephalus; at the age of 4 months a liquid drainage valve system was implanted. The child lies in bed; he has spasticity in his limbs and his active and passive movements are limited. He depends completely on the care provided by adults. He receives kinesiotherapy. The child is subject to observation by a neurologist and by a neuro-surgeon.

The child’s lower and upper limbs are highly spastic and are with diffuse muscle hypotonia. His fine motor skills are not developed. He does not grasp a toy given to him. Atanas holds his hands bent in fists. He is seriously delayed in his psychomotor development. The boy reacts to tactile stimulation by adults. When teased, he does not smile. He is unable to interact with the other children. Atanas depends completely on the care provided by adults. He is fed by a bottle. From time to time he cries when given a shower. He sleeps well.

Orion #

Boy, Age: 3
Premature, Congenital Heart Defect, strabismus, hydrocephalus, general delays
Listed: May 2022
$152.50
has been donated towards the cost of my adoption, including $139.00 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!
Special needs: Prematurity III stage Bronchopulmonary dysplasia; persistent foramen ovale; peripheral pulmonary stenosis; moderate communicating hydrocephalus; retinopathy of a prematurely born child; convergent strabismus.

This is the case of a male child, born prematurely III degree (1180 g), with a complicated perinatal history and pathological neonatal period. Subsequently he developed moderate communicating hydrocephalus and is delayed in his motor and mental development; there are changes in his tone and reflexes.

The child was diagnosed with a congenital heart malformation (persisting foramen ovale and PAC), which required therapy for a certain period of time. His cardiac status has improved. Given the severe prematurity, he has retinopathy of a prematurely born child and strabismus. The ophthalmic status is being monitored. The boy needs to be followed up by a pediatric cardiologist, a neurologist and an ophthalmologist. A systematic motor rehabilitation is conducted.

The child can flip from back to front, he is unable to sit, he is unable to rise on his feet on his own. The boy reaches out and grabs with his hands and can hold toys for a short time. He follows with his eyes and turns his head after moving toys and people; he smiles when they talk to him gently; he winces and listens to a loud sounds and reacts briskly when familiar adults are talking to him. The boy pronounces sounds and random sound combinations. The child is completely dependent on the care of adults. Diapers are used.

Myles

Boy, Age: 5
Country Code: Asia.2
Region: Asia
premature (27 wks) – multiple medical complications, hydrocephalus, epilepsy, retinopathy (vision impairment), CP, hearing impairment, global developmental delays; birth mother smoked cigarettes & drank alcohol during pregnancy.
Listed: Sep 2021
$230.40
has been donated towards the cost of my adoption, including $125.00 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!
Myles was just starting to wake up at the beginning of our Zoom call and as his caregivers slowly nudged and tickled him, he showed us the biggest smile and sweetest little giggle. Four-year-old Myles is not speaking, but we learned from his caregivers that he is a quite boy who prefers not to be disturbed. His favorite toy is his teether, he likes being tickled, and dislikes being moved around.

Myles diet consists of mashed foods, his favorite being fruits.  Myles spends most of his time in his bed or in a support chair. Because he is only allotted one therapeutic device per year, he doesn’t currently have a child walker. With more opportunities to put weight on his legs, he may possibly have the potential for assisted walking in the future.

Myles was born prematurely and has been diagnosed with global developmental delays, cerebral palsy, epilepsy, hydrocephalus and hearing impairment. Myles resides in a nursing home and receives 30 minutes of occupational and physical therapy at a local hospital each week. The agency has much more information on Myles! Could your family be the one he needs?

Vann #

Boy, Age: 3
bilateral cleft of the upper lip with a cleft of the hard and soft palate; cheiloplasty; hydrocephalus; cognitive delays
Listed: Oct 2021
$260.00
has been donated towards the cost of my adoption, including $250.00 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!
Vann smiles and reacts when caregivers interact with him. He can roll around in his crib and is often placed in a walker. He picks up toys, shakes them and tries to manipulate them.

Update Jan 2022:   He’s now independently sitting, standing up in his crib holding on to the rails and taking steps when holding the hands of an adult. He’s receiving daily physical therapy to get stronger and the therapist believes he will soon learn to walk. He maintains eye contact and enjoys interacting with other adults and children Vann has undergone the second stage of cleft surgeries. He’s now eating soft foods from a spoon.  He’s currently living in a group home with children who are more significantly delayed. His social worker believes this will prevent him from developing appropriate communication and social skills, so she is actively looking for a therapeutic foster family for Vann, so that he can continue to reach developmental milestones.

Lennon

Boy, Age: 5
Primary Diagnosis: Other Special Needs
Developmental disorder of speech and language, Other phakomatoses, Umbilical hernia, Congenital malformation of cardiac chambers and connections, Esotropia, Congenital ptosis, malnutrition, anemia, Other disorders of psychological development
Listed: Nov 2020
$137.00
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!

Kellen

Boy, Age: 5
Primary Diagnosis: Hydrocephalus
congenital malformation of the corpus callosum, hydrocephalus, ventricular septal defect, atrial septal defect, congenital talipes calcaneovarus, bilateral inguinal hernia, umbilical hernia, polysyndactyly; preterm
Listed: Dec 2017
$1,061.08
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!
Sweet baby boy!

Fabian

Boy, Age: 3
Primary Diagnosis: Other Special Needs
Fetal alcohol syndrome (dysmorphic)
Listed: Nov 2020
$1,329.50
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!
He has 5 siblings in the family-style children home, they are not adoptable.

Cedric

Boy, Age: 5
Primary Diagnosis: Congenital Heart Defect
Disorder of the Brain; Other developmental disorders of speech and language; Undescended testicle; Accessory thumb(s); Acquired deformity of chest and rib; Ventricular septal defect
Listed: Dec 2019
$3,350.65
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!

Alistair

Boy, Age: 5
Primary Diagnosis: Cerebral palsy
Spastic hemiplegic cerebral palsy; Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures; Unspecified intellectual disabilities; Asthma; Abnormal results of cardiovascular function studies
Listed: Dec 2019
Although there are no official holds in this country, this child has a hopeful family who has a completed homestudy.
$1,049.68
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!

Joel and Jolene

Sibling Group
Ages: 9, 5
Country Code: Asia.2
Region: Asia
Cognitive, speech, motor, socio-emotional delays; sensory integration disorder; vision needs; diagnosis of microcephaly at birth; history of epilepsy
Listed: Sep 2022
$821.12
has been donated towards the cost of my adoption, including $371.12 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!

Some of Joel’s favorite activites include building large castles with Legos, playing basketball and soccer. Joel is EXTREMELY proud of his basketball skills and thinks he is good at dunking the ball! Those who know Joel say he is shy and introverted during initial meetings. After becoming more familiar with someone, he will feel more relaxed and is comfortable carrying on a conversation with them.

Joel has a good relationship with his foster family. He affectionately calls his foster mother ‘auntie’ and foster father ‘uncle’.  Joel enjoys playing games and chatting with his 6 year old foster brother. When his foster family’s 11 year old grand-daughter visits, he enjoys playing board games with her. One of Joel’s fond memories was from when his foster parents took him and his foster brother to “Spider-man: No Way Home.” After the movie he excitedly narrated a large portion of the movie.

Joel has a diagnosis of ADHD and is currently on medication to help with his concentration. Joel is a 3rd grader in elementary school and overall makes good grades. When asked, Joel stated computer class and physical education are his favorite periods. Joel shares that he has 7 close friends at school. During recess, he enjoys playing tag, and a game of cops and robbers. Joel likes being chased because he rarely gets caught!

Jolene enjoys playing with toy cars, riding her bike, playing with bouncy balls, drawing, and listening to stories. Jolene is initially quiet when introduced to new environments. Once she is comfortable, she becomes active and actively engages with familiar adults. Jolene likes to act affectionately towards familiar adults and LOVES to receive hugs from them.

Jolene has a good relationship with her foster parents and 5-year-old foster brother.  She enjoys narrating stories to her foster father and talking with her foster mother about events that took place during her day.

Jolene has a diagnosis of global delay, and vision needs with a microcephaly diagnosis at birth. She has a past history of epilepsy with no current concerns noted. Jolene attends kindergarten and an after school early intervention education program.  Her early education program provides small class size with one-on-one attention and various weekly therapies in OT, PT, speech, and sensory integration. She is progressing with the help of her therapies including in the areas of vocabulary and motor skills. Jolene responds well in therapy and at home to praise and encouragement!

While Joel and Jolene live in separate foster homes, they get to see each other at events and private intimate meetings arranged by the foster agency. When together, they like to play with toy cars and jump rope.

Jeremy

Boy, Age: 3
Country Code: LA-2
Listed: Oct 2022
$22.50
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!
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!

VIDEOS:
https://vimeo.com/maaspecialkids/maa-jeremy1
https://vimeo.com/maaspecialkids/maa-jeremy2
https://vimeo.com/maaspecialkids/maa-jeremy3
Password: Adoptmaa

Tyson #

Boy, Age: 5
Listed: Apr 2021
$27.00
has been donated towards the cost of my adoption!

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

Geno

Boy, Age: 4
Country Code: EE-6
Primary Diagnosis: Other Special Needs
Multiple congenital anomalies, primarily of the urinary system, and developmental delay
Listed: Jun 2022
*** 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 ***

Kohen

Boy, Age: 3
Primary Diagnosis: Spina bifida
$6,009.80
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!
Kohen has had surgery for his spina bifida.  His mental development is normal.

Russ and Ward

Sibling Group
Ages: 4, 4
Primary Diagnosis: Other Special Needs
Twin Boys

Boy 1: disorder of the brain, hypermetropia, astigmatism, atrial septal defect, patent ductus arteriosus, exposure to hiv, malnutrition

Boy 2: disorder of the brain, astigmatism, exposure to hiv, lack of development

Listed: Jan 2020
$2,200.20
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!
This will be a two part adoption: Family must be prepared to adopt boy 1, then have to go back to adopt boy 2. this is because only boy 1 qualifies for expedited availability as both have not yet been listed on the registry for one year. Once adoption 1 is done, the family can file for adoption of the second child immediately as a bio sibling of their child.

Eldon

Boy, Age: 3
Primary Diagnosis: Congenital Heart Defect
Disorder of brain, Undescended testicle, Other specified chromosome abnormalities, Congenital Heart Defect (Atrial septal defect & Other specified congenital malformations of heart), Hypermetropia
Listed: Nov 2020
$1,395.50
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!
He has a severe heart issue, doctors do not give him a chance for heart surgery, by their opinion he needs heart transplantation, and it’s impossible in his home country.

He is such a good kid, his development is pretty good.

Rafi

Boy, Age: 4
Primary Diagnosis: Other Special Needs
Paraplegia; Nonobstructive reflux-associated chronic pyelonephritis; Congenital dislocation of hip, bilateral; Other congenital deformities of feet; Other congenital malformations of spine, not associated with scoliosis; anemia; Other ill-defined heart diseases; Hypermetropia; Renal hypoplasia, unspecified
Listed: Feb 2020
$2,525.40
has been donated towards the cost of my adoption!

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

Kai

Boy, Age: 5
Primary Diagnosis: Other Special Needs
Congenital tracheomalacia
Listed: Oct 2020
$2,578.33
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!
At age of 2 months old he survived a surgery for heart defect

Harlan

Boy, Age: 4
Primary Diagnosis: Congenital Heart Defect
Multiple congenital malformations, not elsewhere classified; Other specified congenital malformations of brain; spastic tetraplegia; epilepsy, Congenital Heart Defect (ASD), Nonrheumatic mitral (valve) insufficiency;
Pain in joints
Listed: Nov 2020
$1,258.60
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!
Harlan has 2 siblings: his half-sister, born in 2010, is not adoptable because she lives in her biological father’s family. His brother, born in 2006, lives in a different orphanage.

Due to this boy’s special news, the governmental authorities may consider the separation of brothers. However, the family is to be approved for 2 children to cover the age of the older brother, (even if they don’t plan to adopt him) in order to separate the boys.