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.

Monte

Boy, Age: 6
Country Code: LA-2
Primary Diagnosis: Fetal Alcohol Syndrome
Fetal Alcohol Syndrome; Microcephaly
Listed: Nov 2022
$45.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Monte has a bright and warm smile. He is described as a social young boy who likes to play with his friends. He also gets along well with adults and is very affectionate with his caretakers. Sometimes he is timid, but he warms up quickly. Monte loves to build things. He follows instructions well and enjoys spending time with his foster family. Contact the agency to learn more about Monte and his special needs!

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

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

Finley

Boy, Age: 2
Country Code: LA-2
Primary Diagnosis: Down syndrome
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!
Finley is a lovely young boy with a bright smile! Finley is waiting for a forever family of his own! Contact the adoption agency to learn more about Finley!

VIDEO: https://vimeo.com/maaspecialkids/maa-finley

Password: Adoptmaa

Daisy

Girl, Age: 3
Country Code: LA-2
Primary Diagnosis: Other Special Needs, Speech Delay
Neglect, Speech and language delays; dextrocardia, gastrostomy and tracheostomy care, unspecified respiratory failure
Listed: Nov 2022
$4.50
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!
Daisy has bright and cheerful eyes. We hope her forever family sees her while she is so young! She will need a family who is committed to caring for her special needs and daily care while she continues to grow and develop. Daisy has speech and language delays, dextrocardia, gastrostomy and tracheostomy care, unspecified respiratory failure, and a history of neglect and abandonment.

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.

Karmen, Kevin & Kendel #

Sibling Group
Ages: 8, 8, 7
Listed: Nov 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 ***
Karmen and Kevin are twins and Kendel is their little sister.
Both girls are physically healthy and developmentally on target for their age.
Kevin has been diagnosed with Duchenne spinal muscular dystrophy and has developmental delays.

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.

Suvi

Girl, Age: 6
Country Code: LA-2
Primary Diagnosis: Skin Condition
Scoliosis; Epidermolisis bullosa simple
Psychomotor delay- language and cognitive
Bronchobstructive syndrome (BOS), Cutis laxa (skin condition); history of pigmentary lesions on the face;
ptosis of upper eyelids that will be corrected for oculoplasty service
Listed: Oct 2022
$26.10
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Suvi loves to paint, go for walks, and play at the park. She likes singing and dancing to children’s songs. She also likes to watch television. Suvi is a beautiful young girl who needs the love and support of a family to continue to grow and develop. Contact the agency to learn more about Suvi and her special needs!

VIDEOS:
https://vimeo.com/maaspecialkids/maa-suvi1
https://vimeo.com/maaspecialkids/maa-suvi2
https://vimeo.com/maaspecialkids/maa-suvi3
https://vimeo.com/maaspecialkids/maa-suvi4
Password: Adoptmaa

Bailey

Girl, Age: 9
Country Code: LA-2
spastic quadriplegia; generalized hyperreflexia; epilepsy; global developmental delays
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!
Bailey accepts physical and verbal contact from others. Bailey likes toys that make noise, and she sometimes smiles at the stimulation of an adult. Bailey will need a family who is able to care for her special needs and provide for her daily care. Agency staff met Bailey in July of 2022. We hope her family sees her soon! Contact the agency to learn more about Bailey and her listed medical needs.

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

Amelia

Girl, Age: 5
Country Code: LA-2
Trisomy 18 / Edwards syndrome; Developmental delay; cognitive delay; microcephaly; pervasive disorder; hearing loss; epilepsy
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!
Amelia is a young girl, born in spring 2017, with beautiful bright eyes. Agency staff met Amelia in July of 2022; they can provide more about this sweet girl and her listed medical needs!

VIDEO:
https://vimeo.com/maaspecialkids/maa-amelia1
Password: Adoptmaa

Finn

Boy, Age: 6
Country Code: LA-2
Primary Diagnosis: Cerebral palsy
cognitive delays, cerebral palsy
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!
Finn is a beautiful boy who will need a special family to care for his medical needs. Agency staff met Finn in July of 2022; they can provide more info on Finn and his medical needs!

VIDEO:
https://vimeo.com/maaspecialkids/maa-finn1
Password: Adoptmaa

Rowan

Boy, Age: 7
Country Code: LA-2
Primary Diagnosis: Epilepsy/ seizure disorder
developmental delays and epilepsy
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!
Rowan is smiley, and loves to clap and listen to what is going on around him. Agency staff met Rowan in July of 2022! Contact them to learn more about Rowan and his medical needs!

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

Elon #

Boy, Age: 7
Primary Diagnosis: Arthrogryposis
Arthrogryposis, delays in 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!
Elon walks independently. He feeds himself and cleans up after his meals. He does not talk at this time, but understands what is said to him and follows simple instructions. He responds to his name. He interacts appropriately with adults and with other children. He attends to tasks and works well 1:1 and in a small group.

Brock

Boy, Age: 8
Country Code: LA-2
Listed: Oct 2022
$90.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Brock is a very social boy, who likes to kick a ball. Brock has continued to develop and grow. Agency staff met Brock in July of 2022! We hope his forever family will see him soon! The agency has additional information available for inquiring families.

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

Jeremy

Boy, Age: 3
Country Code: LA-2
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!
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

Damian

Boy, Age: 11
Country Code: LA-2
Primary Diagnosis: Down syndrome
Listed: Sep 2022
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
Damian has Down syndrome, and is an affectionate and loving young boy. He feels close to his caretakers and loves sharing with them. He loves to give hugs. Contact MAA to learn more about Damian!

There is a $1,500 agency fee reduction for Damian’s adoption with a specific adoption agency.

Raydor #

Boy, Age: 6
Primary Diagnosis: Other Special Needs
Possible Autism, Premature
Listed: Sep 2022
$172.50
has been donated towards the cost of my adoption, including $105.00 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!
Raydor was previously listed on Reece’s Rainbow as Randy.

Raydor’s birth mother was addicted to Heroin and took Methadone during pregnancy. Raydor was born premature and spent the first 5 months of his life in the hospital. Raydor knows his alphabet, numbers and colors in both his native language and English. He can do simple addition problems (single digit plus single digit and single digit plus double digit). He speaks in 2 word sentences and memorizes poems. He loves to build houses and other things with Legos and will stay focused on this task for long periods of time. He plays independently and with other children. He enjoys music and often tries to imitate melodies. Raydor has some behaviors that are commonly seen in children on the Autism spectrum. He has not had any type of formal evaluation for Autism. 

Katrina #

Girl, Age: 9
Primary Diagnosis: Global developmental delays
Listed: Sep 2022
$153.10
has been donated towards the cost of my adoption, including $100.00 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!

Katrina’s physical development and gross motor skills are age appropriate. She talks, but has some difficulty with articulation. Her fine motor skills are developed, but slightly delayed. She is diagnosed with mental delays. She knows and names the colors. She knows the letters of the alphabet and she has started reading. She already counts up to 30 and she writes some numbers. She knows the days of the week, seasons, left vs right, body parts, and can follow directions using instructions such as over/under, front/back, etc. She plays well with other children and enjoys attention from adults. She likes to work on a magnetic board, kinetic sand and active cards. She already colors in a contour and she is very diligent when connecting lines. She can cut and glue ready elements. She can read and the fact that she is being praised for that makes her very happy.

 

She follows the directions of an adult in relation to the hygiene and household activities. She can dress and undress her. She washes her hands and feeds herself independently, she makes attempts for self-serving. She takes care her belongings. She keeps her materials from school in a certain place.

Cattleya #

Girl, Age: 3
Shunt due to hydrocephalus
Listed: Aug 2022
$341.65
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!
Cattleya crawls, pulls to a stand, cruises around furniture and takes steps while holding two hands. She’s not yet walking independently, but she’s trying! She explores her environment and interacts with people and with toys. She babbles, but is not yet speaking any words. She is happy and enjoys interactions. She enjoys musical toys. Medically speaking, while her official diagnosis is “malformative syndrome”, she has signs of craniosynostosis.

Issak & Alek

Sibling Group
Ages: 11, 13
Country Code: LA-3
Primary Diagnosis: ADHD
Listed: Aug 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 ***
These brothers are physically healthy, but needing support for behavioral issues as well as ADHD, childhood depression, and attachment for which they need special care, tolerance, education and continuous treatment to cope with a good quality of life.

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.

Nahla #

Girl, Age: 6
Syndromes of congenital anomalies mainly affecting facial appearance; mental delay, unspecified, significant disturbance of behavior requiring care or treatment; mild to moderate deficit; hyperactive behavior and underdeveloped speech;
Family history: the child’s birth parents abused alcohol, she has been raised in a neglectful environment
Listed: Aug 2022
$255.20
has been donated towards the cost of my adoption, including $230.00 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!
Medical report indicates that the birth mother is an alcoholic. While it does not state that the mother drank during pregnancy, prospective families should be prepared that Nahla may have FAS.

Nahla is physically healthy. She lived in a neglectful home for the first 4 years of her life, before being removed by social services and placed in foster care. She says individual words and some simple phrases. She has made progress in her development since being placed in foster care, but has had to work through behaviors and medical concerns as a result of the previous years of neglect. Progress is being observed in all aspects of her development.

Update Oct 2022:

Nahla’s behavior is characterized by impulsivity and curiosity. Her speech skills present with some deficits. She says the names and denominatives for people close to her – (grandma), (older sister), (uncle), etc. During interaction she uses mimics, gestures, points to what she wants and brings the foster parent to the respective object. She has started to express desires more often, ask questions or express an opinion with simple sentences or two or three words. She understands adults’ speech well and orientates in non-verbal means. She is gradually starting to adhere to personal boundaries and has started to be “shy” in unfamiliar places, as well as set boundaries in her communication with people outside her family circle. She enjoys riding a scooter and bicycle and playing with a ball and at the park. She is able to participate in some playing situations with the biological granddaughter of the foster family. The foster parents are helping her build her skills for independence, as well as self-service skills. The child is unable to eat independently or maintain personal hygiene habits, she is learning to tidy up her belongings and toys. She is able to announce her physiological needs.

Matias

Boy, Age: 10
Country Code: LA-2
Primary Diagnosis: Down syndrome
Listed: Aug 2022
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
Agency staff met Matias in July of 2022. He is an active boy who like to play soccer. He loves to run and jump. Matias also loves to dance.

There is also a $1500 agency grant for Matias’s adoption with a specific adoption agency.

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

Sariah

Girl, Age: 3
Country Code: LA-2
Primary Diagnosis: Genetic Condition (non-DS)
cornelia de lange syndrome confirmed by genetics
Persistent BOS (broncho-obstructive syndrome), sequelae of pulmonary dysplasia plus aspiration cytology for swallowing disorder, hypotonic muscle disorder due to sequelae of hypoxic ischemic encephalopathy, history of resolved hypertrophic heart disease, malnutrition, severe psychomotor delays, history of non-recurrent acute episode convulsive syndrome
Listed: Jul 2022
$140.50
has been donated towards the cost of my adoption, including $115.00 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!
Sariah is an adorable little gal, born in summer of 2019, who is described as affectionate and calm. She has established routines for sleeping. She has right hand dominance and can play independently for 15 minutes. She is not potty trained yet. Sariah can reach for objects in front of her, can turn around, and has good head control. She can move around on a mat without help and follow objects with her eyes. She reaches for objects close to her, can adapt to other spaces, and shakes objects that make noise.

VIDEOS:
https://vimeo.com/maaspecialkids/maa-sariah
https://vimeo.com/maaspecialkids/maa-sariah2
https://vimeo.com/maaspecialkids/maa-sariah3
Password: Adoptmaa

Edmundo

Boy, Age: 11
Country Code: LA-2
Primary Diagnosis: Down syndrome
Listed: Jul 2022
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
Edmundo, born in June of 2011 with Down syndrome, is an active boy who is waiting for a loving family of his own. The agency has a video to see him in action. There is a $1,500 agency fee reduction for Edmundo’s adoption via a specific adoption agency.

Yuri

Boy, Age: 14
Country Code: LA-3
Primary Diagnosis: Other Special Needs
Special Need: Burns
Listed: Jul 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 ***
This handsome 14 years old boy is a practitioner of the Christian religion, he likes sports activities such as soccer and cooperative games, he is characterized by being responsible in the preparation of school tasks and he likes research. His favorite food is ceviche, fries and chicken, his favorite color is green, his favorite toy is drones, his favorite character is Cristiano Ronaldo. He wants to be adopted and have a loving and caring family.

Rose #

Girl, Age: 11
Primary Diagnosis: Other Special Needs, Speech Delay
Mild Mental delays and speech delays
Listed: Jul 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 ***
Rose was removed from an abusive home at 9 years old and could not even speak the language of her birth country at that time. She now speaks in sentences, understands everything that is said to her and has made rapid developmental progress. During the visit with our team member, she was talking about the Mom and Dad that she’s waiting for and having a fun time posing for all the photos (see below). She currently lives with an older foster couple, who she calls grandma and grandpa. They have worked with her to teach her many self-help skills. She’s now in school and doing well working with a resource teacher.

John and Jane

Sibling Group
Ages: 11, 8
Country Code: LA-3
Primary Diagnosis: Other Special Needs
SN: Non-malignant neurofibromatosis, Genetic disorders causing uncontrolled growth of tumors along nerves, Psychosocial and environmental problems, Iris Disorder
Listed: Jun 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 ***
John: He presents difficulties in cognitive processes such as: verbal comprehension, visual space, fluid reasoning, which prevents him from learning according to his peers.

He receives classes and educational support under the tutelage of the educators, allowing him to reinforce each area of development. The child receives constant medical check-ups. Since his admission he receives psychological attention, according to the emotional and psychological needs of the child.

He and his sister have a good emotional relationship. He complies with norms and rules within the Center, respects his peers and the staff that works in the Institution.

Jane: The girl receives the necessary medical care, has been assessed in several areas of medicine such as: Traumatology, Psychiatry, Pediatrics, Ophthalmology, Neurosurgeon, Clinical Psychology, performing frequent health checks, in June 2018 she was diagnosed with Neurofibromatosis, like her brother, in the case of a hereditary disease. The care must be thorough, attend medical check-ups and use the creams prescribed by the specialist, it is possible that this disease will affect future learning.

From the assessment process carried out on the student, she shows difficulties in her cognitive processing skills, evidencing immaturity in learning. Her learning style is slow.

She has a good understanding and develops school activities correctly. It does not make it difficult for her to relate to her peers, she likes to talk and also communicate her feelings and emotions. Respect her peers and staff as well as abide by the rules and regulations of the Special Protection Center. She is attached to her brother.

Mike

Boy, Age: 7
Country Code: LA-3
Primary Diagnosis: Fetal Alcohol Syndrome
PSYCHOMOTOR DELAY SECONDARY TO FETAL ALCOHOLIC SYNDROME
Listed: Jun 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!
Mike is interest in interacting with his peers. He has limitations in intellectual functioning and adaptive behavior.

Eduardo

Boy, Age: 9
Country Code: LA-3
Primary Diagnosis: Other Special Needs
mild cognitive disability, mild delays in general development
Listed: Jun 2022
$25.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Eduardo has been in care since March 2018, with a mild cognitive disability. He has slight delays in general development about 6 years, and is making progress. Under normal weight and short height for age from chronic malnutrition. Astigmatism, myopia and strabismus, wears glasses. Difficulty in reading and writing, math and retaining information. Difficulty to maintain attention. Can become frustrated when can’t perform tasks that peers can. Needs motivation to keep trying. Child has no behavior problems. Gets along with peers. Takes pride in personal appearance. Follows instructions. Reserved with strangers, but affectionate with those he knows. With peers friendly, calm, and supportive. Interest in outdoor activities, sports, especially swimming, board games, puzzles and reading stories. Desires a mother and has an idea of having a brother to play with.

Michey #

Boy, Age: 9
Internal hydrocephalus – post Ventriculoperitoneal shunt condition. heart condition – complete AVSD with partially closed chambers. Cleft palate -surgically corrected. Post bacterial meningitis condition – unspecified and acute pyelonephritis. Delays in all aspects of development.
Listed: Jun 2022
*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2022, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***
$1,035.18
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!
Michey walks while holding one hand of an adult. He can take 2-3 steps independently, but is not yet walking independently. He can pull up and cruise along furniture and objects, and also crawls and scoots on his bottom very quickly to get where he wants to go. He has a very short attention span. He lived in an orphanage for the first 7+ years of his life and received very little intervention or opportunities to learn skills. He’s now living in a group home, where he’s receiving therapy and instruction in basic skills. He enjoys listening to music and playing outside on the swing. 

Marianne

Girl, Age: 12
Country Code: LA-2
Primary Diagnosis: Down syndrome
Down syndrome
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
Marianne is a sweet and beautiful young girl, born with Down syndrome in 2010! Marianne is hoping to find a forever family who loves her unconditionally.

VIDEO: https://vimeo.com/maaspecialkids/maa-marianne1
Password: Adoptmaa

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.

Sadie #

Girl, Age: 3
Primary Diagnosis: Other Special Needs
Progressive ossifying fibrodysplasia
Listed: May 2022
$947.00
has been donated towards the cost of my adoption, including $170.00 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!
Sadie has limited movement in her neck, back and hands/arms (due to limited movement of the shoulders). She has more range of motion in her left arm vs her right. She compensates for her limited mobility. She stands on her toes to reach objects (when she cannot extend her arms) and holds on to a support to bend down or she seeks assistance from an adult. She walks, plays with toys, and interacts with her environment. She can put together wooden puzzles, stack rings and perform other basic tasks. She can take the cap off a pen and tries to draw shapes. She interacts with familiar people. She initiates games such as peek-a-boo. She will point to things she wants to communicate her wants/needs. She dances along to music. She can say some simple single syllable words such as ma-ma, but mostly communicates with gestures. She lived in a home with a younger child for a while and did well with the younger child. The foster family limits her interactions with other people, because they are afraid she will get hurt, due to her physical limitations. She plays well with other people, when she is around them. She does not go to preschool due to the fear her foster family has that she will be injured. She shows a preference to certain objects and TV shows (Peppa Pig and Masha the Bear).

Videos from May 2022 show Sadie walking, playing with toys, putting a puzzle together and interacting with adults. The videos show Sadie’s physical limitations.

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.

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.

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
$127.00
has been donated towards the cost of my adoption, including $100.00 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.