Bailey

Girl, Age: 12

Country Code: LA-2

Primary Diagnosis: Cerebral palsy, Epilepsy/ seizure disorder, Global developmental delays

spastic quadriplegia; generalized hyperreflexia; epilepsy; global developmental delays

Listed: Oct 2022

2025 MACC, Available to Large Families, Available to Single Mothers

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

Katrina #

Girl, Age: 12

Region: Eastern Europe

Primary Diagnosis: Global developmental delays

Listed: Sep 2022

2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Mothers

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.

Janice

Girl, Age: 7

Country Code: Asia.2

Region: Asia

Primary Diagnosis: Cerebral palsy, Global developmental delays

Moderate Cognitive and Motor Delays

Listed: Aug 2022

24 for 2024

Sizable Grants $2,500+

Janice enjoys outdoor activities, especially riding her tricycle, sliding down the slide in the neighborhood park and bouncing around a basketball. When she isn’t participating in a physical activity, Janice likes reading books and singing nursery rhymes with “Twinkle, Twinkle, Little Star,” and “The Butterflies are so Beautiful” being her favorites!

Janice is shy around strangers, but interacts with them once she becomes familiar. Janice acts affectionately towards people she is familiar with and asks for cuddles. Janice has a close bond with her foster family and likes to seek their affection.

Janice has a Cerebral Palsy diagnosis with moderate cognitive and motor skills delays. She currently attends physical, occupational and speech therapies. Janice has made good progress, and she is now able to climb stairs, jump on the ground 10 times in a row, and complete a 4 piece puzzle! At home, Janice will imitate her foster mother’s speech and ask questions.

Could you imagine pushing Janice on the swings at your neighborhood park or teaching her how to ride a bicycle? If you think you could be the right family for her, don’t hesitate to reach out

Jianna

Girl, Age: 11

Country Code: Asia.2

Region: Asia

Primary Diagnosis: Global developmental delays, Speech Delay

Motor delays

Listed: Aug 2022

Jianna’s favorite activity is singing and preforming on stage at church. She has a good sense of rhythm, and she can hum the melody of songs she’s only listened to once or twice! When Jianna isn’t performing, she enjoys riding her bicycle and watching Sailor Moon. Those who know Jianna describe her as friendly and say she LOVES to laugh!

Jianna has moderate cognitive, speech, and motor delays. She currently attends occupational, speech and physical therapy weekly. Jianna is enrolled in elementary school and attends special education classes. Her teacher noted she is able to identify colors, identify objects and their names, and speak in short sentences.

Could you imagine yourself dancing and singing karaoke with Jianna? If you think you could be the right family for her, don’t hesitate to reach out!

Ernest

Boy, Age: 13

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Autism, Blind / VI, Global developmental delays

Listed: Aug 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 ***

This boy wants to be adopted very much, he writes letters for his future family and asks them to come and visit him soon. He is very sensitive and caring child who longs for love and tenderness but sometimes he gets angry and disrespectful… His grades in school are very good but he doesn’t remember about his homework sometimes. He needs a lot of support and supervision from his teacher along with love and support from his future family.

Pattie and Paul

Sibling Group

Ages: 10, 14

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Fetal Alcohol Syndrome, Global developmental delays, Speech Delay

Listed: Jul 2022

Pattie has FAS, hypothyroidism and mental delay.

She completed 3rd grade and needs help with her classes. Her caregivers describe her as kind and nice girl who smiles a lot. She has a positive attitude with her peers and adults. She is very close with her brother.

Paul graduated from kindergarten this year. His health is good, but he has a speech impairment and minor developmental delay. He likes to play outside and enjoys soccer and biking. He loves art and is making progress with learning.

They are nice children who are dreaming of having parents and will do well in a family.

Natala

Girl, Age: 6

Country Code: Asia.2

Region: Asia

Primary Diagnosis: Epilepsy/ seizure disorder, Global developmental delays, Speech Delay

Listed: May 2022

Introducing….Natala! Natala likes crawling, rolling around, and making sounds like she is talking. Sometimes, when she is unhappy, she lets you know by crying and fussing but will calm down quickly once attended to. Natala has good adaptability for a young child and is not shy with strangers. Currently, Natala takes 2 short naps each day, once in mid-morning and once in the early afternoon. Her nap schedule is flexible. She can flip herself over while lying down, stay seated for up to 20 minutes with support, and has recently started crawling! Because she has high muscle tension, her legs sometimes stay lifted slightly in the air while crawling. Among many other capabilities, Natala is able to grasp objects in each hand and pass them from one hand to the other. Although Natala has delayed speech, she has shown progress between her most two recent visits in March and August of 2021. She currently understands a couple of simple words including ‘goodbye’ and ‘kiss’, in her language of course, and has normal hearing. Doctors are monitoring mild vision damage and plan to continue to assess her vision as she develops. Natala has also been diagnosed with epilepsy however since beginning medication, no tremors or twitching have been observed. Natala is currently being cared for by a foster family and has formed appropriate attachment to her foster mother. Young Natala needs a forever family that can support her, love her, and celebrate along with her as she continues to reach milestones. Could you be that family?

Update 2022:

Natala participated in our February 2022 Virtual Superkids trip. She was 2 1/2 years old during the visit. Natala is a special girl who will require lifelong care by her adoptive parents.

Natala expresses her joy through smiling and laughing. She enjoys toys that make sounds and lights up when playing with dolls. She expresses sadness through crying. Natala has global delays in development and non-verbal. She is most comforted and connected to her foster mother.

Bodie # (Barron)

Boy, Age: 8

Region: Eastern Europe

Primary Diagnosis: Endocrine disorder, Global developmental delays

Listed: Apr 2022

Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers

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.

Bodie responds to his name with a smile, to sounds and noise. He keeps an eye on the movement of people and objects in the room. He is described as a calm and pleasant child. He is well attached to his caregivers and responds well to them. When given attention, he reacts positively and with a smile. Most of the time, the child is energetic and physically active. It is difficult for him to stay in one place, constantly moving and exploring.

The child expresses his joy by erratically clapping his hands and by making noises. When held by the hand he makes several steps. (was previously also listed as Barron).

Ronnie and Mary

Sibling Group

Ages: 15, 14

Country Code: EE-2

Region: Eastern Europe

Primary Diagnosis: Global developmental delays

Cognitive Delay, Speech Disorder

Listed: Sep 2021

Ronnie

The girl does not cause any educational problems either at school or in the orphanage. She is very diligent and obligatory. She is happy, independent and caring girl who likes to help with younger children. She is willing to cooperate, she likes meetings with a psychologist and needs time to adapt to a new environment.

She rides a bike, roller-skates, swims, participates in sports and dance activities. Physical activity gives her joy. She has a great artistic talent, but does not believe in herself. She likes to travel and is very curious about life and surroundings, constantly asking questions.

Mary

SN – Moderate intellectual disability, speech disorder

Mary is a very cheerful child. Despite speech disorders, she easily communicates with caregivers or peers. She likes to play with younger children. She carries them in a cart or leads them by the hand. She started learning to roller-skates, likes swimming in the pool, sports and dance activities. She goes to a special school. She doesn’t make any behavior problems. She doesn’t read books on her own, but she likes to see the pictures.

The sisters wish to be adopted together and hope to find a forever family!

Picture of Ronnie coming soon!

Myles

Boy, Age: 8

Country Code: Asia.2

Region: Asia

Primary Diagnosis: Cerebral palsy, Global developmental delays, Hydrocephalus

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

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?

Emma #

Girl, Age: 9

Region: Eastern Europe

Primary Diagnosis: Epilepsy/ seizure disorder, Global developmental delays, Hydrocephalus, Other Special Needs

Condition after herpes-viral encephalitis. Hepatitis caused by CMV. Hypotrophy. Hydrocephaly – of mild degree. Congenital dyserythropoietic anemia. Delayed neuro-psychological development.

Listed: Sep 2021

2025 MACC, 24 for 2024, Available to Large Families, Available to Older Parents, Available to Single Mothers

Emma was recently transferred to a group home where she can receive more specialized care to help her continue to develop and receive appropriate medical care. She is receiving monthly blood transfusions at this time for her anemia. She had surgery to correct clubbed feet in 2020. She can sit unassisted, stand next to a stable support, walk around fixed supports and walk while holding the hand of an adult. Videos from May 2021 show Emma playing with an electronic toy. She is pushing the button to get the toy to make a sound. Her fine motor skills are not well-developed at this time, due to her spasticity. Emma responds positively to adults and other children. She smiles and laughs when adults interact with her.

The agency staff member who visited her during March of 2024, says the following:

Emma is a sweet little girl who needs a loving and supportive family environment. During my brief visit, the child was constantly on the move except for the brief moments when she played with a particular toy or during her brief moments of protest. At the present time, the child’s needs are met at a basic level, with particular attention paid to her medical needs. The lack of systematic and in-depth work of specialists (such as a rehabilitator, occupational therapist, special pedagogue, speech therapist and others) is felt, which the institution currently does not have the opportunity to provide. By falling into a suitable loving family, receiving more attention and adequate care and activities, Emma could show her potential to a greater extent.

Update 8/2024

Special needs: low birth weight – 1800 gr; condition after herpes viral encephalitis; condition after hepatitis caused by CMV; congenital dyserythropoietic anemia; hydrocephalus – mild degree; infantile cerebral palsy – spastic quadriparesis; symptomatic epilepsy; delayed neuropsychological development

Therapy: Convulex 4+4+4 ml., Clonarex 2 x ¼ tablet, Repitend 4 ml – 0,4 ml. Carsil – 2 x ½ capsule daily, EXJADE – 1 tablet daily, Urinal x 5 ml daily, Vitamin D3 x 2

Emma makes steps but always and only with the help of a support. She does not control her physiological needs and wears diapers. She listens to children’s songs and fairy tales and claps with her hands. She holds a toy she has been offered but she would most often put it in her mouth without playing with it.

Emma needs monthly blood transfusions and regular consultations with a neurologist and hematologist.

Taylor

Girl, Age: 10

Country Code: Asia.4

Region: Asia

Primary Diagnosis: Global developmental delays, Thalassemia

Beta-thalassemia trait; ADD; low average intelligence

Listed: Sep 2021

24 for 2024, Available to Single Mothers

Sizable Grants $2,500+

Taylor was born to a mother who tested positive for Anthetamine and Methanthetamine at the time of her birth. She did not experience any type of withdrawal symptoms. The birth mother also smoked throughout pregnancy. Taylor was placed into government care due to her birth mother’s drug use.

When she was 4 years old, she was placed with a local family for the purpose of adoption. She lived with that family for 17 months. The family chose not to finalize the adoption. Taylor was placed in an emergency foster placement for 7 months and then moved into a permanent foster home, where she currently resides.

The previous foster family described her as “a happy and outgoing child who has a very good memory”. Her current foster parents describe her as “talkative, happy and polite”. She seeks out interactions with others. She can play alone appropriately, but prefers to play with other people. She is willing to share her toys. Her gross and fine motor skills are at the appropriate developmental level for her age. She talks in complete sentences and can answer questions and follow verbal instructions. She is diagnosed with ADD and has difficulty staying focused on activities, especially when required to sit still for longer periods of time. She will also “push the boundaries” to see what she can get away with. If she does not get her way, she will throw a “tantrum” to see if the adult will give in.

She is showing signs of the effects of the placement transitions that she has experienced in her young life. She often asks for permission to do even the smallest things. She worries that she is in trouble. The foster family reports that she says she wants to be good. She is seeing a clinical psychologist, who has begun preparing her for a permanent adoption placement. Interest families should be knowledgeable of the effects of trauma and disruption or be willing to obtain continual education on the topic during the adoption process.

Mila #

Girl, Age: 9

Region: Eastern Europe

Primary Diagnosis: Cerebral palsy, Global developmental delays, Hydrocephalus

Hydrocephaly; Strabismus; G-tube feeding; delays in development

Listed: Jul 2018

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***

2025 MACC, Available to Large Families, Available to Older Parents, Available to Single Mothers

Mila turns her head towards sound and looks at people and objects of interest. She recognizes the faces of the staff. She can roll over, but still has difficulty with head control. She enjoys musical toys that spin and will focus on those for short periods of time.

Update 8/2024

Special needs: low birth weight (2410 gr.); congenital anomaly of the central nervous system: moderate ventriculomegaly; cyst of the cave of septum pellucidum and cave Vergae; rejected prior diagnosis of hydrocephalus; brain atrophy; infantile cerebral palsy; syndrome of congenital anomalies mainly affecting the facial area; convergent strabismus; nystagmus; occipital alopecia areata; severely delayed physical and neuropsychological development; severe mental delay

Family history: born from a high-risk pregnancy by a mother with positive serology for hepatitis B and epilepsy (on three medications for epilepsy).

Molly turns independently in bed. Although she is unable to sit independently, Molly maintains a sitting position for a more continuous period at the presence of additional support. She has no stable support in the legs.Molly selectively responds with an appropriate emotional reaction to different situations and objects. She is able to express discontent from internal discomfort through crying. She smiles as a response to a smile, speech and closeness from the caregiver, she positively reacts to positive stimulation. Molly easily handles being moved from one space to another, she is calm and sometimes demonstrates interest. She has formed emotional preferences to certain significant members of the staff, mostly the rehabilitator who works with her, as well as the teacher from the group at the Center for Special Educational Support. Molly laughs at specific sounds coming from a musical toy. She shows preferences for specific children’s songs while she does not react to others.

Molly wears diapers, easily goes to sleep and easily wakes up. She eats food from a spoon

Victoria

Girl, Age: 13

Country Code: LA-2

Region: Latin America

Primary Diagnosis: Global developmental delays

Diagnosed with a mental delay, a non-specified compartmental deterioration, and a language disorder.

Listed: Jan 2020

2025 MACC, Available to Large Families, Available to Single Fathers, Available to Single Mothers

Sizable Grants $5,000+

Frederick

Boy, Age: 15

Country Code: LA-4: Due to the in-country crisis, government offices and courts that process adoptions may be closed or delayed.

Region: Latin America

Primary Diagnosis: Global developmental delays

low muscle tone and has been diagnosed with developmental delays

Listed: Aug 2013

**** 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 ***

Available to Single Mothers

UPDATE JANUARY 2016: Frederick now has a wheelchair that he can move on his own,and he is going to be able to go out to the neighborhood school starting this week! He is making amazing progress.

Frederick has low muscle tone, and he has been diagnosed with developmental delays. He is capable of feeding himself (but he makes a mess!) and just needs more practice to develop that skill. There is concern about core muscle development, but Frederick works hard, so it is believed that he may be able to walk some day.

Frederick is a hard-working little boy who wants to develop his skills. He has developed friendships with some of the other kids in the orphanage (both able-bodied and special-needs kids). He responds well to physical therapy, and in just a couple of months he progressed from simply lying on a mat to attempting to stand and taking small steps. Multiple unrelated children can be adopted together.

Talbot

Boy, Age: 15

Country Code: Asia.2

Region: Asia

Primary Diagnosis: Global developmental delays

Developmental Delays, feeding issues, failure to thrive, left congenital ptosis, laryngomalacia and supraglotoplasty

Listed: Apr 2012

**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

Talbot entered foster care as a result of being removed from his home due to his parent’s inability to provide a safe and stable, loving home for him. He has resided with a foster family since July 2011. He is growing and developing in his foster family’s care. Talbot likes toys that make sound. When he hears music, he dances and laughs out-loud. He enjoys taking walks with his foster family. He is able to say Thank you, Auntie, Mama, and Papa.

Talbot was diagnosed at a few months of age as having feeding issues, failure to thrive, left congenital ptosis, laryngomalacia and supraglotoplasty. According to a October 2011 developmental report, he was delayed in cognition, language, & gross and fine motor skills. He attends weekly occupational and language therapy classes, showing improvement in the past few months. He is able to walk on his own and at the time of the assessment, he was working on climbing stairs. His appetite has picked up and he enjoys eating noodles and biscuits among other foods.

Talbot will do well in a family who is patient, has time to work on developmental growth through play and exploration, and able to access early intervention services.

Mathis

Boy, Age: 11

Country Code: EE-7

Region: Eastern Europe

Primary Diagnosis: Global developmental delays

FAS and delayed development. Mathis recently had surgery to repair his cleft palate. He has physical and psychomotor delays.

Listed: Feb 2016

Mathis has a problem eating and is fed with a tube although he has learned to suck a bottle and can eat mashed food. He still receives liquids from a tube. His language skills are weak. He can walk holding on to something and is crawling. He has started to walk, climb, and manipulate toys and objects. He is doing very well and his development in general is very optimistic.

Description from a visiting family: peaceful, gentle, and enjoys adult attention. He understands the language and is very observant. Mathis is calm, quiet, crawls, responsive, content, alert, survivor, easily comforted.

Bailey

Katrina #

Janice

Jianna

Ernest

Pattie and Paul

Natala

Bodie # (Barron)

Ronnie and Mary

Myles

Emma #

Taylor

Mila #

Victoria

Frederick

Talbot

Mathis

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