Other Special Needs

According to her caregiver, Mariah is a sweet girl, she is such a little “doll”, she likes dresses, shoes, likes to dance and she has an amazing personal charm. But she also has a strong character, pursues a goal, and is very curious about the world. She wants to be independent – she eats her meals alone, uses the toilet herself (and has a good appetite!) – and she also is willing to help.

Mariah has good motor activity, she is physically active, willing to dance and sing. Mariah has a lot of energy, is enduring, does not get tired quickly, and often changes body positions. She tries to be independent.  She does not react with anger to her failures. She is persistent in carrying out instructions and tries to finish what has been started. The girl eats her meals alone, uses the toilet herself, and has a good appetite.

The agency’s representative in country met her in  December 2021 and they have videos and photos to share with an interested family. At the end of the visit while saying goodbye, she quietly asked the representative to find a mother for her.

The agency offers a discount to a special family for this beautiful and brave girl.

Nancy has lived with an experienced foster family since birth. The foster mother was very proactive in getting therapy and services started for Nancy at a very young age. Nancy does not speak, but she understands everything, recognizes people from her immediate environment, laughs with her voice when she likes something. When holding someone’s hand, she can take a few steps. She can crawl and tries to stand up on her own by holding onto a stationary support. She turns easily from back to stomach and vice versa. She sits up and eats from a spoon. 

This little one needs a family to help her reach her full potential. While meeting psychomotor milestones she has other developmental delays.

They have lived in the orphanage since December 2018. Justice is a sweet, social, independent and kind girl. She is very bonded with her sister, Marley. She is a good student and her life is busy with school activities, trips and competitions. Marley is shy and her sister Justice is a role model for her. She likes to play with other children.

The girls want to be adopted and dream about their future family and new life.

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.

Diagnoses include severe prematurity, including damage to the central nervous system –
hydrocephalus; a ventriculoperitoneal shunt was implanted. There is a lag in physical and
neuropsychological development.

Archibald cannot walk independently. He moves by pushing when placed in a walker. Stands up on his own and stands on his feet when in his crib. He can get out of bed by himself. He can go around the whole game room. He can sit for about 15-20 minutes. In terms of fine motor skills, he can pick up a toy himself if it is nearby; he plays for a long time and prefers to manipulate with his left hand. If the toy is at a distance, he tries to reach it. He likes musical toys. He recognizes adults. He has a good emotional tone, he enjoys contact with adults he knows; he loves when they praise him. He gets angry if his toy is taken away and tries to keep it in his possession. Archibald cannot speak but he makes long sounds. In interpersonal relationships he shows preferences for certain adults and initiates contact with them. He plays with toys. The child doesn’t have independent household hygiene habits. He is calm when changing and bathing, as well as in his sleep. Archibald does not take an afternoon nap, he eats everything. He is very stubborn and when he decides that he wants to pick up an object, no matter how heavy and large, he does his best. He still uses a diaper, potty several times a day. His sleep at night is
peaceful. He has daily kinesitherapy and sessions with a teacher. He is followed by a
neurosurgeon.

Viv is a cute little girl who likes watching children’s videos and loves playing outside at the park. She loves music and dancing while sitting. Viv gets excited when playing with dolls and listening to music. Her general development is within her age range, but a little behind because of her skin condition. Contact the adoption agency to learn more about Viv and her listed medical condition!

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.

Update Aug 2023:His long list of medical issues are all related to his premature birth; his weight at birth was just over 2.5 pounds. His medical needs include: bronchopulmonary dysplasia; pulmonary hypertonia; persistent foramen ovale; peripheral pulmonary stenosis; persistent arterial canal (collateral); periventricular leukomalacia; and retinopathy of a prematurely born child. This bright boy can hold toys and play with them purposefully. He begins to babble and recognizes familiar people, greeting them with smiles and laughter. He is calm but expresses displeasure by crying when he is unhappy or his needs are not being met. He is not yet able to feed himself, and though he can roll from front to back, he does not yet sit or stand unassisted.

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.

Zoey is one of the most beautiful little girls you’ll ever meet. She was born with some developmental delays, but then experienced a stroke when she was two and a half. This greatly set back her abilities. However, since then she’s been in a foster family where she’s relearned how to sit, roll, and grasp toys. She is working on self-feeding and becoming verbal again. Although Zoey had a seizure with her stroke she hasn’t had one since, and rarely requires medical care now. However, she may benefit from a better neurologist to understand her brain’s unique functions and abilities. Zoey is not short of opinions and will let you know exactly how she is feeling with tears or laughter! She loves to play and her giggle is absolutely infectious. She loves playing with water, musical instruments, and anything that makes noise. Zoey also loves to eat and isn’t picky at all! She is a social girl who has loved having two foster brothers. Zoey will bring an abundance of joy to any family who chooses to love her forever!

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

Maleah is described as kind and sweet. Maleah has been in and out school due to inconsistent placements. She is excited to learn and share what she understands such as addition. She’s entered the teenage years and is excited to share her opinions.

Single mothers are encouraged to apply for her! Agency staff met beautiful Maleah in February of 2023. Our staff who met her believe she would do best in a home with older children or no children. The agency encourages interested families to contact them, for additional information.

Hanelle was admitted to the Group home in March 2021. The director of the home reported that since then the child has improved significantly – she has become stronger, she has started to eat better; she can now turn her self from the back to the abdomen. There is no support for the legs – when they put her on her feet. If she is put to sit, leaning on pillows, she stays in this position stably. She does not receive any therapies. She has better head control, now. 

The child has adapted to the new environment. At first, she didn’t want to eat. She is eating well now. She likes to be paid attention to, held in her arms and rocked, she likes to be massaged. She seeks attention and tries to attract attention to herself by making sounds. She smiles, even laughs out loud at the teasing of adults. She reacts when they talk to her and when she hears her name. 

She started eating better. She eats pureed common food with both a pacifier and a spoon. They feed her. She prefers to eat sweet things. Hanelle loves mashed fruits and vegetables. They give her adapted and vitamin-enriched milk with biscuits. Drinks water from a pacifier; can’t drink from a glass.

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

Updated May 2019: Harmony was recently moved to a smaller family style center, where is receiving more attention and care. She still goes to the daycare center at the orphanage and will go to school once she turns 7. She is described as very friendly. She is not aggressive at all and interacts well with the other children. She responds to sounds and tone of voice. She can be comforted with a soft tone. She will hold toys and tries to interact with them, but she needs help to know what to do with them. She loves a rocking horse and will play on it for long periods of time. She will laugh and stop rocking to clap her hands in order to show her pleasure. She says some sounds such as “ba-ba”, “ma-ma”, and “la-la”. She enjoys tactile input and responds well to it. She can stand with support and can walk pushing a walker or when someone is holding her hand. She has not had any instruction in how to walk in a way that will accommodate her lack of vision. Since coming to the center, she has learned to drink from a special cup and is eating from a spoon.

Photos and videos from April 2019 are available through the agency

Updated Jan 2017: Harmony tries to sit independently and stands with the help of an adult or holding onto support. She can step aside holding onto support, pushes the walker with help and guidance by an adult. She is visually impaired – holds a toy handed by an adult, studies the objects with her hand. She has delayed neuro psychological development. When she gets upset, she self-harms.

Harmony expresses her emotions with vocalization – vowel sounds and random sounds. When frustrated she can express her discontent. She can tell apart the tone of voice, reacts with a smile to caresses when she’s calm. The child is fed with a spoon by an adult, drinks from a cup held by an adult.

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.

Florence is a beautiful, smiley and easy going girl! She thrives with her title of Princess in her foster home.

Florence is nonverbal but uses other ways to communicate. She smiles and arches when she is happy and will cry when she is in pain, hungry or sad. For example, she usually gets sad if others go on a walk and she thinks she’s not going to go. She likes when you give her simple yes/no questions like which outfit she wants to wear for the day. At school, she has been working on different ways to communicate like using an eye gaze program to speak through a dynavox or trying to use her hand to choose answers.

Florence has a g-tube. In the past, she has eaten meals blended by mouth. Her g-tube was used to give her medicine and water. However, currently she is being fed all food and water via her g-tube as her caregivers are assessing what is safe for her. There are not swallow studies available in her home country so it is a little bit challenging to figure out what is best for her. Her diet is being supplemented with a mix of complan, a powdered-milk nutritional supplement, and real food blends. She is doing well. Also, she does take muscle relaxing medication to help with her spasticity.

Her personality has started to shine through even more so. She likes to laugh. She thinks her friends that do silly things are really funny and often they make her snort when laughing a lot.

She attends therapy four times a week currently for stander time, stretching and exercises. The therapists always say she doesn’t complain unless it is a day where she is clearly uncomfortable before she comes.

Florence enjoys being held by her people and especially when they sing to her or dance with her. Even though she cannot talk, she interacts well with her friends in her foster home! Such a joyful, sweet girl she is.

Brian recognizes familiar adults and has formed an attachment to his favorite caregiver. He is uncomfortable around strangers. He is working with a physical therapist and a teacher on fine and gross motor skills. He can pick up toys and transfer them from hand to hand. His teacher reports that he understands what is being said to him and has recently begun responding to simple directions such as “give me”. He is able to sit unassisted and moves around in a baby walker.

Photos and videos are available through the agency.

Alyssa was a sleepy girl at the beginning of our Zoom call but as her caregivers slowly nudged and called her name, she began to wake up. Two and a half-year-old Alyssa is not speaking, but we learned from her caregivers that she is a cuddly child who loves being held. She will also smile when she hears her name called. Alyssa likes listening to music as it helps to calm her, along with additional cuddles when she is upset. Alyssa seems curious in new environments. She doesn’t interact much with other children due to her mobility. Instead of playing with toys, she would rather be rocked and listen to music.  Alyssa’s diet consists of her formula which she consumes through a nasal feeding tube.

Alyssa is diagnosed with global developmental delays, hydrocephalus and seizure disorder. She resides in a nursing home and receives 30 minutes of occupational and physical therapy each week. The agency has much more information on Alyssa. Could your family be the one she needs?

Polly has been given a diagnosis of childhood Autism and is on several medications. She is now in a day program for children with disabilities and is receiving therapy services. As a result, she’s made progress in all aspects of her development. Polly speaks using simple words and small sentences. She understands everything said to her and can follow 2 and 3-step directions. She is able to express her wants and needs either through words or gestures. She asks questions. She learns new tasks best when a combination of verbal directions and visual demonstrations are used. She prefers playing alone and can play or work on a task for 10-15 minutes at a time uninterrupted. She plays appropriately with toys that interest her: coloring, building with blocks, kitchen/household toys (play kitchen, etc). She feeds herself with a spoon and drinks from an open cup. She’s toilet trained during the day, but still has some accidents when sleeping.

He has a medical diagnosis of Cystic Fibrosis and is behind in all areas of development. Gabe was recently placed in a foster home, and the one-on-one attention combined with proper nutrition has helped him make gains in all areas. He is presently non-verbal and does not yet walk independently. Gabe needs a family of his own and access to the therapies that will help him develop to his full potential.

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).

He lives at the orphanage since 2016. Normal weight and height parameters. Psychomotor development is normal. He is the victim of parental physical abuse and suffers from post-traumatic past. He is under the care of psychiatrist and take medication. No medical diagnoses in his chart, but trauma. You could tell that he is emotionally somewhat fragile.

He is communicative, talkative and charming boy. Positive relationship with peers and adults. His teachers describe him as very good, active and independent student. The computer class, math and English are his favorite subjects. He loves to play soccer, card games and chess. He has a lot of potentials and wants to be adopted. He is highly recommended by his caregivers. The family with an involved, hands-on father will be ideal for this boy. He would do really well as the youngest or only child (or in a family where the other children are grown). He needs an experienced adoptive family who can give him a lot of one-on-one attention and help build his trust in humanity back.

Molly May has made progress in her development during recent months. She is able to sit unassisted, get up on her knees and has begun to start trying to move around in a walker. She is becoming more physically active. She makes eye contact, looks around for families adults and smiles when someone looks at her. She will laugh out loud when an adult plays with her. She watches children’s cartoons and movies on the TV and will get excited and point to the screen when the TV is turned on. She picks up toys and attempts to play with them. She still needs instructions in how to appropriately play with toys. She makes vocalizations in an effort to communicate. She eats soft foods from a spoon.

Molly May has undergone multiple surgeries to repair her cleft lip & palate. She is under the continued care of the doctor who is performing these procedures. She is also under the regular care of a neurologist, who diagnosed her with CP in 2018. She had suffered from “constant shaking” resulting in uncontrollable movements up until a few months ago. The social worker reports that this has greatly improved and that Molly May’s movement are now more calm and she also sleeps calmly too. Videos taken in April 2019 show her interacting with toys.

Photos and videos are available through the agency.

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

A female child with a proven genetic neurodegenerative disease – pyruvate dehydrogenase deficiency (identified homozygous for mutation p.R446* (c.1291C>T).  She was born from the 15 th pregnancy, 12 th birth. . On the second day after birth, transferred to the intensive care unit due to hyperexcitability, hypertonus of the limbs, with convulsive equivalents. With evidence of respiratory distress syndrome and metabolic acidosis. Held oxygen therapy for 5 days. A delay in the NPR was found, mainly in the motor development, with axial hypotonia and hypertonia of the limbs, combined with lactatemia. Submitted material for genetic testing and metabolic screening.Abdominal ultrasound: Pyelectasis (mild) of the left kidney. with microcephaly, developmental delay, tonus changes, elevated lactate and proven pyruvate dehydrogenase deficiency (identified homozygous for mutation p.R446* (c.1291C>T). At the age of 1, a severe retardation in the NPR with quadripyramidal syndrome and microcephaly was formed. Currently, the child has no apparent epileptic seizures, and the EEG shows no epileptiform changes. Remedial nutrition with KetoCal is recommended; reduction of carbohydrate intake. A new hospitalization is forthcoming to start a ketogenic diet with KetoCal.

Ryan is a cute 6-year-old boy, very nice and calm. He can’t see well which makes him very attentive to noise and he has developed a great ability to identify all the sounds he hears.

He likes music, likes to hear the sound of other children playing near him and it makes him smile. He likes to be cradled, and to have his head stroked. He doesn’t like to cry very much, he only cries when he is sick, or when he needs a little attention.

In therapy, he works on range of motion and stretching to prevent further contractures of his limbs, to turn his head to the right, since he tends to lean his head to the left, and to improve functional use of his arms and hands. At school, he uses sensory material and adapted activities to help him develop his academic abilities.

Mina is a beautiful little girl who likes to paint and play “sleepover” with her friends. Mina likes to go to the park and put together puzzles. She also loves to sing and listen to music of all genres, especially tango. Mina enjoys children’s stories and watching her favorite cartoons, which include Masha and the Bear, Puss in Boots, and Blue Shortcuts. Contact the agency to learn more about Mina and her listed medical needs!

Woodrow can sit up independently and will sometimes kneel as well. He occasionally bears weight on his feet, but cannot put his feet completely flat and because his ankles are so tight. He would need surgery before being able to do so. Woodrow doesn’t really scoot or crawl, but he can still make his way across a room by rolling and wiggling.

Woodrow loves to eat and gets quite upset if meal time is late. He doesn’t self feed, but eats pureed food by mouth. It can be a messy affair, but he is quite satisfied when he is done. Woodrow drinks some with a sippy cup or water bottle, but also likes to drink from a regular cup if he is feeling particularly thirsty.

Woodrow is not a fan of bath time and tends to move around a lot as he tries to keep his caregiver from bathing him, particularly his face and head. He is very picky about people touching his head – sometimes he likes a good head massage and other times he will duck away from anyone who tries to touch his head at all. He also does not like anyone touching his face, especially to try and wipe it off after a meal or to brush his teeth. The one exception he sometimes makes is for his caregiver to kiss his cheeks and neck, which he occasionally greets with a big smile.

In the past, Woodrow would often cry and thrash inconsolably for long periods at a time no matter what his caregivers tried. Some changes with medications have helped him drastically. He still does not sleep on a regular schedule, but if he’s awake during the night, he is generally calm, sometimes quiet and sometimes “talking” with his little noises.

Woodrow really likes his feet and will often clap them together. He also uses his feet to protect his head which he hits repeatedly for sensory input. Woodrow does not do a lot of purposeful movement with his hands, but often wrings them.

Woodrow goes to physical therapy and attends a special education class every day. He likes to be pushed around in his wheelchair and enjoys going in the swing.

Woodrow is a ticklish guy and will often reward tickles with a smile. While he is not generally a cuddler, he sometimes enjoys being held and cuddled and will lean in to relax.

Progress with Woodrow has been slow, but he is learning and responding. We continue to pray that he would know that he is safe, loved and treasured. We also pray that a brave and bold family would step forward to pursue his adoption. He is worth it.

This sweet, three-year-old boy has a long list of special needs – Spastic cerebral palsy. Other and unspecified seizures. Congenital laryngeal stridor. Tracheostomy. DNA analysis – homozygosity of UFM1 gene. Feeding via NG tube only. Yes, Isaac needs full care and always will, but he also needs a family to provide that care and the love that every child deserves. Is he your precious son?

Saber is a sweet little boy.  His main diagnoses/conditions are:  epilepsy – grand mal seizures. Infantile cerebral palsy – spastic quadriparesis, severe degree; ROP; cataract in the left eye – condition following surgical treatment; brain cysts; hypotrophy; mixed specific disorders of the psychological development; severely impaired general condition, with severe delay in all areas of development. He is fed via nasogastric tube. He needs constant care, active monitoring by a pediatric neurologist, an ophthalmologist and a physiotherapist.

Sweet Saber truly deserves a wonderful family!  He expresses emotional conditions through mimics. He understands when an adult is in the room and he looks for him with his gaze. He smiles when someone speaks to him or when he is jested. He does not interact with other children, but individual attention by an adult brings him pleasure which he expresses through smiling.

Please help us find this smiley little boy his forever family!

Nilo resides in a professional foster family. She has a congenital absence of her right forearm. Nilo is educated according to the Individual Study Plans of Students with a lower degree of complexity than the educational minimum for the calendar age, tailored to her individual needs. At a moderate pace, with individual help and guidance from the
teacher, she acquires knowledge, skills and competences foreseen in the individual curriculum for each subject of the individual curriculum. The girl distinguishes between the categories of good and bad, she knows generally accepted rules of behavior in social communication. She defines and expresses own desires and needs in words.

Nilo has diverse interests.

Nilo experiences attachment to children and therapists. She is sad when separated from someone. She seeks contact with adults, classmates and older students and engages in joint activities with them, she participates in role-playing games. She has mastered the social role of a student and classmate. Nilo helps her classmates when she sees that they are having a hard time. The comfort zone is the classroom and Montessori room.

The child communicates verbally, expresses wishes, and is often persistent about them, especially about things that spark her interest. When asked a question, she needs time to think about it and reproduce an answer; she constantly asks questions and seeks approval. The answer is not always adequate to the situation. She doesn’t always
understand the meaning of what was said and the execution of a relevant instruction.

Nilo likes a variety of toys, and she possesses different ones. She can play with other children and is cooperative, she shares her belongings. Nilo has developed self-service skills and readiness for academic work. She has established hygiene habits. She eats independently; dresses and undresses; unfastens and fastens; puts on and takes off shoes; she knows the parts of clothing. She can’t tie shoelaces.

She can say that she is in a foster family and that the foster mother raised her. The girl partially understands that foster care is temporary. She listens and accepts information related to the possibility of being adopted and meets potential adoptive parents, but still, she cannot imagine living in a different place.

Joyce LOVES to sing and dance!  Her favorite sing along songs are “Baby Shark”, “Cagabrie Island” and “Jasmine”. Joyce also enjoys riding on a motor scooter because she enjoys looking around at the sights and feeling the wind in her hair!

Those who know Joyce say she has a gentle personality. She likes to act cute and will become lively around familiar people. Joyce has a good relationship with her foster parents and gets excited when their 7 year old grandson visits on the weekend. They get along well and play with each other for hours.

Joyce presents with global delays and has Epilepsy and Thalassemia.  It is suspected she has ADHD.  Joyce attends OT and PT sessions. Joyce attends special education classes at elementary school and an afterschool class. She is making progress with her language skills and can respond to questions with single words.

Are you a family that can support Joyce with growing her language skills? Enjoy singing along to nursery rhymes with her?

Felicity, Kayla, and Yuki are two sisters and a brother in need of a family. They live in a group home for children without disabilities.

Felicity was born in December 2009. The dominant emotions are the positive ones. She demonstrates active social behavior. Sometimes she still demonstrates weaker control of emotions. When frustrated, she reacts with irritation. There is no data for anxiety, depression, or aggression. She is doing well with the maternal language. There are some minimal grammar mistakes. She is able to lead and maintain dialog. She can express sequentially and logically her thoughts and feelings. She is able to express emotions though non-verbal communication. She demonstrates positive self-evaluation. She has the typical characteristics of an extrovert. She enjoys watching TV, drawing, playing computer games as well as playing outside. She is oriented in the behavior of the children and the adults within society. She can attune her behavior towards the requirements of the situation. She participates in games and in the communication of her peers. She is mostly taking the central role. She does not step back from her goals easily. During the school year 2022/2023 she graduated from eighth grade, a class with professional profile. Considering the neglect in her birth family she has some gaps in the knowledge which are expected for her age. At school she works with a resource teacher. She has self-serving skills. She has habits for maintaining personal and environmental hygiene. She has skills to participate in collectively organized household tasks. She wants to be adopted.

Kayla was born in December 2012. She is an emotional child. She does not demonstrate aggression. She is empathic towards the problems of the other kids. She is eager to help her peers if they need it. She is doing well with the maternal language. There are some minimal grammar mistakes. She is able to lead and maintain dialog. She can express sequentially and logically her thoughts and feelings. She can express emotions though non-verbal communication. She is building a positive self-evaluation. She has the typical for her age curiosity and she demonstrates characteristics of an extrovert. She enjoys watching cartoons, drawing, playing board games and computer games as well as playing outside. She is oriented in the behavior of the children and the adults within society. She can attune her behavior towards the requirements of the situation. She is adjusting well in the group of her peers. She participates with big interest in all organized games and events. She can step back from her own goals and actions in line with those of her peers. She can wait for her turn to come. Considering the neglect in her birth family she has some gaps in the knowledge which are expected for her age. She is able to read and write under dictation. She makes minimal mistakes. She is well oriented into her school. During the school year 2022/2023 she graduated from fourth grade. She has self-serving skills. She has habits for maintaining personal and environmental hygiene. She wants to be adopted.

Yuki was born in February 2011. In December 2012, Yuki was a victim in a road accident and suffered a right lower leg fracture. Considering the changes that happened in his life, the adjustment process into the residential facility and in school went with some challenges. In November 2022 he was consulted with pediatric psychiatrist who put the diagnosis for “Other mixed behavior and emotional disorders”. His condition is being followed and therapy may be prescribed as well as work with psychologist. Now he is calm, he is acting with respect towards peers and adults. He observes the rules. With desire he performs all the given tasks in school and in the residential center. The speech and the language skills are well-developed. He was raised in a bilingual environment where d both Bulgarian and Turkish language. He can lead and maintain dialog and he provides enough verbal information. During conversation he communicates freely, he enters contact easily. He is able to express emotions though non-verbal communication. He demonstrates positive self-evaluation. He has the typical characteristics of an extrovert. He enjoys playing on the computer, playing soccer and going for walks outside. With desire he participates in the group activities. He performs the tasks according to his abilities. He likes being praised and to feel helpful, to be in the center of the attention. He is oriented in the behavior of the children and the adults within the society. He can adjust to new conditions. When disappointed he reacts emotionally. He participates in the games of his peers. Not always able to adjust his goals and actions around those of his partners in the game and he may react emotionally and enters into conflict. He finds challenges accepting the failures. During the school year 2022/2023 he graduated from sixth grade, a class with a profile in boxing. He works with a resource teacher there, After the incident he had he has been educating remotely. He is doing well and within the timeframe. He has self-serving skills. He has hygiene habits, but he needs to be reminded. He participates with desire in the activities related to maintaining environmental hygiene. He wants to be adopted.

There is a grant of 7800 euros toward foreign fees (with the agency) and this specific adoption agency will assist with applying for more.

The brothers have been in foster care for many years now and they are such great kids. They want to have a family and to be together as brothers. Next year, because the older one will become 14 in the summer, they will have to move to another town because of his school. There are no options for foster families there and they will have to go to an institution. The social worker is very hopeful this won’t need to happen and that they will be adopted instead.

IRIO – He is social and communicative. He easily makes new friends. In most cases his relationships with the children and the adults are good. According to the foster parents, he communicates well with the children and the adults. They describe him as a well-mannered child, who can assess different situations and adjust his behavior with them. He is aware that there are many social roles in society, which warrant a certain behavior. He participates adequately in the games of his peers. He can follow the instructions and the rules. He prefers games with physical activity, but he can participate in some role plays, too, and symbolic games (he gets into the role of a policeman or a criminal). He seeks the attention of the other children. He enjoys drawing, riding his bicycle, and games with a ball and other sport games. He only likes to be alone if he is using the computer. He fits in well among his peers.

HAMILTON – The boy is calm, observant, and curious about the surrounding world. He is attached to his brother, who is placed in the same foster family. Together they take care of each other, communicate, and play. He talks about his biological family calmly and talks about how they used to live. He did not like the conditions in his home then. He is attached to the foster family, their children, and their grandchild. It is hard for him to accept the pain of others and is always ready to help. When in conflict situations he defends his opinion, he is stubborn. He follows the rules at home and at school. He sometimes presents himself with stubbornness, but he does not argue and is not aggressive. He has an idea of good and bad, and for punishment and justice. He shares his experiences with the foster family and respects them. In his free time, he enjoys watching movies, listening to music, and dancing.

Miriam came into care at six months of age. She was very small and had poor sucking reflex. At the age of 16 months, her skills were at about the 11-month mark. She is listed as having global developmental delay in the moderate to severe range. In April of 2022, Miriam walked without any assistance from anyone for the first time. Everyone was thrilled! Despite her delays, Miriam shows remarkable improvements daily. She is becoming active and physically strong. She is emotionally attached to the staff and relates well to all the house parents and caregivers. Miriam plays and interacts with some of the children. She is sweet and lovely. Her smile makes her even more adorable. The whole team is very fond of her. Miriam needs a family that would wholeheartedly accept her condition and one who is willing to walk her through the struggles and challenges of Noonan Syndrome. The family must be willing to seek the professional help she will need as she grows. Contact the agency to learn more about Miriam!

SEPTEMBER 2023 UPDATE:

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

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

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

We hope just the right family comes forward for Nolan!

September 2023 UPDATE: Simon has updated pictures (at the agency). He has grown up a lot and is using a wheelchair. His write-up states: Simon was diagnosed with cerebral palsy, spastic quadriplegic, and global developmental delay. Despite his condition, he is an active child and has progressed in his mobility through the help of his therapy sessions to her improve his mobility and muscle strength. Simon is enrolled in physical, occupational, and speech therapy sessions. He picks up toy shapes and transfers them from one container to the other in a slow way due to his spasticity. He responds through facial expressions and communicates by pointing to what he wants on his communication board. He understands and follows simple instructions such as take your face towel and wipe your mouth, “up here”, or “high five.” Simon has a good appetite every mealtime but sometimes needs more time as he stocks the food in his mouth before chewing and swallowing if he does not like the food. Due to Simon’s special needs, his child caring agency believes that the prospective adoptive parents will need to show him full support and close supervision since he requires extra care, understanding, and love. He will need to continue therapies and will require special education. He likes to be around many children and would be open to larger families. Simon is unlikely to live independently; However, with the love and care of a family, he would thrive and could live a full life with his family’s support. His agency believes he will make a wonderful addition to a family and will be a much-loved son!
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Simon is a very sweet little boy who currently lives with several older girls and is the last remaining “baby” in his home. He cannot speak, but does communicate through facial expressions and some noises.

A traveling family met Simon and said, “Within the three days we spent at the orphanage, we were able to bond with him to the point he would smile and get excited when he saw us. The older girls told us he can understand what they say to him. He enjoys being held and carried around, but spends most of his day sitting in a baby walker or high chair. He seems very easy going, as we didn’t see him complain about being put in his crib for nap time, etc. The caregivers are working on his motor skills. He can eat with assistance and enjoyed the ice cream we brought! It’s so easy to fall in love with this little boy! We are praying his family sees him soon!”

Simon has spastic quadriplegic cerebral palsy and has had seizures. He takes 30 mg of Phenobarbital once a day. Simon has mild hearing loss of the left ear. Therapy has helped lessen the spasm and Simon can open and close his hands. Simon loves being around people and making faces! When praying before meals, he bows down his head and says “ahh” when everyone says “Amen.” We’re hoping a wonderful loving family comes forward for this special little boy! There is a $500 agency grant for Simon’s adoption with his adoption agency.

Axel has been assessed to have atypical autism against the background of a mild degree initial mental disability. Satisfactory general state of health. Ali understands and follows simple instructions. He imitates speech. He communicates non-verbally by pointing at things. He enjoys in his own way activities such as making things from playdough or clay. He does not get involved in the play and activities of the children in the group. Ali seeks contact with adults and peers in his own way by slapping or by caressing their heads. His play doesn’t match his age. Ali shows no interest in toys or blocks. He prefers to look at pictures and to watch educational videogames with animals. He prefers to do something alone. He likes being alone and does not seek attention. In the 2021/2022 school year Axel studied in the first grade at the elementary school in the town. He has a resource teacher as additional support. He studies under an individual plan for his education. His self-service skills are partially formed. He can eat on his own and prefers to eat with his hands. He needs support and care.

Walt  has been diagnosed with autism and developmental delays. He is nonverbal, does not engage with peers, and prefers to play with rotating, round objects. Walt does not show aggression and expresses warmth toward others on his own initiative. He likes to receive hugs from his foster parent.

Praise is a sweet boy with lots of love to give! His story is sure to touch your heart! He adores his caregivers and has been very responsive to the therapy he has received so far. He has been diagnosed with global developmental delay, but has made great strides in his health and development since his arrival at the baby home. The changes in him are nothing short of praiseworthy! It is clear that with the love of a family and continued therapy, Praise will thrive in life. Could you give this precious boy all the love and care he deserves?

Update November 2015: He demonstrates interest in musical and mechanical toys. He will play for a short time – studies a toy, puts it in the mouth, transfers it from one hand to the other. He likes activities involving music. He recognizes familiar areas of the orphanage and understands his daily routine related to familiar tasks such as eating. He is very happy when interacting with familiar adults.

Update 2018:  Jesse attention span is short-lived and unstable in relation to objects and people. There is some sharing with a close adult.  Jesse responds when called by name.  His memory and speech are poorly developed. When happy, he laughs loud and when anxious, he cries. Sometimes he pronounces unspecified sounds and separate syllables. He is sensitive and emotional and tends to be nervous around strangers.  When given a toy he reaches out and takes it. He is working on the pinch grip. He hasn’t mastered fully the ability to move a toy from one hand to the other. Jesse is fed with a spoon and sleeps calmly through the night.  He cannot control his physiological needs.  Jesse is entirely cared for by the team in his orphanage.

(Jesse was also previously listed as Andy)

This update and new photos were added in October 2022.

Leonard is one of the most clever boys you could ever meet. Although he’s non-verbal in conversations he often sings his favorite songs out loud for everyone to hear. His favorite toys include tennis shoes, books, and anything that spins! He also loves any sort of sensory experience, such as playing in the dirt looking at moving lights, and swinging. Leonard is not difficult to please. He finds joy in all the small moments in life. His favorite days are water days. He could truly sit in the kiddie pools for hours! He loves splashing and experimenting with how the water moves. Leonard is so much fun to play with and be around.

Leonard is gaining more independence everyday. He can eat, walk, and use the bathroom on his own. He has many ways of communicating what he wants using gestures, verbal sounds, and expressions or body language. Leonard is almost never sad or unhappy. His laugh can be heard even in another room, his joy is truly contagious. When he gets to know you Leonard can be very affectionate. He loves to hold hands or lay in your lap. He might also take your hand to show you he wants his head or back rubbed. He knows how to seek out his favorite people, forming clear attachments to those he loves. Leonard would absolutely thrive with the consistency of a forever family who can love him fully and keep him safe always.

Connor is an 11-year-old boy with joy that is contagious! He is very playful and he loves to laugh. His caregivers say that he is responsive to their teaching and he follows the rules. Connor loves music and likes to pretend that he is playing the guitar. He loves when others join in and make music with him! He appreciates sleeping in after a full day of activity. Connor has a diagnosis that includes global developmental delay, but he continues to amaze his caregivers with his determination to learn and do things for himself. Connor is very strong and is able to stand with some support, get himself in and out of his wheelchair, and feed himself. With a little more therapy, Connor will continue to become independent at even more daily tasks. Connor is an absolute inspiration and has so much potential! Could your family give him the love and extra care he needs to reach it?

This update and new photos were added in October 2022.

Anthony has been waiting for a family for a long time. Despite his Cerebral Palsy and Epilepsy he loves to get out of his wheelchair and stretch out on the floor or bed. He is good at moving himself into silly positions, often falling asleep in the funniest ones! Anthony’s favorite toys are those with lights. He loves all colors of lights and often finds them around the room during school. He also enjoys music or being outdoors. Anthony enjoys having people he knows near him, and will often find them and initiate affection with his hand or head.

Anthony has the best smile, but only shows it when he’s truly happy. This might be while he’s being tickled or comforted, during a favorite song, or while feeling the breeze on his face. He has many ways of communicating, such as laughing, crying, and making lots of facial expressions. Anthony is not one to hide how he feels! Anthony would benefit from a family who can care for all his needs, especially as he grows bigger. He’ll bring a sense of love and joy to any household!

Update Feb 2022:  Kinsley is going to be part of the 2022 summer hosting program if not outright matched first! Families in IL, NJ, PA, KY, IN, TN, or MO are eligible to host! Please contact Madison Adoption Agency for additional information on her hosting.

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Kinsley is a beautiful little girl who loves to look pretty. She likes to wear red, pink, and yellow dresses. She also loves accessories like hair clips, earrings, and bracelets. She loves to play with dolls and she also likes to play pretend teacher. Kinsley loves cats. She also loves to watch Princess Sofia. Kinsley is active and likes to swim, ride her bike, and play at the park. We hope this little sweet girl will find her forever family soon!

Additional photos available!

VIDEOS  (Password: Adoptmaa)
https://vimeo.com/maaspecialkids/maa-kinsley1
https://vimeo.com/maaspecialkids/maa-kinsley02
https://vimeo.com/maaspecialkids/maa-kinsley03

There is a $500 agency fee reduction for Kinsley’s adoption with a specific agency!

Kinsley is eligible for a $10,000 grant with the LPA, as long as the family joins LPA!

Kinsley needs a family with an approved home study to be able to lock her file or submit a letter of intent to adopt her. A family without a home study can look at her redacted file. If you are interested in reviewing Kinsley’s file or in adopting Kinsley, the agency would be happy to assist you.

Piper is a beautiful girl with a smile that can light up any room! Piper has a warm, sweet personality, and she adores her caregivers. She absolutely loves being read stories or just talked to. It’s clear that she understands what is being said to her. She enjoys music and appreciates a good nap! Piper has a medical diagnosis that may look concerning at first, but she has already made huge strides strides with some daily therapy and a lot of love! This special little girl will be a blessing to the family God has waiting for her. Could your family reciprocate all the love Piper has to give?

Miriam was born at 28 weeks gestation in early December 2007 in an emergency birth after a placental abruption. She spent five months in the hospital, then lived with her birth family for nine months before entering state care in February 2009. Miriam has been diagnosed with cerebral palsy, affecting primarily the left part of her body, and a glioependymal cyst. She takes medication to address anxiety. Her development is delayed.

After complex surgical intervention, Miriam walks independently and can go up and down stairs while holding on to a railing and sits without support. She uses primarily her right hand and is independently able to eat with utensils, drink from a cup, brush her teeth and use the restroom. She requires assistance with bathing. Miriam is well oriented in the spaces, routines and among the people of her group home. She is emotionally stable but likes to be the center of attention and may show jealousy when other children are prioritized. Although she appears to have an unspecified speech/articulation disorder, Miriam is able to communicate verbally, constantly and curiously asks questions, and can participate in dialogues.

Miriam attends an auxiliary school and says she cannot imagine her life without the opportunity for education.  Her academic knowledge is on a preschool level: she can count to 20 and name all the letters of the alphabet as well as identify colors and everyday objects.  She works with more focus in a one on one setting but can get overwhelmed when tasks are too demanding. She needs many repetitions to acquire new skills. Miriam’s thinking is concrete and situational and her greatest delays are cognitive.

Miriam is friendly, sociable and trusting. She interacts preferably with adults, but also establishes warm connections with peers and joins group activities. Although she is reported to be selective with her relationships, she is well attached to her social worker. She likes to listen to music, play games, and spend time with the group home’s parakeets and yard dog.  Through the services of a non-profit organization, Miriam has the opportunity to go swimming and indoor rock climbing both of which she enjoys very much.

Miriam’s social worker and family therapist note that Miriam is willing to learn new things and would make continued and noticeable progress in a family that can offer her more appropriate interventions and individualized resources as well as a warm and loving home.  Seven years ago, Miriam experienced a disrupted adoption procedure, but her care team believes now that she is more mature, she would understand better the meaning and benefits of adoption and would seriously consider a family interested in making her their daughter.

 

Miriam has waited for a forever family for over eight years. A family interested in adopting Miriam must file their I-800A with USCIS before her 16th birthday in early December.