Uma

Girl, Age: 3
Country Code: Central.Asia.1
Region: Asia
congenital neurological abnormalities, including hydrocephalus and thoracic spina bifida with lower-extremity weakness (flaccid paraparesis).
Listed: Aug 2026
$20.00
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!
This precious little girl has conditions which primarily affect her mobility. She is unable to walk independently and requires assistance with feeding and daily self-care.

Despite her physical limitations, she is described as a warm, affectionate, socially engaged little girl who enjoys interacting with adults and peers, understands simple speech, and is beginning to use words herself.

Tana #

Girl, Age: 6
Congenital anomaly of the central nervous system: Atrophy of the cerebellar hemispheres, cerebellum and corpus callosum. Ventriculomegaly. Epilepsy – Grand mal seizures. Cerebral palsy. Dysplasia of the right hip joint. Accidental noise. Severe neuropsychiatric development delay
Listed: Jul 2026
$684.00
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!
Tana is a sweet little girl whose gentle smile shines through during quiet, loving moments. She responds warmly to soft voices, gentle touch, soothing music, and time spent with caring adults. While she faces profound medical and developmental challenges, she finds comfort in calm interactions and enjoys listening to melodies and musical toys.
Tana has significant medical needs, including cerebral palsy, a seizure disorder, and severe neurological conditions that have greatly impacted her development. She is non-ambulatory, has not developed head control or independent motor skills, and is completely dependent on caregivers for all aspects of her daily care. She is fed through a nasogastric tube and requires comprehensive, ongoing medical support.

Although Tana does not communicate verbally or understand spoken language, she expresses herself in her own ways. She often smiles in response to gentle attention, may make soft vocalizations, and lets caregivers know when she is uncomfortable through quiet crying or facial expressions. She also responds positively to certain therapy exercises and enjoys the comfort of familiar, soothing music.

Tana will thrive in a family that is prepared to provide lifelong love, advocacy, and specialized medical care. She would benefit from caregivers who can celebrate the small but meaningful moments of connection that make her unique.

Jandron

Boy, Age: 1
Listed: Apr 2026
$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!
(Information is from January 2026 when Jandron was 10 months old. He was born in late February 2025)

Jandron was born 5 weeks prematurely to a 20-year-old mother into a highly vulnerable situation. At birth, he experienced respiratory distress syndrome, requiring mechanical ventilation. Jandron has ongoing medical diagnoses of moderate bronchopulmonary dysplasia and recurrent post-viral wheezing, making him dependent on supplemental oxygen. He also has epilepsy, mild encephalopathy, and horizontal nystagmus (involuntary eye movement). Jandron has a history of hospitalizations to treat seizures, bronchiolitis, and wheezing. To manage his health, he takes several daily medications.

Even with his medical issues, Jandron shows beautiful developmental progress–not to mention a BEAUTIFUL smile under the sticker we had to place over his picture. He displays fluid and spontaneous movements of his arms and legs. While he has slight hypotonia (low muscle tone) in his trunk, he successfully rolls from his back to his stomach on his right side. He is also beginning to practice fine motor skills, occasionally using a pincer grip to explore the world around him. He is finding his voice, frequently emitting sweet vowel and syllabic sounds. His responses to auditory stimuli are becoming increasingly consistent. He is a curious observer. He pays close attention to his environment, shows great curiosity toward objects, and responds positively to simple stimuli. He makes wonderful eye contact with his caregivers and rewards them with warm smiles. As a 10-month-old infant with medical needs, he requires full assistance for all daily living and basic hygiene activities.

Jandron is a gentle child with a mostly calm and receptive temperament. Because of his young age and medical history, he relies entirely on his caregivers for emotional regulation. He clearly expresses his feelings, including showing displeasure, and communicates his basic needs through facial expressions and crying. He demonstrates a healthy, positive attachment style with his current caregivers. Jandron seeks connection and instantly calms down when given physical contact and comfort. His ability to connect, look into your eyes, and accept soothing touch shows a profound resilience and a readiness to bond with a permanent family.

While he is too young for traditional hobbies, he has clear preferences that highlight his unique personality. He is an attentive little boy who loves to watch the world around him. He shows a distinct interest in exploring objects with his hands and listening to the sounds in his environment. Above all, his favorite place to be is in the arms of someone who cares for him. He loves physical touch, gentle holding, and the reassurance of a loving voice. He needs a family that is highly sensitive to his medical diagnoses, but more importantly, a family that will cherish his smiles, celebrate his milestones, and offer him the safe, warm home he deeply deserves.

Rowand #

Boy, Age: 8
infantile cerebral palsy – spastic quadriparesis, severe degree; localized symptomatic epilepsy – secondarily generalized seizures; pronounced cerebellar atrophy; atrophy of the large cerebral hemispheres; pseudobulbar paresis; microcephaly; craniosynostosis; optic nerve atrophy; microphthalmia on the left; arachnoid brain cyst with communicating hydrocephalus and atrophy of the temporal lobes; delays in physical, motor, and neuropsychological development; severe mental delay
Listed: Mar 2026
$171.00
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!
Precious Rowand is a boy with complex special needs who is in need of a dedicated family able to provide him with the love, attention, specialized care, and therapies he requires.

Rowand remains in a lying position and is motor-passive. He tolerates interactions – tactile, verbal, musical. He does not initiate interaction when he is awake but remains calm. The boy reacts by crying in moments of discomfort. He reacts to sounds and movement around him.

Rowand is fully dependent on the care of adults. He requires constant specialized care for feeding (via NG tube), body positioning, and systematic motor rehabilitation.

Johnny #

Boy, Age: 2
Primary Diagnosis: Hydrocephalus
Special needs: hydrocephalus – implanted ventriculoperitoneal shunt; macrocephaly; round hemangioma in the scalp area; intermittent convergent strabismus; phimosis; delayed neuropsychological development.
Listed: Feb 2026
$113.00
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!
Meet precious Johnny! He is only 1 years old, turning 2 in the spring. Because of his special needs, he was never raised by his biological family and has spent his entire young life in the neonatology unit, in a children’s home, and now in his current group home for children with medical needs. Johnny is a gentle, sweet boy who needs a loving and devoted family.

Johnny can sit independently and he can assume a hands-and-knees position. He grasps toys and responds with positive emotion during interaction. He has good hand-to-mouth coordination. Johnny can turn from back to belly and vice versa. When standing, he has weak support on his legs.

Most of the time, Johnny is calm; there are no signs of increased anxiety, frustration, or aggression. He uses crying to seek attention or to satisfy needs but calms down quickly when comforted through hugging, gentle stroking, or talking. His sleep is calm.

Yessica

Girl, Age: 9
Country Code: LA-2
Primary Diagnosis: Behavior, Blind / VI
Listed: Jan 2026
$35.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Medical diagnosis of the child: low vision, bilateral amblyopia, astigmatism, hypermetropia, secondary exotropia, and nystagmus (irregular eye movements) with a rotational component, and behavioral disorder.

Information is from September 2024

Summary:  Yessica is a 7-year-old girl who has faced significant instability in her early life. She was abandoned by her biological parents, and then she lived with her grandfather until 2023, when he could not longer care for her needs.

Yessica has specific medical needs, particularly concerning her vision and behavioral health, both of which require consistent management. Yenci has complex visual diagnoses including low vision, bilateral amblyopia, astigmatism, hypermetropia, secondary exotropia, and nystagmus (irregular eye movements) with a rotational component. She underwent surgery for strabismus around April 2024 and currently wears corrective lenses. She has been diagnosed with  behavioral disorder. She takes daily medication for her latter diagnosis. Her weight and height are appropriate for her age. She has received dental treatment for cavities and is in good oral health.

Yessica is currently enrolled in the second grade. She has experienced difficulties with academic performance, including low grades and failing subjects, largely due to challenges with concentration and understanding tasks. She struggles particularly with Language but shows aptitude in math, art, and religion. With increased support at home, her interest in studying is improving. Yessica demonstrates clear language use with coherent content and age-appropriate vocabulary. Her thinking is flexible, allowing her to identify risks and consequences. She is also advancing in reading comprehension. She has adequate fine and gross motor function, showing good coordination and manipulation skills.

Yessica is an affectionate child who is learning to navigate her emotions with professional support. She is currently going to psychiatry and psychology therapy to address behavioral difficulties. She needs support managing frustration and developing assertive responses. She can be impulsive (accelerated behavior), has difficulty staying still, and may struggle with following institutional rules, occasionally displaying rebellious or defiant behavior. Yessica is capable of giving and receiving affection. While she can be jealous with significant figures, she is responsive to dialogue and understands situations after discussion. She has developed skills to express her emotions, needs, and desires more clearly. She can lose motivation easily but is capable of regaining it through encouragement and dialogue.

Yessica has distinct preferences that give insight into her personality and what she hopes for in a family. She enjoys playing with dolls and has a fondness for dresses and shoes. Yessica has expressed a preference for adoption by a nuclear family (mom and dad) or a single-parent maternal family. She is indifferent as to whether the family already has other children. Despite her challenges, she shows a willingness to connect and has a preference for feminine figures, though she is open to a nuclear family structure. A balance of clear, consistent rules with warm affection is crucial to help her feel secure and manage her conduct disorder.

Kenny

Boy, Age: 2
Country Code: LA-2
Down syndrome, surgically corrected congenital heart disease , generalized hypotonia, glycion disorder with gastrostomy management, congenital hypothyroidism, malnutrition in correction, and global developmental delay with impairment in the motor, cognitive, language and social areas
Listed: Jan 2026
*** I am eligible for an additional $2,500 Grant from Reece’s Rainbow! Through 2026, children with Down syndrome under the age of 6 are eligible for this grant. ***
$395.00
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!
Kenny enjoys spending time in his children’s jumper which comes with various sensory stimulation accessories, as well as his crib. He is happy with physical contact, having movements made in his legs, and being lifted up. He has physical, occupational, and speech therapies 3 time a week. Kenny has achieved a notable improvement in his nutritional status. He needs an adoptive family with high emotional, affective, and physical availability, who has a solid support network and preferably experience in the care of children with special needs. It is essential that this family is committed to the active management of the health, therapeutic, and educational services that Kenny requires.

NEW VIDEOS:
https://vimeo.com/manage/videos/1151669660
https://vimeo.com/manage/videos/1151669587
Password: Adoptmaa

There is a $1,000 agency fee reduction for Kenny’s adoption via a specific agency.

Elina #

Girl, Age: 3
Listed: Dec 2025
$935.00
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!

Congenital anomaly of the nervous system (CANS): Spina bifida aperta, condition after surgical treatment; Hydrocephalus, condition after implantation of a ventriculoperitoneal shunt (VPS). Cerebral palsy. Symptomatic epilepsy. Pseudobulbar paresis. Pelvic-reservoir deficiency. Bilateral inguinal hernias. GER. Protein-energy deficiency. Cortical blindness. Profound delay in neuropsychiatric development

Milo #

Boy, Age: 7
Listed: Dec 2025
$172.00
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!
Chronic herpes simplex type 2 encephalitis. Microcephaly. Symptomatic epilepsy. Cerebral palsy – severe quadriparetic syndrome. Profound cognitive delay. Convergent concomitant strabismus. Nystagmus. Atopic dermatitis

Joshua #

Boy, Age: 4
Listed: Sep 2025
$2,003.15
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!
Congenital anomaly of the central nervous system – hydrocephalus; condition after implantation of a ventriculo-peritoneal shunt. Epilepsy. Bronchopulmonary dysplasia. Non-allergic asthma. Cortical blindness. Spastic quadriparesis. Severe developmental delay. Atopic dermatitis.

West

Boy, Age: 7
Country Code: LA-2
Cerebral Palsy, full paralysis; Severe cognitive delay
Listed: Mar 2025
$1,378.50
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!
West is a calm and precious boy who reacts with his eyes when he hears the voices of his caregivers who he adores. He loves to have his face caressed. West will fix his gaze on those he loves dearly. He receives therapies twice a day. Loud noises tend to startle him. West enjoys a calm and peaceful environment. He is beloved amongst all the staff. There is more to West’s gaze than meets the eye; in his eyes is a desire to be wanted. Would you give West the chance to be loved and make those eyes come to life?

VIDEO:
https://vimeo.com/manage/videos/1065191610
Password: Adoptmaa

Agency fee reductions may be available based on the adoptive family’s circumstances (with a specific adoption agency).

Idris #

Boy, Age: 8
Cerebral Palsy – spastic quadriparesis. Localized (focal, partial) symptomatic epilepsy and epileptic syndromes with complex partial convulsions. Severe mental retardation, significant behavioral disorders requiring care or treatment. Optic nerve atrophy.
Listed: Mar 2025
$1,554.00
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!
Idris was born with very low weight and immaturity, complicated neonatal period. Subsequently, with the development of multicystic encephalopathy with microcephaly (based on severe hypoxic-ischemic incidents in the perinatal period), severe spastic quadriparesis and symptomatic epilepsy (mainly tonic seizures). Conducts therapy with Convulex, as a result of which seizures are almost not registered.

The child has severe lag in physical and neuropsychiatric development. Severe mental deficiency.  Needs systematic motor rehabilitation, classes with a speech therapist, psychologist and typhlopedagogue. Weak rehabilitation potential. Followed by a pediatric neurologist and ophthalmologist.

The child can turn from back to stomach and back. Does not crawl, does not sit independently, does not have a four-legged stand. Does not stand up, holding on to a support. Holds a toy placed in the hand for a short time. Lacks a pincer grip. The average mental age of the child corresponds to 3-5 months. The child is mostly calm with accompanying episodes of irritability, expressed through crying. Quickly calms down by the presence and attention of an adult. There are no indications of aggressive behavior or manifestations. Does not utter words, syllables and sound imitations. Does not turn when called by name. Does not initiate contact with other children. The child is completely dependent on the care of an adult. Takes food from an adult with a spoon (less often from a bottle). Falls asleep independently.

There is evidence of a brother with an autoimmune disease – Alopecia areata.

Malachi #

Boy, Age: 3
Primary Diagnosis: Hydrocephalus
Posthemorrhagic extreme internal hydrocephalus; implantation of a ventriculoperitoneal shunt (VPS). Bronchopulmonary dysplasia. Retinopathy of prematurity
Listed: Feb 2025
$1,190.00
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!
He lives in a home for medical and social childcare. He was born to a minor mother who had epilepsy and took anti-epileptic medications during pregnancy. There was a complicated pregnancy and birth, resulting in extreme posthemorrhagic hydrocephalus. A shunt was implanted but failed. A new one was inserted. Malachi is on permanent antiepileptic monotherapy, without convulsive manifestations.

Due to the extreme hydrocephalus, Malachi is in impaired general condition, with significant lag in psychomotor development – no head control, does not turn around, does not sit or stand. He needs specialized care, monitoring by medical specialists, and daily medical rehabilitation. He is usually in a positive emotional state. He coos frequently and continuously. He reacts animatedly to the speech of an adult. He initiates a desire for physical contact by smiling. The boy is completely dependent on the care of an adult. His sleep is peaceful. He takes food with a pacifier. The agency has videos of him.

Mell

Boy, Age: 5
Country Code: LA-2
Primary Diagnosis: Hydrocephalus, Spina bifida
bilateral hip dysplasia with congenital hip dislocation, congenital hydrocephalus, lumbosacral meningocele corrected, congenital malformation of the corpus callosum, hypermetropy (far-sightedness), and malnutrition.
Listed: Oct 2024
$35.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Several videos available from the agency, for serious inquiries!

Info from March 2024:

When Mell was born, his biological parents tried to take care of him even with his special needs, but they lived in a small town far away from cities and hospitals. At his one month check-up, he was diagnosed with congenital malformation of the spinal cord, hydrocephalus, low weight, fetal growth delay, and respiratory syndrome. At one of his following check-ups, the doctor sent Mell to the hospital due to a high fever and inflammation of the brain. Sadly, though they had tried, his parents recognized that they did not have the means of caring for him in the ways he needed, both due to finances and distance from necessary medical care, and they asked Protective Services to care for him. No other family members were able to provide the care he needed as well. Mell was placed in a foster home and is doing well.

Mell has been receiving various types of therapies which have been valuable in his development. When meeting adults for the first time, he becomes shy, but he recognizes familiar people and loves to interact with them. Mell identifies the emotions on people´s faces and interacts accordingly. He is a very expressive child who shows affection in various ways, and sometimes gets jealous when his foster mother gives affection to the other children. According to the professionals who care for him, Mell has the language development of a 12-month toddler. He communicates through crying and screaming and can say some short words such as “mama” and “papa.” He also imitates animal sounds, such as those of a dog or cat. He responds to simple instructions such “Take this” and “Give me that.” Mell identifies different body parts, plays with Play-Dough, and performs other activities that strengthen his fine motor skills. His movements are spontaneous despite the limitations he has in his lower limbs.  Due to his chronological age, Mell requires support, supervision, and guidance to fulfill his daily routines. Mell takes two naps during the day and sleeps throughout the night. He wears diapers all day.

Mell likes to interact with peers or adults and loves to spend time outside. He gets excited when he hears a motorcycle engine as he immediately thinks he is going to go out and gets anxious. He gets upset when his diaper is dirty and when he is not allowed to go out. Mell gets happy with simple things, and he likes to laugh a lot. Mell loves to drink sweet juices. Due to his medical condition, he does not wear shoes but wears very soft socks. He enjoys it when adults help him to kick the ball to play soccer. Mell also likes to play with cars and airplanes.

Lilian and Sonny

Sibling Group
Ages: 11, 8
Country Code: LA-7
Sonny is a quadriplegic child with cerebral palsy and epilepsy.
Listed: Oct 2024
$1,520.00
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!

Lilian is described as happy and communicative girl who is very creative. She interacts positively with adults and other children. She is currently in the fifth grade where she is known to be a good student.

Sonny is a quiet boy though he smiles and babbles to communicate with others. He is a quadriplegic child with cerebral palsy and epilepsy.

The agency can attempt to obtain additional information for interested families.

Kevin #

Boy, Age: 4
Primary Diagnosis: Hydrocephalus, Spina bifida
Congenital anomaly of the nervous system: internal hydrocephaly; condition after ventriculo-peritoneal anastomosis implantation. Holoprosencephaly. Lumbosacral spina bifida aperta; condition after plastic surgery. Lower flaccid paraplegia. Pelvic-reservoir incontinence. Delayed neuro-psychic development
Listed: Sep 2024
$1,614.00
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!
Kevin can sit on his own. He plays with toys. He interacts positively with caregivers. He makes some sounds, but is not yet saying any words.

Brandon #

Boy, Age: 6
Microcephaly. Hydrocephalus. Agenesis of the left hemisphere, persistent foramen ovale, Interatrial defect and Schizencephaly.
Listed: Sep 2024
$2,083.40
has been donated towards the cost of my adoption!

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

Please meet Brandon; he has multiple special needs. Sadly Brandon relies totally on the care of others.  He sleeps in a room with four other children.  The caretaker says he seems to like music and likes the bath.  He can make some sounds for speech.  He has difficulty feeding and swallowing.

The agency staff member that met Brandon said the following:  “According to the caretaker, there is a slight regression, especially in terms of feeding. Unfortunately, I have not been given an opportunity to speak to any of the specialists engaged with the boy and possibly what exactly they are working on. Brandon could have some potential, but it’s very hard to tell.  In any case, he needs a lot of love, a lot of attention and a lot of activities.”  Could you be the family for Brandon?

Bella #

Girl, Age: 10
Primary Diagnosis: Cerebral palsy
Her multiple special needs include Cerebral Palsy and severe quadriparesis.  She is also severely delayed mentally.
Listed: Sep 2024
$2,043.50
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!

Look at the sweet smile on Bella!  Bella spends the majority of the time in her bed or in the special stroller that she can be pushed in.  She is often fed in the stroller as well.  She is fed with a bottle.

Agency staff member said the following:  Given the fact that only a rehabilitator is currently working with the child and the staff at the Home only have time to cover her basic needs, it is definitely very difficult to say to what extent the little girl has developmental potential. In my opinion, Bella liked it when she received personal attention such as being spoken to gently, being teased by me or by my showing her different toys. She had been working on a smile during that time.  Most of the time, both her arms and legs were in motion, and she even managed to roll over in bed. She needs a lot of love and attention and systematic and purposeful activities with specialists.

Dawn and Donna #

Sibling Group
Ages: 6, 6
Listed: Jul 2024
$1,642.00
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!
Dawn & Donna are  twin girls who were born in Ukraine at 29 weeks gestation. They lived in an orphanage in Ukraine until they were 1.5 years old, at which time they were moved to an orphanage in Bulgaria. They were then moved to a different placement in Bulgaria at age 3, where they still reside.

 

Donna’s medical diagnosis includes: Retinopathy of prematurity (ROP) stage 5, post vitrectomy condition bilaterally; secondary glaucoma. Left eye ROP stage4 Nystagmus. Delayed neuro-psychic development. Condition after low birth weight. Self-aggression. Spastic quadriparesis. Iron deficiency anaemia

 

Dawn was born first. Her medical diagnosis includes: cerebral palsy – spastic quadriparesis. Spastic quadriparesis. Suspected hydrocephalus with normal pressure and hypoplasia of corpus callosum. Grade 1 hypotrophy. Convergent strabismus; hypermetropia. Condition following very low birth weight.

 

Update July 2024: After their placement into the foster home on May 14, 2024, the girls have adjusted well and made noticeable developmental progress. They show an attachment to the foster mom and follow her instructions. One of the girls can now walk independently and is well oriented in the foster home. The other girl sits with little support. The girls now eat mashed food from a fork or spoon and chew well. They have learned to speak their first meaningful words and are also observed to repeat syllables. While there’s some jealousy between the sisters when it comes to receiving attention, they are emotionally close and hug/hold hands. Videos from July 2024 show one girl as tenacious in exploring her environment and the other as joyful when playing on the floor. The girls attend therapy twice a week and their foster mom is proactive in seeking additional services for them. They like music and singing and enjoy massage from the foster mom. They are thrilled to be playing in the inflatable pool in the backyard. Their foster mom describes them as positive children who will continue to make progress with the right interventions and lots of love.

From a family who met them in 2023

I met these twins when I visited my daughter for trip one in 10/2023. One twin was active and was able to stand holding on and cruise around her crib. She was able to climb right out of her floor crib and back in herself. It was an activity for her and she did it with great ease. She wasn’t trying to escape at any point and would just flip In and out over and over again. She seemed like what you would expect for a toddler. She stopped what she was doing when someone called her name and turned in the direction of their voice. The other sweet twin was always laying down when I saw her. Sometimes in a crib, sometimes in a seat. My daughter asked for “baby” all the time and they would put this twin in her crib with her to lay together. They said she was more “severe”. She definitely seemed more infantile. They were in a really great place where they got plenty of food and were carried around a lot by the staff there. There were 8 kids on that floor in four rooms. The twins shared a room. I believe they are now in a foster situation. They def were pretty easygoing. They had a lot of musical toys which they seemed to like. The active twin kept herself busy a lot but the quiet twin seemed to love cuddling and other kids being around her. I think some of the delays they have may be related to vision impairments. I would imagine they would do well with siblings.

Esta, Sophie and Luke

Sibling Group
Ages: 13, 8, 7
Country Code: LA-7
Listed: Jun 2024
$808.00
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!
Esta, Sophie and Luke are waiting for a family in Latin America.

Esta is an affectionate child who loves dance, judo, art and making bracelets. She has a strong bond with her siblings and relates well with her caregivers and peers. She is clinically healthy with good physical and motor development.

Sophie shows leadership skills even at her young age when playing with others. She also participates in judo, ballet and other workshops. She also likes to participate in tours to exhibits, the cinema and theater. he also exhibits a strong bond with her siblings and is well-adapted at the institution she lives in.

Luke is an active little boy who loves to play ball. He is bonded with his siblings and interacts well with those at the institution.

The children have experienced trauma in their past and will need to continue to receive counseling to help through the transition to an adoptive family and to continue to work through their past. They are doing well though as they receive services in country. Esta received corrective surgery for a cleft palate and Luke has myopia and strabismus for which he receives care. Aside from her trauma care, Sara has no known needs. All of the children follow the Christian faith.

Seth

Boy, Age: 6
Country Code: Asia.2
Region: Asia
Listed: May 2024
$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!
This little guy is a big fan of cuddle time and giggles in delight when his nanny calls his name! At the age of two he was diagnosed with pediatric lymphoma and was responsive to chemotherapy. Seth is currently 4-years old and has lots of energy! He enjoys taking walks with his nanny, listening to music and playing with toys that light up and make sound. Seth receives comprehensive development services in Taiwan for significant global delays. A family interested in adopting Seth will need to be available for therapies, medical care, and life-long care. Seth is not timid and he enjoys interacting with people so we expect him to have a life full of accomplishments! Seth needs a family to celebrate each milestone he meets!

The adoption agency has additional photos and videos available.

 

Brooklyn and Bailey #

Sibling Group
Ages: 10, 11
Primary Diagnosis: Muscular Dystrophy
Listed: May 2024
$11,884.10
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!
Brooklyn and Bailey are brothers, they reside in a foster family.

Brooklyn has muscular dystrophy and a speech disorder. He has normal mental development. In 2020 he experienced burns over a large portion of his body and had right-sided bronchopneumonia. Therapy: Operative excisional cleaning of the wounds, sterile dressings; intensive treatment of thermal shock; antibiotic therapy. Brooklyn receives additional support in the form of resource teaching. With him a team of specialist work –speech therapist, psychologist, and resource teacher within the limits of the pre-school. The child is for a second year in a row in the same preschool class, because he was delayed from starting first grade because of medical reasons. He likes artistic activities and playing with his peers. He understands and strongly desires to be adopted, even if he does not talk much, his short dialogs are for his future surrounded by his loved ones.

Bailey is a healthy child with age-appropriate physical and neuropsychological development. He has good communication skills, has leadership qualities which sometimes turn bossy, and has a group of friends. He is curious, social and actively interacts with the people around him of different ages. Bailey has the attitude and the mindset for the adoption process with the needed positivity towards providing good living
conditions, including satisfying of the physiological needs, the needs for security, love and belonging, respect and self-affirmation. He understands and strongly desires to be adopted, he often talks about his future, surrounded by his loved ones. The adoption process is so desired and awaited by Bailey. The child is prepared and
ready to have his family, his adoptive parents.

Nany #

Girl, Age: 4
Primary Diagnosis: Blind / VI, Cerebral palsy
Nany has retinopathy of her left eye, cerebral leukomalacia with manifestation of spastic quadriparesis, bronchopulmonary dysplasia and asthma.
Listed: Apr 2024
$2,450.20
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Nany was born with an extremely low weight and a complicated neonatal period. She has retinopathy of her left eye, cerebral leukomalacia with manifestation of spastic quadriparesis, bronchopulmonary dysplasia and asthma. This sweetie needs a very special family.

The agency staff member who met her during March of 2024, says the following: Nany likes music, and it seems to settle her down. She also likes being in the swing. At times she turned to various sounds. She can lift her head slightly while lying on her stomach. Nany is an extremely fragile, sweet and lovable little girl who needs lots of love, attention, understanding, support and lots of cuddles. Given the serious diagnoses, working with additional specialists definitely would ease and help the child’s condition. Nany is in need of a very prepared and supportive family.

Nany’s current adoption agency has grant funding is available for qualifying families.

Eddie #

Boy, Age: 4
Listed: Mar 2024
$2,118.85
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!
Meet Eddie! This sweet little man just turned two years old. He likes to transfer a toy from one hand to the other and will look for a dropped toy. He is able to push buttons on electronic toys, and he reacts positively when adults try to engage him. He is able to roll from side to side and can sit with some assistance. Because of his medical diagnoses, Eddie receives all of his nutrition via a g-tube. He sleeps well and protests at bath time. His diagnoses include Congenital malformation of the digestive system – atresia of the esophagus with tracheoesophageal fistula. Condition following surgical intervention; implanted percutaneous g-tube. Congenital heart malformation – small intraventricular defect. Protein-energy malnutrition. Delayed psychomotor development. He will almost certainly need  more surgeries in the future in order to eat by mouth, and any family considering Eddie should be sure they are prepared to meet his medical needs.

Elise #

Girl, Age: 7
Primary Diagnosis: Genetic Condition (non-DS)
Cornelia de Lange syndrome,
Listed: Feb 2024
$1,031.50
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!
Elise arrived with a unique constellation of traits known as Cornelia de Lange syndrome, primarily affecting her facial features. She’s a delicate soul with a sweet disposition, and her gentle nature is simply heartwarming.

This precious little one thrives on affection — she has an incredible capacity for love and blossoms with nurturing care that includes endless cuddles, tender personal interaction, and thoughtful understanding. She merits a patient touch and activities tailored just for her, which will provide not only pleasure but also enriching experiences.

During our time together, Elise remained serene and composed, displaying a quiet passivity. My playful attempts to tickle and engage her elicited limited response initially, but as patience persevered, her awareness and interaction gradually emerged.

Elise’s life would be beautifully complimented by a loving family atmosphere, filled with unwavering support and encouragement. A home that teems with warmth and offers plentiful one-on-one interaction, a trove of stimulating activities, and specialist involvement, would cultivate her growth and happiness.

To the kind-hearted families contemplating the rewarding path of adoption: envision a life with Elise, where every day is an opportunity to nourish and celebrate a precious child’s potential, and where love knows no bounds.

Izaiah #

Boy, Age: 5
CCFDN syndrome, which includes: congenital bilateral cataracts, facial dimorphism, psychomotor developmental delay, decreased muscle tone and peripheral neuropathy, internal hydrocephalus which does not require neurosurgical treatment at this stage.
Listed: Jan 2024
$1,717.50
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!
Izaiah is now living in a foster family and is receiving physical therapy at a rehabilitation center three days a week. The foster family reports that they are seeing major improvements in his motor skills now that he is receiving support and intervention services. His foster mother reports that he can pull himself up to a standing position using support (example: laying down in the crib and pulls to stand by holding on to the side of the crib). His physical therapist stated that he is making “visible progress” and should soon be independently walking. Izaiah has had surgeries for cataracts in both eyes (2 on the right and one on the left). It is believed he has limited vision from his left eye. He has a diagnosis of internal hydrocephalus, however, his foster mother reports that he was recently seen again by neurology and the diagnosis was dropped. Izaiah understands what is said to him. He smiles and makes eye contact. He says a few single words and also uses gestures and facial expressions to communicate. When asked how old he is he shows two fingers. He is beginning to indicate when he needs to use the restroom, but is still wearing diaper. He holds items in his hands and explores them. He plays with toys and participates in games. He shows an interest in other children.

Mae

Girl, Age: 5
Country Code: LA-2
Primary Diagnosis: Cerebral palsy
Cerebral Palsy; Significant neurodevelopmental delay, but showing significant progress; Recurrent broncho-obstructive symptoms; Fed by gastrostomy; Receiving comprehensive therapies
Listed: Dec 2023
$1,270.00
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!
Mae is a precious little girl, born in September of 2021.  Agency staff met Mae in August of 2023. She is an adorable little girl! We’ve been told she is doing well in her current care center since our staff visited her. Mae is described as a sweet, affectionate, and cheerful young girl. She is always smiling! Mae has managed to adapt to the routines around her required special care. She has made great progress since entering her care center, and she learns quickly through repetition She is a girl who likes to move forward and shows interest in learning new things. It is evident that she manages to bond with her caregivers. Contact us to learn more about Mae and her listed medical needs from her placing agency!

NEW VIDEO:

https://vimeo.com/maaspecialkids/maa-mae20

 

Update: 10/24

Mae is a precious little girl, born in September of 2021.  Our staff met Mae in August of 2023 and again in October of 2024. She is an adorable little girl!  We’ve been told she is doing well in her current care center since our staff visited her. Mae is described as a sweet, affectionate, and cheerful young girl. She is always smiling! Mae has managed to adapt to the routines around her required special care. She has made great progress since entering her care center, and she learns quickly through repetition She is a girl who likes to move forward and shows interest in learning new things. It is evident that she manages to bond with her caregivers. Contact us to learn more about Mae and her listed medical needs!
NEW VIDEOS:

https://vimeo.com/maaspecialkids/maa-mae21

https://vimeo.com/maaspecialkids/maa-mae22

https://vimeo.com/maaspecialkids/maa-mae23

https://vimeo.com/maaspecialkids/maa-mae24

https://vimeo.com/maaspecialkids/maa-mae25

https://vimeo.com/maaspecialkids/maa-mae026

Password:  Adoptmaa

Password: Adoptmaa

Polly #

Girl, Age: 10
Primary Diagnosis: Autism
Listed: Feb 2023
$1,051.00
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!
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.

 

Update 2024: Polly now displays some self injurious behaviors.  They have seen improvements with the addition of multiple medications, but her behaviors can decline as the meds begin to wear off each day and before an additional dose can be given.

Angelo

Boy, Age: 9
Country Code: LA-2
Primary Diagnosis: Other Special Needs
osteogenesis imperfecta and a unspecified conduct disorder
Listed: Oct 2022
$579.50
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!
Update from June 2025: Over the past 3 months, Angelo has made great progress walking. He is doing better and is more confident in himself! He has also come a long way with his communication, making himself understood through signing. He is precious and tender and will continue to blossom!

———————————————————–

So excited we have permission to share Angelo’s pictures!

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!

 

NEW VIDEO:
https://vimeo.com/maaspecialkids/maa-angelo2

NEW VIDEOS: 10/2024

https://vimeo.com/maaspecialkids/maa-angelo3

https://vimeo.com/maaspecialkids/maa-angelo04

https://vimeo.com/maaspecialkids/maa-angelo5

https://vimeo.com/maaspecialkids/maa-angelo06

Password:  Adoptmaa

 

Augustus #

Boy, Age: 7
Primary Diagnosis: Cerebral palsy, Hydrocephalus
Internal hydrocephalus: state after implantation of a VP-shunt; epilepsy; spastic quadriparesis; cortical blindness; delay in the neuro-psychic development
Listed: May 2022
$3,631.50
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!
Augustus was born full term, and was found that he has internal hydrocephalus; at the age of 4 months a liquid drainage valve system was implanted. The child lies in bed; he has spasticity in his limbs and his active and passive movements are limited. He depends completely on the care provided by adults. He receives kinesiotherapy. The child is subject to observation by a neurologist and by a neuro-surgeon.

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

Tyson #

Boy, Age: 9
Listed: Apr 2021
$2,854.23
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Bilateral sensorineural hearing loss (with hearing aid); shunt due to internal hydrocephalus; spastic cerebral palsy

Tyson was born premature and had several complications after birth. He can sit on his own with good balanced reactions. He crawls following the correct motor model. He stands up and walks sideways vertically. He can walk when one of his hands is held and has more control when it’s his right hand being held. He can stand up straight without falling for 2-3 seconds. When walking with a walker, he begins to bend his knees. He purposefully grabs a toy that is handed to him and can switch it from hand to hand. He shows an interest in musical toys and enjoys them. He has started making sounds and simply syllables such as “ma-ma”. He enjoys having someone sing to him and likes to receive hugs. He eats from a spoon. His overall development is delayed.

Photos and videos from August 2020 are available through the agency.

Scotty #

Boy, Age: 12
Primary Diagnosis: Spina bifida
Lumbar spina bifida (surgically corrected), grand mal seizures, spastic cerebral palsy, hydrocephalus
Listed: Mar 2017
$2,037.90
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!
Scotty has little support from his legs. His head control has improved and he can turn from his back to his belly. He sits independently by holding on to the bars of his crib and also makes attempts to stand up. Scotty can hold toys in his hands and tries to clap! He maintains eye contact and recognizes the faces of his caregivers. Scotty expresses appropriate emotions to happiness and agitation and will laugh out loud when teases. He imitates and pronounces combinations of sounds and syllables. Scotty interacts with all children and caregivers. He likes music and toys. Scotty is fed by a spoon and receives additional nutrition from a bottle.

Molly May #

Girl, Age: 11
Primary Diagnosis: Genetic Condition (non-DS)
Trisomy 7; cleft lip & palate; Cerebral Palsy
Listed: May 2019
$5,199.60
has been donated towards the cost of my adoption!

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

Evelyn #

Girl, Age: 12
Primary Diagnosis: Craniofacial disorder
Congenital abnormality of skull and face bones; cerebral palsy. Spastic cerebral palsy; Partial epilepsy-takes medication
Listed: Oct 2019
$2,490.00
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!
Evelyn crawls in order to get where she wants to go. She can stand with support and take steps to the side while holding on to something. She has spastic muscle tone. She picks up objects and transfers them from hand to hand. She does not talk. She responds positively to attention from adults.

David #

Boy, Age: 10
Primary Diagnosis: Cerebral palsy
cerebral palsy; quadriparesis ; epilepsy; Bronchial asthma; delays in all aspects of development
Listed: Feb 2020
$2,866.50
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!
David was declared clinically dead at birth and resuscitated. He currently lives in a group home. He reaches for hanging objects and can hold a toy for brief periods of time. He is very responsive to caregivers. He smiles and shows pleasure when spoken to. He tracts objects and tries to focus on people who are talking to him and objects being presented to him. He rolls from his back to stomach in his bed.

Kinsley

Girl, Age: 14
Country Code: LA-2
Primary Diagnosis: Dwarfism
dwarfism, mild cognitive delay
Listed: Feb 2021
$2,071.85
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!
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.

Victoria

Girl, Age: 14
Country Code: LA-2
Primary Diagnosis: Global developmental delays
Diagnosed with a mental delay, a non-specified compartmental deterioration, and a language disorder.
Listed: Jan 2020
$7,371.00
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!
Reece's Rainbow 20th Anniversary