Victoria

Girl, Age: 13
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!

Elio

Boy, Age: 8
Country Code: LA-2
speech and language delays; Urinary tract infection; Periapical abscess with fistula; Hydronephrosis; Renal dysfunction; Cognitive delay; History of neurogenic bladder; Pyelic Ectasia; Specified Leukocyte Disorder; Coccyx Valgus, 4th toe left Calvalgus
Delayed psychomotor development (associated with prematurity at 32 weeks, fetal distress, breech presentation)
Listed: Sep 2026
$0.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Elio is a child who has had improvements in all areas of development. Health-wise, Elio has shown improvements, as he has not had any new infections. He has been doing well since receiving proper care, and he is responding well to treatment. He is communicating better at a non-verbal level. Elio has made significant progress with his motor development.

The agency’s team met Elio in October of 2024, and they have additional information and videos!

Teressa #

Boy, Age: 6
Primary Diagnosis: Behavior, Blind / VI
Mild mental retardation, significant behavioral disorder requiring care or treatment. Childhood attachment disorder, reactive type. Convergent concomitant strabismus. Unspecified loss of vision in both eyes
Listed: Sep 2026
$0.00
has been donated towards the cost of my adoption!

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

Indy #

Boy, Age: 2
Other forms of congenital hydrocephalus – communicating hydrocephalus. Status post implantation of a valve system for ventriculo-subdural-peritoneal anastomosis. Malfunction of VP [ventriculoperitoneal] anastomosis. Secondary pseudomeningocele. Status post subacute subdural hematoma. Specific developmental disorders of motor function. Convergent concomitant strabismus.
Listed: Sep 2026
$0.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Indy is a sweet young boy who has been cared for in a foster family since infancy. He is generally calm and enjoys spending time with familiar adults. When he feels unsure or needs help, he looks to his caregiver for reassurance and attention. He enjoys shared activities, walks, playgrounds, water play, and bright, interesting toys.

Indy has significant developmental delays related to his medical history, particularly in his motor, communication, and cognitive development. He is an active crawler and can sit independently. He is beginning to pull himself to stand while holding onto furniture and has taken a few supported steps. He continues to need assistance with many age-appropriate daily activities.

Indy does not yet use words or consistently follow simple instructions, but he babbles and enjoys sound-based play. He is curious about his surroundings and shows interest in people and his environment, although his attention span during play is often brief. He can be somewhat cautious with unfamiliar people but warms up when approached gently.

Indy has a significant history of hydrocephalus and has required multiple neurosurgical procedures, including shunt placement and revisions. He continues to require follow-up with pediatric neurology and neurosurgery and ongoing developmental support. His medical team has recommended precautions to protect him from head injuries and certain types of physical activity.

Indy would benefit from a patient, loving family who can provide a stable home, advocate for his medical needs, and support his continued developmental progress. His recent records show encouraging progress, and he is a little boy who enjoys connection, attention, and being included in the activities around him.

Teresa #

Girl, Age: 13
Primary Diagnosis: Behavior, Cerebral palsy
spastic cerebral palsy, childhood hemiplegia, developmental delay, and minimal behavioral disturbances. The girl is in good general health and has no delay in physical development.
Listed: Sep 2026
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Teresa is a lively and affectionate girl who is described as sociable, smiling, and enjoys spending time with others. She has cerebral palsy and developmental delays, communicates primarily through gestures, and understands and follows simple instructions. She walks independently, eats on her own, and helps with simple daily tasks. Because of her positive and radiant personality, she is well-liked by both the adults and children.

Mason #

Boy, Age: 9
Primary Diagnosis: Trauma History
Listed: Sep 2026
**** I am eligible for a $500 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount. To inquire about this child, email childinquiry@reecesrainbow.org ***
Mason is a bright, active, and curious boy who enjoys interacting with others and being involved in activities. He is expressive and able to communicate his thoughts and feelings, especially once he feels comfortable and begins to trust those around him.

Mason enjoys playing football, active games, and video games. He also likes keeping his personal space clean and organized and takes pride in choosing his clothes and looking his best.

Mason is curious and eager to learn. He does well at school and has age-appropriate intellectual development, although he benefits from clear instructions, encouragement, and support when he becomes frustrated or discouraged. Building trust is very important to Mason. He may be cautious with new people and needs time, consistency, and patience to feel safe and comfortable. Once trust is established, he is able to form meaningful relationships and express his emotions.

Mason would benefit from a loving and patient family who can provide consistency, reassurance, and a safe environment where he can build trust and develop a strong sense of belonging. He hopes to have a family who will accept him for who he is and provide the support and care he needs to thrive.

Kali #

Girl, Age: 12
Primary Diagnosis: Behavior, Learning Disability
Other mixed disorders of conduct and emotions. Mixed disorder of scholastic skills.
Listed: Sep 2026
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Other mixed disorders of conduct and emotions. Mixed disorder of scholastic skills.
Kali is a sweet, imaginative, and sociable girl who enjoys spending time with both children and adults. She is kind, polite, and enjoys participating in conversations and group activities.

Kali is active and enjoys physical activities, music, outdoor play, and creative activities. She has a wonderful imagination and especially enjoys play-based and hands-on activities.

She is doing well with her daily routines and continues to develop her independence. At school, Kali benefits from additional support, clear instructions, and encouragement. She responds especially well to individual attention and positive reinforcement.

Kali enjoys building relationships with others and is described as caring and empathetic. She may need patience, reassurance, and emotional support as she adjusts to the idea of adoption.

Kali would benefit from a loving, patient family who can provide consistency, encouragement, and a supportive environment where she can continue to grow in confidence and independence.

Dolly #

Girl, Age: 15
Primary Diagnosis: Behavior, Learning Disability
Other mixed behavioral and emotional disorders
Listed: Sep 2026
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Dolly is a sweet girl who has experienced challenges early in life but continues to grow and learn with support. She has special educational needs and benefits from additional guidance in the classroom.

Dolly can be a little shy and sometimes prefers to spend time on her own, but she enjoys connecting with others and has a positive attitude toward adoption. She enjoys learning and is able to write from dictation, although she works at a slower pace.

Dolly would benefit from a patient, loving family who can provide reassurance, encouragement, and a safe, supportive environment where she can continue to build confidence and thrive.

Andy

Boy, Age: 13
Country Code: EE-11
Primary Diagnosis: Genetic Condition (non-DS)
Fragile X
Listed: Mar 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!
Andy was born with Fragile X Syndrome,and his needs were complex from the start. He was placed in residential care as a newborn.

He has been making progress in his current placement. He enjoys going to school and participating in music class. He may need assistance to focus during school.

Phineas

Boy, Age: 5
Country Code: EE-11
Polymalformative syndrome, with craniofacial dysmorphia; suspicion of Goldenhar Syndrome; Hydrocephaly; upper airway malformation with tracheostomy since 10/4/2021. Currently with cannula. Epilepsy. Gastrostomy. Sensory-neuro deafness – uses hearing aids.
Listed: Mar 2024
$1,025.00
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!
Phineas was previously listed as Phil — he is a sweet boy who was born with a polymalformative syndrome. His condition comes with needs that set him apart, and he was placed in care early on.

Phineas uses a wheelchair in his daily life. He also spends time in a standing frame. He enjoys smiling at people and laughing. Phineas enjoys sensory experiences with tactile or auditory input. He enjoys listening to a maraca or touching a soft stuffed animal.

Mimi and Micky

Sibling Group
Ages: 12, 17
Country Code: EE-11
Primary Diagnosis: Older Child
Listed: Feb 2024
**** I am eligible for a $500 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount. To inquire about this child, email childinquiry@reecesrainbow.org ***
Have you considered adopting siblings?!

Meet Mimi & Micky! They are a delightful duo. Mimi, July 2009, our shining star who reminds us that a little shyness only adds to the charm! She is reported to be clinically healthy.

Her shy sparkle quickly turns to a dazzling ray in the comfort of good company. She’s the heart of our group, spreading joy and giggles with a sense of humor that’s as infectious as her enthusiasm. She has a heart of gold. Her warmth extends to the young ones she cherishes. She’s a caring older sister, always ready to wrap them in a hug or share a playful story.

Ever the social butterfly, she forms deep connections that last, crafting a tapestry of friendships wherever life takes her. It’s no surprise that in every circle, she’s that missing puzzle piece you didn’t know you needed until she arrived.

Meet her younger brother Micky, March, 2014 – a beacon of joy, with a smile just waiting to light up your life! This handsome young man might seem a tad shy at first, but give him a moment, and his true colors shine through, painting laughter and happiness wherever he goes.

Micky thrives in the company of peers, his imagination a treasure trove of fun and games. His spirit of camaraderie embodies a priceless joy that only a loving family can multiply. With football under his belt and his zest for cycling and digital adventures, Micky’s the perfect companion for active days and cozy family nights.

Ames

Boy, Age: 11
Country Code: EE-11
Developmental challenges such as intellectual limitations, learning difficulties, linguistic delays, and special behaviors; maternal mental health issues
Listed: Feb 2024
$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!
Ames is a joyful youngster who displays notable independence for his age, showing advancement in managing personal responsibilities in spite of his cognitive development in areas such as language mastery, social dynamics, and self-regulation. Ames is progressing, revealing a promising trajectory.

His interests are as varied as they are engaging, ranging from the energetic spinning of beyblades to the strategic play of table football, and the creative assembly of Legos. A fondness for stories also defines him—he delights in listening, reading, and sharing tales with others.

Understanding and following rules come naturally to Ames when they are communicated clearly and applied consistently. He flourishes under positive reinforcement and thrives on routine, which helps him navigate his day with confidence. When faced with choices, he benefits from being offered two options to help enhance his decision-making skills.

Adaptable and responsive, Ames shows a commendable capacity for assessing situations; however, he does rely on adult guidance to navigate safely through his environment. Previously having not experienced a traditional family setting, he formed emotional attachments with his caregivers. Ames longs for what many take for granted—a loving family to call his own.

At his current developmental stage, it’s essential to tailor Ames’s transition towards adoption, ensuring the introduction to a potential family is mindful and gradual. Psychotherapeutic support has been assisting Ames in processing his hopes and feelings about family life, laying groundwork for his future relationships.

Lauren

Girl, Age: 14
Country Code: EE-11
Primary Diagnosis: Global developmental delays
Global Developmental Delay with Mild Intellectual Disability, as well as Mild Oppositional Defiant Disorder
Listed: Feb 2024
$36.00
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!
Lauren shines with a warmth that is immediately felt by everyone she meets. Her sweet and easy-going nature makes her quick to bond with both children and adults alike. An inquisitive soul, Lauren’s curious mind draws her to be a helping hand around the home, eagerly participating in day-to-day activities and showcasing a commendable level of independence in her daily routines.

Gifted with considerable communication abilities, Lauren also brings a touch of uniqueness through her passion for dance, expressing herself with joy and confidence in every hip-hop move. This lively interest in the arts highlights her outgoing and engaging personality, which endears her to both peers and adults.

While Lauren delights in being the center of attention and thrives in communal settings, like many children, she’s learning to channel her exuberant impulsivity into positive interactions. Her journey has been one of beautiful transformation. Through consistent support and exposure to stable role models, Lauren has made impressive strides in mastering self-regulation, although the support offered by her environment has its limitations.

The diligent teamwork of dedicated caregivers underlines the progress Lauren has made and underscores the need for continuity in nurturing her personal growth. Particularly crucial is the ongoing dialogue helping Lauren reconcile her emotions regarding her biological family background and shape her aspirations for the future.

Lauren dreams of being part of a forever family—a family eager to provide her with the love, stability, and support she deserves. A family that can offer her a unique place in their hearts and home, affirming her worth and fostering her continued growth, emotionally, socially, and academically.

Elsa

Girl, Age: 13
Country Code: EE-11
Primary Diagnosis: ADHD, Learning Disability
attention deficit/Academic school disorder
Listed: Nov 2024
$2,191.00
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 lovely older girl has an ADHD/ learning disability diagnosis.  She could do great with a family to help her with her schoolwork!

Xander

Boy, Age: 11
Country Code: EE-11
autism spectrum disorder and global developmental delay
Listed: Nov 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!

Eleanor

Girl, Age: 11
Country Code: EE-11
heterozygous variant in the KAT6A gene. Heart issues, global developmental delay, severe language delay
Listed: Sep 2024
$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!
Eleanor is a beautiful young girl who needs a family.

Ariel & Gabe

Sibling Group
Ages: 13, 9
Country Code: EE-11
Primary Diagnosis: ADHD, Skin Condition
Listed: Mar 2024
$1,088.10
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!
Siblings Ariel and Gabe, lived with their mother and older brother until they were placed in residential care over five years ago.

The siblings go to school and enjoy time with their friends. They follow routines for eating sleeping and personal care with minimal support. Their vaccinations are up-to-date and they have routine health checks. Ariel has managed psoriasis with the support of medication and therapies, while also enjoying the gifts of dance, music, and social activities. Gabe has had a minor surgical procedure, that he now manages with medications. He has medications and therapy for behavior support.

Academically, Ariel is in her fourth year and Gabe his second year.
Gabe enjoys watching tv, playing games, painting, and caring for animals. He attends a catechism class and church services. He may have behavior outbursts.

Both children are working through the child preparation plan for adoption.

Anne Marie

Girl, Age: 14
Country Code: EE-11
Primary Diagnosis: Older Child
Listed: Mar 2024
**** I am eligible for a $500 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount. To inquire about this child, email childinquiry@reecesrainbow.org ***
Anne Marie’s life has been marked by many transitions. Anne Marie lived in a family home previously, and then was placed in care of the government due to neglect. Even when the initial transition towards an adoptive family was unsuccessful, Anne Marie returned familiar surroundings with ease.

Anne Marie has a box of keepsakes that is important to her. Her diet is well-balanced, and she manages a minor visual impairment with glasses.

She is a typical teen in many ways — enjoying TikTok, beach outings, cycling adventures, and shared laughter with peers. Her active engagement in Sunday school further enhances her communal ties.

 

Carl

Boy, Age: 15
Country Code: EE-11
Primary Diagnosis: Fetal Alcohol Syndrome
Fetal Alcohol Syndrome
Listed: Mar 2024
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Carl was born prematurely in a home environment lacking the basic necessities; he was moved into residential care homes. He has been diagnosed with fetal alcohol syndrome (FAS), which has impacted his development.

In his current residence, Carl has blossomed into a kind-hearted and friendly child, creating bonds with his caretakers and peers. He partakes in meals with growing independence, embraces dressing routines and self-care; Carl sleeps soundly.

Carl carries a history of medical complexities. Despite an unsupervised pregnancy and a birth weight of less than a kilogram, Carl continues to receive dedicated medical attention across a spectrum of specialties to bolster his growth.

His therapeutic services include speech therapy, psychomotricity, and psychology, extended under the nurturing folds of his supportive abode. Carl delights in equine therapy and the companionship of dogs. Carl is a good student, benefiting from customized learning supports. He also enjoys music, tablets and computers.

Alden

Boy, Age: 7
Country Code: EE-11
Primary Diagnosis: Cerebral palsy, Deaf / HoH
Global cerebral palsy, severe psychomotor development delay, auditive issues
Listed: Feb 2025
$115.00
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!

Rhett

Boy, Age: 8
Country Code: EE-11
Primary Diagnosis: Autism
autism associated with global delay in psychomotor development
Listed: Feb 2025
$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!

Verity

Girl, Age: 13
Country Code: EE-11
Primary Diagnosis: Autism
Childhood autism, deficits in multiple areas
Listed: Jan 2025
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

Bristol

Girl, Age: 14
Country Code: EE-11
Primary Diagnosis: Behavior
Behavioral Issues
Listed: Sep 2025
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

Leo

Boy, Age: 7
Country Code: EE-11
Primary Diagnosis: ADHD, Autism
He has a developmental delay, with preserved skills in the area of locomotion/motor abilities. In addition, manifestations compatible with mild to moderate Autism Spectrum Disorder have been identified, as well as signs suggestive of Attention Deficit Hyperactivity Disorder.
Listed: Jan 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!
Little Leo is only 6 years old. He has a developmental delay, with preserved skills in the area of locomotion/motor abilities. In addition, manifestations compatible with mild to moderate Autism Spectrum Disorder have been identified, as well as signs suggestive of Attention Deficit Hyperactivity Disorder. He is monitored in developmental consultations and is receiving medication. He is also followed in Ophthalmology (routine consultations) and Otorhinolaryngology.

Leo has a calm and affectionate demeanor, showing stable moods and good spirits most of the time. He easily established a close relationship with the adults in his life, accepting physical contact and seeking affection and security from his caregivers. With his peers, he participates more peacefully in group games, having developed skills in waiting, sharing, and respecting rules, showing greater self-regulation. He is more willing to listen, understand, and follow instructions. There are no reports of regular aggressive behavior or tantrums, and it is possible to observe a growing effort on his part to manage his emotions and frustrations.

Leo is a sweet and curious child who shows interest in various recreational activities, such as riding a bike and scooter, jumping on the trampoline, and playing with cars. He likes to try new foods and textures and is receptive to food. He is becoming increasingly independent in his daily routines, enjoying being involved in them and seeking to help adults.

Leo has a brother, they have a very close and affectionate brotherly relationship. As no adoptive family has been found willing to adopt the brothers together, separate adoptions are being considered.

Melody

Girl, Age: 13
Country Code: EE-11
Primary Diagnosis: ADHD
Cognitive delays and attention deficit
Listed: Feb 2026
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

Bailey

Girl, Age: 14
Country Code: EE-11
Primary Diagnosis: Deaf / HoH
Global developmental delay, mild intellectual developmental disorder, bilateral sensorineural hearing loss, strabismus, and gait ataraxis. microdeletion on the short arm
Listed: Feb 2026
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

John

Boy, Age: 14
Country Code: EE-11
Primary Diagnosis: ADHD
ADHD
Listed: Feb 2026
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

Simon

Boy, Age: 12
Country Code: EE-11
Primary Diagnosis: ADHD
ADHD
Listed: Feb 2026
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

Mitch

Boy, Age: 4
Country Code: EE-11
Primary Diagnosis: Craniofacial disorder
trigonocephaly (craniosynostosis) and underwent surgery in 2023. high-arched palate and overlapping teeth. global developmental delay
Listed: Feb 2026
$10.00
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!

Patrick

Boy, Age: 10
Country Code: EE-11
Primary Diagnosis: ADHD
ADHD
Listed: Feb 2026
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***

Dirk and Kaleb

Sibling Group
Ages: 7, 4
Country Code: EE-11
Primary Diagnosis: ADHD, Speech Delay
Dirk has ADHD Behavioral issues; and Kaleb has Mild speech delay, Atopic Dermatitis
Listed: Mar 2026
$60.00
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!
Dirk and Kaleb are brothers who have been living together in residential care since October 19, 2023.

Their shared experiences have created a strong emotional bond, with Dirk often serving as a protective and guiding figure for Kaleb. Both children benefit from continuity, structure, and the support of a stable environment, which helps mitigate the impact of early family instability.

Dirk, the eldest, is curious, active, and cognitively capable, though he requires support with emotional regulation and school learning. Kaleb is affectionate, gentle, and developing independence, thriving in predictable and nurturing settings.

The siblings are covered by a Judicial Trust Measure with a View to Future Adoption, finalized on 10/30/2025, and joint adoption is considered the best path forward to preserve their relationship, provide emotional security, and ensure a stable future for both.

The ideal family would offer emotional stability, structure, and consistency, supporting Dirk’s and Kaleb’s individual needs while keeping their sibling bond intact—a source of protection, comfort, and belonging for both.

Tiana

Girl, Age: 2
Country Code: EE-11
Primary Diagnosis: Genetic Condition (non-DS)
Chromosome 22 Duplication Syndrome
Listed: Feb 2026
$30.00
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!
Tiana is a social, affectionate toddler who enjoys interacting with adults and responds well to familiar caregivers. While she is not yet using words to communicate, she understands simple directions such as “give” and “walk,” and communicates through gestures, pointing during play, and imitation.

A recent and exciting milestone is that Tiana has begun walking, showing growing independence, stability, and confidence. Motor development—especially locomotion—is one of her strongest areas and has allowed her to explore her environment and increase interaction with caregivers.

Tiana has a global developmental delay. At 19 months, her developmental skills were assessed at approximately a 13-month level. She shows progress across areas, with particular gains in mobility. She has a short attention span and prefers sensory-based play, especially activities involving sound and movement. She can be sensitive to noise and visual stimuli but is gradually becoming more tolerant of touch and motion.

She demonstrates oral sensory-seeking behaviors and has a high-arched palate, which may contribute to mouth breathing. Her eye-hand coordination is improving, and she can track and grasp objects, though her exploration remains limited.

Millie

Girl, Age: 12
Country Code: EE-11
Primary Diagnosis: Trauma History
Trauma
Listed: Feb 2026
**** I am eligible for a $500 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount. To inquire about this child, email childinquiry@reecesrainbow.org ***
Millie is a perceptive, curious, active, and fun-loving child. She has a good sense of humor, is affectionate, and does well at school. She wishes to be adopted and says that the waiting makes her feel sad. When asked what kind of family she imagines for herself, she describes a father, a mother, and a little brother.

Dolly

Girl, born 2026
Country Code: EE-11
Dolly has Bardet-Biedl Syndrome, along with several other medical conditions, including: Bronchiolitis obliterans, Kidney disease, Tubulopathy with pseudohypoaldosteronism, Hyperparathyroidism and hyponatremia, Risk of developing diabetes; Strabismus, nystagmus, and myopia (corrected with glasses, which she wears); Moderate to severe AGDPM (non-verbal), with a functional level of approximately 12 to 15 months (GS-II); Global delay in psychomotor development; Bilateral post-axial polydactyly of the feet (six toes on each foot); Stage I arterial hypertension due to renovascular causes
Listed: Feb 2026
$225.00
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!
Dolly is a sweet and friendly girl. She enjoys spending time with her peers and especially likes one-on-one interactions with adults. She is usually in a good mood, and both the children and caregivers are very fond of her.

During the 2024/2025 school year, Dolly attended the 2nd grade. She is well integrated into the school environment and enjoys going to school. She receives support from special education teachers and also benefits from Speech Therapy, Occupational Therapy, and Physiotherapy.

She also has chewing difficulties and is non-verbal. However, she shows some understanding of simple messages, such as recognizing when someone is calling her or playing with her. She makes sounds and vocalizes when engaged or entertained.

Jay, Martin and Ian

Sibling Group
Ages: 9, 7, 6
Country Code: EE-11
Listed: Feb 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!
Jay is currently 8 and shows age-appropriate development. He interacts well with peers and adults and is described as a friendly, affectionate, and polite child. He maintains eye contact, has appropriate vocabulary for his age, and generally presents with a positive mood. His sleep and eating patterns are stable, and he adapts well to changes, though he still struggles at times with managing frustration.

Jay’s psychological assessment shows above-average intelligence. However, he tends to become easily frustrated and distracted, and benefits greatly from positive reinforcement to complete tasks and support his self-esteem. Jay has been diagnosed with ADHD.

Martin is 7, he interacts well with both peers and adults. He is described as friendly, affectionate, and somewhat stubborn, displaying occasional oppositional behavior. He benefits from an assertive and consistent approach from adults and requires positive reinforcement to complete tasks and boost self-esteem. His psychological evaluation shows average cognitive functioning.

Martin has a history of sleep disturbances and oppositional behavior. He currently takes melatonin and risperidone, which have improved his sleep and behavior stability. Medically, Martin underwent adenoidectomy and bilateral myringotomy in November 2023 and continues ENT follow-up due to a ventilation tube in his right ear. He wears glasses for astigmatism and is followed in Ophthalmology. He also attends speech therapy.

Martin is described as emotionally immature, showing attention-seeking behaviors likely linked to early emotional neglect. While initially reserved, he eventually engages warmly and responds well to structured interaction.

Ian is nearly 6 years old. He is a cheerful, affectionate, and communicative child. He attends kindergarten, where he engages positively with adults and peers. Like his brothers, he seeks attention and affection, and shows signs of emotional immaturity—likely the result of early emotional abandonment.

His developmental assessment showed results within the expected range for his age. Ian is described as enthusiastic and motivated, both in structured tasks and in everyday interactions. He responds warmly to attention and maintains appropriate eye contact and spontaneous speech for his age.

Ian was referred to Neurosurgery for dolichocephaly, but surgery was not recommended as the condition does not affect cognitive development. The team attempted to obtain a second opinion, but there has been no follow-up from the consulting doctor. He was also discharged from ENT in March 2024 after an adenoidectomy, and continues to be followed in Ophthalmology for astigmatism, wearing glasses since December 2022. He currently attends speech therapy.

Jay, Martin, and Ian have not had the opportunity to form attachments to parental figures. Instead, their primary psychological and emotional bonds are with each other. As such, joint adoption is strongly recommended to preserve their emotional security and sibling connection.

All three boys have been informed about their adoption plan and have welcomed the idea. They no longer reference their biological family and are beginning to show anxiety and anticipation about the arrival of their new family. During their first meeting with the adoption team, the strong bond among the siblings was evident.

Rita

Girl, Age: 6
Country Code: EE-11
Primary Diagnosis: Deaf / HoH
global developmental delay (mainly motor and speech-language), right spastic hemiparesis related to left cerebral hemiatrophy, bilateral deafness with cochlear implants, and recurrent bronchospasms
Listed: Feb 2026
$10.00
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!
Rita is friendly, sociable, affectionate, and highly expressive. She communicates through facial expressions, gestures, and pointing, and is very attentive to her surroundings and others’ nonverbal cues. She responds well to sensory stimuli with smiles, vocalizations, and interaction, though she has moderate motor limitation on her right side.

Rita is good-humored, loves physical affection, and bonds easily with caregivers. She interacts well with other children, enjoys play, and imitates what interests her. Having experienced a disrupted adoption, she may carry unexpressed fears, but she continues to seek comfort and show affection, indicating strong potential to thrive in a loving, supportive family.

Jaeger

Boy, Age: 6
Country Code: EE-11
Primary Diagnosis: Autism
Autism Spectrum Disorder; Developmental delay
Listed: Mar 2026
$10.00
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!
Jaeger is 5 years old and has shown remarkable resilience despite early life challenges. He was referred to the Child and Adolescent Protection Commission in October 2023 after experiencing domestic violence and severe neglect. Until then, he lived with both parents, and from October to December 2023, he was in the sole care of his father. During this time, Jaeger was exposed to significant alcohol and drug use in the household, as well as chronic health challenges of his mother.

In December 2023, Jaeger was placed under a foster care protection measure. In August 2024, he transitioned from a foster family to a foster care center, where he continues to grow in a safe and supportive environment.

Jaeger has been diagnosed with Autism Spectrum Disorder and receives ongoing care from specialists in neuropediatrics, psychology, genetics, ophthalmology, and otolaryngology. He participates in weekly therapies including music therapy, speech therapy, occupational therapy, and psychomotor therapy. These interventions have led to significant progress, particularly in language development, daily living skills, and emotional growth.

While Jaeger is still developing motor skills appropriate for his age, he can walk, run, climb, and descend stairs. He continues to work on spatial awareness, movement imitation, and spatial orientation. He also experiences challenges with sleep rhythms, which are managed with medication.

Jaeger thrives in structured, predictable environments and benefits from consistent, loving care. His journey shows incredible strength, and he is ready to find a permanent family to support his growth, learning, and emotional development.

Andrew

Boy, Age: 7
Country Code: EE-11
Primary Diagnosis: Cerebral palsy
Cerebral palsy
Listed: Jan 2026
$2,125.00
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!
Little Andrew is a friendly, cheerful, and perceptive little boy. He is currently 6 years old. He was born prematurely and was diagnosed with cerebral palsy in the form of spastic tetraparesis, predominantly affecting the right side (grade 3+), with associated dysarthria. He uses a wheelchair.

Andrew regularly receives physiotherapy, occupational therapy, and speech therapy. He continues to receive follow-up care in neuropediatrics and orthopedics, including the administration of botulinum toxin due to stiffness in the upper limbs. He has hip dysplasia, currently without pain, and underwent surgery for hip stabilization on September 1, 2025. He also continues to receive care in nutrition, ophthalmology, physical medicine, and rehabilitation.

Andrew has a good relationship with both other children and caregivers. In his interactions, he verbally communicates his needs and interests and is able to express discomfort or displeasure.

Andrew is a communicative and expressive child with a reasonable vocabulary and the ability to construct sentences, including negative and interrogative forms. He repeats and learns new words; however, he needs support to improve articulation and diction. To support this, syllabic division exercises are incorporated during games and storytelling activities. He demonstrates a good understanding of his surroundings and, with individualized adult guidance, is able to focus his attention on tasks and interpret simple content.

In the area of autonomy, although Andrew is dependent on adults for his daily routines, he enjoys being involved and participating in tasks. He helps tidy up toys and materials and eats independently at mealtimes using cutlery. He shows greater ease in using a spoon but is also able to use a knife and fork. He can drink independently from a cup or mug.

It is not expected that Andrew will be able to walk; therefore, he uses an electric wheelchair. He demonstrates good autonomy in operating the joystick with his right hand and maneuvers the chair with ease (e.g., anticipating obstacles, navigating around them, reversing, and turning left or right to avoid collisions with people or objects). He has a clear sense of space. The acquisition of the electric wheelchair has been fundamental in supporting Andrew’s autonomy in locomotion. During the summer, he independently accompanied the group on several outings. Additionally, using the electric wheelchair, he is able to accompany an adult while carrying out small tasks (e.g., going to the supermarket or pharmacy).

Despite difficulties with fine motor skills, Andrew shows persistence and interest in exploring objects, toys, and new materials. He enjoys matching and fitting games, stacking objects, and painting with pencils, markers, or brushes using a gross grasp. With assistance, he participates in collage and tearing activities. In drawing, he currently scribbles and does not yet represent the human figure. He also enjoys handling books and is able to turn pages independently to observe the illustrations.

Andrew transitioned to the public preschool network in the 2025–2026 school year following a request for school postponement. According to information provided by his teacher, Andrew adapted well, integrated into daily routines, and maintained positive interactions with adults and peers. However, the teacher noted that Andrew experiences difficulties handling tools during writing and artistic expression activities and is not yet able to perform a fine pincer grasp. As a result, he shows limited autonomy in completing more structured tasks and may resist finishing them (e.g., giving up or becoming distracted). He will soon be evaluated by the technological resources center for possible allocation of an adapted computer.

Josh and Vance

Sibling Group
Ages: 11, 5
Country Code: EE-11
Primary Diagnosis: Other Special Needs
Josh has a Mild developmental global delay
Listed: Mar 2026
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Josh and Vance are two affectionate, resilient brothers who share a special bond and are looking for a nurturing family to help them thrive together.

About Josh:
Josh is a sociable, playful 4th grader who loves hugs, laughter, and outdoor adventures. He enjoys football, walks, and beach outings, and is independent with eating and personal care. Josh has ADHD and receives support for focus and learning, showing great progress in language and social skills.

About Vance:
Vance is a calm, sweet little boy who enjoys quiet play, cartoons, cars, and short walks. He has a gentle personality and is well-adapted to his preschool environment. Vance is healthy overall and continues routine medical follow-ups.

Their bond:
These brothers have been through a lot together and provide each other comfort and companionship. They would thrive in a loving, patient home where their sibling relationship can remain strong.

Josh and Vance are looking for a family that can offer stability, warmth, and support, giving them the chance to grow, play, and flourish together. If your family might be a fit for Josh and Vance, please reach out — the agency would love to share more about these special brothers!

Kevin

Boy, Age: 3
Country Code: EE-11
Listed: Mar 2026
$2,125.00
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 is 3 years old and he is in his first year of preschool at a public school. His integration into the school system has gone smoothly. He is a cheerful, calm, affectionate, and happy child.

Kevin has a global developmental delay; Prenatal microcephaly (cranial magnetic resonance imaging performed in September 2023);
Strabismus and decreased visual acuity – uses ocular prostheses and alternating occlusion

Genetic testing was performed. The results indicate that the child is heterozygous for the identified variants. This does not confirm, but also does not exclude, a possible diagnosis. Analysis of copy number variation (CNV) coverage data did not detect any large deletions or duplications that could explain the patient’s phenotype. A genetic consultation has been requested and is pending.

Mike

Boy, Age: 4
Country Code: EE-11
Listed: Mar 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!
Mike was born via cesarean section at 32 weeks. At birth, he required resuscitation and spent much of his early life in hospitals.

Mike has polymalformative syndrome, complex congenital heart disease, agenesis of the left radius and thumb, agenesis of the right kidney, psychomotor developmental delay, intestinal malrotation, and asplenia, for which he receives prophylactic treatment. He has undergone several cardiac interventions, including pulmonary venous return, Glen surgery, and two catheterizations, and he is expected to undergo another catheterization and heart surgery (Fontan procedure) in the future.

He also has gastroesophageal reflux disease, treated with Nissen fundoplication, and a gastrostomy. Mike receives multidisciplinary care across pediatrics, nutrition, ENT, orthopedics, plastic surgery, child psychiatry, and gastroenterology, with upcoming appointments in genetics and developmental pediatrics. He takes medications including captopril, cetirizine, mometasone nasal spray, amoxicillin, vitamin D, and acetylsalicylic acid.

Mike is a courageous and resilient little boy, making progress every day with dedicated medical care and support.

Danny and Daisy

Sibling Group
Ages: 11, 5
Country Code: Central.Asia.1
Region: Asia
Primary Diagnosis: Microcephaly, Other Special Needs
Danny Diagnosis: microcephaly (post-surgical), developmental delay, speech delay, pigeon chest, astigmatism, nystagmus, and residual encephalopathy. He needs a family who can patiently support him in overcoming his developmental delays and provide access to appropriate medical care and educational opportunities.

Daisy Diagnosis: flat/valgus feet, mild hypermetropia of the right eye, mild astigmatism of the left eye. 

Listed: Aug 2026
$0.00
has been donated towards the cost of my adoption!

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

Danny is described as a friendly boy, likes attention. He tries very hard to do his best at school but his delays make it challenging.

Daisy is developmentally on target. She is a sweet and curious little girl, she loves interacting with kids and adults.

Fine motor skills are somewhat delayed, particularly in activities requiring manipulation of small objects—such as drawing, cutting, and gluing. In the cognitive domain, Daisy shows interest in the world around her. She can count to 10, knows the basic colors and geometric shapes, and distinguishes between animals and household items. She is able to assemble simple puzzles and play with construction sets. A mildly slowed pace of task completion is associated with motor difficulties. Daisy speaks in simple sentences, retells short stories, and learns poems and songs. She understands adult speech and follows instructions. Although she shows interest in other children, she struggles to follow the rules of group play.

Based on vision diagnostics, glasses were prescribed for permanent wear. A follow-up examination by an orthopedist led to the replacement of her shoes with more appropriate orthopedic footwear, selected based on her current condition and foot size.

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
$0.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
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: 5
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.

Goliath

Boy, Age: 7
Microcephaly, CP, epilepsy, blind
Listed: Dec 2023
$5,086.14
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!
Goliath is the cutest, most chill baby ever! He loves cuddles, being bounced on the trampoline, swimming, going for bike rides, being held, and chocolate. He would do great either in a big family with lots of siblings or being the only one to soak up all the attention!

He is a great eater with either blended or soft foods, but not great at drinking liquids. He has a lot of small seizures throughout the day, but is on the max amount of seizure medication that can be found consistently in his country.

In school and therapy he does a lot of sensory activities and is working on using his arms for purposeful movement. He has a stander that he likes to use while playing his toy piano. He doesn’t have an advanced way to communicate yet as he is blind and doesn’t have much purposeful movement but he does let us know when he is happy, mad, or would like something. He mostly only gets fussy sometimes at night time when he wants to be rocked to sleep, when he has to take baths, or when he thinks his food is too spicy.

Update July 2026:
Goliath is growing big and strong while he waits for his forever family. He is getting happier and more interactive in little ways unique to him all the time. Forever the baby of his house, he still loves all of the things mentioned in his previous update- with his all time favorites still being cuddles and jumping on the trampoline. He loves being included in everything and would thrive in a big or small family- around lots of chaos or enjoying soaking up all the cuddles by himself.

Goliath now has a g-tube but still eats small amounts by mouth for fun! Chocolate is his favorite. He is sleeping through the night more, and is very easily comforted when he is fussy.

At school, he is working on increasing his engagement with sensory activities and using his arms more purposefully during play and learning. He especially enjoys when his teachers help him paint or explore sensory materials such as shaving cream. His primary form of purposeful movement is kicking his legs when he knows someone is sitting beside him on the couch. He is quite strong and either manages to move himself a little bit when doing this or at least make the person sitting by him pay him lots of attention :).

He needs access to better medical care for his seizures as he is on the max amount of medication his country has available but still has many small (2-5 second) seizures per day.

Leena

Girl, Age: 11
Country Code: Asia.4
Region: Asia
Primary Diagnosis: ADHD, Autism
Listed: Jul 2026
Leena came into protective care at the age of 1 year after she and her older siblings (not being placed for adoption with Leena) were all hospitalized due to suspected maltreatment. Both parents had histories of drug usage and offenses. Now age 10, Leena has been diagnosed with Austism Spectrum Disorder (ASD) and Attention Deficit Hyperactivity Disorder (ADHD). She is in stable health.
Leena enjoys playing sports, including soccer, skating, cycling and track and field. Social workers and caregivers describe Leena as a cheerful, talkative, helpful, friendly, and playful child who actively participates in sports and games, willingly assists younger children, and contributes to household chores. She receives occupational therapy to assist with fine motor skills, handwriting, motor coordination and other related skills. She has made good progress on finger dexterity as evidenced by her enjoyment of handicrafts—especially making bracelets and necklaces for herself and her toy bunny. She also receives speech therapy for difficulties in oral expression, limited vocabulary, simple sentence structures and restrictive narrative and reporting skills. At the same time, her listening comprehension, language fluency, and speech intelligibility are satisfactory.
Leena is self-motivated to improve but is sensitive to criticism, responds best to simple and clear instructions from trusted adults, and tends to internalize emotions rather than express them directly. She displays notable rigidity, preferring fixed routines and patterns, strict adherence to rules, and often insisting on completing tasks exactly as started or shown. Caregivers recommend that future caregivers adopt gentle, firm, and clear disciplinary approaches to support her emotional regulation and behavioral development.

Jimmy #

Boy, Age: 8
Primary Diagnosis: Behavior, Other Special Needs
Moderate mental delays, significant behavioral disorder requiring additional care or treatment.
Listed: Jun 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!
Jimmy currently lives in a specialized care setting where he receives support for his developmental needs. He is a sweet boy who benefits from a structured environment and caregivers who understand his unique way of interacting with the world.

Jimmy has significant developmental and intellectual delays and requires assistance with most daily activities, including communication, self-care, and personal hygiene. He is nonverbal and communicates primarily through vocalizations, gestures, and his responses to familiar people and routines. While he does not actively seek out interaction with peers, he responds positively to consistent care, attention, and nurturing relationships.

Physically, Jimmy is healthy and has no motor impairments. He enjoys sensory experiences, including time in a dry pool, tactile activities, ball play, and jumping on a trampoline. He is curious about his surroundings and benefits from hands-on exploration and sensory-based activities.

Myles #

Boy, Age: 3
Primary Diagnosis: Behavior, Cerebral palsy, Speech Delay
cerebral palsy; severe mental delays; significant behavioral disorder requiring care or treatment; Expressive speech disorder. Insomnia
Listed: Jun 2026
$0.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Myles is a sweet little boy born in July 2023. Despite facing significant medical and developmental challenges, Myles continues to make progress and has shown determination as he learns new skills.
Myles has been diagnosed with cerebral palsy and severe developmental delays. He requires ongoing therapies and will need a family that is prepared to advocate for his medical, developmental, and educational needs throughout his life. His diagnoses include significant cognitive delays, speech impairment, and motor challenges that affect his mobility and communication.
Although Myles faces many obstacles, he has recently achieved milestones such as learning to sit independently and beginning to pull himself up while holding onto furniture. He enjoys exploring toys, especially those within his reach, and expresses himself through vocalizations and interactions with those caring for him.
Myles will benefit from a family committed to providing a structured, nurturing environment and access to specialized services, including physical therapy, speech therapy, and developmental support. He will need lifelong assistance and care, but with the love and dedication of a family, he can continue to reach his fullest potential.

Grayson

Boy, Age: 4
Country Code: EE-2
Listed: Jun 2024

Adopted Internationally (2026)!

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