Phil and Annie #

Sibling Group
Ages: 10, 4
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 ***
Phil is a wonderful boy with a calm and curious personality. He enjoys socializing and being around friends. Phil is in good physical health. He has an intellectual delay and a history of strabismus (crossed eyes), which was surgically corrected and currently presents with no symptoms.

Annie’s medical history includes a neurological condition with early-onset epilepsy (seizures are currently well controlled with medication), a syndrome of congenital anomalies with predominantly facial involvement, microcephaly, strabismus, and global developmental delays (neurological and psychological). She can stand with support but does not yet walk independently and has limited coordination. She loves interacting with caregivers and is a very sweet little girl.

Jay, Martin and Ian

Sibling Group
Ages: 8, 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.

Mitch

Boy, Age: 3
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!

Axton #

Boy, Age: 2
Special needs: prematurity (2nd degree); low birth weight (1,560 g); microcephaly; congenital bilateral cleft lip and cleft palate (status post plastic surgery); congenital duodenal atresia (status post surgical correction); delayed neuropsychological development.
Listed: Feb 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!
Meet adorable Axton!  Axton has never lived with his biological family and has spent his entire life in hospitals and children’s institutions. His special needs are primarily medical, and his congenital malformations have been successfully treated surgically. Although his neuropsychological and motor development are delayed, Axton is making steady progress.

Axton moves around using a walker and is very active. He sits independently without support. His speech is in the process of development; he pronounces individual sounds and produces a variety of vocalizations.

Axton is cheerful and smiles often. He actively seeks the attention of adults and laughs out loud during playful interactions. He shows good adaptation to new environments and daily routines. Axton is calm and does not display self-aggressive behavior. He independently reaches for toys placed around him, taps them, and explores them with curiosity.

Axton is fed with a spoon by an adult while seated in a high chair. Efforts are being made to teach him to drink liquids from a cup. He falls asleep in a crib, and his sleep is calm.

Bianca #

Girl, Age: 4
Syndrome of congenital anomalies with predominantly facial. Microphthalmi Abnormalities of the thoracic vertebrae. She is missing her left eye ball and right ear.
Listed: Jul 2024
$769.00
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!
Bianca was recently transferred from a large orphanage to a small group home. She’s been making developmental progress in her new home. She can pull to a stand in her crib and cruise along the rail. She will take steps when holding the hands of a caregiver. She reaches for toys and will hold and explore them.

Esta, Sophie and Luke

Sibling Group
Ages: 13, 7, 6
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.

Phineas

Boy, Age: 4
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.

Marcy

Girl, Age: 6
Country Code: EE-2
Primary Diagnosis: Craniofacial disorder, Deaf / HoH
Listed: Nov 2023
$142.20
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!
Marcy is a 4 year old girl with frontal craniostenosis and tuberous sclerosis. Marcy was diagnosed with conductive and sensorineural deafness. Non-orbidity of both eyes. The girl currently does not use corrective glasses, as recommended by ophthalmologists. She is generally cheerful, and is able to imitate gestures and independently eat meals. She struggles with dressing herself and identifying some shapes and colors. Marcy is able to respond to simple commands and messages. She enjoys playing with toys and demonstrates improvement in her coordination. She is very patient and kind. It is recommended for her to wear glasses. Her speech development is delayed, but she can still communicate, and she has demonstrated improvement. Above all she is a nice girl with very many good qualities.

Wayne #

Boy, Age: 9
Repaired cleft lip and palate; mild cognitive delays; speech delays
Listed: Feb 2022
$31.50
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 on development: He enjoys engaging with others in play and initiates communicating. His vocabulary has greatly improved. He continues to learn new words.  He understands instructions and has good active concentration for about 20 minutes. During walks in the park, he enjoys explaining to others what he sees. If he is unable to articulate the words, he uses gestures in a way that can be understood by everyone. He is interested in animals, cars and many different kinds of toys. He is content playing on his own. He very quickly understands how to carry out more complex tasks. He shows a lot of initiative. He has settled in very well to the kindergarten he attends. He is completely independent in self-care to the extent that when he returns home he helps himself to snacks and drinks.

Posie #

Girl, Age: 8
Primary Diagnosis: Craniofacial disorder
cleft lip & palate, facial and skull dysmorphia, seizures, quadriparesis-weakness in all 4 extremities
Listed: Aug 2019
$2,500.85
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!

Evelyn #

Girl, Age: 11
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.

Brian #

Boy, Age: 10
Primary Diagnosis: Craniofacial disorder
Congenital malformation syndromes predominantly affecting facial appearance. Foramen ovale persistens. Transient pulmonary hypertension. Pes equinovarus bilateralis. Severe delay in neuro-psychical development
Listed: Jul 2018
$3,116.62
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!
Brian recognizes familiar adults and has formed an attachment to his favorite caregiver. He is uncomfortable around strangers. He is working with a physical therapist and a teacher on fine and gross motor skills. He can pick up toys and transfer them from hand to hand. His teacher reports that he understands what is being said to him and has recently begun responding to simple directions such as “give me”. He is able to sit unassisted and moves around in a baby walker.

Photos and videos are available through the agency.

Ashford #

Boy, Age: 10
Primary Diagnosis: Craniofacial disorder
Microcephaly
Listed: Sep 2017
$2,610.00
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!
Ashford enjoys the presence of adults and emotionally expresses himself with laughter, crying and sounds. He laughs when tickled and smiles when he sees familiar faces. Ashford is unable to sit, stand, nor does he have head control. He prefers to be on his stomach. He does not have coordinated movement of his arms or legs and has little ability to hold a toy. Ashford’s diagnosis is Microcephaly. He was born prematurely and received intervention at the hospital at birth. Some history of convulsions, controlled with medication. Suspicion of left nasal atresia.
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