Everly

Boy, Age: 11
Country Code: EE-1
Primary Diagnosis: Hydrocephalus
Communicating hydrocephalus; Congenital deformities of feet; Acquired deformity of chest and rib; anemia
Listed: Jun 2020
**** 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 ***

Hernan

Boy, Age: 11
Country Code: EE-1
Primary Diagnosis: Hydrocephalus
hydrocephalus, Spastic tetraplegia, Generalized idiopathic epilepsy and epileptic syndromes, Other chronic tubulo-interstitial nephritis, Congenital malformation of optic disc, Profound mental delays
Listed: Jun 2020
**** 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 ***

Bryan #

Boy, Age: 3
Primary Diagnosis: Cerebral palsy
cerebral palsy – impacting the lower limbs, cognitive delays
Listed: Jul 2021
*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***
$1,980.00
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!
Bryan moves around by scooting on his bottom. He can stand and take a few steps while holding the hands of an adult. He enjoys playing with balls and will hold them, throw them and crawl after them in order to get the ball and throw it again. He says several words and uses them in the correct context. He is very interested in other children and will play with other children and adults.
Photos and videos available through the agency.

Brody #

Boy, Age: 6
Primary Diagnosis: Deaf / HoH
bilateral deafness-choclear implant on the ride side; Moderate mental delay with autistic characteristics; Strabismus
Listed: Sep 2021
*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***
Brody walks independently. He is able to navigate stairs and playground equipment at the park. Most of Brody’s delays seem to be related to being unable to hear and communicate his wants/needs. For example, the foster family reports that he is not aggressive, but he does demonstrate frustration at being unable to communicate with them to express his thoughts and what he wants. He uses some gestures to communicate, such as opening the refrigerator to express that he is hungry. He is supposed to be under the care of a specialist to work with him now that he has the cochlear implant (and to continue to develop his communication skills), but this has not been consistent due to COVID restrictions and the fact that the family must travel to another town for Brody to see the specialist. The foster family does report that Brody seems to be able to hear now that he has the implant and they have seen improvements with the implant in place. Brody does attend a day program for children with disabilities and has recently become more interested in the other children.

Mitchell #

Boy, Age: 5
Primary Diagnosis: Cerebral palsy
cerebral palsy – an ataxic form
Listed: Jul 2021
*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***

Mitchell walks independently with an ataxic gait. He talk using simple words and simple sentences. He plays with toys. He shows interest in his environment and everything happening around him. He seeks contact with familiar adults.

Photos and videos are available through the agency.

Cherlin

Girl, Age: 10
Region: Asia
congenital heart disease (VS, PDA, OSD)
Listed: May 2021
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
Cherlin was diagnosed with congenital heart disease (VS, PDA, OSD) and had successful surgery when she was just an infant. Her heart is now healthy. At age seven, she was described as sunny and active. She is able to do daily tasks (toileting, eating, brushing her teeth, folding clothes, etc.) independently. She runs fast, colors inside the lines, likes dancing and performing, has a good sense of rhythm, and remembers actions correctly. Her communication is good and she understands adult instructions. She is able to draw a circle and count to ten.

Sierra

Girl, Age: 7
Country Code: EE-1
spastic diplegia, Sequelae of subarachnoid haemorrhage, Epilepsy, Congenital malformation of optic disc, Hypoplasia and dysplasia of lung, Cardiomyopathy
Listed: Feb 2018
$2,767.50
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!

Melany #

Girl, Age: 14
Primary Diagnosis: Global developmental delays
Borderline intellectual delays; learning delays
Listed: Apr 2021
*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***
Melany is physically healthy with mild intellectual delays. She is in 7th grade and has worked with a resource teacher online during the 2020-2021 school year. She is described as shy and introverted, though she communicates freely with familiar people. She enjoys talking about topics that interest her and is very friendly. She has friends at school and at the children’s center where she lives. She states that her dreams are to have a family, finish school and become a teacher. When asked what adoption means, she said, “to have a family, to live forever with these people who take care of you and not to be left alone anymore”.

Benson

Sibling Group
Ages: 8
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Disorder of central nervous system, unspecified; Severe intellectual disabilities; Other specified chromosome abnormalities; Frostbite with tissue necrosis of abdominal wall, lower back and pelvis
Listed: Oct 2020
$126.00
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 has a brother born in 2012 who was placed in a different orphanage.  A prospective family should be approved for two — they may be required to be adopted together.

Orren

Boy, Age: 6
Country Code: EE-1
Primary Diagnosis: Congenital Heart Defect
Microcephaly; heart condition (post-op)
Listed: Aug 2020
$1,410.30
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 understands everything and talks back; he follows instructions. He is waiting to get his family.

Brenner and Braun

Sibling Group
Ages: 5, 5
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Diagnoses information listed below
Listed: Sep 2020
$1,655.40
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!
Brenner:
Communicating hydrocephalus
Disorder of brain, unspecified
Portal hypertension
Bilateral inguinal hernia
Other congenital valgus deformities of feet
Congenital tracheomalacia
Cardiomyopathy, unspecified

Braun:
Disorder of brain, unspecified
Unilateral inguinal hernia
Hypertrophy of tonsils
Other non-diabetic proliferative retinopathy
anemia
Heart disease, unspecified

They have a sister, born 2013, she lives with family.

Fulton

Boy, Age: 5
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Other congenital malformations of brain
Listed: Nov 2020
$112.50
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!
By his medical statement his psychological development does not match his age

Lacey

Girl, Age: 7
Country Code: EE-1
Primary Diagnosis: Craniofacial disorder
Cleft palate
Listed: Mar 2021
$2,509.00
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 child shows significant facial features of FAS (fetal alcohol syndrome). This is not a diagnosis, but a cautionary disclosure.

.2

Trina

Girl, Age: 12
Country Code: LA-6
Primary Diagnosis: Other Special Needs
Sickle Cell Anemia
Listed: Mar 2021
$22.50
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!
Trina just glows with positivity! She likes to participate in the activities carried out in the institution, mainly those related to the creative arts such as painting and dancing, she likes to play with her peers and sometimes acts as a leader in social groups. In the psychological report, they describe the girl as responsible, obedient, dedicated, organized and friendly. Trina has a tendency to withdrawal and mild depression, due to the presence of feelings of insecurity, low self-worth and low self-esteem.

Trina also projects a strong need for belonging, parental protection and a strong desire for firm support, these aspects are explained by her life history and have been worked from different approaches by psychology, overall a calm state of mind is reported.

We know that an adoptive family can greatly help Trina feel valued and loved, and will help her improve in these areas with love, security, acceptance and healing.

Photo available from agency!

Trina has Sickle cell anemia, and she was medicated with folic acid. Sickle cell anemia is one of a group of disorders known as sickle cell disease. Sickle cell anemia is an inherited red blood cell disorder in which there aren’t enough healthy red blood cells to carry oxygen throughout your body. While there’s no cure for most people with sickle cell anemia, treatments can relieve pain and help prevent complications associated with the disease. Many people with this condition live very normal lives. Learn more about the illness and living with Sickle Cell by visiting Sickle Cell Speaks.

High altitude risk: The air at high altitudes, such as in an unpressurized airplane or in the mountains at altitudes greater than 5,000 ft (1,524 m), has less oxygen than at sea level. The lack of oxygen can cause cells to sickle which is painful and dangerous for a carrier. For that reason, it is not advisable to place a child for adoption with a family living at higher altitude / mountains.

Raymond #

Boy, Age: 4
Medical Diagnoses: Cerebral palsy secondary to hypoxia at birth, optic nerve atrophy, malnutrition, cleft palate (repaired) 
Listed: Apr 2021
*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***
Raymond is an adorable little guy with cerebral palsy in desperate need of a family who can provide better for his needs. He has so much potential but none of it is available to him due to his current living situation and lack of appropriate resources. Raymond follows simple commands such as “laugh”, “sing”, or “stick out your tongue”. He can stack three blocks and likes to play with toys where he can put smaller objects into larger ones. He is working with a therapist to learn to use a walker. He reacts with a smile to adults who are well known to him. He can babble and imitate animal sounds. Raymond likes to interact with other children and to play simple games. He chews his food well when he’s spoon fed and he drinks from a special bottle. Raymond has lived with the same foster parents since he was a month old. It is not clear from his documents the extent of his visual loss which may be complete or partial.

 

Charleigh

Sibling Group
Ages: 8, 15, 13, 11
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Spastic paraparesis with persistent motor disorders; Congenital malformation of brain
Listed: Jun 2020
$1,171.00
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!
Charleigh has 3 healthy siblings living in a different orphanage: 2 brothers -13 and 9 years old; a sister of 11 years old. As long as all are available they will need to be adopted together.

Trudie and Violette

Sibling Group
Ages: 5, 6
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Younger Sister: Disorder of brain, unspecified; Phonological disorder

Older Sister: Other disorders of nervous system not elsewhere classified; Phonological disorder

Listed: Oct 2020
$1,900.00
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!
These sisters must be adopted together! There are 4 other siblings in a separate orphanage.

Corvin

Boy, Age: 7
Country Code: EE-1
Primary Diagnosis: Other Special Needs
congenital microcephaly; syndrome movements disturbance; severe mental delays
Listed: Jun 2020
$626.00
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!

Dayton

Boy, Age: 7
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Unspecified mental disorder due to known physiological condition; Expressive language disorder; Disorder of central nervous system, unspecified
Listed: Oct 2020
$22.50
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!

Dierdre

Girl, Age: 13
Country Code: EE-1
Primary Diagnosis: Other Special Needs
severe mental delay, autism, congenital heart disease, myopia, strabismus
Listed: Nov 2020
$68.00
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!

Dak

Boy, Age: 13
Country Code: EE-1
Primary Diagnosis: Other Special Needs
severe mental delay, cardiomyopathy, atrophy of visual nerve
Listed: Nov 2020
$351.00
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!

Edison

Boy, Age: 16
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Severe mental delay, scoliosis, strabismus, flat feet, atrophy of visual nerve
Listed: Nov 2020
$124.20
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!

Evander

Boy, Age: 6
Country Code: EE-1
Primary Diagnosis: Congenital Heart Defect
Other disorders of nervous system not elsewhere classified; Ventral hernia; Other congenital deformities of feet; Other congenital malformations of cardiac chambers and connections; Neonatal goiter; Persistent hyperplasia of thymus; Fetal alcohol syndrome (dysmorphic)
Listed: Oct 2020
$101.25
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 has 2 siblings – 17-year old sister and 12-year old brother; Due to his special needs, he may be able to be separated from his siblings, for adoption.

Tyson #

Boy, Age: 4
Listed: Apr 2021
*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***
Diagnosis: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.

Guy

Boy, Age: 12
Country Code: EE-1
Primary Diagnosis: Cerebral palsy
Spastic diplegic cerebral palsy, Severe intellectual disabilities, Microcephaly, Other congenital malformations of brain, Congenital malformation of cardiac chambers and connections, Other specified congenital malformations
Listed: Nov 2020
$178.00
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!

Hank

Boy, Age: 14
Country Code: EE-1
Primary Diagnosis: Other Special Needs
moderate intellectual disabilities
developmental disorder of speech and language
Listed: Jun 2020
$2,226.90
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!

Jayla

Girl, Age: 11
Country Code: EE-1
Primary Diagnosis: Cerebral palsy
severe mental delay, cerebral palsy, concomitant strabismus, astigmatism, contracture joint, unspecified heart disease
Listed: Nov 2020
$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!

Holyanna

Girl, Age: 11
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Severe intellectual disabilities, malnutrition, anemia, Other cardiomyopathies
Listed: Nov 2020
$63.00
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!

Hudson

Boy, Age: 15
Country Code: EE-1
Primary Diagnosis: Deaf / HoH
Sensorineural hearing loss, bilateral; Profound intellectual disabilities; Mixed specific developmental disorders; Other congenital valgus deformities of feet; Exotropia
Listed: Jun 2020
$110.00
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!

Kenrick

Boy, Age: 8
Country Code: EE-1
Primary Diagnosis: Hydrocephalus
Other specified congenital malformations of brain; hydrocephalus; spastic paraplegia; Severe intellectual disabilities; Other congenital valgus deformities of feet; Congenital malformation of optic disc
Listed: Nov 2020
$67.50
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!
He has an older half-sister; she lives with family

Klover

Girl, Age: 12
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Compression of the brain; Unspecified severe protein-calorie malnutrition; Protein-calorie malnutrition of moderate and mild degree; Specific developmental disorders of speech and language
Listed: Nov 2020
$2,640.00
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!

Lincoln

Boy, Age: 8
Country Code: EE-1
Primary Diagnosis: HIV or Hep
HIV; Seborrhea capitis; Disorder of central nervous system; Congenital deformities of feet; Mixed specific developmental disorders; Expressive language disorder; Mixed behavior and emotional disorder
Listed: Nov 2020
$95.00
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!
Lincoln has 3 sisters born in 2009, 2011, 2013 – all are in “a family-type children’s home.” These siblings are not available for foreign adoption but available for domestic adoption. In order to adopt Lincoln, a family would have to get permission for “separating” siblings.

Nadine

Girl, Age: 12
Country Code: EE-1
Primary Diagnosis: Global developmental delays
Moderate mental delay; congenital brain malformation; ventriculomegalia; crossed eyes
Listed: Apr 2015
**** 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 ***
Nadine was recently relisted (March 2021)

Malakai

Boy, Age: 10
Country Code: EE-1
Primary Diagnosis: Other Special Needs
severe mental delays, malnutrition, anemia, rickets, congenital deformation of clavisternomastoid muscle, myopia, hemangioma
Listed: Nov 2020
$99.00
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!

Mateo

Boy, Age: 8
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Disorder of central nervous system, unspecified; Mixed specific developmental disorders; Expressive language disorder; Other mental disorders due to known physiological condition Attention-deficit hyperactivity disorder, predominantly hyperactive type; Other congenital malformations of upper limb(s), including shoulder girdle; Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
Listed: Oct 2020
$14.00
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!
Has two siblings under custody (2003, 2010) and not currently available for adoption.

Nehamiah

Boy, Age: 5
Country Code: EE-1
Primary Diagnosis: Hydrocephalus
Bladder fistula; Stress incontinence; Chronic interstitial nephritis; Chronic kidney disease; Hydrocephalus (condition after shunting)
Listed: Jun 2020
$19.35
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!

Nestor

Boy, Age: 13
Country Code: EE-1
Primary Diagnosis: Other Special Needs
moderate mental delay, epilepsy, microcephalus
Listed: Nov 2020
$34.20
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!

Petey

Boy, Age: 13
Country Code: EE-1
Primary Diagnosis: Other Special Needs
severe mental delay, hypermetropia, atopic dermatitis, heart disease, gallbladder disease
Listed: Nov 2020
$18.00
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!

Harmony

Girl, Age: 5
Primary Diagnosis: Down syndrome
Down syndrome and Congenital Heart Defect (ASD and PFO)
Listed: Mar 2021
$117.00
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!
Update from Feb 2021:  Harmony is outgoing and cheerful. She likes smiling and imitating others’ behavior.  She’s well-behaved, and not yet potty trained. She is attached to her caretakers. She likes here caretakers and cares for others. She has nothing to fear.  She gets along well with others. She likes to play with other kids. She has been living in the orphanage.  Her language skills are delayed, but developing.  She understands simple directions.  She enjoys playing with the other kids, and playing with balls.

Harmony is a precious little girl!   Harmony is described as an active and cute child. At the time her file was prepared (March of 2019), she could stand stably, walk while holding the bed rail, and crawl fast. She liked when her caretaker would accompany her to play. Harmony could discern sounds and make sounds when happy. She liked to pull her familiar caretaker’s clothes, flash her sweet smile, and give hugs! Harmony also liked playing with the child in the bed next to her. She is said to be a good eater and sleeper. We’re hoping to get an update on Harmony and excited to see who her lucky family will be too!

There is a $1,000 agency fee reduction for Harmony’s adoption with her current adoption agency.

Rohan

Boy, Age: 11
Country Code: EE-1
Primary Diagnosis: Other Special Needs
severe mental delay, congenital anomoly the development of the brain, low parapareses, damage of functions of walking
Listed: Nov 2020
$212.40
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!

Sansa

Girl, Age: 14
Country Code: EE-1
Primary Diagnosis: Cerebral palsy
severe mental delay, cerebral palsy, microphtalm, concomitant strabismus, anemia
Listed: Nov 2020
$4.50
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!

Veronika

Girl, Age: 12
Country Code: EE-1
Primary Diagnosis: Cerebral palsy
Moderate mental delays; Cerebral Palsy; hyperkinetic syndrome
Listed: Jun 2020
$90.00
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!

AJ

Boy, Age: 4
Country Code: LA-6
Primary Diagnosis: Other Special Needs
Grade I Osteogenesis imperfecta, controlled asthma, controlled atopic dermatitis, right cryptorchidism (undescended testicle)
Listed: Mar 2021
$90.00
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!
AJ is a calm, loving, shy boy who came into the care when he was about a year old; he was found abandoned. He has favorably adapted to the institution where he is being cared for and he has made significant progress in his motor process.  The boy moves his upper and lower extremities, he can take his feet to his mouth, he crawls, and tries to stay standing with support. The report also states that AJ is a boy who explores the environment, he maintains attention and interacts with people, appropriately responding to the sensory stimuli that are presented to him. AJ likes children’s songs and dances imitating his peers, he likes colorful musical instrument toys.

Photo available from agency!

When the medical report was first performed when he was about one year old, AJ was not walking and a level of delay is reported in the cognitive, language and motor areas that are related to the state of severe malnutrition with which he was found as an infant.

His Grade I Osteogenesis Imperfecta is the mildest form of the condition. Osteogenesis imperfecta (OI) is a genetic disorder characterized by bones that break easily. OI is highly variable. Its signs and symptoms range from mild to severe. In addition to fractures (broken bones), people with OI sometimes have muscle weakness, loose joints (joint laxity), curvature of the spine (scoliosis), brittle teeth (dentinogenesis imperfecta), and hearing loss. A classification system dividing OI into several types is commonly used to help describe how severely a person is affected. Type I is the mildest and most common form of OI.

Talisa

Girl, Age: 12
Country Code: EE-1
Primary Diagnosis: HIV or Hep
HIV disease resulting in encephalopathy; developmental disorder; Esotropia; Myopia; Flat foot; Delayed development following protein-calorie malnutrition; Other specified diseases of gallbladder; Enuresis not due to a substance or known physiological condition; Contracture of joint; Hypothyroidism, unspecified; Other cardiomyopathies; Other specified congenital malformations of brain
Listed: Nov 2020
$9.00
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!
She is a very good girl with good potential to develop.

Tammy

Girl, Age: 8
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Severe mental delays
Listed: Jun 2020
$3,268.27
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!

Thaddeus

Boy, Age: 7
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Disorders of psychological development, Disorder of brain, malnutrition, Microcephaly, Undescended testicle
Listed: Nov 2020
$81.00
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!

Timothee

Boy, Age: 16
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Moderate mental delays, allergy, dermatitis
Listed: Nov 2020
$45.68
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!

Zoriah

Girl, Age: 15
Country Code: EE-1
Primary Diagnosis: Other Special Needs
moderate mental delays
Listed: Jun 2020
$88.43
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!

Santiago

Boy, Age: 3
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Fetal alcohol syndrome (dysmorphic); Congenital deformity of sternocleidomastoid muscle; Disorder of brain, unspecified
Listed: Nov 2020
$236.00
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!

Isla #

Girl, Age: 5
Pierre Robin sequence (cleft lip & palate); strabismus; global developmental delays; strabismus
Listed: Feb 2021
*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***
Isla can crawl, slowly walks, climbs and goes down steps. She does not react to any sounds or to people talking to her. Her report indicates that her hearing is normal, despite repeated observations that she does not react at all to any sounds.When a toy is placed in front of her field of vision, she will reach for it and hold it in her hand.  She enjoys playing with light up toys.