Silvio

Boy, Age: 4
Country Code: EE-2
Primary Diagnosis: Other Special Needs
Extremely premature, tracheotomy
Listed: May 2021
$50.00
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!
Silvio is a Roma boy who was born extremely premature (22 weeks), with a very low birth weight. He spends 6 months at the hospital and fought for his life! He had a tracheotomy procedure and eye Lasik surgery in October 2017.

Last update 2020: Delayed psychomotor development. Visible improvement after rehabilitation. Feeding the by the bottle, playing with toys, rolls out of the back on the stomach and vice versa. He tries to crawl. A very active child who initiates contact. He makes eye contact, focuses his attention on the human face, and smiles back. Video is available from the adoption agency.

Trina

Girl, Age: 11
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.

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.

Brett #

Boy, Age: 6
Primary Diagnosis: Other Special Needs
Mental delays
Listed: Jul 2020
*** 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 ***
Brett lived with a foster family from birth to age 4. He did not attend preschool or receive any interventions during that time. The family was not experienced in how to work with him. He was placed in a small group home at 4 years old. He has thrived in this setting. He has learned many new skills and continues to make improvements in all aspects of his development. He communicates using words and simple sentences. He understands everything said to him and can answer basic questions. He takes care of all his personal hygiene independently (brushes his own teeth, hair, dresses/undresses himself, is toilet trained, etc). He can count to 10, recognize colors and shapes, work puzzles, say his name and age, and also say the names of the other children living in the home. The staff at the group home believe that his mental delays are mild and state that this is because he made such rapid progress once he was placed in the group home and began receiving instruction. The foster family had reported behavior issues, mainly an inability to concentrate. The staff reports no behavior problems and stated that he just needed attention and appropriate instruction. They describe him as very affectionate.

Jax #

Boy, Age: 10
Primary Diagnosis: Other Special Needs
hyperkinetic conduct disorder and a mild mental delay
Listed: May 2015
*** 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 ***
He has been living with a foster family since 2013.

He has a systolic murmur along the precordium; hyperkinetic conduct disorder and a mild mental delay. The child started walking on time, but his speech is underdeveloped. The child cannot stay focused for a long time while playing. He understands and follows simple instructions.

The agency has current medical reports available for serious inquiries.

UPDATE March 2017:   previous Diagnosis of Atypical autism that was changed to hyperkinetic disorder, very interested in motor activities. Responds to positive interactions and praise from familiar adults, but can become anxious in new situations or if a familiar caregiver is not around. He seeks comfort from familiar adults and can become sad if one leaves.

Andy #

Boy, Age: 8
He was diagnosed with spastic quadriparesis, Hypotrophy II degree, Epilepsy, Luxation of the left hip, and physical and cognitive developmental delays. He was born prematurely.
Listed: Jul 2017
*** 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 ***
Andy is very persistent! He tries to reach for a toy that interests him. He is receiving good care and is monitored by a neurologist. Andy really needs someone who can show him what unconditional love looks like and care for him. We hope you can be the one to give him a loving home he deserves!

Norton #

Boy, Age: 9
Primary Diagnosis: Other Special Needs
hyperactive disorder, mild mental disability and a speech delay
Listed: Nov 2017
Norton is a boy who lives with a foster family in Eastern Europe. He loves to play with other children and particularly likes to play with musical toys and cars. He also likes to paint using watercolor paints. He manages to play games for a long time, and he likes to help around the household.

Norton is in good health and is stronger than typical of his age. He can independently move larger items, including furniture. He loves to run and jump, and he knows how to roll over forward and squeeze in narrower spaces. Like many little boys, Norton brushes his teeth twice a day. He can tell others when he needs to go to the restroom, and he eats with great appetite. He naps for two hours in the afternoon and sleeps peacefully at night.

His short-term and long-term memories function at a good level, and Noah can easily remember things related to the lifestyle, as well as past events related to pleasant or unpleasant memories.

Although he has been diagnosed with hyperactive disorder, mild mental disability and a speech delay, Norton has shown progress in his development. He understands everything that is required of him, executing commands correctly. He is persistent in his demands, but he understands when he has violated rules, and he does not oppose correction.

Norton chatters a lot, but he is incomprehensible. He repeats syllables he hears, and he uses gestures to help him communicate with others and make them clearly understand what he wants or wants to do. Norton is working with therapists to improve his speech abilities.

Clifton #

Boy, Age: 9
Born with positive Wassermann test result; he underwent treatment with Penicillin; ectopic left kidney; convergent concomitant strabismus; hypermetropia (long-sightedness); dolichocephaly; Arnold-Chiari syndrome, type I; irritable bowel syndrome without diarrhea; secondary lactase deficiency; food allergy – slight intolerance to foods containing gluten, dairy products and eggs;delayed physical development; generalized developmental disorder; moderate mental delay

specific disorders of motor function development, Moderate mental delay, ectopic left kidney, strabismus

Listed: Mar 2017
*** 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 ***
Clifton lives with a foster family.  He loves to listen to music and dance and is always looking for a dancing partner! His foster family is working on him walking longer distances independently.  He is learning how to play with toys and interact appropriately with other children.  He has few words and does not follow verbal directions.  Clifton is receiving therapy multiple times a week.

Clifton’s gross motor skills are well-developed – he moves around independently, even at long distances, and he has no difficulties walking on different surfaces. He can now run (since the beginning of January 2017). The deficits noted previously in Clifton’s fine motor skills have been compensated to a great extent. He can transfer small elements with a spoon from one bowl into another with an adult’s assistance, he plays with certain materials and toys, he clips and unclips clothes pegs, he looks for an object hidden in the sand and he takes it out with great interest. He holds a pencil and leaves pale traces with it on a sheet of paper. He does great eating with a spoon. Clifton accepts the toothbrush and allows for his teeth to be brushed.

It happens more and more rarely for Clifton to demonstrate anxiety in response to being introduced to unfamiliar places and people. The stereotypic movements he demonstrates when someone initiates interactions with him have decreased significantly. He imitates actions he has observed more often and more successfully than before. Clifton becomes lively and starts dancing whenever someone is singing or plays music.

Clifton is  calm in his new foster family, he often smiles and he laughs aloud while playing with an adult (or with the girls in the foster family). He is especially attached to the foster father and the younger daughter in the family. Clifton has become a lot more sociable in the last 6 months: he seeks children’s attention, initiates interactions, accepts unfamiliar people a lot easier, maintains a smaller distance between himself and others and makes eye contact.

Although Clifton has poor passive vocabulary, he follows simple instructions provided that those are accompanied by nonverbal means of communication. His speech development is at the level of producing chains of syllables. He uses “No” appropriately so as to express his disagreement, he sometimes uses “Yes” and “Give me”. Clifton initiates physical and emotional contact with his foster parents and their children as well as with the specialists working with him. He is especially attached to the foster father and the youngest daughter in the foster family. His interactions with other children have changed significantly – he plays with them for a long time and he is making attempts to cooperate with them.

More photos/file are available from his agency

Jonas #

Boy, Age: 10
2nd-degree prematurity; epilepsy; convergent strabismus; esotropia of the left eye; hypermetropia (long-sightedness); mild mental delay; delayed speech development; other pervasive developmental disorders;
Listed: May 2017
*** 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 ***
Jonas is on several medications.  Jonas’s motor activity completely corresponds to the expected developmental level for his calendar age.  Although his fine motor skills need to improve further, Jonas is able to hold a pencil properly. He can inlay elements with some guidance. He puts cubes one on top of the other. He threads colored rings on a fixed stand, but not yet in accordance with their size.

There are some difficulties in attracting and keeping his attention focused. Jonas plays for a longer period of time whenever he is interested in the respective activity. Jonas orientates well in a familiar environment. He distinguishes between day and night based on his everyday routines – sleeping, meal times, rest. He recognizes the neighborhood around the foster family’s home.

Jonas is reported to have achieved noticeable progress in terms of expressing his emotions and feelings, which are becoming more diverse. He reacts appropriately to smiles and angry faces and also to the tone of voice one talks to him with. He demonstrates his love, attachment and attention for others. He greatly enjoys it when others play with him. Jonas has attached to all members of the foster family.

Rocky #

Boy, Age: 10
Primary Diagnosis: Other Special Needs
Listed: Nov 2017
*** 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 ***
Rocky is a calm, pleasant  boy who lives in a group home in Eastern Europe. He is attached to his caregivers and responds well to them.

Although Rocky was born premature and with low birth weight; cerebral palsy; and speech, motor and cognitive delays, he is making good progress in his physical therapy and other supports. He can walk with minimal support, and his fine motor skills are also improving.

Gemma

Girl, Age: 6
Country Code: EE-1
Primary Diagnosis: Deaf / HoH, Other Special Needs
Other specified congenital malformations of brain; Paraplegia; Pervasive developmental disorder, unspecified; Exotropia; Congenital malformation of optic disc; Ptosis of eyelid; Subclinical iodine-deficiency hypothyroidism; Hypopituitarism; Sensorineural hearing loss, bilateral
Listed: Sep 2020
$617.28
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!
From a family who met her in March 2021:  Gemma is an adorable little girl. She has a bright and spunky personality and is full of laughter and smiles. She loves to be held and embraced and ran to us with hugs. She played ring around the rosy with us, danced in our arms, and loved to be twirled. When given a kiss, she instinctively gives one back. She is so sweet. She loves to play outside, ride a scooter, play in the sand. She says “yes” (in Russian) for most things but she can say other words. She understands everything said to her. She listens extremely well to the nannies and they speak to her as they would a typical 5 year old. She can do the physical tasks a pre-K age child can do (get dressed and undressed, ride a scooter, play with toys, etc). She is toilet trained, though the nannies had her in a pull up while with us. Her vision is impaired and though she can see well enough to get around just fine, she holds things very closely to her face to see them. She has a hearing loss diagnosis but appears to be able to hear everything, though maybe she could still benefit from hearing aids. We were told that she is developmentally like a two year old. This was true in many of her behaviors but we found that she understands much more than a two year old. She has autistic behaviors without an autism diagnosis. She is definitely a sensory seeker; she has a lot of energy and needs to be given tasks and activities to keep her focused. When she is engaged in something she likes, she is completely absorbed in it. She could play the piano for a very long time oblivious to everything going on around her. Though she appears to be in her own world, we were often able to “intrude” into her world and to play with her, to get her to smile and to mimic us and were seeing gains so quickly. Her smile and laughter bring so much joy! Gemma is smart. She can learn. We taught her some basic sign language (“more”) and she began to use it right away without any coaching. She immediately caught on. She will flourish so much in a family who gives her the tools to communicate. She is truly an amazing child, adorable and full of life.

Catriona

Girl, Age: 5
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Hemangioma; Other non-diabetic proliferative retinopathy; Bronchopulmonary dysplasia originating in the perinatal period; Other disorders of nervous system not elsewhere classified
Listed: Sep 2020
$108.00
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!

Nicolette and Oksana

Sibling Group
Ages: 15, 18
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Nicolette – impaired visual acuity; deviated nasal septum; disorders of psychological development – she does not demonstrate any issues
Oksana – thyroid disorders, perhaps; oncology disease; post-op asthenia
Listed: May 2019
$1,516.50
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!
These two sisters must be adopted together! Both girls are very good and friendly.

Santiago

Boy, Age: 2
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!

Wilson

Boy, Age: 12
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Muscular Dystrophy
Listed: Mar 2019
**** 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 ***
Updated pic 2019; Wilson has lost the ability to stand and walk.

Wilson is a sweet, happy, playful boy. He is great with little kids and bigger kids. He loves to play legos, color, watch tv, go to the beach and just be with those who care for him. He spent one summer and winter break with a host family, he bonded well with them. He is affectionate and makes good eye contact.

He has a progressive form of Muscular Dystrophy. He can no longer stand, walk or crawl. He can still sit upright by himself. He does require help dressing, bathing and some help with eating. He is toilet trained but needs help to get to the toilet. He longs to belong and be given love and attention. He adapts well to new adventures, people and places. He will be a blessing to any family.

Wolf

Boy, Age: 7
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Traumatic Brain Injury
Listed: Nov 2020
$2,706.60
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
His special needs are related to the after affects of a head injury by his birth mother; he was severely beaten at early childhood. He requires permanent physical medicine and rehabilitation. He pulls his leg and doesn’t have full use of one of his hands.

He has a pretty good memory and good eyesight.

Vincent, Wade & Siblings

Sibling Group
Ages: 5, 7, 17, 15, 13, 11
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Vincent: Youngest Boy, born 2014: Disorder of brain, unspecified; malnutrition

Wade: born 2016: Disorder of brain, unspecified

Listed: Dec 2018
$1,788.00
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!
Total of 6 siblings: the other 4 siblings are 14 (a boy), 12 (a girl), 10 (a girl) and 8 (a boy). The older 4 have been to the US for hosting.

Vera

Girl, Age: 14
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Birth anomaly brain development, microcephaly with tetraparesis, convulsive syndrome. Mental delays. Convergent squint. Partial optic atrophy. Umbilical hernia.
Listed: Oct 2012
**** 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 ***
Oh sweet Vera! She spends much of her day in the crib and she needs stimulation!! She is living on borrowed time. She has tremendous potential for improvement if only she is given the chance. She will require medical attention and families should expect at the very least physical therapy.

Update June 2013: Vera is doing well! She looks good — but she still spends too much time in her crib. Vera needs a family!

Trudie and Violette

Sibling Group
Ages: 4, 5
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
$1,000.00
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.

Travis

Boy, Age: 14
Country Code: EE-1
Primary Diagnosis: Other Special Needs
congenital defects of the Central Nervous System (CNS)
Listed: May 2011
**** 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 ***
From a family who met him in 2012: When I saw Travis my heart completely broke. I remembered his picture where he was sitting up, and it was obvious that in the time since that picture was taken his health and any ability he once had had deteriorated. He laid nearly lifeless, covered with blankets (mind you it is very hot in the room). I only have the one picture of him because his position never changed. He rarely moved and seemed to be asleep all the time. The only time I ever saw him move he just rocking his head from side to side very slowly as he grinded his teeth…and grinded…and grinded. My instant feeling was that Travis had given up on life, and it breaks my heart.

Every time I saw him there was vomit on the blanket next to his mouth. I suspect it is due to improper feeding. Like Janna, Travis is living at the orphanage on borrowed time.

Please friends, let’s not let Travis give up on life. I don’t know what his future ability would be in a family but even if it never changed isn’t he deserving of the love of a family? Please…someone…rescue Travis.

Update March 2014: He is not doing well. He appeared very drugged. He just rocked his head back and forth and ground his teeth. He occasionally would moan and he was salivating a lot and drooling on himself. He did not respond to me when I approached at all, he just kept rocking his head back and forth…which is why the picture is a little blurry…he never stopped.

Stephen

Boy, Age: 15
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Minimal brain dysfunction, pyramid insufficiency, secondary cardiomyopathy, anomalous chord of the left heart ventricle, hypermobility of hip joints, concomitant alternating convergent squint.
Listed: Mar 2014
**** 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 ***
From a family who met him in late 2013:
Stephen was in Riley’s groupa. We saw him a lot during our 7 weeks of visits. He stood out because he’s 7 yo and taller than the other kids in his groupa of mostly 4-5 yo’s. He is a SWEET, sweet boy. He has a great smile with dimples. He’s not overly active (not hyper). Very obedient/cooperative and follows instructions and the flow of the groupa well. An easy going kiddo. He doesn’t seem to have very significant needs. He functions very “typically”, maybe just mild delays. One thing I’ll never forget about Stephen… one time when we were invited to watch a performance the kids were putting on, we were one of the only people in the audience. He stood there, singing and doing the body motions to the production just as well as could be. He kept looking right at my husband and I like he was performing just for us. He just seemed to love having someone be there for him and encourage him, and nod and smile and let him know he was doing a good job. He was working so hard to do his best and he did so well! It was sweet and sad all at the same time….knowing we weren’t his mama and papa and he didn’t have anyone there to give him that recognition forever, that he so appreciated. He would make such a delightful son! We would have brought him home too but were only homestudy approved for one boy. He’s in a good orphanage that provides good care and services. But who knows where he’ll be transferred to when they no longer have space for him (he’s already over age.) I have pictures and video of him. Such a kind, happy little boy….he needs a family!!!

Stefan

Boy, Age: 12
Country Code: EE-1
Primary Diagnosis: Other Special Needs
parasomnia, severe mental delays, Other atopic dermatitis, Astigmatism
Listed: May 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 ***
He needs a family asap! He requires much time and energy from the adopting family. He is a kind of enervative, cranky and rickety, he likes to be held in arms, he often cries.

This child shows significant facial features of FAS (fetal alcohol syndrome). Please research and prepare yourself for the challenges of children with this condition.

Stanley

Boy, Age: 12
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Spastic tetraplegia; Severe intellectual disabilities; Undescended testicle, unspecified, bilateral; Scoliosis; Astigmatism; Optic atrophy
Listed: Nov 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 ***
Sweet boy needs out of his crib!

Stacie

Girl, Age: 10
Country Code: EE-1
Primary Diagnosis: Other Special Needs
other disorders of the nervous system; atypical autism; Melanocytic naevi of lower limb, including hip; myopia; Abnormal results of cardiovascular function studies
Listed: Aug 2016
**** 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 ***
So sweet!!

Shepard

Boy, Age: 5
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Congenital debility NOS
Unilateral small kidneys
Unilateral inguinal hernia
Atrial septal defect
Listed: Aug 2017
$1,033.50
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!
Sweet baby boy!!

Shawn

Boy, Age: 10
Country Code: EE-1
Primary Diagnosis: Other Special Needs
disorder of the brain; unstable hip; atrial septal defect; Abnormal results of cardiovascular function studies; d50 anemia
Listed: Aug 2016
**** 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 ***

Sandy

Girl, Age: 15
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Mild to moderate delays, FAS
Listed: Oct 2012
**** 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 ***
This child shows significant facial features of FAS (fetal alcohol syndrome). Please research this condition so you are best prepared to help her thrive at home! Won’t she be beautiful with long hair?

New pic January 2017!

Samantha and Kristina

Sibling Group
Ages: 15, 16
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Samantha (the oldest), on the right: Microcephaly, mental delays, crossed eyes, physically capable, friendly and affectionate girl, will do well in family environment. High likelihood of fetal alcohol syndrome.

Kristina, on the left: Microcephaly, Moderate intellectual disabilities, ADHD (hyperactive), Esotropia, Hypermetropia, Cardiomyopathy (unspecified), Scoliosis

Listed: Aug 2010
**** 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 ***
These girls will age out soon!  An I600a MUST be filed by 11/27/2021!

Samantha (the oldest), on the right:     Microcephaly, mental delays, crossed eyes, physically capable, friendly and affectionate girl, will do well in family environment.  High likelihood of fetal alcohol syndrome.

Kristina, on the left:  Microcephaly, Moderate intellectual disabilities, ADHD (hyperactive), Esotropia, Hypermetropia, Cardiomyopathy (unspecified), Scoliosis

Kristina is cognitively delayed, physically capable, helpful, friendly, likes to play, good girl.

The girls are NOT in the same orphanage, but are in the same region and need to be adopted together.

Russ and Ward

Sibling Group
Ages: 3, 3
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Twin Boys

Boy 1: disorder of the brain, hypermetropia, astigmatism, atrial septal defect, patent ductus arteriosus, exposure to hiv, malnutrition

Boy 2: disorder of the brain, astigmatism, exposure to hiv, lack of development

Listed: Jan 2020
$1,135.20
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!
This will be a two part adoption: Family must be prepared to adopt boy 1, then have to go back to adopt boy 2. this is because only boy 1 qualifies for expedited availability as both have not yet been listed on the registry for one year. Once adoption 1 is done, the family can file for adoption of the second child immediately as a bio sibling of their child.

Ryker

Boy, Age: 12
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Childhood autism, Drug-induced tics, Mixed specific developmental disorders, respiratory issues, Other alopecia areata, Umbilical hernia, enuresis
Listed: May 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 ***
Not communicative with children, better with adults, but very “selective” communication – he choses whom he likes and then he may talk to this person and he may absolutely ignore people whom he dislike.

Not much smiling. He speaks.

He is visited by his grandmother but she does not take him home.

Russ

Boy, Age: 15
Country Code: EE-1
Primary Diagnosis: Other Special Needs
goloproentsephaliy
Listed: May 2011
**** 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 ***
Russ’s profile says “goloproentsephaliy” which is unclear, other than there’s some condition with his brain. It’s unclear if it’s a physical or mental condition.  It has been suggested that his ‘goloproentsephaliy’ may actually be holoprosencephaly.

An adoption would have to begin before August 2021!

Rohan

Boy, Age: 10
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!

Roger

Boy, Age: 15
Country Code: EE-1
Primary Diagnosis: Other Special Needs
many facial features of FAS (fetal alcohol syndrome); “childhood autism”; encephalopathy (unspecified disease of the brain); moderate mental delays; Convergent concomitant strabismus (crossing eyes) and hypermetropia (far-sighted); and is said to be anemic.
Listed: Oct 2011
**** 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 ***
Roger is a handsome young man; he has many facial features of FAS (fetal alcohol syndrome). This dear boy is listed as having “childhood autism” — if it is truly autism or autistic behaviors due to orphanage life and his other special needs, we really don’t know.

He is said to have encephalopathy (unspecified disease of the brain), Childhood autism, and moderate mental delays.

He also has vision problems: Convergent concomitant strabismus (crossing eyes) and hypermetropia (far-sighted); and is said to be anemic.

Robyn

Girl, Age: 11
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Congenital malformations of corpus callosum, Quadriplegia, Unspecified intellectual disabilities, Congenital deformity of feet, unspecified Myopia; Alternating esotropia
Listed: Oct 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 ***
Robyn has a brother who has already been adopted.

Rhonda

Girl, Age: 10
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Kidneys dysplasia, chronic pyelonephritis, partial atrophy of optic nerves, secondary cardiomyopathy, crossed eyes, after-effects of brain injury.
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 ***
You can see a marked difference in Rhonda from her time at the baby house, and now at the institution. It is heart-wrenching for us here at Reece’s Rainbow to witness this neglect. Please share Rhonda so we can find a family for her quickly.

Ray

Boy, Age: 9
Country Code: EE-1
Primary Diagnosis: Other Special Needs
FAS, Renal agenesis and other reduction defects of kidney
Listed: Apr 2015
$1,762.50
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!
Ray is facing transfer to the institution.  Please share him so he can find his forever family!

Ravi

Boy, Age: 12
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Congenital chromosomal condition; Severe mental delays; Congenital malformations of palate; Other disorders of optic disc; Chronic inflammation of lacrimal passages
Listed: Jun 2019
$1,003.50
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!
From a family who knows him: Even though Ravi spends most of his days in the same bed, staring at the same ceiling, he’s fascinated by everything that goes on around him. He loves the rare walks he gets outside in the summertime and being held up in the window to watch snow falling in winter. He obviously recognizes his favorite people and cries when they leave. He cannot sit up on his own, and seems to get tired even when held sitting for long. But he scoots all around in his bed, very actively turning his head to where his feet should be, or the other way around to see and hear everything. He is completely non-verbal. Ravi really needs a family and a chance to get out into the world that fascinates him so much!

Rafi

Boy, Age: 3
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Paraplegia; Nonobstructive reflux-associated chronic pyelonephritis; Congenital dislocation of hip, bilateral; Other congenital deformities of feet; Other congenital malformations of spine, not associated with scoliosis; anemia; Other ill-defined heart diseases; Hypermetropia; Renal hypoplasia, unspecified
Listed: Feb 2020
$1,500.65
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!

Quincey

Boy, Age: 10
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Sequelae of inflammatory diseases of central nervous system; severe motor impairment; spastic tetraparesis
Listed: Jan 2019
$1,636.72
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!
From a family who met him Nov 2018: Quincey is one of the most darling, endearing boys we have ever met. He is pure joy and just exudes love and affection. His little giggle is contagious. He begged us to take him home to America- he so desperately wants a family. He loves to show off how he can get into his wheelchair (which he calls his car!) himself and beams with pride. He speaks well, is very bright, and will flourish in a family.

He is so sweet, always look happy and friendly.

Presley

Boy, Age: 13
Country Code: EE-1
Primary Diagnosis: Other Special Needs
Past leukemia, delay of psychological and motor development, skull deformation (almost flat on the back), congenital isotropy of both eyes (crossed eyes)
Listed: Feb 2011
**** 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 ***
What a CUTIE! Presley is a sweet boy with blonde hair and bright blue eyes. He is a very happy and affectionate child. Presley will benefit so greatly from having a loving family! More photos available.

Updated Nov 2013: He is a very sweet child. Seemed to listen to instructions well. Participated in group activities (like dance and singing). Longing for attention, affection, and stimulation. He does not currently have leukemia; but he has mental delays, and his head is very flat.