Girl, born 2017

Spastic quadriplegic Cerebral palsy
epileptic syndromes
severe mental retardation

Listed: Sept 2019

 

$1,922.80 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!

“ihaveawarrior”Boy, born 2005

Kidney Nephrosis

Listed: Sept 2019

White blood cell count is raised. Both kidneys are functioning. He takes medication (hormone therapy) He tires quickly. His face is swollen because of medication. He cannot eat a lot of fried food and cannot play sports. He is sweet and kind and really wants a family.

He has a beautiful singing voice, dreams of being interior designer, and is a huge helper to the orphanage director. Callum loves animals and painting and music. Favorite colors black and grey and white.

He asks the facilitator every time they come if they have a family for him yet.

$2,344.40 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!

Girl, born 2013

Other congenital malformations of brain
Cleft hard palate with cleft soft palate
Polysyndactyly
Other strabismus
Short stature, not elsewhere classified
Profound mental retardation
(Probably has Aperts, though not on her file)

Listed: Sept 2019

$5,141.40 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!

Sibling set!
boy, born 2006
other disorder of psychological development

boy, born 2007
other mixed disorder of conduct and emotions

girl, born 2010
disorder of speech, disturbance of activity

Listed: Sept 2019

These 3 MUST be adopted together!

$121.50 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!

Boy, born 2013

Other congenital malformations of limb(s)

Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures

 

Listed: Sep 2018

$2,057.70 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!

Boy, born 2011

Down Syndrome
Other specified congenital malformations of heart
Moderate Mental Retardation
Enuresis
Deformity of the chest and rib
Deformities of musculoskeletal system
Flat Foot
Esotropia

Listed: August 2019

He is NOT in a “good” place at all and needs to be pulled out asap!

*** I am eligible for an additional $5,000 Grant!  Through 2020, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$2,467.94 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!

Girl: 2009

Diagnosis: Atypical Autism

Listed: Aug 2019

Cora currently lives with a foster family. She has mental delays, some stereotypical movements, and difficulty with eye contact and social interactions. She was diagnosis with Atypical Autism in 2017. She is physically healthy. She is toilet trained and feeds herself. She is described as a happy child who has a contagious smile and laughter. Her caregivers attribute her learning delays to early neglect.

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy: 2014

Special needs: Seizures

Listed: Aug 2019

Anders is a 4-year-old boy and currently lives in a small Eastern European country. He is happiest listening to soft music or playing with toys that make sound! Anders is described as a happy, calm child. Tests show that Anders has learning and motor delays, as well as occasional seizures.

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy: 2017

Listed: August 2019

Diagnosis: Cerebral leukomalacia, feed via NG tubeJasper is a bright little boy, smiling all the time. He holds toys and tries to play with them. He is currently fed with a NG tube. He does have a sucking reflex, but has difficulty with swallowing.

 He can turn without help from his stomach to his back and backwards again. He can hold his head up and control it. He has a weak leg support and cannot stay upright, yet, but can kick with his legs and if put into a walker, can even move to a short distance. He plays with hanging toys when he’s laying on his back. He babbles and makes sounds. He cries at appropriate times, like when he rolls over into the side of the crib and needs help to be moved.

*** 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 on this child, email childinquiry@reecesrainbow.org

Girl: 2017
Diagnosis: cleft lip & palate, facial and skull dysmorphia, seizures, quadriparesis-weakness in all 4 extremities

*** 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 on this child, email childinquiry@reecesrainbow.org

“ihaveawarrior”

Boy: 2015
Diagnosis: DiGeorge Syndrome; heart condition- pulmonary atresia

Listed: Aug 2019

Silas can walk, run, feed himself and is toilet trained. He plays with toys, says simple words and is beginning to use phrases. He’s working with a speech therapist to improve his speech. He can identify part of his body.  He understands simple directions and follows them. He enjoys playing with toys and interacts well with other children. He loves music.

Silas needs to be adopted in order to receive medical care in the US for his heart.

*** 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.

$3,376.80 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, born in  2006, 2008

Mason has a peanut allergy. Both children have delays

Listed: August 2019

Mason & Molly lived with their birth family until 2017, when their father died. Their mother placed them in a group home and stated that she had no desire to continue caring for them. The children are very bonded to each other and live together in a small family style group home. Before entering the group home, the children had rarely attended school and did not have any type of academic foundation. Since being placed in the group home, they have attended school regularly and have worked with specialized teachers to obtain the academic skills that they had previously missed. After a year of intense work, Mason is now only requiring additional support in math and Molly is only requiring additional support in language classes (both her native language and English classes). Both children have their special needs classified as “disorder in school delays”. Both children enjoy playing outside and drawing. They both get along well with the staff and other children. Mason does have a known peanut allergy and also a dust allergy. He takes allergy medication daily.

Photos and videos are available through the agency

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy: 2015

Listed: July 2019

Special Need:congenital heart malformation: ASD, VSD; infantile cerebral palsy – ataxic form; moderate mental delay; autistic manifestations in behavior

Despite his diagnosis of infantile cerebral palsy Teddy walks independently. He climbs on and gets off the bed independently. Teddy examines objects with hands, eyes and mouth. He is able to transfer objects from one hand to another. He is able to hold two toys in his hands and knock them in one another.

When the foster mother leaves the room Teddy would start crying and looking for her.

He likes playing with musical toys and shows excitement when they make sounds. He also looks at and likes some of the TV commercials.

The foster mother feeds Teddy with a spoon and some improvement has been reported, as he is now eating solid food. Teddy loves bananas, biscuits with milk, homemade soups and sops.

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy, born 2013
Other specified disorders of central nervous system
Mixed specific developmental disorders
Unspecified mental disorder due to known physiological condition
Expressive language disorder
Pectus excavatum
Other congenital valgus deformities of feet
Congenital malformation of optic disc

Listed: July 2019

 

$1,421.73 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!

Girl: 2010

Special needs: moderate mental delay- significant impairment of behavior requiring attention or treatment; microcephaly; hyperactive behavior

Listed: 7/2019

 

Gabi is physically healthy with normal physical development. She is radiant and very active.

Gabi responds adequately to praise and punishment. Gabi establishes and maintains eye contact.  She seeks the attention of the people around and she seeks familiar people and their closeness purposefully.

Gabi understands the meaning of words that are often used in her surroundings. She expresses her needs and wishes through vocalization.

In her spare time Gabi likes watching TV, playing on a phone, listening to music and going out for walks.

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy, born 2009

Listed: June 2019

Updated pic January 2020

Congenital chromosomal condition

Severe mental retardation
Congenital malformations of palate
Other disorders of optic disc
Chronic inflammation of lacrimal passages

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!

 

$180.00 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!

Boy: 2017
Diagnosis: Spina Bifida

Yager loves the company of the adults. He likes to be engaged in play and laughs when interacted with. He has a special relationship with one of the staff members, who always accompanies him for operations and for check-ups. While lying on his back, he can turn on his abdomen, he pulls himself up with his arms. The muscles above the waist are very well-developed. He will reach for an adult and when you extend your hands, he immediately pulls himself to the sitting position. He eats from a bottle while holding it himself. When he sees toys, he reaches for them and tries to get them.  If he gets upset he easily calms down if cudded.

He repeats syllables and pronounces sounds. He holds toys in his hands and knocks them together. He can follow simple directions.

Photos and videos are available through the agency.

Boy, born 2014
PRC
Down syndrome, Congenital Heart Disease- mild tricuspid regurgitation, mild pulmonary arterial hypertension, and pericardial effusion(less)

Listed: May 2019

Benson is a beautiful little boy! Benson was said to be a timid little guy who was a little scared of the dark. A nightlight of some sort is helpful for him when it comes to sleeping.

Update June 2019:  Benson is a smiley guy; blessed with a happy, enthusiastic nature and responds with effervescence to interactions with adults and children.  Benson loves social situations and is enjoying some pre-kindy group playtime, several afternoons a week, which involve free playing, manipulative skills, singing, rhythm and socialization.  He is very settled within his family home, and is self-motivated to play, whether with his playmates or alone. Benson perceives happy situations and will often raise his hands in the air and exclaim, “Hooray!” , such as when he attends birthday parties or sees people applauding. He is delightful.

Benson understands his caregivers’ interactions with him, but has a very limited vocabulary.  Benson is very tender-hearted. Benson loves to watch and imitate , slowly improving his cognition with sorting , counting and self-care skills. He has developed lots of physical skills in the last year. He can sit independently, pull himself to stand without help, cruises holding on to furniture/ caregivers’ hands, and can take a few steps without holding on! Benson loves balls and enjoys sitting opposite a caregiver doing rolling, throwing and catching across a short distance.

Update from June 2019:  Video 1, Video 2, Video 3
Benson’s current agency has a $1500 grant available.

*** I am eligible for an additional $5,000 Grant!  Through 2020, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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!

“ihaveawarrior”Boy, born 2016

Other congenital hydrocephalus
other disorders of nervous system
optic atrophy
iron deficiency anaemia

Listed: May 2019

$1,484.75 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!

“ihaveawarrior” Boy, born 2016

Spastic quadriplegic cerebral palsy
Other specified congenital malformationsOther specified congenital malformations of brain
Optic atrophy in diseases classified elsewhere
Chronic viral hepatitis B without delta-agent
Other interstitial pulmonary diseases with fibrosis

Listed: May 2019

 

$1,160.80 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!

girl, born 2006
impaired visual acuity
deviated nasal septum
disorders of psychological development – In real life she does not demonstrate any issues

girl, born 2003
thyroid disorders, perhaps, oncology disease, post-op
asthenia

These two sisters must be adopted together!
Both girls are very good and friendly

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!

paige-2017-cropped

Girl, born 2004
Mental delays. Down syndrome, cardiopathia. Umbilical hernia. Convergent squint.

Listed:  October 4, 2012

New pic May 2019!

Paige had previously been living with her mother until she lost her rights.

She can sit independently and can crawl! Her speech is not well developed but she can partially understand what you are saying.  She has a very short attention span.

Update June 2013:
Lovely Paige has hair now!  She broke my heart.  She was just sitting on the couch rocking back and forth and didn’t respond at all when I came over to her. Poor, sweet thing!! The nannys love her, but she needs more than they can give. I am not sure if the move was hard on her or what but she just rocked and rocked.

*** I am eligible for a $15,000 Older Child Grant! For more information, email childinquiry@reecesrainbow.org ***

Girl, born 2011

Listed September 11, 2015

Phenylketonuria, also known as PKU

New pic May 2019! 

From a volunteer in August 2016:   “I was happy to see that Leena is still the same strong willed young girl as last year. She is available for adoption now! She was a little calmer than last year, but she would still take every chance she got to run around. Just like last year it was obvious that some nurses have a very hard time with her and others love her. She’s much calmer when the nurses like her and she’s easier to handle. It was unclear if she was totally potty trained this year or that she’s still working on it. It was also unclear if she got the diet she needed, but her delays didn’t look worse. Leena is such a wonderful girl! She should be in a family where she has the chance to be who she is, all days of the year.

From a missionary who met her in 2015: “Leena is a strong-willed young girl.  She is stubborn and funny. She loves to explore the world (within the concrete walls she lives between). She has been transferred to this facility in May and she is obviously still getting used to the circumstances of living. She had a lot more freedom in the baby orphanage she came from. Leena can walk (so don’t be fooled by the picture), she can run, she is very energetic. She can drink from a cup. This summer (2015) she was being potty trained. She doesn’t talk. She squeals when she is very excited. She is probably the size of a 3 year old at the moment (summer 2015). She probably understands what is being said to her, but she has a hard time following orders. Due to her PKU she needs a special diet and medicine. The baby orphanage she grew up in, didn’t provide the proper care. So (part of) het mental delays may be caused because of that. The facility she lived in right now, tries to provide the proper care. They do not receive funds for it, so they raise it themselves with a charity fund. They really try to take good care of her. Some nurses really like her. Other nurses have a hard time dealing with her, because of her energetic ways. She likes to move and run around all the time. As soon as you let go of her hand or take her out of her wheelchair, you have to chase her. As soon as you give her an opportunity she’ll take it. Some days she was tied up in a wheelchair and we thought she might have been drugged. She didn’t react, she didn’t smile, she didn’t interact. Until the moment my fiancé pulled her from the wheelchair and it was as if she came alive again. I have not seen any selfharming behaviours and I haven’t seen her hurt other children. I have also not seen her interact with other children at all. The nurses don’t like it when she gets all excited, but for me it was a sign that she was not so institutionalized yet. There was so much fight in her. I hope she finds a family before she loses the strength to fight and before her delays will get worse, due to a lack of a proper diet and medical care.”

$2,014.45 has been donated towards the cost of my adoption!

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

Molly May

Birthday: 2015

Listed: 2019
Diagnosis: Trisomy 7; cleft lip & palate; Cerebral Palsy

Listed: May 2019

Molly May has made progress in her development during recent months. She is able to sit unassisted, get up on her knees and has begun to start trying to move around in a walker. She is becoming more physically active. She makes eye contact, looks around for families adults and smiles when someone looks at her. She will laugh out loud when an adult plays with her. She watches children’s cartoons and movies on the TV and will get excited and point to the screen when the TV is turned on. She picks up toys and attempts to play with them. She still needs instructions in how to appropriately play with toys. She makes vocalizations in an effort to communicate. She eats soft foods from a spoon.
Molly May has undergone multiple surgeries to repair her cleft lip & palate. She is under the continued care of the doctor who is performing these procedures. She is also under the regular care of a neurologist, who diagnosed her with CP in 2018. She had suffered from “constant shaking” resulting in uncontrollable movements up until a few months ago. The social worker reports that this has greatly improved and that Molly May’s movement are now more calm and she also sleeps calmly too. Videos taken in April 2019 show her interacting with toys.

 

Photos and videos are available through the agency.

.

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy, born 2005

Duncan is at risk of aging out!  In order for him to be adopted, an I600a MUST be filed by January 21, 2021!

Malformations of aqueduct of Sylvius (hydrocephalus)
Other congenital malformations of posterior segment of eye
Profound intellectual disabilities

Listed: May 2019

Updated pic from Jan 2020:   He is SO sweet and loves attention!

 

$2,105.60 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!

Age 10; born 2010
Arthrogryposis with knee joint contractures, bilateral club foot, Hypotrophy

Sawyer is able to move around the room by scooting on his bottom. He can talk in sentences, but his articulation is not always clear. He plays with toys, responds when spoken to, follows simple directions, and assists with self-help tasks such as dressing/undressing.
Photo and videos from March 2016 are available through the agency.

Listed, April 2016; Update below, April 2019:

Sawyer has spent his entire life in a large orphanage, where his experiences and interactions have been limited. He’s been attending school and working with a speech therapist for the past 2 years and this has resulted in an increase in all skill areas. Sawyer can talk in simple sentences and answer questions. His articulation is poor, but he’s made improvements with the help of a speech therapist. He can count to 10, identify his body parts, and answer basic questions such as his name and age. He demonstrates imaginative play with toys. His motor skills are delayed due to his diagnosis. He uses a wheelchair for mobility and will also scoot around the room on his bottom. He can feed himself. He can take his shoes and socks off independently. He is described as very social. He works hard during academic instruction. He enjoys interacting with both peers and adults. It is believed that his cognitive delays are due to the environment he has lived in and lack of exposure.

*** I am eligible for an Older Child Grant! Grant funding is dependent on a completed application and available funds. For more information, visit: Other Angels Older Child Grant ***

Boy, age 10
cognitive delays; hypothyroidism

Listed: April 2019

Stan takes medication to manage his thyroid. He’s also on medication for behaviors, and his foster family reports that the medication helps him to sleep better at night, which has improved his overall behavior. He can memorize, retain, and reproduces information. Motor skills are well developed. Self-help skills are well developed. He follows the rules and behaves well in public. The medication he is taking has decreased his mood swings. He talks in complete sentences and is able to ask/answer questions, tell a story, etc. He occasionally mixes up verb tenses and other grammatical errors, but is able to be understood. He is working with a speech therapist at school. He responds well to verbal praise and verbal prompts when he needs correction. He enjoys music and loves animals. He eagerly engages in activities with other children. He likes to put puzzles together, watch TV and play on the computer. He is behind academically at school due to difficulty with attention span.

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy, age 4
Cognitive delays; repaired cleft lip & palate with additional surgeries needed

Listed: April 2019

Drako has undergone surgeries to repair a cleft lip and palate. He is under continues care by medical professionals and will need future orthodontic surgery and other possible surgeries as well related to his cleft issues. Developmentally, his speech, motor skills, and cognitive processing are all delayed. He can crawl, pull to a stand, cruise around furniture/objects, and walk while holding an adult’s hand. He will interact with toys that play music or light up. He babbles, but is not yet saying any words.

Photos and videos are available.

*** 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 on this child, email childinquiry@reecesrainbow.org

Girl, born 2013

Congenital malformation of the central nervous system
symptomatic epilepsy
atactic syndrome
tetraparesis
porencephalia

Listed: Aug 2014

 

$9,565.68 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!

Boy, born 2013

Cerebral palsy

Listed: April 2019

 

 

$77.50 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!

Boy: 2015

Listed: April 2019

Diagnosis: Condition after extreme low weight at birth (prematurity IV degree). Cerebral palsy, spastic form – moderate degree. Bronchopulmonary dysplasia /BPD/. Delayed physical and psychomotor development. Bilateral neuro-sensory hearing loss.  

Aidan has delays in his psychomotor development. He has a potential and if he receives special cares, he will be able to achieve progress. His interactions with others are on an elementary level. The child feels calm in the presence of familiar adults. He is curious and walks around in his walker reaching for different items. The toys which stimulate his tactile sensors are more interesting for him than other toys and items, for example children’s books

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy, born 2009

HIV
Hepatitis C

Listed: March 2019

 

$23.20 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!

Boy, born 2016

Other disorders of psychological development
Disorder of brain, unspecified
Patent ductus arteriosus

Listed: March 2019

He has a brother in a different orphanage born in 2007.  They must be adopted together!

$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!

Boy, born 2009

Muscular Dystrophy

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.

*** I am eligible for an Older Child Grant! Grant funding is dependent on a completed application and available funds. For more information, visit: Other Angels Older Child Grant ***

Boy, born 2010

Nephritic agenesis, one sided
light degree mental delay

 

Listed: Feb 2019

$1,019.70 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!

Girl, born 2016

Holoprosencephaly,
Spina bifida at lumbar part with hydrocephaly.
Spastic tetraplegia
Cognitive thigh deformity
Cognitive hip subluxation one sided.
Cognitive pathology of development of disk of optic nerve
Сoncomitant strabismus

 

 

Listed: Feb 2019

Cassandra has two sisters, who have both been adopted.

$1,583.70 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!

Girl: 2013 – age 5

Listed: Jan 2019

Diagnosis: Seizure disorder-currently on seizure meds; delays in development; ataxic cerebral palsy; ADHD


Shay lives in a foster home. She was hospitalized to look for a cause for her seizures and was diagnosed with ataxic cerebral palsy. She is currently taking medication for seizures, but still has 1-2 seizures each month. She is able to walk and has good gross motor skills. Her fine motor skills are delayed. Her speech is delayed. She uses single words or short phrases to communicate. She has difficulty focusing, which makes it difficult for her to learn new skills. She is very active and needs constant supervision.

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy, born 2008

Cerebral palsy
Spastic lower Paraparesis

Listed: Jan 2018

From a family who met him Nov 2018:   Shaw is a very loving boy who desperately wants a family. He hugged us repeatedly asking, “Mama, America? Papa, America?”

He speaks well, enjoys painting, and can walk with some need for support. He sweetly pushes his friend’s wheelchair and it offers stability for him and assistance for his friend. He’s been raised amongst boys much older than him and has picked up swear words but truly is a beautiful soul. He became jealous of our attention when we were talking with his younger roommate and he bit him. The facilitator would like us to note that he has a family history of mental illness and that his family should consider this in their decision. We are head over heals for this boy and honestly would have brought him home without hesitation were we approved for another adoption. Every adoptive family would be wise to consider trauma-informed parenting and to anticipate both aggression and mental illness. Please, consider whether you could be Shaw’s mama and papa.

He is so sweet, but can be a kind of “difficult” – strong-willing and stubborn. He is a smart boy. He wants to be adopted and asks to find a family for him. At the same time he will choose if he likes a family. I would recommend him to a family with older children – older than him, to show a way to behave. He may be very helpful and careful. I often can see him helping other kids with worse disabilities as he has. But he can lose his temper fast. He has a kind of mental retardation/delay. His biological mother is qualified as mentally disabled due to her schizophrenia.

$19.80 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!

“ihaveawarrior” Boy, born 2011

Sequelae of inflammatory diseases of central nervous system
severe motor impairment
spastic tetraparesis

Listed: Jan 2019

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.

$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!

Girl: 2016; age 2

Listed: Jan 2019

Diagnosis: congenital anomaly of the central nervous system; dysmorphic stigmas(dysmorphic facies, four-finger groove of left hand, six fingers on right leg, longer right foot with a larger surface area); generalized hypotonia and forming hemiparesis on the left.

Sally had one seizure at age one. She’s been on seizure medication since that time and has not had any additional seizures. She touches and grabs with her right hand and moves her right foot. The left hand is almost clenched in a fist. Her muscles are very tight, but she can sit up when placed in that position. She will reach and grab toys with her right hand. She tracks objects that are moving in front of her face. She laughs when adults interact with her. She makes sounds and produces syllabes when imitating someone. She enjoys musical toys and will scoot to get to a toy that is near her when on the floor. She is fed by an adult and can eat from a spoon.

*** 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 on this child, email childinquiry@reecesrainbow.org

Girl: 2013

Special needs: Cerebral Palsy, Leukemia, strabismus

Listed: Jan 2019

Pippy is a precious little girl, born 2013.  Pippy is a twin and was born very premature and diagnosed as having cerebral palsy- spastic diplegia, umbilical hernia, and strabismus.  She now wears glasses to correct the strabismus and has received surgery to correct the hernia.  Pippy was later diagnosed as having acute lymphoblast leukemia.  She is currently in remission, but continues to take medication to prevent her cancer from coming back.  Pippy’s twin brother also has CP and is being cared for by his biological family. Pippy is very delayed in all areas of her development.  She can manipulate objects using her left hand.  Pippy is not speaking at this time.  We hope just the right family sees Pippy and knows that she is their daughter.

UPDATE NOV 2019:

Diagnosis: Acute lymphoblastic leukemia (actively receiving chemotherapy, which will be needed until 2021). Cerebral palsy – spastic diplegia; Gastroesophageal reflux disease, Convergent concomitant strabismus (wears corrective glasses); Delay in neuro-psychic development

 

Pippy is receiving chemotherapy for Leukemia. She was diagnosed in March 2017 and immediately began treatment. She lives in an isolation room at the orphanage to reduce her exposure to sickness. She is considered in remission, but is required to continue to take daily medication. She has a port, weekly blood draws (to adjust medications), and monthly appointments with an oncologist. Pippy also has CP that results in increased muscle tone in all 4 limbs, primarily impacting her legs. She can grab and hold a toy with her left hand. She can manipulate toys by picking up, dropping, pulling a string, picking up ring toys. She understands basic cause and effect, such as knowing to pull a string on a toy to activate the toy. She explores toys with interest. She pronounces several words and can follow basic commands. She enjoys the attention of caregivers.

 

A detailed medical report that outlines her Leukemia treatment, other medical history, and her development are available, along with photos and videos of Pippy. Due to her cancer diagnosis, any interested family would need to provide proof of medical insurance coverage that would adequately cover Pippy’s cancer treatment immediately upon taking custody of her. Her birth country will also require a detailed care plan showing the family has the appropriate resources and support to provide the required medical care for Pippy once home.

*** 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 on this child, email childinquiry@reecesrainbow.org

“ihaveawarrior” Boy, born 2014
Disorder of brain, unspecified
Protein-energy malnutrition of moderate degree

boy, born 2016
Disorder of brain, unspecified

 

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.

$1,180.00 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!

Girl, born 2016

Tuberous sclerosis
Generalized idiopathic epilepsy and epileptic syndromes

Updated pics and video available from Dec 2019

Listed: Dec 2018

She cannot talk yet and in general is pretty “weak”.

$1,747.50 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!

Julian
Age: 2014
Diagnosis: Spina bifida

Listed: Dec 2018

Julian enjoys playing with toys. He is well attached to his caregivers and responds to them when they talk to him. When he is happy, he responds by making noises and clapping his hands. His report indicates that when held by the hands, he will take steps.

Update Jan 2020:

Diagnosis: Spina Bifida; Hydrocephalus: shunt placed: Slight paraplegia of lower limbs; Left kidney agenesis; Vesicostomy.

Julian sits on his own while supporting his weight on his hands. He uses his hands to change his posture and move his body. He stands in the walker. He actively grabs and manipulates toys and objects, tries to use them as intended – shakes to produce sound, pulls the string of a musical toy. Visual-motor coordination is slightly impaired.

*** 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 on this child, email childinquiry@reecesrainbow.org

Ozzie
Age: 2014
Diagnosis: Coffin-Lowry Syndrome


Ozzie has decreased muscle tone. He can’t walk, but has recently started standing up in his crib with support. He smiles and has positive emotions when interacting with adults and when he is with the other children. He pronounces combinations of sounds. He laughs when playing peek-a-boo.

*There is an older child that is believed to be Ozzie’s older brother. However, they are NOT listed as needing to be adopted together. The other child is listed as Ollie  https://reecesrainbow.org/127612/ollie-2

*** 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 on this child, email childinquiry@reecesrainbow.org

Ollie
Age: 2012
Diagnosis: Coffin-Lowry Syndrome

 

Ollie is now living in foster care.He is physically well developed. He has good coordination of his hands and feet. He walks without falling, and can run as well. Climbs up and goes down by the stairs when holding an adult or the railing. He can play with cubes by putting them and taking them out of a cup, but has some problems manipulating with smaller objects. He cannot eat and dress by himself yet, but does make attempts. He understood almost everything and fulfils small tasks. He likes playing hide and seek. He hides behind the door and when he is found, he laughs and stomps his feet. He is interested in musical cartoons and copies the movements of the actors.

*There is a younger child that is believed to be Ollie’s younger brother. However, they are NOT listed as needing to be adopted together. The other child is listed as Ozzie.  https://reecesrainbow.org/127615/ozzie

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy, born 2013

Sequelae of inflammatory diseases of central nervous system
Crossed eyes
Moderate mental retardation

Listed: Dec 2018

$10.35 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!

Boy, born 2014

Other disorders of nervous system, not elsewhere classified
Congenital malformations of aortic and mitral valves
Mental retardation

Updated pics: Dec 2019

Listed: Dec 2018

He has a 15-year old brother and 8-year old sister, we do not have any info on them currently.

Listed: Dec 2018

$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!

Boy, born 2005

Epilepsy
severe mental retardation

Listed: Dec 2018

 

$24.30 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!

Boy: 2016

Listed: Oct 2018

Special needs: genetic metabolic disease – pyruvate-kinase deficiency – homozygote mutation p-R 446; mild to moderate core and periventricular lesions; generalized muscle hypotonia; severely delayed physical and neuro-psychological development;

Josiah moves in space by turning from back to belly and vice versa. He has started forming some of the perceptions about objects from his constant surroundings and everyday life. He connects some objects from his surroundings with the actions performed with them.

When awake, Josiah is mostly calm. He would laugh out loud when jested. During active interactions with adults Josiah pronounces various sounds and random syllables.  Josiah follows a specific dietary regime and has food individually prepared for him. He is fed with a spoon by an adult and has a picky appetite. He is calm during dressing and bathing. Josiah’s sleep is calm.

*** 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 on this child, email childinquiry@reecesrainbow.org

 

Boy: 2014
Diagnosis: Down syndrome

Listed: Oct 2018

Scott spent the first 9 months of his life with his birth family. He was placed in an orphanage at 9  months old. He can sit up unassisted and can stand up with support. He will reach for a toy, hold it in his hand and manipulate it. He likes being held and cuddled. He is babbling and will repeat some basic words such as “ba-ba” and “ma-ma”. He’s been diagnosed with anemia and an iron deficiency.

*** 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. 

$2,025.85 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!

boy: 2010
Diagnosis: Cerebral Palsy

Listed: Oct 2018

Gary is currently living in a group home for children with special needs. He can move around the group home in a gait trainer. Due to his low tone, he can not sit or stand independently. He can roll from back to stomach. He can hold a toy and will manipulate it, though he does not always understand the purpose of the toy. He enjoys interacting with adults and will smile and demonstrate appropriate emotions when engaged in activities.

*** I am eligible for an Older Child Grant! Grant funding is dependent on a completed application and available funds. For more information, visit: Other Angels Older Child Grant ***

For more information on this child, email childinquiry@reecesrainbow.org

Boy, born 2012

Hydrocephalus
Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures

 

Listed: Sep 2018

$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!

Boy: 2007

Listed: Sep 2018

He got very sick in 2015 and went through a number of procedures and while being in a hospital, his mother abandoned him. He is now cured although they keep monitoring him but he desperately needs a family to love and support him and to give back his faith into the family.

 Diagnosis: B-cell Acute lymphocytic leukemia (ALL). Relapse. Status after chemotherapy. Status after Radiation therapy – prophylactic Radiation therapy of Central nervous system (CNS).

Musa is well-mannered and well-meaning child. Follows the daily regime in the CFTA and every day marks progress. His vocabulary is still not very rich because he did not even know Bulgarian until two years ago. He still has some difficulties in choosing the right words. Musa constantly enriches his vocabulary and progresses in this area. His fine motor skills are very well developed, but he still has some difficulties with writing. He is learning to read and already recognizes the individual letters. Musa knows the geometric figures. Now he is able to solve simple tasks with addition and subtraction tasks. Due to the history of his placement and neglect, the child still has difficulties at school and his performance level is lower than this of his peers. But he is willing to learn and does his best.

Musa is quite shy, passive, silent and closed. He has difficulties in communication with strangers and difficult to trust. Musa does not like to be left alone and he is afraid of that. If things do not happen in the way he wanted, it is possible to close in himself. After spending some time in reasoning on what has happened, he realizes that closing in himself, may not be the best way to deal with problems.

In relationship with his peers, Musa is a leader. He has a fighting spirit and likes to win in the games. In his relationship with adults Musa shows respect for their authority. Obeys and seeks for their approval. This has largely contributed to the great progress the child has been making in the past two years.

In his spare time, Musa likes to play soccer. He also plays basketball. He also likes to color and to play on a tablet. His favorite color is blue. Favorite food sausages, dessert – ice-cream and fruit – banana. His favorite footballer is Ronaldo and dreams of becoming a soccer player when he grows up. From the animals he mostly likes dogs.

Musa has difficulties in talking for the adoption, but in general his attitude is positive.

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy: 2011

Listed: Sep 2018

Special needs: hyperkinetic conduct disorder, congenital cardiac malformation – in a condition after surgical correction, atypical autism*

*Abner’s social worker reported that according to the specialists, supervising Abner’s condition and development, the diagnosis of atypical autism is no longer valid and it will be deleted from Abner’s formal paperwork that is to be updated in the following months

Abner likes to keep himself busy exploring! His  favorite activities are the ones that include movement, such as going for a walk. He very much likes to spend time looking through books. He also likes all musical instruments and toys that play melodies and sounds. His favorite toy is a children’s laptop that plays songs. When he hears a melody he tries to dance.

There has been a progress in Abner’s speech development as he has started using a lot of words. He now forms sentences containing 3-4 words, albeit dyslexia is observed.

*** 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 on this child, email childinquiry@reecesrainbow.org

Girl, born 2011

Down syndrome, severe mental retardation, cardiomyopathy

Listed: August 2018

 

*** I am eligible for an additional $5,000 Grant!  Through 2020, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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!

Boy: 2015

Listed: July 2018

Diagnosis: nonspecific reactive hepatitis. Hepatosplenomegalia. Heart malformation foramen ovale, initial lung hypertonia. Condition after hypoxic ischemic encephalopathy 2-3 degree. Hemoragia. Intraventricular bleeding 2 degree. bilateral otomastoidit – mastoidectomy in the right. Retention testicle in the left. Delay in the neuro-psychical development.

Robby is delayed in all aspects of his development, but has begun to make small gains in learning . He will interact with caregivers and other children if an activity is interesting to him. His attention span when working on tasks has begun to increase. He enjoys playing in the sensory room. He learns best with multiple repetitions of a task.

Donations can not be accepted until a family is found for him.

His current agency has videos and pictures that can be shared with interested families

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy: 2015

Listed: July 2018

Diagnosis: Congenital malformation syndromes predominantly affecting facial appearance. Foramen ovale persistens. Transient pulmonary hypertension. Pes equinovarus bilateralis. Severe delay in neuro-psychical development

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.

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy, born 2016

Other specified disorders of brain
Unspecified severe protein-calorie malnutrition
Other specified congenital malformations
Double outlet right ventricle
Other specified congenital malformations of kidney
Chronic obstructive pyelonephritis
Chronic kidney disease (CKD)

Listed: July 2018

$231.30 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!

Boy, born 2017

ventricular septal defect
Neonatal cerebral irritability
Other specified mental disorders due to known physiological condition

Listed: July 2018

 

$1,663.40 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!

Girl, born 2014

Down syndrome
Myopia
Congenital absence, atresia and stenosis of large intestine, part unspecified

Updated pic 2019!  Listed: July 2018

 

Luna has two older brothers; a family could pursue the adoption of all 3 children!  A separation process will need to be done if a family only wanted to adopt Luna.

 

 

*** I am eligible for an additional $5,000 Grant!  Through 2020, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$2,763.84 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!

Girl: 2016
Listed: July 2018
Diagnosis:  Hydrocephaly; Strabismus; G-tube feeding; delays in development

Mila turns her head towards sound and looks at people and objects of interest. She recognizes the faces of the staff. She can roll over, but still has difficulty with head control. She enjoys musical toys that spin and will focus on those for short periods of time.

*** 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 on this child, email childinquiry@reecesrainbow.org

Age: 2
Diagnosis: Cerebral palsy; Microcephaly; Symptomatic epilepsy; Developmental delay

Listed: July 2018

Lisa is a happy and sociable little girl. She enjoys meeting new people and interacts with them appropriately. She responds to her name and verbalizes using sounds and syllables. She follows basic directions. Her motor skills are developing. Videos of Lisa show her playing with a ball and manipulating it appropriately. She currently moves around by crawling. She can take steps when holding 2 hands of an adult and can also move using a walker. She is receiving therapy to help develop her motor skills.
Photos and videos are available through the agency

 

Donations will not be accepted until a family is found for Lisa!

Penn
Boy, born 2007
Diagnosis: mental delays and behavior disturbances

Listed: June 2018

The  child  is  able  to  communicate  with other  children, though his vocabulary is not at age level. He prefers to play alone, but will join in group games willingly if invited. He willingly forms relationships with adults. He has delays in academics, but works hard to learn new skills. His behavior is described as “unstable”

*** I am eligible for an Older Child Grant! Grant funding is dependent on a completed application and available funds. For more information, visit: Other Angels Older Child Grant ***

Boy, born 2013

sweet smile! 🙂

lumbar spina bifida with hydrocephalus
Unspecified personality and behavioral disorder due to known physiological condition
Esotropia
Other acquired deformities of limbs
Flaccid paraplegia
Vasomotor rhinitis
Hypertrophy of adenoids

Listed: May 2018

$148.50 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!

Boy, born 2012

Chronic viral hepatitis B
May also have Cerebral Palsy

Listed: March 2018

 

$2,589.96 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!

Girl, born 2012

Other specified mental disorders due to brain damage and dysfunction and to physical disease

Listed: March 2018

 

$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!

Boy, born 2012

HIV
cerebral palsy
cytomegaloviral disease
moderate intellectual disabilities

Listed: March 2018

What a great smile!

$2,021.00 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!

Boy: 2012

Listed: 3/2018

Special needs: spina bifida aperta-condition after surgical correction of the meningomyelocele region lumbalis; internal hydrocephalus – VP shunt installed; severe muscle hypotonia of the lower limbs; contractures of the ankle joints; lower flaccid paraplegia; convergent concomitant strabismus; esotropia and amblyopia of the right eye – glasses are prescribed and treatment is being conducted; neuro-psychological development – within the norm with regards to the expressive and receptive speech development

Pacen presents as a cheerful and calm boy who doesn’t cry without a reason. He doesn’t have any manifestations of aggressive or self-aggressive acts. Pacen uses separate words, as well as simple sentences in his communication with others. He understands when spoken to and people can have a conversation with him. Pacen uses appropriate social gestures for greeting and good-bye. 

Donations will not be accepted until a family is found.

Girl: 2014

Listed: 2/2018

Special needs: symptomatic epilepsy-partial seizures with secondary generalization; spastic cerebral palsy; hypoxic-ischemic encephalopathy of 2nd degree; profound mental delay;

Kaylyn is in severely impaired condition and her development is delayed in all areas. She is completely dependent on adults’ care. Her sleep is calm and rhythmical. She is fed with a spoon by an adult.

*** 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 on this child, email childinquiry@reecesrainbow.org

Boy: 2007

Date listed: 2/2018

Diagnosis: mild mental delay; hyperkinetic behavior disorder with attention deficit; the child suffered physical abuse and mistreatment; born to a mother with moderate mental delay

Graham is treated with Convulex – 0,5 ml from 50 mg daily, Xanax ½ and Speridan when necessary

Graham takes an active part in the housework at the home. He goes shopping on his own, sets and then tidies up the table, makes his bed, knows how to work the washer, hang and then collect the clothes and tidies his room. One of the main activities that he takes part in is cooking. He is able to cut different types of vegetables in small pieces and follow the instructions of the recipe.  Grahamprefers games involving physical activity. He looks for interaction with his peers. He likes to ride a bicycle and play hide-and-seek. Graham has been acquainted with the process of adoption. His attitude and opinion towards a possible adoption is positive

Donations will not be accepted until a family is found for him.

*** I am eligible for an Older Child Grant! Grant funding is dependent on a completed application and available funds. For more information, visit: Other Angels Older Child Grant ***

Girl: 2007

Listed: 2/2018

Diagnosis: epilepsy –

Giada has grand mal seizures (with small seizures (petit mal) or without them), unspecified; congenital malformation syndromes predominantly affecting facial appearance; genetic syndrome – chromosomopathy or monogenic syndrome; facial dysmorphism; psychological and behavioral disorders related to past trauma.  More information is available from the agency for interested parents.

Giada is on medication for her seizures.

Family history: the child’s biological mother has mental delay, epilepsy- grand mal seizures (she had Depakine during pregnancy) and cerebrovascular disease; the child’s biological father had mental delay and abused alcohol.

Giada is sociable and outgoing girl. She interacts and looks for contact with peers and adults. She is able to cooperate with other children from her class. Giada loves to draw and color, as well as to solve puzzles. She prefers to play with her peers or older children. She loves to play with children younger than her so she can take care of them. She cooperates in games.

Giada knows what adoption means and she dreams about being adopted and have a forever family of her own.

B/c we only have her file for a short time, donations will not be accepted until a family is found for her.

UPDATE: Oct. 2018:

Giada is physically well developed for her age with mild neuropsychological developmental delay. Her Epilepsy (petit mal seizures) is well managed with medication. She has a well developed fine and gross motor skills. She can read and write. She loves to paint and to play sports. She has a well-developed imagination.

She attends a public school and is doing very well there. Her dream is to become a teacher one day. Giada is not shy. She is able to communicate easily and maintain a dialogue with her classmates and adults. She has good hygiene habits.

*** I am eligible for an Older Child Grant! Grant funding is dependent on a completed application and available funds. For more information, visit: Other Angels Older Child Grant ***

Boy, born 2014

sequelae of inflammatory diseases of central nervous system
severe mental retardation
undescended testicle
congenital dislocation of hip
strabismus
atrial septal defect

Listed: January 2018

$1,406.30 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!

Girl, born 2009; Mild Mental Delay
Girl, born 2002 (sister)

Listed: April 25, 2016

Updated pics/info August 2016


Emma is going to be transferred into the school orphanage for mentally delayed children, and it is not the best place to anybody. The orphanage may keep her only till summer 2016, and then she will be transferred!

She is much educationally delayed. She is pretty friendly and calm. But her memory is not good, and it is hard for her to remember any rhymes or poems.

This girl needs a patient family who will love her and care of her. She deserves it!

*** I am eligible for an Older Child Grant! Grant funding is dependent on a completed application and available funds. For more information, visit: Other Angels Older Child Grant ***

girl: 2010

Listed: Jan 2018

Diagnosis: Microcephalous; Moderate mental delays; Speech delay; Behavioral Issues

Malory is a beautiful, giggly girl who lives with a foster family in Eastern Europe. With a contagious smile and laughter, Malory runs, climbs and could be described as an active child.  She enjoys the extra attention she receives from her foster parents. She is physically healthy, and she eats well. Her weight and height are catching up with the standards for her age.

Malory has some developmental delays that her caregivers attribute to early neglect and lack of stimulation. She has difficulty pronouncing some words, and her learning is below the norm for her age.  Malory understands everything her elders say. She cannot talk yet, but she can pronounce separate words and sounds. She knows her name and the people’s names living around her. She plays with the other kids from the group, and she prefers more dynamic games.

Malory gets one-on-one instruction in each subject, participating in different programs – therapeutic, musical and rehabilitation.  She is much calmer then she was before, and she respects the authority of the foster family.

Additional videos are available from her agency.

*** I am eligible for an Older Child Grant! Grant funding is dependent on a completed application and available funds. For more information, visit: Other Angels Older Child Grant ***