There is a very special joy that boys bring to life. Unfortunately, they are often the last ones to be chosen for adoption. We so hope you will find YOUR new son right here at the end of Reece’s Rainbow.

PLEASE HELP US raise grant funds and awareness for these precious, waiting angels. You really can save a life, with even the smallest gift!
You are also invited to send a check (no Paypal fees) to
Reece’s Rainbow, PO Box 146, Combined Locks, WI  54113

“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!

FOR MORE INFORMATION ABOUT THE PROCESS AND/OR ANY OF THE WAITING CHILDREN ON THIS PAGE, PLEASE INQUIRE.

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!

Boy, born 2017

Congenital hydrocephaly, (subcompensated); atonic-astatic syndrome
umbilical hernia; inguinal hernia; mild myopia; average hypermetropia; astigmatism
heart murmur

Listed: December 2017

$110.80 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!

Boy, born 2015

 

Unspecified mental disorder due to known physiological condition
Expressive language disorder
Disorder of central nervous system, unspecified

 

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

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

Boy, born 2016

Other disorders of nervous system not elsewhere classified
Ventral hernia
Other congenital deformities of feet
Other congenital malformations of cardiac chambers and connections
Neonatal goiter, not elsewhere classified
Persistent hyperplasia of thymus
Fetal alcohol syndrome (dysmorphic)

He has 2 siblings – 17-year old sister and 12-year old brother; Due to his special needs, he may be able to be separated from his siblings, for adoption.

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

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

“ihaveawarrior”

Boy, born 2016
H-C
Cerebral palsy

Jesse is definitely a smart boy! He is nonverbal, but already recognizes a lot of letters and their sounds. He communicates by moving his hand closer to the letter or option he is choosing. He is working hard on these skills in preschool, which he currently attends two afternoons each week. He also uses his eyes to communicate. Sometimes I will tell him to look at someone to say please, thank you or sorry and he is always quick to comply, unless he is mad, in which case he will either shut or roll his eyes. If given two choices, I’ll ask him to look at one person for the first choice and another person for the second choice. He is quick to answer, especially if it’s something he really wants. For example, I will say look at Irene if you want your milk or look at Judith if you want more food and he will look at Judith to indicate he wants another bowl of food. Jesse knows the name of all his familiar people and will quickly look at them with a smile if I ask where they are.

Jesse loves to laugh and is quite entertained by the antics of his foster brothers and sister. Every night, I take Jesse into his bedroom to sit by his bed and pray together. Our one year old has a habit of following us in to the bedroom and sitting down beside us until another adult comes to get him. Jesse always anticipates this and as soon as I sit down with him, he watches the door and smiles, until the toddler comes in and Jesse wiggles and dances with joy. Sometimes after Jesse is in bed, his buddy will climb in with him and they both laugh at the craziness of bedtime.

Physically, Jesse can balance in a sitting position for several seconds, with his legs crossed and using his arms for support. He doesn’t do it for long at a time before he tumbles over, but he is always very proud of his accomplishments. He doesn’t roll over, but when he is laying on his tummy (his favorite position!), he can lift his head up and look around. Jesse loves to practice his walking, especially if he can “chase” the other kids around. I support him by holding him under his arms and then he lifts his feet and off we go. Jesse wears AFOs to use his stander every day. He really enjoys this time and rarely fusses while he stands. He has a musical light up toy that he likes to use during this time and he is quick to fuss if one of the other kids tries to take it. He also goes to physical therapy four days a week where he works hard on continuing to develop his skills.

Jesse still wears a diaper, but he is working on potty training and sits on his modified potty every evening before bath time. He will usually use it and always smiles proudly when we praise him for this.

Jesse eats well, with mostly pureed food, although he also likes to eat things like crackers or cookies. He does not self-feed, but if we give him the spoon to hold, he works hard to bring it to his mouth. Jesse drinks from a sippy cup and a water bottle with a straw – he especially loves milk and juice, but nothing too cold!

Jesse enjoys spending time being pushed in a supportive swing and fusses when it is time to get out. He also likes watching movies and going for walks in our stroller. Jesse enjoys story time and holding his baby doll or stuffed lamb. He is an amazing little guy who will definitely be a huge blessing to his family!

$4.50 has been donated towards the cost of my adoption!

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

“ihaveawarrior”Boy, born 2017

At age of 2 months old he survived a surgery due to heart disease

Congenital tracheomalacia

 

 

$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!

“ihaveawarrior” Twin Boys, born 2017

Brenner:
Communicating hydrocephalus
Disorder of brain, unspecified
Portal hypertension
Bilateral inguinal hernia, without obstruction or gangrene
Other congenital valgus deformities of feet
Congenital tracheomalacia
Cardiomyopathy, unspecified

Braun:
Disorder of brain, unspecified
Unilateral inguinal hernia, without obstruction or gangrene
Hypertrophy of tonsils
Other non-diabetic proliferative retinopathy
Iron deficiency anemia, unspecified
Heart disease, unspecified

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

$95.40 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!

Boy, born 2015

hydrocephalus
deafness
blindness
convulsive syndrome

 

 

$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!

“ihaveawarrior”Boy, born 2018

Talipes valgus
atrial septal defect
patent ductus arteriosus

 

He has two brothers and a sister that are under custody and not adoptable at this time

$70.20 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!

“ihaveawarrior”

Boy, born 2017
PRC
brain damage

Ronan is a clever boy and has everyone wrapped around his little finger! He enjoys his mealtimes. He is a boy who knows exactly what he wants and is not afraid to let his caregivers know if he doesn’t like a particular food or texture. He cannot form words yet but is making plenty of sounds. He loves being the center of attention and will cry if his caregivers too far away, indicating he wants to be picked up! They are more than happy to oblige and he spends most of the day cuddled in someone’s arms. Ronan is not crawling yet, but he attends regular physiotherapy sessions to improve his muscle strength and coordination. However, if Ronan does not want to do his exercises, he will kick his legs and scream until his caregivers pick him up. This is something we are working on with him though, as his caregivers know that he needs to do his exercises to improve his tone. We are working on rewarding his therapy efforts with his favorite music and songs. Ronan loves all types of music and will not go asleep without listening to his favorite lullabies. Although he is developmentally delayed, he continues to make good progress and we feel he would thrive with a forever family.

$10.00 has been donated towards the cost of my adoption!

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

Emeric
Birth Year: 2017
Diagnosis: Cerebral Palsy

Emeric can sit up in a special chair with support. He has poor support for his legs. He can hold a rattle with his left hand and shake it. He turns his head in the direction of sound. He has recently started tracking objects with his eyes. He enjoys listening to music. When music plays, he will get very still and listen to it with interest. He laughs and smiles in the presence of familiar adults.

He eats blended food from a bottle.

*** 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 2017

Bladder fistula, not elsewhere classified
Stress incontinence
Chronic interstitial nephritis
Chronic kidney disease
Hydrocephalus, unspecified, condition after shunting

Listed: June 2020

$19.35 has been donated towards the cost of my adoption!

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

Boy, born 2016

consequences of neuroinfection
consequences of inflammatory diseases of the central nervous system
hypertrophy of adenoids
weak hypermetropia of both eyes

Listed: June 2020

$14.00 has been donated towards the cost of my adoption!

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

“ihaveawarrior” Boy, born 2016

Disorder of brain, unspecified
Other disorders of psychological development
Expressive language disorder
Contracture of joint
Congenital dislocation of hip, bilateral
Osteopathy in other diseases classified elsewhere
Other congenital malformations of cardiac chambers and connections
Hypermetropia

Listed: June 2020

$90.00 has been donated towards the cost of my adoption!

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

“ihaveawarrior”Boy, born 2019

Spina Bifida
congenital hydrocephalus, conditions after surgery

Listed: June 2020

 

$45.00 has been donated towards the cost of my adoption!

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

“ihaveawarrior”Boy, born 2016

Spastic quadriplegic cerebral palsy
Other hydrocephalus
Moderate intellectual disabilities
Optic atrophy

$211.50 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!

“ihaveawarrior”Boy, born 2018
PRC
epidermolysis bullosa (EB) and CHD-ASD

Ping is a sweet little boy, with epidermolysis bullosa (EB) and CHD-ASD. Ping was sent to a special home when he was only a few weeks old because he needed nursing care for his skin, extra nutrition, and heart surgery. Ping has had surgery for his heart, but still needs lots of special care for his skin. His skin is easily damaged from ordinary things, like seams on clothing, scratching an itch, and by doing things like rolling over, sitting up, or crawling. During the summer of 2019, Ping started to eat food orally. His nannies are so proud of the progress he’s made! He can sit up independently and loves singing time!

We sure hope Ping’s family finds him and can get him home while he’s still so young!

$544.50 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!

“ihaveawarrior”Boy

Listed: 3/2020

CO-8

Playing with cars is one of Devin favorite activities. He finds colorful toys to be very exciting, especially when these are animals or related to sports. He is very friendly to kids his age and enjoys playing with them. With adults he might be a little shy at first but has no trouble relating once he feels comfortable. Devin enjoys painting. He can spend a lot of time mixing colors and making spectacular artworks. 

Devin gets very excited when someone he cares about comes to visit him. He will receive them with hugs, kisses and lots of smiles. He also likes it when he gets to go out to walk around or play in the park. Devin has a diagnosis of speech and language development disorder and microcephaly with what is suspected to be a cognitive deficit. He would do best in a family that can work with him through all the different parts of his development, keeping in mind his own necessities.

$4.50 has been donated towards the cost of my adoption!

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

OLYMPUS DIGITAL CAMERA

Boy: 2016

Listed: Feb 2020
Diagnosis:  cerebral palsy;  quadriparesis ; epilepsy; Bronchial asthma; delays in all aspects of development

David was declared clinically dead at birth and resuscitated. He currently lives in a group home. He reaches for hanging objects and can hold a toy for brief periods of time. He is very responsive to caregivers. He smiles and shows pleasure when spoken to. He tracts objects and tries to focus on people who are talking to him and objects being presented to him. He rolls from his back to stomach in his bed.

*** 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 2018

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
Iron deficiency anemia
Other ill-defined heart diseases
Hypermetropia
Renal hypoplasia, unspecified

 

Listed: Feb 2020

$432.55 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”

June 2020

Boy, born 2015

Nanism
Williams Syndrome

Listed: Feb 2020

 

$332.90 has been donated towards the cost of my adoption!

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

Boy, born summer 2015

FAS, Hypermetropic astigmatism. Protein energy malnutrition. Changes of retinopathy and retinal blood vessels. Moderate mental retardation with significant impairment of behavior requiring attention or treatment

Nehemiah has grayish-blue eyes and brown hair.   Nehemiah is very active and moving, generally in a positive mood. He likes to walk a lot, walks hand in hand with adults willingly, can do it independently, but in long walks can also use the walking frame. There is no sense of fear in his movements, can climb on different objects (table, windowsill).  Nehemiah likes to exercise, to do backbends and plays alone often. He has short-term steadiness while playing with the toys. He still puts toys in his mouth.  Nehemiah  likes to play with the toy car, to page through the picture books, but only for a short moment. His attention can be attracted by musical toys. He sometimes doesn’t sleep during the day, he likes to play while he falls asleep, sometimes has difficulties to fall asleep in the evening, but sleeps well at night.  Nehemiah  often expresses his feelings with gesticulation and mimicry. He says different sounds, syllables “ta-ta”, “bu-bu”, but doesn’t pronounce words. The boy eats independently, but has to be looked after, drinks unwillingly.

$27.00 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 2014

mild mental retardation. Early organic CNS damage. Physical development delay. Other disturbances in speech and language development. Malabsorption syndrome

Jaylen has blue eyes and light, blond hair.  Jaylen walks steadily, eats independently, also solid food, can speak 4-5 words sentences, is active – loves to ride a push-car, run, play with other kids, wants to get to know everything new around him. Jaylen has successfully started his pre-school education, he attends kindergarten from Monday to Friday. He has adjusted well, he is very happy and eager to go to the kindergarten every day. He studies according to a specialized pre-school education program for children with mixed developmental disabilities. In everyday life a child is able to employ himself constantly. On a daily basis Jaylen needs assistance with changing his diapers as he still continues his potty-training. He needs a little help to get dressed and undressed.

Jaylen has learned to caress a doll or someone from adults or children. In the beginning Jaylen did not know, how to react out his emotions – he threw things away, he was hitting adults and children, also when he was happy to see someone. At the moment Jaylen by movements imitates caresses, gives kisses. Jaylen gets on well with other children, especially with children of his age. Jaylen helps in small daily chores, can collect his toys and put them in places. Jaylen has started to eat hard food; he bites and swallows biscuits, bananas, apples. He shows interest about books, especially about the ones that are with sound. Jaylen starts to show and demonstrate independence. He reacts calmly to new events. He has high level of energy.

$54.95 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: Jan 2020
Diagnosed with autism spectrum disorder (ASD) and has delayed speech

*** 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 2015

disorder of the brain
mild intellectual disability
FAS
Phonological disorder
Other specified disorders of nose and nasal sinuses
Optic atrophy
Hypermetropia
lack of development
Other specified endocrine disorders
Other specified disorders of thyroid
Celiac disease

$52.00 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

Listed: January 2020

epilepsy
valgus deformity
other disorders of psychological development
Undescended and ectopic testicle
Disorder of prostate

He cannot talk. He permanently uses anti-convulsants.  He can feed himself without assistance.

$211.50 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!

“ihaveawarrior”

Boy, born 2017

Listed: January 2020

spastic tetraparesis
Sequelae of inflammatory diseases of central nervous system
Lack of expected normal physiological development in childhood

 

$30.60 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!

Boy, born 2016

Listed: January 2020

disorder of the brain
hypospadias
valgus deformity
craniosynostosis
myopia
iron deficiency anemia

$15.00 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 2017

Listed: January 2020

FAS
lactose intolerance
disorder involving the immune mechanism

$80.00 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 2017

Microcephaly
Mild intellectual disabilities
Umbilical hernia
Strabismus
Nystagmus
Congenital deformity of hip

 

$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!

“ihaveawarrior”Boy, born 2018

Microcephaly
Disorder of brain
Other developmental disorders of speech and language
Esotropia
Anemia
Carrier of viral hepatitis
Congenital hydronephrosis
Abnormal results of cardiovascular function studies

 

$20.35 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!

“ihaveawarrior”Boy, born 2017

Disorder of the Brain
Other developmental disorders of speech and language
Undescended testicle
Accessory thumb(s)
Acquired deformity of chest and rib
Ventricular septal defect

Listed: Dec 2019

$476.65 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!

“ihaveawarrior”Boy, born 2014

Updated pics 12/19!

Generalized idiopathic epilepsy and epileptic syndromes
Mild mental retardation
Convergent concomitant strabismus

Warik has two sisters —
girl, born 2013
girl, born 2017
both healthy

All 3 siblings must be adopted together!

$129.60 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!

“ihaveawarrior”

Boy, born 2019

Arnold Chiari syndrome
probably spina bifida
many other codes

$753.30 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!

 

“ihaveawarrior”Boy, born 2017

Spastic hemiplegic cerebral palsy
Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
Unspecified intellectual disabilities
Asthma
Abnormal results of cardiovascular function studies

$4.50 has been donated towards the cost of my adoption!

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

“ihaveawarrior”Boy, born 2015

Microcephaly
Paraplegia (paraparesis) and quadriplegia (quadriparesis)
Severe intellectual disabilities
Congenital deformity of hip
Optic atrophy
Nystagmus
Abnormal results of cardiovascular function studies

 

$308.70 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!

“ihaveawarrior”Boy, born 2018

Cerebral palsy
protein-calorie malnutrition
Iron deficiency anemia
Astigmatism
Optic atrophy
Exotropia
Other ill-defined heart diseases

$937.00 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 2014

FAS
moderate mental delay
benign neoplasm of neck
two-sided fallen arches
undernutrition

From a family that met him summer 2019: He is adorable, turned 5 this summer. Started walking recently. Has FAS. Cute as a button. Care taker said isn’t violent or doesn’t act out like other kids. Only fusses when it’s time to eat. He walked into my arms without knowing me!

 

$305.00 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: 2016

Listed: Oct. 2019

Special Need: Fetal Alcohol Syndrome

Daniel is a boy whose cognitive and physical development is close to his expected age. He is described as very curious, sweet, gentle, outgoing and has good relationships with other children. He makes good eye contact, speaks in words and sentences, implements instructions and has a sweet personality. Diagnosed with Fetal Alcohol Syndrome and mixed development disorder

Pictures are available from the agency.

$25.00 has been donated towards the cost of my adoption!

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

Boy, born 2017

Patent Ductus Arteriosus
Disorder of the brain
Persistent hyperplasia of Thymus
Hypermetropia

 

$87.50 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: 2016

Listed: Sep 2019

Special Need: spina bifida and lower flaccid paraplegia, hydrocephalus (has been addressed with no concerns), developmental delays

Harry is unable to walk due to being paralyzed from the waist down, but he’s such a lively little boy. Harry loves toys and crawls towards them with excitement. He understands commands and he has a pretty good vocabulary. If on his back, he can sit up with no help. Harry is described as radiant and 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: 2018

Listed: Sep 2019

Special need: Polymalformation, VSD

Tad has been diagnosed with Polymalformative syndrome, Dextrocardia, Ventricular septal defect (VSD), facial dysmorphism, micro-anaphthalmia on the right eye, and dysplastic right ear. Tad is described as a calm boy. Tad has good head control and he can turn from his back to his belly and vice versa. His file states he can reach out and grasp toys and turn to the source of sounds while on his stomach. He reacts to visual, auditory, and tactile stimulation. Tad smiles when interacting with adults and listens to people when they talk. His file states he can pronounce spontaneous sounds and can hold eye contact with objects. He cannot sit up, stand, or walk independently.

*** 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 2015

spastic quadriplegic cerebral palsy, seizures, mild hearing loss

South Asia – Pacific

Listed: Sept 2019

Simon is a very sweet little boy who currently lives with several older girls and is the last remaining “baby” in his home. He cannot speak, but does communicate through facial expressions and some noises.

A traveling family met Simon and said, “Within the three days we spent at the orphanage, we were able to bond with him to the point he would smile and get excited when he saw us. The older girls told us he can understand what they say to him. He enjoys being held and carried around, but spends most of his day sitting in a baby walker or high chair. He seems very easy going, as we didn’t see him complain about being put in his crib for nap time, etc. The caregivers are working on his motor skills. He can eat with assistance and enjoyed the ice cream we brought! It’s so easy to fall in love with this little boy! We are praying his family sees him soon!”

Simon has spastic quadriplegic cerebral palsy and has had seizures. He takes 30 mg of Phenobarbital once a day. Simon has mild hearing loss of the left ear. Therapy has helped lessen the spasm and Simon can open and close his hands. Simon loves being around people and making faces! When praying before meals, he bows down his head and says “ahh” when everyone says “Amen.” We’re hoping a wonderful loving family comes forward for this special little boy!

There is a $500 agency grant for Simon’s adoption with his adoption agency.

$1,250.00 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 2015
PRC
tuberculosis, Pneumonia, Right cerebral hypoplasia, Eczema

Listed: August 2019

Nathan’s spine is slightly lateral bending, but this does not affect his walking ability; he can hold the railing to go upstairs and downstairs; sometimes he can jump in place with both feet; can trot to chase us or toys; can also understand our orders to put the toys to appointed place. If there are new toys he will he happy to point them to us, and show us how to get toys disassembly and assembly; after he gets the toys disassembly and assembly he then hand us to look at his works. We will thumbs up and praise him, then he will laugh more happily. When we teach him to do new playing methods, he will play after watching once.

Nathan has a good memory.  He is good at observing, and he is curious about new things. He likes to be noisy, and he likes to play with us, likes to play outdoors; not afraid of strangers; not afraid of dogs, seeing dogs he will follow dogs to walk. He also likes to watch artist programs, and ball games. Every time he will watch carefully. Sometimes he can imitate us to dance, and he can dance well.

He is curious about new things, and has a strong imitation ability; but he doesn’t have a good sense of danger.   In this aspect he needs to be supervised. He has his own personality; sometimes he is obstinate. Nathan is lovely, optimistic, and clever.

$25.00 has been donated towards the cost of my adoption!

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

Boy, born 2017
PRC
brain hypoplasia

Listed: Aug 2019

On admission, he was diagnosed as brain hypoplasia. He was sent to Cleft Lip and Palate Home for treatment and rehabilitation.  At the age of 1 year, he can roll over and can sit and stand with held; he can grasp a toy with his hand. He can visually move follow the moving toys and sounds; he laughs happily when happy.  He has outgoing personality; he can’t speak, but he has a ready smile; he is obedient and adored.

$9.00 has been donated towards the cost of my adoption!

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

Boy: 2015

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

“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.

$204.80 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!

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: 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.

“ihaveawarrior”Boy, born 2016

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

Listed: May 2019

$339.75 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

 

$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, 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

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 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!

“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.

$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!

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

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

$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: 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

These 3 siblings are only adoptable together!  They are in the same region, but in 2 different cities and 3 different orphanages.

Listed: Sep 2018

Freddie:
Boy, born 2015
Disorder of brain, unspecified
Specific speech articulation disorder

A very good boy, friendly and smart!

 

Carly:
Girl, Born 2012
Disorder of brain, unspecified;
Other congenital valgus deformities of feet
Mild mental retardation
Congenital dislocation of hip, unilateral
Convergent concomitant strabismus

 

Samantha:
Girl, born 2013
Disorder of brain, unspecified
Iron deficiency anaemia
A very good girl, very helpful and friendly, with no significant problems

 

$1,095.75 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!

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

$163.80 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!

Boy, born 2017

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

Listed: July 2018

 

$1,506.40 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!

Boy, born 2014
Blind

Listed: May 2018

Georgie was transferred to his current home in April 2018. He had experienced neglect and under-stimulation in his previous orphanage but already his development is progressing and we look forward to seeing Georgie learn and explore the world. Georgie is functionally blind and has very little light perception. He has been doing so well in his transition into this new chapter of life. Everyday we are more captivated by his bubbly, sweet, gentle disposition.

Georgie is rapidly changing and developing. He is learning how to scoot around, bear weight, and explore with his hands. He had no experience in his previous home with self feeding, but already is making great progress and is self feeding with minimal support. He had no English exposure previously, but in just a month his English understanding is already developing and he responds to several commands. He is weak, but gaining strength. He can pull up to a stand using a surface for support.

Georgie loves making silly noises and often vocalizes silly babbles, finds interesting surfaces to tap on, or picks things up and throws them to hear their clatter. Georgie is very social. He loves to be held and swung around. He sometimes whimpers when he is put down and communicates non-verbally that he wants to be held. He mimics sounds others make and often bursts with excited laughter when playing with other adults and children. We are so excited to see him begin to hit the milestones he is already working towards.

UPDATE July 2020: Georgie has been making steady progress in his language skills. Lately, he has begun to make requests on his own or make jokes in conversations with his teachers, caregivers, and house mom. Georgie’s favorite little joke right now is to reply “JUICE” to each and every question asked of him. He erupts into giggles and repeats the word over and over until tickles and exclamations prompt him to give the real answer that we were looking for. We recently celebrated Georgie’s 6th birthday, and when asked what he wanted to do for his party he answered without hesitation: “DANCE PARTY!” Georgie can count to 10 and is learning his first braille characters!

$2,642.40 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!

Boy, born 2017

Updated pic from June 2020

Listed:  Dec 2017

congenital malformation of the corpus callosum,
congenital hydrocephalus
ventricular septal defect, atrial septal defect
congenital talipes calcaneovarus
bilateral inguinal hernia, umbilical hernia
polysyndactyly

preterm

Sweet baby boy!

$1,061.08 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

Diagnosis: Hydrocephalus, optic nerve atrophy

Evan lives in a baby house in Eastern Europe.  His current diagnoses include: Congenital hydrocephalus – VPS. Horizontal nystagmus. Atrophy of the visual nerve. Moderate muscle hypotonia. Mild mental delay. Delay in the neuro-psychological development.

Listed: October 2017

Evan is interested in what is happening around him. He turns his head in the direction of sound. When spoken to, he listens but does not fix his stare or follow bright objects with his eyes. He is attentive when playing with a musical toy or bright object.  He does not imitate actions with objects.  

Evan can turn from his back to his belly and vice versa, stand up, and reach for a toy that is attached to his bed or given by an adult. He catches the toy after chaotic movements of his hands while trying to coordinate them. He sometimes can place the toy from one hand in the other by himself but sometimes he needs help from an adult. His left hand is no longer in a fist and there are longer periods of time when his fingers are spread out.  

When communicating with an adult, Evan reaches out and touches his/her face and smiles. He is not aggressive but when he wants to be left alone, he will bite his hand.

When provoked, he can imitate syllables but cannot gesture or mimic.  Evan does not react when called by name and does not give a toy when asked.  

Evan is entirely dependent on the staff but will reach toward his food when being fed. 

More information, pictures and videos are available from his 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 2014
Spina bifida of lower lumbar and entire sacral region. Hydrocephalus (with VP shunt) and Chiari malformation. Had operation to release tethered spinal cord. Is catheterized.

Listed: October 2017

February 2020 Update: Zack continues to grow healthy and strong! Ever smiley, Zack is the social butterfly of his home. He adores when visitors come over and he loves making new friends. When going on walks in the neighborhood, Zack will call people as he passes by with a friendly “hello” and huge grin. Zack’s caregiver and teachers often call him a “handsome hero.” He cannot get enough of it! Due to this fact he has begun brushing his hair to the side with his fingers and smiling up at people until they tell him how handsome he is. It is endearing. Zack is truly the sweetest boy. Anytime anyone is sick or seems sad he will ask to sit with them and attempts to cheer them up or offers prayer. He deeply desires to see all of his friends happy at all times.

In classes Zack is currently learning shapes, days of the week, numbers one through ten, and the first five letters of the English alphabet. In play time he often requests blocks in order to build towers. Once they are completed he will call his caregiver in order to proudly show off his creation. When he is not building blocks he loves coloring, making crafts and playing with toy cars. His new favorite sensory play is with shaving cream. On Christmas the staff in his home filled a plastic swimming pool with shaving cream so the children in his home could play with “snow.” Ever since he has begun asking for shaving cream daily in his sensory class.

Recently Zack was gifted a new wheelchair that allows him to more easily reach the wheels. He has begun learning how to push himself in his chair. He is thrilled! While he is still in the early stages of learning this skill, he is already showing amazing progress! Obtaining this skill will be huge in Zack’s independence! He loves practicing and will often request to be taken on walks.  Zack often asks about his future family and is eager for the day that he is able to meet his mom and dad!

July 2019 update: Zack is the naughtiest and happiest boy in his home! He learned all his colours and is now learning his animals. He wants to be more independent! He can scoot backwards to get around by himself. He can make requests in both English and his local language and can translate English words to his local language for his caregiver! Zack loves his caregiver Ammama so much. He always scoots over to be near her and wants to be a part of what she is doing. One day he kept asking Ammama for a new shirt, so when she went on her monthly leave she brought him back a new blue shirt.

$2,058.50 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

Diagnosis: Microcephaly

Listed: September 2017

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

*** 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

Congenital debility NOS
Unilateral small kidneys
Unilateral inguinal hernia
Atrial septal defect

Listed: August 2017

Sweet baby boy!!

 

$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!

Boy, born 2016

Spastic cerebral palsy
cryptorchism
inconclusive laboratory evidence of human immunodeficiency virus of HIV
congenital kidney malformation unspecified
heart murmur

Listed: August 2017

$112.50 has been donated towards the cost of my adoption!

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

Boy, born 2015

disorder of the brain
other osteochondrodyplasia
disease of the gallbladder
short stature
atrial septal defect
cleft uvula

Cutie pie!!!

Listed: Aug 2017

$1,071.20 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 early 2015
significantly premature child, post-haemorrhagic obstructive hydrocephalus, chronic bronchitis, psycho-motor and physical development delay

Listed: July 2017

The boy has greyish-brown eyes and brown hair. The boy smiles a lot, he likes contact with other people, is interested in toys, likes to be outside, enjoys taking bath. When the boy lays on his stomach, he tries to raise his head and hold it for a short time. He eats well porridge or root vegetables with meat, he is spoon-fed. Mostly is seated in a specialized chair with head positioning.

Physiotherapist: tone imbalance. Slight spastic distally, active reflexes, weak torso; Weak head and torso control in all positions against gravity. In lying down on the back position the head is turned to the right, turns to the abdomen without lifting his head from the surface. The head in comparison to body proportionally large. Poor attention and motivation persistence. Interested in flashing, scintillating texture items. Emotionally labile. The development dynamics is minimal.

 

$2,016.10 has been donated towards the cost of my adoption!

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

Boy:  2015

Listed: June 2017

Titus has a congenital cardiac malformation, specifically an intra pericardial septal defect with volume loading of right cavities.  He has also been diagnosed with atactic cerebral palsy and a moderate mental delay.  Titus enjoys holding toys and reaches for a toy if it is out in front of him.  He is able to sit without support and stand up with support.  He smiles and waves his arms and legs when excited and expresses excitement when he hears sounds he likes.  Titus enjoys listening to children’s songs.

*** 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