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Angela

Girl, born 2009
PRC
congenital hip dislocation; mild to moderate delays

Listed: June 2019

Angela is smart, cute and active, and has dimples when she smiles. She gets along well with other kids, and is willing to share food and toys with other kids, willing to do something within her power. She has good physical quality, seldom gets sick, and she is an obedient and cute girl.

From an adoptive family who met her: she was very sweet. She leaves each day to go to regular school in the city. She just finished 2nd grade. She said her favorite class is music class. She walks with a slight limp but gets around very well. When we were visiting she was helping take care of some of the severe needs kids in her class. She seemed shy but she did talk to our interpreter a fair bit.

Additional photos available.

$900.00 has been donated towards the cost of my adoption!

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

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Able

Boy, born 2012
PRC
Down syndrome

Able is a cute little boy who loves to laugh and play games with balls. Able’s caretakers say that he is strong and that he has a lovely smile. Able can walk independently and he has strong imitating abilities. He can dance to the song of ‘Do Re Me’ following the teacher and can take initiative to help his teacher put garbage in the correct place. Abel also helps the other children to put on shoes. Able is always abiding the rules. If there are children who leave their seats in class, Able takes them back to their seats to sit well, and then seats himself. One time in class, Able’s teacher was singing and doing roll call, and another child in class was not concentrating or sitting well … Able went to him and strictly asked him to sit well.

Able can go up and down stairs, throw a ball, and ride a tricycle. Every morning, Able carefully comes down the stairs for exercise. Sometimes he is far behind the teacher. The teacher will squat down, spread her arms, and give a come here sign. Able will then happily run to the teacher’s open arms. Able can doodle with a pen and can put a missing piece of a toy back together.

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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!

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Ravi

Boy, born 2009

Listed: June 2019

Congenital chromosomal condition

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

$13.50 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!

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April

Girl, born 2007
PRC

April seems to be so joyful.  She has ready smile and laughs easily and when she laughs you can see her dimples.  She attends primary school and is on the same level as her peers. For more information on the sweet girl please inquire, for agency contact information.

 

$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!

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Kennedy

Girl, born 2009
PRC
Down syndrome, Congenital heart defect (repaired)

Listed: June 2019

Sweet, adorable Kennedy is a “girly-girl” who just needs her family!  Kennedy has Down syndrome as well as CHD that was repaired in 2011. Kennedy now lives in a family home with 4 other children. She is excited when seeing others and will run over and hold their hands and walk with them. She loves to sing songs and help her teacher hand out snacks. She can walk and run, and walk the balance beam. She loves to “play house”, helps others, and has good self-care skills.

$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!

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Xaria

Girl, born 2010

Congenital hydrocephalus
flail legs
Severe mental retardation
Optic atrophy

Listed: May 2019

From a family that met her April 2019: She was timid and scared of strangers. She has stunning behaviors and needs to be seen by a nutritionalist because she is anemic. She cried when they took her away from us. She is smart, but in her own world a lot. She knew when it was lunch time and kept looking towards the door where they served the food.

She is tiny and beautiful.

$360.00 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!

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Sonny

SonnyBoy, born April 2007
PRC
Post-op Cleft lip / Cleft palate, Deaf

Listed: April 2014

Sweet Sonny is post-operative cleft lip and palate and deaf. Sonny is generally a happy boy, but will cry when he feels wronged. The agency staff observed that he had good interaction with his caretaker. He attends a boarding school for deaf children. He likes doing math problems. Sonny is often bullied by a group of girls, but does not fight back. His caretakers say he shuts down when he is angry. His cleft lip and palate have been repaired. He has good physical and mental development. He can make sounds to communicate and is very independent. He is an affectionate and cuddly little guy!

Update 2019:  Sonny is now 12-years-old! He is athletic and he loves to play sports – especially basketball! He is pretty good at table tennis, too. Sonny’s nannies say he is very outgoing and he makes friends easily. He is a polite young man and he will often help his nannies.

Sonny goes to school outside of his orphanage where he learns math, art, and science. He is focused and actively participates in his classes.  Sonny is deaf but he has found ways to adapt. He knows sign language and he can also communicate by using body language. His nannies usually communicate with him by using body language or writing things down.

*** 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 ***

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Mateo

Boy, born 2010
PRC
Down syndrome

Listed: May 2019

Mateo is a smiley, outgoing, responsible, and very loving boy, with Down syndrome, a right eye sty, and a right undescended testicle. Mateo came into care around three years of age and he has been living in a foster family for quite some time. Since he entered the foster care program, Mateo has made big gains! His foster mother says he is a smart kid and always takes the opportunity to talk about his merits. She works hard with him in order to improve his daily living skills and independence. Mateo likes chatting with people and playing with other kids. He really enjoys dancing and singing too! He is a good helper around the house and he loves taking care of his younger foster siblings, some of whom he has already had to say goodbye to. Mateo is also said to be a good student, who likes talking to his classmates and participating in his classes. He has learned to recognize some simple shapes and some characters. He can also count to 50 and write his full name. Be sure to watch Mateo’s videos to see how well he interacts with other kids and how well he’s doing in school with counting, following instructions, and dancing. We hope that Mateo’s forever family will fall in love with his bright eyes and magical smile and that they will bring him home soon!

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

There’s a $2000 agency grant available for Mateo with his current adoption agency.

$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!

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Chrissie #

Girl: 2016

Listed: 05/2019

Special Needs: Spina Bifida, hydrocephalus- shunt has been placed

Chrissie has Spina Bifida, which impacts her lower limbs. She received a shunt for hydrocephalus. She has experienced recurrent UTIs. This is monitored and treated, as needed.  Chrissie recognizes familiar people and enjoys interactions with staff. She can hold her head up and roll from back to stomach and stomach to back. When asked about her, a caregiver said that she is very tender, likes to cuddle, laughs, and enjoys attention from adults. She makes sounds in an attempt to communicate and responds to singing by making humming sounds to “sing along”.

More 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

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Mayra

girl, born 2017

Primary pulmonary hypertension
Disorder of brain, unspecified

 

$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!

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Nicolette and Oksana

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

$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!

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Grace

Grace RK Girl, born June 2010
PRC
Cleft lip and palate; congenital heart defect (post-op)

Listed: January 11, 2016

Grace was abandoned by the train station when she was ten days old and has been living in an orphanage ever since. Grace was born with a cleft lip and palate, for which her first surgery will occur in May. She also had a congenital heart defect which was corrected this past summer. She does not take any cardiac medication but she sometimes pants and her lips become blue after strenuous exercise so her cardiac issues may not be fully resolved.

Grace is reported to have normal intelligence, potty trained, and she walks and runs just fine. She dresses herself, speaks in 3 – 5 word sentences, likes to sing and play games with other children.

Update from 2016: At 6 years old Grace enjoys looking at books, playing with her friends and has a favorite stuffed toy. She has great self help and fine motor skills, she can dress herself, including jacket and shoes, she can draw lines and shapes. She is an extroverted girl and she really enjoys playing games with her peers. She has many favorite foods, dumplings, noodles, fruit and many more. She had a surgery to repair her cleft lip already, but her cleft palate has not been repaired yet. She studies preschool, she can sing, dance, draw, string beads, and put clothes on dolls. Her upper limbs are flexible, she can walk and run, but not very steadily. She is active and gets along well with other kids,and often helps other younger kids.

$4,092.30 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!

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Leena

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.”

$1,014.45 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!

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Bradlee

Boy, born 2008
PRC
beta thalassemia major

Bradlee is a sensible and well-liked boy, born in August of 2008, who gets along well with the other children in his school and orphanage. He’s not always serious though, as he’s up for a good laugh anytime! Bradlee started attending school at the orphanage in September of 2015. He’s been taking language arts, math, art, music and PE. Bradlee’s teachers say he’s a good student and participates in class. At the end of the first semester of school, he received the “Star of Good Behavior” award! Bradlee is independent with dressing, bathing, and making his bed.

An adoptive mama and advocate has met this child, who she called Brett, and wrote this post about him: https://adoptingthalassemia.com/2018/04/19/smiley-brett/
When admitted to the orphanage Bradlee was initially diagnosed with a heart defect, but later ultrasounds showed it resolved on its own. Bradlee was born with beta thalassemia major and currently receives blood transfusions every two months, as well as chelation medication to treat iron overload.

It is clear Bradlee isn’t getting the care he needs or would get here due to the frontal bossing you can clearly see in the forehead area. If untreated or treated improperly, beta thalassemia major can cause the bone marrow to expand. Bone marrow is where most of the blood cells are produced in the body. The bone marrow expands because it is trying to compensate for chronic anemia. This abnormal expansion causes bones to become thinner, wider, and brittle. Affected bones may grow abnormally (bone deformities), particularly the long bones of the arms and legs and certain bones of the face. When facial bones are affected it can result in distinctive facial features including an abnormally prominent forehead (frontal bossing), full cheek bones (prominent malar eminence), a depressed bridge of the nose, and overgrowth (hypertrophy) of the upper jaw (maxillae), exposing the upper teeth. The affected bones have an increased fracture risk, particularly the long bones of the arms and legs. Some individuals may develop ‘knock knees’ (genu valgum), a condition in which the legs bend inward so that when a person is standing the knees will touch even if the ankles and feet are not. Bradlee desperately needs to find a loving family soon- access to good medical care will be life-saving and life-changing for him!

There is a $2,000 agency grant for Bradlee’s adoption with his current adoption agency. The Cooley’s Anemia Foundation is also giving a $1,000 grant for any child with transfusion dependent thalassemia.

$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!

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MaryKate

Girl, born 2007
PRC
beta thalassemia major

MaryKate is a sweet, spunky, sensible, talkative, and optimistic girl, born in December of 2007. She gets along well with the other children and she enjoys playing aeroplane chess, singling, dancing, and building things with Legos. She does not enjoy running. MaryKate is very responsible and mature for her age. She likes to help her caretakers and teachers. She is independent when it comes to her self care. She can be a little shy at first, but quickly warms up. Many adoptive parents and advocates who have met MaryKate adore her and recall her to be sweet and smart. MaryKate communicates and answers questions well. She attends school at the orphanage and can recite poetry, do addition and subtraction problems, and sing the 26-letter alphabet song in English. MaryKate is obedient and does well in math, reading, Chinese, and English. Her favorite foods are chips, chocolate, and cake, but she also likes grapes, apples, and bananas. She has been to Disney in 2015 and absolutely loved it! She loves Mickey Mouse and hopes to one day be able to go to Disney again!

MaryKate was born with beta thalassemia major. She has been getting transfusions, but not nearly as often as she should be. She is also in great need of iron chelation medication. Her file mentioned a heart defect- VSD as a baby, but it likely resolved on its own as it has not been brought up since. MaryKate would love a family of her own and she desperately needs access to regular transfusions and chelation medication. A family for MaryKate will change her life, but truly save her life too!

Videos available!  A specific agency has a $1000 grant available for MaryKate. The Cooley’s Anemia Foundation is also giving a $1,000 grant for any child with transfusion dependent thalassemia.

$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!

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Ivey #

Ivey
Birthday 2015

Listed: May 2019
Diagnosis: Turner Syndrome

 

Ivey currently lives in a group home for children with special needs and there are no other children her age in the home. She has delays in all aspects of her development. She was born with a heart condition that was surgically corrected. She still takes heart medication and sees the cardiologist for check-ups.

She is also currently on a dairy free diet. The doctor has indicated that milk and dairy products should be slowly reintroduced to observe her tolerance level. An optomologist diagnosed her with a vision impairment, but she does not have glasses or any corrective measures at this time.
Ivey can sit up, pull to a stand and walk around her crib holding on to support. She interacts with toys, but doesn’t know how to play with them appropriately due to lack of instruction. She says a couple of short words and babbles/makes sounds. She makes eye contact, tracks with her eyes, and will interact with a mirror and other toys that interest her.

*** 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

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Molly May #

Molly May

Birthday: 2015

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

 

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.

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*** 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

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Duncan

Boy, born 2009
PRC
beta thalassemia major

May 2019 Written Update:His mental ability is similar to other kids of the same age. He has thalassemia and needs blood transfusion every month. He has a good personality. He is quiet. He listens to the staff, and likes reading, painting, singing, and playing chess. He is well behaved. Duncan has no delays with gross motor or fine motor skills. He attends school. Duncan has a close friend at the orphanage. He knows how to care for others. His social skills are good and he gets along well with others.
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“I love observing others in a big group of people and seeing others happy makes me happy. I am an easy kid who doesn’t need much to be entertained. I just like holding hands and feeling close to people. I’m a total lover, not a fighter! I always listen to what my nannies ask of me and I obey with a smile on my face. I’m gentle with my friends and treat all my belongings with care. People who know me describe me as sweet, shy, loving, happy, kind, and as a good listener.” This was written by volunteers who have gotten to know Duncan well over the years. What a gem of a kid! And don’t get us started on that smile….that smile that pretty much never leaves his face!

Duncan was born in January of 2009 with beta thalassemia major and is transfusion dependent. He needs a blood transfusion approximately every 3 weeks and he receives iron chelation daily. He is easy-going, obedient, and very happy. Unfortunately, Duncan has not been able to attend school outside of the orphanage due to his needs, but does receive schooling inside the orphanage. He knows how to count and can draw, color, and sing songs. Duncan is a polite boy who gets along well with all of his friends. A forever family and the medical care Duncan could receive in the United States would be life-changing for this precious boy!

VIDEOS:
https://vimeo.com/maaspecialkids/maa-duncanupdate
https://vimeo.com/maaspecialkids/maa-duncanupdate2
https://vimeo.com/maaspecialkids/maa-duncanupdate3
https://vimeo.com/maaspecialkids/maa-duncan

There is a $4,000 agency grant for Duncan’s adoption with his current adoption agency.  The Cooley’s Anemia Foundation is also giving a $1,000 grant for any child with transfusion dependent thalassemia.

$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!

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Duncan

Boy, born 2005

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

 

 

$32.00 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!

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Hope

Girl, born 2004

Arnold-Chiari syndrome
spina bifida with hydrocephalus
chronic kidney insufficiency- 3rd stage
spinal bladder
flail legs
congenital hip dislocation
chronic interstitial cystitis

Available in June 2019!!

Everybody who ever met this girl fell in love with her immediately. She is pure love and kindness!

She needs a family who will be able not only love her (which she deserves!) but to provide her with qualified and probably expensive medical care.

$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!

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Sawyer #4-5

Age 9; 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 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

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Stan #

Boy, age 10
cognitive delays; hypothyroidism

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

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Graciella

Girl, born 2015

Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
Other specified congenital malformations of brain
Congenital malformation syndromes predominantly associated with short stature
mixed specific developmental disorder
spastic tetraplegia
Congenital malformation of optic disc

$967.90 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!

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Nora

Girl, born 2013

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

Listed: Aug 2014

 

$8,535.68 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!

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Falconn

Boy, born 2013

Cerebral palsy

Listed: April 2019

 

 

$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!

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Robert

Boy, born 2012
H-C
Cerebral palsy, global developmental delay, microcephaly

Robert is a sweet little boy who loves to smile and laugh. His laugh is contagious and makes you laugh. He loves to play outside and swing. He also likes the zipline. He loves to be a big brother and is sweet with little kids and with babies. He loves to make babies laugh and loves to hold them. He can say a few words but only does it in front of people he knows well and is comfortable with. The words he can say are pretty clear. He will shake his head no if he doesn’t want something or yes if he wants something. He is getting better at responding to directions. He is potty trained. He loves to sit on your lap and cuddle.

Video available.

$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!

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Wendy

Girl, born 2017
PRC
Neonatal brain injury, hypothyroidism, rickets

Two year old Wendy is close with her caretakers and likes being held by them. Her file states that she has sharp reaction to outside stimulation such as sound source and visually following objects. She likes being teased, giggling, and can turn over onto her stomach. Her file indicates that she communicates her emotions by facial expression and reacts to being called.

$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!

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Cynthia

Girl, born 2013
PRC
Down syndrome

Cynthia has been diagnosed with Down syndrome, esotropia of both eyes, and nystagmus. She is described as active, with a ready smile. According to her report in 2016, she can walk stably, crawl, play on big toys outside, and throw a ball with purpose. Her file says her speech is delayed, but can make simple noises to express her emotions. Her file states that she enjoys sunshine, loves playing outside, running, jumping, and laughing. Cynthia’s file says she likes holding her caretakers’ hand and dancing.

*** I am eligible for an additional $5,000 Grant!  Through the end of 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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!

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Jonah

Boy, born 2013
H-C

Jonah is a joy to be around. His smile and laughter lights up the room, especially when he really gets going. He loves to cuddle, get kisses, and to be included on what is going on around him. He has some breathing issues and breathes very loudly but does not regularly use any thing extra to help him breathe. Jonah has struggled with gaining weight his whole life, but lately has been doing better. In December of 2017 he had g-tube surgery and in December of 2018 he had a nissen to help prevent him from vomiting. He is unable to tolerate large amounts of food at a time so he is continuously fed with a feeding pump through his g-tube with a medical formula. Now that he has a nissen he is able to keep more inside him rather than vomiting it back out. Jonah has very high tone but is on medication to help with that as well as goes to therapy multiple times a week for stretching, massage, exercises, and time in the stander.

Jonah can hold his head up on his own, but isn’t steady and will often fall backwards or forwards. He can recover from this on his own but often needs encouragement and occasionally a little help. Jonah can roll from his front to his back or from a side to his back or his front, but cannot yet turn 360 degrees without help. He can also scoot around a little bit whether he is on his back or his stomach. On his stomach he can lift his head up to look around, but does not do so for long periods of time. Jonah needs help keeping his arms in position for supporting his upper body on his elbows. He cannot yet fully sit on his own, but will do most of the work when in a sitting position. Jonah can hold things in his hands, but does not do so for very long. He currently uses a special tomato chair for sitting as well as his wheelchair when needing to be mobile.

Jonah has been going to preschool for just over a year and has been working on communicating and making more and more choices. He can use a yes/no board or make choices between two things by touching the item or card or by looking in the direction of what he wants. He is learning to read just like most five and a half year olds are.

Jonah needs a family who can advocate for his care and love him fiercely. He needs access to more doctors than he has available in the country he is in to address and test some of his needs that cannot be done here.

$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!

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Sasha

Girl, born 2011
H-C
Developmental delays, deaf, VSD, history of seizures

Sasha is a spunky, free spirited 8 year old. She has developmental delays, but is very curious about her surroundings. She is constantly walking around and picking things up to examine them, play with them, or chew on them. She loves to interact when you mimic the things she does as well as being tickled. She laughs and has a fun sparkle in her eye. She also loves watching and interacting with herself in the mirror.

Communication with her is limited since she is deaf and has yet to learn sign language. She understands some signs such as “sit” and “no”, but has yet to repeat signs back to us such as “more” and “food.” Sasha continues to work on those both in her foster home and with her teacher at school, but it has been very slow progress. She also has a VSD (hole in her heart), but her body has learned to live with it well. She has been taken off all her heart medicine, and seems to be doing well so far. She has seen doctors about surgery, but none has been needed so far. She is also on medication for seizures, but under the current combination of seizure medication, she has not a had a seizure.

$5.00 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!

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Barrett

Boy, born 2009
PRC
Cerebral Palsy

Barrett is described as a cute kid with a ready smile. He is said to be able to express himself and speak clearly. Because of his CP he needs help with many of his daily needs. He is not able to walk so must use a wheelchair.

His best friend was recently adopted and he hopes he can also be adopted soon and get the help he needs to live as full a life as possible. Could you be his parents and welcome him into your family?

$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!

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Will

Boy, born 2011
PRC
Down syndrome

His caregiver’s description of him says it all! “He is active and cheerful; has a ready smile; will smile at you if you call him; his smile is moving and makes you feel warm; docile; does not lose temper freely; will be comforted easily; shy in front of strangers; can dance with music; adorable.” Will was born with Down syndrome and no other known health issues.

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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!

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Frederik

Boy, born 2009

HIV
Hepatitis C

 

 

$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!

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Wilson

Boy, born 2009

Muscular Dystrophy

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.

$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!

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Anney

Girl, born 2013
PRC
Cerebral palsy and epilepsy.

Anney’s file states that she is a cuddly girl who loves being held by her caretakers. Her file says she loves to laugh and clap her hands when happy. Her pictures capture her bright and happy smile that light up a room.

$20.00 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!

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Kai and Konner

Boys, born 2008 & 2010
PRC
Blood condition

Kai and Konner were raised by their grandparents and brought into care four years ago.

Elder brother Kai is enrolled in second grade and known as a playful, clever boy who learns quickly. He is learning basic addition, subtraction, multiplication, division, reading and telling time. He enjoys eating snacks and seafood. There are no concerns with his motor development and Kai enjoys various sports, skipping rope and running outdoors. His favorite activities include remote controlled toys and video games. It’s noted that he gets along well with the other children, assists the caregivers, and has good self-care skills.

Younger brother Konner is known to be stubborn at times but playful. Konner avoids candy as he is afraid of tooth decay, but enjoys fruits, sausage, corn and seafood. There are no concerns with Konner’s motor development. He can help with chores and has good self-care skills. He is enrolled in preschool and learning basic math problems, colors, shapes, reading cartoon books and enjoys completing his homework. Similar to his brother, Konner likes to be outside playing in the park, running, skipping rope and playing video games.

The boys take daily medications & have no other health concerns.

Eligible families may qualify for an agency grant, in addition to a $15,000 Child-Specific Grant (exp. 5/15/2019) from the agency.

$10.80 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!

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Philip

Boy, born 2011
PRC
Down syndrome

Listed: Feb 2019

Philip’s file shows he likes interacting in school and playing with his peers. Philips file says that his favorite toys are balls and toy cars. According to his file, he can walk freely on a flat floor, run, and jump.

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$27.10 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!

, , ,

Melody

Girl, born 2013
PRC
Down syndrome

Listed: Feb 2019

Melody is a little peanut who couldn’t be cuter! Melody knows the nanny who takes care of her and is very close to her. She is described as smiley, shy, and energetic. She recognizes the other children in her room and enjoys playing with them. Melody feeds herself with a bottle and likes to eat crackers too. She is afraid of strangers, but will actively ask for hugs from the nanny who cares for her. Being held is one of her very favorite things! Melody will let her nanny know she is not happy if the nanny holds another child first or is too busy to hold her. Melody reacts when called and can understand simple instructions. She is now saying some single words and will say a sentence every once in a while, but it is hard to understand. She is finally walking and appears very small for her age.

Agency staff have met her multiple times and note that she is sweet, has a precious laugh, doesn’t cry much, is often happy, and is a good sleeper. One of our traveling families even had the blessing of meeting her last year. Melody will surely bring so much joy to her forever family!

The agency has several photos — and videos!  NEW VIDEO (make sure to see her beaming smile when she finally gets picked up at about the 41 second mark); and 2018 VIDEO from when a traveling family met her.

Melody’s current adoption agency has a $5000 grant for her adoption!

*** I am eligible for an additional $5,000 Grant!  Through the end of 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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!

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Jayla

Girl, born 2013
PRC
Down syndrome

Listed: Feb 2019

Jayla is an adorable little girl! She loves candy and has a good appetite! She likes to listen to music and play games. Jayla is said to get along well with the others around her, though she is a true introvert who prefers to play alone. At one year old, she could roll over and sit with support. By two years, she could crawl, sit on her own, and feed herself finger foods. She was babbling to the other children. As of November of 2017, she could walk while pushing a rolling toy and her hands are flexible. Her favorite activity is playing outdoors and she enjoys toys that make noise. Jayla has a couple new pictures and a written update (Feb 2019). She definitely needs a loving family and access to resources she needs to thrive.

We hope Jayla’s family sees her soon!  Her current adoption agency has a grant of $5000 for her adoption!

*** I am eligible for an additional $5,000 Grant!  Through the end of 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$5.00 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!

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Ishmael

Boy, born 2013
PRC
Down syndrome

Listed: Feb 2019

Ishmael is a quiet, well-behaved little boy who loves to play outside. He can stand for a long time with his hands holding something for support, feed himself with his fingers, and he imitates simple words. He wraps his arms around his caregiver’s neck as they move around the room. Ishmael is described as a sweet boy who gets along well with other children.

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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!

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Falcon

Boy, born 2010

Nephritic agenesis, one sided
light degree mental delay

 

Listed: Feb 2019

$19.70 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!

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Cassandra + 2 Sisters

Girl, born 2016

Video! 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

She has two sisters, born 2014 & 2015 both are healthy.
These 3 girls MUST be adopted together!

$166.50 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!

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Xander

Boy, born 2012
PRC
Down syndrome; physical developmental delays

Listed: Feb 2019

This little cutie pie is Xander, who was born with Down Syndrome. He came into care when he was about six months old, and joined a foster family when he was 9 months old. He is especially close to his foster uncle. Xander can walk unsupported and ride a trike. He loves to play with others and follows instructions. Xander loves to play outside.

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$145.00 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!

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Jennie

Girl, born 2011
PRC
Down syndrome

Listed: Feb 2019

Precious Jennie needs to find her family! Just watching her video makes your heart yearn to bring her home! Video (pw is jenny)

Jennie was born late 2011 with Down syndrome. She was met by an adoptive mama, who I am sure would love to talk to anyone interested in this sweet girl! Jennie’s photos and video show her darling personality. She seems so outgoing, funny and affectionate! She will be the perfect addition to any family!

*** I am eligible for an additional $5,000 Grant!  Through the end of 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

 

$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!

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Garrison and Hamilton

Boy, born 2014
healthy

boy, born 2012
congenital stenosis of larynx
hearing loss (uses hearing device)
hypospadias

These siblings must be adopted together!

From a family who met them Feb 2019: They are very sweet and seemed happy. They were kind to each other, happily posed for photos, and answered questions. They seem very healthy and I did not notice any obvious developmental delays.

$225.00 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!

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India

Girl, born 2014

Cerebral palsy with severe legs dysfunction
fetal alcohol syndrome
crossed eyes
open oval window

She can walk by herself and understands simple instructions.

$4.95 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!

 

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Paulie

Boy, born 2013
PRC
Down syndrome

Paulie is doing his best to grow in all aspects of his life. Paulie can sit up for a few minutes and he is learning transitional movements from sitting to crawling, moving forward on his stomach and using his arms and legs (one of the steps towards crawling). Paulie doesn’t talk yet, but is headed in that direction. He makes recognizable sounds to communicate. These include clicking his tongue to show happiness. This is a new sound of self-expression to communicate and we are excited because it is an effort he makes towards speech! He does not speak words at this time, but he is using more vocal sounds to express joy or unhappiness. Paulie’s fine motor skills are satisfactory. He enjoys playing with toys that hang on strings or toys that can dangle. Paulie has Down Syndrome but he is working hard to be all that he can be. He has great enthusiasm for life and an even greater smile! Could Paulie be a part of your family?

Paulie’s agency has a $1500 grant for his adoption!

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$20.00 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!

, , , ,

Wayde

Boy, born 2013
PRC
Down syndrome, Congenital heart defect

Wayde’s file indicates that he is a shy young boy who doesn’t like his picture taken. So much so, that he will cover his face if he see’s a camera. His file states that he had difficulty walking at first, but now he can. His file says he loves all types of food, he even will eat chili peppers. Wayde’s file shows that he loves playing so much that if he could, he would stay up all night to play. According to Wayde’s file he is nonverbal.

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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!

, , , ,

Zelda

Girl, born 2013
PRC
Down syndrome

Listed: Feb 2019

Zelda’s file says she is an active young girl, who is extroverted, and has a ready smile. Zelda’s file indicates that she likes to play with others, watch TV, and listen to music. According to her file, she has normal motor function; she can sit, crawl, stand steadily alone, and walk while holding railings. Her file states that she is non-verbal, but will try to imitate words. Her file shows that she can distinguish who is a stranger and who she knows.

*** I am eligible for an additional $5,000 Grant!  Through the end of 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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!

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Journey

Girl, born in 2013
PRC
Down syndrome, congenital heart defect- PDA

Listed: Feb 2019

Journey is a beautiful little girl with a warm smile! Journey is not a picky eater and can feed herself, but won’t necessarily eat as much as she should so she does get some help to make sure she is eating enough to fill her up. She really likes milk and fruits. Journey can walk stably and can go up and down stairs using the handrail. She is said to be calm and cautious. Sometimes if she thinks the stairs, for example, are dangerous she will sit on the stairs and move down with her hands and feet. Journey’s favorite toys are toy dogs and the red plasma car. Because she doesn’t speak much, Journey has trouble expressing her needs and does need some assistance with toileting. She communicates with her gorgeous eyes and through gestures and actions. When people greet her, Journey smiles happily. Journey is an affectionate little girl. For a period of time, she would go down one set of stairs to the office on the second floor when the caretaker was not looking. She would appear suddenly behind one of the workers there and pat the worker. That worker would sometimes then go visit her activity room and Journey would come forward immediately and hug the worker tightly. Her hugs are said to be so tight they are like bear hugs. We can’t wait to see what lucky family is going to be blessed to not only have this little girl in their home and family, but to see those smiles and receive those bear hugs every day!

Video 1 & Video 2

Journey has a $1,500 agency grant for her adoption with the agency who currently holds her file. Other grants may be available based on the adoptive family’s circumstances. Agency grants are awarded as agency fee reductions.

*** I am eligible for an additional $5,000 Grant!  Through the end of 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$203.00 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!

, , ,

Shay #

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

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Cindy

Girl, born 2013
PRC
Down syndrome, CHD

Darling Cindy was born June 2013 with Down syndrome, CHD, and a left wrist deformity. She loves to play hide and seek, and when her caretakers play with her, she is said to laugh loudly and smile.

*** I am eligible for an additional $5,000 Grant!  Through the end of 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

 

$5.00 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!

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Vivi

Girl, born 2013

down syndrome
condition after surgery of atriventricular communication

Listed: Jan 2019

 

*** I am eligible for an additional $5,000 Grant! Through the end of 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$6.30 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!

, , ,

Hazel Mae

Girl, born 2012
PRC
Down syndrome

Listed: Jan 2019

Hazel is an adorable little doll! She has been a part of a foster family and enrolled in a sponsored school called the Grandma program. She is able to go up and down stairs by herself, skip and stand on one foot. She can draw lines, knows big and small, can button and unbutton her clothes, and wash her hands by herself. She is said to be fond of imitating, listening to music and playing with toys. She has a ready smile and gets along well with others. Her favorite activity is watching TV, and her favorite toy is a rag doll. Hazel is ready to be the joy of her new family!

*** I am eligible for an additional $5,000 Grant!  Through the end of 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$247.50 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!

, , ,

Sabrina

Girl, born 2016

sequelae of inflammatory diseases of central nervous system
epilepsy unspecified
other ill-defined heart disease
optic atrophy; myopia; strabismus
delayed development following protein-energy malnutrition
chronic tubulo-interstitial nephritis unspecified

Listed: Jan 2019

$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!

, , , ,

Nolan

nolan-2016Boy, Born September 2004

Nolan is such a handsome boy!  He needs a loving family!

Listed: August 4, 2010

From his medical records:  long-term effects of some early trauma (right-side hemiparesis), mild mental delays, seizures, flat feet, farsightedness

He has fine motor skills, understands everything, he talks but it is hard to understand him.  Nolan is very physically active, happy and cooperative, friends with other children.   A family living in the states who has 3 children, one who is significantly disabled, has taken a special interest in Nolan but cannot add Nolan to their own family due to the needs of their children. Per the family, “Nolan’s eyes and smile caught our heart. He is close in age to one of our own children. We hope this gift will enable someone to give Nolan the chance to live outside an institution.”

A family must have a completed homestudy to commit to Nolan.  Due to the size of Nolan’s grant, 50% of grant funds will be available upon receiving a travel date, and the other 50% upon passing court.

Nolan has a grant of $19,597.50 available towards the cost of his adoption!

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Shaw

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.

$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!

, , ,

Quincey

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.

$477.00 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!

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Daniela

Girl, born 2004

Multiple malformations of the central nervous system
spina bifida
internal subcompensated hydrocephalus
lower flaccid paraparesis
convulsive syndrome
anus atresia

Listed: Jan 2019

$9.90 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!

, , ,

Sally #

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

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Jamila

Girl, born 2011

Listed: Jan 2019

Jamila is listed as having microcephaly as well as hemiplegia on the left side of her body.

She is a vibrant little girl who is full of life and loves being around others. She is active and loves to go on walks around the neighborhood, jump on the trampoline, brush her baby doll’s hair and play hide and seek. She is able to move around independently and can run and walk with ease. She does slightly drag her left foot as she moves around but manages well despite this. Jamila does receive physio therapy where her leg and foot are stretched to help with movement. She attends an on site school 5 days a week where she participates in circle time as well as class time with her teachers. Jamila is able to point to named colors and match colors correctly. She is also working on improving her fine motor abilities through activities such as using the peg board, stringing beads, playing with play doh, and cutting with scissors. Jamila also enjoys finger painting and all types of water and sensory play. She has a very strong bond with her caregiver and good relationships with the other children in her home. Jamila is non-verbal, only able to say “hi” to others to communicate. She does know some signs and is working towards learning more. She can sign to communicate that she wants water and also to ask for help. She has a beautiful face, her eyes, smiles, and adorable dimples steal the hearts of all that come around her. She is a loving girls who seeks out attention and affection from others and would thrive in a family.

$225.00 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!

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Noah

Boy, born 2013
PRC
Down syndrome, CHD

Listed: Jan 2019

Noah is a happy and active little boy, who is just turning 4 years old! Noah was born with Down syndrome and a heart condition, which he had surgery for shortly after arriving at his orphanage. The surgery was successful, and he made a lot of progress as he recovered! Noah loves to roll around on the play mats and play with his toys! He will often hold a ball in his hands and study it while he plays.

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$5.00 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!

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Pippy #

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.

Pippy has a $1,500 agency grant for her adoption with her current agency (Jan 2019). Other grants may be available based on the adoptive family’s circumstances. Agency grants are awarded as agency fee reductions.

Pippy’s agnecy needs a family with an approved home study to be able to move forward with adopting her. If you have an approved home study or a home study in process and are interested in adopting Pippy, please contact her 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

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Sam

Boy, born 2012
PRC
Down syndrome

Listed: Jan 2019

Sam is a shy child with a quick smile who gets along well with the other children. He enjoys playing with balls and swinging, and he likes to play hide and seek. Sam may be a budding musician; he’s shown a keen interest in the electric piano and laughs aloud at the sound when he plays the keys! Sam would benefit from a resourceful family that would be able to provide love, care, and support.

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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!

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Rhiannon

Girl, born 2012
PRC
Down syndrome, CHD (Congenital heart defect)

Listed: Jan 2019

An update from 2016: Rhiannon is a quiet, tiny girl, who appears quite small for her age, and very thin. She has a heart condition, which she has not had surgery for. The nannies say she eats a normal amount, so they are not sure why she’s so thin. When agency staff visited in April 2016, she sat up very stably and was alert, frequently nodding her head and rocking. Caregivers say she doesn’t often reach for toys, but she will react when the nannies make faces or tickle her. She can stand up with support from her nanny under her hands. In the baby walker she can move around very quickly! She will scoot around on her bottom as well to get around, but doesn’t crawl yet. So far she’s not babbling, just making sounds. She does turn to sounds as well.

*** I am eligible for an additional $5,000 Grant!  Through the end of 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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!

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Kristy

Girl, born April 2012

Cerebral palsy

Listed: Dec 2018

Kristy is a cheerful and lovable little girl. She has a deep connection to her caregiver and her face lights up with joy when her caregiver is around. Kristy enjoys snuggling and working on walking using either her walker or the parallel bars with her teacher. It is expected that one day she will become independent with walking using the support of her walker. She is diagnosed with spastic quadriplegic cerebral palsy. Kristy has moderate hearing loss and has a hearing aid to help her hear. Kristy does have some sensory issues which means she has difficulty keeping her hearing aid on for an extended period of time. Her teachers and caregivers work with her on keeping them on and helping her engage in fun activities. Kristy attends an onsite special school where she participates in circle time, sensory play, and individualized instruction. She also receives physio therapy 5 days a week. Kristy loves playing with scarves and waving them in the air to music. She also loves water play with the other kids in the house and laughs hysterically when splashing in the water.

Kristy would make a valuable addition to a family as she has so much love and affection to share with others.

Video available!

$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!

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Erica

Girl, born 2009
PRC
Down Syndrome, postoperative congenital heart disease, brain dysplasia

Listed: Dec 2018

Update (age 7):  Sweet Erica is as cute as can be!  Erica is a cheerful girl who loves to play – she plays well with other kiddos, but she is just as content playing on her own with some building blocks. She always looks at her creation afterwards and is so proud! Her nannies tell us she also loves to get her picture taken. When she sees someone with a camera she gets very excited and begins to pose for a picture – it is very cute!

Erica walks a bit slowly, but she can walk, run, jump, and go up or downstairs without any problems. She can say a few words and can understand what adults say to her. Her limb function appears to be normal and she can put on her shoes, socks, and pants on her own.  Please help Erica find her forever family!

*** I am eligible for an additional $5,000 Grant!  Through the end of 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$5.00 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!

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Marcel

Boy, born 2012
PRC
Down Syndrome, delayed motor development

Listed: Dec 2018

From March 2013:   Under the patient care and training, Marcel has more communication with others and the outside world, and he is interested in some toys. Sometimes when he is doing activity on the cushion, he will reach toys on the shelf when lying on back, and makes the toys make sound. And the sound can make him feel happy. He can also get up the objects and toys near hand, and the put them into his mouth, if he failed to get the toy he can move his body to get. He can follow rolling red training ball, and his sight follow the ball to turn. When lying on back he can raise up head for 2-3 seconds, when lying on back he can touch toys on the toy shelf.   Now he lives happily in this institute, and caretaker takes patient care of him and trains him and forms him some basic motion skills according to his growth. We hope that he can have a family. He is gentle, likes colorful toys.

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$108.00 has been donated towards the cost of my adoption!

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

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Humphrey

Boy, born 2012
PRC
Down Syndrome, Congenital heart defect

Listed: Dec 2018

From July 2014:  Humphrey is active and likes crowed places; he is obstinate and must do things he wants to do; when in our institute, the caretaker who is liked by him took care of him; in foster family, foster parents take care of him.

At 25 months old he could make many sounds; could call mama; could clap hands; at 26 months old: could point to or grasp ears when you ask him where his ears were; at 27 months old: we decided to look for a foster family for his better care and development; on May 9, 2014, the baby was officially admitted to foster family; the family liked him very much and bought him many new toys and clothes; the baby adjusted to new life soon; now he attends our rehabilitation trainings every day accompanied by his mom; he can imitate simple motions such as bird flying, clapping hands and raising hands; at 28 months old: through half a month’s training, he could stand with support steadily; he just will not step forward; during training, he always raise his feet naughtily to ask his mom to hold him.  The baby is adorable and willing to cooperate to do rehabilitation trainings. We believe through working hard together, he will make greater progress.

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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!

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Kraig

Boy, born 2012
PRC
Down Syndrome, congenital left cleft lip/cleft palate, and postoperative repair of congenital heart disease

Listed: Dec 2018

Kraig’s file was prepared in October 2016, when he was four. He is described as an introverted child who will also smile sweetly to his caregiver. He will play with other children, but cries loudly if they take his toys away. He likes an electronic keyboard and rubber ball toy, but will play with them less than five minutes.

Most recently, at the beginning of 2018, Kraig was at a foster home in a major city receiving medical treatment, but was recently recalled back to his orphanage due to new law in his country, in the Spring of 2018.

*** I am eligible for an additional $5,000 Grant!  Through 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$20.70 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!

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KENNA

Girl, born 2017

Sequelae of inflammatory diseases of central nervous system
Other hydrocephalus
Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
Optic atrophy
Nystagmus and other irregular eye movements
Atrial septal defect

Listed: Dec 2018

$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!

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Vincent and Wade & Siblings

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).

These children become available for international adoption in summer 2019

 

$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!

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Dena

Girl, born 2016

Tuberous sclerosis
Generalized idiopathic epilepsy and epileptic syndromes

Listed: Dec 2018

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

$472.50 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!

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Ollie #

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

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Palmer

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!