Boy, born 2010
PRC
hernias (repaired), anemia

Listed: August 2019

Zeke is 8 years old this year and goes to kindergarten. He has a pair of small eyes, but his eyes are bright. He is very clever. He can remember the knowledge taught by the teacher or by mom. He is an obedient child, is active. Every morning he helps mom to fold up a quilt, clean and take care of young sister; he helps sister to put on clothes and he is very diligent. He holds sister’s hands to go to school and helps sister to go upstairs when back home after school; he teaches sister to sing children’s songs, play games, draw and he watches carton with sister together; he puts food onto the plates of sister when having a meal; he is a little sweet guy and is so caring.  He speaks clearly.

Zeke gets along well with classmates in the class; they like to play with him. When his foster mom takes him to play outdoors, he always runs around mom and doesn’t let her out of his sight; he is naughty and adored. He loves sports, loves to run, loves to jump and loves small toys. He likes to take photos and is good at making pose; he always makes a handsome pose to ask mom to take photos for him.

Zeke is very clever. He loves to learn, to use his head and has good memory. He knows the knowledge taught by the teacher and is able to finish his homework alone; he would teach sister to draw and write after school. He is careful in learning; he also likes to play puzzles with sister and spell outs various patterns.

$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 2013
PRC
Congenital Heart Defect, neurogenic bladder

Listed: August 2019

Huxley is introverted, fairly quiet, smart and obedient. He’s shy and doesn’t have great communication yet. He doesn’t like to share with others and he will cry to get attention; if someone grabs his toy, he doesn’t know how to get it back and he only cries there. He has normal sleep and mainly has nutrition porridge.

At the age of 4 and a half, his gross motor ability is increasing, such as riding children’s bike, walking in a line, jumping with one feet and bouncing the ball; he also can help the caretaker to finish simple tasks. His language, understanding and expressions are all increasing; he is able to imitate animal’s sounds and actions.

$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!

Boy, born 2013
PRC
Limb differences

Listed: Aug 2019

The child understands simple words, sometimes the child will follow aunt to speak. Braxton can play in the activity room every day, the child likes playing with other children specially. He likes the blocks especially, but he can not play, so he looks at other children to play blocks, and he likes circle toy. If he wants the toys or other objects, he will shake his arms.

He is shy with strangers. Once he’s familiar with someone, he will move to them, he likes praise, and then accompany him.The child is very clever, sometimes he can help aunt to close the door, knows to call the names of other children who are in the same room with him.

$1,886.90 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!

Girl, born 2016
PRC
premature infant with very low birth weight, hydrocephalus (post-op shunt)

Listed: August 2019

When Minerva came she looked petite and weak, and was hospitalized for care and surgery. She has delayed physical development compared with children of her age, but after the operation her physical health is fairly stable and her motor ability improves day by day.  She is able to raise her head when lying on stomach, and turn over continuously. She likes to roll over to and fro on the mat best.  She is able to sit alone for a moment with both hands against the floor, even occasionally stand for a few seconds with both hands grasping the rail. Her muscular tension is higher, she can not coordinate and control her body well. If her name is called or someone talks beside her ear she is able to turn around her head to locate the source following the sound direction. The muscular tension of her neck has decreased obviously, therefore its turning range is much larger.

If you move a toy with bright colors slowly in front of her eyes she will follow the toy visually. She is able to grasp a toy and shake it to and fro with her hands.  She is an introverted and quiet baby, is able to lie alone for some time without noisy crying, but if she is made to practice sitting with her hands against the floor she will be very reluctant and cry aloud. Her crying is very loud and we can hear it from far away. She also likes to be cuddled by someone and her facial expressions and actions will be much richer while she is cuddled.  Her speech development is delayed. She is a light sleeper.

$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!

Girl: 2018

Listed: 8/2019

Special Needs: adrenogenital disorders, congenital anomalies, anemia, small weight at birth, chromosomal anomaly, syndactyly, developmental delays

We don’t know a lot about sweet Nelly yet, but the agency does have videos of her they can share with inquiring families. Nelly can crawl and can do so well. She loves scooting her way to toys she finds interesting. Nelly can sit up on her own. She enjoys attention and will sometimes interact with other children.

$396.90 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!

Girl: 2009

Diagnosis: Atypical Autism

Listed: Aug 2019

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

*** I am eligible for a $2,000 Grant! ***This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding.

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

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

*** I am eligible for a $2,000 Grant! ***This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding.

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

Siblings, born in  2006, 2008

Mason has a peanut allergy. Both children have delays

Listed: August 2019

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

Photos and videos are available through the agency

*** I am eligible for a $2,000 Grant! ***This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding.

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

Boy, born 2013
H-C
hydrocephalus

Listed: August 2019

Bennett is a very social child. Whenever he sees his friends, he eagerly greets them with a smile, a hug, and a “Happy Birthday!”

He had hydrocephalus as an infant that was treated with a VP shunt. The shunt was later removed but he still has macrocephaly. He does have a history of seizures which are very well controlled by medication. He receives physical therapy twice a week and has made tremendous progress over the past several years. He is fully mobile, can feed himself, and go to the bathroom independently. Bennett wears a helmet to protect his head. He has become fond of his helmet though because he can show off his headstand.

When he is not at home, you will often find him enjoying jumping on the trampoline, playing on the playground or going on a walk. He needs redirection often because he is always on the move. Although he is generally happy, he can get frustrated when people do not do what he wants to do or if he is being asked to do something he is not ready for.

Bennett’s favorite part of school is circle time because he likes to sing songs and answer ALL the questions even if his answer has nothing to do with what was asked. He understands and speaks English as well as his native language. He is known for reciting the four seasons in English quite well. At home, he loves to ask other people to dance and sing with him too. Bennett loves to make people smile!

$1,438.50 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!

Girl, born 2008

S. E. Asia (2)

Listed: July 2019

This silly and playful girl doesn’t like to be alone and prefers to be surrounded by friends. She likes to joke around and giggle. She has been to the beach and the waterpark and enjoys swimming. She loves chocolate milk. She is described as confident and independent by her caregivers.

Poppy has been diagnosed with Thalassemia and receives monthly blood transfusions. She has been in the orphanage her entire life. This silly girl needs a prospective adoptive family with excellent medical, educational, ESL resources, play therapy and have a good understanding of institutionalization and older child adoption.

$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!

Girl, born 2010

S. E. Asia (2)

Listed: July 2019

This sweet child gets along well with peers and with the older girls in the orphanage. She is described as empathetic, obedient, and enjoys giving and receiving hugs from her caregivers. She describes herself as fun, a responsible student, and she enjoys English and Art. She is afraid of snakes and frogs. She has had multiple placements in her life and has been diagnosed with ADHD and is taking medications. She would like a family of her own that includes sisters.

This sweet girl needs a prospective adoptive family with excellent educational resources including ESL support, and have a good understanding of developmental trauma, institutionalization and older child adoption.

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

Listed: July 2019

 

$1,331.73 has been donated towards the cost of my adoption!

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

Girl, born 2012
Down syndrome
CO-7

Listed: July 2019

Bria is a cute little girl, born in August of 2012 with Down syndrome and strabismus.  The agency has additional information; please inquire to learn more about making this adorable little girl part of your family!

Bria has a $2,500 agency grant for her adoption with the agency who listed her; additional grants may also be possible.

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

$1,586.99 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 2006
Cerebral palsy

Listed: July 2019
LA-E9

Mateo has been diagnosed with cerebral palsy.  He received physical therapy to help develop muscle tone and coordination.  He attends a local school and receives support from a private instructor.  Mateo enjoys using his iPad, being read to, and spending time outside.

The adoption agency has more detailed information on this child that they can share with potential families.

$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!

Girl, born 2012
Cornelia de lange syndrome

Listed: July 2019
LA-E8

Lucia has a diagnosis of Cornelia de lange syndrome, which causes developmental delays.  She continues to make great progress with therapy.  She enjoys playing with her favorite doll, and all food.

The adoption agency has more detailed information on this child that they can share with potential families.

$1,008.60 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!

Girl, born 2009
Blind

Listed: July 2019
LA-E7

Rebekah is blind, and has significant delays in speech and motor development.  She can easily become overstimulated.  She enjoys listening to music and receiving hugs from the “aunties” at her children’s home.

 

The adoption agency has more detailed information on this child that they can share with potential families.

$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!

Girl, born 2011
microcephaly, epilepsy, chronic malnutrition

Listed: July 2019
LA-E6

Marisol came into care at this home in 2014, and her physical and emotional health has improved.  Marisol enjoys playing with her dolls, going for walks, and drawing or doing art projects.

The adoption agency has more detailed information on this child that they can share with potential families.

$1,246.95 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, born 2010
Blind in one eye, autism

Listed: July 2019
LA-E5

James is receiving therapy to help him develop his communication and interpersonal skills.  He loves to swim, swing, and play with his special stuffed animals.  He loves chicken noodle soup, plantains, and anything sweet.

The adoption agency has more detailed information on this child that they can share with potential families.

$1,304.95 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!

Girl, born 2009
Cerebral Palsy, cognitive delays

Listed: July 2019
LA-E4

Diana was born to a teenage mother who felt unable to give her the attention and stability she needed.  Diana is unable to speak, but communicates non-verbally.  Diana enjoys being outside, bath time, and hand massages.

The adoption agency has more detailed information on this child that they can share with potential families.

$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!

Girl: 2010

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

Listed: 7/2019

 

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

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

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

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

*** I am eligible for a $2,000 Grant! ***This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding.

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

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.

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

Boy, born 2012
PRC
Down syndrome

Listed: June 2019

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 June 2020, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$31.50 has been donated towards the cost of my adoption!

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

Boy, born 2009

Listed: June 2019

Updated pic January 2020

Congenital chromosomal condition

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

From a family who knows him: Even though Ravi spends most of his days in the same bed, staring at the same ceiling, he’s fascinated by everything that goes on around him. He loves the rare walks he gets outside in the summertime and being held up in the window to watch snow falling in winter. He obviously recognizes his favorite people and cries when they leave. He cannot sit up on his own, and seems to get tired even when held sitting for long. But he scoots all around in his bed, very actively turning his head to where his feet should be, or the other way around to see and hear everything. He is completely non-verbal. Ravi really needs a family and a chance to get out into the world that fascinates him so much!

 

$180.00 has been donated towards the cost of my adoption!

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

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.

Listed: June 2019

$157.50 has been donated towards the cost of my adoption!

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

Boy, born 2012
PRC
Down syndrome

Listed: October 2017

Anderson is a precious little boy who loves outdoor activities like ball games. He can sometimes be active and lively and other times quiet. Anderson has strong imitating abilities. He tries hard to follow along with the morning exercises to music. Whenever it’s time to go outside, Anderson gets very excited and follows the teacher out. He kicks or throws the balls happily. Anderson can hold toys and both of his hands are flexible in regards to fine motor skills. He can use a pen to doodle on a piece of paper. Anderson has been working hard to copy sounds and single words. He is able to independently take off his own clothes and shoes. At the time his file was prepared, he needed some help with dressing and toileting, though he could initially go to the toilet on his own. He can zip well. He is also able to brush his teeth and clean his mouth with minimal assistance. Anderson can join a group game if led and organized by a teacher. He can concentrate well and is not easily distracted. Sometimes he is calm and serious, but when playing with his favorite toys or games he is interested in, Anderson can be active, cheerful, and very excited. Anderson has been living in a foster family and also has a very good friend. Every day, the two go to and leave school hand in hand, often found playing together. Anderson knows how to share and will often share his food with other children. He has a good appetite and likes to eat fruits and cakes. Anderson wakes up at 6:00 a.m. and goes to bed at 8:30 p.m. He is a good sleeper. Anderson is well-loved by the caretakers at his orphanage!  The agency has several videos available of Anderson, as well!

Anderson’s current adoption agency is offering a $1500 grant for his adoption.

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

$600.00 has been donated towards the cost of my adoption!

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

Girl, born 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.

$1,450.00 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!

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 ***

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 June 2020, 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.

$284.00 has been donated towards the cost of my adoption!

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

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

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

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

Listed: May 2019

$1,471.50 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!

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.

Grace has a matching grant of $1000!  When her grant reaches $5092, she’ll receive another $1000!

$6,332.07 has been donated towards the cost of my adoption!

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

Girl, born 2011

Listed September 11, 2015

Phenylketonuria, also known as PKU

New pic May 2019! 

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

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

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

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

Boy, born 2008
PRC
beta thalassemia major

Listed: May 2019

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.

$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!

Molly May

Birthday: 2015

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

Listed: May 2019

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

 

Photos and videos are available through the agency.

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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

Boy, born 2009
PRC
beta thalassemia major

Listed: May 2019

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.
———————–
“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!

There are several videos available.

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!

Boy, born 2005

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

Listed: May 2019

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

 

$562.10 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!

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. 

$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!

Boy, age 10
cognitive delays; hypothyroidism

Listed: April 2019

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

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

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

Girl, born 2013

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

Listed: Aug 2014

 

$9,565.68 has been donated towards the cost of my adoption!

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

Boy, born 2013

Cerebral palsy

Listed: April 2019

 

 

$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!

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

Listed: April 2019

 

Robert is a sweet boy who loves to smile and has a contagious laugh. He happily greets his friends with a double high five and fist bump. Sometimes, he will also jump up for a big hug after.

He understands English as well as his native language. He can say a few words but often only speaks with people he knows well. He communicates nonverbally like with hand gestures and responds appropriately to yes/no questions by nodding his head.   He comprehends everything but is a bit inconsistent with how he responds to directions. Some times this depends on the space he is in or the situation. For example, fast transitions are often a challenge for him so he may freeze until you give him the time to complete the task on his own.

 

His favorite place to be is playing outside. He will often choose to play on the swing, zipline or trampoline. He has been practicing kicking and throwing balls too.

Robert enjoys school. He has mastered drawing circles, tracing shapes, and writing his favorite letter “O.” He can write other letters too though. He also has one on one time for school to practice his letters and numbers. He gets really excited to show off his projects from school and when you compliment him.

Robert is gentle with younger children/babies and children with special needs. He loves to engage with them by singing or dancing with them and will try to hold them.  He is such a happy boy with so much potential! We are praying his family finds him soon!

Video available.

$1,101.50 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!

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

Listed: March 2019

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!

Girl, born 2013
PRC
Down syndrome

Listed: March 2019

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 June 2020, 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!

Boy, born 2013
H-C

Listed: March 2019

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.

$1,235.00 has been donated towards the cost of my adoption!

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

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

Listed: March 2019

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.

$1,098.00 has been donated towards the cost of my adoption!

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

Boy, born 2009
PRC
Cerebral Palsy

Listed: March 2019

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!

Boy, born 2011
PRC
Down syndrome

Listed: March 2019

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 June 2020, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$67.50 has been donated towards the cost of my adoption!

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

Boy, born 2009

HIV
Hepatitis C

Listed: March 2019

 

$23.20 has been donated towards the cost of my adoption!

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

Boy, born 2016

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

Listed: March 2019

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

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

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

Boy, born 2009

Muscular Dystrophy

Updated pic 2019; Wilson has lost the ability to stand and walk.

 

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

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

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

Girl, born 2013
PRC
Cerebral palsy and epilepsy.

Listed: March 2019

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.

$1,305.00 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!

Boys, born 2008 & 2010
PRC
Blood condition

Listed: March 2019

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!

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 June 2020, 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!

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!

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

*** I am eligible for an additional $5,000 Grant!  Through June 2020, 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!

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 June 2020, 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!

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 June 2020, 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!

Boy, born 2010

Nephritic agenesis, one sided
light degree mental delay

 

Listed: Feb 2019

$1,019.70 has been donated towards the cost of my adoption!

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

Girl, born 2016

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

 

 

Listed: Feb 2019

Cassandra has two sisters, who have both been adopted.

$1,482.00 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 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 June 2020, 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!

Girl, born 2011
PRC
Down syndrome

Listed: Feb 2019

Precious Jennie needs to find her family!  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 June 2020, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

 

$100.00 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 2013
PRC
Down syndrome

Listed: Feb 2019

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 June 2020, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$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, born 2013
PRC
Down syndrome, Congenital heart defect

Listed: Feb 2019

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 June 2020, 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!

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 June 2020, 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!

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!

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 June 2020, 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!

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

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 June 2020, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

 

$77.28 has been donated towards the cost of my adoption!

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

Girl, born 2013

down syndrome
condition after surgery of atriventricular communication

Listed: Jan 2019

 

*** I am eligible for an additional $5,000 Grant! Through June 2020, 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!

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 June 2020, 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!

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!

Boy, born 2008

Cerebral palsy
Spastic lower Paraparesis

Listed: Jan 2018

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

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

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

$19.80 has been donated towards the cost of my adoption!

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

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.

$546.30 has been donated towards the cost of my adoption!

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

Girl, born 2004

will age out Nov 2020

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

Listed: Jan 2019

$1,239.20 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!

Girl: 2016; age 2

Listed: Jan 2019

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

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

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding.

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

Girl, 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.

$1,240.00 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 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 June 2020, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$1,510.48 has been donated towards the cost of my adoption!

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

Girl: 2013

Special needs: Cerebral Palsy, Leukemia, strabismus

Listed: Jan 2019

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

UPDATE NOV 2019:

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

 

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

 

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

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

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