Asia Waiting Children “A” thru “K”
As an individual considering becoming a parent to one of these special needs children, I recognize the need to keep confidential any photographs, videos, or any other identifying information I may receive while inquiring about a child’s individual file.
I will not publicly “share” any child’s photograph, video, or child information with anyone or at any time engage in such activity. I will not speak negatively about these children nor post any negative comments on blogs, websites, or other media outlets that would in any way be seen as derogatory.
I understand that there is no identifying information (ie. Birth Name, Complete Date of Birth, Country of Origin, etc) available on this site for any child. This will be provided at time of referral.
In the event I breach any of these terms, I understand that Children’s House International may, in its discretion, discontinue its relationship with me resulting in my adoption being stopped, and I also understand any fees paid to that point will not be refundable. Children’s House International may, in its discretion, also file a court suit against me for breach of this confidentiality statement.
After submitting this confidentiality agreement, you will be redirected to a webpage with information on each waiting child currently available for adoption through Children’s House International along with video links if available.
Submitting this statement of confidentiality does not necessarily indicate that your family meets all of the requirements to adopt. We will review the specific parent requirements with a CHI case manager, and contact us if you have any questions by calling 360-383-0623.
Questions? Call 360-383-0623 or e-mail us HERE.
Agree to Terms
AKAYSHA, female, DOB: Oct. 2012 SN delayed development, abnormal EEG and CT scans
Akaysha especially likes to look at herself in a mirror. What adorable child would not?! She finds her little face quite delightful and also giggles at a good game of peek-a-boo with her caregivers. She responds positively to music and cuddles. She is a good natured baby who doesn’t often cry and she is a robust eater. Akaysha entered her CWI when she was approximately 6 months old. No family, personal nor medical history was found with her and is unknown. She was seen and video recorded on 7/23/2014. She is wobbly when put on the floor to sit until her caregiver helps her sit with more control. Her sweet little self can be seen at the link below.
Akaysha’s reports share:
On admission, she had average physical development, was transferred to Children’s hospital for physical examinations and treatment. PE results: T 36.8 ℃, mild delayed development, sit without help stable, smile when teased, not afraid of strangers. She had average nutrition, clear mind, good mental state, good reaction, stable breath. She had normal skin, no rash, good skin elasticity, soft anterior fontanel, equal size and circle of pupils, sensitive to light, no cyanosis of mouth and lips, no resistance of neck, coarse sound of both lungs without dry or moist rales, heart rate 132 bpm, regular, strong heart sound, no murmur of valves, flat abdomen, normal bowel sound.
Staff gave her scientific feeding, made proper training project, basically adapt to life in this institute. At the age of 8 months, she was transferred into infant nursing program, she can turn over freely, likes sucking fingers, smile when teased, can grasp toys for long time and play. At the age of 9 months, she would look around when being called, look at someone who talk to her seriously, cry when unhappy, quiet after being comforted. At the age of 10 months, she likes look at the mirror, often shake her head facing mirror and laugh out happily. She would dig small holes of toys with her thumb and index finger, always kick her legs. At the age of 11 months, she would grasp her left foot with right hand hardly, she would pull back her feet when being tickled. She can sit against objects, touch adults’ face when sitting on their laps. She likes playing hide-and-seek, giggles when playing. At the age of 1 year, she can have soft rice, quiet when listening to music. She would look at someone who hold her, can stretch her hands for objects in front of her.
Currently, she is 1 year and 1 month old, she is quiet, has a ready smile, seldom cry. She has balanced nutrition, has good physical development. She has routine life, good life habits and balanced diet. She eats table food and continues to drink formula.
ANDERZ, male, DOB: December 2012 SN delayed development
Anderz is a darling 22 month old boy! He’s dressed as though he’s ready to take on the world, and we just can say enough about those squeaky shoes. He’s ready for winter his is puffy coat, we hope this will be his last winter spent in care with no heat.
Anderz originally tested inconclusive for HIV but now tests negative. He has some delays noted on his file but his nannies and the director of the orphanage say he is developing typically for their institution. Anderz should thrive with a loving family who can provide home with the care and attention any baby needs.
BELIZE, female, DOB 6/2008 SN ambiguous genitalia
“Belize is a star; every time there are the activities, we can find her figure in these activities.” This is how Belize is described by her caregivers. The growth report in the file shows the many ways she is indeed a “star”! Belize loves to nurture the younger children and is keenly smitten with flowers and the color red. She knows many English words. She can do math quickly in her head and sometimes will shout out the answer before the other children have a chance to figure it out. She is creative and imaginative. She is a healthy child with a physical difference. She has had a surgery to address this difference. Belize entered her orphanage as a newborn.
Belize’s reports share:
PE on admission: normal muscle force and muscular tension, all was normal but external genital malformations,. Primary diagnosis: hermaphrodism. (in America the medical term used is DSD. When a less-common path of sex development is taken, the condition is often called a “disorder of sex development” or DSD. An excellent resource for education on DSD is DSD Families. Click the link here! Belize has an ultra sound in her file that is helpful. No chromosome tests are included in her file.)
Belize’s physical and cognitive development has been on target. She was able to walk independently at 12 months old. “On admission, she is 2.9kg in weight, 48cm in height, 34cm in head size and 32cm in chest size, fisted tightly and can cry. By the excellent care of the medical staffs and scientific feeding, her physical condition has been improved. At the age of 10months, she can stand with hands holding onto the support and can walk with hands holding adult’s hand. At the age of 12 months, she can walk alone.
In June of 2012, she had performed the surgery with successful process.
At the age of 3 years, she goes to the kindergarten and is a clever and studious child. She likes to go to the writing class. She can write Chinese Characters well, and now she can write these words, such as “zhong”(middle), “xia”(down), “shang”(up), “xiao”(small), “shui” (water), and “huo”(fire). She also can write her own name. Her favorite animal is the monkey, because the monkey can climb the tree, she feels that it’s so wonderful.
Her math is nice, she can perform the addition and subtraction within 10, knows the orders, knows big and small as well as knows separation and reunion. When other children are performing the mathematical arithmetic, she has known to chant out the result while doing the sums in her head for some simple arithmetic. She is a star; every time there are the activities, we can find her figure in these activities. She can speak a lot of English words, such as apple, banana, cat, dog, fish and monkey etc. Her favorite color is red; she always uses the striking color in her drawings; she has good imagination and creativity. In the art class, we can see her own work and she is able to describe her drawing to the teacher and children; her favorite fruit is the apple; she says the apple is so sweet; she likes to eat the fried fish and can pick out the bones of fish.
Belize likes to play games with her friends, would care the younger brother and sister, is very sensible, and has good self-care ability; she can put on clothes and fold up a quilt without help, also can help the teacher to clean. There are flowers in our classroom, she would water these flowers, and loves the flowers very much; she says that she loves them. She is a polite child, can say hello to uncles and aunts on her own initiative; when others helps her, she knows to thanks them; she knows the etiquette of dining, knows to be diligent to trim the nails and have a haircut.
She is going to go to grade one. We believe that she would be better and better.
BENTLY, male, DOB 7/2013 SN: low birth weight, possible premature birth, delayed physical development.
It is likely that Baby Bentley will grow up sharing his birthday cake with America. Our Yankee Doodle Boy has a report written in March 2014 when he was only 8 months old. A current glimpse into his development has been requested but now yet received. Bentley came to his SWI when he was estimated to be a week old. Birth information is not known but from his low weight and development it was possible he was born prematurely. He loves to have people play with him and “bask in the outdoors”. He can follow sounds and has also learned to throw his toys when he wants to make his wishes known. He is also described as curious and active.
Bentley’s reports share:
On admission, he had normal development, average nutrition, clear breathing sound, HR 120 bpm, in order, R 50 times/min. He was 2 kg in weight, 46 cm in height, 36 cm in head size and 34 cm in chest size, was possibility of low birth weight premature.
On Mar.4,2014, he took PE in he is 19 kg in weight, 107 cm in height, 47 cm in head size and 55 cm in chest size, delayed physical development.
He has normal mental development, Bentley was 1 month old when admitted, he has good grasp reflex, loud cry, his neck keep backward and stiff, often keep a fist, has good grasp strength. At the age of 3 months, he can kick quilt, likes to put his hand in his mouth, likes adults talk to him, he would stare at caretaker, make sounds of “gu gu” for response, he cries most loudly when hungry. At the age of 5 months, Bentley is always curious, splash water to play when taking bath, sometimes fight with other kids for attention and toys; his arms and legs are flexible, playing alone on his crib, turn his head when being called, throw toys for attention when unhappy; kick his feet when angry, laugh out loud when happy, can pronounce words with single syllable; he likes playing clap game with caretaker, make sounds of “Ahah} when caretaker speak to him. Currently, Bentley can not sit without help, need to be aided on his back, likes caretaker take him to play and bask outdoors, likes playing toys in the activity room, observe toys given to him, sometimes licks, not afraid of strangers, sing songs and pat him could make him quiet.
Bentley has good physical condition, has not been found to have food or medicine allergy.
Social Welfare Institution
March 20, 2014
BJORN, male, DOB 5/2005 SN: Repaired Hernia
Bjorn is a smart, well-adjusted and caring boy who really wants to be part of a family. Bjorn was abandoned by his family in September 2009 at the door of Children’s Welfare Institute. After admission it was found he had a scrotal hernia, 32 cm in head size, 32 cm in chest size, 51cm in height, and 3.2 kg in weight. His birthday was estimated based on his development.
Bjorn is careful about his appearance and likes to help with the younger children. He is in the first grade of elementary school. Bjorn listens well in class and is diligent and neat in completing his homework. He is not brave when asked to answer questions in class despite his above average knowledge and academic skills. Sometimes he will talk to friends in class, but he is not a disruptive child. Bjorn often helps the teachers and if another child is sick he will take water to him. Every caretaker likes him.
Bjorn has been questioned extensively about his desire to be adopted. He has expressed multiple times that while he loves his friends and staff at the SWI he wants to be adopted. He has explicitly said he is happy to be adopted internationally. This handsome boy will bring joy to the family who makes him their son!
BRITTAN, DOB: 12/2006, male, SN: mild right side hemiplasia, medication controlled epilepsy
Brittan may look somber in his file photos but when a team from Children’s House International met him in April 2014, he was quite the smiler. That smile reached right into the team and shook them smitten! He cheerfully recited a poem and could even speak some English. Brittan apparently likes to be a leader and pretend like he is the teacher. He is described to be intelligent and naturally curious by his caregivers but he has carried the label of “delayed mental development” since an intelligence test give to him when he was 8 months old. CT scans in 2007 showed he had suffered a subdural hematoma. A second CT scan in 2009 found no signs of hematoma. He does have an difference in his sleeping EEG and also his CT scan of the brain. He was admitted to his SWI when he was about a month old. Children like Birttan are exactly why Journey of Hope camps are so vital. In this case, the “on paper” description doesn’t do justice to the “live in action” reality.
Brittan’s reports share:
After admission the doctor on duty named him and did PE for him: 3.9 kg in weight 54 cm in height, 39cm in head size, he has pale face and mild stained yellow, mild nystagmus of both eyes, fast heart rate, SM level II could be found between 2-3rd rib of sternum. Suspected diagnosis: 1) reason for twitching needed to be found, intracranial hemorrhage; 2) reason for stained yellow needed to be found; 3) CHD wait to be excluded
Brittan has a sound sleep, he takes shower once a day, can take off clothes and take shower without help. Since his hemiplegia of right body limiting his right hand and foot, he often has meals and writes with left hand, his right hand just supplement to left hand with simple actions, his right leg is inconvenience, runs with tiptoeing right hand. Brittan can speak fluently, can communicate normally with teachers and classmates, would ask “What is this” initially, curious about anything. Brittan is hospitable to loving people who come to visit, he would show his room to guests, and is polite to them. At home, Brittan can take on responsibility to help other kids collect toys, and take younger siblings to play. Currently, Brittan studies in the senior class of kindergarten, teachers evaluates him as enthusiastic, active, but sometimes break rules, likes walking around. In terms of studying, Brittan knows reading and writing of 1-10, can do additions within 10.
At the age of 8 months, ZHU ZHAO took mental test in General Hospital which shows: delayed mental development, stiff of right body, advise to strengthen on right upper limb rehabilitation training and early education. Aimed at his twitching, he took cranium CT in Fuzhou General Hospital of Nanjing Military Area on Aug.5,2007, which shows: chronic subdural hematoma of left side and cerebral atrophy of left side and expansion of left lateral ventricle. He took CT exam in X-ray Department of Provincial Hospital on Jan.1,2009, which shows: 1.No obvious hematoma signs in the cranium;2. Decreased of left frontal, temporal and parietal lobe, encephalomalacia nidus and partially cerebral atrophy? He took EEG in Provincial Hospital of Fujian on May 5,2009 which shows: Abnormal drug-induced sleep EEG. Details see the medical report. 3 months after admission, Brittan had no heart murmur in heart auscultation, so CHD was excluded. Brittan has not taken vaccinations. He still takes Phenobarbital, his twitching is basically controlled. Currently, he is 111 cm in height, 18 kg in weight, 46 cm in head size, 52 cm in chest size and has 18 teeth, began to grow permanent teeth for 4 teeth. Brittan’s current diagnosis is hemiplegia of right body, epilepsy and delayed mental development.
Brittan is a curious and cute boy, we hope he could be adopted by foreign family, give him better treatment and rehabilitation, allow him to grow happily and have a bright future.
Children’s Welfare Institute
BROOKE, DOB: 6/2011, female, SN: Down Syndrome
Brooke is just way, way too cute! The Children’s House International staff had the delight of meeting her in April 2014. She loved her own little backpack that was packed for her day out. She is able to walk well and interacted cheerfully with other children there. Brooke has the great opportunity to live in a private foster care center where she has one on one care. Brooke loves to SWIM and to give hugs and kisses before bedtime. She was admitted to her SWI when she was approximately 1 month old.
Brooke’s reports share:
After admission the doctor on duty named her and did PE for her: 2.8kg in weight 53cm in height, 35cm in head size, 33cm in chest size , eyes have small palpebral fissure, lateral ear canthus warped, low auricle, face down, Diagnosis: mongolism.
.After admission Brooke was placed with a foster family. Every day she will, draw circles, look at books, read story, sing songs and get a hug and kiss then go to bed . She has a steady sleep, and she likes lying down or lying side to sleep
She is a very lovely child, is also a very helpful child, when she sees something on the ground, she will help you to pick it up, and will help to get tissues, diapers, wet wipes, etc. She is willing to help to fetch what she can. She can imitate adults’ talk, although it is not very standard, but she can make sounds. Particularly when the adult educates other children for misbehavior, she would say to the child, “No!” She knows the names of all the children in the room, can call them out. She can follow the adults to sing songs together, although she can not sing songs very standard, but the musical sound is standard. Now she can respond to us sometimes, when we ask her, “Do you want to play in the car?” (she can sit on the car and push herself away)she will reply “Yes!” She’s very cute, a bit like an adult.
She also can imitate other very great children, when we hold her do any action in front of the mirror, she is very cute. She likes swimming and playing in water very much, she can use her hands and feet to pat the water. When we teach her to swim, we use our hand supporting her chin, (because she can’t swim), let she can float in the water, when we say “do you want to do it again’’, we could not believe our eyes that she bent over the water herself , and used her hand to support her chin, very cute.
She is also a very enthusiastic child and when see some children enter the room, can say hi enthusiastically. She will be very enthusiastic to be held by adults that she knows. She can walk and go up and down stairs alone, she also can drink water and eat herself but needs a little help, and can wash and wipe hands alone. She is a very smart and cute child, she likes to play “love hug”game with her friend Ping Ping.
Brooke is an active girl. We hope a foreign family can adopt her early and give her a warm family, help her gain better education.
Children’s Welfare Institute, Jul.30 2014
CHADWICK, male, DOB 3/2012 SN mild hearing loss of right ear, nystagmus, psychomotor delay
Chadwick is a beautiful baby but he is now a toddler of 2 years old. New pictures are so much in order! A request has been made for current pictures and updates. Chadwick is an active boy who likes to attend his Half The Sky preschool class at the SWI. He was diagnosed with nystagmus and a mild hearing loss in his right ear. Since those reports were submitted the SWI became concerned that his general motor growth was delayed and submitted additional information to be included in his file.
Chadwick had his original file prepared in December 2012 and his diagnosis in the submitted materials was for: nystagmus, and mild right ear hearing loss. Recently the rehabilitation teachers closely observed his daily life. It was discovered that because of the child’s nystagmus, vision may be influenced. He can see things and will reach for toys and play in the yard and will observe around and look at the scenery but he is less responsive than the other children. When familiar people are shouting his name, he will turn around to find the source of sound.
Now at 14 months old he will still not walk alone. With help he can walk some distance. When we tease him with bright colorful toys or call his name, his reaction is big. When he is looking at things, his eyes will wrinkle. The physical exam in the hospital this time shows the result: nystagmus, and mild dysaudia of right ear. (Immediate Evoked Otoacoustic Emission Test)
Chadwick is active, has a ready smile, likes playing alone, he also likes to be cuddled and teased by his caregivers.
Like other children, Chadwick usually like toys, looks for and grabs toys, likes outdoor activities, and likes spending time with his familiar caregivers. He likes his mother to tease him. He is occasionally able to respond correctly according to instructions. Furthermore he attends our nursery class with Half The Sky foundation. They noticed there that when he ate rice and noodles he had some chewing difficulties. We had to take him to the hospital for the relevant inspection of his throat. The doctor diagnosed him having no problem, so it is probably because he does not like or is not yet adapted to eating staple food.
Our rehabilitation doctor now works with every day to train physical therapy. On August 7, 2013, the doctors at Children’s Hospital examined him and said: psychomotor delay.
August 8, 2013
Cheshire, DOB: 5/2008, female, SN: developmental delay
She has a very detailed medical report and seems to be very healthy. She is able to speak her thoughts and emotions and is learning slowly. Cheshire is from a partnered One to One program and we hope to have a video of her soon.
Six months after Cheshire was born, she was found abandoned near a hospital. Police searched for birth parents and relatives without luck. She was admitted to the Social Welfare Institute where they estimated her birth date due to her physical development.
On admission she has average condition, average nutrition, no stained yellow and blooding points of skin, no deformity of skull, no deformity of limbs and spine, and no abnormal findings of anus and external genitalia.
At the age of 6months, Cheshire had average diet and sleep. She was able to roll over on one side, and move her body left and right while on the bed; she can locate the direction of where a sound is coming from.
At the age of 9 months, Cheshire is able to hold her head up with forearms propping and has rich facial expressions when teased. She is able to sit alone, but is still a bit wobbly.
At the age of 11months, she could stand up while holding onto bedrail. At the age of 2years, she can eat biscuit without help and is able to say simple words.
At the age of 3, Cheshire started school and got along well with classmates. Her language skills were poor, but she can express her needs in lengthy sentences. At this time, she is very independent and likes to play blocks alone and have meals alone. At the age of 3.5years, she can express some simple sentences, such as “father”, “mother”, “grandfather” “grandmother” “teacher, I’m here” etc., clearly. She has fairly good thinking ability and memory and can state the names of all students in the class; her body balance is not very well; she can recognize colors, fruits and vegetables.
At the age of 4 years, she has good spirits, average development and is quick in reaction; she can express her needs freely, is fond of dancing and playing with toys; she can recognize “big” and “small, as well as her own name; she can write with a pen, and has average motion; but she can’t jump off the floor with feet; she has average self-care ability, can wash her hands, put on and take off clothes, go to toilet alone, but needs to be reminded.
Now she is 94cm in height, 14.5kg in weight, 43cm in head size, and 50cm in chest size, 14cm in foot length, and has full teeth. The child has normal intelligence development and good physical development, with motor coordination and poor balance ability; she can adapt living environment well. She has routine living schedule, and good living habits, the dieting is balance.
Children’s Welfare Institute
CHESSA, female, DOB: Dec. 2010 SN repaired cleft lip, un-repaired cleft palate, hearing loss
Chessa has spent all of her nearly four years living in her orphanage. She received cleft lip surgery in 2012 but currently has not had her palate repaired. She is only able to drink milk and is not given solid food. Due to her palate issues she has suffered repeated ear infections that have left her deaf. She does not speak because she cannot hear. She likes to play alone or stay with the aunts. She is afraid of strangers. She can walk and climb. She does not run or jump. Chessa has good fine motor skills.
Unfortunately for Chessa she has had an IQ exam that did not account for her lack of hearing. She also carries a diagnosis of mental delay. What opportunities would this girl have if she was taught ASL? What would it be like to be trapped in silence?
Chessa does exhibit some institutional behaviors. She likes to spin and shake her head. It would be impossible to know if this is the result of her silent isolation or if she has some autistic behavior. Chessa has round and big eyes, black and bright, has long eyelashes, making her eyes beautiful. She is gentle, smart and obedient, and is a quiet little girl.
CRISPAN, male, DOB 2/2011 SN post op CHD, hypospadias, arrested development
Crispan is a boy after Cupid’s own heart. Is that an arrow in his hand? Why no, it is actually a scrumptious candied apple. Crispan is a lovely wee lad who likes most to play and be active. In one file photo he looks like he is on the run to find more fun! His heart is working well now since his surgery in March 2013 but a small and systolic murmur can still be heard during his physical exam. Thankfully, he has been in foster care since soon after being admitted to the SWI at approximately 4 months old. He has had the attention of a nurturing family and gets many chances to go out and about and explore the world with them.
Crispan’s reports share:
Crispan joined a foster family from July 15, 2011 until now. Through observation, he has routine life, he takes bath one time every other day before going to bed. He eats staple food he will eat some eggs and fruit after nap. Grapes and apples are his favorite. Before nap he drinks 200ml milk and before go to bed he drinks 280ml milk. He will wake up several times during sleep. He needs to wear diapers while he sleeps.
In the foster home they regularly play music, sing a song to him, and often took him to outdoors to promote his psychological, mental and physical developments. He receives a careful caring. He is growing happily day after a day.
Crispan is active and clever, now he is able to walk and run by himself, he will play with fingers and do sports. He can understand many words, likes eating, sleeping, and bye-bye. He likes drawing, especially drawing lines on paper. He likes building blocks, he can build tower of four blocks, with some help, he can do 8 piece puzzles. In language, he can say “father” or “mother” and understands words meaning. In terms of daily living, he can cooperate with adult activities such as feeding, dressing. Crispan knows how to toilet himself and takes off trousers independently. In social terms, he is not afraid of strangers and unfamiliar environment, and he will familiar with strangers quickly. He likes to interact with people.
Crispan has a Tetralogy of Fallot congenital complex heart disease, during Mar.12, 2013 between Mar.30; he had a surgery and the surgery was successfully. According to the diagnostic report on Oct.30, 2013, Crispan has hypospadias and arrest of development, his lung has a phlegm sound and breath sound also has problems.
Crispan can walk by himself and go upstairs and downstairs all alone, draw lines and build tower of four blocks, say three or five words. He knows having continence of feces and urine in the daytime and corporates in dressing. He is really an active and lovely child with a smile.
On Dec, 2013 the height is 90.5cm, head size:47.2cm, weight:13.3kg, chest size: 48cm.
Signed by Social Welfare Institute
DASH, male, DOB: 3/2011 SN bilateral club feet, deformity of wrists
Dash was abandoned a few weeks after birth. He has been living in an orphanage ever since. On admission he had some jaundice and it was noted that he had normal muscular tension in his limbs but a deformity of both wrists and ankle joints. He has no infectious
After admission, he was cared by the dedicated staff. At the age of 5months, he can visually move following the moving object. Dash was able to grasp and reach for objects but was a bit slower due to his deformity. Dash was a quiet baby who liked to be cuddled.
Now Dash is 3years and 1month, is 70cm in height, 7.4kg in weight, 46cm in head size and 46cm in chest size; he can walk with hands holding onto support, can walk freely in the baby walker, can understand simple instructions, can pick up small things, has a ready smile, begins to speak, can say mom, and can say hello to others on his own initiative. He is shy and has less crying.
DAX, male, DOB 7/2002 SN post operative CHD (Tetrology of Fallot)
Dax is happy, active, sociable boy who has been in his orphanage since he was 6 years old. He entered the institution with a diagnosis of heart disease so it is likely that his birth family could not meet his medical needs although there is no record of his birth family or situation prior to being found abandoned. His CWI directors now feel they may have estimated his age incorrectly and that he is likely 1-2 years younger than they guessed. His physical and social development reflect more a child younger than his stated age. He suffers no current symptoms of heart disease.
Dax has a twinkle in his eye and is occasionally known to tease and make some mischief.
His very best friend is Dixon who is also waiting for a family. Dax enjoys badminton and playing on the playground. He likes to draw. He currently attends Grade 3 in the neighborhood school. In his typical environment he is talkative and active. He is especially verbal and that is described as one of his talents. He is slow to anger and will find a quiet place to sit when he is upset and where he can collect himself. One of his good friends was recently adopted to America and he misses him a lot. He also longs for a permanent family and wishes to be adopted
Dax is part of the One to One Partnership with Children’s Welfare Institution and Children’s House International. There is a group of older children who are registered and waiting for their chance to have a family.
Dax’s reports share:
Dax, male, was found abandoned on Jul 19 2008. After a lot of search by the police station they failed to find his birth parents. He was confirmed as an abandoned baby, and on the same day was sent to Children’s Welfare Institute to be raised. Doctors in this institute decided the child’s DOB as Jul 20, 2002 according to his physical growth.
When admission he suffered CHD and received cardiac surgery on Jun 25 2009, he recovered well. Now he is studying in primary school. He has some good friends in the class, they play together, do the homework together and they are happy. After school they play together and play some mischief.
He is active, has good voice, likes singing and sometimes yells when play happily. He has many advantages, can obey the rules, can unite his classmates, can get along well with his classmates and can tease them happily. Now he has learnt many things, can manage his cabinet, can wash his clothes and clean his house. He is often praised by his teacher.
He likes playing on the court, likes playing basketball, hide and seek and sliding. He wishes to grow up quickly and study hard.
We hope he will be adopted soon and will have a stable family and grow up happily.
Sender: XXX (signature)
Children’s Welfare Institute
Dec 9, 2012
DENZEL, male, DOB 6/2003 SN postoperative myelomeningocele in lumbar region
Denzel is the current unanimously elected president of his dormitory! His presidential duties include helping children get ready for school, helping organize the day and delivery homework. He is also an accomplished ballroom dancer with a gift for rumba. While he entered the SWI as a baby with an infected post-operative incision for myelomeningocele he clearly has not lost the ability to walk, run, or dance. Listen as he shares with you about his delicious lunch (in English no less!)
Physical examination on admission: weight: 5kg, height: 57cm, head circumference: 38cm, chest circumference: 37cm; T36.7ºC, P122/m, R30/m, conscious, fair reaction, medium nutrition, no deformity of head, soft neck, breathing sound is normal for bilateral lungs, no dry or moisture rale, heart rate 122 b/m, regular rhythm, no murmur of all valves, soft abdomen, liver and spleen: not palpable and no enlargement, wound infection in lumbar and sacral region, cannot control defecation and urination, normal muscular tension of four limbs, pathological reflex is not educed; initial diagnosis: postoperative myelomeningocele in lumbar region.
After admission, our medical staff changed medicine for him and gave him treatment according to his condition; we provided considerate care and scientific feeding and we actively treated his URI, intestinal infection and UTI. We fed him with appropriate milk powder and gradually added cod-liver oil, vegetable juice and yolk as supplementary food. At 5 months old: weight: 6kg, height: 62cm, head circumference: 41cm, chest circumference: 40cm; head could turn freely; could raise head. At 7 months old: could hold the bottle to drink milk. At 11 months old: could sit stably. At 18 months old: could stand up straight by holding onto support. At 2 years old: could walk independently and make the sound of ba and ma.
The child rarely cries and likes to be quiet. At nearly 2 years old: mom taught him to walk, but he always stood still and was afraid of stepping forward; everyone encouraged him; someone held food and someone held toy; he looked around and tried to move a small step forward with serious face; under temptation of toy and mom’s encouragement, he walked 5 or 6 steps forward for the first time and mom excitedly held him.
Soon he reached school age; this quiet child soon adjusted life in kindergarten with the help of other children. On the first Children’s Day after entering the kindergarten, he performed sympathy of farmers on stage. He learned a lot in kindergarten and cultivated many hobbies such as singing, dancing and drawing. After class he would draw pictures; every Mother’s Day, he would draw celebration card for mom.
In 2012, he promoted into first grade; he was focus in class; after class, he actively completed homework and actively help other children with homework. In summer holiday of 2012, he attended training class of international standard ballroom dancing and he performed well; in a performance, he performed rumba and moved all mothers presented. In 2013, he won election of head of dormitory with unanimous vote and he helped the teacher with arranging duty day, organizing children to go to school and delivering homework. He is very sensible and kind and he inspires us a lot.
One sentence: Mom I love you, makes us feel so warm and he is active and sensible and he is so close to us. We will strive for future life together.
According to requirements of national disease control department, we have been giving the child vaccinations and detailed vaccination record is attached hereto.
Social Welfare Institute
May 28, 2014
DIXON, male, DOB 4/2003 SN repaired cleft lip, repaired cleft palate.
Dixon is a “can do” kind of boy. He likes to be involved in sports, school work, and even housework. He is an enthusiastic and helpful boy and is extroverted. He is often praised by his school teachers for his work and study habits. Dixon will need speech therapy but hasn’t let his cleft palate keep him from being social and involved in interacting with his family and community. Dixon was admitted to his SWI when he was a toddler and is currently in foster care.
Dixon can be seen at the Sha’anxi Journey of Hope Camp in September 2013 through the following link.
Dixon’s reports state:
Dixon has cleft lips and palate. He took cleft palate repair surgery in October 2003 and cleft palate repair in July 2004 successfully. He was diagnosed with abnormity of seventh chromosome and took bilateral cryptorchidism surgery in June 2007. In order to make him integrated into family life and feel warm of family, we sent him into foster family on Sep.1, 2009.
Dixon is extrovert, likes to interact with others at home. But he couldn’t pronounce clear if in a hurry because of cleft lip and palate. But he still likes to talk with others and his parents correct his pronunciation patiently. He has made good relationship with families so far and lives happily.
Dixon gets along well with other classmates. He is sociable and polite to say hello to adults, help other classmate with enthusiasm. He likes to play basketball and football. He was active in doing labor, can finish homework on time and often got praised by teachers, he will in third grade in September.
Dixon has strong ability of self management, he makes his bed and clear up his clothes everyday and help mother do housework like sweep the floor, wipe table and throw rubbish etc.
Although Dixon lives well here, we sincerely hope he could have a secure home in which his parents love him and he grows healthily and happily.
Social Welfare Institute
ECHO, female, DOB 09/2010 SN 1. facial neuritis on right side; 2. postoperative hydrocephalus; 3. left chronic subdural blood clot. PENDING
Echo is as lovely as her name sounds. She is reported to have normal physical and intellectual development. What is definite is that she a magnificent little girl waiting for a family. You can clearly see this in her video link. Echo has current video and it is just too cute to describe. Watch ECHO show what she can do!! Brilliant ECHO, just brilliant!! PENDING
Echo is part of the Children’s House International and Ningbo SWI One to One Partnership. She was admitted to her SWI as an infant.
Her reports state:
On Oct. 29 2012 she was performed ventricle – abdominal surgery in Children’s Hospital (Tomorrow Plan) to repair her hydrocephalus. From June.28 2013 to July.6 2013, she was treated for the facial neuritis on right side. Now PE: 16.5kg in weight, 98.5cm in height, 51cm in head size and 53cm in chest size, has 20 teeth, moderate nutrition development, normal physical examination. Diagnosis: 1. facial neuritis on right side; 2. postoperative hydrocephalus; 3. left chronic subdural blood clot.
Motor development: can crawl with hand and knees, can walk with hands holding onto handrails, can pick up a pill with her thumb and index finger in left hand and can uses thumb and index finger deftly of left hand; motor of right hand poor; can stand alone steadily; can walk with one hand held; can queue up; like to do excises; can hold a pen with left full hand and scribbles; can imitate drawing lines and imitate drawing vertical lines. (Can walk indepently.)
Adaptability: can use left hand to take the block out of a cup and can put it into the cup again; can beat the block on right hand with the block on left hand, and can build a tower of 3-4 blocks; can cover a bottle with its cap with left hand; can turn book pages over, and can have continence of feces and urine; be fond of watching TV and listening to children’s songs; like to watch cartoon best; when teacher makes the instructions of giving red beads, she can do it well; knows “big” and “small”; when someone calls her, she would smile at once after heard.
Language and sociality: can speak a sentence of 2-5 words, be fond of imitating sounds, such as baba and mama; can express her own needs, such as ” I want to urinate” “I want to drink”; can state the purpose of daily used commodities, such as ” the towel is used for washing face.”; knows what ” No” means; can continence of feces and urine in daily time; can be cooperative when put on clothes; can point to the five sense organs with hand when asked; like to play with children; would share her own toy with other children.
Living habits: get up at 6:30, take a noon nap from 11:30 to 13:30 and go to bed at 19:00; have breakfast at 7:00, lunch at 11:00 and supper at 16:00, with rice add vegetable, meat and fish and bean products for lunch and supper; have supplementary food at 9:00 and 14:00, with Jujube porridge, milk, Langyan soup, all kind of fruits and eggs etc. Usually have good appetite; not choosy to food; have deep sleep; have defecation once or twice and urination 5-6 times.
Comprehensive Evaluation: 1. facial neuritis on right side; 2. postoperative hydrocephalus; 3. left chronic subdural blood clot, normal physical development, normal intelligence development.
Legal representative: XXX
Sealed by: Children’s Welfare Institute
EDUARDO DOB: 11/2012,male SN: Down Syndrome
Eduardo is a new assignment to Children’s House International through an orphanage partnership. He is a very capable toddler whose developmental checklist is highly favorable. He was walking with support in May 2014. He is curious, dexterous, and interactive with other children. His caregivers warmly describe him as “gregarious and cute”. His pictures seem to support this! His favorite activities are listening to music and going to his preschool class, His favorite tos are: balls and toys with sound.
Eduardo’s reports share:
PE on admission: 4.8 kg in weight, 54 cm in height, 37 cm in head size, 40 cm in chest size, Admission diagnosis: 1. Down Syndrome; 2. CHD. He sometimes he has a cold, pneumonia and diarrhea but being cured in time, has no major disease or infectious disease.
Motor development: can raise his head while lying on abdomen, can turn over when lying back, can transfer from sitting to lying on abdomen and transfer from lying on abdomen to sitting, can crawl, sit without help freely, can stand against objects, can stand for a while without help, walk with hand held, can walk without help for a few steps; can grasp toys near him, take a block from a box and take another one; can pick up beans with thumb and index finger, use thumb and index finger deftly, can tear paper; can grasp pen and scribble.
Adaptability: can find sound source, visually follow moving objects, try to find dropped toys, can reach for toys near him; can take two blocks with two hands, transfer toy from one hand to the other, bangs toys together, put blocks in the box, grasp bottle for milk, compare two objects.
Language and social ability: he can visually follow moving people, can tell familiar people and strangers, make sound toward people and objects; tell small part of objects; know his name, turns his head when someone calls him; can feed himself biscuits; know facial expression of adults; can express no; can imitate sound and produce; respond to other’s asking for his objects; can point eye, nose and mouth correctly; can laugh out when you play with him; can take off socks; wave goodbye when guests left.
Personality: active, has a ready smile, fond of imitating, fond of singing, fond of playing toys, gregarious, he is a cute boy.
General evaluation: 1. enlarged liver; 2. Down’s syndrome. Average nutrition development, normal physical development.
Children’s Welfare Institute
Elke, DOB: 2/2008, female, SN: Downs Syndrome
ELEE is such a cutie pie! She is from a partnered One to One SWI and we hope to get additional information on her soon! Watch her video as she sips her milk so politely. She is probably wondering why someone is videotaping such a thing…sipping milk? That’s nothing special, but Ekko stares at the videographer like they’re crazy.
Elke was abandoned near a town center in May of 2008. Police searched for birth parents and family members without success. She was sent to the Social Welfare Institute and on admission she was diagnosed with an umbilica hernia with Downs Syndrome.
Motion development: Can go up and down stairs with holding, can trot, can cross the obstacle over 20cm, can walk on the balance beam under the help, can scribble, can put beans in the bottle, can tear paper with thumb and index finger, can put beads in order, like throwing and pick the ball.
Adaptability: Can recognize her teacher and nurturers, can recognize her classroom and chair, can recognize the kids in the classroom, can know the position of restroom and music room, can recognize big and small, can recognize dog and cat, can imitate well, can wave her body along rhythm, can do the exercise along the music in the morning, can put on and off clothes and shoes, can button, can defecate and urinate, can wash her hands after the restroom, can wash her face.
Language and Social ability: can speak “ayi, mama, xiexie, zaijian”, can understand simple direction, can say “thanks” and “good bye”, can put chair back, can know her position in the line, can clap with other kids.
Immunization: before admission she has been vaccinated with BCG, after admission she has been vaccinated OPV for 3times and booster, MV for primary, HBV for 3times, HAV for once, A+CEMV for once, mumps once, flu for once.
Personality: lovely, ready to smile, timid, cute.
Comprehensive evaluation: Down’s syndrome, average nutrition, normal physical development.
Legal representative: XXX
Sealed by: Children’s Welfare Institute
May 28, 2014
Elliot, DOB: 10/2009, male, SN: Downs Syndrome
Elliot is pictured in his “100 percent NOT nice” t-shirt… but contrary to the bad boy shirt, we think he is a pretty nice guy. Just like his friend Ekko, Elliot has a video of him sipping milk. We will have to talk to our One to One SWI and see what’s up with the videography. However, from the video you can see that Elliot is very healthy and a TOTAL gem. Elliot also has a video of him with Ekko and Emery. They play so nicely together!
Elliot was abandoned near a hospital a few months after he was born (December 2009). Police searched for birth parents and family members without success. He was sent to the Social Welfare Institute and their diagnosis on admission was that Elliot had Downs Syndrome. He was physically healthy and had no history of severe or infectious diseases.
In November of 2010, Elliot received surgery to repair the VSD under GE. He received surgery for his Congenital Heart Disorder and now his status is post-operative.
Motion development: Elliot is able to go up and down stairs, can step by step to go up and down stairs, can paint alone, can tear the paper, can slide, can pat the ball.
Adaptability: Can go to toilet alone, can wash his hands, can take off clothes and shoes, can pick up paper and throw into the trash, can recognize triangle, circle and square.
Language and Social ability: can follow the teacher to count numbers, can learn simple adjective words, such as red, long; can learn fruit, can know to protect flowers, can say hi to visitors, like playing with kids at his age.
Personality: active, like imitation, fond of music, like toys, ready to smile, get along well, like games, lovely boy.
Immunization: he has been vaccinated BCG primary, OPV for primary and booster, DPT for complete and booster, MV for primary, HBV for primary, JEV for complete, HAV once, EMV twice, MMR once, mumps once, flu for once.
Comprehensive evaluation: 1 Down’s syndrome, 2 postoperative CHD, average nutrition, normal physical development.
Legal representative: XXX
Sealed by: Children’s Welfare Institute
May 28, 2014
EMERY, female, DOB 5/2006 SN seizure disorder, arachnoid cyst, limp of lower right leg PENDING
Emery is one of our “E” girls from Children’s House International’s partnership with her orphanage. Her little friends have been matched with their families and CHI now has her file as well. Emery has been registered and waiting for adoption since 2011. A growth update has been requested but currently just a video has been received of Emery playing with her friends Elliot and Ekko. Emery is the child in the left of the video.
Emery is on medication for seizures. Her intellectual and physical development is noted as normal. Emery entered her orphanage when she was estimated to be nearly 4 years old after being found alone on a train.
Emery’s reports share:
Emery, female, was sent to this institute on Mar.17 2010. Physical exam on admission: 14kg in weight, 93cm in height, 48cm in head size, and 50cm in chest size, good nutritional development, normal consciousness, She was hospitalized in Women and Children’s Hospital of because of epilepsy from July.5 2010 to Aug.4 2010; Physical exam presently: 16kg in weight, 98cm in height, 48.5cm in head size, and 50cm in chest size, has 20 teeth, moderate nutritional development, normal intelligence development and physical development, no particulars of nervous system. Diagnosis: intractable epilepsy, arachnoid cyst, limping of right lower limb.
Motor development: she can pick up a pill with her thumb and index finger in right hand, use thumbs and index fingers deftly in right hand, is able to stand alone steadily, can run slowly, can go upstairs and downstairs without help, can walk a straight line on tiptoe; she can hold a pen in left hand and imitate drawing transverse lines, vertical lines and crossing; she can match wavy line with the points, can write number 1, can color and be careful to homework of coloring; every time she makes progress and she has initial ability to draw; she can cut off the thick noodle with the scissors.
Adaptability: she can go to toilet without help and can organize her own clothes after urination; she could wash her hands after toilet on her own initiative, can take the toy to play and then put it to the specified location or the box; she knows “big” and “small”, “long” and “short” as well as “right” and “wrong”; she knows to make an apology and correct when she makes a mistake; she knows red, yellow and green color, knows the change of weather, can count numbers of 1-3 and knows numbers 1 and 2, can read children’s song and poem, with clearly; she can say some English words about the color and the number; she has rich imagination and good creation; she can imitate speaking and doing of the character on the cartoons, likes to play games of role-playing, fond of watching cartoons and listening to a story, can think and say hello to others on her own initiative; she likes to play games with children and is obedient and sensible.
Language and Social ability: she can speak a sentence of 5-10 words, can express her needs, such as “I want to go to toilet” “I want to drink” etc. can ask “what’s it?” on her own initiative, states the purpose of daily used commodities, for example, the towel is used for washing face, the cup is used for drink and the bowl is used for meal; she can introduce her age, name, sex and favorite activity; she can put on and take off clothes, trousers and shoes, knows to washed her own hands before meals and after toilet, and knows why to wash; she knows the sit position and standing position, knows children’s name and gender in the same class, can put away the toys and is able to go to bed alone; she is sensible and there are no concerns; she is polite and can ask for help of the teacher as needed; she can say thanks on her own initiative and would help other children in need.
Personality: active, outgoing, know her own mind, get along well with children and have a ready smile.
Comprehensive evaluation: intractable epilepsy; arachnoid cyst; limping of right lower limb; normal intellectual development; normal physical development
Sealed by: Children’s Welfare Institute
EVERETT, male, DOB 09/2005 SN epilepsy, brain scan difference
Everett is described as “open, active, self-esteemed, brave, strong, and confident”. What a description indeed! When Everett was found, it appeared that he was recovering from an intracranial hemorrhage, the cause of which is unknown. His brain scan shows a difference in his brain structure and “slow wave paroxysmal abnormalities with epileptiform activity”. With this, he has a history of epilepsy but frustratingly the degree, frequency and treatment are not discussed in his file. That information has been requested. Everett appears to be capable of so many things and that new information could really help him. He was admitted to his SWI when he was approximately 2 months old.
Everett’s reports share:
Physical exam on admission: 4.6kg in weight, 55 cm in height, 37 cm in head size, 37cm in chest size, moderate nutritional development, good spirit. Diagnosis on admission: Intracranial hemorrhage healing. In the institute he occasionally had history of cold, pneumonia and diarrhea which has been cured in time. But he has no history of severe and infectious diseases. Now PE: 18.5kg in weight, 110.5cm in height, 45cm in height, 52.5cm in chest size, 22teeth, average nutrition, delayed mental development, normal physical development; diagnosis: 1. Epilepsy; 2. Encephalomalacia; 3. the right maxillary sinus and ethmoid sinus inflammation.
Everett can button, can zip, can string the beads, can paint, can irregular circle, can pick up pills with thumb and index finger of both hands, can use thumb and index finger of both hands deftly, can run and jump, can crawl, can go up and down stairs, can stand for 5 seconds with single foot, can jump forward with both feet, can jump forward with single foot or run with both feet alternately, can walk 2m forward tiptoe against heed alternately, can walk forward and backward straight, and has good balance.
Adaptability: can toilet alone, can put on and off clothes alone, can brush teeth and wash face, can use the food tool alone, can wash his hands, can play toys, can put toys in the original place, can make greetings positively, can introduce himself, can play games with kids, can share, can do what he can.
Language and Social ability: know his gender, can ask “what is this”, can know how to do when “cold, tired and hungry”, can obey the general direction, can express his needs, can speak long sentences, can recite long sentences, like stories, like TV, curious with new surroundings, can answer questions in the class, can know many animals and fruits, can know triangle, round and square, can know weather, can count 1-30.
Personality: open, active, self-esteemed, brave, strong, confident.
Comprehensive evaluation: 1. Epilepsy; 2. Encephalomalacia; 3. the right maxillary sinus and ethmoid sinus inflammation, delayed mental development, normal physical development.
Sealed by: Children’s Welfare Institute
May 28, 2014
FELIPA, female, DOB 8/2009 SN ESTROPIA, SLOW MOTOR REFLEXES
FILIPA was about 10 months old when she was found abandoned at the gate of the hospital. She was placed in a foster family shortly after she was found. Filipa had low muscle tone and was not even able to raise her head. She was withdrawn. Gradually she began to respond to her caregivers and is now a shy girl who is prone to be sick and weak during the summertime. Filipa has some blood work abnormalities that are currently under review. At three years of age she was able to play with other children, point to her body parts, and feed herself. She is currently prone to getting a cold and cough and likes watching TV while sitting close to her foster mother. She is still afraid of strangers and is described as “quiet, shy, and introverted”. At last report she was still unable to walk independently and was not speaking though her receptive speech appears to be very good. Filipa has had a CT scan and has no brain abnormalities.
GIDEON, male, DOB 8/2012 SN Bilateral Cleft Lip/Palate After Repair, Hypospasias
Gideon was abandoned shortly after birth outside the gate of the medicinal plant garden. He was sent to the SWI to be raised. Gideon was born with a bilateral cleft lip and palate. He also was missing his nasal septum. Gideon had his lip, palate and nose repaired in January 2014. He was still categorized as moderately malnourished at that time. His development was also categorized as delayed. We know that at 8 months of age he could sit up on his own, at 16 months of age he could crawl and stand stably. At 16 months of age Gideon could imitate words and had a ready smile. For more information about cleft lip and palate you can go to:
Gideon loves music and playing with toys. He loves to be part of the crowd and to play outside. In foster family, his favorite person is grandma.
GISELLE, female, DOB 6/2006 SN CP
Giselle is an active little girl who is quick to smile! She was found at four years of age after she was abandoned at a hospital. She was only about 25lbs and was only able to walk a few steps. The doctors could not find any physical abnormalities so she was diagnosed with cerebral palsy and central coordination disorder. Giselle was placed directly into a foster family who gave her intensive care and feeding.
Giselle gained strength quickly under the care of the foster family and within six month she could walk more stably with orthopedic shoes. She is able to change her own clothing and knows from facial expressions whether someone is happy or angry. Giselle is fond of music and enjoys watching cartoons. She is quick to react and is energetic. She loves playing games but can be impatient. Giselle especially loves going places with colorful lights and music.
GUIVER, male, DOB 6/2011 SN mild cerebral palsy
Give Guiver a ball and he is ready to play!! Guiver has a diagnosis of cerebral palsy but his caregivers feel that after rehabilitation training, his current development is the same as other children his age. (There is no new medical information in his file that would confirm nor dismiss this.) He is seen in his most current video throwing a ball while walking, kick with one foot while balancing on the other, and walk/scamper around the play room. He does vocalize with those he is playing with. There is NO brain CT or MRI scan in his file. He was given a cerebral palsy diagnosis on his initial admission to the SWI. Guiver was estimated to be 14 months old at the time of admission.
Guiver’s reports share:
On admission the medical staff in this center carried out physical exam for him with the following results: 74cm in height, 8.4 kg in weight, 43cm in head size and 45 cm in chest size, teeth: 5. The preliminary diagnosis: cerebral palsy(flaccid paralysis). His DOB was on Jun 25, 2011 according to his physical condition.
He suffers cerebral palsy, his limb and mental development is delayed compared to normal level. At the age of 1year and 6months, he could grasp toys, could search for sound source if call his name, rarely had motion if lie down. At the age of 2years, he could sit up against object. At present he is 2years and 6months old, he can not walk and crawl, can sit stably without help, likes waving his body, likes riding the rocking horse, can hold the rail and kick his feet; likes clapping or touch his head if lying down, can bang toys together.
His language development is delayed compare to other kids of his age. At the age of 1year and 6months, he could not make sound, had reaction to adult’s speaking. At the age of 2years, he liked hugging, liked interaction with adults to play games, could smile if being teased, could make sound of yaya without mind. At present he is 2years and 6months old, his pronouncing is improved, can call “dad, mom”, can make sound of “wuwu” in the rocking horse. he is open and restless, likes playing games with nurturer, likes listening to nurturer’s singing.
On admission Guiver was diagnosed as having cerebral palsy, limb development delayed compared to other kids of his age. At present his physical condition is good, has no major disease since admission, just occasionally has a cold, fever and cough, not allergic to drugs.
Social Welfare Center
Dec 30, 2013
GULLIVER, male, DOB 3/2012 SN Low Birth Weight (LBW), extra thumb on left hand, undescended testicle, bilateral basal ganglia softening noted on MRI.
Gulliver is ready for his traveling adventure. Indeed he is! He started his journey as a tiny newborn but he is getting stronger and more robust as he grows. Gulliver’s reports were completed in the spring of 2014 but an MRI from July 2014 has been added to the report with no explanation. Clarification has been requested. Video is also anticipated. He is living in Guangdong province.
His reports from April 2014 share:
Gulliver was found at a newborn and reported to the police who then sent the baby to his SWI.
On admission, he had a physical examination: height: 38cm, weight 2kg, head circumference 31.5cm, chest circumference 32cm; conscious; fair reaction; appearance of premature, hexadactylia of left hand, no abnormity of heart and lungs; diagnosis: 1. LBW; 2. hexadactylia of left hand. The doctor estimated the baby’s DOB as Mar. 7, 2012 according to the growth and development.
Under considerate care of our staff, the baby has regular daily routine, fair physical development and normal defecation and urination.
At 6 months old: could raise head when lying on stomach; head could follow sound. At 1 year old: could turn over; could reach out hands to take toy in front of him and put it into mouth; low accuracy. At 1 year and 6 months old: could sit by holding onto support; could bang two toys together; would refuse when trying to take toy from his hands. Now: can sit independently; can stand up by holding onto bedrail; lazy; will lie down after sitting or standing for a while; cannot control defecation and urination.
At 6 months old: knew familiar voce; would smile when being teased. At 1 year and 6 months old: could make the sound of YI and YA; attached to his caretaker. Now he can babble to toys; appears to be active and happy when interacting with familiar people; poor language ability; plain emotion; likes to play toys alone; does not care about things happening around; not afraid of strangers; mild and quiet; likes milk very much; refuse supplementary food; will cry to resist being fed thin gruel.
Social Welfare Institute
Apr. 28, 2014
HAMILL, DOB: 04/2011, male, SN: Repaired CHD, Repaired Cleft Lip/Palate
Who is ready for this bundle of fun? It is obvious from his reports that Hamill is a delight to his caretakers. He is described as “active, smart, cute and sunshine boy”. Hamill loves cars of all types from little push cars to big ride on cars. He will pout if he wants his way, but even this is described as “very cute”! Hamill loves to draw and asks every day if he can have pen and paper and will make drawings for each of the caretakers. He loves to sing and dance and shake his body. He gets along well with the other children and likes to play group games.
Hamill is a loving boy who offers help to younger children in the SWI and likes to assist in feeding the infants. He is able to feed himself and dress and undress. Hamill takes his dishes to the sink after he eats and is potty trained. This little ray of sunshine is inquisitive and asks many questions about everything he sees. He remembers what he is told and will tell the other children the next time he sees the same object. Hamill has good social adaptability and is able to express himself well despite his cleft lip and palate. He is working hard to have correct pronunciation. Hamill will make a fantastic addition to any family!
HEMMING, DOB: 08/2012, male, SN: CHD
Hemming was abandoned when he was just one month old, now we seem dressed in pink but don’t let that deter you for he is all BOY. His big bright eyes are sure to stop you in your tracks! Hemming can’t sit or crawl yet but he loves rocking chairs and making lots of noise with his toys. Hemming seems to be right handed, as he prefers to hold his bottle with his right hand.
Hemming loves the sound of music and can’t wait to learn to dance, for now he shakes his feet to the sound of music and lights the room up with his shinning smile. He recognizes his caretakers and sometimes cries when he sees strangers. Hemming needs a mommy to scoop him up and comfort him from his fears and tell him everything will be OK.
His nannies report that he is a cute and active boy. They hope to find him a family who will love him and give him a happy childhood. They believe he could bring more happiness to his future family.
HELSA, DOB: 09/2012, female, SN: Spina Bifida
Helsa was abandoned when she was about two weeks old. She was born with a spinal meningocele at the L5 level. She was very weak and her meningocele was ulcerated and infected. She underwent repair of her lesion in October of 2012. She has received several months of rehabilitation treatment and is now stronger. She is able to sit up on her own and crawl.
She is able to feed herself finger foods and is becoming much more animated in her personality. Helsa becomes joyful and excited when she is offered a favorite toy. This lovely, big eyed girl is cute and obedient. In an L5 level most of the nerve impulses to muscles are intact except for some small muscles inside the foot and most sensation is intact except the sensation betwooen the first and second toes. While Helsa is too young to determine if she will have issues with continence but her prospects for independent walking is very good! 75% of children with SB have average or above average intelligence.
HERSHEY, DOB:10/2011, male SN: Downs Syndrome
Hershey, an abandoned baby, was born in Oct of 2011. On Apr 28 2012 he was abandoned near his Children’s Welfare Institute. The police station could not find his parents and sent him to our institute to be raised till now.
Body check in the institute: average nutrition, clear mind, dull spirit, no yellow stain and bleeding pot of whole skin, no deformity of skull, anterior fontanel disclosed, appearance of Down’s syndrome, no purple of lips, both lungs(-),not palpable of pathological murmurs, low muscular tension of limbs, could not raise his head, could turn over, no deformity of anus and genital(the child took RMB 200 and a note).
After admission the working staff provided scientific feeding and proper training plan, he was adapted to our institute. At the age of 6 months, he was transferred to infant parenting project to receive early education; at the age of 8months, he could change from supine to prone position, could respond with “aa” if talk to him. At the age of 9months, he could speak “dada” if happy, could make sounds of “enenaa” if do touching practice to him, could hold the toys for a while. At the age of 11months, could pat toys on the shelf, could hold the toys for a while, sometimes could make sounds of “mom”, could hold the milk bottle to drink milk, could put toys into his mouth. At the age of 12months, he could make sound of “henhen” when see other kids eating food, could search for colorful pictures on the wall. At the age of 1 year, he could recognize familiar people, could be happy when see his nurturer, also could giggle.
Now he is 1 year 1month old, can sit against wall, can stare at your mouth if talk to him, has good physical development, has balanced nutrition, has regular life, has good living habit and proper diet.
We vaccinated her regularly according to the requirement of health and epidemic prevention department.
Legal deputy: XXX
Children’s Welfare Institute
Apr 10, 2013
HUTTON, male, DOB 6/2012 SN brain scan difference, mild anemia
Oh this child’s smile is a delightful as the day is long. If he sees you are sad or angry he will try to tease you and kiss your cheek to make you smile too. His favorite place to chill is the rocking chair, especially if there is someone cuddling him there. He is smart and quite attached to his caregivers and little friends. Hutton has a difference in his brain structure but his brain seems to have figured out quite well how to accommodate and take the world by the tail. His developmental checklist is totally impressive. There is nothing on it he can’t do at 20 months except for taking off his own socks and pointing to his eyes, nose and mouth. Hutton was admitted to his SWI when he was approximately 2 months old and has been living with a foster family since February 2014.
Hutton’s reports share:
The PE on admission: 55cm in height, 4.8kg in weight, 38.5cm in head size, 38cm in chest size, and diagnosis on admission: Brain injury syndrome. His DOB was estimated as June 2012 according to physical conditions on admission. After admission, he was given intensive care and scientific feeding, and his physical state was stable. On Nov 21 2013 he had a complete physical exam in Children’s Hospital of the province, he was diagnosed as: Brain injury syndrome.
He is smart, living in the Butterfly home. Now he can walk, can call dad and mom, likes playing, and is attractive. He can tease you if you are angry, also can kiss your cheek. He is not choosy to food, likes sharing food. He likes touching girl’s heads, also occupying the rocking chair. He entered a foster family on Feb 10 2014.
Staple food: rice, vegetables, milk and fruits, not choosy to food
He is extroverted, active, restless, likes playing outdoor, attached to people, likes being cuddled.
Sealed by: Social Welfare Institute
Mar 27, 2014
Jantzen, DOB: 2/2010, male, SN: SN post-surgical sensitive need. Partnership assignment PENDING
Jantzen is so brave that he never cries when getting his vaccinations. He wants to be like his comic hero Black Sergeant who stands for justice! Imagine him running around with a super hero cape flapping behind him in the throes of imaginary bliss as he saves the world. Jantzen is described as very bright and brave to speak up. He is capable in his life skills and with his academics. He is described as much loved by his teachers. His photographs confirm what the reports shares that he has “black and bright eyes and is liked by everyone since he was admitted. He has a ready smile and sweet mouth.” Joy, fun and adventure are written over that face! Jantzen was admitted to the SWI when he was a newborn. Children’s House International has a partnership with his orphanage.
His reports share:
His DOB was estimated as Feb.1,2010 based on his physical development.
PE on admitted: T: deformity of external genitals, normal muscular tension. Primary diagnosis:
hermaphrodism. (The ultra-sound in his file states: unsymmetrical bilateral testis. Prostate could be seen.) In America the medical term used is DSD. When a less-common path of sex development is taken, the condition is often called a “disorder of sex development” or DSD. An excellent resource for education on DSD is http://www.dsdfamilies.org/dsdfamilies/whatisdsd.php . Jantzen has an ultra sound and photos in his file that are helpful. No chromosome tests are included in his file.
On admission, he was 3.0 kg in weight, 50 cm in height, 34 cm in head size, 32 cm in chest size, make fist, could cry and shout. Under the delicate care of medical staff and scientific feeding, he got better physical condition. At the age of 11 months, he can stand against objects, can walk with hands held; at the age of 13 months, he can walk without help.
Jantzen is a smart boy, has black and bright eyes, and is liked by everyone since he was admitted. He has a ready smile and sweet mouth. At the age of 1 year, he always follows caretaker and calls her “mum”.
With Jantzen’s growing up, he went to the kindergarten in 2012, began new life, he adapted to life in the kindergarten quickly. He performs well from putting on shoes and clothing. He eats meals by himself needing no help, can brush teeth, wash face and fold up quilt by himself. Besides, he would help teacher to do things within his power, got love from teachers. Jantzen speaks clearly and loudly, could recite and sing well, Jantzen has learnt many children’s song like “three character primer”, “small swallow”, “fingers” and “dad, where are we going”. He likes cartoon characters in the movie, especially Calabash Brothers, Black sergeant because they are the icon of justice, he hope he could be as powerful and prestigious as them.
Jantzen is talkative no matter on the class or after class, he is bright, brave to speak. Jantzen is strong, he never cries when taking vaccinations, he is obedient and polite, got love from everyone.
Social Welfare Institute
JESSALIN, female, DOB 12/2009 SN Hep B+, language and social delay
Jessalin is back on the hunt for a family. Her family was unable to continue her adoption process due to a change in circumstances. JESSALIN, female, DOB 12/2009 SN Hep B+, language and social delay
Miss JESSALIN always makes our hearts hurt. She is in one of CHI’s partnership programs. Because this is a partnership program we know the children and care in this SWI is pretty tough. Her official special need is Hep B carrier but it’s really her sadness that is the biggest unknown for her and for a family. Her greatest need appears to be getting out of an institutional setting. She doesn’t appear to be thriving there. Her eyes seem to tell us she is delicate and needs one on one care.
CHI first was first assigned her file when she was just turning 3. She didn’t speak or interact and was frankly shell shocked looking in the first video. Then we got an update video in May 2013. The most current video arrived 6/17/2014 with her reassignment. She has not been diagnosed with autism but she is isolating. We don’t know that she isn’t on the autism spectrum. Her future requires a family that can really step into the unknown. Some wee souls have such difficulty in institutional settings. Listen at how loud everything is around her. If she has any sensory sensitivities, she would be really quite overwhelmed.
JILLIAN, female, DOB 10/2013 SN Apert syndrome
Jillian is a gentle baby with a calm personality. The Children’s House International team was able meet her in April 2014 during a Journey of Hope camp with her province. At the time, Jillian was content to have the team touch and talk to her. She tracked the team with her eyes and appeared to have adequate hearing. She is a robust baby who has been in good general health. It was apparent that she likely had Apert Syndrome though at the time the SWI did not have a diagnosis. In July 2014 Jillian was given this diagnosis at her physical exam for adoption registration.
Her SWI was surprised that the CHI team wished to advocate for and sponsor her registration. They couldn’t imagine any family accepting a child with this condition. WHY NOT?! Children with Apert Syndrome can be extremely capable, especially with early intervention! Jillian is ready for her opportunity and there must be a family out there waiting for her sweetness. A good summary of Apert Syndrome can be found at this link!
Jillian’s reports share:
After admission the doctor on duty named her and did PE for her: 3 kg in weight 50cm in height, 33cm in head size, initial diagnosis: 1. deformity of cranium; 2. syndactylism deformity of four limbs; 3. neonatal jaundice; 4. acute bronchitis; 5. Possible eye disease (later marked normal); 6. Possible spina bifida occulta (later excluded).
After admission, she was placed in Infant Group based on her age, she has 3 meals and 1 dessert a day, gets up at 6:00, takes a nap at 11:30 and goes to bed at 21:00; has breakfast at 6:30, lunch at 11:00 and supper at 16:30, desserts at 9:00,14:00 and 20:00. She had formula milk as staple food when admitted, after 4 months old, we added rice paste for her, currently, she has rice paste as staple food, milk, egg custard, fruits jar for desserts. She likes fruits jar, has good appetite, eat much for each meal, she has grown up a lot. She takes bath once in every morning, she likes taking bath, likes patting water with both hands.
After taking bath, Jillian would watch TV sitting on the kids’ chair, she likes watching ads. Jillian has delayed physical development in terms of all indexes, she can support her upper body with upper limbs while lying on abdomen, can suck hands, visually follow dropping objects, she can not turn over of sit without help. She can make sounds, laugh happily when being teased. She took consultation in superior hospital in May 2014, we consider her as Apert’s Syndrome based on her physical condition.
Jillian is 66 cm in height, 7.5 kg in weight, 42 cm in head size, 44 cm in chest size and has 0 teeth. She has been given vaccinations on plan, details see the vaccination record. Spina bifida occulta has been excluded after examination. She took X-ray exam in No.1 Hospital on Jul.24,2014 which shows: deformity of both hands and feet, details see the medical report.
Jillian is a cute girl, we hope foreign family can adopt her, give her a warm and complete family, allow her to take better treatment and education.
Children’s Welfare Institute
KAMMAN, dob 2/2011 SN developmental delay, brain scan difference (large cisterna magna), hearing loss with difference in BAEP test, undescended testicles,
Kamman was part of the Journey of Hope camp in his province. His medical file is over a year old but he does have current video taken 9/2/2014.
An updated medical has been requested. Kamman has an impish grin and outgoing personality. He does have hearing but there is a hearing loss with that test included in his file. He was found and admitted to his SWI when he was approximately 18 months old. He had a rough beginning and lags behind his peers in overall development but is making progress since his admission to his orphanage.
Kamman’s files share:
After admission, the doctor on duty named him and did PE for him: 9.8kg in weight 81cm in height, 44cm in head size, 48cm in chest size, poor development, moderate nutrition, clear mind, dull reaction, able to raise his head, able to sit not stably, not able to crawl and stand; not palpable of bilateral testicles, normal muscular tension; diagnosis: 1. Delayed development; 2.Cryptorchidism (undescended testicles). He was dispatched to infant team for group feeding as no infectious disease was found after the observation period.
After admission he was 18months old, his staple food was porridge, noodles, milk and snack(steamed eggs and fruits). He had good appetite, He has sound sleep and drinks milk once in the night. The nurturer helps him with the defecation and urination, he uses the diaper every day. He takes the bath once every day at 8:30. Now he can not speak, and can make sounds, can understand his name, can turn back if call his name, can show scared and angry expression, can recognize familiar and strange people, can rob his favorite things. He can clap his hands to welcome, can wave his hands and his body to dance. He can walk with holding, can walk to his desirable place with holding the wall or the table. He is active and restless, interested with cartoon, likes watching TV, delayed development and mental retardation compared to other children of his age.
MRI test in Provincial Hospital on Mar 29 2013: 1. Left-right ventricular asymmetry and left ventricular enlargement may be periventricular dysplasia or anomaly; 2. Large cisterna magna; 3. Left-right mastoiditis. BAEP test in Provincial Hospital on Mar 19 2013: abnormal BAEP, bilateral testicles descended into the scrotum. Now he is 11kg in weight, 84cm in height, 46cm in head size, 51 cm in chest size and has 20 teeth. He has been vaccinated.
Kamman is active and beautiful. We hope foreign family can adopt him and make him gain better treatment, grow up happily and healthily.
Children’s Welfare Institute
Jul 14, 2013
KLARXON, male, DOB 7/2001 SN Healthy Older Boy
Children’s House International is in a partnership with Klarxon’s orphanage which is getting quite concerned because he will age out of the adoption system in early July 2015. That is less than 10 months away. Klarxon has been registered for adoption since 2012 but has not had a family commit to his placement. Klarxon entered the orphanage in 2009 after being abandoned at the train station and taken to the police station. From 2009 to 2012 the orphanage published his abandonment notice multiple times in the newspaper but nobody ever came for him.
Klarxon is currently not living at the orphanage. He and his friend Kendrix have both been sent to a special soccer school in another province. Klarxon is a good student and works hard at athletics and is especially skilled at soccer as his many pictures show. Klarxon and Kendrix have both requested to be adopted and as they have lived together like brothers since going to the soccer school, they would like to be adopted by the same family if at all possible. They have both agreed to be adopted individually but dream of going together. They have seen many of their peers adopted throughout the years and have been waiting but not yet chosen.
Klarxon’s reports share:
His study is good, can listen to teacher carefully, can finish his homework on time, can get along well with teachers, can obey the rules and listen to the arrangement.
He is strong as he likes sports. Every afternoon he plays basketball and his skills are good.
He likes working in the student team, can clean the dormitory first every morning. He can join the activity positively and is praised many times. He is confident and ready to smile.
We hope he will be adopted soon and will have a stable family and grow up happily.
Children’s Welfare Institute
Dec 9, 2012