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Asia General Information

The orphan crisis for children with Down syndrome and other special needs crosses every political and continental border, extending through the countries of Asia.  Although many reside in foster homes, they are still discarded and need a forever family of their own.

 

China, Korea, Hong Kong, Taiwan, Thailand, and the Philippines all do an outstanding job of documenting each child’s social history, as well as providing thorough medical history and updates for potential adoptive families.   The process to adopt in these countries is very straightforward and predictable.  We have outstanding agency partners serving these children.  Length of travel and other requirements have been markedly relaxed over the last year, and even allow for single moms and larger families to adopt.

 

Despite all of these positive features, our Asian children are often the last to be chosen.  Please help us raise awareness and find adoptive families for them!

 

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Kolby

Boy, born summer 2016
SE-Asia
Down syndrome

This one year old boy was found at birth at the gate of his current care center. He loves playing with toys that make sounds, and he smiles often. He is described as quite sociable. Upon coming into care, he was found to have Down’s syndrome, atrial septal defect, anemia, and cytomegalovirus. He is said to have no health problems at this time. An adoptive family should have familiarity with Down syndrome.

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

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

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Kenneth

Boy, born 2009

Epidermolysis Bullosa

Hk-2

Listed: June 2017

Kenneth is a happy little boy looking for a home. Kenneth suffers from a severe form of Recessive Dystrophic Epidermolysis Bullosa. He also has severe recurrent blistering all over his body and recurrent buccal ulceration. He is also at risk of skin cancer. His skin is largely affected, especially his back, buttock and legs. Kenneth has Toe Syndactyly Bilateral Feet. He’s able to walk and sit down without assistance. When blistering on his feet is severe, he drags and moves slowly. He uses wheelchair or stroller for outdoor activities. Kenneth also has webbed fingers and has had surgery to separate them.

Kenneth can feed himself with a spoon, turn pages of a book and hold toys. He receives physical therapy and occupation therapy to strengthen his motor skills. Kenneth can eat soft food and when he has a sugar craving, likes chocolate and ice-cream. His other favorite food includes lunch meat, sausage and chocolate milk. He does not like fruits. He has specific bathing needs that need to be done for his wounds. Kenneth is gentle, quiet, loving, shy, polite and friendly. He is a tough child who tolerates daily painful wound care but he never throws temper tantrums. He can entertain himself by watching TV and cartoons and playing with an I-pad.

Photos available for inquiring families.

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him.

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Nikko

Boy, born 2013

Hk-1

Listed: June 2017

Nikko is a sweet little boy looking for a home. Nikko has Congenital Hypoventilation Syndrome and Hisrschsprug’s Disease. He also suffers from Congenital Left Eye, Ptosis and Marcus Gunn Phenomenon.  Nikko has normal vision and hearing.  He is unable to speak but always makes sounds to show his wants or draw others’ attention. He can show where his hands, feet, eyes, ears, month, nose and head. Nikko enjoys eating and loves rice cereal with chopped meat.  He can feed himself with a spoon.  He likes to drink milk, water, and fruit juice. He can stand by himself and walk around by himself for about 10 seconds.

Nikko is not afraid of strangers and welcomes everyone approaching and talking to him.  He also enjoys being held by others and bathing.  Nikko has learned to use smart phone and toy-computer.  He presses the button himself when someone holds the phone for him and asks to take selfie photo with him.  He also plays music and shows people the blinking lights when he is playing the toy-computer. Nikko needs a Trilogy Ventilator, Oxygen Pulse and Oximentry Monitor.  He’s eagerly looking for a new family.

Photos available for inquiring families.

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him.

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Wesley

Boy, born 2002

Hk-3

Listed: June 2017

Wesley was born with multiple medical problems including a chromosomal abnormality, developmental delay, oropharyngeal dysphagia and aspiration (difficulty swallowing), bilateral mild hearing loss, left amblyopia (a lazy eye), left perthes disease (disease that affects the hips), and cleft lip and palate with repair done, and more.

Wesley is a fun young boy looking for a home. Wesley is a friendly boy who likes to interact with his care givers, teachers and other children. He is usually happy and curious about things around him. He is active in class and likes to answer questions. He can mostly do basic things in the classroom such as playing with toys, listening to songs, drawing, and learning words.

Photos available for inquiring families.

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

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Champ

Boy, born 2013
T-A
Premature, traumatic birth, history of seizures

Listed: May 2017

Champ was born one month premature and he suffered from HIE (hypoxic-ischemi encephalopathy) which is basically brain damage caused by lack of oxygen.  All of his medical complications, except for the cleft lip and palate, were caused by his traumatic birth.

Champ has received loving care by foster families.  Focus has been on furthering therapies and working on feeding. In late 2014, he had surgery to place a gastric feeding tube to allow him to learn to swallow.

He currently has therapies; physical, occupational, and speech/feeding, three days a week at a local hospital.  He takes medicine for seizures and muscle spasms.  He has struggled with respiratory tract infections due to aspiration and excess sputum, in the past. Currently he is doing well.

Champ does recognize his name when spoken, the request to raise his head and cough, and praise words like “good boy”, and the words “all done”. He calms when soothed and is able to cry and express dislikes through sounds and body language. He has been given a “Flash” vision test and it was determined that he can see, but the level of clarity cannot be determine from this test. The seizure medicines have caused some vision problems. He is far sighted and possibly has some tunnel vision. He wears glasses for up close vision when we are feeding him and when we show him books, flash cards, and toys.

He is thriving and gaining weight and length well. He is very sweet, smiles sometimes, and loves to be cuddled, twirled and swung. He bonded well with his first foster family and again with his second foster family. He is very aware of people and likes to look at our large dog, the movie Frozen, American football and the Baby First TV Channel. He can focus on things and track items, but he is slow in moving his eyes to do so. His hearing appears to be good, he responds to sounds and startles at loud sounds. He has some tactile sensitivity, but this area continues to improve and he enjoys having his feet massaged. He doesn’t use his hands much, due in part to some sensory issues. I believe with the right therapy, this will improve. He will push away things he doesn’t like, and will sometimes bat at toys and pull things to his head.

From his first foster family:   I think it’s important to share with potential adoptive families that Champ’s condition hasn’t stopped changing and improving since he’s been fostered.  He thrives on love, continuity, and regular stimulation/therapy.  It’s also important to know, something that is hard to see in videos and pictures, that he has a great capacity to give and receive love.  I know many parents who are willing to adopt special needs children, who aren’t daunted by the physical care, are just afraid they will never be able to give or receive love from their adopted child.  With Champ this is not the case.  In the eight months we had him, I can say WITHOUT a doubt that he KNEW and LOVED both of us, and was able to receive the same love from us.

$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!

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Hailey and Hugh

Sibling Pair, ages 9 & 6
T-2sibs

Hailey has developmental delays and vision issues

Hailey & Hugh need to be together!!

Listed: April 2017

These siblings are unfortunately living apart, as the children are housed by age and gender at the facilities. They miss each other a lot and they’re both always happy to see each other when they can get together. They want to be together long term in the same adopted family.

Hailey is described by her caregivers as mild, positive, vivacious and well-behaved. She’s small for her age, wears glasses and has a small vocabulary. She’s easily distracted but has made great improvement in comprehension. Hailey’s a warm-hearted girl who finds pleasure in helping others. She remembers her birth family but is excited to start a new life with an adoptive family—as long as she isn’t separated from her brother.

Hugh is filled with curiosity about the world, often asking “why?” He speaks well and is reported to cooperative and able to follow rules. Like his big sister, he’s easily distracted but he works hard on his schoolwork. He attends primary school and mixes well with the other kids his age. His caregivers describe him as a good boy, energetic and usually happy. He’s been very clear he wants to be adopted with his sister.

There’s a $4000 grant for families who qualify to help with adoption expenses, available from the agency.  Video is available.

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

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

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Mara

Mara-1596Girl, born 2005
T-G
neurodegenerative disease (encephalomyelopathy), scoliosis, global developmental delay (mild-mod.), leg length discrepancy w/low muscle tone, low muscle tone in right hand

Listed: August 3, 2016

Total sweet heart alert! The agency’s team got to see Mara for the second time when they visited in May!

With total politeness she asked for a pack of gummy snacks. A girl that knows what she wants. Soon she was showing off her talent to color! Wow does this girl have skill. Colors all out and organized, color page tilted ever so slightly, and bent into the coloring pose she started her master piece. As we watched she made the most deep-in-thought faces as she decided exactly how she wanted the final product to be.

Mara is such a gentle soul. She has an adorable smirk and wise, knowing eyes. She loves drawing, puzzles and going to school. And she was very, very pleased with her new haircut– she “likes it short because it’s easier to fix and much cooler”. She is so incredibly persistent, such as hard worker. Her foster mom said “She is always like this. She comes home from school and does her work, I never have to remind her. She doesn’t even stop to eat her snack until she has completed all her work.” What an amazing kid!

Mara has a neurodegenerative disease — that is an umbrella term for the progress loss of function of her nervous system. She also has scoliosis. She gets occupational and physical therapy weekly and her foster mom says it has really helped her posture and endurance. Mara walks, goes up and down stairs and can even jump. She has weakness in her arms and legs, but she really impressively compensates when doing daily activities. She is independent with dressing, bathing, and eating.

Unfortunately, we don’t know specifics about Mara’s disease or how fast it will progress. She was seen by a neurologist in 2010, but they were not able to reach an official diagnosis. They refer to it as “encephelomylopathy” in her official paperwork, which is, again, an umbrella term for any disease that affects the brain and spinal cord. Sweet Mara is such a joy. She deserves a family who will be detectives and help determine what is causing her weakness. She deserves a family that will challenge her with puzzles, math problems and lots of therapy. She deserves a family that will be there, whether the disease progresses rapidly or very slowly. She deserves love. She deserves her family.

Mara is a go getter. She is sweet. She is looking for her forever family. Could that be you?

Additional information and photos are available in this blog post 1 and blog post 2.

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

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Kamdyn

Kamdyn Kamdyn2Boy, born 2010
S.E. Asia
Down syndrome

Listed: June 2016

This sweet boy can follow his daily routines and has preferred friends and adults at his care center. Upon coming into care after being found, he was noted to have no right hand, a right leg that was longer and weaker than the left, and to have Down syndrome. His health has reportedly been good. He loves striking two things together to make sounds and climbing. His development is delayed but his gross motor skills are emerging. Recently he has shown improvements in learning to listen and expressing his emotions when upset. This boy is waiting for a family with the resources he needs to reach his full potential.

$427.50 has been donated towards the cost of my adoption!

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

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Kevin

Kevin 6

Kevin 2Boy, born October 2008
K-H
Paresis of the facial nerve on the right side

 

  • Married couples and single women may adopt
  • Adoption process approx 8-12 months
  • Three trips – both parents need to travel for trip one
  • Trip one is 10-15 days
  • Trip two – about 6-8 weeks after trip one, for court
  • Trip three – about 6-8 weeks after trip two, 7-10 days long
  • Total estimated cost is $43,000

$117.00 has been donated towards the cost of my adoption!

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

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Cavan

Cavan 2 Boy, born March 2009
K-H
Ptosis of both upper eyelids

 

 

  • Married couples and single women may adopt
  • Adoption process approx 8-12 months
  • Three trips – both parents need to travel for trip one
  • Trip one is 10-15 days
  • Trip two – about 6-8 weeks after trip one, for court
  • Trip three – about 6-8 weeks after trip two, 7-10 days long
  • Total estimated cost is $43,000

$64.20 has been donated towards the cost of my adoption!

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

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Brendan

Brendan 3 Brendan 1Boy, born October 2013
K-H
feeding disorder, hydrocephalic syndrome, developmental delays

 

Sweet Brendan needs a family ASAP, he is struggling. The family needs to be homestudy ready, and the agency has a couple short videos for interested families.

 

  • Married couples and single women may adopt
  • Adoption process approx 8-12 months
  • Three trips – both parents need to travel for trip one
  • Trip one is 10-15 days
  • Trip two – about 6-8 weeks after trip one, for court
  • Trip three – about 6-8 weeks after trip two, 7-10 days long
  • Total estimated cost is $43,000

$148.50 has been donated towards the cost of my adoption!

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

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Darby

Darby 4Boy, born July, 2013
K-H
Darby has Arthrogryposis – both upper and lower extremities.  Additional pictures available.

  • Married couples and single women may adopt
  • Adoption process approx 8-12 months
  • Three trips – both parents need to travel for trip one
  • Trip one is 10-15 days
  • Trip two – about 6-8 weeks after trip one, for court
  • Trip three – about 6-8 weeks after trip two, 7-10 days long

$109.00 has been donated towards the cost of my adoption!

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

 

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Armand

Boy, born October 2010

Leukoma Cornea (Blindness in both eyes) & Developmental Delays

T-G

 

Armand entered foster care due to inadequate care and parental skills.  He has resided in care since February 2011.

Armand likes to be spoken to and laughs when his name is called. He laughs and smiles when caregivers touch his face and talk to him.

$64.75 has been donated towards the cost of my adoption!

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

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Talbot

Boy, born December 2009

Developmental Delays, feeding issues, failure to thrive, left congenital ptosis, laryngomalacia and supraglotoplasty

T-GLAD

 

Talbot entered foster care as a result of being removed from his home due to his parent’s inability to provide a safe and stable, loving home for him.  He has resided with a foster family since July 2011.  He is growing and developing in his foster family’s care.

Talbot likes toys that make sound.  When he hears music, he dances and laughs out-loud.  He enjoys taking walks with his foster family.  He is able to say Thank you, Auntie, Mama, and Papa.

Talbot was diagnosed at a few months of age as  having feeding issues, failure to thrive, left congenital ptosis, laryngomalacia and supraglotoplasty. According to a October 2011 developmental report, he was delayed in cognition, language, & gross and fine motor skills.  He attends weekly occupational and language therapy classes, showing improvement in the past few months.  He is able to walk on his own and at the time of the assessment, he was working on climbing stairs.  His appetite has picked up and he enjoys eating noodles and biscuits among other foods.

Talbot will do well in a family who is patient, has time to work on developmental growth through play and exploration, and able to access early intervention services.

$29.00 has been donated towards the cost of my adoption!

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

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Heather

Girl, Born December 2003
T-A
Epilepsy, moderate cognitive delay

Listed: November 12, 2011

This BEAUTIFUL girl needs a forever family of her own.   Heather is presently residing in an orphanage.

Health Condition: Heather has been diagnosed with Epilepsy.   She is currently on medication for this condition and reports state that she has not displayed any effects of Epilepsy since April 2009.   Heather has also been diagnosed with Moderate intellectual deficiency. According to reports, she had a brain injury caused by the suspected abuse from her birth father. Her psychological assessments show that she has a delay in cognitive and motor development. Heather has also been diagnosed with congenital myopia, astigmatism and mild strabismus. She currently wears glasses for myopia and astigmatism. The doctor related that astigmatism is mild so it is not necessary for her to have a surgery.

Likes & Dislikes: Heather’s favorite foods are rice with meat sauce, tapioca milk tea, chocolate, pudding, cookies, yakult, and candy. She dislikes carrots, noodles, vegetables, bean curd, and steamed buns. Her favorite activities are playing house, fishing, doing puzzles, drawing, and any active games. Y-W does not enjoy thunder, dogs, being alone, the dark, strangers, or caregivers having raised/angry voices. Heather very much enjoys school, especially singing and dancing. She gets along very well with her school peers.

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

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Cullen

Boy, Born May 2004
T-A

Severe Mental Developmental Delay, Mild Physical Disability, and Epilepsy

Listed:  November 3, 2011

Cullen has been through WAY too many living situations and he needs a true *forever family*.  The agency can provide more details on this for you.

Cullen was born prematurely at 32 weeks gestation and was kept alive on an incubator for 4 days. His birth mother reported that she used amphetamine weekly since 16 weeks gestation, but Cullen was not reported to have any withdrawal symptoms. Cullen was diagnosed with cerebral hypoplasia. The EEG report showed that his brain displayed electronic activity, but no abnormal findings were seen in the brain waves. Cullen was diagnosed with severe mental developmental delay, mild physical disability(lower extremities),  and was suspected with autism but has no diagnosis. He  is on medicine treatment for his epilepsy.

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

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Merlin

Boy, Born October 2007
T-A

Moderate Intellectual Deficiency and Congenital Cardio Disease

From the time that Merlin was born until January 2008, he was hospitalized due to his poor health condition at birth. From January 2008 to January 2010, Merlin lived with his birth mother, who was his primary caregiver.  He presently resides in an orphanage.

Merlin was born at 35 weeks gestation. After birth, he was diagnosed with ventricular and atrial septal defect and patent ductus arteriosus (large). He received several operations. At the age of 2 years, Merlin received frenulum incision due to his speech development delay. He has since been evaluated for speech, cognitive, and motor development. He began receiving therapy for his delays and was evaluated as having moderate intellectual deficiency. He continues to receive therapy while residing in the orphanage. Physically, Merlin has a wide nasal bridge, eyelids slanting downwards, big thumbs, wide gaps between his fingers, and conditions of short attention, motion disharmony, and blurred pronunciation.

$51.00 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!