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Because every family deserves the blessing of a child with Down Syndrome... |
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Cara
Girl, born September 2007
FAS, cognitive delays, anemia, ADD, congenital malformation of ribs NOS: pectus excavatum congenital heart defect: Atrial septal defect
What a little doll! She may be a strawberry blonde? Cara is a sweet little girl with many of the challenges of fetal alcohol syndrome. Facial features, cognitive/academic delays, inattention, and heart condition are all common symptoms of FAS. She previously had a diagnosis of Hep C, but we believe that was preliminary at birth. Families should be aware of this and prepared, but not expect it to be the case. Cara will need to be followed by a cardiologist.
From one of our adoptive families who met her in 2013: Cara seems to be a very bright girl all around. She wanted to sneak out into the room where we were playing with our daughter. They all try When she was told to come in she would quickly sit by our side and say, “but I’m going to sit here nicely and play, I promise.” I felt so bad when they would make her come in. She DID play very nicely. She didn’t throw any tantrums. We gave her a mini slinkie to keep and she was so excited and said thank you and ran back into the room. Her hair is cut much shorter and she is petite. She got her shoes on and off by herself…and fast when told she could play after her shoes were on. She would really thrive in a family. This region waives the 10 day wait usually too which is extra nice.
Cara is facing transfer this year and urgently needs a family to give her the life and future she deserves. This region often waives the waiting period! Married couples only, older parents and large families OK, travel required.
Gene
Boy, born 1998
Gene is described as eager and easygoing.
From someone who met him: To really ‘get access’ to Gene, you need to try hard. Some days he’s living in his own world and it’s hard to ‘reach’ him. But it’s worth the effort. I met Gene in the summer, and the other children in the group were all trying to get my attention, Gene wouldn’t I tried to give some attention to every child in the group, so also to Gene. It took a while before I could get him out of his own world. I grabbed his hand and just stroke his fingers one at a time. He would look at his fingers, and after doing that for minutes, he would finally look at me. He looked who was stroking his hand. Still he didn’t allow me to touch him more than just stroking his hand. Next day I was wondering if he would still remember me and if I could touch his hand again. I didn’t need to ask myself that question, because as soon as I walked in, he came up to me, reaching me his hand. I knew I broke through his wall that kept him safe in his own world. It still took me a while to really ‘open him up’. In November I visited his group again, and again it took me a while to ‘reach’ him. But as I was tickling one of the other boys in his group, he came closer. So I grabbed his hand, to pull him on my lap, next to the other boy, and I tickled him. What happened was amazing! He started to laugh! He laughed out loud, the first time I heard him do that. And he couldn’t stop anymore. His laugh was so contagious and so wonderful to hear it. It brought tears to my eyes. He was so open and he wanted me to tickle him more. Next day I could hardly touch him again, which was hard for me, because I wanted to get him out of his own world again. But I found out that I should not lose hope, because it depends on his mood if he will let you touch him. Another day I could tickle him again and he laughed again. This boy just needs more stimulation to stay out of his own world. Because of the lack of stimulation he normally just sits on the ground and rock back and forth. But he is able to walk, to run around and play games. He can have fun and interact with other children. It just takes a little more. This boy is already in the institute for a long time, and this is the price he paid for it.
He desperately needs a family who will love him and stimulate him. Gene becomes 15 this year! He needs a family committed to him before his 16th birthday, otherwise he’ll be condemned to institution life forever.
Married couples only, large families welcome.
Navid
Boy, born 2003
Cerebral palsy
Navid is described as positive, cheerful, and neat! He appears to be cognitively normal, but with pretty significant CP.
From someone who met him:
Navid is such a happy boy, a little mischievous. He has pretty severe CP, and he spends most of his time in a wheel chair, but he is able to roll over and move around wiggling like a worm. He likes to make jokes. Because he is bound to his wheel chair he doesn’t get a lot of chances to play. Inside the building he can only sit at a table, so what he does most of the time is building with building blocks. At least, he tries to. His fine motor skills are not that good, but he really tries. In the summer of 2012 I trained him to ride his own wheel chair so that he could at least move around a little bit. It made him so happy when he could ride his wheel chair. We walked a lot of rounds together.
He seems to realize that outside the gate of the institution, there’s another world. Sometimes when we were walking/riding around he would steer to the fence and stare through, pointing at the people who were walking on the other side. The people would stare back at him and he would look at me as if he wanted to ask to take him out. I really considered, I could see the desire in his eyes.
But most of the times he is happy and his smile is so contagious. Whenever he is smiling I just want to hold him and cuddle him really close. He loves it when I go with my fingers through his hair, he would lay his head down to my shoulder and smile really sweet. He just loves to be touched. He loves it when you pick him up and dance around with him. He start to giggle louder and louder and his smile reaches from ear to ear.
Julia
Girl, born 2002
FAS (fetal alcohol syndrome), probable secondary CP
Julia has such happy, giant brown eyes and a smile that lights up a room!
From someone who met her: Julia is a girl that I know as the girl with the big smile. Somehow she just seem to smile almost always. She’s a little monkey. Whenever somebody enters her group she would crawl up to that person and just start to climb on him/her. She doesn’t even need you to give her a hand, she’ll just climb up without any help and then she hangs on your neck, looking around, proud, as if she wants to say ‘Did you see that? Do you see where I am?’
Her favorite toy is a doll. She plays with it as if it is a baby. Keeping the doll up straight, putting her down carefully. She feeds and clothes the doll. One of the nurses showed her how she should put a cotton diaper on the doll, she totally loved it. She even sings lullabies for the doll and she’ll ask visitors to do the same. She also loves to play with long hair. She really tries to make ponytails or braids.
Julia is able to walk, but her legs are really crooked, and she needs help to keep standing or to walk. Julia is described as curious and enthusiastic.
Caius
Boy, born April 2012
Arthrogryposis, patent foramen ovale, dacryocystitis
Well, isn’t Caius just a cornucopia of cuteness 
Sweet boy is a wonderful age to join a family and receive therapies and medical care.
Ezra
Boy, born Oct 2011 congenital
internal hydrocephalus operated; anemia; protein-energy deficiency
Ezra has had a shunt placed, and is doing better. His adoption may necessitate consultations with medical personal, to safely transport him home.
From someone who met Ezra in 2013: Ezra is absolutely precious! He is sweet and adorable and oh so lovable! He laughs when his toes are tickled, or when someone around him laughs or talks or sings to him. He often smiles or laughs so hard his chubby cheekers make his eyes close. He ha s learned to blow spit bubbles and coo. It is hard for me to tell if he is able to use his limbs normally, but he is able to move from his back to his side with little or no assistance. He has not yet learned to play with toys, but he has a very strong grip and enjoys holding my finger. I was told he can see, but not very well. I observed his eyes moving rapidly from side to side, and sometimes appearing to be looking in two different directions. In spite of this there were other times in which he appeared to be quite focused and looking right at us. He has absolutely stolen my heart, and I hope that he will find a family that can help him meet his full potential!
These pictures are from May, 2013.
Large families welcome; married couples only. Travel required.
Jefferson
Boy, born April 2006
After-effects of traumatic brain injury, brain contusion, right hemiparesis, ptosis, OS
F06.8, F80.1, F 88.0
In May 2011 the boy fell off the third floor and his condition is the result of the injury. He has some vision and speech impairment but he is a very smart and nice boy.
He is still in the orphanage but will be transferred to the institution soon if we don’t find him a family fast.
Kathleen
Girl, born 2004
Unrepaired cleft palate
Kathleen is described as broadminded and cheerful.
From someone who met Kathleen in 2010: Kathleen is a very loving and social little girl who loves getting attention from adults. Whenever I was in her group, she was always right beside me, participating in whatever I was doing and engaging me in her own favorite activities. Kathleen has kept that silly, playfulness that most institutionalized children seem to lose. She was definitely a little mischievous getting into everything, but was also very quick to follow direction and obviously eager to please. I truly believe she would thrive in a family where she was showered with all the attention she deserves and allowed to simply be the fun-loving, silly little girl God created her to be.
From someone who met Kathleen in 2012: Kathleen is a happy little girl who would love to be able to communicate, but cannot because of an unrepaired cleft palate. She makes noises to communicate to the best of her ability. She is a very sweet little girl, and loves to play outside. Many missionaries who have met her loved her and spoke highly of her!
Sullivan
Boy, born 2001
Sullivan is a sweet, loving little boy. He is described as cheerful and curious. The smile on his face when he is being held is absolutely precious! He is not talking, but appears to be very capable of learning sign language to communicate! He loves to play “If you’re happy and you know it” and made up a sign for this, clapping his hands together.
Sullivan then quickly learned the ASL sign for more. In addition he has a sign for potty, and drink. He does not go right away to strangers, but wants those he is comfortable around to hold him and play with him. He is not able to stand or walk, but crawls to get around. When hurt by another child he will not attempt to defend himself, but will cry in hopes of someone comforting him. Sullivan is a very sweet boy who would do wonderfully in a family!
Bowden #4-2
DOB: 2008
Diagnosis: congenital hydrocephalus
medical records include head circumference measurements plotted throughout his life
UPDATE In 2012, he received a shunt with good post surgical results. His hydrocephalus is now well managed and he’s making good progress in his development. An update on his development will be coming soon.
Bowden has hydrocephalus and delays in his development as a result. However, he has made tremendous gains in all aspect of his development in the past 6 months. He has a significant bond with his physical therapist and responds very well to the rehabilitation program and all the adults that are working with him to improve his development.
Bowden walks with support (holding one hand). He sits independently, crawls and walks in a walker. He climbs up the slide and on other therapy toys independently. He can stand next to an unmoving support holding on with one hand and play with a toy with the other hand. He can get to toys or anywhere he wants to go independently. He uses his left hand more than his right, though he will manipulate objects with both hands. When asked to pick up an object or find a toy, he actively looks for it and correctly identifies the requested item. He follows verbal directions. He cleans up the play area and puts the toys away in a toy box. His report says that he insists on cleaning up without anyone helping him when he’s done playing. He smiles, laughs, cuddles with adults, gives kisses on request, waves “hi” and cheers when given praise. He looks at himself in a mirror, says “hi” to his reflection and then gives it kisses. He loves having the attention of adults and will get sad when his therapy time is done. He loves to listen to music and sings along with the songs. He can perform some of the motions to dances and loves to dance along with any music. He is learning the names of his body parts, will show his teeth when asked if they are clean after brushing and will gesture with his hand when asked to show that he is “this big”. His speech is delayed, but he can say over 10 words. He pronounces a lot of sound combinations and his speech is continuing to develop. He mimics words and 2 word phrases and is beginning to put words together in questions and sentences. He’s had a significant gain in his verbal expression in the past 6 months. He is working very hard to learn to feed himself independently and is successful at feeding himself with a spoon. He needs minimal assistance. He drinks independently from an open cup. He plays well with other children.
UPDATE 2013: Bowden is now TALKING! He loves asking questions and if no one answers him, he answers himself! He’s also learned to feed himself with a spoon. He has a best friend in his group, a little girl who he enjoys playing with. He is now playing appropriately and purposefully with toys and actively participating during learning times. He is showing a curiosity of the world around him and is eager to explore and learn.
UPDATE Feb 2013: He is now living with the physical therapist from his orphanage and she is working with him to help him continue to make progress until a family can be found for him. He still spends his days at the orphanage, In the newest videos, he is walking down the hall holding just one hand of the adult, feeding himself, talking, naming body parts and identifying objects in a book and following verbal directions. He continues to make great progress in all aspects of his development.
We have several photos and videos of Bowden as well as a detailed medical report for interested 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.
Iris
Girl, born 2001
HIV+
Iris is a lovely young lady; she is described as curious and enthusiastic.
From someone who met Iris in 2012: Iris is a sweet girl who loves attention and physical affection. She loves to be hugged and will play with your hair and sit in your lap. She is a big helper within her group, and is a good friend (more like a big sister) to many of the other kids in her group. She is very affectionate with those kids, and will play with them and try to pick them up. She has great play skills, and loves dolls. She also enjoys playing with balloons (hitting them back and forth to other people), and coloring with markers. I have been told she was not burnt, but that she has a birthmark. She is taking medication for her hiv. Her cognitive abilities and social awareness are not what you would expect from a child of her age, and I am not sure how much of this is due to orphanage delays.
Large families welcome. Married couples only; travel required.
Maria
Girl, born 2002
Down syndrome
Maria is a bundle of sweetness and pure energy! She lives her life sort of like a game of bumper kids, not afraid of crawling over, through, or into other children to get where she wants to go. She is otherwise all girl, giggly and sweet, loving to blow kisses or play with dolls.
She is not speaking, but uses some sign language she may have made up to communicate her basic needs, such as thirst or needing to go to the bathroom. She also makes some of the most hilariously adorable facial expressions. She is not able to stand or walk, and she appears to have problems with her hips. She is very flexible, and often sits with one foot above her head. She can get around quite well in a very unique way of holding her feet and scooting along on her bottom, she moves at a very fast pace. She is a sweet girl who does not know about personal boundaries (such as crawling around instead of over the other children) but is nonetheless very loving and would probably do great in a family where she was the youngest.
Porter
BOY, Born August 10, 2005
PORTER HAS BEEN TRANSFERRED TO AN INSTITUTION!
Don’t mind this pink shirt, Porter is a BOY. He is HIV+, stage 3. He is cognitively delayed as well, and has some paralysis on half of his body.
From his medical records: HIV stage 3, without immunosuppression, delay of psychomotor and speech development, bacillosis
Update 2013: Severe mental retardation, HIV, congenital heart disease
Chantelle
Girl, born August 2007
CP dystonic-dyskinetic type, rough delay of static and locomotor activity, mental delay, umbilical hernia, congenital cataract, crossed eyes
Sweet Chantelle has a list of diagnoses, but her main need is a loving family! A family could help her reach her potential and save her from a life in a crib.
Nadia and Nancy (twins)
born August 2007
Both girls have been diagnosed with FAS, pyramidal insufficiency in legs, mental delay, and crossed eyes
What a lovely little pair of pixies! Nadia and Nancy are twins. Please help us find them a family where they can grow up, together!
From a family who met them in 2012:
We saw them successfully feeding themselves borscht. They were sitting up properly and feeding themselves soup with a spoon. One walks and even runs a little stiff/awkwardly but they are absolute DOLLS! The other crawls and socializes. They have deep auburn hair and dark hazel-ish eyes. They are both tall, lean, and long-limbed. One is a bit more shy than the other. Both are BORED and need music, hugs, kisses, and a mama and daddy! They loved our attention and carried around magazine pages. They are beautiful twin girls!!!Oh my heart!!!! My heart is breaking! Someone will be blessed to be their parents!
Large families welcome; married couples only.
Garfield
Boy, born April 2008
Hepatitis C, rough mental delay, fish skin (ichthyosis)
What lovely blue eyes this little guy has … and cute mussed up hair!
Large families welcome, travel required. Married couples only.
Barton
Boy, born December 1997
Rough mental delay, cerebral palsy spastic tetraparesis, partial atrophy of optic nerves
Barton is a quiet boy. He loves to be outside, staring at the sky, following the birds with his eyes. He loves to feel the wind around his and when there’s a leaf on the ground and the wind blows it away, he goes running after it. Barton doesn’t make eye contact but he does listen when you speak to him. He doesn’t talk, but he when you ask him to do something he will immediately do it, come to you and stand in front of you for a moment. When you say ‘well done’ he’ll continue what he was doing before. Barton sometimes seems to live in his own world. He’s not making a lot of social contact with the other children from the group, until somebody turns on the music. He loves music and he will start dancing with the other children of the group.
Barton is fifteen already, so he needs a family fast. He needs a family committed to him before his 16th birthday. This boy can become so much more if he would be supported by a loving family!
Large families welcome, multiple children may be adopted together from the same orphanage. Married couples only; travel required.
Dell
Boy, born October 1999
Down syndrome
From someone who met him in 2012:
Dell is just such an adorable boy. I feel blessed that I could spend time with him. Dell has down syndrome, but he is such a smart boy. He totally loves attention! He’s a little bit mischievous. He will do something that the nurses told him not to do and then he will look at me or them like ‘Did you see what I do?’ Some of the nurses are having a hard time with him because of that, but I just think it’s wonderful. That kind of behavior tells me that he is acting pretty normal. Which child is not searching for the limits and looking what happens when he crosses them? But his behavior is giving him a hard time in the orphanage he’s living in because the nurses are taking care of fifteen children at the time and they just want easy, obedient children. But I think he is adorable and well functioning.
He develops really well. He is healthy boy, well nourished, he talks a lot. He cuddles the little children in the group and carries them around. He loves to play with building blocks and he can make real houses out of them. And he totally loves pictures! He will always put on a really big smile! That smile is so contagious!
Dell is probably the heaviest boy of the group, and that’s why the nurses tell him he’s too heavy to sit on somebody’s lap or be carried around. But Dell loves it to sit on your lap or to be carried around. He loves it when somebody thinks he’s not too heavy or too big/tall. He starts laughing and laughing when you pick him up and twirl him. He enjoys messing up long hair and playing peekaboo.
Last summer an adopting family visited his orphanage and Dell was so fond of the adopting couple. Especially the ‘daddy’. He really called him daddy and every day when they visited their son, Dell would come running after them, hugging them and just hanging around with them as long as he could, until they left or until the nurses told him to come back. This boy would function so wonderfully in a family!
Large families welcome, multiple children may be adopted together from the same orphanage. Married couples only; travel required.
Amos
Boy, born December 1999
Rough mental delay, hydrocephalic syndrome
From someone who met him in 2012: Amos is a wonderful sweet boy! He will do anything you’ll ask. In the summer the children will play outside and the more disabled children are sitting in a big box. Everyday he carries out the carpet to put in the box and he will carry out the benches and chairs to sit on as well. When the ‘outside-time’ is over, he would carry it all back in again. He doesn’t really talk, but I’m pretty sure he would be able to. He does make sounds and he loves to ‘sing’. While singing he makes sounds that could almost be words, but as long as he’s lacking of stimulation, I think he will not talk. He likes to dance around to.
He is a big help for the nurses. When a child has to go to the shower or potty he brings them, when a child falls down, he picks the child up, even without somebody telling him to do that. He is a really social butterfly. He cares about the children around him and I’m sure that he would be an awesome big brother, because that’s what he is for the children in his group.
The only self stimulating behavior that I saw in Amos was sticking things in his ears. You can easily distract him from that by offering him a toy. Once he has a toy, he will not be bored, he can play forever with just one toy.
Large families welcome, multiple children may be adopted together from the same orphanage. Married couples only; travel required.
Artemur
Boy, born January 2002
DS, atrial septal defect, polydactyly of the left hand
Artemur is a handsome boy who has already been waiting far too long for a family of his own!
Large families welcome, multiple children may be adopted together from the same orphanage. Married couples only; travel required.
From someone who met Artemur in 2012: Artemur is a ladies man He loves to greet visitors with a formal “Hello”, a chair for the visitor to sit on, and for the ladies he’ll kiss their hands and sometimes request a kiss by pointing to his cheek. He has ten toes and ten fingers, and appears healthy. He is one of the two highest functioning boys in his group and is a big helper. He is quite verbal, and he has good self-care skills, he is able to feed himself and ask to use the restroom. He likes to play with etch a sketches, toy phones, and bubbles. Artemur would probably do better in a family environment where he can be the youngest in the family.
Augustin
Boy, born February 2011
CP, quadriplegia, microcephaly, cerebral cachexia, seizure disorder
Sweet Augustin has a host of medical issues, but hopefully someone will see past those terms to the boy he is, and the boy he can be! He needs a mama!
Violet
Girl, born July 2003
Diagnosis: hydrocephaly, mental delays
She likes to play, tries to walk alone, but needs assistance. She doesn’t speak, but understands much.
From someone who met her in 2012:
When I walked into the room packed with children, her smile and wave and joy stood out more than all the chaos and heartbreak and noise. She was a darling and I just know she would be amazing to have as a daughter.
Emil
Born December 1999
Diagnosis: cerebral palsy and down syndrome
From someone who met him in 2012:
Emil was the gentlest child ever! Unable to talk but the pleading in his eyes killed me! He grabbed my finger and wouldn’t let go…what a grip! He also got really hit a few times by others wanting my attention, he didn’t retaliate but fell in a heap and moved away, only to return when the coast was clear. I would love to see this child in a nurturing environment!
Emil is able to walk.
Eldridge
Boy, born May 2009
Cerebral palsy
Eldridge also has significant features of FAS (fetal alcohol syndrome), but this is not diagnosed.
Large families welcome, married couples only. Travel required.
Brinli
Girl, born August 2009
After-effects of viral encephalitis in the form of microcephaly, movement disorders syndrome (cerebral palsy syndrome), epileptic syndrome of residual genesis, secondary hypothalamic syndrome, loop of thermal control
Brinli has pretty eyes, and such lovely long fingers. She desperately needs a family to save her from a life spent lying in a crib.
Large families welcome, married couples only. Travel required.
Cherie
Girl, Born Dec 2009
Crouzon syndrome
Sweet Cherie …. she needs a family desperately!
Picture on the left is from December 2012, on the right is from summer 2012.
Cherie needs a family fast! From her medical records: congenital anomaly of the skull, feet and hands. Cleft hard palate, UPU, LLC, aortic defect.
Whitaker
Boy, born October 2010
Cerebral palsy, spastic tetraparesis, optic atrophy, secondary internal hydrocephaly, seizure disorder
Polly #35-0 OD
Girl, born August 2000
Polly is a 12-year-old girl with a mild mental delay who has a developmental disorder of speech and language. She is in need of dental care due to some issues with her teeth.
Polly is relatively well-developed physically when compared to the age norms. The lack of parental care, a mother’s caress and physical and emotional contact in early infancy has affected the child’s psychological development negatively by lowering the quality of her behavioral activity.
There are no significant irregularities as regards Polly’s psychomotor development. She demonstrates satisfactory verbal, non-verbal and eye contact. Her strength is correspondent to her bodily development. The child has normal mobility and well-coordinated movements. She would benefit from active physical activities and sports. The girl has adapted well to her classmates at school. Her attention is unsteady during the classes; she has limited attention span and low stability of concentration and can easily be distracted.
Additional medical information available.
Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.
Robert #34-9 OD
Boy, born December 2002
Down syndrome
Robert is a handsome young man. His general development is delayed. He has good gross motor skills, and his fine motor skills need a bit of assistance; he likes to color. He enjoys listening to music, and dancing. He vocalizes, but his expressive speech is not developed yet.
Robert currently is a student in the fourth grade of a Special School. He has a good orientation in the academic environment and points at objects in the classroom. He understands instructions, but does not always follow them. He knows his name and reacts with a smile when called by name. He takes part in the educational activities with interest but he would soon lose his concentration. He shows positive attitude toward children and adults. He often takes part in organized events. The boy performs simple chores – when assisted and stimulated he cleans his work place and the classroom.
Additional information available from the agency.
Deliya #67-2
DOB: 2008
Diagnosis: Congenital bilateral cataract; bilaterally clubbed feet – surgically corrected; Hypotrophy of bottom extremities; Auto-aggression and stereotypical movements that are common in children with blindness
Deliya has cataracts that could possibly be corrected with surgery. At this time, surgery is not planned in her birth country and she is considered significantly visually impaired at this time. Deliya sits unassisted and has begun to walk while holding on to furniture or touching the wall. She can say 2-3 words and imitates sounds. She does not appropriately play with toys and is considered to be lagging behind in all aspects of her development. However, she cannot SEE and she is not receiving therapy to help her overcome her physical limitations. She seeks out the attention of adults and moves toward their voices. She will respond with touch if other children initiate contact with her.
The agency has several new photos and videos of her.
Dani
Girl, born December 2009
Cerebral palsy, hemiplegia, movement disorders in combination with vision and hearing impariments
Dani has beautiful blue eyes, and a darling little button nose!
Large families welcome, travel required.
Tatiana
Girl, May 20, 2006
Tatiana was born with FAS, but her medical records do not indicate any additional medical complications. She is also HIV positive.
Tatiana is the younger sister of Trudy and Tristan. All three children can be adopted together or separately; they are currently in the same region, but in different orphanages. We hope to find a family where they can stay together!
She is facing transfer to an older child internat very soon, but she can still be adopted from there. Would rather see her in a family! She has been waiting SO long.
From an adoptive family who met her in summer 2011: Tatiana is a sweetheart, and she wants a mama so badly. When we’d go to get our kids, she kept asking “And Tania? And Tania?” She would sob when we would leave her with the groupa. Out of all the kids there, she was the only that I saw playing pretend – eating pretend food, taking care of baby dolls. She is very emotionally fragile, and she seems to get overwhelmed. She is very small and thin. She has big blue eyes, and she desperately wants to be held and cuddled.
From an adoptive family who met her in November 2012:
Tatiana was described by the orphanage director as very beautiful, and she truly is. She was also very enthusiastic when answering questions. She was asked if she has friends and she replied “Da” with her whole body, “Tania have lots of friends”. It was completley adorable. We had given her a pony that moved around on it’s own, and she kept saying “come to Tania, come to Tania”. The biggest hit was the ball that lights up when you bounce it. She would have chased that ball all day! She has a deep voice for such a little girl which I found endearing. It was so ironic, because she is so little and feminine. She has issues with her eyes. Nothing was mentioned in her medical about it. When she turns her head to look at something her eyes bounce around as they try to catch up. She laughs inappropriately, and is very emotional. Has mood swings. Does not understand many simple questions. Her answers did not match the questions, or was unintelligible. She is in constant motion.
Simon
Boy, born Oct 1997
Spinal muscular atrophy, mixed specific developmental disorders (mental delays, very poor speech)
Simon needs a family IMMEDIATELY — he has until October 2013 to be adopted, otherwise he will lose his chance for a family.
From someone who met him in 2012: Simon was so bright, he is amazing! he has great potential and has expressed his desire for a family. He loves gadgets and computers is a typical boy like that! He managed to get into my camera bag (even though it was high on a cupboard) and took my mobile phone apart! He was truly mortified when he couldn’t get it back together and was so sorry…he came straight to me very shamefaced and repentant.
He cannot walk at all; he does not feel his legs and they are very wasted, but he gets around brilliantly in his wheel chair. He talks and is picking up English and draws and writes. He is in the first happy home there with 8 others and so is getting amazing care for his situation.
Griffith
Boy, born August 2008
Minimal hydrocephalus
Griffith is a very nice boy! He has a little bit of an impish look to him in this picture, doesn’t he?
Married couples only, travel required. Large families welcome!
Venetia
Girl, born April 2005
Mild to moderate delays, needs dental work
Sweet girl! She needs a mama to paint her nails and braid her hair. She’s trying so hard to force a smile for the camera.
Frieda
Girl, born September 2002
Mild to moderate delays, Cerebral Palsy
Girl, born September 2003
Girl, born December 2004Adelina
Girl, born December 2002
Mild to moderate delays
Another lovely young lady, still waiting for her forever family.
Girl, born October 2006Soleil
Girl, born January 2001
Mild to moderate mental delays
Soleil comes very highly recommended from the orphanage director. She has shown great progress since she entered the orphanage.
She is running out of time — a family must be found for her before she turns 16!
Havalah
Girl, born June 2005
Mild to moderate mental delays
This little peach is just waiting for a family of her own!
Girl, born December 2004Ryan #6-14
DOB: 2001
Diagnosis: Down syndrome
Ryan is 11 years old. He has been in an institutionHis gross motor skills are well developed. He walks, runs, climbs and prefers physical activities. He exhibits some stereotypical movements. He plays with toys and attempts to manipulate them correctly. He requires 1:1 assistance for academic tasks. He is currently being instructed in how to trace letters, though he still requires assistance with this task. He tries to fit shapes into puzzles. He can arrange blocks and builds towers with them. He likes to arrange the chairs in stacks. He eats independently, though he’s still working on hygiene in related to table skills. He does put away his own dishes once he’s done eating. He can dress himself, but he does not undress himself independently. His personal hygiene skills are not built up at this time. During art class, he requires assistance with coloring and art projects. He can glue items onto paper if the items are pre-cut for him. His emotions and attention are unstable. He is hyperactive and doesn’t always follow the rules. He exhibits difficult behaviors when he doesn’t get his way or doesn’t want to do something. He is sometimes aggressive with objects and with his peers. He enjoys dancing and prefers to participate in activities and play that involve a ball and interacting with children who are more physical.
Additional information: Ryan has been visited by an experienced adoptive family and members from an adoption team well experienced in observing children with special needs. During the visits, he exhibited aggression toward the adults and staff members from the institution. He had difficulty following basic instructions from the staff and often didn’t respond to his name. He did seem to enjoy interacting in small amounts with the adults, though he wanted those interactions on his terms. He did not respond well to restrictions or being made to do things that he did not want to do. He will need a family willing to provide a lot of structure, routine and consistency in behavior management.
Additional photos and videos of Ryan from October 2012 are available.
Duane
Boy, born November 2000
Down syndrome, neurodystrophy, psychological and motor development disorder, alalia
From someone who met Duane in 2012:
Sweet little Duane is the huggiest boy I’ve ever met! He is a determined, strong willed little guy and is up walking and chasing after balls despite some mild CP on his left side that causes his left knee to extend backwards in a painful looking manner. He has an amazing laugh, though it is sometimes a mischievous laugh. He sometimes feels the need to push boundaries, such as throwing balls at the other children, but he is a boy with a lot of love to give, both to the adults and the other kids in his group. He also sometimes gives massages. I feel he would especially thrive in a house where he is the youngest, or at least the smallest child in the home.
Elwood
Boy, born 2008
Sequelae of inflammatory diseases of central nervous system; secondary microcephaly; Fetal alcohol syndrome; tetraplegia; strabismus; Mixed specific developmental disorders
Elwood is a cutie! He needs a mama to love him — and a daddy to teach him to play tee-ball!
Pavel
Boy, born December 2003
Diagnosis: mental delays, CP, tetraparesis, microcephaly, autism
He is a true orphan and knows the love of a family. He is very active, can crawl very well and tries to walk with support (pretty soon they hope he can walk independently- he is very determined!),he can’t talk but can pronounce some sounds. He can cry and show emotion. Motor development not well developed.
Canaan
Boy, born July 2003
Diagnoses: mental retardation, convergent squint, hypoplasia of optic nerves, hypochromic anemia.
This little one is an orphanage favorite and is said to steal your heart when you meet him. He has a wonderful personality and is quite the little helper. He understand speech and he can talk but has speech problems. He is very friendly! He has a short-term memory. He is very active and can service himself with help of adults. This sweet boy lived with his family until his mother passed away in 2009. He knows what it feels like to be loved and taken care of.
He has TREMENDOUS potential and is waiting for his forever family! Please don”t let him go to a mental institution- this little one needs a family!
Nadene
Girl, born July 2005
Diagnsis: mental delays, light degree tetraparesis
Miss Nadene is 7 years old and has regressed greatly in the orphanage; she came here in 2010. She has bad memory and attention. She is very shy and quiet. She needs help often but she can walk with support. She could use the love of a family to really blossom!
Boy, born July 2007Oberon
Boy, born December 2006
Deafness stage 4 — he has a profound hearing loss which means that he is unable to hear human speech, has severe hearing loss in the speech frequencies between 71 and 90 dB HL.
Sociable, friendly, outgoing, cheerful and playful
Oberon is a sweet, active boy. He likes to play with toys. He is helpful, lively and peaceful.
Boy, born January 2006Gabriel L16
Boy, Born December 2001
L16
Handsome Gabriel! 11 years old and really needs a loving, experienced family to give him the life he deserves. He probably has a bit of ADHD, possibly ASD. He is considered relatively low functioning (compared to other children with Down syndrome). But he is active, able, and deserving of a better life than he’s got!
Gabriel will do best in an environment without younger children. He is a big boy and can be assertive at times. He has tremendous potential and I can’t wait to see him blossom in his new family! Interested families should be home study approved prior to commitment. Older parents and larger families welcome!
Nikolajs L15
Boy, Born May 2002
Down syndrome
L15
Nikolajs is 10 years old and waiting for his family to find him. His name means “Victory of the People”. Walks free, is active in the environment which is known to him. Is not able to talk but understands what others are saying, uses gestures when communicates. Expresses emotions by making different sounds and by imitating gestures, likes to imitate different activities, likes dancing or talking by the toy cell phone. Nikolajs also likes playing, has interest in books and magazines. He is calm and he likes to play with his toys alone. Makes role plays – cooperates with other children when wants to. Likes leafing books. Nikolajs knows his digits from 1 to 5 on his fingers. Also points to correct letters when asked. Takes part in sports and culture events at the orphanage.
Full medical and social history available!
Brady L9
Boy, Born April 2001
Down syndrome
L9
Brady is a young man who is 11 years old. He has blue eyes and light brown hair. Brady by nature is calm, kind and he likes tactile communication with an adult.
Brady needs a loving, experienced family of his own. He has heart and pulmonary conditions that desperately need to be addressed. These impact his physical and cognitive abilities, and keep him from achieving his full potential. Full medical and social history available. Families considering Brady should be home study approved prior to commitment.
Older parents, large families, and single moms are welcome.
Christian L11
Boy, Born May 2004
L11
Christian has positive reactions towards the adults with whom he is familiar. Has interest about what surrounds him, though not very big and also not very sustainable. Makes unarticulated sounds. He sleeps well, but has difficulties to fall asleep.
Christian attends school and gets good references from his teachers, he is starting to express his opinion – murmurs when tries to answer. Active and joyful and as most boys – he likes cars and playing with them. Is able to move up and down the stairs, eats self-dependently, though has self-care difficulties (still working on toileting), likes long walks in fresh air but is able to do them only with holding on one’s hand.
Christian has amazing potential….what a joy to get to watch him grow and thrive in a forever family!
Older parents, large families, and single moms welcome. Great program!
Alys
Girl, born February 2003
Mental delays, fetal alcohol syndrome, microcephaly, partial atrophy of optic nerve, birth vitium cordis
Alys is a beautiful, sweet girl who is already 9 years old! She has significant mental delays, FAS, microcephaly and partial atrophy of optic nerve. She could greatly benefit from a family!
Married couples only. Larger families and older parents welcome. Travel required. Families considering Alys should be home study approved (or nearly so) prior to commitment.
Seeley
Boy, born January 2007
CP, mental delays, convergent squint, dysontogenetic cardiopathy, partial atrophy of optic nerve
Another crib baby- this little guy is 5 years old and spends much of his time in his crib. He has significant special needs and could greatly use the love of a family! He was cared for by his mother until early this year (April 2012). He has CP, mental delays, convergent squint, dysontogenetic cardiopathy, partial atrophy of optic nerve.
Braden
Boy, born September 2006
Mental delays, dysontogenetic cardiopathy, convergent squint, umbilical hernia.
Braden lived with his mother until her death before entering the orphanage last year (2011). You can tell he was LOVED and taken care for. He is doing quite well compared to many of the other children which is attributed to being in a family versus institution. Who knows how much he could improve with the love of a family! He also has a caregiver he has attached to.
He is a mobile child and very active. He tries to walk himself. He understand what most people are talking about but he can’t talk in sentences. He can pronounce some words. He can’t service himself, need assistance to eat. He tries to hold a spoon in his hands. He recognizes his caregivers and can follow simple instructions. These are all GOOD things!
Victor
Boy, born May 2003
Mental delays, CP, spastic tetraparesis. Speech, motoric, physical development delays; functional cardiopathia, convergent squint
Another smiler! He has significant delays and has potential to thrive in a family! As all children in this orphanage he is living on borrowed time.
Saul
Boy, born February 2003
Mental delays, CP, birth atrophy of optic nerve, retina dystrophy, contracture of leg joints
Look at that smile! Anytime these children smile that is a GOOD sign!! He is already 9 years old- pretty soon he will be entering an adult mental institution where his chances of being adopted are near impossible.
Geneva L12
Girl, Born October 1999
L12
SO grateful to have this opportunity to share these beautiful older children with you! Geneva is darling….almost 13 years old and growing so well. She is much loved, and attends a school for children with special needs in the 5th grade.
Geneva has a little hyperactivity…she gets bored easily with things and goes from activity to activity. She does not use words or gestures to express her desires. She has such potential to learn to communicate, it would open up her own world and improve her level of frustration. Geneva also has alopecia areata (like Reece!)…she may benefit from Vitamin D therapy and/or steroid treatment for that hair loss.
From her caregivers: Very lively girl, moves all the time. Wants individual attention to be focused on her. Does not react on the admonishments of carers. Girl gladly attends lessons but does not understand the need for them. Does not ‘see’ herself in the mirror. Is not able to repeat movements with her lips and tongue. Has good self-service skills and also tries to help others. Gladly draws with pencils, chalks and also paints. Is trying to learn to ride in the three-wheel bike. Likes walking around the city, going to cinema. Behaves well, eats with fork. She is a singleton, does not participate in the group activities.
Older parents and large families welcome. Parents should be home study approved prior to commitment.
Dante L3
Boy, Born April 2000
L3
Isn’t Dante handsome? My goodness! 12 years old and full of life and potential. Considered quite high functioning by the staff and caregivers. Very smart, active, friendly, helpful…enjoys the computer very much, as well as hockey and basketball. Loves people and playing with other children, but likes to have his own time as well. Speaks well, understands clearly, responds appropriately. He even knows how to ride a bike safely in the street! He is generous with his things, but also takes care of them. (I’m wondering where I can get a child like this!? Wow!)
He does seem to need glasses (he squints a lot). Full medical and social history available.
Praying Dante will not have to wait one second longer now that he has a voice and a chance through Reece’s Rainbow. Older parents and large families welcome, single moms welcome. Wonderful program!
Dixie L2
Girl, Born January 1999
L2
Dixie is going to make a WONDERFUL daughter! She is SO smart, helpful, kind, sociable….she needs a chance to live her life outside of an orphanage. Her speech is very delayed, but she has computer skills and loves to browse through books. She is active outside and enjoys sports and playing. She is a “lttle mommy”, and enjoys helping other children whose needs are greater than hers. Dixie goes to a special needs school where she is in 7th grade. She does have glasses, but she doesn’t like wearing them….sound familiar? 
Dixie is describe as a “keen-witted young lady”. I LOVE that they see her as the 13 year old she is, and not as a child.
Dixie can be adopted by older parents, larger families, and single moms. Families should have experience with international adoption. Full medical and social history available.
Jordan L26
Boy, Born November 2001
L26
Jordan is 11 years old. He has light brown hair and brown eyes. Instead of playing soccer and other games, Jordan clings to a walker because he has vision problems, and it makes him feel so uncertain about the world around him 
Jordan has tremendous potential in a loving, experienced adoptive family.
Diagnosis: Severe mental retardation, significant behavioral changes that require looking after or treatment (F72.1). Down Syndrome. Atrophy of optic nerve. Thrombocytopenia. VCC – atrial septal defect.
Older parents, large families and single moms welcome. A family where Jordan can be the youngest, with older siblings, would be ideal for his learning and attachment. He has missed out on so much in life Families should be home study approved (or nearly so) prior to commitment.
Crystal L25
Girl, Born November 2001
L25
Crystal is so pretty! Dark hair and brown eyes. She does have Down syndrome, but also has many facial features of FAS (fetal alcohol syndrome) as well. Crystal has tremendous potential. She has been significantly impacted by very poor vision and hearing, and that has resulted in lower cognition and physical abilities. Imagine how her world could open up with medical treatment, glasses, and hearing aids!
Crystal can be assertive sometimes, so a family with older children is recommended. Full medical and behavioral info available. Older parents, large families, and single moms welcome. Families should be home study approved (or nearly so) prior to committing for Crystal.
Jill L22
Girl, Born January 2002
L22
Jill is a beautiful young lady who needs a loving, experienced family. She is considered profoundly delayed. She does attend a school for children with special needs, and she does recv therapy and specialized care in her orphanage. She is growing well (size-wise), but she needs full care. She tries to walk but gets tired easily. She has some autistic/institutional behaviors, and craves sensory input.
Full medical and social history available. Wonderful program with a great agency partner. Older parents, large families, and single moms welcome. Families should be experienced with international adoption and the challenges of older children with special needs. Approved home study required prior to commitment.
Thomas L19
Boy, Born November 2003
L19
Hi Thomas! Thomas is 9 years old and waiting for his forever family. He is in 2nd grade now in his school and doing well. He is very active and friendly, smart and helpful! He does have a heart condition that will need attention.
Thomas likes to listen music, fairytales and poems. He tries to recognize letters and digits from 1 to 10 now. Is able to count along if one also is counting together with him, can show the digit, which is needed on his palm, when asked. He also is trying to learn to group shapes and to recognize colors. Thomas likes working with playdough. He gladly participates in sports activities and he likes aerobic exercises. Thomas is good in acquiring and comprehending everything what is new to him.
Self care skills – is able to dress and undress his clothing, but needs some help to button and unbutton his clothes, puts on his boots. Eats and drinks slowly but self-dependently. Toilet-trained during the day, still needs help at night. Thomas is learning how to wash his hands without getting wet and also tries to brush his teeth. Willing to participate in different house-works, he watches how it is done by others and then imitates it.
Thomas walks and runs. Likes going outside. He pronounces simple words and his own name in his special ‘language’. Responds to his name and is active. Understands simple instructions. Repeats words and always wants to do something – playing, imitating sounds and actions. Especially boy likes to improvise dancing. He likes playing alone, then he puts pyramids, draws lines with pencil. He observes other children around him and then imitates what he has seen. Thomas always will find what to do in his spare time. Likes music lessons and he often dances by the music. Learns to put in order toys after he had played with them.
Diagnose: Severe mental retardation, significant behavioral changes that require a looking after or treatment (F72.1). Down’s Syndrome. Compensated hypothyroidism. Celiac disease. Gastritis, duodenitis-helicobacter pylori positive, congenital heart disease, defect of septum of auricle of the heart, cardiovascular incompetence I-II (CVI I-II).
Margeaux L18
Girl, Born December 1999
L18
I so wish we had a better photo of Margeaux! Margeaux is almost 13 years old and is still in a crib She is considered quite low functioning, but it is these children we always see the greatest transformation in! She is able to pull to a stand. Full medical and behavioral information is available. Older parents, larger families and single moms welcome. Margeaux needs a family who is experienced in international adoption and the challenges of children with special needs who have been living in institutional settings. Families should be home study approved (or nearly so) prior to committing for Margeaux.
Margeaux is rapidly approaching the time where she will “age-out” and no longer be eligible for international adoption (by US law). Her life means, and can be, so much more than this! PLEASE do not leave her behind now that she has been given a voice and a chance through Reece’s Rainbow!
Fritz L4
Boy, Born June 2001
L4
Handsome Fritz is already 11 years old. He has blonde hair and hazel eyes. Fritz is blessed to live in a nice orphanage, but he needs a family of his own. He is considered lower functioning, and really needs a family who is experienced with adopting older children.
Fritz may struggle with some sensory or ASD challenges….he is very responsive but needs a lot of self-help and guidance from parents/caregivers. He would probably do best in a family where he can get lots of attention from his parents and older typical siblings….be the focus of the family!
Families should be home study approved (or nearly so) prior to commitment. Wonderful program, outstanding agency partner…older parents, large families, and single moms welcome. More photos and medical info available.
Kent
Boy, born March 
2005
DS: Mental delays, CP, epilepsy, Congenital cerebral cysts. Cardiopathia. Inguinal undescended testis. Bronchiectatic disease.
Sweet Kent is often in his crib but look at that smile! He too lived with his parents for a brief period before they lost rights. Because of his diagnoses he is not cared for properly and could use the love and medical attention a family could offer.
Paige
Girl, born December 2004
Mental delays. Down syndrome, cardiopathia. Umbilical hernia. Convergent squint.
Paige is 8 years old and had previously been living with her mother until she lost her rights. Paige knows what it feels like to be in a family but in her current orphanage she will not receive the love and attention she needs.
She can sit independently and can crawl! Her speech is not well developed but she can partially understand what you are saying. She has a very short attention span.
Married couples only. Older parents and large families welcome. Travel required. Families should be home study approved prior to commitment.
Vera
Girl, born October 2007
Birth anomaly brain develpment, microcephaly with tetraparesis, convulsive syndrome. Mental delays. Convergent squint. Partial optic atrophy. Umbilical hernia.
Oh sweet Vera! She is only 4 years old and has been in this orphanage since spring. She spends much of her day in the crib and she needs stimulation!! She is living on borrowed time. She has tremendous potential for improvement if only she is given the chance. She will require medical attention and families should expect at the very least physical therapy.
Valiant
Boy, born July 2005
Mental delays; consequence of hard degree closed head injury (brain contusion) with tetraparesis. Symptomatic temple epilepsy. Immunity form of idiopathic jaundice. Middle degree anemia. Dysontogenetic cardiopathy
Mr. “V” is 7 years old but looks much younger. As all of these children in this orphanage they NEED families to come adopt them. When the children get older they will be transferred to adult mental institutions (at young ages!) and there will be LITTLE to NO chance of adopting them.
Children in this orphanage need families! They do not receive enough interaction/therapy to help them thrive. They are seen as hopeless but we know that is not true!
Galvin
Boy, born May 2006
Anomaly of brain development with low flail legs, psychomotor and speech development. Protein deficiency anemia. Defect after birth right side cleft lip, soft and hard palate.
Handsome 6 year old Galvin could use a family very badly. He spends most of his days in the bouncy seat and crib. Who knows what his potential could be! Children in this orphanage need families! They do not receive enough interaction/therapy to help them thrive. They are seen as hopeless but we know that is not true!
Shayla
Girl, born March 2004
Diagnoses: deep mental delay. Cerebral paralysis- double spastic form, microcephaly. Strabismus, divergent squint, and Optic atrophy. First degree anemia.
Sweet little Shayla could tremendously use a family and medical attention to help her thrive. She has already been living in this orphanage for 3 years and risks soon having to be transferred to a place where adoption will be next to impossible.
Her speech is not well developed, she holds toys in her hands for brief periods of time (but she sure does love to hold stuffed animals!), she has a reaction when you say her name but she is not able to communicate back but she smiles. She walks with support- can”t walk independently. Children in this orphanage need families! They do not receive enough interaction/therapy to help them thrive. They are seen as hopeless but we know that is not true!
Nick
Boy, born 1998 (most likely in February)
Mild to moderate mental delays
Nick has a sister who has already been adopted to the US.
Nick has some delays, and speaks slowly, and was attending school at one point. His delays may be greater after life in an institutional setting. He would likely thrive in a family!
He is running out of time to be adopted — a family MUST file paperwork for his adoption prior to his 16th birthday.
Alder
Girl, born June 2008
Cerebral Palsy
Alder needs a family, to spare her from a life in a crib, and reach her full potential.
Large families welcome, married couples only. Travel required.
Jolina
Girl, born August 2007
Nervous system disorders, mental delays
Jolina is a darling girl, waiting for her forever family! She has some features of FAS (fetal alcohol syndrome). This is a cautionary disclosure, not a diagnosis.
Lanora
Girl, born August 2009
Spina bifida - Congenital malformation of the central nervous system, myeloradiculomeningocele with rachischisis of lumbar spine; internal hydrocephalus, low paraplegia
Lovely Lanora needs a mama to let her beautiful hair grow out!
Large families welcome, married couples only.
Marnie #29-8
Girl, born Feb 2007
Diagnosis: Down syndrome, repaired heart condition
Marnie was in and out of the hospital the first year of her life due to medical issues surrounding her heart condition. Her heart was successfully repaired when she was a year old and her recent cardiac check up indicated that her heart is functioning normally.
Marnie is currently walking with support and receiving PT to strengthen her leg muscles so that she can walk independently. She has recently started pronouncing sounds and syllables in an effort to communicate. She plays with toys and interacts appropriately with care givers. She is NOT aggressive toward herself nor toward the other children. She eats from a spoon.
Additional photos and video available!
Vaughn
Boy, born January 2007
CO-A
Down syndrome, otherwise reported to be healthy
What a handsome young fella! I adore how he’s standing with his hands in his pockets. Vaughn is already 5, and at a great age to join his forever family. This is a great program with a wonderful agency partner. Hope you will consider Vaughn as your son!
Enoch
Boy, born September 2006
He has strong mental delays, strabismus
Someone needs to save this sweet boy from a lifetime in a crib. He’s chewing on his hands for self-soothing. We have another picture of him that’s fuzzy, but you can see his smile peeking out behind his hands — he has a spark!
Macarius
Boy, born April 2009
Cerebral palsy – Spastic diplegic cerebral palsy
Moderate mental delays; Divergent strabismus; Planovalgus (foot) deformity; malnutrition
Macarius speaks, plays toys and has a positive personality, smiles often. He is a very good boy!
Macarius doesn’t walk, the boy needs a surgery and even with surgery there can be only hopes for his future ability to walk. The doctor in the orphanage says he has good prognoses for the future and his development.
Additional pictures available. Large families welcome, travel required.
Matthew
Boy, born September 2010
Infantile cerebral paralysis, binominal hemiplegia; Internal hydrocephaly; Dysplasia of coxa (hips)
Such a little sweetie … look at those delicate fingers and big dark eyes!
He has possible features of FAS. This is not a diagnosis, but a cautionary disclosure.
Gibson
Boy, born August, 2010
Infantile cerebral paralysis; binominal hemiplegia; post-convulsive syndrome; cognitive delays
Gibson needs a family, or he could spend the rest of his life in a crib. This lovely boy needs a HOME!
Ernie
Boy, born December 2010
Hydrocephaly
Ernie can sit independently. He smiles, plays with toys – and has the most adorable wispy hair!
Ashton
Boy, born August 2010
Spinal bifida of lumbar area with hydrocephaly; lower smoldering paraparesis
An adorable grin on Ashton!
Large families welcome, travel required. Married couples only.
Nevaeh
Girl, born, March 2010
Cerebral palsy, optic atrophy, developmental delays
Ohh, I love her little pouf of hair, what a lovely little girl.
Not sure how much vision she has.
Phillip
Birth Date: 04/12/09
Gender: Male
CO-A
Dysgenesis of the corpus callosum, congenital cervical scoliosis, and hypoplasia of the first finger of the right hand
Phillip was given up for adoption shortly after birth. He is constantly smiling. He is very social and frequently seeks to have company. His weight and height are lower than the normal range for his age, but with a high-calorie diet and a dietary supplement he is expected to reach a normal weight and height. He suffers from a speech delay for which he has been receiving therapy. He is responsive when adults play with him and has been making great progress with the therapy he receives. Phillip is an easygoing little boy who is earnestly waiting to be united with a family that will provide him with the care and love he deserves.
Phillip has a significant language delay, but his vocabulary and verbal productions are increasing. He communicates using single words, gestures, and signs. He recognizes and points out his body parts, imitates animal sounds, follows rhythms, dances and sings songs. He understands and performs routine and simple tasks.
Phillip enjoys to interacting with adults and peers. He looks for help in adults when he has needs.
Video available through the agency for inquiring families.
- Single parents may adopt
- No family size restrictions
- Both parents must travel to the country and stay until completion of adoption — approx 5-7 weeks (one parent may leave after a week or two)
- Estimated total cost $21,000-24,500
- Multiple unrelated children may be adopted together
Matalie 3G
13r4w-3
Date of Birth: June 2004
Gender: Female
Nature: Quiet
Liam
Boy, born March 2006
Cerebral Palsy, significant mental delays
Not a great picture, but Liam is a cutie! Even though he has CP, it’s nice to see him in a place that has him up and about.
Large families welcome, travel required. Married couples only.
Tatumn
Girl, born January 2002
She has moderate mental delays
What a beautiful smile!
Currently Tatumn lives in school orphanage. She is very friendly and easy-going.
Aubree
Girl, born Aug. 1999
Diagnoses: arthrogryposis; mental delay
Aubree is very active, easy-going, and friendly. Currently, she lives in a special school-orphanage.
From one of our adoptive families who visited with her in August 2012: She truly is a ray of sunshine! She comes out to greet us in her wheelchair (she has good upper body strength, her legs are fixed straight out in front of her and are tiny. She doesn’t appear to have AMC in her upper limbs at all. She is extremely friendly and happy, she enjoys singing and dances in her wheelchair. She can also use her upper body strength to scoot around the floor. I am so excited that she is available because I know she will be a wonderful daughter if just given a chance. This girl just exudes love and happiness! The orphanage does provide the children with an education, and even music instruction. We were able to see Aubree perform in a concert that the children gave for their visitors (they have help from humanitarian groups that come in to work on the building and work with the children). If anyone asks about her, I would love to talk with them more about the orphanage and the children there. They have my heart!
*** ADDITIONAL $3000 GRANT AVAILABLE FOR AUBREE’S ADOPTION ***
Collier
Boy, born October 1999
Down syndrome, significant mental delays
This handsome young man has waited a long time for a family of his own!
Large families welcome, travel required.
Cambria
Girl, born January 2005
Anophthalmos (absence of eyes)
What a sweet little girl! She is walking independently.
Married couples only, travel required. Large families welcome!
Jett
Boy, born February 2009
Microcephaly, Congenital hydrocephalus, Pericarditis
Such a handsome boy!
Large families welcome, travel required.
Zoey
Girl, born November 2007
Congenital cytomegalovirus infection, Profound mental delays, Other paralytic syndromes (CP), epilepsy, Microcephaly, Coloboma of optic disc
Sweet love needs a family, or she’s destined to a life lying in a crib. She has a host of needs; a family will need to be well prepared — but she deserves the chance to bloom!
Maiya
Girl, born 2006
After-effects of early organic affection of the central nervous system in the form of intelligence deficiency, atactic syndrome (epilepsy).
She does not talk, only makes sounds; fulfills simple tasks.
Maiya has a sunny smile, doesn’t she? She’s waited long enough — let’s help her find a family of her own!
Jenny
Girl, Born October 2009
CP and Tetralogy of Fallot (heart condition)
Sweet Jenny is waiting for you! She is almost 3 years old, with brown hair and brown eyes. She was born with cerebral palsy and a heart condition, for which she has already had surgery. She is not able to sit on her own, and will greatly benefit from a loving family, medical care and therapy! If she is not adopted, she will remain bedridden for life.
More photos available. Married couples only. Large families and older parents welcome.
Ginger & Jamie (twins)
Fraternal Twins, born August 2007
FAS
FACING IMMINENT TRANSFER!
Ginger and Jamie are 5 years old and waiting for their forever family. They are fraternal twins and can only be adopted together as siblings.
Both children have significant effects from fetal alcohol syndrome. Both of them are very social and friendly. They deserve to be in a family who can care for them!! Both children are cognitively delayed, with vision issues as well.
Ginger (left): brown hair and big blue eyes! severe congenital myopia, organic affection of the central nervous system, nanism of somatic genesis, mental retardation
Jamie (right) brown hair and brown eyes: organic affection of the central nervous system, congenital hypotheriosis, severe myopia, mental retardation.
From a family who met them in 2012:
They were [children] I wanted to remember. We met them both on several occasions during our outside visits. Ginger was all over my hubs, tugging, pulling, hitting, and climbing all over him. To say she wanted attention from him is an understatement. She had lots of energy and always wanted me to pick her up. She always wanted me to hold her hand too! We went on several walks together. She’s a spitfire for sure! Jamie was a lovely little boy. He was always so helpful to the younger kids in their groupa. He loved to push the others on their bikes and was a big help to the nannies. They’re both available and would thrive with lots of love, structure, and attention. I’d be happy to share our experience if any one is interested!
Married couples only. Large families and older parents welcome. Travel required.
Todd
Boy, born December 2010
Blind
Todd is such a handsome fellow!
All we know is that he is listed as “blind” — not sure if he has any vision at all.
Francesca
Girl, born February 1999
Affection of the central nervous system, spastic low paraparesis, myopia, hip dysplasia, mental delays
What a lovely young lady — she’s waited far too long for a family.
Please help find her family before she ages out (at 16)!
Additional photos available. Married couples only; travel required.
Kimberley
P-OD
Girl, born Feb 2007
Down syndrome, congenital heart disease and hypothyroidism. Mental delays.
Report dated 2010
Kimberley is predominantly cheerful. In the orphanage the girl is described as a sociable, smiling, loving, quiet girls, who enjoys being with other persons. Her sleep is normal. She enjoys eating pretty food, so the orphanage gives her vegetables, eggs, iron, etc.. However, they still give her vitamins and avoid foods with lactose.
Her communication is usually through gestures, cries and guttural sounds. General gross motor and fine motor delays, common for a child with Down syndrome.
She participates in group activities and plays in partnership with other children. She is cautious with strangers but she adjusts quickly to their presence.
Kanani
Girl, born April 2008
Anophthalmos of the left eye, optic atrophy of the right eye, spastic tetraparesis
Kanani has been transferred!
Lovely Kanani needs a family to help her reach her full potential.
From a family who met her in May 2012:
Kanani is very sweet girl. She is well cared for in a good orphanage by caring nannies. She gets lots of outside time when it’s warm out but this time is spent lying down in the stroller as she can’t sit on her own. She can hold on to your fingers and seems to just love to have attention although with her eye troubles it is difficult for her to respond. She likes to have her cheek stroked and her hand held. She is quite stiff and in need of physiotherapy and most of all love and attention. We were told that she will be transferred to an institution very soon unless a family is found as children at this orphanage are typically transferred at age 4.
Large families welcome; travel required.
Frankie
P-OD
Girl, approx 12 years old
Down syndrome; Moderate delays
From a report in 2009:
Frankie is a self-sufficient girl, confident, independent, with initiative, restless, with the capacity to interact, she reclaims what she wants, is stubborn and demanding in their desires, impulsive, she plays games for recreation and relationship with her peers. She likes music and dancing.
She has a mental age of 3 ½ years [as of 2009], her verbal language is limited, she shows initiative to communicate, her comprehension is more advanced than her expressive speech.
She moves easily up and down stairs, kicks and throws the ball; her fine motor coordination is poor, she likes coloring, making repetitive lines and activities with the pencil, she uses scissors.
Asher
Boy, born February 2009
Cerebral palsy, spastic low paraparesis, retinopathy
Such a handsome boy! He has such beautiful big eyes.
Large families welcome, travel required. Married couples only.
Leann
Girl, born January 2009
Heart condition – Double discharge of vessels from the right ventricle (after surgery); Urinary/urethra condition – Ureterostomy (after surgery), atrophy of the anus, colostomy (after surgery)
Leann may have some effects of FAS (fetal alcohol syndrome), based on social history.
Additional medical diagnosis available for serious inquiries.
Leann is a very clever, cheerful, jesting girl. She speaks well, and is very sociable.
Update 2013: Leann is one of the loveliest little girls… She chats a lot, laughs, and never complains, even though she has spent most of her short life in and out of hospital . She can run and jump, talk, and she is smart and intelligent.
Carmen #1-9
DOB: 2002
Diagnosis: delays in all aspects of development
Carmen has spent most of her life in a family environment. She was raised by her birth mother until she was 3 years old. At that time, she was placed in a mental institution where the children are generally well cared for. At the age of 5, she was placed with a foster family. The family is missionaries and she lived with them for over 2 years, at which point they had to return to their home country. She moved from their home to another foster home, where she lived for over a year. At the age of 8, she was placed in a group home style orphanage, where she lives today. She was placed in the group home because her foster mother moved to a different town and could not take Carmen with her. The foster mother still visits her when she is able and takes her for weekend trips. She is well loved by therapists and others who’ve been involved in her care over the years and they’ve advocated for her to help her find a forever family.
Carmen is considered delayed in all aspects of her development. She feeds herself and drinks from an open cup. She walks and can go up and down steps independently. She cooperates with all self-help skills such as dressing and undressing. She maintains eye contact and responds to her name. Her speech is delayed, but she understands what is said to her. When she sees something she likes or wants, she will smile and clap. She interacts with the other children and participates in games and group activities. She is making progress in all aspects of her development. Her report has not been updated in over a year, so we are working to get information on her current developmental progress.
Davis
Boy, January 2010
Epilepsy; Congenital cytomegalovirus infection; Acute myocarditis (inflammation of the heart muscle)
Sweet little Davis has so much potential!
Large families welcome, travel required.
Randall
Boy, born 1999
Down syndrome; infantile cerebral paralysis
Randall is a handsome young man who likes to play outside, and is described as gentle with others. He is a sunny, cheerful boy, who also enjoys arts and crafts. He’s non-verbal, but is curious and open-hearted.
From a family who met him in summer 2012:
It took us a few days to really get to know Randall. He was not seeking out all the attention that some of the others were. He was content to swing and sing to himself while waiting patiently for someone to kick a soccer ball with him. Oh how he loves to kick a soccer ball.
He is such a kind gentle boy. He would patiently wait to ask to look through our photobooks. Unlike some of the others he was happy to just look – he didn’t need extra attention while looking through it. He was the most careful with the books always being sure to return them safely.
He has some speech issues. He talks and sings but is hard to understand. I think just before we left he was taken for surgery on his palate which may be why he has speech issues.
In addition to swinging and kicking the soccer ball he loves crafts (stringing tiny beads and coloring) He loved the electronic toys we brought – remote control helicopter and translator. But unlike many of the others he always waited his turn, was careful with the items and always gave it to the next boy when his time was up!
Unfortunately Randall is older – his time is running out!! It’s a pretty easy region – the 10 day wait has been waived in the past – and the boys are taken care of.
Merida
Girl, born May 2003
Bilateral hearing loss, right-sided hemiparesis, cognitive delays
What an adorable young lady!
Large families welcome, travel required.
Kellsey
Girl, born May 2008
Microcephaly; Coloboma of optic disc; Hypoplasia and dysplasia of lung; Ventricular septal defect; Convergent concomitant strabismus; Mixed specific developmental disorders
“Kellen” has been renamed — this is actually a GIRL! Let’s find this little love a family
Quinn
Boy, born March 2005
Congenital hydrocephalus; Coloboma of optic disc; Other paralytic syndromes (CP); Disorder of brain, unspecified; Dislocation of shoulder joint; Atrioventricular block, first degree
Quinn is 7 years old — let’s help him find his family. Every child deserves a loving family to call their own.
Landon
Boy, born March 2009
Spina bifida; Congenital hydrocephalus; Other paralytic syndromes (cerebral palsy); Acute myocarditis; malnutrition and other nutritional deficiencies
Precious boy! Landon needs a family to help him grow, and keep him healthy.
Large families welcome; travel required. Married couples only.
Elias
Boy, born August 2011
inflammatory diseases of central nervous system; Congenital hydrocephalus; Other disorders of optic [2nd] nerve and visual pathways; Carrier of viral hepatitis B
What a sweet baby Elias is!
Elias is in a fast region that often waives the 10 day wait. Married couples only, travel required.
Additional photos available.
Aven
Boy, born June 2009
Dandy-Walker syndrome; hydrocephalus; Hypoplasia and dysplasia of lung; Atrial septal defect; Congenital subluxation of hip; chronic viral hepatitis B without delta-agent; Convergent concomitant strabismus; Bilateral inguinal hernia; Tetraplegia, unspecified
This little boy has a laundry list of issues, but I’m confident there is a family out there who will be able to look at this picture and see a child, their son.
Large families welcome, travel required.
Waniya
Girl, born October 2007
Cerebral palsy; Mixed specific developmental disorders; Coloboma of optic disc
Waniya (pronounced Wa-NEE-ya) — a Lakota (Sioux) name that means “breath of life.”
Waniya is a gem; she needs a family to reach her true potential.
Daisy
Girl,