|
Because every family deserves the blessing of a child with Down Syndrome... |
![]() |
Jewell

Girl, Born April 24, 2006
Mirabel

Girl, Born August 2009
Miss Mirabel is also a real cutie! What a great smile she has
From her medical records: congenital malformation of the central nervous system, cerebral hernia, hydrocephaly subcompensated, flail legs
Married couples only. Large families and older parents welcome. Travel required.
Kristopher
HIV+, heart defect, vision issues (blind in one eye), moderate mental delay
Kristopher is a handsome young man with blonde hair and brown eyes. He is very active and is said to be always happy, but he is quite delayed. Kristopher has significant vision issues, which may or may not be correctable.
From a family who met him in October 2012:
Kristopher is a super-sweet boy who is 5 but looks 2 and is happy ALL the time. He needs to live near a large medical facility, have heart surgery (unless it’s too late), and probably needs a small family that can commit to pretty full care for him. He is darling!
Photo from April 2011. Additional photos available.
Lynne
Girl, Born July 2, 2007
I HAVE BEEN TRANSFERRED TO THE OLDER CHILD ORPHANAGE/SPECIAL NEEDS HOME.
From her medical records: minimal brain dysfunction, delay of psychological and speech development (may have slight mental delay), patent foramen ovale, crossed eyes.
Brett
Boy, born September 2007
Brett is a handsome young man who was born with CP. He is very smart, he gets around on his own by crawling, but he is not able to walk. Therapy will do wonders for him! He deserves to have a family!
From a volunteer who knows him: He plays with other children. He speaks with separate words. He understands the addressed speech. The boy is curious, likes classes. He loves when his nurse reads for him, he likes making pyramids.

Update December 2012:
Brett is very smart and curious. He has some learning and language delays associated with institutional life, but he does speak in complete phrases around people he trusts. He enjoys cars, coloring, and games. He got very excited when we showed him pictures of dogs and other animals, so he might do well with pets.
A family considering adopting him should be prepared to deal with some institutional behaviors and traumas. This is the area where Brett might need the most assistance in understanding rules, family, and nurturing relationships.His physical disability limits his lower body, specifically his legs and feet, but he is very strong in the upper body and crawls very quickly. He is a very active kid who needs some physical therapy, appropriate equipment, and perhaps braces to get where he needs to for walking. He is able to pull himself to standing. The orphanage has worked with him on potty training and he seems to be doing well with it.
More photos available, married couples only.
Nicholas
BOY, born November 9, 2006
Nicholas is officially diagnosed with FAS (fetal alcohol syndrome). His delay is considered significant. He needs a loving family to help him achieve all he can be. He does not appear to have any asdditional medical complications from his FAS. This picture makes him seem to have vision problems, but I think it’s just a bad picture.
If you are unfamiliar with FAS, please spend some time researching this condition. Just as with Down syndrome, FAS and FAE have a wide variation of effects on each child, both medically, physically, and cognitively. This is typically dependent on how long during the pregnancy the mother consumed alcohol, and of course, how much. There is no way to know this ahead of time.
Noah (13)
Noah is a sweet boy with light brown hair and big blue eyes. He was born with CP and is significantly cognitively delayed. He is not able to walk at this time, but loves to be held and loves attention and affection. His possibilities are endless!
Kenneth
Boy, Born November 27, 2006
Photo dated Feb 2010. Kenneth is a blonde haired, blue eyed cutie who was born with FAS. Kenneth does have some spasticity on his left side, and will greatly benefit from therapy and a loving family to encourage him! He is diagnosed with hydrocephaly, but this is a result of the FAS. He is not in need of a shunt to correct (the doctors say).
As you can see from this updated picture, Kenneth is doing GREAT! He wants a mama and papa of his own.
If you are unfamiliar with FAS, please spend some time researching this condition. Just as with Down syndrome, FAS and FAE have a wide variation of effects on each child, both medically, physically, and cognitively. This is typically dependent on how long during the pregnancy the mother consumed alcohol, and of course, how much. There is no way to know this ahead of time.
Kiril
Angelina
Miss Angelina has spina bifida. She has blonde hair and giant blue eyes!
From her medical records: Congenital dysfunction, myelocele of lumbosacral part of spinal cord (had surgery); internal hydrocephalus, flail legs with dysfunction of pelvis/hips, delay of psychological development.
More photos available.
A family who met her in 2011 says she’s the happiest child, always smiling and laughing.
Dixon #2-3
Boy, Born March 22, 2001
Diagnosis: Down syndrome
From his medical records: Elementary thinking processes are observed. He can’t speak but pronounces separate sounds and some syllables. He knows his name and reacts when called. He carries out very elementary orders come here, give me your hand, and lie down. He distinguishes praise and reprimand. He is not oriented for a place and time. His attention is unstable, his memory is mechanic. He gives his hand for a greeting. He walks independently and has good general motorics. The fine motorics are limited. In emotional aspect the child is calm and quiet. He rejoices at the attention he is paid but prefers to play alone. He likes to play with toys by turning them from all sides. He looks at his hands with a great deal of interest and entertains himself by making different movements with them. The child is taken care of entirely by the personnel. The child is included in the project Granny and grandchild and learns how to eat independently. A speech therapist works with the child in order to develop his speech skills. The training how to eat on himself continues.
SINGLE MOMS, OLDER PARENTS, & LARGE FAMILIES WELCOME, EASY TRAVEL
MULTIPLE CHILDREN CAN BE ADOPTED AT THE SAME TIME WITH LOW COST
Leo

Boy, Born December 4, 2002
Violetta
Oh sweet girl
Violetta is 4 now and is facing transfer this year. She urgently needs a family!
From her medical records: FAS, syndrome of movement disorders in form of two-sided pyramidal insufficiency, condition after surgery: abdominal incision, bowel resection (September 19, 2008), end-to-end abdominal anastomosis as a result of enterocolitis and serous peritonitis, examination stage and assumption of partial optic atrophy, slight protein-energy malnutrition, defficiency anemia.
Daniel #14-2

Boy, Born April 9, 2001
From his medical records: The physical development of the child lags behind considerable from the indexes for the age. The child walks independently and climbs up stairs with support. The movements of the child are not coordinated. The fine motorics are not perfected. The child doesn’t have notions of time built up. He orientates well in the space. He recognizes his image in the mirror and looks at it with an interest. He has perceptions for the main colors but cannot name them. The child is with insufficient ability for concentration of his attention. His active attention is attracted and kept with difficulties. The child is communicative, initiates with ease contacts with the personnel, the other children and with strangers. He likes the contacts with adults. He is not conflict and has good behavior in the group. He is prone to exhibiting whims and to be unhappy. He protects a toy that is taken away from him. The intellect of the child is with deficit corresponding to the diagnosis of Down Syndrome. He shows attachment, joy, anxiety and guilt. He is calm and observes the play of the other children. He plays with them and enjoys contacts with them. He carries out simple orders come here, give me your hand, and sit down. The child doesn’t have skills to serve himself built up, needs constant support. He can eat independently. He can’t put his clothes on and take them off on his own but cooperates when changed. He reacts to his name. He orientates in the daily routine. He doesn’t signal his physiological needs. The child understands the speech of the others when expressed elementary. He carries out orders and verbal commands. He pronounces single words by imitating. He is communicative, seeks contacts, and shows preferences in the interactions with the other children and the personnel. He has expressive mimics by which shows his emotions and attitudes. The child likes to listen to songs, laughs loud and claps with his hands. He moves in time with the music and is very lively and energetic. He attracts the attention of the adults by pulling them or patting them with his little hand because he can’t speak. He pronounces separate syllables: ma, ba, da as well as words from repetitive syllables: mama, baba.
SINGLE MOMS, OLDER PARENTS, & LARGE FAMILIES WELCOME, EASY TRAVEL
MULTIPLE CHILDREN CAN BE ADOPTED AT THE SAME TIME WITH LOW COST
Andrew
Boy, Born December 3, 2001
Ruslan

Boy, Born November 12, 2002
Diagnosis: Down syndrome
ALREADY TRANSFERRED, PLEASE ADOPT ME SOON!!
Ruslan is a handsome young man who is in desperate need of a family right away. He has strabismus, and is also a CARRIER of Hepatitis B. (www.webmd.com) He is asymptomatic at this time. We are trying to get more details on his Hep B….he is living in the general population of children, so they don’t appear to be very concerned about him transmitting it to other children. (Typically, children with blood-born viruses such as Hep B and HIV are isolated in special orphanages and never available to be adopted, so we are thinking that maybe he tested positive at birth and hasn’t been retested, or he isn’t showing any outwards symptoms).
From a nurse in the infectious disease unit in a pediatric hospital: *** Hepatitis B is something that children in the USA are routinely vaccinated for. If parents have not received the vaccinations, they can easily go to their physician and receive the series. With these vaccinations transmission is extremely minimal as vaccinated parties can have immunity to Hepatitis B. Titers (simple blood test) can also be drawn after taking the vaccines to make sure immunity has been acquired. Hepatitis B is also treatable with medications and people can also just be carriers of the virus. This health condition is labeled chronic, but with proper medical treatment and simple precautions it is very treatable and the risk of transmission is minimal at most. ***
Ruslan has already been transferred out to the institution due to his age, but he can still be adopted!! Families considering Ruslan should be home study complete/approved prior to commitment, as his needs will be great. Please open you heart to little Ruslan….he needs you!
Nastya
Girl, Born July 27, 2005
Colin
Boy, Born December 16, 2002
Daniel

Boy, Born January 2006
HELP! I HAVE ALREADY BEEN TRANSFERRED!
Daniel is facing a bedridden life in the mental institution without your help! Poor Daniel struggles with many health complications, but he can truly reach his full potential with a loving family. He has CP and hydrocephalus, along with some symptoms of epilepsy.
From his medical records: congenital hydrocephalus, spastic tetraparesis, movement disorders, symptomatic epilepsy, severe mental delay, partial optic atrophy.
From an adoptive family in summer 2012:
Daniel is not doing well. His head has enlarged quite a bit and both times I saw him he was lying down in a raised toddler bed. He clearly needs medical help for the hydrocephalus.
This region typically waives the 10 day waiting period for children with special needs.
Dylan #17-3

Boy, Born August 2, 2001
Main diagnosis: Down Syndrome, Severe lagging behind in his mental development; probable FAS in addition to the Down syndrome.
Glenn

Boy, Born August 16, 2003
Down syndrome
Glenn has blonde hair and blue eyes. He has Down syndrome, and struggles with the effects of FAS. With this comes strabismus and a valvular heart defect. Despite this, he is doing well, mobile and active and friendly.
As with all children living in these difficult conditions, this child’s cognitive development has regressed significantly since he/she was younger. It is of crucial importance that any family considering the adoption of an older child from the mental institution setting be well prepared for what to expect with regards to how the neglect and lack of adequate medical care and nourishment has affected this child. These children all have TREMENDOUS potential for improvement, and deserve to have a life outside these four walls.
Updated 2012:
Sweet Glenn is such a love! Despite multiple medical conditions he is doing pretty well! He loves to hug and understands commands. His finger motor skills are not well developed. He can eat and use the bathroom independently. He is currently not speaking very much but it does not sound like he attends any speech therapy. He does need help changing his clothes but he is practicing!
This little guy could greatly use a family to help stimulate his speech and his fine motor skills.
These children are truly living on borrowed time, and families should be home study approved before an official commitment can be made for this child.
Marlowe #18-1

Boy, Born August 28, 2001
Diagnosis: Down Syndrome, Inborn cardiac malformation – persisting arterial channel, Lung hypertonia, Severe lagging behind in his development. Photo taken May 2009.
SINGLE MOMS, OLDER PARENTS, & LARGE FAMILIES WELCOME, EASY TRAVEL MULTIPLE CHILDREN CAN BE ADOPTED AT THE SAME TIME WITH LOW COST
Alex
Boy, Born May 30, 2001
Vlad
Boy, Born September 22, 1999
***Vlad is also an OLDER CHILD, and will have no opportunities if he ages out. His "orphan and HIV status" will follow him the rest of her life. Please give Vlad a chance to grow up knowing the love of a family and having basic the opportunities that he deserves. ***
For more info and parent support on adopting and raising a child with HIV, please visit http://www.projecthopeful.org/
Brett #19-1
Boy, Born August 23, 2001
Diagnosis: Down Syndrome, Severe lagging behind in his development, Alopetio areata
Brett was born premature at home and taken to an open field, where he was abandoned. He was there for 6 hours before being rescued and taken to a local hospital, where he was treated for shock, hypothermia, bug bites all over his body and difficulty breathing. Once released from the hospital, he was placed in an orphanage and later transferred to a mental institution, where he lives today. From a physical standpoint, he suffered several bouts of bronchitis and other sicknesses as a young child. He does have alopecia (hair loss), but does not have any other health problems at this time. Based on one of the video clips, it appears that Brett is able to pop his hip out of socket, as his can turn his leg at an unnatural angle. He can walk and move freely around in his environment.
Brett suffers from many delays as a result of spending over 10 years in an institutionalized setting. He walks, plays with toys, communicates using gestures and interact with adults at will. He is NOT aggressive. The staff cares for all his basic needs and he is not receiving any academic instruction or any noted therapies at this time.
Several photos and videos of Brett from December 2012 are available.
SINGLE MOMS, OLDER PARENTS, & LARGE FAMILIES WELCOME, EASY TRAVEL
MULTIPLE CHILDREN CAN BE ADOPTED AT THE SAME TIME WITH LOW COST
Alexey

Boy, Born April 11, 2001
Alexey is consdered significantly delayed. He is fully mobile, and oh so handsome! But he has been given a second chance at life, saved from the mental institution and living in this well-kept school setting.
From a family who met him, Sept 2012:
Alexei is really a handsome guy and I think he knows it! He was playing ball with his groupa and is very active. When he was given a cookie from us he said thank you appropriately and made perfect eye contact. He will be a joy to any family with sons at home!
Update June 2013:
Alexey has a very big sweet tooth! He would not put down his lollipop to take a picture- when asked he told us politely “No, thank you.”
Darina
Girl, Born October 2007
Oh Darina, how she has regressed
(( We had such a darling photo of her from two years ago, and to see her like this now breaks my heart. She could have come so far and been spared this ;(
Darina struggles with CP. She has compensated internal hydrocephaly as well. She is not able to walk on her own. From her medical records: congenital brain abnormality, atopic-astenic syndrome, delay of mental and motor development, microcephaly, hip dysplasia, congenital isotropy of both eyes, koch valga to the left (foot position)
Darina is facing the institution soon and will remain bedridden for life if she is not adopted
Grant

Sealey
Sealey needs a family….he has severe CP, and is diagnosed with congenital brain malformation; anencephalea (no cerebral cortex). He is not able to walk and needs full care. It wil be so wonderful to see him blossom in a loving family. He is facing the institution very soon.
MORE PHOTOS AVAILABLE
Kolya #7-2

Boy, Born August 12, 2004
Main diagnosis: Down Syndrome. Asthma with prevailing allergic component. Lagging behind in his neuro-psychical development. Abnormally low weight; full medical records available
SINGLE MOMS, OLDER PARENTS, & LARGE FAMILIES WELCOME, EASY TRAVEL
Samson

BOY, Born August 28, 2004
Samson is also blessed to still be at the baby house. He was born with CP and strugges with epilepsy. He has optic nerve subatrophy, and will do great in a family who has experience with vision impairments! The caregivers say he has a great personality! Samson has so much potential!
MORE PHOTOS AVAILABLE
Mikale #38-2
DOB: 2003
Diagnosis: Down syndrome
Mikale has been transferred to a mental institution. He attends a specialized school. He interacts well with other children and does not have any behavior issues. He’s non-verbal, but he understands what is said to him and follows directions that are given to him. He plays appropriately with toys and enjoys blocks most of all. He feeds himself and assists with setting the table and also with cleaning up the toys. He seeks out adults and other people to interact with. He is physically healthy, with no past or current health concerns.
Additional photos and videos from January 2013 are available for interested families.
SINGLE MOMS, OLDER PARENTS, & LARGE FAMILIES WELCOME, EASY TRAVEL. MULTIPLE CHILDREN CAN BE ADOPTED AT THE SAME TIME WITH LOW COST.
Tanner #31-1

Boy, Born July 26, 2001
Lagging behind in his neuro-psychical development.
Nolan

HELP, I HAVE BEEN TRANSFERRED!!
Boy, Born September 2004
Nolan is such a handsome boy! He needs a loving family!
From his medical records: long-term effects of some early trauma (right-side hemiparesis), mild mental delays, seizures, flat feet, farsightedness
He has fine motor skills, understands everything, he talks but it is hard to understand him. Nolan is very physically active, happy and cooperative, friends with other children.
A family living in the states who has 3 children, one who is significantly disabled, has taken a special interest in Nolan but cannot add Nolan to their own family due to the needs of their children. Per the family, “Nolan’s eyes and smile caught our heart. He is close in age to one of our own children. We hope this gift will enable someone to give Nolan the chance to live outside an institution.”
Matvey
Boy, Born August 28, 2004
SIGNIFICANT RISK, PLEASE ADOPT ME SOON!!
Matvey is such a cute little boy, with blonde curls! He is cognitively delayed, but does not seem to have any official diagnosis other than that. He has amazing potential!! He was transferred to another region in 2010.
Yuri

For more info and parent support on adopting and raising a child with HIV, please visit http://www.projecthopeful.org/
Jason

Boy, Born April 10, 2003
HELP! I have been transferred to a remote institution, with no hope of finding my family without you!
Jason spends his time either in a crib or in a stroller, sitting outside.
He needs a lot of love and attention … He is a good, sweet child, but he has a lot of self-injuring behaviors. Unfortunately, he is often restrained because he hits himself really hard.
Update Nov 2012: Jason is learning to walk with support!
From a family who visited with him in June 2013: I saw Jason this morning. I got to take him for a walk in the stroller, play with him, feed him (twice!), and get him ready for his nap. He is wonderful. He loved it when I made my hand crawl up his belly and tickle him under the chin. I was rewarded with loud laughing and a huge smile. He liked to have me rub his feet, and whenever I would stop he would stick his little foot up for more. He makes noises but he does not talk. He can walk if he holds both of your hands, but he prefers to crawl as he can go faster. He is the king of the bouncy seat. He sits in it whenever he can, and he shooed away another child who came too close.
He is about the size of a four year old and is in a 4/5 shirt. He’s heavier than I thought he would be, but I can carry him easily. I’m totally in love.
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Evan
Diagnosis: cerebral palsy, epileptic syndrome, significant mental delays. Unable to walk, spastic/tight muscles. Evan is blessed to still be at the baby house (as of March 2010), but once he is transferred, he will spend the rest of his short life bedridden. Please consider being a loving family for Evan!
From a missionary who visited with him in March 2012: Evan is also in the boys new house where just 9 children are. He was gentle, lovey, cuddly and just so sweet. He is severely delayed but a gentle delight to be around and he loved stacking blocks with me. He was picked on quite a bit by the others who I saw hitting him. Felt so desperate for him.
From a family who met him in summer 2012:
One of the boys I worry most about is Evan. He appears to have cerebral palsy. He is stiff and a bit distorted. He does not have the luxury of PT and OT to help him function better. He sits hour after hour in a wheel chair. He will not be one that is given a job on the grounds like the others. As he gets older and bigger he will be moved to a bed and left there. He will be put in a diaper and left in bed – fed there and left – the diaper changed once or twice a day. He will no longer be taken outside he will just be left to lay there.
As I pushed our son’s wheelchair back to the house I waved at Evan. His eyes came to life – he was noticed. Later when I returned he waved and smiled. After that I made it a point to include Evan as much as possible. I would push his wheelchair to where the group was. If we were playing with balloons I would make sure he had one. He soon learned to pop the balloon. He thought it was hysterical. It also got him attention – everyone would look.
Of all the kids there I think he has the most room for improvement. With a family that will stretch him and help him I think he has a ton of potential! He is speech delayed also but again has so much potential.
Irina


Girl, Born March 5, 2005
Adam #16-1

DOB: 2001
FULL MEDICAL INFO AVAILABLE
SINGLE MOMS, OLDER PARENTS, & LARGE FAMILIES WELCOME, EASY TRAVEL
MULTIPLE CHILDREN CAN BE ADOPTED AT THE SAME TIME WITH LOW COST
Janie (26)

Janie (26)
Girl, Born March 8, 2006
If you are unfamiliar with FAS, please spend some time researching this condition. Just as with Down syndrome, FAS and FAE have a wide variation of effects on each child, both medically, physically, and cognitively. This is typically dependent on how long during the pregnancy the mother consumed alcohol, and of course, how much. There is no way to know this ahead of time.
Camille

Girl, Born June 4, 2007
Camille is a beautiful girl who deserves a life outside of this crib! She is diagnosed with hydrocephaly and CP. She has a precious smile (please inquire for more photos) and a will to survive and THRIVE!
From her medical records: hydrocephaly, symptomatic epilepsy, deep mental delay, kidny development pathology, extra right kidney, partical otrophy of vision nerve, flat feet
Victoria
Victoria (43)
Kiril

Boy, born July 2003
Little Kiril was born with microcephaly (a small head) as a result of FAS (fetal alcohol syndrome). He is considered significantly delayed. He has brown hair and brown eyes, and so desperately wants to know life outside of this orphanage. He is a darling little boy, and the orphanage director would so love to find a family for him soon. He is able to stand, and can walk with help, but his speech is very delayed. With therapy and a loving family and educational opportunities, Kirill has so much potential in life!
Kiril has been transferred to a special needs school, not an institution. We have several other children waiting there who could be adopted with him.
If you are unfamiliar with FAS, please spend some time researching this condition. Just as with Down syndrome, FAS and FAE have a wide variation of effects on each child, both medically, physically, and cognitively. This is typically dependent on how long during the pregnancy the mother consumed alcohol, and of course, how much. There is no way to know this ahead of time.
UPDATE fall 2012:
Kiril is making progress, he can walk independently, he tries to service himself, tries to hold a spoon and eat by himself. He doesn’t speak, but tries to repeat words. He is very nice, quiet, not aggressive and very handsome, all caregivers love him.
He needs a family NOW.
Talia (26)

Talia (26)
Girl, Born March 17, 2007
Fetal Alcohol Syndrome
This darling little girl is 5 years old now. She is walking and active, and is waiting for her “forever family”. She was born with FAS, and has many of the facial features common to this condition. Talia is actually diagnosed with FAS, so there must be documentation of consumption during pregnancy in the records.
If you are unfamiliar with FAS, please spend some time researching this condition. Just as with Down syndrome, FAS and FAE have a wide variation of effects on each child, both medically, physically, and cognitively. This is typically dependent on how long during the pregnancy the mother consumed alcohol, and of course, how much. There is no way to know this ahead of time.
Talia is living in the same orphanage as Janie is and they can be adopted together.
Arlene
Oh, Arlene…..from her medical records: after-effects of congenital toxoplasmosis, complex secondary hydrocephaly, episyndrome, hernia
Update June 2012: doing GREAT! Growing and happy, and needs a family!!!
This region typically waives the 10 day waiting period for children with special needs. Please consider one (or more!) of these beautiful angels from orphanage 41.
MORE PHOTOS AVAILABLE
Lorena

Girl, Born November, 2005
Wendy (6)
Girl, Born June 25, 2006
Wendy is a beautiful girl with sandy blonde hair and blue eyes. She was born quite premature (not sure which gestational week, but it is listed as “4th stage”). She has CP and is completely blind, with congenital cataracts in both eyes, optic sub-atrophy, and microcephaly.
Despite all of these odds stacked against her, she is an orphanage favorite and is well loved. She will really blossom in a loving family, and learning to use her other senses will open up the world around her. Wendy is already 6 now, and is facing the institution soon. She needs a family right away!
Anderson

Andrey
Boy, Born November 29, 2002
From our facilitator who has visited with him:
HIV. His life story is very typical The boy doesn’t have brothers and sisters. His mother abandoned him at the delivery house, the father was registered after the mother’s words. Loves to construct, to draw, very assiduous, wants to know everything about What? Where? When and Who? Hardworking, can focus his attention and be concentrated on the most important things. Among children he is very supportive and friendly. For more info and parent support on adopting and raising a child with HIV, please visit http://www.projecthopeful.org/
Miranda

Girl, Born August 25, 2004
Cerebral Palsy
SIGNIFICANT RISK, PLEASE ADOPT ME SOON!!
What a beautiful little girl! Wispy blonde hair and bright blue eyes! Miranda is healthy and developing well out side of her CP. She is an orphanage favorite. Waiting for more info on her ability to walk/speak, etc.
She has two younger siblings, their status is not known.
She was transferred from her baby home, and still waits for her family. She has been listed for SO long!!
Valery

Girl, Born September 27, 2006
Kaleb #6-5
DOB: September 2003
Down syndrome
Kaleb’s gross motor skills are developed. He walks, goes up/down steps with minimal assistance and runs. He spends most of his time choosing to sit in a child’s chair. He requires 1:1 assistance with academic tasks. He is attending a special needs school. He enjoys group music activities. He eats with assistance and is on a restricted diet to assist with constipation issues. He is a calm child. He does not exhibit any auto-aggression. He responds to his name. He makes eye contact, but he does not talk. He likes to play with cars, balls, stuffed animals and on the swing. He prefers to spend his time alone instead of interacting with other children.
Addition photos and videos from October 2012 are available of Kaleb.
Nana

Wyatt
Boy, Born May 2004
SIGNIFICANT RISK, PLEASE ADOPT ME SOON!!
Diagnosis: HIV. He takes daily medication ART (antiretroviral therapy). Very smart, tells poems, can draw, write, is good in mathematics, participates in children’s activities, likes encouragement.
For more info and parent support on adopting and raising a child with HIV, please visit http://www.projecthopeful.org/
Marty #6-7
Boy, June 27, 2002
Marty has Down syndrome and at the age of 5 months old was given a diagnosis of CP based on his delayed motor development and horizontal nystagmus (both of these things are common in children with Down syndrome).He is described as a quiet and even-tempered child who has adapted quickly to the routine and daily schedule at the institution. He is able to walk independently. He assists with dressing and undressing himself and is learning to feed himself as well. He goes to the toilet when reminded to do so by the staff. He is not yet speaking but demonstrates understanding and follows basic requests.
He plays with other children and interacts well with adults. He responds to his name and loves attention from the caregivers. He has a special bond with one specific care giver. He loves to play with toys and shows a preference for stuffed animals.
Marty has already been transferred to an institution.
SINGLE MOMS, OLDER PARENTS, & LARGE FAMILIES WELCOME, EASY TRAVEL
Sergey
Sergey needs a loving family who can help him achieve his full potential. He is destined to be bedridden for his very short life if he is not adopted. he is able to sit on his own and does his best to get around. He is significantly delayed and really needs a family! Sergey is facing imminent transfer to the institution.
From his medical records: congenital brain anomaly, spastic tetraparesis, simptomatic epilepsy, generalized tonic clonic seizures, cryptorchidism, adenoid vegetation, bending-movable contractures of the hip joints, deficiency anemia, mental delay
Nate (26)
Nate is a handsome young man! He was born with CP, and has some vision problems as a result of CMV (cytomegalovirus). He has brown hair and big brown eyes. He is not able to walk on his own, but he will truly blossom in a loving family, who can provide the therapy and encouragement he needs. We are hoping to learn if he is being treated for the CMV, but he is asymptomatic at this time.
Jared (26)

Jared (26)
BOY, born May 1, 2007
This handsome young man, with dark hair and dark eyes, was born with a rare genetic condition called Stickler Syndrome. His medical records also indicate microcephaly, a common symptom of SS.
Individuals with Stickler syndrome experience a range of signs and symptoms. Some people have no signs and symptoms; others have some or all of the features described below. In addition, each feature of this syndrome may vary from subtle to severe.
A characteristic feature of Stickler syndrome is a somewhat flattened facial appearance. This is caused by underdeveloped bones in the middle of the face, including the cheekbones and the bridge of the nose. A particular group of physical features, called the Pierre Robin sequence, is common in children with Stickler syndrome. Robin sequence includes a U-shaped or sometimes V-shaped cleft palate (an opening in the roof of the mouth) with a tongue that is too large for the space formed by the small lower jaw. Children with a cleft palate are also prone to ear infections and occasionally swallowing difficulties.
Many people with Stickler syndrome are very nearsighted (described as having high myopia) because of the shape of the eye. People with eye involvement are prone to increased pressure within the eye (ocular hypertension) which could lead to glaucoma and tearing or detachment of the light-sensitive retina of the eye (retinal detachment). Cataract may also present as an ocular complication associated with Stickler’s Syndrome. The jelly-like substance within the eye (the vitreous humour) has a distinctive appearance in the types of Stickler syndrome associated with the COL2A1 and COL11A1 genes. As a result regular appointments to a specialist ophthalmologist are advised. The type of Stickler syndrome associated with the COL11A2 gene does not affect the eye.
People with this syndrome have problems that affect things other than the eyes and ears. Arthritis, abnormality to ends of long bones, vertebrae abnormality, curvature of the spine, scoliosis, joint pain, and double jointedness are all problems that can occur in the bones and joints. Physical characteristics of people with Stickler can include flat cheeks, flat nasal bridge, small upper jaw, pronounced upper lip groove, small lower jaw, and palate abnormalities, these tend to lessen with age and normal growth and palate abnormalities can be treated with routine surgery.
Another sign of Stickler syndrome is mild to severe hearing loss that, for some people, may be progressive (see hearing loss with craniofacial syndromes). The joints of affected children and young adults may be very flexible (hypermobile). Arthritis often appears at an early age and worsens as a person gets older. Learning difficulties, not intelligence, can also occur because of hearing and sight impairments if the school is not informed and the student is not assisted within the learning environment.
Stickler syndrome is thought to be associated with an increased incidence of mitral valve prolapse of the heart, although no definitive research supports this.
Vitaly
Boy, Born January 14, 2005
Little Vitaly is so handsome, with his dark hair and eyes! Vitaly was born with CP and is not able to walk at this time. He is moderately cognitively delayed, but will regress every day he is in this place. He is already living in an institution, and he needs to be rescued desperately. Otherwise he will never have a chance to walk, never have the opportunity for surgery or therapy.
Susana
Girl, born August 2006
Mixed hemangioma of face and neck, Chronic viral hepatitis C, Other specified deforming dorsopathies (carriage defect), Astigmatism, Iron deficiency anemia
Susana is a friendly and sociable girl!
Tera #26-5
Age: 12
Diagnosis: dysplasia of right pelvic joint – condition after surgery. 50 % degree of disability without others’ help, was determined
Tera is 12 years old. She just completed 5th grade and is doing very well in all aspects of her development. She has age appropriate gross motor skills. She sings, recites rhymes and says her favorite subjects are math, drawing (crafts) and physical exercise. She can read and write well.
Additional photos and videos from June 2013 are available for interested families.
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.
Decker
Boy, born Sept 2012
Down syndrome
We don’t have a full update on little Decker — it’s not known if he has any additional health needs.
What a little lovebug!
Pippa
Girl, born January 2001
HIV
Pippa is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
Gina
Gina has a sunshiney smile! She has cerebral palsy, and needs a family to help her reach her full potential.
More pictures available, but she is seated in this chair in all the pictures we have.
Gina will be available for international adoption when she turns 5, in September 2013.
Wesley
BOY, born January 2008
From his medical records: internal hydrocephalus, multi cystic encephalomalacia, convulsive disorder, hernia, secondary cardiomyopathy, patent foramen ovale, anomalous chord of the left heart ventricle, secondary optic atrophy
Wesley is now available for international adoption, as he is 5 years old.
Clyde
Boy, born December 1998
HIV
Clyde is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
Shawn

Boy, born August 2001
HIV
Shawn is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
Zach

Boy, born August 2005
HIV
Zach is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
AnnaMarie
Girl, born December 1998
HIV, crossed eye
AnnaMarie is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
Jude
Boy, born March 2002
HIV
What a shy smile this handsome boy has.
Jude is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
Trisha and Tyler


Girl, born November 2000
HIV
Such a beautiful girl!
Trisha has an older brother (born 1999), who is healthy. They will be available to be adopted together, in early 2014.
Trisha is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
Cooper
Boy, born July 2001
HIV
Oh my gosh, isn’t he CUTE! Look at that smile, and those freckles!
Cooper is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
Murray
Boy, born August 2001
HIV
Isn’t he handsome!
Murray is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
Patience
Girl, born 2004
HIV, mild mental delays
Patience has parentage of mixed backgrounds (her father was reportedly a visiting foreign exchange student) and she is treated poorly because of her skin color. She is not in a great orphanage; she desperately needs a family.
From a family who met her in 2012:
She’s precious and sweet, but was terrified. They said she doesn’t talk hardly at all ever- my guess is selective mutism. She was definitely the racial minority, no apparent physical disability at all, very smart, receptive language skills seemed awesome. We just adored her and felt so sorry for her.
She would press up close to us and slide one little dark hand over and touch my knee and then the others would yell at her and she’d cringe and her eyes would cloud over and she’d slide to the back of the pack and just watch. We just loved her. Truly.
Ariel

Girl, born July 2008
Goltz syndrome, severe mental delays, multiple malformations of upper and lower limbs, umbilical hernia, nasal septum deflection, congenital ptosis of the right eye, coloboma, hypermetropia of both eyes, dacryocystitis of the right eye, macula papilloma
Little Ariel is severely delayed and has a host of medical issues; she will need a family with access to good medical care.
Sven #HA

Boy, born Oct 2002
Diminished intellectual capacity. Calm, affectionate.
Slightly delayed intellectual capacity for his age. The child is very calm and good, no aggression is observed, he is very loving and sensitive. Very much likes to color and draw, has very good sense of color. During the day he likes to draw and to order puzzles. At school lags behind, his attention is easily distracted.
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.
Clive #HA
Boy, born January 2001
Controlled epilepsy (Grand mal seizures, medicated), light mental delays.
Clive is said to be calm, affectionate. He displays deficiency in the basic cognitive functions – thinking, memory, attention, perceptions, imagination. The fine motor skills are also not well developed.
He is a very intelligent child, responsible towards school, has no absences, he discusses and shares with the educators and conducts a conversation. He works with a resource teacher at school. His character is calm, balanced, alert and affectionate.
Clive is a student in the 5-th grade and is well adapted in the school environment. He starts working slowly, with endeavor. He works on adapted program on language, literature and mathematics. He knows how to add and subtract. He has an affinity towards music and loves to sing. He is contact with the other children and adults. Doesn’t enter in conflicts with the other children, he is polite, follows the general rules and norms for conduct. Knows the hierarchy in the institutions – school, he behaves well.
Clive is well developed physically, positive and well-wishing, very friendly and easily makes contact.
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.
Darren #HA
Boy, born March 2010
Hydrocephalus
Darren is very calm and smiling, but doesn’t sit or walk – he only lays because his head is too heavy.
He is happy when he sees the members of the staff, recognizes familiar people from strangers. He feels good when being around other children and adults. Grabs a toy when given to him and holds it for a while. Turns his head towards the direction of a sound. Makes active and passive movements with the limbs. Has a calm daily and night sleep.
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.
Jacques #401 OD
Boy, born 2006
neuropsychological, motor and speech development delays
Jacques has severely delayed neuropsychological, motor and speech development. His behavior corresponds to that of an infant. He makes several steps independently and walks when held by one hand. He doesn’t speak, but produces monotonous sound combinations. He sometimes seeks adults’ physical closeness.
Cliff #397 OD
Boy, born 2008
This almost 5-year-old boy has infantile cerebral palsy, microcephaly, club feet, congenital megacolon and hypotrophy.
Cliff laughs aloud when jested and smiles when involved in interaction. He follows moving objects with his eyes. He listens to adults’ speech. He has a good appetite. His sleep is calm.
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.
Lucy and Linus #399 #400 OD

Lucy is a 5-year-old girl (born 2007) who has congenital microcephaly, infantile cerebral palsy, severe mental delay,delayed psychomotor development, multiple malformation syndrome. She rolls from back to belly and vice versa independently. She remains in a seated position for a short time when provided with some support. She shows interest in toys – she grabs and holds a toy in her hand, waves it around and examines it closely. She responds emotionally to seeing a familiar adult.
Linus is a 4-year-old boy(born 2009) who has microcephaly, congenital anomaly of the central nervous system, delayed psychomotor development, severe mental delay, multiple malformation syndrome. When put in a baby walker he steps on the floor with his whole feet and starts to slowly go around the room in the walker. The boy remains in a seated position for a short time with an adult’s assistance. He follows each and every movement of a person or an object with his eyes and head. He loves to watch the other children playing and moving around.

These siblings have very similar diagnoses. Biotinidase deficiency is suspected. There is an emotional bond between the children and they often hold hands, smile, laugh, look for each other with their eyes and jest with each other when they are placed side by side.
Because we only have these files for a short time, they will not be able to receive donations until a family is found for them.
Carl #394 OD
Boy, born 2001
History of seizures, speech delays
Carl is an 11-year-old boy, who takes epilepsy medication, hasn’t had a seizure ever since he was placed in the institution where he is at present (June 2009); has a speech difficulty; interacts freely with both familiar and unfamiliar people; loves playing with all children; shows a great interest in being involved in different activities; likes logic games; has normal physical development.
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.
Ethan
Boy, born November 1999
HIV, astigmatism
Ethan is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
Ally
Girl, born Aug 25, 1997
HIV, non rheumatic carditis
She is aging out but says, “YES, I want to be adopted!”
A family will need to have paperwork filed PRIOR to her birthday in August; otherwise she will not be able to be adopted.
Ally is in the same orphanage with several other available children. Interested and approved families could adopt multiple children together.
Marv
Boy, born October 2001
Crossed-eyes, development delays
From someone who met him:
Marv is a very sweet, happy boy. He loves to play soccer, even though his vision problems make that very difficult for him. He has been living in a boarding school for typical kids, and receiving his own private lessons, but recently was transferred to a facility in another region specifically for children with special needs. His favorite class is math, and he gets great grades in math. His least favorite class is Ukrainian. He is said to learn more slowly than other children, which is why he has required private lessons.
He is cheerful, friendly, and sociable. He said several times he would like to be adopted by an American family.
Hattie
Girl, born December 2009
Down syndrome, congenital heart defect — atrial septal defect, after surgery
Oh what a precious little sweetheart! Love the bows in her hair!
Update June 2013:
Hattie was in our daughter’s groupa and seems so sweet. She often was in the stroller when her groupa was outside, but sometimes the nannies would take her our of it. She can sit independently, stand with support and was able to walk with one hand held assist. She would follow us with her eyes and look at us when we were nearby. She needs a mama and papa to love her and help her grow.
She is so pretty — her pictures don’t do her justice!
Laynie #65-5
Age: 6
Diagnosis: Delayed development
Laynie is described as having a positive attitude toward herself and others. Her motor skills are well developed. Her speech is delayed, but she speaks using single words and simple sentences. She’s attending kindergarten and has the assistance of a resource teacher. She mimics the actions of adults and plays games with other children. She enjoys looking at books. She follows verbal directions, asks questions and is beginning to memorize short poems and songs.
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.
Abraham #59-3
Age: 3
Diagnosis: Combined defect (cleft lip, soft palate and hard palate) – surgically corrected, delays in development
Abraham has had 6 surgeries to correct his cleft and palate issues. He makes some vocalizations, but does not have any developed speech at this time. He has well developed motor skills: walks, runs, goes up/down steps unassisted. He eats independently and drinks from a cup. His attention is unstable and he does not interact with the other children. He does interact with known adults, and has a 1:1 caregiver that spends time with him several days a week. He has been evaluated by a psychologist and diagnosed with moderate mental delays.
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.
Evan #65-2

DOB: 2008
Diagnosis: Craniostenosis
Family history: biological sibling has the same genetic condition
Evan is 3 years old. He is on a special diet due to episodes of vomiting that led to a diagnosis of a metabolism problem. He sits up, crawls, walks with assistance and enjoys being placed in a walker. He reaches for toys and plays with them for periods of time once they are given to him. He is making sounds and babbling, but does not yet have purposeful speech. He loves to interact with adults and will pout when they do not give him the desired attention. He imitates the actions of adults. He has a 1:1 caregiver that works with him daily.
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.
Easy travel, larger families, older parents and single moms welcome.
Liam #56-1
DOB: May 2007
Liam was born with a cleft lip. He has undergone genetic testing and extensive evaluations and consultations with specialists. There is no official medical diagnosis that has been found. The neurologist found “slightly increased muscle tonus of the right leg and extended reflexogenic zone.” His ears are described as “specifically modified”, though his hearing is not effected. Otherwise, all testing and reports have come back clear/healthy.
Liam has delays in his motor skills and his cognitive development. He sits up and moves around in awalker. He’s not yet walking independently. He reacts when spoken to, answers to his name and pronounces some random syllables and words. He laughs loudly and holds toys and observes them closely. His medical report states: “He needs a family.” Yes, he does!
UPDATE: We have new photos and VIDEOS of Liam!!! He is very small for his age. However, in the videos, he is very alert and responsive to the staff. Several additional photos and videos are available of Liam.
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.
Ruby #56-2
DOB: May 2007
Diagnosis: Hydrocephalus-shunt is in place, opthamolgist prescribed glasses
Ruby’s legs are said to be “spastic”, though no further explanation is given. She rolls over and when on her stomach, can supports herself on her arms while holding her head up. She reaches for toys and holds them. She laughs out loud and she is begining to make purposeful sounds in an effort to communicate. She has a volunteer that works with her and she recognizes this person as soon as she sees her.
We have several photos and videos of Ruby.
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.
Corwyn
Boy, Jan 2009
Down syndrome
Oh, hello handsome!
Update June 2013:
Corwyn is completely adorable. He is very interactive. He can walk by himself and keeps up well with some of the other kids in his groupa. He always smiled at us when we walked by him or his groupa. He also often would say hi and bye, sometimes waving when we were walking by him. He enjoys playing with a pull car, playing with a ball, and spinning. One day when we were outside on the playground, he came up to us and stood at the other end of the sea-saw horse toy, rocking it with his hands. He would do really well in a family and needs a mama and papa soon.
Reign
Girl, born December 1999
Cerebral palsy, deep mental handicap
Bedridden and quiet, so heartbreakingly alone.
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Velia
Girl, born August 2000
Down syndrome and cerebral palsy
From someone who met her:
She was in an almost empty room, just with another child next to her. She was rocking and gnawing at the bars of the cot and such a sad sight to behold. My heart just collapsed for her!
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Salome

Girl, born March 1998
Microcephaly, cerebral palsy, deep mental handicap
Salome needs the care and attention of a family, to provide the medical interventions and therapy she so greatly needs.
From someone who met her:
Her thinness is heart stopping! She was twisted and sucking on a bottle, such a lost and forgotten soul! Obviously in such desperate need!
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Pearson
Boy, born Dec. 2004
Moderate mental delays
He is a very good boy, communicable, calm and friendly.
Della

Girl, born June 2002
Down syndrome, deep mental handicap, deficiency anemia, hypostatura
From someone who met her:
I called her the crying girl as she was sobbing uncontrollably and just being ignored, she had a pencil which she kept turning over and over as she sobbed, it was heartbreaking. This place too cold and hard for such a child!
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Phoenix
Boy, born May 2002
Cerebral palsy, spastic tetraparesis, epilepsy, hydrocephaly, deep mental handicap
From someone who met him:
Bedridden but still able to smile. They seemed particularly keen for me to photograph this child and kept turning his head for a better shot! I sensed that they too spot the potential within this child who smiled from inside his limited life. Somebody please go get this boy out of this cot!
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Solomon
Boy, born March 2001
Significant mental delays, sequela after viral encephalitis, cerebral palsy, tetraparesis, epilepsy
He was a truly desperate sight. He sat rocking back and forth and moaning and staring into space. I wonder how a real life in a family could break the shell he is now locked in. My heart breaks for him even now!
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Morris
Boy, born 2001
Significant mental delays, hydrocephaly, spastic paresis and inborn partial optic atrophy
From someone who met him:
He is a quiet child who smiled every time I looked his way.
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Delmar

Boy, born January, 2004
Down syndrome, mental delays, inborn partial optic atrophy of both eyes
From an adoptive family who visited with him in June 2013: I met Delmar today. He is really tiny … maybe the size of a 3 year old, very petite in build. He was quite shy and didn’t want to come near me. He moved away when I tried to touch his hand. He was more open with the therapist who was there (a guy). Mostly he just sat on a mat, rocking and looking into space. Occasionally he waved his hands around. He’s a beautiful little boy, and was adorable in a tiny pair of overalls.
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Kendall

Girl, born January 2006
cerebral palsy, bigeminal epilepsy, deep mental handicap, inner hydrocephaly, convergent squint
Kendall is a true orphans, as her mother has passed away.
From someone who met her:
She was gorgeous, when I spent time with her she had been taken into the playroom by a caretaker and she was lapping up every single second, she couldn’t stop laughing and grinning; it was a joy to watch! when I compare to pictures I received of her later in her cot it does not look like the same child! She needs a life and love, she could bloom, I know it!
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Iggy
Boy, born Aug 1997
Cerebral palsy, microcephaly, mental delays
What a smiler and an utter sweetheart!
He grinned and laughed and his disposition did not match up to his circumstances or surroundings. In my short time with him he was an utter ray of sunshine.
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Nehemiah

Boy, born January 2000
Cerebral palsy, difficult mental handicap
From someone who met him: When I met him I was heartbroken! More than any child in the institution the sight of this thin boy with his hands tied and blood on his sleeves made me weep! My own child self-harms and I think I connected with this sight…it could have been my angel!! The staff told me he was tied for his protection, as he hurts himself; the holes on his sleeves obviously points to this… my own child has a self-harming syndrome and lives a wondrously happy and fabulous family life! Yes it needs managing but this child in front of me was desperate and my heart literally broke! He needs help and the life I know he can lead!
From an adoptive family who visited with him in June 2013: I met Nehemiah today. He is in a groupa with 7 other boys. In the playroom he sat on a mat with a stuffed lion. He didn’t really interact with me at all. Occasionally he would begin to cry loudly. Luckily, the caregivers responded to him quickly. He has sores all over his hands and wounds on his face. He’s a very attractive little guy, though.
COMPLETED & APPROVED HOME STUDY REQUIRED PRIOR TO COMMITMENT. 10 day wait often waived here. Married couples only, larger families welcome.
Jonathan
Boy, born March 2003
Sequels of encephalitis, convulsive disorder, sensorimotor alalia, deep mental handicap
A terribly sad rocking child whose face showed so much sorrow behind the eyes it was heart wrenching! He moaned and rocked and seemed untouchable! His eyes haunt me even now! How I wish I could have spent more time with him. He so needs a family to wipe away that sorrow.
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Fabio

Boy, born November 2002
Cerebral palsy, spastic tetraparesis, microcephaly, deep mental handicap, carditis, biliary dyskinesia
He was in the same room as Bobby and seemed quite quiet. I would love to see him outside of those stifling rooms.
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Mario
Boy, born May 2001
Mental delays, inborn hydrocephaly, cerebral palsy, anemia
When I met him he was in the institution, but he has since moved to the first happy home (after another boy was adopted) so he is in a much better situation. I know emotionally he suffers, as he cries an awful lot.
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Blaine
Boy, born Sept 1999
Cerebral palsy, deep mental handicap, hydrocephaly, complete vascular leukoma, corneal staphyloma, inborn optic atrophy
This child is rather calm, but always smiles when somebody touches him, and always tries to walk with somebody’s support.
From a family who met him in June 2013: I met Blaine today. When I arrived at the orphanage he was being stretched by the therapist. He seemed to really like the therapist and would crawl to him and hold up his hands so that he could stand up. He can walk if you hold both his hands, and I saw him in a gait trainer, too. It’s very difficult for him to walk as he doesn’t seem to be able to fully straighten his legs. Blaine smiles a lot and seemed to be a pretty happy kid. He did get mad about something and have a tantrum, but it passed quickly. He rocks a lot and makes repetitive noises. He came over to sit by me and took my hand from another child’s so he could hold it. He was very interested in my iPhone.
From someone who met him: He was a bundle of smiles, just desperate to interact with us. [One of the men] picked him up and swung him, they obviously have built up a relationship and he shrieked with laughter…it was joyous! He was made to sit next to Tania for a picture, she hated it but he was just fine! He would blossom in a family and with a life!
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Miriam

Girl, born August 2007
Congenital malformations, deformations and chromosomal abnormalities, myopia
Miriam also has significant signs of FAS, although that is not diagnosed
From someone who met her:
I loved this child but she seemed so lost…she had only just arrived at the institution when I visited and she was bewildered! She is TINY. She is the child we all talk about, the child plucked from the baby house at 5 and left in a cot! She is the child forgotten and alone!
I was told she could walk, in fact she is the only child in the bedridden building who can walk, and then without warning she was swooped from her cot and paraded in front of me. A recent update says she is still moving and can still walk and she cries if she doesn’t get her walk! And she is still laughing and playing; but for how much longer?
She needs OUT! She needs a Mama, NOW!
Families should be HS approved (or close to it) prior to commitment. 10 day wait often waived here. Married couples only, larger families welcome.
Kammy #69-2
DOB: 2007
Diagnosis: Alopecia; Developmental delays with behavior concerns
Kammy walks, runs, feeds herself, puts her own shoes on and washes her hands independently. She holds a pen and colors inside the lines when coloring. She plays appropriately with toys. Her speech has recently improved. She can say her name and several phrases and her level of understanding as also improved. She quickly memorizes songs. She constantly seeks out adults and engages them in order to get them to play with her. Her pretend play skills are developed and she will use toys to act out things she’s seen in the past. Her report indicates that she has been diagnosed with behavior problems and takes medication for behavior. However, there is no mention of any negative behaviors or behavioral concerns in her developmental report.
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.
Garrett
Boy, born Sept 2004
Coffin Lowry Syndrome, Hydrocephalus, moderate mental delays
Garrett does not speak, but understands speech addressed to him. Garrett can be adopted with Troy and Sammy.
From an adoptive family:
I met Garrett in May 2012 and I will always remember how sweet he was. He was usually the first one to greet me with a hug when I visited. He was always so excited to show off for me. When the care-taker announced that they were all going outside he promptly put his shoes on and helped some of the other kids with their shoes as well. He and the other boys in his group (Troy and Sammy) are very well loved by one of their care-takers and it shows. It is obvious that they have been taught manners and cooperation and they are very kind to one another. They are taught at least several days a week so do not let the diagnosis deceive you, they are fairly smart boys. They all have obvious delays but never had any problems following instructions and they understood everything they were told and all seemed to love to be helpful. When I show our son (who was adopted from this group) their pictures he remembers their names and tells me they were his friends. He told me he wants them to be adopted and to come to the U.S. How I pray that happens for Garrett and the other boys! Garrett is so sweet and innocent, I hate to see what will happen to him if he ages out of the orphanage.
Sammy
Boy, born Feb 2005
Asthma and Moderate mental delays; Subcompensated hydrocephalus; possible FAS
What a great grin! Sammy can be adopted together with Troy or Garrett.

From an adoptive family:
I met Sammy in May 2012 and he was one of the sweetest kids I had ever met. Always ready with a smile and a hug! I brought things for all the kids in his group and he waited so patiently for his turn and gave me a big hug after. He was very kind and gentle with all the other kids, especially the one girl in the group. He and the other boys in his group (Troy and Garrett) are very well loved by one of their care-takers and it shows. It is obvious that they have been taught manners and cooperation and they are very kind to one another. They are taught at least several days a week so do not let the diagnosis deceive you, they are fairly smart boys.
They all have obvious delays but never had any problems following instructions and they understood everything they were told and all seemed to love to be helpful. When I show our son (who was adopted from this group) their pictures he remembers their names and tells me they were his friends. He told me he wants them to be adopted and to come to the U.S. How I pray that happens for Sammy and the other boys! Sammy is so sweet and innocent, I hate to see what will happen to him if he ages out of the orphanage.
Rebekah #69-3
DOB: 2006
Diagnosis: Cerebral Palsy
Rebekah was born premature at 27 weeks and has quadriplegic CP. She is delayed in all aspects of her development.
Additional information about her abilities and development are coming soon.
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.
Sutter

Boy, born 1998
Cerebral palsy
More information coming soon.
Sutter is easygoing, organized
Sutter is a really smart boy. He likes to make puzzles and he can solve them really fast. His favorite game was copying a picture and rebuild it with little colored pins on a board with holes. If you try to fool him, he will say ‘no’ and start to laugh contagious. I’m sure that he would be able to participate in some kind of education.
He had several operations as a child, which improved his locomotion, but after his growth spurt he lost some of his mobility again. He tries to walk with crutches and he gets PT for it. With the right medical care I’m pretty sure he would be able to walk.
Some days he is really kind for the other children in his group and then he acts really helpful. Other moments he tries to get all the attention. He would do very well in a family, where he gets the attention he deserves.
Sutter becomes 15 this year. He needs a family committed to him before his 16th birthday, otherwise he will never be able to join a family, his chanced are gone then and then he is condemned to institution life for the rest of his life.
Additional photos and video available. Married couples only, travel required.
Henrietta
Girl, Dec 2009
Congenital brain malformation (corpus collosum agenesia), spastic tetraparesis, epileptic syndrome, optic nerves atrophy, equinovarus, condition after exudative pericarditis, hypotrophy, deficiency anemia, mental retardation, convalescent bronchial pneumonia.
Rowen
Boy, December 2011
Cerebral palsy, symptomatic epilepsy (frontal lobe, focal) with partial seizures with secondary generalization
Another adorable baby boy!
Large families welcome; married couples only.
Harbin
Boy, May 2011
Cerebral palsy, symptomatic epilepsy (secondary generalized seizures), optic nerve atrophy, crossed eyes.
Hello, sweet baby! Aren’t you just precious?
Large families welcome; married couples only.
Anders
Boy, Sept 2012
Congenital cleft lip and palate with sucking and swallowing disorders, open arterial duct of minimal sizes, open oval window
Anders is still so young — he needs medical intervention!
Large families welcome; married couples only. Travel required.
Sawyer

Boy, born Jan 2011
Compensated normal pressure triventricular internal hydrocephalus
We’re awaiting additional medical information, as he appears to have some digits fused together on his right hand.
This darling boy has the most soulful eyes, doesn’t he?
Stephen
Boy, born June 2006
Minimal brain dysfunction, pyramid insufficiency, secondary cardiomyopathy, anomalous chord of the left heart ventricle, hypermobility of hip joints, concomitant alternating convergent squint.
Large families welcome; married couples only.
Mollie
Girl, born Sept 2008
Minimal brain dysfunction, dyslalia, deficiency anemia
Will be available when she turns 5 years old, in Sept 2013.
Bryannah #8-3

DOB: 2001
Diagnosis: Down syndrome
Bryannah has been in a mental institution since 2011. She has been in orphanages her entire life, but was just recently registered for adoption in 2013. She has waited 12 years for a chance to find a family! She walks, plays with toys, responds to her name and attends a special needs school each day. She is not talking and still requires help with daily self-help skills.
The agency also has a video available.
Kraig #29-10
DOB: 2009
Diagnosis: Cerebral Palsy- spastic quadriplegia /more visible in the upper limbs, Retinopathy II type – Total detachment of both retinas; delayed development
Kraig is 4 years old. He is considered blind as a result of an injury during birth and surgeons in his home country have determined that his eyes can not be repaired. He is sociable, especially with adults he knows. He walks holding on to one hand of an adult and around an immovable support. He will take several independent steps and it is very likely that the only reason he is not 100% independent with his walking is due to his hesitation to walk since he can not see where he is going. He shows interest in the surrounding environment and listens to its noises. He eats from a spoon and is learning to feed himself. He can get the spoon to his mouth, but is still learning how to scoop food onto the spoon while compensating for his lack of vision. He plays with toys. He babbles and says some syllables spontaneously. He interacts with adults. He follows verbal directions and will play games in which he has to follow verbal instructions (raise your hands, clap your hands, etc). He enjoys music.
Several photos and a detailed video from April 2013 are available.
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.
Tiya #71-1
Girl, DOB: 2004
Diagnosis: mental delays
Tiya has been living in an institution since 2009. Her report indicates that she has mental delays, with no official diagnosis/cause. She had strabismus. Last month, she underwent corrective eye surgery. She walks and has good motor skills. She talks in simple sentences and understands everything that is said to her. She does not show aggression toward other children. She sings songs and enjoys music. The director of the institution reports that Tiya is very kind and doing very well in kindergarten.
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.
Connor #28-3
Boy, DOB: 2007
Diagnosis: cerebral palsy & mild mental delays
Connor is 6 years old. His physical delays are minimal. He walks, runs & climbs stairs. His fine motor skills are also developing. He works puzzles, builds towers with blocks and draws lines. He is learning to fold clothes. He likes movement games/activities and participates in games with his peers. He understands what is said to him and follows simple directions. He says a few words. He feeds himself with minimal assistance.
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.
Olive #38-2

Girl, DOB: 2007
Olive just turned 6 years old. Her motor skills are well developed: she walks, runs, goes up/down steps, throws a ball and climb. She is able to manipulate puzzles, turns pages in a book and perform other basic fine motor tasks. She can identify some parts of her body when asked to point to them. She can also identify objects in her environment in this manner. She pronounces some syllables, but is not yet saying complete words. She understands what is said to her but does not initiate communication. She has instances of auto-aggression. She mimics dance and movements during music time. She participates in games such as jumping rope and other “active” games.
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.
Doug #33-4
Doug has already been transfered to a mental institution!!!
This precious little boy has already been through several major transitions in his short life. He was raised by his birth family until he was 16 months old. He was then placed in an orphanage for young children for 7 months. A month before his 3rd birthday, he was transfered to a mental institution, where he currently lives.
Doug has moderate mental delays with no known cause. He walks and runs and climbs on objects. His visual-motor skills are developed but he still has difficulty with fine motor tasks. His speech is delayed and he is not talking at this time. He has recently begun showing an interest in toys and playing with them. He spends time each day in the sensory room. He does not like for the staff to try to direct his activities and prefers to do his own thing. He does play appropriately with toys and manipulates them in the correct ways. His favorite toys are balls, blocks, cars and trucks. He recognizes staff members and smiles at them. He seeks out interactions with them and will cuddle with them too. He tries to get them to follow him and to engage them in whatever activity he is doing. He doesn’t yet seek out any interaction with the other children. He eats from a spoon and drinks from a cup with some assistance from the staff.
At 27 months of age, his skill level was tested at:
motor skills- 2 years
speech development- 5-6 months
cognitive development: 10-12 months
$18.00 is available towards the cost of my adoption!
Because we only have this child’s file for a short time, he will not be able to receive further donations until a family is found for him.
Monacella
Girl, born January 2009
Brain malformation (corpus callosum agenesia, optic septal dysplasia, ventriculomegalia, cerebral hemisphere hypotrophy), spastic tetraparesis with severe movement disorders Q 04.8, symptomatic focal partial epilepsy with complex partial and rare secondary generalized seizures G 40.2, optic nerves atrophy, convergent squint.
Sweet girl has a laundry list of diagnoses; she needs a family, or she’ll spend so much of the rest of her life in a crib. She’s got sparkle — a family could help her truly shine!
Carter
Boy, born Nov 2011
Cerebral palsy, double hemiplegia G 80.0.
What a little sweetheart! Don’t you just want to scoop him up!
Bryson
Boy, born December 2008
Delay of psychological and speech development, hip dysplasia, atrial septal defect (condition after surgery).
Bryson will be available when he turns 5 years old, in December 2013.
Cyrill
Boy, born July 2011
After-effects of meningocephalitis, tetraparesis, internal hydrocephalus, Hirschsprung disease, thymomegalia
Roland
Boy, Feb 2009
After-effects of neuroinfection, spastic tetraparesis with severe movement disorders G 09, symptomatic focal epilepsy with secondary generalized seizures, medicamental remission G 40.2, mental delays, partial atrophy of optic nerves.
Posey
Girl, born Nov 2008
Cerebral palsy, double hemiplegia with severe movement disorders, symptomatic epilepsy (frontal lobe, focal) with partial seizures with secondary generalization, significant mental delays, optic nerves atrophy.
This sweet girl needs a family to help her bloom!
Kree
Girl, born November 2008
Brain malformation, corpus callosum agenesia, delay of psychological and speech development, pyramid insufficiency, hip dysplasia, convergent squint.
What captivating eyes she has!
Royce
Boy, born Sept 2010
Cerebral Palsy
Sweet little guy, he’s sitting in a high chair in this picture. He needs the love and support of a family!
Leif
Boy, born January 2010
Cerebral Palsy
Dear Leif needs a family to help him reach his full potential — he also is in need of dental care
Travel required, married couples only.
Jeremy
Boy, born Oct 2011
Q90.0 DS; G93.8 Other specified disorders of brain; I51.8 Other ill-defined heart diseases (open foramen ovale); L20.8 Other atopic dermatitis
Look at those big blue eyes!
Jeremy is a very smart and good developed boy without severe health issues besides of DS. Everybody in the orphanage loves him! They will be happy if he is adopted to a loving family.
Kathryn
Girl, born Oct 2005
HIV
Kathryn has a sister who was born in 2002, and is healthy. They may be adopted together, or Kathryn may be adopted on her own. The girls are in the same region, but live in different orphanages.
Cameron
Boy, born Feb 2011
Congenital hydrocephalus, paraplegia and tetraplegia (spastic tetraparesis), partial atrophy of optic discs of both eyes, additional chord of the left heart ventricle, hernia.
Vance
Boy, born 2001
Down syndrome
Vance is a cute, outgoing boy, with a winning smile! He loves to play outside – particularly swinging and playing soccer. He enjoys drawing and playing with puzzles and bricks.
Vance has a significant speech delay, but interacts with others using gestures and expresses himself well.
Piper
Girl, born October 2007
Hydrocephalus, spastic tetraparesis, epilepsy, adenoid vegetation, congenital partial atrophy of optic discs, recrudescent bronchitis in remission
Congenital heart disease (ASD), secondary cardiopathy.
Piper dear, where is your mama? Sweet girl has a lot of needs; a family could drastically change her life — otherwise, she is one who could be destined to spend her life in a laying down room.
Lydia
Girl, born September 2007
Cerebral palsy
This little love is riding in a stroller — we don’t know much about her mobility. Her wispy hair is beautiful, isn’t it?
Shadrach
Boy, born June 2010
Microcephaly, spastic tetraparesis, epileptic syndrome with frequent seizures, chronic subdural hematoma
This sweet little tyke needs a family to love an care for him — he’s said to have frequent seizures, so a neurologist should be overseeing his care and medications.



















Girl, Born September 2008
















Boy, born August 2000
Boy, born January 1999
Boy, born Sept 2000



