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Because every family deserves the blessing of a child with Down Syndrome... |
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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.
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.
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.
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!
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
BOY, Born October 26, 2004
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!
Evan

Boy, Born June 2003
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.
Kyle #7-1

Boy, Born March 11, 2004
Main diagnosis: Down syndrome, stabismus
Kyle has already been transferred to a mental institution.
Kyle was born with a heart condition and anal atresia, but both have been surgically corrected and he is now perfectly healthy. Kyle walks, pronounces combinations of words and seeks out physical contact and attention. He has difficulty with his attention span and his development is delayed. However, he still shows a desire to learn and interact.
Several photos are available. Profile and most recent photo updated in 2012.
SINGLE MOMS, OLDER PARENTS, & LARGE FAMILIES WELCOME, EASY TRAVEL
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 is on a gluten free diet for symptoms of Celiac disease.
Kaleb’s gross motor skills are developing, but delayed. He started walking when he was 4 years old and still requires assistance going up and down steps. He can run, but it is with a “clumsy” gait. He spends most of his time sitting in a child’s chair. He requires 1:1 assistance with academic tasks. He eats with assistance. He is a calm child. He does not exhibit any auto-aggression. He responds to his name but doesn’t usually follow verbal instructions. 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.
Alaric
Boy, born January 2013
Down syndrome, congenital heart defect (Atrial Septal Defect 3 mm. He does not need heart surgery)
What a sweet little bald baby boy!
Married couples only; large families welcome.
Brandon #6-16

Age: 1
Diagnosis: Down syndrome
*updated information on his development is coming soon*
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.
Beatrice

Girl, born October 2011
No eyes, no nose; congenital heart defect (open oval window)
Sweet little Beatrice! Imagine being stuck in a crib all day….with little opportunity for stimulation anyway, but also having no sense of vision or smell either! Imagine what reconstructive surgery will do for this angel…..the gift to know the beauty of the world around her and the smell of *home*.
Beatrice is doing well medically, she is a good weight so far, but REALLY needs a family! She makes sounds, likes to communicate and interact with others.
The sooner she can get into a family, the better, so she can get the therapy she’ll need to blossom.
From a family who met her in Oct 2012: “I got the pleasure of meeting Beatrice today and such a beautiful baby girl she is. When I looked at her all I could think about as she moved her adorable lips as though she was taking a bottle after waking up from a nap was if she could only get adopted in America the opportunities and what surgery would do for this little girl. Her life would be changed let alone saved. When I visited her it was very emotional even for the staff at the school and tears ran down their face and I held her hand and she squeezed my fingers. She is very loved her and the staff can only hope and pray she finds a forever family to give her all the opportunity and chances in life she so deserves. I have personally adopted and am adopting from this school now twice and it is an incredible school to work with and the children are loved and cared for but when her time is up when she ages out her future will be grim. I pray this precious girl will find her forever family.”
A family that visited her orphanage in May 2013 observed that Beatrice was able to stand in her crib. They also saw that the arm braces have been removed, that she could sit up unassisted and could grip toys in both hands. During a verbal interaction with Beatrice, the family observed that she turned toward their voice in response.
Married couples only. Large families and older parents welcome, travel required. More photos available!
Davin #390 OD
Boy, born March 2003
This 10-year-old boy is in good physical and neuropsychological development, despite his congenital bone malformations. He has several innate bone malformations: narrow shoulder girdle; distanced asymmetric mammillas; left arm – forearm aplasia with two finger rudiments; rights arm – hypoplasia of the wrist with syndactyly; legs – his feet are underdeveloped. He is very friendly and enjoys drawing and telling stories.
He is expressive, ambitious, sensitive and has a sense of dignity. At times he might be stubborn. He has a very charming sense of humor.
He keeps on asking everyday if there is finally an adoptive family for him and he looks forward to meeting his Mommy and Daddy.
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.
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!
Nettie #226 OD

DOB: 2005
Diagnosis: delays with no specific diagnosed special needs
Nettie was raised by her family after birth. She was placed in an orphanage at 13 months old and transferred to another orphanage for older children when she was 4 years old. Her gross motor skills are well developed. She walks, runs, kicks a ball and plays sports. She can dress and undress herself and put her shoes on and off. She folds her clothes and is learning to make her bed. She washes her hands and brushes her teeth. She feeds herself, but does not yet clean up after herself after meals. She plays appropriately with toys and participates in games with other children. She sometimes have a difficult time understanding the rules of the games. She colors with colored pencils. She understands everything that is said to her and follows simple verbal directions. Her speech is significantly delayed and her inability to communicate with the staff and other children cause great frustration. She is hyperactive and moves quickly between activities. It is difficult for her to learn due to her lack of focus and hyperactive behavior. She is described as impulsive with non-purpose driven behaviors. She has a difficult time “warming up” to strangers and is very attached to familiar staff. A very detailed psychological report is available.
UPDATE 2013:
She has moderate mental delay. Her physical development is normal. She walks stably and takes part in the gymnastics activities. She goes up and down the stairs stably. Good coordination of the legs and the arms.She can dress and undress, put on and off her shoes. She also tidies up her clothes on a chair. She has delayed speech development. She understands the meaning of words and sentences but it is difficult for her to pronounce sounds and words, She can’t yet focus her attention on a given object even for a short time; she doesn’t have the required discipline.
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!
Pete # CAN
Boy, born 2011
Down syndrome
Pete was born in June of 2011 and is diagnosed with Down Syndrome. He is post-operative for a heart condition at his last post-operative appointment in September it showed very good results.
Pete is calm and active when he wakes up and smiles when spoken to, touched or played with. He engages people with his gaze and follows their movements. He reaches for hanging toys and grabs the toys when they are given to them. He can grab his feet with his hands.
Pete is active and can turn over, stand with support and holds his head high and stable. He vocalizes loudly and likes practicing his voice.
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!
Fallon #11-42

DOB: 2007
Diagnosis: mental delays
The picture on the left is from April 2013
Fallon spent the first 3 years of her life in an orphanage that was known to provide very minimal care to the children. When she was 3 years old, she was transferred to an orphanage for older children. Then, at age 5, she was placed in foster care with an older couple.
Fallon’s report indicates that she has global delays. She walks. She can say a few words that are difficult to understand and communicates her wants/needs using gestures. She follows verbal instructions. She imitates other children and enjoys music and dancing. Her report indicates that she now wears glasses. She has no health concerns.
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.
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.
Tristan # CAN
Boy, born June 2008
Neuro-Psychological Delays
Tristan’s information is from a report dated January 2012. The full report and videos are available for review from the agency.
During his first year, Tristan’s physical development was on target. He pronounced words by imitation. After 1 year, he did not learn new words and did not pronounce them with purpose. In 2010, he was taken for a Psychological consultation. At that time he was diagnosed with mental retardation. Individual psycho-pedagogical activities are recommended. The concern for Tristan is that he is delayed in his neuro-psychical development. He pronounces several short words and can perform elementary verbal orders if he wants. He can hold a pencil and leaves marks on a sheet. There are several videos included with the full file that show this skill. He can hold a spoon while eating. He performs observed actions with toys. He can throw a ball in a box. The child runs considerably well. He can climb up stairs and goes down with support.
During the last months Tristan eats well. His lack of appetite has been resolved and the child has good weight graph. During the past period the child established privileged bond with one of the nurses. Under the program “Granny’s Grandchild” from 15th September 2011 with the child works a woman for four hours a day. The work is individual. These contacts influenced the child in a positive manner. He feels good in their company. He is enjoying their presence and trusts them. He is looking for a contact with both of the women and makes attempts to have their attention. For surpassing his lagging behind in the neuro-psychical development the individual work with the child must go on.
Because the agency only has this child’s file for a short time (mid-May), he will not be able to receive donations until a family is found for him.
Kody #1-7 CAN


DOB: 2008
Diagnosis: developmental delays
Kody was born premature at 27 weeks gestation. His birth mother smoked during the pregnancy and her amniotic sac ruptured 3 days before delivery. He was breech and delivered via C-section in poor condition and weighing just 2 pounds. Many of his delays are consistent with a child born at this early gestational age.
Today, Kody is healthy, though he has occasional respiratory infections. He’s had eye surgery for strabismus. His motor skills have been delayed as a result of being premature, but he is now walking well independently. He reaches for objects, tracks them with his eyes and has good visual motor skills. He picks up objects and studies them intently. If he is unfamiliar with an item/toy, he will shake it, turn it and check it out in detail to attempt to figure out what it does. He is using combinations of sounds and putting syllables together to make simple words. He does not have any true purposeful speech yet , which is a source of frustration for him when he’s trying to communicate his wants/needs. Sometimes he gets upset and other times, he just shuts down and won’t communicate at all. He enjoys interacting with adults and laughs loudly when being played with. He has a good attention span and will focus on the adult interacting with him or what he’s playing with. He initiates games with adults. He drinks from a cup unassisted and eats with a spoon. He has difficulty with chewing. He has a 1:1 caregiver that spends time with him daily.
The agency is able to request additional information for a serious inquiry. There are also videos available with a full file request.
Because the agency only has this child’s file for a short time (mid-May), he will not be able to receive donations until a family is found for him.
$108.00 is available towards the cost of my adoption!
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.
Harry and Will (twins)

Twins, born Oct 2010
Epilepsy
The boys had prenatal exposure to HIV; but they are testing negative. They have some features of FAS, but this has not been diagnosed, but a cautionary disclosure.
Such cute boys! They’ll liven up a household for sure!
The boys have an older sister (born in 1998) who has no special needs. She is available for adoption, but they may be separated.
Large families welcome; married couples only.
Tadee
Girl, born February 2004
Chronic Hepatitis B
Tadee is a lovely young girl, hoping for a family of her own! Her hair is adorable, with the multiple braids.
Jaysen #378 OD
Boy, born June 2004
This 8 years old boy has been diagnosed with Fraccaro syndrome. He demonstrated a delayed neuropsychological development and hypogonadism, symptomatic epilepsy and mental delay. He needs a lot of positive emotions, individual work and positive reinforcement in order to master new skills and habits, and further acquire knowledge. His physical development is not correspondent to his biological age. He can sit independently but it is hard for him to walk on uneven surface and he is not always able to go down the stairs. This is main reason he cannot take part in sports games. He knows his name and responds with eyes when called by his name, especially when call by a familiar adult. He cannot speak yet and can pronounce a few words only.
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.
Amaris #377 OD
Girl, born September 2005
Her neuropsychological development is delayed. She has a surgically corrected heart malformation a weeks after she was born.
History of seizures, and increased muscle tone.
This 7-year-old girl is in a satisfactory general condition. She walks independently and takes part in music and dynamic games. She initiates contact with a caregiver in game play activity. She cannot speak and makes inarticulate sounds. She likes to play along with musical and singing toys.
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.
Ivy #379 OD
Girl, born May 2003
Hydrocephalus
This girl is almost 10 years old and her neuropsychological development is delayed as a result of her congenital condition – hydrocephalus. She is small for her age. She seeks other people’s closeness and responds with a smile when meeting unfamiliar adult. Her speech is underdeveloped and she doesn’t use language as a means of communications. She tries to imitate sounds and says the word “mama”…. She studies a special educational program at school. She sleep good and wakes up calm and joyful. She likes to play alone or observe the other children playing.
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.
Autumn #380 OD
Girl, born October 2005
Blind (fourth degree of Retinopathy), Delayed physical and neuropsychological development
This 7 years old girl can walk independently. She attends special school and follows simple instructions. She likes the adults and wishes to spend most of her time in the group with children. The girl doesn’t always like physical interactions. When she wants to be left alone she would wave her hands, spin around and cover her ears with hands. The child likes going out for walks. She is calm while traveling or when visiting a place she hasn’t been to before. She likes musical toys. She knows her name and react to it but doesn’t always like it when someone addresses her directly. She makes sounds which might be interpreted as joyful or expressing displeasure. She doesn’t speak, she repeats syllables in imitation – “pa-pa”, “ma-ma-ma”, “da-da-da”, “o-pa”.
She shows preference to food – she likes sweets, pudding, and chicken and already tries to eat independently but needs adult’s assistance. She is fed by a spoon. She hasn’t yet mastered her skills to get dresses and undressed. She takes her shoes off.
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.
Bert and Ernie

What a handsome pair of boys! And so young!
Boy, born February 2008
Bert has cerebral palsy; we don’t have any specific information
Boy, born March 2009
Younger brother, Ernie, is healthy. He is only available to be adopted WITH his brother.
Large families welcome; married couples only.
Sinclair #375 OD
Girl, born April 2005
Cerebral palsy and moderate mental delay
Listening to quiet music relaxes her. She seeks contact with another children from her group. She attends Daycare center for Children with disabilities but she is dependable on the care of adult. She repeats others’s movements – giving a hand, clapping and raising both hands. She recognize her caregivers and rejoices in their presence. She will feel and do much better in a family setting where she will get a personal attention.
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.
Alonzo #373 OD
Boy, born 2006
Alonzo is a 7-year-old boy who has a number of congenital bone abnormalities.
Despite the deformities he can effectively use his limbs – he walks independently, goes up and down the stairs while holding onto the railing or an adult’s hand. His fine motor skills are not very well developed. He has good social and emotional skills. He sleeps good and has a good appetite. He likes to play with another children. He loves to play ball – he kicks a ball and throws the ball with both hands. During the school 2012/2013 he is a student in the preparatory class of the Primary school at the Home for Children with Physical Disabilities.
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.
Jeanette

Girl, born 2003
HIV, strabismus, congenital cataract (blind in right eye)
Mild to moderate mental delays, FAS, tuberculosis of the lymph nodes
Update March 2013:
Jeanette was exposed to alcohol prenatally. She has issues with impulsivity/understanding consequences. She is well-liked where she is, but needs additional support to succeed in school. It’s recommended that Jeanette would do great with older children whom could help correct her behavior and could model appropriate behavioral for her.
She is very sweet and loves to draw, and color. She pays great attention to detail in her drawings and when she is doing something she like to do like drawing she can sit still for a very long time doing it. She is also very funny and dramatic. She loves to act and dance and sing and make goofy faces and act silly to make people laugh. She could do well in a family but they would need to be prepared for FAS (fetal alcohol syndrome).
Corbyn
Boy, born Sept 2008
HIV+
Corbyn will be available for international adoption this fall, when he turns 5!
Large families welcome, married couples only.
Thatcher
Boy, born April 2012
Down syndrome, congenital heart disease (operated)
What deep, dark eyes Thatcher has! Don’t be fooled by his pink outfit, he is a BOY!
Devora

Girl, born February 2002
Mental delay, HIV
Creative, eager
Devora is a real sweetie pie! She loves to have her head rubbed, and enjoys being tickled. Her smiles and giggles are absolutely heart melting! She does not talk, stand, or walk as far as I could tell. Her idea of mischief is to kick off a shoe or hide her arm inside of her sweatshirt, and she’d giggle as these things were corrected.
She seemed to find it very amusing when I would ask her where her hand was, then say “There it is” as I removed it from inside of her shirt. This became a game, and she would giggle as she hid her arm again as soon as I removed it from inside of her shirt. She is a very content little girl, and something as simple as a spiky ball could put a big grin on her face. I never saw her upset as long as she was allowed to play in either her bed or her chair, but she would become upset if I tried to move her to a more unfamiliar area to play.
Mason and Madison

Mason
Boy, Jan 2001
Cardiac abnormalities: mitral valve prolapse of 1 stage, supplemental oblique chord of the left ventricle. Scoliosis.
Madison
Girl, born Sept 1997
Abnormal development of cardiac system: mitral valve prolapse of 1 stage, humpback.
They are currently in the same orphanage, and need to be adopted together.



















Girl, Born September 2008










Boy, born Jan 2013
Boy, Dec 2012
Girl, born 1998