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Hunter, Forest and Ridge

30809005259_130809005814 30809010039

 

Hunter-001ForestRidge-001Brothers – they need to be adopted together!

They are said to be “very good boys”!

Listed: August 11, 2013

Hunter, The oldest, was born in March 2004:  Hyperkinetic disorders/Hyperkinetic conduct disorder; Nonorganic sleep disorder/Emotional sleep disorder; Benign intracranial hypertension; Other specified diseases of gallbladder; Flat foot

Hunter likes to eat a lot. He and his brother Forest have a lot of energy. He really likes to do arts and crafts and play games. Most of the time he has a very sweet disposition. He is very keen to interact with adults. That being said if an adult is too rough with him things will start to escalate. If an adult tries to swat at him or restrain him in someway he may attempt to bite. Hunter can speak pretty well but he can’t always communicate what’s going on with his emotions. Hunter responds best to strong male figures. An attentive dad is key to a positive adoption for him. He is in grade 4 here but he can’t read, write, do math, or anything like that right now. He is schooled by himself and school mostly consists of arts and crafts. He is not unintelligent but very delayed. He likes soccer. He would be great in an attentive family where he and his brothers will get much attention and where they will be by far the youngest children. I would adopt him myself if I could be as focused on him and his brothers as he needs a dad and mom to be and if we had the space for them along with our current 3. He enjoys picking fruit and cleaning in the orphanage. He is never been far from the orphanage and he is interested in coming to America. He has communicated that he really wants to come to America and really wants a papa.

Forest, the middle boy, was born in Aug 2006:
Mild mental delays; speech disorder

Forest likes to eat a lot. He does school the same way his brother Hunter does. He is considered to be in the second grade. Very sweet but also very active. Like his older brother, he needs to need a lot of attention to keep him from unintended harm. He likes to be outside. He has minor institutional self harming tendencies like scratching himself to leave marks. He does not do that a lot though. Forest loves to give hugs and kisses and hold hands with the adults.

Ridge, the youngest brother was born in Aug 2008
Stenosis of pulmonary artery; currently he does not require surgery. Tuberculin skin test – positive?

Ridge likes to clean. He was mopping the floor with an adult sized mop as I wrote this. He is a very small but sweet boy. He’s a very peaceful and charming child. He is not in school yet but he seems to be the most intellectual of his brothers. He will likely do better in school then his brothers when he gets the chance. He is so cute it is hard to imagine him spending another day without a family. When the boys orphanage shuts down Ridge will be separated from his brothers for several months because he is not old enough to go with his older brothers. I expect this will be a very traumatic time for him, so if a family could come for him as soon as possible that would be best. No family should hesitate to adopt these children as long as they are available to give the time and attention that these children deserve. If that is done the children will flourish.

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

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Clark

30730200600 (2)30730200600 (1)Boy, born September 2011

Cerebral palsy, retinopathy, premature, severe myopia.

Listed: August 2013

He cannot sit or stand.

$2,724.07 has been donated towards the cost of my adoption!

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

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Rhyder

30728134755rhyder-2017-croppedBoy, born February 2003
Congenital malformation of entodermal canal, anus atresia (colostomy in 2003)

Listed: August 5, 2013

New pic January 2017!  Isn’t Rhyder handsome?   He needs a loving family to help him with his medical needs.  14 years old now.  Rhyder is a very nice boy!  He has had several operations, and currently wears diapers.  He has “Absolutely normal mental development.”

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

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Avery

guardianangel30728131506Boy, born June 2004
HIV
Listed: August 5, 2013

 

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

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Virgil

30806220620virgil-2016Boy, born May 2006 Congenital cerebral hernia, hydrocephalus,  flail legs, slight mental delay, equinovarus, adenoid vegetations of I stage, paralytic strabismus, slight astigmatism, anemia,  TB-infection, congenital heart disease (open oval window), diffuse goiter of I stage

Listed: August 11, 2013

This lovely boy has a long list of diagnoses, but SO much potential for growth in a loving family!  MORE PHOTOS AVAILABLE.  Married couples only.  Travel required.  Older parents & larger families welcome.

 

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

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Wylie

30818205146wylie-2016-croppedBoy, born May 2009
hydrocephaly, epysyndrom, spastic tetraparesis, congenital defect of brain development

Wylie has a handsome boy who is facing transfer soon.  VIDEO:  https://youtu.be/XEt-iY-OHtk

Listed: August 2013

From a family who visited him in 2015:  He is calm when being walked around but becomes over stimulated easily. He is getting close to being transferred and this will be terrible for him. In the baby house the caregivers have more time to spend with him. In an institution I can see him just being constantly sedated… This handsome little guy needs out now!!!!

From a family who met him in 2014:

Wylie is a sweet boy, and obviously loved by the nannies. They often stooped down to talk to him, and walked hand in hand with him. He walked constantly, clapping his hands and smiling. He exhibited what I would describe as autistic tendencies. I don’t recall ever hearing him speak. One day he wondered out of his groupa (apparently the door wasn’t latched) into the common area we were visiting out son in. My husband took his hand and led him back. He has a special place in our hearts and we pray someone will see him and choose him. I would be glad to talk to anyone interested. He is precious. He’s at a great baby house, that is very pro-adoption, and in a faster region than most.

*** This child has significant facial features of FAS (fetal alcohol syndrome).   This is a cautionary disclosure to better prepare our potential adoptive families.  Families considering this child should research and be prepared for the challenges that can come with this condition.   You can learn more about FAS here: http://en.wikipedia.org/wiki/Fetal_alcohol_syndrome  and post to our Facebook group to ask other adoptive parents about the challenges and blessings of children with FAS. ***

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

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Rylan

30816163201Boy, born Sept 2008
microcephaly with internal hydrocephalus, hyperkinetic behavioral disorder (ADHD), mental delays

 

*** This child has significant facial features of FAS (fetal alcohol syndrome).   This is a cautionary disclosure to better prepare our potential adoptive families.  Families considering this child should research the challenges that can come with this condition.   You can learn more about FAS here: http://en.wikipedia.org/wiki/Fetal_alcohol_syndrome  and post to our Facebook group to ask other adoptive parents about the challenges and blessings of children with FAS. ***

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

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Carolina

Carolina 2013 (3)carolina-2017Girl, Born May 2006

Listed: August 6, 2010

Carolina is such a beautiful girl; beautiful brown hair with olive skin.  She has cerebral palsy, and does wear AFO’s on both feet.

From her medical records: Cerebral palsy, convergent squint, mental delay.   She can walk by supporter or holding one hand.  She says separate words, understands simple speech, is affectionate and friendly.   Physical therapy and a loving family will bring MIRACLES for this little girl!

Carolina was transferred in 2011 to a boarding school (not an institution).

New pic January 2017!  

UPDATE August 2013:

Carolina is a beautiful girl! She is about 4ft tall and about 50lbs. Her CP affects her mostly from the knees down. She does have cytomegalovirus. This was reconfirmed last year, but we were not able to find out if it is active, or if she merely was exposed while her mother was pregnant with her. CMV does cause brain damage if a baby is exposed in utero, so a family needs to be prepared for that, or for the fact that is IS transmissible when it flares. She is very strong and she does make her likes and dislikes known. Her biggest love is candy…but not chocolate! She likes white chocolate a lot though. She likes dolls, and can undress them herself. She has good use of her hands. She gets around by crawling or knee walking, which is great. Knee walking shows her hips are nice and strong. She loves to “dance.” Dancing, to her, is an adult bouncing her up and down for as long as you can stand to do it. She gets quite unhappy when you stop to take a break. The nannies make her walk a bit while holding onto hands, but her legs and feet are just not able to line up with her being so tight. She is very strong. She loves cell phones and will try to snatch them at any opportunity. A toy cell phone that plays music would be nice for her. She speaks, though it is like a toddler. She repeats the same few things over and over, but she does say a couple other words and used them correctly. She understands much more though and the caretakers speak to her in complete sentences. She just loves to move and bounce and be twirled around. She likes BIG movements. She was very briefly startled by my husband, but quickly discovered he could bounce her around longer and higher than I could…and so she quickly preferred him!

Carolina does have some institutional behaviors that a family needs to be prepared for. Her moods change quickly, and when she gets upset, she can throw herself to the floor, even injuring herself. She will hit, pull hair,etc if she is upset. She will throw large toys as well. The caretakers love her, but did express that she would likely not engage or interact with kids bigger than her, and would be likely to assert herself over anyone smaller. That is just how life in these places is. Families without small children would be best for her. An involved, hands-on Papa would be ideal, and a trampoline would be out of this world for her.

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

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Lucie

30818222451lucie-2016Girl, born Jan 2009
Cerebral palsy, Epilepsy, partical optic atrophy , cross-eye, mental delay, possible FAS

Listed: Aug 19, 2013

VIDEO:  https://youtu.be/y43CZ_uQ7ig

updated medical 5/15: added cardiomyopathy and atopic dermatitis

What a pretty smile Lucie has!  She could do so well with a family.  Lucie has recently been transferred to the adult institution.  We must find a family for her!

$405.14 has been donated towards the cost of my adoption!

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

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Chantelle

21221095254 Chantelle 2013 (3) 21221095254 Chantelle 2013 (2)Girl, born August 2007
CP dystonic-dyskinetic type, rough delay of static and locomotor activity, mental delay, umbilical hernia, congenital cataract, crossed eyes

URGENT!  CHANTELLE IS FACING TRANSFER

Sweet Chantelle has a list of diagnoses, but her main need is a loving family!   A family could help her reach her potential and save her from a life in a crib.

 

From a family who met her in fall 2013:
Chantelle is mostly kept in a laying room although I did seen her out in the main groupa room laying down in a gated play area. I believe she can roll around. I saw her holding things in her hands as well. She has a calm, sweet spirit and I had her smiling in the first minute of seeing her. I touched her precious little face and told her I loved her and she smiled. The other kids seem to love her and they liked going into the laying room to take pictures of her with me.  Chantelle so needs a family now! She won’t be kept at the baby house much longer. She is soooo beautiful, the pictures really don’t do her justice.

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

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Nash

Nash 2015Boy, born 2004

Hydrocephalus

Listed: August 20, 2013

July 2016: NASH HAS BEEN TRANSFERRED TO THE INSTITUTION :(

 

From a volunteer who visited with him in July 2014:  ” Nash is still this very small boy. He has the size of a pre schooler. He is really cute though. He loves to have a man around. He showed my boyfriend all around the place. He loves to blow little wind mills and play games together. He doesn’t really speak the language they speak in his country, but he does make all kinds of ‘words’. He actually tries to make you understand and every now and then there will be an actual word in it, which makes it easier to understand what he says. He is potty trained and he understands language and knows quite well how to read the body language of the nurses. He’s a big help for the nurses, he carries toys inside and pushes wheelchairs. We suspect that he has some kind of visual impairment. He had the glasses of my boyfriend on for a moment and he seemed to be able to see much more, but I’m no eye doctor, so I can’t say for sure. All I can say is that this boy desperately needs out. He is quite healthy and he needs a family where he can blossom. He is an amazing boy and I have tons of pictures and a couple videos of him, where he shows his own goofy self. So please don’t let this boy wait any longer. Many of his friends from the orphanage have been adopted, but he is still listed. I want him out there! I want someone to see his potential and love him all the way home!

From a family who met him in Dec 2013: He seemed to be rocking more persistently. I noticed when music was being played or when we would actively engage him play he would rock nervously. However, he is a wonderfully sweet spirited child and is eager to please. He would always great us with a formal, “hello” and then lead us to take a seat. He never missed an opprotunity to rush out of the groupa and jump in our laps or include himself in whatever game we were playing with our boys. He so desperately wants to be loved. He called me, “Mama” and it broke my heart…how I wish I could have taken this precious boy as well. There were many days that we noticed him strapped to a chair or straight jacketed; I am not sure why because I never saw any self injurious behavior from him. He is very impulsive and easily excited but his joy simply radiates a room. He desperately deserves to be loved, valued and wanted….he only aims to please. The first thought that came to mind upon meeting him was, “He does NOT belong here”….he is so smart…though his speech is often slurred; but only slightly. He seems to be minorly effected by his hydrocephaly and gets along very well. His poor little hands do shake though; probably as a result of the pressure on his brain. I am unsure if he has been shunted or not; I felt around his head one day and did not feel the bump that would indicate he has. If he has not been shunted then that makes his case even more urgent. He desperately needs out! This boy has ALL the potential in the world…he just needs the right parents to break him free!  I also have a video with him in it, if a family is interested.

From someone who met Nash in 2012:  Nash is a wonderful little boy. He is always quick to excitedly greet visitors with happy squeals and a formal hello, and is quite insistent visitors take a seat in the chair he brings over to them 🙂  He is very helpful and obedient, and will sometimes bring toys over to the smaller kids in his group who cannot get toys for themselves. He is very talkative, but a lot of what he says is sort of like “Nash”-ese. He has no problem getting his point across, however, if it is important to him that you understand him! He likes to play with just about any toy; balls, legos, cars, light up toys, you name it he will play with it. He enjoys being silly and laughing, and especially thrives with one on one attention. He is generally a happy little guy, but does not like messes or rule breaking, and is not afraid to tell the other children “No” or try to right their wrongs if they are misbehaving. He very much aims to please! I feel Nash would adjust easily to and thrive in a family!

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

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Faye

30818162858Girl, born July 2008
Microcephaly

 

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

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Todd #21-12

 

Boy, Born 2007

Good general condition, hydrocephalus with a shunt installed, spina bifida aperta, lower limb paraplegia, congenital anomaly of the excretory system – agenesis of the left kidney, hypotonic right ureter, osteogenesis imperfecta (which has not been genetically proven), convergent strabismus, logorrhoea, delayed neuropsychological development.

Listed: Sept 11, 2013

Todd can sit independently. He talks and easily carries on conversations with adults. His intellectual development is right at the “normal” level on testing. He has a caregiver that works 1:1 with him daily.

Families who have visited the orphanage where he lives report that he is a very smart and friendly little boy. He is able to carry on a conversation and answer questions appropriately and plays hand held video games.

Update, 2016:
Todd recently turned 9 years old.  He engages in symbolic and role play, which includes the activities and roles typical for his environment (how a doctor’s visitation goes; how one gets medical supplies; how one organizes a birthday party; what happens during the lesson with the resource teacher).   He knows the staff members. He takes the initiative in meeting new people. Todd eats independently. He eats common food. He chooses his clothes depending on the season and the temperature in the building. Todd leads a dialogue and asks a lot of questions.He loves telling stories and improvising depending on the specific interests of the person he is communicating with.

Additional photos and videos are available.

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

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Asher

Guardian Angelasher1Boy, born February 2009
Cerebral palsy, spastic low paraparesis, retinopathy

New picture from March, 2016

 

Such a handsome boy!  He has such beautiful big eyes.

 

$2,234.38 has been donated towards the cost of my adoption!

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

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Irina

irina2015-3Girl, Born March 5, 2005

Listed: prior to 2010

Cleft palate, possible FAS

From a volunteer who visited with her in August 2016:  Irina’s update from last year is still very accurate. Her introvert and shy behaviors got more though. She prefers not to interact at all. It took me half of our trip to get her to trust me enough to walk around the building with us and she would still not look at me. She avoids any eye contact. She did enjoy the attention though. She still loves to sit on someones lap. She has grown even more than last year. This year she had become too heavy for me to carry her.

I think Irina wants to get out of the facility. She was transferred to this facility a couple years ago. Before she lived here, she lived in a ‘normal orphanage’ with a special needs group. When they lost their funding she was transferred here. When we take her for a walk she walks to the gate and she just stares at the world outside of those gates. She realizes there is an entire world out there. One day the nurses saw us at the gate though and they yelled at us for minutes. We were not allowed to take Irina there, she could walk away. The gate is closed and locked and we were there with her, so there was no way she’d walk away, but from that day on Irina was even more closed and she lost most of the initiative while walking. She even lost her interest in the swing. She needs someone she can trust, someone who she’ll know will stay and will love her. She has already been listed for so long! She needs a family!

From a volunteer who visited with her in July 2015:  ” Irina is a beautiful girl with dark hair and big dark eyes. She has a cleft palate. She is a precious and happy little girl. She loves personal attention. She is craving attention and physical touch. If it was up to her she’d be held and hugged all day. She can react really shy to people who talk to her and especially when yelled at, she will become really introvert. She is a really sweet girl. Irina is a physically quite healthy girl. She is well nourished, she can walk, run, swing, etc. Her physical development is good, compared with the other children in the same facility. She seems to have a strong body. She knows how to use a swing properly and can swing by herself. She enjoys it a lot. She can play accurate with toys, like dolls, or pretend play with kitchen tools. She knows how to walk stairs. She can dress and undress herself. She can drink from a cup and eat by herself. She is potty trained and will tell if she has to use the bathroom. She doesn’t talk, most likely because of her cleft palate. She doesn’t make noises, but her eyes express a lot about how she feels. And her smile will tell you when she enjoys something. She understands what is being said to her and she can follow orders. When Irina is in the group, she’ll try to stay away from the others. She prefers to play by herself, but she is also capable of interacting with other children or adults. She prefers to play with children who are smaller or younger than her, probably because they are no threat to her. Last year I saw how she was being bullied by other (bigger) children. She tries to flee from bullies (and from yelling), but there is nowhere to go. This year she is doing much better. She has grown physically, which made her less of a target for the bigger children. Maybe also because new smaller children are in the group now. Sometimes she’s still the target of bullying and harming behaviour, but at other moments she will show these behaviours herself. She can be a bully to the smaller children herself. I think this is her way of showing that she is stronger now, but this is no good development. The longer children are in this facility, the more harming behaviour they show. Irina is still able to receive love, but time is ticking away. She needs a family. She would thrive in a family where she could be ‘the baby’.”

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.

Irina has been transferred to the older child internat now.   Elinor, Devora, Julia,  Sullivan, Artemur, Duane, Abner and Irina may all be in the same region.

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

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Kanani

kanani-2016Girl, born April 2008

Anophthalmos of the left eye, optic atrophy of the right eye, spastic tetraparesis

Kanani has been transferred!

NEW PHOTO DECEMBER 2016

Lovely Kanani needs a family to help her reach her full potential.

From a family who met her in May 2012:  Large families welcome; travel required.Kanani is very sweet girl. She is well cared for in a good orphanage by caring nannies. She gets lots of outside time when it’s warm out but this time is spent lying down in the stroller as she can’t sit on her own. She can hold on to your fingers and seems to just love to have attention although with her eye troubles it is difficult for her to respond. She likes to have her cheek stroked and her hand held. She is quite stiff and in need of physiotherapy and most of all love and attention. We were told that she will be transferred to an institution very soon unless a family is found as children at this orphanage are typically transferred at age 4.

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

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Todd

Boy, born December 2010

Blind

Todd is such a handsome fellow!

All we know is that he is listed as “blind” — not sure if he has any vision at all.

$3,089.10 has been donated towards the cost of my adoption!

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

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Valery

Girl, Born September 27, 2006

Valery was born with CP and spina bifida.  She has significant strabismus and “progressive hydrocephaly”.  She is not able to walk, and is significantly delayed in all aspects.   But she is still beautiful and deserving and can truly thrive in a loving family, with access to adequate medical care and nutrition.   Valery will remain bedridden for life, and will likely not survive the transfer to the institution.   Won’t someone consider being her “forever family”?

Listed: June 20, 2010

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

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Stella

stella-2016Girl, born 2010

Down syndrome

Listed: August 3, 2016

VIDEO:  https://www.youtube.com/watch?v=SSDRmbGeQds

From a family who met her in Feb 2019: I think she is developmentally delayed and seems to be somewhat lost in her own world. She does smile when tickled, held my hands to play a game rowing back and forth, and she giggled when I clapped her hands. She is sweet, doesn’t cry often. She doesn’t like change or new places, but is content to be in her own area and hang out. She likes other kids to be around. She does not seem to hear or see very well. She does hear somewhat because she makes noises when it is silent, but doesn’t respond much to silly noises or her name. She reached for her nanny when I was holding her. She sits, stands, and when walks while holding hands. She is fed via NG tube but they are working with her to eat by mouth and she is making progress. She is adorable and sweet and so deserving of a family. I do very much believe that she will progress with a family willing to give her the help she needs. She has some autistic tendencies like repetitive movements of her hands. Personally I do not believe it’s full autism but maybe more like sensory issues because of her hearing and sight issues.

From a family who met her in February 2017:  ” She is what would be considered “low functioning”. I would describe her as autistic, although autism is not listed in her chart. She is currently fed via tube inserted into her mouth to her stomach. She was sick with a flu type virus and sent to the hospital. Prior to that visit she was eating regularly by mouth. After a week at hospital being fed by tube she has had difficulties swallowing. She is small. The size of a thin two year old. She does gently reach for your hand and make some eye contact and interaction. She has VERY low tone and does not sit up on her own. She is gentle. She does not yell or cry according to nannies, she is gentle with other children and mainly keeps to herself. Playing with her hands.”

From a missionary who met her in December 2016:  “Strabismus. Low tone. Very cuddly and mushy! Can stand with some support. I showed them some therapy positions and exercises for them to do to get her to weight bear on her feet and I can tell that they have been doing it. Her nose and eyes were excessively yucky and I suspected that her hearing was impaired from fluid. I discussed it with her doctors and they were going to follow up on it. She makes sounds, no language. ‘Lower functioning’ (but I hate to say that). The orphanage workers love her and I think that is a problem in that they carry her about. She is in a baby house with typical peers. I believe with some medical attention and therapy she is capable of progressing.”

*** I am eligible for an additional $5,000 Grant!  Through June 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

$7,288.60 has been donated towards the cost of my adoption!

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

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Annie #

Girl: 2005

Listed: Feb 2019

Diagnosis – Chronic viral Hepatitis B without Delta agent.

Annie was placed with the same foster family since age 4. She is presently in 7th grade. She is doing well in school. She goes regularly to school and likes it there. She is reading and writing very well. Her grades in school are average. Her favorite subjects in school are Arts, Music, Sport and Bulgarian language and literature. She is very polite, social and open girl.

She is a great child – very charming and beautiful and at the same time smart and very nice child without any signs of initialization  or emotional deficit.  She wants to be adopted very much and I hope that a family for her could be found no matter of her age.

*** I am eligible for a $2,000 Grant! ***This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding.

For more information on this child, email childinquiry@reecesrainbow.org

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Tina #

Girl: 2017

Listed: Jan 2019

Special needs:  Down syndrome. Congenital cardiac malformation – Tetralogy of Fallot. State after surgery treatment of congenital cardiac malformation. Greatly delays in physical and neuro-psychic development.

She is extremely sweet and charming little baby girl. She needs more time to get to use to new people. When she expresses her emotions she usually makes sounds and syllables. She makes eye contact. She reacts to people, but quickly gets tired and shifts her sight away. She usually moves into the space by turning from back to stomach. She is able to hold upright her head. In general this is her way to move around, she cannot crawl. She turns around but usually she is more apathetic (the staff thinks that this is mainly due to her heart condition). She holds a toy put into her hand and when she drops some toys she is looking for it.

This precious little girl deserves attention and love, as every child of course, but she definitely shows much more necessity for cuddling. She is infant baby with diseases, which need special cares and monitoring and once she has her own forever family soon, she will make a big progress!!!!

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding.

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

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

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Ashley #

 

 

Girl: 2013

Listed: Jan. 2019
Diagnosis: Dandy Walker; Congenital cytomegalovirus infection

Ashley was severely neglected by her birth family for the first 3 years of her life. The doctor responsible for her care at the Baby Home indicated that once she was removed from the family, she began making progress by first learning to walk and then developing new skills. They have seen a great increase in skills over the past few months and believe she has a lot of potential.. She attends a preschool class at the orphanage.

According to the doctor at the orphanage, the Dandy Walker Syndrome diagnosis has not been proven and no changes have been found in the brain and the eyes of the child.

Ashley walks, runs, and climbs up/down stairs. She can build a tower of cubes, put circles on a pin and push the right buttons of a busy box.

Ashley is very curious; she will initiate contact with an adult or other child first. She does not isolating herself from the other children, but she prefers to be on the periphery of the game and not in the center. Ashley attends preschool preparatory group within the Baby Home. In the group, she appears as an active, open child with a positive character.

Ashley understands, what is required of her, but not always implemented the task. She reacts to her name and performs simple task at her will. The child is making sounds and pronounces syllables, for now. A

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding.

For more information on this child, email childinquiry@reecesrainbow.org

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Dominik #

Boy: 2017

Listed: Jan 2019

Diagnosis: Down syndrome; heart condition-surgically repaired; pancreas annulare

Dominik was diagnosed at birth with Down syndrome, pancreas annulare with malrotated intestines. He underwent further testing, which found multiple heart defects. His heart was surgically repaired when he was 5 months old. The pancreas annulare is not causing any health issues at this time.

Dominik can roll over from back to belly and is beginning to attempt to crawl. He can sit unassisted and has recently started bearing weight on his feet. He reacts to sound and follows toys with his eyes and by turning his head. He’s beginning to babble and make sounds. He laughs and cries to show emotion. He likes rattles, toys that play music/make noise, and fabric that makes a crinkle sound. He will reach for toys, pick them up or take them from someone offering them to him and explore them by shaking them, bringing them to his mouth, etc.

Medical report and videos available through the agency.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding.

$27.00 has been donated towards the cost of my adoption!

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

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Shay #

Girl: 2013

Listed: 01/2019

Shay
Age: 5
Diagnosis: Seizure disorder-currently on seizure meds; delays in development; ataxic cerebral palsy; ADHD


Shay lives in a foster home. She was hospitalized to look for a cause for her seizures and was diagnosed with ataxic cerebral palsy. She is currently taking medication for seizures, but still has 1-2 seizures each month. She is able to walk and has good gross motor skills. Her fine motor skills are delayed. Her speech is delayed. She uses single words or short phrases to communicate. She has difficulty focusing, which makes it difficult for her to learn new skills. She is very active and needs constant supervision.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding.

For more information on this child, email childinquiry@reecesrainbow.org

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Silas #

Boy: 2017

Listed: 01/2019

Silas
Age: 1
Diagnosis: hydrocephalus, shunt, mild possible seizure activity observed (not officially diagnosed); increased muscle tone in all 4 limbs

Silas is closely followed by both a neurologist and a neurosurgeon. He’s sees the neurologist every 3 months and the neurosurgeon every 6 months. He can roll over unassisted. He smiles and reacts with pleasure to caregivers and to music. He is making sounds and some syllables such as “ma-ma”, “no-no”, “ba-ba”, etc. He loves music very much. It calms him, and at the same time makes him move in a rhythm even lying down. He kicks with his feet in time – there are active movements of the limbs. He loves the Sensory room, where he likes the different sounds and images. He does not like being alone. He feels much better in a group along with other kids, where it is louder, more moving and more colorful. He expresses emotions especially when is cuddled.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding.

For more information on this child, email childinquiry@reecesrainbow.org

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Tabitha

Girl, born 2015

down syndrome
speech delay
atrial septal defect
iron-deficiency anemia
abdominal hernia

Listed: Jan 2019

$76.50 has been donated towards the cost of my adoption!

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

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Vivi

Girl, born 2013

down syndrome
condition after surgery of atriventricular communication

Listed: Jan 2019

 

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

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

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Lionel

Boy, born 2018

other specified disorders of brain
microphthalmos

 

Listed: Jan 2019

$90.00 has been donated towards the cost of my adoption!

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

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Enzo

Boy, born 2018

congenital hydrocephaly
congenital defect of development of corpus callosum
torticollis

 

Listed: Jan 2019

 

$18.00 has been donated towards the cost of my adoption!

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

, , , ,

Sabrina

Girl, born 2016

sequelae of inflammatory diseases of central nervous system
epilepsy unspecified
other ill-defined heart disease
optic atrophy; myopia; strabismus
delayed development following protein-energy malnutrition
chronic tubulo-interstitial nephritis unspecified

 

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

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

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Nolan

nolan-2016Boy, Born September 2004

Nolan is such a handsome boy!  He needs a loving family!

Listed: August 4, 2010

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.”

A family must have a completed homestudy to commit to Nolan.  Due to the size of Nolan’s grant, 50% of grant funds will be available upon receiving a travel date, and the other 50% upon passing court.

Nolan has a grant of $19,597.50 available towards the cost of his adoption!

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Shaw

Boy, born 2008

Cerebral palsy
Spastic lower Paraparesis

Listed: Jan 2018

From a family who met him Nov 2018:
Shaw is a very loving boy who desperately wants a family. He hugged us repeatedly asking, “Mama, America? Papa, America?”

He speaks well, enjoys painting, and can walk with some need for support. He sweetly pushes his friend’s wheelchair and it offers stability for him and assistance for his friend. He’s been raised amongst boys much older than him and has picked up swear words but truly is a beautiful soul. He became jealous of our attention when we were talking with his younger roommate and he bit him. The facilitator would like us to note that he has a family history of mental illness and that his family should consider this in their decision. We are head over heals for this boy and honestly would have brought him home without hesitation were we approved for another adoption. Every adoptive family would be wise to consider trauma-informed parenting and to anticipate both aggression and mental illness. Please, consider whether you could be Shaw’s mama and papa.

He is so sweet, but can be a kind of “difficult” – strong-willing and stubborn. He is a smart boy. He wants to be adopted and asks to find a family for him. At the same time he will choose if he likes a family. I would recommend him to a family with older children – older than him, to show a way to behave. He may be very helpful and careful. I often can see him helping other kids with worse disabilities as he has. But he can lose his temper fast. He has a kind of mental retardation/delay. His biological mother is qualified as mentally disabled due to her schizophrenia.

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

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

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Quincey

Boy, born 2011

Sequelae of inflammatory diseases of central nervous system
severe motor impairment
spastic tetraparesis

From a family who met him Nov 2018:
Quincey is one of the most darling, endearing boys we have ever met. He is pure joy and just exudes love and affection. His little giggle is contagious. He begged us to take him home to America- he so desperately wants a family. He loves to show off how he can get into his wheelchair (which he calls his car!) himself and beams with pride. He speaks well, is very bright, and will flourish in a family.

He is so sweet, always look happy and friendly.

$477.00 has been donated towards the cost of my adoption!

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

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Daniela

Girl, born 2004

Multiple malformations of the central nervous system
spina bifida
internal subcompensated hydrocephalus
lower flaccid paraparesis
convulsive syndrome
anus atresia

 

$9.90 has been donated towards the cost of my adoption!

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

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Sally #

Girl: 2016

Listed: Jan 2019

Age 2
Diagnosis: congenital anomaly of the central nervous system; dysmorphic stigmas(dysmorphic facies, four-finger groove of left hand, six fingers on right leg, longer right foot with a larger surface area); generalized hypotonia and forming hemiparesis on the left.

 

Sally had one seizure at age one. She’s been on seizure medication since that time and has not had any additional seizures. She touches and grabs with her right hand and moves her right foot. The left hand is almost clenched in a fist. Her muscles are very tight, but she can sit up when placed in that position. She will reach and grab toys with her right hand. She tracks objects that are moving in front of her face. She laughs when adults interact with her. She makes sounds and produces syllabes when imitating someone. She enjoys musical toys and will scoot to get to a toy that is near her when on the floor. She is fed by an adult and can eat from a spoon.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding.

For more information on this child, email childinquiry@reecesrainbow.org

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Garrett #

Boy:  2016

Diagnosis: Down syndrome, polysyndactyly

Garrett is an adorable little boy, born in November of 2016 with Down syndrome, polysyndactyly (webbed fingers/toes) – 3rd and 4th fingers on both hands and 2nd and 3rd toe on both feet, congenital cardiac malformation – open foramen ovale with preserved chamber function (the foramen ovale is already closed), and motor developmental delays.

Garrett turns from his back to his belly and vice versa. When lying on his belly, he leans on his elbows. Garrett reaches for a toy he is being handed or for hanging objects. He takes two toys, one in each hand, and knocks them together. Garrett is overall a pleasant little guy and individual attention from an adult makes him so happy. He loves to smile back at adults when they are smiling at him. He cries at separation, but quickly calms down. Garrett has syllable-repetition speech. He accepts food from a bottle and is gaining weight. His sleep is calm.

His file is currently with multiple agencies. One agency is offering a $1500 agency fee reduction.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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

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

, , , ,

Pippy #

Girl: 2013

Special needs: Cerebral Palsy, Leukemia, strabismus

Pippy is a precious little girl, born 2013.  Pippy is a twin and was born very premature and diagnosed as having cerebral palsy- spastic diplegia, umbilical hernia, and strabismus.  She now wears glasses to correct the strabismus and has received surgery to correct the hernia.  Pippy was later diagnosed as having acute lymphoblast leukemia.  She is currently in remission, but continues to take medication to prevent her cancer from coming back.  Pippy’s twin brother also has CP and is being cared for by his biological family. Pippy is very delayed in all areas of her development.  She can manipulate objects using her left hand.  Pippy is not speaking at this time.  We hope just the right family sees Pippy and knows that she is their daughter.

Pippy has a $1,500 agency grant for her adoption with her current agency (Jan 2019). Other grants may be available based on the adoptive family’s circumstances. Agency grants are awarded as agency fee reductions.

Pippy’s agnecy needs a family with an approved home study to be able to move forward with adopting her. If you have an approved home study or a home study in process and are interested in adopting Pippy, please contact her agency.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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Tobias #

Boy:  2013

Diagnosis: Untreated Recto-vesical fistula and anal atresia that has resulted in a colostomy bag for stool output and chronic kidney conditions including untreated kidney reflux. A vesicostomy was placed for urine output. These conditions are possibly repairable with appropriate medical care.

Tobias is developing well. He talks in sentences and answers questions appropriately. He has difficulty pronouncing some words, but is able to get his point across.  His gross motor skills are well developed. He walks, runs, goes up/down stairs, kicks a ball, throws a ball, and “drives” around in a kid car outside. His fine motor skills are also well developed. He can hold a pen correctly and draw tiny circles on paper. He can thread beads, make things with with putty/play dough, and put his hair up with a hair tie. He has an imagination and demonstrates pretend play skills in his videos. He loves sunglasses and will even attempt to make sunglasses out of twigs when playing outside.He also takes twigs and makes bracelets and rings to wear. He is learning his colors and shapes and can already properly identify some of them. He knows body parts and can count. He can also identify some animals. He interacts well with other children and adults.

The team member who visited him described him as, “Cheerful, sweet, very funny and always smiling”.

Photos and videos are available through the agency.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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Leon #

Boy:  2017

Diagnosis: hydrocephalus; motor delays

Leon is living in an orphanage that is known for a lack of care to children. Despite this, his emotional development seems to be doing well. He was recently moved out of the section of the orphanage for babies and in with the toddlers. He enjoys interacting with the staff and the other children. He plays with toys. He eats from a spoon. He is crawling and can stand with support. His motor delays are said to be due to high muscle tone.

Additional photos and videos are available through the agency.

 

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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MARCOS

Boy, born 2014

Disorder of brain, unspecified
emotional disorders
mild mental retardation

 

He doesn’t have any siblings.  He is available early 2019.

$0.90 has been donated towards the cost of my adoption!

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

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KENNA

Girl, born 2017

Sequelae of inflammatory diseases of central nervous system
Other hydrocephalus
Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
Optic atrophy
Nystagmus and other irregular eye movements
Atrial septal defect

 

$90.00 has been donated towards the cost of my adoption!

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

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Vincent and Wade & Siblings

Boy, born 2014
Disorder of brain, unspecified
Protein-energy malnutrition of moderate degree

boy, born 2016
Disorder of brain, unspecified

Total of 6 siblings: the other 4 siblings are 14 (a boy), 12 (a girl), 10 (a girl) and 8 (a boy).

These children become available for international adoption in summer 2019

$180.00 has been donated towards the cost of my adoption!

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

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Nannette and Pamela

Girls, born 2013 and 2014

Both girls have diagnosis:
Other disorders of nervous system in diseases classified elsewhere

Wonderful children!

The girls will be available in summer 2019

 

$45.00 has been donated towards the cost of my adoption!

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

, , , ,

Dena

Girl, born 2016

Tuberous sclerosis
Generalized idiopathic epilepsy and epileptic syndromes

Listed: Dec 2018

She cannot talk yet and in general is pretty “weak”.

$135.00 has been donated towards the cost of my adoption!

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

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Patricia #

Patricia
Age: 2016
Diagnosis: Hydrocephaly, heart condition

 

Patricia is currently fed via an NG tube 4 times a day. The staff believes that she could learn to eat by mouth if a family was able to work with her on the skill. She can not sit up, but she does move her legs and her hands.  Patricia is very alert and aware of people. She tracks people and objects with her eyes and also looks when she hears voices. She responds to touch by smiling and making happy noises. When a toy is placed in her hand, she attempts to bring it to her mouth. She enjoys when someone sings to her and responds with smiles and sounds.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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Julian #

Julian
Age: 2014
Diagnosis: Spina bifida

 

Julian enjoys playing with toys. He is well attached to his caregivers and responds to them when they talk to him. When he is happy, he responds by making noises and clapping his hands. His report indicates that when held by the hands, he will take steps.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

, , , ,

Liam #

Liam

Age: 2015
Diagnosis: mental delays, asthma, strabismus

Liam was born with a cleft lip & palate. It has been surgically repaired. He has delays in his development and is currently working with a speech therapist to improve his speech. His medical report mentions decreased hearing, which could be the underlying reason for his language delays and slow developmental progress. He does not react to toys that make sound nor turn in the direction of the sound. He plays with cubes by putting them in and taking them out of a cup, but has some problems manipulating with smaller objects. His play is mainly throwing objects and chasing them. He enjoys playing  with balls and cups.  He enjoys physical interactions with adults (hugging, jumping with them holding onto him, swinging, etc).

Photos and videos are available through the agency.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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Ozzie #

Ozzie
Age: 2014
Diagnosis: Coffin-Lowry Syndrome


Ozzie has decreased muscle tone. He can’t walk, but has recently started standing up in his crib with support. He smiles and has positive emotions when interacting with adults and when he is with the other children. He pronounces combinations of sounds. He laughs when playing peek-a-boo.

*There is an older child that is believed to be Ozzie’s older brother. However, they are NOT listed as needing to be adopted together. The other child is listed as Ollie  https://reecesrainbow.org/127612/ollie-2

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

, , , ,

Ollie #

Ollie
Age: 2012
Diagnosis: Coffin-Lowry Syndrome

 

Ollie is now living in foster care.He is physically well developed. He has good coordination of his hands and feet. He walks without falling, and can run as well. Climbs up and goes down by the stairs when holding an adult or the railing. He can play with cubes by putting them and taking them out of a cup, but has some problems manipulating with smaller objects. He cannot eat and dress by himself yet, but does make attempts. He understood almost everything and fulfils small tasks. He likes playing hide and seek. He hides behind the door and when he is found, he laughs and stomps his feet. He is interested in musical cartoons and copies the movements of the actors.

*There is a younger child that is believed to be Ollie’s younger brother. However, they are NOT listed as needing to be adopted together. The other child is listed as Ozzie.  https://reecesrainbow.org/127615/ozzie

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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Palmer

Boy, born 2013

Sequelae of inflammatory diseases of central nervous system
Crossed eyes
Moderate mental retardation

 

$10.35 has been donated towards the cost of my adoption!

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

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Orion

Boy, born 2014

Other disorders of nervous system, not elsewhere classified
Congenital malformations of aortic and mitral valves
Mental retardation

He has a 15-year old brother and 8-year old sister, we do not have any info on them currently.

 

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

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

, , , , ,

Devin

Boy, born 2005

Epilepsy
severe mental retardation

 

 

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

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

, , , ,

Conrad

Boy, born 2018

Arthrogryposis multiplex congenita
Other specified disorders of brain

 

$27.00 has been donated towards the cost of my adoption!

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

, , , ,

Josiah #

Boy: 2016

Listed: Oct 2018

Special needs: genetic metabolic disease – pyruvate-kinase deficiency – homozygote mutation p-R 446; mild to moderate core and periventricular lesions; generalized muscle hypotonia; severely delayed physical and neuro-psychological development;

Josiah moves in space by turning from back to belly and vice versa. He has started forming some of the perceptions about objects from his constant surroundings and everyday life. He connects some objects from his surroundings with the actions performed with them.

When awake, Josiah is mostly calm. He would laugh out loud when jested. During active interactions with adults Josiah pronounces various sounds and random syllables.  Josiah follows a specific dietary regime and has food individually prepared for him. He is fed with a spoon by an adult and has a picky appetite. He is calm during dressing and bathing. Josiah’s sleep is calm.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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Scott #

Scott
Boy: 2014
Diagnosis: Down syndrome

Scott spent the first 9 months of his life with his birth family. He was placed in an orphanage at 9  months old. He can sit up unassisted and can stand up with support. He will reach for a toy, hold it in his hand and manipulate it. He likes being held and cuddled. He is babbling and will repeat some basic words such as “ba-ba” and “ma-ma”. He’s been diagnosed with anemia and an iron deficiency.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

$54.00 has been donated towards the cost of my adoption!

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

Gary #

Gary
boy: 2010
Diagnosis: Cerebral Palsy

Gary is currently living in a group home for children with special needs. He can move around the group home in a gait trainer. Due to his low tone, he can not sit or stand independently. He can roll from back to stomach. He can hold a toy and will manipulate it, though he does not always understand the purpose of the toy. He enjoys interacting with adults and will smile and demonstrate appropriate emotions when engaged in activities.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

, , , ,

Ryan #

Boy, born 2012

Listed: Oct. 2018

Diagnosis: remission after brain tumor; VP shunt; epilepsy

Ryan has no mental issues. His memory, thinking and intellect are normal for the age. He has very good communication skills; communicates easily entering into dialogue; telling his experiences, can define in words how his body feels. Among the children, he feels comfortable, looking for contact with his peers. Ryan’s games varied – typical boyish type, calm and connected with movement. He plays with a variety of toys – with keys, buttons, sound and light effects, musical etc. The child enters role in the story game. His current interests are aimed at police and fire trucks and accessories related to these items. He has good self-service skills. He eats clean, serves with a spoon and fork. He can dress and undressed by himself, puts and takes off his shoes. Controls and communicates his physiological needs, he is potty trained. His day and night sleep is calm and he falls asleep easily.

When Ryan was 2, a tumor was surgically removed from his brain. He went through chemotherapy procedures. Ryan has been experiencing a number of other physical problems, like changing the VPS 3 times because of the chemotherapy, Ataxi (lack of coordination during walking), Epilepsy symptoms and Strabismus. He is in a stabilized general condition, but needs constant specialized care and actively monitoring of his health. He is receiving physical stimulation and other supports and has made good progress. Ryan can walk with minimal support and his fine motor skills are improving as well.

Ryan is a calm and pleasant child.  He is well attached to his caregivers and responds well to them.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

, , , ,

Simon #

Boy:  2016

Simon
Age: 2
Diagnosis: Cystic Fibrosis; Ileostomy

Simon reacts to his name and to noises around him; he listens and tries to identify where the sound comes from. He smiles when he sees a familiar face. He feels nervous around strangers and looks for support from an adult he knows. He has recently learned to pull to a stand, can cruise by stepping laterally, and can take steps to walk while holding the hand of an adult. He moves around the room in a baby walker. He reaches for toys, holds and plays with them. He is very curious and seeks the attention of the caregivers. He laughs out loud and responds positively to affection. He likes to be cuddled. He has formed an attachment to specific caregivers. He is not verbal at this time, but does make sounds to express his emotions and to get attention. Simon is on a dairy free diet. He eats 6 times a day and is fed with a spoon.

The agency has detailed medical information regarding Simon diagnosis, along with additional photos and videos of Simon.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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Calvin

Boy, born 2012

Hydrocephalus
Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures

 

 

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

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

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Freddie, Carly and Samantha

These 3 siblings are only adoptable together!  They are in the same region, but in 2 different cities and 3 different orphanages.

Freddie:
Boy, born 2015
Disorder of brain, unspecified
Specific speech articulation disorder

A very good boy, friendly and smart!

 

Carly:
Girl, Born 2012
Disorder of brain, unspecified;
Other congenital valgus deformities of feet
Mild mental retardation
Congenital dislocation of hip, unilateral
Convergent concomitant strabismus

 

Samantha:
Girl, born 2013
Disorder of brain, unspecified
Iron deficiency anaemia
A very good girl, very helpful and friendly, with no significant problems

 

$1,095.75 has been donated towards the cost of my adoption!

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

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Ace

Boy, born 2013

Other congenital malformations of limb(s)

Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures

 

 

$1,004.70 has been donated towards the cost of my adoption!

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

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Bryant

Boy, born 2018

lumbar spina bifida with hydrocephalus

 

$1,117.96 has been donated towards the cost of my adoption!

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

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Dawson

Boy, born 2015

Blind

 

Listed: Sept 2018

$1,001.50 has been donated towards the cost of my adoption!

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

 

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Knox

Boy, born 2003

Down Syndrome
astigmatism
convergent concomitant strabismus
scoliosis
flat foot (pes planus)

*** I am eligible for a $15,000 Older Child Grant! For more information, email childinquiry@reecesrainbow.org ***

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Musa #

Boy: 2007

Listed: Sep 2018

He got very sick in 2015 and went through a number of procedures and while being in a hospital, his mother abandoned him. He is now cured although they keep monitoring him but he desperately needs a family to love and support him and to give back his faith into the family.

 Diagnosis: B-cell Acute lymphocytic leukemia (ALL). Relapse. Status after chemotherapy. Status after Radiation therapy – prophylactic Radiation therapy of Central nervous system (CNS).

Musa is well-mannered and well-meaning child. Follows the daily regime in the CFTA and every day marks progress. His vocabulary is still not very rich because he did not even know Bulgarian until two years ago. He still has some difficulties in choosing the right words. Musa constantly enriches his vocabulary and progresses in this area. His fine motor skills are very well developed, but he still has some difficulties with writing. He is learning to read and already recognizes the individual letters. Musa knows the geometric figures. Now he is able to solve simple tasks with addition and subtraction tasks. Due to the history of his placement and neglect, the child still has difficulties at school and his performance level is lower than this of his peers. But he is willing to learn and does his best.

Musa is quite shy, passive, silent and closed. He has difficulties in communication with strangers and difficult to trust. Musa does not like to be left alone and he is afraid of that. If things do not happen in the way he wanted, it is possible to close in himself. After spending some time in reasoning on what has happened, he realizes that closing in himself, may not be the best way to deal with problems.

In relationship with his peers, Musa is a leader. He has a fighting spirit and likes to win in the games. In his relationship with adults Musa shows respect for their authority. Obeys and seeks for their approval. This has largely contributed to the great progress the child has been making in the past two years.

In his spare time, Musa likes to play soccer. He also plays basketball. He also likes to color and to play on a tablet. His favorite color is blue. Favorite food sausages, dessert – ice-cream and fruit – banana. His favorite footballer is Ronaldo and dreams of becoming a soccer player when he grows up. From the animals he mostly likes dogs.

Musa has difficulties in talking for the adoption, but in general his attitude is positive.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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Abner #

Boy: 2011

Listed: Sep 2018

Special needs: hyperkinetic conduct disorder, congenital cardiac malformation – in a condition after surgical correction, atypical autism*

*Abner’s social worker reported that according to the specialists, supervising Abner’s condition and development, the diagnosis of atypical autism is no longer valid and it will be deleted from Abner’s formal paperwork that is to be updated in the following months

Abner likes to keep himself busy exploring! His  favorite activities are the ones that include movement, such as going for a walk. He very much likes to spend time looking through books. He also likes all musical instruments and toys that play melodies and sounds. His favorite toy is a children’s laptop that plays songs. When he hears a melody he tries to dance.

There has been a progress in Abner’s speech development as he has started using a lot of words. He now forms sentences containing 3-4 words, albeit dyslexia is observed.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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Emilia

Girl, born 2011

Down syndrome, severe mental retardation, cardiomyopathy

Listed: August 2018

 

*** I am eligible for an additional $5,000 Grant!  Through June 30, 2019, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant***

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

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

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Robby #

Boy: 2015

Listed: July 2018

Diagnosis: nonspecific reactive hepatitis. Hepatosplenomegalia. Heart malformation foramen ovale, initial lung hypertonia. Condition after hypoxic ischemic encephalopathy 2-3 degree. Hemoragia. Intraventricular bleeding 2 degree. bilateral otomastoidit – mastoidectomy in the right. Retention testicle in the left. Delay in the neuro-psychical development.

Robby is delayed in all aspects of his development, but has begun to make small gains in learning . He will interact with caregivers and other children if an activity is interesting to him. His attention span when working on tasks has begun to increase. He enjoys playing in the sensory room. He learns best with multiple repetitions of a task.

Donations can not be accepted until a family is found for him.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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Gracelyn #

Girl, born 2015

Gracelyn is a beautiful little girl who has Down syndrome, West syndrome and Cerebral Palsy.

 

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

$1,506.65 has been donated towards the cost of my adoption!

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

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Brian #

Boy: 2015

Listed: July 2018

Diagnosis: Congenital malformation syndromes predominantly affecting facial appearance. Foramen ovale persistens. Transient pulmonary hypertension. Pes equinovarus bilateralis. Severe delay in neuro-psychical development

Brian recognizes familiar adults and has formed an attachment to his favorite caregiver. He is uncomfortable around strangers. He is working with a physical therapist and a teacher on fine and gross motor skills. He can pick up toys and transfer them from hand to hand. His teacher reports that he understands what is being said to him and has recently begun responding to simple directions such as “give me”. He is able to sit unassisted and moves around in a baby walker.

Photos and videos are available through the agency.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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Gavyn

Boy, born 2016

Other specified disorders of brain
Unspecified severe protein-calorie malnutrition
Other specified congenital malformations
Double outlet right ventricle
Other specified congenital malformations of kidney
Chronic obstructive pyelonephritis
Chronic kidney disease (CKD)

Listed: July 2018

$42.30 has been donated towards the cost of my adoption!

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

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Declan


Boy, born 2017

ventricular septal defect
Neonatal cerebral irritability
Other specified mental disorders due to known physiological condition

Listed: July 2018

 

$1,045.00 has been donated towards the cost of my adoption!

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

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Luna

Girl, born 2014

Down syndrome
Myopia
Congenital absence, atresia and stenosis of large intestine, part unspecified

Listed: July 2018

 

$1,008.84 has been donated towards the cost of my adoption!

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

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Mila #

Girl: 2016
Listed: July 2018
Diagnosis:  Hydrocephaly; Strabismus; G-tube feeding; delays in development

Mila turns her head towards sound and looks at people and objects of interest. She recognizes the faces of the staff. She can roll over, but still has difficulty with head control. She enjoys musical toys that spin and will focus on those for short periods of time.

*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. 

For more information on this child, email childinquiry@reecesrainbow.org

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Asher and Emerik #

Asher: 2009 & Emerik: 2003

Listed: July 2018

Asher has pulmonary valve stenosis. He is monitored by a cardiologist.
He attends school, where his favorite class is reading. He enjoys playing outside with his friends. He is described as being very social. He enjoys sports and dreams of being a soccer player.

Emerik does not have any special needs.  He enjoys sports, music, watching TV and playing on the computer. He works hard in school, but is behind academically. His social worker attributes this to a lack of education in his early life with his birth family. He is described as shyer than his brother and as a result, it takes him longer to make friends. When asked what he wished for, he said a bike and that he’d like it to be red or black.

Photos and videos are available through the agency

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