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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.

$2,818.32 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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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!

*** 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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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.

*** 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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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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Giovanni

Boy, born 2018

Down Syndrome
Atrial septal defect- condition after surgery 12/18
Disorder of brain, unspecified

 

Listed: July 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!

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Daniel #

Boy: 2017

Special Needs: Third degree immaturity; first degree hypotrophy; intraventricular hemorrhage; Child Cerebral Palsy; epilepsy; delayed neuro-psychic development; strabismus; bronchial asthma.

Listed: July 2019

The child keeps his head upright in a child chair in the wheelchair. He is unable to stand on his feet. In bed he can turn and roll. The boy is calm, with good emotional tone. He responds positively to contact: he laughs when teased by an adult and is happy with someone he likes.

 

*** 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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Davi #

Boy: 2017

Special Needs: Down Syndrome

Listed: July 2019

Davi is all smiles! He is an adorable little boy born in June of 2017 with Down syndrome. He is mobile and his fine motor skills are developed. He tracks well with his eyes and he knows and reacts to his name. He can reach out for someone’s hand to put his in their, and say ”bye.”  Davi has a good daily routine. He will sit on the potty and sometimes use it. He is also said to be a good eater and calm sleeper.  Davi pronounces syllables and interacts well with adults. He follows patterns that are shown to him and he imitates movements. For instance, he sits on the swing and he walks with a stroller. Davi is a calm, active, and positive child. He adapts easily and is not aggressive.  We hope Davi’s family sees him and brings him home while he is still so young!

His current agency has a $1500 agency grant available for Davi’s adoption, and also requires that families interested in adopting him need an approved home study to apply.

$22.50 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!

*** 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.

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Gabi #

Girl: 2010

Special needs: moderate mental delay- significant impairment of behavior requiring attention or treatment; microcephaly; hyperactive behavior

Listed: 7/2019

 

Gabi is physically healthy with normal physical development. She is radiant and very active.

Gabi responds adequately to praise and punishment. Gabi establishes and maintains eye contact.  She seeks the attention of the people around and she seeks familiar people and their closeness purposefully.

Gabi understands the meaning of words that are often used in her surroundings. She expresses her needs and wishes through vocalization.

In her spare time Gabi likes watching TV, playing on a phone, listening to music and going out for walks.

*** 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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Ravi

Boy, born 2009

Listed: June 2019

Congenital chromosomal condition

Severe mental retardation
Congenital malformations of palate
Other disorders of optic disc
Chronic inflammation of lacrimal passages

$13.50 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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Antonio #

Boy: 2017

Listed: June 2019

Diagnosis: Congenital abnormality of the central nervous system – hydrocephalus permagna. Condition after implantation of a ventriculoperitoneal shunt. Symptomatic epilepsy. Convergent concomitant strabismus. Atopic dermatitis. Second degree prematurely born baby.

This is the case of a male child born prematurely – 2nd degree with hydrocephalus diagnosed prenatally. At the age of 2 months he had a liquor drainage surgery with implantation of a VP-shunt. He is delayed with reference to all indicators of the physical and neuro-psychic development. Nasogastric-tube feeding is applied due to missing nutritional reflexes.

This is a child with hypertensive – hydrocephalic syndrome. Liquor draining surgery has been done. The child was fed by way of nasogastric-tube until the age of 1 year and 8-9 months; after that he was taught to eat with a spoon. The child has visual and hearing perceptions. He is unable to control his head. He is unable to flip from back to front or to sit. He is delayed in his physical and neuro-psychic development – speech and motor skills.

He reacts when spoken to and when touched and smiles.

*** 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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Lazar #

Boy: 2017

Listed: 06/2019

Special needs: Down Syndrome

Lazar is a handsome boy seeking a family that can give him the time, attention and love needed so he has the opportunity to thrive!

Lazar was born in  2017..  He has a diagnosis of Down Syndrome, Trisomy 21, Regular Form.  His doctors report that his general condition is relatively good.  He is delayed in his motor function as a result of the diagnosis of Down Syndrome.  He is able to roll from front to back and back to front but is not able to sit or stand on his own.  At birth, a consultation with a cardiologist showed a congenital heart defect described as a Foramen ovale.  At 1 month of age, a follow-up cardiologist visit showed there was no longer a congenital heart defect.  Additional reports regarding Lazar describe that when you pay attention to him and talk to him, he smiles and babbles happily.

Children with Down Syndrome need ongoing and consistent intervention in order to reach their full potential.  And all children deserve the chance to grow-up in a family.

Lazar is waiting for his forever family to find him and bring him home.  Several videos of Lazar are available through his placing 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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Garth #

Boy: 2017

Listed: 6/2019

Special needs:Williams – Beuren Syndrome

Garth is able to turn from back to front on his own; he can sit on his own but needs something to hold on; he is able to stand holding onto a support and makes some steps. When standing on his feet he joggles. He grasps toys and plays with them, passing them from one hand to the other. He can move around in a baby walker. He is expected to start walking soon. The boy attempts to reach a toy placed nearby by crawling but he is unstable and falls aside. Every day he receives physical therapy. His physical therapist and his pedagogue work on his motor development and he has improved a lot. His doctor said that he is hyperactive which is typical for his main condition. He can pronounces random specific sounds; there are no syllables or imitation. His doctor expects that at some point he may start speaking. This child is given pureed food; he is fed by an adult with a spoon. He eats well and has a good appetite.

*** 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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Oakley

Boy, born 2015

updated pics 4/19!

Disturbance of cerebral status of newborn, unspecified
Congenital cataract

 

 

$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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Xaria

Girl, born 2010

Congenital hydrocephalus
flail legs
Severe mental retardation
Optic atrophy

Listed: May 2019

From a family that met her April 2019: She was timid and scared of strangers. She has stunning behaviors and needs to be seen by a nutritionalist because she is anemic. She cried when they took her away from us. She is smart, but in her own world a lot. She knew when it was lunch time and kept looking towards the door where they served the food.

She is tiny and beautiful.

$360.00 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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Yager #

Boy: 2017
Diagnosis: Spina Bifida

Yager loves the company of the adults. He likes to be engaged in play and laughs when interacted with. He has a special relationship with one of the staff members, who always accompanies him for operations and for check-ups. While lying on his back, he can turn on his abdomen, he pulls himself up with his arms. The muscles above the waist are very well-developed. He will reach for an adult and when you extend your hands, he immediately pulls himself to the sitting position. He eats from a bottle while holding it himself. When he sees toys, he reaches for them and tries to get them.  If he gets upset he easily calms down if cudded.

He repeats syllables and pronounces sounds. He holds toys in his hands and knocks them together. He can follow simple directions.

 

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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Chrissie #

Girl: 2016

Listed: 05/2019

Special Needs: Spina Bifida, hydrocephalus- shunt has been placed

Chrissie has Spina Bifida, which impacts her lower limbs. She received a shunt for hydrocephalus. She has experienced recurrent UTIs. This is monitored and treated, as needed.  Chrissie recognizes familiar people and enjoys interactions with staff. She can hold her head up and roll from back to stomach and stomach to back. When asked about her, a caregiver said that she is very tender, likes to cuddle, laughs, and enjoys attention from adults. She makes sounds in an attempt to communicate and responds to singing by making humming sounds to “sing along”.

More 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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Benson

Boy, born 2014
PRC
Down syndrome, Congenital Heart Disease- mild tricuspid regurgitation, mild pulmonary arterial hypertension, and pericardial effusion(less)

Benson is a beautiful little boy! Benson was said to be a timid little guy who was a little scared of the dark. A nightlight of some sort is helpful for him when it comes to sleeping.

Update June 2019:  Benson is a smiley guy; blessed with a happy, enthusiastic nature and responds with effervescence to interactions with adults and children.  Benson loves social situations and is enjoying some pre-kindy group playtime, several afternoons a week, which involve free playing, manipulative skills, singing, rhythm and socialization.  He is very settled within his family home, and is self-motivated to play, whether with his playmates or alone. Benson perceives happy situations and will often raise his hands in the air and exclaim, “Hooray!” , such as when he attends birthday parties or sees people applauding. He is delightful.

Benson understands his caregivers’ interactions with him, but has a very limited vocabulary.  Benson is very tender-hearted. Benson loves to watch and imitate , slowly improving his cognition with sorting , counting and self-care skills. He has developed lots of physical skills in the last year. He can sit independently, pull himself to stand without help, cruises holding on to furniture/ caregivers’ hands, and can take a few steps without holding on! Benson loves balls and enjoys sitting opposite a caregiver doing rolling, throwing and catching across a short distance.

Update from June 2019:  Video 1, Video 2, Video 3
Benson’s current agency has a $1500 grant available.
$63.00 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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Bohdi

Boy, born 2016

Other congenital hydrocephalus
other disorders of nervous system
optic atrophy
iron deficiency anaemia

$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!

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Lennox

Boy, born 2016

Spastic quadriplegic cerebral palsy
Other specified congenital malformations
Other specified congenital malformations of brain
Optic atrophy in diseases classified elsewhere
Chronic viral hepatitis B without delta-agent
Other interstitial pulmonary diseases with fibrosis

$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!

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Mayra

girl, born 2017

Primary pulmonary hypertension
Disorder of brain, unspecified

 

$10.00 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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Nicolette and Oksana

girl, born 2006
impaired visual acuity
deviated nasal septum
disorders of psychological development – In real life she does not demonstrate any issues

girl, born 2003
thyroid disorders, perhaps, oncology disease, post-op
asthenia

These two sisters must be adopted together!
Both girls are very good and friendly

$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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Paige

paige-2017-cropped

Girl, born 2004
Mental delays. Down syndrome, cardiopathia. Umbilical hernia. Convergent squint.

Listed:  October 4, 2012

New pic May 2019!

Paige had previously been living with her mother until she lost her rights.

She can sit independently and can crawl! Her speech is not well developed but she can partially understand what you are saying.  She has a very short attention span.

Update June 2013:
Lovely Paige has hair now!  She broke my heart.  She was just sitting on the couch rocking back and forth and didn’t respond at all when I came over to her. Poor, sweet thing!! The nannys love her, but she needs more than they can give. I am not sure if the move was hard on her or what but she just rocked and rocked.

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

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Leena

Girl, born 2011

Listed September 11, 2015

Phenylketonuria, also known as PKU

New pic May 2019! 

From a volunteer in August 2016:   “I was happy to see that Leena is still the same strong willed young girl as last year. She is available for adoption now! She was a little calmer than last year, but she would still take every chance she got to run around. Just like last year it was obvious that some nurses have a very hard time with her and others love her. She’s much calmer when the nurses like her and she’s easier to handle. It was unclear if she was totally potty trained this year or that she’s still working on it. It was also unclear if she got the diet she needed, but her delays didn’t look worse. Leena is such a wonderful girl! She should be in a family where she has the chance to be who she is, all days of the year.

From a missionary who met her in 2015: “Leena is a strong-willed young girl.  She is stubborn and funny. She loves to explore the world (within the concrete walls she lives between). She has been transferred to this facility in May and she is obviously still getting used to the circumstances of living. She had a lot more freedom in the baby orphanage she came from. Leena can walk (so don’t be fooled by the picture), she can run, she is very energetic. She can drink from a cup. This summer (2015) she was being potty trained. She doesn’t talk. She squeals when she is very excited. She is probably the size of a 3 year old at the moment (summer 2015). She probably understands what is being said to her, but she has a hard time following orders. Due to her PKU she needs a special diet and medicine. The baby orphanage she grew up in, didn’t provide the proper care. So (part of) het mental delays may be caused because of that. The facility she lived in right now, tries to provide the proper care. They do not receive funds for it, so they raise it themselves with a charity fund. They really try to take good care of her. Some nurses really like her. Other nurses have a hard time dealing with her, because of her energetic ways. She likes to move and run around all the time. As soon as you let go of her hand or take her out of her wheelchair, you have to chase her. As soon as you give her an opportunity she’ll take it. Some days she was tied up in a wheelchair and we thought she might have been drugged. She didn’t react, she didn’t smile, she didn’t interact. Until the moment my fiancé pulled her from the wheelchair and it was as if she came alive again. I have not seen any selfharming behaviours and I haven’t seen her hurt other children. I have also not seen her interact with other children at all. The nurses don’t like it when she gets all excited, but for me it was a sign that she was not so institutionalized yet. There was so much fight in her. I hope she finds a family before she loses the strength to fight and before her delays will get worse, due to a lack of a proper diet and medical care.”

$1,014.45 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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Ivey #

Ivey
Birthday 2015

Listed: May 2019
Diagnosis: Turner Syndrome

 

Ivey currently lives in a group home for children with special needs and there are no other children her age in the home. She has delays in all aspects of her development. She was born with a heart condition that was surgically corrected. She still takes heart medication and sees the cardiologist for check-ups.

She is also currently on a dairy free diet. The doctor has indicated that milk and dairy products should be slowly reintroduced to observe her tolerance level. An optomologist diagnosed her with a vision impairment, but she does not have glasses or any corrective measures at this time.
Ivey can sit up, pull to a stand and walk around her crib holding on to support. She interacts with toys, but doesn’t know how to play with them appropriately due to lack of instruction. She says a couple of short words and babbles/makes sounds. She makes eye contact, tracks with her eyes, and will interact with a mirror and other toys that interest her.

*** 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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Molly May #

Molly May

Birthday: 2015

Listed: 2019
Diagnosis: Trisomy 7; cleft lip & palate; Cerebral Palsy

 

Molly May has made progress in her development during recent months. She is able to sit unassisted, get up on her knees and has begun to start trying to move around in a walker. She is becoming more physically active. She makes eye contact, looks around for families adults and smiles when someone looks at her. She will laugh out loud when an adult plays with her. She watches children’s cartoons and movies on the TV and will get excited and point to the screen when the TV is turned on. She picks up toys and attempts to play with them. She still needs instructions in how to appropriately play with toys. She makes vocalizations in an effort to communicate. She eats soft foods from a spoon.
Molly May has undergone multiple surgeries to repair her cleft lip & palate. She is under the continued care of the doctor who is performing these procedures. She is also under the regular care of a neurologist, who diagnosed her with CP in 2018. She had suffered from “constant shaking” resulting in uncontrollable movements up until a few months ago. The social worker reports that this has greatly improved and that Molly May’s movement are now more calm and she also sleeps calmly too. Videos taken in April 2019 show her interacting with toys.

 

Photos and videos are available through the agency.

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*** 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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Duncan

Boy, born 2005

Malformations of aqueduct of Sylvius (hydrocephalus)
Other congenital malformations of posterior segment of eye
Profound intellectual disabilities

 

 

$50.00 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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Sawyer #4-5

Age 9; born 2010
Arthrogryposis with knee joint contractures, bilateral club foot, Hypotrophy.

Sawyer is able to move around the room by scooting on his bottom. He can talk in sentences, but his articulation is not always clear. He plays with toys, responds when spoken to, follows simple directions, and assists with self-help tasks such as dressing/undressing.
Photo and videos from March 2016 are available through the agency.

Listed, April 2016; Update below, April 2019:

Sawyer has spent his entire life in a large orphanage, where his experiences and interactions have been limited. He’s been attending school and working with a speech therapist for the past 2 years and this has resulted in an increase in all skill areas. Sawyer can talk in simple sentences and answer questions. His articulation is poor, but he’s made improvements with the help of a speech therapist. He can count to 10, identify his body parts, and answer basic questions such as his name and age. He demonstrates imaginative play with toys. His motor skills are delayed due to his diagnosis. He uses a wheelchair for mobility and will also scoot around the room on his bottom. He can feed himself. He can take his shoes and socks off independently. He is described as very social. He works hard during academic instruction. He enjoys interacting with both peers and adults. It is believed that his cognitive delays are due to the environment he has lived in and lack of exposure.

*** 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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Stan #

Boy, age 10
cognitive delays; hypothyroidism

Stan takes medication to manage his thyroid. He’s also on medication for behaviors, and his foster family reports that the medication helps him to sleep better at night, which has improved his overall behavior. He can memorize, retain, and reproduces information. Motor skills are well developed. Self-help skills are well developed. He follows the rules and behaves well in public. The medication he is taking has decreased his mood swings. He talks in complete sentences and is able to ask/answer questions, tell a story, etc. He occasionally mixes up verb tenses and other grammatical errors, but is able to be understood. He is working with a speech therapist at school. He responds well to verbal praise and verbal prompts when he needs correction. He enjoys music and loves animals. He eagerly engages in activities with other children. He likes to put puzzles together, watch TV and play on the computer. He is behind academically at school due to difficulty with attention span.

*** 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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Drako #

Boy, age 4
Cognitive delays; repaired cleft lip & palate with additional surgeries needed

Drako has undergone surgeries to repair a cleft lip and palate. He is under continues care by medical professionals and will need future orthodontic surgery and other possible surgeries as well related to his cleft issues. Developmentally, his speech, motor skills, and cognitive processing are all delayed. He can crawl, pull to a stand, cruise around furniture/objects, and walk while holding an adult’s hand. He will interact with toys that play music or light up. He babbles, but is not yet saying any words.

Photos and videos are available.

*** 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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Graciella

Girl, born 2015

Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
Other specified congenital malformations of brain
Congenital malformation syndromes predominantly associated with short stature
mixed specific developmental disorder
spastic tetraplegia
Congenital malformation of optic disc

$967.90 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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Nora

Girl, born 2013

Congenital malformation of the central nervous system
symptomatic epilepsy
atactic syndrome
tetraparesis
porencephalia

Listed: Aug 2014

 

$8,535.68 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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Falconn

Boy, born 2013

Cerebral palsy

Listed: April 2019

 

 

$10.00 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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Adrian #

Boy: 2015

Listed: 4/2019

Diagnosis: Condition after extreme low weight at birth (prematurity IV degree). Cerebral palsy, spastic form – moderate degree. Bronchopulmonary dysplasia /BPD/. Delayed physical and psychomotor development. Bilateral neuro-sensory hearing loss.  

Aidan has delays in his psychomotor development. He has a potential and if he receives special cares, he will be able to achieve progress. His interactions with others are on an elementary level. The child feels calm in the presence of familiar adults. He is curious and walks around in his walker reaching for different items. The toys which stimulate his tactile sensors are more interesting for him than other toys and items, for example children’s books

*** 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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Izak

Boy, born 2017

possible HIV infection or contact with smb. HIV positive
encephalopathy of unspecified aetiology

atrial septal defect
ventricular septal defect

 

$150.00 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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Frederik

Boy, born 2009

HIV
Hepatitis C

 

 

$23.20 has been donated towards the cost of my adoption!

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

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Damian and his brother

Boy, born 2016

Other disorders of psychological development
Disorder of brain, unspecified
Patent ductus arteriosus

He has a brother in a different orphanage born in 2007.  They must be adopted together!

$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!

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Wilson

Boy, born 2009

Muscular Dystrophy

Wilson is a sweet, happy, playful boy. He is great with little kids and bigger kids. He loves to play legos, color, watch tv, go to the beach and just be with those who care for him. He spent one summer and winter break with a host family, he bonded well with them. He is affectionate and makes good eye contact.

He has a progressive form of Muscular Dystrophy. He can no longer stand, walk or crawl. He can still sit upright by himself. He does require help dressing, bathing and some help with eating. He is toilet trained but needs help to get to the toilet. He longs to belong and be given love and attention. He adapts well to new adventures, people and places. He will be a blessing to any family.

$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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Falcon

Boy, born 2010

Nephritic agenesis, one sided
light degree mental delay

 

Listed: Feb 2019

$19.70 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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Cassandra + 2 Sisters

Girl, born 2016

Video! Holoprosencephaly,
Spina bifida at lumbar part with hydrocephaly.
Spastic tetraplegia
Cognitive thigh deformity
Cognitive hip subluxation one sided.
Cognitive pathology of development of disk of optic nerve
Сoncomitant strabismus

Listed: Feb 2019

She has two sisters, born 2014 & 2015 both are healthy.
These 3 girls MUST be adopted together!

$166.50 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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Jennie

Girl, born 2011
PRC
Down syndrome

Listed: Feb 2019

Precious Jennie needs to find her family! Just watching her video makes your heart yearn to bring her home! Video (pw is jenny)

Jennie was born late 2011 with Down syndrome. She was met by an adoptive mama, who I am sure would love to talk to anyone interested in this sweet girl! Jennie’s photos and video show her darling personality. She seems so outgoing, funny and affectionate! She will be the perfect addition to any family!

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

 

$10.00 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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Adele

Girl, born 2008

Down syndrome

 

 

 

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

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Garrison and Hamilton

Boy, born 2014
healthy

boy, born 2012
congenital stenosis of larynx
hearing loss (uses hearing device)
hypospadias

These siblings must be adopted together!

From a family who met them Feb 2019: They are very sweet and seemed happy. They were kind to each other, happily posed for photos, and answered questions. They seem very healthy and I did not notice any obvious developmental delays.

$225.00 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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India

Girl, born 2014

Cerebral palsy with severe legs dysfunction
fetal alcohol syndrome
crossed eyes
open oval window

She can walk by herself and understands simple instructions.

$4.95 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 – age 5

Listed: Jan 2019

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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Vivi

Girl, born 2013

down syndrome
condition after surgery of atriventricular communication

Listed: Jan 2019

 

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

$6.30 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!

, , ,

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!

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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

Listed: Jan 2019

$10.00 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.

$4.50 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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Quincey

Boy, born 2011

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

Listed: Jan 2019

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.

$486.00 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

Listed: Jan 2019

$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; age 2

Listed: Jan 2019

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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Pippy #

Girl: 2013

Special needs: Cerebral Palsy, Leukemia, strabismus

Listed: Jan 2019

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.

Listed: Jan 2019

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

Listed: Jan 2019

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

Listed: Dec 2018

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

$5.40 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

Listed: Dec 2018

$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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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”.

$585.00 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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Julian #

Julian
Age: 2014
Diagnosis: Spina bifida

Listed: Dec 2018

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

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Liam #

Born 2015
Diagnosis: mental delays, asthma, strabismus

Listed: Dec 2018

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. 

$250.00 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!