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Other Angels Girls, 0-5

Everyone loves a precious little girl they can dress up in frilly dresses and hair bows. They capture the hearts of every daddy in the world! Here are some who are waiting for their family at the end of Reece’s Rainbow. Their special needs include such things as arthrogryposis, CP, spina bifida, FAS (Fetal Alcohol Syndrome), Autism, and other diagnoses.

You really can save a life, with even the smallest gift! You are also invited to send a check (no Paypal fees) to Reece’s Rainbow, PO Box 4024, Gaithersburg, MD 20885

“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!

FOR MORE INFORMATION ABOUT THE PROCESS AND/OR ANY OF THE WAITING CHILDREN ON THIS PAGE, PLEASE INQUIRE.

Pippa

PippaGirl, born March 2012
PRC
Hydrocephalus; Meningocele

Pippa is an active and lively little girl and she loves to talk and smile. She has started to learn to talk, and she can say simple two-syllable sounds. Her pronunciation of single syllables is clear. She is a bit introverted and shy with strangers, but after a while she will be fine.

Although she has myelomeningocele and hydrocephalus, she has already had two surgeries and has a shunt for fluid drainage. She can sit well, and she can freely crawl back and forth in the room. She loves to imitate others around her. When she hears music, she will rock her body along with the rhythm; it is so cute. She loves to share toys and play with other children.

$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!

Fern

Fernuodated filepicture2Fernupdated file pictureGirl, born Aug 2010
Cerebral palsy
PRC

She can laugh aloud. She waves her head when happy. She grasps little toys with left hand and put them into her mouth to bite them. She can sit alone for a short time. She looks around when someone speaks to her.

Fern has a good physical state, has balanced nutrition, has a routine life every day, good living habits but is choosy about food.

 

From an adoptive parent who saw her in April 2014:
Let me start by saying my heart broke for this little one. She is unable to sit up or feed herself. She cannot walk. She was brought to me in the crib. She smiled when I spoke to her and she grabbed my hand when I placed mine in hers. She laughed when we tickled her and she seemed to enjoy my attention. The nannies say she can smile and laugh when tickled. She can chew and swallow food. She has a familiar caretaker and smiles when she is with her. She is described as a very content child. She is easy going.

Note: Fern’s updated file pictures do show her sitting up, although she may be supported by leaning on the wall in one picture. She desperately needs a family who can get her out of the crib and into therapy so she can be all that she can be!

$103.95 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!

Cherie

cherie1 cherie2

Girl, Born Dec 2009
Crouzon syndrome

 

Sweet Cherie …. she needs a family desperately!

Picture on the left is from December 2012, on the right is from summer 2012.  Additional pictures available.

 

Guardian AngelCherie needs a family fast!  From her medical records:  congenital anomaly of the skull, feet and  hands. Cleft hard palate, UPU, LLC, aortic defect.  Hydrocephalus

 

UPDATE OCT 2014:
She was born end of 2009. She was born via c-section and a full term baby with Aperts Syndrome and Hydrocephalus. She has had multiple surgeries to include a separation of both her pinkies from her other fused fingers. She uses her hands and feet very well to get what she wants. She had a shunt placed for her hydro as well. Soon after her first surgery the shunt failed and after some time they did a second surgery. The surgery did not go well and a significant amount of brain damage was sustained and the second shunt was not able to be placed as a result of the damage. She also has difficulty with sight. Mostly though she threw any toy or object near her. She crawls and scoots to get around and does not speak but makes noises. She seems to know her name but does not make eye contact when her name is called. We were told she likes “baby toys”- things with bright lights, colors, noise, and also that she likes music. She is able to eat regular soft foods but is spoon fed, she is able to use a sippy cup. She currently spends most of her time in her stroller. We were told that she is developmentally around 18 months but we think more like 8-10 months from what we saw in 3 hours. She is a very sweet wonderful little girl who needs a family who can meet her needs and love her well.

$10,008.00 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!

Chloe

41128135744 Chloe (1)Girl, born 2010

Congenital heart defect: Ventricular septal defect, Atrial septal defect; Convergent concomitant strabismus; Mental and physiological delays; Acquired deformity of chest and rib

41128135744 Chloe (2)

 

$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!

Lyla

Lyla 1Girl, born August 2007
PRC
Learning delays/low IQ

 

Lyla is a beautiful little girl who is 5 years old. She came into care just last August, and was found to be a normal, healthy little girl who was developmentally on target. She adapted to the orphanage life quickly. She was “tested” after being at the orphanage only 3 months, and they said she had  ”clear pronunciation, fluent, restless, no abnormal action, flexible hands and feet, understand general objects and use of some objects, poor initiative action”…then they slapped her file with a low IQ number. Lyla can speak in full sentences, understands directions, cares for her needs, helps out with the children younger than she is, and is a delightful little girl. She attends kindergarten and lives with a foster family.

Lyla loves to play games, loves to go to school, and is a very happy little girl. I am not sure what they expect of her as far as “initiative” is concerned…but considering the changes in her life these past months, she seems to be doing very well! Lyla needs a family to love her, and enjoy every minute of having this sweet girl as their daughter.

$96.00 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!

Ruby

41128135617 Ruby (2)

41128135617 Ruby (1)Girl, born 2010

Congenital malformation syndromes due to Fetal alcohol syndrome, Other pervasive developmental disorders, Lack of expected normal physiological development, Iron deficiency anemia, Cardiomyopathy, unspecified

Available for adoption in spring 2015

Note: Ruby has a healthy sibling brother, who is *NOT* adoptable for adoption, due to his paperwork. A family who commits to Ruby should be prepared for a possible delay in country, due to “separation” of siblings.

 

$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!

Mildred

MildredOLYMPUS DIGITAL CAMERAGirl, born February 2011
Cerebral palsy, microcephaly, pseudobulbar syndrome, focal symptomatic epilepsy

 

Mildred is so young — she could really thrive with the love and care of a family!

 

$7,668.95 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!

Annabelle

Annabelle March2014aAnnabelleGirl, born July 2009
PRC
Amblyopia (both eyes); congenital nystagmus (both eyes)

Annabelle is a beautiful little girl. Her caregivers report that she is blind, but can see some light and objects. She will giggle and smile when a camera flash goes off, so it does appear that she can see light. Annabelle’s development is delayed, but from caregiver reports, she spends most of her time in a crib or in one area. So it is quite possible that some of her delays are from institutionalization.

From an update in late 2012, Annabelle is able to sit and stand with support and can play while on her stomach. She is a quiet child who does not communicate much. She may need to have her hearing checked. She has never seen an eye doctor. Annabelle needs a family who can get her in to see medical specialists. Are you the family who can giver her the attention she needs and deserves so she can blossom and reach her full potential?

March 2014 update-
Annabelle shows delays and can only see light. She is very outgoing and enjoys playing with kids and adults. In a current video, she can be seen standing up as well as trying to repeat a few words. Annabelle loves hugs!

$450.00 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!


 

The Reece’s Rainbow Prayer Warrior Ministry was created with three goals in mind:

  1. To lift the daily needs of each waiting child up in prayer
  2. To lift Reece’s Rainbow up in prayer
  3. To lift the families whom God is preparing for each waiting child up in prayer

 

Rona

S

SGirl, born July 2010
PRC
Cerebral palsy (low muscle tension)

Rona is a ray of sunshine! She is a little shy and timid, but is very friendly to those she is familiar with. She likes to play with toys, especially rag dolls. Rona underwent rehabilitation for her cerebral palsy and she can now walk on her own! She is steadily growing to taking care of herself and the nannies are proud of her progress. We hope Rona finds her home soon!

$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!

Lora

40225195110 (6)

Girl, born February 2009
Slight mental delay, crossed eyes

 

What a dolly!

Lora will be available for adoption in July 2014.

$270.00 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!

Jenny

Guardian AngelGirl, Born October 2009

CP and Tetralogy of Fallot (heart condition)

 

Sweet Jenny is waiting for you!  She is almost 3 years old, with brown hair and brown eyes.   She was born with cerebral palsy and a heart condition, for which she has already had surgery.   She is not able to sit on her own, and will greatly benefit from a loving family, medical care and therapy!  If she is not adopted, she will remain bedridden for life.

 

More photos available.  Married couples only.  Large families and older parents welcome.

$1,312.40 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!

Hester

40316105637 (1)40316105637 (2)Guardian AngelGirl, born July 2011
Disorder of the brain, congenital deformity of the hip, bilateral hearing loss, exotropia

 

Hester is darling!  She can hear.

 

$283.50 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!

Gigi

Gigi (2)Gigi (1)Girl, born July 2012
PRC
Hydrocephalus, bilateral blindness, developmental delays

Gigi is sweet little girl who has excellent hearing abilities! She can kneel on both knees and sit on her own. Gigi responds to her own name, and whenever she hears music, she get really excited and laughs! She loves to play with others. We hope Gigi finds her forever family!

$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!

Kendall

KendallGuardian AngelGirl, age 2
PRC
Missing right eye, left eye deterioration, hearing loss

Kendall just turned 2 years old. Although she is a quiet girl, she is close to her caretakers. Her left eye has corneal degeneration and she is missing her right eye. She also still has trouble with her hearing and it has made it hard for her to keep up with the other kids her age. She can stand up on her own but needs a little help walking around.

She is really good at recognizing the voice of familiar people and when she hear musics, she likes to dance around. She is ready and waiting to dance into her families heart.

$46.35 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!

Carole #26-38

OLYMPUS DIGITAL CAMERACaroleGirl, 4-years old

Deaf, Cerebral palsy

Update November 25, 2014.

The girl was in a stroller where she stays most of the time. She was calm, didn’t make a sound, and she looked very sweet. Our representatives had the chance to talk only with the nurse of the institution who had been working there only for a month. She told me what she likes to play with, how she likes to sit, and what she likes to eat. She either stays in the stroller, on a bed, or a mattress on the floor. The nurse says she doesn’t really likes to play with toys. When she was placed on the mattress and the bottle was moved she tried to reach in the only way she could, which was on her back pushing the back of her head in the mattress and pulling herself with neck muscles. It wasn’t a very efficient way of moving but she apparently really liked the empty bottle : ). The nurse moved it further in order for her to show us what she can but that kind of moving was the only thing we saw, except that she tried to turn from front to back once. The nurse told us she liked to play with a packet of tissues and tried with one, but she didn’t show any interest in and kept holding the bottle.

She didn’t feel comfortable lying on her stomach, and didn’t know what to do, at least she held her head up. She does not know how to crawl, and almost didn’t move when she was lying on her front.

She is not very spastic – passively her legs moved pretty easy. Her hand was also not very spastic, the dominant hand is her left one, she uses it to grab (the bottle) and to reach for things; her right hand is a bit more spastic and her fingers are flex almost in a fist, although it was easy to open them. She suffers from severe hypotrophy of the muscles of all her limbs, the fact the nobody works with her at least for her physical development is the main reason she is in the state she is in right now. From what we understood, even in the home where she lived before no specialist really worked with her seriously.
She is very sweet little girl. The best care for her is not provided in the institutions she was placed before and is now placed. Her physical and neuro-psychical condition is declining due to the lack of professional work done with her.

She really deserves a family, which will take care of her and provide for all her needs. She has significant potential for improving her condition if she is placed in a family environment and professional work is done with her.

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.

Dorothy #503

Shylah 503DorothyGirl, born June 2010
Epilepsy, Cerebral Palsy, Recurrent urinary tract infections, Hypotrophy second degree, Delay in the neuropsychological development

Dorothy walks independently, tries to run; understands and follows simple instructions; manipulates with toys and objects; holds a pencil and scribbles with it; produces random sounds.  The child manifests emotional deficit – performs stereotypic movements, demonstrates self-aggression. She likes listening to music and she tries to dance. She loves to swing on a swing and does so with great pleasure.

Since her placement in a foster family, Dorothy has started responding to emotional stimulation with far more diverse facial expressions as compared to before. She is currently in a process of enriching her notions and acquiring self-service skills and habits. Some progress is seen as regards her social and emotional development as well as her fine motor skills.

Additional information is available from the agency.

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.

Anah

AnahGirl, born July 2010
PRC
Impaired intelligence, motor and speech

Anah is a little love bug! She loves being held when she is sad and is easily comforted. Anah loves to eat! She is not picky and will eat any and all foods. She likes to watch TV and listen to music. Anah’s motor development is lacking. She is only able to sit on her bed and she cannot stand. Her language abilities are also rather lacking and she is unable to talk. We hope a family will open their hearts to little Anah!

$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!

Lanora

OLYMPUS DIGITAL CAMERAGirl, born August 2009
Spina bifida - Congenital malformation of the central nervous system, myeloradiculomeningocele with rachischisis of lumbar spine; internal hydrocephalus, low paraplegia

 

Lovely Lanora needs a mama to let her beautiful hair grow out!

Large families welcome, married couples only.

$1,472.00 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!

Kiki #

KikiGirl, born August 2010

Kiki first lived with her mother.  In 2013 she was placed in an institution that takes care for special needs children. She suffers from epilepsy and mental delays. There is a delay in her motor and neuropsychological development. She shows increased muscle activity, cannot speak, although she makes attempts and makes some sounds.  She has learned to walk and now runs. She is on drug treatment for her epilepsy.  Needs an adult’s help with dressing and toileting. She is relatively happy, calm and is not a problem child. She does not fear to interact with adults who knows. Suffers from strabismus and will probably need glasses or surgical correction.

Kiki has features consistent with a diagnosis of FAS (fetal alcohol syndrome).  This is not a diagnosis, but a cautionary disclosure.

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.

Lucie

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

 

What a pretty smile Lucie has!  She could do so well with a family.

 

$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!

Rianne

RianneGirl, born May 2011
PRC
Right eyeball atrophy; Small left eyeball

Rianne’s eyeballs have atrophy, her vision abilities are low, she can sense light, and she is only able to see a rough image of objects. She is unable to see things that are far away. She is able to pull other children’s hands. Her hand is frequently waving in front of her eyes. She will use a hand to grab another hand, she is able to normally grab hold of things, she can complete a few fine movements, and her left and right hands can transfer things back and forth. She can take crackers and fruit to eat by herself. She can crawl, turn her body over, walk by herself, and run. When she is in a classroom, apartment, or other familiar surroundings, she can find toys.

Rianne can currently say “mama,” “jie jie sister,” and “ge ge brother.” When we carry out a few simple exchanges with her, she is also able to understand. Through sounds, she can frequently distinguish familiar people that are near to her. She is able to remember her nannies and teachers that take care of her. When she is teased, she will laugh, twirl around and dance. Through distinct sounds, she can find familiar nannies to hug. She will reject strangers.

Rianne is a lively and active child. She likes to snatch toys from other children. When the nannies interact with her, she will frequently have a big smile. When the child cries, she likes it when people hug her, take her hand to twirl her around, and she likes musical and bright toys. She is afraid when people lift her up over their heads. She is especially interested in music. She especially likes to watch TV, but due to her low vision, she is only able to see the light, and hear the sounds. She likes to listen to the children’s songs.

$99.00 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!

Lola

LolaGirl, born March 2009
PRC
bilateral microctia, curvature of the spine, post-op esophageal and anal atresia

When Lola came into care she was diagnosed with esophageal and anal atresia. She had an operation to correct both of these in 2011, and recovered well after some good nutrition therapy. Lola has a difficult time hearing because of her bilateral microctia, but she is able to follow instructions and hear her caregivers. When the doctors looked at her heart, they saw that she has left ventricular false tendons, but other than that her heart looked healthy. Lola’s file says that she also has a curved spine, but is able to fully walk, run, and jump. Lola really enjoys being active and independent!

$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!

Mary Ellen #23

OLYMPUS DIGITAL CAMERAMary EllenAge: 2
Diagnosis: Arnold-Chiari syndrome; hydrocephalus (shunt installed); spina bifida aperta-surgically repaired; stabismus; frequent bladder infections that are being treated

UPDATE:  “She is turning two in February. She speaks her first words and loves any attention she can get. She had surgical correction of her spine and a shunt installed to reduce fluid on her brain.”  “Recently the shunt that keeps her from having too much fluid on her brain failed and she underwent surgery again. The sweet baby who sought contact is now avoiding eye contact. While her physical issues have been met her emotional needs are suffering.”

UPDATE 2014:

became clear that following the revision of her VP shunt at the end of 2013, there are some negative effects on her vision and possibly her hearing. She does not fixate her eyes or follow a moving object with her eyes anymore. Her condition as of now will have to be further clarified.

She is not speaking, does not tolerate even being touched without screaming, has ZERO reaction to sound and no indication that she has any vision (doesn’t track objects moving in front of her face or even blink). We only have a very short video clip of her that is current, but the little girl in the photo you have posted and the info at the top of her report is sadly no longer the same child that is available for adoption. I desperately want to see this little one find a family, but her needs should be very clearly listed upfront.

Photos and videos are available, along with detailed medical reports.

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.

Rachel

Rachel_RKwebreadyGirl, born October 2012
PRC
Apert Syndrome

Meet Rachel! She has been diagnosed with Apert Syndrome and hand and foot deformities. Because of her special needs, Rachel’s development is behind other children, but she has an active personality just waiting to blossom! Rachel loves taking showers and playing in the water. She can’t hold toys well but she likes to bat at them with her hands, and she loves any toy that makes noise. Rachel especially loves to be held. In fact, her caregivers tell us that is her favorite thing to do! Rachel loves nothing more than to sit on someone’s lap and be loved. Rachel needs a family to snuggle with her and help her become all she is meant to be. Could your family welcome this sweet little girl into your life?

$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!

Leigh

LeighGirl, born October 2008
PRC
Cerebral palsy

 

Leigh turned 5 in October. She came into care when she was just 2 years old. Leigh get massages every day to help her legs get more flexible. She is able to crawl around and is working on walking, but she is not quite there yet. Leigh is able to follow directions given by her caregivers and she likes to play with her friends. Her new favorite thing to do is crawl around and get into everything!

$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!

Penda

Penda (2)

Penda (1)Girl, born December 2012
PRC
Blind, mild heart defect

Penda can sit independently for a short while and stand with support under the armpits. Her growth and development are behind same-age children in the orphanage. Penda knows her name and will listen attentively when she hears her name. She will laugh when people tickle her and she makes noises as she tries to talk. Penda is attached to her foster mother. She is waiting for a family who can help her learn the skills she will need to make her way in the world. Are you the family she is waiting for?

$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!

Dani

21114214213 DaniGirl, born December 2009
Cerebral palsy, hemiplegia, movement disorders in combination with vision and hearing impairments

DANI IS FACING TRANSFER!

They really want a family for her in the orphanage before she has to be transferred.

 

Dani has beautiful blue eyes, and a darling little button nose!

Large families welcome, travel required.

$1,278.45 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!

Lulu

Lulu (2)

Lulu (1)Girl, born May 2011
PRC
Post-op congential retinal glioblastoma; Artificial eye

Beautiful Lulu was abandoned in January of 2013 and was preliminarily diagnosed with leukocoria in her right eye and an artificial left eye.

Her hands are nimble and she can use one hand to grab the other. She normally grabs things and plays with toys on her own. She can do a few fine motor movements and she uses her fingers to grab onto and pick things up. Her left and right hands can pass things back and forth between them. She can grab onto cookies as well as fruit and eat them. She can walk on her own and she likes to jump and play in her crib. Lulu has post-operative retinal glioblastoma, an artificial eye and both her eyes cannot see things.

Lulu can call out, “ma ma” and sometimes she will baby talk. She understands what the nannies say and she especially likes to play together with the nannies; and when they tease her, she will smile happily. The child remembers the sounds of people she’s acquainted with and when she hears someone she’s familiar with, she will want to be held. She rarely cries and when the child is crying her heart out, if you grab a toy and give it to her, grab something to give her to eat or hold her she will be ok.

Lulu is a lively little girl who loves to smile and is especially likeable. She is very gregarious and she likes to play together with other little children. However, sometimes she is a bit shy. She is especially interested in sounds and likes to listen to music

$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!

Sarea

Guardian AngelGirl, born May 2009
PRC

postoperative hydrocephalus, postoperative meningocele (spina bifida), optic nerve atrophy, Cerebral palsy

 

At the first sight, we were impressed by her black eyes. Her eyes were big and black, which seemed to talk. As she grew up, we found her hair was beautiful, black and soft. Till now we do not cut her hair. The caretaker likes dressing her and do various hair style for her.

She received the surgery of meningocele and hydrocephalus. Now she is diagnosed as cerebral palsy and optic nerve atrophy. Her motion ability is poor and limbs are not powerful. She can turn over, can lie on the stomach, but can not sit. Additionally her mental development is delayed. She can not speak, just makes some unconscious sounds, she seems to dislike toys and not sensitive to the sounds.  Now she can eat the fixed food, mainly vegetable, meat, egg, noodles, oatmeal, porridge, rice, etc. She also likes fruits. She rarely has illness. She is slight, and shorter than other children of her age.

Though she has lots of disadvantages, she is still a lovely and happy baby. She likes smiling, especially when someone is talking with her and teasing her. When someone is hugging her, she is quiet and listening to adults’ talk, sometimes she touches the person’s face. She likes noisy, always turns her head to the sounds. When no one plays with her, she will be upset and call unhappily.

Though she is a disabled child, she is lovely as other healthy child. She has the same feeling, desires to be loved and cared. We hope she would grow up healthily and happily and she would have a family with warm and love. We believe she can adapt new place and bring happiness to the family. Bless Sarea!  Wish she can find her parents soon and have a family. Wish she is peaceful all her life.

$69.81 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!

Susy

Susy 1 Susy 2Girl, born Nov 2009
PRC
Cerebral Palsy

Susy is diagnosed with Cerebral Palsy (CP). Her CP seems to be fairly moderate. Susy was found when she was about two years old. Too little tension in her muscles prevented her from sitting or standing on her own, so that spring she received intensive therapy for three months through which she made very significant progress with her motor skills. She’s described as even-tempered and patient, although she still struggles to do some things the other children do easily. She’s thought to be clever and loves to laugh and smile with the nannies, touching their faces for connection. Emotionally, she’s right on track with her peers. Susy likes watching TV and listening to music, being held, and going outside to play. She rarely cries, unless she’s hungry. Her caregivers say she is well-loved and that they are deeply impressed by how much progress she’s made. She can sit unassisted and walk holding hands. It would be amazing to see the changes in this child with the love and support of a family and some good physical therapy.

The following is an update that just arrived (10/2014) for Susy: She can move around with a walker and stand up with assistance. She cannot feed herself yet. She can only smile. She knows how to read the face of adults. She can reach to get stuff from other kids. She is afraid of strangers.

$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!

Elle

ElleGirl, born Sept 2008
PRC
Dandy-Walker syndrome, hydrocephalus, Thalassemia, speech delays

 

Elle needs regular blood transfusions for her Thalassemia.  Additional medical information available.

$135.29 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!

Holland

Holly post-surgeryHolly 2Girl, born Oct 2011
PRC
Blind (retinal glioblastoma; secondary retinal detachment; glaucoma; left eyeball after enucleation)

 

Holland has delayed development. When admitted, she was 4 months old. At that time, she could make the sound of “gugu” if being teased and could hold your fingers if you touched her hand. At the age of 8 months, she could turn over and sit alone, hold the milk bottle to drink milk, and jump if you held her arms. At the age of 1 year, she could crawl forward and backward, knew her name, and could respond if you called her name. At the age of 1.5 years, she could walk with holding hands, imitate speaking, and could understand simple language. Now she can walk alone, can speak simple sentences. Her cognitive ability is not good due to her visual impairment. She likes toys with sound. Holland is quiet, lovely, shy, and sometimes likes toys and music. She likes playing games with familiar people and can smile when happy. Under careful care of everyone, she is growing up healthily and happily. She has built stable and close relationships with the nurturers.

$95.85 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!

Brinli

Girl, born August 2009

After-effects of viral encephalitis in the form of microcephaly, movement disorders syndrome (cerebral palsy syndrome), epileptic syndrome of residual genesis, secondary hypothalamic syndrome, loop of thermal control

Brinli has pretty eyes, and such lovely long fingers.  She desperately needs a family to save her from a life spent lying in a crib.

 

Large families welcome, married couples only.  Travel required.

$38.70 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!

 

Audra

Audra Audra 2Girl, born March 2010
PRC
Anal atresia, limb diferences(hands and feet) ear deformity

Guardian Angel4 year old Audra is waiting for a family. Is she cute or what!?!?! Audra is diagnosed as having congenital anal atresia with recto-perineal fistula; polydactyly of both hands; syndactyly of both of feet; deformity of both ears. Audra can dress and undress herself. She is a very cooperative child and she has a good appetite. She very much enjoys dragon fruit with peanut butter. When eating, she eats nicely and she likes to stay clean. Audra is very clever and nice. She can speak well and she can understand Chinese and some English. She lives in a foster family, where she likes helping. She will close the cupboards once they are filled and is curious about new things. She likes to go explore and touch things that are new to her. She loves rag dolls and her blanket, which she likes to sleep with. Audra likes to look at herself in the mirror when she is wearing nice clothes. Audra is good at sharing toys with other children. She can walk steadily and can go upstairs and downstairs without help. Audra loves to dress-up! She is active, lovely, and a favorite! Could this little princess be your daughter?

$270.00 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!

Hannah

Girl, Born September 7, 2008

Hannah is a darling girl who needs a family.   MORE PHOTOS AVAILABLE.

From her medical records:  absence of rectum, cranial bones deformity, multiple development pathologies, severe dermatitis, delay of development but she is very smart and active
Hannah is a very friendly girl. She likes to play different toys, with other children of her group. She is very smiling, easy-going girl. She understands everything, but she does not talk yet. She is a smart girl. She is walking independently.

Hannah was born with deformed cranial bones.   Hannah is very smart, she is nearly walking, and has striking blue eyes and a smile to warm your heart!   She has severe dermatitis, from what they are not sure.    She was also born without a rectum, and presumably uses a colostomy bag at this time.  She will definitely need to be seen by a gastroenterologist once home.

From an adoptive family who visited with her in June 2010:  “ Hannah is a precious little angel that despite her challenges, is unbelievably full of life.  She loves her walker, especially moving “lightening fast” down the hallway, to the playroom, whenever she has the chance.  She is a little spit fire…who has a mind of her own;) We took her pacifier (which she loves) out of her mouth to snap a few pictures and she made herself perfectly clear that she wanted it back:)  She is developing very well and  walks by holding on to her caretakers finger.  She can hold a ball/toy and is very social little girl.  She happily perked and stood up to her feet (while in her walker) when I bent down and spoke to her.  When my camera flashed, she threw her little hands up to her face and smiled.  She is an absolute favorite of her caretakers and the Orphanage Director.   The “blue” on her skin is an anteseptic that is applied as a result of her extreme skin allergy.  Given the chance, this little one will grow by leaps and bounds.  She sure stole my heart!”

UPDATE 2013:
Hannah is doing well, she is still in the orphanage and will be available for adoption when she turns 5 in September.  She is a sweet girl! Unfortunately, pictures cannot reflect it, but she is very charming!  We would be happy if a good family could adopt her ASAP!

We got to meet Hannah while touring the special needs floor of the baby house in April 2011.  She is obviously adored by the staff, and is well cared for.  She was super tiny and a little shy, but that didn’t stop her from approaching our daughter who had traveled with us.  Although I didn’t hear her make any sounds, she was very expressive and they quickly and easily responded to her.  She appeared to fully understand what they were saying to her as well, and did respond with head nodding and shaking a few times.  Not only was she walking on her own, she was strong and steady.  Able to get up and down, chase the ball, run off with the ball in her hands.  She is currently living in a caring environment with a great therapy floor, able to help her to meet her milestones and goals.  She will be transferred between the age of 5 & 6 as all children are from this facility.  The reality of where she will go, and the group where she will be fit into should a family not arrive for her BEFORE she is transfer is not good.  She will quickly regress there.

$10,009.00 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!

Posey

30417092736Girl, born Nov 2008

Cerebral palsy, double hemiplegia with severe movement disorders, symptomatic epilepsy (frontal lobe, focal) with partial seizures with secondary generalization, significant mental delays, optic nerves atrophy.

 

This sweet girl needs a family to help her bloom!

 

$66.60 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!

Joanna

40929144350 JoannaGirl, born 2012
Hydrocephalus
Will be available December 2014 / January 2015

 

$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!

Annie

Annie (3) Annie (2)Girl, born 2009
PRC
cerebral palsy, epilepsy

Annie was found abandon at 1 yr old. Her evaluation in July 2012 stated….. During the test the patient can smile when teased, muscular tension of whole body is high, can not keep her head vertical stably, when held to stand her feet is crossed, when lying on stomach she does not use her forearms to support, she can not roll over, can not sit alone.  She can not get things on her own initiative, can not evaluate her adaptability.

From someone who knows her:
She’s doing really well. She’s on medication to control her seizures and it’s working fine. I have never seen her have a seizure, but I believe it has happened occasionally when she has been febrile with a cold or virus. Of course, does need her medication to keep her stable.  She loves her wheel chair.

Annie’s personality is loving and sweet. She is happiest if somebody will just spend time with her – laughing playing and cuddling her. But she is not whiny when other kids are getting the attention either, so she would be a great fit for a large family. She just enjoys movement and action, whether it involves her, or is going on around her.  One of her favorite games is when you push her wheelchair really fast between two people – she laughs so much at this!

She’s bright and has a great understanding of everything, but cannot communicate verbally.

Her disability is definitely severe, but she is emotionally very healthy. We would so love to see her in a family. Eventually she will need to leave our home, as she is absolutely not palliative, and we desperately want to see that move take her to a loving home! She is really such a beautiful child. She is like sunshine, she warms everyone around her. Even though she is trapped inside a body which will not do what she needs it to do, the beauty of her personality will not be contained. If we can find a family who can manage her physical needs, they will be so blessed by this precious daughter. It makes me so sad to think of her future if she has to remain in  her birth country.

$280.80 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!

Priscilla

Guardian AngelPriscilla

Girl, Born February 2010

WONDERFUL new photo of Miss Priss!

updated medical: congenital malformations of her spinal cord/musculoskeletal system/eye/hip, lactose intolerance, nephritis, diverticulum of bladder, mental delays

Pretty Priscilla!

From her caregivers:  communicative; adequate reactions.  Character: cheerful, active, friendly, communicative, likes to play with different toys.

Update Nov 18, 2014:

Priscilla is doing very well. She is a kind of shying but a smart girl. She understands everything but her speech ability is not understandable to me as she is very quiet. She has survived her blood issues she had few years ago.

She will be 5 years old in February 2015, and it would be great if a family will be ready to adopt her by that time. She really needs a family asap because her intellectual potential may be lost due to nobody really cares of her mental development and IQ in the orphanage. They care of her general health condition pretty good though.

More photos available.

$1,346.95 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!

Brenda #1-9

Brenda 2014 (2)BrendaAge: 4
Diagnosis: microcephaly, mental delays

Brenda has delays in her development. She walks, runs, climbs stairs independently. She is able to thread larger rings, to pull circle out of the tray, to fill and empty box, to turn the pages of a book with thick covers, to arrange a tower of 2-10 cubes, arranges puzzles. She prefers to play by herself. Her speech is delayed, though she does respond to her name. She feeds herself with a spoon and drinks from a cup.

 

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.

Lynda

30815195533Guardian AngelGirl, born Dec 2008
Hydrocephalus, Severe mental delays

 

She is a very sweet and kind girl and extremely needs a family.  She will be 5 this December, so any new family may commit to her and start preparing a dossier.

She has siblings, but none are available for adoption; 2 older sisters live with birth mother and 1 younger sister has been adopted.

From a family who met her in summer 2013:
She was in my kids’ groupa.  She is the sweetest little thing and needs out of there ASAP!!!  She has the most noble quiet nature about her.  She is mentally delayed but has so much potential.  She was one of the least favored children in the orphanage and she is desperate for love.  On one occasion she wandered over to the play shelter where we were playing and was trying to eat our daughter’s cookie.  We didn’t have any extra (we brought treats for the groupa every three days or so) so my husband just picked her up to distract her and as soon as he did, she threw her arms around his neck and rested her head on his shoulder just soaking in the attention.  I can’t bear the thought of her being transferred!  She already has it bad enough.

 

$2,678.25 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!

Marilee #474

474_Ph_Dec13Girl, 1.7- year-old
Congenital hydrocephalus (no indications for a surgical correction at present); microcephalus; suspected infantile cerebral palsy; convergent concomitant strabismus; specific developmental disorder of motor function; delayed neuropsychological development.

Marilee vocalizes (vowel sounds such as “a-a-a”), although she does not yet produce defined syllables or connected syllables. She does not cry in a loud and clear voice. Her eye contact needs to improve further. Marilee does not yet respond to being called by name. She responds visibly to touch and relaxes greatly when someone holds her in their arms. Marilee is being monitored by a team of specialists at the orphanage.

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.

Lollie

photogirl

Girl, born May 2011
H-C
Siezures; other undiagnosed issues

Lollie is learning how to sit; when you put her in a sitting position, she can now sit for several seconds. She has an epileptic syndrome and is on medication for seizures, but has not had any seizures since being admitted to our care. She has a vision impairment, but with glasses is able to see much more of her world. Lollie is nonverbal, but she will make contented noises to express herself.

$61.20 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!

Victoria (Meryl)

photogirlGirl, 5 years old
CO-A
Syndrome 3C (cardiac malformations, cerebellar hypoplasia, and cranial dysmorphism) or
Ritscher–Schinzel syndrome,[2] is a rare condition, whose symptoms include heart defects, cerebellar hypoplasia, and cranial dysmorphism.

Victoria is a sweet 4-year-old girl who is kind, affectionate, funny, and lovable. She has been living in a foster home since she was 2-months-old, and is very affectionate with her foster family. She loves playing with her foster siblings, and gets along very well with the children closest to her age. Her foster mother describes her as a happy, obedient, sociable child, and they enjoy having her in their home.

Because Victoria has Syndrome 3C, a condition that is characterized by cardiac malformations, cerebellar hypoplasia, and cranial dysmorphism (3C’s), her development is not up to age level. She has been going to therapy to develop her speech skills. She also has Enuresis, which affects her bladder and urination control.

Victoria interacts well with other children and loves to watch TV and play. She can eat, brush her teeth, and dress herself independently. She loves doing her homework and schoolwork, and can concentrate on a task or an activity. She is an extremely outgoing child, who is respectful and always follows directions.

Sweet Victoria is looking for a forever family that will provide her with love and affection, kindness and guidance. She will bring lots of laughter, many smiles, and tons of hugs to your home!

Photo available from the agency, for serious inquiries.

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her. 

Judy

JudyGirl, born October 2012
H-C

Judy is a sweet little girl. She appears to have some delays, possibly cerebral palsy, and does not currently have much muscle control. She cannot hold her head independently, but her control is improving. She cannot roll over, but can roll to her side. As her nutrition level increases, we are hopeful that this will improve. Judy loves to interact with those around her and will eagerly watch you until you pay attention to her. She has a great giggle and a precious laugh and is completely adorable!

$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!

Antoinette #24-33

Antoinette  (2) Antoinette  (1)Girl, 2 years
Cerebral palsy, blind, deaf

March 2014 update:

No physical activity and initiative. Muscle tone – quadri-hypertonus and normoreflexia. Takes a passive seat with adherence, has elbow support but shows poor balance reactions. Gripping reflex – upon touch with, grips for a short while. Visual – motor coordination /hand-to-hand; Hand-foot-thigh; Hand-foot-mouth /. Visual analyzer – horizontal nystagmus, amaurosis, atrophy of optic nerve. Does not follow and fixate a bright object. Does not wince and does not orient in the direction of strong acoustic stimulus, bilateral sensorineural hearing loss. Pronounced “seeking” reflex and pathological oral automatisms. Speech production – coo sounds and vocalizations. Affective reactions – heavily decreased mimical facial expression, responds to tactile stimulation, “facade” smile is observed briefly.

Autonomy – positioned entirely by an adult. She feeds with an appetite and permanently gains on weight. Sleep – short periods of wakefulness.

Update, August 2014: Within a month this little girl has made a progress, which is encouraging. Also, the staff working with her shared that according to them she is not deaf but probably with decreased hearing!!!

The agency has an updated report on file and video! Antoinette needs a family that will give her a chance!

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.

Rose

RoseGirl, born Sept 2011
PRC
Cleft lip / cleft palate, Cerebral Palsy

Rose is 2 years old and she loves to smile! She has a cleft lip and palate and Cerebral Palsy (CP). Her CP makes it hard for her body to move so right now she cannot sit or stand on her own. It can also be hard for her to talk with her cleft lip and palate. Rose loves when her caretakers go outside with her, and she loves when they call her name. Rose laughs and smiles at people when they talk to her, and especially when they play bells. She can roll over, hold her own toys, and hold her head up like a champ!

$45.68 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!

Leilani

30118214804

Girl, born March 2009
hydrocephalus (with shunt), spastic tetraparesis, convulsive disorder, Hep.B, valgus feet, optic discs atrophy

 

 

 

$1,329.42 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!

Susie

Susie Photo 1 March 2014 (1)SusieGuardian AngelSusie was born prematurely at 27 weeks gestation in June 2011. She has been diagnosed with multiple malformations of the brain, including agenesis of the corpus callosum, porencephaly, hydrocephaly, and hematomas. A catheter and shunt have been placed to allow fluids to drain from Susie’s brain. Susie has epilepsy, is blind, has no head control, and has significant developmental delays, but she reacts when someone speaks to her and loves music. Additional photos and reports are available upon request from the agency.

Please note: Married couples are given preference due to child’s court appointed guardian in this case.

$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!

Vikki

girlsillouettenophotoGirl, born August 2010

Significantly delayed psychomotor development; Pineal cyst

The agency can request further information for serious inquiries. We are so excited to be able to advocate for these children!

$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!

Helen

Helen2014Girl, born Dec 2008guardianangel
PRC

 

Helen was born with encephalocele, which is type of neural tube defect that occurs very early in fetal life where the embryo’s cells that form the skull do not come together to close over the brain. The result is a defect in the bones of the skull, causing brain tissue to protrude from the skull.

Helen loves to make herself laugh. She enjoys spending her time playing, humming, and observing things around her. She is doing well and getting strong. She is able to walk with help and has recently been able to pull herself up. She loves to go outside to the playground and practice her walking. Her smile is so cute and her laugh so hearty.

Helen has had surgery, and additional information is available about her surgeries and hospitalizations.  She has vision concerns, and has recently begun speaking a few words.

$3,801.44 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!

Nevaeh

Neveah (1)Nevaeh (1)Girl, born, March 2010
Cerebral palsy, optic atrophy, developmental delays

 

Ohh, I love her little pouf of hair, what a lovely little girl.

Not sure how much vision she has.
From a family who met her in early 2014:
She needs out! She is skeletal and looks to be in very poor condition. Neveah just cries and cries if you get near her. Also, she appeared to be heavily sedated. She had a toy tied to her wrist/hand, and her hands were bound to not scratch herself. So, so sad.

$145.00 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!

Judith

40730094950Girl, born 2012
CP, dual hemiplegia
Judith cannot walk or sit independently. But she shows interest in toys and reacts to speech addressed to her.

 

$5.00 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!

Tesia

Tesia

Girl, born Feb 2011
Down syndrome, Cleft Palate, bilateral ear deformity, growth delays, developmental delay

Tesia has a diagnosis of Down Syndrome, but a prospective family needs to be open to the possibility of a different medical diagnosis as Tesia exhibits many characteristics of children who have been diagnosed with Treacher Collins, although TC is not mentioned specifically in her record.

Tesia was found abandoned at around 10 days old. She is a timid, shy and quiet little girl who likes to play with toys especially balls, sand and slides.

Tesia2

Tesia is able to walk and is reported to be toilet trained. She can search for the source of a sound and can make sounds on her own, but did not use words as of the report date. Tesia likes to be cuddled and spoken to. She is waiting for a family of her own who can snuggle with her as they tell her “I love you!”

$364.50 has been donated towards the cost of my adoption, including $180.00 from Angel Tree donations!

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!

Tenley #476

Tenley_2014 Tenley23 years old

polymalformative syndrome, a condition after surgery for atresia of the esophagus and the anus, plastic reconstruction, esophagogastroanastomosis, colostomy, restoration of the colon. She has vesicoureteral reflux, hydronephrosis and megaureter in the left. 2-degree hypotrophy; significantly delayed neuropsychological development.

Tenley turns from back to belly and from back to a sideways position. She does not yet make attempts to crawl or stand up independently. She cannot take a sitting position independently yet. However, she is stable once placed in a sitting position. Her legs support her. When placed in a standing position, she can remain standing while holding onto a fixed support. She makes steps while held by both hands by an adult.

As regards the child’s speech, she mostly produces sounds and sound combinations. She responds to voices, although she does not yet differentiate being called by name.

She reaches for, takes by herself or insistently tries to reach a toy. She plays with toys continuously (looks at them closely, transfers them from one hand into the other, examines them with her mouth). She prefers plastic toys. She reacts positively to music (children’s songs).  She tolerates the presence of other children or adults. The child does not always demonstrate readiness to interact or play together with an adult. She has low frustration threshold.
The child eats with an adult’s assistance. She does not yet announce or control her physiological needs.

Updated pictures and information coming soon.

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.

 

Marisol

MarisolGirl, born November 2009
P-OD
overall delay and cerebral atrophy
Development: Sat without support: 7 months
Crawled: 12 months
Stood up by using furniture around: 16 months
Walked: 20 months
Language: At the age of 30 months vocal and syllabic sounds that are repeated if she is doing something that she likes and entertains her. She is able to say “chao” o “adios” (good bye) and “ma” or “mama”

Evaluation: 05/2013
Global Developmental Delay: Main delayed areas are language and communication (vocabulary). Areas with more progress are gross and fine motor. Areas with more noticeable improvement are: social adaptation, cognition, language (referred to response to communication with others and abilities of communication)

Affective Emotional: Cheerful child who loves receiving affection. The keepers report that she always shows a great need of affection, attention and closeness. Playing is still primitive consisting of hitting the blocks, putting them in line, put objects in and out, etc. She likes music and dances when she listens to it. She can play with other children around but still struggle playing with them.

Note: According with Adoptability report dated 2012:  requires a family with no kids that will give her a personalized affective attention that she can adapt to, progressively.

Marisol is currently available for adoption and waiting for her  forever family! The central authority in the children’s country of origin are the legal custodians and guardians of the children and Open Door has been given the privilege to assist in finding permanent homes for these children.  Agency has photos and videos and will be happy to share them with an interested family.

$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!

Athena

AthenaGirl, born Feb 2010
PRC

Athena is a sweet little girl who has been diagnosed with congenital cleft palate and a slightly dilated ventricular system.

Athena is an active child who likes riding on the wood horse in the institute. She likes playing with toys and rattles and her favorite toy is the toy bee. Athena likes communicating and playing with her caregivers. She likes to crawl and receive hugs too.

$58.90 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!

Tina #417

IMG_0201SAMSUNGDOB: 2009
Diagnosis: Rubinstein-Taybi syndrome

Tina has been diagnosed with Rubinstein-Taybi syndrome, which is characterized by short stature, learning difficulties and distinct facial features. She was born with a heart condition that was surgically repaired. She can roll over and support herself up on her hands. All 4 of her limbs appear to have weak muscle tone, which could be a result of spending prolonged amounts of time in her crib. She will hold a toy in her hand and watch it. She makes eye contact with caregivers and eats from a spoon.

Additional photos of Tina are available.

Update from a family who met her in Nov 2013:
We visited her first during our November visit to Bulgaria. She is absolutely beautiful. She is very sweet and was happy to be held. She clearly has likes and dislikes and is able to make that clear. We spent a lot of time walking with her when she got restless from laying or sitting for too long. I was able to feed her one afternoon. She has some feeding issues and needs to eat pureed or soft foods. She enjoys eating and showed, by her eagerness, which foods were her favorite. She did not show any signs of recognizing her caregivers and showing any varying emotion for different people. We were told that she has not connected to any of her caregivers or show recognition of them. We had an evaluation done on her medical file by our local International Adoption Center. They told us that given what is reported in her MRI that she has fluid where she should have brain matter so her functioning level will likely not make major gains. I can’t say enough how lovely she is and sweet. She showed preference for toys and loves to put things in her mouth! We very much enjoyed our time with her.

 

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.

Gina (Missy)

Gina 2014 (2)Gina 2013Girl, born September 2008
Cerebral palsy

 

Gina has a sunshiney smile!

More pictures available, but she is seated in this chair in all the pictures we have.

From a family who met her in August 2013:
Precious Gina is so willowy and gentle. She is being loved and cared for in her baby house. She is soon to be transferred, though. Her groupa goes outside twice daily on nice days and she sits in a stroller staring at the leaves and feeling the breeze. When touched and cuddled, she moves her head toward you. Her skin is soft, and her hands are so gentle. She blinks with delicate eyelashes and seems to be trying to clear the fog to see you. I got to see her several times and each time her face lit up with a smile and she moved her chest side to side rhythmically to acknowledge her joy at being noticed. She is so full of life, and needs more therapy to help her reach her full potential. Gina deserves so much more than what she has been given. If only her mom and dad could look into her eyes and see how much life is behind them. She is a treasure, and is in desperate need of a family as she approaches the age of transfer. The institution she is headed for will not offer her anywhere near what she has now. Please see Gina before she is lost forever.

Gina received massage therapy regularly, is in diapers, and could use some dental care. She is very thin, but is being offered excellent nutrition. She is in a region that we felt comfortable having just mom stay for much of the travel. More pictures and a video available.

From a family who met her in early 2014: 
I did get to see her several times while the door was open to the groupa’s play room. She is so very skinny now. When she was left in her crib she was usually crying and trying to roll over. One day there was a sweet nanny holding her and singing to her. She had the biggest beautiful smile and was loving being rocked and sung to! Her hair looked like it had grown out some. She had really beautiful, sweet curls.

Gina is now available for international adoption as she recently turned 5.

$305.15 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!

Abigail

Abigail Photo 16 Nov-2014 - Nov 2014 - AAbigail Photo 1 - April 2014Abigail was born in January 2011 and has been diagnosed with spina bifida and hydrocephalus for which she has received a shunt. Abigail also takes medication for epilepsy, but has not had any seizures since beginning treatment. She may need a surgery to correct her strabismus.

Abigail was recently seen by an orthopedic surgeon who noted that her spinal deformity and spina bifida are severe. He believes that Abigail is paraplegic and will not be able to walk in the future. Her spine will need treatment to correct its position and improve her sitting posture as well as upper body skills. Abigail is able to use her hands very well, moves around freely on the floor and sits unassisted. She struggles with solid food because she does not chew very well, but reportedly has no trouble eating cookies and candy. While Abigail is very vocal, only about 50 words in her vocabulary are completely clear to understand.

Abigail is a bright and engaging child. She speaks in complete sentences, explores, and knows exactly what is asked of her. Abigail is interested in everything, likes to talk on the phone, plays with toys, and sings. She is known as the social butterfly of her orphanage, always smiling and joyful.

From a family who met Abigail in May 2014: Abigail is a little diva! She is so tiny for her age, but her personality is explosive. She is very smart. She told me all the names of the caregivers and children. When she sees someone she shouts, “Come” and taps on the ground next to her. She is so loving, compassionate, and so kind. She frequently hugs the other children on her own doing. She doesn’t have too much use of her legs at this time, but can scoot on her bottom. She has noticeable curvature of her spine. She needs that corrected. It could improve her physical abilities a lot. We put her in a walking position and she could put some weight onto her legs. She laughed so hard at herself when she was “walking.” She uses a little wooden toy with wheels like a wheelchair. She rolls around everywhere, even getting into the shoes as most young girls would. She had a nasogastric tube in her nose while we were there. A virus was going around and she wasn’t drinking enough so they put it in the children to make sure they were getting enough liquids. They said it was temporary and she normally eats and drinks fine. She also can feed herself and loves chocolate. Whoever adopts Abigail will be so blessed. I think she will excel in a family, and the reward for being her mom would be the biggest blessing to anyone.

From a family who met Abigail in October 2014: Abigail is the size of an infant in both height and weight. She’s a social child, engaged and engaging. She communicates constantly and purposefully, but her speech is very hard to understand. She has a lovely smile. Abigail gets around quite well by scooting on her bottom. When she saw another child upset and crying, she moved over to her and gave her friend a long hug.

Additional information is available directly from the agency.

Married couples only due to child’s court appointed guardian in this case.

$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!

Marsha #4-62

MarshaAge: 4
Diagnosis: polymalformative syndrome, chromosomopathy and developmental delays

 

Marsha’s birth mother was just 16 years old when Marsha was born and raised her for 3 years. After several hospital stays, Marsha was placed in the orphanage. She has delays in all aspects of her development, but has been making steady progress since entering the orphanage. She is walking independently, playing with toys and seeking out the attention of caregivers appropriately. She is not yet talking, but is learning to feed herself. Updated photos and videos will be available soon.

Quinn

Girl, born January 2009
PRC
Cerebral palsy (High tension in all four extremities); Brain atrophy (slight) and hydrocephalus

 

Quinn was 1 when she came to the institute. In the beginning, she cried often during bed time and at night. In her second month here, she slept well through the night. She could produce basic sounds, and move her head around. Her eyes could follow the movement of toys. At two, she could find the source of a noise and understood when the caretaker called her name.  Due to the tension in her limbs, she still could not sit or stand by herself. The caretaker monitors her when she is using a walker.

Quinn is shy and quiet.

$94.50 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!

Clara #29-12

ClaraAge: 2
Diagnosis: Microcephalus; Infantile cerebral palsy; Severe delay in development

 

She pronounces sounds. She sits with help and in a positioning therapeutic chair. She can keep her head up when put on her stomach. She eats with good appetite but has unsatisfactory weight gain. She is calm when asleep and awake. Clara has recently started keeping her head up for longer periods of time. She can turn only from back to stomach. She sits only with support. She pronounces accidental sounds. She follows with a look moving objects for a short time and doesn’t reach out to them. She holds a toy put in her hand but doesn’t bring it up to her eyes or manipulate with it.She reacts positively to physical touch and when someone talks to her. She smiles and vocalizes in response.

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him.

Nora

40819143326 NoraGirl, born 2013
Congenital malformation of the central nervous system, symptomatic epilepsy, atactic syndrome, tetraparesis, porencephalia

 

 

$101.25 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!

Henrietta

30421112308Girl, Dec 2009
Congenital brain malformation (corpus collosum agenesia), spastic tetraparesis, epileptic syndrome, optic nerves atrophy, equinovarus, condition after exudative pericarditis, hypotrophy, deficiency anemia, mental retardation, convalescent bronchial pneumonia.

 

$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!

 

Yvette #413 OD

413 YvetteGirl, born January 2009

infantile cerebral palsy, symptomatic epilepsy, nystagmus, delayed physical and neuropsychological development. She takes a medication so as to prevent the seizures. She has daily rehabilitation, remedial massages and gymnastics.
In the last 4-5 months Yvette has started performing active movements with the hands – she reaches for and grabs a toy that has been handed to her. She turns from her back to one side. She loves it when someone talks to her and caresses her and she then produces joyful sounds. She maintains stable eye contact. She pronounces several one-syllable words.

 

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.

Malinda #

MalindaGirl, born 2012
West syndrome / infantile spasms; delays in neuro-psychological development, hypotonia, facial dysmorphia, nystagmus (inconstant), systolic murmur

 

 

 

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.

Gabby #HA

Gabby_smGirl, born 2009

microcephaly; cerebral palsy – spastic quadriparesis; Congenital heart malformation, severe developmental delays

 

Sweet Gabby has some significant needs.  Gabby was at one time declared unfit for travel by medical professionals. A family would need to be prepared for that possibility.

The agency has additional information and videos available for inquiring families.

From a family who has met her:   I have met this child and reviewed all of her medical records. I’ve spoken at length to the director (who is a doctor) about her needs. I have touched her and spoken to her and prayed over her. I’ve written an accurate description of her here, if you’d like to accurately reflect her needs. She is completely unresponsive to touch and voices.  It sounds cruel, but the reality is that all she does is breathe. She did not move the entire time I was in the room. There was no reaction at all to my touch. Her eyes fluttered, but I honestly think it was involuntary eye movement. I am not a doctor and I would LOVE to be wrong.  But US doctors have looked at her brain scans and said that she does not have a brain”.

Because we only have this child’s file for a short time, she will not be able to receive donations until a family is found for her.

Chelsea Anne

Chelsea AnneGirl, born February 2009
PRC
Developmental Delay

Chelsea Anne is a precious little girl who came into care when she was 3 years old. She loves to walk around and watch her friends play. She is not able to speak to her friends or caregivers and sometimes she can follow their directions. Chelsea Anne likes to twirl things in my fingers and she especially loves when she has a soft shirt to play with. Chelsea Anne has a difficult time self-soothing so sometimes she will bang on items to help herself calm down. She is working on getting more independent and eating independently. She is very helpful when it’s time to get dressed!

$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!

Monacella

30417230923 MonacellaGirl, born January 2009

Brain malformation (corpus callosum agenesia, optic septal dysplasia, ventriculomegalia, cerebral hemisphere hypotrophy), spastic tetraparesis with severe movement disorders Q 04.8, symptomatic focal partial epilepsy with complex partial and rare secondary generalized seizures G 40.2, optic nerves atrophy, convergent squint.

 

Sweet girl has a laundry list of diagnoses; she needs a family, or she’ll spend so much of the rest of her life in a crib.  She’s got sparkle — a family could help her truly shine!

$41.00 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!

Mackenzie

Mackenzie Photo 6 rec. 1-22-014Girl, born November, 2008
Cerebral palsy and congenital developmental defect (cleft palate, right sided syndactyly).

Due to Mackenzie’s difficulty gaining weight, she did not have an operation for her cleft palate, but with time it has closed on its own. As her cleft palate closed itself, she is now able to eat almost everything, and has started to gain weight better. She stands only holding on something, but is able to crawl and scoot around well. She is very smiley and likes to be loved. She knows her name and reacts to it. She seems to know the caretakers, but her reactions and the way she plays corresponds to a one year old child. She plays with toys; but when she sees something new, she wants to take it to her mouth first. She does not speak and does not make sounds. Additional photos, video and report available upon request from the agency.

Comments from a current traveling family: “While visiting with our daughter [in the same orphanage] we had the chance to spend some time with “Mackenzie”. Wow… She is an amazing little girl with such a will for life. She shows such determination in everything she does and truly lives her life not letting anything get her down or in her way. She is such a happy little girl with the most contagious beautiful smile. Her diagnosis does not define her and it is clear that she will live life to the fullest if given the chance. She loves when she is talked to, loves listening to music and embraces the touch of others. She is loved dearly by everyone around her while she waits patiently for her forever family.”

From a family who met Mackenzie in May 2014: Mackenzie is a sweet and loving girl.  She can now pull to a stand without assistance and cruise along stable support.  She is even able to wobbly walk while pushing a walker.

$40.50 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!

Aura Lee

40404202845 Aura LeeGirl, born July 2009
Microcephaly, spastic tetraparesis

 

Oh, isn’t she lovely?

Aura Lee is doing very well.  She knows her nannies, smiles at familiar adults.  She can sit down and stand up with help.  She does not have mental delays.

Aura Lee has features consistent with FAS (fetal alcohol syndrome).  This is not a diagnosis, but a cautionary disclosure.

Aura has developing speech — she can make separate sounds, and will repeat after an adult.

$274.61 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!

Cate

CateGirl, born July 2011
PRC
left eye ptosis, atrophy- retinoblastoma

Cate is just over 2 years old. The doctors believes she has ptosis, left eye atrophy, and possible retinoblastoma of her right eye. She hasn’t received any treatments for her eyes.

Cate can keep up with the kids her age. She can walk around and knows exactly what toys to pick out of the toy box. She knows how to talk and get along with others, but is very shy and prefers to stay quiet around strangers.

$89.20 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!

Mandy

Girl, Born 2010

syndactyly of hands and feet, steeple tower head, psychological and motor delay, Congenital heart defect (patent foramen ovale, secondary defect of interatrial septum)

Many will be available in early 2015.

We are so glad to finally be able to relist Mandy! She was born with multiple skeletal anomalies, including fused/webbed hands.

 

The girl is smiling, laughing. She reaches for toys. She walks in baby-jumper.    Doctors consider that surgery may help to separate her fingers on the hands.   They give a positive prognosis regarding her mental development.  More photos are available.

This region typically waives the 10 day waiting period for children with special needs.   

$1,317.80 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!

Donna

30119084859July 2011
hydrocephalus (internal hydrocephalus as a result of suffered meningitis); spastic tetraparesis; prematurity; retinopathy of prematurity; collapse of lungs; prenatal infection;

heart disease:  open arterial duct (condition after surgery on August 10, 2011), open oval window, anomalous chord of the left heart ventricle

 

Look at that white-blond hair!  So pretty!  Donna desperately needs a mama.

 

$40.50 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!

Lizzi Belle

Lizzi Belle (2)

Lizzi Belle (1)Girl, born August 2009
PRC
Intellectual delays, possible cerebral palsy, possible autism

Lizzi Belle was first thought to have Down syndrome, but that was not the case. However, she has very severe intellectual delays, possible CP, and possibly autism. Lizzi Belle cannot speak, cannot walk, is not toilet trained, and according to the nannies…”unable to communicate with the outside world”. A family for Lizzi must be willing to love her unconditionally, and care for her needs for many, many years to come. It is impossible to say what the future holds for Lizzi Belle, but it will certainly be brighter with a family to love her! This photo is an older photo, but the agency has a new video to share.

$100.00 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!

Scarlett

ScarlettGirl, born February 2009
Congenital hydrocephalus; Spastic tetraparesis

 

What a little doll!  She just turned 5 years old, and is now available for adoption.

Miss Scarlett needs a family of her own.  Married couples only, large families welcome.

 

$25.00 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!

Ysabelle

Girl, born 09/24/08
T-HSA

Ysabelle is a very special girl looking for a forever family. She was born into a very poor family who cannot take care of her medical expenses. She suffers from cerebral palsy, atopic dermatitus, and intraventricular hemorrhage. From all accounts, she is a loving, sweet girl who loves to interact with other children and adults. She receives lots of therapy, and her teacher shows a lot of tenderness and care towards her. Ysabelle just started eating solid food, and can stand, walk, and squat with help. Her language development is behind, but they hope that with more social interactions her vocabulary will improve. Ysabelle needs a family who would be willing to dedicate themselves to providing therapy and lots of love.

 

$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!

Lolita

Lolita (1)Girl, born 12/2008
PRC
Brain dysplasia; post-operative congenital heart disease

5 year old Lolita is looking for a special family that will be hers forever. She is diagnosed with brain dysplasia and post-operative congenital heart disease. Lolita was abandoned at 4 years of age…can you even imagine? She had a surgery for her CHD before arriving at the orphanage. She can walk alone without help, but her step is a bit abnormal. She is curious and observant of her surroundings.Lolita is reserved, but gets along with her caretakers. Guardian AngelWhen asked

Lolita (2)

something, she will shake her head. Currently she is receiving preschool education in the center. Lolita can feed herself and use the bathroom independently, but her language is delayed. She has trouble with pronunciation and is only saying simple words. She will receive speech training to help her with this. Lolita has fine muscular tension of the limbs, but her motion is fairly flexible. Her fine motor of the upper limbs is poor. She enjoys going for walks outside and building towers with blocks. Lolita is gentle, cute, and quiet. She has a sweet smile. She likes to watch TV, listen to music and she is an easygoing child.

$1,079.20 has been donated towards the cost of my adoption, including $1036.00 from Angel Tree donations!

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!

Sabine

30818212820Girl, born Nov 2009
Epilepsy, left cross-eye

 

*** 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. ***

 

$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!

Mercy

Guardian Angel

mercy-2014Girl, Born July 4, 2009

 

Mercy has been waiting TOO long.  So glad to have a new pic of her, but she needs OUT.

 

Many photos available of her.    From her medical records:  Myelocele of lumbosacral part of spinal cord (spina bifida, had surgery); flail legs; optic nerve atrophy; congenital hips dislocation, clubbed feet.

 

$5,117.40 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!

Anna

AnnaGuardian AngelGirl, born January 2011
PRC
Spina bifida (post-op)

 

Anna has no sensation in her lower limbs but her upper limbs has full range of movement. She can sit independently but cannot walk. She has no sensation regarding toileting. Her mental and language development is all age appropriate according to her update completed December 2013. Her foster mother says that she is active and gentle. She listens well but will cry when her foster mom leaves. Her foster mother says that as long as she tells Anna that she will be back and when she will be back that she will quiet down and accept that her foster mom is leaving. Anna is a beautiful girl that longs for a family to call her own.

For interested families, the agency has 2 videos of Anna and an update from December 2013.

Anna would greatly benefit from treatment and therapies at a children’s hospital like Shriner’s in the US. This little girl would have a bright future with the love and care of a family.

$121.50 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!

Mary

MaryMary

Girl, born May 2011
PRC
Post-op anal atresia/fistula, vision impairment, neoplasm of right ear

Mary is a sweet little girl who has been diagnosed with postoperative anal atresia/fistula, vitreous opacity of right eye, a neoplasm of right ear, and congenital microphthalmus of both eyes. She is able to crawl around but cannot walk on her own just yet. Mary still needs support while standing up and if she is helped can walk slowly. Mary uses a walker and with it is able to go places, sit, and stand up. She is learning how to eat with a spoon. Mary cannot see things that are far away due to her vision impairment. She gets along well with others and enjoys playing with the other children. Her caretakers think she is very energetic and active.

$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!