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 277, Monrovia MD  21770

“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.

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Olive

Girl, born 2016
sweet baby!

 

dyskinetic cerebral palsy
other specified retinal disorders
anemia
atrial septal defect

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

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

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Sierra

Girl, born 2015

spastic diplegia
Sequelae of subarachnoid haemorrhage
Epilepsy
Congenital malformation of optic disc
Hypoplasia and dysplasia of lung
Cardiomyopathy

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

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

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Eden

Girl, born 2014

Eden is completely blind and has profound hearing loss. She received bilateral cochlear implants and is responding to sound and making many new sounds, although not yet saying any words.

Eden has delayed milestones as a result of having no visual or auditory input for so long, but we are excited to see how she progresses over the coming months. She attends an on-site preschool every morning. She can sometimes get overwhelmed by the new sounds she is hearing, and when she feels this way, she tries to take her speech processors off. Eden has some self-stimulating behaviors. She loves to splash in the water and is getting better and better at walking independently with her guide cane. She loves to swing and rock in her rocking horse. She loves to cuddle. She has started to take several steps on her own, and also while holding onto a push toy (pre guide cane) or her cane.

$10.80 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!

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Kristen

Girl, born 2017

disorder of the brain
cleft palate
congenital absence of hand and finger
optic atrophy
other lack of expected normal physiological development
ventricular septal defect

 

$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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Sahana #

Girl: 2013

Listed: Jan, 2018

Her special needs are infantile cerebral palsy, symptomatic epilepsy and hypotrophy.  Sahana is not yet speaking and is fully dependent on her caretakers. She is spoon fed pureed foods because of her inability to swallow whole foods. Sahana enjoys music and reacts positively when she is sung to or music is being played. She is described as calm, especially in the presence of adults

B/c we only have her file for a short time, donations will not be accepted until a family is found for her

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Addison

Girl, born 2014
PRC
Epilepsy, delays

Addison is a petite and precious three-year-old girl who loves to be cuddled. When Addison was younger, she could walk independently and she had good fine motor skills. She could take small things out a bottle, turn the pages of a book, and take off her own socks. Addison loved to wave hello and goodbye, clap her hands, and blow kisses. Her nanny adored her and often took her to play on the playground. Addison could speak simple words, such as mom and sister and she could understand the adult’s instruction. She was described as cooperative, active, full of expression, and adored. Addison was sometimes mischievous and would occasionally lose her temper, as any 2-3 year-old would. She enjoyed the rocking horse and playing with balls.

In April of 2016 she started having seizures and was sent to the hospital for treatment. She does have a CT scan in her file which was normal, but once Addison came back she was like a different child. She had stiff limbs and couldn’t walk or sit. She was able to make small guttural sounds and could visually track moving people. The orphanage decided to have her start rehabilitation training. Addison started receiving acupuncture and massage therapy and her muscular tension improved. She can now hold her head up when lying on her stomach and responds to toys that make sound. She knows her name and will look when called. She still makes good eye contact, but has less facial expressions than she used to. She now imitates making sounds and recognizes people. She is still attached to her favorite nanny and enjoys when the nanny spends time with her. She will cry when the nanny leaves. Her nanny spoon feeds her porridge and she often bites the soon tightly and sometimes has trouble swallowing.  The agency has received a recent update. This sweet little girl has been through so much without a family by here side. It is our hope that the perfect family for her comes forward and meets her where she’s at and helps her reach her fullest potential!

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

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

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Lexie

Girl, born 2013
PRC
Blind

January 2018 Written Update:   Lexie will be 5 years old in February. She has been attending preschool for 1 ½ years. She comes to school Monday-Friday from 8-4:30 pm.  For a little while she was in foster care organized by another nonprofit that works in her orphanage but for the last year she has been living in the orphanage. There are currently 9 children attending this school. Most of the other children came when they were older and have additional special needs. None of the other children are verbal and we believe this has affected her development as well. She doesn’t have any peers she can interact with. Even though the other children are older than her they are developmentally behind. She can speak in short sentences. She can make some requests and sometimes answer simple questions. In the last few weeks we have seen a change in her behaviors. She used to be a very happy little girl who played easily on her own or with teachers. She used to be able to follow commands and two step directions. She could sing along to songs. Now she seeks people out and wants to be with someone all the time. If they don’t respond right away she will start hitting herself indicating she needs someone to be with her and help her regulate. She is generally happier when she has a person with her. The teachers have had to assign her a teacher as her hands were becoming bruised and swollen. The teacher is worried about how the orphanage is affecting her and she has brought her out of the orphanage on weekends and she has never hit herself when they are together outside of the orphanage. They have a really sweet relationship and she is comforted by her when she is upset.

There is a $1,000 agency grant for Lexie’s adoption with her current agency. Other grants may be available based on the adoptive family’s circumstances. Agency grants are awarded as agency fee reductions.

The agency has videos available, too.

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

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

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Sidney #

Age: 2015

Diagnosis: Low birth weight, Cerebral Palsy, Deafness

Listed: Dec. 2017

Sidney is 2 ½ years old and resides in Eastern Europe. Her current diagnoses include low weight at birth (3rd degree); Post-hemorrhagic hydrocephalus; VPA; Infantile cerebral palsy (spastic quadric paresis); Deafness in the left ear and highly reduced hearing in the right ear; Delay in the neuro-psychological development.

          Sidney is very active!  She moves around by turning or pushing herself. She does not have good leg support when placed in a walker. She reaches out to toys, grabs them and manipulates with them for long periods of time. She purposefully hits the toy on a hard surface.

          Sidney has a good emotional state. She initiates contact with adults and is happy when seeing familiar people enter the room. She pronounces continuous combinations of sounds.  Sidney falls asleep easily and her sleep is peaceful. The child is calm when bathed or dressed/undressed. She is fed by an adult, but she is picky!

        B/c we have her file for a short time, donations will not be accepted until a family is found for her.

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Jessie #

Girl: 2015

Jessie has been diagnosed with Microcephaly, Strabismus, Epilepsy and global developmental delay, but she is showing great progress.  She is a joyful, calm and positive  little girl who is growing up in a foster family in Eastern Europe.

Listed: December 2017

Whether she is meeting new people or at home, Jessie is calm and laughs easily. There is no unjustified anxiety. She expresses appropriate emotions in social contacts with other children and verbalizes positive emotions through sounds and syllables.

Jessie is a warm and cuddly little girl.  She knows how to charm other people and receives lots of attention. Jessie has some issues concerning her general motor skills, but she is showing great progress. She can move using a walker, but she is starting to take a few steps with support, too. She has tremendous power in her legs, and the specialists think she will soon start running around.

Jessie  is receiving support and interventions from specialists (therapist and psychologist) in the local community.

B/c we only have her file for a short time, donations will not be able to be accepted for her until a family is found.

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Margaret #

Girl: 2016

Diagnosis: Cerebral Palsy, epilepsy

Listed: December 2017

Margaret was born with some complications and has been diagnosed with Spastic Cerebral Palsy, Strabismus and Epilepsy. She had to receive help when eating, and she continues to use a G-tube at the moment when she eats.

Margaret is a warm and cuddly little girl. Almost 2-years-old, Margaret knows how to charm her caregivers, and she receives lots of attention. She is currently living in a baby home in Eastern Europe.

Margaret was born with some complications. She had to receive help when eating, and she continues to use a G-tube at the moment when she eats.

Music and musical toys make Margaret very happy, which she expresses by smiling and making baby sounds. Margaret has global delays and receives support and intervention from specialists in the orphanage.

 

B/c we only have her file for a short time, donations will not be able to be accepted until a family is found for her

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Sade #

 

Girl: 2013

Listed: July 2017

Sade has been diagnosed with Holoprosencephaly and is currently residing in a specialized facility where she received medical care and permanent rehabilitation services. Sade enjoys interacting with adults and will communicate with them by touching their face and laughing when they tease her.  She happily observes other children at play and displays a mostly calm personality.  It has been reported that, although her movements are stereotypical, she is staring to develop control over fine motor skills and her gross motor skills are improving as well. Sade needs a family that will nurture her and help her get the ongoing care that she needs.

 

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Liesl, Kurt, Brigitta and Louisa

4 Siblings

girl, born 2013 — mild mental delays

boy, born 2012 — alalia

girl, 2007 — alalia, She cannot talk

girl, born 2005 — moderate mental delay

They must be adopted together!

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

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Karen #

Girl: 2014
Listed: July 2017

Karen loves social interaction and receiving lots of love and attention.  She has several special needs conditions, which include CP, microcephaly, epilepsy and Strabismus. Despite these challenges, she is able to do many things.  She can crawl to get around and walk with assistance.  She also does well playing alone with toys and if one catches her attention she will spend a long time studying it and playing with it.  She especially enjoys noise maker toys.  Karen is non-verbal and her communication consists of syllabic patterns. She makes attempts to repeat different sounds and syllables.  She has no trouble bonding with her caretakers and does not have any issues with eating or sleeping.

 

B/c we only have her file for a short time, we will not be able to accept donations until a family is found for her

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Penelope

Girl, born 2013

Thoracic spina bifida with hydrocephalus
Congenital vertical talus deformity
Chronic tubulo-interstitial nephritis
mixed developmental disorder

Listed: June 2017

$112.50 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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May

Girl, 2 years old
Atrial Septal Defect, premature birth, delayed psychomotor development

Listed: May 2017

May was born prematurely and was faced with numerous surgical procedures, e.g. cardio surgical procedures and hernia repair. She has been diagnosed with loss in the intracardial and atrial septum. In 2014, she underwent a pulmonary banding and ligation of the arteries with success. Because Maya was born prematurely, she is delayed in psychomotor development. She attends rehabilitation programs and she receives numerous exercises to stimulate her development in all areas. The last psychological opinion made in 2015 indicated delays in psychomotor development, but it was stressed that she has spent most of her life in hospitals and was a premature baby. It is believed she will improve greatly both socially and physically if she is put in a stable and loving environment with more physical and social stimulation. It would be very helpful for her to be established in a family where she would receive more frequently extensive stimulation at home and with therapy. She stays at the child care facility where there are children with severe health problems, so the level of attention given to her is lower than recommended.

$49.50 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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Gianna

Girl, born 2015

congenital hydrocephalus
tetralogy of fallot
congenital malformation of pulmonary artery
patent ductus arteriosus
congenital cerebral cysts
congenital malformation of corpus callosum

Listed: May 2017

She had heart surgery done recently and she started to make huge progress right after it.

$1,263.10 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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Harlow

Girl, born 2013
PRC
Congenital retinal degeneration, developmental delays

Listed: April 2017

From the agency:  When the update came in, it was hard to read. But I powered through. Until I saw this:

Please describe his/her personalities in detail? No personality
No personality. No personality. I kept reading it over and over again. No personality. This cannot be so. Her referral, from two years ago, describes her as “giggles when she is touched; lovely when she smiles; enjoys that someone accompanies and plays with her.” Now, no personality.

In continuing to read the update, and comparing it to the two year old referral, it is pretty clear that Harlow has been forgotten. She does not go to school. She cannot perform any fine motor skills simply because she cannot see. She cannot perform most gross motor skills simply because she is given no chance to. She spends her days in her crib. Alone.

I am fairly certain that it should not read ‘no personality,’ but instead should read ‘no spirit,’ or ‘lost spirit,’ or ‘crushed spirit.’ It is not her personality that is lacking, but her spirit slipping away. She has been given up on by those around her, and has no other option but to give up on herself.

Harlow lives in dark, quiet solitude. No place for a child. She has lost hope. But we have not. We still see potential. We still see hope. And we will continue to share about Harlow until a family – HER family – sees it too.

The update is concluded with:

Anything else you think the family should know about this child? No
A response laden with hopelessness and doubt. A response lacking any type of love or compassion for this child. This soul whose spirit is in there somewhere, but if she stays where she is, will soon be gone forever.

$2,241.00 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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Gigi

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

Listed: Nov 2014

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!

Update 2017:  Gigi is able to walk on her own but cannot climb stairs.  She can sing children’s songs and count.   She needs assistance in taking care of her own needs (such as eating, dressing, toileting).  She can only repeat other people’s words.  She hasn’t had any hospitalizations or medical events.  She has never had seizures.  She is completely blind.

$1,118.80 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!

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Even if you can’t adopt,

you can be a guardian angel for an orphan with special needs!

The Guardian Angel Program is part of our Prayer Warrior Ministry. To find out more about being a Guardian Angel, please CLICK HERE

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Cecylia

girlsillouettenophotoGirl, born 2014

hypoxia, posible hydrocephalus.  Delay global development.  Probable Cerebal palsy;  minimal emotional contact

$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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SCARLET

guardianangelscarlett-2017-croppedGirl, born 2013 & Boy, born 2011

Scarlet:  Epilepsy, FAS.  She is severely handicapped

Rhett is healthy – Rhett has been adopted

VIDEO!  January 2017: Shareable video link: https://youtu.be/OyGhFHu_A0E

New pics January 2017!!  

$2,341.10 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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Kenzie

kenzie-2016Girl, born 2015

Thoracic spina bifida with hydrocephalus; Lumbar spina bifida with hydrocephalus; Sacral spina bifida with hydrocephalus
Congenital heart defect: atrial septal defect; other malformation of the tricuspid valve; heart failure

Look at that hair!  Adorable!

Precious baby girl!  What a gift to have her listed so young.

At the age of two days old, she was operated. Now the hole in her spinal column is closed, but she needs the second step, next surgery. Mentally she is developing normal, she can grab things, she does the baby talk, she makes eye contact, she cries very seldom.

She can not sit, she always lays in her crib. She is a good eater, she has some baby fat. Her caregivers say she is not a cry baby, and seems to be happy.  She was also previously listed as “Samantha.”

$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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Sloane

sloaneGirl, born 2014

spina bifida; hydrocephalus; congenital malformation of the central nervous system; congenital hip dislocation; convergent squint

Listed: July 26, 2016

$73.00 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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Eleanor

girlsillouettenophotoGirl, born December 2013

Distal urethral acidosis. Nephrocalcinosis. Hearing loss on both sides. Heart defect. Hypotrophy. Slightly delayed psychomotor development. Reduced muscle tension.

$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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Leelee

leeleeGirl, born 2014
Spina bifida

Listed: Sept 20, 2016

Leelee went directly to Family Orphanage from the hospital after birth. She was born with spina bifida in the sacral, without hydrocephalus, operated on the first day of life. Because of neurogenic bladder, she is systematic catheterized.

Leelee is very cheerful and open, easily makes contact with new people. Leelee willingly playing with dolls, cradled them, she takes in the stroller and swings them, loves also look books. Motor development girl is behind schedule. Currently Leelee already able to run, although there she imbalance. It comes and goes down the stairs holding the railing with both hands, climbs up on a chair and goes down with him.

Leelee uses single words, which include the names of familiar people, actions, and everyday objects.

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

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

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Leigha

LeighaGirl, born January 2014
CO-1
Shaken Baby Syndrome

 

Listed: Dec 23, 2015

$2,071.10 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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Rachel

Rachel_RKwebreadyGirl, born October 2012
PRC
Apert Syndrome

Listed: Oct 2014

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?

$41.40 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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Kimmy #

Girl, born 2013

This 4 years old girl has been diagnosed with PDD – Pyruvate dehydrogenase deficiency (PDD), Spastic quadriplegia with axial hypotonia, microcephaly and dismrphic facies. She has rehabilitation every day and is on a special Pyruvate dehydrogenase diet due to the PDD.

Listed: Dec 6, 2016

She is a little sweet girl with big brown eyes, white skin and auburn hair. She has small feet and such tiny legs.  She is very sociable and emotional child, who loves attention and loves the contact with adults and children. The staff reported that she grabs a toy with her right hand and holds it for a short time. She really loves to be tickled on the legs and laughs with voice. She can stay in a sitting position in chair alone.

UPDATE 2017:OLYMPUS DIGITAL CAMERA

Kimmy stands with the help of an adult.  She is relaxed, calm and laughs.  Kimmy pronounces different sounds with a melody and likes communicating with adults. She likes games and songs.  The family history of the child is that one sibling was diagnosed of a brain tumor and passed away and another died of pneumonia.  Kimmy has a delay in physical and psychomotor development and she requires special care.  Kimmy received a microcephaly diagnosis and the presence of metabolic encephalopathy was suspected.  She has also been diagnosed with infantile cerebral paralysis – spastic quadriparesis type.

 

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.

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Kitt

guardianangelkitt2-300x2952x Girl, born 2013

features of hypotrophy, dysmorphism face and hands, cataracts, circulatory system defect

kitt-197x3002x

Listed: Dec 7, 2016

 

Oh my, what a darling girl!

During holiday, Kitt has made good progress in the area of movement – and she’s learned to walk on his own.  Kitt understands instructions, complies with them, plays, and has her own ideas.  She is receiving early intervention.

$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!

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Gretel

gretel-221x3002xGirl, born 2015
FAS (Fetal alcohol syndrome)

Listed: Dec 7, 2016

Gretel does not crawl, she can turn onto her belly, goes to a kneeling position, on hands and knees, swings. Gretel is fed through a g-tube (surgery in February 2016), also takes a small amount of food or liquid with a teaspoon.

Gretel develops physically, has significantly improved eye contact; she is calm, serene, responds well to a massage, very fond of massage hands and feet, then reacts with laughter. Massage is a problem within the oral cavity and oral feeding. The girl does not like this, but the appropriate action (stimulation of chewing and swallowing) and quiet, slow feed, is making progress. She is now able to eat a small amount of mixed fruit or soup with a teaspoon.

Gretel begins to make sounds, they are not yet purposeful, the girl usually murmurs, laughs and cries.

$473.50 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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Maggie

Maggie (2)

Maggie (1)Girl, born September 2013
PRC
Cleft palate, repaired cleft lip, CHD (PDA), delays

Listed: Oct 2015

Maggie is a precious little one who has just turned 2. She arrived at the orphanage when she was about 6 months old; a frail and quiet baby girl. She was found to have a cleft lip and palate, CHD (PDA), and the ring finger and middle finger of her left hand fused. She had the lip surgery in 2014, but no palate surgery yet, to our knowledge. Her heart defect, Patent Ductus Arteriosus, is not at all uncommon. An x-ray of her hand showed mostly adhesion of the adjacent skin of the two fingers. Maggie has delays of both motor skills and speech. It is difficult to say if the delays are due to her known medical issues (plus unknown care for her first 6 months), or if there may be another cause. We do know Maggie needs help. She needs a family to love her unconditionally, and medical care plus therapies to help her reach her full potential. Maggie needs a family.

$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!

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Luisa

girlsillouettenophotoGirl, born June 2012

Global developmental delay. Very poor speech development. Neurodevelopmental disorders: cognitive, language, motor, emotional, observation towards the overall development of the disorder. The low level of visual perception. Decreased levels of auditory function. There is a disturbance in the field of small and large motor skills.

$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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Mira

girlsillouettenophotoGirl, born September 2014

After  birth she had respiratory failure, respiratory distress syndrome, underwent congenital pneumonia, jaundice, found intrauterine fetal infection, ASD II (congenital heart disease). Observation in the FAS. Cysts found in both compartments of the brain, anemia. Has recommended a neurological consultation. Reduced muscle tension. Good general condition.

$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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Mabel #

Girl: 2015

Listed: 2/2018

Diagnoses: Multiple congenital anomalies, not specified otherwise and affecting the skeleton (genetic testing: 46XX, normal female karyotype, normal test for micro-deletions); Multiple reduction defects – missing paroxysmal segments of the bottom extremities and radial beam of the right hand (missing right and hypoplastic left femur, anomaly of the right palm with one finger and phocomelia of the left hand, bilateral phocomelia of the bottom extremities, hemimelia of the right hand); Moderate external hydrocephalus – no surgical treatment necessary; Hypoplastic parenchymal organs and organs of the secretion system; Facial dysmorphism and hemangioma on the forehead; Moderate developmental delays.

Personality, development and abilities: Mabel’s motor skills are on target, with deficits only related to her defects of the skeleton. She likes listening to children’s songs and is curious about the activities going on around her. She is interested in toys and activities. She participates with interest and attention in activities related to music, speech, early childhood arts and constructive activities; When seeing a familiar person, she smiles and says simple words and sentences. Mabel is emotionally related (bonded) to certain members from the staff. She brightens when there are children around her. The child is emotional and happy when with a familiar adult. She laughs out loud when teased. She has emotional and social personality. Mabel seeks contacts with the other children and with adults using smiles, words and simple sentences. She recognizes people with whom she has interacted. Her speech development is at the level of pronouncing syllables, words and simple sentences. She understands the speech of others and can be persuaded with words. She has started orienting in time and space; she knows her routine. She focuses her attention on objects and actions that she is interested in.

Donations will not be accepted until a family is found for her

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Kaylyn

Girl: 2014

Listed: 2/2018

Special needs: symptomatic epilepsy-partial seizures with secondary generalization; spastic cerebral palsy; hypoxic-ischemic encephalopathy of 2nd degree; profound mental delay;

Kaylyn is in severely impaired condition and her development is delayed in all areas. She is completely dependent on adults’ care. Her sleep is calm and rhythmical. She is fed with a spoon by an adult.

 Donations will not be accepted until a family is found for her.

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Kahlia #

Girl: 2016

Diagnosis: Cerebral palsy; Spastic quadriparesis; Microcephaly Severe hydrocephaly; Severe mental retardation; Optic nerve atrophy

Kahlia lives in Eastern Europe and is 2 years old. She is completely dependent on the adult that cares for her. She doesn’t move on her own, feed herself, communicate or respond to communication. Kahlia has cerebral palsy, microcephaly, hydrocephaly, and severe vision problems. She doesn’t play with toys or hold them. She doesn’t have an attention span or focus on any one object. She is bottle fed.

Donations will not be accepted until a family is found for her.

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Elaine

elaine-300x2482xGirl, born Feb 2013

The girl moves crawling and pushing handles. She can independently sit. She learned to move around using a wheelchair (knows how to turn, go forward and backward). She passively stands – able to set and maintain the torso axis. Attempts to walk with walker.  She have muscle flaccidity and paralysis from the waist down. The child has no feeling in the lower extremities.

Listed: Nov 22, 2016

Elaine is a cheerful, lively emotionally, so her smile quickly gaining the sympathy of adults.

Strengths of girl is cheerful mood, rich facial expressions, varied emotional expression, gratitude, seeking contact with another person, the pursuit of overcoming obstacles.

$154.00 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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Hasini

Girl, born July 2012
PRC
malnutrition, developmental delay, oral deformity. ametropia and double strephenopodia

Hasini was wearing orthopedic shoes for rehabilitation as of the time her file was prepared. Hasini had a CT scan come back normal. There is a very good possibility that she has what is called Moebius Syndrome, which affects the muscles that control facial expressions and eye movements.
Hasini is described as gentle and quiet. From her outdated file: Hasini can sit stably for a long time now. She can use her left hand to go from lying down to sitting and can flexibly turn over. She likes to crawl backwards. When she is happy, she would grab the bed handrail to rock her body. She can clap and can grasp the toys attached to her bed. She can understand simple instructions. For example, if the caretaker asks her to put her hands down, she will do it. If tell her “we need to stand up,” she will give her hand to the adults because we have to help her up. She can make the “a” “e” “na” sounds. She falls asleep quickly. Hasini is afraid of strangers, but after some time, she gradually accepts the strangers. She likes playing with other kids.

A recent update states that she moved from foster care back to the orphanage recently. The update was not very positive, but Hasini has only been with them for a few months. The inability to make facial expressions may cause confusion for those who try to care and interact with her. Hasini needs a family who can see the beautiful little girl she is. Those with Moebius Syndrome do not smile with their mouths, but with their hearts. Will you be the lucky family who gets to see Hasini’s heart smile?

$11,013.30 has been donated towards the cost of my adoption!

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

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Jackie

guardianangel

Girl, born 2013jackie2-chac-e1460663796192
PRC
Anal atresia, congenital heart defect

Listed: Sept 15, 2015

Jackie will be turning two years old shortly. She was abandoned at a hospital when she was one day old. She was born with a hand deformity, anal atresia and a heart defect. Jackie received surgery for her anal atresia, but she doesn’t have bladder or bowel control yet and wears diapers. Jackie had surgery to correct her ventricular septal defect when she was one year old and has reportedly fully recovered, takes no heart medication and has no restrictions on her activities. Jackie also has deformities on her left hand. She is an active little girl who can crawl and say a few words. Her mental development is delayed in comparison to her peers. Jackie has a ready smile, likes to play with her toys and loves hugs. Could she be your daughter?

From an August 2016 update-Jackie’s mental development is normal on target. She is walking independently. Jackie is not potty trained yet. She’s wearing diaper. She pees and poops regularly.  She had surgery done for anal atresia, and it’s successful. Jackie has no need to follow up on her heart surgery as it was successful. No medication or further surgery needed. Her communication is normal. She can make simple communication with adults.  Jackie is gentle and quiet.

$491.50 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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Laina

girlsillouettenophotoGirl, born May 2014

Laina has delayed psychomotor development and hypertonia. She has significant hearing loss in her left ear, with almost no reaction; her right ear has normal hearing. Laina has slightly dysmorphic facial features. She has a congenital heart defect –Patent ductus arteriosus.
With these diagnoses, it’s possible that Laina has Down syndrome, although it’s not diagnosed in the information the agency currently has.

$1,025.00 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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Maddie

Maddie update 2015Girl, born March 2014
H-C

Listed: Jan 13, 2015

Update Feb 2018: Maddie is a sweet little girl who has developmental delays. She has not been diagnosed with anything particular, but she does appear to have cerebral palsy of some degree. She prefers to keep her head tilted to one side and tends to be very stiff, however she does great at tummy time and will lift her head up to look around. Maddie also loves to be held and can easily be soothed when you pick her up for some cuddles. Maddie does have a lot of muscle spasms, but we do not think this is seizure activity. She has started a muscle relaxer medicine which seems to be helping her a lot. Despite her delays, Maddie is very observant of her environment; she can often be seen looking at those around her and she has gotten good at tracking people and objects with her eyes. Maddie cannot yet sit up on her own, but when put in a crawling position, she will often move her legs forward like she is trying to crawl. She also bears weight on her legs when put in a standing position. She often is all smiles when she gets to have time in the stander. Maddie is an easy going baby, except sometimes at meal time when she does not want to eat, but she will gobble down anything that has peanut butter in it. She smiles so big when we sing songs and will make herself known if she doesn’t get to see the pictures when we are reading books. Maddie knows who her people are and prefers them over anyone else. She loves kisses and will instantly return the favor with a big smile. Sometimes when she really gets going she will let out a belly laugh that forces you to laugh as well.

$1,168.40 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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Nora

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

 

 

$111.25 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!

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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