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 146, Combined Locks, WI  54113

“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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Sierra

Girl, born 2015

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

Listed: Feb 2018

$1,012.50 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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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.

Listed: Feb 2018

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.

Jan 2019 update: Eden has started moving around the home with purpose more independently.  She is now able to climb up 3 flights of stairs while holding onto the rail for support.  She is also able to come down the stairs, also holding onto the rail for support.  Eden has always been quite the acrobat and has now learned to climb on the sofa in the home and will stand while holding onto the back and jump and giggle.  She has also learned to find a low hanging disc swing in the home and climb on it.  She loves the swing and will vocalize sweet sounds as she enjoys the motion.  Eden continues to work with her guide cane and still needs encouraging and prompting to use the guide cane throughout the day.  She takes daily walks down the street with her teacher. She mostly enjoys the walks, unless she is tired, then she cries to be picked up and comforted.  Eden continues to wear her processors allowing her to hear and she often responds to the sounds of toys falling on the floor, familiar voices, and music.   She does require frequent prompting to complete activities in her classes.  Eden also continues to demonstrate some aversions to a lot of textures. This is addressed in the home through a lot of opportunity for sensory play.  She enjoys having lotion rubbed on her, sensory brush actives and water play.

$2,251.50 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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Addison

Girl, born 2014
PRC
Epilepsy, delays

Listed: January 2018

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!

$1,006.42 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!

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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.

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

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

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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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SCARLET

guardianangelscarlett-2017-croppedGirl, born 2013

Scarlet:  Epilepsy, FAS.  She is severely handicapped

Scarlet was originally listed with her brother, Rhett.  Rhett has been adopted.

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

New pics January 2017!!  

$6,343.60 has been donated towards the cost of my adoption!

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

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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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Minerva

Girl, born 2016
PRC
premature infant with very low birth weight, hydrocephalus (post-op shunt)

Listed: August 2019

When Minerva came she looked petite and weak, and was hospitalized for care and surgery. She has delayed physical development compared with children of her age, but after the operation her physical health is fairly stable and her motor ability improves day by day.  She is able to raise her head when lying on stomach, and turn over continuously. She likes to roll over to and fro on the mat best.  She is able to sit alone for a moment with both hands against the floor, even occasionally stand for a few seconds with both hands grasping the rail. Her muscular tension is higher, she can not coordinate and control her body well. If her name is called or someone talks beside her ear she is able to turn around her head to locate the source following the sound direction. The muscular tension of her neck has decreased obviously, therefore its turning range is much larger.

If you move a toy with bright colors slowly in front of her eyes she will follow the toy visually. She is able to grasp a toy and shake it to and fro with her hands.  She is an introverted and quiet baby, is able to lie alone for some time without noisy crying, but if she is made to practice sitting with her hands against the floor she will be very reluctant and cry aloud. Her crying is very loud and we can hear it from far away. She also likes to be cuddled by someone and her facial expressions and actions will be much richer while she is cuddled.  Her speech development is delayed. She is a light sleeper.

$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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Nelly

Girl: 2018

Listed: 8/2019

Special Needs: adrenogenital disorders, congenital anomalies, anemia, small weight at birth, chromosomal anomaly, syndactyly, developmental delays

We don’t know a lot about sweet Nelly yet, but we do have some videos of her we can share with families. Nelly can crawl and can do so well. She loves scooting her way to toys she finds interesting. Nelly can sit up on her own. She enjoys attention and will sometimes interact with other children.

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Annie

Girl 2016

Special Need: spina bifida (surgically corrected), anemia, minor delays, potential autism.

Meet sweet little Annie! Annie loves to laugh, give hugs and kisses, and play with her toys. She is living with a foster family who she is very affectionate towards. Annie talks and walks well. She can hold a cup and drink from it. She recently was tested for childhood autism and the results pointed toward this diagnosis. Behavioral therapy was recommended. We have videos of Annie to show potential families.

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Posie #

Girl: 2017
Diagnosis: cleft lip & palate, facial and skull dysmorphia, seizures, quadriparesis-weakness in all 4 extremities

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

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

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Chrissie #

Girl: 2016

Listed: 05/2019

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

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

More photos and videos are available through the agency.

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

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

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Ivey #

Ivey
Birthday 2015

Listed: May 2019
Diagnosis: Turner Syndrome

 

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

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

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

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

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Molly May #

Molly May

Birthday: 2015

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

 

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

 

Photos and videos are available through the agency.

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

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

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Graciella

Girl, born 2015

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

$967.90 has been donated towards the cost of my adoption!

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

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Nora

Girl, born 2013

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

Listed: Aug 2014

 

$8,535.68 has been donated towards the cost of my adoption!

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

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Wendy

Girl, born 2017
PRC
Neonatal brain injury, hypothyroidism, rickets

Two year old Wendy is close with her caretakers and likes being held by them. Her file states that she has sharp reaction to outside stimulation such as sound source and visually following objects. She likes being teased, giggling, and can turn over onto her stomach. Her file indicates that she communicates her emotions by facial expression and reacts to being called.

$10.00 has been donated towards the cost of my adoption!

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

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Cassandra + 2 Sisters

Girl, born 2016

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

Listed: Feb 2019

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

$166.50 has been donated towards the cost of my adoption!

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

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India

Girl, born 2014

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

She can walk by herself and understands simple instructions.

$4.95 has been donated towards the cost of my adoption!

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

 

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Shay #

Girl: 2013 – age 5

Listed: Jan 2019

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


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

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

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

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Sabrina

Girl, born 2016

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

Listed: Jan 2019

$10.00 has been donated towards the cost of my adoption!

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

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Sally #

Girl: 2016; age 2

Listed: Jan 2019

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

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

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

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

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Pippy #

Girl: 2013

Special needs: Cerebral Palsy, Leukemia, strabismus

Listed: Jan 2019

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

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

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

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

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

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KENNA

Girl, born 2017

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

Listed: Dec 2018

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

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

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Dena

Girl, born 2016

Tuberous sclerosis
Generalized idiopathic epilepsy and epileptic syndromes

Listed: Dec 2018

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

$585.00 has been donated towards the cost of my adoption!

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

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Mila #

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

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

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

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

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Lisa #

Age: 2
Diagnosis: Cerebral palsy; Microcephaly; Symptomatic epilepsy; Developmental delay

Listed: July 2018

Lisa is a happy and sociable little girl. She enjoys meeting new people and interacts with them appropriately. She responds to her name and verbalizes using sounds and syllables. She follows basic directions. Her motor skills are developing. Videos of Lisa show her playing with a ball and manipulating it appropriately. She currently moves around by crawling. She can take steps when holding 2 hands of an adult and can also move using a walker. She is receiving therapy to help develop her motor skills.
Photos and videos are available through the agency

 

Donations will not be accepted until a family is found for Lisa!

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Becky #

Girl: 2015
Special needs: spina bifida; hydrocephalus, condition after VP shunt; convergent concomitant strabismus

Listed: May 2018

Becky is a calm child, with positive emotional tone. She is able to demonstrate various reactions of content and discontent. She smiles when spoken to and laughs out loud when jested. Becky recognizes her caregivers and calls them by their names. She is sociable and loves being around adults and other children in her group. A significant increase of words in the child’s passive and active vocabulary has been observed in recent months. The number of words she can pronounce is constantly increasing. She understands adults’ speech. Becky answers questions appropriately. She initiates verbal interaction on her own and performs simple instructions. Becky enjoys playing with toys and she can play continuously with them. She plays with toys in accordance with their purpose. Becky is not a picky eater. She has good appetite and is gaining weight. Her sleep is calm.

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

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

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Joely

Girl, born Sept 2013

oculo-auriculo-vertebral (OAV) syndrome (known as Goldenhar syndrome)

South Asia – Pacific

Listed: May 2018

Joely is full of energy and vibrancy. Joely was born with a cleft palate, a deformed/missing right ear, a small meningocele (soft fluid filled mass) at the back of her head, and Congenital Heart Disease – Atrial Septal Defect (ASD). In February of 2014, Joely was diagnosed by the genetics doctor with Oculo Auriculo Vertebral Spectrum. In 2017, she had an operation to repair her cleft palate; however, there are still two small holes in her palate which will need to be repaired again. Her surgeons have stated that her meningocele would need an operation in the future, but that it is not urgent. Her doctor recommends continual regular monitoring and checkups with a pediatric cardiologist, but does not see the need for surgery at this point. She shows no signs of heart problems at this time. Joely is fit and active and does not tire easily.

Because of Joely’s delays, she currently has weekly occupational and speech therapy as per recommendations. She really enjoys her sessions. Despite her wide range of medical concerns, Joely is really thriving. She started attending the local nursery school this year and is adapting well. Her teachers are very fond of her and she holds her own in a class of her peers. Although she is talking, her speech is delayed and she is often difficult to understand, especially for strangers. Her house parents understand her well. Joely is more than capable of making her needs and wants known using a combination of words with facial and hand gestures. She is independent and likes to do things by herself if she can, but will willingly accept help when needed. She follows her daily routine well. She has become more affectionate over the last 6 months and enjoys all the activities at the child caring agency, especially singing in the nightly devotions. Despite the holes in her palate, Joely is a good eater and enjoys all kinds of foods. She has friends within the center but can be a little rough with younger children. She does well with older children, as she models their behavior. She can be boisterous at times, but she has shown a much higher level of self-control since she started nursery school. Joely will continue to develop and catch up with the consistency and love of a forever family who have good medical resources and therapists at hand.

*Photos and video are available for seriously interested families. Joely is from a small Asian country. Per her country’s regulations, pictures and videos can only be shared with seriously interested families directly and are not allowed to be shared publicly. Joely’s file is listed with multiple agencies with a sending program from this country and approval is dependent on the head of adoption in this particular country.

There is a $500 agency grant for Joely’s adoption with a specific agency.

$1,000.10 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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Olivia

Girl, born 2013
PRC
Microphthalmia, delays

Listed: March 2018

Olivia is an energetic, smiley, and beautiful little girl who likes listening to music and playing outside. She is especially close to her caregivers and loves to be cuddled and tickled by them. Olivia is diagnosed as having microphthalmia, which means that both of her eyes are very small and underdeveloped. She also has very low muscle tone. She is able to stand with support, but she can’t walk yet. Her caregivers have been working with her, but she still struggles to move independently. She can sit up for about 30 minutes, but she gets tired and often needs support. She knows her name, responds when called, and can follow simple instructions. She can make sounds like “ah,” but doesn’t say any words. She gets excited when her caregivers tell her it’s snack time or time to go play! Olivia has some feeding issues. She mainly eats soft foods like mashed vegetables. She has a hard time swallowing and needs food chopped up for her. She really likes to hold her bottle herself. Olivia is in a school program in her orphanage during the week days and lives with a foster family on the orphanage grounds the remainder of the time. Olivia is making progress, but what she needs most is a family who can provide her with love and therapies that are simply not available in her orphanage!

Olivia has a $500 agency grant, with her current adoption agency. Olivia needs a family with an approved home study to be able to hold her file or move forward with adopting her.

$1,458.70 has been donated towards the cost of my adoption!

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

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Raven

Girl, born 2017

hydrocephalus
Peripheral chorioretinal dystrophy of retina

Listed: March 16, 2018

 

update: she just had a shunt put in – 2018!

Paperwork should be ready in a couple of

months!

$1,282.89 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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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.

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

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

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DeeDee

Girl, born 2014

HIV
renal hypoplasia – unilateral
spastic diplegic cerebral palsy

DeeDee has such beautiful eyes!

 

Updated Jan 2018:  Deedee has a brother born in 2013, do not know his special needs yet.

Listed: December 2017

$1,141.98 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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Jozy, Rowan and Reisen

rowan-reisenjozyGirl, born 2013
HIV

boy, born 2008
mental delays

boy, born 2010
mental delays

Listed: Jan 26, 2017

The dynamic duo – here come Rowan and Reisen. Their smile can light up a room and they are certain to win you over with their little boy charm. Both love cars and chocolate. Rowan has been hosted before last summer; Reisen just recently arrived at the orphanage. Both boys have some developmental delays, but are teacher’s favorites. Rowan has grown leaps and bounds since he was last hosted in the US, in every way possible.

Rowan: Loves cars, Happy & Playful, Speech delays; Reisen: Outoging lil bro, Artistic explorer, Friendly

From Dec 2016:
They appeared to be very hyper, having serious behavioral issues and mental delays. They changed families during hosting program because first hosting family couldn’t handle them.

Their sister can be adopted separately from them but adoptive family needs to have approval for three children in order for us to be able to separate them. She lives in a different orphanage from them.

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

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Maddie

Girl, 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.

Maddie update 2015

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.

$2,514.70 has been donated towards the cost of my adoption!

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

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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