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.

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.

$3,005.00 has been donated towards the cost of my adoption, including $505.00 from MACC 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!

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!

$1,808.42 has been donated towards the cost of my adoption, including $802.00 from MACC 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!

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 ***

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

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

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!!  

$6,846.52 has been donated towards the cost of my adoption, including $502.92 from MACC 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!

Girl, born 2016

HIV

 

$562.50 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!

Girl: 2016

Special Needs: Autism

Bethany is a sweet little 3-year-old from Bulgaria. She enjoys playing with her toys and will often imitate what the older children are doing. She also like to have close contact with other children and adults in her home. Bethany was diagnosed with autism and would need some special attention from her new family. Would you consider welcoming her into yours?

*** 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

Girl: 2014

Diagnosis: Congenital abnormality of skull and face bones; cerebral palsy. Spastic cerebral palsy; Partial epilepsy-takes medication

Evelyn crawls in order to get where she wants to go. She can stand with support and take steps to the side while holding on to something. She has spastic muscle tone. She picks up objects and transfers them from hand to hand. She does not talk. She responds positively to attention from adults.

*** 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

Girl, born 2019

Deletion from autosomes, unspecified
Patent ductus arteriosus
Other congenital malformations of cardiac chambers and connections,
Organic emotionally labile (asthenic) disorder

Listed: Oct 2019

$103.50 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!

Girl, born 2015

Microcephaly
Epilepsy, unspecified
Congenital malformation of optic disc
Optic atrophy
Astigmatism
Other ill-defined heart diseases
Mixed specific developmental disorders
Convergent concomitant strabismus

Listed: Oct 2019

$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!

Girl, born 2017

Spastic quadriplegic cerebral palsy

Other generalized epilepsy and epileptic syndromes

Listed: Sept 2019

 

$555.00 has been donated towards the cost of my adoption, including $500.10 from MACC 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!

Girl: 2017

Listed: Sep 2019
Diagnosis: non-obstructive hydrocephalus, Quadriparetic syndrome, delays in psycho-motor development

 

Stephanie rolls from back to stomach/stomach to back, crawls short distances mainly by pulling herself with her left arm, and sits with minimal support to her back. When placed in a walker, she can move it backwards with her legs. She will hold a toy that is handed to her, but once she drops it, she often doesn’t look for it. If she finds a toy in her space, she will grab it. She is making sounds and producing basic syllables. She laughs and smiles when caregivers interact with 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

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!

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 the agency does have videos of her they can share with inquiring 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.

$225.00 has been donated towards the cost of my adoption!

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

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

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.

.

*** 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

Girl, born 2013

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

Listed: Aug 2014

 

$9,035.68 has been donated towards the cost of my adoption, including $500.00 from MACC 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!

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!

Girl, born 2016

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!

$967.60 has been donated towards the cost of my adoption, including $548.00 from MACC 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!

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

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

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.

UPDATE NOV 2019:

Diagnosis: Acute lymphoblastic leukemia (actively receiving chemotherapy, which will be needed until 2021). Cerebral palsy – spastic diplegia; Gastroesophageal reflux disease, Convergent concomitant strabismus (wears corrective glasses); Delay in neuro-psychic development

 

Pippy is receiving chemotherapy for Leukemia. She was diagnosed in March 2017 and immediately began treatment. She lives in an isolation room at the orphanage to reduce her exposure to sickness. She is considered in remission, but is required to continue to take daily medication. She has a port, weekly blood draws (to adjust medications), and monthly appointments with an oncologist. Pippy also has CP that results in increased muscle tone in all 4 limbs, primarily impacting her legs. She can grab and hold a toy with her left hand. She can manipulate toys by picking up, dropping, pulling a string, picking up ring toys. She understands basic cause and effect, such as knowing to pull a string on a toy to activate the toy. She explores toys with interest. She pronounces several words and can follow basic commands. She enjoys the attention of caregivers.

 

A detailed medical report that outlines her Leukemia treatment, other medical history, and her development are available, along with photos and videos of Pippy. Due to her cancer diagnosis, any interested family would need to provide proof of medical insurance coverage that would adequately cover Pippy’s cancer treatment immediately upon taking custody of her. Her birth country will also require a detailed care plan showing the family has the appropriate resources and support to provide the required medical care for Pippy once home.

*** 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

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

$1,096.00 has been donated towards the cost of my adoption, including $1006.00 from MACC 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!

Girl, born 2016

Tuberous sclerosis
Generalized idiopathic epilepsy and epileptic syndromes

Listed: Dec 2018

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

$1,085.65 has been donated towards the cost of my adoption, including $500.65 from MACC 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!

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

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!

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!

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

Girl, born 2014

HIVrenal 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

$1,641.98 has been donated towards the cost of my adoption, including $500.00 from MACC 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!

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 ***

Girl, born March 2014
H-C

Listed: Jan 13, 2015

Update August 2019: Maddie is such a sweet girl with an easy going personality. She has spastic cerebral palsy and microcephaly. Maddie prefers to keep her head tilted to one side, but has made a lot of progress in her ability to move it to look the other way. She tends to be very stiff but 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 takes a muscle relaxer medicine which seems to help 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 on her own, but can sit supported on a chair or a bench with a little help in the right places. She attends therapy three days a week for stretching, exercises, and stander time. Sometimes she loves it and sometimes she hates it. Maddie is an easy going girl, 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.

In December 2018 Maddie got a g-tube. She still eats blended food by mouth the same as she used to, but we use her g-tube to ensure she gets enough liquids and consumes all of her medicine. By mouth she has trouble swallowing thin liquids. Maddie is a petite girl, but has had a good growth spurt in the last year.

Although Maddie does not talk, she knows how to communicate. She will smile when happy and will cry to alert discomfort or hunger. She has been working hard in school to learn so many things. Maddie can read and spell almost any one syllable word and her name. Every single week last year she came home from school with a 5/5 on her spelling test. She knows opposites, what happened next, and basic addition and subtraction as well. To show off these skills she uses magnetic letters on a magnetic board and will choose the next letter with her hand. Maddie also likes to use her yes/no board for simple questions and being able to be given choices like what movie she wants to watch that day. Maddie is so smart. With access to more communication devices she will tell great stories.

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.

$3,024.70 has been donated towards the cost of my adoption, including $505.00 from MACC 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!


 

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