It is our true belief that there is a “forever family” for each of our waiting orphans with special needs.

The purpose of Reece’s Rainbow is to raise funds as adoption grants, to help potential adoptive families with the high cost of giving these children the life they so richly deserve.Your donations and advocacy turn the child on the left into the child on the right! This page includes the profiles of those children with larger grant funds available.

Put on your WARRIOR shoes and help us find families! PLEASE SHARE THIS PAGE, that others will see it and take that leap of faith to save a child in need.

Melissa

Girl, Age: 13
Country Code: LA-3
Primary Diagnosis: Genetic Condition (non-DS)
Cornelia de lange syndrome
Listed: Jul 2019
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
$4,242.10
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!
Melissa is an extremely loving girl!  She enjoys playing with her dolls.  Although she likes all food, she loves chicken and rice.

Melissa has a diagnosis of Cornelia de Lange syndrome, which causes developmental delays.  She continues to make progress with therapy.

Melissa was previously listed on Reece’s Rainbow as “Lucia.”

Natasha

Girl, Age: 6
Cerebral Palsy, Epilepsy
Listed: Jan 2024
$4,268.00
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!
Natasha is a pretty little girl, with very calm with big eyes and beautiful white teeth. She is very special. She doesn’t smile at everyone. She must first know you, and trust you, but her smile is fascinating. She loves to drink juice and she likes to eat sweets. She really likes music. She likes to be pampered by her foster family and only cries if she needs a little attention.

In therapy, she works on ways to improve her functional mobility, and increase the functional use of her arms. At school, she does a lot of sensory activities to work on ways to respond and communicate better and fixate her eyes on objects to learn.

Goliath

Boy, Age: 6
Microcephaly, CP, epilepsy, blind
Listed: Dec 2023
$2,786.14
has been donated towards the cost of my adoption, including $0.00 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!
Goliath is the cutest, most chill baby ever! He loves cuddles, being bounced on the trampoline, swimming, going for bike rides, being held, and chocolate. He would do great either in a big family with lots of siblings or being the only one to soak up all the attention!

He is a great eater with either blended or soft foods, but not great at drinking liquids. He has a lot of small seizures throughout the day, but is on the max amount of seizure medication that can be found consistently in his country.

In school and therapy he does a lot of sensory activities and is working on using his arms for purposeful movement. He has a stander that he likes to use while playing his toy piano. He doesn’t have an advanced way to communicate yet as he is blind and doesn’t have much purposeful movement but he does let us know when he is happy, mad, or would like something. He mostly only gets fussy sometimes at night time when he wants to be rocked to sleep, when he has to take baths, or when he thinks his food is too spicy.

Christian

Boy, Age: 6
Cerebral Palsy, history of Epilepsy, possible visual impairment
Listed: Dec 2023
$2,648.00
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!
Christian is a handsome boy, calm and very adorable with his beautiful smile. He often falls asleep. He is sensitive to noise. He jumps and cries when he is picked up to change position. Nevertheless, he likes to listen to music, he likes to be rocked and he likes when people communicate with him.

At school, he progresses slowly with his sensory exercises which he likes and are helping him to stay awake longer than before. In therapy, he works on functional mobility, which helps him raise his hand to touch an object. He has consistently shown slight improvement in engagement with increased stimuli. He is responding more to toys and people by raising his head, laughing, smiling, and keeping his eyes open.

Woodrow

Boy, Age: 11
Primary Diagnosis: Blind / VI, Cerebral palsy
Microcephaly, Cerebral palsy, Optic Nerve Atrophy
Listed: Sep 2023
$2,648.50
has been donated towards the cost of my adoption, including $0.00 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!
Woodrow can sit up independently and will sometimes kneel as well. He occasionally bears weight on his feet, but cannot put his feet completely flat and because his ankles are so tight. He would need surgery before being able to do so. Woodrow doesn’t really scoot or crawl, but he can still make his way across a room by rolling and wiggling.

Woodrow loves to eat and gets quite upset if meal time is late. He doesn’t self feed, but eats pureed food by mouth. It can be a messy affair, but he is quite satisfied when he is done. Woodrow drinks some with a sippy cup or water bottle, but also likes to drink from a regular cup if he is feeling particularly thirsty.

Woodrow is not a fan of bath time and tends to move around a lot as he tries to keep his caregiver from bathing him, particularly his face and head. He is very picky about people touching his head – sometimes he likes a good head massage and other times he will duck away from anyone who tries to touch his head at all. He also does not like anyone touching his face, especially to try and wipe it off after a meal or to brush his teeth. The one exception he sometimes makes is for his caregiver to kiss his cheeks and neck, which he occasionally greets with a big smile.

In the past, Woodrow would often cry and thrash inconsolably for long periods at a time no matter what his caregivers tried. Some changes with medications have helped him drastically. He still does not sleep on a regular schedule, but if he’s awake during the night, he is generally calm, sometimes quiet and sometimes “talking” with his little noises.

Woodrow really likes his feet and will often clap them together. He also uses his feet to protect his head which he hits repeatedly for sensory input. Woodrow does not do a lot of purposeful movement with his hands, but often wrings them.

Woodrow goes to physical therapy and attends a special education class every day. He likes to be pushed around in his wheelchair and enjoys going in the swing.

Woodrow is a ticklish guy and will often reward tickles with a smile. While he is not generally a cuddler, he sometimes enjoys being held and cuddled and will lean in to relax.

Progress with Woodrow has been slow, but he is learning and responding. We continue to pray that he would know that he is safe, loved and treasured. We also pray that a brave and bold family would step forward to pursue his adoption. He is worth it.

Thea #

Girl, Age: 4
Primary Diagnosis: Global developmental delays
Microcephaly
Listed: Aug 2023
$3,150.93
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!
A female child with a proven genetic neurodegenerative disease – pyruvate dehydrogenase deficiency (identified homozygous for mutation p.R446* (c.1291C>T).  She was born from the 15th pregnancy, 12th birth. On the second day after birth, transferred to the intensive care unit due to hyperexcitability, hypertonus of the limbs, with convulsive equivalents. With evidence of respiratory distress syndrome and metabolic acidosis. Held oxygen therapy for 5 days. A delay in the NPR was found, mainly in the motor development, with axial hypotonia and hypertonia of the limbs, combined with lactatemia. Submitted material for genetic testing and metabolic screening. Abdominal ultrasound: Pyelectasis (mild) of the left kidney. with microcephaly, developmental delay, tonus changes, elevated lactate and proven pyruvate dehydrogenase deficiency (identified homozygous for mutation p.R446* (c.1291C>T). At the age of 1, a severe delays in the NPR with quadripyramidal syndrome and microcephaly was formed.

Currently, the child has no apparent epileptic seizures, and the EEG shows no epileptiform changes. Remedial nutrition with KetoCal is recommended; reduction of carbohydrate intake. A new hospitalization is forthcoming to start a ketogenic diet with KetoCal.

Mahleah

Girl, Age: 16
Country Code: SE.Asia.2
Region: South Asia
Primary Diagnosis: Older Child, Other Special Needs
$3,270.56
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!
Maleah is a medically healthy, active, tall and athletic beautiful teen girl!  More than anything she wants to be part of a family, and is open to both a two parent family as well as a single Mom.  Maleah has overcome much hardship and adversity in her past and needs a strong, committed family who is well-versed in trauma.  Maleah adores younger children and would benefit greatly from cousins or younger friends in the community!  Agency staff has met and spent time with Maleah and were immediately struck with the incredible potential this young woman has, if only given the opportunity!  Maleah will turn 16 in October 2025, making her ineligible for international adoption to the US at the time.  Her family must be ready and willing to race to her in time!

Mina

Girl, Age: 8
Country Code: LA-2
Developmental delays/malnutrition; Arthrogryposis; Osteogenesis Imperfecta; Bilateral club feet; Congenital Glaucoma
Listed: Mar 2023
$2,702.50
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!
Mina is a beautiful little girl who likes to paint and play “sleepover” with her friends. Mina likes to go to the park and put together puzzles. She also loves to sing and listen to music of all genres, especially tango. Mina enjoys children’s stories and watching her favorite cartoons, which include Masha and the Bear, Puss in Boots, and Blue Shortcuts. Contact the agency to learn more about Mina and her listed medical needs!

The agency staff met lovely Mina in August 2024. She was very talkative and outgoing. She doesn’t allow her special needs to limit her. Mina, born in November of 2016, knows how to start and maintain a conversation. She is very observant and knows how to ask questions and engage in it and the context. She uses very sophisticated words for a seven year old – it was impressive!! She knows how to count in English from one to ten, knows some colors in English, and knows the colors in Spanish. She has a great memory and can remember facts. Mina can easily express her thoughts and ideas.

Mina likes to paint and play “sleepovers” with her friends. Mina likes to go to the park, put together puzzles. She also loves to sing, listen to music of all genres, especially tango. Mina enjoys children’s stories and watching her favorite cartoons (Masha and the Bear, Puss in Boots, Blue Shortcuts).

VIDEOS:
https://vimeo.com/maaspecialkids/maa-mina
https://vimeo.com/maaspecialkids/maa-mina2
https://vimeo.com/maaspecialkids/maa-mina3
https://vimeo.com/maaspecialkids/maa-mina4
https://vimeo.com/maaspecialkids/maa-mina5
https://vimeo.com/maaspecialkids/maa-mina6
https://vimeo.com/maaspecialkids/maa-mina7
https://vimeo.com/maaspecialkids/maa-mina8
https://vimeo.com/maaspecialkids/maa-mina9
Password: Adoptmaa

Mina also has a $500 agency fee reduction, with a specific adoption agency.

Zoey

Girl, Age: 7
Country Code: Africa-1
Region: Africa
Developmental Delay, Post-stroke
Listed: Jan 2023
$3,632.50
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!
Zoey is one of the most beautiful little girls you’ll ever meet. She was born with some developmental delays, but then experienced a stroke when she was two and a half. This greatly set back her abilities. However, since then she’s been in a foster family where she’s relearned how to sit, roll, and grasp toys. She is working on self-feeding and becoming verbal again. Although Zoey had a seizure with her stroke she hasn’t had one since, and rarely requires medical care now. However, she may benefit from a better neurologist to understand her brain’s unique functions and abilities. Zoey is not short of opinions and will let you know exactly how she is feeling with tears or laughter! She loves to play and her giggle is absolutely infectious. She loves playing with water, musical instruments, and anything that makes noise. Zoey also loves to eat and isn’t picky at all! She is a social girl who has loved having two foster brothers. Zoey will bring an abundance of joy to any family who chooses to love her forever!

Janice

Girl, Age: 7
Country Code: Asia.2
Region: Asia
Moderate Cognitive and Motor Delays
Listed: Aug 2022
$2,877.00
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!

Janice enjoys outdoor activities, especially riding her tricycle, sliding down the slide in the neighborhood park and bouncing around a basketball.  When she isn’t participating in a physical activity, Janice likes reading books and singing nursery rhymes with “Twinkle, Twinkle, Little Star,” and “The Butterflies are so Beautiful” being her favorites!

Janice is shy around strangers, but interacts with them once she becomes familiar. Janice acts affectionately towards people she is familiar with and asks for cuddles. Janice has a close bond with her foster family and likes to seek their affection.

Janice has a Cerebral Palsy diagnosis with moderate cognitive and motor skills delays.  She currently attends physical, occupational and speech therapies. Janice has made good progress, and she is now able to climb stairs, jump on the ground 10 times in a row, and complete a 4 piece puzzle! At home, Janice will imitate her foster mother’s speech and ask questions.

Could you imagine pushing Janice on the swings at your neighborhood park or teaching her how to ride a bicycle?   If you think you could be the right family for her, don’t hesitate to reach out

Salvador

Boy, Age: 6
Country Code: LA-2
Primary Diagnosis: Blind / VI
Norrie’s disease; neurodevelopmental delays; blind
Listed: Jul 2022
$2,675.34
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!
Agency staff met sweet Salvador in July of 2022. Salvador receives physical, occupational, and language therapy weekly. He is doing well with advances in development. He walks, jumps, and climbs the stands. He combines words, counts numbers from 1 to 20, and says about 25 words. Salvador can feed himself with help. Contact the adoption agency to learn more about this sweet boy!

VIDEOS:

https://vimeo.com/maaspecialkids/maa-salvador1
https://vimeo.com/maaspecialkids/maa-salvador2
https://vimeo.com/maaspecialkids/maa-salvador3
https://vimeo.com/maaspecialkids/maa-salvador4
https://vimeo.com/maaspecialkids/maa-salvador5
https://vimeo.com/maaspecialkids/maa-salvador6
https://vimeo.com/maaspecialkids/maa-salvador7
https://vimeo.com/maaspecialkids/maa-salvador8
https://vimeo.com/maaspecialkids/maa-salvador9

Password: Adoptmaa

Sadie #

Girl, Age: 6
Primary Diagnosis: Other Special Needs
Progressive ossifying fibrodysplasia
Listed: May 2022
$2,777.00
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!
Sadie has limited movement in her neck, back and hands/arms (due to limited movement of the shoulders). She has more range of motion in her left arm vs her right. She compensates for her limited mobility. She stands on her toes to reach objects (when she cannot extend her arms) and holds on to a support to bend down or she seeks assistance from an adult. She walks, plays with toys, and interacts with her environment. She can put together wooden puzzles, stack rings and perform other basic tasks. She can take the cap off a pen and tries to draw shapes. She interacts with familiar people. She initiates games such as peek-a-boo. She will point to things she wants to communicate her wants/needs. She dances along to music. She can say some simple single syllable words such as ma-ma, but mostly communicates with gestures. She lived in a home with a younger child for a while and did well with the younger child. The foster family limits her interactions with other people, because they are afraid she will get hurt, due to her physical limitations. She plays well with other people, when she is around them. She does not go to preschool due to the fear her foster family has that she will be injured. She shows a preference to certain objects and TV shows (Peppa Pig and Masha the Bear).

Videos from May 2022 show Sadie walking, playing with toys, putting a puzzle together and interacting with adults. The videos show Sadie’s physical limitations.

Augustus #

Boy, Age: 7
Primary Diagnosis: Cerebral palsy, Hydrocephalus
Internal hydrocephalus: state after implantation of a VP-shunt; epilepsy; spastic quadriparesis; cortical blindness; delay in the neuro-psychic development
Listed: May 2022
$2,631.50
has been donated towards the cost of my adoption, including $0.00 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!
Augustus was born full term, and was found that he has internal hydrocephalus; at the age of 4 months a liquid drainage valve system was implanted. The child lies in bed; he has spasticity in his limbs and his active and passive movements are limited. He depends completely on the care provided by adults. He receives kinesiotherapy. The child is subject to observation by a neurologist and by a neuro-surgeon.

The child’s lower and upper limbs are highly spastic and are with diffuse muscle hypotonia. His fine motor skills are not developed. He does not grasp a toy given to him. Atanas holds his hands bent in fists. He is seriously delayed in his psychomotor development. The boy reacts to tactile stimulation by adults. When teased, he does not smile. He is unable to interact with the other children. Atanas depends completely on the care provided by adults. He is fed by a bottle. From time to time he cries when given a shower. He sleeps well.

Kellet

Boy, Age: 10
Country Code: Asia.2
Region: Asia
Primary Diagnosis: Sensitive Special Need
Listed: May 2022
$2,780.99
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!
Introducing Kellet! Kellet is a medically healthy 6-year-old boy who is active and very curious about new people and environments. He likes playing with younger children and is able to interact and share toys with peers. Kellet likes adventures and challenges and takes initiative to play with others. He has age-appropriate gross and fine motor skills; he can pour water without spilling, draw meaningful pictures, run and climb stairs without rails for support, throw and catch a ball, and much more! He also has good verbal expressions and age-appropriate language development. He can count from 1 to over 100! Kellet can also engage in back-and-forth conversation and tell a story by looking at pictures. He sleeps deeply at night and eats the same food as adults for three meals a day. We hear that Kellet has good focus at school and can follow class progress and teachers’ instructions.

Update May 2022:

Kellet was seen as a part of virtual SuperKids in February 2022.  Kellet recently turned 7!  Kellet is in first grade and his favorite subject is Math!  He is doing well in school and enjoys his friend group.  His social worker shares that she is impressed by his patience and involvement with activities during their time together.

Kellet shows his imagination through art and storytelling as he recently drew a picture for his best friend, who is a mermaid and lives in the sea!  Kellet expressed a desire to also be a mermaid, so he can be with her all the time!  How sweet is that?!  Kellet enjoys imaginary play through dress up with peers and enjoys playing with Legos.  Kellet is enthusiastic about life, playing games, and has a high level of attentiveness.  He lives in an area where he is able to hike and run in the outdoors- activities that he appears to enjoy!

Kellet has foster siblings.  When they are available, Kellet enjoys spending time with them.

Tristan

Boy, Age: 14
Country Code: EE-2
Primary Diagnosis: Other Special Needs
Listed: May 2021
$2,822.34
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!
He lives at the orphanage since 2016. Normal weight and height parameters. Psychomotor development is normal. He is the victim of parental physical abuse and suffers from post-traumatic past. He is under the care of psychiatrist and take medication. No medical diagnoses in his chart, but trauma. You could tell that he is emotionally somewhat fragile.

He is communicative, talkative and charming boy. Positive relationship with peers and adults. His teachers describe him as very good, active and independent student. The computer class, math and English are his favorite subjects. He loves to play soccer, card games and chess. He has a lot of potentials and wants to be adopted. He is highly recommended by his caregivers. The family with an involved, hands-on father will be ideal for this boy. He would do really well as the youngest or only child (or in a family where the other children are grown). He needs an experienced adoptive family who can give him a lot of one-on-one attention and help build his trust in humanity back.

Taylor

Girl, Age: 10
Country Code: Asia.4
Region: Asia
Beta-thalassemia trait; ADD; low average intelligence
Listed: Sep 2021
$3,531.00
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!
Taylor was born to a mother who tested positive for Anthetamine and Methanthetamine at the time of her birth. She did not experience any type of withdrawal symptoms. The birth mother also smoked throughout pregnancy. Taylor was placed into government care due to her birth mother’s drug use.

When she was 4 years old, she was placed with a local family for the purpose of adoption. She lived with that family for 17 months. The family chose not to finalize the adoption. Taylor was placed in an emergency foster placement for 7 months and then moved into a permanent foster home, where she currently resides.

The previous foster family described her as “a happy and outgoing child who has a very good memory”. Her current foster parents describe her as “talkative, happy and polite”. She seeks out interactions with others. She can play alone appropriately, but prefers to play with other people. She is willing to share her toys. Her gross and fine motor skills are at the appropriate developmental level for her age. She talks in complete sentences and can answer questions and follow verbal instructions. She is diagnosed with ADD and has difficulty staying focused on activities, especially when required to sit still for longer periods of time. She will also “push the boundaries” to see what she can get away with. If she does not get her way, she will throw a “tantrum” to see if the adult will give in.

She is showing signs of the effects of the placement transitions that she has experienced in her young life. She often asks for permission to do even the smallest things. She worries that she is in trouble. The foster family reports that she says she wants to be good. She is seeing a clinical psychologist, who has begun preparing her for a permanent adoption placement. Interest families should be knowledgeable of the effects of trauma and disruption or be willing to obtain continual education on the topic during the adoption process.

Leon

Boy, Age: 11
Country Code: LA-2
Primary Diagnosis: Down syndrome
Listed: Dec 2020
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
Leon loves to play games with his peers. He also loves riding on his toy motorcycle. He loves to see motorcycles and hear motorcycles when he goes on his walks outside. He loves to watch the cars go by on the streets too. Leon also likes to paint, especially with his hands. He likes to drum along to music. Leon is ready to share his big heart with a forever family!

Jesse #

Boy, Age: 12
Primary Diagnosis: Cerebral palsy, Hydrocephalus
Jesse has Moderate external hydrocephalus; Arachnoid cyst – cortical atrophy; Infantile cerebral palsy – spastic quadric paresis; Hypotrophy; Delays in the neuro-psychological development; Severe mental delay.
Listed: Jun 2015
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Update November 2015: He demonstrates interest in musical and mechanical toys. He will play for a short time – studies a toy, puts it in the mouth, transfers it from one hand to the other. He likes activities involving music. He recognizes familiar areas of the orphanage and understands his daily routine related to familiar tasks such as eating. He is very happy when interacting with familiar adults.

Update 2018:  Jesse attention span is short-lived and unstable in relation to objects and people. There is some sharing with a close adult.  Jesse responds when called by name.  His memory and speech are poorly developed. When happy, he laughs loud and when anxious, he cries. Sometimes he pronounces unspecified sounds and separate syllables. He is sensitive and emotional and tends to be nervous around strangers.  When given a toy he reaches out and takes it. He is working on the pinch grip. He hasn’t mastered fully the ability to move a toy from one hand to the other. Jesse is fed with a spoon and sleeps calmly through the night.  He cannot control his physiological needs.  Jesse is entirely cared for by the team in his orphanage.

(Jesse was also previously listed as Andy)

Posie #

Girl, Age: 7
Primary Diagnosis: Craniofacial disorder
cleft lip & palate, facial and skull dysmorphia, seizures, quadriparesis-weakness in all 4 extremities
Listed: Aug 2019
$2,500.85
has been donated towards the cost of my adoption!

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

Molly May #

Girl, Age: 10
Primary Diagnosis: Genetic Condition (non-DS)
Trisomy 7; cleft lip & palate; Cerebral Palsy
Listed: May 2019
$4,195.10
has been donated towards the cost of my adoption, including $0.00 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!
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.

David #

Boy, Age: 9
Primary Diagnosis: Cerebral palsy
cerebral palsy; quadriparesis ; epilepsy; Bronchial asthma; delays in all aspects of development
Listed: Feb 2020
$2,857.50
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!
David was declared clinically dead at birth and resuscitated. He currently lives in a group home. He reaches for hanging objects and can hold a toy for brief periods of time. He is very responsive to caregivers. He smiles and shows pleasure when spoken to. He tracts objects and tries to focus on people who are talking to him and objects being presented to him. He rolls from his back to stomach in his bed.

Bria

Girl, Age: 13
Country Code: LA-2
Primary Diagnosis: Down syndrome
Down syndrome and strabismus
Listed: Jul 2019
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
Our sweet Bria, born in August of 2012,  finds joy in connecting with nature. Dancing allows her to express herself freely, while walking to the local farm brings a sense of peace. Bria’s laughter is infectious, spreading joy and warmth to those around her. Bria’s comfort in both observing and participating in play activities suggests a personality that values both independence and social interaction. She willingly engages with others, regardless of age. Bria shows affection spontaneously and reciprocates when it is given to her, which suggests that she is capable of forming healthy relationships and bonds with others.

Bria may not be able to speak with words, but her actions speak volumes. Her gestures and expressions convey her emotions and needs in a way that her caretakers understand. Her ability to dress herself independently shows her determination and self-sufficiency. Bria may communicate differently than others, but her message is clear: she is capable, strong, and deserving of love.

When faced with unfamiliar faces, Bria can feel overwhelmed and anxious. She may struggle to trust new people. It is important for those around her to be patient and understanding, allowing her the time and space she needs to feel comfortable and secure in new environments. With time and support, Bria may learn to develop stronger social skills. We think she is truly a special person to know!

NEW VIDEO:

NEW VIDEOS:
https://vimeo.com/maaspecialkids/maa-briaupdate
https://vimeo.com/maaspecialkids/maa-briaupdate2
https://vimeo.com/maaspecialkids/maa-briaupdate3
https://vimeo.com/maaspecialkids/maa-briaupdate4
https://vimeo.com/maaspecialkids/maa-briaupdate5
https://vimeo.com/maaspecialkids/maa-briaupdate6

Password: Adoptmaa

Bria has a $2,500 agency grant for her adoption with the agency who listed her; additional agency grants may also be possible.

Bennett

Boy, Age: 12
Primary Diagnosis: Hydrocephalus
Listed: Aug 2019
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Bennett is a very social child. Whenever he sees his friends, he eagerly greets them with a smile, a hug, and a “Happy Birthday!” He had hydrocephalus as an infant that was treated with a VP shunt. The shunt was later removed but he still has macrocephaly. He does have a history of seizures which are very well controlled by medication. He receives physical therapy twice a week and has made tremendous progress over the past several years.

He is fully mobile, can feed himself, and go to the bathroom independently. Bennett wears a helmet to protect his head. He has become fond of his helmet though because he can show off his headstand. You will often find him enjoying jumping on the trampoline, playing on the playground or going on a walk. He needs redirection often because he is always on the move. Although he is generally happy, he can get frustrated when people do not do what he wants to do or if he is being asked to do something he is not ready for.

Bennett’s favorite part of school is circle time because he likes to sing songs and answer ALL the questions even if his answer has nothing to do with what was asked. He understands and speaks English as well as his native language. He is known for reciting the four seasons in English quite well. At home, he loves to ask other people to dance and sing with him too. Bennett loves to make people smile!

Simon

Boy, Age: 10
Country Code: SE.Asia.Pac
Region: South Asia
Primary Diagnosis: Cerebral palsy
spastic quadriplegic cerebral palsy, seizures, mild hearing loss
Listed: Sep 2019
$2,660.30
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!
September 2023 UPDATE: Simon has updated pictures (at the agency). He has grown up a lot and is using a wheelchair. His write-up states: Simon was diagnosed with cerebral palsy, spastic quadriplegic, and global developmental delay. Despite his condition, he is an active child and has progressed in his mobility through the help of his therapy sessions to her improve his mobility and muscle strength. Simon is enrolled in physical, occupational, and speech therapy sessions. He picks up toy shapes and transfers them from one container to the other in a slow way due to his spasticity. He responds through facial expressions and communicates by pointing to what he wants on his communication board. He understands and follows simple instructions such as take your face towel and wipe your mouth, “up here”, or “high five.” Simon has a good appetite every mealtime but sometimes needs more time as he stocks the food in his mouth before chewing and swallowing if he does not like the food. Due to Simon’s special needs, his child caring agency believes that the prospective adoptive parents will need to show him full support and close supervision since he requires extra care, understanding, and love. He will need to continue therapies and will require special education. He likes to be around many children and would be open to larger families. Simon is unlikely to live independently; However, with the love and care of a family, he would thrive and could live a full life with his family’s support. His agency believes he will make a wonderful addition to a family and will be a much-loved son!
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Simon is a very sweet little boy who currently lives with several older girls and is the last remaining “baby” in his home. He cannot speak, but does communicate through facial expressions and some noises.

A traveling family met Simon and said, “Within the three days we spent at the orphanage, we were able to bond with him to the point he would smile and get excited when he saw us. The older girls told us he can understand what they say to him. He enjoys being held and carried around, but spends most of his day sitting in a baby walker or high chair. He seems very easy going, as we didn’t see him complain about being put in his crib for nap time, etc. The caregivers are working on his motor skills. He can eat with assistance and enjoyed the ice cream we brought! It’s so easy to fall in love with this little boy! We are praying his family sees him soon!”

Simon has spastic quadriplegic cerebral palsy and has had seizures. He takes 30 mg of Phenobarbital once a day. Simon has mild hearing loss of the left ear. Therapy has helped lessen the spasm and Simon can open and close his hands. Simon loves being around people and making faces! When praying before meals, he bows down his head and says “ahh” when everyone says “Amen.” We’re hoping a wonderful loving family comes forward for this special little boy! There is a $500 agency grant for Simon’s adoption with his adoption agency.

Summer

Girl, Age: 13
Country Code: EE-7
Primary Diagnosis: Other Special Needs
FAS and mixed development disorder, premature birth
Listed: Feb 2016
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Summer is quiet, friendly and always smiles when she is seen by an adult. She almost eats without help – but she eats slowly. She almost goes up and down the stairway by herself. She does not want to always participate in all activities and needs extra motivation. She expresses her feelings with mimics and movements. She has started to speak and pronounces some words. Summer loves music, reading, books and swinging on the horse.

She wants adult’s attention and likes to lean on an adult, sit in their lap, and give hugs. Her fine and gross motors skills development are adequate. She is friendly with adults and children.

Lena

Girl, Age: 10
Country Code: EE-7
Primary Diagnosis: Down syndrome
Listed: Oct 2020
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
$2,697.24
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!
This little girl with Down syndrome is described as brave, loving and interested in activities. She adapts well to a new environment and enjoys coloring, painting, musical activities, singing and playing with toys and dolls. She is developmentally delayed and needs a loving family to help her reach her full potential.

Anthony

Boy, Age: 15
Country Code: Africa-1
Region: Africa
Primary Diagnosis: Cerebral palsy
Cerebral Palsy, Microcephaly, Epilepsy, Left Hemiplegia/Visual Impairment
Listed: Jul 2020
$2,696.50
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!
This update and new photos were added in October 2022.

Anthony has been waiting for a family for a long time. Despite his Cerebral Palsy and Epilepsy he loves to get out of his wheelchair and stretch out on the floor or bed. He is good at moving himself into silly positions, often falling asleep in the funniest ones! Anthony’s favorite toys are those with lights. He loves all colors of lights and often finds them around the room during school. He also enjoys music or being outdoors. Anthony enjoys having people he knows near him, and will often find them and initiate affection with his hand or head.

Anthony has the best smile, but only shows it when he’s truly happy. This might be while he’s being tickled or comforted, during a favorite song, or while feeling the breeze on his face. He has many ways of communicating, such as laughing, crying, and making lots of facial expressions. Anthony is not one to hide how he feels! Anthony would benefit from a family who can care for all his needs, especially as he grows bigger. He’ll bring a sense of love and joy to any household!