Joyana

Girl, Age: 3
Country Code: Asia.2
Region: Asia
Primary Diagnosis: Craniofacial disorder, Global developmental delays, Speech Delay
Motor Delay
Listed: Aug 2022
$1,025.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
MACC Availability 2023
Joyana’s favorite activities include playing on a yoga ball, hugging her ragdolls and playing with toys that light-up and make sounds. Joyana also likes nursery rhymes, with “A Mud Doll (Ni-Wa-Wa)” being her favorite! When she hears her caregivers sing Ni-Wa-Wa, she will sing along to the words ‘wa-wa’ and sway her body to the beat. Joyana is shy in new environments and around new people, but happily plays once she has warmed up to them. She has a close bond with her foster family and enjoys playtime with her 3 year old foster sister.

Joyana has cognitive, motor and speech developmental delays. Joy currently attends occupational therapy, and her caregivers hope she will start physical therapy soon. In the meantime her caregivers continue to work with her to practice and improve her muscle strength and endurance. At the time of this report, they were helping Joy learning to climb up and down stairs by herself! Joy has a surgical history of craniosynostosis surgery and polydactyly surgery (12/2020).

Can you imagine singing nursery rhymes with Joy as part of your nightly bedtime routine?

Michey #

Boy, Age: 10
Region: Eastern Europe
Primary Diagnosis: Congenital Heart Defect, Craniofacial disorder, Down syndrome
Internal hydrocephalus – post Ventriculoperitoneal shunt condition. heart condition – complete AVSD with partially closed chambers. Cleft palate -surgically corrected. Post bacterial meningitis condition – unspecified and acute pyelonephritis. Delays in all aspects of development.
Listed: Jun 2022
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers
Michey walks while holding one hand of an adult. He can take 2-3 steps independently, but is not yet walking independently. He can pull up and cruise along furniture and objects, and also crawls and scoots on his bottom very quickly to get where he wants to go. He has a very short attention span. He lived in an orphanage for the first 7+ years of his life and received very little intervention or opportunities to learn skills. He’s now living in a group home, where he’s receiving therapy and instruction in basic skills. He enjoys listening to music and playing outside on the swing.

Posie #

Girl, Age: 5
Region: Eastern Europe
Primary Diagnosis: Craniofacial disorder
cleft lip & palate, facial and skull dysmorphia, seizures, quadriparesis-weakness in all 4 extremities
Listed: Aug 2019
$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!
Inquire About This Child
Available to Large Families, Available to Older Parents, Available to Single Mothers, MACC Availability 2023

Evelyn #

Girl, Age: 9
Region: Eastern Europe
Primary Diagnosis: Craniofacial disorder
Congenital abnormality of skull and face bones; cerebral palsy. Spastic cerebral palsy; Partial epilepsy-takes medication
Listed: Oct 2019
$125.00
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!
Inquire About This Child
Available to Large Families, Available to Older Parents, Available to Single Mothers, MACC Availability 2023
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.

Brian #

Boy, Age: 8
Region: Eastern Europe
Primary Diagnosis: Craniofacial disorder
Congenital malformation syndromes predominantly affecting facial appearance. Foramen ovale persistens. Transient pulmonary hypertension. Pes equinovarus bilateralis. Severe delay in neuro-psychical development
Listed: Jul 2018
$25.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Inquire About This Child
Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers, MACC Availability 2023
Brian recognizes familiar adults and has formed an attachment to his favorite caregiver. He is uncomfortable around strangers. He is working with a physical therapist and a teacher on fine and gross motor skills. He can pick up toys and transfer them from hand to hand. His teacher reports that he understands what is being said to him and has recently begun responding to simple directions such as “give me”. He is able to sit unassisted and moves around in a baby walker.

Photos and videos are available through the agency.

Ashford #

Boy, Age: 8
Region: Eastern Europe
Primary Diagnosis: Craniofacial disorder
Microcephaly
Listed: Sep 2017
$1,005.00
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!
Inquire About This Child
Available to Large Families, Available to Older Parents, Available to Single Fathers, Available to Single Mothers, MACC Availability 2023
Ashford enjoys the presence of adults and emotionally expresses himself with laughter, crying and sounds. He laughs when tickled and smiles when he sees familiar faces. Ashford is unable to sit, stand, nor does he have head control. He prefers to be on his stomach. He does not have coordinated movement of his arms or legs and has little ability to hold a toy. Ashford’s diagnosis is Microcephaly. He was born prematurely and received intervention at the hospital at birth. Some history of convulsions, controlled with medication. Suspicion of left nasal atresia.

Nannette

Girl, Age: 15
Country Code: Asia.1: This country is currently not actively processing adoptions, due to COVID.
Region: Asia
Primary Diagnosis: Craniofacial disorder
Post-op congenital right cleft lip, right microphthalmia; scar hyperplasia post systemic inflammatorome. cicatricial alopecia; post inflammatory depigmentation macule; Malnutrition
Listed: Jan 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 ***
Available to Single Mothers
From her 2012 file- Nannette has normal body and intellectual development. At the age of 4 years, she can take care of herself, have a meal, go to toilet, read, and draw lines and scribble. She can walk and run. Nannette’s Language, personality and emotion development is delayed. She is introverted and not talkative. Usually when she communicates with adults, she can understand adults, but she responds less or responds in a low voice, we can’t hear clearly. When Nannette gets along with children, she is talkative and usually happy. In her diet, she has good appetite and good digestion; when it’s time for meal, she is anxious about, even loses her temper. In life, Nannette is an obedient child, and often willing to help the aunt to do something that she can do, such as putting away milk containers, taking diapers, picking up garbage and taking out the trash and so on. Now with her growing slowly, she can learn from imitating continuously, and learns more and more. Now she can draw lines and scribbles and sing children’s songs and so on.

Marielli

Girl, Age: 12
Country Code: Asia.1: This country is currently not actively processing adoptions, due to COVID.
Region: Asia
Primary Diagnosis: Craniofacial disorder
Post-operative cleft palate
Listed: Nov 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 ***
Available to Single Mothers
Beautiful Marielli has a contagious giggle. She loves to play with her foster mommy and giggles every time a toy block falls from her head. Like most toddlers, she wants to play the game on repeat. She shows how she wants to play again by grabbing her foster momma’s hand and motions to do it again. One of her favorite times of day is bath time! The sweet girl loves to splash and splash.

She is social, active and definitely not shy. She is often comforted by being held and snuggled when she is upset. Marielli was fortunate to be a part of Love Without Boundaries cleft exchange in 2012 and has had her cleft palate repaired already. Her file states that she congenital cleft palate (now repaired) and poor brain development. She is sure to be an absolute joy to a family. Who is ready to giggle and splash with Marielli?

An update received in the fall of 2015 states that Marielli is now living with a foster family. She is reported to be a healthy little girl who rarely gets sick. Compared to children of the same age, Marieli is still very delayed. She does crawl, stand, and walk with assistance. Marielli is cooperative with her caregivers, but rarely talks and says few well-pronounced words. She is happiest when her caregivers play with her, offer her toys, or hug her. Marielli has quite an appetite and eats a wide range of foods. There is a small hole in her palate, so some foods are difficult for her to eat. It is said that she is receiving rehabilitation training, but no details were given. Marielli has a fear of meeting strangers and her caregivers say she has an introverted personality.

Kraig

Boy, Age: 11
Country Code: Asia.1: This country is currently not actively processing adoptions, due to COVID.
Region: Asia
Primary Diagnosis: Craniofacial disorder, Down syndrome
Down Syndrome, congenital left cleft lip/cleft palate, and postoperative repair of congenital heart disease
Listed: Dec 2018
*** I am eligible for a $15,000 Older Child Grant! For more information or to inquire about this child, please email childinquiry@reecesrainbow.org ***
Available to Single Mothers
Kraig’s file was prepared in October 2016, when he was four. He is described as an introverted child who will also smile sweetly to his caregiver. He will play with other children, but cries loudly if they take his toys away. He likes an electronic keyboard and rubber ball toy, but will play with them less than five minutes.

Most recently, at the beginning of 2018, Kraig was at a foster home in a major city receiving medical treatment, but was recently recalled back to his orphanage due to new law in his country, in the Spring of 2018.

Jonie

Boy, Age: 11
Country Code: Asia.1: This country is currently not actively processing adoptions, due to COVID.
Region: Asia
Primary Diagnosis: Craniofacial disorder
Post-op cleft lip and palate; unsteady gait
Listed: Feb 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 ***
Available to Single Mothers
Jonie is diagnosed with post-op cleft lip and palate and an unsteady gait (she was not quite walking at the time her file was prepared). Jonie loves to be held and would talk non-stop whenever someone held her. In fact, if she wasn’t the first one held, she would cry loudly in her crib. Smart girl knew how to get someone’s attention! When learning how to stand, she would laugh happily. Her favorite thing to do is to play outside. Jonie loved watching the children swing and her eyes were full of curiosity. When in the playroom, she always looked for her favorite toys and would sometimes get upset when she didn’t get her favorite toy. A hug from the aunties cheered her up! In March 2013, she had her cleft lip and palate surgery. It took her a little time to warm back up once she came back from surgery, but it wasn’t long and she was walking around and talking a lot again. Jonie loves going on the swing- the higher she goes, the happier she will be, often not wanting to stop. Jonie is an active, clever, lively, and lovely child in need of a forever family!

Grace

Girl, Age: 13
Country Code: Asia.1: This country is currently not actively processing adoptions, due to COVID.
Region: Asia
Primary Diagnosis: Craniofacial disorder
Cleft lip and palate; congenital heart defect (post-op)
Listed: Apr 2013
$8,706.55
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!
Inquire About This Child
Available to Single Mothers
Sizable Grants $7,500+
Grace was abandoned by the train station when she was ten days old and has been living in an orphanage ever since. Grace was born with a cleft lip and palate, for which her first surgery will occur in May. She also had a congenital heart defect which was corrected this past summer. She does not take any cardiac medication but she sometimes pants and her lips become blue after strenuous exercise so her cardiac issues may not be fully resolved.

Grace is reported to have normal intelligence, potty trained, and she walks and runs just fine. She dresses herself, speaks in 3 – 5 word sentences, likes to sing and play games with other children.

Update from 2016: At 6 years old Grace enjoys looking at books, playing with her friends and has a favorite stuffed toy. She has great self help and fine motor skills, she can dress herself, including jacket and shoes, she can draw lines and shapes. She is an extroverted girl and she really enjoys playing games with her peers. She has many favorite foods, dumplings, noodles, fruit and many more. She had a surgery to repair her cleft lip already, but her cleft palate has not been repaired yet. She studies preschool, she can sing, dance, draw, string beads, and put clothes on dolls. Her upper limbs are flexible, she can walk and run, but not very steadily. She is active and gets along well with other kids, and often helps other younger kids.