Bianca #

Girl, Age: 3
Syndrome of congenital anomalies with predominantly facial. Microphthalmi Abnormalities of the thoracic vertebrae. She is missing her left eye ball and right ear.
Listed: Jul 2024
$769.00
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!
Bianca was recently transferred from a large orphanage to a small group home. She’s been making developmental progress in her new home. She can pull to a stand in her crib and cruise along the rail. She will take steps when holding the hands of a caregiver. She reaches for toys and will hold and explore them.

Esta, Sophie and Luke

Sibling Group
Ages: 12, 7, 6
Country Code: LA-7
Listed: Jun 2024
$808.00
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!
Esta, Sophie and Luke are waiting for a family in Latin America.

Esta is an affectionate child who loves dance, judo, art and making bracelets. She has a strong bond with her siblings and relates well with her caregivers and peers. She is clinically healthy with good physical and motor development.

Sophie shows leadership skills even at her young age when playing with others. She also participates in judo, ballet and other workshops. She also likes to participate in tours to exhibits, the cinema and theater. he also exhibits a strong bond with her siblings and is well-adapted at the institution she lives in.

Luke is an active little boy who loves to play ball. He is bonded with his siblings and interacts well with those at the institution.

The children have experienced trauma in their past and will need to continue to receive counseling to help through the transition to an adoptive family and to continue to work through their past. They are doing well though as they receive services in country. Esta received corrective surgery for a cleft palate and Luke has myopia and strabismus for which he receives care. Aside from her trauma care, Sara has no known needs. All of the children follow the Christian faith.

Phineas

Boy, Age: 4
Country Code: E-11
Region: Europe
Polymalformative syndrome, with craniofacial dysmorphia; suspicion of Goldenhar Syndrome; Hydrocephaly; upper airway malformation with tracheostomy since 10/4/2021. Currently with cannula. Epilepsy. Gastrostomy. Sensory-neuro deafness – uses hearing aids.
Listed: Mar 2024
$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!
Phineas was previously listed as Phil — he is a sweet boy who was born with a polymalformative syndrome. His condition comes with needs that set him apart, and he was placed in care early on.

Phineas uses a wheelchair in his daily life. He also spends time in a standing frame. He enjoys smiling at people and laughing. Phineas enjoys sensory experiences with tactile or auditory input. He enjoys listening to a maraca or touching a soft stuffed animal.

Marcy

Girl, Age: 6
Country Code: EE-2
Primary Diagnosis: Craniofacial disorder, Deaf / HoH
Listed: Nov 2023
$45.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Marcy is a 4 year old girl with frontal craniostenosis and tuberous sclerosis. Marcy was diagnosed with conductive and sensorineural deafness. Non-orbidity of both eyes. The girl currently does not use corrective glasses, as recommended by ophthalmologists. She is generally cheerful, and is able to imitate gestures and independently eat meals. She struggles with dressing herself and identifying some shapes and colors. Marcy is able to respond to simple commands and messages. She enjoys playing with toys and demonstrates improvement in her coordination. She is very patient and kind. It is recommended for her to wear glasses. Her speech development is delayed, but she can still communicate, and she has demonstrated improvement. Above all she is a nice girl with very many good qualities.

Wayne #

Boy, Age: 8
Repaired cleft lip and palate; mild cognitive delays; speech delays
Listed: Feb 2022
$31.50
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!
Update on development: He enjoys engaging with others in play and initiates communicating. His vocabulary has greatly improved. He continues to learn new words.  He understands instructions and has good active concentration for about 20 minutes. During walks in the park, he enjoys explaining to others what he sees. If he is unable to articulate the words, he uses gestures in a way that can be understood by everyone. He is interested in animals, cars and many different kinds of toys. He is content playing on his own. He very quickly understands how to carry out more complex tasks. He shows a lot of initiative. He has settled in very well to the kindergarten he attends. He is completely independent in self-care to the extent that when he returns home he helps himself to snacks and drinks.

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!

Evelyn #

Girl, Age: 11
Primary Diagnosis: Craniofacial disorder
Congenital abnormality of skull and face bones; cerebral palsy. Spastic cerebral palsy; Partial epilepsy-takes medication
Listed: Oct 2019
$1,490.00
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!
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: 10
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
$2,116.62
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!
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: 10
Primary Diagnosis: Craniofacial disorder
Microcephaly
Listed: Sep 2017
$1,610.00
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!
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.