Lexi

Girl, Age: 4
Country Code: LA-6
Region: Latin America
Primary Diagnosis: Deaf / HoH
Listed: Sep 2025
$0.00
has been donated towards the cost of my adoption!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
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Available to Large Families, Available to Single Fathers, Available to Single Mothers
Lexi is a bright-eyed 4-year-old girl with bilateral hearing loss and developmental delays, but these do not diminish her joyful spirit. Lexi communicates in her own unique ways and is curious about the world around her. Lexi will thrive in an environment where she receives consistent, patient attention and where her efforts to communicate are celebrated. She’s looking for a family who will provide a nurturing and stimulating home, eager to support her continued development and help her reach new milestones. With love and encouragement, Lexi has the potential to blossom and bring immense joy to her adoptive family.

Sebastian

Boy, Age: 4
Country Code: LA-6
Region: Latin America
Primary Diagnosis: Autism
Listed: Sep 2025
$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!
Inquire About This Child
Meet Sebastian, a delightful and active four-year-old-boy from a Caribbean island who is eagerly awaiting his forever family. Sebastian is a vibrant little explorer who loves to move! He’s remarkably coordinated, climbing stairs, and showing great dexterity as he twists and unscrews things. Sebastian is also a curious learner who enjoys imitating actions and is already showing a keen eye for color, happily sorting objects. He’s growing by leaps and bounds, blossoming into a bright and engaging individual who will bring so much joy to a loving home. Sebastian possesses a wonderful range of emotions, openly expressing his happiness and other feelings, and he’s beginning to form connections with those around him. He is ready to flourish in a supportive and nurturing adoptive family where his unique strengths can shine even brighter. Sebastian has been diagnosed with mild autism.

Rio

Boy, Age: 8
Country Code: LA-6
Region: Latin America
Primary Diagnosis: Down syndrome
Listed: Sep 2025
*** I am eligible for an additional $5,000 Grant from Reece’s Rainbow! Through 2025, children with Down syndrome ages 6-9 are eligible for a $5000 Older Child Grant! ***
$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!
Inquire About This Child
Rio is an 8-year-old boy from a Caribbean island who thrives on connection and enjoys interacting with others. Due to Rio’s diagnosis of Down Syndrome, he is delayed in his development, but he brings an innocent wonder and playful spirit to every interaction. Rio is looking for a forever family who will cherish his unique qualities and support his continued growth. He would flourish in a home where patience and understanding are a priority, and where he can continue to explore and learn at his own pace.

Deacon

Boy, Age: 8
Country Code: LA-6
Region: Latin America
Primary Diagnosis: Deaf / HoH, Limb differences
Club foot, hearing impaired, general delays, scoliosis
Listed: Jul 2024
$618.00
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
Deacon, born January 2017, is a cheerful and loving little boy, who is often smiling! He interacts well with both children and adults and likes to give and receive hugs and kisses. He enjoys all kinds of play, especially musical activities, and his favorite toys include balls, cars, and blocks. Due to the pandemic he is receiving educational instruction at the orphanage. When he was found at one month old, Deacon was admitted to the hospital immediately due to sepsis. While there he was diagnosed with left club foot, malformative syndrome, and possible spina bifida occulta due to a pit on his sacrum. He began weekly casting for his club foot, then received a tenotomy in April 2017, and wore a harness to keep his feet in correct position. However, he needed casting again in 2020, and then began AFO therapy. Later he was diagnosed with dorsolumbar scoliosis and moderate bilateral hearing loss. Deacon is reported to be moderately delayed for his age, but at four years old has achieved many milestones! He can kick a ball, and go up and down stairs while supervised by an adult. He is able to build with blocks, scribble, shape play-dough, and hold a glass and a spoon to feed himself. He can communicate basic needs through short phrase such as “give me water” and “let’s go” and is reported to speak well. When presented with a picture he can identify elements by name, and recognizes several body parts and animals.

Deacon has seen many specialists, but has not received a conclusive diagnosis tying together his needs yet; they feel the most likely diagnosis is Klippel-Feil syndrome or Jarcho-Levin syndrome, but have also considered arthrogryposis and mucopolysaccharidosis. He needs a family open to his orthopedic needs who will get him the care and treatment he needs as he continues to grow!

Trina

Girl, Age: 16
Country Code: LA-6
Region: Latin America
Primary Diagnosis: Other Special Needs
Sickle Cell Anemia
Listed: Mar 2021
$604.50
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!
Inquire About This Child
24 for 2024
Trina just glows with positivity! She likes to participate in the activities carried out in the institution, mainly those related to the creative arts such as painting and dancing, she likes to play with her peers and sometimes acts as a leader in social groups. In the psychological report, they describe the girl as responsible, obedient, dedicated, organized and friendly. Trina has a tendency to withdrawal and mild depression, due to the presence of feelings of insecurity, low self-worth and low self-esteem.

Trina also projects a strong need for belonging, parental protection and a strong desire for firm support, these aspects are explained by her life history and have been worked from different approaches by psychology, overall a calm state of mind is reported.

We know that an adoptive family can greatly help Trina feel valued and loved, and will help her improve in these areas with love, security, acceptance and healing.

Photo available from agency!

Trina has Sickle cell anemia, and she was medicated with folic acid. Sickle cell anemia is one of a group of disorders known as sickle cell disease. Sickle cell anemia is an inherited red blood cell disorder in which there aren’t enough healthy red blood cells to carry oxygen throughout your body. While there’s no cure for most people with sickle cell anemia, treatments can relieve pain and help prevent complications associated with the disease. Many people with this condition live very normal lives. Learn more about the illness and living with Sickle Cell by visiting Sickle Cell Speaks.

High altitude risk: The air at high altitudes, such as in an unpressurized airplane or in the mountains at altitudes greater than 5,000 ft (1,524 m), has less oxygen than at sea level. The lack of oxygen can cause cells to sickle which is painful and dangerous for a carrier. For that reason, it is not advisable to place a child for adoption with a family living at higher altitude / mountains.

AJ

Boy, Age: 8
Country Code: LA-6
Region: Latin America
Primary Diagnosis: Other Special Needs
Grade I Osteogenesis imperfecta, controlled asthma, controlled atopic dermatitis, right cryptorchidism (undescended testicle)
Listed: Mar 2021
$590.00
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
24 for 2024
AJ is a calm, loving, shy boy who came into the care when he was about a year old; he was found abandoned. He has favorably adapted to the institution where he is being cared for and he has made significant progress in his motor process.  The boy moves his upper and lower extremities, he can take his feet to his mouth, he crawls, and tries to stay standing with support. The report also states that AJ is a boy who explores the environment, he maintains attention and interacts with people, appropriately responding to the sensory stimuli that are presented to him. AJ likes children’s songs and dances imitating his peers, he likes colorful musical instrument toys.

Photo available from agency!

When the medical report was first performed when he was about one year old, AJ was not walking and a level of delay is reported in the cognitive, language and motor areas that are related to the state of severe malnutrition with which he was found as an infant.

His Grade I Osteogenesis Imperfecta is the mildest form of the condition. Osteogenesis imperfecta (OI) is a genetic disorder characterized by bones that break easily. OI is highly variable. Its signs and symptoms range from mild to severe. In addition to fractures (broken bones), people with OI sometimes have muscle weakness, loose joints (joint laxity), curvature of the spine (scoliosis), brittle teeth (dentinogenesis imperfecta), and hearing loss. A classification system dividing OI into several types is commonly used to help describe how severely a person is affected. Type I is the mildest and most common form of OI.