Adrena

Girl, Age: 16
Country Code: LA-2
Primary Diagnosis: Older Child, Trauma History
Listed: Dec 2024
**** I am eligible for a $500 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 ***
Adrena, who is now 15, came into care with her older sister when it was discovered that she and her sister were being abused in their home. Her sister is now aged-out of the system and while they stayed in touch initially, unfortunately they do not know her current whereabouts. While Adrena is clinically healthy, she has a lot of trauma in her past and will need at least counseling when she joins a new family to help her work through her past and transition into the new family and life.

This report is two years old, from when Adrena was 13; she is now at risk for aging out, as she is 15 years old.
Adrena is starting 9th grade. She is one of the best students of her class. The teachers have stated that Adrena is known for being responsible, respectful, helpful, kind, and always willing to learn new things. She feels comfortable being the leader of a group of peers within the academic environment. She is an independent girl who fulfill her daily routines without any help or supervision. Adrena takes good care of her personal belongings and has great hygiene habits. Whenever a task is difficult for her, she keeps trying and does her best to finish it. She can stay focused on one task and does not like to leave anything unfinished. Adrena recognizes authority figures, and she is respectful and obedient towards them.

There are no concerns regarding Adrena’s motor, language, cognitive and social development. She loves to give and receive affection from people who are emotionally close to her. Adrena gets shy when meeting people, and she usually waits until someone else takes the initiative to start a conversation. It is hard for her to express her feelings and emotions to people she is not familiar with. She interacts positively with adults, peers, younger children, and animals, but has stated that she prefers to interact with peers and not so much with younger children. Adrena is able to handle her emotions, frustrations and impulses in an age-appropriate manner. According to the foster mother, she is usually happy, does not get mad easily and is not anxious. Adrena has stated that she is afraid of being placed with her biological father again. When asked what her ideal family would be, she said one with a mom, dad, older sister and a dog of her own.

Adrena loves to spend time outside playing sports, especially soccer and volleyball. She likes to eat out, and while she doesn’t have a favorite food, she likes to try new things. She also likes to paint, do arts and crafts, and listen to hip-hop music. Adrena wants to go to college even though she does not yet have a clear idea of what area/subject she likes the best.

Kyle #

Boy, Age: 9
Primary Diagnosis: Hydrocephalus
Microcephaly. External hydrocephalus. Delay in neuropsychological development. Moderate mental delays. Suspicion for Seckel’s syndrome
Listed: Dec 2024
$180.00
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!

Evan #

Boy, Age: 11
Primary Diagnosis: Cerebral palsy, Limb differences
Spastic cerebral palsy, severe. Moderate mental delay. Congenital malformations of the foot
Listed: Dec 2024
**** 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 ***

Hans

Boy, Age: 6
Country Code: LA-2
Hydrocephalus; Epilepsy; Cerebral palsy; Macrocephaly, hip dislocation; gastrostomy
Listed: Nov 2024
$41.20
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!
Information in this report is from November 2024

Hans was born to a young teenage girl who, tragically, had already given birth to a child at a very young age. Due to her chronological age and emotional immaturity the mother was not able to fully understand her responsibility, and despite the support of her family, the bond between Hans and his mother was not positive. After Protection Services became involved, it was evident that the biological mother and her family were not able to take care of the child due to his special needs, economic struggles and already caring for Hans’s older sibling. He, therefore, came into care at the age of 3 years old. There is no information about the biological father.

Hans is not enrolled in school due to his medical diagnoses. Hans loves to receive affection, and he responds through smiles. He is totally dependent on others to fulfill his daily routines. He communicates through guttural sounds, screams or by crying. Hans cries whenever his diaper is dirty. Hans´s gross and fine motor skills are not developed. The child cannot hold his head up, and he cannot crawl or walk. He has some body movements, and the foster mother has received training on how to stimulate his motor development. He does not like to be held and prefers when people change his body position without holding him for too long. Due to Hans’s medical diagnosis, he has a severe cognitive delay and is not able to interact with other children. Hans receives occupational, physical and speech therapy. Hans takes daily medication.

Hans likes to listen to soft music. He needs a family who can always take care of him due to the severity of his condition.

Everly

Girl, Age: 3
Country Code: LA-2
Primary Diagnosis: Global developmental delays
High neurological risk, Encephalopathy, Hypoxic ischemic, Diffuse atrophy by neuroimaging, Global neurodevelopmental delay, Hypotonia, Movement disorder, Swallowing disorder, Strabismus, Moderate acute malnutrition
Listed: Nov 2024
$198.00
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!

Everly is an adorable little girl with a bright smile. Everly was born prematurely, and has several special needs. She loves bath time. She also loves affection. Everly is continuing to grow and develop. We hope a loving family sees her while she is so young.

Elsa

Girl, Age: 12
Country Code: E-11
Region: Europe
Primary Diagnosis: ADHD, Learning Disability
attention deficit/Academic school disorder
Listed: Nov 2024
$2,191.00
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!
This lovely older girl has an ADHD/ learning disability diagnosis.  She could do great with a family to help her with her schoolwork!

Eloise

Girl, Age: 2
Congenital right clubfoot, Spina Bifida, Hydrocephalus- ventriculoperitoneal shunt, Congenital bilateral hip dislocation – hip reduction plus harness
Listed: Nov 2024
$135.00
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!
Eloise is a joyful, affectionate, and calm child, who enjoys the simple pleasures of life such as music, dancing, and storytelling. Her sunny disposition radiates through her interactions, whether she’s playing freely in the park, lying peacefully on the grass, or engaging with her peers. Despite any initial nervousness around new people, her warm and gentle demeanor quickly puts others at ease, leading to the formation of close emotional bonds, particularly with her foster mother.

Eloise’s ability to communicate her needs and emotions through gestures and sounds demonstrates her keen self-awareness, and her empathetic nature is evident when she comforts her loved ones. Though faced with medical challenges, Eloise has proven to be remarkably resilient.

VIDEOS:
https://vimeo.com/maaspecialkids/maa-eloise01
https://vimeo.com/maaspecialkids/maa-eloise02
https://vimeo.com/maaspecialkids/maa-eloise03
https://vimeo.com/maaspecialkids/maa-eloise04
https://vimeo.com/maaspecialkids/maa-eloise05
https://vimeo.com/maaspecialkids/maa-eloise06

Password:  Adoptmaa

Agency fee reductions may be available based on the adoptive family’s circumstances.

Katy

Girl, Age: 5
Country Code: LA-3
Primary Diagnosis: Other Special Needs
Mucopolysaccharidosis syndrome type IV, and mild cognitive scoliosis
Listed: Nov 2024
$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!
Katy is a very intelligent and curious girl.  She loves going to the pool on sunny days.  Her favorite foods are soup and smoothies.

Martin & Rafael

Sibling Group
Ages: 10, 7
Country Code: LA-3
Primary Diagnosis: Learning Disability
developmental delays
Listed: Nov 2024
$1,018.00
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!
Martin was born in 2018; he is a curious and playful kid.  He likes playing outside and loves to eat hot dogs and to drink fresh juice.  Martin has mild developmental delays and attends a regular school.

 

Older brother Rafael (born in 2014), likes being outside and jumping on the trampoline.  He loves chicken, rice, and cake.  Rafael has developmental delays and is currently attending a special education school.

Valeria

Girl, Age: 14
Country Code: LA-3
microcephaly, epilepsy
Listed: Nov 2024
**** 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 ***
Valeria is a very protective girl.  She loves drawing and doing art projects.  Valeria currently has a feeding tube.

Update in 2025 states that she no longer has a feeding tube, and is doing really well!

Valeria was previously listed on Reece’s Rainbow as Marisol.

Steven

Boy, Age: 15
Country Code: LA-3
Primary Diagnosis: Blind / VI
Blind in one eye, autism
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 ***
Steven is receiving therapy to help him develop his communication and interpersonal skills. He loves to swim, swing, and play with his special stuffed animals. He loves chicken noodle soup, plantains, and anything sweet.

The adoption agency has more detailed information on this child that they can share with potential families.

Steven was previously listed on Reece’s Rainbow as James.

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.”

Cheyenne

Girl, Age: 13
Country Code: LA-2
Mild cognitive delay
Listed: Nov 2024
**** 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 ***

Information in this report is from March 2024

Cheyenne, 12, came into care in 2020 when her mother left her with a woman and it became clear that she was not returning. In the child investigation, it was discovered that Cheyenne had been the victim of abuse by both a non-family member when she was young and a minor relative though there is not much information regarding the later situation. Due to being moved around so much and the chaotic environment of the biological family, Cheyenne was not consistently enrolled in school which has affected her cognitive development.  Cheyenne is now enrolled in school, and she is in 4th grade where she is respectful, responsible, and motivated at school. In 2023, she was given an IQ test and scored 63, which led to a diagnosis of mild cognitive delay.  At the age of 11 when the test was performed, it was estimated that she had the cognitive development and maturation of a 7-year-old.  She goes to cognitive therapy to overcome her diagnosis of mild cognitive delay due to the family environment she grew up in.

Cheyenne has adjusted well to her foster family and being in a positive family environment. For example, while she likely did not attend religious services in the past, she enthusiastically attends Catholic services with her foster family and participates in spiritual activities such as praying the rosary with the family. Her foster family has helped her work on her social development, interaction with others, taking responsibility for her actions in a positive way, etc. It is noted that Cheyenne had a habit of lying to avoid negative consequences; however, great improvements were made in this area. While she still gets anxious when confronted about any inappropriate behaviors, Cheyenne is no longer afraid to accept the consequences of her actions. It is upsetting to her when someone lies about her. She is cooperative and strives to be obedient, and she is getting better at managing her emotions, impulses, and frustrations. She gets sad when others positively talk about their biological families, and she just wants to find her forever family. She is afraid of feeling alone.

Cheyenne is very affectionate and sweet. She is friendly and has wonderful skills to be a leader inside and outside her foster home. Cheyenne interacts positively with adults, peers, younger children, and animals. Cheyenne is quiet and feels good when she finishes the tasks assigned to her. She is independent and fulfills her daily routines on her own.

Cheyenne enjoys participating in recreational or playful activities with her peers. She especially likes riding her bicycle and playing soccer. She also likes to draw and dance. Cheyenne loves to eat spaghetti, rice with chicken, and oatmeal, but she does not like to eat broccoli. Cheyenne has stated that she would love to become a Chef to express her love through food.

Dezi

Boy, Age: 7
Country Code: LA-2
severe mental delay, significant behavioral disorders, overall developmental delay, overall developmental disorder, epilepsy, Soto Syndrome
Listed: Oct 2024
$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!
Information in this report is from July 2024:

Dezi lived with his biological parents and older sibling until he was almost four years old. While his parents tried to take care of him, money was always lacking and ultimately, his parents knew they could not meet Dezi’s healthcare needs. In order for him to get all the help he needs and to have a better life, his parents relinquished him to protective care services in July 2022.

Due to the child´s medical diagnosis, he is not enrolled in school. There were two times were Dezi attended a special school, but his needs were much greater than what the teachers could manage. Dezi´s adjustment to a foster home was challenging but his current foster mother has done a great job with him. He has developed a strong bond with his foster mother and regulates his emotions in accordance with what she is doing or how close she is to him. He is now able to give and receive affection, which is a great achievement, and he even sometimes gets jealous when his foster mother pays attention to the other children. Dezi’s language is almost nonexistent, but he says a few words such as “ma.” He communicates mostly through facial gestures and by pointing at things he wants to grab or do. When Dezi gets upset, he cries and has “tantrums,” throws objects, and lays himself on the floor. Dezi is not comfortable being around people he is not familiar with. If he likes somebody, he will usually pull that person by the arm to start a game. Dezi likes to play with other children for short periods, and he is not aggressive towards them. He gets anxious when he is not familiar with an environment. He gets upset when he is not allowed to do something or eat at different moments throughout the day.

Dezi is very active, he changes from one activity to another in short periods, it is very hard for him to focus his attention on one specific thing. There are no concerns regarding his gross motor development, he is still working on his fine motor skills. He needs guidance and support to fulfill his daily routines though there are some activities that he can do on his own, such as eating with no help and dressing up. He sleeps throughout the night without any inconvenience. Dezi does not wear diapers during the day as he can go to the bathroom alone but needs help to clean himself up; he wears diapers during the night. He does not like animals.

Dezi’s favorite show is Paw Patrol. He gets happy when he gets new toys, especially cars even though toys do not usually last a long time because he plays roughly with them. He likes to wear clothes with Superman logos or drawings. Dezi has a good appetite and eats every kind of food. He likes to play with water.

Nicholas

Boy, Age: 7
Country Code: LA-2
Primary Diagnosis: Autism
alleged autism during childhood, unspecified behavioral issues, neurofibromatosis (non-malignant), acromegaly and pituitary gigantism, overall developmental delay, and allergic rhinitis
Listed: Oct 2024
$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!
(Information below is from March 2023 when Nicolas had just turned 4 years old.)

Nicholas was placed in a foster home when he entered protective care as a newborn due to familial issues. He is now enrolled in pre-k. Due to his complex medical condition, his academic development is limited. Nicholas tries to be independent in some daily activities, such as dressing himself, but for the rest of his care he needs constant supervision, support, and guidance both due to his age, his developmental delay and suspected autism.

Nicholas is a loving and affectionate child toward people he knows and he expresses his love through kisses, hugs, and by clapping. He has a strong need to be near his foster parents and sometimes gets jealous when they are holding another child. He does not like to be around too many people or in places where the noise is too loud. If he is interested in interacting with an adult, he will find a way to call for attention. He communicates through sounds, screams, and some syllables. Sometimes Nicholas gets upset when toys or objects are not organized or placed in the same spot he left them. Nicholas needs an adult to supervise his behavior while he is interacting with other kids, as he needs someone to remind him to behave positively and be patient with others.

Nicholas is constantly moving around and loves to explore his surroundings. He gets easily frustrated when his daily schedule changes. He is very interested in water and on many occasions, he has submerged objects or documents in water. It is reported that his body movements appear to be tough and not well coordinated. He is able to follow simple instructions. He can play with toys and other objects and his fine motor skills are still developing. He spends his time organizing toys and objects by color and size. He is afraid of climbing up and down the stairs. Nicholas still wears diapers but is currently being potty-trained. He goes to bed around 10:00 pm and wakes up at 6:30 am. It is important to give him his medication in the evenings before bedtime. Nicholas loves to listen to music, eat, and explore cell phones.

Fera

Girl, Age: 15
Country Code: LA-2
Primary Diagnosis: Older Child
Listed: Oct 2024
**** I am eligible for a $500 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 ***
Information in this report is from April 2024 (Fera was 13 at the time).

Fera did not attend school until 2021 but has already progressed to the fifth grade! Her academic development has been great. She gets anxious when she has tests at school or when she is asked about her Indigenous community. It bothers her when she is not able to complete homework on her own. Fera recognizes authority figures; she is respectful and obedient toward them, including her teachers. She can stay focused on one specific task and follow simple and complex instructions.

Fera is known to be very responsible. She is an independent girl, who does not require help to fulfill her daily routines; she is a great helper around her foster home. She has good sleep and eating habits. Fera manages her impulses and frustration in accordance with her chronological age. She is usually calm and collected. When situations bother her, she simply moves to a different place and abstains from any interaction. Fera takes good care of her personal belongings and is well organized. She has good hygiene habits.

There are no concerns regarding Fera’s motor, language, cognitive and social development. Fera is currently clinically healthy, she does not take any medication. Due to a tuberculosis episode, she goes from time to time to see the pneumologist. While she is clinically healthy, it is important to realize that all children available for adoption has a history of trauma and likely will need psychological/mental health services once they are home.

Fera is shy by nature—she is quiet and takes her time to feel comfortable and interact with others. She is very selective with her group of friends or people she trusts. She keeps a low profile and does not feel comfortable being the leader of group. She is able to give and receive affection, and she does not get jealous when her foster parents pay attention to the other children. She interacts positively with adults, peers, younger children, and animals. Seeing homeless children or stray animals wandering on the street makes Fera sad. She is also afraid of the dark and deep waters.

Fera enjoys spending time with her friends, especially when she gets to go to the pool or the river with them. She especially likes going to birthday parties she is invited to at times. She also enjoys simple things like going for a walk. Fera is talented at painting. She says would like to become a veterinarian and take a beauty course to learn how to do different hairstyles.

Evan and Michael

Sibling Group
Ages: 14, 16
Primary Diagnosis: Older Child
Listed: Oct 2024
**** I am eligible for a $500 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 ***
 EVAN — Diagnosis: clinically healthy
MICHAEL — Diagnosis: clinically healthy IQ71

Kortni and Kevin #

Sibling Group
Ages: 15, 13
Primary Diagnosis: Older Child
Listed: Oct 2024
**** I am eligible for a $500 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 ***
 KORTNI
Diagnosis: Other mixed disorders in behavior and emotions.
 KEVIN
Diagnosis: Other mixed disorders in behavior and emotions. Kidney stone with ureteral stone.

Everett #

Boy, Age: 14
Primary Diagnosis: Autism
autism and severe delays in intellectual functioning; non-verbal
Listed: Oct 2024
$1,000.00
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!
Everett resides in a center for children. He is a healthy, good-looking boy who has autism with severe delays in intellectual functioning. He makes sounds but has no speech skills. He shows stereotypical mannerisms of rocking, hand fluttering, and hyperactivity. He plays by himself and does not interact with others. He seldom reacts to his name. Sometimes he self-harms or shows frustration. He does not sustain attention for very long. He needs assistance in feeding, clothing and self-care. He needs close attention. He needs a loving family.

Videos are available.

Mell

Boy, Age: 4
Country Code: LA-2
Primary Diagnosis: Hydrocephalus, Spina bifida
bilateral hip dysplasia with congenital hip dislocation, congenital hydrocephalus, lumbosacral meningocele corrected, congenital malformation of the corpus callosum, hypermetropy (far-sightedness), and malnutrition.
Listed: Oct 2024
$35.00
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!
Info from March 2024:

When Mell was born, his biological parents tried to take care of him even with his special needs, but they lived in a small town far away from cities and hospitals. At his one month check-up, he was diagnosed with congenital malformation of the spinal cord, hydrocephalus, low weight, fetal growth delay, and respiratory syndrome. At one of his following check-ups, the doctor sent Mell to the hospital due to a high fever and inflammation of the brain. Sadly, though they had tried, his parents recognized that they did not have the means of caring for him in the ways he needed, both due to finances and distance from necessary medical care, and they asked Protective Services to care for him. No other family members were able to provide the care he needed as well. Mell was placed in a foster home and is doing well.

Mell has been receiving various types of therapies which have been valuable in his development. When meeting adults for the first time, he becomes shy, but he recognizes familiar people and loves to interact with them. Mell identifies the emotions on people´s faces and interacts accordingly. He is a very expressive child who shows affection in various ways, and sometimes gets jealous when his foster mother gives affection to the other children. According to the professionals who care for him, Mell has the language development of a 12-month toddler. He communicates through crying and screaming and can say some short words such as “mama” and “papa.” He also imitates animal sounds, such as those of a dog or cat. He responds to simple instructions such “Take this” and “Give me that.” Mell identifies different body parts, plays with Play-Dough, and performs other activities that strengthen his fine motor skills. His movements are spontaneous despite the limitations he has in his lower limbs.  Due to his chronological age, Mell requires support, supervision, and guidance to fulfill his daily routines. Mell takes two naps during the day and sleeps throughout the night. He wears diapers all day.

Mell likes to interact with peers or adults and loves to spend time outside. He gets excited when he hears a motorcycle engine as he immediately thinks he is going to go out and gets anxious. He gets upset when his diaper is dirty and when he is not allowed to go out. Mell gets happy with simple things, and he likes to laugh a lot. Mell loves to drink sweet juices. Due to his medical condition, he does not wear shoes but wears very soft socks. He enjoys it when adults help him to kick the ball to play soccer. Mell also likes to play with cars and airplanes.

Lilian and Sonny

Sibling Group
Ages: 10, 7
Country Code: LA-7
Sonny is a quadriplegic child with cerebral palsy and epilepsy.
Listed: Oct 2024
$520.00
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!

Lilian is described as happy and communicative girl who is very creative. She interacts positively with adults and other children. She is currently in the fifth grade where she is known to be a good student.

Sonny is a quiet boy though he smiles and babbles to communicate with others. He is a quadriplegic child with cerebral palsy and epilepsy.

The agency can attempt to obtain additional information for interested families.

Jana

Girl, Age: 7
Country Code: LA-2
Edwards Syndrome (Trisomy 18 by translocation) and pulmonary dysplasia, fully dependent on oxygen. Epilepsy, gastroesophageal reflux without esophagitis, nausea and vomiting, urinary tract infection, gastrostomy, congenital malformation syndromes associated mainly with short stature, hypothyroidism, and spastic cerebral palsy.
Listed: Oct 2024
$610.00
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!

Information in this report is from March 2023 when Jana was 5. The adoption agency has medical records and pictures for Jana dating back to 2019.

Jana entered care at one year of age due to abandonment and negligence. Within her foster home, it is evident that Jana likes to interact with others. In her own special way, Jana is able to share and receive affection. She communicates with others through body language and eye movements. The foster mother has learned to read her body movements to identify if something is bothering her. Jana responds to stimuli generated through loud voices. Due to her medical diagnoses, she needs constant supervision and guidance to fulfill all her daily routines. Jana´s gross and fine motor development is delayed. Her cognitive development is severely damaged due to her medical diagnoses. She wears diapers all day. Jana spends her days seated in her wheelchair or laying down in her bed when she sleeps. She receives therapy and medication through her gastrostomy.

According to the foster mother, Jana loves to receive massages. She likes when people speak to her in a soft voice. Jana enjoys going outside for short periods.

Declan

Boy, Age: 8
Country Code: LA-2
Primary Diagnosis: Down syndrome
Down syndrome
Listed: Oct 2024
*** 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! ***
$751.50
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!
Our sweet Delcan, was born in May of 2017 with Down Syndrome. We are so excited to share his referral with interested families.

There is a $1,000 agency fee reduction for Declan’s adoption with a specific agency. Additional agency fee reductions may be available based on the adoptive family’s circumstances.

VIDEOS:
https://vimeo.com/maaspecialkids/maa-declan10
https://vimeo.com/maaspecialkids/maa-declan11

Password: Adoptmaa

Rose and Sawyer #

Sibling Group
Ages: 16, 15
Listed: Sep 2024
**** I am eligible for a $500 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 ***
Rose
Diagnosis: school skills disorder
SAWYER
Diagnosis: school skills disorder. Other mixed behavioral and emotional disorders

Kevin #

Boy, Age: 3
Primary Diagnosis: Hydrocephalus, Spina bifida
Congenital anomaly of the nervous system: internal hydrocephaly; condition after ventriculo-peritoneal anastomosis implantation. Holoprosencephaly. Lumbosacral spina bifida aperta; condition after plastic surgery. Lower flaccid paraplegia. Pelvic-reservoir incontinence. Delayed neuro-psychic development
Listed: Sep 2024
$614.00
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!
Kevin can sit on his own. He plays with toys. He interacts positively with caregivers. He makes some sounds, but is not yet saying any words.

Nate

Boy, Age: 5
Country Code: LA-7
Primary Diagnosis: Cerebral palsy
Premature birth, Cerebral palsy
Listed: Sep 2024
$32.50
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!
Information in this report is from Summer 2024:

Nate was born prematurely at 27 weeks gestation and was hospitalized for two months. After living with his mother for two months, he came into protective care at 4 months old after his mother abandoned him in the care of a neighbor. Initially she visited him occasionally, but the last visit was in 2022. Nate lives with a foster family.

Nate has unidentified cerebral palsy, but it doesn’t hold him down! While at 8- months-old he showed significant delays in neuro-psychomotor development, today he has shown significant development. He is being monitored a team of specialists including a neuro-pediatrician, orthopedist, physiotherapist, psychologist, speech therapist and nutritionist, in addition to receiving specialized educational care. Nate can now move around with some independence and is in the process of adapting to the use of an orthotic equipment, which may help his locomotion. According to the physiotherapist’s report, Natey crawls, sits in a W position with balance, stands with support and walks sideways. He has the potential to use a walker for home distances and a wheelchair for community distances.

Socially, Nate is an extroverted child who loves to participate in activities and communicate. He can focus on activities. He understands what is asked of him and responds coherently within his ability. He demonstrates caring and affection with other children and adults. He is observant to what is going on around him. Nate lives in a house where there are children younger than him and this fact limits his social interactions, which has significantly compromised his progress.

It is believed that Nate has great potential for development, as long as there is proper stimulation. The possibility of starting family life through adoption at this time is considered extremely important for the progress of the child’s physical, social and cognitive development.

Eleanor

Girl, Age: 10
Country Code: E-11
Region: Europe
heterozygous variant in the KAT6A gene. Heart issues, global developmental delay, severe language delay
Listed: Sep 2024
$20.00
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!
Eleanor is a beautiful young girl who needs a family.

Owen

Boy, Age: 4
Country Code: LA-2
Primary Diagnosis: Down syndrome
Down Syndrome; Hypothyroidism; Swallowing Disorder; Taking medications
Listed: Sep 2024
*** I am eligible for an additional $2,500 Grant from Reece’s Rainbow! Through 2025, children with Down syndrome under the age of 6 are eligible for this grant. ***
$937.50
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!
Owen, born in February of 2021, is curious and eager to learn. He has a natural sense of wonder and a genuine enthusiasm for life. His playful spirit brings joy to those around him, and his kindness shines through in everything he does. Owen’s open-mindedness and willingness to try new things make him a joy to be around. We are excited for him to bring his light to a loving family.

VIDEO:
https://vimeo.com/maaspecialkids/maa-owen1
Password: Adoptmaa

Bowie #

Boy, Age: 8
Vision issues, cerebral palsy, seizures
Listed: Sep 2024
$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!

Please meet this cute boy named Bowie.  He was diagnosed with congenital cataracts in both eyes.   However he underwent surgical treatment with implantation of intraocular lenses. There is suspected Glaucoma.  He is also diagnosed with Children’s cerebral palsy – Quadri pyramidal syndrome. Grand mal seizures with or without petit mal seizures.

Bowie can sit up independently from a lying position. He can stand up by holding on to various objects. He walks independently but it is uncoordinated. The child lags in neuropsychological development. He accepts bodily closeness with pleasure.  It is pleasant for him to be held by an adult. The presence of children in his immediate space does not bother him, but he does not show interest in them and does not initiate interaction. He is soothed by riding in a pram or listening to favorite children’s songs.  He prefers the environment to be quiet.  He becomes nervous and anxious around loud noise.  He is entirely dependent on the care of an adult.

Mira #

Girl, Age: 11
Primary Diagnosis: Trauma History
Listed: Sep 2024
Mira is physically healthy. She lived in a neglected environment for the first 7 years of her life. She has delays in her speech, but she understands everything said to her and speaks in short sentences. She is in 2nd grade in school (in her country, children start school at age 7). She can read and write. She plays the piano and enjoys the lessons. She says when she grows up, she wants to a police woman and a piano player. She has good self-help skills and no behavior concerns.

Brandon #

Boy, Age: 5
Microcephaly. Hydrocephalus. Agenesis of the left hemisphere, persistent foramen ovale, Interatrial defect and Schizencephaly.
Listed: Sep 2024
$1,033.40
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!

Please meet Brandon; he has multiple special needs. Sadly Brandon relies totally on the care of others.  He sleeps in a room with four other children.  The caretaker says he seems to like music and likes the bath.  He can make some sounds for speech.  He has difficulty feeding and swallowing.

The agency staff member that met Brandon said the following:  “According to the caretaker, there is a slight regression, especially in terms of feeding. Unfortunately, I have not been given an opportunity to speak to any of the specialists engaged with the boy and possibly what exactly they are working on. Brandon could have some potential, but it’s very hard to tell.  In any case, he needs a lot of love, a lot of attention and a lot of activities.”  Could you be the family for Brandon?

Bella #

Girl, Age: 9
Primary Diagnosis: Cerebral palsy
Her multiple special needs include Cerebral Palsy and severe quadriparesis.  She is also severely delayed mentally.
Listed: Sep 2024
$1,043.50
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!

Look at the sweet smile on Bella!  Bella spends the majority of the time in her bed or in the special stroller that she can be pushed in.  She is often fed in the stroller as well.  She is fed with a bottle.

Agency staff member said the following:  Given the fact that only a rehabilitator is currently working with the child and the staff at the Home only have time to cover her basic needs, it is definitely very difficult to say to what extent the little girl has developmental potential. In my opinion, Bella liked it when she received personal attention such as being spoken to gently, being teased by me or by my showing her different toys. She had been working on a smile during that time.  Most of the time, both her arms and legs were in motion, and she even managed to roll over in bed. She needs a lot of love and attention and systematic and purposeful activities with specialists.

Pah

Boy, Age: 5
Country Code: Asia.4
Region: Asia
Listed: Sep 2024
$100.00
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!

Pah is a lovely little 4-year-old boy in need of a permanent home. He has been with his foster family since he a little baby. He is bonded to his foster family as well as another foster child in the home who is 3 months younger than him.

Pah currently is in good normal health. However, when Pah was 22 days old he showed peripheral pulmonary artery stenosis, small patent foramen ovale (PFO), and secundum atrial septic defect 1.5 mm. On the follow-up echocardiogram in April 2022, the results showed normal heart anatomy and function. As of his August 2024 child checkup, his hearing and vision were reported to be normal. While Pah’s physical health remains good, he has been diagnosed with Autism Spectrum Disorder (ASD) in August 2023, for which he attends Child and Adolescent Psychiatry therapy. During the same evaluation, he was assessed to have a mild delay in gross motor skills as well as a mild delay in oral language. He had been previously diagnosed in 2022 with Borderline Developmental Delay. As observed, he can speak clearly, except that he may mispronounce some words.  He is able to hold conversations with adults and express his needs and feelings in sentences.  He can also follow instructions. Pah receives speech therapy about 2 times per month, and physiotherapy and occupational therapy 3-4 times per year at school. Pah can walk and run confidently.  He can jump forward 12inches with both feet, stand on one leg, walk upstairs and downstairs with alternative feet by holding onto the handrail, throw and catch a ball, and kick a ball forward 5 feet away. He can also climb up the rope net.  In terms of fine motor skills, Pah can build a tower of 9 blocks, remove bottle caps, hold a pen to draw, turn pages one by one, and thread beads.

Pah is described as a happy, outgoing but also stubborn child who has shown improvements in his emotional expression. He has become more accepting of reasoning as he gets older. Due to his ASD features, Pah has a set way of doing things. He also tends to cry easily over trivial things such as when he cannot find a toy or complete a task on his own. Pah shares a normal relationship with the other foster child in the home. They have typical sibling-like rivalries and will sometimes fight over toys. He shares a close relationship with the foster mother and accepts her guidance and follows her instructions. Overall, Pah is generally an easy child to take care of. He is well-behaved and manageable most of the time except that he tends to cry easily and can also be quite stubborn at times.

Pah performs well in his self-care tasks. Being able to drink from a cup and a straw, he can feed himself with spoon and a fork. He can wash and dry his hands with a towel; put on and take off his clothes, shoes and socks; brush his teeth and wash his face. He has finished toilet training and does not need to wear diapers. He can go to the toilet by himself. He only needs assistance in bathing, washing his hair and cleaning after a bowel movement.

Pah is attending pre-kindergarten at a nursery school.  As described by the teacher, Pah has some close friends at school and enjoys a satisfactory relationship with his teachers. He can follow school rules and routines.  Being attentive in class, he enjoys participating indifferent activities.  As described, Pah is sometimes sensitive to the teacher’s reminders and sometimes is emotional about this. Pah knows lots of colors, shapes, fruits, animals, food and body parts. He also knows some concepts such as “big-small,” “up-down,” etc. He can recite the numbers from 1 to 50 and recognize some letters and numbers. He can tell others his name and age.

Families with a home study prepared for any international country can submit for consideration of Pah. The agency program specialist can explain the child/family matching process in his country.

Thomas

Boy, Age: 15
Country Code: Asia.4
Region: Asia
Primary Diagnosis: ADHD
Listed: Sep 2024
**** I am eligible for a $500 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 ***
Thomas is described as a lovable, active, cheerful and sociable 14-year-old boy who enjoys various sports such as basketball, hiking and cycling. In addition, he also enjoys playing computer games, singing and watching YouTube videos. When he smiles and laughs, a deep dimple can be seen on his right cheek. He shows frequent and appropriate eye contact when interacting with others.  Thomas readily helps out in the classroom at school where he performs well academically and has developed positive relationships with his peers. His involvement in sports has not only helped Thomas to understand the importance of collaboration and cooperation, but also supported him in regulating his body sensations for better emotional regulation and stability.

Thomas has been living in the same foster home since 2012 and has developed close relationships with various members of the foster family. However, he understands that the foster family is only temporary, and he longs for a permanent family to love and care for him. Thomas actually had a family identified for him, but the adoption process was taking a long time and eventually the family decided that caring for a teenager was beyond their capacity. Now Thomas is seeking a loving family who can provide him with stability and guidance while honoring his cultural heritage and connection with past caregivers. As Thomas has grown up with his current foster family and has seen them maintain a relationship with their biological children who are now adults living overseas, he hopes for a family who will allow him to maintain contact with his foster family over social media and he hopes to visit them when he is older.

With committed caregivers by his side, it is believed that Thomas will build meaningful relationships with his adoptive family and thrive to his fullest potential. Thomas has a diagnosis of ADHD, but his medication has improved his ability to sustain attention and reduced his hyperactivity. Thomas shows age-appropriate development and self-care skills and enjoys generally good health. We believe that there is a family out there that can provide the love and stability that Thomas needs and deserves. He
shows so much potential and has consistently expressed a desire for a forever family.

Samson #

Boy, Age: 3
hydrocephalus, spina bifida in the lumbosacral area –condition following implantation of a VP shunt and closing of the spinal defect; lower flaccid paraplegia; pelvic reservoir incontinence; delayed psychomotor development; delayed psychological development.
Listed: Aug 2024
$1,015.00
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!

Update Nov 2024:  Samson was recently moved from a large orphanage to a small group home for children with disabilities. He  loves attention and responds with joy with staff interacts with him. He is described as a calm and radiant child.

Samson sits independently and can stay in this position for extended period of time. He reaches for distant toys by directing his hands and turning his torso towards the desired direction and after that he pulls the toy. He prefers toys with buttons, which make sounds, light or melody, as well as toys with movable elements, which he can spin. He initiates interactions with adults, whom he likes and with children. Samson enjoys being praised and reacts with discontent when something is being denied or forbidden to him. He is fed via baby bottle and spoon.

Salazar #

Boy, Age: 10
Mild to moderate mental delay. Delay in expressive speech. Hyperopia. Astigmatism.
Intermittent heterotropy. Low birth weight, moderate mental delays
Listed: Aug 2024
$100.00
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!
Salvador has resided with a foster family since July 2018.

He was born with low weight and with pathological neonatal period. The child has a
physical development within the lower limit of the norm and mental delay in mild to moderate degree (IQ-41). Phrase speech is not developed, he utters single words; lags behind in the development of habits, skills, emotional and social development.
Uses optical correction due to intermittent heterotropy and astigmatism of the eyes.

The child walks stably and independently. There is delay in the development of the fine motor skills. The emotional status of the child is mostly positive – he is calm and curious. He does not show aggression, he is adaptive. He understands phrasal speech, utters single words, but does not speak. The child is able to play by himself, but he also is looking for the company of other children. Participates in the game process. He feeds himself, his personal hygiene is well-maintained. He controls physiological needs.

Roman

Boy, Age: 13
Country Code: LA-2
anxiety disorder; unspecified emotional and behavioral disorder
Listed: Aug 2024
**** 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 ***

Report is from August 2024 — Roman, 12, lived with his biological and an older brother until he was 7 years old. At that time, the place where his mother worked burned and she had to leave his brother with that child’s father, and she moved to a different town with Roman. Unfortunately, she could not find a stable job or place to live and she sought assistance from Protective Services. Roman was previously hosted by a family, but that family opted not to adopt him. More information is available.

Roman is in the 4th grade. It has been observed that Roman has great leadership skills, especially at school. Most of his teachers have stated that Roman has a lot of potential but his lack of motivation hinders his progress and development. However, Roman has great skills in math. He recognizes authority figures; he is respectful and obedient towards them. He can follow simple and complex instructions. There are no concerns regarding his motor, language, cognitive and social development.

Roman is an affectionate child after he has built a positive relationship with an adult. He can verbally express his feelings and emotions; however, when there are situations of high emotional demand, he limits the externalization of what he is feeling. Roman is still learning to manage his frustration and impulses, but good improvements have been observed. Roman is shy when meeting people but can easily overcome this behavior once he feels the adult is trustworthy. He interacts in a positive way with adults, peers, younger children, and animals. Roman gets anxious when he does not get what he wants immediately or when something he was expecting does not end up happening. Roman is sad when remembering his biological family, and this connection is part of why the hosting family did not choose to adopt him. Roman is afraid of dark, thunder, rain, and heights. In order to fall asleep, he needs some light or a stuffed animal.

Roman loves it when he gets to go to amusement parks, the movies or the pool. Roman likes to ride his bike, listen to music, and watch TV. He has stated that he would like to improve his drawing skills.

Sal & Monty

Sibling Group
Ages: 10, 9
Country Code: LA-5
Primary Diagnosis: Trauma History
Listed: Aug 2024
$788.00
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!

Sal and Monty are eager to go to a family as soon as possible! These brothers from Latin America are currently 8 and 7 years old.

Sal and Monty came into care in late 2020 after their teacher reported noticing repeated physical injuries with one of the children. At that time, protective services investigated and found that the children living with their mother who had previously lost custody of them due to abuse when Sal was only a year old.

Sal

Sal is currently 8 years old. He is predominantly affectionate, sociable, and respectful. He likes to play and interact a lot, and he is very interested in learning new things and being accepted by his peers. He shows autonomy and confidence to perform routine activities by himself, and he only asks for help for the things he cannot manage. He is well bonded with his younger brother. He expresses affection toward Monty, plays with him, and is attentive to his well-being. Sal is currently enrolled in a Montessori school and is in the 3rd grade. He continues to work on following the rules and order within the environment. Sal has a tendency to downplay incidents where other children have been aggressive or abusive toward him, and he often does not report such incidents to adults. He tends to normalize these types of negative rough or violent interactions and does not remove himself from the situation. However, the caregivers have been working with him on this situation and he is improving as well as learning measures on how to protect himself from any abusive situation.

Sal has been diagnosed with attention deficit hyperactivity disorder for which he is taking medication. He suffers from atopic dermatitis, has dry skin on his cheeks, currently treated with symptomatic management with the use of moisturizing creams. The child has compound hypermetropic astigmatism and currently wears glasses.  He also has a low weight and height for his age.

Monty

Monty is 7 years old little boy who is described as kind, giggly, and playful. Monty is also enrolled in the Montessori school with his brother and he is in the 2nd grade. At school, he is polite and cordial as he is at home, establishing effective bonds with his classmates and guides. He has a stable mood and is affectionate with his caregivers and most people at the foundation where he lives. He is also able to communicate things that bother him and stand up for himself. He has a good relationship with his older brother Sal, trusts him, and likes to be taken care of by him. His favorite activities are playing soccer with his brother, drawing, and playing video games. His favorite characters are Hulk and Spiderman.

Monty was evaluated by neurology after presenting motor coordination with lag and decreased strength in his lower limbs. A decrease in the strength of both legs with frequent falls was identified, with no apparent alterations in sensitivity. Sensory and motor neuro conduction velocity studies and electromyography of bilateral tibial and peroneal nerves were performed, resulting in a diagnosis of severe sensory-motor polyneuropathy for which he requires follow-up by neurology and rehabilitation (to read about this condition, visit this site:  Sensorimotor polyneuropathy: MedlinePlus Medical Encyclopedia. He has also been diagnosed with mixed astigmatism and low weight/height for his age.

Hope

Girl, Age: 11
Country Code: Asia.4
Region: Asia
Primary Diagnosis: ADHD
Listed: Aug 2024
**** 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 ***

Hope is a bright, assertive, and courageous girl with many endearing qualities and undiscovered traits. She is highly active and enjoys a range of sports activities, including running, swimming, and hiking. In her spare time, she loves engaging in craft work like origami. Her recent obsession with Sudoku has highlighted her strong logical thinking skills.

Despite facing challenges such as eczema, ADHD, and ODD, Hope is managing with her prescribed care routine. She thrives better with individual attention and consistent, firm, yet gentle care. She has shown significant improvement since being moved from an orphanage to her current foster home where she is adhering to rules and routines, and slowly learning how to live in a family atmosphere.

Hope was previously approved for adoption overseas. However, due to concerns the family had regarding her psychological/mental health once in-country, they withdrew their petition to adopt. A further report about Hope’s emotional development and readiness for adoption after the previous withdrawal will be ready by September.

Now, Hope is seeking a loving family who can provide the consistent, gentle care she needs to flourish. Hope’s institutional upbringing has shaped her attachment and emotional needs, but with the right support, she has the potential to thrive in a family environment. Given that adoptions from her country take approximately two years to complete, while Hope is entering her pre-teen years now it is important to realize she will be a teenager when adopted.  Interested families need to be willing to learn and be well aware of the challenges of adopting an older child so her family will have the capacity to support her emotional and behavioral needs. It is also recommended that the family be well-equipped with trauma-informed care and understand issues related to delayed adolescence and the impact of long-term institutionalization. This includes understanding family roles, including those of a father and mother, and sibling relationships.

CHI has given this child the pseudo name Hope because we and her social service staff in HK believe that with the right family who understands her past and can provide her with and affection with proper rules and routines, Hope can overcome her difficult past and achieve great things. We look forward to finding a family that can offer her the stability and care she deserves. CHI has past child studies to provide to seriously interested families.

 

Jaxon

Boy, Age: 8
Country Code: LA-2
Primary Diagnosis: Deaf / HoH, Down syndrome
Down syndrome; Bilateral sensorineural hearing loss; Language delays- communicates through sounds, signs, and screams; Von villebrand disease; Other specific leukocyte disorders, Gastrostomy; Hypothyroidism; Other specified disorders of the kidney and ureter; Other types of infantile paralysis
Listed: Aug 2024
*** 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! ***
$1,036.50
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!
Jaxon has a warm smile and readily shares it with anyone around him. He is also affectionate. He does not like to feel limited or subject to restraints. Jaxon likes to explore and laugh a lot with the people he recognizes as close.

VIDEOS:

https://vimeo.com/maaspecialkids/maa-jaxon01

https://vimeo.com/maaspecialkids/maa-jaxon02

https://vimeo.com/maaspecialkids/maa-jaxon003

https://vimeo.com/maaspecialkids/maa-jaxon004

Password: Adoptmaa

There is a $1,000 agency fee reduction for Jaxon’s adoption, with a specific adoption agency. Additional agency fee reductions may be available based on the adoptive family’s circumstances.

Wyatt

Boy, Age: 9
Congenital Zika, Cerebral Palsy, Epilepsy
Listed: Aug 2024
$1,252.00
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!
Wyatt is a child with a lot of energy. He is very handsome with long hair and a beautiful smile. He loves music and anything that makes noise around him. He thoroughly enjoys interacting with people who talk to him and will make noise in response to them. He loves many activities including the trampoline, swings, going for a walk, and playing with other children.

A therapist works with him weekly. He presents with many neuromuscular deficits that impact his ability to move his arms. He is able to move his left arm a little to touch objects; however, he does not pick up and hold objects yet. Movement is also limited in both legs, with his right leg having less mobility. He is unable to sit, stand or walk. He is able to hold his head up for short periods of time; however, he is making great progress with this. Wyatt is extremely motived during his therapy sessions.

Cognitively, he is extremely aware and currently does very well in school. He knows shapes, colors, some letters and numbers. He can identify them and answer questions using eye gaze with 2 choices. He loves to laugh at kids when they are running around. Sensory materials and adapted activities are helpful in school to further develop his academic abilities.

Liamo

Boy, Age: 4
Country Code: LA-2
spastic cerebral palsy, microcephaly, overall developmental delay, epilepsy, gastrostomy, and blindness.
Listed: Jul 2024
$20.00
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!
Info is from January 2023; the agency can get updated information when there is a serious inquiry.

Liamo was placed into protective care upon discharge from the hospital when he was born. At the time of his birth, he suffered severe asphyxia. His mother’s pregnancy was unplanned and she had not received any prenatal care. His parents were unable to grasp his medical diagnosis and condition, they were not in the position to care for his medical needs. No one in the biological family was able to care for him either.

Liamo is a child who needs constant supervision. His oxygen levels needed to be always monitored; however, oxygen support has been removed and he seems to have a better mood. He has not had any seizures but does have some spasms during the day. He cannot stay in a seated position. Despite his diagnosis, Liamo loves to receive affection. He communicates through babbling and other sounds. He needs support to fulfill all daily activities. He wakes up very early in the morning and is still not able to sleep throughout the night. Liamo wears diapers all day.

Liamo can kick his legs and with the help of external support equipment he can stay in a seated position for a period of time. His neck control is getting better, as he now can hold his head up for 40 to 50 seconds. He can grab objects with his hands without applying pressure. Liamo goes to occupational, physical, and speech therapy. He gets easily uncomfortable when he needs to wear more clothes, he prefers to wear very light clothes. He turns his head when he hears a strong noise. He takes daily medication. Liamo likes to change positions constantly and likes to participate in activities where there are sounds involved.

Ally

Girl, Age: 15
Country Code: LA-2
Primary Diagnosis: Older Child, Trauma History
Listed: Jul 2024
**** I am eligible for a $500 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 ***
Ally, now 14, lived with her mother and stepfather in their indigenous community until her parents separated. At that time she went to live with her grandparents who used physical punishment with her. Her mother started a new relationship with a man and they were negligent and abuse toward Ally. At that time, Ally suffered from enuresis (bedwetting), and whenever she would hear the word punishment she would wet herself. She entered into protective care at the age of 7 and her biological mother showed no interest in fulfilling the requirements to regain custody. Ally is now said to be clinically healthy, but as with all children in care, she has suffered trauma from her abusive and difficult past.

Ally is enrolled in school; she is in 8th grade. Her academic performance is good, and her main interest is art—she loves to draw and paint. Her least favorite subject is math. She has a positive relationship with her teachers and classmates. Ally does not get jealous when her caregivers pay attention to other kids, and she is able to give and receive affection. She is an independent girl who fulfills all her daily routines without help. Ally has good sleep and eating habits. She manages her frustration and impulses in accordance with her chronological age. She stays focused and does her best to complete every activity even if it is challenging.

There are no concerns regarding her motor, language, cognitive and social development. She used to go to psychological therapy, but every goal was achieved and she no longer needs this type of support. It is still difficult for Ally to fully express her feelings and emotions verbally, but a great improvement has been shown. At the moment there are no specific triggers that will cause her to feel anxious. In the past, the thought of being reintegrated with her biological family was a cause of anxiousness.

Ally does not get shy when meeting new people but might wait for others to take the initiative to start a conversation. She recognizes authority figures and is respectful and obedient towards them. She interacts positively with adults, peers, younger children, and animals. Ally has great hygiene habits and takes good care of her belongings.

Ally loves playing sports like basketball, and she is part of her school team. She likes to walk outdoors and is very interested in learning English. Ally is currently clinically healthy and does not take any medication. Ally is very aware of fashion and likes to wear clothes that are aesthetically correct. She likes to listen to K-pop.

Ally will need a family who is motivated to get paperwork done quickly as she is 14.5 years old and in danger of aging out of being able to immigrate to the U.S. While we do not anticipate any problems (we can never guarantee), a family must be committed to completing a home study and dossier in a efficient manner so the process can have time to complete.

Sani

Boy, Age: 11
Country Code: LA-2
Primary Diagnosis: Blind / VI, Trauma History
Vision loss, trauma history
Listed: Jul 2024
$34.00
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!
Intelligent, extroverted, spontaneous, resilient, loyal, a dreamer, creative, affectionate, loving, self-efficient, autonomous, astute, brave, perseverant, with a restless mind to learn new things and face new challenges, and with great capabilities. Despite extreme difficulties in life, this is how Sani is described even though being a victim of severe child abuse of various types—including abuse that led to vision loss —could have led him to be otherwise described. Sani came into protective care in 2022 at the age of 7 years old. He is now 9 years old.

Sani is currently enrolled in the 4th grade. According to his teacher´s report, the child is loved by his classmates. He uses his cane to walk around and there are no major concerns regarding his motor, language, cognitive and social development taking into consideration his diagnoses of secondary vision loss and severe child abuse syndrome. He has great communication skills and can verbally expresses his feelings and emotions with people he is very familiar with. Sani recognizes authority figures, but many times has trouble being respectful and obedient, especially if he does not agree with an instruction given by them. Sani can easily make new friends and has leadership skills among his peers.

Sani goes to psychological therapy. He is still learning to take full responsibility for his consequences, and sometimes he lies to avoid any kind of discipline. Sani is learning to manage his impulses and frustration. If there is a situation that he cannot handle emotionally, he will start yelling or behaving in a hostile way with his peers. Whenever he throws a tantrum, he sometimes experiences psychomotor agitation and uses bad language. Whenever there are situations that make him feel anxious, he bites his sleeves, has sweaty hands or has motor restlessness. He gets upset when he needs to continue pushing to do his best in order to fully know the Braille system. He is afraid of being in a dark room alone. Because of his severe history of child abuse, it is recommended that Sani be the youngest child in the family though this may be negotiable depending on a family’s experience with children from abuse. Sani has expressed that he would like a family with two heterosexual parents and he would like to have siblings.

Sani likes to play soccer and enjoys building with Legos and also engaging in conversations with adults. He likes to listen to music in English or Portuguese since he has expressed his desire of learning new languages. Sani favorite colors are blue, white, black and orange. He loves to practice soccer, swimming, martial arts such as capoeira and riding his bicycle. He even likes to breakdance as evidence in a video sent with his profile. Sani is good at playing musical instruments. He would like to become a scientist, learn about biology and astronomy and also speak different languages.

Anna

Girl, Age: 11
Country Code: LA-2
Primary Diagnosis: Autism, Speech Delay
autism, language and speech developmental delay, moderate mental developmental delay, expressive language disorder.
Listed: Jul 2024
**** 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 ***
Anna, now 10 years old, entered the Protection Services for the first time when she was a newborn baby as her mother used drugs while pregnant. She lived with her grandmother for a while, but reentered care at 13 months old.

Anna is known for being a happy girl. Anna is not enrolled in school as it has been difficult to find an Institution that can work with her diagnosis and special needs. However, when she was enrolled in school, it was noted that she behaved positively and recognized authority figures. Anna loves to give and receive affection, and she does not get jealous when her foster mother pays attention to other children. Her closest bond is with the 12-year-old daughter of her foster mother. She needs support and supervision to fulfill her daily routines. Anna has a good sleep and eating patterns; however, she very occasionally wets the bed. Anna sometimes throws objects to the floor when she feels frustrated. She can follow simple instructions. Due to her diagnosis, it is hard for her to stay focused on one specific task.

Anna can keep her balance and walk, and she tries to jump but is not fully able to do it. She can run slowly and up the stairs if an adult holds her hand. Her fine motor skills are still developing. Anna is not able to hold scissors, but she can grab pencils and color. She needs help with dressing and hygiene. For the most part, Anna communicates through signs and very short words; it is not hard to understand what she wants. She goes to speech therapy. Anna recognizes familiar faces, and she does not get shy when meeting new people. She can play with younger children or with peers, but she gets upset when other children take her belongings. She recognizes her foster mother as an authority figure. She likes dogs as long as they are away from her, and she gets nervous when pets are near her.

Being told she looks pretty or that she is beautiful makes Anna happy. She loves to have her hair done in pretty styles and enjoys wearing new clothes. She likes to watch children’s movies and videos of people doing exercises. She is very good at swimming. Anna´s favorite foods are spaghetti and chicken with rice. She loves to listen to music and do puzzles.

Jean-Luc #

Boy, Age: 7
Primary Diagnosis: Epilepsy/ seizure disorder
Pyruvate dehydrogenase deficiency – homozygote for mutation p.R446 (disorder of pyruvate metabolism and gluconeogenesis). Microcephaly. Epilepsy
Diagnosis: Pyruvate dehydrogenase deficiency – homozygous for mutation p.R446 (disorder in the metabolism of pyruvic and gluconeogenesis). Microcephaly. Epilepsy.

A male child, born 2460 g., with a congenital genetic metabolic disease (pyruvate dehydrogenase deficiency), leading to a disorder in the absorption of sugars and carbohydrates. The child is on a strictly individual ketogenic diet (rich in fat and completely excluding carbohydrates). He is fed with special diet milk – Ketocal.

When conducting electroencephalography, epileptic activity was registered, which is why constant anticonvulsant therapy with Trileptal is being carried out. No epi-seizures have been observed after its initiation.

The child lags behind in physical, neuropsychiatric development and motor skills. He needs follow-up by a pediatric endocrinologist and dietician and a pediatric neurologist.

The boy has pronounced axial muscle hypotonia, hypertonia of the limbs. He sits up independently, but still does not stand up in the crib. He is placed in a walker and permanent rehabilitation is carried out. He is calm, does not isolate himself in the children’s group. He shows discontent when he does not like something, but quickly calms down. The child’s sleep is peaceful.

According to a Psychologist’s last Individual Characteristic from November 2024: “ …Over the past months, progress has been reported in the child’s general and fine motor skills. He stands up on his own on a stationary support and steps to the sides, holding on to the stationary support. The child moves by crawling. He can sit alone without support. He spends his waking hours with the other children in the group and he likes it very much, calm and smiling.

Jean-Luc is smiling, radiant, calm. He stands next to the children and does not isolate himself. There is no joint play yet. He cannot initiate contact with the children by himself. He shows dissatisfaction when he does not like something. He enjoys teasing from a familiar adult. During activities, he is involved, but is not active and shows little interest.

Listed: Jul 2024
$45.00
has been donated towards the cost of my adoption!

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Diagnosis: Pyruvate dehydrogenase deficiency – homozygous for mutation p.R446 (disorder in the metabolism of pyruvic and gluconeogenesis). Microcephaly. Epilepsy.
A male child, born 2460 g., with a congenital genetic metabolic disease (pyruvate dehydrogenase deficiency), leading to a disorder in the absorption of sugars and carbohydrates. The child is on a strictly individual ketogenic diet (rich in fat and completely excluding carbohydrates). He is fed with special diet milk – Ketocal.
When conducting electroencephalography, epileptic activity was registered, which is why constant anticonvulsant therapy with Trileptal is being carried out. No epi-seizures have been observed after its initiation.
The child lags behind in physical, neuropsychiatric development and motor skills. He needs follow-up by a pediatric endocrinologist and dietician and a pediatric neurologist.
The boy has pronounced axial muscle hypotonia, hypertonia of the limbs. He sits up independently, but still does not stand up in the crib. He is placed in a walker and permanent rehabilitation is carried out. He is calm, does not isolate himself in the children’s group. He shows discontent when he does not like something, but quickly calms down. The child’s sleep is peaceful.
According to a Psychologist’s last Individual Characteristic from November 2024: “ …Over the past months, progress has been reported in the child’s general and fine motor skills. He stands up on his own on a stationary support and steps to the sides, holding on to the stationary support. The child moves by crawling. He can sit alone without support. He spends his waking hours with the other children in the group and he likes it very much, calm and smiling.
Jean Luc is smiling, radiant, calm. He stands next to the children and does not isolate himself. There is no joint play yet. He cannot initiate contact with the children by himself. He shows dissatisfaction when he does not like something. He enjoys teasing from a familiar adult. During activities, he is involved, but is not active and shows little interest.

Gene

Boy, Age: 13
Country Code: LA-2
Listed: Jul 2024
**** 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 ***

Gene’s information is from a report in June 2024 — the agency does have older reports as well.  Gene was 7 years old when he entered care due to neglect. He spent most of his days on the streets and there were behavioral issues within his family of origin. His father was in jail and his mother was involved in criminal activities as well as drug usage. While she said she was going to make changes in her life to regain her son’s custody, she did not follow through. Gene is now 12 years old.

Gene is in the 4th grade. He struggles academically. It is difficult for him to understand new concepts and therefore is unmotivated to do his best. He still has trouble pronouncing properly many words. In 2020 he was diagnosed with mild cognitive developmental delay, but this diagnosis was overruled though an IQ test is pending. He can get easily distracted if he does not like a specific activity. There are no concerns regarding his motor development. His language development is behind, it is difficult for him to comprehend a reading assignment; and he mispronounces some words. In the middle of the night, it is necessary to wake him up to go to the bathroom so that he will not have any accidents. Gene has been learning to manage his frustrations and impulses in a better way. Gene interacts in a positive way with his peers. Gene recognizes authority figures; he is respectful and obedient towards them. It has been observed that Gene interacts positively with adults, kids his age, younger children, and animals.

Currently, Gene goes to therapy, and he has been diagnosed with unspecified mixed behavioral issues for which he takes daily medication. He gets anxious whenever he is not permitted to do something he wants or whenever he does not fully understand a task. He gets upset when he feels he is being attacked, but he has not become aggressive. Gene is afraid of being alone, getting lost and being in the dark. Whenever he feels sad it is because he longs to have a family.

Gene loves to participate in any recreational activity, including sports. Some of Gene’s favorite activities are playing soccer, going to the park, playing cops and robbers, making bracelets and painting. When he grows up, he would like to be a professional soccer player or a chef.