Lennon

Boy, Age: 5
Primary Diagnosis: Down syndrome
Listed: Oct 2025
*** 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. ***
$0.00
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!

Lennon is a cheerful, active, and loving child. He always responds with a smile to those who take care of him. He sleeps well at night and takes a nap after lunch. He is a good eater. Some of his favorites are watermelon and beans. He likes to listen, sing, and dance. It is evident that Lennon relates to music. He follows the rhythm with his hands by clapping. dancing, jumping, and singing. He likes to feel the volume of the songs in a regulated way, paying careful attention to the beat. He loves to play with balls, specifically throwing them. He also likes to role play. He likes to feel well-dressed and receive compliments on his fashion.

So many pictures and videos are available for this darling boy, with the agency!  The agency also offers families a reduced fee / grant for families.

Cicilia

Girl, Age: 2
Country Code: LA-2
Primary Diagnosis: Down syndrome
Listed: Oct 2025
*** 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. ***
$0.00
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!
Cicilia has a stable state of mind and is described as tranquil and joyful. Sometimes she cries when a need is not met, or she expresses discomfort. She gives and receives affection through non-verbal expressions like smiles, kisses, caresses, and hugs. She loves to interact through clapping or smiles and does a great job sharing with other children. She struggles a bit with gross and fine motor but receives physical and occupational therapy at home for 40 minutes, 3 afternoons a week. She loves children’s music, children’s television, going to the park, and exploring new surroundings. She has a good appetite and loves to snack. She gets a little antsy when food is not given right when she wants it.

The agency who listed Cicilia also offers additional fee reductions / grant opportunities to families.

Brianna #

Girl, Age: 3
arthrogryposis multiplex congenita (AMC); polymalformative syndrome; congenital hip luxation; atopic dermatitis; significant delays in neuropsychological and physical development
Listed: Oct 2025
$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!

Darling Brianna sometimes turns herself to a side position. She grabs toys with both hands and handles them. A smile is observed when interacting with an adult. She looks at herself in the mirror. She pronounces vowel sounds. She enjoys individual attention, and she gets upset if she is not paid attention to or if she is left alone in the crib after she has been paid attention to. She tries to initiate contact with her eyes and facial expressions, and she responds to her name.

The position of Brianna’s legs doesn’t allow her to sit and she doesn’t straighten her head, but sometimes she rotates her torso laterally to some extent.  She reaches and grabs a toy handed to her by an adult or placed in her immediate environment and handles it briefly. She follows moving objects and people with a glance and a turn of the head.

Brianna is described as “absolutely adorable, easy to communicate with, and curious about new people and new toys.” Her caregiving staff says she is a calm and gentle child and is “everyone’s favorite in the house where she lives!” Please help us find Brianna’s family!

Amari

Girl, Age: 7
Country Code: Africa-3
Region: Africa
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! ***
$45.00
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!
Amari is currently 7 years old. She was found abandoned at one-and-a-half years old in March 2020.

Joshua #

Boy, Age: 3
Region: Europe
Listed: Sep 2025
$903.15
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!
Congenital anomaly of the central nervous system – hydrocephalus; condition after implantation of a ventriculo-peritoneal shunt. Epilepsy. Bronchopulmonary dysplasia. Non-allergic asthma. Cortical blindness. Spastic quadriparesis. Severe developmental delay. Atopic dermatitis.

Dario #

Boy, Age: 2
Primary Diagnosis: Blind / VI, Cerebral palsy
spastic cerebral palsy, bronchopulmonary dysplasia, retinopathy of prematurity, and convergent strabismus
Listed: Sep 2025
$0.00
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!
Dario is a sweet and gentle two-year-old boy who greets the world with a warm, kind smile. He’s actively exploring his environment including walking and standing while holding onto support, turning over in bed, and sitting up on his own. Dario’s curiosity shines through as he uses a palm grip to explore objects, bringing them to his mouth to learn more about their textures and shapes.

Beyond his physical achievements, Dario is a bright and engaging little boy. He’s communicative, actively seeking attention and focusing intently on things that pique his interest. His memory is impressive, especially for the location of objects, and he readily connects people and items with his past experiences. Dario loves to play and interact, showing his joy with smiles and laughter, and he uses sounds and gestures to connect with those around him.

Amelia & Scarlett

Sibling Group
Ages: 6, 6
Region: Africa
Primary Diagnosis: Other Special Needs
Sickle Cell Disease
Listed: Sep 2025
$0.00
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!
These 6-year-old twin sisters from western Africa are ready to bring double the joy to their forever family! While they might greet you with a touch of initial shyness, don’t let that fool you. Beneath their gentle exteriors lie curious minds and warm hearts that blossom quickly. Their caregivers consistently remark on their intelligence and enthusiastic approach to learning. Amelia, the more contemplative of the pair, loves playing with her dolls, watching Disney films, and creating colorful masterpieces with her drawing. Scarlett, with her inquisitive nature, is full of thoughtful questions and energy. She has a passion for dance and loves playing with Barbies. Imagine the joy of witnessing these two smart young girls explore the world around them. If you’re looking to open your heart and home to not one, but two little girls ready to learn, grow, and share their unique personalities, perhaps Amelia and Scarlett are the perfect fit for your family.

Amelia and Scarlett have been diagnosed with Sickle Cell Disease, which is currently managed with daily medication.

Wisdom

Boy, Age: 2
Country Code: Africa-3
Region: Africa
Primary Diagnosis: HIV or Hep
Listed: Apr 2025
$70.00
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!
Widsom is HIV+, has sickle cell anemia, and is Hep B positive. The agency has extensive medical information on him as of November 2024. The videos of him do also seem to indicate cerebral palsy. At the time of listing, he is nearing two years of age.

West

Boy, Age: 6
Country Code: LA-2
Cerebral Palsy, full paralysis; Severe cognitive delay
Listed: Mar 2025
$49.50
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!
West is a calm and precious boy who reacts with his eyes when he hears the voices of his caregivers who he adores. He loves to have his face caressed. West will fix his gaze on those he loves dearly. He receives therapies twice a day. Loud noises tend to startle him. West enjoys a calm and peaceful environment. He is beloved amongst all the staff. There is more to West’s gaze than meets the eye; in his eyes is a desire to be wanted. Would you give West the chance to be loved and make those eyes come to life?

VIDEO:
https://vimeo.com/manage/videos/1065191610
Password: Adoptmaa

Agency fee reductions may be available based on the adoptive family’s circumstances (with a specific adoption agency).

Idris #

Boy, Age: 7
Cerebral Palsy – spastic quadriparesis. Localized (focal, partial) symptomatic epilepsy and epileptic syndromes with complex partial convulsions. Severe mental retardation, significant behavioral disorders requiring care or treatment. Optic nerve atrophy.
Listed: Mar 2025
$244.50
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!
Idris was born with very low weight and immaturity, complicated neonatal period. Subsequently, with the development of multicystic encephalopathy with microcephaly (based on severe hypoxic-ischemic incidents in the perinatal period), severe spastic quadriparesis and symptomatic epilepsy (mainly tonic seizures). Conducts therapy with Convulex, as a result of which seizures are almost not registered.

The child has severe lag in physical and neuropsychiatric development. Severe mental deficiency.  Needs systematic motor rehabilitation, classes with a speech therapist, psychologist and typhlopedagogue. Weak rehabilitation potential. Followed by a pediatric neurologist and ophthalmologist.

The child can turn from back to stomach and back. Does not crawl, does not sit independently, does not have a four-legged stand. Does not stand up, holding on to a support. Holds a toy placed in the hand for a short time. Lacks a pincer grip. The average mental age of the child corresponds to 3-5 months. The child is mostly calm with accompanying episodes of irritability, expressed through crying. Quickly calms down by the presence and attention of an adult. There are no indications of aggressive behavior or manifestations. Does not utter words, syllables and sound imitations. Does not turn when called by name. Does not initiate contact with other children. The child is completely dependent on the care of an adult. Takes food from an adult with a spoon (less often from a bottle). Falls asleep independently.

There is evidence of a brother with an autoimmune disease – Alopecia areata.

Malachi #

Boy, Age: 2
Primary Diagnosis: Hydrocephalus
Posthemorrhagic extreme internal hydrocephalus; implantation of a ventriculoperitoneal shunt (VPS). Bronchopulmonary dysplasia. Retinopathy of prematurity
Listed: Feb 2025
$90.00
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!
He lives in a home for medical and social childcare. He was born to a minor mother who had epilepsy and took anti-epileptic medications during pregnancy. There was a complicated pregnancy and birth, resulting in extreme posthemorrhagic hydrocephalus. A shunt was implanted but failed. A new one was inserted. Malachi is on permanent antiepileptic monotherapy, without convulsive manifestations.

Due to the extreme hydrocephalus, Malachi is in impaired general condition, with significant lag in psychomotor development – no head control, does not turn around, does not sit or stand. He needs specialized care, monitoring by medical specialists, and daily medical rehabilitation. He is usually in a positive emotional state. He coos frequently and continuously. He reacts animatedly to the speech of an adult. He initiates a desire for physical contact by smiling. The boy is completely dependent on the care of an adult. His sleep is peaceful. He takes food with a pacifier. The agency has videos of him.

Paul #

Boy, Age: 2
Primary Diagnosis: Blind / VI
Iris coloboma
Listed: Jan 2025
$90.00
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!
Paul can crawl, pull to a stand, walk holding the hand of an adult and has recently started taking steps independently. He knows where his toys are kept in the house (toy boxes) and will go to them to get his toys. His fine motor skills are well developed. He transfers small objects from hand to hand and has a pincer grasp. He shows an interest in toys and outdoor activities, such as swinging. He enjoys cause and effect toys. His speech is starting to develop. He “babbles”, saying syllables such as “da-da” and “ba-ba”. He is attached to familiar people and expresses his emotions in age appropriate ways. He was recently prescribed glasses to help with his vision issues.

Owyn #

Boy, Age: 4
Primary Diagnosis: Hydrocephalus
Listed: Jan 2025
$25.00
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!
Precious Owyn is looking for a special family.

He is diagnosed with hydrocephalus and has some other medical issues that require in-depth care. The adoption agency has a lot more photos and more information about his needs and video footage.  A specific adoption agency also has grant funding in the amount of $2500 available.

Amelia #

Girl, Age: 9
Primary Diagnosis: Hydrocephalus
Hydrocephalus with Verticulo-territorial shunt implantation; delayed in her physical and neuropsychological development
Listed: Jan 2025
$90.00
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!
Amelia is reported to be “just as sweet as she can be.” The agency has a new report from November 2024 as well as photos & videos that can be shared with inquiring families.

A specific agency also has grant funding available in the amount of $2500.

Melanie #

Girl, Age: 5
Primary Diagnosis: Hydrocephalus, Spina bifida
spina bifida, hydrocephalus, psychomotor developmental delay, urinary incontinence
Listed: Jan 2025
$112.50
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!

Meet smiling Melly.   She had surgical treatment for correction of a meningocele.  A ventriculoperitoneal shunt was also implanted to treat hydrocephalus. Unfortunately after surgery Melly’s lower limbs are paralyzed.

Melly moves independently in a wheelchair. She can pull herself up with her hands She enjoys contact with children and adults.  She plays with toys, handles them, and can throw them.  Melly pronounces various sounds and syllables although she points to make her needs known. She can maintain interest in an activity for 15-20 minutes.

Millie, Aaron & Ayana

Sibling Group
Ages: 10, 12, 14
Country Code: LA-2
Primary Diagnosis: ADHD, Trauma History
Millie is clinically healthy, Aaron has ADHD, and Ayana has been diagnosed with Oppositional Defiance Disorder.
Listed: Dec 2024
$31.50
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!
Millie, Aaron and Ayana came into care in 2020 due to their parents’ drug usage and failure to adequately care for them. At that time, the children had not been in school, which meant that Aaron and Ayana were academically behind and placed in a grade lower than is age appropriate. However, all three children have done well in school considering their situation.

While there is no plan to separate the children, Millie and Aaron have expressed not wanting to be with their older sister as she mistreats them. The child study for the oldest sister recognizes that she has mistreated then, but also notes that she has made some progress since being in therapy and also since the children have lived in a positive family environment. Continued therapy is needed and is being received. The children have expressed wanting a family with a mother and a father as this is what knew before coming into care, but this is not set in stone.

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.

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.

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.

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.

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.

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.

Dawn and Donna #

Sibling Group
Ages: 5, 5
Listed: Jul 2024
$144.00
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!
Dawn & Donna are  twin girls who were born in Ukraine at 29 weeks gestation. They lived in an orphanage in Ukraine until they were 1.5 years old, at which time they were moved to an orphanage in Bulgaria. They were then moved to a different placement in Bulgaria at age 3, where they still reside.

 

Donna’s medical diagnosis includes: Retinopathy of prematurity (ROP) stage 5, post vitrectomy condition bilaterally; secondary glaucoma. Left eye ROP stage4 Nystagmus. Delayed neuro-psychic development. Condition after low birth weight. Self-aggression. Spastic quadriparesis. Iron deficiency anaemia

 

Dawn was born first. Her medical diagnosis includes: cerebral palsy – spastic quadriparesis. Spastic quadriparesis. Suspected hydrocephalus with normal pressure and hypoplasia of corpus callosum. Grade 1 hypotrophy. Convergent strabismus; hypermetropia. Condition following very low birth weight.

 

Update July 2024: After their placement into the foster home on May 14, 2024, the girls have adjusted well and made noticeable developmental progress. They show an attachment to the foster mom and follow her instructions. One of the girls can now walk independently and is well oriented in the foster home. The other girl sits with little support. The girls now eat mashed food from a fork or spoon and chew well. They have learned to speak their first meaningful words and are also observed to repeat syllables. While there’s some jealousy between the sisters when it comes to receiving attention, they are emotionally close and hug/hold hands. Videos from July 2024 show one girl as tenacious in exploring her environment and the other as joyful when playing on the floor. The girls attend therapy twice a week and their foster mom is proactive in seeking additional services for them. They like music and singing and enjoy massage from the foster mom. They are thrilled to be playing in the inflatable pool in the backyard. Their foster mom describes them as positive children who will continue to make progress with the right interventions and lots of love.

From a family who met them in 2023

I met these twins when I visited my daughter for trip one in 10/2023. One twin was active and was able to stand holding on and cruise around her crib. She was able to climb right out of her floor crib and back in herself. It was an activity for her and she did it with great ease. She wasn’t trying to escape at any point and would just flip In and out over and over again. She seemed like what you would expect for a toddler. She stopped what she was doing when someone called her name and turned in the direction of their voice. The other sweet twin was always laying down when I saw her. Sometimes in a crib, sometimes in a seat. My daughter asked for “baby” all the time and they would put this twin in her crib with her to lay together. They said she was more “severe”. She definitely seemed more infantile. They were in a really great place where they got plenty of food and were carried around a lot by the staff there. There were 8 kids on that floor in four rooms. The twins shared a room. I believe they are now in a foster situation. They def were pretty easygoing. They had a lot of musical toys which they seemed to like. The active twin kept herself busy a lot but the quiet twin seemed to love cuddling and other kids being around her. I think some of the delays they have may be related to vision impairments. I would imagine they would do well with siblings.

Brooklyn and Bailey #

Sibling Group
Ages: 9, 10
Primary Diagnosis: Muscular Dystrophy
Listed: May 2024
$5,006.50
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!
Brooklyn and Bailey are brothers, they reside in a foster family.

Brooklyn has muscular dystrophy and a speech disorder. He has normal mental development. In 2020 he experienced burns over a large portion of his body and had right-sided bronchopneumonia. Therapy: Operative excisional cleaning of the wounds, sterile dressings; intensive treatment of thermal shock; antibiotic therapy. Brooklyn receives additional support in the form of resource teaching. With him a team of specialist work –speech therapist, psychologist, and resource teacher within the limits of the pre-school. The child is for a second year in a row in the same preschool class, because he was delayed from starting first grade because of medical reasons. He likes artistic activities and playing with his peers. He understands and strongly desires to be adopted, even if he does not talk much, his short dialogs are for his future surrounded by his loved ones.

Bailey is a healthy child with age-appropriate physical and neuropsychological development. He has good communication skills, has leadership qualities which sometimes turn bossy, and has a group of friends. He is curious, social and actively interacts with the people around him of different ages. Bailey has the attitude and the mindset for the adoption process with the needed positivity towards providing good living
conditions, including satisfying of the physiological needs, the needs for security, love and belonging, respect and self-affirmation. He understands and strongly desires to be adopted, he often talks about his future, surrounded by his loved ones. The adoption process is so desired and awaited by Bailey. The child is prepared and
ready to have his family, his adoptive parents.

Nany #

Girl, Age: 3
Primary Diagnosis: Blind / VI, Cerebral palsy
Nany has retinopathy of her left eye, cerebral leukomalacia with manifestation of spastic quadriparesis, bronchopulmonary dysplasia and asthma.
Listed: Apr 2024
$1,356.70
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!
Nany was born with an extremely low weight and a complicated neonatal period. She has retinopathy of her left eye, cerebral leukomalacia with manifestation of spastic quadriparesis, bronchopulmonary dysplasia and asthma. This sweetie needs a very special family.

The agency staff member who met her during March of 2024, says the following: Nany likes music, and it seems to settle her down. She also likes being in the swing. At times she turned to various sounds. She can lift her head slightly while lying on her stomach. Nany is an extremely fragile, sweet and lovable little girl who needs lots of love, attention, understanding, support and lots of cuddles. Given the serious diagnoses, working with additional specialists definitely would ease and help the child’s condition. Nany is in need of a very prepared and supportive family.

Nany’s current adoption agency has grant funding is available for qualifying families.

Eddie #

Boy, Age: 3
Listed: Mar 2024
$1,100.85
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!
Meet Eddie! This sweet little man just turned two years old. He likes to transfer a toy from one hand to the other and will look for a dropped toy. He is able to push buttons on electronic toys, and he reacts positively when adults try to engage him. He is able to roll from side to side and can sit with some assistance. Because of his medical diagnoses, Eddie receives all of his nutrition via a g-tube. He sleeps well and protests at bath time. His diagnoses include Congenital malformation of the digestive system – atresia of the esophagus with tracheoesophageal fistula. Condition following surgical intervention; implanted percutaneous g-tube. Congenital heart malformation – small intraventricular defect. Protein-energy malnutrition. Delayed psychomotor development. He will almost certainly need  more surgeries in the future in order to eat by mouth, and any family considering Eddie should be sure they are prepared to meet his medical needs.

Elise #

Girl, Age: 6
Primary Diagnosis: Genetic Condition (non-DS)
Cornelia de Lange syndrome,
Listed: Feb 2024
$0.00
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!
Elise arrived with a unique constellation of traits known as Cornelia de Lange syndrome, primarily affecting her facial features. She’s a delicate soul with a sweet disposition, and her gentle nature is simply heartwarming.

This precious little one thrives on affection — she has an incredible capacity for love and blossoms with nurturing care that includes endless cuddles, tender personal interaction, and thoughtful understanding. She merits a patient touch and activities tailored just for her, which will provide not only pleasure but also enriching experiences.

During our time together, Elise remained serene and composed, displaying a quiet passivity. My playful attempts to tickle and engage her elicited limited response initially, but as patience persevered, her awareness and interaction gradually emerged.

Elise’s life would be beautifully complimented by a loving family atmosphere, filled with unwavering support and encouragement. A home that teems with warmth and offers plentiful one-on-one interaction, a trove of stimulating activities, and specialist involvement, would cultivate her growth and happiness.

To the kind-hearted families contemplating the rewarding path of adoption: envision a life with Elise, where every day is an opportunity to nourish and celebrate a precious child’s potential, and where love knows no bounds.

Goliath

Boy, Age: 6
Microcephaly, CP, epilepsy, blind
Listed: Dec 2023
$2,786.14
has been donated towards the cost of my adoption, including $0.00 from MACC donations!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Goliath is the cutest, most chill baby ever! He loves cuddles, being bounced on the trampoline, swimming, going for bike rides, being held, and chocolate. He would do great either in a big family with lots of siblings or being the only one to soak up all the attention!

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

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

Anne #

Girl, Age: 3
Spina Bifida, hydrocephalus-shunt placed
Listed: Dec 2023
$1,940.00
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!
Anne is delayed in all aspects of her development. She recently began eating from a spoon, and the NG tube was able to be removed. She enjoys attention from staff. She smiles when caregivers speak to her. She reaches and grabs objects, but is not yet playing with toys.

Vernon #

Boy, Age: 5
Spina bifida; hydrocephalus- shunt; delays in all aspects of development
Listed: Dec 2023
$1,018.00
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!
Vernon crawls using his upper body. He plays with toys and interacts with familiar adults. He responds to his name by turning toward the person calling him.

 

Update 10/24

He has several special needs including congenital internal hydrocephalus and spina bifida aperta (thoraco-lumbar). Vernon is undergoing daily rehabilitation. His condition is monitored by a pediatric neurologist, a neurosurgeon and a pediatrician.

Vernon can turn independently from his back to his stomach and vice versa. He has good head control. He can purposefully grab a toy and hold it.  He enjoys personal attention from an adult, laughs loudly at teasing and reacts with displeasure when left unattended. He is mostly calm. No aggressive behavior was recorded. When he is called by name, he turns toward the direction of the sound.  He reacts to a noise stimulus. He speaks syllables and long sound combinations.

Woodrow

Boy, Age: 11
Primary Diagnosis: Blind / VI, Cerebral palsy
Microcephaly, Cerebral palsy, Optic Nerve Atrophy
Listed: Sep 2023
$2,648.50
has been donated towards the cost of my adoption, including $0.00 from MACC donations!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Woodrow can sit up independently and will sometimes kneel as well. He occasionally bears weight on his feet, but cannot put his feet completely flat and because his ankles are so tight. He would need surgery before being able to do so. Woodrow doesn’t really scoot or crawl, but he can still make his way across a room by rolling and wiggling.

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

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

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

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

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

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

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

Walt

Boy, Age: 9
Country Code: EE-6
Listed: Aug 2023
*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***
$1,510.00
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!

Walt  has been diagnosed with autism and developmental delays. He is nonverbal, does not engage with peers, and prefers to play with rotating, round objects. Walt does not show aggression and expresses warmth toward others on his own initiative. He likes to receive hugs from his foster parent.

Joyce

Girl, Age: 10
Country Code: Asia.2
Region: Asia
Listed: Dec 2022
$1,047.00
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!
Joyce LOVES to sing and dance!  Her favorite sing along songs are “Baby Shark”, “Cagabrie Island” and “Jasmine”. Joyce also enjoys riding on a motor scooter because she enjoys looking around at the sights and feeling the wind in her hair!

Those who know Joyce say she has a gentle personality. She likes to act cute and will become lively around familiar people. Joyce has a good relationship with her foster parents and gets excited when their 7 year old grandson visits on the weekend. They get along well and play with each other for hours.

Joyce presents with global delays and has Epilepsy and Thalassemia.  It is suspected she has ADHD.  Joyce attends OT and PT sessions. Joyce attends special education classes at elementary school and an afterschool class. She is making progress with her language skills and can respond to questions with single words.

Are you a family that can support Joyce with growing her language skills? Enjoy singing along to nursery rhymes with her?

Ashton

Boy, Age: 7
Country Code: LA-2
Primary Diagnosis: Hydrocephalus
Hydrocephalus and Developmental delays
Listed: Nov 2022
$748.50
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!
Ashton is an adorable little boy who is described as a social child who loves to be around others who give him affection. He shares with the people around him. He loves to hear music and pleasant sounds. He likes painting and watching animated shows. Contact the agency to learn more about Ashton and his special needs!

NEW VIDEOS:
https://vimeo.com/maaspecialkids/maa-ashton3
https://vimeo.com/maaspecialkids/maa-ashton4
https://vimeo.com/maaspecialkids/maa-ashton05
Password: Adoptmaa

OLDER VIDEOS:
https://vimeo.com/maaspecialkids/maa-ashton1
https://vimeo.com/maaspecialkids/maa-ashton2
Password: Adoptmaa

Bailey

Girl, Age: 12
Country Code: LA-2
spastic quadriplegia; generalized hyperreflexia; epilepsy; global developmental delays
Listed: Oct 2022
$67.50
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!
Bailey accepts physical and verbal contact from others. Bailey likes toys that make noise, and she sometimes smiles at the stimulation of an adult. Bailey will need a family who is able to care for her special needs and provide for her daily care. Agency staff met Bailey in July of 2022. We hope her family sees her soon! Contact the agency to learn more about Bailey and her listed medical needs.

VIDEOS:
https://vimeo.com/maaspecialkids/maa-bailey001
https://vimeo.com/maaspecialkids/maa-bailey002
https://vimeo.com/maaspecialkids/maa-bailey003
https://vimeo.com/maaspecialkids/maa-bailey004
Password: Adoptmaa

Katrina #

Girl, Age: 12
Primary Diagnosis: Global developmental delays
Listed: Sep 2022
$2,065.10
has been donated towards the cost of my adoption, including $0.00 from MACC donations!

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

Katrina’s physical development and gross motor skills are age appropriate. She talks, but has some difficulty with articulation. Her fine motor skills are developed, but slightly delayed. She is diagnosed with mental delays. She knows and names the colors. She knows the letters of the alphabet and she has started reading. She already counts up to 30 and she writes some numbers. She knows the days of the week, seasons, left vs right, body parts, and can follow directions using instructions such as over/under, front/back, etc. She plays well with other children and enjoys attention from adults. She likes to work on a magnetic board, kinetic sand and active cards. She already colors in a contour and she is very diligent when connecting lines. She can cut and glue ready elements. She can read and the fact that she is being praised for that makes her very happy.

 

She follows the directions of an adult in relation to the hygiene and household activities. She can dress and undress her. She washes her hands and feeds herself independently, she makes attempts for self-serving. She takes care her belongings. She keeps her materials from school in a certain place.

Augustus #

Boy, Age: 7
Primary Diagnosis: Cerebral palsy, Hydrocephalus
Internal hydrocephalus: state after implantation of a VP-shunt; epilepsy; spastic quadriparesis; cortical blindness; delay in the neuro-psychic development
Listed: May 2022
$2,631.50
has been donated towards the cost of my adoption, including $0.00 from MACC donations!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Augustus was born full term, and was found that he has internal hydrocephalus; at the age of 4 months a liquid drainage valve system was implanted. The child lies in bed; he has spasticity in his limbs and his active and passive movements are limited. He depends completely on the care provided by adults. He receives kinesiotherapy. The child is subject to observation by a neurologist and by a neuro-surgeon.

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

Alan

Boy, Age: 14
Country Code: EE-2
Primary Diagnosis: Other Special Needs
Listed: Dec 2021
$667.00
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!

Alan is amazing 10 years old boy who had a rough start with an unstable and unhealthy environment. He is the victim of parental physical abuse and suffers from post-traumatic past

He connects well with both peers and adults. He is calm, helpful and kind. The boy eagerly learns about nature, sings songs, makes interesting art works, uses computer programs well.

He needs a forever home to support him as he continues to overcome negative experiences of his past and shower him with the love every child deserves.

He has a lot of potentials and wants to be adopted. He is highly recommended by his caregivers. The family with an involved, hands-on father will be ideal for this boy. He would do really well as the youngest or only child (or in a family where the other children are grown). He needs an experienced adoptive family who can give him a lot of one-on-one attention and help build his trust in humanity back.

Emma #

Girl, Age: 9
Condition after herpes-viral encephalitis. Hepatitis caused by CMV. Hypotrophy. Hydrocephaly – of mild degree. Congenital dyserythropoietic anemia. Delayed neuro-psychological development.

Listed: Sep 2021
$2,190.50
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!
Emma was recently transferred to a group home where she can receive more specialized care to help her continue to develop and receive appropriate medical care. She is receiving monthly blood transfusions at this time for her anemia. She had surgery to correct clubbed feet in 2020. She can sit unassisted, stand next to a stable support, walk around fixed supports and walk while holding the hand of an adult. Videos from May 2021 show Emma playing with an electronic toy. She is pushing the button to get the toy to make a sound. Her fine motor skills are not well-developed at this time, due to her spasticity. Emma responds positively to adults and other children. She smiles and laughs when adults interact with her.

 

The agency staff member who visited her during March of 2024, says the following:

Emma is a sweet little girl who needs a loving and supportive family environment. During my brief visit, the child was constantly on the move except for the brief moments when she played with a particular toy or during her brief moments of protest. At the present time, the child’s needs are met at a basic level, with particular attention paid to her medical needs. The lack of systematic and in-depth work of specialists (such as a rehabilitator, occupational therapist, special pedagogue, speech therapist and others) is felt, which the institution currently does not have the opportunity to provide. By falling into a suitable loving family, receiving more attention and adequate care and activities, Emma could show her potential to a greater extent.

Update 8/2024

Special needs: low birth weight – 1800 gr; condition after herpes viral encephalitis; condition after hepatitis caused by CMV; congenital dyserythropoietic anemia; hydrocephalus – mild degree; infantile cerebral palsy – spastic quadriparesis; symptomatic epilepsy; delayed neuropsychological development
Therapy: Convulex 4+4+4 ml., Clonarex 2 x ¼ tablet, Repitend 4 ml – 0,4 ml. Carsil – 2 x ½ capsule daily, EXJADE – 1 tablet daily, Urinal x 5 ml daily, Vitamin D3 x 2
Emma makes steps but always and only with the help of a support. She does not control her physiological needs and wears diapers. She listens to children’s songs and fairy tales and claps with her hands. She holds a toy she has been offered but she would most often put it in her mouth without playing with it.
Emma needs monthly blood transfusions and regular consultations with a neurologist and hematologist.

Zeek #

Boy, Age: 6
Primary Diagnosis: Hydrocephalus, Spina bifida
Spina Bifida; shunt placed for hydrocephalus
Listed: Sep 2021
$2,067.50
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!
Zeek is being taught to use a wheelchair. He can currently turn, but has not yet mastered going forward and backwards. He is also learning to pull his torso up and move around when in his bed or on the floor. He can physically handle toys. He picks them up, transfers them between hands, looks for them and retrieves them if he drops them. He can push buttons and activate sensory toys. He follows simple directions such as “give me”. He plays peek-a-boo. He enjoys interacting with the staff. He will hold out his hand for a hand shake, make kissing noises, and reaches to be held. He uses his hands to show how big he will grow up to be when asked by an adult. He is pronouncing sounds and syllables.

Updated May 2022: Zeek was recently moved from a large orphanage to a small group home, where he’s now receiving more interaction and attention. His language skills have started developing. He can now say several words. He enjoys interacting with staff and responds when he receives attention. He enjoys music.

Tyson #

Boy, Age: 8
Listed: Apr 2021
$1,854.00
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!
Bilateral sensorineural hearing loss (with hearing aid); shunt due to internal hydrocephalus; spastic cerebral palsy

Tyson was born premature and had several complications after birth. He can sit on his own with good balanced reactions. He crawls following the correct motor model. He stands up and walks sideways vertically. He can walk when one of his hands is held and has more control when it’s his right hand being held. He can stand up straight without falling for 2-3 seconds. When walking with a walker, he begins to bend his knees. He purposefully grabs a toy that is handed to him and can switch it from hand to hand. He shows an interest in musical toys and enjoys them. He has started making sounds and simply syllables such as “ma-ma”. He enjoys having someone sing to him and likes to receive hugs. He eats from a spoon. His overall development is delayed.

Photos and videos from August 2020 are available through the agency.

Scotty #

Boy, Age: 11
Primary Diagnosis: Spina bifida
Lumbar spina bifida (surgically corrected), grand mal seizures, spastic cerebral palsy, hydrocephalus
Listed: Mar 2017
$1,037.90
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!
Scotty has little support from his legs. His head control has improved and he can turn from his back to his belly. He sits independently by holding on to the bars of his crib and also makes attempts to stand up. Scotty can hold toys in his hands and tries to clap! He maintains eye contact and recognizes the faces of his caregivers. Scotty expresses appropriate emotions to happiness and agitation and will laugh out loud when teases. He imitates and pronounces combinations of sounds and syllables. Scotty interacts with all children and caregivers. He likes music and toys. Scotty is fed by a spoon and receives additional nutrition from a bottle.

Molly May #

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

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Molly May has made progress in her development during recent months. She is able to sit unassisted, get up on her knees and has begun to start trying to move around in a walker. She is becoming more physically active. She makes eye contact, looks around for families adults and smiles when someone looks at her. She will laugh out loud when an adult plays with her. She watches children’s cartoons and movies on the TV and will get excited and point to the screen when the TV is turned on. She picks up toys and attempts to play with them. She still needs instructions in how to appropriately play with toys. She makes vocalizations in an effort to communicate. She eats soft foods from a spoon.

Molly May has undergone multiple surgeries to repair her cleft lip & palate. She is under the continued care of the doctor who is performing these procedures. She is also under the regular care of a neurologist, who diagnosed her with CP in 2018. She had suffered from “constant shaking” resulting in uncontrollable movements up until a few months ago. The social worker reports that this has greatly improved and that Molly May’s movement are now more calm and she also sleeps calmly too. Videos taken in April 2019 show her interacting with toys.

Photos and videos are available through the agency.

Mila #

Girl, Age: 9
Hydrocephaly; Strabismus; G-tube feeding; delays in development
Listed: Jul 2018
*** I am eligible for a $2,000 Grant! ***
This grant is offered by Reece’s Rainbow, for children in this specific country. Grant funds are dependent on available funding. For more information, email childinquiry@reecesrainbow.org ***
$853.00
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!
Mila turns her head towards sound and looks at people and objects of interest. She recognizes the faces of the staff. She can roll over, but still has difficulty with head control. She enjoys musical toys that spin and will focus on those for short periods of time.

Update 8/2024

Special needs: low birth weight (2410 gr.); congenital anomaly of the central nervous system: moderate ventriculomegaly; cyst of the cave of septum pellucidum and cave Vergae; rejected prior diagnosis of hydrocephalus; brain atrophy; infantile cerebral palsy; syndrome of congenital anomalies mainly affecting the facial area; convergent strabismus; nystagmus; occipital alopecia areata;  severely delayed physical and neuropsychological development; severe mental delay
                                                                                                                        
Family history: born from a high-risk pregnancy by a mother with positive serology for hepatitis B and epilepsy (on three medications for epilepsy).
Molly turns independently in bed. Although she is unable to sit independently, Molly maintains a sitting position for a more continuous period at the presence of additional support. She has no stable support in the legs.Molly selectively responds with an appropriate emotional reaction to different situations and objects. She is able to express discontent from internal discomfort through crying. She smiles as a response to a smile, speech and closeness from the caregiver, she positively reacts to positive stimulation. Molly easily handles being moved from one space to another, she is calm and sometimes demonstrates interest. She has formed emotional preferences to certain significant members of the staff, mostly the rehabilitator who works with her, as well as the teacher from the group at the Center for Special Educational Support. Molly laughs at specific sounds coming from a musical toy. She shows preferences for specific children’s songs while she does not react to others.
Molly wears diapers, easily goes to sleep and easily wakes up. She eats food from a spoon

Kaylyn #

Girl, Age: 11
Primary Diagnosis: Cerebral palsy
symptomatic epilepsy-partial seizures with secondary generalization; spastic cerebral palsy; hypoxic-ischemic encephalopathy of 2nd degree; profound mental delay;
Listed: Feb 2018
$2,004.50
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!
Kaylyn is in severely impaired condition and her development is delayed in all areas. She is completely dependent on adults’ care. Her sleep is calm and rhythmical. She is fed with a spoon by an adult.

Josiah #

Boy, Age: 9
Primary Diagnosis: Genetic Condition (non-DS)
genetic metabolic disease – pyruvate-kinase deficiency – homozygote mutation p-R 446; mild to moderate core and periventricular lesions; generalized muscle hypotonia; severely delayed physical and neuro-psychological development;
Listed: Oct 2018
$1,000.10
has been donated towards the cost of my adoption, including $0.00 from MACC donations!

Your gift will serve ALL of the children, as 10% of each Waiting Child Donation is shared with our Voice of Hope fund, as well!
Josiah moves in space by turning from back to belly and vice versa. He has started forming some of the perceptions about objects from his constant surroundings and everyday life. He connects some objects from his surroundings with the actions performed with them.

When awake, Josiah is mostly calm. He would laugh out loud when jested. During active interactions with adults Josiah pronounces various sounds and random syllables. Josiah follows a specific dietary regime and has food individually prepared for him. He is fed with a spoon by an adult and has a picky appetite. He is calm during dressing and bathing. Josiah’s sleep is calm.

Isaac #

Boy, Age: 12
Primary Diagnosis: Cerebral palsy
Craniosynostosis with microcephalus; Infantile cerebral palsy – spastic quadric paresis; Suspected atrophy of the visual nerve on both eyes; Delay in the physical and neuro-psychical
Listed: Jun 2015
**** I am eligible for a $5000 Older Child Grant ****
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
Isaac is a sweet little boy living in an Eastern Europe orphanage. He cannot sit without support or turn between his stomach and back. There is little support in the legs. Isaac doesn’t have an attention span and doesn’t focus on his surroundings. He reacts to touch but doesn’t when verbally addressed. He doesn’t understand speech but sometimes makes sounds. Isaac is mostly calm and smiles. He doesn’t interact with the children and adults around him.

There is little reaction with toys and no playing when in his possession. Isaac is completely dependent on the help of the staff.

Condition after a brain hemorrhage. Cyst in the left cerebral hemisphere. Microcephaly. Spastic quadriparesis. Cryptorchidism. Anemic syndrome. Behind in his neuro-psychical development. When put on his belly or held, he keeps his head up. He slightly turns to one side but doesn’t turn independently from back to stomach and vice versa. He doesn’t try to sit up and doesn’t get up to a standing position. He doesn’t have good support in his legs. He starts after loud sound but doesn’t turn his head to the direction of the sound. He listens to the speech of adults. He doesn’t look at an adult leaning over him. He doesn’t follow with a look moving objects or people. He reacts to touch. He is calm and doesn’t cry without reason. He reacts positively to interactions and laughs loud. Photos and videos from June 2015 are available through the agency.

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.