These beautiful children have already waited so long for a family to call their own! Every year it gets harder and harder to find experienced adoptive families for them. Your donations make it possible to re-write the course of their lives.
Donate online via Paypal or send a check to Reece’s Rainbow, PO Box 146, Combined Locks, WI 54113
*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!
Want to be a Prayer Warrior for any of these children? Click here!
Jordan
Contact the adoption agency to learn more about Jordan and his special needs! We sure hope someone brings this cutie pie home while he’s still so little!
NEWER VIDEO:
https://vimeo.com/maaspecialkids/maa-jordanupdate
Password: Adoptmaa
Sal & Monty
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.
Ryan
He likes music, likes to hear the sound of other children playing near him and it makes him smile. He likes to be cradled, and to have his head stroked. He doesn’t like to cry very much, he only cries when he is sick, or when he needs a little attention.
In therapy, he works on range of motion and stretching to prevent further contractures of his limbs, to turn his head to the right, since he tends to lean his head to the left, and to improve functional use of his arms and hands. At school, he uses sensory material and adapted activities to help him develop his academic abilities.
Salvador
VIDEOS:
https://vimeo.com/maaspecialkids/maa-salvador1
https://vimeo.com/maaspecialkids/maa-salvador2
https://vimeo.com/maaspecialkids/maa-salvador3
https://vimeo.com/maaspecialkids/maa-salvador4
https://vimeo.com/maaspecialkids/maa-salvador5
https://vimeo.com/maaspecialkids/maa-salvador6
https://vimeo.com/maaspecialkids/maa-salvador7
https://vimeo.com/maaspecialkids/maa-salvador8
https://vimeo.com/maaspecialkids/maa-salvador9
Password: Adoptmaa
Samuel
Samuel is an energetic and strong willed 5 year old boy who loves outdoor activities, playing with robots, puzzles and watching movies! Samuel said he would like to become a policeman when he grows up.
Samuel is not shy! He enjoys interacting with new people and likes playing in groups. His foster father said Sable “feels especially loved when there are more people interacting with him.”
Samuel resides in a foster home and has a 2 year old foster sister. He has a close bond with his foster parents and often expresses his affection to them.
Samuel has developmental delays and suspected ADHD. He attends occupational and speech therapy. During a recent visit with his social worker, he demonstrated his ability to string beads together, stack blocks and draw with a pencil. His articulation and pronunciation have improved, and he is able to clearly express himself. Sable also attends group therapy to help improve his interpersonal skills.
Archibald #
hydrocephalus; a ventriculoperitoneal shunt was implanted. There is a lag in physical and
neuropsychological development.
Archibald cannot walk independently. He moves by pushing when placed in a walker. Stands up on his own and stands on his feet when in his crib. He can get out of bed by himself. He can go around the whole game room. He can sit for about 15-20 minutes. In terms of fine motor skills, he can pick up a toy himself if it is nearby; he plays for a long time and prefers to manipulate with his left hand. If the toy is at a distance, he tries to reach it. He likes musical toys. He recognizes adults. He has a good emotional tone, he enjoys contact with adults he knows; he loves when they praise him. He gets angry if his toy is taken away and tries to keep it in his possession. Archibald cannot speak but he makes long sounds. In interpersonal relationships he shows preferences for certain adults and initiates contact with them. He plays with toys. The child doesn’t have independent household hygiene habits. He is calm when changing and bathing, as well as in his sleep. Archibald does not take an afternoon nap, he eats everything. He is very stubborn and when he decides that he wants to pick up an object, no matter how heavy and large, he does his best. He still uses a diaper, potty several times a day. His sleep at night is
peaceful. He has daily kinesitherapy and sessions with a teacher. He is followed by a
neurosurgeon.
Jeremy
The agency has additional medical information and videos available.
Wayne #
Christopher
Christopher now has a $500 agency fee reduction for his adoption; Additional agency fee reductions may be available based on the adoptive family’ circumstances!
Dawson
Dawson is a 5 year old boy who is active and cheerful. He has been diagnosed with fetal hypotrophy, myopia, and nystagmus. He demonstrates curiosity and is very observant. His psychomotor development is good for his age. He moves independently, both walking and running. He struggles with maintaining balance, but he has improved in coordinating his movement. He hasn’t reached age-appropriate communication skills, but he has made significant progress in this area. He can imitate gestures and words and he understands basic commands. His emotions are becoming more complex. Dawson can remember the names of his peers and caregivers. He eats meals independently and is getting better at changing clothes without help. He is making steady progress and has demonstrated the ability to aquire new skills.
Ben
Ben is a determined and easy-going child despite his significant medical and developmental needs. He is described as having a gentle temperament and finds contentment in simple pleasures like listening to children’s songs, sleeping peacefully and engaging with his caregivers.
Ben has been diagnosed with Chromosome 2q deletion with developmental epileptic encephalopathy, and global developmental delay. His developmental age is estimated to be under 3 months. Ben also experiences visual impairment due to right eye congenital ptosis. While these conditions necessitate using a manual wheelchair and a gastrostomy feeding tube, they do not diminish his indomitable spirit. is a courageous fighter who has persistently strived for survival and shown constant improvement in his health. As of December 2023, he has successfully been weaned off oxygen therapy. Furthermore, the ward nurses report that Ben exhibits consistent progress in his motor development under the guidance of therapists. This highlights Ben’s progress in his development through appropriate stimulation. It is believed Ben will gain more opportunities to explore and develop his potential once he starts attending school. To learn more about Chromosome 2q deletion, here is one of many articles available online: GARD Rare Disease Information – Chromosome 2q deletion – National Organization for Rare Disorders (rarediseases.org)
With a loving, committed family who is open to acquiring the necessary medical knowledge, his care staff believes that Ben will receive the support he needs to continue flourishing. Ben’s gentle nature, resilience, and evident potential make him a truly special child deserving of a forever home filled with unconditional love. While some development is expected, Ben will need lifelong care from his loved ones.
A family with a home study for any country can submit for consideration of this child. If matched, the family would need to update their home study to this specific country.
Seth
The adoption agency has additional photos and videos available.
Brent #
Brent lives in a family environment. He eats pureed food and can drink from a cup. He can crawl very fast on his hands and knees although he does not walk without support. He can pull himself to standing when he desires to do so. He is frightened easily by loud sounds. He does not have a specific activity that he enjoys.
There are no manifestations of aggression, but there are manifestations of auto-aggression, most often expressed as hitting his head against the wall, the bed frame, but not with his hands. Brent loves to go outside and he is taken in a wheelchair to do so.
The in-country staff member made the following personal observations:
Brent is cared for at a basic level. Unfortunately, I don’t get the impression that the child is being worked with systematically and purposefully. There is no connection and exchange of information and guidelines between the Day Care Center and the Family-type Accommodation Center for children with disabilities. Brent needs a loving and caring family environment. He needs a family that would be willing to pay attention to him, play with him, and patiently and purposefully help and teach him.
AJ
Photo available from agency!
When the medical report was first performed when he was about one year old, AJ was not walking and a level of delay is reported in the cognitive, language and motor areas that are related to the state of severe malnutrition with which he was found as an infant.
His Grade I Osteogenesis Imperfecta is the mildest form of the condition. Osteogenesis imperfecta (OI) is a genetic disorder characterized by bones that break easily. OI is highly variable. Its signs and symptoms range from mild to severe. In addition to fractures (broken bones), people with OI sometimes have muscle weakness, loose joints (joint laxity), curvature of the spine (scoliosis), brittle teeth (dentinogenesis imperfecta), and hearing loss. A classification system dividing OI into several types is commonly used to help describe how severely a person is affected. Type I is the mildest and most common form of OI.
Sven #
Dorie, Nathan, Iggie
Nathan: Strong motor skills – correct for age. Walks, runs, overcomes obstacles. He participates in games, wants to attract attention and is upper active. Perception and hand-eye coordination – within the normal range for age. The boy notices details, differentiates shapes and colors. Recognizes pictures, selects pairs. He connects the pictures. He places the blocks in the holes of the puzzle. Builds block structures – simple and complex at the age level. Slight speech delay. Social behavior and emotional zone – age appropriate. There is a great need for a relationship, attention and contact. Sometimes he is too impulsive and reacts hypersensitive.
Iggie: Low birth weight, FAS
Strong motor skills – the boy walks independently, runs, overcomes obstacles with a slightly lower fluency. He imitates simple, single body movements, claps his hands, raises his hands up, stomps his feet, enjoys simple games with adults, keeps up with the group. He puts circles on the pyramid, builds a tower from blocks, creates a row (“trains”). He scribbles with a crayon without imitating the direction and shapes, but he likes to draw with adults.
Speech shaping – reacts to sounds from the environment, looks for the source of the sound, reacts to musical sounds. Active speech at the word stage – repeats many one and two-syllable words on command. Points to parts of the face, says the correct words (ear, eye, etc.). Social behavior and the emotional sphere – visible improvement of contact and relationships, establishing contact without difficulty. He is cheerful, establishes basic relations with children, reacts positively to games, and imitates. Develops the basics of independence in everyday activities. Eats by himself.
The children experienced neglect and abuse before coming to the orphanage.
Bodie # (Barron)
Bodie responds to his name with a smile, to sounds and noise. He keeps an eye on the movement of people and objects in the room. He is described as a calm and pleasant child. He is well attached to his caregivers and responds well to them. When given attention, he reacts positively and with a smile. Most of the time, the child is energetic and physically active. It is difficult for him to stay in one place, constantly moving and exploring.
The child expresses his joy by erratically clapping his hands and by making noises. When held by the hand he makes several steps. (was previously also listed as Barron).
Reggie
reduction anomalies.
games with other children. His speech is undeveloped and difficult to understand. Reggie is unable to concentrate or
understand abstract problem solving. He needs help learning appropriate skills to regulate his emotions. He is currently attending a preparatory kindergarten group and attends a football club because he is very mobile and inquisitive. Reggie receives speech therapy and special education support (at least 5 times a week). He speaks with slurred speech and has a developmental delay. Irregular speech speaking in 2-3 word sentences with a poor vocabulary. He follows instructions, completes a 9-piece jigsaw puzzle correctly, knows colors, builds a tower of 10 blocks. He asks the name of an unknown object, can jump on one leg (both right and left). His fine and gross motor skills are insufficiently developed, self-regulation is impaired, impulse control is weak, attention span is short, he is interested in toys and names them, but does not play with them for long periods.
Alfie
https://vimeo.com/maaspecialkids/maa-alfie
Password: Adoptmaa
Agency fee reductions may be available based on the adoptive family’s circumstances.
Geno
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 ***
Silvio
Last update 2020: Delayed psychomotor development. Visible improvement after rehabilitation. Feeding the by the bottle, playing with toys, rolls out of the back on the stomach and vice versa. He tries to crawl. A very active child who initiates contact. He makes eye contact, focuses his attention on the human face, and smiles back. Video is available from the adoption agency.
Myles
Myles diet consists of mashed foods, his favorite being fruits. Myles spends most of his time in his bed or in a support chair. Because he is only allotted one therapeutic device per year, he doesn’t currently have a child walker. With more opportunities to put weight on his legs, he may possibly have the potential for assisted walking in the future.
Myles was born prematurely and has been diagnosed with global developmental delays, cerebral palsy, epilepsy, hydrocephalus and hearing impairment. Myles resides in a nursing home and receives 30 minutes of occupational and physical therapy at a local hospital each week. The agency has much more information on Myles! Could your family be the one he needs?
Monte
VIDEO: https://vimeo.com/maaspecialkids/maa-monte
Password: Adoptmaa




















































