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!
Christian
At school, he progresses slowly with his sensory exercises which he likes and are helping him to stay awake longer than before. In therapy, he works on functional mobility, which helps him raise his hand to touch an object. He has consistently shown slight improvement in engagement with increased stimuli. He is responding more to toys and people by raising his head, laughing, smiling, and keeping his eyes open.
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.
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 #
Owen #
Finn
VIDEO:
https://vimeo.com/maaspecialkids/maa-finn1
Password: Adoptmaa
Now that Finn is 8, he has a $500 agency fee reduction for his adoption; Additional agency fee reductions may be available based on the adoptive family’s circumstances!
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




































