It is our true belief that there is a “forever family” for each of our waiting orphans with special needs.
The purpose of Reece’s Rainbow is to raise funds as adoption grants, to help potential adoptive families with the high cost of giving these children the life they so richly deserve.Your donations and advocacy turn the child on the left into the child on the right! This page includes the profiles of those children with larger grant funds available.
Put on your WARRIOR shoes and help us find families! PLEASE SHARE THIS PAGE, that others will see it and take that leap of faith to save a child in need.
.2
Elaine is the youngest; HIV, Other disorder of speech; Abnormal results of cardiac function
Down Syndrome; heart condition – operated
Cerebral palsy; symptomatic epilepsy; mental delay
Traumatic Brain InjuryHe has a pretty good memory and good eyesight.
hydrocephalus (shunted), spastic tetraplegia, epilepsy unspecified, optic nerve atrophy
They have a younger sibling who is not available.
Other congenital hydrocephalus; other disorders of nervous system; optic atrophy; anemia
Communicating hydrocephalus; Paraplegia; Epileptic seizures related to external causes; Other congenital deformities of hip; Optic atrophy; Other visual disturbances; anemia
Other congenital malformations of limb(s); Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
She gives thumbs ups, is speaking a few simple words, and blows kisses. She needs help getting dressed, but puts on her own shoes. She has started potty training. She is good at imitating and her caregivers describe her as sweet and engaging.
Nancy needs a family of her own. Anyone’s life would be brighter with Nancy’s hugs in it! Additional information and photos can be found in this blog post.
Recently, the orphanage’s physical therapy team has been working on the right side of his body, which seems a little weaker than the left. He is not able to hold things in his right hand. Kenny’s mental development is age appropriate. His physical development is good – he can crawl, sit, and walk holding on. Kenny is very attached to his nannies and loves to play with the 10 children in his room. Can Kenny be the son you’ve been searching for?
Ezrah has an extroverted personality, is active, likes to play games with peers; he likes colorful toys with making sounds; he responds actively to stimulation of new things or strangers.
In an update from January 2016: Ezrah isn’t receiving any therapies for his conditions, and can’t yet stand or walk on his own. He gets around very well by crawling using his arms. Ezrah can speak in simple phrases, and express his ideas easily, as well as follow simple instructions from caregivers
April 2016 update: Ezrah is active and outgoing. Ezraht’s mental development is the same as kids the same age. His lower limbs make it so that he cannot walk. He knows and will tell adults when he needs to go to the bathroom. He can use the baby toilet by himself. Ezrah is well behaved and obedient.
He cannot walk, but he can move on his bottom with hand coordination. His fine motor skills are good and he can pick up rice. He cannot go to school due to his special need. Ezrah has good emotional development. He can read faces. He is attached to his foster mother and will share food with her. Ezrah can express his needs well and can follow simple directions. He is a very smart child! He can call the familiar people properly. Ezrah likes to play games with his foster family and other kids. He has been in the same foster family since March of 2014. He is not on any medication.
Brody is learning well and is he learning how to crawl. He can hold his own bottle and toys and likes to be active. He is not making sounds yet but he always has a ready smile.
Johnny has a diagnosis of Down syndrome with developmental delay, a gastrostomy and thyroid profile within the normal upper limit for his age. He is a little late for his age on his speaking and would do best in a family that can help him work on this. His family must be very loving and work consistently on his development.
Video available.
Cerebral palsy and temporal lobe epilepsyUpdate Feb 2018: With lots of patient attention, we are finally seeing Jubilee make an effort to be part of the world around her. She is doing so much better lifting up her head during tummy time. She has also started making some small but intentional hand movements when we are holding her with a toy in her lap.
Updated August 2019: Jubilee is a sweet 6 year old girl. She goes through phases where she is very happy and smiles a lot, and then goes through phases where she doesn’t smile very often. She is quite opinionated and will always let us know when she is uncomfortable, hungry, etc. She is adored by everyone that knows her. Her nannies love to dress her up, do her hair, and take her for walks. At school she is working on making choices, using her hands to reach out, and focusing her eyes on one thing at a time. In therapy she is also working on purposeful movement, range of motion, standing, and several other things.
Down syndrome and strabismushttps://vimeo.com/maaspecialkids/maa-bria
Password: Adoptmaa
Bria has a $2,500 agency grant for her adoption with the agency who listed her; additional grants may also be possible.
The agency has a video available of Bailey! There is a $2,500 agency grant for Bailey’s adoption with a specific adoption agency.
Spina bifida of lower lumbar and entire sacral region. Hydrocephalus (with VP shunt) and Chiari malformation. Had operation to release tethered spinal cord. Is catheterized.In classes Zack is currently learning shapes, days of the week, numbers one through ten, and the first five letters of the English alphabet. In play time he often requests blocks in order to build towers. Once they are completed he will call his caregiver in order to proudly show off his creation. When he is not building blocks he loves coloring, making crafts and playing with toy cars. His new favorite sensory play is with shaving cream. On Christmas the staff in his home filled a plastic swimming pool with shaving cream so the children in his home could play with “snow.” Ever since he has begun asking for shaving cream daily in his sensory class.
Recently Zack was gifted a new wheelchair that allows him to more easily reach the wheels. He has begun learning how to push himself in his chair. He is thrilled! While he is still in the early stages of learning this skill, he is already showing amazing progress! Obtaining this skill will be huge in Zack’s independence! He loves practicing and will often request to be taken on walks. Zack often asks about his future family and is eager for the day that he is able to meet his mom and dad!
July 2019 update: Zack is the naughtiest and happiest boy in his home! He learned all his colours and is now learning his animals. He wants to be more independent! He can scoot backwards to get around by himself. He can make requests in both English and his local language and can translate English words to his local language for his caregiver! Zack loves his caregiver Ammama so much. He always scoots over to be near her and wants to be a part of what she is doing. One day he kept asking Ammama for a new shirt, so when she went on her monthly leave she brought him back a new blue shirt.
A traveling family met Simon and said, “Within the three days we spent at the orphanage, we were able to bond with him to the point he would smile and get excited when he saw us. The older girls told us he can understand what they say to him. He enjoys being held and carried around, but spends most of his day sitting in a baby walker or high chair. He seems very easy going, as we didn’t see him complain about being put in his crib for nap time, etc. The caregivers are working on his motor skills. He can eat with assistance and enjoyed the ice cream we brought! It’s so easy to fall in love with this little boy! We are praying his family sees him soon!”
Simon has spastic quadriplegic cerebral palsy and has had seizures. He takes 30 mg of Phenobarbital once a day. Simon has mild hearing loss of the left ear. Therapy has helped lessen the spasm and Simon can open and close his hands. Simon loves being around people and making faces! When praying before meals, he bows down his head and says “ahh” when everyone says “Amen.” We’re hoping a wonderful loving family comes forward for this special little boy! There is a $500 agency grant for Simon’s adoption with his adoption agency.
Shiloh also enjoys water play. With the assistance of her teacher, she splashes water around a sensory bin; using cups, shovels, and other water toys to manipulate and move the water. Her favorite game is when her caregiver counts to three and then leans her backwards. As her caregiver starts to count, a grin will flash in anticipation of being “thrown” backwards. Shiloh is a deep lover of life and friendship and would thrive in a family of her own.
UPDATE July 2020: Georgie has been making steady progress in his language skills. Lately, he has begun to make requests on his own or make jokes in conversations with his teachers, caregivers, and house mom. Georgie’s favorite little joke right now is to reply “JUICE” to each and every question asked of him. He erupts into giggles and repeats the word over and over until tickles and exclamations prompt him to give the real answer that we were looking for. We recently celebrated Georgie’s 6th birthday, and when asked what he wanted to do for his party he answered without hesitation: “DANCE PARTY!” Georgie can count to 10 and is learning his first braille characters!
She wants adult’s attention and likes to lean on an adult, sit in their lap, and give hugs. Her fine and gross motors skills development are adequate. She is friendly with adults and children.