Daylan
Kelvin Philip
Travis
Louis
Nolan
Nicholas
Kenneth
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Brody and Auggie
Auggie born March 2005: Rough mental delay, partial atrophy of eye nerves, cerebral palsy, Epilepsy-FAS
Haile
Ryland
Artie
Kipper
Aleah
Paulo
Adalia
Valery
Joshua
Noah
Molly
Jan 2019 Update: In March 2018, due to increasing hip pain and subluxation of her hip joints, Molly underwent a major double hip surgery: femoral derotation and osteotomy to correct the alignment of her hips and femurs. She was in a spica cast (immobilizing her hips and knees) for over a month. She then spent much of the year re-gaining the strength and movement that she had lost while immobilized. She is a fighter and persevered through significant discomfort over the past year. She maintained her joyful, sweet spirit throughout! Molly celebrated her 12th birthday in December. She was very excited to receive a new traditional dress for the occasion and to get henna designs drawn on her arms. She loves getting fancy and looked so gorgeous! Molly was also very enthusiastic about her cake as she loves all sweets. Over the past year, Molly developed a new interest in make-up and will request to wear it by reaching up and rubbing her hand on her lips and cheeks. She also was introduced to the movie “Frozen” and it has become a favorite. She will “sing” (vocalize) along to favorite songs such as “Let it Go”. Molly may not stand out as one of the youngest or one of the sickest, but she is so worthy of a family. She would be a beautiful addition to a family and a beloved daughter, sister, and cousin.
July 2020 Update: Molly has had a great summer! She is enjoying her classes where she is working on following patterns, reading, categorizing items, and using alternative communication and sign language to engage in pretend play. Molly’s teenage sass is undeniable! She is very insistent when she wants to watch a new movie or when she wants her make-up done. She also gets so excited whenever a new dress is brought to her home and she is persistent to have her photo taken and shown to everyone! She loves being with the little kids of the home, especially helping an adult to push them in the swing or dancing with them sitting in her lap on her wheelchair.
Wendy
Stephen
Stephen was in Riley’s groupa. We saw him a lot during our 7 weeks of visits. He stood out because he’s 7 yo and taller than the other kids in his groupa of mostly 4-5 yo’s. He is a SWEET, sweet boy. He has a great smile with dimples. He’s not overly active (not hyper). Very obedient/cooperative and follows instructions and the flow of the groupa well. An easy going kiddo. He doesn’t seem to have very significant needs. He functions very “typically”, maybe just mild delays. One thing I’ll never forget about Stephen… one time when we were invited to watch a performance the kids were putting on, we were one of the only people in the audience. He stood there, singing and doing the body motions to the production just as well as could be. He kept looking right at my husband and I like he was performing just for us. He just seemed to love having someone be there for him and encourage him, and nod and smile and let him know he was doing a good job. He was working so hard to do his best and he did so well! It was sweet and sad all at the same time….knowing we weren’t his mama and papa and he didn’t have anyone there to give him that recognition forever, that he so appreciated. He would make such a delightful son! We would have brought him home too but were only homestudy approved for one boy. He’s in a good orphanage that provides good care and services. But who knows where he’ll be transferred to when they no longer have space for him (he’s already over age.) I have pictures and video of him. Such a kind, happy little boy….he needs a family!!!
Samantha and Kristina
Kristina, on the left: Microcephaly, Moderate intellectual disabilities, ADHD (hyperactive), Esotropia, Hypermetropia, Cardiomyopathy (unspecified), Scoliosis
Nate
Jewell
Haven
Poor Haven; sweet little girl. Such a pretty girl burdened with such medical and cognitive difficulties, and no mama to love her through them.
From our team who visited there: Haven is afraid of strangers and would not interact with us.
Gabrielle
Eric
Eric has been transferred now . The daily suffering and mere existence is heart-wrenching. Try to imagine a life like this! Eric will remain bedridden for life… he needs a family quickly!
Elijah
He can walk and likes music and playing with mobile phones. He likes watching TV and doesn’t speak much.
Elijah really responds well to a male caregiver — he needs a Papa of his very own!
From a missionary who visited in August 2014: ” A beautiful little boy. He is doing so much better, he loves to walk. He needs someone to hold his hand as is too scared to walk alone just yet. He still has some self harming behaviors and lets you know when he’s not happy! But most of the time he is calm and has the cutest giggle. “
From someone who met him summer 2013:
Elijah is a beautiful, sweet child. He is nonverbal but he occasionally makes some noises. Unfortunately, when I saw him he had to be restrained most of the time because he would hit himself and bang his head … hard. He now has a one-on-one caregiver, and I hear he is doing very well. Elijah likes to watch tv, and he loves musical toys. When you play music for him, he just lights up in a huge smile. He has an infectious laugh. While I was visiting, Elijah had surgery to fix a malfunctioning shunt. I was able to visit him in the hospital. The dedication of the man who is now his personal caregiver was amazing. Elijah can walk with support, and he loves to be held and cuddled. This little blond-haired child looks like an angel, and he would bring nothing but joy to a family’s life.
Easton
Carolina
Brandon
New photo Jan 2017. Brandon has been transferred. This is what institutional orphanage life is like for disabled children. Drugged. Hungry. Restrained. Unstimulated. Uneducated. Immobilized. Broken. PLEASE help us by sharing these children and helping them find families. It doesn’t have to be this way!
Brandon is a sweet little boy who was born with CP. Brandon is socially and emotionally delayed. Whether his delays are simply from institutionalization or have a congenital basis is unknown. Only when he is a wanted part of a loving family and given access to proper medical and educational interventions can his true potential be revealed.
He is also said to have significant speech delays. He has crossed eyes and astigmatism.
Willow
Willow arrived at this orphanage in early February 2013. She loves music and loves to dance. She has responded well to the pre-school program taught at the orphanage. She has a bright smile and a contagious laugh. When visitors come, Willow is delighted to swing with them or go on walks in the neighborhood.
From a missionary who visited with her in 2013: ” I’ve met Willow! Seriously, this girl ALWAYS smiles. Whenever I would come near her she’d just grab my hand and grin at me. She wants to go exploring so bad, but she can’t walk. She would just point at stuff and grin at me to try to get me there. She is a sweetie pie. my roommate got to feed her lunch one day. She is a happy little girl who went from being scared of others near her to loving the attention! “
Grayden #
Daphne
Daphne was born with CP. She is not able to walk and is significantly cognitively delayed. She is described as an affectionate and responsive child, and she would so benefit from having a loving family of her own.
Liam
Not a great picture, but Liam is a cutie! Even though he has CP, it’s nice to see him in a place that has him up and about.
From a family who met him in 2014: This little guy tried for 5 minutes to get my attention before I could come over to him. Although he is mostly nonverbal, his receptive language is good, and he was able to follow instructions and respond to our conversation. I asked what he could do physically, and he immediately began pushing the cover back and trying to flip over, to show me he could roll, and pull up on the side of the bed. He is very sweet, and so very much wants OUT of the bed and to be up walking, but without proper medical intervention and regular therapy, he won’t be able to. His outgoing, sunny personality is absolutely wonderful! His biological mother died 4 years ago, and he entered the orphanage then, so he had that solid foundation of a loving mom during the important years. From a CP perspective- all four limbs are involved, and he has high tone in his torso that makes it difficult for him to sit up, because when he gets excited, his tone kicks in and it flattens him back out. He also has significant spasticity in his legs, particularly in his heel cords and hamstrings. That is something that in the USA might be treated with a medicine like Baclofen, which would allow him more flexibility. He’s very affectionate and easygoing, and constantly tries to get up and move around like the other kids. He just really needs a family to help him reach his potential!
Virgil
Preston
After-effects of inflammatory diseases of the central nervous system; optic nerve atrophy; conductive and neurosensorial hearing loss; atopic dermatitis; cryptorchidsm; severe mental delay
Sergey
Roger
He is said to have encephalopathy (unspecified disease of the brain), Childhood autism, and moderate mental delays.
He also has vision problems: Convergent concomitant strabismus (crossing eyes) and hypermetropia (far-sighted); and is said to be anemic.
Genevieve
She loves to participate in dancing and singing with the class, always front and center, leading the other children and keeping perfect time with the steps. Her inner beauty radiates to all around her!
Ruthie
Sandy
New pic January 2017!
Kyle
He needs a family to begin the adoption process prior to December 2021 — when he turns 16.
Arnold
This little cutie does not look happy about posing for the camera! Arnold is said to have “lower paraparesis” – which may be anything from CP affecting his lower limbs to paralysis.
Julie
February 2020 Update: Julie is just as friendly as ever! When people she knows or visitors enter the room, she grins from ear to ear and calls them over to say hi. Julie is a girl who can make everyone laugh! She is spunky, funny, and oh, so sassy. Julie continues to work on her letters, numbers, shapes, and colors in class. She can now count to 10, she can identify 15% of the English alphabet, and identify basic colors. She is bonded to her primary caregiver and gets along with the other children in her home. She loves to hold babies and play with other children her age. She can sit independently and crawl. She receives physical therapy 5 times a week where she working on tall kneeling and strengthening her back muscles. She can bear weight on her legs during physical therapy with the help of AFOs. Julie had hip surgery in July 2019. She is working daily with her physical therapist to regain strength in her legs, core, and arms. Through a variety of exercises, she is sitting independently again and has started to crawl. Julie also stands with assistance while wearing AFOs during therapy. Julie is one tough cookie and she is working hard to be even stronger than she was before.
Julie is funny and sassy. She is a friendly child and always greets visitors with a big smile and waves them over to say hello. She has good use of her hands and is able to complete tasks such as feeding herself and is working on pre-writing skills. Julie attends an on-site school where she works with her teacher on learning her English alphabet and shapes. She can count up to 5 and identifies basic colors. Julie likes to look at books and play with toys, especially baby dolls and blocks. She speaks full sentences in her native language, and speaks 70 plus English words. She understands most of what is being said to her in both English and her native language. She is bonded to her primary caregiver and gets along with the other children. She loves to hold the babies and play with other children her age. She can sit independently and crawl. She receives physical therapy 3-4 times a week where she working on tall kneeling and strengthening her back muscles. She has recently started bearing weight on her legs during physical therapy with the help of AFOs. Julie is also in the progress of potty training and has been doing really well with this.
Rebekah
Rebekah feeds herself independently and calls people by name. She can identify objects and colors. She is independent in indicating her needs and independent in her self care. She is attending on site school where she can write numbers 1 to 200. She loves counting things. She knows and writes all of her upper and lower case letters. She is reading and writing 3 letter words. She can spell her name. She doesn’t want to miss out on what is happening, she is eager to be a part of the fun. She enjoys sitting with adults and telling stories. She loves to color, draw and write. She is proud to be a helper and to be independent. She is working on pre-vocational skills of washing dishes and sweeping and fine motor skills like beading, threading, and cutting with scissors. She is well liked by all the staff and is helpful in the home. She has several very close friends with whom she gets all very well.
Lorena
Lorena will remain bedridden for life if she is not adopted. A family would need to begin the adoption process prior to NOVEMBER 2021 to adopt Lorena.
Krista
Russ
Grant funds depend on available funding; the link above, shows the current available amount!
To inquire about this child, email childinquiry@reecesrainbow.org ***
An adoption would have to begin before August 2021!