Boy, born 2012
Severe mental retardation
Tetralogy of Fallot
Spastic tetraplegia
Talipes equinovarus
Hypopituitarism
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!
Boy, born 2011
hydrocephalus
Spastic tetraplegia
Generalized idiopathic epilepsy and epileptic syndromes
Other chronic tubulo-interstitial nephritis
Congenital malformation of optic disc
Profound mental retardation
Boy, born 2015
congenital microcephaly
syndrome movements disturbance
severe mental retardation
Boy, born 2012
S. E. Asia (2)
Listed: Aug 2019
Phineas is described by nannies as an observant child who has positive relationships with peers and caregivers. He enjoys being with his caretakers and knows/understands their individual personalities and is challenging for him when he has a new caregiver. He gives and receives affection with individuals he likes. He participates in the orphanage activities and loves to explore. He can express his feelings if his caregivers encourage it and knows some self-care.
Phineas has been diagnosed with ADHD and currently receives medication for treatment. This little boy needs a loving family that can provide a nurturing environment, felt safety, and knowledge regarding older child adoption.
Boy, born 2011
S. E. Asia (2)
Listed: Aug 2019
Brandt loves riding bikes and playing soccer and plays for the soccer team at his school. His caregivers describe him as a cheerful child who is talkative and very sweet He attends 1st grade and his favorite class is where they learn the ABC’s. He is not a fan of coloring or drawing and when he doesn’t like an activity at school, he prefers to go to the bathroom and clean. He is calm and loving with other children and he enjoys social activities and helping with chores.
Brandt had a complicated birth history, and was premature. He typically wears glasses. Brandt needs a prospective adoptive family with excellent educational resources including ESL support, and a good understanding of developmental trauma, institutionalization and older child adoption. He needs a family that is open to some unknowns.
Boy, born 2013
Expressive language disorder
Moderate mental retardation
Undescended testicle, bilateral
Convergent concomitant strabismus
Astigmatism
Lack of expected normal physiological development
Listed: March 2020
Boy, born 2013
sweet smile! 🙂
lumbar spina bifida with hydrocephalus
Unspecified personality and behavioral disorder due to known physiological condition
Esotropia
Other acquired deformities of limbs
Flaccid paraplegia
Vasomotor rhinitis
Hypertrophy of adenoids
Listed: May 2018
Boy, born 2013
Other specified disorders of central nervous system
Mixed specific developmental disorders
Unspecified mental disorder due to known physiological condition
Expressive language disorder
Pectus excavatum
Other congenital valgus deformities of feet
Congenital malformation of optic disc
Listed: July 2019
Ollie
Age: 2012
Diagnosis: Coffin-Lowry Syndrome
Ollie is now living in foster care.He is physically well developed. He has good coordination of his hands and feet. He walks without falling, and can run as well. Climbs up and goes down by the stairs when holding an adult or the railing. He can play with cubes by putting them and taking them out of a cup, but has some problems manipulating with smaller objects. He cannot eat and dress by himself yet, but does make attempts. He understood almost everything and fulfils small tasks. He likes playing hide and seek. He hides behind the door and when he is found, he laughs and stomps his feet. He is interested in musical cartoons and copies the movements of the actors.
*There is a younger child that is believed to be Ollie’s younger brother. However, they are NOT listed as needing to be adopted together. The other child is listed as Ozzie. https://reecesrainbow.org/127615/ozzie
*** 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 on this child, email childinquiry@reecesrainbow.org
4 Siblings
girl, born 2013 — mild mental delays
boy, born 2012 — alalia
girl, 2007 — alalia, She cannot talk
girl, born 2005 — moderate mental delay
They must be adopted together!
*** We are eligible for an Older Child Grant! Grant funding is dependent on a completed application and available funds. For more information, visit: Other Angels Older Child Grant ***
Boy, born 2012
disorder of the brain
atrial septal defect
valgus deformity
organic disorder of personality and behavior with cognitive delays
Listed: April 2017
New picture (left) May 2017.
Boy, born February 2012
PRC
indirect inguinal hernia of right side; postoperative sensitive special need; DSD
Listed: March 2015
Lennox is described as smart, clever, quiet, and pleasant. In March of 2014 he had surgery for one of his special needs. Lennox is a handsome and active boy who has a ready smile. The caretakers and other kids all like him very much! His agency has asked for an update and hope to have one soon!
Boy, born 2013
Cerebral palsy
Listed: April 2019
Boy, born Feb 2011
PRC
Cerebral Dysplasia
Listed: Feb 2015
Legend is a great little boy who loves to listen to sounds and music! He is drawn to toys with sounds and exciting noises and will give you the biggest smile when he has one! Legend is shy but active and is able to crawl on his hands and knees. Legend has cerebral dysplasia but he’s not letting that get him down! Legend will continue to grow and thrive in his forever home!
Boy, born September 2011
PRC
Cerebral Palsy
Listed: Jan 2015
Tyran is a sweet little boy who is 3 years old. He has a diagnosis of cerebral palsy which appears to affect his gross motor skills. His report was done when he was about 17 months old, and at that time he was sitting without support, but was unable to crawl or stand. Tyran’s fine motor skills are good, with the exception of transferring an object from one hand to another. He is a very bright little guy, whose receptive speech is very good. He was able at 17 months to say “nainai” (grandmother) but it was not very clear. Tyran lives with a foster grandmother who loves him, but he does not appear to have access to any needed therapies. Tyran needs a family not only to love him as he grows, but can provide the therapies he will need to reach his full potential.
Boy, May 2011
Cerebral palsy, symptomatic epilepsy (secondary generalized seizures), optic nerve atrophy, crossed eyes.
Listed April 21, 2013
Hello, sweet baby! Aren’t you just precious?
Large families welcome; married couples only.
Boy, born April 2013
PRC
Heart arrythmia, past CMV, Strabismus
Olaf is an adorable little guy. He has been hospitalized a few times due to heart arrhythmia (it is apparent when he runs a fever), and once with CMV (cytomegalovirus) from which he recovered. Olaf has strabismus (crossed eyes) which should be corrected; either with glasses, or an outpatient surgery.He is growing, and developing well. At 13 months he was crawling and standing with one hand supported. He could stand for long periods of time. Olaf loves toys, and he really loves his nanny! He could imitate words, and his favorite toy was a toy cell phone. (Note to prospective parents – guard your phones!) Olaf is ready to be loved by his own parent(s), and will keep you busy! Are you ready to give this little cutie some warm hugs?
Boy, born 2012
disorder of the brain, unspecified
other specified mental disorders due to brain damage and dysfunction and to physical disease
hypospadias
Listed: April 25, 2016
He is not available until summer 2017!
Unless a medical codes changes
Boy, born 2012
Microcephaly
Spastic Tetraparesis
updated pics/video Aug 2016
Video
Listed: April 25, 2016
Boy, born 2011
Symptomatic epilepsy, Epilepsy and recurrent seizures
Boy, born 2012
Abnormal development of hand, congenital radial clubhand with right forearm shortening; balanic hypospadias; positive HCV, PCR antibodies are negative; pyelectasis
Boy, born 2012
HIV
cerebral palsy
cytomegaloviral disease
moderate intellectual disabilities
Listed: March 2018
What a great smile!
Boy, born 2012
Chronic viral hepatitis B
May also have Cerebral Palsy
Listed: March 2018
Boy, born 2011
Other disorders of nervous system
Mild mental retardation
Other congenital valgus deformities of feet
Divergent concomitant strabismus
Listed: Sept 22, 2016
Boy, born 2011
Sequelae of inflammatory diseases of central nervous system
severe motor impairment
spastic tetraparesis
Listed: Jan 2019
From a family who met him Nov 2018:
Quincey is one of the most darling, endearing boys we have ever met. He is pure joy and just exudes love and affection. His little giggle is contagious. He begged us to take him home to America- he so desperately wants a family. He loves to show off how he can get into his wheelchair (which he calls his car!) himself and beams with pride. He speaks well, is very bright, and will flourish in a family.
He is so sweet, always look happy and friendly.
Boy, born 2012
PRC
Cerebral palsy
Listed: Aug 2015
Maximilian is an adorable little guy who recently turned 3 years old. He came into care as a newborn, and was diagnosed with CP. Max has good fine motor skills, excellent speech (although they say he has a short tongue tie), and is able to walk…but not for long distances. Max’s head tilts to the right; this could be a result of the CP. Maximilian is a delightful little boy, whose cognitive skills are on target. His receptive speech is great, and he follows instructions well. He can easily express his needs. The nannies describe him as “strong and brave”. They also said when he sees the other kids walking and doing things he would like to do he wants to be like them. Max works very hard when exercising…he wants to be strong and able to run and play with his friends. Max need a family, good therapy, and treatment to straighten his neck. Max needs you!
Boy, born 2012
Listed: August 2017
FAS, disorder of the brain, cardiac murmur, cardiomyopathy, exposure to TB, congenital deformities of hip, anemia
He needs a smile!
Boy, born 2011
FAS, Internal hydrocephalus, congenital brain malformations, slight mental delay, crossed eyes
So so sweet!!
New pic December 2016!
Shareable video link: https://youtu.be/joWms-lQA0E
Boy, born 2012
hydrocephalus (shunted), spastic tetraplegia, epilepsy unspecified, optic nerve atrophy
Boy, born 2012
Microcephaly
Listed: July 2017
Boy, born 2012
Microcephaly, spastic tetraparesis
Listed: October 5, 2014
Boy, born 2011
Congenital hydrocephalus
paraplegia and tetraplegia (spastic tetraparesis)
partial atrophy of optic discs of both eyes
additional chord of the left heart ventricle
hernia
Listed: June 2017
Look at the curls on this doll! Cameron is in urgent need of medical care!!
Boy, born 2013
Sequelae of inflammatory diseases of central nervous system
Crossed eyes
Moderate mental retardation
Listed: Dec 2018
Boy, born 2012
Hydrocephalus
Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
Listed: Sep 2018
Boy, born 2011
Severe delay of physical and mental development
Listed: Aug 25, 2015
VIDEO: https://youtu.be/i4KTSYVhRmU
From a family that met him 6/15:
We spent about a week with this sweet boy when we were adopting our son in June 2015. He is so desperate for love. He called me momma and begged my daughter and me to hold him. We loved on him as much as possible and he soaked it up. He picked up English words very quickly, and remembered day after day that I had hand sanitizer in my purse and asked for it by saying, “soap!” He loved to play ball with my kids, and the nannies would let him push the baby carriage around during walks. He has the most infectious giggle I’ve ever heard. He walks well, but the nanny indicated that he has issues with his knees. It didn’t stop him, though!
He needs a good, patient, and loving family to give him what he needs. He is so skinny and needs good nutrition. He has very minor orphanage behaviors, but from the progress he made just being with us for a few days, I know he will flourish in a caring family. He will be transferred to a horrible place (the director of the orphanage told me it is horrible), likely very soon, since he’s almost 4.
This region is beautiful and very cost efficient. The orphanage director is lovely. The facilitators are amazing, and the judge is hilarious and wonderful! You will be able to stay in a hotel and walk to the orphanage and enjoy the beauty and culture of a wonderful town.
LOTS of videos available!
Boy, born February 2012
PRC
Limb difference
Listed: May 26, 2015
3 year old Quinntavius is missing his right hand. It looks as if he may have ptosis (droopy eye lid) of his left eye, but that is not a formal diagnosis. Quinntavius likes to look at picture books and be read to. He really enjoys going outside and playing and basking in the sunshine. Quinntavius has good fine motor skills and is very observant.
He knows his name and likes hearing his named called. Quinntavius has good expression and is very curious. He is a quiet boy and doesn’t cry often. He can combine actions with words, such as shaking his head no and saying no. He really likes to play with toys, especially blocks, and he enjoys rolling balls. Quinntavius sounds like a wonderful little boy who doesn’t let anything stop him. Now he just needs a forever family of his own! Video available from spring 2017.
microcephaly
Generalized idiopathic epilepsy and epileptic syndromes
Other congenital malformations of cardiac chambers and connections
Other congenital malformations of cardiac septa
Iron deficiency anaemia
Other lack of expected normal physiological development
Optic atrophy
Boy, born 2012
PRC
tethered cord release (post surgery) / cystostomy
Listed: Dec 2015
Riley is an active, and incredibly adorable, little boy who is 3 years old! He came into care when he was about 8 months old. He was already crawling, and standing with support. Riley received surgery for a tethered cord in May of 2013. After his successful surgery,when they removed his catheter, they found there was an apparent urethral injury. They performed a cystostomy (a surgically created connection between the urinary bladder and the skin which is used to drain urine from the bladder in individuals with obstruction of normal urinary flow). Riley recovered well, and was returned to his foster family. He is a smart little guy who is very social. His fine motor skills and speech are on target. Riley is attached to his foster dad, and loves to play with the other children in the foster home. Riley needs a family of his own!
OCTOBER 2017 UPDATE: Percy is a very bright and cheerful boy. He has an adventurous personality, is eager to try new things, and has an open disposition that is friendly, but not inappropriately so. He is not afraid of foreigners from overseas and was immediately interested in learning English with American volunteers in school and was one of the first to master the alphabet song. He has a good ear for language and has soaked up everything he can learn in English and he retains it (colors, shapes, animals, clothing, parts of the body, etc.). He has a great sense of humor, loves to laugh, and gives a loud “Good Morning!” and hard high five whenever he sees his English teachers. He has learned to read some characters in his native language, knows his numbers, has started basic math and knows many songs and dances from school. Percy lives with an attentive foster family who would love to see him adopted as they know that he needs medical treatment from pediatric specialists. He interacts appropriately with peers, is silly and fun with his little friends, but not unkind.
Boy, born January 2012
PRC
meningocele (post surgery) / hydrocephalus (post surgery)
Listed: Nov 5, 2015
Rory is a handsome, engaging, and active boy who is 3 years old. He came to the orphanage at around 6 months old, and they discovered he had already received surgery for a meningocele, and had a shunt placed for his hydrocephalus. Rory was able to sit unassisted, and before long was crawling. He is having casting procedures to correct his club foot, so he is temporarily using a wheelchair. You can see in his video that being sidelined from the action is almost more than he can stand! Rory has undescended testicles, which need to be corrected as soon as possible. His shunt has been trouble-free. Rory (without the cast) is able to stand with assistance, but is unable to walk at this time. He is incontinent. Rory has no cognitive delays, is a bright and social boy. Before his recent cast, he would get around by crawling and moving with his knees in a kneeling position. Physical therapy would be so beneficial for Rory! He needs a family! Video is available from the agency.
Boy, born 2012
Hydrocephaly, congenital heart defect (operated)
Boy, born 2011
Mental delay, brain dysfunction, speech delay
Listed: February 1, 2016
Joey has 3 or 4 siblings that must be adopted with him!
Sisters: D (born 2009), A (2007), brother Y (2006) (and one younger brother, whose status is unknown)
From a family that met him 12/15:
Joey is a tiny, smiley little guy who loves attention and hugs! He was so happy to sit on my lap for a hug, to show me the little stuffed animal and toys he was holding and to have his picture taken! He is verbal and said things like, “Cheese!” when having his picture taken, and “Can I see?” to see the photo stored in the camera. He will make a sweet addition to any family and he will simply thrive with the love of a Mama and Papa poured into him!
Boy, born 2012
Delay of psychological and motor development, crossed eyes
Girl, born 2009
mild mental delays
Listed April 27, 2015
Samuel has an older sister who has already been adopted.
Boy, born 2012
severe mental delays, malnutrition, anemia, rickets, congenital deformation of clavisternomastoid muscle, myopia, hemangioma
Boy, born 2011
severe mental delay
congenital anomoly the development of the brain
low parapareses
damage of functions of walking
Boy, born 2014
Other specified congenital malformations of brain
spastic paraplegia
Communicating hydrocephalus
Severe intellectual disabilities
Other congenital valgus deformities of feet
Congenital malformation of optic disc
He has an older half-sister; she lives with family.
Boy, born 2014
Disorder of central nervous system, unspecified
Severe intellectual disabilities
Other specified chromosome abnormalities
Frostbite with tissue necrosis of abdominal wall, lower back and pelvis
He has a brother born in 2012 who was placed in a different orphanage.
Boy, born 2014
Disorder of central nervous system, unspecified
Mixed specific developmental disorders
Expressive language disorder
Other mental disorders due to known physiological condition Attention-deficit hyperactivity disorder, predominantly hyperactive type
Other congenital malformations of upper limb(s), including shoulder girdle
Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
Has two siblings under custody (2003, 2010) and not currently available for adoption.
Boy, born 2014
Phonological disorder
Portal hypertension
Iron deficiency anemia secondary to blood loss (chronic)
Boy, born 2016
Microcephaly
heart condition – operated on
He understands everything and talks back; he follows instructions. He is waiting to get his family.
Boy, born 2011
Listed: June 2020
Communicating hydrocephalus
Congenital deformities of feet
Acquired deformity of chest and rib
Iron deficiency anemia, unspecified
Boy, born 2014
FAS
moderate mental delay
benign neoplasm of neck
two-sided fallen arches
undernutrition
From a family that met him summer 2019: He is adorable, turned 5 this summer. Started walking recently. Has FAS. Cute as a button. Care taker said isn’t violent or doesn’t act out like other kids. Only fusses when it’s time to eat. He walked into my arms without knowing me!
Boy, born 2014
sequelae of inflammatory diseases of central nervous system
severe mental retardation
undescended testicle
congenital dislocation of hip
strabismus
atrial septal defect
Listed: January 2018
Boy, born 2013
diagnosed with congenital brain disorder (callosal agenesis, polymicrogyria)
Spastic tetraparesis
Epilepsy syndrome
Speech delay
Listed: April 25, 2016
Updated pics/info/video August 2016
Poor guy! He was looking miserable! He is getting worse than before. He needs good diagnostic and medical care.
Video
Boy, born 2012
Listed: April 2016
Congenital malformations of corpus callosum; Other reduction deformities of brain
Congenital hydrocephalus, unspecified
Cerebral palsy, unspecified,
Atrial septal defect
Congenital deformity of hip, unspecified
Convergent concomitant strabismus; Other disorders of optic disc
Boy, born 2013
Multiple congenital arthrogryposis, internal hydrocephalus, open oval window
updated pics Jan 2015 and medical info:
Multiple congenital arthrogryposis, thymic hypoplasia, hypoplasia of abdominal wall muscles, crossed eyes, additional chord in the heart.
He had surgery. He is developing well. Smart boy. Needs out asap.
From a family that met him 11/15:
“Mathis” (he will be 3 years old in winter) also has delayed speech and mental delay. He did not use any words while we were there. He cannot sit, crawl, stand, or walk. We did not see him move about the floor, he needed to be held. This is frustrating for him. We did not observe him using his hands. I tried to place toys in his hands a he did not grab them. He did not laugh or smile.
Boy, born August 2013
PRC
Motor delays
Rigby is a precious little one who is 22 months old. He came into care when he was about 10 months old…wheezing, and in need of help. After some TLC from the nannies, there was improvement in his health and motor skills. He was still behind his peers, but had become a very engaging and social baby. At 17 months of age, Rigby could roll over, sit with some support, and play with toys. Rigby was not able to crawl or walk at that time. He loves to be around the other kids. The more action, the better! The nannies have noticed he has high muscular tension and uncoordinated movements. There was no formal diagnosis made in his file which had resulted from a thorough exam. Rigby is an active, loving, happy little guy who really needs a family and some good therapy to help him with his gross motor skills. He needs to come home.
Boy, born 2011
FAS, Specific disorders of mental development
Boy, born 2013 (wearing blue socks-pink shorts) No diagnosed special needs
Girl, born 2010 (wearing dress) FAS, Microcephaly, low paraparesis
New pic January 2017!
Boy, born late 2012
congenital malformation of corpus callosum,
delay of psychological and motor development
Bobby’s two brothers are no longer available for adoption, as they have gone into domestic foster care.
Boy, born 2013
Internal progressive hydrocephalus with brain atrophy, condition after shunting, ventriculitis, microphthalmia, congenital retina malformation, crossed eyes, mental delay
New photo 2019
Update: Ronan is walking! Video.
New picture, late 2017: Ronan looks good — what a smile!!
Boy, born 2011
After-effects of encephalitis, spastic tetraparesis, hyperkinetic syndrome, crossed eyes, hip joints contracture, deep mental delays
Boy, born 2012
FAS, Renal agenesis and other reduction defects of kidney
Listed: April 16, 2015
New pic January 2017.
Ray is facing transfer to the institution. Please share him so he can find his forever family!
Boy, born 2011
CP, Mild cognitive disorder, probable FAS
Flaccid hemiplegia, Other vitreous opacities
Griffin can walk with help, understands simple instructions, can say separate words.
Listed: July 2014
Updated pic from summer 2019, he is being hosted in the US! Griffin is extremely sweet and affectionate. He shows a lot of intelligence and is very resourceful. He was understanding and speaking some English in the two weeks he was with us. He can walk and run, but would absolutely thrive with orthotics and physical therapy. He also managed stairs well, as long as there is a railing. His favorite things to do are swim (needs a life vest), jump on the trampoline, and listen to music. Oh, and eat, of course!
From two of the families that hosted him, we believe he would do best as the youngest and smallest child or as an only child. There was some aggression and anger in certain situations. We also believe there should be no animals in the home. Or caution with line of sight supervision.
He has mixed maturity and typically fell between 2-4 yrs old behaviorally and emotionally. Sometimes older, often younger. He completely deserves to be babied and spoiled and loved on. He would absolutely thrive and blow expectations out of the water.
Boy, born Nov 2011
Cerebral palsy, double hemiplegia G 80.0.
Listed: May 2014
What a little sweetheart! Don’t you just want to scoop him up!
Boy, born November 2012
PRC
Congenital optical atrophy of both eyes
Listed: May 2014
Josh is a cute, very active and extroverted little boy. He has congenital optic atrophy of both eyes but he can still track light. Josh loves to play games with his caretakers and he rarely gets fussy. Josh can crawl around and even go in reverse too! He likes to sit up and play with toy balls that make sound. It he can hear it then he can follow it. Josh understands simple dialogue and can recognize familiar people by their voice. He is sensitive and happy most of the time. Josh likes to suck on his fingers when he gets tired and his favorite thing to do is listen to music.
Boy, born January 2012
PRC
tuberous sclerosis; infantile spasms, and psychomotor development delay
Ollie’s report states that he has good development. He gets along well with others and is closest to his caregiver. He is a quiet child who likes music and enjoys his swim lessons.
Boy, born May 2011
PRC
Cerebral Atrophy of bilateral frontal lobes (but normal development)
Lew does not speak much yet. He can make “Yiyi-yaya” sounds and point to the objects he wants. He can express himself with other ways. For example, if someone took his ball, he will make “yiyi-yaya” sound to caregivers and pointed to the ball and ask the caregivers to get it back. When you get it back for him, he will laugh to you He can stand up without any help, he can walk alone (al little waddled) and walk hand in hand with other kids. He can pick up a very small object from the ground. He can hold a ball and raise it up and throw it out, then pick it up and repeat.He is a little bit shy and can be very cautious with strangers. He is very open and happen when he is with caregivers and kids he is familiar with.
There is a video available of Lew: http://youtu.be/N6L8vMOvv78
Boy, born September 2013
spastic quadriplegic cerebral palsy; congenital pes planus; hearing loss, unspecified; optic atrophy; strabismus; other specified congenital malformation of the heart
Listed: Feb 2014
From a family who met them July 2017:
Finley is precious and has the most adorable dimples! He walks very well and we are told has recently made incredible progress! The nannies love him and say is very friendly and helpful, and especially enjoys helping to set the table. He is soft spoken, but communicates well. We adored him!
Fern is doing so well! We were told he has improved dramatically with a change in medication. His smile just lights up the room! Updated pics, video and info 7/17!!
Fern: Boy, born 2016
other specified congenital malformations, atrial septal defect, patent ductus arteriosis, laryngeal hypoplasia
congenital hydrophenosis, congenital vertical talus deformity, esotropia, vitamin deficiency, cytomegaloviral disease
Boy, born June 2011
Cerebral palsy dyskinetic (hyperkinetic) type
Listed: Jan 2013
What a little love! Another one who is so young and will greatly benefit from therapy and a family. Someone scoop him up!
Boy, born January 2011
Cerebral palsy – spastic diplegia; blindness of both eyes; hernia; valgus feet; cardiovascular system malformations
Listed: Jan 2014
Boy, born September 2011
Cerebral palsy, retinopathy, premature, severe myopia.
Listed: August 2013
He cannot sit or stand.
Boy, born February 2012
Congenital hydrocephalus, spastic tetraplegia, epileptic syndrome, open oval window
Boy, born Oct 2011
congenital
internal hydrocephalus operated; anemia; protein-energy deficiency
Listed: Jan 2013
Ezra has had a shunt placed, and is doing better. His adoption may necessitate consultations with medical personnel, to safely transport him home.
From someone who met Ezra in 2013: Ezra is absolutely precious! He is sweet and adorable and oh so lovable! He laughs when his toes are tickled, or when someone around him laughs or talks or sings to him. He often smiles or laughs so hard his chubby cheekers make his eyes close. He ha s learned to blow spit bubbles and coo. It is hard for me to tell if he is able to use his limbs normally, but he is able to move from his back to his side with little or no assistance. He has not yet learned to play with toys, but he has a very strong grip and enjoys holding my finger. I was told he can see, but not very well. I observed his eyes moving rapidly from side to side, and sometimes appearing to be looking in two different directions. In spite of this there were other times in which he appeared to be quite focused and looking right at us. He has absolutely stolen my heart, and I hope that he will find a family that can help him meet his full potential!
These pictures are from May, 2013.
Even if you can’t adopt,
you can be a guardian angel for an orphan with special needs!
The Guardian Angel Program is part of our Prayer Warrior Ministry. To find out more about being a Guardian Angel, please CLICK HERE
Boy, born August 2011
inflammatory diseases of central nervous system; Congenital hydrocephalus; Other disorders of optic [2nd] nerve and visual pathways; Carrier of viral hepatitis B
Listed: June 2012
What a sweet baby Elias is! Elias is in a fast region that often waives the 10 day wait.
Additional photos available. Video
CONTACT
Reece's Rainbow
PO Box 146
Combined Locks, WI 54113
CLICK HERE to contact us.
Your questions will be directed to the appropriate team member.
PO Box 146
Combined Locks, WI 54113
CLICK HERE to contact us.
Your questions will be directed to the appropriate team member.
