There is a very special joy that boys bring to life. Unfortunately, they are often the last ones to be chosen for adoption. We so hope you will find YOUR new son right here at the end of Reece’s Rainbow.

PLEASE HELP US raise grant funds and awareness for these precious, waiting angels. You really can save a life, with even the smallest gift!
You are also invited to send a check (no Paypal fees) to
Reece’s Rainbow, PO Box 277, Monrovia, MD 21770

“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!

FOR MORE INFORMATION ABOUT THE PROCESS AND/OR ANY OF THE WAITING CHILDREN ON THIS PAGE, PLEASE INQUIRE.
The majority of these children posted here can also be adopted by CANADIAN FAMILIES! Please inquire!

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Ollie

Ollie (1)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.

 

$50.00 has been donated towards the cost of my adoption!

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!

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Griffin

griffin-2016Boy, born 2011Griffin (1)
CP, mental delay, probable FAS

Griffin can walk with help, understands simple instructions, can say separate words.

Updated pics 10/16, from a family that met him:   He walks, he talks, he answered questions appropriately, he is Great! He loved my husband. We told him we would try to find him a family and he was SO shocked!  We need him out before he gets transferred in a couple of months!!  Griffin is very high functioning and has a personality of gold!

Update 7/16 – He really needs out asap! He has very little time left before he is moved to the institution! He is making good progress! He can walk by himself and he talks pretty well too! Don’t let him face institution!

$108.00 has been donated towards the cost of my adoption!

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!

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Gabriel

Gabriel 2

Gabriel 1Boy, born December 2011
PRC
postoperative lumbosacral meningomyelocele; hydrocephalus; Chiari deformity; left down limb deformity with paralysis; nervous bladder

 

Gabriel has delayed limb and intelligence development. At the age of 3 months, he could smile if being teased and could turn his head. At the age of 6 months, the center arranged his rehabilitation training. He could control his head,turn over, could not sit alone, had right lower limb deformity, club feet, and normal left lower limb. At the age of 9 months, he could grasp his toys, hold his bottle to drink, and smile at familiar people. At the age of 1 year, he could imitate adult’s action, hit the toy blocks, and giggle if happy. At the age of 1.5 years, he could sit alone after a period of rehabilitation training, crawl and stand with holding, but still could not walk. Now he can imitate speaking, understand simple directions, and can recognize some common objects. Gabriel is open, lovely, likes music and toys, and likes playing games with familiar people. He can smile if happy and can wave his hands and feet when he hears the music. He has built stable and close relationships with the care takers.

$450.00 has been donated towards the cost of my adoption!

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!

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Kristoff

KristoffGuardian AngelBoy, born November 2011
PRC
Cerebral Palsy

 

Look at this heart breaker. He has mild cerebral palsy and is just too cute. The agency has updated photos and a development report. Can’t you just picture him rocking his way into your heart?

 

$45.00 has been donated towards the cost of my adoption!

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!

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Breckin

breckinchristmas16-breckin-Boy, born February 2011
H-C
Cerebral Palsy

Breckin has cerebral palsy, but he can sit up and stand with assistance. He can even take a few steps if you hold onto his hands! He cannot yet feed himself, but he has practiced holding his own spoon and sippy cup and has made great progress.

Update Jan 2015:
Breckin has cerebral palsy, but he can sit up and stand with assistance. He can even take a few steps if you hold onto his hands. He has been receiving regular therapy and loves this time. Breckin is making great improvements – he now has a modified crawl that he uses to get all around his house and can quickly move to wherever he wants to be. He can also pull himself up to stand and does this often. Breckin does not yet feed himself, but he has practiced holding his own spoon and sippy cup and has made great progress. Breckin is a happy little guy who loves to play.

$40.01 has been donated towards the cost of my adoption!

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!

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Bentley (L)

B301 BentleyBoy, born Nov 2011
Encephalopatia due to mother’s alcohol use, Inborn hypotrophia, CMV infection (citomegalovirus), Specific mixed developmental disorder, Bilateral Neuritis cochlearis, Low weight and height growth, Heart murmur

Listed: September 5, 2013

As of June 2013:
Bentley is mostly passive, his muscles are weak. He can not sit, stand or walk on his own. He does not like to have a close contact with a person, cries when is picked up. Bentley likes to sit in a special chair and rock. Sometimes the boy pronounces accidental sounds. Does not picks up yet toys in to his hands, when is talked to – does not react. Sometimes when he sits alone it was observed that he started to smile. He needs help while eating and drinking. Child’s motor development is delayed, compared to his age.

The picture is older; the agency hopes to have an updated picture soon.

$204.00 has been donated towards the cost of my adoption!

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!

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Rory

OLYMPUS DIGITAL CAMERABoy, born June 2011

Cerebral palsy dyskinetic (hyperkinetic) type

 

What a little love!  Another one who is so young and will greatly benefit from therapy and a family.  Someone scoop him up!

 

Rory has 4 older siblings; 2 of them are in the same region and available for adoption.  His available brothers were born in 2006 and 2003.

$1,149.50 has been donated towards the cost of my adoption!

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!

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Josh

JoshBoy, born November 2012
PRC
Congenital optical atrophy of both eyes

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.

$25.00 has been donated towards the cost of my adoption!

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!

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Sanders

SandersBoy, born June 2012
PRC
Post-op spinal meningocele, hypophrenia

Sanders is an adorable little boy who turns 2 in June. He can walk holding onto a railing. Sanders is still very young so it is too early to tell if he has full control of his urine and bowel movements. He is at the perfect age to start early intervention programs and therapies. He is just waiting for his family to see him and help him start building his skills.

 

$50.00 has been donated towards the cost of my adoption!

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!

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Chase

Chase (8) Chase (15)Boy, born October 2011
PRC
Delayed psychomotor

Are you ready for this cuteness? Say hi to 2.5 year old, Chase! Chase is listed as having psychomotor delays. Chase is very mobile and has good movement. He has received daily therapy over the past year to help with his motor skills and is learning to crawl and walk. It takes him some time to learn these skills. While he does not learn quickly, he does try. He is not potty trained yet, but when they put him on the toilet, he will go. Chase lives in the orphanage and he seems to be a very happy boy. He does not seem to be slowed down by his special need.

$45.00 has been donated towards the cost of my adoption!

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!

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Vinny #

Boy: 2015

Diagnosis: Infantile Cerebral Palsy – spastic quadric paresis. Muscle hypertonia. Delay in the neuro-psychological development. Hydronephrosis 1st degree

 

Vinny is an adorable little boy that is living in an orphanage in Eastern Europe. He has poor muscle tone and active movements. Coordination is poor as well due to walking on his toes when trying to step (with help). He is diagnosed with Cerebral Palsy. At the age of 3 months old, he began reacting to sound and looking at objects. Vinny has good control of his head and can roll on his stomach and back. He does not attempt to walk and he has trouble sitting without support. He has spastically increased muscle tone. He does well holding objects but does not pass them hand to hand, but rather to his mouth. Vinny has a good attention span and does well with recognizing individuals. His behavior is calm and very playful when being interacted with. He listens when being communicated with and tries to interact back with syllables and noises. Vinny is a picky eater and very dependent on the work staff.

 

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him.

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Kelton #11-57

Boy: 2013

Listed: 4/2017

Kelton is very curious and is a happy boy most of the time.  He is unable to walk without aid, but he tries to get around when he sees and interesting toy near him, and will grab and play with a toy for long period of time.  This social boy enjoys playing with and receiving attention from other kiddos and his caretakers. He has been diagnosed with Spina bifida and Hydrocephaly.   Precious Kelton is ready to join a loving families that can provide for his needs.

Videos of Kelton are available upon request.

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him.

 

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Augustin

Boy, born 2012

disorder of the brain
atrial septal defect
valgus deformity
organic disorder of personality and behavior with cognitive delays

 

$0.00 has been donated towards the cost of my adoption!

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!

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Branson #

Branson 

Age: 2
Listed: 3/30/2017

Diagnosis: Premature birth, strabismus, reflux, right-sided hemiparesis

Branson is from Eastern Europe.  He was born prematurely at 28 weeks and suffered neonatal respiratory distress syndrome, mother-fetal infection, intraventricular hemorrhage IV degree complicated with porencefal cyst 53/23 mm, pneumonia, retinopathy, and gastroesophageal reflux disease. Branson has strabismus, is allergic to Augmentin, and has not received some of his vaccinations due to low birth weight, bronchopulmonary dysplasia and bronchial asthma.  There is no data that the child was ill with any of the typical children’s diseases such as whooping cough, varicella, measles, rubella, parotitis.  There is no data that he has had Tuberculosis, seizures or convulsations, including from fever.  Branson has had bronchopneumonia with acute respiratory insufficiency during autumn-winter and bronchopneumonia dysplasia that evolved in bronchial asthma.  Videos are of available of this child.

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him

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Scotty #

Boy: age 2

Diagnosis: Lumbar spina bifida (surgically corrected), grand mal seizures, spastic cerebral palsy, hydrocephalus

Scotty has little support from his legs.  His head control has improved and he can turn from his back to his belly.  He sits independently by holding on to the bars of his crib and also makes attempts to stand up.  Scotty can hold toys in his hands and tries to clap!  He maintains eye contact and recognizes the faces of his caregivers.  Scotty expresses appropriate emotions to happiness and agitation and will laugh out loud when teases.  He imitates and pronounces combinations of sounds and syllables.  Scotty interacts with all children and caregivers.  He likes music and toys.  Scotty is fed by a spoon and receives additional nutrition from a bottle.

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him.

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Maximus #

Boy: 2012

Moderate cognitive and speech delay

Maximus like to play with musical toys.  He understands his name and reacts when called.  He can point to body parts when asked too.  Maximus is nonverbal, but can point to pictures of familiar objects.  He prefers to interact with adults and shows affection when they are familiar to him.  He is introverted when interacting with other children still.  He eats independently and is potty trained.

 

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him.

 

More photos/file are available from his agency

 

 

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Clifton #

 Boy: Born 2012

specific disorders of motor function development, Moderate mental delay, ectopic left kidney, strabismus

Clifton lives with a foster family.  He loves to listen to music and dance and is always looking for a dancing partner! His foster family is working on him walking longer distances independently.  He is learning how to play with toys and interact appropriately with other children.  He has few words and does not follow verbal directions.  Clifton is receiving therapy multiple times a week.

 

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him.

 

More photos/file are available from his agency

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Paddy #

Boy:Born July 2012

Hydrocephalus, Thalassemia, astigmatism

Paddy can turn over on his own, and sits independently. He will walk holding hands or using a walker, but does not like to walk over uneven surfaces.  He likes musical toys and has recently started imitating simple actions like a ring stacker.  Paddy likes to interact with familiar adults and may pout when they leave.  He eats mashed food and drinks from a cup.

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him.

More information and pictures may be available from his agency.

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Mayson #11-61

maysonAge 2:
Diagnosis: Hemophilia B & esophageal atresia

Mayson is 2 years old and is living in an orphanage where the doctors and staff work diligently to address his medical needs. He has a gastric feeding tube (G-tube) and this is how he receives all of his nutrition. He walks, says a few simple words, follows simple directions, and engages with staff and other children.

A full medical report, photos, and videos are available through the agency.

from a family that met him 2/2017:
He is a very happy and social child with a bright smile.  He watches people a lot, especially in new situations.  While he is a bit shy at first, it doesn’t take much for him to join in.  When he gets excited and smiles, you can’t help but smile and laugh with him!  He seems to form bonds and likes to be included in activities.  He’s very easygoing.
$274.50 has been donated towards the cost of my adoption!

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!
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Anthony #

anthonyBoy, age 1.5
Neonatal, cerebral schemia; hydrocephalus; ventriculoperitoneal shunt

Anthony is an adorable, sweet 1 year old! Anthony has a lack of development physically and neurologically. In late 2015, a ventriculoperiteneal shunt was placed and he has been free of seizures since then. He cannot sit upright by himself and does not talk, but responds to sound. Anthony is tube fed due to lack of suck reflex. He does not react well to teasing or tactile stimulation by smiling but by irritation and crying.

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him.

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Zachary

zacharyBoy, born 2012

Phenylketonuria (PKU)

Available end of summer 2017!

 

 

$47.50 has been donated towards the cost of my adoption!

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!

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Landon #

landonBoy, age 2

Probable Opitz Syndrome GBBB resulting in fronto-nasal dysplasia, hypertelorism, & male karyotype, MLPA-N. Hypospadias penis, surgically corrected in 2015. Accidental heart noise at birth, no longer present.

Landon enjoys interacting with the other children and is interested in music. He is a happy child and is developing appropriately for his age. Detailed medical information on Opitz syndrome is available along with several videos for any interested families. Could you be Landon’s forever family?

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him.

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Boyd #

boydBoy, age: 1 year 8 months

Congenital malformation syndromes predominantly affecting the facial area (high forehead, dolichocephaly, bigger nose, microretrognathia, macroglossia); pes equinovarus; severely delayed neuropsychological development; severe generalized muscle hypotonia more affecting the lower limbs

Listed: Jan 2017

Positive dynamics in Boyd’s status and improvement of his muscle tone have been observed in the last months. Boyd has marked slight increase in his spontaneous motor activity, too.

Boyd’s caregiver and the head nurse from his ward share that he has been making a constant, albeit very slow, progress in his development since his placement in the orphanage. They both share that Boyd is like a baby and needs a lot of patience but they both believe he also has the potential to continue progressing in his development. Boyd would greatly benefit if he is adopted by a family who can meet his medical needs but also provide him with proper stimulation and personal attention. Most of all, little Boyd needs a forever family who would accept and love him unconditionally.

Because we only have this child’s file for a short time, he will not be able to receive donations until a family is found for him.