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 more than $10,000+ in grant funding 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.

Grants:(click to visit)
Grants over $2500+
Grants over $5000+
Grants over $7500+
Grants over $10,000+
Grants over $15,000+
Grants over $20,000+

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Aura Lee

Girl, born July 2009
FAS, Microcephaly, spastic tetraparesis

Listed April 7, 2014

NEW PHOTO DECEMBER 2016:  Aura Lee has already been transferred to the adult institution.  You can clearly see her wasting away, from that beautiful chubby-faced toddler she was before.

Status from April 2014:  Oh, isn’t she lovely? Aura Lee is doing very well.  She knows her nannies, smiles at familiar adults.  She can sit down and stand up with help.  She does not have mental delays.auralee-2016

Aura has developing speech — she can make separate sounds, and will repeat after an adult.   Aura Lee has features consistent with FAS (fetal alcohol syndrome).  This is not a diagnosis, but a cautionary disclosure.

Aura Lee will not be marked family found until a family has a completed homestudy and is USCIS approved – she does not have time to wait!!

$10,700.78 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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Hasini

Girl, born July 2012
PRC
malnutrition, developmental delay, oral deformity. ametropia and double strephenopodia

Hasini was wearing orthopedic shoes for rehabilitation as of the time her file was prepared. Hasini had a CT scan come back normal. There is a very good possibility that she has what is called Moebius Syndrome, which affects the muscles that control facial expressions and eye movements.
Hasini is described as gentle and quiet. From her outdated file: Hasini can sit stably for a long time now. She can use her left hand to go from lying down to sitting and can flexibly turn over. She likes to crawl backwards. When she is happy, she would grab the bed handrail to rock her body. She can clap and can grasp the toys attached to her bed. She can understand simple instructions. For example, if the caretaker asks her to put her hands down, she will do it. If tell her “we need to stand up,” she will give her hand to the adults because we have to help her up. She can make the “a” “e” “na” sounds. She falls asleep quickly. Hasini is afraid of strangers, but after some time, she gradually accepts the strangers. She likes playing with other kids.

A recent update states that she moved from foster care back to the orphanage recently. The update was not very positive, but Hasini has only been with them for a few months. The inability to make facial expressions may cause confusion for those who try to care and interact with her. Hasini needs a family who can see the beautiful little girl she is. Those with Moebius Syndrome do not smile with their mouths, but with their hearts. Will you be the lucky family who gets to see Hasini’s heart smile?

$11,013.30 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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Felicity

Felicity (1)FelicityGirl, born February 2011Felicity (2)
PRC
Down syndrome

Updated April 2016:
Felicity is a very cute little girl, who warmed up to our staff quickly when they visited in April 2016. Another little girl put a crown on her head at the nanny’s request, which Felicity didn’t seem to mind! She is diagnosed with Down syndrome, as well as a heart murmur. She is able to walk and run well. Her speech is not always clear, but staff heard her say “mama” very clearly. Caregivers say it seems like she tries to put 2-3 words together, but they can’t always tell. She’s a very social little girl, who loves to be playing with other kids. A natural little leader, she can become loud trying to get the other children’s attention and get them to follow her! She follows basic directions, but isn’t receiving any formal teaching yet. When asked to point to parts of the face (eyes, ears, nose, mouth) she could do so. Our staff watched her put together duplo blocks very well!

There is a $4000 Child Grant that may be available to families through the agency.

$14,623.76 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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Colby

Colby 2016ColbyBoy, born August 2008
PRC

Listed: Feb 22, 2013

Colby is a precious boy who has been diagnosed with Down Syndrome and Patent Ductus Arteriosus (Congenital Heart Defect). From observation, the heart condition has no obvious affect on daily life.

Colby is active, extroverted, and smiles often. When Colby hears music on the radio, he dances with joy. He does well in dance class and has a good sense of rhythm. Colby also enjoys playing games with other children and likes to watch cartoons.

Update 2016:
Colby is very good at imitating; in his music and dance class, he learned a whole entire dance routine after being shown the first time! He has come a long way since his early days at the orphanage. At first, he was withdrawn and did not actively engage with others. Nowadays, he’s quite active and extroverted—he actively participates in all classroom activities. Although he was diagnosed with Down syndrome and has cognitive delays, his language ability has greatly improved. Every day before school, he’ll wave and say goodbye to his foster mom. When he comes home from school, he’ll say “hello mother” and “hello father” in his native language. Colby knows all the names of his foster family members, and can name common objects and foods. He has some challenges with expressive language but he’s quite good at understanding others. He has great self-care skills such as putting on his clothes and shoes, using the restroom, brushing his teeth, washing his face, and feeding himself. Colby gets along well with other children and likes to play games with them. His report states that he has a congenital heart defect but that it does not have any obvious effects on his day-to-day life; he hasn’t received surgery for his heart as of May 2016. An agency staff member met him on a recent Journey of Hope trip to China and found that he’s quite talented and showed off his martial art and rollerblading skills! He can speak words and simple sentences, but also communicates through pointing, touch, and body language. He’s been living with his foster family for about 5 years and they shared that he’s a great helper around the house and loves outdoor activities.

$10,155.95 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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Hannah

14088420_10153821829092606_9221273545580412810_nGirl, Born September 7, 2008guardianangel

NEW PIC JANUARY 2016!

Hannah is a darling girl who needs a family.   MORE PHOTOS AVAILABLE.
Listed: Aug 6, 2010

From her medical records:  absence of rectum, cranial bones deformity, multiple development pathologies, severe dermatitis, delay of development but she is very smart and active.    Hannah is a very friendly girl. She likes to play different toys, with other children of her group. She is very smiling, easy-going girl. She understands everything, but she does not talk yet. She is a smart girl. She is walking independently.

Hannah was born with deformed cranial bones.   Hannah is very smart, she is nearly walking, and has striking blue eyes and a smile to warm your heart!   She has severe dermatitis, from what they are not sure.    She was also born without a rectum, and presumably uses a colostomy bag at this time.  She will definitely need to be seen by a gastroenterologist once home.

From an adoptive family who visited with her in June 2010:  ” Hannah is a precious little angel that despite her challenges, is unbelievably full of life.  She loves her walker, especially moving “lightening fast” down the hallway, to the playroom, whenever she has the chance.  She is a little spit fire…who has a mind of her own;) We took her pacifier (which she loves) out of her mouth to snap a few pictures and she made herself perfectly clear that she wanted it back:)  She is developing very well and  walks by holding on to her caretakers finger.  She can hold a ball/toy and is very social little girl.  She happily perked and stood up to her feet (while in her walker) when I bent down and spoke to her.  When my camera flashed, she threw her little hands up to her face and smiled.  She is an absolute favorite of her caretakers and the Orphanage Director.   The “blue” on her skin is an anteseptic that is applied as a result of her extreme skin allergy.  Given the chance, this little one will grow by leaps and bounds.  She sure stole my heart!”

UPDATE 2013:
Hannah is doing well, she is still in the orphanage and will be available for adoption when she turns 5 in September.  She is a sweet girl! Unfortunately, pictures cannot reflect it, but she is very charming!  We would be happy if a good family could adopt her ASAP!

We got to meet Hannah while touring the special needs floor of the baby house in April 2011.  She is obviously adored by the staff, and is well cared for.  She was super tiny and a little shy, but that didn’t stop her from approaching our daughter who had traveled with us.  Although I didn’t hear her make any sounds, she was very expressive and they quickly and easily responded to her.  She appeared to fully understand what they were saying to her as well, and did respond with head nodding and shaking a few times.  Not only was she walking on her own, she was strong and steady.  Able to get up and down, chase the ball, run off with the ball in her hands.  She is currently living in a caring environment with a great therapy floor, able to help her to meet her milestones and goals.  She will be transferred between the age of 5 & 6 as all children are from this facility.  The reality of where she will go, and the group where she will be fit into should a family not arrive for her BEFORE she is transfer is not good.  She will quickly regress there.

$11,117.40 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!