Friday, December 30, 2011

Waiting Little Boys!

Agency G

MILES DEC 2007 Thal B Major

Guillermo DOB: Oct. 2009 SN: He has bilateral microtia, but can hear in his right ear. He also has a cyst in his left eye, but it does not cause him any problems

Oliver and Hudson (TWINS) Had an adnormal brain scan DOB Feb 2010 Oliver and Hudson came into care when they were one month old. Their development has been a little slower than other children, however they are progressing well. Both boys can crawl and walk with support. They can babble and play with blocks. They love toys that make noise and to crawl everywhere!

Agency CC

XJW 5/29/2010 Cleft palate, repaired cleft lip, mild hydrocephalus

ZZY0911.1.4 DOB: 11-19-10 BOY SN: Ear deformity/hearing problem

Agency B

Landon April 2011 Cong proctatresia, hypospadias and rectum urethral fistula

Daniel Jan 2008-missing fingers on left hand

Will Feb 2010 Left microtia, ankylotia

Johnny June 2010 Cleft lip and palate

Shaun July 2010-Deformed & Dysaudia of ears, CHD (PF)

Rhett Aug 2009 cleft lip and palate

Zander-July 2010 Urogenital issue(enorchia of left side), treated anemia

Charlie-June 2010 treated club foot, delay,unknown anus surgery in past, normal defacation

Shane Nov 2009 cleft lip, palate, HepB carrier, birthmark on back of head

Agency AA

Lance Jan. 2011 cleft lip and palate. He has not yet had surgery to correct this

Nathaniel DOB: 4-19-10 SN: post-op cleft lip; cleft palate; ecphyma in front of his left ear

Agency AS

Dalton boy 2.5 repaired cl/cp

Agency W

Chet 2/2011 Heart Defect and Hernia. Chet is a small child in comparison to his peers. He is an outgoing boy who is happy when anyone stays with him, talks to him, or shares toys with him. He especially likes toys with music and bright colors. He has congenital hear disease and a special, sensitive issue. He needs a family to aid his physical and mental development. Due to his age, it is thought that he will adapt quickly to a new environment.

If  anyone would like more info on any of these little boys please send us an email at

Taylor and Ashton

Friday, December 23, 2011

Wonderful Waiting Kids

Wendy 13 years old

Wendy will AGE OUT in 9 months. PLEASE help spread the word. She needs her family now before her chance is lost forever!!

Wendy is outgoing, active and restless, is ready to help others, always with happy smile on her face. She is satisfied with present life, but she also hopes that she would have her own loving parents as other classmates in school, hopes that she could see anxious mother outside of school who is await for her after school and then go back home with hands held by mother.
**sniff...sniff...she wants a mama to love her!!**
Special need: age..she is healthy

Macy 8 years old

One year ago, Macy entered a foster family and she adapted to the life there very fast. Now she receives early education in Half Sky in the institute. Under the good education and guidance of the institute, she can no go up and down stairs, take on and off clothes and bath alone. She remembers which floor she lives on and other children’s name. She can hold a pen to draw a sun, count 1-5 and tell red. Macy can ride a tricycle and pat balls.Macy is shy and introverted and exchanges little with other children. . She says “auntie, I want the grandma” most. Entering the foster family, her most close persons are the father. She likes to go out with the father and likes to play with other children. She would tell the mother if other children slip out to play. She is a little bit shy and dare not to greet strangers. Under the reminding of others, she can say hello. She can say her own name. She has little words but can express her needs in simple language.
Special Needs: white spots of cornea of the right eye, atopic dermatitis, delayed physical development

JB 2.5 years old

JB was born with glaucoma, cataracts, and clouded retina. We were able to get surgery for him and his sight has been gradually improving. He can now see with wearing glasses and has eye drops every day.He has some special needs as he has hydrocephalus, development delays, and limited sight. Under the excellent care of the foster family, he is strong day by day. (a loving christian family ;)

Special Need: leukomalacia (hydrocephalus); postoperative glaucoma and cataract.

Jane 9 years old

Jane is clever girl, intellectual developed well. She currently lives with her foster family. She is shy, talks little to stranger, but she will chat with familiar people sometimes, play house with friends always. She is clever, will help to do what she could do and send wishes to senior citizens, loved by adults. She likes to play very much, sliding board and dolls, she could take good care of younger kids, is a kind girl with a loving heart.

She is clever, will help to do what she could do and send wishes to senior citizens, loved by adults. She likes to play very much, sliding board and dolls, she could take good care of younger kids, is a kind girl with a loving heart. But all of these days she seem to have psychological problems. Once there are strangers who know her visit at home or school, she would looks very anxiety and tension as well as hide herself. In the early of September of 2010 she studies in grade one in primary school. But she can’t adapt the visiting of the strangers. If she meets this, she would hide herself under the desk or cry, which affected normal teaching seriously, and on November of 2010 she quits school; now she can’t go to school. Everyday she does housework and plays at home with foster mother. Her studies don’t been improved.

She is in desperate need of a loving family!!! A family who can pour themselves into making her secure in who she is...a precious child of God!!

Special Need: Hep B carrier (she also has a growth on her face in front of her ear)

Sebastian/Wilson 3.5 years old

Under the excellent care of caretakers, Wilson has routine life, and the body development is good, motion of limbs is normal, has normal defecation and urination, but due to the reason of retard development, his development index is not to the standard. He currently lives with a loving foster family.

Special Need: Post operative cleft lip and palate (it is uncertain if his palate has been repaired, yet); retard mental development

Rose 4 years old


Precious Rose was abandonded at 2 years old. She had a finding note with her that stated: "she is ill but the family can not support her and hope to be sent into a institute."

Through rehabilitation and exercises, Rose can walk with a walker. After supper, she would practice walking with a roll booster in the rehabilitation park. Now she knows to go to the toilet by herself. She can also dress herself in summers. The clothes in winter is much tough, she can not dress herself in winter due to the problem of the legs. Rose is very beautiful and intelligent without showing out. She would speak much with familiars but not with strangers. Now she can play jokes and act as a spoiled child. The teachers like her very much. She is a quite girl and is very smart in learning.
She is still inconvenient in walking but this has not influence her happiness. She is smart and cute and people love her very much. I asked her “do you want a foreign family?” she said “yes, I am. And I want a family with mother, brothers and papa”

Special Need:
disabled lower limbs
The bilateral sides are symmetrical; no abnormal findings are about the gap between joints. Diagnose: no abnormal findings are about the feet and both ankle joints.)


Fielder 6 years old

Fielder likes to be cuddled by the caretaker or people she is familiar with. At that time, he is very happy, would put his head on the shoulder of the caretaker. Fielder has motor, language and mental development delayed compared with other kids (this info. is 4 years old...waiting for an update). He had his cleft lip repair 5 years ago but his file does not state if his palate has been repaired, yet.

Special need: postoperative cleft lip (waiting on an updated to see if his palate has been corrected)

Grayson 6 years old

Precious Grayson was abandoned at 2 months old and his dob was determined by a note attached to him. He has normal mental development. He lives with a foster family and his file states: he learns much knowledge, he has good acceptability in the kindergarten, he will write the word taught by teachers, and has good imitate ability, likes to sing and dance, and assemble the toys, and no finding of the symptom of the cerebral hyperplasia.

Grayson also likes singing, watching cartoons, likes snacks; in kindergarten, he is kind of naughty in the class, but he can remember all the new words taught in class. And also writes them at home showing to his foster mom. Now he is in first grade, he is sensible, gets along well with his classmates, and he is very glad to play games with his classmates. He loves assembing robots, and toys such as Armor Warriors. He is not picky of foods, can brush his teeth, wash his face and fold up his own clothes.He is very clean.

Special need: history of cerebral hypoplasia (now he has no symptoms)


Wei 10 years old

Just look at this sweet peanut...he has the most precious smile! He has been waiting a long time for his forever family! This adorable guy is waiting in a phenominal orphanage...he's waiting in our Solomon's orphanage...a LWB orphanage ;)He is an extroverted, outgoing and active child. At school he abides by the school rules and participates in all kinds of group activities with average comprehensive scores. He likes classes such as fine arts, physical education, and his favorite sport is basketball. In the WI, he is well behave and follows the recommendations of our caregivers. He is able to put away his bed neatly and cleanly, and helps other children as well. He has good adjusted ability. Since he has cleft palate, he can not speak that clearly yet could be understood. He gets along well with other children and classmates.

Special need: postoperative cleft lip, cleft palate III

A Lian almost 3 years old

She is absolutely perfectly created by OUR LORD!!! No mistake made...she was known by our Maker long before He fashioned her in her mother's womb. But you know what...most people don't see her that way...they see a little girl who is not complete...I ASSURE you, she is complete...wonderfully and fearfully made!!! PLEASE help spread the word about this precious one!!!
This is beautiful, amazing A Lian. I have been advocating for this sweet one for a while and still she does not have her forever family. I have this tiny video of her
and it bring me to tears...tears of joy because there is NO doubt she is a bundle of beautiful joy...tears of longing...longing for her to have a forever family to love her!
Sweet A Lian is almost 3 years old and was born with Down's Syndrome. Here's a little bit of info. on this little miracle: A Lian is a completely adorable child. She loves to cuddle and give kisses, and though sometimes solemn, her whole face scrunches up in a ready smile and laugh when interacting. She can dance with the music, and cooperates when the caretakers dress her. She eats with a good appetite, can peel the skin off of fruit by herself, and can drink with a straw. Any family would be blessed to have this sweetheart. A Lian is physically healthy. No heart or thyroid issues have been detected. A Lian - Just learned to walk. She seemed to enjoy walking around with the walker that was present. Wide base of support when walking with arms up in a high guard position (typical for newly acquired walking ability). Wide base of support while sitting. Is able to get on both knees and reach and play in that position. Can go into a 1/2 kneeling position, which is an age appropriate transition movement. Will climb up to get a toy. She is curious and likes to explore. Loved lying in the fresh, warm, clean pile of diapers on the floor. Will scribble circles when given a pen/pencil. Loves to interact with the adults and enjoys just being carried around and played with on your lap.


For more info on any of these precious little ones please email me at TSW1203@AOL.COM or email Stacy at

Wednesday, December 14, 2011

Sorry for being MIA

Life has been crazy lately with finals I promise to add children sometime tomorrow after my last final, but in the mean time WASATCH has created a site for their waiting children please go check it out if the link does not work copy and paste it into your browser.