Monday, January 30, 2012

Abigail Hearing impaired beauty MATCHED!!!

This sweet little girl has waited far to long for a family to call her own. Her Mama and Baba have to be out there somewhere. She was born December 2007 (same month and year as my princess was). She just turned 4 years old and is deaf. I do not know her type of deafness but think about all the opportunities she would be able to have with a family. She is special focus so she can be adopted by someone who is wanting to reuse their dossier or adopted along with another child. Please please consider adding this little one to your family she has been waiting on the shared list for over a year with no one choosing her as their daughter.

SHE HAS BEEN MATCHED WITH HER FOREVER FAMILY CONGRATS TO THEM AND HER!!

If you want more info on her please email my personal email tsw1203@aol.com and be sure to include the name given to her on the blog, SN, and DOB. I will then be able to connect you to those who have more info on her.

Friday, January 27, 2012

MIA

For the next few days I will be MIA! My computer has a virus and is at tech support getting fixed so bear with me as it is fixed and hopefully restored to normal!! I will return next week posting children waiting for families in the mean time please check out the other advocates under the tap at the top.

Wednesday, January 18, 2012

Fred waiting in China

Fred will turn 14 in October, so we need to find him a family ASAP! All the WACAP staff members who met him fell in love with this kid. He'd make a great brother and son for some family. We know they're out there - but maybe they just haven't seen HIM yet! http://www.wacapadoption.com/345859/2012/01/17/and-still-he-smiles-meet-fred.html They have one photo on their secure website, and families are welcome to request his file with no obligation for more info and photos of this great kid!

From the WACAP website:

Fred is an outgoing Asian boy who wasn’t shy when talking with us. He attends a school outside the orphanage and they report that he is quite smart and an above-average student. Fred’s favorite subject is math. He enjoys playing when outside of school especially with a ball. He has many friends of all ages. Although he has dwarfism, Fred is very active and likes to run. He says that some of his favorite things are snacks and new clothes. Fred says that nothing makes him sad. When he sees an injustice for himself or others, he tells the teachers. His caregivers report that he is a hearty eater. He was very polite and always smiled at us when he saw us walk by during our visit at the institute. At 13 years old, Fred needs a family very soon or else he'll be be deemed ineligible for adoption. Unfortunately, there are very few options for an orphan with dwarfism in his country.
Visit WACAP’s waiting child webpage to see a picture of Fred.
Fred is listed with WACAP through a special partnership project with his orphanage. Fred is part of the Special Focus program. There is a $4,200 Promise Child grant for eligible families for this adoption. Even if you might not typically meet the requirements to adopt from Fred's country in Asia please ask about exceptions! There is no obligation or fee to view his information. Please ask about Fred – ID# SP.FY.1098.32310.01 Interested families should contact https://mail.wacap.org/owa/redir.aspx?C=7a75cda8071e4d16aaba4f7e21a36656&URL=mailto%3aCkids%40wacap.org or https://mail.wacap.org/owa/redir.aspx?C=7a75cda8071e4d16aaba4f7e21a36656&URL=mailto%3aFamilyFinders%40wacap.org or call
WACAP toll free: (888) 440-8231

Tuesday, January 17, 2012

Build A Menu

Build a Menu is a wonderful organization started by a friend of mine to help families create meals specific to their their daily needs while staying on a budget. They also donate part of the money they make to a charity of your choice that helps orphaned children. So far the charities that you can pick from are Starfish Foster Home, WACAP's Promise Fund, Starfish Foster Home , WACAP's Promise FundPathway Youth & Family ServicesShow Hope, CompassionArms of Hope, Annabelle’s WishNot For Sale. and Lifesong for Orphans. Please consider signing up with them today not only will you create a family friendly meal plan on a budget but you will be helping many orphaned children around the world like the ones advocated for on SWW! Please click HERE for their website.

Taylor

Friday, January 13, 2012

Waiting Child Onika

Onika is a beautiful 7 year old girl waiting right here in the USA for a family!! She is waiting in the State of Idaho but families from any state may inquire to adopt her!

She is aescribed as a "social butterfly," Onika is a smart girl who loves showing off her abilities at school. She can be very sweet and likes to please others. Onika enjoys coloring, drawing, riding her bike and puzzles. Her favorite doll is Raggedy Ann.

Onika's adoption team is searching for a couple or single parent that can provide the structure and routine in which she thrives. Because she loves to engage in conversation with adults anytime and anywhere, she will need parents who will encourage her social skills within safe boundaries.

Onika also needs a family environment where she can be the sole focus for a while. An emotionally secure couple or single individual with no pets would be ideal, especially if at least one parent has had some experience working with children who have experienced substantial abuse and neglect at an early age.

Onika's team wants to consider families where she can be the only child. It will be important that her parent(s) are realistic about the emotional and behavioral challenges ahead. She needs a stable parent or parents who have the understanding, commitment, humor and creativity to withstand day-to-day difficulties. Her family will need a strong support network, which should include adults who can provide occasional respite. This will prevent burnout for her parent(s). Good emotional support will be so important to ensuring Onika is able to thrive. So too will be the ability to follow through with professional appointments and discipline strategies. With access to excellent support services, her parent(s) can maintain commitment as they help her make sense of her past, present and future. With these resources in place, this "social butterfly" can take wing and soar!

Please if you would like to know more on this beautiful girl go HERE

Sunday, January 8, 2012

Beckett

Could this sweet boy be your son?
Updated Photo (He no longer has his baby curls but is still just as handsome)

Beckett was born February 2009 in Russia. He is described as calm and loves to caress
What a sweet curly-top he was!  Beckett has giant blue eyes and a sweet personality.  He is diagnosed with some vision loss in one eye and some hearing loss in one ear. More pictures are available!

Beckett does NOT have Down syndrome.
Please consider Beckett, he will so greatly benefit from medical care and a loving family.
Please go HERE to learn more about him

Requirements to adopt from the Russian region he is currently living in:

3 trips are required 
  • 1st trip, Both parents for 5-7 days
  • 2-3 month wait for the judge to appoint the court hearing
  • Both parents travel for 2nd trip about 7 days, both parents leave after the court hearing
  • 30-day waiting period is NOT waived for special needs
  • Only one parent would need to return after the 30-day wait
  • Up to 5 young children in the home if the family income is sizeable (the adopted child being the 5th child)
  • Both parents must be younger than 60 years
  • Parents may NOT be currently on anti-depressants; prior history of anti-depressants may be permitted on a case-by-case basis
  • No criminal background (DWI's acceptable on a case by case basis)
  • EASY TRAVEL IN-COUNTRY
  • Fee includes orphanage donation
  • Married couples and single heterosexual mothers may apply
  • Un-related children may not be adopted simultaneously
  • Total program and travel fees approx $35-40K
  • Thursday, January 5, 2012

    Sweet Xander

    Xander is Starfish babies that I got the privilege to meet this summer, he incredibly sweet and adorable.

    XANDER
    He was born September 2009 with a type of Spina Bifdia and Hydrocephalus. He is able to sit up and has some feeling in his lower limbs. He is by far one of the sweetest little guys I have ever met. His eyes will go right to your heart. He is so sweet and gentle natured. I have more pictures and a video on him from this summer. He is waiting agency specific please email me at stillwewait@aol.com for more info!

    Such a cutie and was always happy!

    Blowing bubbles!

    See what I mean with those beautiful eyes of his!

    Newer pic from a fellow volunteer who visited he can stand with some support

    Those eyes get me every time love this boy!

    Tuesday, January 3, 2012

    Are you Lizzy's Family?

    Lizzy has stolen my heart she is beyond beautiful and I know her family has to be out there somewhere. She was born in Russia and has Down syndrome and may or may not also be HIV+. She can be adopted by both married couples and Single Heterosexual Mothers. Please please help me find this little ones family she is still so young and would benefit so much from having a family and not knowing what it is like to grow up in an orphanage.

    Here is what RR says about her

    Girl, born October 2010
    Hazel eyes
    Black hair
    Character is calm
    I love how she has grown! Old picture is from March 2011, and new one is from June. She would so benefit from a family while she is still so young!
    Lizzy has Down syndrome and is listed as HIV+; however since she is still so young that may just be that her mother was HIV+

    LOTS more photos available! Please go HERE to learn more on her or email me at stillwewait@aol.com

    Taylor

    Monday, January 2, 2012

    What About Now?

    What is holding you back from adopting?
    1.      -We don't have the funds/don't want to take away from our other children
    2.      -It's not for us/Were not called to adopt
    3.      -I couldn't love a child that isn't born from me
    4.      -I could not handle a special needs child
    5.      -We are not special people
    6.      -We cannot handle another child
    7.      -We don't have the time to
    8.      -What people would think of us (applies more to those adopting a child of a different race or culture)
    Many of these excuses are what people are using every day to keep them from adopting a child that needs them more than they could ever fathom.

    I know that everyone who follows SWW is not a Christian or affiliated with a religion but it is SWW motto that Every Child Deserves a Family no matter where they are from or what their special need may be. Each child is special in his or her own way.

    1.      Funds will come they always do people who have very little bring home children every day. If God calls you he will provide for the adoption. You can hold fundraisers, hold auctions, benefit dinners etc...
    2.      Everyone is called to care for the orphan it is not an option it is a command to care for the orphan and the widow in their distress... James 1:27. IT IS NOT AN OPTION but a command he doesn't say do it if you can fit it into you schedule or if you have time care for them. Even if you cannot adopt you can give to an orphan to help better their life or donate to a family adopting a child.
    3.      If you were handed a child who needed  you right now you would cuddle them every woman would a sweet innocent baby what isn't there to love. Love might not come immediately but over time it will. Love comes softly and over time it builds slowly.
    4.      Sure you could Special needs may sound scary but in reality many of the children adopted from the Special needs program are normal healthy children with cosmetic issues such as Missing finger, Cleft Lips, Club foot, Birth Marks, Ear Deformities. Underneath their special need they are a normal child who wants to be loved and accepted some children do have more severe needs that require more extensive surgeries such as Heart Defects, Spinal Related Issues, and Hydrocephalus. Some Children have intellectual needs that are not correctable and then there are need that do not require medical intervention at all such as missing limbs and digits, ear deformities that do not affect hearing, birthmarks, Age yes being over the age of 6 is a special need in many countries and even being a boy can be a special need.
    5.      It does not take special people to love a child and to provide for their needs. No one person is perfect those that adopt just want children to love and to share their love with
    6.      Yes another child will bring more work, laundry, expense in general. But with that there are extra kisses and hugs, another child to watch grow and mature, and more love all around.
    7.      Well you had the time for that vacation didn't you why couldn't you make time for one more little one.
    8.      Honestly who cares what they think of you people will either love you are hate you why try to please everyone.
    So What About Now what is your excuse not to adopt and do as you are called. If you are called God will provide. 2012 is a brand new year and yes no one ever said it would be easy but will you tell God no and let a small child sit and waste away because you are too caught up in your current life to break and cry for the orphan. Will you answer his call before it is too late for a child?

    In these few days of 2012 children have been abandoned without left to survive on their own and grow up in orphanages that DO NOT care for them whether they live or die.

    So what about now are you going to sit back and let another child suffer or will you answer the call that has been commanded and help a child that needs you.

    Adoption does not take a special person all it takes is a person that is willing to love and care for another.

    "An adopted child is not an unwanted child but rather a child that is prayed for and loved before they are ever known."

    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 stillwewait@aol.com


    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



    SHE WANTS A MAMA, PAPA, & BROTHERS!!!

    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.


    video



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

    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 http://wasatchadoptions.blogspot.com if the link does not work copy and paste it into your browser.

    Saturday, October 22, 2011

    Please considering Helping this Family bring home their Daughter

    Many of the people remember the little girl Pearl who was advocated for on here! Well, as you know she has been matched and the family happens to be one that I dearly love and admire! They are stepping out on faith to bring Pearl home and went against the norm of waiting until they had the finances to do so. Please consider helping them bring her home it is possible for you to win one of the TWO iPads that someone generously donated so every penny will go to their adoption cost and not to buy the iPads. The deal is $2 for 1 ticket OR $10 for 6 tickets.  Drawing will be December 1st.  Here are the prizes
    1st Prize - 32 GB iPad
    2nd Prize - 16 GB iPad

    Please go to the family's blog for more on how to enter http://www.thebarbeebunch.blogspot.com/

    Saturday, October 15, 2011

    Boys 3 and under who are waiting

    Please note that these children may or may not be matched at this time. Due to the rapid changing of the shared list and since we have moved blogs we are unable to always keep this post updated. If you know of a child who has been matched listed here let us know stillwewait @ aol.com. Thank you!


    Shared list boys
    2009, June 14th, Boy
    SN: CHD -
    2010, June 5th,
    SN: Cleft lip, Cleft palate, Crossed eyes, Heart disease

    L Mao Kids
    Brennan male, age 3 right hand and left ear deformity-MATCHED

    L non mao kids agency specific- 
    Freddy male, age 1 congenital deformity of right corners of mouth, congenital atresia and defect of right outer ear and auricular tube.

    Jimmy male, age 3 congenital glaucoma of right eye, pinnal deformity of right ear

    Mark male, age 3 cleft lip/palate

    L Shared list kids
    Nathan Male, Age 22 months Heterochromia Iris, Dysaudia

    Larson Male, Age 3 Polydactyly Right Hand, Deformity of Left Auricle

    Lincoln Male, Age 22 Months Postoperative CHD

    Jeremiah Male, Age 2 Postoperative Meningocele

    Nate Male, Age 2 Post-Operative Cataracts on both Eyes


    C hope Kids,
    Dang He is a 3-year-old boy with cleft palate III and a deformity with his left foot. DOB 11/9/2007
    Yang Fu is a 1-year-old boy with a post-operative meningocelein and has had surgery to drain his hydrocephalus meningocelein is in the lumbosacral area. DOB Sept 1 2010

    Dang Qing is a 2-year-old boy with post-operative hydrocephalus.
    Sui Xiu is a 3-year-old boy with congenital heart defect and special needs. CHD; syndactylia of right index and middle fingers (CHD and exclusion of right syndactylia can be done); bilateral undescended testicles; short penis DOB Feb 20,2008

    Dang Guo is a young boy with poor msucular tension in his extremities DOB July 14, 2010
    For more info on the CHI boys click on the link below

    MATCHED: Boy limb differences 3 years old

    B Waiting Children email X for more info on them xqcai @ comcast.net

    Hayden Born Jan 2011 Albinism

    Nicholas-born Sept-2008 CHD (TOF)

    Jackson born Dec 2009 hydrocele, hernia, Laryngomalacia
    Thomas born Feb 2008 deformity of external ears
    Aiden born Nov 2010 Albinsim
    Isaac born Jun 2011-Urogenital issue
    Cade-October 2010-congenital limb deformity
    Jayce Feb 2011 post-op CHD, post-treatment club feet, umbilical hernia, questionable hearing test on left
    Craig-March 2010 hand and foot deformity
    Shane Nov 2009 cleft lip, palate, HepB carrier, birthmark on back of head
    Noah April 2010 facial angiomatosis IQ test at 9 mths indicates delay

    Owen born December 2009 Hydrocephalus
    Jason 2-11 history of CHD minor hypospadia-hernia
    Heston Jan2010 post op anal atresia(imperforated anus), CHD
    Jared March 2010 deafness, hypospadia, hernia
    Zander born June 2008 premature
    Asher born February 2009 growth delay

    S W Kids
    Jake is 20 mths old He was born 10-22-2009 Jake's SN: post op club feet and possible arthrogryposos or reflex concern. He is currently living at New Hope Foundation. http://www.hopefosterhome.com/babies/jake.htm

    Ryan
    DOB: 12/25/2009 Special Need: Deformed Auricles
    FOr more on these little boys please visit the link below.

    FOR MORE INFO ON AY OF THESE LITTLE ONES EMAIL ME TSW1203@aol.com
    Due to recent changes with the C3WA I can no longer post agencies.