This Week's Waiting Kids! :)

All of these BEAUTIFUL children are two and under, most from BAAS and some from Lifeline.


First is sweet Howard, who is a year old, about to be two in May. He's with BAAS. Here's what's written about him:




Howard was born in May of '09. He has repaired cleft lip and un-repaired cleft palate. He is described as an active and bright child with a ready smile.


Next is adorable Jenna, who is also with BAAS and is almost a year old. Here's what's written about her:




Jenna was born in March of 2010. Her special need is postoperative congenital anal atresia. She had surgery in May of 2010 and received “rectovestibullar fistula repair and anoplasty” under GA and the surgery was successful. At present she recovered well and defecates normally. In November of 2010 she had a complete physical exam. The final diagnosis about her: rectovestibullar fistula repair, postoperative congenital anal atresia, congenital deformed cranium: absent callosum, foliaceous holoprosencephaly, dilation of cella lateralis. At present Jenna has plump face, red lips and fair skin, and she looks lovely.




Now she has good physical development, has 2 teeth, can roll over, can raise her head, can walk alone quite steadily, has some grasping ability, can grasp the small toys near hand, can visually follow moving people, can respond when her name called and will shake her head to express refusal when others give her the food she does not like.


This is precious John, who's a year old and is also with BAAS. I am not completely sure he is available, but, here's what's written about him:

John was born in May of '09. His special needs are cleft palate and repaired cleft lip and HBV carrier. John is a lovely boy with good appetite and ready smile.

This is cutie Anthony, who is almost two. He is also with BAAS. Here's what's written about him.

Anthony was born in March of '09. He has albinism. He is a lovely boy who likes to play with his own hands.

This is beautiful Lily, who will be three in a little less than a month. She is with BAAS. Here's what's written about her:

Lily was born in Febuary of '09. Her special needs are post operative congenital heart disease (valvular pulmonary stenosis); severe sensorineural hearing loss in both ears; tympanitis and mastoiditis in both ears. Lily's current height is 73.5cm, weight is 10.5kg, head size is 44cm and chest size is 50cm.



She lives at the orphanage right now and her physical development is good. She can sit, stand and walk on her own. She can only say Ma Ma. She likes to be with people she knows, and likes to play with other children. She is a bright and lovely child.

This is adorable Phil, who is going to be three in about a month, also. He is also with BAAS. Here's what's written about him:

Phil was born in Febuary of '09. He has albinism. He lives with a foster family and is very attached to his foster mother.

This is precious Sean, who is two. He is with BAAS. Here's what's written about him:

Sean was born in October of '08. He has β thalassemia. He lives with a foster family and is an active and bright boy.

This is beautiful Ting, with BAAS, who will be three in less than three months. Here's what's written about her:

Ting was born in March of '08. Her special needs are postoperative anaplasty of crossfoot in both sides, dislocation of hip joint in both sides. Ting had surgery on September 17th of 2010. The surgery was basically successful. However she still cannot walk after the surgery.



She cannot sit as steadily as before the surgery and will need to rest just sitting for a little while. The orphanage took her back to the hospital for recheck and was told the surgery was not a problem but it would take a while to recover.

This is cutie Zane, from BAAS, who is two. Here's what's written about him:

Zane was born in October of '08. He had CHD: aortic stenosis (mild to moderate), VSD (perimembranous part), PDA, pulmonary stenosis, permanent left superior vena cava, and anomalous muscle band of right ventricle.



In March of 2010 he received aortoplasty, valvuloplasty of pulmonary valve, VSD repair and ligation of ductus arteriosus under GA CPB. The surgery was successful. After operation his general condition was good. He is being cared for at the Philip Hayden Foundation. He is a lovely and active little boy.

This is precious Zachary who is two, and is with Lifeline.

Zachary has CHD. Look at that smile! :)

This is adorable Joseph, who is two and is with Lifeline.

Joseph has scoliosis, and also has a $1,500 grant with Lifeline.

This is cutie David, who is two, and is with Lifeline.

David has "deformed left forearm and left hand bilaterla oblique inguinal hernia." He has a $1,500 grant with Lifeline.

This is precious Michael, who is two, and is with Lifeline.

Michael has CHD. Sweet Michael has a $1,500 grant with Lifeline.

Next is adorable Jeremy, who is one and a half and with Lifeline.

Jeremy has a meningocele. This little beam of sunshine also has a $1,500 grant with Lifeline.

This is cutie Christopher, who is one and a half. He, too, is with Lifeline.

Christopher has Post Operative Spina Bifida, umbilical hernia. He also has a $1,500 grant with Lifeline.

Please pray for these kids. Some of them with the more major SN's, such as CHD, B Thalassemia and such really need to get out of China to get good care. If you want more info on them, leave a comment with your email and after I read it, I won't publish it, for your privacy. :) Also, someone left me a comment requesting information on sponsoring some children that I had on a post, but they left no way of contact for me. Can you please leave me a comment with your email? Thank you! :) If anyone wants to sponsor, let me know and I can get some info to you! Just leave a comment with your email address, and, again, I will not publish it after reading.

A quote for you today:

"I am a little pencil in the hand of a writing God who is writing a love story to the world."

-Mother Teresa

Jesus loves you!

Blessings,

Joy :)