Saturday, November 27, 2010

Kids with Anemia but a focus on Thalassemia

Today's Kids all have some form of Anemia but there is a focus on Beta Thalassemia today and its description is below followed by wonderful kids who wait!!

Thalassemia is an blood disorder passed down through families (inherited) in which the body makes an abnormal form of hemoglobin, the protein in red blood cells that carries oxygen. The disorder results in excessive destruction of red blood cells and anemia.

There are many forms of thalassemia. Each type has many different subtypes. Both alpha and beta thalassemia include the following two forms:

•Thalassemia major
•Thalassemia minor
You must inherit the defective gene from both parents to develop thalassemia major.

Thalassemia minor occurs if you receive the defective gene from only one parent. Persons with this form of the disorder are carriers of the disease and do not have symptoms.

Beta thalassemia major is also called Cooley's anemia.

Treatment
Treatment for thalassemia major often involves regular blood transfusions and folate supplements.

Persons who receive significant numbers of blood transfusions need a treatment called chelation therapy to remove iron from the body.

Now on to a few whonderful kids who have Beta Thal that wait these children are agency specific please email me if you would like more info on them and to find out which agency has their file tsw1203@aol.com

First up is the Beautiul Danielle (MATCHED CONGRATS TO THE FAMILY)
Danielle was born 2/10/2010 still a baby she has beta thal and a port wine stain on the left side of her face. Isn't she simply beautiful she just needs parents to put a smile on her face! Still havent figured out why she is still waiting




Next up is the Handsome Sean

Sean was born 10/12/2008 he has beta thal and lives with a foster family. He is described as smart!


Next is Robert, Bob for short
Bob was born 2/23/2007 and his sn is Beta Thal. He is quite the cutie and looks like a heart stealer.



Next is the lovely Laila
Laila was born 1/1/2008 still a baby she is beautiful she has Beta Thal along with G6D deficiency which I think is another type of anemia.



Next is the cutie Simon
Simon was born 2/15/2008 he was born with a cleft lip and palate and Beta Thal. He looks like a mommy's boy and really needs someone to make him smile.



More agency specific no pictures on these little ones I do not know the exact blood disorders these children have but can direct you to the agency that has their files

Gender: Male
Date of Birth: 6/2009
Special Needs: Blood Disorders, Cleft Lip/Cleft Palate

Gender: Male
Date of Birth: 4/2009
Special Needs: Limb Differences, Blood Disorders

Gender: Male
Date of Birth: 1/2005
Special Needs: Blood Disorders

Gender: Male
Date of Birth: 8/2003
Special Needs: Cleft Lip/Cleft Palate, Blood Disorders

Gender: Male
Date of Birth: 3/1999
Special Needs: Blood Disorders

Gender: Male
Date of Birth: 9/1997
Special Needs: Blood Disorders (Ages out in Sept of next year)


Shared list Kids with Beta Thal: Please keep in mind the shared list is ever changing and at anytime these kids can be matched or moved to an agency specific list without my knowlegde please ask you agency if you would like more info on these little ones below!

Lizzie was born 9/30/1997 she ages out in september and looses the chance of ever finding a family then.



Next is Hannah. Hannah was born 7/2007 she does not have Beta Thal but another form of anemia. On hold for a family


Next is Mia. Mia was born 11/2006 and she also does not have beta thal but another form of anemia that is not listed.


Next is Ethan. Ethan was born 01/2006 and he has Beta Thal.


Claude is up next he was born 11/03/2005 his sn is Beta thal.




Sam is up next he was born 08/2004 and does not have beta thal but another blood disorder.


These next kids have no pictures but are all on the shared list unless otherwise noted I do not know somes exact birthday but can find it out if you would like it. Some may have Beta Thal and others may have a different blood disorder

Gender: Male
Date of Birth: 8/2003
Special Needs: Club foot/feet, Blood Disorders

Gender: Female
Date of Birth: 10/1998
Special Needs: Spina Bifida, Blood Disorders

Gender: Male
Date of Birth: 2/2005
Special Needs: Blood Disorders

Gender: Male
Date of Birth: 6/2008
Special Needs: Sexual Development differences, Blood Disorders

Female
10/25/2004
βThalassemia

Female
8/1/2006
β-thalassemia, slow motor development (can’t walk), slow physical development (height couldn’t reach the standard)

Female
8/12/1998
suggested to have combined Mediterranean Anemia (MA) (thalassemia) test to exclude MA. 3) Positive HbsAg, HbeAg and HbcAb

Male
1/4/2005
thalassemia

Female
3/18/1998
β-thalassemia and medium anemia, low growing development

Male
7/10/1999
G6PD deficiency

Female
11/9/2008
mild alimentary anemia;cerebral palsy;mentally development delay

Female
12/15/2003
Intellectual development delayed,concomitant esotropia,mild anemia

Male
10/6/2001
Anemia. Require oral drug treatment; Normal( low level for developmental index)

Female
9/29/2005
Right cross eye; congenital microcornea; adherent leucoma, motor retardation, minor anemia,SHE HAS A TWIN SISTER LISTED BELOW

Female
9/29/2005
blind (left eyeball has been removed), mental retardation, minor anemia, TWIN SISTER

Male
3/16/2008
deformity of right foot (two toes of right foot), delayed motion, slight anemia

Male
3/26/2006
Mediterranean anemia

Female
1/4/2004
b-Mediterranean anemia

Male
5/12/2007
ß-Mediterranean anemia; growth retardation (4 items unqualified); intelligence development normal

Male
8/4/2006
β-Mediterranean anemia

Male
4/25/2005
Mediterranean anemia

Male
6/6/2004
congenital anopsia of both eyes, slow development, anemia

Female
4/1/2001
Mild CP, malnutritional anemia

Male
6/14/2000
Postoperative cross-foot, HB positive, mild anemia

Male
11/30/2008
mild anemia; left eyeball atrophy, right eyeball congenital glaucoma

Friday, November 26, 2010

An Orphan's Wish Boy

Meet LUKE!!!


Luke – August 2007
Luke’s special need is clubfoot and mild cerebral palsy.

Luke arrived at the clubfoot casting unit in August 2010. After settling in, he soon began charming the carers and earned his nickname of Mr. Happy. He is a giggly little boy who loves to go around on his tricycle. Luke just had surgery to repair a hernia in his diaphragm and is doing well. We are looking forward to seeing him gain weight, grow and to continue with the casting treatment for his clubfoot. He brings much joy to the House of Love and would bring much joy to his family too.

You can read more about Luke and see more pictures of our Mr. Happy at the following blogposts: home again, recovering, surgery, and our little Mr. Happy.

If you are interested in reviewing Luke’s file, please contact Betty Betz at FTIA for more information. FTIA’s standard agency fees are reduced by $1,800 for the adoption of a child with special needs.

The Ugly Truth of Diseases.

This story BROKE.MY.HEART. It is the horrible truth of children with HIV/AIDS all around the world.
from : http://master.dailychilli.com/news/7638-the-lonely-life-of-a-six-year-old-boy

The lonely life of a six-year-old boy

Ah Long carrying firewoods down the mountain path to his home
A six-year-old HIV carrier, has been living alone since his parents died of AIDS.

The boy, known as Ah Long, does his own washing, cooking, studying and he also rears some chicken.

He lives in his parents' house at the foothill village of Malu Mountain in Liuzhou in Guangxi Province, China.

Ah Long has an 84-year-old grandmother, who visits him quite frequently and cooks for him.

The granny has also planted some vegetables near the house for Ah Long.

Ah Long making a fire to cook dinner

Ah Long making a fire to cook dinner


Ah Long does know what AIDS is.

All he knew was that his friends never want to be near him, doctors did not want to treat his wounds and his only family member – his granny – refused to live with him.

He was also rejected by the nearby primary school.

The only companion the boy has is a dog called Lao Hei.

Ah Long playing with Lao Hei in front of their house

Ah Long playing with Lao Hei in front of their house


Due to his complicated family background, the Welfare Department has declined to take care of the boy.

Ah Long studying in his room alone

Ah Long studying in his room alone

He receives 70 yuan (RM33) monthly subsistence allowance from the civil bureau but it is not enough.

After Ah Long's story was published in Chinese newspapers, a couple announced that they would adopt the boy.

However, it has yet to materialise.
*****************************************

When most hear the word HIV/AIDS it sends fear through them. It is a "silent killer" who wouldn't be afraid of it?! So many have such unrealistic views on the disease. You can't get HIV/AIDS by hugging, kissing, sharing drinks, touching, or any of the basic things. It is not a disease you can just catch like a cold. Yet, so many people think it is. So many orphans in the world never get homes because of the title "HIV+" or even worse "AIDS +" that one little 'title' costs so many children the chance of having a family. To be honest HIV/AIDS has always SCARED ME TO DEATH. I had NO idea what HIV/AIDS was. I only knew that it could kill you. Now I am much more educated on the subject. It is not a disease that should terrify you. Infact it is very manageable. Most children with HIV can live NORMAL lives and have normal life expectancy. HIV/AIDS orphans are continually thrown to the side and looked down on in all societies. Do you think those children can help the disease their parents gave to them? Do you think it is what they want? All the pain, the medicines, the looks, etc. Do you think they chose that? They didn't. They can't help it. So why do we all judge them and refuse to accept them just like they are? Why do we wait and refuse to open our hearts to children who NEED homes just as much as EVERY OTHER ORPHAN IN THE WORLD. Just because they are HIV/AID+ it does not make them less deserving. So why do we think it does?

This is an AWESOME video on HIV/AIDS awareness. I would suggest watching it. It is awesome information.

Tuesday, November 23, 2010

BELLA URGENT!!!


She is 13 years old and in Shanghai. She is an orphan living in an orphanage. Bella has six months to find a family. If this doesn't happen by February, she no longer be eligible for adoption. AT ALL, EVER.




Let's not let that happen. Let's spread the word, give her a chance at a mother, a father, siblings, and an education.




She is listed with a friends agency. They have used them twice and would not hesitate to use them again. For more info please leave a comment or email me (tsw1203@aol.com). The CCAA is willing to make exceptions for those over age 55 and that do not meet certain requirements for the China program. The agency is willing to transfer her file order to find her a family!!!

Sunday, November 21, 2010

Still WE Wait



In America everything is put over the top. It is overrated. Everything can always be bigger and better. Everything can be improved or redone from what they are now. Everything. We can never be happy with what we have. We always need the "next big thing."
God loved us so much. He put us here for ONE main purpose. To serve Him. To share HIS glorious news. To tell the World about how wonderful He is. To share His Love! Yet still WE all wait. We sit on our couches watching tv, playing video games, eating excess amounts of food, living life to the very fullest. Forgetting the MAIN reason we are here. We are not here to eat, to party, to watch tv, to buy that new laptop, to get the new cell phones, or to make ourselves happy. We are not here for that!
We all seem to live in this fairy tale and take the thing of "Oh, someone else will do it" over our concince. We forget that children are starving, crying, orphaned, begging for love. We forget that we are living so wonderfully while others suffer. We forget that we waste SO much. We throw plates of food away because "you weren't hungry." We take SO much for granted. We take for granted the next meal, the warm bed, the air condition, the love our families offer. Everything we have could be GONE. Gone in the BLINK OF AN EYE. Everything you build your life around could disappear in a flash. Without you even knowing what hit you it could ALL BE GONE.
Jesus does not tell us to leave it to others. He does not tell us to just hit that "donate" button. He doesn't tell us to just ignore the crisis of everyone in the world. He tells us to pick up our cross and follow Him. We are commanded in James 1:27 to look after the orphans and widows in their distress. He commands us!!
So why do WE still wait?

Thursday, November 18, 2010

A Young Man Who Needs a Home!

There is a young boy, Joseph, that desperately needs a home. He has Pulmonary atresia, Velo-Cardio, Facial Syndrome, a voice problem. He is turning 12 this May. From what people who have seen him and talked with him say, he is sweet, intelligent, very polite child and a big helper with the little kids.

We just found out that Joseph's adoption papers have returned to the CCAA by an adoption agency, because nobody was interested in him. Please help us to spread the words out that he is available for adoption, he is a sweet boy who desperately needs a forever family! Whoever is interested in him will need their agency to contact the CCAA for his paperwork.

This is what the gal from the foster facility says about him... "He can't speak clearly, it's hard to understand him, the doctor said he might need an operation to fix it and it's not a hard one but he has to wait until his heart is fixed (he has had one heart surgery 4 years ago, and needs one more)
He likes anything related to Ultraman and Transformer, Legos, he like to build toy airplanes and boats and draw, he is very particular about his food, he likes to eat noodles and potatoes and doesn't like meat that much, he is a very neat and kind boy, he is not the smartest kid in his class but does well with all the subjects, gets along with others."

Chinese name: Dang Feilong (党飞龙)
Date of Birth: 05/08/99
SN: Pulmonary atresia, Velo-Cardio, Facial syndrome, voice problem
SWI: Luoyang orphanage of Henan province





Wednesday, November 17, 2010

The Waiting Child by Debbie Bodie

I saw you meet your child today You kissed your baby joyfully and as you walked away with her I played pretend you'd chosen me. I'm happy for the baby, yet Inside I'm aching miserably I want to plead as you go by, "Does no-one want a child of three?" I saw you meet your child today In love with her before you met And as I watched you take her out I knew it wasn't my turn yet. I recognize you from last year! I knew I'd seen your face before! But you came for a second babe. Does no-one want a child of four? I saw you meet your child today But this time there was something new A nurse came in and took MY hand And then she gave my hand to you. Can this be true? I'm almost eight! And there are infants here, you see? But then you kissed me and I knew The child you picked this time was me.

Millions of children are waiting simply because they are older! Could you be the family an older child is dreaming and praying for? In countries around the world there are HEALTHY children waiting and their special need is AGE! They are considered special needs because they are not under 4 how sad it is to think that they are waiting simply because they are older. Here are some of the older children waiting!

These are just a small number of the children who wait all of these children are on China's shared list and can be found by an agency who has access. Not every child listed below is 100% healthy some have special needs that can be controlled on medication, may require surgery or more surgery, or they may have needs that do not affect their over all health at all missing limb digits, ect. I cannot guarantee that any of these children are still available or if they are on the shared list some may be on agency specific list and I am not aware if they are.

Male
1/24/2001
healthy

Male
7/9/2001
Healthy (older child)

Female
8/9/1997
healthy

Male
6/5/1999
healthy

Male
3/3/2000
Healthy (older child)

Male
8/28/1998
Healthy (older child)

Male
3/9/2001
Healthy (older child)

Male
10/15/1998
Healthy (older child)

Male
5/3/1998
Healthy (older child)

Male
3/7/2000
Healthy (older child)

Male
8/12/1998
Healthy (older child)

Male
11/10/1997
epilepsy

Male
11/24/1999
underdevelopment of left lower limb. Healthy

Male
12/5/1997
Healthy (older child)

Male
7/30/2000
Healthy (older child)

Female
6/12/1998
healthy

Male
12/16/1999
healthy

Male
6/19/1998
healthy

Male
9/22/2000
healthy

Male
12/18/1997
Healthy (older child)

Male
7/22/1998
healthy

Female
5/16/2000
chinese says epilepsy

Female
6/11/2000
chinese says epilepsy

Male
1/9/1997
Healthy (older child)

Female
9/30/1997
β thalassanemia

Male
3/4/1998
Healthy (older child)

Male
7/10/1999
G6PDdeficiency

Male
6/23/2003
postoperative cleft lip and palate repair

Male
7/1/1999
Cleft Lip/Palate

Female
7/2/2000
Cleft Lip/Palate

Male
3/1/1999
Healthy (older child)

Female
7/1/1998
basically normal (HB carrier)

Male
1/10/2004
congenital repair of cleft lip postoperative

Male
4/1/2004
Postoperative cleft lip and cleft palate(both sides)

Male
12/10/2002
postoperative cleft of lip and palate

Male
1/5/2003
postoperative CHD

Male
9/4/2000
CHD-DORV/ASDF/VSD post operative; Hep-C virus carrier; curvature of penis

Female
5/3/2001
severely and profoundly deaf of both ears

Male
2/20/1997
Basically normal (right ptosis)

Female
2/2/2005
Epilepsy

Male
11/19/2004
HBV infection, postoperative congenital cleft lip, congenital cleft palate III

Male
12/17/2003
Cleft Lip/Palate

Male
3/10/2001
cleft lip and palate

Female
1/19/2000
postoperative cleft lip

Male
9/1/2004
postoperative torticollis

Male
5/5/2005
congenital cleft lip and palate, post operation of congenital cardiac

Male
12/14/2004
deformed right eye

Female
1/17/2001
Postoperative congenital heart disease

Male
8/4/2003
albinism achromodermia

Male
8/1/1999
Healthy (older child)

Female
5/1/2001
1 left TEV

Male
1/4/2005
thalassemia

Male
1/15/2002
Hep. B carrier

Male
4/29/2001
congenital deaf mutism

Female
9/30/1997
1 CHD: good postoperative recovery of VSD repair, minor incompetence of TV 2 HB

Male
7/15/1998
Healthy (older child) , superficial caries of dentin,accessory tooth

Male
8/24/2000
albinism

Male
1/18/2000
Hepatitis B Positive

Male
9/5/2003
delayed speech

Male
7/19/2002
slightly poor motor balance

Male
7/28/2003
DST is abnormal ,the result as above,other is normal

Female
12/10/2000
congenital ankylodactyly

Male
10/4/1998
HBV

Male
10/9/2002
left undescended testis

Male
7/14/1997
Operative cleft lip and palate

Male
12/20/1998
congenital deaf and mute

Male
7/11/1998
congenital cleft lip and cleft paltae repaired;;pigeon chest

Male
5/5/1998
Healthy (older child)

Male
3/15/2004
postoperative congenital cleft lip and palate

Male
7/1/2001
inborn mute and deaf

Male
7/31/1998
postoperative congenital cleft lip and palate;bilateral cryptorchidism

Male
4/30/2002
Muscle atrophy of both lower limbs

Male
6/8/2000
postoperative congenital heart disease

Male
8/21/2003
postoperative cleft lip ;left cleft palate III degrees

Male
9/19/1999
Healthy (older child)

Male
12/30/1998
Healthy (older child)

Female
11/30/2001
CHD

Male
1/29/2004
thalassanemia

Male
4/25/2005
Mediterranean anemia

Female
8/30/2000
slightly low right muscular tension

Male
5/2/1998
Hepatitis B Positive

Male
9/23/2000
post-op right oblique inguinal hernia

Male
5/1/2001
Healthy (older child)

Female
4/16/1999
Hepatitis B Positive

Female
6/19/1999
Healthy (older child)

Female
7/30/2000
post-operative cleft lip and palate II repair

Male
5/23/1998
Healthy (older child)

Male
8/4/2000
Healthy

Male
8/22/1999
Healthy (older child)

Male
5/9/1999
Healthy (older child)

Male
3/7/2000
Healthy (older child)

Male
12/27/1998
Healthy (older child)

Male
10/5/1998
Healthy (older child)

Male
8/29/1997
Healthy (older child)

Female
8/1/1997
epilepsy

Female
3/20/1997
Healthy (older child)

Female
11/19/1998
Healthy (older child)

Female
8/7/1997
Operative cleft lip and palate

Male
5/17/1998
deformed feet

Male
11/10/2001
congenital deaf-muteness; congenital hypospadia

Male
1/28/1999
Healthy (older child)

Male
7/9/2001
Healthy (older child)

Male
1/24/2001
healthy

Female
8/9/1997
healthy

Male
6/5/1999
healthy

Sunday, November 14, 2010

Korean Children

Today's post will feature a few children that are waiting in Korea. Korean Requirements You must be married couple. Parents age must be 25 - 45 and no more then 4 children at home. Per Korean law I cannot post the child's picture here but I do have pictures of all of these children but no medical info other then what is posted here if you would like more info on any of these children you have to contact the agency for more information. I cannot guarantee that any of these children have not been matchedd with their families but if anyone finds out they have or if you need to know an agency that a child is with and it is not listed here please email me at tsw1203@aol.com and I can find out for you. If the agency is known it is listed beside the child.

Boy 12-02 09 murmur, lesion in chest (to be removed)Holt Adoption Agency

Girl 12-06-09 Premature (34 wks) Welcome House Agency ( she looks like she would be a handful her picture is adorable) Matched With her Family congrats to the family!
Girl(2y) August 11, 2008 chomosomal abnormality, DGS, ASD (waiting on AAC's list Name Madison)

Boy(1yr) March 14th, 2009 Premature, Hydrocephalus w/Shunt (waiting on AAC's list Name Shane)

Boy 9-25-09 Delay

Girl 10-08-09 Small Head, CHD risk cognitive delays (agency unknown but I can find out for an interested family)

G07-13-09 Delay-tested 8 mths @ 11mths (Amy@Welcome House (215) 249-0100 ext.119 prefer families in VA, DE, PA)

Boy 09-22-09 Background issue to consider Agency: Children's Home Society

Girl 03-13-07 Premature & COng Syphillis Agency: Children's Home Society

Boy 05-02-09 Premature, CHD, COng Rubella Agency: Children's Home Society

Girl 04-13-07 Macrocephaly & CHD Agency: Children's Home Society

Saturday, November 13, 2010

Special Needs Resource Videos

Spina Bifida

Albinism

Thalassemia


Click on the name of the SN to be directed to the video these are only a few and as LWB adds more I will post them here!

Friday, November 12, 2010

The Forgotten.



Forgotten : disregarded: not noticed inadvertently
Children all over the world are simply forgotten. Orphans.
I cannot and will not forget them. I simply can't. I refuse to. I will fight with everything in me until they all have a home.
Once you have held an Orphan, Touched an Orphan, LOVED an Orphan, been LOVED by an Orphan, put a face with the name of an Orphan your life is changed. Whether you like it or not. The fairytale days of "poverty and orphans aren't a big deal. they are ok by themselves" is shattered. I know this first hand. In 2007 when my family went all the way to China to adopt a little Orphan girl my world was rocked. I have never been the same. From the time I walked into that civil affairs office and saw all of the beautiful, precious, children of God sitting there...alone. hungry. begging for love. my life was changed. never again was I going back to the sitting on the couch flipping the channel when the commercials we all know about came on. Those days were gone. God changed my heart.
He broke me into 10000 pieces for the Orphan. the Forgotten.
He called me. Of all of the other humans in this world the ruler of the Universe called me! He called US to help the Orphans in widows! Many of us sit back and enjoy our wonderful, happy, sugar-coated lives in America. That is not for me.
I love America, yes.
But I love Jesus so very much more.
Are you willing to leave your comfort zone for Him?
Please join me in refusing to forget the forgotten. One child at a time. One by One until they all find a home.

Monday, November 8, 2010

Little ones in China who are under 3 and waiting

All of the children today are under the age of 3 with managable SN's as long as the family educates themselves on the SN. Please remember that. I am cannot guarentee the avaiablity of any child because the shared list changes every few mintues and at any time these children can be locked or moved to an agency specific list. The majority of the little ones listed are boys with a few girls with more then one need. Please consider adding on of the 1500 hundred children on the shared list to your family. Children marked as new do require a Log In Date in order to view their file. I have decided to not post pictures of these little ones because I do not have a photo of all of them.

GENDER: M
SN: congenital absence of right arm
LID Required
DOB: October, 2009





Gender: Male
SN: post-operative cleft lip, cleft palate, developmental delay
LID Required
DOB:January, 2009






Gender: Male
Date of Birth: 8/2009
Special Needs: Limb Differences (assuming it deals with fingers or his arms he can walk) maybe a club foot I do not know for sure


Gender: Male
Date of Birth: 7/2009
Special Needs: Birthmarks/Nevus (small mole like spot on his face)



Gender: Male
Date of Birth: 6/2009
Special Needs: Blood Disorders, Cleft Lip/Cleft Palate (anemia)



Gender: Male
Date of Birth: 4/1/2009
Special Needs: Limb Differences, Blood Disorders (congenital absence of the right radial bone and deformities in his right upper limb)



Gender: Female
Date of Birth: 2/2009
Special Needs: Spina Bifida



Gender: Male
Date of Birth: 2/2009
Special Needs: Spina Bifida



Gender: Male
Date of Birth: 1/2009
Special Needs: Cleft Lip/Cleft Palate



Gender: Male
Date of Birth: 12/2008
Special Needs: Spina Bifida



Girl 2-12-09 Cleft Lip Palate Hehp B



Girl March 2009 right clubbed foot, arthrogyposis of arms

12-02-09 Pre op Spina Bifida (SB of thoracalimb) Was still on Shared list as of Oct. 25th 2010

Girl: 05-29-08 TOF un repaired, extra thumb

Girl June 09 development delay (could be with anything growth, motor, or physical)

Boy: 04-06-09 Albinism

Boy: albinism 5.3.2008

Boy: 03-28-08 albinism

Boy born 2/20/2008, albinism

Boy 12-09-08 Albinism

07-29-09 post op Imp. anus B

03-26-09 hydrocephalusabsence of septum

10-02-08 Post op def hands.feet

10-2-08 maldev right eye

01-2009 cleft hands and feet

01-2009 spina bifid, club foot

06-08 laryngeal web, developmental delay, kidney cyst

11-10-08, absence of right arm

3-12-07dev delay

11-7-08 cleft lip & Pal, mild Thalassemia

3-2-09 CP hernia

04-2009 club feet, hands

07-2009 pre-op Meningocele

Male
1/10/2009
1 cleft palate; 2 repaired cleft lip; 3 growth development delay



Female
6/29/2009
delay development



Male
3/29/2010
congenital cleft lip and palate Ⅱ°



Male
12/13/2009
congenital cleft lip and palate in right upper side, III degree, and congenital cleft palate in both sides, II degree in the left and III degree in right side



Female
1/2/2010
heterotropia; lower indexes, possible cerebral palsy



Male
1/4/2009
post-operative congenital cleft lip,cleft palate



Female
3/14/2010
congenital cleft microphthalmia, blue-sclera syndrome; HB



Female
10/29/2009
delay development of motion function



(most likely because she is intustiaized)



300
Female
1/23/2009
Spinal meningocele



357
Male
7/26/2009
post-operative congenital cleft lip,cleft palate; 1. low weight, weak, need nutrition improvement to change the condition; 2. delay mental development, increase training, test blood routine in regular time; 3. CHD, follow up.



360
Male
2/7/2009
cleft lip and palate Ⅲ°, hernia on right side



366
Male
1/25/2009
1. deformity of upper limbs 2. CHD



370
Female
6/12/2009
craniofacial dysostosis



373
Male
2/14/2009
post-operative CHD



379
Male
6/5/2009
androgyneity

'

Male
4/9/2009
CHD (post ligation of ductus arteriosus); hypospadia



Male
8/8/2009
cleft lip and palate, cross foot in both sides



Female
7/10/2009
androgyneity



Male
4/18/2009
Congenital Heart Dis



Male
8/15/2009
1, absence of right hand, deformity of short left hand; 2, redundant prepuce.



Female
12/23/2009
1. congenital cleft lip and palate; 2. congenital CHD, VSD, and acleistocardia



06-2008 Boy post op cl-cp

5-2009 Boy amb gen (male chrom)

03-2009 Boy limb diff (no fingers right hand, thumb & pinkie on left)

02-2009 Boy past femure fracture

10-2008 Boy light port wine (his name is Zhang Liming)

07-2009 Boy post op imp anus

Boy ambiguous genitalia 6.9.2008

Boy Cl-Cp Hep B 5-4-09

Boy 01-21-09 post op Sb, & dropsy-hydroceph

Boy 03-30-09 malformed hands-ft

Boy 05-20-09 muscular atrophy of left lower limb, hairy moles

Saturday, November 6, 2010

Shared List/Special Focus kids!

Today's Kids are from Korea and China I will label where the child is from. All of these first little ones were born in 2009 unless otherwise listed!

Gender: Female
Continent: Asia China
SN: Hearing impaired

Leah is a very pretty little girl. This young lady has good growth and development. Though she has severe hearing loss in both ears, she is obedient, sensible, helpful and curious and loves to explore new things. She is outgoing with a ready smile and is gregarious, getting along well with others. She is a good independent problem solver. I have watched this little girl sti on a list for way to long she is beautiful and just needs a mom and dad to make her smile!! Born in 1998

Gender: Female
Continent: Asia China
SN: Hearing Impaired
Marie is a cute young lady has big eyes and a round face. Though she is congenitally deaf, her general health is good. She is very shy and likes to be alone. Though she has some learning difficulties, she is very good at handcrafts. Born in 1997 ages out begining of the year

Gender: Male (Karl)
Continent: Asia China
Special Needs: Heart Defects, Cerebral Palsy

Gender: Male (Sam)
Continent: Asia China
Special Needs: Limb Differences

Gender: Male (Luke)
Continent: Asia China
Special Needs: Birthmarks/Nevus


Gender: Male (Max)
Continent: Asia China
Special Needs: Blood Disorders, Cleft Lip/Cleft Palate

Gender: Male (Eric)
Continent: Asia China
Special Needs: Limb Differences, Blood Disorders

Gender: Female (Sally)
Continent: Asia China
Special Needs: Micro/Macro cephaly

Gender: Male (Noah)
Continent: Asia Korea
Special Needs: Heart Defect an Cleft Palate

Gender: Male (Caleb)
Continent: Asia China
Special Needs: Sexual Development differences, Micro/Macro cephaly

Gender: Male (Logan)
Continent: Asia Korea Born 2010
Special Needs: Physical dev delays

Gender: Female (Alexia)
Continent: Asia China
Special Needs: Spina Bifida

Gender: Male (Mitchell)
Continent: Asia China
Special Needs: Spina Bifida

Gender: Male (Andrew)
Date of Birth: 1/2009
Continent: AsiaChina
Special Needs: Cleft Lip/Cleft Palate

Gender: Male (Cameron)
Date of Birth: 12/2008
Continent: Asia China
Special Needs: Spina Bifida

Gender: Female (Callie)
Date of Birth: 11/2008
Continent: Asia China
Special Needs: Deaf/hearing impaired

I will try to add more kids later but if you would like more info on any of these little ones please let me know. Email me at tsw1203@aol.com and be sure to include the name and SN of the little one you would like to know about and country if other then China.

Monday, November 1, 2010

Starfish Boy waiting

Many of you know that this summer I volunteered at Starfish foster home in Xi'an China. Well, one of the many children I worked with is currently waiting for a forever family. He is 2 and so sweet. Thomas was born with TOF one surgery is complete and he may need another one in the future he also has an exposed bladder which I do not know if it has been repaired or not since I have left. He is so sweet and really needs a mom and dad to love on him. He was one of the many children that I fell for!! Please email me if you want anymore info on him or where to find his file. tsw1203@aol.com. He is on the Shared list as of December 17, 2010