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Author Topic: Team Smile Train  (Read 3117 times)
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carien
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« on: December 05, 2010, 01:21:50 PM »

There are many teams  who have there  own topic. Team Smile train so-far didn't have one . David the founder (is that the correct word) of Team Smile Train can tell you much more about it then I can.

As a Dutch I never heard about Smile train this wonderful organisation who helps children with clefts. We try to raise awareness for this organisation. Some of the members wanted to start an own fundraiser.
So far we raised over 3000 dollar that means we helped 12 children who will have a change in life because I think those children have absolute no future without an operation.


If you want to know more about is you can find us here
http://www.kiva.org/team/smile_train

If you want to join us you are very welcome
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David2051
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« Reply To This #1 on: December 06, 2010, 07:50:18 PM »

Thanks for starting this thread, Carien!  I thought I would post a couple patient stories from Smile Train.  You are right, these kids wouldn't have any chance at a normal life without the work of Smile Train.  I think they have provided surgeries for about 600,000 kids.

Quote from: www.smiletrain.org
Angelica Joy, 2 years, Philippines
 
For Angelica Joy (AJ) Fabroa, getting the operation needed to fix her cleft lip was a challenge. The youngest of four children, AJ was born in the Philippines into a poor, hardworking and loving family.
After Angelica's Cleft Lip Surgery  When AJ was born, her father started crying at the sight of her cleft lip. He and his wife were devastated, but neither of them lost hope because they knew her cleft could be treated. Knowing that AJ would have trouble feeding, they placed her in the care of a local mission that treated children with clefts. However, because AJ had been underweight since birth and had a weak body, the local mission evaluated her and would not operate.
  When AJ and her parents returned a second time, again she could not pass the physical due to her low body weight and they were told to hospitalize her. AJ’s parents could never afford to pay for the cost of a hospital stay and so they began searching for another alternative.
  Soon after, a local council official visited their small community and told AJ’s parents about The Smile Train Cleft Care Program run in conjunction with the Philippine Band of Mercy. In a matter of weeks, AJ finally received the surgery to repair her deformity.
  Today, little AJ is a healthy and happy two-year-old, who can eat normally and is starting to talk. Because of the determination of her family and The Smile Train, the Fabroa family can all smile together!

Quote from: www.smiletrain.org
Bhavani, 6 months, India


Thirupathi Rao and his wife were a happily married couple. They settled in a small village in the Krishna district of Andhra Pradesh in India. They are agricultural laborers and whenever they manage to get work, they earn less than $2.00 per day.
  Their first child was a healthy boy. But when Mrs. Rao gave birth to her second child, the family was shocked to see that the baby girl had a disfiguring facial deformity. They thought it was a curse from the gods and they were so despondent about the whole issue they wanted to abandon the child.
  Luckily for the baby girl, her mother learned about The Smile Train cleft project through other members of her village who also had a child born with a cleft.
  The baby girl was brought to Vijetha Hospital at Vijayawada and was examined by the chief surgeon and the director of the project Dr. P.M.C. Naidu.
  After the surgery Bhavani’s family was thrilled to see her with a normal looking lip and their joy could not be translated into words. They no longer feel like they have been cursed, but rejoice when they see their beautiful baby girl smile!
« Last Edit: December 07, 2010, 01:40:06 PM by David2051 » Logged

Join Team Smile Train!  http://www.kiva.org/team/smile_train  :-)

“send a postcard and receive a postcard back from a random person somewhere in the world!” http://www.postcrossing.com/

Learn more about ovarian cancer. Educate for early detection.  http://ovariancancerin.org/

Be a bone marrow donor, save a life.  http://bit.ly/4Amit

Change a child's life, be a sponsor.  http://children.org/
David2051
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« Reply To This #2 on: December 09, 2010, 01:39:58 PM »

A message I posted to the team recently...  For me this image is the embodiment of Kiva, and I am grateful to all the people who make Kiva possible.  :-)

Quote
Several years ago I had a box of Christmas cards with this image on them.  It is, perhaps, rather unlikely for a Christmas card, but this Norman Rockwell image seems very significant to me.  I didn't have the sense to keep one of the cards, but the inscription inside said something to the effect that with all of our differences, we are all the same in wanting peace in the world.  This image to me seems to represent the very best spirit of Kiva.  I hope this holiday season will bring unity and peace.
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Join Team Smile Train!  http://www.kiva.org/team/smile_train  :-)

“send a postcard and receive a postcard back from a random person somewhere in the world!” http://www.postcrossing.com/

Learn more about ovarian cancer. Educate for early detection.  http://ovariancancerin.org/

Be a bone marrow donor, save a life.  http://bit.ly/4Amit

Change a child's life, be a sponsor.  http://children.org/
carien
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« Reply To This #3 on: December 10, 2010, 02:20:18 AM »

Here is a story of a young girl called Marceline



http://www.operationsmile.org/gift-catalog/video.html


It only takes less then a hour to give her back here live
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carien
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« Reply To This #4 on: January 30, 2011, 02:38:04 AM »

This week our team reached 3500 dollar that means with our team fundraiser we managed to help 14 children so far. 14 lives we changed
14 children who have a change in live now.


That's something to put a smile on your face today


 Smiley Smiley Smiley Smiley
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JohnAtKiva
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« Reply To This #5 on: January 30, 2011, 11:48:41 AM »

This week our team reached 3500 dollar that means with our team fundraiser we managed to help 14 children so far. 14 lives we changed
14 children who have a change in live now.  That's something to put a smile on your face today

Wow, that's amazing carien!!  Where did you do a fundraiser?  I'd love to contribute!

John
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carien
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« Reply To This #6 on: January 30, 2011, 12:59:36 PM »

Hi John it you can find it on our team page but here is the link


http://bit.ly/TeamSmileTrain2010


In Holland when the train is to late the have to give you some money back for half an hour 9 dollar en for one hour 18 dollars I was always to lazy to ask the money back but since I donate it to Smile Train I ask it back with a bog smile


 Smiley Smiley Smiley Smiley
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David2051
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« Reply To This #7 on: January 30, 2011, 01:51:50 PM »

Wow, that's amazing carien!!  Where did you do a fundraiser?  I'd love to contribute!

John



Hi John!  

The link to the fundraiser page is on our team page.  http://www.kiva.org/team/smile_train

The direct link is here.  http://bit.ly/TeamSmileTrain2010     Hmmm, I guess maybe I should make a new link, that seems a bit dated now, doesn't it?  lol

So far we have had 50 donations made through this page, which I think is great!   Thumbs Up

There is also a guest book on this page where people can leave encouraging messages.  Thanks for your interest in the mission of Smile Train!

 Thank You

(oops, I see Carien posted already...)  
« Last Edit: January 30, 2011, 01:55:30 PM by David2051 » Logged

Join Team Smile Train!  http://www.kiva.org/team/smile_train  :-)

“send a postcard and receive a postcard back from a random person somewhere in the world!” http://www.postcrossing.com/

Learn more about ovarian cancer. Educate for early detection.  http://ovariancancerin.org/

Be a bone marrow donor, save a life.  http://bit.ly/4Amit

Change a child's life, be a sponsor.  http://children.org/
David2051
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« Reply To This #8 on: January 30, 2011, 02:06:58 PM »

Here is an interesting article.  The contrast between treatment in the developed versus the developing world is stark. 

Cleft palate requires early intervention


Berks County, PA  -  Dear Dr. Reitz: I read an article in the Reading Eagle about a woman who donated money to a charity for children with cleft palate. How common is cleft palate and how is it treated? - Joan, Bernville

Dear Joan: Cleft palate is a genetic defect in the growth of the fetus that causes incomplete fusion of the roof of the mouth. Cleft lip (sometimes called hare lip because it looks like a rabbit's lip) is a similar birth defect causing incomplete fusion of the lip. Cleft palate and cleft lip can occur both simultaneously or independently.

Facial clefting occurs in one in 1,000 births and treatment requires a team of medical specialists including orthodontists, oral surgeons, plastic surgeons and speech therapists. The cause is most likely genetic, however it is believed alcohol consumption, smoking, or drug use by a mother during pregnancy can contribute to a child having clefting.

Cleft palate is first diagnosed on an ultrasound before birth. Babies born with a cleft palate have a difficult time feeding and usually require a special bottle or plastic oral appliance. Babies with just a cleft lip usually can be breast-fed. Treatment usually starts within the first few weeks after birth with orthodontics to narrow the gap. The timing of surgery is decided by the surgeon, however it is usually performed within the first 18 months. Cleft lip usually is surgically repaired within the first three months after birth.

By the numbers, you can see facial clefting is a very common birth defect. In fact there are quite a few famous people who are affected. Most people are aware that actor Stacy Keach has a cleft lip, however an Internet search revealed a long list of famous people that have cleft palate including comedian Cheech Marin of Cheech and Chong, newscaster Tom Brokaw, Indianapolis Colts quarterback Peyton Manning and possibly gunslinger Doc Holiday.

The Reading Eagle article mentioned the organization "Smile Train" that treats poor children with facial clefts in developing countries. Cleft lip and palate are a major problem in developing countries because many children do not receive treatment, and unrepaired clefts make it difficult to eat and speak. A donation of $250 is enough to help one child live a better life.

Fortunately, in the United States available medical care helps children born with facial clefts have a good prognosis, with 80 percent developing normal speech. Proper prenatal care is the best method of reducing the risk.
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Join Team Smile Train!  http://www.kiva.org/team/smile_train  :-)

“send a postcard and receive a postcard back from a random person somewhere in the world!” http://www.postcrossing.com/

Learn more about ovarian cancer. Educate for early detection.  http://ovariancancerin.org/

Be a bone marrow donor, save a life.  http://bit.ly/4Amit

Change a child's life, be a sponsor.  http://children.org/
JohnAtKiva
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« Reply To This #9 on: January 30, 2011, 03:21:12 PM »

Hi John it you can find it on our team page but here is the link
http://bit.ly/TeamSmileTrain2010

Hi John!  The link to the fundraiser page is on our team page.  http://www.kiva.org/team/smile_train

Thanks carien and David!  I made a contribution. :-)  What a wonderful cause...

John
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