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Lung transplant gives teen hope.



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Old Apr 27, 2008, 11:41 AM
oramar's Avatar
Granny Gidget
Join Date: Nov 1998
Lung transplant gives teen hope.

Double lung transplant gives teen hope after a lifetime of struggle

On Good Friday Samantha Moschetta received a double lung transplant.

And days later, for the first time in years, she was able to walk far enough from Children's Hospital in Pittsburgh to buy Italian ice and chai tea.

The 17-year-old Penn Hills girl returned home on a recent Friday as an example of transplant success.

But that success tops off a lifelong struggle with cystic fibrosis that required daily determination to survive the potentially deadly disease. She had to undergo daily life-sustaining treatments from her parents, David and Betsy Moschetta, and significant expenditures of time and energy just to live a burdensome life.

Samantha's future remains uncertain due to the difficulties inherent with lung transplants, coupled with continuing problems that cystic fibrosis imposes on digestion.
But hers is a story of how persistence and determination -- and her absolute refusal to give up -- paid off.

Today Samantha literally breathes more freely than she has for most of her 17 years. It provides her incentive to resume a relatively normal teenage life, including possibly returning to high school and getting a driver's license.

Full Story:
http://www.post-gazette.com/pg/08118/876605-114.stm


Last edited by brian : Apr 27, 2008 at 11:51 PM. Reason: added breif article bit
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Old Apr 27, 2008, 02:29 PM
StudentNurseBean (Female)
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Join Date: Apr 2006
Re: Lung transplant gives teen hope.

wow, great

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  #3  
Old Apr 30, 2008, 11:25 AM
Registered User
Join Date: Apr 2005
Re: Lung transplant gives teen hope.

Wow, super news!! My 25 yo son in law died in Jan after fighting CF and it's ravages, ironically, he was to be actively listed on the transplant list that week.
It will never be an easy life, even with the transplant but the CF community has a saying.. "Breathe Easy," and the people with transplants say that the first unassisted breath after the transplant is awesome!
May is National Cystic Fibrosis Awareness Month and Great Strides Walks will happen throughout the month to raise funding for research. The CF foundation receives no gov't funding since it's considered an "orphan" disease, 97 cents of every dollar raised goes directly for research. Please, please go to CFF.org to see /learn more about this horrific genetic disease and keep my daughter in your prayers! Thank you.

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Lung transplant gives teen hope.

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