A Walk In My Not-So-New Shoes

Saturday, June 05, 2010

I'D GIVE YOU ONE

I just love this video ...

Posted by Kelly's Venture at 11:27 a.m.
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About Me

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Kelly's Venture
My name is Kelly and I was diagnosed at the age of 3 with Cystic Fibrosis (CF). On February 22 2008, I was blessed with a new life. I received a double-lung transplant at Toronto General Hospital, Toronto, Ontario and have been living life to the fullest since then! This blog serves as a little snippet of my life, living with CF, and enjoying my new lungs! Hope you enjoy!
View my complete profile

CF & TX LINKS

  • Canadian Cystic Fibrosis Foundation
  • Canadian Transplant Assocation
  • CarePages - Patient Support Pages
  • CCFF: Resources for Individuals Seeking Lung Transplant
  • Eastern Newfoundland & Labrador CCFF Chapter
  • Toronto General Hospital Lung Transplant Program
  • Trillium Gift of Life Network

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      • BREATHING
      • I got the job ... PERMANENTLY!!
      • I'D GIVE YOU ONE
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Molly

Molly
Our silly ol' girl ... came to live with us on Oct. 14, 2006

Beatrice

Beatrice
Our newest pug ... came to live with us Mar. 23, 2009!

WIllow

WIllow
Adopted May 8, 2010 ... and not a pug!

Sally LIttlefoot

Sally LIttlefoot
Chaning it up a little ... adding a hedgehog to the mix ... Apr. 15, 2011

Rosie

Rosie
Newest addition, adopted July 29, 2011 ... 4 doggies and counting!

OUR PAST PUGGERS

I've always owned pugs ... well, pugs have OWNED me ;). These are our fur babies who have crossed over the Rainbow Bridge ...

They all hold a very special and permanent place in my heart ...

Neffie

Neffie
First rescue pug (RIP little girl: August 7 1998 - June 7 2010)

Bertha

Bertha
Our precious girl ... came to live with us on Oct. 14, 2006 (RIP Oct. 13, 2003 - Jan. 13, 2009)

Sharlie

Sharlie
1st and only black pug (RIP little lady: Oct. 16, 1993 - May 25, 2007)

Teddy

Teddy
1st pugger ... Mr. Teddy Bear (RIP little man: Mar. 30, 1992 - Oct. 4, 2006)

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WHAT IS CYSTIC FIBROSIS?

"Cystic fibrosis (CF) is the most common, fatal genetic disease affecting young Canadians. CF is a multi-organ disease affecting primarily the lungs and the digestive system. In the lungs, CF causes severe breathing problems. A build-up of thick mucus makes it difficult to clear bacteria and leads to cycles of infection and inflammation, which damage the delicate lung tissues. They must follow a demanding daily routine of physical therapy to keep the lungs free of congestion and infection.

In the digestive tract, CF makes it extremely difficult to digest and absorb adequate nutrients from food. Thick mucus blocks the ducts of the pancreas, preventing enzymes from reaching the intestines to digest food. Therefore, persons with CF must consume a large number of artificial enzymes (on average 20 pills a day) with every meal and snack, to help them absorb adequate nutrition from their food."

- Canadian Cystic Fibrosis Foundation (CCFF)
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