A Walk In My Not-So-New Shoes

Friday, September 03, 2010

GOD & DOG

This is such a sweet video ... absolutely love it! So very true!

Posted by Kelly's Venture at 6:14 p.m.

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About Me

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!

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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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Molly

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

Beatrice

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

WIllow

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

Sally LIttlefoot

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

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

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

Bertha

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

Sharlie

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

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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