thejoysofhavingcf.blogspot.com

The Joys of having CF

The Joys of having CF. Saturday, July 25, 2015. The Hardest Post By Far Part 2. When I left off with my previous blog post Part 1. I was beginning to talk about the start of a lot of changes, so let's continue, and I do apologize if when I left off I had people worried. My right arm, the arm that they couldn't get an IV in, all those little holes are from numbing medicine. I believe we counted 11 needle marks in my right arm. So after 7 days in the hospital.my longest stay in a very long time, I went...

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The Joys of having CF | thejoysofhavingcf.blogspot.com Reviews

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The Joys of having CF. Saturday, July 25, 2015. The Hardest Post By Far Part 2. When I left off with my previous blog post Part 1. I was beginning to talk about the start of a lot of changes, so let's continue, and I do apologize if when I left off I had people worried. My right arm, the arm that they couldn't get an IV in, all those little holes are from numbing medicine. I believe we counted 11 needle marks in my right arm. So after 7 days in the hospital.my longest stay in a very long time, I went...

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The Joys of having CF | thejoysofhavingcf.blogspot.com Reviews

https://thejoysofhavingcf.blogspot.com

The Joys of having CF. Saturday, July 25, 2015. The Hardest Post By Far Part 2. When I left off with my previous blog post Part 1. I was beginning to talk about the start of a lot of changes, so let's continue, and I do apologize if when I left off I had people worried. My right arm, the arm that they couldn't get an IV in, all those little holes are from numbing medicine. I believe we counted 11 needle marks in my right arm. So after 7 days in the hospital.my longest stay in a very long time, I went...

INTERNAL PAGES

thejoysofhavingcf.blogspot.com

1

The Joys of having CF: Feb 9, 2015

http://thejoysofhavingcf.blogspot.com/2015_02_09_archive.html

The Joys of having CF. Monday, February 9, 2015. As I Sit Here. As I sit here tonight, in the light of the hotel room, watching Full House and drinking a coffee chiller, the night before my long doctor's appointment tomorrow, I'm reflecting on the last two months. Just two months ago I had thee worst PFT's of my life. Still considered good but not to MY standards. Tonight the thoughts in my mind keep replaying; have I done what I needed to improve them? Am I doing ALL that I know I am capable of?

2

The Joys of having CF: Reflection, Hope, & Celebration

http://thejoysofhavingcf.blogspot.com/2015/05/reflection-hope-celebration.html

The Joys of having CF. Friday, May 1, 2015. Reflection, Hope, and Celebration. Today is the start of Cystic Fibrosis Awarness. It is the month where Facebook turns "purple", but it's also a time where I reflect on my life, and where I am, and where my future is going. I reflect on my goals and dreams for the future. It reminds me to not take each day for granted and live it to the fullest. Also, it reminds me of those who have lost their battle with CF. Those who fought a tough fight. View my complete pr...

3

The Joys of having CF: Mar 6, 2015

http://thejoysofhavingcf.blogspot.com/2015_03_06_archive.html

The Joys of having CF. Friday, March 6, 2015. Today March 7, 2015 marks my 20 year anniversary of being diagnosed with CF. I was four months old, and when I was diagnosed the life expectancy was not very good. In fact my parents were told I may not live to graduate high school. But I've never really been one to worry to much about statistics. Now don't get me wrong there's been many tough times, but in the end, those times just make us stronger. I was also diagnosed on my uncles birthday; the same uncle ...

4

The Joys of having CF: Great Turnout

http://thejoysofhavingcf.blogspot.com/2015/05/great-turnout.html

The Joys of having CF. Saturday, May 2, 2015. Here is a picture of all the people who walked today and raised money for a cure. I hope everyone has a great weekend and if you haven't had your CF walk yet, I hope there's great turnout. Subscribe to: Post Comments (Atom). The Joys of having CF. View my complete profile. I was asked once, "If you could tell the world one thing about Cystic Fibrosis, what would it be? Interested in my book? Contact: paige cf 94@yahoo.com.

5

The Joys of having CF: The Hardest Post By Far Part 2

http://thejoysofhavingcf.blogspot.com/2015/07/the-hardest-post-by-far-part-2.html

The Joys of having CF. Saturday, July 25, 2015. The Hardest Post By Far Part 2. When I left off with my previous blog post Part 1. I was beginning to talk about the start of a lot of changes, so let's continue, and I do apologize if when I left off I had people worried. My right arm, the arm that they couldn't get an IV in, all those little holes are from numbing medicine. I believe we counted 11 needle marks in my right arm. So after 7 days in the hospital.my longest stay in a very long time, I went...

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thejoysofhavingcf.blogspot.com

The Joys of having CF

The Joys of having CF. Saturday, July 25, 2015. The Hardest Post By Far Part 2. When I left off with my previous blog post Part 1. I was beginning to talk about the start of a lot of changes, so let's continue, and I do apologize if when I left off I had people worried. My right arm, the arm that they couldn't get an IV in, all those little holes are from numbing medicine. I believe we counted 11 needle marks in my right arm. So after 7 days in the hospital.my longest stay in a very long time, I went...

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The Joys of Having Two Daughters. Like us on Facebook for post updates: https:/ www.facebook.com/pages/The-Joys-Of-Having-Two-Daughters/171121616308159. And I thought boys were bad. All the dirt of boys, plus the attitude. Monday, October 6, 2014. I have a teenage daughter. My name is Kristen and I have a teenage daughter. After spending way too much "at work" time googling the interwebs for answers, I have come up with one. But there will be mistakes and there is nothing I can do about it. We have this ...

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