Wow, it's 2011. This year is going to be the best year by far. More memories are going to made this year than any other year. 2011 is going to be a year to remember! In probably 2-2 1/2 months we will be going to Bora Bora, Tahiti(still waiting to hear exact dates, just know sometime in March). This year I have made some resolutions for myself. I always say I'm going to do something and it never fails, I never follow through with them. BUT this year I WILL follow through with my resolution.
This year my resolutions are:
1) No more "food" from McDonalds, Hardees, or Burger King!!!!
2) No Hospital! Stay healthy(i am currently the healthiest i've been in my Whole. Entire. Life. I want to keep it that way. My lung function is currently 97% which is awesome, but when I go to the doctor Wednesday the 6th, my goal is to have my lung function at 98 or 100%)
3)Become Fit(now i'm not over weight by any means, I love my appearance and everything, I just want to take better fit of myself, do more excercising, and start back up with my 1/2 mile run everyday-starting in Spring).
So I just wanted to welcome everyone to 2011, and do a little update :) I will post more after my dr. appt on Wednesday :)
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Contact: paige_cf_94@yahoo.com
The Joys of having CF
About Me
- Paige
- My name is Paige. I have Cystic Fibrosis. I am a fun loving, small town girl with big dreams...trying to live my life to the fullest. I am a Christian. My family is my priority. I love to travel. I want to see the world. I enjoy spending time with my family & friends. In March 2011 I went on my Make~A~Wish trip to the most beautiful island in the world, Bora Bora. I have written a book called, Growing up with Cystic Fibrosis the first 13 years. It's about living with Cystic Fibrosis (an incurable illness). I wrote the book to help people. I have recently started to get involved with public speaking. I believe that my purpose in life is to help people, and to make a difference. I believe that God put me on this earth for a reason, and i'm not going to let him down.
A Powerful Statement
"I was asked once, "If you could tell the world one thing about Cystic Fibrosis, what would it be?" And it is this. That CF hurts. It hurts physically when it feels like sandpaper is scraping your lungs with every breath. It hurts mentally to plan for and get excited about a life you may never lead. It hurts to fall in love because ...CF can be an extraordinary burden on anyone who is not meant to deal with it, most times resulting in rejection and loneliness. It hurts to watch dozens of friends lose this fight that they never deserved or asked for. But most of all, it would hurt to not have been blessed with the chance to experience life through a CFer's eyes: No love is half-given, no day is not lived to its fullest and NOTHING is taken for granted." ~posted by a fellow CFer
Interested in my book?
Contact: paige_cf_94@yahoo.com
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