The journey of two CFers

About Me

Hey everyone! Lauren and Alexandria are starting a CF blog about our lives with Cystic Fibrosis and how we became very close friends! :) We will be posting new posts every chance we get so keep checking in! Lauren writes in yellow and Alexandria writes in green/blue. Thank you! <3
Turn volume up at 0:38.

Thursday, October 15, 2009

Ever wondered?

So I'm pretty sure that everyone has at least thought about this once, well everyone with CF or any other type of illness.
Have you ever thought about what it would be like if we were born "normal?"
There's so many things that would be different in my life if I never had Cystic Fibrosis.
Here's some examples...
1.) I could be deathly afraid of needles.
2.) I would probably care more about myself than others.
3.) I would complain about having a cold.
4.) I wouldn't have to get up at 4:30 am on school days.
5.) I would think Pseudomonas, Xopenex, Pulmozyme(ect.) were all foreign words. :)
6.) I wouldn't make people wince daily when I cough.
7.) I wouldn't have to miss more than 60 days of school each year.

And the list could go on and on!!
If you really think about it, you could be thinking all day.
It's really amazing how different we are from people, but even if I am different, I would never give up the life I have.

That is unless a cure ever comes out.
Until then, I'm going to live my life the way I'm supposed to.
I'm going to live my life as a strong CFer!

Little facebook App.

People with blue eyes last the longest in relationships. They are kind, pretty or handsome, very good kissers and are really hot. They are very funny, outgoing and don't care what people think or say. They love to party.They are very satisfying and love to please. Are straight up WARRIORS((aka wolves)) when they need to be.They are bad to the bone. Peaceful with low phisical endurance. Spirtual intense computer lover.

I have blue eyes and that's what the app. said. It's actulley 100% true.
But one thing I love about it is the "straight up WARRIORS" part. It seems like everything I do relates back to CF. It doesn't matter what it is, but I always find myself thinking about it.

So that's all I have to say for now :)
Just thought I'd share.