cfprincess.blogspot.com

cfprincess

The journey of a young woman with a chronic disease, Cystic Fibrosis. Saturday, July 10, 2010. Everything you had in your world and it is all taken away from you. that hurts. Everything you ever cared for, and it dissapears, it hurts. Wednesday, July 7, 2010. It's hot and muggy. Sticky, and slow moving. It's not making for much of a good day as far as the CF pain crap goes. I need the wind, I think today is a good beach day. Theres a bit of stuff to update you on, but I'm to warm to write anymore. But my...

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cfprincess | cfprincess.blogspot.com Reviews

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The journey of a young woman with a chronic disease, Cystic Fibrosis. Saturday, July 10, 2010. Everything you had in your world and it is all taken away from you. that hurts. Everything you ever cared for, and it dissapears, it hurts. Wednesday, July 7, 2010. It's hot and muggy. Sticky, and slow moving. It's not making for much of a good day as far as the CF pain crap goes. I need the wind, I think today is a good beach day. Theres a bit of stuff to update you on, but I'm to warm to write anymore. But my...

<META> KEYWORDS

1 cfprincess

2 ridin' solo

3 posted by

4 cfprincess xxo

5 no comments

6 today

7 livelaugh love breathe

8 everything is just

9 so difficult

10 1 comment

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cfprincess,ridin' solo,posted by,cfprincess xxo,no comments,today,livelaugh love breathe,everything is just,so difficult,1 comment,labels cf clinic,pain,prom,prom planning,labels prom,then wednesday sucked,pfts,dale,two best friends,2 comments,kayla

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cfprincess | cfprincess.blogspot.com Reviews

https://cfprincess.blogspot.com

The journey of a young woman with a chronic disease, Cystic Fibrosis. Saturday, July 10, 2010. Everything you had in your world and it is all taken away from you. that hurts. Everything you ever cared for, and it dissapears, it hurts. Wednesday, July 7, 2010. It's hot and muggy. Sticky, and slow moving. It's not making for much of a good day as far as the CF pain crap goes. I need the wind, I think today is a good beach day. Theres a bit of stuff to update you on, but I'm to warm to write anymore. But my...

INTERNAL PAGES

cfprincess.blogspot.com

1

cfprincess: Prom Planning !

http://cfprincess.blogspot.com/2010/06/prom-planning.html

The journey of a young woman with a chronic disease, Cystic Fibrosis. Tuesday, June 22, 2010. Prom Prom Prom, everything is all about prom for the last week, and finally it's here in one more night! I can't wait. Even though I still feel like crap, it's one night that will make me forget about being sick. Well until I have to take pills or insulin. lol. Today at school is all of prom committee setting up and decorating, so thats where i'm headed! I'll be sure to write all about it.

2

cfprincess: Another week down, Another one on it's way

http://cfprincess.blogspot.com/2010/06/another-week-down-another-one-on-its.html

The journey of a young woman with a chronic disease, Cystic Fibrosis. Friday, June 11, 2010. Another week down, Another one on it's way. So CF clinic sucked. Now todays just.another day. That's all the last week has been. just a lot of sleep and catching up on lost sleeping time. Rest has been much needed, but I still feel completely drained, so it's time for more sleep. Subscribe to: Post Comments (Atom). View my complete profile. Another week down, Another one on its way.

3

cfprincess: June 2010

http://cfprincess.blogspot.com/2010_06_01_archive.html

The journey of a young woman with a chronic disease, Cystic Fibrosis. Sunday, June 27, 2010. I had SOOO much fun at prom with Dale. It was a day where we both got to be happy and get our pictures taken with a couple friends and dance together and just have a good time. After prom we went out for supper at jackastors with the same friends and just all around, it was SUCH a good time. So of course it had to end. But my pain is getting to be extremly unbearable, so I am out for the night! So CF clinic sucked.

4

cfprincess: April 2010

http://cfprincess.blogspot.com/2010_04_01_archive.html

The journey of a young woman with a chronic disease, Cystic Fibrosis. Friday, April 2, 2010. This is MY story. Thats a quick few things about me, and it would be great to hear from anyone if you are reading this. Subscribe to: Posts (Atom). I am 15 years old, I live in Canada and I have Cystic Fibrosis. I love to read, and I loovvee being in the sun. View my complete profile. This is MY story.

5

cfprincess: May 2010

http://cfprincess.blogspot.com/2010_05_01_archive.html

The journey of a young woman with a chronic disease, Cystic Fibrosis. Tuesday, May 25, 2010. My “alright that’s enough! I wrote this awhile back before I ever had a blog and though I would post it for you guys to see what you thought. tell me what you think! 8221; moment and realize what they have to do to stop these times. I have recently had my “alright that’s enough! My way of coming about it is a bit strange; I just told myself. 8216;alright Megan enough is enough why are you suffocating. This young ...

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The journey of a young woman with a chronic disease, Cystic Fibrosis. Saturday, July 10, 2010. Everything you had in your world and it is all taken away from you. that hurts. Everything you ever cared for, and it dissapears, it hurts. Wednesday, July 7, 2010. It's hot and muggy. Sticky, and slow moving. It's not making for much of a good day as far as the CF pain crap goes. I need the wind, I think today is a good beach day. Theres a bit of stuff to update you on, but I'm to warm to write anymore. But my...

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