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FightforRoses | Living life with Cystic Fibrosis

Living life with Cystic Fibrosis

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FightforRoses | Living life with Cystic Fibrosis | flyingpenguin20.wordpress.com Reviews

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Living life with Cystic Fibrosis

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1

Let me explain… | FightforRoses

https://flyingpenguin20.wordpress.com/2014/02/07/let-me-explain

Living life with Cystic Fibrosis. Gotta love the morning routine. →. Let me explain…. If you were to meet me face to face, you would simply see a 32 year old female. I am a mother, a wife, and also a fighter.not the average 32 year old. I suffer or live (however you want to put it) with Cystic Fibrosis, I did not have. Trouble when I was younger, now is a different story,more and more I start to feel it. Dragging me down, almost like I’m drowning in it. Thanks for reading.every little bit helps. Gotta lo...

2

BEST BEFORE… | FightforRoses

https://flyingpenguin20.wordpress.com/2014/02/19/best-before

Living life with Cystic Fibrosis. HELLO IS ANYBODY OUT THERE…. A HEDLEY KIND OF THERAPY →. Living with a unexpected expected expiry…. My parents were told when I was diagnosed at 16months, I wouldn’t live past 5, that I would not walk for a long time because I was just to underdeveloped. While within a month of the right treatments I was running and playing and ahead of my expected motor skills… Then my parents were told I would not make it past 18…. One thought on “ BEST BEFORE…. Enter your comment here.

3

I got the antibiotic blues…da da….. da dum…………….. | FightforRoses

https://flyingpenguin20.wordpress.com/2014/02/09/i-got-the-antibiotic-blues-da-da-da-dum

Living life with Cystic Fibrosis. Gotta love the morning routine. QUICK HIDE……. →. I got the antibiotic blues…da da…. da dum……………. So I am on yet another course of antibiotics, aside from daily inhaled one…. I go through stages before I succumb to the antibiotics…. Waiting and being stubborn has gotten me in big trouble with my lungs (A story for another day), and still I worry and hesitate…. I am hoping I feel more energized tomorrow, cause I always know that tomorrow is a brand new chapter. You are com...

4

The good, the bad, the greatful | FightforRoses

https://flyingpenguin20.wordpress.com/2015/03/11/the-good-the-bad-the-greatful

Living life with Cystic Fibrosis. PUT EM UP……. The good, the bad, the greatful. Ok, it has been way to long since I have last wrote on here. Life has been crazy for this cfer. My health has been doing pretty great considering. I got really sick in September of last year; I lost 10 pounds in two weeks. I got a lot of comments like Wow I wish I could do that… Yeah well I wish I couldn’t do that…. I guess it is because your body blocks out the pain. The only thing I am sure of is that I will work my but...

5

Gotta love the morning routine.. | FightforRoses

https://flyingpenguin20.wordpress.com/2014/02/08/gotta-love-the-morning-routine

Living life with Cystic Fibrosis. Let me explain…. I got the antibiotic blues…da da…. da dum……………. →. Gotta love the morning routine. Everyone says it is great to have a morning routine…Yeah well once I would like not to have one, but I can’t. 4 thoughts on “ Gotta love the morning routine. February 9, 2014 at 4:22 pm. Oh man, I hear you! My “morning routine” frustrates me to no end too. Juggling motherhood and CF is definitely no picnic. It’s a great list of lots of different CF blogs and a fun wa...

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cfblogroll.blogspot.com cfblogroll.blogspot.com

Cystic Fibrosis Blogroll: Featured Blogger: Kristy Of "Life in a Bubble of Fun"

http://cfblogroll.blogspot.com/2013/07/featured-blogger-kristy-of-life-in.html

Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll! How To Get Your Blog Listed. Tuesday, July 30, 2013. Featured Blogger: Kristy Of. Life in a Bubble of Fun". Today's Featured Blogger is Kristy from Life in a Bubble of Fun. First, tell me a little bit about yourself and your child with CF! My name is Kristy, I am a stay-at-home-Mum married with three children aged 6, 5 and 2. How old was your child when they were diagnosed with CF? The specialists at the Chi...

cfblogroll.blogspot.com cfblogroll.blogspot.com

Cystic Fibrosis Blogroll: Anything Is Possible: A CF Patient Interviews Her Parents About Life, Family, and Raising A Child With CF

http://cfblogroll.blogspot.com/2014/11/anything-is-possible-cf-patient.html

Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll! How To Get Your Blog Listed. Thursday, November 6, 2014. Anything Is Possible: A CF Patient Interviews Her Parents About Life, Family, and Raising A Child With CF. I was recently contacted by Erin Evans, a 31-year-old CF patient who works for the Cystic Fibrosis Lifestyle Foundation. Erin sent me a blog post that she'd written for the CFLF blog. See full interview here. Posted by cindy baldwin. One Breath at...

cfblogroll.blogspot.com cfblogroll.blogspot.com

Cystic Fibrosis Blogroll: Organizing the CF Blogroll

http://cfblogroll.blogspot.com/2013/10/organizing-cf-blogroll.html

Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll! How To Get Your Blog Listed. Monday, October 28, 2013. Organizing the CF Blogroll. I never could have imagined when I began this blogroll just how much it would take off! We now have about a hundred bloggers who have been added to the CF Blogroll, with more requesting to join on a regular basis. I don't know about you, but I love the opportunity to have so many CF blogs in one place! Life With Cystic Fibrosis.

cfblogroll.blogspot.com cfblogroll.blogspot.com

Cystic Fibrosis Blogroll: We're still here!

http://cfblogroll.blogspot.com/2014/10/were-still-here.html

Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll! How To Get Your Blog Listed. Tuesday, March 1, 2016. Friends of the CF blogroll,. I've had a few people ask me if I'm still adding blogs to the blogroll, and the answer is YES! I'm also always happy to feature any blogger from the blogroll who is interested. Send me an email or leave a comment here and I'll forward a copy of the interview questions! Hope to see YOUR blog here soon! Posted by cindy baldwin.

cfblogroll.blogspot.com cfblogroll.blogspot.com

Cystic Fibrosis Blogroll: Featured Blogger: Kayla of "One Breath at a Time"

http://cfblogroll.blogspot.com/2013/02/featured-blogger-kayla-of-one-breath-at.html

Do you have cystic fibrosis (or a child or spouse with CF) and a blog? Add it to the CF Blogroll! How To Get Your Blog Listed. Tuesday, February 5, 2013. Kayla of "One Breath at a Time". If you'd like to be a Featured Blogger, leave a comment or e-mail beingcindybaldwin AT gmail DOT com, and we'd love to feature you! Today's Featured Blogger is Kayla of " One Breath At A Time. I "met" Kayla through the CF Blogroll and am excited to be able to feature her today! First, tell me a little bit about yourself!

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FightforRoses | Living life with Cystic Fibrosis

Living life with Cystic Fibrosis. The good, the bad, the greatful. Ok, it has been way to long since I have last wrote on here. Life has been crazy for this cfer. My health has been doing pretty great considering. I got really sick in September of last year; I lost 10 pounds in two weeks. I got a lot of comments like Wow I wish I could do that… Yeah well I wish I couldn’t do that…. I guess it is because your body blocks out the pain. The only thing I am sure of is that I will work my butt off and nev...

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