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confessionsofacfpatient.blogspot.com

Confessions of a CF patient

Confessions of a CF patient. It's not the amount of breaths you take, but the moments that take your breath away'. Sunday, 19 February 2012. So it's been 6 months since my transplant on 20th February and I have been so busy! In November I was back in hospital for 2 weeks because my lung function wasn't increasing as much as they hoped so they gave me iv's (thank god I still have my port) and 3 days worth of Iv steroids. These left a horrid taste in my mouth and felt like I had been chewing and suckin...

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Confessions of a CF patient | confessionsofacfpatient.blogspot.com Reviews
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Confessions of a CF patient. It's not the amount of breaths you take, but the moments that take your breath away'. Sunday, 19 February 2012. So it's been 6 months since my transplant on 20th February and I have been so busy! In November I was back in hospital for 2 weeks because my lung function wasn't increasing as much as they hoped so they gave me iv's (thank god I still have my port) and 3 days worth of Iv steroids. These left a horrid taste in my mouth and felt like I had been chewing and suckin...
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1 the thoughts
2 the drugs
3 the girl
4 the signs
5 the year
6 since transplant
7 xmas was amazing
8 hahaha
9 posted by
10 sophie anne
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the thoughts,the drugs,the girl,the signs,the year,since transplant,xmas was amazing,hahaha,posted by,sophie anne,3 comments,xxxx,2 comments,no comments,arriving at harefield,the novalung,4 comments,1 comment,haha,older posts,justgiving.com/danny gannon
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Confessions of a CF patient | confessionsofacfpatient.blogspot.com Reviews

https://confessionsofacfpatient.blogspot.com

Confessions of a CF patient. It's not the amount of breaths you take, but the moments that take your breath away'. Sunday, 19 February 2012. So it's been 6 months since my transplant on 20th February and I have been so busy! In November I was back in hospital for 2 weeks because my lung function wasn't increasing as much as they hoped so they gave me iv's (thank god I still have my port) and 3 days worth of Iv steroids. These left a horrid taste in my mouth and felt like I had been chewing and suckin...

INTERNAL PAGES

confessionsofacfpatient.blogspot.com confessionsofacfpatient.blogspot.com
1

Confessions of a CF patient: The Year...

http://www.confessionsofacfpatient.blogspot.com/p/this-year-2010.html

Confessions of a CF patient. It's not the amount of breaths you take, but the moments that take your breath away'. This is a list of things I want to do or am looking forward to doing in 2010:. See the musical Avenue Q - January. See the musical Legally Blonde - February. See pitbull in concert - 9th May. Chelsea stadium tour - 16th June. Raise money for CF. Holiday to York - 30th October. Holiday to Spain - 25th June. Getting weight to 50kg. See JLS in concert - December. My 22nd birthday - 12th July.

2

Confessions of a CF patient: January 2012

http://www.confessionsofacfpatient.blogspot.com/2012_01_01_archive.html

Confessions of a CF patient. It's not the amount of breaths you take, but the moments that take your breath away'. Saturday, 14 January 2012. Learning to walk, talk and breathe again. My scar was tight and i couldnt straighten too well but the main struggles were with the drains and attempting to walk. Day by day things got easier and I was able to do more and get about my room on my own as I had things to hold on to. The last week was spent teaching me how to walk up and down stairs. It was sooo...Pleas...

3

Confessions of a CF patient: Learning to walk, talk and breathe again.

http://www.confessionsofacfpatient.blogspot.com/2012/01/learning-to-walk-talk-and-breathe-again.html

Confessions of a CF patient. It's not the amount of breaths you take, but the moments that take your breath away'. Saturday, 14 January 2012. Learning to walk, talk and breathe again. My scar was tight and i couldnt straighten too well but the main struggles were with the drains and attempting to walk. Day by day things got easier and I was able to do more and get about my room on my own as I had things to hold on to. The last week was spent teaching me how to walk up and down stairs. It was sooo...Wow J...

4

Confessions of a CF patient: May 2011

http://www.confessionsofacfpatient.blogspot.com/2011_05_01_archive.html

Confessions of a CF patient. It's not the amount of breaths you take, but the moments that take your breath away'. Thursday, 26 May 2011. Me and my Scottings have been together now for 5 years. We celebrated by going to Scotts favourite place (the cinema) and then my favourite place (a restaurant) haha! As of today, I am needle free! Thats good teamwork ;). Feels sooooo much better - have gone shorter and blonder. Thats such good progress already and i really hope she continues to do well. I was so e...

5

Confessions of a CF patient: Since transplant

http://www.confessionsofacfpatient.blogspot.com/2012/02/since-transplant.html

Confessions of a CF patient. It's not the amount of breaths you take, but the moments that take your breath away'. Sunday, 19 February 2012. So it's been 6 months since my transplant on 20th February and I have been so busy! In November I was back in hospital for 2 weeks because my lung function wasn't increasing as much as they hoped so they gave me iv's (thank god I still have my port) and 3 days worth of Iv steroids. These left a horrid taste in my mouth and felt like I had been chewing and suckin...

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Confessions of a CF patient

Confessions of a CF patient. It's not the amount of breaths you take, but the moments that take your breath away'. Sunday, 19 February 2012. So it's been 6 months since my transplant on 20th February and I have been so busy! In November I was back in hospital for 2 weeks because my lung function wasn't increasing as much as they hoped so they gave me iv's (thank god I still have my port) and 3 days worth of Iv steroids. These left a horrid taste in my mouth and felt like I had been chewing and suckin...

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Confessions of A Cf wife

Confessions of A Cf wife. Tuesday, December 20, 2011. Deep inside I have these horrible thoughts of "what if". I keep telling myself that if he is at least finished with this step then we are one step closer to the next. I keep thinking we are going to miss out on something and it is going to be too late. I wish that I had someone tell me that these jumbled most random thoughts were normal. Anyways.Better thoughts tomorrow as I must put on my "Positive Pants" Ha :). Tuesday, November 22, 2011. The other ...

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