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Since transplant by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis Well I need to get back to the land of blogging....I haven't blogged in ages about what I have been doing and I promised myself that I would carry on doing this blog after ... Read on »
Learning to walk, talk and breathe again. by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis On E ward, i didnt sleep well for the first week. Its hard to sleep in hosp anyway but i was on lots of medications that affected me and plus it was the first time i had be ... Read on »
Recovering from a transplant - Intensive Care by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis I went to sleep at 2pm on Saturday 20th August 2011 holding onto my mummy and Scott. I had spoken to my dad and my little brother. Scott went home straight away as he said ... Read on »
Im back.....and breathing!!!! by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis Wow!!! Its been just over 3 months since I last blogged, and im sorry, but I have a very good reason...I had my double lung transplant!!!! It WAS NOT an easy ride as I will ... Read on »
What a washout....literally by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis Ive been pretty busy actaully since Harefield so this post may be a longish one!! The day finally came that i had been looking forward to since xmas. I had brought my ... Read on »
Harefield 2 day assesment by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis My appointment for my 2 day assesment for going on the transplant list was for Monday morning so we went up on the sunday night again and stayed in the onsite housing. As s ... Read on »
24 hour oxygen and acting posh by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis So I have been doing lots of little odd jobs...putting stuff up on ebay, going bank, seeing friends for lunch, posting off the stuff i sold blah blah blah. Got stuck in man ... Read on »
5 years together by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis 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!! We d ... Read on »
Chelsea charity match by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis I will start with the health side of things. Im feeling alright at the moment. Im still on iv's as i agreed to have a 3rd week just to get my chest as clear as possible. My ... Read on »
Documentary on BBC3 by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis I havent done much at all since starting these ivs which is a good and bad thing really. Good because i should be resting and taking it easy so my body can recover and not ... Read on »
Oxygen - check! by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis Bugger it...my chest had a big old flip out and im now on iv's, possible daytime feeds and oxygen. It got worse and worse over the long bank holiday weekend so i warned Lan ... Read on »
Shopping, Sun and Easter by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis No matter how ill I feel or how bad life seems, it always seems that little bit more bareable when the sun is out. Not that im feeling overly ill, its just a fact! Ive ... Read on »
My little bro is fundraising by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis My little bro Danny has managed to get a place on the Cystic Fibrosis football team for a charity match at Chelsea FC stadium: Stamford Bridge!! They will be playing agains ... Read on »
Relief??? by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis Ok...i dont know if thats the right word. I seem to be saying that phrase alot lately and its only because im feeling so many different emotions so i dont really know how t ... Read on »
I cant see by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis Im writing this with blurry vision and seeing black splodges on the page so if spelling is not great or i make no sense at all, then that is why!! Dont worry im not g ... Read on »
Harefield - the 1st meeting by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis I havent hardly been home or sat down for too long in one place since my last blog on monday and im knackered so this weekend, i have done very little other than watching t ... Read on »
Everyone is snotty!!! by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis Im surronded by coughing people and im attempting to avoid them as much as possible but when one is your best friend, one is your mummy and the other is your boyfriend, it ... Read on »
Transplant talks by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis Yes the time has come where transplant has been mentioned and appointment came through the post on friday for me to go to Harefield hospital for a day appointment to talk t ... Read on »
Only 4 weeks by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis Arghhhhh!!! Only 4 weeks roughly since leaving hospital and im starting iv's again on friday. Big fat bumholes!! I believe that its still the same infection i had in hospit ... Read on »
Owner of an iphone by Sophie-Anne Posted in: Blog Posts in Cystic Fibrosis Yay!! I finally managed, after walking to a million different phone shops with Scott, to get an iphone and sort out my shitty blackberry contract. It took me days to figure ... Read on »