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At War with Cystic Fibrosis

Thursday, 1 January 2015. Meeting One Direction, Christmas and the New Year. I'm so bad at keeping up with this blog; that's a New Years resolution for me - update my blog more frequently! I have lots to tell you :-)! Where shall I start? A month ago, we asked for a blood gas to be taken, as I hadn't had one done for 6 weeks and I had been having some terrible headaches. We found the CO2 levels to be high (9.2 kPa) which probably caused the headaches! I've been on and off a number of antibiotics as usual...

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At War with Cystic Fibrosis | harrietsheehan.com Reviews
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Thursday, 1 January 2015. Meeting One Direction, Christmas and the New Year. I'm so bad at keeping up with this blog; that's a New Years resolution for me - update my blog more frequently! I have lots to tell you :-)! Where shall I start? A month ago, we asked for a blood gas to be taken, as I hadn't had one done for 6 weeks and I had been having some terrible headaches. We found the CO2 levels to be high (9.2 kPa) which probably caused the headaches! I've been on and off a number of antibiotics as usual...
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1 photos and videos
2 facts about me
3 bucket list
4 hello everyone
5 happy new year
6 hmmm
7 haha
8 thank you
9 love
10 facebook
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photos and videos,facts about me,bucket list,hello everyone,happy new year,hmmm,haha,thank you,love,facebook,twitter,personal instagram,art instagram,1 comment,tweet,i'm getting stronger,hi everyone,i'm so excited,i can't wait,idkharriet,no definitely not
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At War with Cystic Fibrosis | harrietsheehan.com Reviews

https://harrietsheehan.com

Thursday, 1 January 2015. Meeting One Direction, Christmas and the New Year. I'm so bad at keeping up with this blog; that's a New Years resolution for me - update my blog more frequently! I have lots to tell you :-)! Where shall I start? A month ago, we asked for a blood gas to be taken, as I hadn't had one done for 6 weeks and I had been having some terrible headaches. We found the CO2 levels to be high (9.2 kPa) which probably caused the headaches! I've been on and off a number of antibiotics as usual...

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At War with Cystic Fibrosis: November 2014

http://www.harrietsheehan.com/2014_11_01_archive.html

Thursday, 6 November 2014. During the past couple of weeks or so I have been continuing to make some progress, although the past week has been difficult because I have been struggling because my nausea has got worse again. I have been continuing to work on building some strength and 10 days ago I walked for the first time in months (since before my last stay in intensive care)! It felt so amazing to walk after so long! And Dad helping me walk! Here’s how my weight gain has gone:-. Some of my blood results.

2

At War with Cystic Fibrosis: Back Home At Last

http://www.harrietsheehan.com/2014/02/back-home-at-last.html

Wednesday, 26 February 2014. Back Home At Last. So, it’s been three weeks, now! I was discharged from hospital, after 150 days, on January 31st. I also like being closer to friends, and hopefully I can visit some of my friends soon. It feels really strange being back at home after so long. Last Thursday, I was sick a lot, and this caused my NG tube to come up. I had another one put down, but before I did, I ate something (a choc-au-pain), and I noticed that I. Being on oxygen is a nuisance, and Mom and D...

3

At War with Cystic Fibrosis: Drawing Boards and Twitter...

http://www.harrietsheehan.com/2014/03/drawing-boards-and-twitter.html

Saturday, 1 March 2014. Drawing Boards and Twitter. Just a quick blog post to tell you what I've been up to for the last few days! For the last 3 days, my friend I met through Twitter, Chris, has been helping me get lots of celebrities to tweet me! Chris had a heart and lung transplant 6 years ago. I'm really grateful for all his hard work and time helping me! He's very brave and caring.an amazing person! Here are some of the tweets that I've recieved:. You can follow Chris here. Thank you for reading!

4

At War with Cystic Fibrosis: January 2015

http://www.harrietsheehan.com/2015_01_01_archive.html

Thursday, 1 January 2015. Meeting One Direction, Christmas and the New Year. I'm so bad at keeping up with this blog; that's a New Years resolution for me - update my blog more frequently! I have lots to tell you :-)! Where shall I start? A month ago, we asked for a blood gas to be taken, as I hadn't had one done for 6 weeks and I had been having some terrible headaches. We found the CO2 levels to be high (9.2 kPa) which probably caused the headaches! I've been on and off a number of antibiotics as usual...

5

At War with Cystic Fibrosis: Photos and videos

http://www.harrietsheehan.com/p/pictures.html

Me with my Mum, Dad and sister in New York, where my Dad ran the marathon for the Cystic Fibrosis Trust in 2008. Me and my Mum in France on holiday in 2012. Me and Gemma Collins from TOWIE at the Clothes Show Live in Birmingham in December 2012. My stamp to get in to the X Factor Live Finals in November 2012 - my dad and I had to queue for ages in the cold! Me, Dad and Dappy at his concert in Bristol in December 2012. It was an amazing night - I love Dappy! Me and my lovely (cheeky! Little sister, Imogen.

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Everything Happens For A Reason: Bucket List

http://misskmgammon.blogspot.com/p/my-bucket-list.html

My bucket list consists of things I've wanted to do or things I've done, now I've had my transplant i hope I can accomplish all of them! See one direction live - Seen them at Wembley 6/6/14 and Cardiff 6/6/15. Go to Disneyland/Disney World. See disney on ice. Watch a show in theatre- Jack And The Beanstalk 17/12/14. Have my nosed pierced - pierced on 18/09/14. See Mcbusted live - Saw them in Cardiff 06/06/15. Spa break with mum. Hot air balloon ride. Go to X Factor Final - Went in 2013. Get a small tattoo.

misskmgammon.blogspot.com misskmgammon.blogspot.com

Everything Happens For A Reason: Radiotherapy Appointment

http://misskmgammon.blogspot.com/2015/06/radiotherapy-appointment.html

Monday, 1 June 2015. But I am very excited to see One Direction and Mcbusted live on Saturday! This is the mask I will wear whilst i have radiotherapy. As always, thank you for reading. Royal Devon and Exeter Hospital. 1 June 2015 at 13:45. Ur so brave Katie. Sending hugs for your journey ahead xx. 1 June 2015 at 15:33. Best wishes Katie, hope all goes well. From here in Australia. 2 June 2015 at 16:42. Subscribe to: Post Comments (Atom). Live Life Give Life. Rest In Peace Katie-Marie Gammon. Hey Guys, I...

misskmgammon.blogspot.com misskmgammon.blogspot.com

Everything Happens For A Reason: Happy New Year :)

http://misskmgammon.blogspot.com/2015/01/happy-new-year_9.html

Happy New Year :). Friday, 9 January 2015. I hope you all had a great Christmas and New Year! In my last post I said was in hospital but they let me home for Christmas and Boxing Day! I am starting very strong methyl pred tomorrow to hopefully treat it and make me well enough to go to Disneyland on the 4th February! Thank you so much to everyone who has messaged me, I am very thankful to have great people in my life and always will be forever grateful to my donor xxx. As always, thank you for reading.

misskmgammon.blogspot.com misskmgammon.blogspot.com

Everything Happens For A Reason: Cystic Fibrosis Awareness Month

http://misskmgammon.blogspot.com/2015/05/cystic-fibrosis-awareness-month.html

Cystic Fibrosis Awareness Month. Tuesday, 5 May 2015. May is Cystic Fibrosis Awareness month… I did a post about it last year but i'm going to do a post about it every year! I really hope one day there will be, we need to make as much awareness as possible for this horrible illness! When I was born the doctors told my parents that the life expectancy was around 13 years old, in my case this was true because i needed a lung transplant when I was 13! As always, thank you for reading,. Live Life Give Life.

misskmgammon.blogspot.com misskmgammon.blogspot.com

Everything Happens For A Reason: May 2015

http://misskmgammon.blogspot.com/2015_05_01_archive.html

A Happier Post :). Wednesday, 27 May 2015. Hope you are all well? Yesterday Faith and Kerri came to visit because we haven't seen each other since October last year! We went to pizza hut of course had a massive catch up, it was lovely to see them, we are going to see them again in August because we're going to a friends wedding, which is exciting! Not sure how its going to be without Zayn in the band though but I will still love them! It is a must see! Me and Faith 3. As always, thank you for reading.

misskmgammon.blogspot.com misskmgammon.blogspot.com

Everything Happens For A Reason: April 2015

http://misskmgammon.blogspot.com/2015_04_01_archive.html

Friday, 24 April 2015. My last post ending in that I hoped my lung function wouldn't drop again, well it did and then GOSH wanted to see me, so we went up and we saw Paul this time and they didn't know what was wrong still. Please everyone sign up to be an Organ donor, it saves so many lives, click. *HERE*. If you want to sign up :). As always, thank you for reading. Labels: Great Ormand Street Hospital. Subscribe to: Posts (Atom). Live Life Give Life. 160; Im sorry I havent posted anything in a while!

misskmgammon.blogspot.com misskmgammon.blogspot.com

Everything Happens For A Reason: One Direction, McBusted & My Friend Emily xx

http://misskmgammon.blogspot.com/2015/06/one-direction-mcbusted-my-friend-emily.html

One Direction, McBusted and My Friend Emily xx. Monday, 8 June 2015. I hope you've all had a lovely weekend! On Saturday I went to Cardiff to see One Direction On The Road Again tour and McBusted were their open act whilst they were at Cardiff. Dad drove me and Olivia up there, we was worried as the day before there were 45 mile tailbacks but thankfully it wasn't too bad but the seeing 1D and Mcbusted live one word. BRILLIANT! It was so good! Please can you keep Emily and her family in your thoughts at t...

misskmgammon.blogspot.com misskmgammon.blogspot.com

Everything Happens For A Reason: A Happier Post :)

http://misskmgammon.blogspot.com/2015/05/a-happier-post.html

A Happier Post :). Wednesday, 27 May 2015. Hope you are all well? Yesterday Faith and Kerri came to visit because we haven't seen each other since October last year! We went to pizza hut of course had a massive catch up, it was lovely to see them, we are going to see them again in August because we're going to a friends wedding, which is exciting! Not sure how its going to be without Zayn in the band though but I will still love them! It is a must see! Me and Faith 3. As always, thank you for reading.

misskmgammon.blogspot.com misskmgammon.blogspot.com

Everything Happens For A Reason: February 2015

http://misskmgammon.blogspot.com/2015_02_01_archive.html

Goodbye Reflux, Hello Sloppy Food. Sunday, 22 February 2015. I hope you are all well! I'm going home tomorrow but decided not to go back to college until next week as i'm in quite a lot of pain where they did the keyholes to. A picture of what a Fundoplication is. I'm back up at GOSH again in about 2 weeks for another lot of Antibody-Mediated Treatment, I will have this every month for a few months to hopefully say goodbye to these Antibodies! As always, thank you for reading. Great Ormand Street Hospital.

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At War with Cystic Fibrosis

Thursday, 1 January 2015. Meeting One Direction, Christmas and the New Year. I'm so bad at keeping up with this blog; that's a New Years resolution for me - update my blog more frequently! I have lots to tell you :-)! Where shall I start? A month ago, we asked for a blood gas to be taken, as I hadn't had one done for 6 weeks and I had been having some terrible headaches. We found the CO2 levels to be high (9.2 kPa) which probably caused the headaches! I've been on and off a number of antibiotics as usual...

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