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Living with Cystic Fibrosis - Landing

Living with Cystic Fibrosis depicts my story, offers advice and provides an insight into the every day life of a CF patient.

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Living with Cystic Fibrosis - Landing | livingwithcf.com Reviews
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Living with Cystic Fibrosis depicts my story, offers advice and provides an insight into the every day life of a CF patient.
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2 living with cystic fibrosis
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Living with Cystic Fibrosis - Landing | livingwithcf.com Reviews

https://livingwithcf.com

Living with Cystic Fibrosis depicts my story, offers advice and provides an insight into the every day life of a CF patient.

INTERNAL PAGES

livingwithcf.com livingwithcf.com
1

Stay Informed - Living with Cystic Fibrosis

http://www.livingwithcf.com/stay-informed.html

Living with Cystic Fibrosis. One of the most popular features of Living with Cystic Fibrosis is my frequently updated blog in which I detail up to the minute information with regards to my Cystic Fibrosis journey. By publishing a blog I can continue to document my thoughts and feelings whilst providing a personal insight into the day to day responsibilities of a CF patient. Join the dozens of people already subscribed to the Living with CF blog. ENTER YOUR EMAIL ADDRESS. 2012 Living with Cystic Fibrosis.

2

Medication - Living with Cystic Fibrosis

http://www.livingwithcf.com/medication.html

Living with Cystic Fibrosis. Medication, physiotherapy, inhalers and nebulisers. Coping with the relentelss demands that CF forces upon you is daunting. It relies heavily upon self discipline and time management. For anyone dealing with CF, striking the correct balance regarding your day to day routine is crucial. Creon 25,000 · 30-45 Daily (Average). Azithromycin · One tablet Daily. Vitamin A D · Two tablets Daily. Tocopherol · One tablet Daily. Otherwise known as Vitamin E, this tablet helps to fight.

3

Treatment - Living with Cystic Fibrosis

http://www.livingwithcf.com/treatment.html

Living with Cystic Fibrosis. Like all CF patients, I undergo a daily treatment routine to help prevent Cystic Fibrosis from causing prolonged problems and below you will learn of the current treatment and medial devices that I use to maintain my health. What exactly is a Portacath? What is it made from? How long does it last? The device is made up of three main parts. The outer shell is made from stainless steel or titanium, to ensure it is strong and secure. Within the shell there is a silicon b...An Ac...

4

Story - Living with Cystic Fibrosis

http://www.livingwithcf.com/story.html

Living with Cystic Fibrosis. Throughout my life I have had to cope with Cystic Fibrosis, there have been many difficult times and I have had to make tough decisions. There are many others in the same situation as me. Being a teenager with CF is hard, you have to cope with taking time off school, considering the impact your illness has on your family, and your social life with your friends. Education has proven to be somewhat of a turbulent time in my life as I have not always been able to manage the pres...

5

Living with Cystic Fibrosis - Blog

http://www.livingwithcf.com/blog.html

Living with Cystic Fibrosis. An impromtu hospital admission and life as a University student. With Christmas just around the corner, I thought I’d look back on a year of transition. A lot has happened in twelve months, and the blog post. I wrote back in December of last year indicates what a busy year it has been for me. It's a long day when your a patient! Whilst I can’t claim to have enjoyed my time on the ward (nobody likes hospitals! Having returned home from University one evening feeling as if my b...

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After a fantastic three years of documenting my life with Cystic Fibrosis I feel this. Website has, for now at least, served it's purpose. Having received thousands of. Visitors and hundreds of messages of support, www.livingwithcf.com. Is no longer being maintained. A huge thank you to everyone who has supported me through my illness. And followed my progress. During the time I have been documenting my life with CF,. University and am now finally pursuing my passion. Here's to finding a cure.

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Living with Cystic Fibrosis | Hmong, Torah, Cystic Fibrosis

Living with Cystic Fibrosis. Hmong, Torah, Cystic Fibrosis. My Passage to Yexus (Yeshua)…. January 31, 2010. Here we are again…. Well, I’m starting to get tired so I’ll go and see if I can get some sleep…. Posted in Cystic Fibrosis. January 17, 2010. Shortness of breath…. Posted in Cystic Fibrosis. December 30, 2009. How I’ve been feeling…. Got the tune up I’ve been dreading for in the back burner for a while and I’m ready to take on the cold weather of MN winter. Or so I thought. November 30, 2009.

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