Questions & Answers – Part 2

April 22, 2009

Finally! Back in business. It feels really good to be writing again and this post I am going to answer some of the other questions that were asked when I put out the call for any Questions people might have about living with Chronic Illness, this website or myself. Hopefully the Part 1 answers satisfied, I […]

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Questions and Answers

March 13, 2009

I put the call out on Monday for any questions that you guys might have about living with Chronic Illness or anything else you wanted to know about me. I had a few through email and one through the comments. I am will try to answer all questions as best as possible but will split them up […]

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OK, breathe, Lily, breathe….

March 9, 2009

So I was meant to be going home today but it did not happen. I seemed to have picked up a lurgy somewhere around here (hospital hazard) so I am going to be campaigning to go home Wednesday now instead. Not being able to go home brings up all that stuff that I have written […]

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Hospital and Isolation

March 6, 2009

Living with Chronic Illness, especially Cystic Fibrosis, means that hospital admissions are a fact of life. I don’t like it but it is something that I have to do for me to have something of a normal life outside of here. I need to spend time here to recharge and renew my batteries. I need […]

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Growing up in Hospitals….

March 4, 2009

During this hospital admission I am lucky to have an old friend in at the same time. He also has CF and we have known each other since I was 11 years old! Almost 16 years! Goodness! I am grateful to be able to catch up with him as I have lost many of the friends […]

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