The World is a Blur

Just after Christmas, I was moved back out of my single room. Pete and Courtney were visiting at the time. Unable to move my head, and with eyes that would not focus, I was still very unaware of my surroundings. Although I had now been in ICU for several weeks, I was completely unaware of…

Nits!!!

The only thing worse than an itch, is an itch you can’t scratch! On the 29th December 2011, Ali arrived with an unusual smirk on her face – a combination of pity and mild (maybe moderate) amusement. She walked over, looked at me, and told me she had some bad news. My kids, and the…

And So It Continues ……

 Over the first few days, word of my condition spread far and wide. A special friend, Jen, set up a support page on Facebook in my honour. It not only served as a place for people to leave me well-wishes and words of support, but also a place where friends could find information on my…

Letting Go Of Dreams

One of the hardest things about a new disability is letting go of dreams. I know we all give up dreams as our lives take different paths to those we had planned. And I know that I just need to create new dreams that are achievable for the ‘new us’. I grew up in a…

Groundhog Day

I have been procrastinating over posting this. This post has no clear theme or structure. It is just bits and pieces that went on day to day and feels a little messy. I guess it reflects my reality in those early days. On my 5th day in ICU, Steve brought the kids up to see…