For all my wanging on about this being a real time blog about having a brain tumour and what it's like to undergo treatment, I've left it way too late to write this post, but then when I decided on a real time blog I a) didn't realise how little would actually happen during treatment;... Continue Reading →
Waiting for the shoe to drop
Although I knew full well that it takes around two weeks for any radiotherapy side effects to show themselves, it's hard not to interpret each and every twinge during the first half of my six weeks of daily radiotherapy as A Sign. Is this tired feeling a symptom of the treatment, a side effect of... Continue Reading →
The Mould Room
And speed up everything did. The day after meeting Paula, the mask fitting, an MRI and CT scan were arranged for the following two days. None of us could work out why it would take two days to make the mask. E suggested it's made on the first day and I get to go back... Continue Reading →
It’s not a given
The thing about brain tumours is that there are over 120 types. Granted, adult primary brain tumours tend to be one of a handful of types, but multiply that by all the different places in your brain they could occur, and times that by the age and underlying health of the person who owns that... Continue Reading →
Maggie Macmillan
I'm writing this while a third of the way in to 30 sessions of radiotherapy, and the side effects of getting a high strength blast of x-rays to the brain every day are starting to kick in. Please bear with me if it's a bit rambling and it takes a while to get new posts... Continue Reading →
Results day
As the biopsy results appointment drew near, things did not get any easier. I know several people with brain tumours. From close friends to friends of friends I've never actually met, each have different tumours and outcomes. Some good and some very bad. Because of our similar deficit, the one who played most on my... Continue Reading →