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It's summer and many people are celebrating the fact that we are experiencing an unusually warm period of weather. The heatwave might be...
Children in Need night, for everyone, is emotional. For myself, it's always a little bit extra hard as 'ME anniversaries' do sti...
Unrest - My thoughts 'Unrest' is a documentary on ME. A very brave woman, Jennifer Brae, documents her journey through the ...
ME Awareness Day has come around again and it feels a bit strange this time. I'm used to doing something 'big' to try raise awar...
Adventure Time I've managed to put a little bit of energy aside to type up my absolutely incredible time I had last week at the Calver...
Well, it's been awhile since I've been blogging. But, I'll get back into the swing of it once I have a bit of extra time (an...
Today, I feel rough. Why's that? I only went to go see Beyonce last night! It's not often I get to go out never mind do anything big...
#MillionsMissing is a global protest held today, dedicated to the millions of Myalgic Encephalomyelitis (ME) and Chronic Fatigue Syndrome (...
'So you're ill...every day?!' she says with a confused look across her face. 'Yes, every day' I reply. I don't kn...
December Volunteering I had to take quite a step back on my voluntary work lately because of my health, but I've had a great team o...
Linking into the last post, I have some rather exciting news about a little project I've been working on. I've been working wit...
Today is a little blog post inspired by the little things in life which are getting me through at the moment. I've had a bit of a ...
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