I’ve never built a New Year Resolution list before, likewise I’ve never truly celebrated the New Year before either (and to be honest we’re not planning on doing anything tonight, even though I’d love to go down to the pub for a drink).
So this is why I’m here; to compile a list of things that I’m hoping to achieve in the coming year.
Continue reading ‘The start of my New Year Resolution List!’
Edit 6/1/10: Updated to reorder some of the paragraphs and generally make the post a little bit more ‘readable’.
I’ve been pondering about posting this for several days now. I feel it’s important to portray what my illness is, and how it effects me, but it’s just super depressing, and I don’t want to bring down the tempo of my blog. But I’ve decided to go ahead and write this up, and hope it helps at least one person understand how debilitating it can be for us.
I suffer from an illness called Myalgic Encephalopathy (M.E). It’s also known as Chronic Fatigue Syndrome (C.F.S), or Post-Viral Fatigue Syndrome (P.V.F.S). I simply refer to my illness as M.E as it’s so much simpler.
Continue reading ‘M.E and my life’
