A very brief overview of Chronic Fatigue Syndrome
Quiet
I've been quiet for a while now, I've just not had the energy to write, let alone think of something to write about. I try to be helpful with the things I write, either with the ways I'm managing things or just sharing my experiences, lately, I've been struggling with both.
My GP’s Prescribed Levothyroxine
The last 3 weeks have been interesting. After 8 years I'm finally getting some treatment that may or may not help me.
I went back to the GP, again
It seems every year or two I decide I've had enough with being ill and force myself to go back to the doctors. It's never led anywhere. They run the same few blood tests which all come back normal so they tell me to just look after myself. Well, this year, I had enough.
2020
It's been one hell of a year, but we've made it.
Merry Christmas
Merry (belated) Christmas
Why I Play Football Even Though I’m Ill
It might sound odd hearing about someone with Chronic Fatigue Syndrome, or any chronic illness/disability, playing football, any sport actually, but I do try to play as often as possible. Which isn't very often.
Long Covid, CFS, and Worries
A post from a time of frustration about Long Covid and my associated worries.
An Unintentional Hiatus
I realised about a month ago, in fact it was at the start of Lockdown 2: Electric Avenue when I realised that I hadn't made a post on here in ages.
Why do I use CFS and not ME?
Why do I use the term Chronic Fatigue Syndrome and not Myalgic Encephalomyelitis?
Going Private
Going private for my healthcare has been on my mind a lot recently.
