M.E. (Myalgic Encephalomyelitis) is something very few who haven’t lived within its reach truly understand. Like many other chronic illnesses, nobody on the outside can really see its true effects, the worst is mostly played out behind closed doors and in dark rooms. Before I carry on, I just want to note that, like many […]
This year, my 25th one, was the year I always told myself I’d have ‘caught up’ by… whatever that means. It’s like I thought life was a game of monopoly, with houses to gather with each year. The dating one, the driving one, the job one, moved out one, home-owner one, car, relationship, child… And […]
This started off as an appreciation post for my new power-chair, but it’s become so much more. I hope you’ll bear with me, as I think it’s an important topic to cover whatever your current health status. I’m sure it’ll come as no surprise that farms and faulty health aren’t exactly a match made in […]
This week is M.E. Awareness Week, culminating in M.E. Awareness Day on Sunday, (Myalgic Encephalomyelitis, also known as Chronic Fatigue Syndrome/CFS; although, that name feels a bit like calling a flood a ‘chronic puddle’, but that’s a debate for another time). I was going to let it pass by without saying anything. I worry about […]
This blog post is a bit of a personal one, it’s something which has been on my mind for quite some time. I feel like it’s something we all need reminding of every now and then, I know I certainly do, so I thought I would finally get it off my chest. Here goes… A […]