Luckily in this day and age we have a lot of resources and equipment at our fingertips. As someone with a disability, there’s quite a few items I need in my everyday life to help it run more smoothly. Now, I don’t have unlimited funds (if only) so I don’t have every product that could…
Category: chronic pain
Stationery Galore: Huge Haul
If you’re a stationery lover, I can guarantee you will adore this post. It’s very picture heavy but I’m sure that won’t be a problem with any of my fellow stationery addicts. I’m pretty sure that I’ve lost at least a week of my life browsing Etsy and I’m totally okay with that as I’ve found…
The ‘Done’ List: Acknowledging Achievements
I’ve always been overly critical of myself; I give myself a hard time and feel guilty if I spend a few hours resting. As someone that suffers with chronic pain, I should be used to chilling out and letting myself recover but I put a lot of pressure on myself, and never give myself credit…
One Year Follow-Up: Stanmore Pain Management and Rehabilitation Programme
Can you believe that it’s been a year since I spent three weeks in rehab? Where has the time gone? I distinctly remember the nerves I felt the weeks leading up to the programme as if it was last month. The apprehension, the anticipation, the terror. I was terrified, I’ll openly admit that; it was…
I’m Not Superhuman: Not All Disabled People Can Be Paralympians
Let me start this off by saying that this is not a post slagging off the Paralympics. The athletes that partake in the games are absolutely amazing and I tip my hat (I’m not wearing a hat, but let’s pretend I am) to all of them. My problem is with the media and how Paralympians…
How Aren’t You in Pain?
As I lie here with my left knee heavily braced, the pain surging through my whole leg, pulsating, agonising, my mind begins to wander. I only ever voiced this a few months ago and as soon as I said it out loud, I realised how ridiculous it might sound to someone who doesn’t know me….
I’m Really Flexible and it’s NOT Sexy
I have Ehlers-Danlos Syndrome type 3; the hypermobility kind, the stupidly bendy ‘how don’t you snap?’ one. Some people will probably call the majority of us with EDS 3 – double-jointed, but that’s a myth, I mean, how can you have double the amount of joints? I’ve written quite a few posts on EDS, and…
Proprioception and Ehlers-Danlos Syndrome
When I was diagnosed with EDS type 3, (hypermobility, HEDS, whatever you want to call it) ten years ago I was naive enough to think that Ehlers-Danlos would be the strangest words I’d hear regarding my condition. Alas, my nineteen year old self soon learned a lot more; proprioception being one.What is proprioception?Basically, proprioception is…
What Disability?: The Adaptability of Children
I spent last weekend with my three year old nephew, Kaine, and it got me thinking about how he sees me. I’m his Auntie Sarah, I use crutches, I use an electric wheelchair, I wear splints and take tablets, but most of all, I make a huge fuss out of him, I buy him toys…
Medication Made Me Say It
I’ve said quite a few hilarious things when I’ve been slightly off my face on prescription drugs. This is completely different to my Brain Fog series, because brain fog happens on the daily, and here I’ll be sharing silly things I’ve said/done when I’ve taken really strong medication and the effects it has on my…