It was sort of inevitable that I’d be writing about COVID – 19 and the lockdown, let’s face it it’s all anyone can think about right now. So here’s my take on COVID – 19, lockdown and how it’s affected my life.
So let’s start with the practical bits: The events I’d planned to attend have now been cancelled or postponed (fingers crossed this thing eases by October so the rescheduled Cage Warrior 114 card can go ahead and we can celebrate mine and my mum’s birthdays at the same time). My university is now closed with all lectures and exams online AND I’ve left Birmingham and moved back to the family home for the foreseeable future. While this might be a bit of an annoyance as I’m used to my own space and schedule having lived on my own for most of the last 5 years now, but I know it was the right decision. I’m 90% an introvert so staying inside is something I can do pretty easily by choice; I mean I spend most Saturday nights watching MMA by myself rather than clubbing or at a bar. But of course there is no choice in this situation and THAT’S the bit that’s going to be a struggle. Those of you who regularly read this blog will know I spend what feels like half my life on a train, but that isn’t possible right now, so the wanderlust is building up a fair bit right row. So I guess it’s just time to stockpile wanderlust in this lockdown and use it all up when I can.
Now on to the more specific bits: What does COVID – 19 mean for me in terms of my disability? Well I have cerebral palsy which according to the list below would make me somewhat high risk for the virus (but not shielding level high risk) and vulnerable which meant I should stay inside as much as possible. It didn’t specify if it was a specific type of cerebral palsy that would make people vulnerable but I chose not to take the risk and begin isolating/quarantining/whatever the appropriate word is. I have to admit that that scared me a fair bit. I’d never seen my disability as something that made me vulnerable or significantly affected my life before, it was just sort of this thing that existed as part of my life and meant I got a cool set of wheels. But seeing my condition on that list and knowing what that said about the effect this virus could have on me was a reminder that I wasn’t entirely invincible.
The really REALLY scary part about this is not the way it is impacting me, but the way it’s impacting my family. My mum’s autoimmune disorder means she’s at the highest risk if she gets COVID – 19 and has to shield for 12 weeks. I’d known it was coming after hearing that those with autoimmune conditions were high risk and knowing the condition she has, but hearing that she’d actually got the text about shielding still came as some weird kind of shock even though I knew it was coming. We don’t always get on 100%, we’re too similar for our own good and we both drive each other up the wall more often than not, but god do I love that woman. The thought of her getting this virus and potentially losing her, and losing both my parents in the space of 2 years, terrifies the entire life out of me. The reminder that the woman who made me invincible may not actually be as invincible herself as I always thought she was is an eye opening wake up call that I wasn’t expecting to affect me in quite the way it has.
PLEASE stay inside and observe social distancing so I can be close to my mum again and her and other high risk people (and everyone else) can safely leave their house at some point this year.
Stay Safe, Stay Inside, Wash Your Hands and Stay Invincible!
Em (Invincible Woman On Wheels)