Covid 19: Lockdown And Chronic Illness

I wanted to write about the impact of the Covid 19 lockdown on me personally, because it would seem from friends points of view or from reading various social media comments that people might think it hasn't made much of a difference to those that would normally be housebound alot anyway. At least from my … Continue reading Covid 19: Lockdown And Chronic Illness

Invisible illness. Seeing is believing.

They say seeing is believing. So how do I show someone that I have an invisible illness? How do I explain it in a believable way? It's crazy that something so very real, incredibly painful and hugely debilitating to me can be disbelieved by others simply because they can't see it. I believe it because … Continue reading Invisible illness. Seeing is believing.

10 things I wish I knew about life after Guillain-Barre Syndrome.

When I was diagnosed with Guillain-Barre Syndrome back in 2016 I'd never even heard of it. I asked the doctor to provide me with some information I could read and I was promptly provided with a print out from the internet about the condition. Paralysis, difficulty breathing, loss of bladder function, severe pain, possible death....it … Continue reading 10 things I wish I knew about life after Guillain-Barre Syndrome.