All the following “Mini Posts” are originally posted via my social media accounts (Instagram and Facebook), meaning they are a lot shorter than my blog posts. As some people who read my blog don’t have Facebook or Instagram I decided to share them on here so you can read them too. 

Welcome to life with Chronic Lyme disease!This photo is the absolutely smallest insight into what it’s like to live with

I was scared that letting go of all my illness labels and identification meant I would have nothing to write

I realised recently just how much my illness takes up rent space in my mind. It’s kind of hard for

It’s so easy to get wrapped up in all the things we still need to do to get to where

Today somebody was able to get out of bed for the first time in years. Today somebody found the courage

Today officially marks seven years of illness. Seven years to the day when I got glandular fever aged 16 which

One of the hardest things about being chronically ill is not knowing the end date to it all; the “chronic”

May you never forget how far you have come. May you never discredit your progress or growth. May you never

There comes a point where the time passed becomes bigger than what the heart can bear. Three years housebound was

So many things may not have changed this year. You may be in the same place physically; still trying to

Whatever you did or didn’t achieve this year, I hope you choose to rise above that. I hope you choose

I get so many messages from people saying things like, “I wish I was as positive as you”, “I wish

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