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. 

When I was 19, a couple in a restaurant started chatting to me. They asked me what I did, and

What a difference a year makes, from functioning at 5% to 30% today 🌟🌈 ~ This time last year I

Something that I think is overlooked with illness is how much it affects your family. It wasn’t just my friends

I’ve been thinking a lot about the fact that while my life has not stopped these past few years, a

Whatever you’re feeling right now is okay. If you’re grieving, give yourself time to grieve. If you’re sad, give your

These past 3 months have been everything and more ☺️🌟 Ever since I got glandular fever, aged 16, I’ve seen

I’m all too aware that many of us in the chronic illness community struggle with fatigue, both mentally and physically,

Others may look at you and see you in ways you do not wish to be defined. But this does

Me and my book have only gone and got itself a podcast episode!! The incredible Hayley and Tom from Spoonie

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

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