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.
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15-07-2020
Whatever you’re feeling right now is okay. If you’re grieving, give yourself time to grieve. If you’re sad, give your
08-06-2020
These past 3 months have been everything and more ☺️🌟 Ever since I got glandular fever, aged 16, I’ve seen
03-06-2020
I’m all too aware that many of us in the chronic illness community struggle with fatigue, both mentally and physically,
31-05-2020
Others may look at you and see you in ways you do not wish to be defined. But this does
12-05-2020
Me and my book have only gone and got itself a podcast episode!! The incredible Hayley and Tom from Spoonie
03-05-2020
Welcome to life with Chronic Lyme disease!This photo is the absolutely smallest insight into what it’s like to live with
07-04-2020
I was scared that letting go of all my illness labels and identification meant I would have nothing to write
22-03-2020
I realised recently just how much my illness takes up rent space in my mind. It’s kind of hard for
11-03-2020
It’s so easy to get wrapped up in all the things we still need to do to get to where
16-02-2020
Today somebody was able to get out of bed for the first time in years. Today somebody found the courage
06-02-2020
Today officially marks seven years of illness. Seven years to the day when I got glandular fever aged 16 which
26-01-2020
One of the hardest things about being chronically ill is not knowing the end date to it all; the “chronic”
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