Let’s talk about Sunflower Lanyards for hidden/invisible disabilities @hiddendisabilities_anz Last year I wrote a blog post about tips for travelling with chronic illness. I asked you…
Another year another endometriosis awareness post This year I was actually inspired by an article I wrote a few years back for Eureka St. I wanted…
Gender inequality in the healthcare system is something I have been passionately advocating for, especially this year. I’m pleased to share that as part of the…
It’s October, which means it’s Dysautonomia Awareness Month! You’ve probably heard about Dysautonomia by now because I’ve been advocating and sharing infographics every October for years…
Travelling and chronic illness aren’t quite a perfect match. So I wanted to share some top travel tips I and other chronic illness pals have found helpful!
Let’s talk … DISABILITY PRIDE MONTH Despite being an invisibly disabled individual myself, I personally have not really been aware of Disability Pride Month before. I…
I have been bullet-journalling for a while now and post about my spreads on my instagram stories which has meant I have had a few questions…
So I haven’t found self-isolation too hard, stressful or different from my normal life. Why? Because my life changed when I was officially diagnosed with Myalgic…
A few weeks ago I was reflecting on how much my life has changed since becoming sick. Of course it has changed for the worse… but…
I am sick of medical professionals not understanding my condition, actually scratch that… I am sick of medical professionals not even knowing what my condition is.…