[Image description: pale pink background with black bold heading reading 'change', beneath it in a handwriting font reads 'isn't always a bad thing'. There is a black illustration of a wildflower on the left hand side.] Hello my lovelies, As you may know if you have read my recent blog post titled 'politicizing disabled bodies' [...]
Hello my lovely folx, how are you all doing today? I know it has been long time, no see here on the blog - but that's a topic for another time entirely. As today, I bring frustrating and angering news relating to my IG account, and the action taken by the platform to censor yet [...]
As a disabled womxn I oftentimes used to feel left out of the conversations regarding sex, relationships, and sexual health. So earlier this year I took it upon myself to change that in a small capacity, not just for myself- but with the hope that it would serve as representation in a small way for [...]
I write today regarding my project, which aims to provide a platform for individuals to join the conversation about sexuality and sexual health as a disabled person; as there is a significant lack of disabled representation in discussions surrounding these topics. Sexual wellbeing and owning our sexuality is just as important as any other aspect of health and wellness[...]
Hello, my name’s Lori- AKA ‘Bud to Bloom’, a UK based disability, and mental health blogger living with Ehlers Danlos Syndrome, ME, and a host of other comorbidities. My journey with chronic illness started at age 13, and like many spoonie warriors it appeared to come from nowhere. However after a few years I was [...]
I never thought I would make it to 20, I had developed this prophecy that I wouldn't make it through the difficulties endured during my mid teens.
As a young girl I spent a lot of time daydreaming about the future, my future - and how perfect everything was going to be 'by then'. Watching cheesy American teen movies about the toils of high school students for rich, white, and straight cis women gave me a highly unrealistic expectation of what my [...]
I slowly began to hate using my walking stick, crutches, walking frame, and wheelchair - I failed to invest in my comfort and sense of self-expression because I was living in a state of denial. I didn't WANT to think of a future with mobility aids; it felt like I would be giving in.
May 9 - "This past weekend has been rough - my body feels like it's falling apart beneath my skin, uncontrollable; fighting against itself - the epitome of connective tissue disorder." Warm weather is a rarity in northern England, so I try my very best to go into the garden whenever my PoTS and ME [...]
"How have your disabilities affected your relationships?" To understand how my relationships have been affected as a result of my disabilities, it's important to understand that my conditions have caused a shift in my relationship with myself. Chronic pain is difficult - the constant struggle to get through the days, some easier to navigate than [...]