Hello lovelies, I just want to begin by thanking those of you who expressed their support for my recent blog post regarding self-nurture and feeding my inner child. If you are following my Instagram account, or have read my newest blog publications, you'll likely be aware of the fact I have battled mental illness for [...]
Tag: chronicfatiguesyndrome
Ways I Make My Self Care Accessible
Hello lovelies! I hope you're all doing as well as can be expected - especially those out there who're frontline workers or folx in lockdown. It can be incredibly stressful, and I've began go feel the effects of 10 months shielding from the rest of society, and enduring 3 national lockdowns. Being disabled creates a [...]
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 [...]
Disability and Sexuality, part 1
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 [...]
Needing a carer from a sick person’s perspective | ME Association
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 feel it in my bones (announcement)
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 [...]
“Disabled people have sex?”
In March and April I had the amazing opportunity to write blog posts for Intimately - an accessible and inclusive underwear company. Both posts centred around sex with disability - the first about embracing one's sexuality with a disability, and the second about navigating sex with disability. Photo credit: Hannah Todd Photography This blog post [...]
Finding Strength in Stripes: A collaborative piece sharing the stories of those with EDS/HSD
My love for writing has been a constant throughout my life, however, it wasn't until March 2018 that I decided to turn this passion into an active hobby in order to share my experience with issues concerning topics close to my heart. Fast-forward to the present day and I have had the privilege of meeting [...]
The EDS Chronicles: Losing trust in professionals (1/2)
Hello Blooms, I have felt a great sense of hesitation whenever I think about writing a blog post about the topic I shall be discussing today with you all. Yet at this point whenever I feel hesitant to talk about how I feel, I just go ahead and do it. I'm sick of hiding behind [...]
Mental Health Double Standards
Hello Blooms, UM...I HAVE A QUICK QUESTION Why do we respect suffering in silence; not wanting to 'trouble' anyone with a so-called problem? Why do we expect this of ourselves yet encourage other people to talk to us about anything that is on their mind? We are upholding the negative stereotypes we are actively trying [...]
