Today, I want to lay down some goals with you all for the upcoming month. I'm hoping the month goes to plan and I'm excited for what it brings, the small adventures and large, and the future feats I'll be setting myself up for. This August I'm free of the education system and have no… Continue reading Things I’d Like To Achieve This August
On what is not far off of the year anniversary for my 'Rare Disease Talks' post where I spoke about BBC's Casualty's representation of Ehlers-Danlos Syndrome, Fibromyalgia and Postural Orthostatic Tachycardia Syndrome (PoTS), I'm back with another*. This one varies slightly, with the representation being served upon a reality television show, but I think this… Continue reading Rare Disease Talks: RuPaul’s Drag Race (2019)
This month, I'm asking you to be aware of the chronic and mental health conditions I battle with, and educate yourself.
I vouched at the beginning of last year that i'd be transparent on mental health, disability, recovery, and even started an instagram account to log all of that. Ironically, it's chronic illness that's caused the downfall of that account due to a lack of spoons to post and update, constant brain fog and a lack… Continue reading The Side Of Chronic Illness You Don’t See On The Internet
(1/2) As a disabled person, you get a lot of people knowing little about you casting judgement. Sometimes this is as you're merely going about your day, and sometimes it's facing accessibility issues; unfortunately, yes, they are intertwined more than one would hope, but today I'm here to speak of the former. I'm using this… Continue reading Everyday discrimination.
I feel more than lucky to be a part of the blog tour for Sophie Sabbage's book 'Lifeshocks'. To fulfil my part of the tour, I was lucky enough to interview Sophie about her latest book and shed light on her previous publication, 'The Cancer Whisperer'. An interview with Sophie SabbageHave you always wanted to… Continue reading Lifeshocks: An interview with Sophie Sabbage
Rare diseases. They're called 'rare' for a reason, and not usually talked about much, apart from on said awareness days or weeks where people care for the most minuscule of moments. One thing that will always resonate with me was an experience I had in my last year of sixth form. I remember, one day… Continue reading Rare Disease Talks: BBC Casualty (2018)
just a small town girl on a journey of self discovery, and self love. i’ll be sharing my journey through this planetary existence, along with the things that make me happy, DIY creations, home decor, my journey to wellness from physical and mental illnesses, and everything in between.
Coping with chronic & mental illness oh and a cat...
‘Though she be blind, yet she is not invisible.’ - Francis Bacon
A Research Blog
A critical theorist and activist collective.
Have courage and be kind
my little spot on the internet for lifestyle
Adventures of An Aspergers Husband & a CP Wife
Theatre-Books-Life
My absurd life with mast cell activation syndrome
Live life unfiltered and embrace your flaws, because.....perfect is boring!!!
My world in a little bloggy nutshell 🌏
a foundation for growing up
...A glimpse into my world.
