Happy pride month!I’m aware that it may be news for many of my readers/followers that I’m queer, non-binary, and I’m also disabled.I’ve made blog posts in the past discussing topics such as growing up queer and disabled however as my style of content production has evolved, I have taken to finding empowerment and comfort in [...]
Tag: wheelchairuser
DISABILITY AND SEXUALITY – PART 2
My relationship with my sexuality has always been disorganized, even before I became legitimately disabled by my conditions. I grew up feeling like I needed to fit into a mold I wasn't shaped for, and a body I didn't even understand was objectified by many people around me from a young age.
Valentine Gifts for Spoonies
Valentine's day is approaching, and whether you choose to celebrate it or not - either that be with a partner, or put a platonic twist on it and have a fun filled day to celebrate your love for your best friend, it's always nice to ensure you have put thought and effort into the way you choose to share your love and affection. I like to think I'm a good gift giver, and I absolutely love celebratory holidays, therefore I thought it wise to share some suggestions I have for a fellow spoonie in your life, with an emphasis on independent businesses.
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 [...]
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 [...]
Bloom’s recommended – Letter to Pain Management — tearydawn
I don’t know how to articulate my feelings and experiences in the small amount of time that we’re allotted. I wish I could take you home for a few days to see exactly what my life is like and what I go through. It’s not obvious in a half hour appointment where I’m simply sitting […] [...]
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 [...]
The EDS Chronicles: Dating Shouldn’t be a Chronic Pain
Blooms, Over the past few months, I have been relatively busy over the past few months - attending hospital appointments, travelling to Scotland for a family graduation, seeing friends before the uni year commenced, and OH I downloaded Tinder. My experience with Tinder has been interesting - I've had only decent encounters with people who [...]
