It’s a tale as old as social media itself that we only post the glossy parts; I’ve felt strangely anxious about the warm, generous response to my story on
@1granary about living with endometriosis and working in fashion. I think I’m still in partial denial—scarred by years of medical gaslighting, still wanting to believe I’m more than my endo, even though it dictates every moment of my emotional and bodily life. There’s also the sticky paradox that I exist within an industry that continues to perform on conforming, flattened images of women so foreign to the unruly, painful, cut-up one I live in.
By the time a doctor finally listened to me, endo had claimed part of my intestines, bladder, uterosacral ligaments, ovaries, fallopian tubes, and appendix, requiring serious surgery to remove the lesions and parts of the affected organs. From then on, it’s been an endless carousel of more surgeries and doctors’ appointments, bed-ridden days of pain, paralysing fear that I might lose more of me with every twang of discomfort, and constant experimenting with diets, medications, everything. And ofc, the days when I just say fuck this all and call my mum for a good old cry. But this is all at the cost of my career.
That being said, in a weird way I’m grateful for it. It’s given me compassion, a deep love for the fleshy body and complex human within—and I so fiercely believe we need to value the perspective that those of us with chronic illness and disability bring to this industry.
Because really, we’re all only ever temporarily abled.
And I want to thank the editors and PRs I work with who, despite all odds, have allowed me to carve out a fruitful career—through patience, grace, and the value they see in me. I can’t help but count my lucky stars that I get to work with such extraordinary humans.
And for all my endo warriors: I hear you, I see you. I wish I could find a cure for this cruel, cruel disease—but in the meantime, I promise I’ll never, ever stop fighting for us.