Help Jasmine raise money

Endometriosis tried to stop me, but unfortunately for everyone, I’m stubborn and mildly unhinged.

Hi! I’m Jasmine—though many people know me as Jazz.

I’m a 34-year-old woman who was recently diagnosed with endometriosis after enduring symptoms for 18 years. For nearly two decades, I navigated a healthcare system that too often dismissed my pain, seeing multiple doctors and specialists before finally receiving a diagnosis through my GP and a referral for further care. My diagnosis was based on my symptoms, and I’m currently awaiting another referral to a specialist —care that will likely include endometriosis excision surgery to remove lesions affecting my organs and tissues.

My story is not unique. Endometriosis is widely underdiagnosed, misunderstood, and underfunded, leaving countless people to suffer in silence. My journey has been painful and, at times, deeply isolating—but it has also ignited my determination to speak out, demand better care, and raise awareness for those still searching for answers.

Please stand with me. Together, we can amplify voices, challenge stigma, and push for earlier diagnosis, better treatment, and real change. Join me in this fight to end endometriosis.