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"You should have had that out a long time ago."
These were the words Laura Shennan's surgeon told her after she woke up after an elective partial hysterectomy, a procedure she had wanted for over a decade. It was the validation she needed after years of debilitating pain that impacted nearly every aspect of her life.
"I first got my period when I was 11 and from day dot it was an extremely horrible experience for me, every single month."
Laura is one of the nearly one million women in Australia who suffer from endometriosis, a condition that is still widely misunderstood and has an average seven-year delay between symptoms and diagnosis.
"For as long as I can remember, I have always had to take one or two days off school or work when I had my period," Laura said.
"I've taken so much sick leave that you can track my periods on my leave history. And, if I actually got sick, I would have to take unpaid leave as there would be no sick leave left."
Like many sufferers of endometriosis, Laura experienced an array of crippling symptoms, including migraines that would arrive so violently she'd have to ghost her colleagues for two days. "The pain would come on so quickly I didn't even have time to set an out-of-office. My colleagues would all be asking where I was."
























