Most people think period pain is normal, but for someone with Endometriosis, it’s far beyond “normal cramps.”
What is it?
Endometriosis happens when tissue similar to the lining of the uterus (endometrium) grows outside it — on ovaries, fallopian tubes, bladder, or even intestines.
This misplaced tissue still behaves like the uterine lining → it thickens, breaks down, and bleeds during each menstrual cycle. But unlike normal periods, the blood has no way to exit the body, leading to inflammation, scarring, and adhesions.
Symptoms (often ignored or misdiagnosed):
Severe pelvic pain (especially during periods)
Heavy or irregular bleeding
Pain during sex or urination
Digestive issues (bloating, constipation, diarrhea)
Infertility in some cases
Constant fatigue
Why is it overlooked?
Many women are told “it’s just bad period pain”
Average diagnosis delay = 7–10 years
Lack of awareness among patients AND healthcare providers
Impact on life:
It doesn’t just affect physical health — it impacts mental health, career, relationships, and fertility plans. Women silently push through exams, jobs, or household work while fighting pain so sharp it feels like knives inside.
Treatment options:
Currently, there’s no permanent cure. But treatment can help manage symptoms:
Painkillers & hormonal therapy (like birth control pills, IUDs, GnRH agonists)
Surgery (laparoscopy to remove lesions)
Lifestyle changes (diet, stress management, exercise)
Support groups for emotional wellbeing
Why talk about it?
Because 1 in 10 women worldwide live with endometriosis, yet it remains under diagnosed and stigmatized. Awareness can help more women seek help early and push healthcare systems to prioritize women’s health.
MBH/AB