Hey Girl, Hey— It’s March!​
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March is National Endometriosis Awareness Month, a time to recognize, educate, and uplift those living with endometriosis, especially Black women whose pain is often dismissed.

Endometriosis is a chronic condition where tissue like the uterine lining grows outside the uterus, causing painful periods, pelvic pain, fatigue, and fertility challenges. It affects about 1 in 10 people with uteruses, and while exact numbers for Black women aren’t fully known due to underdiagnosis, thousands, even hundreds of thousands, are living with it, often for years without answers.

However, there is good news for people living with endometriosis. There are hormonal and non-hormonal treatment options for endometriosis, depending on the desire for fertility. Talk to your health professional today about your options.

Sisterly Health Truths:

• Underdiagnosed: Black women are often diagnosed later than white women due to bias, myths, and dismissal of pain.

• Years of pain: Delays and misdiagnoses can lead to unnecessary physical, emotional, and reproductive harm.

• Pain is real: Severe or persistent symptoms are not “just periods” and deserve attention, validation, and care.

Trusted Resources & Local Care:

🔗 Endo Black, Inc. – A Black-women-led nonprofit that advocates for and educates Black women and women of color about endometriosis. They provide community support, educational materials, and programs addressing disparities in diagnosis and care.

🔗 Endometriosis Foundation of America (EndoFound) – A national organization focused on awareness, early diagnosis, research, and advocacy. They offer educational events and campaigns aimed at reducing stigma and improving clinical outcomes.

🔗 OHSU Endometriosis Info (Oregon) – Provides comprehensive information on symptoms, treatment options, and access to specialized care, including gynecologic and surgical management through Oregon Health & Science University.

Sisters, let's treat ourselves to good health!