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Midlife Wellness & PolicyUniversity of Michigan School of Public Health

25 Years of Data Show Black Women Face Worse Menopause Symptoms and Less Treatment

February 14, 2023

A 25-year review of SWAN study data reveals that Black women experience more severe hot flashes, higher rates of hypertension and depression during menopause, and are less likely to receive treatment for any of these conditions.

Read the original article at University of Michigan School of Public Health

Kairos™'s Take

Kairos™'s perspective on this story

Twenty-five years of data from the Study of Women's Health Across the Nation (SWAN) paint a troubling picture of how race shapes the menopause experience in America. A review by the University of Michigan School of Public Health found a consistent pattern across a quarter century of research: Black women are more likely to experience hot flashes but less likely to receive treatment for them. They face greater risk of hypertension during the menopausal transition but are less likely to receive hypertension treatment. They have higher rates of depression but are less likely to receive mental health services.

These disparities persist even after controlling for socioeconomic status. Researchers found that Black and Hispanic women still reported worse menopausal symptoms than non-Hispanic white women at comparable income and education levels, suggesting that factors beyond access and affordability, including provider bias, clinical knowledge gaps, and structural racism, contribute to the treatment gap.

The consequences extend beyond symptom burden. Untreated menopause symptoms accelerate cardiovascular disease, bone loss, and cognitive decline. When these conditions go unmanaged in populations that already face elevated baseline risk, the health disparities compound over decades.

Addressing this requires interventions at every level: policies that improve access, training that reduces provider bias, and tools that empower patients to document and advocate for their own care. The SWAN data demonstrates that the problem is well documented. What is lacking is the systemic response.

The Tracking Connection

Kairos™ contributes to health equity by putting clinical-quality health tracking directly in the hands of patients. When a woman can present documented symptom severity, treatment gaps, and longitudinal trends to her provider, the conversation shifts from subjective assessment to objective evidence. Kairos does not solve systemic racism in healthcare, but it gives every user the same quality of health documentation regardless of background, reducing the information asymmetry that enables disparate treatment.

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