Although it’s been framed as a “middle-aged white woman’s disease,” migraine doesn’t discriminate; it affects one in seven people across all genders and race. But the right diagnosis is often more difficult to find for people in marginalized communities.
In the second of a two-part episode, Sarah Shaw and her doctor Courtney White, MD, discuss the need to educate the medical profession, especially in Black, Brown, and low-income communities, on the many symptoms of migraine so they can better serve patients in the BIPOC and LGBTQA+ communities.
Some highlights in this episode:
: 53: How Sarah found out she was having a migraine attack2:00: “The emergency room is the worst place to go when you have a migraine attack.” — Dr. White4:00: The younger generation of migraine patients benefit from social media4:44: What patients with chronic illness have taught Dr. White5:36: “The medical system is not fair for anybody, but especially for low-income people.” — Dr. White6:35: What does a good provide- patient relationship look like?7:12: Creating a comfortable atmosphere for patients to be able to speak up7:58: Sarah discussing how doctors made her feel ashamed8:24: Migraine and the healthcare system9:44: How a podcast like ours helps people dealing with migraine in Black and Queer communities10:19: “Migraine does not discriminate, and that even though it's been framed as a middle-aged white woman's disease, that's not the only population.” — Dr. White11:48: Migraine disease affects men, women, non-binary people, all races, there is no discriminationJoe Coe, Director, Education and Digital Strategy at GHLF: [email protected]
Sarah Shaw, BIPOC Patient Advocate, Community Outreach Manager: [email protected]
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