“Is the system failing women… or was it never built for us in the first place?”
“Why do so many women feel dismissed when they finally ask for help?”
Women make up over half the population, yet their symptoms, pain, and lived experiences are still too often minimized, delayed, or misunderstood in healthcare. In this episode, we dig into the uncomfortable truth behind inequity in women’s medicine and what starts to change when women finally start talking to each other.
This conversation is bigger than hormones. It’s about the entire system women are navigating.
In this episode, we break down:
• Why women’s symptoms are more likely to be dismissed or misattributed
• The historical exclusion of women from medical research and clinical trials
• How outdated diagnostic models still shape modern care
• Why conditions like endometriosis, autoimmune disease, and heart disease are so often missed or delayed
• What current research actually shows about gender bias in diagnosis and treatment
• How social media and online communities are changing patient advocacy
We also sit down with Claire Brown, founder of MOVE Realty and creator of the Little Rock Power Women’s community, which has grown into a space where over 30,000 women share real healthcare experiences, support each other, and call out gaps in care.
Claire shares:
• Why she started the Power Women community
• What women are really searching for when they join
• The most common patterns she sees in shared healthcare experiences
• How community changes the way women advocate for themselves
• Whether online conversations are creating awareness or real change
A few realities that frame this conversation:
• Women account for about 75% of autoimmune cases
• They are 5 to 8 times more likely to experience thyroid disorders
• Around 80% of osteoporosis cases occur in women
• Depression and anxiety are diagnosed nearly twice as often in women
• Women are more likely to experience delayed diagnosis across 100+ diseases
• Studies show women often wait longer, receive less pain medication, and are more likely to be misdiagnosed, especially in emergency and cardiac care
• One study found 93% of women reported feeling dismissed when seeking medical help
And this isn’t random. It’s systemic:
Women were historically excluded from research, underrepresented in clinical trials until the 1990s, and often studied through male centered models of disease. Even today, symptoms like fatigue, pain, and hormonal changes are still frequently minimized or attributed to stress or anxiety.
But here is what matters most.
When women compare experiences, patterns emerge.
And when patterns emerge, silence breaks.
This episode is about that shift.
Because being told “everything looks normal” should not be the end of the conversation.
Practical takeaways:
• Track your symptoms and patterns over time
• Ask follow up questions when something feels off
• Seek second opinions when needed
• Do not accept dismissal as diagnosis
• Find providers who listen beyond lab results
• Trust your lived experience as data, not emotion
Share this with the woman who has ever been told “it’s all in your head.”