Loading...
Loading...
A UX research case study exploring how to help women with PCOS connect with fellow patients and empathetic gynecologists.
UX Designer & Researcher
Solo Project
Course Project

“”|
It wasn't until I started talking to people that my perspective shattered. One by one—my cousins, my close friends, and other women in my life revealed that they too had been diagnosed. They were all fighting the same battles, but completely in private. I had no idea.
It made me wonder: how many more were suffering in silence?
I realized the core of the problem wasn't just medical—it was the profound isolation that came from a condition no one was talking about. This project is my attempt to break that silence.
Polycystic Ovary Syndrome affects millions of women worldwide, yet awareness and support remain critically low.
PCOS is the most common endocrine disorder among women of reproductive age
The majority of women with PCOS don't know they have it
Women with PCOS are significantly more likely to experience depression
And projected to reach 78 million by 2036

I followed a structured UX research process over 5 weeks to deeply understand the problem space.
Desk Research, User Interviews, Market Analysis
User Personas, Empathy Maps, Journey Mapping
HMW Questions, Card Sorting, Site Mapping
Information Architecture, User Flows
Usability Testing, Iteration
I conducted qualitative research with 13 participants across 4 stakeholder groups to understand the full ecosystem of PCOS care.
Ages 15-30
Of daughters with PCOS
Healthcare providers
Via video/phone calls

The research revealed that the challenges of PCOS extend far beyond the physical symptoms.
Almost all interviewees experienced anxiety, depression, and low self-esteem. Parents and even some doctors weren't aware of this connection.
Gynecologists recommend healthy diet and exercise, but don't explain how to actually implement these changes in daily life.
Most women switched gynecologists at least twice, often starting with family friends who weren't the right fit.
Majority of interviewees reported experiencing body shaming by family or friends, significantly impacting mental health.
At diagnosis, most adolescents didn't know what PCOS was, nor did they know other women who had it—despite its prevalence.
Obesity causes PCOS, but PCOS also induces obesity. Stress triggers recurrence. The only breakthrough point is lifestyle change.
“There were times when I felt constantly anxious and depressed but could not tell anyone.”
“My gynac gave me very basic information and told me to google about PCOS on my own.”
I identified 4 distinct user segments within the PCOS awareness and support ecosystem.

I created detailed personas for each stakeholder group, combining interview insights into actionable user representations.




I analyzed 5 competitors—2 direct (PCOS-specific) and 3 indirect (general women's health)—to identify gaps and opportunities.

To empower young females with PCOS and their families by increasing awareness about the condition's links to lifestyle, genetics, and mental-physical health issues and by connecting them with fellow patients & experienced gynecologists which will foster shared experiences, reduce mental health issues, and promote happier lives despite PCOS complexities.
I framed key opportunities as 'How Might We' questions to guide solution ideation.

I used card sorting with 8 participants to validate the information architecture before designing user flows.




This project concluded at the information architecture stage. Here's what would come next.
Create high-fidelity mockups based on the validated information architecture, focusing on a warm, supportive visual language.
Test prototypes with target users to validate design decisions and identify pain points in the user experience.
Build a minimum viable product focusing on the community feature—the highest-impact, lowest-effort solution identified.
This project reinforced that the most valuable insights come from listening, not assuming. Every interview challenged my preconceptions about what women with PCOS actually need—it wasn't better tracking features, it was connection and understanding.
Healthcare design requires extra care with language and visuals. Body positivity, avoiding triggering imagery, and creating safe spaces for vulnerable conversations became central to every design decision.
Starting with my sister's story wasn't just narrative technique—it was the foundation of genuine empathy. Personal connection to the problem space made me a more thoughtful researcher and designer.
Design isn't just about solving problems—it's about understanding people first.
If you'd like to discuss this project or explore working together, I'd love to hear from you.