Welcome back to Living With Pilonidal Cyst Disease! In this episode, I dive deeper into understanding pilonidal cysts — from my own perspective, not as a medical professional, but as someone who’s lived through it.

I share what it felt like to experience symptoms, how I first noticed something was wrong, and the impact it had on my daily life — physically, mentally, and emotionally. I also talk about the journey from the very first cyst to surgery, and the after-effects that most people don’t discuss.

This episode is for anyone curious about pilonidal cysts, going through it themselves, or supporting someone who is. It’s a raw, honest account of what it’s really like — because no one should have to feel alone in this experience.

Disclaimer: I am not a medical professional. Everything shared here is based on my personal experience and is not medical advice.

As someone who lived/lives with pilonidal cyst disease and how lonely I felt through my journey, I felt the need to share my story. I always longed for that success story especially as a teenager going through this horrible disease. I finally decided it was time to share my own story, my feelings and my success.

Making this was not easy as this brings up some terrible trauma and it makes me very vulnerable sharing my story but I know even if this helps just one person, I am doing the right thing.

I really hope you enjoy it and please feel free to ask me any questions you have!