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Living With Pilonidal Cyst Disease

Living With Pilonidal Cyst Disease

Von: Ashley Kellestine
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This is my story on living with pilonidal cyst disease. I know how isolating and lonely it can feel and for a while now I’ve wanted to share my own success story to help those who are in the midst of this disease. The people who need to hear a success story, the ones who are feeling alone right now.Ashley Kellestine Alternative & Komplementäre Medizin Hygiene & gesundes Leben
  • Episode 3: The Flare-Ups That Ruled My Life
    Feb 6 2026

    In this episode, I talk about flare-ups — what they actually feel like, how they start, and why they’re so much more than “just pain.” I share my personal experiences with flare-ups, from the physical symptoms to the mental spiral that comes with waiting, uncertainty, and fear. This episode dives into the reality of living through repeated flare-ups, emergency room visits, lancing and drainage, and the emotional toll of never knowing when the next one is coming. If you’ve lived through a flare-up, are currently in one, or are terrified of the possibility, this episode is for you.


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

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    8 Min.
  • Episode 2: Understanding Pilonidal Cyst Disease – From My Perspective
    Jan 30 2026

    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.

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    10 Min.
  • Living With Pilonidal Cyst Disease
    Jan 27 2026

    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!

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    23 Min.
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