The Cycle. Endometriosis Podcast

First, I’d like to say thank you for this podcast. Hearing stories from different Endo warriors lets me know that I am not alone. Endometriosis is one of those topics that isn’t talked about enough. Not enough people know about this disease and the effects it has on us mentally, physically, and emotionally. Doctors tend to minimize our symptoms and/or gaslight us into thinking the symptoms that we experience are not “that bad”. ER Doctors and even OBGYN specialists are not as knowledgeable so it’s a constant cycle of pain, ER visits, cysts, pain meds, birth control, and surgery. All while having to work and live a normal life. I’m currently going through a 3 week flare and honestly, this podcast is the only thing that’s keeping me sane. One day, I hope to share my story!

I’m 42 and feel I’m so late in receiving a diagnosis of endometriosis and having an expert excision surgery. This heartfelt podcast of personal stories has really helped me cope with my experience of the past 12 years leading up to this moment, xo

I am 22 and have been diagnosed with endo, pcos, and interstitial cystitis. I was diagnosed back in december and was pretty clueless to what all this is. I thought I was going crazy and most of my symptoms might’ve been in my head. This podcast has brought me so much knowledge and comfort. thank you so much for doing this

Dr Fenske brought me so much hope. Thank you from the bottom of my heart!