GhostlyMarie
Peer Supporter
So, I’ve been dead set on doing the work since October of last year and so far so good! My mental health is a lot better, I have stronger boundaries, I don’t care about my symptoms being present or not, I do whatever I want regardless of what my mind or body tries to tell me I can or can’t do.
I want to preface the rest of my post by saying I know 100% that my symptoms are TMS. Back in 2022, I had an “allergic reaction” to an antifungal cream on my nethers that catapulted me into pelvic pain that turned chronic after doctors couldn’t help or figure out what happened. Honestly, I feel like if I had just waited, I would have healed and been fine but no, I went to see doctors who scared the crap out of me and introduced me to vulvodynia, IC and Pudendal Neuralgia and it messed me up.
Before this happened to me, I was 100% healthy and “normal”. No one can convince me that I went from being a healthy, athletic young woman to destined to be in chronic pain for the rest of my life overnight. It doesn’t make sense. IT DOESNT MAKE SENSE. Okay, rant over haha
Anyhoo! Presently, my symptoms have been happening more frequently lately. At first I thought this new increase in pelvic symptoms might be extinction bursts but I’m not so sure. I started a new job recently and though it is rather stressful, I have been allowing myself needed breaks and moments to check in with myself throughout my day. So, I’m not sure if maybe these just are a cluster of extinction bursts (although my symptoms stay localized to my pelvic floor and never really moves elsewhere) going on or if maybe my nervous system is becoming dysregulated due to life stuff. Every time my symptoms arise, I smile and say “hi” to them and then I proceed to tell myself out loud that I am okay and everything okay. That I’m safe.
I must note now that right after I wrote that my symptoms never move, my scalp started itching in random places haha
anyway! Has anyone ever experienced a cluster of extinction bursts before? I’m curious about your experiences!
I want to preface the rest of my post by saying I know 100% that my symptoms are TMS. Back in 2022, I had an “allergic reaction” to an antifungal cream on my nethers that catapulted me into pelvic pain that turned chronic after doctors couldn’t help or figure out what happened. Honestly, I feel like if I had just waited, I would have healed and been fine but no, I went to see doctors who scared the crap out of me and introduced me to vulvodynia, IC and Pudendal Neuralgia and it messed me up.
Before this happened to me, I was 100% healthy and “normal”. No one can convince me that I went from being a healthy, athletic young woman to destined to be in chronic pain for the rest of my life overnight. It doesn’t make sense. IT DOESNT MAKE SENSE. Okay, rant over haha
Anyhoo! Presently, my symptoms have been happening more frequently lately. At first I thought this new increase in pelvic symptoms might be extinction bursts but I’m not so sure. I started a new job recently and though it is rather stressful, I have been allowing myself needed breaks and moments to check in with myself throughout my day. So, I’m not sure if maybe these just are a cluster of extinction bursts (although my symptoms stay localized to my pelvic floor and never really moves elsewhere) going on or if maybe my nervous system is becoming dysregulated due to life stuff. Every time my symptoms arise, I smile and say “hi” to them and then I proceed to tell myself out loud that I am okay and everything okay. That I’m safe.
I must note now that right after I wrote that my symptoms never move, my scalp started itching in random places haha
anyway! Has anyone ever experienced a cluster of extinction bursts before? I’m curious about your experiences!
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