I very rarely see posts from anyone with somatic ocd. is there anyone else out there who struggles with this?

Anyone else struggle with somatic OCD and any pain/feeling slightly different is so noticeable and you feel like you’re just going to collapse or something? Like my ocd always convinces me that any sort of pain is related to some kind of illness that can cause a bad outcome or even death. If so, please share your tips of how to improve with this type of ocd 😭

Hi guys, This is my first post on here, as I’ve been scared to be vulnerable in this way. I’ve had a lifelong journey of mental health, diagnosed with a myriad of things, and misdiagnosed with others. When I got diagnosed with OCD, things started to click and treatment has been going well. There’s still a disconnect, things I do that are different than others and aren’t compulsion or obsession related. The reason I’m posting is to ask if anyone has been diagnosed with OCD/Autism and how you navigated that comorbidity. Thank you to anyone who shares

My OCD diagnosis is still very new, but now that I know what it is, it is clearly something I’ve had for as long as I can remember. Contamination/bugs and health have been a consistent theme since childhood, but religious/existential themes emerged during adolescence. Around that same time, there was also a good deal of trauma, and during middle school I started experiencing hallucinations. Tactile (like bugs crawling on me or biting me, an eyelash being stuck in my eye, but nothing was really there); visual (like moving shadows or things that would dart past in my periphery, and then I would just have intrusive thoughts of scary things around corners or under things); and auditory (an angry male voice that grumbles or yells indistinctly, or a high pitched noise like a microphone/speaker feedback but muffled and less sharp). Because of the religious denomination I grew up in, I initially assumed these were demons and tried to address it that way, but when I was 14 or 15, it occurred to me that those voices/sounds sounded like the way I felt, and the visual/tactile experiences happened during times of stress too — and so all of those experiences could just be seen as an expression of a fragmented part of myself. That acceptance didn’t make them go away — I still experience them now and I’m in my 30s — but it made those experiences less scary and more manageable. I also see now how these all pop up specifically when OCD obsessions are super triggered and when I’m super sleep deprived. Anyway! Since this diagnosis, and talking about the hallucinations at all, are new to me, I am wondering who else has had similar experiences. I don’t really know how much of the hallucination experience is OCD versus trauma, but it seems like this might all make sense under the “quasi-hallucination” label.