- Date posted
- 3y
OTO
Recently learned about ocular tourrettic OCD. This makes so much sense with my symptoms-I feel freer knowing that this is part of OCD and that it can go along with other subtypes.
Recently learned about ocular tourrettic OCD. This makes so much sense with my symptoms-I feel freer knowing that this is part of OCD and that it can go along with other subtypes.
What's that?
I am newly diagnosed with OCD as a 33 year old female I was fat oses with bipolar at 15 and never really identified with it much and totally relate to ocd. I wish i would have known long ago so I could have gotten treatment earlier. Now that I know and am aware and can see what’s off and what are compulsions and my insatiable need for reassurance it’s so overwhelming- it feels like my mind is a prison and attacks me with a new pure o quest as soon as I wake up I’m optimistic I’ll be able to get better but it just feels like it’s time sucking and joy stealing disorder I know I’m not alone here I feel like a crazy person replaying and replaying things I want to know if you can relate or if you have been at this for a while and actually feel like you are breaking free from this Thanks for the read
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.
I would like to raise awareness for an OCD subtype that is almost never talked about and is not included in the official OCD subtypes. This subtype includes obsessions about: 1. Thinking that something is wrong with your brain 2. Being convinced that you have forgotten how to think 3. Being convinced and paranoid that you have lost your inner voice 4. Being extremely afraid that you have lost the ability to feel 5. Being hyperaware of every thought, tracing it back to see how it occurred 6. Being convinced that something is wrong with you when something doesn’t go the way you expected it 7. Thinking that you are not thinking about it in the right way when trying to think your way out of it Compulsions include: 1. Mentally trying to figure it out 2. Trying to prove to your self that nothing is wrong with you 3. Putting your life at a stop until you figure it out 4. Excessive googling, using chat bots, reddit, researching, reading books & trying to find the missing piece of the puzzle I am sure there are other people who relate to this. This subtype isn’t mentioned anywhere and it’s really confusing for those experiencing it. Please, if you feel or think in a similar way like this post and reply in order to raise awareness.
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