Skip to main content

From a Catatonic State

I can't move, even to lift my eyelids. I'm only semi-aware of what's happening around me, but I'm fully awake, fully aware of my thoughts, and fully aware of what's happening to me.
My therapist calls this a catatonic state, and it's happened to me in moments of extreme stress since I was a kid. It's been happening to me more often, though, lately, and it's easier to slip into this state when I'm both exhausted and delusional.

I'm always resisting becoming delusional. I have intrusive thoughts 24-7, and I always have to think harder than neurotypical people to tell the difference between fantasy and reality. When I'm exhausted, I can't keep this up anymore, and the lines blur. Because the delusions I slip into are often terrifying, I can slip into a corresponding catatonic state.

A catatonic state is not sleep paralysis. I'm awake before it happens. Sometimes, I'm chatting with friends in the car one moment and catatonic the next, and they often don't realize that anything's wrong or think that I've just gotten quiet.

Being catatonic is, itself, scary. I'm trapped in my head with frightening thoughts, but I can't move or speak to engage in any of my usual distractive or coping mechanisms.

My psychiatrist made some medication changes to try to help with this.

My psychiatrist prescribed a small dose of Ativan at bedtime to help with this. I have reservations, as it can be addictive, but I think she's right that it's needed.
We already have me on general anti-anxiety/anti-depressant and anti-psychotic medication, and I religiously utilize my coping mechanisms and thought exercises.

So far, Ativan helps a lot with the fear I experience in the evenings, and it can often prevent this catatonic state. However, it can make me equally unresponsive in a tired and detached state that makes it hard to form words or engage with the world around me. 

Psychiatric medication can have heavy side effects, like this lethargy, and sometimes my family and friends discourage me from taking it as a result. I'm not always open with everyone about the breadth of my psychiatric symptoms, but those who know are usually in favor of me taking the medications.

Psych meds are really needed for me, and so is therapy. Please don't discourage people from seeking that help. You never know what's happening in their brains.

Comments

Popular posts from this blog

Depressed?

Am I depressed? I told my psychiatrist I wasn't at my last appointment because there are things that can pierce through the haze of mental illness and make me feel alive- poetry mostly. I asked my friends and family if there are things that make them feel alive, and a lot of them had long lists: time with loved ones, hiking, making art, making music, cooking, playing with pets... I have one thing, but I'm so grateful to have that thing. If you have something that makes you feel alive, hold onto it, and if there are days where depression is so thick, your one thing barely makes a dent, do it anyway. It's your secret weapon in an invisible war. But I digress. I told my psychiatrist I wasn't depressed because I can enjoy poetry, and it can make me feel alive. I can also sometimes enjoy my other hobbies. However, upon further reflection, I think I must be depressed because I can't do anything. I sleep 16 hours a day, but is that from depression or because I have tr...

Change

This is a vent blog, but maybe it will give some insight into the types of changes that are hard as an autistic person: This week has been a barrage of change. I notice the tiny changes that I'm told allistics don't notice, and there were also a lot of bigger changes. First, I got a new student, which is a pretty common change; it happens about every 6 weeks. Then, I tried to do a lesson with an existing student, but our software wouldn’t work. Work told me the software had permanently discontinued service to our company, and I had to download and learn a new software, so I did. Several days later, though, they told me that the original software had been reinstated. This week, 4 lessons got rescheduled by students, my roommate was coming and going on a new schedule, and I was sleeping on a new bed. I started a new major project for work, and service techs came with noisy drills and disrupted my routines. I'm working way more hours than I can handle, and it's t...

Increasing my Testosterone Dosage

TW: Body changes, sexual changes, suicide mention   I started low-dose testosterone on February 1, 2016 . My step-dad had just taken his own life, and I felt the need to take control of mine. I was on testosterone for a long time before I was sure that I really wanted to be on it- that it was the decision that would reduce dysphoria the most for my nonbinary self. Part of this indecisiveness came from my autism; I've always had trouble making decisions due to being overwhelmed by the options and fearing regret. I talked a lot with my therapist about my uncertainty around testosterone, and the ongoing theme was that I was happy about the current changes; I was just afraid that I would regret future changes. So, I stayed on testosterone, reasoning that I could always go off of it if the changes started causing dysphoria from being too masculine. Since then, I've started trying my hand at online dating. Through answering the many, many questions on the sites, building my profil...