I’ve done a lot of things today that cause me anxiety (hello University and the saldo of my bank account), so what could be a better moment to finally do one more: tell people what’s going on in my strange head at the moment.
At first I need to apologize once again. I haven’t been able to do pretty much anything since, well… since the year turned, I guess, and now it’s August. My sense of time is gone. I crashed pretty hard and had to drop everything - my studies, my thesis, my friends, my martial arts, my teaching, and finally even my job. Now I’m trying to once again pick up the pieces and see what can be salvaged. It’s exhausting. The last few years have been nothing short of nightmarish in the field of my mental health.
What’s wrong with me then? As you might remember, I’m bipolar, and lately I’ve been in the grip of a crippling depression that’s lasted for years. I also suffer from severe anxiety and have PTSD, which causes its own problems from panic attacks to uncontrollable shaking. Add to this my spine which is basically fusing its vertebrae together (if I stop moving and taking my meds, that is exactly what will happen) and several other lesser concerns with my health and social relationships and what we end up with is the human wreck that I currently am.
I still haven’t given up though, I’m going through psychotherapy (again/still) and I have a small army of mental health professionals trying to figure out what to do with me short of locking me up (that’s been on the table too). Right now I’m at the tail end of a month-long treatment regime where they’ve been trying to set my brain straight with magnets. As you might recall, they’ve poked at my head with electricity and several different modes of therapy before, and since the ECT (Electroconvulsive Therapy) took a heavy toll on my memory (which perhaps caused more problems than it fixed), the doctors thought that they’ll zap me with something a bit more benign this time.
TMS (Transcranial Magnetic Stimulation) doesn’t have any of the severe side effects that ECT has, you don’t need to be anesthetized during the treatment and it’s advertised as a “painless” treatment. Well let me tell you that painless it is not, at least not for me. In other ways it is a lot more hassle-free, but the first two weeks I felt like someone was either stabbing my eye with a hot poker from the inside of my skull or that I was getting root canal on all of the teeth in my lower left jaw simultaneously. The treatment cycle lasts for approximately a month and I’ve received it five days per week about half an hour at a time.
The treatment is given in a chair that is suspiciously reminiscent of a dentist’s chair. At first the nurse or doctor glues this sensor on your face and then pokes your head with a metal stick, drawing marks for the camera that follows the sensors on your face and in their hand. The camera looks a lot like a slightly concerned, benevolent alien hovering over you and trying to figure out what kind of fascinating little animal you are. With the sensors and the alien camera (and in my case, also previously taken MRIs) they can pinpoint the location where the magnetic stimulation will be directed to.
When they’ve made sure the magnetic coil is in the right place, they start with the impulses: a few seconds at a time followed by about twenty seconds of rest. Apparently my facial nerves are weird and this pain-free treatment is usually everything but pain-free, but it’s manageable. The hospital where my treatment has been given gives you the option to try to watch TV at the same time to distract you from the root canal, which basically has just made me really hate daytime TV with a passion. Still, it could be a lot worse. Compared to the ECT it’s a walk in the park.
During treatment the pain levels vary massively. Sometimes it’s the stabby stab to the eye and sometimes it’s like someone’s lightly scratching your scalp. The weirdest part is how it somehow scrambles your brain and makes it impossible to focus on any one thought. It’s like your thoughts are in freefall. It resembles the weird semi-dreaming state when you’re just about to fall asleep and your brain is firing impulses and images all over the place but nothing really makes sense. Quite a trip.
After treatment I’ve had some headaches but compared to my usual migraines they’ve been light. The scrambled thoughts follow you for a while after the treatment is over, but it’s nowhere even close to the state after ECT when you can’t really remember who or what you are. A few minutes sitting in the cafeteria helped me to collect myself and I was allowed to go home without a chaperone. After ECT I wouldn’t have known where I lived, after TMS I could find the right tram stop after only some light confusion.
Well, has it worked? I think it’s too early to tell, but I’m trying to set myself up for success and kind of pretend it works and see if it sticks. I still have three treatment sessions to go through, but I’m ending my sick leave and trying to get back to, well, life one small step at a time and see how it goes. I might write another entry after a couple weeks and try to analyze how my mental state has evolved. Right now I’m mostly just confused and slightly apprehensive and very anxious, trying to channel it all into hope somehow.
So now you know what I did last summer. Here’s to hoping it works.