Being hospitalized brings up such mixed emotions. In a way, it’s a relief; you get a break from life for a while. But then you realize that when you get out, life is going to be the same, if not worse. Missed school, missed exams, late bill payments. Whatever anxiety was reduced quickly comes back tenfold.
As I rode in the back of the ambulance for an hour and a half, my mind kept coming back to two things. The first, why the fuck do these people care about me? I didn’t get it. Why did my friend care enough to take time out of her day to bring me what I needed? Why did she care enough to comfort me when was scared to go? Why did the therapist care enough to wipe my tears away? Why did my therapist care enough to not give up on me? Why did my psychiatrist care enough to save me? Why won’t they just let me be? Why is it so wrong to die? What good am I to these people, to the world?
The second thing stemmed from a conversation I had with the nurse while I was waiting for transport a couple of hours prior. In our conversation, I told her about my writing work with HealthyPlace, my articles on DID. I’m normally very hesitant to share my professional work with anyone on the outside ever since it was used against me. But I trusted her, so I told her about my diagnosis and my writing.
She read through a few of my articles. Then she stopped and asked if she could ask me a question. I told her it was okay. Then she asked me “why don’t you take your own advice?”
It took me a minute to process. I understood her point. I’ve spent the last two plus years writing about DID, sharing ways to improve communication, work with your system, ask for help. I gave people with DID hope that life could be doable. Yet I had done very little of what I had written. I was giving others hope when I myself was hopeless, telling others to do things I gave up on doing. Why? Because I was different. Because I didn’t think I was worth it. I wasn’t being realistic with myself or with anyone else, and that bothered me.
I held on to both of those thoughts throughout my entire hospital stay. People care. I matter. It probably helped me get through the hospital stay more than anything else did.
I realized early on that the hospital wasn’t the place for me. The first night when the psychiatrist did my intake, she not only made me feel guilty for leaving my brother, but she also didn’t know what DID was. Instead of explaining it, I told her to forget about it. I didn’t have to energy to fight her on anything, or to educate her on things she should have already known. I told her about my heart condition, and my need for sodium-laden fluids. She told me they didn’t do special diets there, and I’d have to deal. At that point, I was done.
The only positive of hospitalization, aside from the friends I made, was being weaned off of my heart medication. The psychiatrist I spoke to the following day agreed that the medication can have severe side effects in rare instances, and can cause increased suicideality and worsening depression. While I had that before the medication, I certainly didn’t need anything making it more apparent. I appreciated that this psychiatrist listened to me instead of brushing me off as knowing nothing.
I did feel a little bit better once I weaned off of the medication. I was still suicidal, and still very much depressed, but I knew that staying inpatient wasn’t going to help that in any way. I had already been there a week, and it was hell. I wasn’t allowed to leave the floor because I was considered a fall risk. I couldn’t go to outside groups or go to the cafeteria for meals. It was isolating. I called my friend every night. That helped me get through. I knew she couldn’t visit because I was sent somewhere considerably far away; it hurt, but I understood it. I cried the first two nights I was there, but after that, it got easier. I learned of her son’s plan to come in an armored truck and help me break out; I halfway wished that plan was possible.
I was placed as a dual diagnosis patient — which I had to explain several times that I was there for PTSD, not for substance abuse (which, unfortunately, I just discovered they have added DD to my medical record). Most patients there were dual diagnosis — a telling sign of the opioid crisis and its aftereffects. Psychiatric facilities here now have more patients with drug or alcohol abuse than they do general psych. It definitely changes the experience, and the needs of DD patients become priority, at the expense of other patients.
They wanted me to stay longer. I knew I wouldn’t be able to do it. I was starting to get stir crazy. One of the patients had become indirectly threatening towards me. It started to feel more unsafe as the days went on. I did everything I was supposed to, so they discharged me, with an appointment the next day for intake at the program I was in before I was hospitalized.
It wasn’t as easy to come back to life as I thought it would be. I felt like a failure. I had to restart program. A program I had been in since August. I saw so many people come and go, and I was still there. And now to be there again, starting all over. Why can’t I just get over everything already? Why can’t I just be cured?
I wish I could say I climbed out of rock bottom, but I’m not sure I have.
I care. You matter. That’s it, KJ.
And you know this: if we swapped chairs, you would say the same to me.
Bringing an extra chair to wherever you are. TS
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I would say the same to you because it’s true for you. Sometimes I’m not so sure it’s true for me.
An extra chair sounds nice. I can carry one of those fluffy ones.
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So I just spent ten minutes looking at fluffy chairs!!! I love them! I want to call them pouffes!
Know that I throw popcorn at you every single time you doubt my friend Crystalie. Ha! TS
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Fluffy chairs are awesome.
And I love popcorn. I will gladly catch it.
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Hi, KJ! So glad to see you in print again! And a great article (that will help me!)
https://www.healthyplace.com/blogs/dissociativeliving/living-with-did-dissociative-living/2018/01/why-its-difficult-to-ask-for-help-when-you-have-did/
We are halfway through winter today! Hugs TS
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Hugs. How awful they couldn’t accommodate your medical diet for POTS…that was dangerous and irresponsible and could have thrown you into medical crisis. Ugh.
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Exactly! Fortunately they had endless saltine crackers, so I consumed way too many of those, plus mixed salt packets in cups of water to get by.
The night nurse happened to be familiar with POTS and was astonished they were not accommodating anything for it. They could have prescribed sodium tablets, if anything.
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I have my salt tabs as a prescription on my records. Maybe it would be good to get yours as such, even if you buy them through Amazon, in case you ever have something like that again. How truly awful. I hope someone complains about them.
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That’s a good idea. I’ll get them as a backup.
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