Freezing out but my room is a sauna
It’s 10 degrees out or there abouts. I had to turn down the heat because my room is so damn hot. I can’t stand the heat. I am grateful for it but I rather be cold. It is what I grew up with as my room didn’t have a radiator. I had to have multiple blankets on me to keep warm during the winter. I didn’t mind. I liked it.
I can’t sleep mostly because of pain. I had a study interview today about chronic pain. It went well, though we went over the time by a half hour. I didn’t mind. It was good talking to someone about my pain. They wanted to know more about my use of social media and how I talk about my pain and so I told her. It was a good interview. I hope they learn what ever it is they are trying to learn.
I am really tired but I just can’t sleep because of the heat and pain. My foot is killing me. I had to have something to eat so I went downstairs. That aggravated my foot. Then I went back up the stairs which didn’t help matters. I took another pain pill hoping to speed up the other two that I took. Lately, the regular pain meds are having no effect on me as they don’t make me sleepy anymore. It still works for my pain but it seems that it takes longer to do so. I am worried now that I am tolerant to the meds and need to find something else.
I went to bed around midnight and it’s still hot in my room, despite lowering the heat. I didn’t lower it too much, just one degree. I fell asleep and just woke up now, 6 hours later. That must be the latest I have slept in a while. I am not going to go back to sleep because I need to leave the house around 0850. I might take a shower, though I am really not wanting to. It’s going to be freezing in the bathroom as there is no heat so I will take it tomorrow when the temps are below 20 degrees. It’s 12 degrees right now. I still haven’t decided if I am going to wear my long johns or not with my jeans or sweat pants. I haven’t decided what I am going to wear. These decisions are always hard for me.
I might make a cup of tea just so that I have a little caffeine on board. Think Earl Grey would be nice. I haven’t had that in a while. I still have to pack my bag for the hospital. I have decided to use my suitcase so I need to transfer every thing from my backpack to it. Then I need to stuff my blanket in. I think I will put the blanket in first and then put the clothes on top of that. I might be snowing on Monday so I think a suitcase would be better for my travels than my backpack and bag. I still will take a backpack for my journal and coloring books. That might kill some time while I am there and don’t want to go to group or something.
Today would have been the day I would try to kill myself. I feel defeated that my plan didn’t work out and that it would just make me sick rather than kill me. I hated when I have botched plans. It really sucks. I just feel like a loser. Now I got to figure out another way to die and hope I succeed.
I have thought about getting a haircut but I am getting low on funds and it’s going to be two weeks before I get paid again. I still need to pay for my prescription that I will be picking up today. And I need a refill on my Neurontin as I am running low. I need to email my neurologist to get that script because my PCP’s office won’t prescribe it to me. Ridiculous. I hope she will allow me to take 1200 mg at night as I have been taking that to help with the burning pain. It seems to work at least 24 hours so I have good coverage. Some nights I don’t need to take it because it’s not every night that I have the pain.
As I prepare for my hospital admission, I got to take my meds with me because I don’t want to take a million pills. I also need to fill out my medication list and how I take my meds because I don’t want there to be a hassle with my pain meds. I really wish the doc wrote that I take 2 tabs every 6 hours rather than 1 tab every 4. 1 tab doesn’t do shit for me. We’ll see how the docs at the hospital decide to write the order. They all have the same computer system now so it’s going to be difficult to get my meds the way I take them. It’s so frustrating. I’ll also have to prepare for taking my psych meds differently than what I take them at home. Man this is going to be so annoying. I am going to be a zombie in the morning and a night owl at night. Not looking forward to this at all. I am going to ask my psych today when I see her if I really need to go in or not. I know I am still feeling suicidal and the hospital will be a respite from my urges, but I just hate the medication piece of the puzzle. It always gets fucked up. And it’s frustrating to fix because I usually have to wait 24 hours for the changes to occur. Annoying!!