pain and sleep ramble

Got things done today

Last night I started the process of changing the bedding and sheets on my bed. See, half of my bed I use as my “office”. It has books, journals, my laptop and a couple of other items. So clearing it off was the real problem to changing the linen. Once I did that, I got the comforter off the bed and washed it. I knew it would take a couple cycles to dry in the dryer. I already had a set of clean sheets. Trouble was that today after I took my shower, I didn’t want to do anything. I had a rough night sleeping and thought a shower would wake me up. It had the opposite affect. But once the comforter was drying, I knew I had to change the sheets. I forced myself to do it and it went quicker than I thought it would. Usually I only have one clean set of sheets because I always put the clean sheets somewhere and forget where I put them. But the last time I washed my sheets I put them in my bureau where it wouldn’t get lost and hopefully the clean smell would stay on it. Score for me.

This is hard because it always hurts my back when I do change the sheets. It would be easy if I didn’t keep my bed as an “office” but it is easier to work from my bed than from a desk. I know sleep docs would have a fit if they knew. But I won’t see them as I know my problem with sleeping comes from my mood disorder than any other cause. Last night, I slept a few hours and was up at 0230. I wrote a nice blog, something about demons and that is all that I remember of it. I was in a lot of pain when I wrote it and also was a little drugged up with my pain meds. But I had to write. It was the only way I would get back to sleep. Around 7ish, I was finally ready to call it a night. I wish my sleep schedule would be normal but when I am in pain, all bets are off. And I was in so much pain last night it woke me up. Then I started getting cramps in my neck that just wouldn’t allow me to go back to sleep. It was a really bad night. Probably the worse since being home from the hospital. And I was so angry at my treaters. Angry that they had kept me alive. Angry that I was in so much pain and couldn’t sleep. Angry that I couldn’t vent with someone because it was 3 in the morning. I was so WTF at everything.

I am to have a lunch date with my aunt this week. But I don’t think it is going to happen because I have my appointment with my PCP this week. It’s an appointment I am not looking forward to. My blood pressure is still borderline high to high at times. It seems to be worse in the evening. I don’t know why. I will mention that to him as well. He isn’t going to be happy with me because I gained a few pounds while in the hospital. I have been trying to work it off but it’s been so difficult as all I want to do lately is sleep because my nighttime sleep schedule is so fucked up. Maybe I will go for a walk tonight. It can’t hurt. Well, I suppose it can. I just never know what will jack my pain up. Sometimes it is over activities. Sometimes its doing NOTHING but resting. I just don’t get it. I know that if I go up and down the stairs more than a few times, I will hurt. My ankle just doesn’t like the normal flexion it is supposed to have. But I really have no idea why I woke up in excruciating pain last night. I am so baffled. I know part of it is because I was sleeping on my left side (I usually sleep on my right). But I was in a deep sleep and for me to be woken up in severe pain, I just don’t get it. I wish I could talk to some doctor about it to help me figure it out. My PCP is useless when it comes to trying to figure out my pain. But then, he is not a pain specialist. And the pain specialists don’t have any answers for me either. So I am stuck with figuring it out on my own. I need to become a pain expert and study pain but the brain is so damn complicated. I am lucky if I remember the structures of the brain. I can’t even remember the amygdala from the gyrus. It has been too long since I looked at it and its pathways. My memory is not the same as it once was. I used to have photogenic memory. Now, I am lucky to remember things such as when I had lunch or breakfast.

They say not to use the word “demons”

They say not to use the word “demons”

In recent news about suicide, attempt survivors are asking that the word “demons” not be used and that the real “thing” be used. I forgot the term as it was many days ago and I don’t have that much of an attention span that I used to have. It got me thinking about my blog as the word “demons” is used.

I don’t really care what these people say, I am still going to have my blog and though I don’t talk about the “demons” in my blog, I mostly talk about how I feel, which is often suicidal. These suicidal tendencies often come out in the middle of the night, when I can’t sleep, and when I am in pain. I would write some horrible stuff and get a lot of people concerned.

Tonight the “demons” are out. I am hating everyone that has kept me alive the past few weeks. Though I could kill myself now. It doesn’t make a difference with the time frame. I am in excruciating pain and just want to end things. I am so tired of fighting pain. It used to be just psychological that the fight was about. Now, it is both physical and psychological and I am sorry but I can’t keep fighting both. It is too hard. I know that I will feel better in the morning, when I get a few hours of sleep. But right now I could write an email to my psychiatrist and tell her how much I hate her for keeping me alive. I could text my therapist with the same hate. But instead of doing that, I am just going to blog until I fall asleep.

What makes my life so special that I can’t commit suicide? Robin Williams was special. He did the deed. So do a lot of people, every year. They say that 39,000 people will take their life in a year in the US. And the number of attempts are in the hundreds of thousands. Or maybe it is a hundred thousand. We just won’t know because it is so underreported. Many people survive their attempt and often don’t seek medical attention afterward. It is so hard to kill the human body. It boggles my mind when I hear of homicide, though. Seems like that should be higher than suicide but it is not (and please correct me if I am wrong).

But aside from the global effect of Williams’ death, I still feel like it is my turn to die. I really don’t want to live knowing I am going to be in pain the rest of my life. It’s too much of a burden to think about. But I am lucky that all I need are a few pain pills to ease my pain. It doesn’t get rid of the pain entirely, but just enough that it takes the suicidal feelings away. I just took these meds but it takes a half hour or more to work. Chronic pain is a big risk factor for suicide. I know because I live with it every day. My treaters know that. That is why I am hating them at this moment. My foot is throbbing up a storm. I don’t know if it has to do with the weather change. My body can’t tolerate huge gaps of temperature changes. But I have no control over that and I am not about to move to another state. Yes, moving to California might help my pain but it will be isolating because I have a few friends there and most of my family are here. Isolation and being suicidal do not mix. That is why I stay at home. It is a preventative factor for my suicidal brain.

I don’t know why I am up at 3 in the morning. I woke up in pain and still my pain meds have not kicked in. The “demons” are still around me, wanting me to try and take my life. But that will involve getting out of my cozy bed and I am too tired and in too much pain to do so. I guess you can say I am too lazy to take my life. So I write about it instead. I won’t write about the methods that have been swirling around my brain. But one of them include the method Williams chose. He is a brave person. It takes a lot to kill yourself. I am not giving him praise, the media has already done that. But I am happy for him. People in the hospital didn’t understand that. And maybe you might not either. I am happy for him because HE is no longer suffering. HE succeeded where I am a failure. His suffering has ended while mine is still going on.

He died as a complication of depression. I like that term. “Complications of depression” yes, I like that term very much. But I doubt it will be used for my death. The throbbing has escalated. My foot is now on fire. And there is no extinguisher in the world that can put out the fire. So I take another pill. I hope that I am sleeping soon.

Do I

Do I

“Do I” is a song by Luke Bryan, one of my favorite male artists. Every time I hear the song, I wonder if my therapist and I are still a good fit. I think we are as we have been together for so long, but I often wonder if I am too much for her to bear or that I am a burden to her.

I went to Starbucks for the first time in four weeks. All my baristas were gone from the Davis location. I was so bummed not to see familiar faces. I hope they were off that day or just on vacation. I will be super bummed if I have to deal with new people. I will go there tomorrow and see how they make a clover coffee. I won’t order their reserve, just the Pike. I seem to like that better than their regular iced coffee, probably because it is made fresh.

I am still feeling good. Today on Mental Health chat on Twitter, the discussion was bipolar disorder. I have been diagnosed with bipolar as I have had some hypomanic episodes. I have never been full blown manic. I had one episode while I was in the hospital. I was really jocular and upbeat. I was also really racy and despite taking Ativan regularly, it still didn’t alter my mood. This lasted until I took some pain meds and then I crashed, hard over this past weekend. It was fun while it lasted and I wish I still felt that great. I felt like nothing could touch me. Suicide was furthest from my mind and I felt like I was on top of the world, even though I was in a psych hospital. It was very strange. I was expecting to go down, but I wasn’t expecting to be “that” down. I was really tired and just needed to rest but I was too restless to actually sleep. I took a prn to calm down some and finally was able to get some rest. Everyone was telling me I looked tired and down. With my anticipated discharge on Monday, I was thinking that it was not going to happen. I really didn’t want to leave the hospital feeling the way I did this weekend. It was such a major depressive episode that I didn’t want to chance leaving the hospital and then acting on my thoughts. So I had to practically beg to stay one more day. My case manager asked me why I wanted to die. I told her to end the pain and the indignity that I was feeling with my disability. I really just wanted to say “are you fucking kidding me”? This hospitalization, I experienced everything I do when I am home. I crapped my pants, leaked urine, was suicidal more than a few times, and was overall, severely depressed. The hypomania was a godsend. I just wish it lasted longer than it did. But it never does and the longer it lasts, the worse my depression is. I think I had a total of 12 hours of it. Not long enough to do any financial damage or anything, but enough to let me know I was alive again, that something inside me wants to keep going no matter what the suicidal thoughts might be.

My writing partner has suggested that I write a book about coping as a suicide attempt survivor. I have been giving it some serious thought and I think I can write it. I don’t know if I am going to write it in blog form or book form yet. Depends on how much I can actually write. But a large part of what works for me is already out there but people don’t utilize it. For example, I gave the crisis response plan (see this blog about it) to one of the patients because it was less confusing than what the hospital was giving out about distress tolerance. The hospital uses DBT type of works, which is fine for some people but may not fit for everyone. And, who the fuck is going to look at a piece of paper when they are in crisis mode?? I know I am not. I have been there too many times. But I have found that the crisis response plan has been helpful to me since David Jobes uses it in his work with suicidal patients.

One of the mental health counselors was interested in my book and the SSF, Suicide Status Form (see my comparisons of psychological pain scales for more information). I wish I could publish it on my blog but it is not available in electronic form and I would be violating copyrights. I use this in my therapy when I am suicidal. It helps because it gives my therapists some way of knowing which areas are causing me to want to die. I think it would be wonderful to use in an inpatient stay but I don’t get to make those types of decisions. Anyway, this MHC and I were talking about it and it was so good to talk about clinical stuff with someone again rather than just stuff about me. It was like being back in academia again where exchanging ideas is so important for learning. I just wish my treatment team was on board with my ideas for my treatment than just saying that I have to stay away from suicide stuff. I told them that I can’t. It is apart of me like breathing. I am always thinking about what is best for me and I am always searching for an answer to end the suicidal thoughts. Just telling me to stop is not going to work. I read clinical stuff as well as blogs because I want to keep abreast of the latest research. Even though I am no longer a member of the AAS, I still keep up with the suicide research. I wish I could afford their membership but I am on such a fixed budget that I can’t. I also would love to have the archives of suicide research journal but again, I can’t afford membership. It totally sucks. I was hoping that the sales of my book would provide me with additional income but it hasn’t taken off the way that I wanted it to. I have not reached my goal of selling 100 books, though I am half way there. While I was in the hospital, I sold two books. Not my personal copies, just through Amazon. I did bring one with me to give away but I never did. I still have it. My book signing has not gone well. It brought extra income just to buy food and the essentials. The struggles of the writer. I just have to find the right audience to get my book sold.

I am planning on getting my book reviewed by the AAS (American Association of Suicidology). It will be sent out next week along with a book for my editor. I have been meaning to send it out but things always seemed to get in the way. I wasn’t planning on being in the hospital for so long. I really thought I was going to stay a few days and that would be it but they had other plans when I told them I was going to kill myself when I got out. Hospitals tend to frown upon that. I put them in a “bind”. Sorry, but that was how I was feeling. I really was in bad shape and all that I was feeling felt normal to me. Looking back, I see that I wasn’t as rational as I thought I was. I guess that small overdose was the wake up call for my outpatient treaters to put me in the hospital.

still inpatient 2

It’s Sunday and I am still here. I probably will be here for a while as I found out last night that there is no set discharge date for me. This upsets me. I talked with my pdoc and told her that even though she is on vacation, I want to be discharged and that I will email her every day until I see her on the 22nd. I am still having suicidal thoughts and stuff but they are lessening. I think the new medication is helping me. I really want to be in my own bed again.

Since I have a bunch of time on my hands while I am in here, I have written a lot in my journal and written a few letters to my therapist. She is on vacation also. I really miss her and hope that when I get out of here I can borrow my sister’s car and see her. I haven’t seen her since June. She misses me as much as I miss her. I am trying my best to get out of here and still be safe.

I had an ankle flare up the other day and I can’t seem to calm it down. It is bugging the crap out of me. I had the doc change my medication orders so I take two pills instead of one. This has helped me tremendously. I feel like I can now be better now, least where my pain is concerned.

I wrote out a treatment plan for my case manager last night, I am hoping that it shows that I am trying to work on my issues. I know that this unit cannot work on ALL my issues but I just want to work at least on a little bit so that feel a little better. If I can work on the self-hate and “like” myself a little bit, I think that will decrease my suicidality enough that I can be okay. I will find out tomorrow if this plan is going to be acceptable to my treaters. It is the only think that I have going for me. If they tell me they cannot work with me on this a little bit than I have no other choice than to sign a 3 day and leave AMA [against medical advise]. Course, it might back fire on me and lead to a court commitment but I will worry about that later. Hopefully it doesn’t come to that.

Last night was rough for me as I wanted to write out my will and testament and a good bye letter to my friend. Actually, it was more to write out what I want him to do in case of my demise. My contact person talked me out of doing this. She wanted me to work on a self-compassionate letter instead. I have yet to write this. I might work on that today, though it is going to be difficult.

I had a tough day with family. One of my cousins called and wanted me to visit him but when I told him I was in the hospital, it was like I did it on purpose and didn’t want to see him as he told me in advance he was coming up {he lives in Virginia}. I felt very upset by this. I then told him not to tell my aunt about my being in the hospital because I don’t want her to know. He then flipped out about that. It was like a no win situation with him that just left me feeling upset. Then my sister texted me wanting me to tell her what medication I was on. I just felt like I was being bombarded by family. I didn’t answer my sister’s text.

I talked with my contact person. It was the same one I had last night. She is good and I like talking with her. I told her I was feeling depressed and wasn’t sure if I could keep my safety outside the hospital, which is true. I still am having suicidal thoughts and plans. I don’t know if I would act on those plans but I know that they are still there. I really feel like I should do something. I am feeling agitated and perturbed. I told my contact person that my “normal” voices aren’t there. I am missing them very badly and I think that is what is making me feel perturbed. I hope they come back so that I have someone to talk to. I feel lonely without them.

I am thinking of a good friend tonight. I found out she has suffered a stroke and is in the ICU. Her left side is affected and so is her speech. She is a very religious person so I know that god will take good care of her. I just hope she doesn’t suffer. If you bloggers can send her good thoughts, I would most appreciate it.