Incompetence and needs: A story of transference

Incompetence and needs: A story of transference

My therapist read my Thanksgiving Eve blog and was basically horrified to find that she is inadequate for my needs. She wanted me, again, to see another therapist that was local as seeing someone in person on a regular basis might be more helpful to me. I nixed the idea because I don’t want to start over with someone new. She said it would be more as an adjunctive way. I don’t give a fuck, I am not setting out to see a new therapist. Then she brought up the whole CBT therapist idea. Nixed that too.

It got me thinking about what I need from my therapist. Frankly I don’t know. We have been struggling with my suicidality for so long that it just goes on without a resolution. It got me thinking about the CAMS philosophy and frankly, even though my therapist has been collaborative, she really hasn’t been. She acts more like a friend than a therapist at times. It has been driving me crazy since she took up the majority of the session with her guilt talk, whether it was directed towards me or her, I am not sure. She feels like she is failing me. Hence her incompetence.

There is more to solving suicidality than filling out the SSF forms. Again she brought up if she only knew how to get me to “open up” and write the answers she needs on the stupid forms, she will feel better. But that is not how it works. The SSF just provides you with problems that need solving so that you don’t end your life. The therapist and client are to work together to solve these issues so that life becomes more tolerable rather than intolerable, a “life worth living”. I’m never going to reach that stage of treatment because maybe I am too stubborn to give up my suicidality long enough to find a life worth living. I just go about my daily business of drinking coffee, writing this blog, taking care of my family and then dealing with a stupid therapist twice a week that drives me absolutely fucking insane with her idiocy.

Maybe we have been together too long and can’t see the forest for the trees. We are wrapped up in something and our path has gone so far astray that we just can meet anymore eye to eye. Maybe we are too close because my heart was really breaking today while she was droning on and on about seeing another therapist and how she was basically failing me. Yes, she is a pain in the ass. She is an idiot, but who isn’t really? I texted her that tomorrow will be our last session. I seriously doubt she will take me seriously. I don’t even know what no therapy will look like. I don’t want to know but what else can I do? Go on with a therapist that hates me on some level for calling her out?

Usually you bring up stuff and it gets dealt with and then you move on from it somehow, someway. A few years ago, we were at this impasse. The same issues were covered today. They haven’t moved on because they haven’t been dealt with. I know what needs to be done but I am just too much of a chicken shit. And there we have the needs piece again. I could list them and they would have NOTHING to do with the list from Shneidman. But I feel insecure and my therapist, even though she won’t admit it, does too. That was evident today and it was killing me inside. It broke my heart.

I know I have called my therapist a lot of names in this blog today, but I still believe she is right for me because we have a connection. Granted right now, that connection is a little frail but we are still tethered. The last time we talk about this, we went over Shneidman’s needs. He had 20 of them and I think I boiled them down to less than 10 that affected me, because part of his theory was that frustrated needs causes suicidal thinking. A lot has happened to me this year, more than any other year to date. Problem is that we just talk about shit in circles and we just go around and around because we are just on this merry-go-round that doesn’t have a stop.

People go to therapy for different reasons. I have a whole slew of them that are basically being neglected and possibly fueling my suicidality. I could list them but if you read my blog or my tweets every day you can probably figure out what the major ones are. I know my therapist can’t do shit about my physical pain, neither can my psychiatrist. I have trauma history, a death in my family that still hasn’t been quite dealt with, PTSD that I don’t think is managed, etc. just to name a few. I read blogs from fellow friends that suffer the same kinds of things that I struggle with yet they are dealing with differently. One of my blog friends has severe PTSD and has anxiety that tears her apart at times. My anxiety, though not a principle symptom, has becoming more of a problem lately because of my damn pain syndrome. It drives me to suicidal thinking. And there is no cut off valve when that level has been reached. So far I have managed but I still plan and strategize my suicidal plan because it comforts me to know I have a way out. I still don’t know what is going to happen this week. I know I have put off my plan but it’s back on again because, why the hell not if my therapist is pulling away from me, even though she says she is not.

In my head, I think I have spoiled my therapist. I bring her treats and indulge in her fantasy that I won’t kill myself. Maybe we both are trapped in that fantasy because I am still here either way you look at it. I have tried to bring her the reality my death will bring and even tried to say if I die, here is the help you need to find. I once brought her an article about it that she refused to read. She doesn’t think I will kill myself. Maybe that is what is keeping me going but it is also draining me to keep up this front week after week. I want to die very badly, to get away from myself because there are so many things I can’t stand about me. Being in pain every single day and night is also taxing me. Knowing the fact that my pain syndrome has changed course on me hasn’t helped matters. All I can do is what the voices tell me to do at the end of the day. So far I have ignored them, but one of these days, I will give in and things will finally be at peace. For me anyways.

Sleepless night filled with pain

Sleepless night filled with pain

I slept about three hours last night. I just couldn’t get comfortable because of pain and then I had to drive to my therapist’s office. I got some Starbucks before I left town. The pain was unreal last night. I had like four different types of pain going on in various parts of my foot and ankle. At one point, I had to keep it off the sheets because it was causing pain. I took Neurontin and my pain meds as well as Ativan. You would think that combo would knock me out but it didn’t. I didn’t go to sleep until 0530 or so. I swore if I was still up at 6, I was going to cancel the Zipcar and call it a day.

Therapy went kind of bad. We were talking about all sorts of things which were okay and then I brought up my book and how I should probably put a picture of myself on the back cover. I hate pictures of myself because I feel that I am really ugly and fat. I hate the way I look. She immediately goes into therapist mode and I am “diagnosed” as having body dysmorphic disorder. She wants to do exposure therapy to help me see that I am not what my head believes. Sorry, all my life I have been called ugly and fat. I don’t think exposure therapy is going to help. She got on her high horse, like this was going to be the mission for the next few weeks. I dread this idea. For one, I hate taking selfies. They never come out right and if I try to smile I just look like a dork. I think I look better with a serious face. Anyways, I don’t have to have a picture on the book but I was entertaining the idea.

I hate looking at myself. Even when I do have a photo of myself on Facebook or Twitter, it doesn’t last long. I can only stare at myself for so long before I get sick of it. So then I change it to a logo of some sort, usually sports related. I can’t even stand looking at myself in the mirror. I just feel so hideous. I even told my therapist today, I can’t believe she likes to look at me for 50 minutes.

I gave her some of the pumpkin fluff that I made. I actually gave her all that was left because I couldn’t eat it anymore. It was too rich and I couldn’t only have small portions of it at a time. I had some of it before filling the container with it. It was so yummy. But I won’t be making it again. I much prefer cake.

The ride home went well. I took the highway both ways so I made perfect time both ways, though I nearly got into an accident when I reached my town. Fucking driver just rolled through a stop sign and kept going. Idiot. I came home in plenty of time to return the car. But before I did, I had to eat something. I hadn’t had anything since 5 when I had some apple pies and whatever I had with the pumpkin fluff. Not enough to call it a meal.

Knockout

Knockout

I went to Harvard Square today with the hopes of meeting my Twitter buddy. I did a lot of walking for an hour but it was worth it. I must have spent at least a half hour walking around the bookstore, just looking at books. I came across one called “Knockout: Mental in Massachusetts”. Its author is B.C. Scott and it is just as anonymous as the author wanted it. It was a fantastic little book, just under 120 pages. It was written in the style that my second book is, roughly 850 words or so per chapter. It was a quick read and I loved it. The person has an eating disorder, bipolar I, BPD, and PTSD. Her life was interesting as she was untreated for her manic episodes for most of her life. She was rarely down and when she was down, thoughts of suicide went through her mind. She thought of it and if she attempted, she doesn’t say. I know a lot of Bipolar I’s that think of killing themselves but never attempt. I hope she is one of those.

I didn’t get to meet my Twitter buddy because he had to see a patient at the hour he was free. He felt bad but I understand. I am literally two stops away from him so I am sure I will see him in the future. Plus, I love the bookstore that is a little ways from his office. That is where I found Knockout in the psychology section. It wasn’t supposed to be there but I guess fate had it there for me. I wasn’t going to buy it at first. There was no price tag on it or even a UPC code as it was made “on demand by Paige”. It’s their version of Amazon on demand books, self publishing. It cost $20 so I know I am going to sell my second book for $25 as it will be close to 200 pages. I love how the author writes about writing in her book and where she goes to do her writing. She doesn’t sound that much different than me, except she has the support of her family with her illness behind her, mostly her parents. That is something that I will never have, but I have learned to live without.

On the way home, it started to rain. I was going to stop in Starbucks for a coffee and something to eat but my leg started hurting and there was a long line. I couldn’t bear it so I left. I wait for the bus in my Square but it never came and I was really hungry. I just had a bagel at like 10 and then a pumpkin scone at Starbucks while I was waiting for time to go by to go to Harvard. I hardly ate anything and my stomach was getting angry with me. I really wanted steak tips but the line at the restaurant I went to was again long because it was dinner hour. So I went to Chipotle for a steak burrito. It was very good, even though I got sour cream and guacamole on my face while eating it. My sister sent me pics of quiche so when I went home (an hour later because the bus was late), I had some of that.

I emailed my psychiatrist early this morning because I didn’t have my trilafon. I now know it isn’t her fault so I told her stupid Epic was the reason and could she please call it in. I provided the pharmacy’s number and within an hour, my script was ready. I picked it up on the way home. My allergies were bad so I also got some Benadryl. It’s make me drowsy as I type this because it’s the gel cap kind. I only took 25 mg because I knew it would make me sleepy. The other Benadryl that I have is expired so I am not sure it has been doing anything. It has helped me sleep but nothing for my allergies.

I had therapy this morning. We talked a lot about the concerned asshole. She is the one that gave me the idea of writing the letter to this jerk off. She doesn’t want me to give up my blog either. I was talking to another blog reader who went through the same experience I went through. She doesn’t want me to give up my blog because of this asshole. I am sure the jerk is probably saying “better to be angry at me than be dead”. FUCCK YOU I say. You only prolonged my death. There will be other episodes, except you aren’t going to know about them. It just won’t be this weekend, you fucker.

I bought a new album today to help my mood. It’s called “Fighter” by David Nail and this guy is unreal. I love his songs and one of them is a Lady Antebellum song on their 747 album, I think. He sings it so good. I love Lady A and I wish they would stop giving away their songs to other artists. It wracks my brain because I am singing the song with Lady A but it’s not Lady A so it’s driving me nuts!! Like Martina McBride has their song “It Ain’t Pretty”. Every time I hear it, I am wondering when Hilary Scott is going to come in (Lady A’s singer). I still can’t decide who sings it better. I love Martina McBride but her vocals just sounds strange after you hear Hilary Scott’s voice.

I want to thank my readers for being there (except the one that called the cops, you can go to hell). Your support makes this blog worthwhile and doesn’t feel like I am wasting my time with it.

Writing Itch 2

Writing Itch 2

I have been trying all sorts of things to get my mind of the writing itch, I even tried writing in my journal but nothing has scratch it so it calms down.

I am listening to the ball game because it usually calms me down, even though I get excited while listening. They have a new player on the team and I am excited to hear how he pans out.

I have been trying hard on what to write and I still got nothing so this might just be a rant of sorts or just a random thoughts put on a computer screen. Today I read about how my favorite actor, Wil Wheaton was having trouble finding work as an on-screen actor. He really misses being an actor. I miss seeing him on the screen. I wish they would give him a chance because I really think he is a good actor. But I guess as young actors age, they don’t find work so easily. He is busy writing, which has kept him busy. I guess it’s better than doing nothing. And I know how hard it is to write. But he is more creative than I am. I write every day but I don’t think it’s substantial. I have questioned whether what I write really helps people because I don’t get many likes like I used to and my comments are down.

I don’t know if people reading this right now have read my previous blog of the day. I am reading a chapter on the psychologist/psychiatrist Adler. He has a unique perspective of how to treat diagnosis by treating the whole person rather than the diagnosis. It’s kind of what my therapist has been doing, treating me as a person rather than a diagnosis. My psychiatrist also does the same thing. She has been the most liberal psych that I ever had, but the she has been the ONLY outpatient psychiatrist I ever had. I say liberal because she is not a drug pusher like some psychiatrists are. She rather you take less medication than more. That is why I was kind of shocked that when we restarted the Zoloft, I thought she wanted me on 50 mg and instead she wanted me on 100 mg. That is the only time that we kind of disagreed but I am glad I am on 100 mg because it is helping me cope better. It hasn’t really “cured” me of my depression, like most medications, but it does relief some of the symptoms.

I was reading an old notebook that had some journal entries about therapy way back in 2001. It talked about my therapy sessions and what was going on then. I found that despite the years, I am no better. Even though I was reading some blogs from last year, things are the same as far as being depressed and suicidal. I want to “fix” myself but have not been able to find the right treatment even though I have been in treatment. Medication and talk therapy only goes so far. I think that if I wasn’t in chronic pain all the time, I would most likely be better off. I guess you really have to be careful what you wish for because there were times before Cauda Equina Syndrome entered my life that I sometimes wish I was in physical pain than in emotional pain. I had no idea how debilitating physical pain could be. I thought it would be “easier” because there are medications for physical pain. But the daily pain that I have is so exhausting. Even with me trying to take a shower this afternoon was tiring and painful. I could barely stand for 10 minutes to shower. I had to sit for a little bit before I could shut the water off and dry myself. It was terrible. I don’t wish this on my worst enemies. I knew back then in 2000 that I had a bad back. I never should have gone to a chiropractor but I did because it was some relief. I should have stopped going when I was better but they just suck you in for more adjustments because it’s “better for your health”. Yea, right. I wouldn’t recommend them for shit now and especially if you have herniated discs in your back or neck. That is just causing trouble.

This month marks sixteen years that I have known my therapist. We met for the first time but unfortunately, I couldn’t see her right away because of insurance issues. I was so thankful that in January she was still accepting patients. I really don’t know what I would do without her. She has been my voice of reason at times, even though she can be a real pain in the ass as well. She has saved my life numerous times, by telling me she cares for me and sometimes she loves me. I know it’s a kind of love that two people have because I love her, too, though I don’t show it often. I was pretty much in love with her the day I met her. I remember a session where I finally admitted my feelings for her and the next day I saw her, she wore a mini skirt and her legs were and are gorgeous. She doesn’t wear skirts anymore, least not short ones since she is married but good god almighty, I could hardly speak that day. And I was totally like, you got to be kidding me. I got her a birthday present that I will give her at the end of the month when I see her again. Her birthday is this weekend. Got to love Google for helping me find these things about her.

There is a LOT of stuff that I have given her over the years. She must have a file cabinet just for my letters alone. I used to write to her all the time when we were seeing each other. That was when I had a car and she was local, not out in the boonies like she is today. I do miss seeing her but talking on the phone is fine. I think it’s better because I have more face to face contact with her when I see her than I did before. I still might look at the floor than talking with her but there is definitely more face contact. Before I would just spend the entire session looking at a chair or the floor or something on her rug. Anything but her face. It was too scary because I didn’t want the connection. Now that we have the connection, I can look at her without worry, though it still is scary at times.

I sent her the link to my blog again about Chronic pain and suicidality. I want her to read it before our next session because I think it’s important for her to know. She didn’t have time to read it on Monday or before today’s session. If she doesn’t read it, I feel like why bother sending her stuff. Same with the letters. That is why I don’t write them anymore because she doesn’t read them or it takes her a long time to get to them. I know she only has a few minutes between sessions but I just feel like she is missing out on my work if she doesn’t read what I send her. I rather her be late to session than her not reading my blog or letter. If I am putting effort into this thing, the least she can do is try to read it.

I counted my antipsychotic pills (trilafon) and found that I will run out before I see my psychiatrist again. I will have to email her to send another script sometime next week. I thought I wouldn’t run out but if I am taking 2 a day, I will run out. I need to take 2 to keep the paranoia and voices down. I find that it works best if I take it twice a day than once a day. I know my psych just wants me to take it once a day but it doesn’t cover me the whole day. I have tried to just take it at night because that is when the voices are at the worst. It just doesn’t seem to hold me and then a few hours later I will need another dose because I am still up battling the voices so I can sleep. I don’t want to bother her as she is on vacation. She did ask me if I was set on meds and I thought I would be okay with the trilafon but I miscalculated. 30 pills only gets you so far in two weeks. Some days I need 12 mg because the voices are so damn bad. I have been getting musical hallucinations lately that have been god awful. I hear a song over and over like it is playing but it’s not. And it plays the entire song over and over. I have tried listening to music to stop it from playing but it doesn’t help. Then there are a battle between what is in my head and what is actually playing on my MP3 player. It sucks. Least the lyrics haven’t changed so that is good. Sometimes the lyrics will tell me to do things, even if I have heard the same song a million times. It’s just odd. But it’s just part of the psychosis. And it’s worse at night than during the day. Everything is worse at night. My pain, physically and mentally, the voices, the songs, the paranoia, the delusions. Everything.