RACTHOUGHTSING

Quick update: it went great – 100 times better than I could possibly have hoped for. Not only did they not have to give me any shots to numb my mouth during the teeth cleaning, but they told me I no longer have gum disease. On top of that, they did not 2, but 6, fillings – at the gumline of each of my top upper teeth. It was fabulous. A bit sore, now, but the impact to my self-esteem is huge. I no longer feel embarrassed to smile.

Well, so much for thinking I might be able to get by with Trazedone and Claritin :-(

I’ve been waking up with a song stuck in my head and racing thoughts for the past few days, and this morning was the worst, yet. I’ve been growing more distracted at the same time — and perhaps a bit moodier.  And my heart is racing, and I’m shaky. And this is very, very uncomfortable. The very worst of it seems to dissipate as I wake up, but most of it will probably stick with me throughout the day.

I’m concerned about myself, this morning. Will these old, familiar (but absent, for the most part, on my Seroquel/Lamictal/Neurontin regimen) go away if I stop taking the Trazedone and Claritin? One small hope along with the concerns, though, is that it will stop once I start my period, which is likely to be late this month because of all the changes and stress over the past few weeks. Racing thoughts have always peaked right before my period.

So — no Claritin today, and I’ll try half a Trazedone instead of the full 100mg pill before bed, tonight.  I’ll try switching to Unisom (my old stand-by from my pre-psychophamacuetical days) over the next few days, or maybe I’ll try Melatonin, instead.  I’ll try taking something else for allergies — or even taking nothing for allergies. Allergies are a common topic of conversation in Austin, Texas, especially this time of year. While the optical migraines, itchy skin, runny nose, and watery eyes are miserable, they are nothing compared to how uncomfortable I feel when my asthma gets worse on top of it (as it always does). This time of year I have the triple-play of mold, cedar, and artificial heating, and I have yet to find a way to feel better for any long period of time. Claritin works minor miracles, but I can’t tolerate it for more than a few days at a time (if the racing thoughts don’t happen, extreme irritability does). Although this sounds extreme, it’s actually quite common in this part of the country.

And just to get all of my whining in, for the day, my internal thermostat has gone wonky. It’s 41 degrees outside and we’ve had our heater set on 73 for the past 24 hours, and I’m sitting here in my husband’s sweatshirt, flannel pajama bottoms, and socks; sitting here drinking hot coffee, and freezing. Wishing it was 104 outside again, as it seemed to be for most of the summer. I don’t have much tolerance for cold – in fact I started looking for beams of sunlight to stand in during my smoke breaks when the temperature finally dropped below 90 last September – but this has been one of the coldest Decembers on record in Austin.

I’m heading off for my second round of dental work this morning. I’m taking what would normally be 3 separate appointments (one for root scaling and planing in both sides of my mouth, and one for 2 fillings I’m having done) and combining them in to one. While I do not expect it to be a pleasant experience and while I know my mouth will be sore and my teeth will be extra sensitive for the next few days, I do look forward to having this dental work behind me.

I need to leave here in about 45 minutes; in the meantime, I’m going to go crank the heat up to 77, wrap up in a fuzzy comforter, and plop down on our sofa under the heating vent.

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Serohell

I have something I need to admit to, here: I didn’t take my medication as prescribed, last night. Instead, I doubled up on my Seroquel and skipped my Neurontin and Lamictal. I’ll explain why in a new post, but first let me talk to you about Seroquel.

Oh how I love my Seroquel. It is the most reliable sleep aid I have ever encountered. Because of Seroquel, I can guzzle my beloved Diet Coke and iced tea from the moment I wake up until the moment I go to bed without having to suffer through caffeine-induced insomnia. Because of Seroquel, I can choose to go to bed at 3am without worrying that I’ll waste a moment of my precious bedtime tossing and turning. Because of Seroquel I never have to thrash around for hours on end in a torment of stress-induced rumination. It knocks me out, nearly every time. It doesn’t produce a “high”, but neither does it make me feel queasy or leave an odd taste or sensation in my mouth (a-la Ambien or Lunesta), and it doesn’t have any impact at all on the number of hours I am able to sleep at a stretch. I don’t build up a tolerance to it. I am never tempted to take it during the day.

In fact, Seroquel causes only two problems in my life that really bother me: 1) I am completely unable to sleep without Seroquel and haven’t been able to stop taking it since I started taking it many years ago; 2) Over the past several months I have developed a side-effect that is absolutely horrible: I lose the ability to swallow about an hour after I take it.

My dependency on Seroquel bothers me a lot, and it’s a problem I’ve read about again and again in posts all over the Internet by other people who take it. In fact, I often wonder if taking Seroquel for a long period of time changes something in your brain chemistry so that you are, literally, unable to ever fall asleep naturally again. I went through a period of several months, last year, when the only psycho-pharmaceutical I was on was 25mg of Seroquel. That’s the lowest dose of Seroquel you can take, and the pill itself is so tiny that it really can’t be cut in half. People who take Seroquel as a mood stabilizer are often prescribed 800mg or even 900mg of the drug per day (I can’t imagine how that would impact me – I would be catatonic, unable to function at all). When I tried to stop taking that 25mg per day I suffered extreme withdrawal symptoms, the worst three of which were intense itching all over my body coupled with intense joint pain all over my body, along with complete insomnia. I think the longest I made it without Seroquel was three days.

The problem of being unable to swallow started a few months ago, and it is the most miserable, awful feeling. The smooth muscles in the back of my throat simply stop working. I can usually trigger my swallowing reflex by sitting up and drinking something, but not always.

I haven’t spoken to my doctor about this problem because I know it means that I should stop taking Seroquel, and I can’t imagine how I would do that. I keep postponing the conversation because, after all, I do eventually manage to fall asleep despite the horrid sensation (that’s how thoroughly it knocks me out). I’ve also wondered if maybe it’s the combination of Seroquel and Lamictal and Neurontin, all of which I take before I go to bed. I started trying to space my medications out because of this side effect, so I usually take my Lamictal and Neurontin about a hour before I take my Seroquel. Spacing out my medications helps a little, but not a lot.

At any rate, since I got a wild hair and decided not to take my Lamictal and Neurontin last night, I arbitrarily decided to double up on my Seroquel, instead. My thinking was that I would be awake off and on all night because of withdrawal from Lamictal and Neurontin, and that doubling up on my Seroquel would help me sleep through it.

And this is what happened: I stumbled to bed, closed my eyes, took a few deep breaths, and then had the sensation that no matter how deeply I breathed I wasn’t getting enough oxygen. The sensation scared me so I sat up to gather my senses, and that’s when I realized that the real problem was that I couldn’t swallow at all and, more than that, my throat was collapsing every time I laid down. And then my legs got restless. I was kicking and kicking and kicking. Oh God, the misery! I got up and weaved in to the kitchen where I tried to drink a little water, and it was like this: fill my mouth with water, tilt my head back, wait and wait and wait for the swallow reflex to kick in and then gulp. I tried eating a flour tortilla, thinking that the chewing action might kick my muscles back to life, but gave up when I realized that I was at risk of choking myself. By then I was so sedated I could barely keep my eyes open. I said a little prayer, put faith in the fact that I’ve never heard of anyone dying from 200mg of Seroquel, and went to bed. My last waking thought was wishing I hadn’t taken the Seroquel.

I slept in, today. Awakened at 12:50, which is 4 or 5 hours later than I normally sleep (thank goodness it’s Sunday). Why in the hell did I decide not to take my Lamictal and Neurontin, last night? It doesn’t make any sense. I haven’t done anything like that in a couple of years. Why now?

Well, the simple answer is doubt. And I’ll write more about that in my next post.

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Mad Shrink

I haven’t feeling feeling great. Lots of trouble getting sleepy at a reasonable hour, and lots of trouble waking up too early. There was even one night last week when my Seroquel never took affect, which happens from time to time. I couldn’t focus yesterday. My speech was slow and my thoughts were slower. I had a little panic attack during my first break (because I was caught at work in this state). I tried to reach my doctor but her receptionist said the doctor’s calendar was locked in the doctor’s office, with the doctor, who was on a conference call. When I called back later the receptionist apologized and said she’d forgotten to get it from the doctor. Not that the doctor is going to be in, since next week is a holiday.

I have a chip on my shoulder about my psychiatrist. For one thing, she called me a couple of months ago and chewed me out because my pharmacy had contacted her. The situation was this: my doctor had given me new prescriptions for my medications, since my old ones had expired. When I called the pharmacy to get the prescriptions refilled they didn’t see the new ones on file, so they faxed a form to my doctor’s office seeking approval to refill them, then called to let me know they were waiting on said approval. When the pharmacy called me I corrected their error and they filled the prescriptions. The doctor called to tell me to tell the pharmacy never to contact her for a prescription, then went on to rant – and, really, I do mean rant – about how faxes from pharmacies cost her a lot of time and money, and about how pharmacies only do this to line their own pockets. I explained that it had been a mistake but she didn’t seem to hear me. It was a very odd call.

What I wish I had said to her was “Are you f’in kidding me? You charge $140 dollars for 30 minutes of your time, and you’re complaining to me about a fax?” Instead, I apologized.

So, the whole dollar amount thing… what I’m wondering, is, how does she justify it? 30 minutes per session means sixteen sessions per day, which comes out to $44,800 per month in client billings. Let me add that my doctor, like most other psychiatrists, does not accept insurance. Now, tack on to that the fact that she charges $25 per 5 minutes of phone consultation (i.e., if you don’t have time to make an appointment and need her to call you back). Now, tack on to that the fact that you are charged for missing an appointment with less than 48 hours’ notice. Now, tack on to that the fact that she charges $400 for an initial interview with first-time clients. Now, tack on to that the fact that you share your office office space and receptionist with 10 other doctors (so your overhead is nice and low). Combine all of this with the fact that your office hours are Monday through Friday, 8am to 5pm, meaning that those of your patients who work (i.e., most of them) are likely to ask you to call them occasionally, and are not unlikely to miss an appointment here and there… Holy crap, lady, how much money do you make every month, and why in the world would you think I give a s**t about your dislike of the fax machine?

Of course, I’ve signed the same financial agreement with every other psychiatrist I’ve seen. They like to be sure they get their money. I’ve actually paid much more for a doctor’s visit, in fact. I think what steams me is that it feels as if I’m being taken advantage of. It feels as if these psychiatrists are saying, “You patients really suck. You’re horrible to be around! I will charge you for the time I spend rolling my eyes when I think of you.”

I should add, though, that my doctor seems to be a pretty good doctor. Of course, she did forget who I was once, and that was after she’d been my doctor for a little over two years. Still, we all have our moments.

Psychiatry in the real world is nothing like psychiatry as portrayed in the movies, in books, or on television.

More about this subject in another post. Meanwhile, I’ll simply wait for this latest whatever-state-I’m-in to pass. Again.

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I had a lunch hour think about my doubts yesterday; the ones that plague me about the history of my struggle with this illness.

I should mention that this is not the first time I’ve had a good long think about my accepting my diagnosis. I should mention that the thoughts are uncomfortable and confusing. I should mention that I have a history of swinging back and forth with my conclusions, and with my approach to managing my symptoms. I usually end up assigning my conclusions to either “I don’t have bipolar disorder, I just have a low character”, or “blame everything on bipolar disorder”.
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As I sat in my car, eating my Quarter Pounder With Cheese, considering the either-or questions about my diagnosis, I felt an uncomfortable tension in my torso. It almost felt like fear, and I could practically hear my own subconscious warning me that I was coming dangerously close to a conclusion about myself that could lead to stopping my medication again. I remembered the horrible withdrawal symptoms I’ve experienced in the past when I’ve suddenly decided that I just have a low character. I remembered the frustration of malfunctioning reason and judgement, the utter inability to focus on anything for more than an hour or two at a time – and the reverse, the hyper-focus on a wonderful intention, and getting pretty far down the road toward accomplishing some goal, and then suddenly becoming totally unable to complete the project.

If I had done nothing more than listen to that internal voice I wouldn’t have given the questions in my mind much more thought, but I ignored it while I ate my lunch. I thought about that first Paxil pill I took back in 1996 and wondered, regretfully, if all of the problems I went through were 100% caused by the medications I used, off and on, throughout all the worst years. I wondered if I took that medication, went on and off the medication, because I needed an excuse for the destructive, self-indulgent decisions I was making right and left. I even wondered if the mental health professionals I consulted during those years led me in to a lake of fire. I wondered if the medications I’ve been taking all these years have permanently damaged my brain, rendering me unable to function without them.

In other words, I spent a lot of time thinking about personal responsibility, yesterday. The very phrase was like a light from a distant source, shining down on the ground somewhere in front of me. A light I wanted to follow.

And so I took a deep breath, and here’s what I decided to consider as I move through the next few days:

  1. I think a lot better, and feel a lot better, on the medications I’m taking right now
  2. There’s no need for me to think about my medications, right now
  3. Ruminating about a period in my life that was awful won’t help me move forward
  4. I don’t practice much personal responsibility in my life – but that doesn’t really have anything to do with my character

Funny, but once I’d reached this point in my thinking I felt better, not worse. Taking as much personal responsibility as I can for my decisions big and small is something that is within my control every moment of every day. Personal responsibility is the opposite of helpless, and taking personal responsibility for the choices I make about my life feels good.

Taking charge of the choices I make about my ability to live a full and happy life despite having bipolar disorder means, to me, right now, doing exactly what I’m doing with this blog. It means stepping out of the shadows of my past, my fears, and my assumptions. It means not accepting the isolation I’ve surrounded myself with for so long, or my unwillingness to expose myself to rejection or failure because I’m different.

It means thinking well of myself.

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I spent some time on research over the weekend (and on finding a way to display that research in this blog). What little information I focused on was astounding and is still on my mind. The possible discovery of a gene that would point to an entire subtype of bipolar disorder that might be treated with anti-inflammatory treatment. A radically decreased estimated lifespan. Double and even triple risk of heart disease, kidney failure, asthma (all of which can also be impacted by faulty immune system responses, including inflammation). Even evidence that poor test results for blood lipids could be a hallmark of bipolar disorder.

Personally, I have both asthma and horrid cholesterol levels, and heart disease and immune disorders run in my family.

I’m no scientist, so I’m trying not to come to my own conclusions about what I’ve read but a few questions do keep spinning through my mind:

  • What would it take for physicians of all kinds to collaborate and plan care for their patients? And I’m not just talking about prescriptions, here. I’m talking about agreeing on risk factors to monitor, and non-pharmacological therapies, and overall support and monitoring
  • Why does the psychiatric community continue to focus on what appears to be outdated information: that is, that mental illness is all in our heads, and that medication designed specifically to sedate, to alter mood and perception, are our only options for treatment?
  • Why do mental hospitals continue to focus on warehousing, group therapy, and “one size fits all” psychopharmacology for their patients?
  • Why does bipolar disorder not immediately set off warning bells — why do our doctors not immediately test for those diseases and illnesses research so clearly shows are associated with it?

These questions, unfortunately, play in to my general distrust of the medical community – something I am working on overcoming. They also, however, lead to my next topic; one that Barb touched on when she commented on my last post: my own responsibility to commonsense self-care. Do I exercise? Not right now. Do I make an effort to eat a healthy diet? Rarely. Do I try do maintain a healthy sleep schedule? Never.

It would be easy to blame science for my health issues, and it would be easy to blame bipolar disorder for my poor self care. These are excuses I have to admit that I use every day. I don’t quite smoking because I’m afraid of a manic episode (something that’s happened in the past). I eat cinnamon rolls all day because I need the pleasure they give me to get through my work day. Ditto fountain Diet Cokes. I don’t cook healthy meals because I’m too tired. I don’t clean house because I have important creative business to attend to, like this blog.

Blame and excuses, like shame and guilt, have little place in a healthy life. When I was in therapy we focused a lot on these cornerstones of immobility, and I actually made some progress away from them. Now, having been off the therapy wagon for a number of years, I find that I’ve built on those cornerstones and now have a pretty solid foundation of unhealthy habits on which to live my life.

I hope we continue to make strides in the case for the inextricable links between physical and mental illness, and I hope our doctors catch up soon. It is important, though, not to get sidetracked by the questions they present.

Which is why, this week, I have the following goals:

  1. Cut out the cinnamon rolls
  2. Go to bed an hour earlier every night
  3. Begin the search for a therapist
  4. Continue my research, and blog every day
  5. Read and comment on a different blog every day

Does anybody else struggle with a tangle of medical, mental, and self-care issues? I’d love to hear about it if you do.

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Episodes associated with mental illness are traumatic. It isn’t a topic that gets discussed, much, but I wonder if our current approach to treating mental illness – the medication, the therapy – lacks an important focus. I wonder if we should place an equal emphasis on rehabilitation, in much the same way we focus on rehabilitation for patients who have experienced head trauma.

I am too often a flower that refuses to bloom for fear of the sun, or for fear of a freeze. It doesn’t matter that’s it’s partly cloudy and warm outside; I remain resolutely closed. And why is that? When I was younger I tended to open with abandon. Every episode, when I was young, was going to be the last episode. It wasn’t until the episode that seemed it would never end that I lost my nerve.

It began the summer I turned 30. The Austin of that year was all thrumming heat, tropical flowers, vivid greens and blues and saturated, woody browns. Everything was the most everything anything had ever been in my life. The most beautiful. The most in control. The smartest. The fastest. The most successful. The richest. The busiest. The most in demand. Under the circumstances, I was convinced that this, finally, was what it meant to be a grownup; that everything that had come before had come because of a lack of skill.

It didn’t last, of course. The summer turned into a desperate fall, which led to rapid cycles of hard-edged mania and soggy depression, until all time turned into a mixed episode. I became a sobbing bag of fury, obsession, self-hatred, psychosis, impulsiveness, and suicidal ideation.

It lasted for 4 years.

I remember feeling so angry. I couldn’t seem to go all the way crazy, and I couldn’t seem to get better. My perceptions were skewed all over the place and so was my judgement, and that was overwhelmingly frustrating to me because it meant that nothing ever turned out the way I thought it would. I was hearing and seeing things all the time, things I could never find, and I didn’t know that they were hallucinations. Sounds of every kind were intensely irritating to me. I didn’t trust anyone. At all. I had lost any friends I might have made the summer I turned 30, and although I couldn’t stop thinking about killing myself I couldn’t seem to do that, either. And there was this intense agony in my body all the time, a kind of odd, terrible, horrible need to stretch out and run that stretching out and running did absolutely nothing to sooth. And I was paranoid — oh but I was paranoid. It wasn’t just that I believed everybody hated me. I believed everybody hated me for no other reason than that everybody was cruel and mean and awful and that they would hurt me if they could.

Interspersed throughout those 4 years of hell were hours, even days, when all of my symptoms were at bay. These respites were spent recovering in a kind of useless way because I knew the next onslaught would appear shortly. I was exhausted.

One night I walked outside and stood in the middle of my parent’s driveway. I was crying, and my fists were clenched tight, and I felt full of rage towards the idea that the rest of my life would be eaten by this affliction. “I will be better than this, I WILL BE BETTER THAN THIS” I said out loud (though softly). It was an incredibly histrionic moment for me, and I knew it was, which is why I had chosen to experience it in the middle of my parent’s driveway, sometime after midnight, with no one to judge me but me and what may or may not have been an imaginary angel hovering a few feet over my head, all bronze feathers and sympathy.

It wasn’t as if no one had ever prescribed medication for me before; I had simply never followed anyone’s instructions because I didn’t trust anybody. And yet my absolute determination to “BE BETTER THAN THIS” somehow gave me the idea that I didn’t have to trust somebody to try what they suggested. I didn’t have to trust a doctor to follow doctor’s orders, in other words. So I picked a doctor – somebody who at least looked like I thought a doctor was supposed to look – and for once I did as I was told. Because of the medication, I was able to build a bunker in my very own bed out of pillows, stuffed animals, and the complete works of JRR Tolkien and (eventually) spend entire weekends in my own apartment. One thing led to another, which led to another, and another, and eventually I found myself in what passed quite nicely as the place you actually do get to when you’re mentally ill and you’ve learned a few coping skills.

The problematic thing about what I think of as bipolar trauma is that it keeps recurring, though the period between episodes may change from hours to months, and the ferocity of the symptoms may vary unpredictably. I may not have visited with my big, bronze angel since then, but neither has that period turned out to be an anomaly. In fact, my life went out of control again quite slowly this last time, but no less emphatically.

By process of elimination, and by forcing myself to get back out into the world again, I have been forced to accept that there are some things I can no longer clearly differentiate between. I honestly don’t know the difference between, for instance, who means me harm and who is simply standing there, not giving me a second thought. I honestly don’t know how I am perceived by the world around me, and I’m not sure of my place in the world. I can pretend that I have my bearings for long periods of time, but I don’t have any idea if I am successful in that pretense. Therapy might give me some insight into my fears, but I am not aware of a therapy that might help me to train my brain to bypass the pathways damaged by my experiences.

I am forced to admit that I can’t simply choose to bloom again. When should I bend to the shade? When to turn to the sun? Without answers I’m afraid I will remain at the mercy of my own determination and the sympathies of angels, wherever they may be.

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Episodes associated with mental illness are traumatic. It isn’t a topic that gets discussed, much, but I wonder if our current approach to treating mental illness – the medication, the therapy – lacks an important focus. I wonder if we should place an equal emphasis on rehabilitation, in much the same way we focus on rehabilitation for patients who have experienced head trauma.

I am too often a flower that refuses to bloom for fear of the sun, or for fear of a freeze. It doesn’t matter that’s it’s partly cloudy and warm outside; I remain resolutely closed. And why is that? When I was younger I tended to open with abandon. Every episode, when I was young, was going to be the last episode. It wasn’t until the episode that seemed it would never end that I lost my nerve.

It began the summer I turned 30. The Austin of that year was all thrumming heat, tropical flowers, vivid greens and blues and saturated, woody browns. Everything was the most everything anything had ever been in my life. The most beautiful. The most in control. The smartest. The fastest. The most successful. The richest. The busiest. The most in demand. Under the circumstances, I was convinced that this, finally, was what it meant to be a grownup; that everything that had come before had come because of a lack of skill.

It didn’t last, of course. The summer turned into a desperate fall, which led to rapid cycles of hard-edged mania and soggy depression, until all time turned into a mixed episode. I became a sobbing bag of fury, obsession, self-hatred, psychosis, impulsiveness, and suicidal ideation.

It lasted for 4 years.

I remember feeling so angry. I couldn’t seem to go all the way crazy, and I couldn’t seem to get better. My perceptions were skewed all over the place and so was my judgement, and that was overwhelmingly frustrating to me because it meant that nothing ever turned out the way I thought it would. I was hearing and seeing things all the time, things I could never find, and I didn’t know that they were hallucinations. Sounds of every kind were intensely irritating to me. I didn’t trust anyone. At all. I had lost any friends I might have made the summer I turned 30, and although I couldn’t stop thinking about killing myself I couldn’t seem to do that, either. And there was this intense agony in my body all the time, a kind of odd, terrible, horrible need to stretch out and run that stretching out and running did absolutely nothing to sooth. And I was paranoid — oh but I was paranoid. It wasn’t just that I believed everybody hated me. I believed everybody hated me for no other reason than that everybody was cruel and mean and awful and that they would hurt me if they could.

Interspersed throughout those 4 years of hell were hours, even days, when all of my symptoms were at bay. These respites were spent recovering in a kind of useless way because I knew the next onslaught would appear shortly. I was exhausted.

One night I walked outside and stood in the middle of my parent’s driveway. I was crying, and my fists were clenched tight, and I felt full of rage towards the idea that the rest of my life would be eaten by this affliction. “I will be better than this, I WILL BE BETTER THAN THIS” I said out loud (though softly). It was an incredibly histrionic moment for me, and I knew it was, which is why I had chosen to experience it in the middle of my parent’s driveway, sometime after midnight, with no one to judge me but me and what may or may not have been an imaginary angel hovering a few feet over my head, all bronze feathers and sympathy.

It wasn’t as if no one had ever prescribed medication for me before; I had simply never followed anyone’s instructions because I didn’t trust anybody. And yet my absolute determination to “BE BETTER THAN THIS” somehow gave me the idea that I didn’t have to trust somebody to try what they suggested. I didn’t have to trust a doctor to follow doctor’s orders, in other words. So I picked a doctor – somebody who at least looked like I thought a doctor was supposed to look – and for once I did as I was told. Because of the medication, I was able to build a bunker in my very own bed out of pillows, stuffed animals, and the complete works of JRR Tolkien and (eventually) spend entire weekends in my own apartment. One thing led to another, which led to another, and another, and eventually I found myself in what passed quite nicely as the place you actually do get to when you’re mentally ill and you’ve learned a few coping skills.

The problematic thing about what I think of as bipolar trauma is that it keeps recurring, though the period between episodes may change from hours to months, and the ferocity of the symptoms may vary unpredictably. I may not have visited with my big, bronze angel since then, but neither has that period turned out to be an anomaly. In fact, my life went out of control again quite slowly this last time, but no less emphatically.

By process of elimination, and by forcing myself to get back out into the world again, I have been forced to accept that there are some things I can no longer clearly differentiate between. I honestly don’t know the difference between, for instance, who means me harm and who is simply standing there, not giving me a second thought. I honestly don’t know how I am perceived by the world around me, and I’m not sure of my place in the world. I can pretend that I have my bearings for long periods of time, but I don’t have any idea if I am successful in that pretense. Therapy might give me some insight into my fears, but I am not aware of a therapy that might help me to train my brain to bypass the pathways damaged by my experiences.

I am forced to admit that I can’t simply choose to bloom again. When should I bend to the shade? When to turn to the sun? Without answers I’m afraid I will remain at the mercy of my own determination and the sympathies of angels, wherever they may be.

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I went shopping for interview clothes, today. I didn’t bother looking through my closet to see if I actually needed anything, first. I simply took a shower, put on makeup (a rare occurrence), took a blow drier to my hair (another rarity), held my head up high and pointed the car towards Macy’s.

Macy’s was not my first choice. My first choice was Anthropologie; however, Macy’s is much more affordable. And a lot closer. And since it was getting close to rush hour, and I’m still unemployed, and I need to be practical about anything I purchase these days, I headed to Macy’s.

I told myself that today would be a good day to shop. My hair is long, now, and that’s the real kicker: I feel far more beautiful than I did a year ago. And I did have on makeup. Also, I actually wore a jacket I purchased at Anthropologie back when we still had money. And heels. And my new (cheap but at least they’re new) jeans.

The problem really started the first time I passed a mirror and saw myself out of the corner of my eye. I looked nothing like I had looked when I left home. I was hunched over. I had no neck. I was greyish-brown all over. And that’s when it happened. That’s when it always happens: I turned in to a freak of nature.

I became certain that everyone in my vicinity was distracted by my freakishness, disturbed by my presence. Became certain that even beyond the ‘freak’ judgement they were all throwing my way was the immediate certitude they all shared that I was digusting; weak, self-indulgent, reprehensible.

Now, I should interject here that I am aware, when this happens, that it is a symptom of insecurity. I went to a dressing room and stared at myself face-on in the mirror until I liked what I saw again, but that only fixed things for a few minutes. I felt guilty and ashamed for wanting to buy something for tomorrow’s interview. I felt guilty and ashamed for being so fat. I felt guilty and ashamed for not knowing how to put a simple interview outfit together; for being so unsure about weather to wear panty hose, a dress, a skirt, slacks, a blazer… I began to fixate on my body in front of the mirror. The slackness everywhere. The fat stomach that pouches out in such an ugly way even when I don’t know it’s doing it, even when I thought it wasn’t (but that was before I caught a sideways glimpse of myself). The hair that turned dry, brittle and flyaway the minute I stepped in the store.

As I continued shopping I became certain of one other thing: that nobody will hire me. Nobody. That it doesn’t matter who I meet in an interview – I will be rejected because of the disgusting freak thing. And because if that doesn’t drive them away, my paranoia will.

The intensity of my insecurity is such that it messes with my ability to think clearly, to speak clearly, to make sense. I know I come across as someone with something to hide. I added ‘criminal’ to the list of things I figured the other customers I passed were labeling me. If and when I did see someone who appeared to work at the store, I assumed they were simply following me at a discrete distance to ensure that I didn’t steal something.

Last night I told David that I was going to write down every fear I have about going back to work, and about interviewing for a job. So I’ve started this post to do just that. The hope, by the way, is that I will be able to face these fears head on. That I will be able to sort the wheat from the chaff.

God but I feel so strongly that I have lost myself somewhere along the way. And yet, that doesn’t make any sense at all. With the exception of a year (one, single year) when I first moved to Austin, almost all of my clothes shopping expeditions since I was a teenager have felt the same way. From 107 to 177 and everywhere in between – I simply panic when I am shopping. But panicking about finding a job is something new.

It feels pretty much the same, though.

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