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Folk don’t want the messy truth. Not that I have seen, at least not my messy truth. They want uplifting tales of hope, poignant tales of sorrow, struggle and overcoming into victory and joy that carries them up with it, and a shiny list of tools to get there. I can’t offer that.

I remain trapped in the journey. I slog along in a morass of something beneath evolved, thrashing in some sort of swamp with no enlightened path shedding a glow of epiphany through the sagging webwork of moss and spiderwebs that is my mind. I present my sense of hopelessness.

There was a bridge over it for a while, a stable earthen construction bordered by smooth logs, lifting the pilgrim over the marsh but not too high, following the vagaries of life but not dropping too low, and it seemed worthwhile to try to be a better person because it appeared possible. But the things chased me, the memories, mistakes, all I’ve done wrong, the shame, and they wouldn’t stop. The earthwork ended, and I fell straight in. Now the things have me again. They surge behind, around and in front, darkening my mind, eroding my thought and eating the hopes and the goals in front of me. They are monsters that chew, swallow and dissolve my lessons and my resolutions without cease.

In 2001 the people in my life suffered my psychosis, which lasted years. At the end of it I was exiled. I was expected to be ashamed of and accept responsibility for behaviors I could not control but only scream at from a tiny cage in my mind as I watched in horror. I was/am so sorry for the lives that I affected in such bad ways. I was/am ashamed, too, but I couldn’t let go of the idea that I was sick and that it was so unfair to be judged for having a disease. I very much wished I was dying of cancer instead of going around with the Sword of Suicide dangling over my head. People would sit at my bedside and call me brave for surviving as long as I had. Instead they spit on me, and if I’d succumbed to my illness they would have spit on my grave. My attempts to make amends were laced with bitterness and, justifiably, every one was refused. The worst part is, nowadays when I have a relapse episode, the self-loathing and bitterness return. How self-centered it all is. The mixed episodes have been returning with greater frequency, the brain fog is overwhelming, and now I’m in crisis again, which has not happened to me in a very long time. Hence this post, probably.

Here is what I am doing. DBT tool: mindfulness. DBT tool: Opposite action. Other tools: Masking, since it seems to be the only way to get along. Focusing on gratitude, gratitude, gratitude. Lifting other people up and cheering them on whenever possible. Forcing myself to go outside and play.

Most of these things have worked for a while but are now falling apart.

So for today, I have no tidy conclusion. I was trying to write things with tidy conclusions but that made me quit writing altogether. It was no more than a feeble attempt at masking anyway, only on the page. Then I tried writing my messy truth and no one wanted it. But that’s okay. Why should they?

Authenticity all the way.

My wish for you is that you are secure in the knowledge that you are valuable, no matter how you feel. Have a wonderful day.

Fear and loathing in the presence of my betters

Microscopic image of synovial fluid

Last week, three sales and technical reps came to my workplace. I’d been informed they were coming at a certain time and was as mentally prepared for this horrific event as I could be. These meetings usually take place in the conference room. There’s a good-sized table with decently spaced-apart chairs and plenty of light by which to watch people’s faces and see all their materials. Best of all, it’s a non-clinical area and you can have your water bottle with you.

My department is also a room. It’s filled with benches and safety cabinets and incubators and agars and analyzers and a microscope. I’m back here because microorganism wrangling is a one-person job and I need to work alone. I often keep the lights dimmed because overhead lights are just … cruel. I’m fortunate to have a choice. There’s even a window, a decadent luxury in a lab. But the room has one horrible feature: the workstation is against the wall opposite the door. Not only is my back to the ever-open door, but a biological safety cabinet and bookshelf loom at my back, between me and the doorway; I can’t see it even when I turn around. Whenever anyone comes into the department, they round this tower and appear beside me and I startle so hard my butt catches air. Sometimes they speak suddenly just before manifesting, which has the same effect. The adrenaline spark is so intense that it hurts—a lot—exploding through my body and brain, slamming into my fingertips and toes and the crown of my head. Every nerve shrieks at once. It’s comparable to touching an electrified livestock fence multiple times a day.

Invariably they act surprised by my reaction, though it happens every single time they come in unless they do me the courtesy of knocking or dinging the call bell I have on the counter by the door for that very reason. There are two or three people who accommodate me in this simple way before they come on around. The rest gasp or laugh or say, “I didn’t mean to startle you,” or all three at once. Sometimes they appear offended that I should be startled by them, as if they have the right to have me not be startled by them.

Then they start talking about whatever they have come to interrupt me with. My heart is pounding and my face is so flushed I feel like my eardrums are going to burst. I’m trying to slow my breathing while the pain recedes from my nerves, which feel like tiny stick people flailing their arms and screaming as they are dragged back into a wormhole. I scramble to shift my focus to what the other person is launching at me and redirect my thoughts from the microorganisms I’ve been pondering.

But none of these terrible things were going on when, sitting at my workstation in the low light, I heard unfamiliar voices out in the corridor mingled with those of the two supervisors. It’s time for the meeting, I thought, proudly calm, and grabbed my notebook and went to the door.

With big smiles they greeted me, Super1 and Super2 and three female sales reps from the biotech company. Grinning back, I focused on each one’s name and face and promised myself I’d remember. And instead of then proceeding to the conference room where I could see them, they formed a phalanx and advanced at once into my dark domain. There, the supervisors toured the shadowy beings around my department as if I were not even present. Nobody thought to turn on the lights.

When our happy group came back around the biological safety cabinet toward the doorway, they stopped. Maybe they were talking about the analyzer they were standing next to; I don’t even remember. All I remember is that I tried to say something, felt irrelevant, and we continued standing right there in a close, roughly ovoid configuration, me trapped against the incubators between Super1 and a sales rep, with no escape.

I’m fairly certain I have various conditions that have never been diagnosed in addition to my bipolar. Maybe they aren’t anything. But they are challenging obstacles for me all the same. One of these is acute claustrophobia in groups of people. Another one is intolerance of standing in one position for any amount of time unless I’m in the woods. Another one is insomnia and chronic exhaustion.

Well, the conversation went on. I waited for Super1 to make a move to head to the conference room, and he didn’t. I slowly realized, to my utmost dread, that they had in effect started the meeting right here, huddled together in this dark, compressed space. I was okay for a few minutes, but fatigue set in along with the claustrophobia, right on time.

I was still struggling to maintain an interested demeanor well after it became clear to me that no one was interested in my dredged-up ideas about anything. I quit trying to contribute and turned my attention to fighting the claustrophobia. There was no direction I could move. Super1 lounged against the incubator on my left, an option I didn’t have because I was at the space between the incubators. The rep to my right seemed to close in on me. She could almost brush my sleeve. Panic arose and I was quickly exhausted trying to suppress or at least hide my frenetic panting. With the hyperventilation, strangely, came the imperative to yawn. Yawning, I’m aware, is universally interpreted as a sign of disrespect rather than complete exhaustion in such settings. I’m also aware that fighting the urge to yawn is a challenge shared by everyone, which made my failure to subdue a couple all the more socially unacceptable. My self-consciousness was justified when one of the impeccable reps snickered, openly watching me struggle.

By then, I could no longer stand still. Oh, how I wanted to. But I couldn’t. My legs were spasming. I squiggled and fidgeted like my son in first grade before starting Adderall.  Their talk was gibberish. My ears roared with the effort to hold back yawns, to still my restless legs and arms. And yet I found myself fixated equally upon my own misery and the plight of the third of the visitors.

Unlike me, she had perfect composure the entire time standing business-casual in those skinny high heels she was wearing. They were the sort of shoes, I thought, one might wear to a meeting in which one expected to be sitting at a table in a conference room. Standing there like that for so long on a concrete floor could be nothing but torture. I was stuck on it like I get stuck when someone mentions they have to go to the bathroom and then lets events carry them along and doesn’t get around to going. All I can think is GO TO THE BATHROOM PLEASE.

I needed that lady to get off those heels as much as I needed to crouch on the floor, yawn big, and then run around the benches screaming.

I was shaking inside, dizzy and near tears by the time the meeting seemed to be wrapping up. There were sporadic “Well, it’s been really great finally meeting you,” sorts of remarks, and “Here’s my card,” mixing in with final pitch fragments and answered questions. Any second, we’d all exchange final handshakes and they’d be out the door. And I wasn’t glad. I was desperate.

But Super2 suddenly had a burning question. It was very important. No, that’s not what I’m asking. I’m asking this.

Yes, what about this? Super1 agreed. Clarify, clarify. And the wheels began turning once more, and the conversation rumbled back to life, and I held back my tears with no idea what anyone was saying. I felt like I was about to pass out. Eventually the shifting around, closing of notebooks, and handing off of brochures resumed, and this time it was for real. The meeting was over. But the terror was not. They all started socializing. “You driving back this evening? Where to?” “What’s your sales territory?” “What motel are you staying in? Here’s what to do while you’re in town. Oh, you brought your bicycle? Let me tell you about the trails!”

I was still standing there. I could not even chew my leg off. I was well and truly trapped, and I could no longer hold back my tears. But a coworker appeared with a specimen for culture as if a guardian angel had shoved her in the door to rescue me with a task only I could perform. I sidled unsteadily past the woman next to me, surveyed the items in the hood, and then whispered to the aide, “Bring me another one. Say it’s STAT!”

But that interruption was the catalyst. The meeting actually broke up. For they all were as full of it as I was, having been caught in a PCR amplification loop of polite small talk that seemed inescapable. But they could play the game. It’s all just body language and concealing the tells. They could do it. They could pretend they were okay, and with engagement and endurance. I could not. That’s the difference between “normal” and me. I dove headfirst into setting up that culture. I waved the slide in the air to dry it for staining. I tooled around the bench a few times. Then I stepped out into the bright hallway.

There they all were! Clustered around Super2’s office door! Well, I’m sure she had questions and inconsistencies to point out and they were all quailing before her acumen.

I zoomed to the breakroom, chugged water, and looked at Bluesky for a minute. I went to the bathroom, not because I needed to (I didn’t; I was frankly dehydrated) but because it was a door I could get behind and lock.

Some days, I can’t see a way forward. This is one of those days. Climate is stressful. Future uncertain. I can’t bear the thought of going to work. I’m afraid of losing my job. I don’t know why, and I don’t know how long I can hang on. I need change.

What to do, what to do. Call my provider’s crisis line? My self-esteem is too low to consider wasting their time.

When this happens, I have a hard time finding the solution-oriented person I’ve learned to become after 50 years of this. So, grasping at straws, I bang my way through piano music, making it up on the spot sometimes, almost invariably some repetitive doom-laden lacrimose storm front in the key of A minor. I update my Linkedin in the hope of finding some sort of freelance work in case the worst-case scenario comes to pass, and everything in my profile looks amateur and stupid. I immerse myself in tasks around the house that are normally satisfying, but I’m still hyperventilating.

When these feelings overwhelm, I can’t help worrying. I can’t help worrying that I’m relapsing. This feels like a mixed-manic shitshow.

And watching the world around me, it seems evident that I’m not alone, that this is nothing special. But your life matters. Go ahead and call the crisis line, if you are in my boat.

National Suicide Prevention Lifeline: 800-273-TALK (8255)

NAMI Help Line: 800-950-6264

Visit www.nami.org for tons of resources.

I routinely experience rage at work. This particular time, it was at the words of a person, not the bleep of an analyzer, and I like this person very much, so I made an effort and kept it to myself (sort of); my abrupt departure from the room may have been a tell. This happened a little while back, but I’ve been thinking about it quite a lot.

I don’t even remember what the overall conversation was about, but the switch flipped when the co-worker put on their wisest face and said, “Everybody’s a little bipolar.” I looked at them. “No,” they said, looking even wiser. “I mean it.”

I work in a field that attracts social misfits, recluses, and scientific types with organized and exacting tendencies. Often, all in the same individual. We laugh, we suffer, we generally understand each other, and I know that no offense was meant. I said nothing, only got up and left. “Slacking in the break room,” and all that. So perhaps I overreacted.

Now I get that the word “bipolar” means two-sided. Everyone does have their two sides, their ups and downs. That might make one, in fact, “a little bipolar.” So they weren’t wrong. People living with bipolar disorder do not own the word. But it did hit a nerve. Because when the term is used casually, as a joke or an insult or to talk down about oneself, it references the disorder and contributes to stigma.

And it brought to the fore an even more common one, because I so often hear it: “I’m so OCD about this.” Every time I hear this, I swear that the next time someone says it, I’m gonna ask.

“Do you know what OCD stands for? You’re literally using a condition, which can ruin lives if severe enough or untreated, as a casual adjective. Worse, you’re using this adjective for a slight self-deprecation. You absolutely cannot do that.” Well, everyone, as it seems to me in the moment, does!

We have sensitivity trainings galore. About race, culture, gender, religion … why not about mental health? You wouldn’t say a company meeting is a pow-wow. How is it any more acceptable to say anyone is “OCD about” anything? I would argue that it is not. That’s misappropriation too. Besides being terrible grammar, once you spell it out.

Sure, I’m grinding on something here. There are probably many of us living with these challenges who don’t get offended by this language, or are inured to it, or use it this way themselves, because they can. But I suspect there are many others, like me, who are disturbed or triggered. Use of these terms in casual conversation seldom lands as complimentary. Think about that. It’s a symptom of the stigma, deeply entrenched.

I don’t think it would be a terrible idea to educate the workplace about use of these terms.

????????????????These earrings personify the bipolar experience for me. When I am manic, I am like the skeletor face and when I am depressed I am the personification of the drooping mask…even though we are required to wear masks in our day-to-day life I don’t know about you, but it is nearly impossible for me to wear a happy face in all arenas.

For the longest time I was reluctant to wear these earrings because I thought they were too weird and Aztec pagan, but recently I realized they are the perfect expression of my personality. Someone from outside could look at these and think they are weird or cool. But no one but myself will know what they truly signify. And I don’t know about you but sadly being bipolar is part of my identity.

I think, from DBT class and a lot of other blogs, that bipolar shouldn’t define a person. You can use your social and behavioral skills to mask it and not rock the boat for anyone else. But, right or wrong, being bipolar is part of who I am. I cannot escape from this, no matter how acceptably I behave; no matter what positive philosophy I adopt.

And I truly do believe that these positive philosophies are the way to go. Bipolar DOES NOT own you. But for my part, though it doesn’t own me, it is still a part of who I am and I do get sick of all the “positivity” and “cheerleading”. Does that make me a person who gives up? I don’t think so. Being aware is OK. It keeps a person ready to think a moment before reacting to something.

Because you are aware. Awareness isn’t a failing. Acknowledgement is not a failing. Acknowledgement is important and really the best way to help yourself.

Acknowledgement is not the same thing as characterizing oneself. I have been guilty of this. Acknowledgement does not give the disorder its power. Its power comes from characterizing yourself.

You are more than your bipolar disorder. But acknowledging it, even gaining personal power from the knowledge and experience, are good things, in my opinion as a person who has struggled with self-hatred and inferiority from this disease.

So I do like my earrings. They don’t mean the same thing to everyone.

Nothing does.

There is power in personal symbols.

 

About the Letters.

this is a share off of Facebook.

"I am angry enough to die." - Jonah 4:9

“I am angry enough to die.” – Jonah 4:9

I am like a bucking horse – I mean, a horse that bucks. Almost every horse bucks, eventually, during his or her life. Some are forgiven; some are not. I’m like one of our rescue horses, given to instantaneous bucking fits, no warning, just instant bronc mode. Sometimes though, I give warning, crow-hops, but in general, these warnings are ignored.

I figure I must live in a state of forgiveness for my bucking, or I would be shot or abandoned by now. Committed to an asylum or sent to the sale barn. Yet it doesn’t feel like I’m being forgiven. It feels like I am kicked and beaten every time I’m down. That I’m still here argues for forgiveness. These repeated beatings argue for unforgiveness.

Things begin to happen, but like my stories, they go nowhere. I need to be sent to a sale barn. A sale barn for useless, problem wives, to be auctioned off, packed into a truck, and taken away on a journey that will end in slaughter. Humane or inhumane matters not, since being stuck in this life is in itself inhumane.

Today, I hate being bipolar. Today, it seems bipolar is me, so I must hate myself and my life. I have tried and tried not to let bipolar get me down, but it’s apparently hopeless. Apparently, I am supposed to be grateful for my disease because it is teaching me so much about life – that would be useful to me if I didn’t have the disease, but as it is, such knowledge is useless!

Suicidal ideation was happening! I was so mad at hubby and frustrated with my earlier behavior that I wanted to pop a bullet into my brain, the very horror I had believed would never manifest again.

I would have gone past considering it, I think, if the family wouldn’t lose everything without my disability check. Or, if I didn’t owe them all better for having lived with and tolerated me and my disease for so long already. Or, if I didn’t owe God for dying for my sins. Or, if I didn’t care about ruining my children’s lives.

I cannot believe God tolerated Jonah’s anger and simply explained to him why it was unjustified. But he did. For that, God only deserves gratitude on the part of Jonah and of me.

 

 

It turns out that yes, indeed, I am manic, very much so, and have been for a while now.  Mania is not always a good thing, even though many of us are medicated to the point that it seems we are kept below the threshold of “normal” in terms of happiness and productivity. Thus we long for the mania to return, or even hypomania, for which I have wished repeatedly during my prolonged depressive periods.

My mania lately has taken a freaky form: Anxiety, right-brained reactivity and destructive impulsivity that has now resulted in me truly hurting someone and forever burning a bridge that was important to many people. I am filled with remorse, and many things, particularly horses, will be no longer enjoyed without that prick of sorrow and guilt that I have set myself up for with my actions taken in the throes of mania.

I have medicated myself rather heavily in order to accept the constant yelling I am getting from my hubby and myself right now. Everything I say is responded to by hubby as “you aren’t hearing a word I am saying,” and “it’s like talking to a rock!” and “Stop it” You are being ridiculous.” Ridiculous, ridiculous, ridiculous are all my concerns as I watch him doing what I believe to be further damage over the phone, and insisting that I abdicate what I feel is important responsibility without offering a different solution to take the place of my abdication. I wish he would stop it but there is nothing I can say that isn’t “ridiculous.” I also know he is trying to do helpful things that will lead to the solution of our current problems more productively than the things I did, in the hopes of keeping me out of the hospital again. God bless him!

So, thanks to my understanding doctor who has prescribed me some extra medication (extra risperidone and clonazepam) to help me react without anger or bitterness or dangerous breakdowns to these triggers, I am able to use the extra medicine she prescribed to enable me to control myself, namely, my tongue for the most part. I have little doubt that when the crisis is passed, I will be able to return to my normal tiny dosages, as I don’t like taking the refuge of extra medication. I would prefer to handle my crises with mindfulness, wise mind, essential oils, prayer and so forth. But now I need to feel as little emotion as possible or the anxiety would get out of control. Of course, it can also be argued that in this circumstance, anxiety and fear and crippling remorse are warranted and normal, too.

I am reminded of the words of Jesus, and I pray every day that he will help me guard my tongue. He said if a part of the body offends, then cut it off. Not sure if he was being literal or speaking in a parable. Sometimes I wish I could cut out my tongue. I feel it has caused me to do damage beyond forgiveness. I will never receive the forgiveness of the person I have hurt, but I know my heavenly Father will forgive me.

To be Christian about this for a moment: “I [God] live in a high and holy place, but also with him who is contrite and lowly in spirit, to revive the spirit of the lowly and to revive the heart of the contrite. I will not accuse forever, nor will I always be angry, for then the spirit of man would grow faint before me–the breath of man that I have created.” – Isaiah 57: 15-16

There is some spiritual help for me and for others who have done horrible things through the erroneous impulses that accompany mania. Deeds done while in the manic state should never be written off just to being manic. We should take responsibility for what we have done, for we have done these things.

There may have been one way in which my destructive impulses have worked out for good and that is what my husband reminds me of when he is being compassionate toward me, and it comforts me but only a little. How I wish for the good mania, the type that doesn’t result in craziness.

Yet I know too, that this will pass, just as I know my normal, functional times will pass, and that my depressive periods will pass. Everything passes and turns into something else with bipolar. You can count on not staying a certain way forever; there will always be a change, and sometimes for the better. Take encouragement from that. Remember to take a breath, mindfully, seeking wise mind to operate from. Hopefully wise mind will become a habit. It has not happened for me during my manic freakouts, but that does not mean I will not be able to achieve this with the help of the good Lord. Many others have succeeded at this and I know that I can too.

 

 

Reasons why Bipolar is difficult to diagnose:

It has different components, which manifest at different times, so often the doctor has only what s/he sees at a given time to go on, eg:

– has similarities to other illnesses such as major depressive

– when presents as psychotic, any disorder which includes psychosis

– may present as a normal, well person, etc.

This can also apply to someone who is seeing a psychologist for crisis evaluation or a psychiatrist for emergency med management, you can seem normal then too. How? Read on if you wish. (Be warned, it’s another of my personal horror stories, very recent)…

All few of you who read this blog know I’ve been struggling for some time now with a great depressive epoch, and have recently found that some of the symptoms of my “depression” are actually more symptoms of mania. . .. therefore I’m rapid cycling like the wheels of a bicycle racer near the finish line. (please forgive the obvious metaphor, I’m not too creative at the moment, heh).

My life is unpredictable, my family never knows what will happen next. I don’t either. I know something is wrong with my meds, yet I’m reluctant to have them adjusted, especially by a doctor who no longer is familiar with my case, because of the release I’ve experienced on my current meds from cognitive dysfunction, and having regained a lot of my lost memory on the current regimen.

Yet, I sensed a crisis impending so my husband, who also sensed it, did what we both had sworn we’d never do. . . call that place for crisis help again. In this oddly rare instance, a “crisis counselor” was not available, though we’d expressed our reluctant understanding of the need to jump through that deplorable hoop before seeing a psychiatrist. It turned out that we were referred to the main crisis guy, over the phone, who mysteriously was able to produce an opening in the psychiatrist’s schedule on the spot!

Wonderful, we thought. So we saw her, and she, after only a few minutes, pronounced me normal and doing well and no adjustment of my meds was needed and she would see me again in 6 months. No opportunity to dispute that was apparent. Period. Then (unbeknownst to us) she canceled my previously scheduled appointment with my regular psychiatrist, which had been coming up fairly soon. A week later, I had the crisis my husband and I had feared.

Something triggered my destructive half, and I knew I was losing it fast. I felt rage and frustration and knew I was going out of control. So I went to an area where someone had stacked T-posts without consulting me and where I did not want them, and began heaving them out of there. What I was doing appeared like random destruction, to observers, but I had every intention of re-stacking them in a more appropriate place when I was done heaving them out of the stupid place. The kind of thing I had been counseled to do, take out my feelings in a safe way without hurting myself or exposing my family to my “episode”.

The observers (hubby and daughter) did not know what I was doing or why, and so hubby attempted to interfere with my work. Well, he successfully interfered with it, and there I went, set off. An argument ensued, which quickly escalated into something beyond my control and I began to self-harm in my usual way when out of control, which is to start bashing my head into things.

I was being yelled at to “just stop it! Please stop!”

What my interferer didn’t know was just how hard I WAS trying to stop it. I was bashing my head into the horizontal 2x4s of the horse stall wall instead of the 8×8 cemented support post that I FELT COMPELLED to bash my head into. For example. Also, how when I was smashing the bowl in the kitchen, my body/brain was screaming at me to smash WINDOWS. And other things, which I was given to understand made me a bad person who was acting out on purpose. It ended up hours later with me lying on the thin, softening ice of our stock pond trying to “cool off” but preferably go to sleep there and actually perish of hypothermia.

Unfortunately, my crying kids found me there and begged me to get off the ice. I was heartbroken, for them, but could not move. Then my husband showed up and was a little more belittling than I felt he need be. I felt, soon after I had been gotten into the house, that I was being treated the way Therapist K had treated me all those months ago, calling the police to the mental-health facility, like I was a sub-human animal who was acting out on purpose.

The horror of the whole thing for me was that I had all these self-harm/suicide prevention strategies hard-wired (I thought) into my brain. And yet they were not sufficient.

All this about a week after the psychiatrist had pronounced me normal and in no need of a medication adjustment. Boy were we glad I had another appointment already scheduled with my usual psychiatrist  (who was to be leaving the institution soon).

The next day, of sound mind, it occurred to me that I’d better check that. Make a call to confirm that appointment, since I already knew the system was broken, the front desk people were overworked, and the policies were often stupid and usually detrimental to the mental health patient.

So I called to confirm the appointment and surprise, surprise, there was no appointment. My recently-visited psychiatrist had cancelled all other appointments in favor of the one six months away. I was a bit disappointed about that, considering what had happened last night, and insisted the appointment be rescheduled since I had been suicidal. Oh, no, that appointment was already filled, did I want to be put on a cancellation list?

I explained how important it was that I see a psychiatrist immediately, so I got an appointment for three weeks hence. And I was told I am on the cancellation list, although I’m pretty sure that if I were, I’d have gotten in by now.

My husband has tried very hard to get through to them. Not even my new therapist, who had replaced Therapist K on my case because she was of a more appropriate age and qualification, had anything at all helpful to offer him. So he went to the head crisis  guy, who found him to be in crisis himself! My poor husband, doing all he can with what he has, and has been doing so for 19 years! What greater love can there be from a mortal than that I am blessed with from him???? ❤ ❤ ❤

So, there’s an example of how bipolar can present in ways that result in incorrect diagnoses with potentially disastrous results. In my case, I had the diagnosis, but my status was incorrectly evaluated, or rather, not evaluated at all, because of how I seemed when I walked into the consultation room. So a patient, with or without a diagnosis, should be very sure to make certain the doctor hears the whole enchilada and doesn’t have to go only by what he/she sees in the consulting room.

Waiting to be made Good

despairing here abandoned

trapped in the deeps

between the firmaments

the points of life above

the speckled infinities within

drowning in the deeps

waiting maybe for the spirit of God

to move across the face of the waters

for an evening and a morning

I don’t know where my soul is

to seek, or find or knock, or open

or any redeeming thing

anything would be welcome here

an hallucination for a Comforter

a seizure for an angel

my soul is a world without form, and void

and nothing earthly can fill it

or give shape to it; it shall all be torn away

endlessly old I can scarce believe

in becoming new

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