Bipolar 2 From Inside and Out

Posts tagged ‘being overwhelmed’

Music Charms the Troubled Mind

Once I knew a man whose wife was going to leave him. I knew he was in a lot of pain and despair about it, though he also turned into a huge asshole before everything was said and done. He was also suicidal for a time.

One day when I was trying to talk him through a bad patch, I asked whether he might turn to music to help him. “What?” he said. “Do you think I should listen to country music and cry in a beer?”

I wasn’t suggesting that at all. I just knew that he was a singer and songwriter of talented amateur status and was known for this in various circles. I honestly thought that music might help.

On the other hand, I always forget, when I am on the downswing, how much music can do for me. It soothes and heals, but it also lets me tap into the emotions that I have been suppressing.

Do I have the inexplicable blues that are part and parcel of my condition? There’s a song for that. Am I feeling unrequited love? Unrequited lust? There’s a song for those too. Is the world spinning too fast for me? Do I need to know that everything will be all right? Or do I just need to know that someone, somewhere and somewhen, has also felt this way? I can turn to music.

“Music, uniquely among the arts, is both completely abstract and profoundly emotional. It has no power to represent anything particular or external, but it has a unique power to express inner states or feelings. Music can pierce the heart directly; it needs no mediation.”
– Oliver Saks, Musicophilia

Saks also says, “The power of music, whether joyous or cathartic, must steal on one unawares, come spontaneously as a blessing or a grace.” There he and I part company.

Music can certainly steal on us unawares, whack us upside the head with a memory, a feeling, a piercing stab of emotional intensity, all the stronger for being unexpected.

But we can also choose to bring music into our lives when nothing else seems to touch us. We can tap into those memories and feelings – good or bad – and let the music wash over us as we listen and feel.

According to scientific experiments with fMRI, music uses more parts of the brain than almost any other activity. The neural connections fire all over the place – more so if one is playing an instrument, but even when just listening. The memory centers, artistic areas, language centers, emotional areas – even the motor complexes – are stimulated.

My problem is remembering all that music can do for me. When my emotions are dulled, flattened by the steamroller of depression, I sometimes forget that I can be any other way. The music I love is always there for me. I can bathe in it, wallow in it, be uplifted by it, float on it, join in with it, feel it emotionally and viscerally and intellectually all at once or one at a time. It can express the things that I just can’t.

When you’re depressed is a time for writing bad poetry. Or you can let good poets and songwriters take you with them as they explore the human condition in ways you’re not capable of. I think that’s why they do it – create their art. The really good ones anyway.

There’s also something to be said for music as distraction. A song from years ago – even a frivolous one – can take you away from your troubles, even if only for a moment. This is not the time for exploring new musical avenues. Remembering that things once were good can feed your sadness, your depression, but it can also give you perspective. If you took joy in this music once, there will come a time when you will again. And maybe that time is now.

Perhaps the most amazing power of music is to provoke catharsis. Certain songs leave me sobbing like a baby. They don’t even have to be sad songs, though many of them are. “The Mary Ellen Carter” by Stan Rogers is about as life-affirming as you can get, but it can still turns me into a weeping puddle. (https://www.youtube.com/watch?v=Fhop5VuLDIQ) His song “Lies” has nothing to do with my situation personally, but its evocative power touches me nonetheless. (https://www.youtube.com/watch?v=D79XOc1vKzQ) And almost no one I know can make it through Kathy Mar’s “Velveteen.” (http://www.last.fm/music/Kathy+Mar/_/Velveteen)

Afterwards, I feel drained and, if not exactly better, less emotionally constipated, I guess you’d say. Clearing away a bit of blockage can be cleansing. If music can do that – and it can – then I don’t care if its country with a beer, jazz with a glass of wine, or hip hop with an energy drink. Even easy listening with a glass of milk, if that’s your thing.

So thank God and Apple for iTunes. And here’s hoping that my Swiss cheese of a memory will give me a nudge in the right direction when I need it next time.

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A Response to the Dalai Lama

This Friday, my Facebook newsfeed included a quotation from the Dalai Lama.

Depression seems to be related to fear, anger and frustration. When you’re in a bad mood, even if you meet with your friends, you don’t take pleasure in their company. But when you’re in a good mood, even if things go wrong, you can cope with them without difficulty. This is why putting yourself in a good mood, making a point of developing a sense of loving kindness gives you greater inner strength.

While I respect and admire the Dalai Lama, on this subject he is wrong.

I wrote a blog post to tell him and his followers so. I posted it on Blogher.com. (Blogher is a site for women bloggers that sometimes syndicates content. It is more general than what I usually post here, so I wrote something special for them.)

As I researched, trying to find when and where the Dalai Lama said this (I couldn’t), I discovered several articles about research into depression and Buddhist principles and techniques.

One was an article by Kathy Gilsinan at The Atlantic
(http://www.theatlantic.com/health/archive/2015/07/dalai-lama-neuroscience-compassion/397706/). It talked about “high-amplitude gamma-oscillations in the brain, which are indicative of plasticity.” What that is or has to do with depression, I don’t know. It sounds like “handwavium” to me.

One that made more sense was this, from Jeanie Lerche Davis at
WebMD: http://www.theatlantic.com/health/archive/2015/07/dalai-lama-neuroscience-compassion. (The feature was reviewed by Louise Chang, MD.)

While meditation can help many who are depressed, it’s not a sure-fire cure, [Charles W.] Raison [psychiatry professor and co-director of Emory’s Collaborative for Contemplative Studies] tells WebMD. “In fact, many people with mood disorders find they can’t do meditation when they’re depressed.” Their thoughts are too overwhelming. They are anxious, nervous, and can’t sit – and likely they need antidepressants, he says.

That’s more like it.

In my response to the Dalai Lama, I said,

Real, clinical depression is not about being in a “bad mood.” It’s true that a truly depressed person does not find pleasure even in ordinarily pleasurable things, such as meeting with friends. But we cannot simply put ourselves in a good mood.

That’s the hell of depression. We want to enjoy the good times. We want to put ourselves into a place of inner strength. But we can’t. Not without help.

In fact, your advice is hurtful to depressed people. Too many times we have been told, “Cheer up.” “Smile! You’ll feel better.” “Think about someone else for a change.” “What do you have to feel bad about?”

Don’t you think we would if we could?

Remarks like these remind us that we have an illness and we cannot cure ourselves by willpower alone – no more than a person with hepatitis or tuberculosis or even schizophrenia can. We need help, and most of us need medication.

You do a disservice to people with depression when you tell them to put themselves in a good mood. You, an enlightened spiritual leader, may be able to do it, but we can’t.

Certainly we can benefit from practicing loving kindness and developing inner strength.

But without treatment for depression, how many of us can do that?

It angers me when people say that depression – or any mental disorder – is something people can or should be able to cure with an attitude adjustment. I’ve heard it too many times from people in my life, and I’m sure you have too.

What’s really disappointing is that someone like the Dalai Lama, with his legion of followers and enormous credibility, is perpetuating this old way of thinking.

This lie.

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Sense of Self

The air is still and blankets all my sense.
I’m muffled, muzzled in the sheltering dark
But dare not hope for fire, with bright, intense,
loud flames that rend the silence with a spark.

I breathe or not. It’s sometimes hard to tell
When swathed in dimness. Stifling, musty scent
Fills up my nostrils and my brain as well –
Which cannot will the veil be shredded, rent

to save from suffocation. How shall I
Withstand this cycle till the day appears
And breezes blow the dust away from my
Stopped ears and eyes and lungs, plugged full with fears?

Pull off the cover and let free the soul.
Take broken breath and heal it into whole.

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I Have This Friend . . .

To have a friend, be a friend.

That’s how the saying goes, and it goes double for friends with mental disorders.

But.

There are limits. Boundaries. You may call them self-serving or self-saving, but there they are.

When you are depressed, you neglect friends, and I have certainly done that. I permanently lost one friend over it. But another kept reaching out to me and I eventually responded. (We then had a good game of “I’m a bad friend.” “No, I’m a bad friend.” She thought she hadn’t reached out often enough. I was glad she put up with my silence as long as she did, until I was able to reach back.)

But I have this friend. We used to be tight. When we were both depressed, we shared our misery and so lessened it. But now that the Pit of Despair is no longer my permanent abode…I have to limit my contact.

Why? My social skills have never been terrific, but now I frequently find myself walking that invisible line between Bad Friend and burnout.

Why is it so hard to be a Good Friend?

First, there is the Disaster Report. Whenever I talk to her, I hear a litany of all that is going wrong in her life. Almost never anything else. I’m no fan of relentless positivity, but its opposite is sometimes hard to bear too, even though I’ve been guilty of the same.

Then there is the fact that any suggestions are pushed away, denied as impossible, dismissed as unworkable. Granted, we have completely different styles of coping, but I feel discounted, unheard. Eventually I gave up sharing anything but a few of my own tribulations, some awful jokes, and commiseration.

Then I get off the phone or off Facebook, usually after half an hour or so. That’s about my limit.

I still keep reaching out. I don’t want to be a Bad Friend. I know I can’t fix her, or even her day-to-day difficulties, the kind even non-depressed people have. But I sure wish there were a way I could help, short of climbing down into the Pit with her. I hope that listening, even half an hour at a time, does some good.

And when I talk to other friends of mine, I try to remember to ask how their day was and what’s new in their life and have they seen any good movies and what is a mutual friend doing. I try to listen if they have something to share, good or bad, and I try not to overwhelm them or play whose-life-sucks-the-most. I try to be a Not-Bad Friend, even if I do have to lean on my friends, at times pretty heavily.

And they do likewise, when they can.

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Mr. Fix-It

Him: I just groomed the cat. I used a cat-a-comb.

Me: *total silence*

Him: Hey, honey! I just groomed the cat – with a cat-a-comb!

Me: *more silence*

I was depressed, and he was trying to cheer me up. Using exactly the same joke that had gotten no response only seconds before. I don’t know why he thought it would work better the second time.

Many men have the instinct that, when confronted with a problem, they will try to solve it. When something is broken, they will try to fix.

I wasn’t broken, exactly, but I was deep in the Pit of Despair, aka the lower mood swing of my bipolar disorder. At that stage I am immobilized, uncommunicative, and utterly humorless.

The fact that Dan had worked in hospitals and psychiatric facilities was actually a bad thing, despite what you might expect. He had run laughter therapy groups, he knew the jargon, and he sincerely wanted to be helpful.

But he didn’t know – viscerally – what depression was like. How it felt in your body and mind and soul, how it damped down your personality and blunted your reactions and removed your ability to view life as anything other than miserable. Certainly not funny.

Later Dan learned all this when he experienced his own bout of clinical depression and became another one of my Prozac pals. But until then, he would occasionally come shrinking at me, until I had to tell him to stop. I could accept a hug, but not a joke or a “remedy.”

But all that was early in our relationship and before I had begun to heal or even get proper treatment. And I literally would not have made it this far without Dan. I need him and likely always will.

When it’s Pit of Despair time again (which it sometimes still is), he checks on me to see if I need that hug, or some food, or a kind word, or just to be left alone. When I am better, he still does the cooking and shopping, and reminds me to eat regular meals and take showers and tells me I smell nice after I do. Sometimes he can coax me out of bed with a tape of The Mikado or out of the house with lunch at Frisch’s. If I’m too nervous to drive to my appointments, he takes me. When I’m together enough to work, he keeps the house quiet and fixes food when I need a break and validates me for being able to bring in money, even when it’s difficult.

But he can’t fix me. And now he knows that.

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Churchill’s Dog

Winston Churchill famously compared depression to a black dog. Here’s a video that takes that metaphor and runs with it.

Andrew Solomon, author of The Noonday Demon: An Atlas of Depression, says, “Depression minutes are like dog years, based on some artificial notion of time.” He goes on to describe how the simple act of getting out of bed and taking a shower can consume hours, leave you exhausted, or be simply impossible without help.

The Noonday Demon

There’s even a Black Dog Institute in Australia, which is a non-profit organization that provides information about depression, bipolar disorder, suicide, and other topics.

Home

There are other metaphors. J.K. Rowling, creator of Harry Potter, talked about depression and dementors. Here’s a link to a post I wrote about that.

Read Your Way to Sanity

The black dog is with me now.

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Not Waving but Drowning

Consider this a trigger warning. The third section is going to talk about some difficult stuff, although in mostly general terms.

Here’s a list of how I know how bad my mood disorder is at any given time. Being bipolar, I cycle in and out of these phases, along with periods of reasonably competent functioning and even, occasionally, contentment or even happiness.

There are basically three stages of increasing dysfunction.

Starting to Sink
My sense of humor takes a hike.
I need more alone time.
I take mega-naps.
I forget that music can help.
I snap at my husband.
Noises irritate me.
I can force myself to work.

Floundering
I don’t want to eat.
I turn off my phone.
I sleep up to 14 hours a day.
Attention span is one hour (or one average book chapter).
I can trick myself into working.

Going Under
Can’t sleep.
Can’t work.
Can’t read.
Attention span: 15 minutes max.
Thinking “Maybe the plane will crash and I won’t have to deal with this anymore.”
Regretting I flushed my stash of pills.
Urge to cut.

Fortunately, I am well-medicated enough that category 3 doesn’t happen nowadays, though I remember it clearly and am appalled. At that point, the only things I can do are keep seeing my doctors and taking my meds. And remember to thank my husband when I come out of it.

(The title of this post is from a poem by Stevie Smith. The last two lines are: I was much too far out all my life / And not waving but drowning.)

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The Universe vs. Me

I set out Friday to drive from Ohio to Michigan – about a 3-4 hour drive, depending on traffic.

Five miles out, the Saturn stopped working. Called husband and AAA. Towed to local mechanic. Probably bad clutch.

So we switched my luggage to my husband’s Blazer. About 30-40 miles away from home, car stopped working. Called cell phone emergency road service. Towed to nearest garage. No idea what’s wrong with it, or if the random mechanic is any good.

So my husband picked me up and put my luggage in the back of his ’84 pickup. Halfway home, the radiator blew. I had a meltdown. Called AAA. Towed home. Had pizza delivered.

That’s it on the vehicles. Not even a bicycle left.

Also, there is No Money, except maybe enough to pay the mortgage and health insurance for February.

I have my Abilify, but it hasn’t kicked in yet.

A couple of friends suggested that this was the universe’s way of telling me not to go to Michigan, thereby avoiding something even more heinous that would happen there.

My questions regarding this theory are:

Did the universe really want us both stranded at home, with no way to get to the store or pharmacy, or for that matter, to the other cars?

Did the universe really want Dan to miss more work and lose more pay, especially since he lost nearly a month’s pay going to stay with his mother while she recovered from surgery?

Did the universe really want us to invest yet more money in the cars, when we just bought two of them new wheel bearings?

My answer: No.

The universe is not conspiring against us. This is not divine retribution for a life of sin. This is not bad karma because I was a cannibalistic serial killer in a past life. This was not caused by some higher power that knew I shouldn’t go to Michigan because the place where I was going to stay would spontaneously burst into flames in the middle of the night.

But sometimes it sure feels like it.

I believe there is no larger “because.” Just the fact that we have crappy vehicles and can’t afford the upkeep.

I have no idea what to do, except go to bed, finish having my meltdown, and stay there till the Abilify revs up.

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The Abilify Saga Continues

It turns out, Abilify works for me. Except now I have to work for Abilify. To afford it, I mean.

I now wake up around 7:30 or 8:00 instead of 10:00. I can concentrate long enough to read whole chapters of books, and am enjoying that immensely. I am able to get showered and dressed and go out to run a few errands. I can decide what to eat and even recognize when it’s time for me to eat.

And I can work. I have taken on a mega-project, which has required my attention up to eight hours a day, researching, writing, editing, and proofreading. I don’t know how well I’m doing (there are some differences of opinion about that), but I’m doing it, goddammit.

I may be pushing myself a little too hard, despite the new energy and focus. The other day I had to force myself, one pitiful step at a time, to address a dozen Christmas cards. “You have the list, you can put the addresses on the envelopes. You’ve got enough stamps, you can surely put them on the envelopes. (Don’t call me Shirley.) Better put return addresses on. You can do that much, then stop. You can slip the cards into the envelopes. How hard can that be? You had them printed with your names, so you don’t really have to sign them if you don’t want to and won’t have to fake your husband’s signature because he’s not here. That would be too much. Now lick the envelopes. All you have to do is stick out your tongue. Might as well take them to the mailbox. You need to get cat food out of the car anyway. Okay, now you can crash. Egg sauce, Ted.”

Many’s the year when all that was Just Too Much. According to the Mystic Law of Reciprocal Cards, we get about four nowadays, and are very grateful for those.

And grateful for the Abilify. Except it’s $800 a bottle, even for the tiny dose I’m taking. I got one free month and one discounted month ($650) from the manufacturer and have spent a lot of time since worrying and seeking solutions.

There will (we hope) be a generic in April. Yay.

I know someone who was taking it and has some left over.

I know someone in Canada.

Will my doctor prescribe a higher dosage so I can break them in half and stretch them (and the cost) out?

I may have at last solved the problem. After hours on the phone and hours more on hold, we finally have new insurance. It costs about as much per month as a bottle of Abilify, but the drug benefit kicks in before we’ve paid the deductible (which is way lower than previously). So our many, many other drugs will magically shrink to $15 per – or less with mail-away – and we’ll come out ahead. A little. Probably. If I can keep up the pace on work.

Plus, now we have dental, and oh lord do I need that. But that’s another story for another time.

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Happy Humbug

It’s a truism that holidays are difficult, not to say hazardous, for those of us with mental disorders. But there are a variety of reasons and a variety of reactions and – dare I say it – a variety of coping mechanisms.

First, let me say, that despite the fact that I was already depressed or bipolar as a child, the holidays were marvelous. Our granny, maiden aunt, and uncle lived a few hours away and we spent Every Holiday there. (My uncle drank, but not when we were kids.)

On Thanksgiving, we’d arrive, the adults would eat themselves into a coma, and then nap while we kids were sent of to the movies.

Christmas was similar, except that we’d get up, open presents from our parents (and “Santa” for the biggies), pile into the car, and head to granny’s. The adults would eat themselves into a coma, and then nap while we kids were sent of to the movies. (I specifically remember The Sting and The Andromeda Strain, during which I saw my first picture of a naked male butt.)

There was no tension involved – no grand dining table, no fancy dress, no distant relatives, no formal manners. We’d simply fill a plate with home cooking, perch on a sofa (which was called the davenport) or chair, and chow down.

My birthday falls between Thanksgiving and Christmas, but poised well enough between the two that it was never combined with either one. Back then, birthdays were simple – cake and frosting from box mixes, four to six neighbor kids, presents (no gift bags), and maybe a couple of party games. (It was at someone else’s birthday party that I was traumatized during a game of Pin the Tail on the Donkey.)

How could anything in later life measure up to those?

Well, it couldn’t. My first Thanksgiving away from home was when I was at college, and we ate lasagna, not turkey. I believe it was the first time I had lasagna. Ever.

Since then all the holidays have gone downhill, or I have.

Any more, they’re a chore, a relentlass gray blob from November through January. (Halloween starts it off. I can’t get with that either.)

For years, I kept up some of the traditions for my parents’ sake. My mother in particular loved everything to do with Christmas – the Macy’s parade, the tree with my father’s favorite old smudge-faced angel on top, crocheted holiday sweaters and snowflakes and handmade ornaments from her foreign penpals and neighbors and church friends.

.muzz3

My first Christmas in my own apartment, I had a small fake tree. When I got married my husband and I tried to get into the spirit with surprise gifts and selecting and decorating my mother’s tree and inviting a divorced friend to dinner with us.

But I was sinking rapidly. At various places I worked, all the ladies sported store-bought Christmas sweaters and sweatshirts (Halloween ones, too) that I thought were just awful. But one year, in a desperate attempt to fit in, I bought holiday sweaters on sale in January to wear the next year. Of course, by then I had lost the job.

Dan and I continued the tradition of dining with our friend John, but our venue changed to Chinese restaurants, where we were kept company by Jews, pagans, atheists, and, no doubt, other depressives and bipolars.

One year Dan was visiting his mother and I was on my own. I tried. I really did. I trotted out a festive holiday sweater and little wrapped-present earrings, and went out to a buffet that offered turkey and beef and ham. But I sat by myself and listened surreptitiously to my iPod. And not holiday music, either. By then about all I could stand was the Christmas jazz from the Charlie Brown TV show.

This year, we ate out on Thanksgiving – but not at the swanky hotel buffet we sometimes took my mother to, or any of the other mega-buffets. We went to a diner that John used to love. I had pork chops and lemon pie. On Christmas I’m likely to be by myself again and may just get festive with a Stouffer’s mac-n-cheese.

Comfort food seems appropriate, and the cats like to lick the dish. Then for dessert – Zoloft and Ativan and Lamictal and Abilify and Ambien. Yum. Visions of psychotropics dance in my head.

 

P.S. I wrote about a Thanksgiving with John on my other blog. If you’d like to see it, go to http://janetcobur.wordpress.com/2014/07/25/thanksgiving-ratatouille-and-a-near-death-experience/

And if you’d like to see my rant about the “War on Christmas,” go to http://janetcobur.wordpress.com/2014/11/09/lets-call-a-truce-on-christmas/

 

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