Bipolar 2 From Inside and Out

Promises Made

September 15, 2024

My husband and I have a pact regarding suicide. No, it’s not a suicide pact of the kind you read about in the newspapers. This is a pact aimed at preventing suicide.

Dan and I both have brain illnesses. He has depression, and I have bipolar disorder. We both take meds for them and are reasonably stable a reasonable amount of the time.

That wasn’t always true, however. At one point or another, we each have considered killing ourselves.

Dan’s episode happened when he lost a job that had started out successfully and well, but devolved into chaos, disappointment, and bad feelings. On the day he was let go, he was so upset that the people where he worked called an ambulance to meet him at our house and take him for a psych evaluation. But Dan has worked in some psych units, so he knew how to answer their questions without setting off any alarms that would cause them to keep him there.

Much later, however, he told me that he really had been suicidal at the time.

My brush with suicide came after my mother died. In the aftermath, Dan did something I thought was dishonest (I won’t go into details), and I catastrophized. I didn’t approve of his action and was alarmed when he said he would do it again in the same circumstances. I felt that if that happened, I would be compelled to drop a dime on him. Then he would be disgraced, lose his job, maybe even be subject to legal consequences. I couldn’t live with the thought of that, so I decided the only thing I could do was fix the situation and then kill myself.

If it seems like those are crappy reasons for suicide, well, they are, but they didn’t seem like it at the time. That’s the insidious nature of suicidal thoughts.

We didn’t just have thoughts, however. We had plans for how to do it. (When we were able to talk about it later, it happened that our plans were almost identical.)

What stopped us? I can’t speak for Dan, but I kept postponing the act until I had settled on a method. Then my meds kicked in and I didn’t feel the need anymore.

Now we have a pact. If either one of us thinks about suicide in the future, we’ve agreed to tell each other, generally by saying, “I’m having bad thoughts.” That’s our code for it. (If we have lesser bad thoughts, we say, “I’m having bad thoughts, but not the really bad ones.”) That’s our pact. We will let each other know if we’re feeling bad enough to consider it so we can get help for ourselves or for each other.

And when we say those words, we know to take them seriously and to talk about what we’re feeling and why. We help each other consider other, less lethal, responses. Fortunately, we have both abided by our pact.

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Where Does the Money Go?

September 8, 2024

Though it embarrasses me to write this, it’s true that when I’m hypomanic, I overspend. That’s one of the ways I can tell that I’m actually hypomanic, when I go on spending sprees. Online shopping is my downfall.

I buy things for myself. I’m still in search of the perfect bra, and I like to have a good supply of underwear. I buy exotic jewelry—amber, picture jasper, zoisite—this despite the fact that I almost never leave the house. I end up wearing the jewelry to my doctor’s appointments. And I know it doesn’t really go with my t-shirt collection.

I buy books. Lots of books. I have an e-reader with almost 2,000 books on it. I know I’ll never read all of them, but I can’t resist something really interesting or by a favorite author.

I buy presents. I see things online that I think my husband might like, buy them, and squirrel them away until his birthday or our anniversary or Christmas. Half the time I don’t even know what he’ll do with them. My latest purchase for him was an articulated copper trilobite. I figure he has a curio cabinet and, if he can’t figure out anything else to do with it, he could put it there.

I buy presents for friends, too. Recently I bought carved stone guitar picks, for no reason, for two of my dear friends who play the guitar. And I sent a friend one of his favorite treats for his birthday.

Has this gotten me into financial trouble? I’d have to say yes. We’ve had some financial reverses recently, but truthfully, we could have absorbed them better if we still had the money I spent. There’s no room left on our credit cards. At the end of the month, things get tight and we have to watch every penny until our Social Security comes in.

Of course, my husband has his own fits of reckless spending. He buys presents, too, mostly for me or his mother. And he buys lots of garden supplies, everything from individual plants to truckloads of mulch. He also indulges in fossilized wood, spheres of polished stone, antiques, and the like. He can’t resist the discount shelves at the grocery store and brings home expensive (but bargain!) delicacies like canned banana leaves and pumpkin pasta sauce. We both like to eat out.

So, how do I try to keep these hypomanic spending jags down? I do try.

First of all, I take my meds faithfully. They include a mood leveler, which I hope will cut down on the hypomania.

Second, I listen to my husband. He often notices when I’m teetering on the edge of hypomania and tells me so.

Third, I try to spend the least amount possible when I do spend money. I buy books when they are discounted to $3 or less. (When we ran out of money at the end of last month, I didn’t even look at the ads for bargain books, just deleted them.) I buy underwear only when it is on a closeout sale. I use gift cards when I have them.

I also try to set limits. I try not to buy things that cost more than $25. (Sometimes I don’t make it.) I watch for sales, free shipping, and 2-for-1 offers. When I consider a larger expense, I talk it over with my husband. (Sometimes he enables me, however.)

Then too, I’m the one who pays the bills and monitors the credit cards and bank account. Sometimes I miscalculate, but I almost always know how much is in the bank and what bills are due and when. There are times when I tell my husband how much we can spend on groceries for the week (not that he always sticks to what I tell him).

Of course, the consequences of my hypomanic spending increase my anxiety, to the point where I’m almost immobilized. (That’s where I am right now.) I’m not sleeping well, or some nights at all. But I am trying to find ways to bring in more money to supplement our Social Security and my husband’s job. But my work is unpredictable and so are my earnings. There are steady months, but right now my assignments are in a slump.

Oh, well. I guess overspending is better than hypersexuality.

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The Varieties of Grief

September 1, 2024

Loss and grief affect us all. If you’re lucky enough that they haven’t yet, they’re coming. You won’t know when or why or how, but they’re unavoidable. There’s no way to prepare for them, either. Loss and grief rock your emotional balance and your mental health.

You’ve no doubt heard of Elizabeth Kubler-Ross’s Five Stages of Death and Dying—denial, anger, bargaining, depression, and acceptance. (Some people say there are seven stages, including the usual five plus shock and guilt.) The stages apply to other kinds of grief besides death and dying.

The thing is, not everyone experiences grief in the same way. You may not experience all five (or seven) of the stages or not in the order they’re usually presented. You might skip anger, for example, or begin with depression. It depends on the type of loss you’re experiencing and your psychological makeup. If you suffer from clinical depression, for example, it’s easy to get stuck in that stage of grieving a loss. If you have anger management issues, you might experience that before you get to denial, or you might skip over bargaining.

Nor is there a time limit on grief. The experts say that six months to a year is a “normal” time for grief to last. Obviously, this is not hard and fast. If it takes you two years or more to return to full functioning, that’s how long it takes. No one should push you to “get over it” in what they consider to be an acceptable length of time (but they probably will).

That said, there is a condition called Prolonged Grief Disorder. When grief lasts for years and interferes with your daily life and functioning, you may be suffering from it. If this is the case, you should consider getting professional help.

Grief enters your life in any number of ways, and not always ones you expect. Here are some of the common and less common ones.

Death

Death is what you usually think of when you consider grief and loss. This is usually the death of a loved one, but it can even be caused by the death of a public figure such as John F. Kennedy or someone you look up to and admire even if they’re not a family member or close friend. Even the death of a beloved pet can lead to very real grief that often is not understood by others.

Loss

There are kinds of loss other than death. If you work at your dream job and the company suddenly goes under or you are let go, you can feel grief and go through the same stages of grief as someone who experiences a death. You might be in denial, for example, or experience a period of bargaining or anger. Losing your home to financial reversals or a natural disaster is another example.

Health

If your health deteriorates severely, you can experience grief or a sense of loss over the things you used to be able to do. If you lose a limb, for example, or are paralyzed by disease or accident, you can feel grief over your new situation and again, denial, anger, bargaining, and depression. Even normal aging and the loss of abilities that often accompany it can cause you grief.

Relationships

The death of a relationship can also cause grief. Whether it’s by divorce, estrangement, or abandonment, you suffer because of the loss. You could obsess over the good times you spent together or be troubled by memories of the relationship when you least expect them, such as when you encounter a reminder of the person.

Ambiguous Grief

Ambiguous grief occurs when the outcome of a situation is unknown. A missing child is an obvious example. You don’t know whether they’re still alive or whether they’ve been abducted and killed. You bounce between hope and despair. You may be angry at God for allowing the situation or at the police for not solving the case quickly. If you have a loved one who is homeless and experiencing a serious brain illness, you may not know where they are or if they’re safe. You imagine the worst. You could blame yourself, even if it’s not logical. Bargaining is one typical response, a case of the “if only’s.”

There are support groups for many kinds of grief, such as for the bereaved, crime victims, or those with a family member in hospice. (This could be called anticipatory grief.) Other kinds of grief, such as grief over the loss of a job, home, or friend, usually don’t have any kind of support group. Friends and family members may try to offer support, but that’s not the same as a group with a mental health professional as a facilitator. Being with other people who have also experienced a particular variety of loss or grief can be a profound relief or lead to healing and acceptance. At the least, it’s a safe, nonjudgmental space where you can process your feelings.

Grief is deeply personal. Although there are commonalities to the experience, there is no one blueprint for grief. What you experience is in some ways unique to your situation. Length and depth of grieving can’t be quantified or predicted.

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Sleeping or Not

August 25, 2024

Sleep is one of the most problematic aspects of bipolar and many other brain illnesses. With bipolar disorder, you tend to sleep too much when you’re depressed and not enough when you’re manic. For adults, the recommended amount of deep, restorative sleep is 7–9 hours. That allows someone to have the proper proportion of REM sleep, which is when you dream and when your brain consolidates memories and experiences.

To this, many of us say, “Hah!”

Right now, I’m torn between the two extremes. I’ve been having mixed episodes, so there are days when I want to stay in bed all day. On other days, I can’t get that restful, uninterrupted sleep. I wake up at around 2:00 a.m. and can’t get back to sleep until at least 6:00. I take a nap in the afternoon, and then can’t get to sleep until around 2:00. Or I’m so exhausted that I go to bed by 8:00 and again wake up at 2:00. Once in a great while I go to bed around 9:00 and wake up in time to see my husband off to work at 5:30. Those are the good days.

It’s true that I’ve had a lot of stress lately. Financial, legal, health, and emotional problems have been piling up for both me and my husband. I read at night after taking my bedtime meds, and I feel sleepy in about half an hour. But when I put down my book and try to sleep, I get racing thoughts about every impending disaster—and there are plenty to choose from. The anti-anxiety med I take does nothing, even if I take a second one (which my doctor allows).

If and when I finally do get to sleep, it’s not restful and restorative. I know that I do enter REM sleep, because I dream. One night recently, every single impending disaster combined into a vision of ultimate dread. It wasn’t just that everything that could go wrong did. They all were over the top, all my fears taken to the extreme with vivid color and sound. Worst of all, I couldn’t talk to my husband about my disturbing dream as I usually do. He was dealing with the same fears and facing the same disasters. It seemed unfair to dump my terrors on him. Although he was involved in the dream, I didn’t want him to think I was blaming him.

Along with the terror dream, I’ve had the normal variety of unpleasant dreams that express frustration or inadequacy—missing a plane, losing a competition—the kind that I can generally shrug off. Now, however, they seem to linger in the back of my brain all day.

There is one thing that helps, but I know I shouldn’t do it. That’s taking a sleeping pill. I don’t currently have a prescription for it, though I did in the past. I stopped taking it when I learned that I slept okay without it. But I still had half a dozen pills and didn’t get rid of them. I thought I might use them if I needed to sleep on a long flight. Instead, I remembered I had them during the current series of crises. And they work. But I have to dole them out carefully. I don’t see my psychiatrist until next month, and he doesn’t prescribe over the phone. I tried to make an appointment to see him earlier, but I don’t have transportation on the days he sees clients.

My best bet at this point is to hope that some of the crises resolve before my appointment and I don’t need the sleeping pill anymore. There’s a chance that some of them will, but then again, they may not resolve in our favor. It looks like more hamster brain for me.

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Prayer and Bipolar Disorder

August 18, 2024

My mother believed in the power of prayer, and thought I should do more of it. I can’t say she was wrong. She prayed for self-improvement (for God to take away her bitterness at a relative) and for social issues (returning prayer to schools). I don’t know whether she ever prayed for an end to my bipolar disorder (she kept most of her praying private between her and God), but I never have. I don’t think it works that way.

So, what do I think about bipolar disorder and prayer? I think there are many things about bipolar disorder that you could pray about.

You could pray that science finds better treatments for bipolar disorder.

You could pray that you find a support system that helps you (or give thanks for the one you already have).

You could pray that you find a therapist, or a therapy, or a psychiatrist, or a medication that helps you. (Though I would recommend putting some effort into doing this one yourself as well as praying.)

You could pray that you have the strength to get out of bed in the morning or the peace to sleep at night.

You could pray for understanding of what you’re going through—from another person, an employer, the world at large, or even yourself.

You could pray that you don’t do too much harm while in the grip of mania or depression.

You could pray that you will recognize when someone is reaching out to you and that you will have the ability to accept.

You could pray that you have the courage to reach out to someone else, and the wisdom to keep reaching.

In my opinion, what you can’t do is “pray away” the bipolar disorder. If you’ve got it, you have to find a way to live with it. If prayer helps you do that, more power to you. But, again, in my opinion, prayer is not a cure for the disorder. There are some things that are meant for religion or philosophy to make better, and things that science has a better shot at.

You can point to various miraculous remissions of cancer or other diseases, or make the argument that removing demonic possession would now be called healing of mental illness. And if those give you comfort or hope, again, good for you.

St. Dymphna is the patron saint of the mentally afflicted (though personally, I think she should be the patron saint of abused children). If she, or God, or some other higher power of whatever religion or denomination or sect can lessen your suffering, go for it.

I just don’t believe that you—or I—personally will be cured of bipolar disorder by prayer.

Feel free to disagree with me.

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Meltdown

August 11, 2024

I haven’t had a meltdown in a good, long while. And I’d prefer to keep it that way. But this week, I had one.

What brought it on? As usual, too many crises all hitting at once. One of every kind—financial, legal, emotional, work, medical, and family. The kind with no obvious solutions.

Individually, I’ve had versions of all these crises before, and gotten through them somehow. I’ve developed any number of coping mechanisms that I can pull out of a hat if I need to. But the hat holds only so much. I can’t keep pulling things out of it if there are no more in there. Hence, the meltdown.

I often turn to my husband when I have a meltdown, but this time I can’t. He’s having a meltdown of his own. It isn’t identical to mine, but they do overlap. Neither one of us has much to offer the other. We do try to support each other to the extent of our abilities. But there’s no denying that we’re both depleted, with not much ability to soothe or strategize.

One thing I could do, and did, was call on a friend so I could let it all out. I’ve known him for years, and he’s seen this happen to me before. And, wonder of wonders, one of the first things he asked was whether I needed advice on my problems or just a listening ear. I chose the listening. What I needed most at that point was to let it all out. And I did.

Once that happened, I was able to pick myself back up and start coming up with solutions. Moving money around. Getting a lawyer. Gathering phone numbers and making calls. Taking notes. Helping my husband calm down when he was having a panic attack and a meltdown of his own.

Another thing I did was reconnect with my therapist. I hadn’t had a session in a few years. She had moved to another practice, I was fairly stable, and our sessions had gotten shorter and shorter because I just didn’t have issues that needed addressing. I had sensibly put the new practice’s number in my phone, just in case. I used it, and within a day heard back from her. I have an appointment scheduled for next week.

I know I’ve done the right things, the things most likely to help resolve the problems, but somehow that doesn’t help yet. I need to get all the assorted crises worked out or at least put on hold before I can return to something resembling stability. Next week will be a rough one, and my phone friend may just get another call. I don’t want to overburden him, but honestly, it’s been years since he’s dealt with me in the middle of a meltdown. I anticipate that Monday will be particularly difficult, with two crises, one major and one relatively minor coming to a head then.

I’m trying to shut down my emotions as much as possible in order to get through all this. I know that’s not ideal, but honestly, I don’t see how I’ll manage without doing that. Of course, that makes the meltdown afterward more likely and potentially more severe. I need to make sure that all my meds are refilled and try to establish a better sleeping schedule, which has been eluding me lately.

Time to make phone calls now, and more later. Wish me luck.

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Ratting Out Max

August 4, 2024

I knew Max and his wife Sheila for a long time. We went to large gatherings together. We all loved mysteries and fantasy books and swapped them back and forth. Max and I both studied martial arts and compared styles. Whenever I wrote an article for a martial arts magazine, he had me autograph it. When they moved to a big house in the country, I spent time there. We went antiquing. I got to know their children, some of whom are still my friends today.

When I was editing a magazine, both Max and Sheila wrote for me. Max sent me copy in envelopes addressed to Fearless, Crusading Editor and variations thereof. He called me a lot too, about the magazine or just to talk, back in the day before bosses monitored their employees’ phone calls quite so assiduously.

They weren’t just a couple to me. They were individual friends. And they trusted that I wouldn’t go running to the other if they told me personal things. I didn’t tell Sheila that Max had a financial reverse that he hadn’t told her about. I didn’t tell Max that Sheila had a medical issue she wasn’t ready to discuss. I figured such things were theirs to work out. And I didn’t tell Max that Sheila meant to divorce him on a certain date. Again, it seemed to me that it was not my place to be a go-between.

It wasn’t an amicable divorce. Max didn’t want a divorce at all. Sheila was adamant that she did. Max asked me to find articles on how bad divorce was for the kids and talk to Sheila. I never did. I didn’t feel it was my place.

Then one day Max called me. I knew it was going to be a serious, difficult conversation. In it, he expressed suicidal ideation. I tried all the things you’re supposed to do. I asked if he had eaten or slept recently. I encouraged him to do so. I asked if he could listen to the music he loved. I asked if he had talked to his psychiatrist or a religious counselor. I asked if he had a plan.

He did. There was a gun in the house.

And I ratted him out.

I knew the name of his therapist, and I called him. And I called Sheila, and I told her. I didn’t want her to come home from work and find his dead body.

Max forgave me for calling his therapist. He never forgave me for calling Sheila. I saw him in public a few times after that, and he was dismissive and rude. I didn’t try to maintain the connection after that.

I stayed close with Sheila for a while until she gave up on my depressive behavior, fearing that I might be suicidal, too. But that’s another story.

To this day, I miss Max’s presence in my life. I read a book or an article and think, “Max would like that.”

And to this day, I can’t feel regret for ratting him out. I feel I did what I had to for my friend. If the same situation arose today, I would do exactly the same, even though it meant losing my friend. At least he’s still alive.

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Murder and Mental Illness

July 28, 2024

Murder is associated in the public mind with brain illnesses, particularly schizophrenia, bipolar disorder, and PTSD. David Hogg, anti-gun activist and mass shooting survivor has a lot to say about the topic: “If you believe it’s mental illness, call your reps and ask that they fund mental h[ealth] programs in our schools and communities. I don’t agree it’s mental illness that causes these shootings But we do need more funding for mental health programs to reduce the growing rate of suicide.”

Hogg has said that systemic poverty, race, and hatred are bigger motivators of mass shootings than mental illness. He also notes, “I do think it’s important to note the shooter at my high school had tons of mental health stuff. From my understanding, … there were school psychologists, there were therapists, there were all these different things involved. And I don’t think one more therapist would have made the difference for him. We need to put our politics aside, and get something done.”

The assassination attempt on former President Trump has stirred up the debate again. The assumption that mental illness is the cause of public acts of violence persists. The usual suspects include bullying, psychotropic medication, and social isolation. There have also been a lot of conspiracy theories and blame tossed around. It was Democrats. It was a “false flag” operation. It was staged. It was a foreign plot. The injury was minor. The injury almost took his life. (There may well be more I haven’t heard.)

I fully expect the mental illness hue and cry to start. In fact, it’s already begun. There have been reports that Thomas Crooks sought information on major depressive disorder and was bullied at school. (He was 20 years old when he fired at Trump. Apparently, he committed no violence while at school.) I stress that these are not facts. They have only been reported in the media and tempered by the term “allegedly.”

Personally, I don’t accept such reports at face value. Media reports in the aftermath of a shooting have so often turned out to be unwarranted, misguided, or premature. I prefer to wait for more reliable, less heated reporting that comes from official sources who have actual knowledge of the situation.

I will say that major depressive disorder is a disorder that leads to violence against oneself rather than others. Even if the Crooks did have it (not proven), it seems unlikely that it was a factor in the incident. Depression more often results in suicidal ideation or attempted or completed suicide than in homicide. That he might have been seeking “suicide by cop” is even more unsupported so far and probably unknowable.

It may be true that Crooks had a mental illness, but we don’t know that yet—if we ever will—and there are other possible explanations for his actions, including garden-variety hatred, violent extremism, and political motivation.

What I do think we know is that mental illness will once again be assumed to be the cause by both the public at large and the media. They may even find some psychological “experts” who never met Crooks and never treated him to expound on his diagnosis or motivation in media interviews. That’s usually the course these things follow. Lilliana Mason, a political scientist at Johns Hopkins University, said today, “It sounds like he was relatively isolated and troubled, sad and looking for attention.”

I also firmly believe that this incident will make no difference whatsoever in the debate on gun control. And if mental illness is the cause, it will be acknowledged as a Bad Thing but will not result in any initiative that would provide funding for better care of those with SMI. A massive tut-tut and a hearty shrug are about all I expect.

I’d love to be proved wrong.

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What Does FINE Mean?

July 21, 2024

I get tired of acronyms—letters that spell out a word and may also stand for the first letters of a word. NASA is okay with me, but I dislike SMART goals, TSA, ATF, and every other government agency. Even more annoying are ones that go on too long and are mystifying to those not already in the know. For example, HHGttG stands for Hitch-Hikers Guide to the Galaxy to SF (science fiction) fans or SMoF (Secret Masters of Fandom).

There are also lots of slogans that make more or less sense, depending. Just Say No. Just Do It. Me Too. Hold My Beer. Keep on Truckin’.

Plenty of acronyms are associated with mental illness, too. SMI. AOT. CARE Courts. BPD. There’s also the infamous FINE. When someone asks how you are and you tell them, “fine,” what that really stands for is Freaked out (or fucked up), Insecure, Neurotic, and Emotional (or empty).

One acronym I’ve been seeing lately is ASK, which stands for Acknowledge, Support, Keep-in-touch. It’s meant to be the “Stop, Drop, and Roll” of how to help a friend who’s having emotional difficulties. I’ve seen PSA (another acronym) ads promoting it on Showtime and MTV (another acronym that is no longer valid). As slogans go, it’s not too bad, although Acknowledge seems a little vague until it’s explained, but Support and Keep-in-touch are pretty clear.

The acronym ASK is associated with the Active Minds organization. Their website is easily findable if you enter “Active Minds” into Google. (The search term ASK brings up too many unrelated hits.) The website it takes you to offers interactive YouTube and “digital experience” links that demonstrate the principles.

Less memorable is ALGEE Assess risk, Listen nonjudgmentally, Give reassurance and information, Encourage appropriate help, and Encourage self-help. It’s a “Mental Health First Aid Action Plan” for helping someone in mental or emotional distress. Assess risk refers to risk of suicide, which may be too complicated a task for non-professionals. The second E, Encourage self-help, refers to suggesting “self-care, self-help strategies, or other ways to get support, such as going out for coffee to talk things over.” Personally, I think the acronym ALGEE is not very memorable and the explanation of the letters is not exactly intuitive.

The slogan that I found most puzzling (although it did get my attention, so it was effective there) is “Seize the Awkward.” The phrase focuses on the idea that, while it may feel a little difficult or awkward to speak to a friend about mental health concerns, you should accept that feeling as natural, then move past the awkwardness and start a helpful or meaningful conversation. The Seize the Awkward website has a lot to offer. There are nine ads for young adults featuring popular or famous spokespeople from music, sports, and other categories. The Ad Council has also provided GIFs, Instagram images, and posters you can use to spread awareness on your own site or location. There is a Campus Toolkit which includes resources on break-ups, loss, suicide, LGBTQ suicide, and racism.

I hereby retract my objection to Seize the Awkward because of its memorability and thoroughness. It’s wonderful. Right up there with Just Do It.

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My Brazen Hussy Phase

July 14, 2024

This is me in my Brazen Hussy phase, back in my college days. The piano player is a friend that I sometimes went places with. (We tried dating once, but it was a total bust.) We decided to recreate a saloon girl-type photo at the piano in the student union building. There was a lot of hooting and cheering as we got in position. I didn’t have a saloon-girl outfit, so I dressed Western instead. The vest was one my mother made for me out of various calico fabric scraps. I don’t remember just when or where I got the leather hat, but it went with me throughout college and beyond.

My Brazen Hussy phase was the first time that hypomania hit, except for the many times that it appeared as anxiety before I went to college, and after.

As many people do the first time they experience hypomania, especially the sexual kind, I rather enjoyed it. I flirted and dated, which I never did in high school. I joined a sorority and went to frat parties. I enjoyed my first kiss and then many more. I had a mad crush on a musician and eventually got to know him too. He was exciting and passionate and awakened something in me that never even seemed to exist before. When he broke up with me, I went into a deep downward spiral. I won’t say that was why I took a year off college, but I was confused about my future, and that surely didn’t help.

Back in my hometown for the next year, I got my hypomanic mojo back. I engaged in what I knew was a risky relationship with a coworker. I kept up with him for years and told him about my former life as a Brazen Hussy and about my depression. We went out during the former and he stuck with me through the latter. But he always said he wanted Brazen Hussy Jan rather than timid, depressed Jan.

I was back in Brazen Hussy mode when I met the man who would become my husband. We were with a couple of women who already knew him and greeted him with a kiss. “Don’t I get one too?” I asked boldly and got one. He kissed me again around the campfire and followed me around all weekend. I basked in the attention. It was exactly what I needed at the time.

Shortly thereafter, I moved back to my hometown. But we conducted a long-distance relationship until finally he moved out to be with me and, eventually, we married.

I won’t say I never went back into Brazen Hussy mode again. Hypomania still affected me. I still got mad crushes and flirted outrageously. Finally, however, I was diagnosed with bipolar and properly medicated. I won’t say the Brazen Hussy mode went away entirely, but episodes were fewer and further between and easier to understand.

I didn’t originally mean this post to be so confessional, but hypomania and hypersexuality are a very real part of bipolar disorder that I didn’t miss out on in my younger years. And that I sometimes miss in my later years. I know that not having those surges of intense feeling is better for me. Nowadays, however, when my bipolar disorder kicks up, it’s generally bipolar depression. I’m a lot more settled now and don’t have much room in life for hypomania. When I experience it now, it usually manifests as anxiety again or mild euphoria and overspending.

But I’d be lying if I said I didn’t miss my Brazen Hussy phase from time to time.

Category:

Mental Health

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