Bipolar 2 From Inside and Out

Posts tagged ‘husband’

Following My Moods

When I was a teen and undiagnosed with bipolar disorder, I had a weird reaction to people around me – I would pick up their moods and personalities and found myself mimicking them. I suppose it was a way for me to try on other personalities that I might someday integrate into my own, when I was stable enough to do so.

When I was a little older, I began journaling, which quickly turned into blogging. My journals were repetitive and boring, consisting mostly of “Felt depressed. Went to post office.” It didn’t seem helpful to me, though I know journaling is helpful to a lot of people. It helps them express what is happening to them and how they feel about it. In that way, it’s like a diary. Going back over a journal after, say, a year or so of writing (not necessarily every day) can help a person track their moods and their triggers. People can note their physical surroundings and emotional response and note whether seasons or weather, food and drink, interactions with certain persons, or other life circumstances have an effect on their moods and can help identify events that bring on depression or mania.

There are variations of this. One friend of mine used Facebook as his “diary.” He would look back through a year of his posts and conversations to determine when depression had struck him (there were fewer posts during those time periods).

In my own case, my husband and I have noticed that our moods follow each other’s. When I am depressed for a few weeks, he becomes depressed, too. When I am hypomanic, his mood lifts and he finds more joy in his own life. We do things together, like baking or watching our favorite TV shows together or going for day-long or even weekend getaways.

The same is true the other way around. When Dan is depressed or angry or just plain surly, I find it extremely difficult to maintain even a level mood. His mood creeps in and takes over mine. I sometimes try to maintain a level mood when this happens, but it is very difficult. I find myself struggling not to lose whatever peace or joy I have. I find myself frustrated by his depression or annoyance, to the point where I want to tell him to snap out of it. (I try not to do this. It doesn’t help anyway.)

If we both hit lows at the same time, or experience anger simultaneously, it gets fairly ugly. That’s when we fight, or both retreat to our rooms, or spend time away from each other, indulging in our own pursuits. Admittedly, such contemporaneous moods don’t hit very often, but when they do, it’s hell.

Both of us have learned techniques to respond to these “following” or simultaneous moods. We generally need more space or alone time. We ask each other for what we need and if the other is able to give it (hugs, for example). We offer what we are able to do, if there is indeed anything we realize might help.

Mostly, though, we just wait for the moods to pass and for both of us to return to a level state. I continue taking my meds and writing my blogs.

Interestingly, it was my husband who first noticed these “following” moods. Over the years, he has become pretty perceptive about both our feelings. It may help that he has studied and even worked in psychological settings for a while (no, that’s not where we met), but I think his real education has been living with me for almost 40 years. In all that time, you begin to notice patterns.

At one time my blogs did record my day-to-day (or week-to-week) feelings and actions. Sometimes they still do. But anymore, I find myself exploring other aspects of bipolar disorder and mental illness in general. I don’t believe I’ve said all there is to say about my feelings and symptoms, but this blog has allowed me to stretch out and consider the wider world of mental health.

Apparently, my husband is getting better at it too.

Laughing Out Loud

There’s nothing funny about bipolar disorder. In fact, one of the ways that I know I’m having a spell of bipolar depression is that my sense of humor flies out the window. Nothing brings a smile or a laugh – not my husband’s awful jokes. Not my friend Tom’s silly songs. Not a funny movie like Arsenic and Old Lace.

I have been in a spell of depression for a little while now. As I mentioned last week, part of it may be reactive depression. But here’s the thing. Reactive depression feels the same as bipolar depression. You have the same sense of misery, loneliness, helplessness, hopelessness, anomie. But you know what caused it and that it will end pretty soon, relatively, unless you tip over into a true depressive episode, which can last a lot longer than that.

But yesterday I laughed. And that was a good thing. It didn’t pull me completely out of my depression, but it let me know that escape was possible, and maybe even starting.

It happened like this:

My husband and I were sitting on the couch, watching TV. I was not enjoying it. Then a commercial came on about “man-boosting” pills that increase testosterone. It promised everything: strength, leanness, stamina, and outstanding performance in the bedroom.

Dan turned to me and said, “Hey, honey. Maybe I should try some of that. Improve my performance in bed-woo-woo-woo!

I turned and looked him straight in the eyes. I said, in a solemn, deadpan voice, without a trace of a snicker: Woo. Woo. I never got to the third Woo because we both dissolved in giggles. And it felt good – not only that I could laugh, but that I could make him laugh. Just thinking about it made us laugh all over again.

Today I am back to feeling overwhelmed, if a little less miserable, but still functioning on some kind of level. I don’t think my depression is over with. But for just a moment, I saw a ray of hope. Yes, it was over something stupid. Yes, I delivered the line with a flat affect. No, I didn’t know it was going to be that funny. I even thought Dan might be offended that I was making fun of him. But the important thing is that we both laughed. 

What I’m saying is that laughter, by itself, is not a cure for depression, however much the memes and the positive thinkers tell you that it is. But if laughter happens to you, it at least reminds you that the depression will end sometime – maybe quicker than you think. The giggles are building blocks that will help you climb up out of your hole, or at least see that there is a way out.

That’s a lot of philosophizing about two words (or syllables, really), and I’m not sure the magic would happen again if either one of us said Woo. But I am taking the memory of that moment with me, for whatever strength it can give me and whatever amusement will stay with me when this depression ends.

All Mixed Up

Leigh-Prather/Adobestock.com

As I mentioned a few posts ago, my psychiatrist and I are working on a medication change that will, I hope, pull me out of bipolar depression. The medication that we changed was a mood-leveler, which sounds like a productive way to start.

We’re increasing the dose, which means it shouldn’t take the time it would for the old drug to “wash out” of my bloodstream (and/or brain) while we’re waiting for the new one to kick in. I’ve been that route before, and it’s miserable.

While I haven’t noticed my moods becoming exactly stable since the change, I have noticed certain effects. I am able to get through the minimum of what I need to do each day, though nothing more. And I have noticed that I am getting irritable. This does not happen so much when I’m depressed. When I’m depressed, I don’t care enough about anything to be irritable.

In fact, irritability is one of the ways that hypomania manifests for me, before I get to the euphoria/super-productive/reckless spending stage. I get snappy with my husband about all his annoying habits, like never giving me a straight answer to a simple question. (What are you watching? A movie. What did you get at the store? Food.) I think he thinks he’s being funny, but I find it frustrating. Not that I don’t have annoying habits too, especially when I’ve either depressed or irritable.

So, I guess in one way, the irritability is a good sign. It doesn’t mean I have level moods yet, but it seems to mean that I’m not totally stuck in the depression. (I explained to my husband what was happening with me, and he seems to understand more. Though it remains to be seen if he’ll answer simple questions informatively.)

I think what I’m experiencing is a phenomenon know as mixed states. If to be depressed is to care about nothing and mania is to care about everything, a mixed state is some hellish combination of the two. Imagine being immobilized and jumpy all at the same time. That’s what it’s like, paradox that it is.

I haven’t had mixed states too often in my life, though I have had emotions that swerve drastically from happy to depressed in an instant (which is an extreme version, I think, of what’s known as ultra-rapid cycling). This is something different, though.

Now, I use up all my spoons early in the day and nap, or I stay up but go to bed at around 8:00. Ordinarily, if I went to bed that early, I’d read for a couple of hours, but these days half an hour or 45 minutes is it, tops.

Still, I think (or hope) that this mixed state of affairs is a step along the way to level moods that are higher than the numbness and not-caring of depression. It’s not comfortable to go through, but then neither is depression or mania, even hypomania.

It’s been about six weeks since the change in my medication. Within another four to six weeks, it will likely become apparent whether the change, once set in motion, will have an outcome I can live with. Until then, I need to spend my spoons as wisely as I can and try to remember not to snap at my husband, even when he’s being annoying.

Bipolar Conversation

This morning a podcast called Bi-Polar Girl was uploaded, and I was the interviewee. (You can find it on Apple, Amazon, and other podcast sources.) Here’s a look at what was like.

  • Prepping. Before we recorded the podcast, my anxiety kicked in, and I tried to overprepare. I bombarded the hosts with emails asking what I should be prepared to talk about or what questions they were going to ask me. Basically, they told me we were going to “wing it” and have me tell my story.
  • History. The thing we talked about most was when I started showing signs of bipolar and when I was diagnosed. I explained that I was showing signs of it as early as my high school years, how I decided to seek treatment after college, and how I was mistakenly diagnosed with major depression for years before receiving the proper diagnosis and medication.
  • Meds. We discussed medication in some detail – pill-shaming, how every person reacts to meds differently (so it’s useless to “recommend” a particular drug to friends or support group members). We talked about the side effects of various medications, including the fact that the most-feared one seems to be weight gain. One particular point of discussion was how many people are afraid that taking medications to treat their disorder will stunt their creativity or turn them into “zombies.” Snowflake (one of the hosts) and I agreed that our creativity and ability to work were actually improved while on medication, because it enabled us to focus and do more creative work.
  • Family. We also talked about the fact that I have no children and my reasons for that. (We also introduced some of our pets during the Zoom call, or they introduced themselves. Just try to keep an animal out of a Zoom call.) I shared that I felt it would be unfair to a child to have a nonfunctional mother, that I was afraid of going off antidepressants while pregnant, and postpartum depression afterward. Snowflake shared her story of medications, potential side effects, pregnancy, and postpartum depression.
  • My publications. I talked about my blog and my books, Bipolar Me and Bipolar Us. In particular, we discussed gaslighting, which features in my second book, and how people with bipolar are more susceptible to it. Both Snowflake and I shared how we had encountered gaslighters in our own lives.
  • Groups. Chacoman, the other host, questioned me about whether I was involved in any local or regional support groups, and I had to admit that I’m not. Now, during the pandemic, group meetings are problematic at best, but I don’t react well to groups at any time, due to my anxiety (which is how my hypomania manifests). In my case, outreach is limited to my blogs and books, and membership in online support groups.
  • Miscellaneous. We got off topic a number of times. I don’t want to make it sound like the interview was all serious or grim. We also talked about our pets, positive relationships, college memories, and even politics.
  • Plans. I talked about how my next book will be a mystery, with a bipolar main character, and received positive feedback on the idea.

All in all, it was a good experience, worth overcoming my anxiety for. I had only participated in a podcast once before, a not-altogether-successful interview about my first book with an interviewer who had obviously not read it and was more interested in whether any of my family members were also creative. (It was supposed to be a podcast about first-time authors.)

This was not the same sort of thing at all. I told my story, as the hosts had recommended, and we had a genuine, far-ranging conversation about not just my own experiences with bipolar disorder, but with how others cope with it as well. Actually, I learned a lot about myself, from how much my anxiety – and especially social anxiety – still affect me, to how much my teen years illustrated my journey into depression.

So, here’s a big thank you to Snowflake and Chacoman for the opportunity to share with them and their audience. I would absolutely do it again. It helped me step out of my comfort zone and, I hope, will help the listeners as well. It’s a form of outreach that I had never considered, but one that I found valuable – and just plain fun!

 

 

When My Carer Needs Care

By Farknot Architect / adobestock.com

My husband is the mainstay of my support system and, in large part, my caregiver. I cannot count the things he has done for me and does for me every day. We’ve been married for over 35 years and during that time he has helped me through daily life, major depression, anxiety attacks, loneliness, irrational thoughts, school, therapy. He makes sure I practice self-care and cares for me as needed.

Recently, though, he needed my help and care. The other day he experienced distressing eye-related symptoms – a large “floater” (dark spot) in his vision and unexpected flashes of light. What could I do about it? First, I answered his request to get a flashlight and look in his eye, but I saw nothing.

Next I arranged an appointment for him at our eye doctor. Dan used to be terrible at admitting when he needed medical treatment, but since a heart scare he’s been much more amenable to seeing a doctor. That particular evening, he was scared and cranky, and made up excuses. He left his phone in the car. That’s okay. I had mine right there. He didn’t know the number. That’s okay. I have it programmed into my phone. I waited on hold. “Forget it,” he said. “Never mind,” I replied. “I’ve got nothing else to do.” He said he didn’t see the floater any more. I pointed out that his eyes were closed. I got through to the doctor and made him an appointment for the next day.

Naturally, I drove him to the appointment, as they would have to dilate his eyes. Then, afterward, I drove him on several other errands (including an appointment with a different doctor) and made sure he ate lunch. I canceled one of the errands and put off others when I saw how tired and nervous he was getting. I took him home and tucked him in bed. (The floater turned out to be nothing truly alarming, just an effect of his aging eyes. He named it “Freddie the Free-Floater.”)

Dan has done almost exactly the same for me, many times. I could usually make my own appointments, but he encouraged me to do so. He has driven me to appointments countless times. He makes sure I eat. When I run out of spoons, he cancels or postpones errands, or even runs them for me. He reminds me when I need to have a lie-down or to sleep or to shower.

It was unusual for me to be the caregiver in this situation, and at times difficult, but I didn’t begrudge it. How could I possibly?

Of course, later in the day, I had a crisis and a mini-meltdown of my own, and there was Dan, ready to be with me, talk me through it, and make sure I didn’t skip a meal.

I know this is what marriage is supposed to be – partners helping each other through their individual and mutual times of difficulty. I also know that mental illness can put a terrible strain on a relationship. I admit that I am very needy at times, and was even more so at other times in my life.

But this time I got to be the strong one and take care of his needs before my own. And I was pleased and proud to be able to do that. Often there’s little enough that I can do for him, except offer him encouragement and remind him that I love him and appreciate him and all he does for me. If he asks for something he needs, I try to make sure he gets it (except for the $900 woodchipper, I mean). And I do what I can that benefits both of us – working to bring in money, paying the bills, doing computer research, handling phone calls, reminding him of appointments when I can – mostly stuff that involves computers and phones and recordkeeping and occasionally knowing where missing stuff is. And reassuring him when he gets trapped in the depression that he also suffers from that I love him and that he is strong and good and that he needs to take care of himself, and that if he can’t, I will try and do my best.

Asking for What You Need

I saw a post on a bipolar Facebook page that asked what coping mechanisms people used. There were the usual responses about self-care, which is certainly a fine coping mechanism. But it’s far from the only one.

I’ve learned any number of coping mechanisms over my years in psychotherapy. There’s “looking at how far I’ve come.” There’s “leaving the room when my anxiety gets too bad.” And there’s always one of my favorites: “petting the cat.”

But the answer I put down was “asking for what I need.”

It’s a good coping mechanism because no one can read minds. No one else knows what I need. And, short of them guessing and hoping to hit on the right thing, the only thing I can really do is ask.

I can ask my therapist whether we can work on my anxiety today. I can ask my friend to check in on me daily for a while. I can ask my husband for a hug, or alone time, or some distraction.

Of course, I don’t always know what it is that I need at any given time. At times like that, I can simply ask for things that might help or have helped in the past, like the aforementioned hug or alone time. My husband has been with me for so long and is so familiar with my bipolar disorder that he knows a number of things that are likely to help, and he can suggest them. If all else fails, he suggests I go to bed, or read, or listen to music, all things which can calm or center me. Sometimes he simply puts on my favorite movie, to help draw me out.

Closely tied to the mechanism of asking for what I need is the technique of negotiation. I may know what I want or need, but the other person may not be capable of providing it, or at least not right then. If a friend can’t take my phone call, I can suggest an alternative: Call me after 10:30 or sometime tomorrow. If I need distraction and my husband has to go to work, he can suggest that we go out to lunch the next day.

We’ve developed a shorthand for such situations. When the only thing I can do is say, “help,” he responds with, “help how?” If I can then come up with a suggestion, I do. A lot of the time he is able to provide what I need. But sometimes he just isn’t. Maybe he isn’t able to get me out of the house for lunch. So instead I say, “I need comfort food.” He usually says, “You can get that.” Or he may respond with what it is that he can do: “There’s cheese and crackers here. Will that do?”

Asking for help isn’t easy, and Lord knows negotiating for what you need isn’t either. Both take lots of practice. And there is always the possibility that another person simply cannot supply what you need. That’s where self-care comes in. I know down deep that a nap, or comfort food, or music may help me, and if no one else can provide them, I can usually do it myself.

Receiving help may not be easy, either. Asking for what you need can make you feel, well, needy. And receiving help from someone else may make you feel guilty or unworthy. But the fact is that you – all of us – need help at times and that learning how to ask for and accept help is a valuable skill. And a totally valid coping mechanism.

When Trauma and Mental Illness Happen Together

Couples who experience serious trauma may go through the experience together, but they do not always stay together afterward. The death of a loved one, infidelity, the onset of a disease – many things can test a couple’s ability to cope with the event and with each other.

Serious mental illness can also be a relationship killer. Dealing with symptoms, treatments, medications, setbacks, hospitalization, mood swings, and just generally going off the rails is more of a task than many couples can handle.

Combine serious trauma and serious mental illness, though, and what you’ve got is a recipe for a new level of disaster.

One of the potential pitfalls is two people who grieve in different manners or on different timescales. One partner may feel it necessary to process events aloud and at length, while the other may prefer to process feelings internally, without conversation. One person may take a year to get over a death, while the other is still grieving after three or more.

Then there’s couple who have different agendas when it comes to whatever is troubling them both. One may feel that moving on is the best response to a traumatic event, while the other person can’t let go of the past.

Many relationships crack and break apart under the strain. And those are just for couples who don’t have mental disorders.

Now take an example (not completely at random) of a couple who have lost their home in a natural disaster. He suffers from depression. She has bipolar disorder. He grieves the loss of their home and all their belongings to a point that she considers excessive. She kicks into hypomania and focuses on the small details of their situation. He thinks she doesn’t grieve. She thinks he needs to help her address the future.

It will be easier for this couple to stay on track and stay together if they can talk about what has happened and what is happening. That may well involve talking with other people – a trusted friend, a professional counselor, even each other. But it’s important that both people feel that they are being listened to and, more importantly, being heard. And that’s not always something that the other partner can provide.

If the couple can talk to each other, their communication skills will be severely tested. Depressed people and those with bipolar disorder both tend to isolate in times of stress. Processing feelings may not be either person’s greatest strength. And those different timescales and differing agendas are likely to throw up roadblocks should they try to talk about it all.

Being aware that trauma and mental illness both have detrimental effects on a relationship may help. Although even previously strong relationships can be stressed to the breaking point, stepping outside oneself to try to understand the other person can be enlightening. Feelings that seem callous or stubborn or flippant or shallow can just be different ways of dealing with trauma. Thinking the way you feel is the only way to feel will severely impede healing.

If it sounds like I am trying to remind myself of all these things, well, I am. We lost our home in a tornado, and my husband and I were dealing with mental difficulties before that happened. I feel that I must be on alert now for any signs that our relationship is cracking. But it’s not just my problem. The disaster, and the mental disorders, and the relationship are things that we share. They have led to a tangle of emotions and reactions that aren’t predictable or rational or even helpful.

We know the basic things we need to do – take our meds, practice self-care (and help each other do so as well), talk when necessary and be alone when that is what’s needed. We have to keep our eyes on what’s important: our mental health and getting through these difficult times intact both personally and as a couple. And we need to see the humor where there is any. But this isn’t the ordinary sort of disagreement that lasts a day or a week. It’s something we’ll be working on long-term.

Wish us luck.

Emotional and Mental Work

I am weary to my bones and to my soul. As the spoonies say, I’m so out of spoons I can’t eat soup.
Physically, I haven’t done that much to wear myself out. A little light housecleaning. Running some errands. Answering emails and making phone calls. No heavy lifting, unless you count the time I had to help my husband push the washer back into place.
No, the heavy lifting I have been doing is emotional and mental. Make no mistake, that is work and it is exhausting. I am responding to a physical and emotional crisis that happened almost exactly a month ago. After the disaster (a tornado destroyed our house), my husband has done almost all of the physical heavy lifting.
The mental work is stuff that I’m easily capable of doing on a good day: dealing with bureaucracy, organizing the trivia of paperwork and daily life, paying bills, etc. Now, however, there is so much of it to deal with that I am falling behind. I haven’t kept up with sorting our receipts. I haven’t returned the phone call about the hole the cable guy made in the wall. I haven’t even listened to the voice mail about it. I haven’t responded to a friend’s request to look over an official letter she is writing.
The emotional work is entirely different. My husband is dealing with issues of grief, loss, and anger regarding the loss of our house and our possessions. Somewhere inside, I must be having similar feelings, but his are closer to the surface and he is able to express them more.
And I am having some difficulty dealing with this. First of all, angry men distress me, even if I’m not the object of their anger. It’s a throwback to other times and other relationships, a button that was pushed and has stayed mostly stuck in that position. Dan is doing his best to accommodate this quirk, trying to keep his voice down and his conversation rational when we speak of it. But I hear him when he is alone in his study, bellowing or wailing in emotional pain about something I do not fully understand.
My husband and I are operating from different places, with differing agendas, regarding the loss of our house and belongings. He invests his memories and emotions in things much more than I do. I look at what can be replaced and he looks at the irreplaceable – artifacts from his trips to Africa and Israel, for example. Those can’t even have a price put on them and there is no way to replace them. His grandfather’s diamond ring could be physically replaced, but not the sentimental value he attaches to it.
I do understand this, though not at the gut level he does. I do (or did) have possessions that meant a lot to me – a guitar, paintings a friend did, some carvings in semi-precious stones, some photos, of course (though some are stored on my computer, which survived). And I think the salvage company did a poor job of inventorying what they had to throw away and keeping what was small but important, letting us participate in the process. But my anger doesn’t extend to revenge fantasies.
All these feelings, both expressed and unresolved, are sapping my strength and my energy. I have gone back to my therapist for reminders of my coping mechanisms and validation on what I have been able to do – and to have a safe space to vent when all of this does begin to spill over.
And now I have decided to go back to work, on a reduced schedule at least. I don’t know if this is a good idea or a bad one, but it seems a necessary one. Perhaps it will provide a missing piece of familiarity in my life, something to anchor me. Perhaps a different kind of work will distract me from what I have been dealing with.
I know there’s still a lot of emotional and mental labor to do, but with help from my husband and my therapist, I believe I will get through it, especially if I pay some attention to self-care: taking my meds regularly, sleeping and eating regularly, taking breaks when I need them, taking comfort in our cats, and trying to eat the elephant one bite at a time.
This is one of the biggest elephants I can remember, though.

When Will My Breakdown Happen?

For those of you who follow this blog, this is another chapter in the saga of our experience with the Memorial Day tornado, which destroyed our house. My husband, who lives with depression, and I have been coping very well so far.

I saw my psychiatrist on Saturday. During the session, I mentioned that I hadn’t had a breakdown yet, but that I knew it was coming. “I hope not,” he replied.

Frankly, I think he’s being unrealistic. I keep saying it will come when we are settled in a living space, which we now are (a rental house) and when I don’t have to deal with insurance, housing, furniture, landlords, finances, utilities, and the thousand-and-one things that I’ve been in charge of dealing with. (Dan has been in charge of the more physical stuff, like salvage at our dearly lamented former house. He’s better at that and I’m better at working the phones and the computer.)

I think my brain will want to decompress with a crying jag and a couple of days in bed, at the very least. I plan to start work again next Monday, so it will likely happen during this next week. I know you can’t schedule these things, but I hope that’s the way it works out.

Dan is already at the ragged edge. He went back to work a couple of weeks ago, though physical health problems interfered with that somewhat. On Saturday he slept the whole day, having worked all night without sleep, owing to our moving out of the hotel and into the house in just a couple of hours. His emotions are also closer to the surface, too. He’s expressed anger at the salvage people and a need to cry when he sees what’s left of the house and our belongings.

Much as I dislike having breakdowns, or mini-melt-downs, or whatever you call them, I think sometimes they are both necessary and inevitable. When a bipolar brain gets too clogged up with the effort of coping during especially trying circumstances, it seems only natural that when the stress lets up even a little, that brain will need to let out all the feelings that have been suppressed while dealing with the crisis.

Bottling up your feelings is generally not a good idea, but sometimes you just have to in order to keep going. But like a shaken bottle of soda, the pressure builds up and there has to be a way to release it. The metaphoric bottle may simply explode, spraying shrapnel and its contents over everyone and everything within reach. This is not pretty, but it is understandable.

Keeping your feelings suppressed too long – putting them in a box and sitting on the lid – is not healthy, either. If you don’t allow yourself to feel the emotions and deal with them, they may fester and spring out of the box at the most inopportune time. Or you may turn off your emotions entirely and not be able to feel anything – including relief and satisfaction, in addition to the distress, anger, and/or despair that are in that box. A lot of us, including me, have done this for years in the course of our disorder. Feeling nothing but numbness can seem appealing if the alternative is chaos and pain.

So, in a way, I am hoping that I do have a bit of a breakdown, in a safe space where I can rage, weep, isolate, and grieve what we have lost. I don’t think I’ll be quite whole again until I have gone through the emotions that I’ve been putting off.

This week I’ve made an appointment with my psychotherapist, whom I stopped seeing about a year ago. I hope that she will be able to help me process the process, as it were. I think it’s definitely time for a “check-up from the neck up.” Maybe in her office, I will find that safe space and begin to feel the feelings that I know are hiding somewhere deep inside me.

 

Disaster in Dreams

On May 27th, our house was destroyed by a tornado. I was on the second floor of the building at the time and the roof came off. I emerged without a scratch.

On June 12th, I had my first dream about the tornado.

Up until then, I had been coping with the disaster, putting one foot in front of the other, dealing with what must be dealt with, eating the elephant one bite at a time. Now, it appears, my disorder or my subconscious has caught up with me.

As is typical with dreams, there are both similarities and differences with real life. As for the similarities, the dream took place in a wooden building and I was on the second floor. I wasn’t wearing shoes at the time. (In the dream I was looking for a pair of boots that fit me. In real life, I was able to slip on a pair of shoes before the rescuers ordered me out.)

But there were significant differences. In the dream, I was not in my house but in a riding stable that shows up on occasion in my various dream landscapes. I was waiting for a horse to ride, which may have been related to my desire to escape.

In real life, I had little to no knowledge that the tornado was coming. I heard about it with no time to get downstairs to a safe place. I put a pillow over my head and hoped for the best. I was alone when the roof blew off.

In the dream, I knew that the tornado was coming. I could see it through a window or maybe through a skylight (which is what our great room became).

The biggest difference, though, is that in the dream I was terrified. I panicked. I screamed. There may have been someone there with me in the dream, but no one who could help me. In real life, I was alone, though rather calm, but as soon as he could, my husband came for me and then the rescue squad came for us both.

I’m not a Freudian when it comes to interpreting dreams and in this case, I didn’t have to be. It was frighteningly literal. Clearly, my conscious mind had fed my subconscious mind all the details it needed to recreate the event in a slightly altered but basically straightforward form.

I had been proud of myself for keepin’ on keepin’ on, doing the things that had to be done. But by the time the dream hit, the mundane details were 90 percent taken care of. We were in a residential hotel instead of a shelter. Our cats, who also survived (there was a part of the dream about missing cats), were with us. The insurance company and rental agents and salvage people were on the job and on the spot. My husband was keeping track of physical details while I worked the phones and the bureaucracy. A friend remarked how well I was handling it all, without having the breakdown everyone including me had expected.

Since that dream, I’ve been more troubled by phenomena like wind, thunder, and lightning. There is less coping to do to distract me and my disorder takes over. Even as I write this, there are high winds and I worry about the hotel’s roof blowing off. (We are on the top floor, which may have been a bad idea. They said it was the “quietest” floor.)

I’ve also had a bad-hotel-experience dream which was almost amusing in its details but seems to me to be a symptom of a deeper disquiet with our current living situation.

My husband and I are not on the same page with all this. His memories reside in things much more than mine do and I cannot be entirely sympathetic with his grief over the losses we suffered. To me, we rebuild and refurnish and salvage what we can and let go of the rest. He’s had his meltdowns too, though he remains solicitous of mine. As far as I know, his dreams are untroubled, though his daily life is, to the extent that he’s considering seeing a therapist. (A local college is offering free counseling to tornado victims – or survivors, however you prefer to think about it.)

I do not like the loss of my composure. I do not like the dreams or the fact that I am having them. I have expected them but was still not ready for them to come. I’m now having trouble getting to sleep at night.

I know this was inevitable but I do not like it. I’m lucky that it held off long enough for me to function effectively. I wonder how long it will be with me. Other traumas I have suffered have recurred in my dreams for literally decades. I hope this one is different.

 

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