Bipolar 2 From Inside and Out

Posts tagged ‘depression’

Emotional Numbers

What’s the relationship between mood and emotions? How is the mind involved? Is it even possible to sort them out?

These days, people talk a lot about one’s Emotional Quotient, or EQ, also known as emotional intelligence, or EI. EQ is defined as “the capacity to be aware of, control, and express one’s emotions, and to handle interpersonal relationships judiciously and empathetically.” Emotions are “a natural instinctive state of mind deriving from one’s circumstances, mood, or relationships with others.” Mood is “a temporary state of mind or feeling.” Obviously, the definitions overlap somewhat.

All of these terms are used by the general public. EQ is the currently popular term. You can find any number of “tests” online that claim to determine your EQ. Often these are phrased in terms of your “personality” and may refer to enneagrams or other psychological theories. Other searches revert back to showing you your IQ, even if you were looking for EQ tests. Many of them charge money to show you the results. I’m not interested enough in my EQ to spend the money, though I took one of the tests. I might ask my therapist if she has a handle on what my EQ might be. I’d be happy with a subjective evaluation such as Excellent, Good, Average, Poor, or Terrible. Anything more, like a circular chart with bright-colored segments, I believe I’ll pass.

How do EQ and IQ tests compare? Healthline says, “IQ tests measure your ability to solve problems, use logic, and grasp or communicate complex ideas. EQ tests measure your ability to recognize emotion in yourself and others, and to use that awareness to guide your decisions.” So, completely different things. A person with a high IQ could have a low EQ and vice versa.

So, what else do the experts say about the difference between moods and emotions? “Moods can last for hours while emotions last anywhere from seconds to minutes, at most.”

There I would disagree.

At least, I have an opinion. An emotion is something I feel for a defined amount of time, usually a short one. My husband and I disagree and I feel an emotion of annoyance. But it seldom lasts for mere seconds. It can dissipate within a minute or last for several hours, depending on when we talk it out.

A mood lasts longer than that. Now that I’m relatively stable, my moods may last longer than a week, but less than years. Right now, I’m having a mood of anxiety, which has lasted for nearly a month, which doesn’t show much sign of pulling back, and which I’ve had to discuss with my therapist and my psychiatrist.

Moods certainly can last for more than seconds or minutes – hours, days, weeks, or longer – but emotions can last a long time too. Have you ever held a grudge? It’s not a fleeting emotion. It’s not a mood, but it can last for potentially years – even the rest of your life. What’s left? A state of mind? A personality trait? A decision?

In my research, I did come across a piece about EQ and various disorders. It was on a site that promotes a treatment center for drug abuse, so I don’t know how accurate it is. But it said that empathy, being a major component of EQ, will change in a person with depression. They may feel more empathy for a person who is also suffering, but less for a person who isn’t. This leads to numbness, they say, which may further impair one’s mental health.

In cases of ADHD, the center says, people may have trouble reacting to emotional stimuli and engage in “inappropriate behavior” for a situation. Without treatment and EQ, they may still feel internal restlessness.

Anxiety and EQ, they say, are complicated. Low EQ may mean detachment from things that threaten safety and self-esteem. On the other hand, people with anxiety and high EQ may have a tendency to be so empathetic that they overthink and lack the ability to self-regulate.

The treatment center says it can improve EQ and thereby improve self-awareness, self-regulation, motivation, empathy, and social skills, all in the context of addiction recovery. Whether this is true – whether raising EQ is possible and promotes benefits in understanding and behavior – is, as far as I can see, far from settled. It’s also unclear to me in which order this would happen. Would treating the mental condition raise the EQ, or would raising the EQ help treat the mental condition?

I also encountered a study that said high EQ is positively associated with good general physical health. Yet another investigated the correlation among EQ, a sense of belonging, and mental health among college students. Rejection in particular was associated with poor mental health outcomes.

I’d like to see more on the subject.

How I’ve Experienced Group Therapy

I’m not great at group therapy. I’ve tried, but I never managed to get anything from it.

It may be familial. My father had a particularly vicious cancer, multiple myeloma, which he survived for a dozen years, a lot longer than the doctors thought he would back then.

The hospital where he was diagnosed and treated offered support groups for cancer patients. I remember one called “Make Today Count” (which I think implies a certain recognition of mortality that’s not really encouraging – but I’ve never faced it myself).

My father refused to go. Adamantly. Of course, the choice was up to him, but he chose not to get involved and made no apology for it. It wasn’t that he couldn’t accept help. He just relied on family and friends for it – people he knew and had a connection with. I’m sure that support helped him to survive as long as he did, and I can see how a group of strangers, even if they had the same or similar conditions, wouldn’t appeal to his independent streak. It wasn’t that he didn’t have a positive mental attitude, either. No one could have been more determined that he was going to persevere for as long as possible. No one could have been more confident that he would prevail. And no one could have kept doing the things he loved for as long as possible.

I have had experiences with group therapy, but they have not been successful. When I was in college and experiencing a depressive phase, I went to a group offered by the university’s health services. I was skeptical at first. One woman’s problem was that she didn’t know whether she should marry a rich guy or a poor guy who had both proposed to her. (I’m not denying that she was conflicted, but I wondered how much a mental health group could help. Maybe individual therapy could have helped her clarify her thinking, but then again, I just don’t know.)

The other thing I remember was that once the group facilitator issued us a challenge – which of us could role-play meeting another person and holding a conversation with them. My hand went up, and I performed the task easily. I had reached the point where I could fake my way through simple social encounters, so it wasn’t all that difficult. The facilitator looked impressed and slightly disbelieving. It was something I already knew how to do, so it didn’t actually help me with my problems. I don’t know if it helped anyone else either.

Another time, when I was out of college and in private therapy, my therapist was going on vacation and recommended a group I could go to while she was away. They took us through a relatively simple exercise – making a drawing of our life journey. As I recall, we used only symbols, no words.

When I finished, I burst out crying uncontrollably and didn’t know why. I don’t remember anyone there helping me process what I was feeling. Maybe I expected too much from a therapy group. Maybe they weren’t equipped to handle a meltdown. But it was a thoroughly upsetting and unhelpful experience, and I didn’t go back.

Another group I attended a few times struck me as a bit peculiar. The participants each related a difficult situation they had been in and the symptoms they experienced, then told how they would have handled it previously and how they handled it now. There were lots of quotes from a book they all carried like a bible. There was no discussion – just the facts and the quotes. (Once I offered someone a piece of gum or a mint and they pointed to me, chuckled, and said, “Dry mouth!”) Again, I didn’t find it really helpful.

At this point, I’ve pretty much given up on therapy groups. Perhaps, like my father, I am simply not a group person. I know there are those who will say that I simply haven’t found the right group. They may be right, but I have stopped looking.

There are lots of mental health groups – not therapy groups, of course – on Facebook and elsewhere on the internet. I’ve become the moderator of one (https://www.facebook.com/groups/HopeforTroubledMinds – come check it out if you want to). What founder Tony Roberts and I try to do is offer a place for people with brain illnesses to learn from and share their experiences, with a faith component. Tony, who is much more in touch with the faith-based communities than I am, provides most of that part of the content. I facilitate by curating articles from around the internet on anxiety, depression, PTSD, bipolar disorder, psychosis, and general mental health. I post memes that relate to mental health or offer encouragement – or sometimes ones designed to bring humor to the subject. And I ask questions intended to spark discussion. I hope it helps.

And I also hope that other people have had better experiences than mine. I’d love to hear about them.

What Is Resting Sad Face?

Resting bitch face is a thing, you’ve probably heard. Some people – usually women, though I suppose some men have it too – look mean when their face is still and their muscles are slack. People who see them assume that they are grumpy at the least or maybe sulky or angry – hence the name resting bitch face.

I have resting sad face. Once when I was working at a restaurant, the manager saw me sitting while on my break and told me that I should smile. I replied that I was paid to smile at the customers, not on my break. Of course, that was a bad response, though I know that women are often told to smile more (men, not so much). I probably would have gotten along better with my coworkers if I had smiled more.

But I was suffering from depression at the time, or at least the depressive phase of bipolar disorder, and was untreated. Smiling was something I had neither the inclination nor the energy to do. Sad was my natural expression.

When I didn’t have resting sad face, I had resting worried face. (A different manager asked me, “What does a girl your age have to worry about except ‘Am I pregnant?'” As it happened, that was the one thing I knew I didn’t have to worry about.) I was also suffering – again, untreated – from an anxiety disorder.

What I haven’t had is the mask of “smiling depression.” Many people with depression pretend to be happy most of the time, at least in public. You can see it dramatized in depression medication commercials when someone holds a happy face symbol in front of their face. (In real life, I’ve noted that the depression or sorrow sometimes leaks out around the eyes, though, even past the mask.)

There are two different kinds of smile – the “Duchenne” smile (named after a 19th-century scientist whose major contributions centered on mapping the muscles that control facial expression) and the “Pan Am” smile. The Duchenne smile is the sincere smile of a truly happy person. It’s easy enough to tell when someone is giving you a Duchenne smile. The muscles at the corner of their eyes crinkle, making little crows’ feet. It happens automatically when you think of a happy memory or greet a person you like a lot.

The Pan Am smile is the one where the smile does not reach the corners of the eyes. (It got its name from airline attendants who were required by their job to smile at all times, whether they were at rest or not, happy or not.) No one has resting Pan Am smile face. It’s impossible. It takes a number of facial muscles to smile and when you’re resting, you don’t use those muscles. No, the Pan Am smile takes intention.

The Pan Am smile, however, is the one a person uses when they do have smiling depression. (I used it once when, at a different job, we were all posing for individual portraits. My results were so fake-looking that the photo was never used. They didn’t even let me see it, much less anyone else.)

I’m kind of hoping that these days, I have at least resting neutral face. That sounds like the right expression for a stable person.

Can I Choose My Emotional Reactions?

Back before he started on his path to learning how to live with me, my husband used to refuse to say he was sorry if he hurt my feelings. “I didn’t mean to,” he would say.

“If you stepped on my toe without meaning to, you’d say you were sorry,” I replied.

“Yes, but if I stepped on your toe, I’d know I hurt you.”

“I tell you that you hurt my feelings. That’s how you know you did.”

“I can’t control your reactions. I say something and you react with hurt.”

“I can’t choose my reactions when you step on my toe. It hurts and I say ouch. It’s the same when you hurt my feelings.”

We’d go around like this for a while.

Later, he came around to the idea that I couldn’t control my reactions. There were things that he couldn’t see inside me, from my emotional triggers to my bipolar disorder. At last, he admitted that I couldn’t control my reactions and learned to apologize even for things he didn’t mean to do.

Later still, he claimed that maybe I couldn’t control my emotional reactions, but that I had control over what I did about them. I maintained that I couldn’t necessarily do that. My feelings were hurt and I cried. I could choose whether or not to leave the room or stop speaking to him, but the tears were not optional. They were not something I could choose or control. Believe me, I’ve tried.

Our admittedly small example has larger implications. There seems to be a lot of things we’re supposed to be able to control. In the illustration above, your mind, your relationships, your emotions, your actions, and your words are said to be things you can control.

I would disagree with some of that. As my experience with my husband showed, I couldn’t control my emotions – I didn’t choose them. I can’t control my relationships. There’s another person involved, with a lack of control over their emotions as well.

And my mind. When you live with serious mental illness (SMI), you’re acutely aware that, a lot of the time, you can’t control your mind. From overthinking at one end of the continuum to psychosis at the other, the mentally ill mind does what it will. Personal choice can’t control it. We’re not able to reach inside and change our brain chemicals or the past traumas that influence our minds and our choices. Sometimes medication and therapy can’t control the mind either.

There are also a lot of memes – and people’s opinions and statements – saying that we can control whether we are happy or not. “Choose happiness.” “The only difference between a good day and a bad day is your attitude.”

I’m not even sure that’s true for people who don’t have SMI. Emotions aren’t something that can easily be switched on and switched off. Before I was correctly diagnosed and properly treated, I simply had to go through a spell of depression and wait for it to pass. It’s still largely true for me, except that now I know that the depression will pass, and a lot sooner than it used to.

I don’t think that it’s a good idea to deny your emotions, either. If you feel hurt or sad, let yourself feel that feeling and work through it. It may be trying to tell you something – that you’re angry for a reason, for example, and need to address that reason. Or if you’re sad, recognize that there’s something making you sad and stay with that sadness for a while. Forcing yourself to behave cheerfully denies the reality of your emotions and merely puts a mask on them. And that’s not healthy. Sooner or later, those feelings will leak out from behind the mask or shatter it.

I’ve always been a great believer in choice. But there are things I don’t think a person can or should have to choose. Emotions and our reactions to them are not within our control. Our actions are – leave an abusive relationship, seek help for mental illness, take medication every day, and so much more.

But not everything about us is subject to choice, and I think it’s better to recognize that than to deny it.

(And for those of you who are curious about it, my husband and I have chosen to work on our individual and mutual problems and have accomplished 40 years of struggle and working together to control what we can accept and what we can’t. We choose that struggle and that work every day.)

Feeling Better Than Average

I was chatting online with a friend the other day and asked how she was doing. Knowing that we both suffered from depression and complicated lives, I didn’t expect a throwaway answer like “fine.”

What she said was, “better than average.” She didn’t have time to say more because she was in the waiting room for her therapy appointment. I would say that I have been better than average lately, too.

But it all depends on what “average” means, doesn’t it? For me, an average day (or week or perhaps even month) means I don’t have extreme depression or hypomania, don’t leave my house but can if I have to, and am able to work on my writing. To an “average” person – if there is such a thing – it may not sound like much, but it is my baseline, my average. Better than average means that I have intentionally gotten dressed in something other than pajamas and gone somewhere, have a handle on our finances, and made a lot of progress on my writing. Today, I would say, is an average day. Not great, not awful, but average.

Average is a good place for me to be. It means I’m fairly stable, not troubled overly by symptoms of my bipolar disorder. Better than average is okay, too, though it makes me more wary of whether I may be going over the edge into hypomania. Any better than “better than average” and I know I’m in its grip. “Below average” translates to “low” for me, and means that I’m on the lookout for depression to descend.

My friend, though, has been having an average year that would not be average for me. Her baseline is a lot lower than mine, with several years of family and financial crises, career reverses, and severe depression. Occasionally, she has been even lower than just below average. So, to hear her say that life has been above average of late is encouraging but not necessarily terrific. I hear her “better than average” as saying, “not as bad as usual” – though still not good.

She doesn’t have bipolar disorder, but I can’t remember a time when she was truly better than average by any reasonable definition, at least not in the last ten years or maybe longer. It’s one of those situations in which all I can do for her is listen if she wants to talk. So to hear her admit that she feels better than average seems like something to be celebrated, even though I fear that it is illusory and bound not to last.

I’ll be interested to hear the next time we talk what made her feel above average and whether it has lasted. Was it a momentary improvement in one of her many difficulties? Was it something her therapist can help her maintain? Has her dopamine or serotonin or whatever kicked in? Has her baseline truly gotten better? Or will I see a retreat to her normal below-average (or worse) baseline?

I can’t help feeling that it’s too soon to celebrate. But I do so want it to be real and to celebrate with her. Even if the improvement is only temporary, I know how good that feels and the hope it gives. And I wish that for her. I hope the next time she’s in touch with me, she still feels at least better than average.

Do My Friends Really Like Me?

There have been times in my life when I thought I didn’t have a friend in the world, and my disorder was the cause of it. I was just too weird, too odd – unlovable. I didn’t fit in anywhere, with anyone.

Actually, it started in my childhood. I had the idea that my parents only loved me because they had to – because I was their child. Ergo, if I weren’t their child, they would never love me. This was very untrue and unfair, I now realize, but I lived the early part of my life believing it.

I had very little evidence that I could make friends. I just never seemed to get the hang of it. There were kids in the suburban neighborhood where I lived, but we didn’t form what you would call lasting friendships. As I recall, there were two sisters who tried to humiliate me with a cruel prank involving a Ouija board and tape-recorded “messages” from the beyond.

In third grade, children threw stones at me. I had to have three stitches in my forehead. Another kid chased me around the schoolyard with a hypodermic needle that I hope was imaginary. My “best” friend in junior high school literally kicked me in the ass in front of a group of younger kids, which led to the first major meltdown that I can remember.

Though now, looking back, high school was the time when I began to embrace my oddity. I wasn’t diagnosed yet, so I didn’t know that the depressive and manic episodes were responsible, but I was learning that there were people who would accept me regardless. I had a tight little group of three or four friends, most of whom are still my friends to this day. They taught me that lasting friendship was possible. In college, I acquired another tight little circle of friends – and one disastrous train wreck of a relationship that left me with defective coping mechanisms such as self-harm.

Since my diagnosis, I’ve found more friends. Several have not been able to adjust to my mood disorder and have broken off contact. It hurt badly, of course, but I could see their point. When I was at my lowest point, I was not able to be a good friend to them either.

So, how has bipolar disorder been involved in my friendships (or lack thereof)? First, with all the chaos inside my head and my constant need to deal with it, I didn’t have much energy left to find friends. When I did get close to people, I ended up pushing them away with my erratic behavior. Only a few kindred souls stuck with me.

I suffered from imposter syndrome too. I thought that it might look like I had friends, but they would soon realize how damaged I was and leave. Or I believed that I was faking being a friend and really had no idea how to go about it.

I ghosted people without intending to when I went into a depressive episode. If I met them when I was manicky, I might be the proverbial life of the party, entertaining with my peculiar sense of humor. The next time they saw me, though, I might be an uncommunicative, weepy lump.

Still, there are people who have known me through the whole range of my moods and my disorder, and I am confident that they are my true friends. They really like me (shades of Sally Field!) and some even love me. I have Facebook friends that I keep in touch with regularly. They provide me a link to the outside world. I have IRL friends whom I see occasionally (we tend to live in different states). I even have a few friends nearby.

I love my friends. Because of how hard they’ve been to come by, I value them greatly. They have stood by me. They have invited me to dinner, to their parties, and on their vacations. They have comforted me when I was down, distracted me when I was anxious, and enjoyed my company when I’ve been stable. They’ve cried on my shoulder and I have cried on theirs. They’ve bought my books. Some have even lent me money when I really, really needed it. They have become my family of choice.

I treasure every one of my friends – especially my husband, who is my best friend. I wouldn’t be where I am today without them.

What’s Really Scary

It’s very nearly Halloween and there are lots of scary things out there, from costumes to movies. But here’s what I find scary.

My number one fear is the return of my bipolar symptoms, especially the depression. I’ve been mostly stable for years now, with only occasional and relatively mild symptoms when I relapse. But I still remember what it was like and I don’t want to go back there. The misery and the hopelessness. The numbness and the pain. The lack of joy, or contentment or, for that matter, even blankness.

Hypomania isn’t as scary, though I know it can and does recur from time to time. I don’t have a history of extreme symptoms and, with my husband’s help, I’m able to navigate the ones that do occur.

I can handle it if I get mild “breakthrough” symptoms when I encounter triggers. I have coping mechanisms in place, including simply waiting for them to pass, because I know they will. That trust in my resiliency – and my medications – has grown over the years.

Still, there’s always the thought in the back of my mind that the efficacy of my meds could wane. I could crash again. There’s no guarantee.

Then there’s the fear that I could develop a batch of new symptoms, triggered by God only knows what. I know that some people with bipolar disorder have hallucinations, hearing or seeing things that aren’t there. One friend of mine has heard voices for years, and another one is visited at times by an imaginary animal. (He doesn’t mind it; he says it’s always been pleasant.) Again, not likely, but then again, my brain has already been proven to be glitchy.

Of course, I do find other things scary. I am terrified of bees, wasps, ticks – anything that impinges on my dermal boundaries. I’ve been stung once and suffered no symptoms beyond the usual, but it did nothing to allay my fears. In fact, I took beekeeping in college, hoping that I would get over the fear. That didn’t work either. I still freeze, shake, scream, cover my head, or run. It’s a phobia, though not a crippling one. It doesn’t bother me enough to try eradicating it via therapy. Besides, if the beekeeping class didn’t help with desensitization, I’m not sure what would.

But there are less personal fears that I have too.

Some are societal problems. Stigma regarding serious mental illness still exists. And although people increasingly seem to be concerned about “mental health,” it turns out what they really mean is usually substance abuse or crime. Initiatives and funding tend to focus on those problems, sometimes to the exclusion of actual brain illnesses – except maybe schizophrenia, and then only as it relates to violence or homelessness. Of course, those are real problems, but there are a lot more people who need to be helped that aren’t getting attention, funding, or treatment.

Speaking of treatment, that’s another subject that’s frightening. It just isn’t available in many locations. I don’t know what the situation is regarding available beds in my geographic area, but I doubt there are many, given national trends and the complete lack of an inpatient ward at the hospital nearest me. If I did experience more extreme symptoms, I’m not altogether sure I could get good, prompt treatment.

Finding a psychiatrist or a therapist can also be difficult, bordering on impossible. When Dr. R., my longtime psychiatrist, retired, I tried to find a new one. I called the doctors he recommended, but none had openings. I turned to my primary care physician, who at least agreed to continue my psychotropics until I could find a psychiatrist. Six months later, I got in to see someone. And that was only for med checks. I had slightly better luck finding a therapist, but it was by no stretch of the imagination a breeze. Fortunately, both have managed to avoid retiring.

Call me a pessimist (okay, I’m a pessimist), but I also fear that things aren’t going to get much better anytime soon.

Three Days in the Life

What’s it like to have bipolar type 2? Here’s a look at three typical days.

It’s a day when I’m depressed. I wake up late and try to decide whether to get out of bed. I do so in order to take my meds, since I have to go to the bathroom anyway. If I have anticipated this depression, I will have left a box of Cocoa Puffs by my bedside, and these constitute my breakfast.

If I stay in bed all day, I am bored, because I can’t even focus enough to read. Everything I try to read means nothing to me. If I get up, I spend a large part of the day on the sofa, watching horrible reality shows that remind me that there are other people with crappy lives too. I skip lunch. I forget that I have an iPod with thousands of songs on it. I skip therapy appointments because I’m unable to get up and dressed and drive there. I feel numb and useless and pathetic. My brain reinforces this belief.

In the evening, I cry. I weep. I sob. Snot runs from my nose. I have circling thoughts about every stupid, embarrassing thing I’ve ever done. I try to wait till my husband’s asleep so he won’t hear me crying. I wake in the middle of the night, still crying.

I have anxiety attacks too, particularly when I’m in bed at night. I wake gasping. My husband holds me and strokes my hair until I fall asleep again. It’s really all he can do for me.

My psychiatrist and I keep trying different meds, but none of them does more than take the edge off a little. I still can’t function.

There is nothing I can do to change any of this. I can’t cheer up. I can’t even see a time when I won’t feel this way. This goes on every day for months. For years, even. I’d hope for an end to this, but I have given up on hope.

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It’s a day when I’m hypomanic. I wake up early, not exactly refreshed, but with a more-than-usual alertness. I take my meds, then go downstairs and have a muffin and a container of yogurt for breakfast.

I go to my computer and start writing. I may have an assignment – typing or ghostwriting – or I may just work on new blog posts. The momentum of writing stays with me and presses me to keep going. I write lots, but badly. Maybe I forge ahead and write another blog post or volunteer for more typing. I forget that I need lunch.

I jump around from project to project. I scroll and scroll through Facebook. I check my email every few minutes. I go to clothing websites and order underwear and pajamas and blouses. I look at jewelry, too. I check my bank account at least four times.

I don’t read, because nothing holds my attention. I watch competition shows because of the excitement. I try to listen to music, but I can’t finish one song without flipping to another.

I may notice that I’m hypomanic and try to control it. This goes on for a week or so. I hope it ends soon.

______________________________________________________________

It’s a day when I’m stable. I wake up after nine hours of sleep and take my meds. I have a bowl of oatmeal and a cup of tea for breakfast. I check my calendar and see what I have scheduled for the next few days, such as an appointment with my therapist or finishing my writing or typing assignment. I have peanut butter and fruit for lunch.

I do my work. I reread what I wrote when I was hypomanic and immediately start revising it – if I haven’t already submitted it. I take on new assignments and try to space them out so they’re not overwhelming. Sometimes I even succeed. I keep a calendar on my computer with dates of appointments for both me and my husband, when assignments are due and when bills need to be paid, and which week is recycling week.

I meet with my therapist once a month via video chat and see my psychiatrist four times a year for medication updates. The only time I miss one of those is when my car is at the mechanic.

I’m very close to “normal.” I hope this goes on forever.

This post first appeared on The Mighty.

Are Holistic Approaches to Mental Health Useful?

Well, first of all, the answer to that question depends on what you mean by “holistic.” If you mean treatment that considers the mind, body, and soul, I certainly have to say yes. All three are inextricably intertwined and healing one tends to heal the others as well.

Certainly, the mind is involved – that’s implicit in the word “mental.” To many, this means the brain as the location of the mind. Increasingly, this also means thinking of and referring to mental illnesses as brain illnesses. And the competing theories of what causes depression and bipolar disorder, for example, have had something to do with the brain. Perhaps neurotransmitters in the brain are not behaving the way they are supposed to, or processing traumatic events causes brain illnesses (certainly true in PTSD), or genetics is responsible. whichever it is, the brain is involved.

It’s not controversial to say that the body and the mind are linked in the most profound ways. What affects one affects the other. Mental illness has demonstrable effects on the body, all the way from not being able to care for oneself physically to having a shortened life span. Treatment programs for mental illness often include an exercise component, which causes physical changes in the body and brain. Depression in particular is known to be alleviated by even small amounts of exercise. The exercise partially relieves the depression, which makes it more likely that the depressed person will be able to exercise. It’s a cycle that benefits both the body and the mind.

As far as the soul goes, I don’t feel theologically competent to make any definitive statements. I do know, however, that many people find that spiritual practices such as prayer help them cope with the effects of brain illnesses. It may be subjective, but what works, works. I personally don’t believe that prayer cures mental illness, but even if it just makes the sufferer feel more at peace and more comforted, that’s a component of healing that’s important.

Holistic healing that recognizes the interconnectedness of these three aspects of the person is, in my opinion, more likely to be more effective than any one of them alone.

Then there’s the other thing people often mean when they say “holistic healing.” To many, holistic healing means avenues of treatment beyond the scope of Western medicine. Herbal medicine, meditation, homeopathy, acupuncture, yoga, and crystal healing are among the avenues that have been explored.

There is certainly some validity to herbal medicine. It’s been practiced for thousands of years and the results are well-known, particularly by indigenous peoples who have passed that knowledge on throughout the years. Chamomile, lavender, passionflower, and saffron have been studied for mitigating anxiety or depression in cancer patients, with favorable risk-benefit profiles compared to standard treatments. Ginseng is another popular herb for relieving mental conditions. St. John’s wort has been used as a treatment for depression for hundreds of years, and so has valerian for anxiety. And there are many vitamins and supplements such as B vitamins and zinc that might have beneficial psychological effects.

Unfortunately, there hasn’t been a lot of rigorous scientific study of plant-based medicine. For people who gather herbs and plants from the wild, there’s no telling the potency or amount of the active substance that may be present. Even in herbal products sold at health food stores, there is little standardization, so you don’t always know what you may be getting in terms of dosage.

Meditation and yoga are popular adjuncts to talk therapy and/or medication for psychological problems. In fact, these days, they seem to be promoted as a panacea for mental health. They’re particularly popular recommendations in corporate settings, where they’re seen as a low-cost alternative to more expensive treatments that would affect the company’s health insurance costs.

Nonetheless, meditation and yoga do have beneficial effects on mood disorders such as anxiety and depression, and may be helpful for conditions such as PTSD as well. Any amount of exercise is commonly recommended for people with depression and bipolar disorder. The effects are cyclical. The more one exercises, the more one feels able to get going with exercise. Yoga, being low-impact, is something that can be tried by nearly everyone. I’d still say they are adjuncts to traditional treatments for mental illnesses rather than a first-line approach.

Then there are practitioners of alternative medicine. These therapies range from acupuncture to chi balancing to aromatherapy to biofeedback to reflexology to reiki. Let’s start with one that has some science to back it up.

Acupuncture and its cousin acupressure have solid adherents behind them. Johns Hopkins Medicine says that acupuncture is useful in treating anxiety, depression, insomnia, nervousness, and neurosis, though more studies need to be done. And who am I to argue with Johns Hopkins? If they say it’s effective or even promising, I’m willing to say it falls inside the spectrum of helpful approaches.

Reflexology, not so much. The idea that there are areas on the feet that correspond to body parts and can be helped by foot massage is not scientifically proven for health in any body parts, either anatomically or physiologically. (It hasn’t been disproven either, but you can’t prove a negative.) It’s based on the idea that “energy lines” throughout the body somehow combine in the feet (or hands) to produce a map of the body. It is recommended for anxiety and stress relief.

On the other hand, the massage practice of concentrating on muscles that are tensed is much more well-documented. The Mayo Clinic has said that it can reduce stress and anxiety, and even mentions it as a treatment for depression and seasonal affective disorder (SAD). The thing is, any practice that reduces stress is good for relieving anxiety. Whether or not massage has any effect on serious mental illness (SMI) is doubtful.

Relief from tension is, of course, possible when a person believes that a particular technique can reduce it. So if you believe in aromatherapy, for example, it may help you relax. It’s the placebo effect. I’d rather stick with massage.

Then there are approaches that simply don’t work. Homeopathy is supposed to work on the theory that if a substance is good for the body, introducing a single drop of it into water will be effective in the treatment of a disorder. Never mind the science (though there are rigorous studies that say homeopathy simply doesn’t work), the math doesn’t support this. Diluting a substance to the extent that there are minuscule, millionth amounts per glass of water – or even less – just isn’t sufficient to do anything. If there are larger concentrations of the substance, in which there can be alcohol or heavy metals like iron and lead, there may be drug interactions or serious side effects. In 2017, the FDA alerted consumers that some homeopathic teething tablets contained excessive amounts of the toxic substance belladonna. Belladonna is also said to be a treatment for bipolar disorder and schizophrenia.

Crystals are another way that alternative practitioners attempt to cure assorted diseases and conditions. Jasper and tiger’s eye are recommended for anxiety and lepidolite or citrine for depression. Smoky quartz is even said to relieve suicidal thoughts. I wouldn’t count on it. Again “energy fields” of the body and “vibrations” of the various stones, minerals, and crystals are supposed to combine to affect mental and physical health. I own and wear any number of crystals for their beauty, but have never felt any healing effects. The only benefit I see is if a stone is carried in the pocket as a “worry stone,” which the person can rub to induce a calming effect, an early version of the “fidget spinner,” as far as I can see.

Still, proponents of these alternatives to traditional Western medicine will continue to hope for beneficial effects. The National Center for Complementary and Integrative Health says that Americans spend over $30 billion annually on alternative health care. I say, “Let the buyer beware.”

What If My Symptoms Come Back?

It’s inevitable. Once you’ve dealt with a mental illness, you’re afraid it will come roaring back, even if you’ve been stable for a long time. You wonder if your medications will stop working. You dread “breakthrough” episodes that will put you back in the same awful space you thought you had escaped from. You have flashbacks or dreams that take you to places you thought you had left far behind. You imagine you hear someone call your name and wonder if it’s a symptom. Sometimes, something you never thought of as a trigger will catch you by surprise and send you right back to the dark place, the anxious place, the out-of-control place.

Those fears are not unwarranted. All of those things could happen. For many people, they do. For most, the thoughts pop up at odd moments, even when you’re doing well. They’re unpredictable. That’s part of what makes them so scary – the knowledge that you have no control over these thoughts of recurrence.

It certainly happens to me. I obsess over my own thoughts. I fear dropping back into depression. I wonder if I’m exhibiting hypomanic behavior without realizing it. I overanalyze nearly every feeling I have if it has the slightest hint of a symptom of bipolar about it.

That’s when it’s good to have a strong support system – a person or persons you can talk to and check in with. Someone who recognizes your baseline behavior and when you start to depart from it. Someone who understands your disorder and what the symptoms might be.

I’m fortunate to have a support system in place, though it consists of only two or three people at this point – my therapist, my husband, and to some degree my prescribing psychiatrist. I see my psychiatrist only four times per year for med checks, but I can tell him when I think I’m experiencing symptoms and ask whether he thinks it’s something that warrants a change in meds.

I see my therapist approximately once a month, and she has a better handle on intrusive thoughts and whether they are irrational or not. She provides a “sanity check” for me. Most of the time, she reassures me that they’re normal (or nearly so). Sometimes, she tells me if I should bring them up with my psychiatrist the next time I see him. Mostly, she listens, which is what I think a good therapist does.

The mainstay of my support system, however, is my husband. He understands bipolar disorder from years of living with me and living through my mood swings. He knows my baseline level of behavior and when I begin to depart from it. For example, he can recognize when I am starting to get hypomanic and suggest to me that I might be beginning an episode. Or, if I feel like I might be getting manicky, I can ask him if he sees the symptoms in me or not. If I’m having delusions that other cars are swerving into my lane, he can suggest I take an anti-anxiety med.

Four former members of my support system are no longer there, two because they recognized my symptoms increasing and were not able to deal with them, and two lost to death. Even though my husband and my mental health providers help keep me on an even keel, I do miss the additional input. I need reassurance when I am doing well and help when I begin to veer off course.

This month, however, I am doing better. I just postponed my therapist appointment because I have no pressing issues that need addressing this month. May it stay that way.