Author: Lori Lynne

Where to begin? I am a drug addict in recovery who also lives with a mental health diagnosis. Finding hope, meaning and joy in my process means learning to judge myself and my life by a very different set of criteria from the ones I was taught to use. I connect with the world by writing, exploring creative work such as Tarot, and keeping an open mind to new tasks. I hope something I do will help someone out there feel less alone!

I is for Inconsistency

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Case in point: how many days/letters I just skipped. This is a fact of life. Anything I start has a good chance of not getting completed the way I or others envision it. I have to either abandon a project or be willing to come back to it humbly, again and again if necessary, owning my past neglect and trying not to make excuses for it.

We all have to do it. We tackle our horrific bathroom, chiding ourselves for letting it get this bad. We try to save a dying plant, knowing it wouldn’t be dying if we’d been more diligent about its care in the past. We start exercising again, bemoaning the body that would be so much stronger if we hadn’t stopped.

Yes, we all do it. But when I’m coming out of a depressive dip–or a series of them with some good old procrastination in between–it’s a big barrier to get over. It’s bad enough when it’s a chore, or paperwork, or my health, but it’s worse when it’s relationships I neglected.

This is a topic I’ve written about before and will probably write about for the rest of my life: finding the balance between appropriate remorse and destructive shame. Not being someone who saunters around saying, “Well, this is just how I am!” but also not hiding away from the world and refusing to give what I can.

F Is For “Fuck It”

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The ultimate metamorph, the “fuck it” feeling can be good or bad, destructive or liberating. It can be the moment of casting aside recovery efforts and popping a pill, or the moment of turning away from a useless argument to direct your efforts to more important things.

Recklessness. Apathy. Liberation. Anger. Dismissal. Rejection. Exasperation. Spontaneity. It can mean any of them. And any of its meanings could be playing out in a healthful or unhealthful way.

“Fuck it” is not appropriate when faced with politics…but it’s appropriate when looking at the hundredth headline about the same thing when what you really need is sleep.

“Fuck it” is not appropriate when faced with a difficult relationship…but it is when the same specific argument has happened a hundred times and you have to start looking for a solution that doesn’t involve convincing the other person you’re right.

“Fuck it” isn’t useful when it comes to your health…but it is when you hear the same outdated lecture from your doctor for the hundredth time after they’ve forgotten your logical response to it for the hundredth time.

“Fuck it” isn’t good as a general approach to parenting…but it makes a lot of sense when your kid’s finally dressed for preschool, except they insist on wearing their rain boots on a sunny day, and it was time to leave five minutes ago, and it’s just not worth it.

We need the “fuck it” feeling or it would be hard to let go of anything. Oh, there are more serene ways to let go–but they require a level of confidence and self-acceptance that few of us can sustain all the time. Whatever emotion comes with of “fuck it” helps shut up that voice telling us we can’t stop until it’s solved; until we win.

E Is For Elephant in the Room

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You know the one. Someone brings up the topic of addiction, or mental illness, or meds…and suddenly the elephant is there, pointing its trunk right at you, and there’s an awkward pause in the conversation. Or maybe you’re watching a movie with friends, and the plot introduces something to do with the condition(s) you have, and you feel tension in the room as others wonder how you’re reacting and you wonder whether the fictional character is changing the way they see you. Or you’re at a support group meeting and someone’s sharing about the horrible things Person with Condition X has done to them and people who know you flick their eyes towards you and away and you’re there thinking, “Well, Person with X sounds to me like a total asshole who just happens to have Condition X.”

I’m only one of many who experience this kind of thing. An even more pervasive version is experienced by a Black woman I know who finds it incredibly frustrating to be the only person of color at a gathering because people see her as a “representative” and expect her to react to and weigh in on any remotely race-related topic. She can’t just be in the group as herself.

Sometimes the elephant is present when people know just a little about me and what I have. They’re curious to know more, but they’re uncomfortable about asking. Every decision point makes them unsure whether they will offend. Meanwhile, every misconception they’ve absorbed in their earlier life is coloring how they see me and their judgment of whether I’m a safe person to invite closer.

So when my book is polished a bit more, can I just carry it around and force every new acquaintance to read it? Unfortunately, I don’t think it works that way.

D Is For Despair

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Sometimes despair looks like roses.

It did for me, one day in 2011, when I looked at the roses in my yard for what I thought would be the last time as I prepared to leave and carry out my plan for suicide. (Spoiler alert, I didn’t go through with it.)

Despair looks different on everyone. It can look like slumping on a couch, surrounded by paraphernalia of one’s substances of choice, staring into the distance. It can look like careening through one destructive relationship or hookup after another. It can look like sitting at a computer all night, whether working or gaming, not wanting to see the external world or another person’s face. It can look like a perfectly normal life and come through in nothing but occasional body language cues and microexpressions.

One person’s hallmarks of despair might not indicate despair on another person. They might just be in a fallow period, or a mentally hyperactive period, or be acting out a bit following a breakup.

How is despair different from depression, or grief? I think it’s different because it’s more than a set of phenomena like symptoms, emotions, or behaviors. Despair is any or all of those things grown into a worldview; a set of beliefs. Beliefs about what life is, what possibilities do and don’t exist, and the worth of one’s own self and experiences.

If emotions are weather, despair is geographical change. Sometimes it sets in abruptly, like an earthquake, but more often its effects are slow and insidious. And sometimes it lifts or alters abruptly, with a change in circumstances, but it can also recede as subtly as it came.

That’s what it was like for me. The return of hope was so quiet, so gradual, that it was a shock when I realized it was there.

C Is For Cannabis

~ Lori Lynne ~ 2 Comments

Okay, first, for the record, cannabis is awesome. I am so glad it’s getting legalized more and more. I agree with those who argue that, as a recreational drug, it’s less harmful than alcohol. I’m glad dispensaries carry such a variety in so many forms. I have many friends who benefit from its medical use, whether it be smoking it for nausea or applying CBD oil to aching joints. My own daughter may start using it for her migraines. Cannabis needs to stay legal, get cheaper, and be the subject of research to plumb its possibilities.

But please stop pressuring me to use it. Tell me how well it’s worked for you, once or twice–sure. But let it go after that.

I know many strains won’t produce euphoria. I know all that, I swear. But this one woman keeps telling me I should smoke it for my anxiety, which implies a strain that does something…and for me, an anti-anxiety effect would create a constant temptation to overuse, because I’m an addict and I react in certain ways to things that produce short-term changes. I stay away from certain psych meds for the same reasons. I just can’t use an “off” switch in a responsible way.

It’s true that I belong to a recovery community that views cannabis with a lot of suspicion, so peer influence plays a role in my caution. If I should develop a condition where cannabis really is the only thing that will help, I’ll have to navigate complicated choices. But I am not there yet. Recovery is a lifelong task of risk/benefit analysis.

B Is For Brain

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Does changing my brain mean changing who I am?

I believe in some type of consciousness that surpasses matter. But in everyday life my emotions, thinking ability, and creativity are profoundly influenced by the physical qualities of the lump of soggy goo that lives inside my skull. It requires fuel. It responds to its chemical environment. When I get sick, it loses function. When I took drugs, it responded to that. And when that lump of soggy goo developed bipolar disorder, it changed my life on so many levels I can’t imagine a hypothetical self without it now.

There’s a novel in which the protagonist, an old man, gets his brain transplanted into the body of a young, beautiful woman. He had his original brain and all its memories, but that brain was now bathed in a different chemical soup. The author chose to have the character, a heterosexual man in his old body, become bisexual with a strong preference towards men. The explanation given was twofold: a bond with the previous owner of the body, and the influence of female hormones.

Do I think that explanation is realistic? No, and I think some of the author’s attitudes about gender are quite dated, but it is food for thought. How much of our sexuality, for example, lies in the body, how much in the brain, and how much in a mysterious entity that is neither? Extrapolating, how much of my very identity lies in each?

I don’t mean to define myself by a diagnosis in a self-defeating manner, nor do I mean to discount the role of attitude and insight in my quality of life. I’m simply saying that understanding that I’m coping with a certain kind of brain can help me structure and create a life that suits it as well as possible. I know there’s a huge amount I can do to influence it–but I’m still starting with my individual lump of soggy goo.

A Is For Acceptance

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I used to think acceptance was the coward’s way out. It would be wrong for me to accept my conditions or their limitations, because that would mean I was giving up instead of fighting, fighting all the time, fighting to create a “normal” life like all the inspirational stories out there tell us a disabled person is supposed to do.

The culture I live in glorifies fighting. When a person develops cancer, their process is framed as a battle. Their perceived job is to fight–and if the cancer proves to be terminal, the battle is lost. Death is framed as a failure. For millions like me, life with compromises is seen as a failure. Accepting that I cannot work full-time, or spend too long in certain environments, means stepping away from the meritocracy and accepting a role of someone who’s not in the race.

Settling into a regimen of care that doesn’t fix everything but has been sustainable for years is seen as a failure. I’m supposed to be trying things, constantly seeking alternative treatments, and spending my life in an endless search for a cure instead of living it.

Of course, there’s a balance needed between accepting and fighting. There are many battles to fight every day. If a heavy depression has kept me from washing my hair for days, accepting my greasy locks and itchy scalp isn’t the best choice. Better to fight the inertia, if I can, and drag myself to the shower. Ditto for hundreds of other arenas where I take on my demons to win the prize of some meaningful action.

But accepting myself, in general–accepting that I have the life I do–is key, no matter what it costs.

No Help To Be Had

~ Lori Lynne ~ 2 Comments

This morning I made calls to ten more therapists whose names were given to me by the network my health care plan referred me to because they have no more capacity. I have now contacted about fifty therapists and found no openings in a process that has lasted six months. Even before that, my visits had been dropped to one every six weeks.

The pandemic has ripped the band-aid from several wounds in our society, and I hope this is one of them. There is something fundamentally wrong about mental health care for the non-wealthy; it has been wrong for a while, but this is a tipping point. The ERs are going to be flooded more than they already are–mental health ER visits have increased markedly in many areas.

California’s process for licensure as an MFT or social worker is one of the longest and hardest in the nation, and structured in a way that makes it nearly impossible to achieve working part time because if you don’t finish in six years they make you start over. Counselor trainees, and anyone not working in out-of-pocket private practice, are overworked to the point of breakdowns. Usually, their one goal is to get into private practice and escape their hell.

What is the answer? Peer counseling? A lower-level licensure to work with clients who mostly need coaching and someone to listen? What the hell do we do about this? I want to help, but licensure has been off the table for a while because I can only work part-time. I know I could do useful counseling, if there was a framework to do so. But there isn’t.

Grief Time Warp

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My sister died a month ago. It seems like a very long time, but it also feels as if it happened yesterday.

Grief makes time do strange things. So does depression. So does mania, for that matter. All of these things make our already subjective sense of time much more subjective. But there’s another way grief changes time–you get caught in memories.

I’ve always been resistant to talking about my childhood. Even when I tell my story to a group of fellow addicts or some other group, I act as if I sprang into being as a teenager. “My childhood was better than some, and worse than others,” is the most I will say before moving on.

But I did have a childhood, and my sister was part of it, as were her conflicts with other family members. When she left home to join the military, it affected us all. When her addiction developed and she began to go in and out of destructive behavior, that affected everyone too. When I developed an eating disorder, I looked to her as an example when she was doing the recovery thing. When I myself became a drug addict decades later, I felt even closer to her no matter how little we were talking.

This month has been hard. Not just because I’m sad, but because her death has ripped off the band-aids on all sorts of toxic family stuff. But I am called to strength now. I need to bring passion to my recovery work, because the addiction that slowly destroyed her body still wants mine. After nine years clean, it still waits, and watches, ready to catch me if I fall into self-pity or run too far away from my feelings.

Stop Writing Right Now!

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That’s what my brain has been telling me for a few days. Whether it’s the result of my latest biochemical dip, or the stage of my projects, or environmental factors, is unimportant. And there’s no writer who doesn’t live with frequent self-doubt. Still, I hate it when the “stop writing” thoughts take over for days at a time.

They lay out, in excruciating detail, an array of reasons why my two big writing projects a) suck and b) are meaningless.

Sometimes they focus on the book and tell me it’s boring, self-absorbed, and won’t actually help anyone. Sometimes they focus on the poetry compilation and tell me it’s trite and not topical any more; that the pandemic means nobody cares about addiction even though overdose rates continue to rise.

I’ve done some reading about the nature of thoughts, especially the usefulness of being aware that what I think of as a thought is, in fact, nothing more than a set of words. It has no power. Whether a true story or a false one, it is a story.

I don’t beat myself up for buying into thoughts more when I’m in a depressive dip. It makes sense that my defenses get exhausted then. But it helps to know that I’m doing it; to see the process happening and know it is a process.

The Conversation’s Getting Harder

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Ever since the pandemic began, I’ve felt an unusual amount of pressure to keep it together. Not surprising…health care workers of all kinds are overloaded, so it makes sense that as a concerned person I’d want to avoid making them work harder.

Non-emergency mental health appointments are very difficult to get. My health care system dropped my video visits to once every six weeks, then none. I either cope on my own or, if I feel as if I’m going to harm myself, I am supposed to go to the packed, overwhelmed ER. There’s nothing in between.

I am all right, relatively speaking, so far. But I continue to be worried about others who need more care to manage their conditions—and when my symptoms rise, I’m afraid for myself too.

The conversation about needing help is harder to have these days, especially when extreme political turmoil is added to pandemic stress:

Person With Mental Health Issues: I’m not sleeping.

World: Duh. Nobody’s sleeping right now.

PWMHI: I’m…feeling really depressed.

World: Duh…

PWMHI: I’m anxious all the time. I can’t sit still. I really have the urge to use drugs.

World: Join the crowd.

PWMHI: …. (Struggles to find words to convey that their symptoms are more than just feelings, that they’re in danger from them. Gropes for words that might get them some understanding without making them look like a selfish person who just wants attention.)

World: Are we done here?

Splat

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It happens so quickly. One moment, I’m me. I’m dealing with symptoms, but have a decent sense of self at the center of it all. Then a question comes up. Someone wants to know if I’m up to doing an optional, often recreational, thing. It might be as simple as watching a certain movie. But I freeze.

Am I up to it? Is my brain able to cope with whatever the thing is at the moment? I stare at my questioner like a deer in headlights as my brain whirls. What’s worse, to turn the person down or to try the thing and have it not work out? I think about all the reasons I should say yes; all the times I’ve had to say no in the past…and as I struggle to find words, I’m plastered against a wall of shame like a bug on a windshield.

Still staring at the person who waits for a reply, I’m consumed with hatred for the cycle of apologies that shapes my days. I despise that the necessity for some apologies remains, no matter how well I take care of myself or how much I grow in self-acceptance. I go through a miniature version of the anger and shame I felt when I was first diagnosed, or when I first realized my condition wasn’t going to let me do certain jobs.

At last I answer the question. But whatever my answer is, my mini-crisis churns inside me and tries to taint my experience.

Why Am I Surprised?

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I know how this works. I’m hypomanic for a while. I get all sorts of great ideas for projects. I even work on some of them. My mind whirls with possibilities…then comes the crash.

Then come the nights of less and less sleep as the exciting part of hypomania turns into a complete inability to focus on one thought for amy length of time. Then the disorientation. Then the onset of a depressive phase.

I know how this works. So why is a tiny part of me still taken aback when it happens? Why am I surprised that now my mind is sluggish, or that I react to questions with a “deer in headlights” expression? Why am I surprised that the happy projects of a few days ago seem as far away as the moon and just as unattainable?

Why can’t I accept that I, in effect, have lost a good part of my intelligence for a few days? That I’m going to be physically clumsy and have to take care not to fall and hurt myself?

No matter how much acceptance I achieve, there’s a part of me that fights. I don’t want to be like this. I don’t want to slog through the days ahead and wait for the spark to return. I don’t want to be spending way too long writing this post because of the constant typos my fumbling fingers are making.

I don’t want it, but that’s the way it is.

Leaving the Box

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I have lived most of my life in boxes. Some were shaped like rehab. Some were shaped like psych wards. Many had no physical structure at all, only walls and flaps made of compulsive rituals.

I have lived most of my life obsessed with the next pound, the next pill, or the next scheme to fix myself and leave the realm of brokenness behind forever.

Wars happened while I dwelt in my boxes. Cultures changed, the planet suffered…for most of my adult life I have been on the sidelines, self-absorbed. I don’t say that to beat myself up, only as a simple truth.

There are a lot of limits to what I can do now, but I do believe I have left boxes behind. Even when I have episodes, even when I’m overwhelmed, I am still part of the general community.

I get to experience the fear and anger we all feel. I get to experience ordinary human joys and sorrows. I get to look at myself in the mirror and notice the mundane signs of aging.

I hope I never stop visiting my former boxes, because many friends known and unknown are still in them. But I don’t live there anymore.

Timelessness

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Today is Monday. This has been a public service announcement.

I’m in shock that it is November. My impressions of the last months are separated not by date but by vague phases of no-fires, fires, no-fires, election, and dark, all silhouetted against the pandemic.

For those like me who don’t have structured employment, this timelessness can be a hazard. “Make a schedule,” advice articles say. Yes, I’ll get right on that as soon as I master basic self-care and achieve some sort of consistent energy level.

I am lucky I don’t live alone, or it would be worse. My spouse, who is working from home, gives a few clues—if I do not hear his voice on the constant remote meetings he endures, it must be the weekend.

I have other clues as well. If I’m logging in to my writing group, it must be Friday. If I’m logging in to a certain support group meeting, it’s Tuesday. But there’s still a feeling of timelessness.

Who Counsels the Counselors?

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I’m not working in the counseling field right now. I may never be able to work in it again; I don’t know. But my experience from both sides of the relationship makes me acutely aware of both sides of the mental health crisis which is a secondary effect of the pandemic.

In the last six months, the therapist my health plan allows me to see (a sad once a month) has been replaced three times. There are no longer any therapists there qualified to run certain groups, the only type of help available more often. Counselors all over are quitting many jobs like rats leaving a ship because their client overload and working conditions become too much to handle.

The people who need ongoing therapy for their conditions need it more than ever. People who didn’t need help before now need some. And it’s getting worse as those who marshaled all their strength and white-knuckled it through the last six months feel their grip begin to slip.

Counselors have always faced a high risk of burnout. They must fight to protect their psyche against “vicarious trauma” that builds up when engaging with a client’s trauma. Well, I’ve heard it said that we are all experiencing low-level trauma right now. That means that the stress on the counselors now is not just a matter of time and energy. It’s a matter of extra injury to their minds and souls.

Five Minutes

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I just sat down and wrote a list of five-minute activities. It felt pretty cheesy, but I need to find the willingness to pick one when I feel adrift instead of turning to eating or video games.

As I’ve written before, I’m fine with video games to a point. And I know where that point is; I’m not getting any fun or relaxation out of the game if I pass it. So unless I’m in near-crisis and just have to buy time, it is better to get up and do something else.

Why five minutes? It’s an attempt to break through the block that says something’s only worth doing if I’m going to go the whole nine yards. A walk has to be a long one, scrubbing a toilet has to involve cleaning the whole bathroom, etc. This perfectionism feeds into the “well, I’m not feeling up to all that, so I’ll wait for a time when I am.”

I’ve been ignoring my physical therapy exercises for a hip pain. The whole routine takes a half hour twice a day and feels as far from me as the moon. But wouldn’t it be better to do a few of the stretches than nothing?

Nonzero is always, always better than zero for me. Staring disgustedly at a poem draft for five minutes is light-years ahead of not bringing it before my eyes at all.

Passing for Normal

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I felt normal today because I got to drink coffee from my favorite place, something I haven’t done since February. There were tables very far apart, so I sat drinking and feeling a breeze on the lower part of my face. Such a normal thing that I’ve missed a lot. It made me think of other times I’ve felt normal, or—more likely—just felt as if I looked normal.

I remember passing for thin. Around 2013, I was at the tail end of a very low-calorie diet that took my weight down close to “ideal.” I took a ballroom dance class but never lost the feeling of being an imposter. The body I had, even as it moved while held in someone’s arms, felt like an illusion tricking them.

I remember passing for normal as a mom, mostly when my daughter was little and I’d sit in the park exchanging innocuous facts with other mothers while laughing at toddler antics. Although I was far, far from okay on the inside, the outside looked wholesome.

I remember passing for a normal person at a ball game. The SF Giants were in the playoffs and I was in the stands with my spouse and daughter. I wore an old orange Giants T-shirt of his. I was in orange, just like everyone else. I felt happy to be part of the crowd.

And oh, God, I remember passing for normal at jobs, back when I could. Wearing an ID badge, nodding at meetings, writing up notes. Helping others. Looking competent and adult between my secret anxiety-attack bathroom breaks.

2000 Words

~ Lori Lynne ~ 1 Comment

I’m revising an interesting chapter in my memoir/outreach book this week.

In the chapter, I’m 44 years old and in rehab (again) for painkiller and sleeping pill addiction. I’ve arrived here with the absolute conviction that it will not work; that this is just a way station between life and death. My plan is to stay long enough to clear my mind so I can write a few goodbye letters. Then I’m going to leave and kill myself so my family doesn’t have to deal with my addiction and mental illness any more.

All right…in 2000 words or so, describe this state of mind to a reader well enough to draw them in and give them a shadow of understanding. Convey the numb and matter-of-fact certainty of one’s worthlessness and lack of hope. Use images and scenes to increase a sense of reality. Make everything you’ve already written coalesce into this moment. Do this while making sure the writing is free of melodrama or self-pity.

Ready? Go.

Are They All Right?

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I can’t stop thinking about people from my past. Wondering if they’re okay, what they are doing, how they are dealing with the pandemic. Whether they live alone or with others, whether they’re working. Do they have enough money, how is their health, how are they coping spiritually?

I can reach out to some, if I get up the nerve. “Hey, it’s me, I know we drifted apart decades ago, but how’s it going?” People would understand even if they think it’s weird. These are weird times, after all.

But in a few cases, I can’t for fear of harming the person by bringing up memories that might disrupt their current life. The most painful case is an ex-partner from my mid-twenties. There’s a lot I would like to say to him and a lot I’d like to apologize for, but I’ve never tried because I don’t want to risk negative consequences for him. But I miss him, almost three decades later.

Thoughts of him normally come and go, but they’re so strong now. I don’t know whether he’s married or has kids, if he has a job, if he is struggling to care for an elderly parent…I know nothing. He could be sick. He could be dead.

Over the years, I’ve often pushed away the thought of hiring a PI or paying a website to get just a few pieces of information without him knowing. Just enough for me to know whether he’s within reach of OK. But it feels unethical.

I know I’m probably not alone. I hope other people are braver than me, and free from reasons to hold back.

Yes, I Play Animal Crossing

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I admit it—my daughter and I both find comfort in video games right now. I know a great many people, especially creative ones, who look down on those who play. I know there are valid issues surrounding the effect of both games and other media on the human brain.

That being said, I find video games good for anxiety management. There are times I can’t focus on writing, or wholesome leisure activities like reading poetry. When friends say they’re playing too much during the quarantine, I understand how they feel, but I don’t beat myself up about how long I play.

Animal Crossing: New Horizons came out on the Nintendo Switch console just as the shelter in place was beginning. Because of this, it’s even more popular than it was expected to be. When I can’t sleep, or desperately need something to do with my hands, I’m on my virtual island.

I see it as harm reduction. Sure, gathering pretend resources and building things that aren’t real are not the best thing to do with the times I’m not able to work, but I could be doing worse. I could be relapsing on drugs. I could be overeating and making myself sick. I could be dwelling obsessively on the world’s situation to the point of convincing myself there’s no point in staying clean.

If the worst thing I’m doing is catching fish to sell to a capitalist raccoon, I’ll take it.

What I Deserve

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Do I deserve coronavirus?

As the pandemic becomes more real and more obviously not going to go away any time soon, I’ve started to be more afraid of getting sick. I’m lucky enough to be sheltering in place except for trips to the grocery store, and I live in an area where folks are obeying the mask rules. But I have an illogical conviction that I’m going to get sick. Seriously sick.

I know it isn’t illogical to think I’ll be exposed if this goes on long enough. And I’m somewhat vulnerable because of being over fifty and having diabetes. But my odds are still decent for having a less catastrophic illness than my imagination portrays.

When I sat and unpacked this feeling a bit, I realized it comes from the part of me that thinks I deserve to get sick. That I don’t deserve to stay healthy when so many “better” people aren’t.

Survivor’s guilt. I know it. I’ve tasted it often when thinking of my fellow addicts who died, or fellow mental illness sufferers who didn’t make it through a bad episode. Especially when I think about the roles privilege played in my survival—white privilege, education, health insurance, etc. Regardless of how hard I worked, these other presences can’t be ignored.

And there’s no doubt privilege plays into my survival odds in the pandemic as well. Racial and economic inequities are achingly clear. So it makes sense that I’d have these thoughts. But too many of them are dangerous for me because they feed depression and apathy. Self-care is sliding. I’m not going out for walks. Sleep is worse than usual (and usual sucks.)

Writing sucks too. But today I did small revisions on a segment. And I wrote this.

Control, See?

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I am desperate for some shred of control over my life, my future, my daughter’s future…control I do not have.

Some can take this desire for control and turn it into concrete action, no matter how small, toward improving the situation.

Sometimes I manage that, especially if I can define writing as a beneficial action. Said definition is of course a matter for ongoing debate. I can also make masks, however inexpertly, or clean, or cook meals for my family.

But as many of us do, I’m also seeking control in other spheres of my life. Spheres not directly related to the big problems; spheres where I can have a feeling of control.

Cue the eating disorder.

I’m hearing it from many sufferers…the stress is driving them to more frequent binges, or to more restrictive behavior if that’s a problem, or both.

I knew I’d never make it through these months staying the same weight. Maintenance is not my strength. I’m either going to gain a lot of weight or lose some. In an effort to choose the latter, I put myself on a stricter regimen a couple of months ago.

It’s helping me avoid binges. I’ve even lost a few pounds. But I’m achingly aware of how I cling to the faint sense of control it gives me. I’m thrilled when I lose a pound; I’m worried and upset when I don’t. In the face of this overwhelming world, my brain dwells on such a trivial thing.

I understand. I know it’s what brains do sometimes. I know I’m not alone. But it’s humbling to watch myself race in a circle, knowing full well why I’m doing it, yet still racing.

Chapter of the Week

~ Lori Lynne ~ Leave a comment

Every Friday, I get to hang out with a few other writers and read the latest chapter of my book to them. The hanging out is done online right now because of the pandemic, but it’s still enough for me to make sure I at least revise a chapter for the week.

I’m at a stage where I’m going through the book chronologically and doing tweaks and consolidations. It’s the first time my group is hearing the chapters in order, because the first round of chapter segments were created and shared in haphazard fashion. Sometimes they skipped decades forward or backward.

Going in order is harder. It’s scary to be marching forward, one chapter a week, knowing that at some point I’ll reach the end of pre-written stuff for revision and have to write a few missing chapters at the end. Then an introduction. And then it will be a fucking manuscript.

And I’m doing this during the pandemic, with the future so uncertain, and my critical voice shouting that no one’s going to want to read anything about any other subject besides this for the next indefinite number of years.

Calla Lilies

~ Lori Lynne ~ Leave a comment

(Reposted from my archive, Not This Song)

My daughter brought me calla lilies on Mother’s Day.

It was 2011, and instead of carrying them into my room or proudly displaying them on the breakfast table she held onto them tightly during a long car ride.

She and her father signed in and had the bouquet inspected, then waited while I was notified that my visitors were there. Only then did she get to give them to me. Only then did she get to be hugged, and hear how beautiful they were, and see me read the little poem she wrote on the homemade card shaped like a butterfly.

That is Mother’s Day in rehab, and I can never see calla lilies without thinking about that day. I wasn’t the only one getting cards and flowers, and I wasn’t the only one to gaze at them with a mixture of emotions too tangled to articulate.

Mother’s Day is hailed by therapists as one of the most stressful days of the year for a reason–none of us is without feelings on the subject of the mother we had and/or the mother we are. Told by commercials and companies how we should feel about our mothers and children, we writhe in discomfort with our more complicated internal landscape.

Complicated it may be, but it’s a pretty fair bet that being institutionalized isn’t in any of our personal “what kind of mother I want to be” manifestos. It kind of kicks things up a notch in terms of regret.

After that day’s visit was over, I looked at the smooth whiteness of the lilies beside my bed with a kind of doubled vision, seeming to see bouquets like it in many other places. I knew that many children wouldn’t get to deliver one at all due to the rules of the rehab, or hospital, or prison their mother was currently inhabiting.

I’m happy to be at home on Mother’s Day this year. Didn’t get any lilies. Don’t want any. But she can give me flowers, or a hug, or a thorough trouncing in video games, any time she wants to, because I am here.

Mothers who can’t be at home today, I remember you. I know better than to judge your love for your children based solely on where you are. Don’t give up.

Children, fathers, grandparents and all who visit, I remember you. Thank you for your love and effort.

Happy Mother’s Day.

Masks

~ Lori Lynne ~ Leave a comment

I am sewing masks, the way many people are lately. I don’t sew very well, and I swear like Samuel L. Jackson whenever I stab myself with a pin, which is often.

I am asking myself frequently whether it’s worth the amount of time, frustration and literal blood it takes for me to produce a small fraction of what I see better sewing folks and/or those with more physical and mental stamina are producing.

It has been many years since I approached what I think of as a “normal” level of productivity. Because my disability is mostly invisible (unless you live with me) I struggle with internalized ableism and hold myself to a standard I will never meet.

I know I’m not alone. I know I shouldn’t compare myself to others. But sewing’s the least of it…I pour myself into my writing in little chunks, knowing I’ll never be able to put in the kind of hours, or networking time, or number of events others can.

These feelings are normal for me. They don’t get argued away. I just have to make sure my deeper beliefs coexist with them: Yes, what we do matters. Yes, every little bit helps. Write the book. Write the poem. Make the mask.

Holding On

~ Lori Lynne ~ Leave a comment

So what’s the pandemic like through the eyes of a mental patient and recovering addict?

Well, there’s a lot of pressure to keep myself together, of course. Strong voices telling me this is NOT the time to have an episode or need a meds adjustment. And certainly not the time for a relapse on drugs.

It’s scary, because while not doing drugs is something I can control to a degree by practicing recovery techniques, the mental health thing is under less control. I can take my meds religiously. I can try to eat well and get a little exercise and do things that connect me to what I value. I can do all this, and it still might not be enough because neurochemical shit happens sometimes.

Meanwhile, all the “normal” people around me are experiencing levels of anxiety they aren’t used to. They need me to be functional so I don’t drain their energy away from managing their own stress.

“One day at a time,” is more real than it’s been for a while. I try to make plans…what part of mask sewing I’m going to work on today, what I’m going to eat for lunch, whether I’ll go for a walk. And while I do that I’m acutely aware of the degree of privilege I have compared to some of my fellow sufferers.

I have loved ones in my house. I have access to the medicines I need. For now, my family isn’t in danger of losing our home or not having enough food. I’m lucky.

Do you hear that, brain? We’re lucky. Now show your gratitude by refraining from any shenanigans until further notice.

Things I’m Not Doing

~ Lori Lynne ~ 1 Comment

Right now, a drug addict paces in the ER, so desperate for a fix that COVID-19 holds no terror for them.

Right now, some sick person is waiting too long for an ambulance because two paramedics are running up to an addict’s apartment to Narcan them for the third time this month.

Right now, an addict is spamming one of their doctors’ overloaded phone lines with demands for prescriptions.

That addict could be me.

It’s been more than eight years since I got clean. Since I experienced the magic mix of luck, grace, privilege, and yes, hard work too, that helped me (so far) beat the odds.

If I were still deep in my addiction right now, I could do any of the things I’m thinking about. It would feel like a matter of survival to get the drugs I needed, and the threat of deadly illness to myself and others would feel very far away.

Someone who routinely takes a handful of pills they know might kill them isn’t exactly dialed in to any logic of self-preservation, let alone consideration of others.

I’m not doing anything great in the pandemic so far. I don’t work in an essential business like health care or food acquisition. I’m one of the many whose most useful contribution is to stay the fuck home and take really good care of myself to minimize the chances of getting sick, or having to go the ER for any other reason.

But at least I’m doing that instead of being an active liability. And if all I’ve accomplished in the past eight years is just developing the ability to be less of an asshole at a time like this, I’ll take it.

Sidelines

~ Lori Lynne ~ Leave a comment

Yesterday, I heard an opinion that those like me who live with mental illness won’t suffer as badly during the pandemic as those who are used to being happy and productive.

The logic goes like this: we’re used to feeling bad, we’re used to sitting on the sidelines and not being able to do much, so how is this different?

I didn’t know how to react when I heard this. I wanted to talk about what it’s like to be seen as a constant liability to the world. I wanted to point out that right now a lot of mentally ill people are trying extra hard not to be a burden on an overloaded system. When their symptoms torment them, the knowledge of the crisis feeds their shame and lowers their resistance to judgment and stigma.

There is no time to be mentally ill while the world burns, the thought repeats. So what if they’ve run out of their meds, or if the only thing keeping them going was that therapist they can’t go see now.

They will not ask for help. They will try to cope as best they can. Some will fail to make it through.

Let Us Write Together

~ Lori Lynne ~ 1 Comment

You are loud today, world.

This is not a week when I can even try to defy you, blot you out or forget you.

There is no muffling the parts of your voice that shriek at me not to write. That tell me it won’t matter, that any story I tell is unimportant. That thinking about the projects I cherish is shallow and self-absorbed.

You are here in the room with me, humming and babbling and singing.

So get comfortable.

I have found extra chairs.

Sit here, pandemic.

Read over my shoulder, climate change.

Correct my spelling, cruelty. Play with my paper clips, ignorance. Have a mint, fear.

Let us write together.

The Sin of Happiness

~ Lori Lynne ~ 1 Comment

I have a secret. A dirty, dirty secret. One that’s been embarrassing me more than my drug addiction, or mental illness, or other general faults and vulnerabilities.

I’m happy.

Writing that makes me immediately feel the need to write that I’m also sad, frustrated, angry, worried, afraid, et cætera. As is normal for the times we are living in. And those things are true.

But, at certain moments, I’m happy. And when I am—here’s the REALLY embarrassing part—I think I’m happier than I’ve ever been in my life.

The last five years have brought a flowering of creativity and the growth of a completely illogical degree of self-acceptance. Never total, never unchallenged, but there.

As the world goes to shit around me, I’m having fleeting experiences of joy and wholeness. My superego tries to tell me I’m shallow and self-absorbed for feeling these things. My heart is not listening.

Meeting a Reader

~ Lori Lynne ~ Leave a comment

I had another “first” last week; the first of many new experiences for someone who’s never written a book before.

I was at a sort of cheesy group mindfulness class. Most of us had been referred there because we suffered from depression, addiction or other conditions, and didn’t get to see a one-on-one therapist very often on our health plan.

So, one woman in the class talked about not thinking the techniques we’re learning would work for her. I’ll paraphrase what she said:

“Okay, so maybe this homework will help with my depressive thoughts and feelings. But what if I have depression and addiction? What if I have depression and addiction and trauma to deal with? I’m supposed to just let it all in? It’s too much. I could never address it all at once. But if I stop working on any of them they sneak in and sabotage me.”

Her voice was edged with both resentment and resignation. Resentment because she was already feeling dismissed and expecting to be patted on the head and told to go play like a good girl. Resignation because even as she spoke, she didn’t think speaking up was going to do any good.

I wanted to let her know she was not alone. I wanted her to know someone understood what it’s like to deal with multiple conditions. Understood the “it’s too much” feeling, understood what it was like to feel different no matter what therapy you’re trying. What it’s like to throw yourself into treating one thing and work your ass off only to be tripped up by one of the others, until you’re where she is: a place of “it’s too much.” And I wanted to tell her there is life and growth coexisting with that place.

I said some things. I named the different conditions I live with. But what I really wanted to say to her would have taken a long, long time.

What I really wanted was to give her my book. Have her take it home, curl up and read it cover to cover and know she wasn’t the only one to feel some of what she felt.

The contents of my book are what I wanted to say to her. And that makes me feel that, no matter how hard the writing and editing is, I am on the right track.

Safe

~ Lori Lynne ~ 1 Comment

“Safe space” is a concept these days, and I’m for it. But is there really such a thing as a safe space for me?

I’ve been struggling lately with the fact (as I’ve mentioned) that I no longer feel safe talking about any kind of physical or mental health issue with some people. From now on, when certain people greet me and ask how I’m doing, I am in perfect health and having a good day. Like a gazelle in a herd, I must not show weakness or injury lest I be targeted by wolves.

“But wait,” I interrupt myself, “isn’t it important to be authentic about your issues? Might you be missing an opportunity to be helpful to someone?” Well, I don’t put up shields lightly. This is a case where I’ve shared my truth several times and had it discounted.

So that’s become a space that is safe for me to talk about writing, but not other things. There are spaces where I can talk about addiction, but too much talk of psych treatment might get me rejected. There are therapy spaces where I can talk about mental health, but have to hold back on talking about my writing lest I be accused of intellectualizing.

Sometimes being unsafe is the right thing to do, of course. Sharing honestly in a recovery meeting may help someone feel less alone, so it can be worth consequences to me. I have to weigh the risks and benefits and make a choice about how transparent to be.

The book in progress, of course, represents a choice to be extremely transparent. It’s possible to do because I can tell myself that no matter how many “unsafe” places it ends up, it has a good chance of also reaching places where it could help someone else feel a little safer. A little more seen.

When Truth Doesn’t Matter

~ Lori Lynne ~ Leave a comment

“Wait a minute,” I can hear readers thinking. “This author’s all about self-disclosure and authenticity and all that jazz. Truth has to be important to them.”

You’re right. Truth, in general, is of paramount importance. But I’ve recently been given food for thought about one particular circumstance in which truth may be a bit irrelevant.

Cognitive-behavioral therapy has been very popular for a while, and is helpful for many people. A central principle of CBT is to question your negative thoughts and assumptions, learn to recognize illogical thinking, and use various techniques to decrease the number and severity of negative thoughts you have.

In other words: get into the habit of believing, and trying to prove, that your negative thoughts about yourself or your life are not true (or at least vastly exaggerated.)

Although I find many of the techniques useful, I have encountered two issues with this. First, since the goal is to change my thinking, I feel like I’ve failed when negative thoughts are still such a big part of my consciousness. Second, the content of some of my negative thoughts is true and trying to argue with it doesn’t help at all.

My planet really is in trouble. I really do regret not writing for decades. Relatives really are going to get harder to deal with as they age. I really did irreversibly fuck up my body in some ways. The odds of my book getting published really are low.

Anyway, I just finished a book called “The Happiness Trap” that was recommended to me. I tend to avoid self-help books, as a rule, but I decided to give it a try. It advocates that we don’t try to argue with our negative thoughts, or control how often we have them, but rather work on coexisting with them and using mindfulness techniques to be less affected by them.

It suggests that when I’m aware of a negative thought I’m having or story I’m telling myself, I don’t ask myself whether it’s true or not–only whether, at this moment, it is helpful.

When Advice Hurts

~ Lori Lynne ~ 1 Comment

I’m coping with some health stuff right now. Nothing worrisome in the long term, but I’m on my third antibiotic since early December. I’m frustrated at the decrease in creativity caused by fatigue and discomfort. That’s not all, though.

I had to cancel a writing group meeting last Friday. Instead of saying anything about the infection, I lied and said I had to go out of town.

Why did I lie? Because I was tired.

I didn’t want the lectures I knew I’d be given if some of them knew I was (a) sick and (b) using Western medicine. Lectures I’ve heard from these folks before.

I didn’t want to hear I wouldn’t have these problems if I were vegan. Or if I took the right supplements. Or did homeopathy.

I didn’t want to hear that all my ills are caused by dairy, or not doing yoga, or my childhood vaccines.

I don’t make any medical decision, including using antibiotics, lightly. I use the knowledge I have (including my degrees in biology) to weigh the data and make my choices. But people seem to see me as some sort of compliant, brainwashed sheep if I choose a treatment a doctor recommends.

Many of these people are kind. They don’t realize they’re hurting me. Not just frustrating and infantilizing me, but hurting me. They don’t realize that when they keep repeating advice, this is the message I receive:

“Because you’re making some kind of choice that differs with my opinion, everything you are suffering is your fault. You didn’t get sick; you made yourself sick. You deserve no kindness, only judgment.”

Yes, I get that message loud and clear, whether I should or not. And it makes me feel so fucking alone. Because these are the type of people who also belong to the “all psych meds are evil and you can cure your mental health condition with positive thinking and vegetables” school of thought.

Which means I’ll never, ever be able to please them. Because even if there should come a time when meds don’t need to be in my toolbox, I’ll still be standing firmly on the side of their responsible, case-by-case, nonstigmatized use by others.

Now, if you’ll excuse me, it’s time for the sheep to go take the next dose of her evil antibiotic. Baa.

The Meatball Challenge

~ Lori Lynne ~ 2 Comments

Read this whole post, because I need your help with the meatball.

I don’t enjoy the holidays much. There are exceptions (I made it to a party last night and hopefully committed only minor social blunders) but I’m low-key to the point of denial most of the time. Oh, I like getting together with some of my relatives and playing games and having a nice meal, but (just as with Thanksgiving in my country) I don’t like being told that I have to do it on a particular day. Or being bombarded with how much more holiday-related fun other people with more energy and different families seem to be having. Or the endless question “Are you ready for the holidays?”

As if they were a college final exam or something.

At any rate, silly humor helps me when I am stressed, so I turn to the meatball challenge. The way it works is, you take a well-known line from literature or poetry and substitute the word “meatball” at an appropriate place.

“But soft! What light through yonder meatball breaks?”

“O Meatball! My Meatball!”

“Because I could not stop for a meatball, it kindly stopped for me…”

“Quoth the Meatball: Nevermore.”

You get the idea. Why “meatball?” I have no idea. It just works, maybe because it’s so arbitrary and pointless.

Right now I’m trying to do it a bit differently. You see, Christmas carols are one of the few things I enjoy about this time of year. Archaic language, religious references and all, I love that they’re songs a lot of people know. So I’m doing the meatball challenge with holiday song titles. It’s fun, but I’m running out of carols I know. So if anyone can help, please comment a title for me. Maybe even share so I can get more. Thanks in advance.

Joy to the Meatball!

Third Time’s the Charm?

~ Lori Lynne ~ 1 Comment

Today I wrote the third version of the few pages that mark the beginning of a new phase of my book. The first version got okay feedback, but I and my fellow writers agreed the voice wasn’t quite right.

So I wrote it for a second time. I changed the voice and changed the tone in a way I thought would sound more personal. I put in some new, clever stuff as well. Satisfied, I stuffed the stapled pages into my backpack and brought them to the group.

They hated it.

I wasn’t even surprised–by the time I finished reading the section out loud, I knew it wasn’t working. What had escaped me at the keyboard became obvious to my ears. I hadn’t just failed to improve it; I’d made it much worse.

So today I wrote a third draft. It’s different from the first two; it doesn’t try to cover as much and it’s definitely more personal. (Cried while writing it, which is usually a good sign I’m being authentic.) But I have no idea whether it works or not.

What’s really hard is that I haven’t got a plan for what to do if this isn’t better. I’m pretty sure I’ll need to put it aside for a while and try to work on another section, but I don’t want to. I want to be happy with this piece before I do later ones.

And I want a pony.

Sick Squared

~ Lori Lynne ~ Leave a comment

Being sick is depressing, sure. For me, though, being sick is clinically depressing.

Maybe those of us with mental health issues are more sensitive than usual to the tiniest changes in our brain chemistry. If we’re on meds, maybe illness changes the way our bodies metabolize them. Whatever the reason may be, even a minor illness seems to guarantee a sharp depressive dip for me.

It was just a bad cold, for heaven’s sake. Severe congestion, touch of fever, no huge deal, only lasted three days…but I’m clawing my way out of leftover mental fog, compulsively pessimistic thinking, and hair-trigger anxiety.

Yesterday was the first day I actually thought about my writing projects again, and it wasn’t pretty. Every gloomy, nihilistic, they’re-no-good-and-even-if-they-were-it-wouldn’t-matter thought I’ve had about them came cascading down at once.

I know what to do; what I’ve had to do thousands of times. Baby steps. Little things like this. Do not try to tackle everything that has piled up, or I’ll end up crawling back under the covers.

I want my brain back to its best functioning now–but what I’ve got is a blog post and a sink full of clean dishes. And that’s probably it for today.

First Principles

~ Lori Lynne ~ Leave a comment

What helps me when I get overwhelmed by my writing projects, or by life in general? Sometimes nothing…I get to be overwhelmed for a while. I do mindless things, try very hard to choose mindless things that are not self-destructive, and generally buy time until the intensity of the feeling passes.

But when the overwhelm is about my books, it helps if I can go back to what I call my first principles: Why am I working on these projects? What is my duty in regards to them? Do I understand that I am not in control of how they are received when the time comes to send them out? Am I willing to do my best, with no guarantee that they will be published or widely read? Am I willing to resist comparisons and fight insecurity when I hear of fellow writers’ productivity, networking and other successes?

The insight I had (and was questioning) about the structure of my nonfiction book has crystallized into an updated plan. This is exciting, and it’s making me more connected to the book’s arc…which, in turn, sends my mind into the future where the book’s a book and I’m querying agents et cætera. This is not the time for those thoughts. Maybe some writers can do it, but I know I need to concentrate on getting a draft of the book done.

I’m not trying to seal off any knowledge of or respect for the realities of the publishing industry. I’ll continue to get feedback from other writers, but right now I know I’ll hamstring my creativity if I try too hard to write for anyone but me and the people I’d like to help.

Inspiration or Hypomania?

~ Lori Lynne ~ 1 Comment

Both of them present the same way: I have an idea. An amazing idea. The best idea I’ve had in a long time. My head begins to whirl with plans for executing it, alternative plans, and alternatives to the alternatives. I sleep even less than usual because the ideas keep chasing themselves around in my head.

Eventually, one of two things happens: If it’s just inspiration, I question it obsessively, but (hopefully) eventually overcome procrastination and insecurity to take some step toward carrying it out. If it’s hypomania (a symptom of my condition, Bipolar II) I just whirl and whirl until I eventually burn out and crash. After I come back from whatever self-destructive crap I might have done while crashing, the idea seems ridiculous or lackluster.

But what if it’s not either-or? What if it’s a little of both?

The large-scale planning of my book continues. It’s reached the next level after a recent attempt at rounding out a chapter instead of focusing on shorter segments. For several days, I could tell my brain was in high gear, no matter what I was doing. I did mindless things quite often in an effort to slow down and relax, but while I was doing said mindless thing the thoughts were churning in endless circles.

Then a breakthrough seemed to happen: I had a vision for a new way of organizing the chapters that would be more blended and less choppy. It calls for changes about what goes where, using the 90,000 words I have so far as raw material but not necessarily in their current segments.

Evidence on the side of inspiration: I’m already making a lot of notes and at least trying to get the ideas down in some form, which counts as action.

Evidence on the side of hypomania: My brain fucking hurts and I really want to go eat donuts to club it into silence.