Reclaiming my body, or: ¡Viva la Revolución!

a cure for what ails you, abuse, anxiety, dissociation, memories, personal experiences, ptsd, relationships, therapy, three hopeful thoughts

Sometimes, EMDR can take a while.

This week, my therapist and I tried to pin down a common theme in some of my more disturbing memories of X. We essentially started freestyling at each other, throwing out possibilities and ultimately ending up…pretty stumped. She thinks it all goes back to what she calls “the rabbit hole”–dysfunctional patterns with my mother and my other relatives that began when I was a child and are coloring how I interact with the world even now, twenty-odd years later. We also had a really great conversation about body autonomy and ownership, and how I’ve been seeing myself as a commodity for so long and “going along to get along” for pretty much my entire life.

My existence has been defined by one thing: the need to protect myself at all times, to defuse all the bombs, to take all the right steps so I don’t fall into a crack or a lava pit or inadvertently provoke someone else’s rage. I make myself as pleasant and agreeable as possible because I grew up learning that rocking the boat meant someone screaming in your face.

I am a nice person, yes. The whole thing isn’t fake or some survival mechanism from long ago. I don’t see a reason to be unkind to people, when giving a stranger a compliment takes less time and brightens someone’s day. But I am gentle with others because I am so often afraid. As a child, survival meant being quiet, being kind; never confronting, never correcting.

My therapist and I have also spent the last few weeks working with my deep-seated body image issues. It’s a topic I don’t often talk (or write) about because there’s a mountain of shame that comes with it. However, I try to be transparent in my posts and other communication with you, readers, so let me bring you up to date.

My family-of-origin is weird in a bunch of ways. Even if you’re relatively new to the blog, you’re probably aware of this. But one of the most pervasive and insidious messages I received as a child was that my stomach was ugly and needed to constantly be “held in.” You know, like how you sometimes suck in a bit to zip up a new pair of jeans? Like that, except all the time.

Long story short, we were at Disney World when I was nine or ten and was wearing this cute little biker-shorts-and-crop-top deal, neon green and black. I thought I looked so cool with my white bucket hat, despite the fact that it was 95 degrees and I was wearing, well, a bucket hat. We were posing for a picture in front of some palm trees and one of the relatives who’d brought me on the trip poked my stomach and said, “Suck that in.”

Again: I was, like, nine or ten when this happened.

And I had been holding in my “gut” every day for the next twenty years. I was terrified to let anyone see me not “holding it in.” Even as a 90-lb freshman in high school, I still held it in. I was terrified of sleepovers–with friends in school, and with lovers later in life–because I knew I would not have complete control of my body and what it looked like while I slept.

It took two long, very difficult EMDR sessions, a ton of self-care, and lots of encouragement and positive feedback from my fella, but I am slowly letting go of the compulsion to suck in my stomach at all times. As I write this, I’m slouched over like an overstuffed possum* (thanks to our wedding food tasting this weekend!) and I do not care. I know no one here is going to judge me. I am comfortable that I am not some hideous trog if I’m not pretending like I don’t have organs in my abdominal cavity.

The way I view my body changes from day to day, of course, but the last week has felt effortless.

But this is only the first step. My body has never been truly my own. Over the course of my life, I have allowed others to pick at me like gulls on a whale carcass: this one takes my body but nothing else–they use my flesh and forget that I am human. That one only likes me when I’m not sad. This person takes for granted that I will always forgive them. And it goes on and on, the give-and-take-but-mostly-take that made up all but the last three or four years of my life.

Think about that for a moment. Twenty-five years of feeling vaguely “other” in my body, like I was driving a leased car. Mine, but not really mine.

And I have allowed–even willingly participated in–this parceling-out of me, of my body, of my mind, of my experiences. I have done this because submission means safety. If I don’t really care either way, I’ve long said, what does it hurt? Why not let someone else make the decision? Why even bother giving an opinion, if it will make this person happy?

It’s funny that I am just now realizing how dysfunctional this mindset is. Having those thoughts on occasion is natural. Having those thoughts form the basis for every interaction you have with another human being is probably not the healthiest way to go about this whole “life” thing.

Those patterns are why it’s so scary to have finally found a partner who wants all of it at once–even the parts of myself I find the ugliest and most shameful. I am learning that it’s okay to express my opinions, even if I’m not 100% sure the other person shares them. Wedding planning has, on the whole, been full of great opportunities for me to test out the whole “assertiveness” thing without the stakes being too high. For the first time in my life, I feel safe disagreeing with my partner because I know it will not immediately lead to a breakup or abuse.

So, my assignment moving forward is to nurture myself, to keep being me, to keep doing the things I enjoy without worrying so damn much about how it’s going to look or who’s going to judge me. I’ve been doing this, to some extent, for a while (my guy and a certain friend can attest to me publicly howling and barking like a dog through a bronze metal sculpture last summer). I vowed last year to make absurdity common in my life and to ask “Why not?” more often than “Why?” when thinking about doing something. I want to be freer. I want to feel that my body is my own. And most importantly, I want to keep being stable and happy.

Now that you know a bit more of my tragic backstory, readers, how many links have you been able to make between your early childhood experiences and the person you are today?

* This guy right here:

possum-150200

We came home from the tasting and just kinda slouched on the couch like this while the cats prowled hungrily, begging for leftovers.

 

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On Vulnerability

a cure for what ails you, abuse, anxiety, memories, ptsd, therapy, three hopeful thoughts

There are so many words in the English language relating to innocence and vulnerability, and most of them can bring me way down if I’m not careful. They provoke some ancient anxiety that I’ve come to realize, with the help of my excellent therapist, are linked to what she calls my “wounded younger self.” (I was incredibly skeptical of inner child work at first, but it is incredibly effective and incredibly healing.)

“Little” is an adjective that, when paired with certain words that also remind me of innocence, usually messes me up emotionally. That’s the word that got under my skin tonight.

I’ve been feeling kind of “off” the last few days. I recently blocked my mother completely on my phone–including the second number I thought she’d deleted until she used it to contact me after I blocked the first number–and was treated to some really unsettling dreams on Monday and Tuesday night.

Monday’s main feature involved me skipping my grandmother’s birthday party because my mother was going to be there and I knew she’d be drunk. Tuesday’s late-night horror show involved a healthy helping of guilt because I was hiding from her (in a Target, of all places) while she wailed and lamented that she “couldn’t believe [I] didn’t want to talk to her.”

Naturally, this put me in a pretty weird headspace today. Wednesdays are my big clinical days and I do group as well as individual client work. As such, I generally store my feelings away to deal with later and do a pretty good job of not thinking about them at all during the day because I’m 100% focused on my clients. (Side note: I adore them, and I’m bummed that I’m leaving my practicum site in a few weeks!)

On the drive home from class this evening, though, those neglected feelings reared their ugly collective heads and roared.

The anxiety and guilt were so powerful that I considered just going to bed early and sleeping it off.

Instead, I took a shower.

I focused hard on those thoughts and attempted to get a good, cathartic cry in. Nothing happened.

I turned the focus to that wounded younger self I mentioned and took the opportunity to literally hug myself while I waited for the conditioner to work its magic on my decidedly unruly hair. I decided to speak aloud because I’m home alone most days during the week and hey, I knew the cat wouldn’t judge me. (Audibly, anyway.)

I told my younger self that it’s okay. I told her I love her and that I’m sorry she felt like no one could keep her safe. I told her that I’m going to do it. This changed into me speaking to whatever hypothetical future child I’ll end up having. I promised that child to take the best care of it I can and to make sure it never feels afraid or lonely.

And I cried. Instead of stifling it or trying to be tough, I gave myself over to it completely–ugly, wracking sobs. After a while, those sobs turned into relieved laughter that I’m sure sounded like I’d finally gone completely ’round the bend.

I think there’s something to be said for having a good cry.


On Monday, I spoke to my clients in group about the concept of “ghosts”–they had all shared some intense and profound stories about their deepest wounds, their secret shames, their most painful memories. I told them that while they can haunt you, they can’t physically hurt you. You can start to let go of them.

I led them in one of my new favorite exercises, which is “HA!” breathing. Basically, you take a deep breath and push that breath out while making a “HA!” sound. I opened the group with the exercise and invited them to imagine themselves yelling at someone or letting frustration out. I demonstrated (because I am not afraid to look silly anymore), and they loved it. After the big, intense sharing session, I led them in the exercise again, this time instructing them to imagine the “HA!” on the exhale as them blowing out part of their ghosts.

I’m glad it was a hit, and I encourage you all to try it, readers. Howling into the void or, as I called it, “therapeutic yelling,” is incredibly cathartic.

 

Life as a haunted house

a cure for what ails you, abuse, anxiety, dissociation, memories, personal experiences, ptsd, relationships, therapy, three hopeful thoughts

I’ve been having the nightmare again.

In it, I could be seventeen or twenty-nine. In it, I am standing in my childhood bedroom, looking out the window at the front lawn. There’s a weird unstuck-in-time feeling; it could be morning or late at night, but the sky is a flat indistinct expanse over the rooftops and trees. The lighting is confusing, too–is it dusk? Dawn? Just a cloudy afternoon?

His old, beat-up white Buick rolls up to the curb and my stomach twists in on itself, the knots fluttering like anxious birds.

What did I do this time?

He could be in a good mood, or a bad mood, or both, or neither. He could be smiling while walking up to my front door but then want to talk to me, right up close (as Stephen King wrote in my favorite novel of his, Rose Madder).

Or maybe it’s fine. Maybe he’s just going to pick me up and we’ll go hang out with friends or sit in his car down by the river, just talking for hours.

But I know damn well it’s not fine.


I am all ages, all the time. My therapist says that I need to nurture my wounded inner child, which I thought sounded stupid and New Age-y until I actually started trying it out. It’s effective–when I get anxious or depressed, I look at my younger self and pull her close.

You didn’t do anything this time, or any time. It’s going to be okay.

I wish believing was as easy as speaking.


On Thursday, the anxious snakes took up residence in my belly as I cleaned the apartment. My fiance had had a rough day on Wednesday and I knew he was feeling crappy, and also that it had nothing to do with me. He wasn’t rude or snappy with me, but he wasn’t really in the mood to spend much time talking during our nightly phone call. I knew this wasn’t my fault.

But the ghosts, the echoes, they spun a different story. As I swept and cleaned the kitchen floor (which, with two cats, is a neverending chore), the words kept flowing into my mind.

I have to do this right or he’ll be upset.

My fella? He never gets upset with me, ever. I think we’ve had maybe one argument in the entire three years we’ve been together. He is sweet and gentle and kind. We coo over the cats together, make a game out of going grocery shopping, laugh at hideously dark things that we know aren’t supposed to be funny.

But the trauma said,

Do it right, or else. Or else he’ll be mad. Or else no one will love you.

I paused many times during my cleaning spree to speak aloud to myself, to that wounded, younger part.

He is not like X. You were a baby. It was not your fault.

Sometimes, it works, but I’m pretty sure it’s just me handing a squalling child a piece of candy to shut it up. I don’t actually deal with the feelings. I invalidate and suppress and push, push, push until they go away.

My therapist and I have done three EMDR sessions now, and it seems to be a magic bullet for me. The first two sessions dealt with my childhood and centered around two specific disturbing memories and the phrase, “My mother’s anger is not my fault.”

Today, we dealt with X and the nightmare, which has been occurring with alarming frequency. I recently took an elective on domestic violence, and I know that’s what’s stirred all of this up again.


The ghosts are not happy when you call them out. They want to stay hidden and rattle the windowpanes, throw a few dishes when you’re not watching too closely.

And they expect to get away with it.


Today, we embarked on a grand journey of the hell I lived from ages 17 to 19. We worked on the phrase, “I didn’t do anything wrong.” I’m mostly believing it now, but only as it pertains to that one image. I know we have more work, so much more work, to do before I’m healed.

But the most upsetting part isn’t the actual image or the memory. The worst part is how young I was, how vulnerable. X saw that. He latched onto it. He told me his tales of woe and wept insincerity, and I bought it. He took my kindness, my urge to nurture and pacify, as weakness.

I don’t often cry in therapy, but when I do, it’s because that girl back then was so young. She was a baby, even at 17, and I feel overwhelmingly protective of her, this past-me. I’m not sure if it’s because I’m more self-aware now or if it’s some sort of misplaced maternal instinct, but when we’re focusing on a memory in EMDR, I see myself standing beside her. By round three of EMDR*, I have my arms around her and I am holding her close. I am telling her that it’s okay, that she didn’t do anything wrong, that she is good and lovable and so much more than what the trauma says.

And as the session progresses, the frightened, anxious self–the part that believes she did something wrong–becomes defiant. It was amusing the first time it happened in our first session, when the five-year-old self in the memory we used actually kind of yelled back at my mother.

This time, the wounded self snapped, “If he’s pissy, it’s because he’s an asshole. I didn’t do anything wrong.”

This defiance, my therapist says, is a good sign. I think it is, too. Also, it makes me chuckle–I’ve always been pretty stubborn, and time and time again, I’ve seen that if I’m pushed and threatened enough, I will gain the strength and courage to fight back.

As much as I hate that I’m going to be in therapy for a while (my insurance is awesome, but the co-pays add up), as much as I hate that other people dealt enough damage to put me there, I recognize that I am fighting back. That is so much. That is everything.

I am fighting the ghosts. One day, I will drive the last of them from my house and I will finally feel the peace most people take for granted. Right now, I’m actually feeling pretty peaceful–I went into therapy feeling very tense, and as I drove home, every muscle in my body felt loose and relaxed in a way I don’t often get to experience while I’m awake.

I’m going to leave you with this thought, readers. People may have done damage to you, but you are not damaged. You can fight. And I’ll fight right alongside you.

We’ve got this.


* We typically do three or four rounds with the same memory and the same phrases. Your mileage may vary, but my sessions go like this:

  • On a scale of 1-10, how distressing is the phrase (for example, “What did I do this time?”) to you now?
  • On a scale of 0-7, how believable is the phrase you’d like to replace it with? (For example, “His anger is not my fault.”)

I use the hand buzzers because I’m migraine-prone so the blinking light isn’t great (and I find that closing my eyes helps me visualize the memory we’re using). Headphones with alternating sounds between the left and right side can also be used, but since unexpected or loud sounds in my left ear makes the dissociation spike for some reason, we ruled that out.

Bilateral brain stimulation is awesome! The brain is so amazing, how it can bend into impossible shapes, at impossible angles, and not break.

Love your brain, your beautiful “broken” brain, readers.

 

A Wild Blogger Recognition Award Appears!

Authoress, bipolar disorder, endometriosis, rapid-cycle bipolar disorder, stigma, three hopeful thoughts

Jeanette at My Life with PTSD & Bipolar: Mental Health Matters kindly nominated me for
Write a brief story about how your blog began. I’ve been running The Dissociated Press for five years now (holy cats, time flies!) and have been documenting my journey to mental health–or at least, relative stability and improved daily functioning. When I started this blog in 2013, my life was a total mess. I was in an unhappy marriage and missing a lot of work because I was freshly diagnosed with bipolar 1 and adjusting to my new medications. I ended up losing that job, which was a major low point.

There have been a lot of low points throughout my blog-writing history, but things have dramatically improved in the last couple of years. I escaped from that unhappy, unsupportive marriage, enrolled in graduate school for clinical mental health counseling at a great school, and got engaged to a lovely, wonderful man.

I still hit depressive episodes from time to time, but unlike my pre-medication, bad relationship days, I take comfort in the knowledge that my life is so much better than I ever could have imagined. I have a wonderfully supportive partner, and his family is incredibly encouraging of me sharing my journey. My classmates have expressed appreciation for my candor, and I’ve been able to help a lot of people through my disclosures.

Advice for new bloggers is something I haven’t really thought about, but my main piece of advice is to write for yourself first and foremost. TDP has evolved over time–at first, it was a place for me to get my thoughts and experiences out into the ether in hopes of finding others who were also struggling.

Also, I like to focus on and directly address my readers as a group in my posts and always try to end a post with a positive thought or insight. It prevents the blog from feeling dreary and helps promote the overall message: recovery is possible, and recovery never looks the same for everyone. Your journey matters. Your message matters. Your experiences matter.

As I’ve gotten healthier and stopped focusing so much on my illnesses (which are still a main focal point of the blog, albeit in a different way), I realized that my relatively small following was a great audience for information about the stigma surrounding mental illness.

I realized that everyone, but especially others living with my specific conditions (PTSD with depersonalization/derealization and rapid-cycling type 1 bipolar disorder) could benefit from learning about the latest news and treatment options. I’m building up quite the library of scholarly articles and studies, and if there’s enough interest, I plan to post a few quick-and-dirty rundowns of them.

Again, I can’t thank Jeanette for this nomination–it came out of nowhere and I feel very honored about the whole thing and appreciate being recognized for my work. Validation and recognition for what I’m doing always feels nice! Also, the badge image is really cute.

My Picks for Nomination:

The Global PTSD Survivor Blog

Bloomin’ Uterus (a blog about endometriosis, which I also have)

Ruth at PTSD – Accepting, Coping, Thriving

 

 

An Audio Post!? 4-7-8 Breathing Exercise

a cure for what ails you, anxiety, authoress in motion, ptsd, three hopeful thoughts

Hey readers! I haven’t posted any sort of “There’s a real person in here!” content in a really long time, so here’s a quick clip of me walking you through an even quicker breathing exercise. Click below for the transcript and let me know what you think!

(Side note: I love transcribing stuff because it makes me uncomfortably aware of my verbal tics. Sorry ’bout that.)


News Day Tuesday: BLOOM by Anna Schuleit

a cure for what ails you, bipolar disorder, major depression, memories, News Day Tuesday, ptsd, rapid-cycle bipolar disorder, stigma, three hopeful thoughts

Hey readers! This week, we’re doing something a little different for News Day Tuesday.

I stumbled across Anna Schuleit’s beautiful BLOOM project from 2003 (yes, I know I’m super late to the party). Today, I want to celebrate that project.

In 2003, artist Anna Schuleit installed 28,000 (28,000! Yow!) potted flowers throughout the psychiatric ward of the Massachusetts Mental Health Center (MMHC).

Anna Schuleit’s installation project was created within the entire building of MMHC, on all floors, inviting former patients and employees, staff, students, and the general public, to re-visit the historic site once more before its closing. There was also a symposium at a nearby venue, and an open forum on the front steps of MMHC, during which the patients were invited to tell their stories. The events were dedicated to the memory of the thousands of patients of MMHC, and included as many of them as we were able to contact, as well as the doctors, nurses, support staff, researchers, students, and the general public. The project was a non-profit effort run entirely by volunteers and all of the events were free and open to all.

Source

As people living with mental illness, some of us with more than one, we know the therapeutic power of telling our stories, of having a voice when we’re so often voiceless. Mindy Schwartz Brown wrote some beautiful poetry about her experiences at MMHC, which you can read here. One poem in particular, “Asylum,” touched me deeply.

ASYLUM
(for Anna)

How did this edifice become “home” to its inhabitants-
the renowned multiply degreed,
the haplessly homeless dually diagnosed,
the walking wounded,
the worried well,
the happy go lucky who cleaned floors,
cooked lunches,
took blood pressures.

How could it contain all of the
the egos,
the disintegrated, the inflated,
occupying one space in parallel play?
MD, SPMI
Ph.D, BPD
MSW, DBT
Tell me in this soup, where does one find one’s ME?

DSM IV, Anybody going for V?
What’s the code for those who close hospitals
then open prisons for the sick?

We all feel so much better now,
knowing our brains are
faulty and we are not.
Structural errors ,
neurotransmittor deficits,
viral origins,
genomic misconfigurations.

So now can we all be friends?
Can we do lunch?
Just as we would with a diabetic?

October 3, 2003

Mindy Schwartz-Brown © 2003

The pain of not being recognized is one we know all too well. The lines “We all feel so much better now, / knowing our brains are / faulty and we are not” struck a chord with me that resonated all the way through my body and down into what some people call the soul.

We are the ones who are forgotten. We are the ones who are hiding in plain sight, not out of our own desire to be invisible, but of the desire of others to make us invisible. We make others uncomfortable, particularly when we don’t outwardly fit the mold of the “mentally ill person.” Whenever I reveal that I have bipolar I and CPTSD to someone, I am typical met with one of two reactions. The person either recoils–the discomfort in their eyes is stark and harrowing–or they tell me how “brave” I am.

I am not brave. I simply live. What choice do I have? I do not want to die, though there are plenty of people who view living with a mental illness as a fate worse than death–and I find that more disturbing than anything going on in my attic. There have been countless times when the hauntings have gotten so noisy that I feel as though my mind may literally split in two. Still, I live. Our lives have worth. We have worth.

I’d like to end by including a few photos of Schuleit’s installation. I spent a great deal of time yesterday perusing the photos and reflecting–not on my own experiences, as I have never been inpatient, but on what others’ experiences might have been like as they lived out their day-to-day at MMHC.

bloom-by-anna-schuleit-red-mums-640x920

bloom-by-anna-schuleit-white-tulips

bloom-by-anna-schuleit-blue-hallway

All images above copyright Anna Schuleit.

Tell me your stories, readers. It’s important.

News Day Tuesday: New treatment for PTSD?

a cure for what ails you, News Day Tuesday, personal experiences, ptsd, rapid-cycle bipolar disorder, three hopeful thoughts

Good morning, readers!

This week, I rustled up an article about some exciting developments in PTSD research.

Basically, scientists are looking at glutamate (one type of those fun little things in your brain that sends signals) and how alterations in glutamate levels affect PTSD. What this means for us is that PTSD is now being studied on a molecular level, which means that new treatments could be on the horizon!

My PTSD is generally well-controlled, as far as “controlling” it goes. I’m still mad-jumpy and don’t have a good time in crowds (the dissociation spikes, and sounds that hit my left ear first seem to make it worse, though my previous psychiatrist had no idea why). I still feel depersonalized/derealized every single day, though the level of detachment varies widely. I haven’t been able to pinpoint exactly what it is that makes it better or worse, but admittedly, I’ve been super lazy about charting it.

However, I’m sleeping soundly for the first time I can remember. I think a lot of us can relate to the hypervigilance and, by extension, light sleeping. Loud noises still startle me awake and my fiance sometime scares the bejeezus out of me by touching me–gently–to wake me up. But! and this is good news–the sounds of the cats wheezing or vomiting or fighting don’t wake me in a panic. It’s more of a “God, this again?” reaction, which, while not fun, is better than waking up with a racing pulse and momentary confusion about where I am.

As far as journaling about symptoms goes, I’m still trying to figure out a system. How many times in a day should I note what’s going on upstairs? I don’t want to become obsessive about it, as I did with my mood journal when I was first beginning treatment for bipolar disorder. At the same time, I want to make sure I have an accurate log of my symptoms and the events that may have caused an increase/decrease in the weird floaty feelings of unreality.

That being said, it’s sometimes hard to notice the changes because they’re subtle. Because this has been chronic for six years now, it often takes an absolutely massive spike before I notice anything is off. On a related note, I often don’t notice the symptoms decreasing because hey, it’s my “normal” now.

Any ideas or tips, readers? Should I follow the standard day/time/preceding events/level (on a scale of 1-10) format I’ve used in the past for mood tracking? What system(s) do you use?

I look forward to hearing from you! I’ll see you next week and as always, stay safe and remember to say one nice thing to yourself every day. Today I have two: “My new DIY manicure is bangin'” and “I am surviving my fiance’s work trip with zero negative emotions!”

It’s important to focus on the positive, especially when our emotional weather is often stormy.

News Day Tuesday: BiAffect App Links Keystrokes with Bipolar Episodes

a cure for what ails you, bipolar disorder, News Day Tuesday, rapid-cycle bipolar disorder, three hopeful thoughts

Greetings, readers!

It was a bit of a challenge to find an article for this week, but I finally stumbled upon something that could make a huge difference in how we track our moods. There’s a new app called BiAffect that uses your keystrokes, frequency of texting, and social media app patterns to track manic and depressive episodes.

To find out whether a user might be experiencing a manic or depressive episode, the app tracks typing speed, how hard keys are pressed and the frequency of the use of backspace and spellcheck.

chicagotribune.com

I know there are a lot of people who dislike the idea of being tracked in any sense, which is totally fine. However, I feel a bit more comfortable with it knowing that it comes directly from a research group. It’s only available for iPhone, which is kind of a bummer because I’m a die-hard Android user.

I wish something like this had been around in 2013, when I was deep in the throes of exhausting rapid-cycling episodes. I was newly diagnosed, but the challenge of finding the right combination and doses of medication, the loss of my job (probably due to my cycling), and the overall disintegration of my marriage had more or less temporarily erased any benefits or relief I found from my diagnosis.

One of my long-time friends mentioned that he noticed I was posting a lot more on Facebook when I was manic than when I was depressed. Like, a lot. Even now that I’m stable and successfully medicated, I still pay close attention to what and how often I post. When I’m more energetic and feel like interacting with others, I find myself wondering if it’s because I’m manic, hypomanic, or just…not depressed.

When you’re living with bipolar disorder, it’s a constant question of Column A, Column B, Column C, or a bit of each. You learn to analyze your moods and energy levels, and this tracking can quickly become obsessional.

I see this app as a double-edged sword. On the one hand, it would save those of us who pay attention to our moods a ton of work. On the other, those of us who are prone to preoccupation and overall obsessional thinking could end up checking in a lot more often than usual.

If BiAffect is released for Android, I’m for sure going to jump on it, at least for a trial run. It seems like it could be a useful tool for mental health care providers and patients alike–rather than having to drag in pages and pages of mood diaries, we could pop open an app and have the data right there at our fingertips (literally). And, at least in theory, it seems like any sort of self-report bias would be removed, or at least mitigated. I know I’ve been guilty of fibbing a bit in my mood diaries due to the shame that comes from realizing just how sick I am.

What do you think, readers? Would you give something like this a spin, or do you find it intrusive? Let me know! I’ll be keeping an eye on this one.

Until next time, stay safe and remember to be excellent to yourself.

News Day Tuesday: Sick Days

a cure for what ails you, major depression, News Day Tuesday, ptsd, rapid-cycle bipolar disorder, stigma, three hopeful thoughts

Hey readers! I’ve gotten really bad about posting regularly and as we all know, structure is crucial when you’re living with a mental illness (particularly bipolar disorder). I made myself a super-nifty planner before I started school in January and am actually going to start using it to keep myself on track. What this means for you is that hopefully, I won’t disappear for weeks at a time!

Anyway, today’s article addresses the stigma against physicians taking sick days for mental health. While it focuses on doctors in Australia, the topic is extremely relevant to anyone who has ever taken or needed a “mental health” day. According to the article, doctors (unsurprisingly) feel uncomfortable taking sick days for self-care, even when they begin to feel burned out and can’t deliver their usual level of care to patients.

“I’m completely supportive, but I’ll admit I’ve never been brave enough to take a mental health day,” one doctor said, adding, “How can you dump your workload on a colleague who is going through much the same things as you are?”

– abc.net.au

I find this extremely relatable because I’ve always felt awkward calling into work or needing to leave early because my brain has decided that doing anything other than crying in bed is just not going to happen. It doesn’t happen often, but I’ve always felt the need to claim another reason–usually migraines, which I used to get several times a week–because we’re conditioned to believe that depression, anxiety, and other disorders of the mind are not a valid reason for absences. We’re taught to believe that we need to suck it up and get on with our lives, even if that means hiding in the bathroom to cry or have a panic attack.

Naturally, this poses a huge problem for anyone in the workforce, but it’s especially problematic for health care providers. It’s something I’ve often thought about as my clinical practicum draws closer. How can I best serve my clients if I’m experiencing the same symptoms as they are?

I also fear that even in a mental health facility, where one would expect supervisors to be a bit more sympathetic, I’ll come across as weak or unsuitable for the job because of what’s going on in my brain. There’s an indescribable level of self-loathing and shame that comes with mental illnesses, and I’m sure all of you can relate. It’s the feeling of being less-than, the feeling that you don’t deserve to have a job because some days, you just can’t handle the world. You begin to question everything about yourself–am I being weak or overly sensitive? Am I doing this whole “adult” thing wrong? The fear of losing your job is a constant presence, which only makes things worse.

So what can we do about it? Unfortunately, there’s no easy answer to that question. One would hope that with increased media exposure, employers will become more understanding, although every boss is different and there are zero guarantees.

When I was first diagnosed with bipolar disorder, I loved my job. I was working as an editor at a translation company, but my symptoms were so severe that I actually had what I called my “Oh shit, I cried at work!” kit, which I kept in my desk so I could patch myself up after crying jags. Some of the items included eye makeup, because it’s embarrassing to have streaked makeup after crying (even though I became very good at crying without messing up my face). Although my employer was aware of my struggles, I still lost that job due to absences, which sent me into a horrific downward spiral that took over a year to break.

Since then, I’ve become quite anxious about divulging any information related to my mental health to anyone at any job…and that’s problematic by itself. Why should we feel ashamed of something that’s beyond our control? The answer lies in the stigma.

It’s going to be a long, uphill battle, though the fact that today’s article even exists gives me hope. Exposure and time are the only things that are going to remedy this issue. It’s an unhappy thought, but I sometimes find myself wondering if mental health issues will ever be considered as legitimate as something as simple as food poisoning when it comes to work absences.

I’d like to end on an up note with another quote from the article: “If we can’t help ourselves, how can we help others?”

Self-care is so important, readers. The Compassion Project offers a list of self-care activities that you can check out to build a plan for yourself. Here are some of my favorites.

  • Reading
  • Baking (I’m a huge stress baker, though I haven’t done it in a while)
  • Knitting or embroidery
  • Crafting
  • Cuddling with a pet
  • Going for a walk (which you can even do at work–take a five-minute break to stretch your legs)
  • Doing a crossword puzzle

What are some of your favorite self-care activities? Let me know–I’m always looking to add to my list!

As always, readers, stay safe and I’ll see you next week.

28.

Authoress, ptsd, three hopeful thoughts

Today is my 28th birthday. I generally don’t put much stock in them–it’s just another day when you get past a certain age, in my opinion. But my fella made today really special (breakfast and a mini scavenger hunt to my gift!), so it’s the best birthday I can remember.

Birthdays are significant to me for one reason: they’re proof that I’m still alive. It might seem silly to most people, but as quite a few of you know, those of us afflicted with PTSD tend to also be plagued by the belief that we’re just not going to live very long.

For me, this feeling of dread started when I was in my mid-teens. I thought I wouldn’t make it to sixteen, then nineteen, then twenty-one…and here I am at twenty-eight, having endured three lifetimes worth of horror and survived it all. Every year on this date, I take a moment to marvel at that.

It’s kind of incredible. And you, my readers–all of you–are incredible for hanging on and being alive. Remember that when the bleakness starts to press close and you feel like you’re buried above ground. You are still here, and you should be so proud of that.

Until next time, readers, stay safe and lovely.