My Grief and Loss Is Intertwined With My Mentally Illness

I admittedly don’t know what loss and grief are like for most people. I have been battling my mental illnesses my entire life, so I don’t know what it is like to exist without them. Whenever I hear people offering their condolences and reassuring others that it gets easier over time, I can’t help but wonder if that’s actually the truth for some people because I know it is not a universal truth. Things most assuredly don’t ever feel like they get any better for me.

I have struggled with many types of loss throughout my life. Loss of innocence stolen too soon. Loss of safety and security. Loss of home, relationships, friends. Loss of babies who grew inside me but never got to take a first breath. Loss of both my parents a decade ago. And most recently, the loss of both of my emotional support animals. To say I am intimately familiar with the feelings of loss and grief is an understatement.

My depression often leaves me teetering between periods when I am raw and over-emotional, feeling everything too strongly, and periods where I shut down and am numb to the world, unable to process any emotion at all. Because of this, my grief often comes in waves. When there’s a lull in the storm of emotions, I often assume my heart has begun to mend, only to have it tear wide open again as another wave hits. My numbness deceives me into believing the worst is over for days at a time, only to awaken one day feeling raw and overwhelmed once again. And as is often the case with rough seas during a storm, multiple waves often crash seemingly at once, as older pain rides in on the heels of new.

My anxiety makes me question every loss I have experienced and meter out assumed personal accountability for ever heartache I have ever experienced. I over-analyze and criticize myself for things I have convinced myself after the fact that I could have, should have done differently. I find myself worried again and again that my actions or inaction will repeat the patterns of old losses and create new ones. Yet, instead of those fears promoting change, they often spark my fight or flight response, causing me to flee. Or worse yet, I become like a deer frozen in the headlights, terrified that any choice I make, to stay or to go, to act or not act, will ultimately be wrong.

My PTSD has caused me to relive some of the more traumatic losses of my life multiple times over the years. When those moments are triggered again in my memory, it is as if I am reliving those experiences again in real time. Having a flashback of old losses renews and resets the whole trauma for me.

It is not that I am dwelling on the pain and losses of my life. I try to focus on positivity as often as possible. I have a mental wellness toolbox full of techniques and exercises intended to help keep me grounded and centered. I spend time with family and friends, partake in hobbies and activities, and otherwise attempt to distract my mind from the pain I often feel. I thoroughly embrace and practice the art of self-care. I never sit home intentionally focused on those feelings of loss and grief. Yet somehow, those emotions seem to know about every crack in my armor, seem to always find a way back in.

I am not intentionally avoiding facing my grief and loss, either. I have spent many hours over the years talking about my feelings in therapy. I have further processed my emotions many times over by writing about them and the impact they have had on my life. I am not walling myself up, building an unfeeling facade that cracks under the pressure of pain. I have attempted numerous times to process my emotions, to rationalize with myself and heal. But the healing never comes.

I have allowed myself to feel both sorrow and rage. I have forgiven myself and others. I have accepted that I cannot change the past. I have done every single cliched suggestion thrown out there about moving on and letting go.

I want to heal. I don’t want to keep hurting over so much in life. But I honestly don’t know how to shut any of it off. Every time I think it is over, another wave hits or a different wave. It could be a few hours, a few days, sometimes as long as a week. But those waves of grief and loss always manage to find me, old waves and new, compounding on each other and seemingly ever-increasing as my heart develops new cracks.

And the moments are so seemingly random and sporadic that there’s no way to brace for them or adequately prepare.

My fiance and I were binge-watching old seasons of Hell’s Kitchen and came upon an episode where the contestants were preparing a dinner service for a young lady’s sweet sixteen. As quick and as simply as flipping a switch, my entire mood and demeanor shifted. One moment, we were laughing and joking, engrossed in the show. The next, my eyes were welling up with tears. I couldn’t stop thinking about how I never got my sweet sixteen, the sweet sixteen my mother had promised me for years. Three months before my sixteenth birthday, my father walked out on our family and cut all ties. I tried numerous times between that February and my birthday in April to get in touch with him but he always dodged my calls. I called up his work on the day of my birthday, sure that he wouldn’t deny me on that day, only to hear him in the background tell his co-worker “tell her I’m not here”. My sixteenth birthday was the first time I tried to kill myself.

Just like that, every emotion, every feeling of heartbreak and loss came rushing back.

My fiance lost his father to cancer shortly after we got together. The cancer, the hospice, everything triggered the loss of my father again and again. He’s still grieving the loss of both his parents and every time I attempt to comfort him and ease his pain, my own grief for the loss of my own parents renews.

For the last decade, I had two sugar gliders registered through my doctors as emotional support animals. I could take them everywhere with me, which helped immensely with both my depression and anxiety. One passed away roughly three months ago, the other last week. Losing them was like losing part of my heart. I cried inconsolably and went numb in waves, sobbing until my eyes ran dry and my voice went hoarse more than once. I watched the clock with pained precision, unsure what to do with myself each day when feeding time rolled around. I beat myself up horrendously for the fact that they passed at all, as if I could have spared them old age and death by sheer willpower alone. The truth is that they hadn’t been sick at all. They were just old and the time runs out for all of us eventually. Yet I still felt to blame for them not living longer, not living forever. I found myself taking in two sugar glider rescues last night, not because I was over the loss of my Lilo and Stitch or because I assumed they would fill the hole that loss left in my heart, but simply because I desperately needed that distraction. I needed new babies to keep me busy, new babies to love and to care for, a new purpose to keep going. Their adoption was bittersweet, though, because I am still raw from losing my other babies. But at least when feeding time rolls around again, I have something to focus on other than my grief.

An old friend from high school killed himself. The last time I spoke to him was less than a week before he died. Whenever I think of him, I wonder whether he would still be here today if I had said anything differently or called to check on him again. It doesn’t matter that we had grown somewhat apart over the years, living separate lives, and barely talked anymore. We used to be close so I feel responsible because I didn’t maintain that friendship better, didn’t reach out more, didn’t try harder. The rational part of my brain knows that line of thinking is irrational, but a larger part of my brain and my heart just won’t let go of those thoughts.

So many things can set off waves of grief, some large and obvious, others seemingly small and trivial. I’ve found myself sobbing uncontrollably over Hallmark commercials or sights and sounds, songs or movies that reignite memories. Empathizing with the pain of others reignites my own. As simple as that, in a flash, those feelings refresh and the grief is renewed. I can be fine one moment, laughing and joking, and be biting the inside of my cheeks the next in a futile effort to fight back tears.

I know mental illness is a liar and a master manipulator, capable of twisting truths and spinning lies. I know deep down that I am not responsible, directly or indirectly, for many of the losses in my life and that hindsight is 20/20. But my rational side knowing these things does not stop these emotions from flowing or my grief from being felt. And therein lies the problem. I can rationalize all I want but I cannot shut these feelings off.

Perhaps I’m just wired differently. Perhaps I’ve been broken too many times, been cracked to the core so often that I am incapable of fully healing. Perhaps some wounds just never heal. I honestly don’t know. I just feel like I’m in perpetual mourning, eternally haunted by every loss I’ve experienced in my life, whether one at a time or intertwined and flowing as one.

I honestly don’t know if those promises that things will get better is an old wives tale, something people just say when the silence becomes too heavy and they need some words, any words, to cut the tension and the pain in the room. I don’t know if for some people it does actually get better over time. I just know that for me, as someone struggling with mental illness, grief and loss never seem to fully go away.

Coronavirus Has Become The Great Equalizer For The Mentally Ill

For years now, I have attempted to combat the stigma associated with mental illness.  Again and again, I have given real world examples, approached the subject from differing angles, even used charts and graphs, hoping to help those who have never experienced it themselves better understand.  Yet, sadly I still often feel like I fall short.  While those who are living with mental illness have contacted me numerous times to thank me for putting their experiences into words, there are still those who could not wrap their minds around what it was like to live with our diagnosis.

That is, they couldn’t fully understand until this pandemic hit.

Day after day, for months now, I continue to see postings, comments and tweets that could have been written by any one of the millions of people who struggle every day with various mental illnesses.

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People talk about being worried all the time, sometimes not even knowing what it is that they are worried about, only that the ever-present feeling of dread is looming there, hanging over them.

People talk about being afraid of their world falling apart, the economy crumbling, their job not being there after all of this is over.  They worry about not being smart enough to home school their kids, and of the dangers of sending them back to school in the height of the pandemic. They worry about the house not being clean enough if they have to do a video conference with their co-workers or whether they are even capable to adequately work from home for any length of time. They worry about bills accumulating faster than money comes in and the continuous threat of losing their homes due to evictions and foreclosures.

Even seemingly little things like running to the store for food or toilet paper feel huge.  The world outside doesn’t feel safe.  What if the store is out of whatever we need when they get there?  What if they bump into someone sick? What if they bring the virus home?  The sound of someone nearby coughing makes them jump and want to run back home to safety.  Many even put off going out for days until they absolutely have to, the dreaded eventual trip weighing on them.

People talk about being worried incessantly and excessively about their loved ones and friends, of imagining worst case scenarios of their illnesses and deaths, even though they know they are currently safe and healthy.

Though the common sense part of their brain keeps firing off, trying to remind them that everything is currently okay, and that things will likely eventually be okay again, they cannot help but feel like everything they are worried about is not only possible but probable.  Everything seems to be hanging heavily and even little things feel too big to handle some days.

They feel restless. Their mind runs nonstop.  Even reading the news feels overwhelming, yet they struggle to look away because they feel an urgency to stay informed.  They feel like they have no control over their lives, as if everything is spiraling down into chaos, getting crazier by the day, and there’s absolutely nothing they can do to stop it.

They talk about the confusion of differing information out there, of never knowing what to believe, who to trust, and being fearful of choosing incorrectly and it leading to disaster.

People talk about being continuously exhausted as the pandemic drags on and on, about wishing things would just be over but fearing there is no end in sight. They’re tired of thinking about the coronavirus, tired of worrying about it, want it to just go away. Yet it continues to loom, to linger, to threaten their peace of mind and their very sanity.

All of that is anxiety.

THAT is what people who live with an anxiety disorder go through every single day over a multitude of things in our lives.

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People talk about that feeling of hopelessness.

They feel trapped at home without any real purpose. They are constantly dragging throughout the day.  They can’t stay focused. They are eating and sleeping all the time or not at all.  Some complain about not even enjoying their favorite foods anymore or their favorite shows no longer bringing them any joy.

Some feel all alone.  Many of those feel isolated even with others around, afraid to talk about what they are feeling and going through because they don’t want to seem crazy.  They pull inwards, trying to cope and to put on a brave face, even though they feel like they are falling to pieces inside.

Homeschooling has become overwhelming – they don’t remember school being that hard and feel inadequate because they are struggling to help their kids with basic subjects.  They feel they are letting everyone down by not being enough. Yet the thought of sending kids back to school feels equally as disastrous. It is as if no matter what choice they make, it’ll be wrong, that every option is equally bad and hopeless.

Life itself feels exhausting to them.  There’s times they just feel numb to it all.  Other times, they just want to cry.  Often, they just resort to sleeping, or mindlessly scrolling through social media or watching random shows, though they can barely recall afterwards what it was that they saw.  They feel they are just going through the motions and desperately wish life would just get back to normal – though they know there is nothing they could do to change anything.

Some people are attempting to regain control of their lives, to go out and do something, anything, to reclaim the life they once knew. Yet, while out and about, they are distracted by all that could go wrong, by wanting to return to the safety of their homes. Though part of them desperately wants to enjoy their time out, their thoughts and feelings hang heavy on them, throwing a dark cloud over it all. They feel guilty for everything – for even trying to go out, for trying to have fun, for being too lax or not taking enough precautions. They apologize to others for sucking all the fun out of what could have potentially been a nice day, feeling they somehow seem to be ruining everything they touch.

They see other people being productive, using their downtime wisely to accomplish so many things. They wish they could get things done, as well, but seem to have no desire, no drive to do anything. They find themselves procrastinating and then beating themselves up for their inactivity, which in turn makes themselves procrastinate more, caught in an endless loop where nothing gets done and then they beat themselves up for that lack of productivity.

All of that is depression.

That is what people struggling with a depression diagnosis go through on a regular basis.

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I have seen people talk about wanting to be productive during this downtime, taking on a multitude of projects, more than any one person could legitimately handle, convinced they have the time and energy to do it all, only to crash into an overwhelmed, discouraged heap days later with everything half completed.  They go through cycles of manic, larger than life aspirations and heavy, depressing reality.

People talk about feeling irrationally angry, of feeling fed up about everything and nothing in particular at the same time. They find themselves continuously annoyed with everyone in their life and even the pandemic as a whole.

They describe many of the feelings common with depression, but with an entirely different mess added to the mix. They talk about having feelings that boomerang and yo-yo from one end to another, or sometimes both extremes at once. They talk about feeling so much, in so many directions, that they cannot even put it all into words.

Those highs, lows and extremes are all aspects of bipolar disorder.

People struggling with bipolar disorder often find themselves experiencing a wide variety of emotions and extremes with no rhyme, reason, pattern or predictable duration.

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The list goes on and on of ways this pandemic has helped mirror mental illness in the everyday lives of people who have never experienced it before and struggled to understand it. In the last few months, I have seen these sentiments appear and reappear throughout the country as pockets of positive cases sprung up and the epicenters continued to shift. No matter where the worst of the pandemic currently resides in the country, though, the narrative has remained largely the same.

Whenever I see people talking about their struggles during this pandemic, I want to call out “YES! Yes to this tenfold! That is exactly what it is like!” in hopes of turning it into a teachable moment.

At the same time, I find myself saddened, because I wouldn’t wish any of these experiences on anyone else, even if they are temporary and likely to end when this crisis is over.  I know what it is like to live with anxiety and depression every single day for years on end. I grew up seeing my mother struggle with bipolar disorder and now watch my fiance battle it on a daily basis. I am intimately familiar with many of the struggles of living with a mental illness. It breaks my heart to see so many others going through these struggles because I know firsthand how hard it can be.

As strange as it sounds, though, beneath it all, this pandemic has given me a strange sense of unnerving calm. For the first time in my life, I don’t feel entirely odd, different, unbalanced or crazy.  For the first time, I don’t feel singled out, the odd woman out in a world where everyone else seems to be breezing through life, coping much better than I could ever dream. For the first time, everyone else can finally understand all the feelings I go through every single day.  At least in that one aspect, the pandemic has become the great equalizer for those of us with mental illness.

I can only hope that their memories do not fade, though, once all of this is over.  Perhaps now that more people understand and have experienced many of the feelings commonly associated with mental illness even on a temporary basis, they will be more empathetic to the struggles many of us face every single day. Though even if those memories do eventually fade away, I hope everyone currently struggling to cope with the weight of the pandemic knows, as those of us in the mental health community often reassure each other, that none of you are alone. Though there are no easy answers or solutions to much of what you are feeling, we understand and we are all here, even if physically apart, to offer our support. Please never be afraid to seek help if you find you cannot cope on your own. Stay strong.

How I Spent My World Mental Health Awareness Day

I woke up early.  Not fifteen or twenty minutes early or even when the rising sun peeked in my window.  I woke up around three in the morning, not because any alarms were set or any loud noises woke me from my slumber.  My sleep is always spotty and restless, frequently dotted with anxiety and depression-laden nightmares.  Most nights, I’m lucky if I get more than five hours of sleep. Last night was no different.

I laid there feeling empty and stressed for hours, my thoughts racing, unable to get back to sleep.  When his alarms began going off three hours later, I resigned myself to the fact that there would be no more sleep for me today.

I helped him get ready for work, timidly smiling as I ushered him out the door. I said nothing about how I was feeling because I did not want to burden him with things he had no control over.  Easier to smile and to pretend, even though I know deep down I’m not kidding anyone.  Not myself. Not him.

After he drove away, I sat on the couch ruminating about everything I have to do today.  I sat there immobile for hours, beating myself up for all those things I should be doing.  I put a movie on, but it turns out it was for background noise more than anything, because I cannot recall anything about it.

I sat, I laid this way and that, I tossed on the couch for hours, not even quite sure why I was in such a funk today.  I felt lost and alone, the world utterly hopeless, which made no sense because things truthfully aren’t going that badly right now.  Yet those feelings were there all the same.  I couldn’t shake them, couldn’t stop them, any more than I could mute all those thoughts racing through my mind.

It was noontime before I managed to pull myself up.  There were days mountain climbing would take less effort.  I had been awake for 9 hours, out of my bed for six.  I was already exhausted and ready to climb back into bed.  Yet I managed to prepare some fresh salsa and straighten up the small mess I made on the counter today, piling those dishes on the side.  The dishes from yesterday still sit in the sink.  I ruminate about whether I’ll be able to wash them today.  I know I should.  But some days I just don’t have the energy.

I spent the majority of the afternoon watching an old series on television.  I know that I’ve seen it all before, which is a good thing because re-watching those episodes today was a blur.  I tried playing a game.  I tried checking my social media.  The truth is that I have no interest in anything today, no ability to focus on anything.

I want to scream and shout.  I want to cry.  I want to laugh at the pure insanity of it all.  I want these feelings to stop, this pain to stop.  I desperately want to be happy, to not have my mental illness always leaving a thick, dark sludge over everything in my life.  It taints everything.  Even the most delicious food tastes bland, the most upbeat music feels melancholy.  I don’t understand why my own mind would do this to me, why it wants me to hate my life, to hate myself.

It’s an hour until he is due back home.  All I have to show for the day so far is a container of salsa.  Strangely, even that feels like a victory.

I tell myself I will get to those dishes right after I finish writing this.  I don’t know if I will but I’m trying to be hopeful and positive.  I’m not sure I really feel it or believe it, though.  People say “fake it until you make it”.  I do it every single day when I try to encourage myself that today will be better, that I will be better today.  It all feels like lies because nothing ever seems to get better.  Yet part of me remains hopeful.

I breathe deeply and try to re-center myself.  I wash the tears from my face.  I mentally prepare myself to paint that smile back on my face, to pretend I am doing better than I truly am.  I know that, as long as I can force a grin and my cheeks are not salty from tears, he will assume today at least wasn’t an absolutely horrible day and not bring it up.  I actually prefer that today because I’m not even truly sure what has me so shaken to the core.  I wouldn’t even know what to say if he asked what was wrong.  I just know those feelings are there.

I do a mental tally of what foods we have that would be quick and easy because I’m not sure I have the energy to make anything more than that.  Truthfully, I don’t think I even have the energy to do that, but I’m terrified of letting him down, of disappointing him, of him thinking for even a moment that I am as worthless as I feel inside.

I catch myself, reminding myself that he would never say that, never think that.  That is my depression talking.  Part of me knows my depression lies, yet those sentiments always feel so real.

I settle on an easy dinner and turn back to do one last proofread.  I tell myself that writing this is a huge accomplishment, that I should be proud of myself for opening up at all.  It doesn’t feel like an accomplishment, though.  It feels like nothing, a waste of time.  I feel like a waste of space.  I question why anyone would even want to read this, to hear anything I have to say.

Again, I catch myself.  Easily, a dozen times a day I realize I am spewing that narrative, buying into depression’s lies.  Part of me wants to scream “shut up! Shut up! SHUT UP!”.  Unfortunately, though, stigma already has many people assuming that those with a mental illness are crazy.  I can’t feed their ignorance and their fears.  Still, I wish my mind would go silent.

I’ve done very little today beyond battling my own mind.  That, and beating myself up for everything that I haven’t done.  It feels like I’ve gone ten rounds with a heavyweight champion.  I’m already exhausted and ready for bed.  Ironically, I know when I finally get to go to bed, I won’t even be able to sleep.  I’ll lay there like I do every night because my mind never shuts up.  The words might alternate between despair and emptiness, but the endless chatter always remains.

Today is supposed to be World Mental Health Awareness Day, but in truth it could be any random, generic day to me.  They all bleed together, all feel the same.  The intensity varies day to day but the struggle is always there.  The world only schedules awareness one day a year but it is my reality every day.

Four Days on Suicide Watch

Everything had been building up for months, years.

It was not that I didn’t have wonderful things in my life to be grateful for. I had healthy, compassionate, intelligent children that were growing into incredible adults before my eyes; I had reconnected with my first crush ever who has turned out to be the love of my life and we have a wedding to plan; I had finally found my calling as a mental health advocate and had the start of a promising writing career; I finally understood my struggles with my mental illness, having found a clinic that not only helped me to find the answers I needed, but also actually gave me hope for the future. In so many ways, my life was finally looking up.

However, it was overshadowed by a lifetime of struggling. I had been battling my own brain my entire life. And in recent years, the government and my insurance company, as well. It felt like all I ever did anymore was fight everyone, again and again. It seemed never-ending. I was so exhausted from fighting all the time, never getting to catch my breath, never getting a break.

Add to that discovering not one but two meningioma tumors on my brain. I had survived years of abuses that left deep scars that would never fully heal. My fiance and I were facing a possible pending eviction caused directly by the government’s prolonged inaction in my case and direct refusal to comply with a judge’s previous fair hearing decision in my favor.

The straw that broke the camel’s back, however, was the fairly consistent presence of someone toxic in my fiance and my lives under the guise of one of his  childhood friends who was hell-bent on causing problems in our relationship, repeatedly trying to split us up.

To give a little background on the situation, she had known him since she was thirteen and had a crush on him for close to thirty years, bordering on stalkerish. When he was staying with his parents following the end of his marriage, she would intentionally show up hours before he was due home from work and say she would wait in his bedroom for him as an excuse to sleep in his bed. Though they never had any type of a relationship because he never saw her THAT way, for years, she regularly borrowed hats and shirts from him and kept them, much like a girlfriend would normally do. Despite having a crumbling relationship at home she should have been devoting her attention to, she tried repeatedly over the years to supplant herself into my fiance and his family’s lives in any way she could whenever she could, often causing drama in the process.  Though he later forgave her to an extent, she even played a crucial part in the break up of his first marriage.

From the time we got together, she had been trying to cause problems between us and split us up. The first time I met her was a month into our relationship, shortly after his father went into hospice. She pulled me aside and tried to convince me that I had no idea what I had gotten myself into or the mess he was going to be so I should just walk away before I got in over my head. She told me he was mentally unstable, that she knew him well enough to know I could not handle what was in store. She seemed thrown aback when I told her I had known him longer than her and I was in it for the long haul.

When she could see I was not going anywhere, she switched tactics. Over the course of the next year, every single time she came over she would make negative comments about me and my mental illness, lecturing me that I needed to stop being lazy and do something with myself and my life. Whenever my fiance and I would both jump in to defend me and attempt to explain the disability diagnosis my doctors had given me, she would interject that she worked in mental health, too, and she “knew what she was talking about”. She worked in a mental health care adjacent position, as a glorified overnight babysitter at a facility that housed mentally or physically disabled adults, a job you didn’t even need a high school diploma or any certification to get, yet she swore repeatedly that she knew better than all my doctors over the years. She frequently trivialized my mental health writing as a waste of time and criticized everything from the cleanliness of my apartment to my cooking, as if nothing I did even remotely met her standards.

As if the constant attacks were not enough, she also was constantly attempting, albeit admittedly very poorly, to  blatantly flirt with my fiance in front of me. She would try to run her fingers through his hair and insist he let her cut it, to which he would pull away and say I will cut his hair when he needs it done. When he stopped shaving for no shave November and the couple months afterwards, she commented repeatedly that he should shave because he looks so much better clean shaven, that she prefers him that way, even offering to do that for him, as well. She was forever reaching out to touch him, swat at him or rub him with her hand while she talked, trying to take sips out of his drinks like a girlfriend might do and regularly found excuses to lift her shirt or drop her pants in front of him under the pretense of showing off numerous bug bites and bruises. She would often announce wildly inappropriate things that people wouldn’t normally discuss with friends, like she had just shaved her nether regions or talk about having sex, watching porn or masturbation when she came over.

We tolerated much more than we should have because honestly we felt sorry for her. She was always desperate for attention and, according to her, her problems were always ten times worse than everyone else’s.  For example, when we attempted to explain about my doctors finding my brain tumors, she cut us off by saying, “That’s nothing! Did I tell you I had to bring my car back to the shop again?!” as if car problems were somehow worse than brain tumors. She was loud, obnoxious, crass and crude with no concept of respect or boundaries, always saying or doing whatever she could think of to get all eyes on her. She was always talking badly about someone when she came over, usually my fiance’s ex-wife, even though she was supposedly still good friends with her, to the point where we began watching everything we said around her to avoid becoming part of her gossip. She also had severe substance abuse issues. In a year and a half of seeing her once to twice a week on average, I never once saw her even remotely sober regardless of the time of day – she was always drunk, high or both. We knew from everything she had talked about that things were bad for her at home, that her relationship was in shambles.  A lot of people had written her off already over the years for her behavior but we understood that she had a lot of issues so we tried to cut her some extra slack.

I had tried my best to be kind to her. On more than one occasion, I took the time to show her sons my sugar gliders and explain more about them. I even watched her youngest once for over an hour while she ran an errand. If we had leftovers when she stopped by on her way to work, I would send her with a plate or bowl. She would regularly fill her purse from treats I had put out in snack bowls. I baked her family Christmas cookies and sent her with extra for both home and work. I once even lent her an old pair of pants that were too big on me so she had something clean for work when she stained her own. I listened sympathetically when she complained of relationship issues, health problems or other stresses, trying to extend an olive branch of friendship. I even did my best to overlook her steady barrage of flirtation with my fiance because I realized it must have been hard to see someone you crushed on for decades happily with someone else.

But despite all my attempts at kindness, both her attacks on me and her inappropriate flirtation with my fiance not only continued but steadily increased. What originally may have been one off-handed comment about her believing my disability was nonsense became full-fledged rants. She began making snippy and snide remarks and telling us to stop whenever my fiance and I were affectionate to each other as if she resented anyone else showing him attention or love.  Over time, it had all became too much to bear. When my fiance and I began contemplating marriage, she declared we were not ALLOWED to both get married a second time because she had never even been married a first. When we officially announced our engagement, she responded by referring to me as (please excuse my language) his “fuck buddy”, saying outright that the only thing I did for him was give him my “roast beef curtains” and insist that he deserves better than me. That was the last straw and we agreed she was no longer welcome in our house or our lives.

For two weeks afterwards, she did not come around. Then late one night, well after one in the morning when we were already in bed, we heard a drunken knock at our kitchen window. We both knew exactly who it was because she was the only one we knew with the audacity to think that would be acceptable. I was livid and wanted him to tell her to leave immediately. He wanted to quietly let her in to avoid her making a drunken scene in our apartment building, to wait to tell her she was no longer welcome here another time, during more reasonable hours when she might be somewhat more sober and perhaps slightly more reasonable. Everything quickly escalated.

We were both beyond stressed at the time, not at all with each other but rather with life circumstances in general, topped off by our unwelcome, uninvited guest. Beyond all my own issues, he had been struggling terribly, as well. He had a lifelong battle with his own mental illness. In the last year, he had lost first his father then his job. The family dog that had been his parents’ for well over a decade had to be put down and he was struggling to keep his truck, one of his last physical connections to his deceased parents, on the road and in working order. We were both well beyond our breaking points on many fronts and the culmination of everything with her pushed us right over the edge. We fought terribly, something we don’t often do even in a mild sense.  It may have been the worst fight of our entire relationship. Afterwards, I retreated to the bedroom to cry, locking the door so I could be alone.

I did not have any plans to commit suicide. The thought honestly had not even crossed my mind.  I was not trying to hurt myself in any way. I loved my fiance and my children more than I could ever put into words and would never have wanted to hurt them in any way, either. I was hurt, angry and distraught over our fight, disgusted that we had tolerated someone so blatantly toxic for so long, and I was exhausted and overwhelmed with life in general.  I just wanted to be alone, wanted to try to calm down, to catch my breath, to stop feeling like I was free-falling through a world where I was never allowed to just be happy, never allowed to just rest and be at peace.

I dumped the basket of pills out on the bed and fished out various bottles of my take-as-needed anti-anxiety medications. In between sobs, I took a few. Then I vomited.

Seeing the pills floating there on top, I took a few more to replace the ones I had lost. I continued to sob and to vomit. To vomit and to take more pills to replace the others.

At this point, I was no longer thinking clearly, caught in a nightmarish loop, wanting desperately just to calm down, to stop feeling like this, and to get some much needed rest.

Eventually, sleep came. I started to feel dizzy and thought to myself, “..finally.. they are starting to kick in..”  It is the last thing I remember for almost two days.

I woke up a day and a half later in the hospital. He was seated at my bedside, looking ragged, like he hadn’t slept in days.

Baby! You’re awake! Oh my god I love you. I am so sorry about everything. How are you feeling? What do you remember?

I was confused and disoriented. On oxygen. Had a bunch of tubes and wires all over my body.  It took me a few minutes to realize where I was and what was going on. I could not remember anything since taking the pills, crying and throwing up repeatedly. I was not even sure what day it was.

I can’t believe you don’t remember any of it. I had to kick down the door, to call the police.

My chest hurts.

I can only imagine. One of the cops did a sternum check, pushing really hard on your chest, hoping for a reaction to the pain. You were completely unresponsive.

My throat hurts.

You had tubes down your throat. They had to restrain you for a bit because you started to flail and grab at the tubes. You have no idea how much you scared me baby. What you looked like, laying there hooked up to all those machines, all those wires and tubes. I thought I was going to lose you. Please don’t ever scare me like that ever again.

I wanted to talk about it all, to explain, but my voice was raspy, my throat raw. It hurt to talk. I couldn’t stop coughing. I wanted to insist I hadn’t meant for any of this to happen, to swear I wasn’t suicidal like I had been all those years ago before we were even together. I wanted to apologize for scaring him, for fighting over stupid things like people who were inconsequential and irrelevant. All I could do though was cry as he held me close, my tears flowing freely with his.

I had lost a day and a half.

But more importantly, I tarnished our relationship in a way I can never take back. The sight of me laying there unresponsive, of being carted out on a stretcher, of my laying there as the doctors frantically worked to revive me, will forever haunt his nightmares.

I spent the next day in intensive care as they closely monitored my heart, followed by three days on a secure floor on suicide watch. Again and again, I tried to explain it all to whoever would listen, to insist I was not suicidal.  However, protocol required a few days of observation no matter what was said.

My heart was constantly monitored, my vitals taken every few hours. My IV was moved numerous times as my veins collapsed and fresh bruises appeared up and down my arms. I was stuck in bed for the first couple days upstairs while I waited for nurses to find me clothes other than hospital gowns. The clothes I had arrived in had been cut off me in the emergency room when I arrived. I could not wear other clothes from home until after I was cleared for discharge.

I was not allowed many other items often taken for granted such as a phone charger or silverware. Well-intentioned staff reached out repeatedly to try to convince me life was worth living. Meanwhile, they rushed to confiscate any cans or other sharp items from meal trays and to take endless notes on everything I said and did to assist with my psychological evaluation. I had a constant companion, a nurse or aide to sit with me at all times to prevent me from possibly further harming myself. Though I was never by myself during those four days, I had a lot of time to lay in bed alone and think.

I was not suicidal but I have been in the past. I did not intent to harm myself, but I had in the past. Intentional this time or not, I found myself in the same place and, like my previous attempts in the past, it had not solved anything. On the contrary, it made everything much worse. It hurt the people I love, scared my fiance and my children to death.

I didn’t get any time to calm down, didn’t get that moment of peace I had desired so badly. The majority of the problems had not gone anywhere. I lost a day and a half, woke up in pain and discomfort only to face new problems created by my own actions.

I was extremely lucky just for the fact that I am still here to tell my story. I could have just as easily become a statistic that day. My story could have just as easily ended with my obituary, the words and questions of others left unanswered, adrift in the wind.

I cannot apologize enough for what I put everyone through. I feel stupid, ashamed, that I should have known better. There are no words that could adequately express my remorse. I would do anything to take back that night but there is nothing I could ever say or do that would erase the past.

I would love to say there is no excuse for my actions but when my depression and anxiety reach certain levels, I no longer always think clearly. I become increasingly overwhelmed, the world feels largely hopeless and I am no longer able to cope. Even when I am not actively suicidal, which I have not been for years now, I struggle regularly with suicidal ideation, not exactly wanting to die but no longer wanting to continue living my life the way it is, either. Though I never meant to fall apart like I had that day, unfortunately once I reach a certain point, I react before rationalizing the repercussions of my actions.

I would love to say there is an easy solution to this, that I could take a magic pill or think some happy thoughts and my mental illness would just fade away and disappear. I wish I could say it was a temporary phase even that I would eventually get over. My mental illness is caused in part by a genetic mutation. I was born with it and I will have it until the day I die. There is no cure for me. It is permanently hardwired into my genetics. I can receive therapy for past traumas and current issues, I can take medication to provide my brain with the chemicals my body cannot make itself, I can fill my coping toolbox with techniques and strategies for dealing with harder days and attend things like tai chi and yoga classes until the day I die. Yet I will always have a mental illness. It is a lifelong, permanent diagnosis for me.

Mental illness is my cross to bear. Though I truly appreciate that my loved ones are willing to stand by me and support me through my struggles with my mental health, it is not fair or right for them to suffer like they have for my diagnosis. Although I never intended to do so, I severely hurt everyone that matters to me. They all have tried to be compassionate and understanding, to forgive me for an illness that often wreaks havoc in my life, for a condition frequently beyond my control.

However, I am not sure I will ever be able to forgive myself.

Since getting out of the hospital, my fiance and I have not talked much about the incident beyond him being thankful that I am okay and asking me to please never scare him like that again. I have reassured my children that I am okay, as well, trying to minimalize the severity of it all to lessen their fears. Again, I wish there were some magic words I could say to take away the pain and panic in their eyes. I fear no apology will ever be enough.

It took almost a week before we could even sleep in our bedroom again. While I was in the hospital, he slept on the couch when he could sleep at all, the spilled pill bottles, vomit and towels still sitting where they were when the ambulance carted me away. I insisted on cleaning it up myself when I came home, my mess, my problem, but going into that room felt like crossing into an alternate nightmare dimension. Nevertheless, I fought my way through a bevy of anxiety attacks and breakdowns to clean it all up. Even after everything was cleared away, no trace remaining, we opted to sleep in the living room for the next week on our air mattress. We knew what had happened in there, we had lived through it, yet we were still not quite ready to fully face it.

The first couple nights that we returned to the bedroom, I couldn’t sleep at all. He continued to cling tightly to me all night while he slept, as he had done every single night since we returned home from the hospital, as if he was terrified that I would disappear forever if he let go for even a moment. I laid awake both nights, silently crying for the pain and fear I had placed in his heart. A month later, my anxiety still rises whenever I enter that room, my sleep restless and plagued by nightmares old and new.

I know I need to change many things, to put safeguards in place to prevent something like this from ever happening again. I cannot change the fact that I have a mental illness, but there are other things I can address, precautions I can take. I never want to hurt my loved ones like that ever again. For instance, no more locking myself away when I am upset. No more taking extra dosages of medication early, even if I have thrown up the dose I just took. No more tempting fate when I might be too emotionally irrational to think clearly.

I have a constant pressing need now to reassure him that I am okay, that he doesn’t have to worry. I catch him looking at me, watching me, more frequently now, and checking in on how I am feeling. We are trying to heal from this, to move forward, though I’m not sure we can ever completely move past it. He almost lost me that day. He is always going to worry just a little bit more now.

We have also agreed to remove certain toxic people completely from our lives, those who prefer to add drama and conflict rather than happiness and support. We learned the hard way that some people will take advantage of our kindness and tolerance, repaying us tenfold with cruelty and drama. The nail in the coffin of that childhood friendship was hearing from mutual friends that she had been going around laughing and bragging about “putting me in the hospital”, proud of the part she played in my breakdown. We will never again allow anyone like that into our lives. Whatever it takes to never find ourselves in that situation again.

Some people say that suicide is selfish because all it does is pass the pain onto others. Other people attempt to explain that those who make attempts just don’t want to hurt anymore themselves. Many nowadays recognize that suicide is often a tragic byproduct of mental illness. I have been suicidal. I have been in those moments of desperately wanting the pain to stop. I have had suicidal attempts in my past and now an unintentional attempt because I was upset, irrational and not thinking clearly. I have lost loved ones to suicide, and known others who have lost people they loved deeply, as well, so I understand all too well how devastating it can be from the outside looking in. Regardless of where you fit in the equation, suicide is always heart-wrenching and tragic.

One thing I can tell you, whether you are suicidal or not, whether your attempt is intentional or not, the result is always the same. Pain. Pain for everyone you love, everyone who loves you. Pain for yourself should you survive. And not just physical pain from tubes and tests and IVs. Emotional pain as you see that haunted look in their eyes, that kernel of doubt that appears every time afterwards that you insist you’re okay. Pain that will continue for years, that will likely never go away, whether you’re around to see it or not.

Pain and overwhelming loss for everyone who has ever cared for you. They will never be the same. You might carry physical scars from your attempt, but theirs will run much deeper and never fully heal. Those close to you will retrace all your interactions, looking for signs, real or imaginary, to explain what happened. They will question whether they should have said this or should not have said that. People who you have not seen in ages will question if they should have reached out, as if they could have magically known things were bad and somehow made a difference. They will all blame themselves for your actions and choices. Whether you die or not, they will be forever haunted by that one choice you made, something completely beyond their control. Yet, in their pain, they will embrace that blame, caught in a cycle of imagining every scenario that could have prevented it.

To those contemplating suicide or just on that edge of not being able to cope with life anymore, please know that I understand completely how hard it can feel, especially when you’re struggling with mental illness. You are not alone. But I wouldn’t wish the kind of pain I caused on anyone, not my worst enemy, not my loved ones or yours. Once it has happened, though, you cannot ever take it back. Even if they don’t lose you, your relationships will never be the same. I cannot change the pain I’ve caused, but perhaps, by sharing my story, you can spare your loved ones from the same fate.

Please be careful. Be careful with yourself and be careful with your loved ones. Life is a fragile thing, a light that can be snuffed out in a moment.  It may be hard sometimes, downright unfair. But life is also precious. As is love. Don’t take either for granted.

I know all too well that mental illnesses are rarely rational. When we are upset, we often react based on pure emotion. So take precautions now, during the calm before the next storm. Do not leave ways to harm yourself readily accessible when you might find yourself too emotional to think rationally. Don’t set yourself up to fail or to hurt yourself or those you love.

I thankfully am very lucky to still be sitting here, able to share my story. Many others have tragically lost their battles with mental illness without ever having a chance to tell their tale. Their stories are told in yearly mental health statistics and on memorial pages created by those they left behind.  We’re all in this boat together and we only have two choices. We can either become a statistic or we can keep going, keep fighting, and find some way to make a difference in this world, even if only to show others that it is possible to survive our diagnosis. There are too many mental health statistics and enough pain already in this world. If we have to choose anything, let’s choose life and love.

Much love, compassion, hope and faith that even if this does not find you well, it finds you strong enough to keep living. ❤

Fear of the Unknown – Wedding Planning Anxiety

As a young girl, I dreamt of my wedding day many times over.  My friends and I had mock weddings in our backyards and on the playground, pretending our dandelions were expensive bouquets and using whatever we could find as makeshift veils.  We would practice walking down the aisle, improvising imaginary heartfelt vows that professed undying love.  It was thrilling to imagine that one day, when we found our real life prince charming, he would sweep us off our feet and we would get to plan our wedding for real.

I have never planned an actual wedding before.  I was married once before but I never did get the fairy tale wedding of my dreams.

My ex-husband and I got married more out of obligation than any deep-seated desire to be wed.  After struggling to find his way in life, he stopped in at a recruiting station on the way home from work one day and decided on the spot that he wanted to go into the Air Force.  We had a young son together at the time.  The Air Force had a steadfast rule against recruiting single parents.  Upon learning this fact, he came home from the recruiter’s office that afternoon to explain his dilemma.

It was followed by a simple “..so do you wanna get married or what?”

I was not one to stand in the way of his future or his happiness so I agreed.

Not a very heartfelt proposal followed fairly closely by an equally eloquent wedding a few days later, a simple hand-fasting in his mother’s living room, followed a store bought sheet cake.

I had a wedding gown that I had previously purchased when my ex and I had casually tossed around the idea of possibly getting married one day.  I had found it on sale, a virtual steal, already altered for another bride with a similar frame who changed her mind at the last moment.  The dress originally retailed for a few thousand but had been marked down to just over a hundred because it sat in the store, unpurchased, for so long.  It seemed like kismet to find a gown already tailored to my exact proportions.  It was beautiful and elegant, everything a young girl would imagine her wedding dress to be.  Yet it sat in the closet on my first wedding day, never even made it out of the box.  It seemed silly, bordering on asinine, to even put it on when the rest of the few people in attendance were not dressed up at all.  I have since gotten rid of that gown because it stood as a painful reminder of everything my wedding should have been but wasn’t.

This time around, I want to do it right.

By right, I don’t mean some over-the-top fancy gathering where everyone is dressed to the nines and I’m paraded around in a dress that costs nearly as much as a new car.  I honestly don’t even need another fancy wedding gown, though I do want to wear something simple yet beautiful to mark the occasion.

I don’t need an expensive bouquet.  Nor do I need a fancy big cake with multiple tiers and arches.  I’m actually partial to wildflowers.  And we both love cheesecake.  I’m open to compromises as long as I am not compromised right out of my wedding day altogether.  I refuse to ever do that again.

By right, I mean a wedding that’s planned out, on my terms, incorporating things that mean something to both Marty and me.  I want to be surrounded by our family and friends.  I want to have music we’ll both happily sing along to and food we’ll both enjoy.  I want it to be a day full of love, laughter and happy tears.  I want it to be a day that I will cherish forever, look back upon years from now and smile.  I don’t want some rushed, generic ceremony with no heart done out of obligation.  I want a real wedding.

That being said, I have no idea how or where to begin.  I have a vague idea of some concepts I would like to incorporate but I have yet to weigh which are realistic and which are not, not to mention what will be affordable.

We don’t have a lot of money to dedicate to the day, but even that is fine by me.  We will manage.  After all, a marriage is supposed to be a celebration of love, not of wealth.  But I don’t want to disregard the day as unimportant, either.  It marks an important milestone in our lives and should be treated as such.

I’m thrifty by nature and crafty at heart.  I love to save wherever I can, whether by hitting sales or doing things myself.  I even find all these bridal giveaways fun in their own “probably never going to happen but it’s nice to dream” sort of way. However, the field ahead of me is largely unexplored and I fear it may be full of landmines I am not expecting.

I fear cutting corners like George Castanza in Seinfeld, opting for cheaper envelopes with toxic glue.

I fear taking on a project that turns out to be more than I can handle, of wasting time, resources and money that would have been better spent somewhere else or done by a professional.

I fear forgetting something critical to the ceremony, or even worse, someone important.

I even fear having everyone object at the ceremony, telling him to run while he still can.

I’ve barely scratched the surface of planning this wedding.  I still have over 9 months to go and an entire wedding to plan.  Yet in my head I have failed miserably at it many times over in a thousand different ways.

I know deep down that it is just my anxiety and not reality.

My anxiety has a knack for making mountains out of mole hills, of making even the simplest of tasks feel overwhelmingly impossible.  My anxiety holds me on the verge of sheer panic, racing through my mind everything and anything that could possibly go wrong.  And that is on an average day.  Throw a once in a lifetime milestone like marrying the love of my life into the mix and my anxiety goes into permanent overdrive.  I only have one shot at this and I cannot let my anxiety get the better of me, pushing me to give up before I have even begun.

I know I am capable of doing this.  I’m more than competent at planning and organization, even meticulous when I need to be.  I am creative and artistic.  I have a good eye.  I am overly sentimental, bordering on downright sappiness, so I would never intentionally leave anything or anyone meaningful out.  Most importantly, I know Marty as well as I know myself so I know better than anyone else how to create a day that would mean the world to both of us on multiple levels.

Yet my anxiety rages on.

My plan at this point is simple.

I have to take things one step at a time, one task at a time.

Focus on what matters.

I am not striving for perfection.  I don’t need everything to be perfect.  I just need more than a rushed wedding in a living room with a generic sheet cake so my new spouse can ship off to basic training.

I need a wedding that will mean something to both Marty and to me.

I know I can do this if I set my mind to it, take my time and work it out one piece at a time.

The problem is that I honestly have no idea how to do it quite yet.  And not knowing where to even begin is probably the scariest feeling of all.

Except perhaps letting him down.

That scares me even more.

But that’s when I hear his voice, calming me, soothing me.  Telling me whatever I do will be perfect.  That he will love me no matter what.  That all he wants is for me to be happy.  That all he wants is to spend the rest of his life with me.  He has that miraculous power over me to bring me back from that edge, to lull me back to reality, to give me the peace of mind I so desperately need.

I know in my heart that no matter what happens on our wedding day, what truly matters is that it marks the first day of the rest of our lives together.  I know that no matter what happens, it will be perfect because we will be together.  Everything else is just details that I will iron out along the way.

I just wish my anxiety would stop trying to convince me otherwise.

anxiousbride

This Piece Was Originally Written For The Anxious Bride on 8/11/18.

When Will Insurance Companies Realize Fighting Against Patient Care Is Not Cost Effective?

Other than my ongoing battle with mental illness, I have been relatively healthy my entire life.  I don’t drink, smoke or do drugs.  Prior to the last couple years, other than mental health doctors, I rarely went to the doctors at all beyond basic check ups.  Other than medications for my mental illness, I have rarely relied on any medication stronger than acetaminophen or an antacid, and only then if absolutely necessary.  Due to this fact, I had little experience with battling my insurance company for most of my life.  These last two years, however, have been a real eye opener.

I have struggled with severe depression and anxiety my entire life.  For years, I was labelled “treatment resistant” because no medication I took ever seemed to work.  A couple years ago, my meds doctor at my mental health clinic sent me for a genetic test to help determine what prescriptions might work better for me based on my genetic make up.

The test came back with an unexpected result.  I had a genetic mutation that rendered my liver incapable of metabolizing folic acid in any usable amount.  Broken down folic acid, called l-methylfolate, is used by the neurotransmitters in the brain to help moderate moods.  Because my own body could not metabolize folic acid into l-methylfolate in any usable amount, the neurotransmitters in my brain had been literally starving for what they needed for the majority of my life.

It was a fairly easy fix.  There’s a pill on the market of broken down folic acid.  It is, on average, under $200 a month.

It is something my body cannot make on its own and my brain needed to function properly.  Yet my insurance company fought me on it for almost 9 months.  In the meantime, my doctor had to prescribe me a collection of high dose antidepressants, anti-anxiety and sleep aids in hopes that together they might even slightly touch my mental illness.  I had a revolving combination of medications, anywhere from four to six prescribed at a time, with the dosages being steadily increased.

The cash price of the one anti-depressant alone that I took during that time runs on average $250-$300 per month.  The one anti-anxiety medication I took runs between $45-$85 per month.  The one sleep aid ran around $20 a month. Other medications we tried ran between $10-20 apiece.  Altogether, I was taking between $450-$500 a month worth of medications that were barely able to do anything for me because my insurance company did not want to pay less than $200 a month for the medication I truly needed.

After almost 9 months of fighting and multiple appeals and fair hearings, I finally got my prescription approved.  These days, I am taking my l-methylfolate, along with one moderate but inexpensive antidepressant and a natural sleep aid.  Altogether, the cost is still under $200 a month.  I honestly cannot fathom why the insurance company would have opted for 9 months to pay over double that amount on a less effective treatment instead of just approving what my doctor had initially prescribed me, what I truly needed.

I wish I could say that this was an isolated incident but over the past couple years, I have had multiple run ins with my insurance company in regards to my treatment.  Though relatively healthy for the majority of my life, these last two years have been plagued with multiple health issues, issues my insurance company has chosen to fight me on, as well.

Two years ago, I was rushed to the emergency room in severe pain.  It turned out that a large cyst had grown on my ovary.  Within the cyst, a mass of tissue had begun to grow, as well.  Together, they had put increasing pressure and weight on my ovary, contorting it and damaging not only the ovary itself but also on the veins around it.  The ovary was damaged beyond repair.  There was a concern that the mass within the cyst might be cancerous.  Rather than doing a biopsy then surgery that would prolong my suffering, my doctor opted to remove the ovary first then biopsy the mass on it afterwards.

Again, it was an easy fix.  The ovary had to come out.

Yet the insurance company dragged their feet for over two months.  For over two months, I was in constant agony, on bedrest, slowly awaiting the pre-op tests to get approved, let alone the surgery itself.  For over two months, I had to take pain medication and see my doctor almost weekly to check my blood pressure, monitor my pain levels and make sure no infection had set in.  For over two months, I had to have a coordinated care provider come to my house to assist with things I could no longer do for myself because I could barely move on my own without excruciating pain.

The ovary, along with the cyst and the mass of tissue within it, had to be removed.  The insurance company ended up having to cover numerous extra doctor appointments more than was necessary, along with added prescriptions and periodic home health care assistance, all because they delayed the approval of treatment that was ultimately going to be needed to begin with.  Dragging their feet and delaying approval did not save them any money.  Quite the opposite.

Most recently, during a ct scan it was discovered that I have two meningioma tumors on my brain.  Though 80% of meningiomas are benign, doctors still have to test them to make sure they are not.  I first saw a neurologist who, in turn, referred me to a neurosurgeon for testing.  The neurosurgeon ordered both an EEG and an MRI with and without contrast to be done so they can get a better look at my tumors.

It has been almost two months since the meningiomas were discovered.  The EEG was completed, yet we’re still waiting for insurance approval for the MRI.  Meanwhile, my neurologist keeps scheduling appointments because, until he knows for sure that they are benign, he has to keep monitoring me for signs of seizures or other averse effects.

Best case scenario – if they are small enough and benign, it is considered watch and wait, with them being periodically monitored and measured once or twice a year to look for changes.  Worst case scenario – they are malignant, I need surgery and radiation.  But until the MRI is done, it is a case of *Schrödinger’s tumor – we won’t know whether it is benign or malignant until the doctors get in there for a better look.

Meanwhile, I keep going in for more or less useless appointments where my doctor keeps checking in to ask how I am feeling and checks my vitals, then we sit around discussing how the insurance company still hasn’t approved the MRI.  Yet, he can’t put off these appointments until he knows for sure whether we need to worry about these tumors or not.  So the insurance company is getting billed for appointment after appointment to check in on how I am doing while we wait for the MRI instead of just approving the MRI that will ultimately be needed anyway.  These tumors are not going to go away on their own.  The MRI is needed to fully diagnose them and my neurologist is not going to allow me to fall between the cracks just in case they are malignant and surgery is needed.

I honestly do not understand why insurance companies fight patients and their doctors on treatment that is needed.  It is not like any of my treatment was something ordered on a whim.  There was a prescription for a substance my brain needed that my body could not make on it’s own.  There was a surgery to remove an organ that was irreparably damaged and causing me severe pain.  And there was a test needed to determine whether the tumors on my brain are benign or malignant.  Three cut and dry cases of treatment that was very much needed and not in the least extravagant or superfluous.

Yet, the insurance company’s decisions in each of these three cases over the last year has cost them, each time, much more than it would have cost them if they had approved the treatment the doctors in each case recommended.  If a prescription, a test or a procedure is ultimately needed and there is no other possible recourse to resolve the issue, why would the insurance company either deny it outright or drag their feet in approving it?  It will only end up costing them more in the long run.

I with I could say my experiences were isolated incidents.  In the course of my battles over the past two years, I have spoken to numerous others who have been and are currently fighting their insurance companies, as well, for the treatment they need.  It appears to be more commonplace than most people realize.

When did it change that healthcare became more about trying to cut corners and save money than in treating the patient and doing what was best for their health?  Has it always been this way?  Wealth over health.  Profit over people.  It’s honestly disgusting, despicable and deplorable.  Having been relatively healthy for the majority of my life, I never realized what a struggle it can be to get the treatment you need covered.

While I understand and acknowledge that fraud is rampant in medicine today and insurance companies need to validate claims before approval is given, once there is proof to support the medical treatment requested, it makes little sense to drag out or deny the claim further.  Insurance companies could ultimately save substantially more money not by fighting patients on the treatment they require but by approving and expediting it so that their overall treatment and recovery takes less time and costs less money.

 

* Schrödinger was an Austrian scientist in the early to mid 1900’s.  He developed a theory made popular in recent popular nerd culture, called the Schrödinger’s cat paradox in which a cat is sealed in a box with a flask of poison and a radioactive source.  According to his theory, it is accurate to assume that the cat is simultaneously both alive and dead because either option is probable.  Until you open the box and check, you do not know for sure.  I referred to my meningiomas as Schrödinger’s tumors because, until the MRI is done, there is no way to know for sure whether they are benign or malignant.

Love.. When You Both Have A Mental Illness

Everywhere you look nowadays, you see stories about Ariana Grande’s whirlwind romance with Pete Davidson.  And almost everyone seems to want to put in their two cents on the matter, claiming everything from the fact that they’re too young to they’re moving too fast.  So many opinions abound.

More than anything, though, I keep seeing people chiming in about the fact that they both have mental illnesses that they have spoken publicly about, as if their illnesses play a large part in their relationship in some negative way.  Ariana Grande has spoken out about her struggles with anxiety and post-traumatic stress disorder.  Pete Davidson has shared his experiences with borderline personality disorder.  Yes, they both have mental illnesses but they also have found love.  And two people loving each other is not a bad thing.

There are many people that buy into the stigma surrounding mental illness, assuming that everyone struggling with one is crazy, unbalanced or even dangerous.  Some assume that nobody can have a healthy relationship while they have an unhealthy mind and that two mentally ill people coming together is a recipe for disaster.

I once even had a friend tell me specifically that “two unhealthy people cannot have a healthy relationship”.  Based on their premise, because I have a lifelong mental illness diagnosis that has its roots in my genetics, I have no hope of having a healthy relationship, especially if I fall in love with someone else who is struggling with an illness, as well.  If he were to be believed, I was destined to be alone.

As someone who struggles with mental illness who is in a relationship with someone else who is mentally ill, as well, I can tell you from my own personal experience that is not the case.

I have depression, anxiety and PTSD.  He has been diagnosed with bipolar disorder and PTSD.  We have both struggled with our illnesses for years, even being hospitalized for breakdowns at different points in our lives.  Yet, in each other we have found a love unlike anything either of us had ever experienced before.

We knew each other years ago as children.  He was my older brother’s best friend for a time and my first crush.  In our teens, life sent us in different directions and we lost touch for many years.  We found each other again a year and a half ago, after twenty five years apart, and sparks flew.

Like Ariana Grande and Pete Davidson, we’ve had people look at our relationship with judgment because we moved so fast.  He found me online again, listed as a friend of a friend he might know and we reconnected.  For two days, we talked non-stop whenever we had a moment to spare.  On the third day, we arranged to get together in person.  We’ve been together ever since.  As they often say “the rest is history”.

A month and a half later, we found ourselves living together.  We hadn’t planned it that way honestly.  His father had inoperable end-stage cancer and was placed in hospice.  There was no way I was going to leave his side for even a moment and make him endure that alone.  I had lost my own father to cancer a few years earlier, following his own brief stay in hospice.  Going through that together brought us even closer.

All the people from the outside looking in saw were two people who jumped ridiculously fast into a relationship.  They don’t realize that we knew each other as children and had a pre-existing familiarity and closeness that was brought back to the surface again.  The don’t accept that facing hardships together as we had done brings people closer.  They don’t consider that we have physically spent more time together in the last year and a half together than some couples have after dating for years.  They don’t see how we are with each other behind closed doors and how close we’ve continued to grow with each passing day.  Some people come directly from a place of judgment and automatically think it’s irrational to be so serious after such a short time.  Or worse, they label our choices as “crazy”, as if our love was just another way our mental illnesses have presented themselves.

Because of our mental illnesses, we’ve both always felt different, broken, damaged.  We both never felt we quite fit in or that anyone else could truly understand what we’re going through.  We’ve both felt so lost and that life should not be this hard.  We both have struggled for years to stay positive when it felt like our world was spiraling down into a dark abyss.  We both had numerous people in our lives who just couldn’t understand, who told us it was all in our heads, that we just needed to get over it and suck it up.

The difference now is that we both have someone we can talk to about everything we’ve been through.  Someone who truly gets it because they have been there themselves.  Someone who listens without judgment because they understand all too well how much that judgment hurts.  Someone who sees us not as damaged and broken, but for the big hearts and beautiful souls we have inside.

With that level of love and acceptance comes an incredibly strong bond.

We’re able to open up to one another and talk on a level that we never had before, to share experiences and traumas we’ve kept to ourselves for years.  In each other, we’ve found the one person we can completely be ourselves with, say anything to, without fear of rejection.

We both have a portion of our mental illness that is unique to us.  I have a generalized anxiety disorder and he has bipolar disorder.  Though I have not struggled with his disorder myself, my mother had bipolar disorder so I had some experience with his illness, at least from the outside looking in.  We have patiently explained to one another everything the other didn’t understand and offered tips to one another for how to support us when we are struggling.  We listen intently to each other and are supportive to each other because we both know very well how it feels to have nobody there who understands.

The depression side of his disorder I understand all too well.  The manic side not so much, though I had learned early on in life to spot the shifts in my mother because she shared his diagnosis.  When he has a manic episode, I am always there to offer support and encouragement.  He often becomes hyper-focused on one task or another and I intervene to make sure he does not lose himself, putting off self-care and disregarding his basic needs like eating.  On the rare occasion that his mania presents itself as rage, I do my best to deescalate the situation in a non-confrontational way.  No matter how his mania presents itself, I offer a calming presence to soothe him and bring him back down again, often rubbing his back, head and shoulders to help him relax.

When my anxiety makes me think irrationally, he is there to talk me down, to help me see reason.  Following anxiety attacks, when I desperately just need the quiet presence of someone else, he holds me closely without judgment and reassures me everything is okay.

Depression hits us both pretty hard.  In the past, we’ve both dealt with people who never understood and who insisted it was all in our heads.  But we both know the signs.  We can see in each other when our depression is raging strong.  And we are both there for each other how we always wished someone would have been there for us for all those years.  We are gentle, kind and compassionate with each other because we’ve been there ourselves and we understand how hard it can be.

We both are plagued by PTSD, as well.  Nightmares of past trauma are especially hard for us both.  When either of us is battling the demons of our past, the other can see the signs, intervene and offer comfort and support.  When our pasts are haunting us, we can talk openly about it on a level that we never were able to with anyone else.

On days either or both of us are struggling particularly hard, we have learned to lean on each other without judgment.  We each pick up where the other leaves off.  We have developed an ever-shifting balance in our relationship.  On days we both are struggling, we curl up together and lean on each other for comfort.

We cheer each other on for our successes and support each other in our struggles.  We encourage each other to stay strong, to keep fighting and to get the treatment we each need.  Neither one of us judges the other for the ways our illnesses present themselves because we understand all too well and empathize with each other on every level.  We not only offer each other support but we’ve become proactive in each other’s treatment, as well.  We’ve attended doctors appointments with each other and helped bring up concerns the other may not have noticed or may have been too uncomfortable to discuss.  We love and support each other in every way.

Yes, we jumped into a relationship that became serious relatively quickly.  But it was not because our mental illnesses had us thinking irrationally.  In each other, we saw someone who finally understood everything we had been battling our entire lives.  In each other, we found that one person who could accept us completely for who we were, loving us not despite our mental illnesses but because of every single thing, mental illnesses included, that made us who we were.  In each other, we discovered what we had been needing, what we had been missing, our entire lives.  Pure unconditional love.

When you find something like that you don’t question it.  You don’t hold back, think on it or weigh options.  You thank the heavens for placing someone in your life and in your path that makes you finally feel not just that it’s okay to be you but that there’s not a single other person in this world you’d rather be.  You run with it and you love them back completely because life is short.  We have to make the most of it.  And a love like this is too good to pass up.

Yes, we may lean on each other more than others do because of our conditions, but that doesn’t make our relationship unhealthy.  We give each other exactly what we each need.  We might both have mental illnesses, but we both are so much more than our diagnosis.  And now we are both blessed to have found someone who can truly see that.

After all, mental illness is just another medical diagnosis and one that is largely treatable.  The only thing that makes mental illness different from other illnesses is that it presents itself in the brain instead of the body so it’s not as easily visible.  People with different medical conditions live their lives and find love every single day.  Those with a mental illness are no different.  People who have a mental illness are just as worthy and deserving of love as anyone else.

So please don’t judge others, or their relationships, based on the fact that one or both of them have a mental illness.  Don’t let the overwhelming stigma surrounding mental illness turn you into a naysayer that pronounces doom and gloom on two people in love just because they both happen to share a similar medical condition.  Instead, celebrate that, despite the fact that there are millions of people walking this earth, they were able to find that one person who loves them completely for who they are.

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Having A Positive Mindset Will Not Cure Depression

Many people assume that those who are suffering from depression are just caught in the wrong mindset, that we’re being Debbie Downers and Negative Nancys, wandering through life with a Trelawney*-sized penchant for doom and gloom.  They assume a great deal, if not all, of our mental illness could be solved simply by trying a little harder and adopting a more positive mindset.  I can tell you firsthand that is not the case.

I have been told by multiple people over the years that I am the most positive, cheerful, upbeat little depressed person that they have ever met.  I refuse to be a victim.  I am a fighter.  A Survivor.  Even in the roughest of circumstances, I still search for something positive to cling to like a life preserver in rough waters after being thrown overboard during a raging storm.  I am a firm believer that there is always something positive to be found if you look hard enough.  Even on the worst days, I am that one person you can count on to offer an encouraging smile and to point out something good to be grateful for in life.

I do not intentionally surround myself with negativity.  Over the years, I have systematically removed many so-called friends and family from my life who found more pleasure in knocking others down rather than helping each other up.  I’ve chosen instead to surround myself with people who believe in kindness and compassion, those who prefer to cheer openly for the success of others rather than privately snickering over their defeat.

I don’t carry within myself an undue amount of anger, hurt or resentment.  If someone has grievously injured me, I have learned to just remove them from my life as a doctor might amputate a gangrenous limb.  I do not allow their cruelty to continue to fester and grow but rather I accept that they do not deserve a place in my life and I continue onward without them.  I have accepted that not everyone belongs in my life and that some people were merely meant to play the passing role of a teacher of harsh realities.  I refuse to waste undue amounts of energy dwelling on the cruelty of anyone who would not give me a second thought.  I choose to focus the majority of my energy on improving myself and my future rather than dwelling on other people or a past I cannot change.

I have trained myself to consciously focus on happiness and positivity every single day.  Every day I strive to accomplish three goals.

  1. Every day, no matter how rough the day might feel, I look for at least one reason to smile, one thing to be grateful for in my life.
  2. Every day, I try to reach out and do something kind for someone else without expecting anything in return.  This could be as simple as holding open a door or reaching out to someone else to see how they are doing.
  3. Every day, I make sure to tell at least one person in my life that I love and appreciate them.

At my core, I have a very positive mindset.  I have a fundamental belief in the strength and resilience of the human spirit, that we as a species are stronger than we realize and are survivors at heart.  I carry within myself a genuine hope that one day things will get better and I am proactive in working towards that goal.  I encourage not only myself to power through and not give up on a daily basis, but I reach out to others, as well, through my writing.

I also have friends and family that I have opened up to about my illness.  I do my best to be honest with where I am at mentally and emotionally at all times.  I have constructed a support network of people I can reach out to if I need help so I am not facing everything alone.

I have not given up on myself.  I not only see my doctors regularly, but I push myself as much as possible to attend wellness activities such as yoga, tai chi, meditation and art classes.  I take my treatment seriously.  My wellness and emotional toolbox is chock full of useful techniques to use when I am struggling.

I make sure to eat regularly even if I am not feeling particularly hungry so that my body receives the nutrients it needs.  I do not smoke or use drugs and very, very rarely do I drink any alcohol, let alone have more than one drink.  I practice self-care and engage in hobbies such as writing, sketching and painting so I have positive outlets to focus my attention upon so I do not lose myself along the way.  Over the years, I have learned to love myself and to treat myself gently, with the same kindness and compassion I would show others.

I have not surrendered to my mental illness or turned a blind eye to it, pretending it is not there.  I read up on the latest studies on a regular basis.  I belong to multiple online support groups that share not only encouragement but share information, as well.  I want to remain knowledgeable about my illness so I can make educated decisions about my ongoing and future treatment.

My mindset is not an issue.

I am fighting every single day.  I am like the cancer patient who pushes herself to eat even though her chemotherapy has left her feeling nauseous because she knows it is what her body needs or to go for a short jog because she is determined to not let her illness defeat her.  I am like the woman with rheumatoid arthritis so bad that every step wracks her body with pain who still goes out to work in her garden because she doesn’t want to lose herself to her illness.  I am no different than many other people with hundreds of different debilitating diseases, illnesses and ailments who are fighting the good fight every single day not only to survive but to find some way to truly live despite their diagnosis.

Again, my mindset is not the issue.

All the positivity in the world will not negate my illness.  A wellness toolbox full of handy tricks will not fix it.  It is a medical condition that needs medical treatment.  As good as things like having a support system, a positive attitude, eating well, exercise and engaging in healthy hobbies might be for someone’s emotional well-being, they will not cure mental illness any more than they would cure cancer or arthritis.  I have learned to cope with my illness to the best of my ability but I still need ongoing treatment.

The main difference between other more widely accepted ailments and mental illness is that my condition stems not in my body but in my brain. That, and the stigma attached to mental illness that prevents others from viewing it as a legitimate, treatment-worthy condition.  Because it cannot readily be seen by the naked eye, it is often doubted, minimized and trivialized, treated largely as a joke.  Though it may be considered an invisible illness, I am fighting it every single day.

From the time I wake up every day, I am fighting my own mind.  As much as I struggle to stay positive and focused, a very real part of me is trying to convince me that the world is hopeless.  Whenever I attempt to reach out to friends and loved ones, it tells me that I am a burden to them, that I shouldn’t bother, that I should leave them in peace.  It pushes for me to isolate, to hide my pain, to succumb and surrender to it.

There are days I am overwhelmed with emotions.  I feel everything so deeply and there appears to be no way to turn it off.  I have this intense need to cry, to weep not only for myself but for everyone else struggling, for everyone who’s lives have been made harder by my illness and for everyone else who has lost their battles along the way.  On those days, my world is overflowing with so much pain that it is overwhelming.

On other days, I feel nothing at all.  I find myself trapped in a dark void where nothing feels like it matters, least of all me.  There is no joy in that darkness, no light, no hope.  I struggle to even move because I feel swallowed up within its depths.  Everything on those days feels like an insurmountable obstacle.  Even simple tasks like eating make no sense because everything tastes bland, like nothingness.  That voice within my head echos through the darkness, asking what’s the point.

No mater how much the sun is shining, my world always feels dark, cold, hopeless and full of despair.  No matter how many times I tell myself that it isn’t truly the case, it still feels that way.  It is like my mind has constructed its own alternate reality and has taken me hostage within its walls.  I feel helpless like I have no control over my own life, let alone my body or my mind.

Every single day, I have to fight myself to even get out of bed.  It isn’t a case of laziness or just not wanting to get up.  The weight of everything I want to do and need to do rests so heavily on my shoulders that I often find myself immobile, incapable of action.  Every single day I am beating myself up for everything I know I should be doing but cannot manage to bring myself to do.  I desperately want to get up, do things and be productive, but the weight of my illness pins me down.  It then uses my inability to function against me as evidence that I am worthless and a waste of space.

Every single day, my mental illness presents itself in very real and physical ways as well.  My body is always as exhausted as my mind.  I ache all over.  My anxiety frequently has my head spinning and my heart pounding.  When confronted with stress, my chest tightens and my thoughts race.  My stomach is always in knots.  I regularly experience nausea and vomiting and have a recurring bleeding ulcer.  I have absolutely no desire to eat most days or to even do anything at all for that matter.  Every night, I struggle to get to sleep and to stay asleep.  I am plagued by horrible nightmares on a regular basis.  No matter how much rest I might get, I always feel sluggish, like I am running on empty.  It is like my own body has betrayed me.

My world feels hopeless.  I feel helpless.  I feel lost and alone.  I feel broken beyond repair.  There is not a single day that I do not have to remind myself multiple times that this is not reality.  This is my mental illness.  There is not a single day that I am not fighting with myself, pushing myself to do something, anything, even if it is just to pull myself out of bed and eat something.

I am not consumed by negativity, nor am I lazy or weak.  I have not given up on myself or the world.  I have hope for my future and a strong will to fight.  I am doing my best.  I refuse to let my mental illness beat me.

My mindset is not the issue.

My mental illness is.

I struggle every single day not because I am not trying hard enough to have a positive mindset but because I am ill.

 

*For those unacquainted with Sybill Trelawney, she is one of many wondrous creations from J. K. Rowling’s Harry Potter universe, the Divination professor who at one time or another had foreseen the death of every student at Hogwart’s.  Whenever I imagine anyone embracing hopelessness and envisioning a world full of nothing but doom and gloom, I think of Trelawney.

 

To the Mother I Never Knew..

As Mother’s Day came and went this past year, I once again found myself with conflicting feelings.  Part of me wanted desperately to join in with friends who were fondly honoring their moms or mourning the mothers they had lost over the years.  Another part of me, however, felt numb and empty, because I never had that type of cherished bond with my mother.  I honestly never knew her.

No, my mother didn’t die when I was born.  She passed away 8 years ago this Thanksgiving Day.  No, she didn’t give me up for adoption nor did she abandon me.  The truth is that my mother was there throughout the majority of my childhood and sporadically at best throughout my adult years.  I just never really knew her because the woman she truly was was buried deep beneath often untreated, always undertreated, mental illness.

Growing up, my mother was one of my biggest abusers, both mentally and physically.  She was prone to severe mood swings that would shift into bouts of rage at the drop of a dime.  She had bipolar disorder.

We were estranged for the last few years of her life.  I could no longer handle the abuse nor did I want my children subjected to it.  It seemed that her medication was never quite balanced nor were her moods.  It always felt like what little treatment she did receive was not helping, was not working, and she was doing very little to proactively work towards correcting anything.  She felt to me like a ticking time bomb, one I was afraid would go off at any moment and I did not want my children caught in the crossfire.

Over the years as I have struggled with my own mental illnesses, I have come to deeply regret those feelings.  I was diagnosed with depression, anxiety disorder and PTSD, labelled treatment resistant for years.  No medication ever seemed to work.  It wasn’t until the last year or two that I discovered via genetic testing that my resistance was caused in great part to a genetic mutation.  I’ve often wondered since then if my mother suffered from the same mutation.

The truth is that mental illness changes a person, or perhaps more appropriately it snuffs that person out, dimming their light and dulling their soul.  The person that you are is trapped underneath, desperately needing to come out, wanting to shine.  But there is this dark hopelessness that oozes over everything, making it impossible to fully be the person you truly are.

I think about my own children and how my diagnosis has affected them.  They have only seen glimpses of the real me over the years.  The creative me who would spend half the day drawing huge murals with sidewalk chalk on the tennis courts at the park with them on summer days.  The silly me who would make paper pirate hats and eye patches, transforming our dining room chairs into a pirate ship to celebrate Talk Like A Pirate Day with them.  The nurturing and educational me who would catch tadpoles in buckets with them to show them how they turned into frogs.

More than anything, though, they saw my mental illness.  They saw the mom who was too exhausted just from going through the daily motions of life to do anything fun.  They saw the mom who opted for quiet family days indoors watching movies or playing board games because I was physically and mentally unable to do anything more.  They saw the mom who often emerged from the bathroom drying my eyes as I attempted to hide the tears I could never seem to stop from flowing.

They were vaguely aware of the person I truly was but they knew my mental illness well.

I remember when I first started taking the medication I needed for my genetic mutation and I had my first truly happy moment.  It was the first time in my life I ever felt that sludge of mental illness be lifted off of me, albeit for a short period of time.  The medication is not a panacea.  It in no way cures or stops my mental illness.  However, it does give my mind the ability to fight back in a way that it never could before.

That moment of happiness was beyond blissful.  I laughed, cried and hugged my boys, asking them again and again if that was truly what happiness felt like.  I had never experienced anything else like it.  That sludge continues to lift here and there sporadically and I have a genuine hope for the future now, that there might be a day when there’s more periods of happiness than illness.  But for now, more days than not, I still struggle.

I have heard from people that knew my mother at the end of her life, in those last couple years, that she had finally gotten the treatment she needed.  Her medication was finally balanced.  She was happy and more herself than she had ever been before.  She was doing crafts with the neighborhood children and even developed a fondness for Harry Potter.

Part of me envies them because I never knew that woman.  I never had the pleasure of meeting her.  All I ever knew was the sludge and taint of her illness.  On Mother’s Day, I mourned the ghost of a woman I never even met, a woman I would have loved more than anything to know.

Please keep in mind that when you’re dealing with people who are struggling with mental illness that they are not completely themselves.  The person they truly are is in there somewhere, beneath their diagnosis, fighting to get out.  Please don’t ever assume that we’re just not trying hard enough, that we’ve already given up or that we’ve lost who we are along the way.  It is a daily battle, a constant fight, against your own mind.  It is a never-ending struggle to push your way through a thick layer of darkness just to come up for air.

Looking back, I truly regret becoming estranged with my mother.  I had done what I thought was best at the time, trying to shield my children and myself from an illness that was not her fault.  She had no more control over her bipolar disorder than I do over my own mental illness.  I am sure she was trying harder, fighting more, than I ever realized.

To the mother I never knew – I’m sorry I was not there when you needed me.  I’m sorry that I allowed my fear to dictate my actions and choices and that I abandoned you when you needed me most.  I’m sorry I was not more compassionate and understanding of all that you were going through.  Most importantly, I am sorry I never had the pleasure to truly meet you.  Happy belated Mother’s Day.

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An Average Day Living with Depression and Anxiety

From time to time, I come across random memes that try to explain what it is like to live with both anxiety and depression.  Though everyone who has been there always nods in agreement because we understand the struggle behind those few words, unfortunately no meme could ever adequately explain what it is truly like to live with both.  Even simple, average days can feel unbearable and insurmountable.

Upon waking up today, I began jotting down random ways both my depression and anxiety presented itself throughout the day and how they interacted with each other.  This was just an ordinary day.  I did not expect anything monumental to occur.  I just wanted an honest portrayal of an average day living with both depression and anxiety.  Yet by the end of it, I am thoroughly exhausted.  Not because my day was particularly eventful but because the mental illnesses inside my head have left me yet again mentally and emotionally drained.

Anxiety is waking up far too early because the cat has dislodged the bedroom curtain, inviting the sun to shine in my face.  Anxiety is laying there as my mind begins to race, picking up where it left off the night before.  It is knowing there will be no more sleep today because I cannot shut my brain back off.  It is thinking of everything I should have done or still need to do, panicking over all that I might have forgotten and everything I know I won’t get to today.  Anxiety is my mind on an ever-playing loop reminding me of all that I’m doing incorrectly and all the ways my life could go wrong.  It is wanting to scream within my own head a hundred times a day “Oh God! Oh God! Make it stop!” even though I know full well that it will never stop.

Depression is laying there for hours after I wake, unable to move despite anything I might have to do that day.  Being hungry or having to go to the bathroom is irrelevant.  I’m not being lazy.  Though part of me knows I should get up, my depression has rendered me immobile.  I carry within myself a strange sort of apathy for the world again today though I’m not entirely sure where it came from.  Whenever one part of my mind attempts to prompt me into action, another louder part responds back, asking “What’s the point?”  That part of my brain reminds me that everything is hopeless, nothing will ever get better, that everything is a waste of time.  As much as I don’t want to listen, don’t want to believe, that voice is boomingly loud and self-assure.  It convinces me for hours that it is better to stay in bed than to start yet another day of misery.

Together, I have a combination of steady stress, apathy, hopelessness and despair.  I have one part of myself revving up, pushing for action, warning me of everything that could go wrong if I do not do something and another part refusing to budge at all because it cannot see the point.  Together, it is the combination of the panic of Chicken Little’s sky falling and that deer, frozen in the headlights the moment before it is plowed down by a tractor trailer.  It is a constant go go go and stay stay stay, a battle of opposites where I cannot help but feel the game is rigged and no matter what I do, I’m going to lose.  And all of that occurs before I even pull myself out of bed.

My depression and anxiety continue on throughout the day, sometimes sporadic, other times constant, wreaking even greater havoc whenever their paths cross.

Depression is barely eating for a couple days because I have no appetite or because I simply cannot see the point of wasting food on myself that someone else might enjoy more.  Anxiety is realizing I haven’t eaten much in days and worrying that I might be making myself sick and not wanting to saddle anyone else with taking care of me.  Together, I find myself going through bouts of not eating and then binging to make up for it.  Grazing on whatever is nearby, not because I want to eat or even that it is good for me or tastes good but because I know that I have to put something in my body.  I eat some soup straight out of the can without heating it up, because it is quick, close and convenient, telling myself that I’m making less dishes to wash, but in reality, I just don’t care.  Nothing tastes like it should anyway.  I’m just eating out of obligation so that nagging voice in my head will shut up.

Depression is wearing the same sweater for three days, making excuses that it is my favorite or most comfortable.  In reality, I have no plans to go anywhere.  Laundry is already piling up and wearing clothes longer means I can put off  washing clothes for yet another day.  My depression insists this is reasonable.  Anxiety is panicking and rushing to hand wash a spot out in the sink when I accidentally spill something on it.  One part of me is willing to wear that sweater until it is threadbare and worn, while the other cannot stand the thought of it being ruined or stained.  Though the two sides are so contrary that they make no sense together, somehow they both exist in my head.

Depression is having my laundry and dishes build up for days because I just don’t have the will or the energy to do them.  Anxiety is rushing to spot clean the apartment because someone is coming over even though I know there’s no way I could get it all done in time.  When combined, I find myself rushing to clean until the last possible moment, trying to tuck away, hide or set aside messes I don’t have time to deal with, breathlessly asking them to “please excuse the mess” as they come through the door.  That small amount of anxiety-fueled exertion to clean is enough to wear me out for days.

Depression is putting off showering for days because it’s not like I have done anything or that I am going anywhere to warrant it.  Anxiety is feeling like I have to do things such as pulling my hair back in a braid so that it doesn’t get tangled or unruly.  Between the two, I look more put together than I am, provided nobody comes too close.  I apply extra deodorant “just in case” and take an extra long shower when I finally do get in there, my anxiety trying to squeeze days of self-care into one tank-worth of hot water.

Depression is feeling completely alone sometimes, even if someone is right there with me.  It is simultaneously wanting to never let go of them and wishing they would just go away because I believe they would be better off without me.  Anxiety is wanting to talk to them, to tell them how bad things truly are, but being terrified it will scare them away, terrified I’ll somehow mess everything up.  Between the two, I find myself feeling lost and alone, afraid to speak up.  I’m afraid to let them in and afraid to let them go.  Even when they’re right next to me, I’m isolated and afraid.

Depression is sitting there for hours in a fog, unable to retain much of anything my mind has pulled in.  It is re-reading the same page or watching the same scene multiple times, before giving up because it all doesn’t really matter anyway.  There is a lack of enjoyment in everything.  Life feels stale and empty.  I go through the motions of living though it feels like a pale reflection of life.  Anxiety never shuts up, like a perpetual snooze alarm set to go off whenever my mind attempts to focus on anything else.  It is a constant distraction, constant reminder of everything I haven’t done, should have done, should be doing right now and should be doing later.  Between the two, I have constant distractions and a complete lack of interest.  It often feels virtually impossible to keep myself on track because my mind is all over the place and has no desire to cooperate.

Depression is putting off making phone calls for hours because I dread having to deal with other people on my low days.  When my depression is bad, any interaction is a struggle.  Anxiety is dwelling on those phone calls the entire time leading up to them and for hours afterwards.  It is having trouble verbalizing what I mean, reiterating some things repeatedly and forgetting others completely.  Between the two, I have scraps of paper filled with information that I keep with me whenever I make important calls because I’m afraid I might forget something important and I dread the possibility of having to call back again.

Depression regularly leaves me feeling physically worn out, tired and sluggish.  No matter how much I try to rest, I still feel drained.  Anxiety has me jumpy and jittery, my leg bouncing a mile a minute.  My body always feels revved up and over-wound, my mind won’t stop racing.  Between the two, I can never seem to get comfortable, never feel fully rested.  I cannot sleep well because my body never powers completely down.  Yet I cannot seem to harness that energy, either.  It is a nervous energy that serves no practical purpose beyond blocking me from even momentary peace.

Throughout the day, I am in a constant battle within my own mind.  It screams at me with the fierceness of a drill sergeant, nags at me with the persistence of an old world grandmother who believes they always know best.  Contradicting everything they throw at me and forcing myself into some semblance of functionality sometimes takes every ounce of willpower I have inside of myself.  I am fighting to do all I can, the best that I can, battling against my own mind to keep going though my depression urges me to throw in the towel and give up.  I know I will never accomplish everything my anxiety thrusts my way, but I have to keep encouraging myself that I have done something and that is good enough.  I cannot allow my depression to weigh me down or my anxiety to beat me up.

It has been an average, uneventful day.  I didn’t even manage to pull myself up out of bed until after ten in the morning.  It is barely ten at night and I feel exhausted.  It has been twelve hours, barely half a day.  Very little has been accomplished beyond a load of dishes, a handful of phone calls to schedule appointments, some basic self-care and one small glimpse of my mental illnesses, written down for all to see.  Yet I consider it a victory to have gotten through yet another day, managing to accomplish what I did.  I feel exhausted already and ready for bed.  It is not that the day was particularly eventful or busy.  It is the constant battle within my head and my body that has worn me out.

Perhaps the most frustrating thing about living with depression and anxiety is that, even after sharing this, there will be some people who still don’t get it, who will insist it is just mind over matter.  They will suggest I just need to be more positive, just need to stay focused and try harder, to have more faith in God or to just stop making excuses.  Some people cannot seem to grasp that this is not anything I am intentionally doing to myself.  I would not wish this on my worst enemy if I had one.  I cannot wish away my diagnosis with happy thoughts, sheer willpower or positive mantras. The fact is that this is a medical condition that I struggle with every single day.   Some days are harder than others but even the simple days like today are not easy when I’m waging a constant war within my own mind.