When the Holidays Are Marred by Loss and Complex Grief

Written For The Mighty on 11/19/2020.

Holidays are usually seen as a happy time, when friends and family get together to celebrate. They are a time filled with the warm glow of decorations, delicious foods to fill our stomachs and wonderful memories in the making with the people we love. 

But sometimes everything is not that simple. When you lose someone you hold dear during the holidays, it creates a dark cloud that looms over the entire celebration, making it harder to enjoy it as you otherwise would.

Loss is hard any time of the year. But a loss during the holidays can be especially painful because everyone else expects you to be happy during the holidays. It is hard to celebrate anything when you don’t feel festive inside. It can feel near-impossible to smile when all you want to do is cry. It is hard to be around others who are happy and festive when you feel anything but, leaving you to wonder if it is just better to stay home and not ruin anyone else’s time.

Holidays are often rooted in nostalgia. Current celebrations bring back memories of other times, better times, when your loved ones were still there to celebrate with you. The sights, sounds, tastes and scents alone can make their absence even more glaring and jarring. What once were joyful recollections you shared together of other years become gut punches that leave you fighting back tears.

It can be doubly hard when you carry conflicting feelings about the person you lost. People often say that you should never speak ill of the dead, disregarding the fact that rarely in life is anything solely black or white, good or bad. The vast majority of relationships in our life exist somewhere within the realm of grays, where they are not one or the other but rather a complex combination of both. When your grief is complex, it makes mourning that much more difficult. 

My mother passed away 10 years ago Thanksgiving day. 

All my childhood holiday memories revolve primarily around my mother. She was the cook, the baker, the decorator, the present-wrapper. The holidays were largely constructed and orchestrated by her two hands. Almost every holiday tradition I’ve carried with me throughout my life originates with her. There is not a single major holiday I celebrate that does not have her fingerprints all over it.

She was my mother. She taught me to cook and bake, to sew, knit, embroider, darn and craft. She implanted in me my stubborn will to keep fighting and my love for the holidays as a whole. She is a big part of the person I am today.

She was also one of my primary abusers throughout my childhood, physically, verbally and mentally. She is one of the reasons I struggle with post-traumatic stress disorder (PTSD) and depression. She is proof that very few things exist simply as black or white. 

She is my mother. I love her as every little girl loves her mother. And at the same time I hate her. I love her for all that she has taught and given me, and I hate her for all that she’s put me through. I miss her with every fiber of my being and at the same time I could never forgive her for the darkness she put over the holidays for me. 

To better help you understand our relationship, I feel it is important to divulge a little background. Growing up, my mother was very abusive. She was struggling with often untreated, always undertreated bipolar disorder with frequent bouts of rage and I was her primary target. Our entire house was a war zone where the only way to be heard was to yell louder than the next person, and the only way to shut someone up was to lash out with the meanest, cruelest thing you could think of. After over 20 years of combat, my father walked out on our family shortly before I turned 16. My mother retaliated by driving to his work and shooting him twice. She spent the next few years bouncing between jail and mental institutions until it was ultimately pleaded out. But the damage had already been done and my life had been changed forever.

Her actions that day made it very clear to me exactly what she was capable of doing during her bouts of rage. Yet she still refused to seek help, frequently breaking down into tears or exploding with anger with no prior warning at the drop of a dime. For years, I watched in fear for my own life and the lives of my children until I finally admitted to myself that I did not feel safe. My mother and I had been estranged for a couple years when she passed away.

My mother’s death was officially listed as an accidental overdose of prescription drugs. My mother suffered from a lot of maladies and had medicine for all of them. She took dozens of different medications over the course of the day. Presumably, she had taken her medication for the day, forgotten, taken them again, forgotten and repeated this pattern multiple times before succumbing to an overdose.

I do not believe it was an accident. My mother had always been meticulous with her medication, separating it into containers designating not only days of the week, but times of the day, as well, so that she never missed a dose. 

I believe she killed herself that Thanksgiving morning 10 years ago and that, in the process, she robbed my holidays from me. 

Every year now when the holidays roll around, I struggle to enjoy them. My entire holiday season is marred by her loss.

I love her. Everything I do during the holidays comes directly from her. Yet she also hurt me worse than any other person ever has and made me feel largely unsafe in this world. She wasn’t all bad. I miss her. I feel guilty for not being there when she died. There’s an emptiness in my heart that nothing seems to fill, yet I also carry so much anger towards her. From Thanksgiving through New Years, my emotions are continuously all over the place, repeatedly being pulled one way then the other. I want to be happy, be festive, to enjoy the holidays with my family, but it’s a constant struggle.

It’s become a matter of taking everything one day at a time, sometimes one minute at a time. Allowing myself to feel everything that I am feeling because all my feelings are valid. And accepting that sometimes I’m just not in the right mindset and I need to pull back, regroup and recharge. I have learned to be gentle with myself. I do what I can when I can, and forgive myself for the things I am just not able to do during the holidays. I do my best to live in the moment and embrace the joy, but I don’t pretend that the darkness isn’t still lurking in the shadows, as well. It isn’t easy, but it is better to acknowledge and face all of my feelings, good and bad, than to shove them down deep inside and pretend they aren’t there. I celebrate when I can and step away when I cannot.

After all, none of us has to be festive all of the time — especially when we are not feeling it.

Republished on MSN on 11/20/2020.

Republished on Zenith News on 11/19/2020.

Republished on The Mental Guide on 11/2020.

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.

———-

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.

———-

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.

———-

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.

Sorry Not Sorry: My Mental Well-Being is a Priority

It has been a rough couple months.  Horribly frigid and snowy weather, as well as a revolving door of various sicknesses in my home, have combined with my mental illness to create a perfect storm.  I endured what felt like a never-ending rotation of maladies, downward spirals and utter numbness. There were many days I felt like I could barely function at all.  I usually love the holidays but this past year, the festivities felt hectic, rushed, hollow and empty.  As much as I beat myself up for not being more present, more in the mood, more cheerful and jovial in general, I just could not snap out of the funk I was in.  And the guilt of it all was eating me alive.

After two and a half months of struggling to get from day to day, unable to even inspire myself to write, I am finally emerging like the groundhog in early February to start anew.

Periodically, this happens to me.  When life gets hard, I pull in on myself, much like an armadillo rolling in on itself for protection or a cell phone going into power saver mode so it doesn’t shut down completely.  This cycle has repeated itself from time to time throughout my life.  Whenever everything would get hard, I would pull inward, isolating and conserving my energy in order to survive.  On the other end of this pattern would always inevitably come unfathomable guilt and pressure to make my recent absence up to everyone.

I have struggled my entire life with depression, always feeling as if I was broken, as if I was always letting everyone down by not always being able to do, to be, everything others needed and expected of me.  I consistently felt like a failure.  Like I didn’t even deserve to be on any list of priorities.  After every struggle I endured, I always felt like I was playing catch up, that I owed it to everyone else to use whatever energy I could muster to make it up to everyone else for letting them down yet again.

Christmastime this past year was especially hard.  I usually do a marathon cookie bake as part of my holiday traditions.  Three days of baking. Fifteen types of cookies, plus candies and fudge. Everyone in the house getting sick delayed the grocery shopping and my baking was put off until the last minute.  What is usually three comfortable yet full days of baking was ultimately crammed into a panicked day and a half.  Pushing myself that hard utterly burnt me out.  I existed in a heavy fog of numbness for the remainder of the year.

Speaking afterwards to my doctor, she inquired, “If you only had half the time, why didn’t you just bake half the cookies?”

I started to explain that people were expecting the cookies.  My kids love all the cookies every year and give away boxes to their friends. My fiance needed cookies to bring into work.  We had friends and family that we gave boxes to every year.

She countered by asking why I exactly felt so obligated.  Was anyone was paying for the cookies in any way or if I was just doing it out of the kindness of my heart?

I began defending myself again, insisting that I didn’t want to let anyone else down.

In a perfect check-mate moment, she asked, “What about letting yourself down? Is doing for others out of the kindness of your own heart really worth burning yourself out and running yourself down?  At what point do you fit into the equation? If you only had half the time, why couldn’t you just bake half the cookies?  You’re still being kind to others that way.  But you’re also being kind to yourself.”

Our conversation bounced around in my head for hours. Days. Weeks.  Again and again, I pondered where I fit into the equation of my life and why I didn’t seem to matter at all in most cases.

I ultimately determined that I needed to restructure my priorities in order to find a place for myself in the equation.  I had to be willing to reserve what little energy I do have during rough periods on what should be most important in my life – my family and myself – without becoming guilt-ridden afterwards.  The addition of “myself” towards the top of my list of priorities is honestly fairly new and admittedly still somewhat uncomfortable.  For much of my life, I was on the bottom of the list, if I appeared at all.

That was a feeling that I desperately needed to address.

Whenever I struggle to apply my own self-love or self-care, I stop to consider what I might tell someone else in my situation.  I would never discourage anyone else from pulling back in order to take care of themselves.  I would never accuse anyone else of being a bad person for wanting to matter, too, or for feeling like they sometimes had to prioritize themselves in order to make it through to tomorrow.

Let’s be honest here.

Wanting to matter, too, is not being self-centered.  Wanting to do self-care when you need it does not mean you don’t care about others, as well.  Nobody is saying you can only choose one or the other, help others or help yourself.  The two are not mutually exclusive.

Not writing for a couple months honestly ate at me very badly.  I felt terribly guilty, like I was letting my readers down by not writing more content, not sharing my journey more frequently.  But after that pivotal talk with my doctor, I am no longer guilt-ridden.

The truth is that I had a few months where I was struggling badly.

I had a few months that I desperately needed to devote any energy I could muster into self-care and self-preservation.

That doesn’t mean that everyone else doesn’t matter, as well.  When I have enough time, enough energy, enough willpower to reach out and advocate for others, I still will.  I cherish every time someone has reached out to me letting me know my words have impacted their life. This journey is too important to give up.

I will still help others whenever I can.

But I must help myself, too.

I cannot carry the world on my shoulders, struggling to keep others afloat if it means I go under and drown.

I will always prioritize my family because they are the cornerstone of my world, but from now on, I will be prioritizing myself, as well.

I cannot help others if I cannot help myself.

I will take care of myself whenever I need, however I need.  If that means I do not write for a period of time, so be it.  If that means I only bake half the amount of cookies because I only have the time and energy to do that much, then that is all I will do.

Over the last decade, I have grown my hair out repeatedly, only to cut and donate it when it gets long enough to do so.  My hair was down to my mid-back, with perhaps nine months to a year to go until my next donation.  However, the meningioma tumors on my brain have been causing pressure migraine headaches in increasing frequency of late.  The added weight of all my hair does not help.  As much as it would be nice to donate yet another ponytail to help others, realistically it would not be fair to myself to endure almost a year more of harsher migraines in order to make another donation.  I can still help others, just not at a detriment to myself.  In an act of self-care, I cut my hair shoulder-length.  The intensity of the majority of my headaches has lessened noticeably since then.

I have entered a new period of my life, one where I learn to value myself as much as I have valued others in the past.  I will learn to set my goals and expectations based on what I feel I can handle instead of what others have decided to expect.

I will set new limitations and boundaries so that assisting others no longer harms me.

I will no longer put myself out there beyond my own capabilities in any way that will ultimately hurt myself in the process.

I will prioritize my mental health guilt-free.

I won’t ever again apologize for having to take care of myself.

Sorry not sorry.

My mental well-being matters.

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.

Having a Family Isn’t Exhausting – My Depression Is

My youngest just started college.  He took a train upstate for a weekend visit after his last class this past Friday.  I spent the two days prior trying to build up my energy preserves before his arrival.  We didn’t have a particularly eventful weekend, yet I was worn out by the time he left.  It isn’t that he is exhausting.  My depression is.

Even when my children were younger, I found myself building up reserves of whatever energy I could muster, saving whatever I could for them.  It seemed like I was eternally exhausted, forever worn out and hanging by a thread, trying to scrounge up whatever motivation I could manage in a feeble attempt to be the mother I felt they deserved.

We took frequent long walks to parks throughout the city, many day trips to area museums and festivals.  Yet I always felt like I fell short, like I never was able to do even a portion of what I wanted to do with them.  More than anything else, we had quiet family movie nights or game nights at home, days spent home playing in the backyard or drawing with chalk on the sidewalk out in front of the house because I was too exhausted to do anything else.

The fact is that my depression is both physically and mentally exhausting.  I am engaged in a never-ending battle with my own brain.  I begin most days already feeling like I am running on empty.  Even my sleep is restless so I never fully recharge.

On the average weekday morning these days, I am up when my fiance’s alarm goes off.  I scurry around for an hour or so, helping him get ready for work.  It gives us a little extra time to spend together on days when he’ll be gone most of the day.  When he leaves, I collapse on the couch, where I spend a good chunk of my day.  It isn’t that helping him get ready is exhausting.  My depression is.

An hour before he is due home, I muster up what little energy I have left to somewhat straighten the house and start dinner.  There’s always easily a dozen things I wish I had done throughout any given day that will get put off to another day.  I truly wish I had the energy to do more.  Most days, I’m amazed I managed to do as much as I have.

The truth is that I spend most of my time alone in a fog of depression.  I often use up what little energy I do have on my family so by the time they leave I am tired, exhausted, worn out.  Some days, I am caught in a funk, immobile and numb.  On other days, I wait until I have the house to myself to break down and cry, sobbing throughout the day.  Either way, I find myself crumbling and falling apart moments after my family is out the door.

Shortly before they’re due home, I dry my eyes and paint on a smile.  I straighten my hair and tidy the house.  I try my best to hold everything together for them even though I usually feel like I am falling apart inside.  By the time they come through the door, I am already wishing I could climb into bed.  It is exhausting.

I often do my best to keep the true extent of my struggles to myself because I don’t want my family to worry about me or to suffer over my pain.  I don’t want them to question whether they are doing enough for me or whether they have been supportive enough.  They know about my struggles with depression yet I still try to shield them to the best of my ability.  My mental illness is not their fault.  I always feel like I must protect them from it, shield them from it, save them from the worst of it.

I conserve my energy for my family in part because I want to be strong for them.  It is bad enough that I feel weak and helpless – I don’t want them to see me that way, as well.  My family brings out the best in me so I want to give them the best of me in return.  A large part of me is also honestly terrified of letting my family down, of being too broken, too much of a mess to be the person they need me to be, the person they deserve to have in their lives.

Please know that they have never said or done anything to make me feel this way.  I know that these feelings, too, are products of my depression.  I prioritize others over myself because my depression makes me devalue myself.  I internalize everything, blaming and beating myself up far worse than anyone else ever could.  My depression makes me feel like a failure, tells me that no matter how much I do, it will never be good enough, never be enough in any way.

Unfortunately, though, recognizing that it is my depression is not enough to stop these feelings or the behaviors that result from them.  Depression is an illness.  Calling a duck a duck will not make it disappear.  A diabetic labeling their illness will not magically balance their sugar levels any more than someone with a mental illness acknowledging their symptoms will instantly change how they feel inside.  It is good to acknowledge the illness so you understand why you feel the way you do, but comprehending an illness will not make it go away.

Perhaps, in time, I will acquire more self-care and coping skills so that I do not always feel like I am running on empty.  Perhaps, as well, I will heal more and become somewhat more functional again.  But in the meantime, I only have just so much energy to give and I choose to give the majority of it to those who reside in my heart.

I do not resent my family for soaking up the majority of my energy each day.  It is my own choice to do this.  I do this not because I feel that I have to but rather because I want to do so.  My family means the world to me.  I would do anything for them – even give them the last little bits of myself that I have left for the day.

Because on a lot of days, that is exactly what it is.  Those little stores of energy I have managed to reserve for them are the only true sparks of myself I am able to muster.  When they are used up, there is nothing left of myself for myself.  All that remains is my depression.

I know many people will say that I must take care of myself as well.  I’ve been reminded often that “you can’t fill from an empty cup”, implying that I cannot truly be there for anyone else until I have tended to myself first.  But, for me, taking care of my family *IS* taking care of myself.  It is an all too common sacrifice for those of us living with depression.  We give the best of ourselves to our children, our partners, our family and friends because in our hearts we believe that they bring out the best in us so they deserve nothing less than our best in return.

Depression is exhausting.  Most days, I have very little of myself to give the world.  I give all I can to my family, even if it leaves little to nothing for myself.  I do this because I am my best self when I am with my family.  I am more myself when I am with them than I ever am when I am alone.  If I only have a little of myself to go around, I want to share it with those who love and accept me, depression and all.

Republished on The Mighty on 11/2/18.

Riding Out the Storm

Today is not going to be a good day.

It’s not even nine o’clock in the morning yet, but I already know this for a fact.

There are some people that will insist it is too soon to know anything for sure, that I should pick myself up, brush myself off and face the day with a positive attitude and a brave face.  There are others who will insist it is all in my head, telling me that I will be fine once I get up, get out there and start moving.

There are some who will insist I am being melodramatic, making mountains out of mole hills.  If you have never experienced these storms firsthand, never fought to survive them, you have no idea how bad they can get.

But I know these days all too well.

I’ve struggled with depression my entire life.

I’ve wrestled with this beast many times over, fought this monster again and again.

And I know today will be yet another epic battle.

Today, I will be lucky if I can even pull myself out of bed.  The world feels completely overwhelming, my life utterly overbearing.  Everything seems hopeless and futile.  I feel like I am suffocating under the weight of all the problems and issues I have been attempting to juggle and resolve.  I am mentally and emotionally exhausted beyond words.  The lies depression tells have already begun gusting and blowing around me, their sheer force threatening to knock me down.

I am wrapped in a blanket.  I will be lucky if I can pull myself up at all today.

I am caught in a rising tide of emotions, being pulled back and forth between feeling way too much and being completely numb to it all.  The tears come in waves, the struggles crashing into me, threatening to knock me overboard.

As each wave recedes, I sit here catatonic, drenched in my own tears, unable to even fully process everything I am feeling anymore.

The pain and the numbness each wash over me in turns.  Every time I think I could not possibly feel anything more, I am flooded with more anguish and strife.  Each time I think the agony will never end, I find myself trapped in that moment of stillness again, that nothingness, staring into that void, feeling empty and numb.

I rock back and forth, thrown around in that sea of depression, each crashing wave threatening to pull me down into its depths.

I am trapped in that storm front, between the hot and the cold, feeling too much and feeling nothing at all.

You cannot stop those storms when they hit, but you can feel them in the air when they’re about to arrive.  You know they are coming so the best you can do is prepare.

I cancelled my afternoon appointment.  Otherwise, I know I would spend the morning fighting with myself to get up, get moving, and ultimately tearing myself apart for being unable to do so.  When I dragged myself to the bathroom, I brought back granola bars and my water bottle on the way back through.  I grabbed an extra blanket, extra tissues and the television remote.  There is little time to prepare but I do my best.

I have curled up on the couch, wrapped up tightly, nourishment on hand, ready to ride out this storm.

There’s an old saying that “into every life a little rain must fall” but this isn’t just a little rain.  It is a hurricane.  A tsunami.  A nor’easter.

I would evacuate if I could but there is really nowhere to go.  Like Eeyore, these storm clouds follow me everywhere.  The storm will come.

There will be flooding.

But I won’t let myself drown.

I’ve learned long ago not to push myself during these storms, not to foolishly attempt to wander out when they get bad.  I don’t beat myself up for what I cannot do or where I am incapable of going.  I cannot control the storms raging inside me any more than I can mother nature outside.  They come from time to time because they are part of my depression.

It is always harder to go out in the storm so I try to avoid it whenever I can.

I have learned to batten down the hatches, board up the windows and take care of myself the best that I can.  I have learned to take care of myself to the best of my ability, making sure I have what I need on hand.  I have learned, as well, to not beat myself up for not feeling capable of navigating through these storms.  It is better that I stay home, stay safe and warm, then to attempt to venture out and drown in the sea of my own depression.  Especially when the skies appear clear to everyone else so nobody else even realizes I’m drowning.

No storm lasts forever.

I will ride this one out and I will be okay.

Because I am a survivor.

I have survived other storms and I will survive this one, as well.

I refuse to drown in my own depression.  I will do whatever I must to stay afloat.

The Depression Chart – Helping Others Understand Depression

*Ever since I created my Anxiety Chart, I have been asked by readers to create a similar chart for depression.  After much thought and consideration, this is the chart and accompanying graph that I designed.

Many people do not understand depression, assuming it is just random bouts of sadness and crying.  Unless someone has suffered through their own struggle with depression, it is near-impossible for them to truly understand how debilitating it can be to live with that diagnosis.

One of the hardest parts of explaining depression is that it is neither rational nor is it predictable.  It is hard to provide relatable examples because the feelings connected with depression would feel wildly irrational to anyone not experiencing them at that moment.  It is also impossible to predict or predetermine depression because it often comes unexpectedly in waves.

Therefore, instead of providing a chart with relatable examples, the chart I devised shows the increasing intensity of this mental illness.  My hope is that the statements provided at each level, combined with the descriptions included, will help those who have never struggled with depression understand how our frame of mind is magnified as our condition worsens.

It is also important to note that depression is not all sadness and hopelessness.  Instead of providing a chart listing levels 1-9, I have split this chart in half.  There is a 1-4N to designate worsening stages of numbness and a 1-4D to describe stages of downward spiral.  This chart is extremely simplified, yet illustrates how, as depression worsens, the intensity of the condition increases.  However, unlike conditions like anxiety that worsen in one direction, depression can and does frequently occur in both the realms of numbness and hopelessness to varying extents.

It is also important to note that depression is not linear.  It comes in waves and spikes.  It is not uncommon to struggle with days of increasing numbness, only to wake up the following day in the midst of a downward spiral.  Depression randomly alternates between the two, with no rhyme or reason to the length or intensity on any given day.  Some days you feel nothing at all, other days you feel everything too strongly.  There’s no way to predict when you will be pulled in either direction or how long either will last.

There will be days when someone might even feel fine, or even just more functional.  On other days, you might be unable to pull yourself out of bed or might seem to cry over everything.  There are days that feel like a struggle and others that feel completely impossible, days where you find yourself crying a little bit more and days you just want to give up.

When describing increased emotional pain, the best example I can think of is to compare it to the pain of loss.  Milder stages of depression might be akin to losing something that matters to you, perhaps something of sentimental value.  As depression increases, imagine the pain of losing a beloved pet, your parents, your spouse or your child.  Imagine the ache and the pain, the feeling in that moment of things never being okay again, of wanting to give up, to crumble under the weight of that pain.

Except the person you are mourning is yourself.  Your happiness and who you used to be.  And the loss comes again and again in waves, sometimes mild, other times so severe that the tears and the pain feel like they will never stop.

At the same time, you loathe and disgust yourself.  You feel worthless, a waste of space.  Your own mind lies to you, convincing you that the world would be better off without you in it.  That is where rationality parts ways.  Everyone can understand loss, pain and grieving.  But it is hard to wrap your head around losing yourself, let alone hating yourself, unless you have spiraled down to those depths yourself.

Yet those feelings are there, along with a tremendous amount of guilt.  You feel guilty that you are such a mess.  You feel guilty for subjecting everyone else to your mess, as well.  Often, you are also ashamed of your illness because you feel you should be stronger, more capable, better than you are.  That shame often leads you to lie or minimize the intensity of your suffering for fear of being judged.  Depression makes you feel like a failure just for being sick.

When someone is struggling with depression, their very perceptions become distorted.  It is common for everything to feel much worse than it actually is.  Think back to when you were a little child.  Things on the counter felt up way too high, the door knob out of reach.  Even simple things like tying your shoes were a struggle and felt like a monumental task that took maximum effort and concentration.  That is how everyday tasks feel when you have depression.  Everything feels harder.  Every problem feels bigger.  You feel small and helpless.

Think back, too, to when you were a young child and were upset with your parents, when you felt completely misunderstood and all alone in the world.  Think back on the time when your four or five year old self was convinced you should run away, that nobody would care if you were gone. Think back to any other point in your life, as well, when you felt completely alone, when you had no help, nobody there.  With depression, those feelings are ever-present.  Your mind tells you that nobody understands, that you are alone in the world.  Depression isolates you by telling lies that you do not matter.

Think back to the last time you were sick, laid up in bed with a bad flu or stomach bug.  Remember how physically and mentally exhausting it felt to even move or pull yourself out of bed?  How easily you found yourself worn out, just wanting to lay back down and sleep?  How you put off going to the bathroom for hours because you didn’t even want to move?  How you ate frozen waffles or canned soup for three days because you just did not have the energy or the desire to cook a real meal?  That is what depression is like, too.

The numbness, however, is hard to explain to anyone who has not experienced it firsthand.  If you’ve ever had someone or something upset you so much that you no longer cared, magnify that lack of concern tenfold.  It is similar to that catatonic shock following an accident or trauma.  You feel nothing, lost, blank, numb.  Eventually, you mentally shut down.  You are immobile, held hostage, trapped in your own mind.  You have no interest or motivation to do anything.  You see no point in even trying.

I wish there were more relatable examples I could give but it is impossible to rationalize the irrational.  There are some examples that are somewhat similar in one way or another, but even those don’t quite equate.  The best I can do is to illustrate the directions depression can go and to quantify how bad it can get.

When trying to explain depression, the best someone who is struggling can do is to explain how close we are at the given moment to either shutting down or wanting to give up.  The worst part is that the status can change in a moment’s notice on any given day.  There is no way to predict when it will veer off in either direction, let alone the severity of the bout.  You cannot even predict what will cause your condition to worsen, or whether it will even be something large or small.  Something as tragic as a great loss is just as likely to cause a period of numbness as a simple broken plate is to cause a severe downward spiral.  There are times we are honestly not even sure why we are feeling the way we do, only that the depression is there.  There is no rhyme, reason or rationality to any of it.

It is not something that a person can control in any way, either, let alone simply snap out of on their own accord.  Depression is a mental illness.  It is a medically-diagnosed condition that severely affects the ability to cope with life, negatively impacting and impairing both thoughts and behaviors.  Having a mental illness is no different than having any other type of illness.  Much like a diabetic has a pancreas that is malfunctioning, when a person has a mental illness, their brain is not working correctly.  The only difference is the organ affected.  Both conditions need medical treatment.

I understand how difficult it must be for someone who has never suffered from depression themselves to understand. Depression seems irrational because it is.  It doesn’t make sense, even to those of us struggling with it every day.  We find ourselves on a roller coaster ride that is speeding out of control, flying up and down every which way, with no way to stop or slow down.  Nobody asks for a mental illness.  Depression is not something anyone has done to themselves or is causing because they are not trying hard enough.  We don’t understand how we even ended up on this ride, let alone how to get off.  How can we adequately explain something we don’t even understand ourselves?

The confusion surrounding depression is also in part due to the stigma attached to mental illness in general.  For years, anyone with a mental illness was labeled as lazy, crazy, dangerous or a joke.  Either way, they were not taken seriously.  Mental illness was a dirty word that wasn’t discussed openly.  People fear or mock what they don’t understand.  The lack of education about medical conditions like depression led to wide-spread ignorance and misinformation.  Unfortunately, once that cat is out of the bag, the damage is done and it will take much longer to properly educate people about mental illness than it took to originally spread the falsehoods and misconceptions.

I understand fully that depression makes no sense to someone who has never experienced it themselves.  It honestly makes no sense to us, either.  But please know that depression is much more than just merely feeling sad from time to time.  With depression, you sometimes feel everything so strongly that it is completely overwhelming, the emotions feel agonizingly painful and never-ending, and the world feels utterly hopeless.  Other times, someone with depression is completely numb, feeling absolutely nothing at all.  Either way, everything feels much harder, more intense.  Depression is exhausting, both physically and mentally.  Perhaps worst of all, you feel helpless to do anything, like you have no control over your own mind.  And depression is not linear.  It goes up and down, every which way, changing direction and intensity on the drop of a dime.

I wish I could provide a chart that was more relatable for those who have never experienced depression, but, as I have stated before, there really is no way to rationalize the irrational.  The best I can do is to lay out what depression is like in a very simplified form and hope for your empathy, compassion, understanding and patience.

Republished on The Mighty on 2/18/19.

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Republished on Core Wellness on 2/18/19.

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Republished on MSN on 2/24/19.

Please Give Mental Illness The Same Respect You Would Give Other Illnesses

Not everyone understands what it is like living with a mental illness. I get that. Most people, at their core, mean well and are trying to help in one way or another.  Whether they are attempting to be supportive or trying to snap someone back into their perceived “reality”, they just don’t know what to say.  I understand that completely, too. But using tired old cliches about life that don’t apply to living with a serious illness does not help at all.  Nor does it help to offer outdated advice that has been proven to be both ignorant and ineffective.  They do much more harm than good. It not only minimizes our condition and our struggles, but it also tells us that you neither understand what we are going through nor do you take our illness, or us, seriously.

Please do not tell us that “everyone has problems sometimes“, “into everyone’s life a little rain must fall“, or that “nobody said life was fair“.  Likewise, please don’t tell us “it is what it is” or “everyone gets depressed sometimes“, as if our diagnosis is an everyday, trivial, meaningless bit of happenstance that is unimportant and should be paid no mind.  A mental illness is not an average, run of the mill problem, a typical bump in the road of life that everyone faces at some point and is easily cast aside or overcome. It is a medical diagnosis, a medical condition that drastically affects every aspect of our lives.  You wouldn’t tell someone with cancer that everyone has problems sometimes, laughing it off like it was nothing. You would show an appropriate level of concern over their health and well-being. You would encourage them to see a doctor and take care of themselves. You would be supportive. You wouldn’t dream of minimizing their condition because, left untreated, it could have deadly consequences. So could my mental illness and it deserves to be treated in the same regard.

Asking us if we’ve “just tried being happy“, telling us we “need to just learn to focus on the positives” or otherwise suggesting we’re not trying hard enough misplaces the blame on us for our diagnosis. The patient is never to blame when their body goes haywire and runs amuck. We understand that sometimes our bodies malfunction, become unbalanced, and horrible things like tumors occur.  You can’t will away cancer with a positive outlook and trying harder won’t make tumors disappear. The same goes for mental illnesses.  We don’t tell someone with cancer that it is “all in their head“, “mind over matter“, and expect them to become healthy again by sheer willpower alone. We encourage them to see a doctor immediately, get everything taken care of and treated so their body can work properly and be healthy again. Untreated cancer can eat a person alive from the inside out, deteriorating their health and destroying the quality of their life in every way. So can mental illness. The only difference is cancer mainly attacks and destroys the physical body while mental illnesses primarily attack the mind.

Please don’t judge us on our appearance, telling us that we “don’t look sick” or that we “just need to smile more” as if our diagnosis is even remotely dependent on our outward appearance.  Also, please don’t tell us that we “don’t look all that sad to you” or that we “looked just fine the other day” because we have briefly managed to put on a brave face or wear a mask to hide our pain.  Having a good day here and there does not negate all the bad ones.  Invisible illnesses are still illnesses.  Like many other serious health conditions inside the body, you cannot often or easily see mental illness with the naked eye.  Not seeing a tumor growing inside someone does not make it any less real or dangerous.  Not seeing a diabetic’s pancreas malfunctioning does not mean it is not happening or that they do not need treatment.  Someone with cancer or another serious medical condition occasionally smiling, laughing or briefly enjoying life does not mean that they are instantly cured and tumor-free.  Just because you cannot see our mental illness does not mean we are not suffering.

Asking us “why can’t you just be normal?” or suggesting that we “need to stop feeling sorry for ourselves” not only blames us for our diagnosis but treats us as if we’re somehow broken or flawed and it is all in our head.  Nobody asks to have a mental illness nor does anyone want to be sick.  We are not doing this to ourselves.  We are not having pity parties. Please don’t suggest we’re just looking for attention or tell us that “the only one we’re hurting is ourselves” either, as if we’re intentionally sabotaging our own happiness by entertaining the absurd idea of some make-believe malady.  Mental illness is a very real medical diagnosis, one that is often completely beyond our control.  Our behavior did not cause it any more than a person’s attitude or imagination can cause tumors.

Please do not suggest we should just “snap out of it and get over things already“, either.  A person cannot snap out of a mental illness diagnosis any more than they can snap out of diabetes.  There is no set time frame that someone should be better, or even show marked improvement.  Like diabetes, a mental health diagnosis often lasts a lifetime.  And the healing process with most illnesses is not linear.  A diabetic can alternate between periods of stability, and episodes of sugar spikes and crashes, dangerous highs and lows that drastically and dangerously impact their health.  Similarly, even when in ongoing mental health treatment, a series of good days can be interrupted by periods of downward spiraling or numbness, and worsening symptoms as we attempt to balance medications and work through both past and new traumas.  Along the same lines as the fact that we refuse to take the blame for our illness, we are also under no obligation to heal on anyone else’s schedule or whim.  It is our illness, our treatment, and we will take as long as we need to take to heal fully and properly, even if it takes a lifetime.

Do not remind us that “every cloud has a silver lining” or tell us to “look on the bright side“, suggesting that we need to look for something positive at the core of our struggle.  Likewise, please never tell us that “what doesn’t kill us makes us stronger” or tell us that “it is God’s will“, as if our suffering was some divine gift or that it will be worth it in the long run.  Again, it is an illness, a medical diagnosis.  You would not confront a diabetic who must have their feet amputated due to their condition and suggest that they would somehow come out stronger for their loss.  You would not imply to a patient who cannot keep down any food because they are undergoing chemotherapy that the silver lining is that they always did want to lose a few pounds.  You would not tell anyone that their illness was a blessing in disguise, that they should be grateful for their suffering and pain.  Comments like those would be not only wildly inappropriate but also extremely insensitive, as well.  You would offer the person suffering your compassion, sympathy and support.  People with mental illnesses deserve the same.  There is nothing positive about our diagnosis or our struggle so please don’t insist we look for a silver lining or a bright side that is not there.

Please don’t tell us that “other people have it worse“, as if our struggle is insignificant because someone else has struggled more.  Don’t ask us “what do you even have to be depressed about?“, expecting us to justify our diagnosis or quantify our suffering so you can determine its validity.  A mental illness is a bonafide medical diagnosis that deserves acknowledgement and actual medical treatment regardless of its severity in comparison to someone else’s.  It is always a serious health condition that can continue to worsen if left untreated.  You wouldn’t shrug off anyone’s cancer diagnosis as trivial or be so unsympathetic as to suggest their tumors were insignificant because someone else had larger ones.  Cancer is always taken seriously.  Mental illness should be, as well.

If we trust you enough to open up about our diagnosis, please don’t shut us down by telling us “there are just some things you just shouldn’t talk about” or reminding us that “some things should be kept private“.  That is ignorance and stigma talking.  Yes, we understand that mental illness is uncomfortable to discuss.  So is any other serious medical diagnosis.  The difference is that families and friends will discuss other illnesses and the impact they will have on everyone’s lives.  We sincerely apologize for any discomfort our diagnosis might give you, but please know that we are not confiding in you hoping you can solve it or make anything better.  We are sharing our diagnosis because we consider you an integral part of our lives and we want you to be aware of everything that is going on.  Don’t tell us that we shouldn’t talk about mental illness as if it is something we should be ashamed of having.  The biggest reason this diagnosis has become so rampant in society today is because no one talked about it for far too long.  No one talked and nobody sought treatment.  But silence won’t make the problem go away.  Health issues don’t vanish because you refuse to acknowledge them.  It will only make it worse.

Please stop shaming us for our diagnosis altogether or our efforts to seek treatment.  Don’t tell us that “all we really need is some fresh air and some running shoes” in order to feel better.  Don’t tell us that “only weak people rely on medication” or suggest we try vitamin regimens, scented oils or other homeopathic remedies instead of what we have been prescribed.  We have seen actual doctors.  Medical professionals have given us a verifiable medical diagnosis and prescribed us the appropriate medications to treat that diagnosis.  You wouldn’t shame a diabetic for using insulin to balance their body so please stop shaming us for taking our prescriptions to balance our minds.  You wouldn’t tell a cancer patient that they didn’t need chemo, to just go for a brisk run or take a nice, long bath instead.  That is because it is widely accepted that chemotherapy is used to treat cancer and insulin to treat diabetes.  If you are willing to accept other medical diagnoses and treatments as valid, please accept ours, as well.

Please don’t attack us, demanding to know “what have you even done with yourself lately?” or otherwise question why we are not able to function as well as a healthy person.  Don’t interrogate us about what we have and have not accomplished recently, either, as if our level of productivity must meet your standards or our activity must be on par with yours.  Having a mental illness takes a lot out of a person, both mentally and physically.  It is perfectly acceptable for someone who has just undergone chemotherapy to spend a day in bed if they so need it.  If a diabetic has a sugar crash and feels under the weather, others will suggest they go lay down and feel better.  Healing and recovery time is acceptable for all other illnesses.  It should be for mental illnesses, too.

For so many years, mental illness was treated as something shameful, something you just didn’t discuss, something whispered about in dark corners.  With the continuing rise of suicides, addictions and other mental health crisis in our society, mental illness is being spoken about today on a scale previously unimaginable.  I understand that it might take some time for everyone to fully understand how to openly discuss our diagnosis with both compassion and respect after being shrouded in secrecy and stigma for so long.  When unsure how to proceed, many people turn to old cliches and outdated advice that they believe have stood the test of time.  However, many of those statements and sayings are not at all appropriate or applicable to mental illnesses.  If you are unsure what to say to someone with a mental illness, a good place to start would be to ask yourself if you would say those words to someone else with any other serious illness.  If you cannot imagine saying it to someone with cancer or diabetes, for example, it’s a good bet that it is not an appropriate response to our diagnosis, either.

After all, people with mental illnesses are not asking for special treatment.  We are just asking to be treated with the same courtesy you would treat anyone else who is ill.

I Have Depression.. But I am Happy..

I have struggled with depression my entire life, in part due to a genetic mutation passed down to me from my parents that affects the way my body metabolizes specific chemicals my brain needs to moderate my moods.  I regularly go through horrendous downward spirals where I feel completely broken and worthless, where life feels utterly hopeless.  I struggle with long periods of numbness where I have difficulty functioning or even finding the motivation to get out of bed.  On bad days, I will cry until my face is sore and my voice is hoarse, and it is unlikely I will be able to accomplish much more than basic self-care.  I am battling an illness that warps my very perceptions of life and continuously exhausts and pains me both physically and mentally.

But I am happy.

I have an amazing fiance who is very supportive of me and my diagnosis.  I have healthy, kind, smart and all-around wonderful children who have grown into incredible adults.  My fiance’s children are both amazing, as well. Together we have all formed a beautiful, blended family that I love with all my heart and am proud to call my own.  I have a team of doctors who actually listen to me and a treatment plan that is slowly but surely helping improve my quality of life.  And I have a blossoming writing career that has given me a true sense of purpose and an ability to help others in need.  I have many wonderful blessings in my life to be grateful for, many reasons to be happy.

Yet I have been diagnosed with depression.

That is because a mental illness like depression has nothing to do with happiness.  Depression is not caused by being in the wrong frame of mind or just not trying hard enough to be happy.  Having a depression diagnosis has nothing to do with feeling sad, a little blue or under the weather.  People with depression aren’t being Negative Nancys or Debbie Downers who just need to learn to lighten up and look on the bright side.  My diagnosis wouldn’t just disappear if I just tried to smile a little harder or maintained a more positive outlook on life.  My depression has nothing to do with whether or not I am happy.

I have trained myself to find reasons to smile everyday.  I am usually the first to look for something positive in even the roughest of situations.  No matter how hard my own day might feel, I always try to show compassion and kindness to others.  If nothing else, I am grateful each day I wake up and thankful of all the loving and supportive people in my life and share that sentiment regularly.  I am hopeful for the possibilities the future may have in store for me, as well.  Some of my friends lovingly joke that I am the happiest, most positive little depressed person they know.

Yet I continue to struggle with my depression diagnosis.

My brain does not care whether or not I am happy or grateful, whether I am hopeful, compassionate or kind.  My mental illness is caused by my brain not working properly, much like a diabetic’s pancreas malfunctioning causes their condition.  I have no more control over having a mental illness than someone else having diabetes, heart disease or another medical condition they may have been passed genetically.  Yes, events in my life may have further exasperated my mental illness, much like having excessive sugar might worsen a person’s diabetes or having foods high in cholesterol might affect the severity of heart disease, but my condition preceded any of the traumas and abuses I have endured over the years.  I have even sought treatment to help resolve those issues to the best of my ability, yet my depression has remained.

Because depression is an illness, a medical diagnosis with both mental and physical causations.

It is not all in my head.

It is not a state of mind or an emotion.

Depression isn’t about being sad.

The cure for depression is not happiness.

Like any other illness, depression needs ongoing medical treatment.  Doctors need to not only diagnose the condition, but also to isolate and treat both the mental and physical reasons for the illness, as well. Though doctors often utilize psychological treatments like therapy, meditation and mindfulness, they usually also include psychiatric methods and medications to help treat the physical causation.  That is because doctors recognize mental illnesses such as depression as a verifiable disability that deserves a comprehensive, multi-pronged treatment.

In cases like mine where my depression has a genetic causation, my diagnosis is permanent.  I was born with it much like some children are born diabetic.  You would not blame a child for being born with a pancreas that was incapable of functioning properly so please don’t blame me for the fact that I was born with organs that malfunctioned, as well.  The only difference in my case are the organs affected.  No matter how happy I am or how positive my outlook is on life, my liver will never be able to metabolize the substances my brain needs in order to function properly.  I will have this medical diagnosis and need ongoing treatment until the day I die.

If I confide in you that I am struggling with depression, please don’t try to encourage me to try to be happier and more positive, or point out all the blessings I have in my life.  I am happy and grateful already.  You do not need to remind me to be hopeful for the future because I already am.  Please don’t blame me for my diagnosis either, insinuating that I wouldn’t be ill if I just tried a little harder.  I did not ask for this diagnosis, nor did I cause it.  What I need from you is the same compassion, understanding and support you would give anyone else with any other medical diagnosis.

Because, though I am already happy, knowing you were doing your best to be supportive and treat me with the same respect you would someone struggling with other illnesses would make me even happier.

Republished on the Mighty on 4/4/19.