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.

Advertisements

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.

mightylogo

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.

depressionchart

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.

depressiongraph

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.

mightylogo

Republished on The Mighty on 2/18/19.

yahoolife

Republished on Yahoo: Lifestyle on 2/18/19.

yahoonews

Republished on Yahoo: News on 2/18/19.

yahoofinance

Republished on Yahoo: Finance on 2/18/19.

Core-Wellness-Logo-228

Republished on Core Wellness on 2/18/19.

mamamia

Republished on MamaMia on 2/23/19.

msn-logo-simple-png

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.

mightylogo

Republished on the Mighty on 4/4/19.

When You’re Struggling With Mental Illness, A Good Therapist Can Make All The Difference

For years, I struggled with my mental health treatment.  Not only was I considered “treatment resistant” because no medication my doctors prescribed seemed to even touch my illness, but I had become increasingly disillusioned with the therapy aspect, as well.

In theory, I have always believed therapy was a good thing.  Better out than in, as Shrek says.  I believed that people need to be able to talk about the issues in their life so that they did not build up, escalate and cause further issues down the line.

However, my personal experiences with therapy and counseling were disheartening to say the least.

When I was a child, my mother briefly took our family for therapy together.  On the very first appointment, when my brother and I both attempted to speak up and share our perspectives on the situation, we were cut off.  Our “family therapist” informed us that they were the parents, we were the children, that whatever they said goes and that our opinions on the matter were irrelevant.  From that point on in his sessions, I didn’t even bother participating because he made me feel irrelevant, as well.  The whole experience left a horrible taste in my mouth and made it harder for me to trust or open up to therapists from that point on.

As a teenager after my mother shot my father, I was briefly placed in counseling again.  The therapist that time did not seem interested in who I was or how I was feeling.  They simply wanted to know whether I had any plans to try and harm myself or anyone else.  Once they felt reassured that I was not a danger to myself or others, they saw no reason to see me any further.  Again, I was left feeling like I did not matter.

In my twenties, I had my first serious breakdown and my first true glimpse into the mental healthcare system.  I now not only was assigned a therapist but a meds doctor, as well.  I also had doctors that I saw for group therapy sessions.  I had a bonafide mental health team.

My therapist was always watching the clock and would interrupt me each session when we had ten minutes left, telling me to “wrap it up” because our session was almost over.  She chose the direction of our sessions, insisting we always talk about current issues because she didn’t believe I was ready to talk about my past.  I had no control over my own therapy.  I felt irrelevant to the whole process, like I was just going through the motions of getting help and she was only listening because she was being paid to do so.  If I ever needed to contact her in between sessions, I was directed to leave a voice mail, though her mailbox was often too full to leave one.

My meds doctor was equally as bad at listening.  He would prescribe me whatever the current flavor of the month antidepressant might be.  When I would explain that it was not even touching my symptoms, he would continuously up the dosages or add other prescriptions into the mix until the side effects became unbearable and I felt like a walking zombie.  Every time I spoke up explaining that nothing was helping and that I felt worse than before I began taking anything, I was disregarded and told that I had to give the medications time to work.

My “therapy groups” were laughable at best.  Everyone in the groups were told that we were not allowed to talk about anything too personal, nor were we allowed to discuss any topic that might be triggering to anyone else.  What we were left with was a room full of people sitting there uncomfortably, some wanting to cry, others wanting to rage, as we all muttered through gritted teeth that we were fine because none of us felt we were allowed to say anything more.

The mental health clinic I attended also had an impatient wing at an area hospital.  I was admitted there a handful of times over the years.  As bad as their other services were, those stints on the mental health floor of the hospital were the worst.  It always took over a day to get my medications approved so I felt even more unbalanced from the start.  On an average three to seven day stay, I only saw a doctor for ten to fifteen minutes on the day I was admitted and again on the day I was released.  In between, the only option for any sort of therapy were groups.  I was assigned groups with the same rules as my outpatient groups so nothing was ever talked about or resolved.  No one was allowed in their rooms during the day so you had hallways full of clinically depressed people walking endless laps around a secured wing, biding their time until their next mandatory group or meal.  Patients openly sobbed or sat around with numb expressions as if life itself no longer made sense.  Nurses sat in a large locked cubicle in the center of the wing, laughing and talking among themselves and largely disregarding the patients unless they had to intervene with a “behavioral issue” or direct someone somewhere.  There was no real treatment.  It was a corral to hold the mentally ill until the staff could pass them off to be someone else’s problem.

More than once, I stopped going to my treatment over the years.  I felt irrelevant, unheard, unhelped.  It all felt like a complete waste of time.  However, with or without treatment, my mental illness raged on and periodically I found myself having another breakdown and needing treatment again. Unfortunately, there was not a large selection of mental health clinics in the county where I lived, and the others all had long waiting lists, so whenever I needed mental health treatment I was sent back to the same clinic that had already previously let me down.  Over time, I became so disenchanted with the mental healthcare system that I just couldn’t see the point anymore.  I may have had a bonafide mental health treatment team but I walked away without any real treatment for my illness.

A couple years ago, I had yet another severe breakdown, this time thankfully in another county.  With the help of a coordinated care provider, I was able to get an appointment at a clinic that normally had a long waiting list and was not currently taking new patients.  Again, I would be assigned a mental health team.  I wasn’t going to hold my breath, though.  I had been through this process many times before.  My expectations were low.

I have never before been so pleasantly surprised or so grateful to be proven wrong.  The difference was like night and day.

My meds doctor actually listened to my previous experience with different prescriptions and did not try to push a large pile of pills on me.  Instead, he had me take a genetic test to determine what medications would work best for me based on my genetic make up.  Lo and behold, based on the results of this test, over half of the medications previous doctors had placed me on were listed as causing moderate to significant interactions for me.  The genetic test also revealed a genetic mutation I had that greatly contributed to my treatment resistance.  We worked together to create a treatment plan that actually suited me.

All my groups encouraged open dialogue, even if the topic was grief or pain.  My groups laughed together and cried together.  We fought our battles side by side and all felt heard.  This clinic offered a wide variety of groups beyond traditional therapy groups, as well, such as transforming anxiety through art, meditation, tai chi and yoga.  I found myself signing up for every group I could fit into my schedule.  Not only were they treating my mental illness, they were contributing to my mental wellness, as well.

My biggest blessing and godsend at this new clinic was my therapist. She lets me control the flow of our appointments and choose what I feel I need to address each week, never prodding or rejecting the topics I select.  She made allowances with her scheduling so that if we ever went over the session time, she never had to cut me off or make another patient wait.  She understood my struggles with verbalizing sometimes in between appointments and readily agreed to communicate via email or texts because that was what worked best with me.  Whenever I have emailed or texted her, she has responded back in under a day.  Most importantly, she truly listened and cared.

When I was struggling to find housing, she brought in resources and connected me to organizations that might be able to assist me.  She helped me navigate through registering my sugar gliders as emotional support animals.  She took the time to introduce me to others I would be attending groups with so I did not feel so awkward about not knowing anyone there.  When I was on bedrest following surgery, she did sessions over the phone so that I did not have a lapse in treatment.  She has helped and intervened with more than one personal crisis time and again. She regularly went above and beyond in every way imaginable.

Perhaps the grandest gesture she had done was only a couple months into our visits.  My mother had passed away on Thanksgiving day 2010.  In one of our early sessions, I had expressed to her how hard this day still was for me years later.  On Thanksgiving, she took time out of her day and her own family celebrations not once but twice to reach out and call to make sure I was okay.

Again and again, she has shown me that I wasn’t just a patient that mattered during those 50 minutes penciled in on her schedule.  She helped me to feel like I mattered even when I had trouble mattering to myself.  She always made me feel like my mental health was a priority, that I was a priority.  I have never felt more heard.

I honestly feel like I won the therapist lottery.  In under two years time, I have gone from hating therapy and thinking it is a joke to believing it can truly make a difference in someone’s life.  My life.  Everyone’s life.  Whenever I hear anyone talk about needing a therapist, I refer them to my clinic, insisting that even if there is not an opening right away, they are worth the wait.  I often share stories about my experiences with my therapist that end in “what therapist does that?!”.  The only difference is that now my stories come from a place of gratitude instead of disbelief and disgust.

There are wonderful therapists out there.  There are clinics that genuinely want to help their patients heal, who see them as people that are suffering instead of a steady flow of dollar signs in and out the door.  I understand how easy it is to become disillusioned with the mental healthcare system when it feels like you are unheard and irrelevant to your own treatment.  I’ve been there.  I went through a revolving door of sub par and inadequate treatment for years.  But please know that not all clinics and not all doctors are like that.  Some genuinely care about their patients and their well-being.

If you are feeling unheard or untreated, please don’t give up hope.  Don’t stop your treatment because your doctor is not hearing you or is not working in your best interest.  Keep looking.  Find a new doctor.  Your mental health matters.  Don’t settle for clinics that make you feel irrelevant.  Find a place where you feel heard, where you feel like you truly matter.  Find a place that makes you look forward to getting the treatment you need.  Trust me – It can make a world of a difference in your life.

I want to end this piece by taking a moment and thank Mary B. and everyone else at my mental health clinic for making such a dramatic impact on my life.  You are all truly a blessing not only to me but to all those whose lives you have touched.  Thank you sincerely.

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.

mightylogoRepublished on The Mighty on 9/14/18.

msn-logo-simple-png

Republished on MSN on 9/14/18.

yahoo

Republished on Yahoo on 9/14/18.

yahoolife

Republished on Yahoo Lifestyle on 9/14/18.