Coronavirus Has Become The Great Equalizer For The Mentally Ill

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

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

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

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

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

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

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

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

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

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

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

All of that is anxiety.

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

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People talk about that feeling of hopelessness.

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

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

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

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

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

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

All of that is depression.

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

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

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

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

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

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

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

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

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

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

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

Fear of the Unknown – Wedding Planning Anxiety

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

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

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

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

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

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

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

This time around, I want to do it right.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Yet my anxiety rages on.

My plan at this point is simple.

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

Focus on what matters.

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

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

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

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

Except perhaps letting him down.

That scares me even more.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

 

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

Love.. When You Both Have A Mental Illness

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Republished on The Mighty on 6/28/18.

Republished on Yahoo Lifestyle on 6/28/18.

Republished on Yahoo News – Canada on 6/28/18.

Republished on Yahoo News – India on 6/28/18.

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.

Republished on The Mighty on 9/14/18.

Republished on MSN on 9/14/18.

Republished on Yahoo on 9/14/18.

Republished on Yahoo Lifestyle on 9/14/18.

An Average Day Living with Depression and Anxiety

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Anxiety is Often Completely Irrational

Anxiety is often irrational but the fact that it does not always readily make sense does not stop it from rearing its ugly head.

Sometimes all it takes is something going badly once.  Every single time I’m in a similar situation afterwards, my anxiety is heightened and part of me fears that something bad will inevitably occur again.  Other times, I can have something bad occur repeatedly and nothing is ever triggered.  Each new time something bad happens again, I find myself honestly surprised at the outcome.

There’s no rhyme or reason to which will occur.  It is not based on the severity of the bad result.  It is not based on how pivotal the event was to my life.  Though I have struggled for years to understand my anxiety and pinpoint what causes it, I have not been able to discern any common factors to make it easier to predict my anxiety in the future.

A recent example of how my anxiety presents itself occurred a couple weeks ago. While preparing to shave my legs in the shower, I found a tick on my leg just below my kneecap.  Thankfully, he didn’t appear to have been there for long. I was able to get him out fairly quickly and easily.  There have been no rashes or bullseye rings around the site since then to warn of conditions such as Lyme disease.  All in all, I was pretty lucky. The whole situation was resolved quickly and without further or lasting complications.

This was my first experience finding a tick on myself in my lifetime.  It obviously was an isolated occurrence, unlikely to be repeated again any time soon.  I don’t spend a lot of time in wooded areas or anything where I’d be likely to pick up another tick.  Yet every time I have stepped in the shower since then, my anxiety easily goes up two points.

Whenever I step into the shower now my heart starts to race.  Though I begin an inner monologue telling myself that I am just being silly and paranoid, I can feel my chest start to tighten.  I stand under the stream of water, close my eyes and practice my conscious breathing techniques trying to calm myself back down.  I struggle to fight the urge to scour every inch of my skin again and again looking for other ticks.

I know it is irrational.  I know my anxiety in this situation makes no sense.  I know that, logically, I am highly unlikely to find another tick even upon a thorough inspection.  I know it was an isolated incident.  But logic plays no part in how my mind and my body begin to react in these situations.

I don’t even know if my anxiety in this particular situation will fade somewhat over time or if it will continue to grow.  Sometimes my situational anxiety will dull somewhat over the course of time.  Other times, however, it remains consistent or even grows and expands upon itself, merging with other anxieties over time.  Again, I have never been able to find any rhyme, reason or pattern to how my anxiety presents itself.  There’s no way to predict what lies ahead.

All I know is that, thanks to one random, errant tick, I have become increasingly apprehensive about taking my showers over the last couple weeks.  And I know that as much as I try to be rational and reason with myself, I cannot rationalize with my anxiety.  It comes and goes as it pleases, always leaving a mess in its wake.

That has always been one of my biggest issues with explaining my anxiety to other people.  Everyone always attempts to apply logic to the situation to “help me see how ridiculous my anxiety is”.  You cannot rationalize the irrational.

Though sometimes portions of my anxiety will eventually fade over time, I have carried others with me for decades.  A good portion of my anxiety revolves around never truly feeling safe.  In this aspect, it has merged with my PTSD because in my head security equates to safety.  Due in a large part to the abuses of my past, I have noticed that I subconsciously react to my anxiety over not feeling safe in many ways. For example, I always leave my shower curtain somewhat ajar so I can see the pathway directly to the door.  I often find myself jumpy and apprehensive when seated with my back to doorways because I carry within myself an ever-present fear of someone approaching me unaware.  I check locks repeatedly, especially before going to bed, because I cannot  relax, get comfortable or fall asleep if I am even the slightest bit anxious about my safety.

I have not experienced anything in the scope of sexual abuse or physical abuse since I was a child that would warrant such anxiety.  There is no rational explanation for why I need to have a clear view of the door from my shower or why I must watch the pathways to my location like a hawk.  It has been decades since I have had anything happen and I am no longer that little child who cannot fend for herself.  But my body and mind will not accept that reality as fact.  To this day, whenever I am presented with certain situations, my anxiety is automatically heightened.  It doesn’t matter that it is irrational.  It doesn’t matter that I can even clearly see that the situation is irrational and call myself on it.  My mind and body still react as if there is something to fear.

I understand that others mean well when they try to reassure me that there really is nothing to worry about or make comments about my overreacting.  I’m aware of that fact myself.  But they might as well be telling me the sky is blue because I can see that, as well, yet I have as little control over that as I do over my anxiety.  There is nothing anyone else could say to me that I have not said to myself a hundred times over.  I know somewhere within myself that it is irrational.  But that does not stop my mind and my body from reacting as if it was the most rational thing in the world.

I don’t need anyone else to tell me that my anxiety is often irrational.  Trust me, I have those bases well covered.  What I need more than anything is compassion and understanding, along with acknowledgement that I am doing my best to use everything I possess in my mental wellness toolbox to soothe myself and bring myself back down out of a panic.  I know my anxiety is often irrational.  Please believe my when I say I am not doing it intentionally to make my own life or anyone else’s harder.  It is a mental illness.  I have virtually no control over how my mind and body react in certain situations.  The last thing I need is judgment or lectures about how I just need to be more rational and calm down.  Because let’s face it – You cannot reason with something that is unreasonable.  You cannot rationalize the irrational.  All the common sense in the world will not negate anxiety.  It is a medical condition.

Minimizing Our Illness Only Hurts Ourselves

We have all been there. We are having a rough day, feeling under the weather. Our mental illness is wreaking havoc, making it difficult to even function. Yet when someone asks if we’re okay, we force ourselves to smile and reassure them that we’re fine.

Our eyes are puffy from crying and our world feels like it is collapsing beneath our feet. Yet, instead of being honest about how we are feeling, we force ourselves to smile and we make a half-hearted joke about allergies and it being that time of year.

We laid in bed for hours the night before, unable to sleep because our anxiety had our mind racing for over half the night. When we finally managed to pass out from exhaustion, our sleep was spotty, restless and riddled with anxiety-laden nightmares. Yet when someone points out we look tired, we force ourselves to smile and remark about how there’s never enough hours in the day to sleep as much as we would like.

Our stomach rumbles reflexively because we haven’t eaten in a day and a half because we have no appetite or desire to eat. When someone notices the sound, we force ourselves to smile and make an offhanded comment about it being a busy day, too busy to find time to eat yet. We reassure them we’ll eat plenty to make up for it later, even if we have no intention of following through.

We spend three days mostly curled up in bed, barely able to function. When someone checks in to see whether we’re okay, we run our fingers through our disheveled hair, force a smile and mutter something about just getting over a cold or the flu because somewhere in our mind we rationalize that a fake physical ailment sounds more believable and justifiable than a real mental one.

Someone remarks on the fact that we were wearing the same outfit when they saw us last a few days ago. We force a smile and reply that it’s our favorite or most comfortable one and joke about it being laundry day.

We force smiles and ask people who stop by for a visit to please excuse the clutter and the mess as if we have just been too busy to clean instead of being honest that we just haven’t had the physical or mental energy to do much of anything around the house in days.

We know when things are bad. We can see when our functionality begins to slip. Yet, instead of being honest with those around us, more often than not we minimize our struggles or even outright lie about their existence.

We isolate and make excuses about being busy with life. We avoid friends and family so they don’t see how bad things truly are. Again and again, we make excuses and downplay the severity of our condition as if we’re doing other people, or ourselves, an enormous favor by shielding them from the truth.

Many times every day, in virtually every interaction we have with others, we minimize our illness and the effect it has on our life supposedly for the comfort of others. We have so many excuses for doing this. We don’t want to put our drama on anyone else. We don’t want others to worry. We don’t want to be a burden. We don’t want to be accused of being an attention-seeker or throwing a pity party. We don’t have the words to adequately explain what is going on inside us or just plain don’t want to talk about it. We’re embarrassed of our diagnosis and don’t want to be judged or treated like a joke. Whatever our reasoning, we press our lips into a pained smile, pretending things aren’t all that bad and we lie.

We press our lips together in fake, forced smiles. We say we’re okay even when we know without a doubt that we’re not. We claim that we’re hanging in there, doing our best to stay positive and keep going, acting as if there’s nothing to worry about even as our world feels like it is crumbling around us.

What good does lying or minimizing our struggles really do?

Time and again, we wish others understood exactly what we are going through. In rare moments of unfettered honesty, we tell others they could not possibly understand how bad it is unless they experienced it for themselves.

But how is anyone supposed to ever understand or empathize if we keep hiding the harsh reality of the situation from them? We cannot simultaneously spare them the agony of the truth and accuse them of just not understanding how bad things really are. If we want others to understand how bad things truly are, we have to be completely  honest about it. Not partial truths, not sugary sweet versions of the truth but the whole unadulterated, ugly truth.

Because in reality, their comfort is not our responsibility. Our responsibility is our own well-being. We are doing ourselves no favors by hiding how we are doing from those who care about us. Likewise, we are doing them an injustice by hiding the truth from them. If someone is checking in about our well-being, they obviously care. If they care and are trying to be there, they deserve the truth. Not some watered down version of it but the whole truth and nothing but the truth.

Will our honesty make others uncomfortable? Most likely. But let’s be honest here. Mental illness is not pretty. It is dark and scary. It torments us to our very soul. Being honest about the effects of our diagnosis is not going to be pretty. But it is real. And reality can sometimes be very disconcerting. It can be a hard pill to swallow. But the truth is the truth and, as the saying goes, the truth can set you free.

Time and again, we complain about the stigma surrounding mental illness and how so many people do not take our diagnosis seriously. Perhaps we hold part of the blame ourselves. If we want others to truly understand what it is like living with mental illness, we need to start being completely honest about it.

I know it can be scary putting everything out there. There’s a great deal of vulnerability in sharing the whole, unfettered truth of the situation with others. But unless you’re completely honest about how you truly are, you cannot ever expect anyone else to understand exactly what you are going through.

Republished on The Mighty on 6/25/18.

Republished on Yahoo Lifestyle on 6/25/18.

A Trip to the E.R.: Physical Vs. Mental Ailments

This last week has been yet another stark reminder of how differently people view and react to mental illnesses versus physical ones, especially in medical settings like the emergency room.

Please bear in mind that I am by no means a frequent flyer in the emergency room. The last time I was in the E.R. was about two years ago when I had a large cyst and tissue growth on my left ovary that had twisted and contorted it, causing severe pain. I was in no way crying wolf or looking for attention. My E.R. visit resulted in a surgical referral and the removal of that ovary.

My mother was a hypochondriac. She had doctors for everything and scheduled appointments with specialists on the drop of a dime. Somewhere along the way in my journey to not become her, I became the polar opposite in that aspect. I avoided doctors and only sought medical treatment as a last resort. I once tried to walk off appendicitis for a few hours as bad stomach cramps. On some level, I know it is irrational and that I need to make my health a bigger priority, but I still struggle to go to the doctor unless it is absolutely necessary.

Last week, I had a bit of a scare. I had gotten upset after a spat with my partner and had gone for a walk to calm down and clear my head. Somewhere along the way, though, my head began to hurt and spin. I knew I was upset but the details felt distant and fuzzy, as if the facts were lost in my head somewhere yet I was unable to access them. The harder I tried to root out facts, the more my head spun and the more confused I felt.

While I do struggle often with losing numbers, words or specific facts as a result of my mental illness and have also had memory issues following anxiety attacks and PTSD flashbacks as well, I have never experienced anything like this before. When I realized I could not even recall my own name, it sent me into a panic. I knew something was seriously wrong so went into the first business I saw and asked the clerk to call 911 for help.

An ambulance arrived to take me to the hospital. Their initial fear was a stroke. They started running multiple tests and sent me for a CT scan. As tests began to come back ruling out the prognosis of a stroke, the demeanor of the staff treating me began to change drastically.

Their next possible prognosis was that it was purely a mental issue or that I was lying about the severity of my condition, putting on some sort of act for attention. Despite the fact that I was visibly agitated and distressed at being unable to recall even basic facts, their demeanor changed. All of a sudden, they became outright accusatory and began to question whether I was telling the truth. One nurse went so far as to tell me point blank that they would have to start doing uncomfortable and painful tests, including taking my temperature rectally, putting in a catheter for a clean urine sample (though I had given them one in a cup not twenty minutes prior) or even putting a needle in my back to withdraw fluids for tests “unless I had something I wanted to confess”.

As I laid there in a state of panic not because of the possible upcoming uncomfortable tests but rather because my brain just was not working like it should, I could hear that nurse at the desk nearby laughing with her coworkers about how she was “going to get a rectal thermometer and make me talk”, the results of my CT scan came back.

It turns out that I have two meningioma on my brain, tumors between the surface of my brain and the inside of my skull. The larger of the two is in the falx region, in the front of my head, which deals with memory. The smaller of the two is in the middle, presiding predominantly over balance.

Neither was particularly large thankfully, but when housed in the small space between my brain and skull, even smaller tumors could cause issues. Apparently in my already agitated state following the spat with my partner earlier, there must have been just enough pressure put on the memory portion of my brain to cause a temporary memory loss.

The whole demeanor of the staff treating me shifted once again, becoming very serious and somber. They gave me some sedatives and anti-anxiety medication to calm me and slowly the fog began to clear. They began bringing in paperwork and test results for me to bring to my primary doctor to get a referral for a neurologist, stressing the urgency of the situation. Though they informed me that something like eighty percent of meningiomas are benign, even benign tumors continue to grow and could cause temporary or even lasting damage to my brain if left untreated. Ultimately, I’ll need surgery regardless of whether biopsy results conclude the tumors are benign or malignant.

The whole situation made me nauseous, even beyond the fact that I have tumors on my brain. Just the fact that I was only taken seriously when they feared for a physical condition like a stroke or when the tumors were found on my brain was appalling. As I had mentioned earlier, I have had memory issues related to my mental illness in the past, though thankfully never quite to this extent before. However, following PTSD flashbacks or severe anxiety attacks, my brain is always fuzzy and muddled, as well, and I often have periods of impaired memory afterwards. The fact that professionally trained medical staff at an emergency room would treat any condition they believed had a mental origin less seriously, let alone as a joke, is beyond disgusting to me.

I did not make a scene or call them out on their obviously shifting behavior, in part because the very idea that I had tumors growing on my brain left me in a state of shock. Even more so, like many others struggling with mental illness, I have sadly become accustomed to my mental health not being taken seriously. However, it is deeply disconcerting to me that emergency personnel at a hospital would be so openly cavalier about anyone’s mental health, treating their patients as a joke.

I walked away from this situation with a few distinct feelings and thoughts in my head. First and foremost, I have a newfound anxiety and wariness about going anywhere alone until this is resolved, particularly when upset. I was lucky that I was in an area with easy access to other people and was blessed to have maintained enough reason to know to ask for help. But I carry with me now an ever-present fear that next time I might not be as lucky, especially considering that I regularly operate under conditions of extreme anxiety and depression due to my mental illness.

I also am distinctly aware of all the unknowns in my foreseeable future. I am not sure exactly where I go from here. I understand the basics. Get a neurology referral, get an MRI, get a  biopsy, have surgery, possibly radiation if needed. But I have no idea of the time frames of anything just yet and probably won’t until tests and biopsies start coming back. I don’t deal well with the unknown. Not being able to plan to any degree heightens my anxiety to dangerous levels.

There is a strange sense of underlying optimism, as well. Somehow I know I will get through this, that I’m a tough cookie. I come from strong stock. Both my parents survived multiple types of cancer and other ailments before they passed. My time is not up yet. I have too much left to do. I have a lot of fight left in me.

However, I am very aware of the fear growing inside me, too. Cancer scares me to the core. I remember going to the hospital day after day when my mother had part of her lung removed due to lung cancer, watching her fade in and out in the CCU, not sure whether she would make it or not. I remember reconnecting with my father just in time to watch cancer wreak havoc on his body, going through repeated cycles of surgeries and chemotherapy. His cancer always seemed to be one step ahead, reappearing again and again in different areas until it eventually killed him. I’ve seen cancer eat away at and kill multiple friends over the years, as well. Cancer is, by far, my biggest fear and it is now on my doorstep.

More than anything, though, I came away from this with a harsh reminder of the stigma that still surrounds mental illness, even in medical facilities. When they believed my issue was a mental one, I was a joke they saw fit to threaten with unneeded, uncomfortable and painful tests as a way to get me to “come around”, expecting my condition to magically cure itself and disappear under threats of unpleasantness. It took finding tumors on my brain, something they could physically see, for my condition to finally be taken seriously.

Republished on The Mighty on 6/17/18.

Republished on Yahoo Lifestyle on 6/17/18.

Republished on Yahoo Finance on 6/17/18.

Republished on Yahoo Sports on 6/17/18.

Anxiety & Jumping to Conclusions

When someone suffers from an anxiety disorder, our minds are always in overdrive, racing at top speeds trying to figure everything out. For each and every problem that presents itself, our brains reason out hundreds of possible reasons why, usually settling on the worst possible scenario or the one that bears the most personal responsibility. We see ourselves as broken and flawed so we naturally assume the fault ultimately must always rest with us.
When a friend does not acknowledge our messages or respond back right away, our mind races to decipher what we must have done to upset them without realizing it. We ponder whether we’ve been such awful friends, caught up within our own misery and personal problems, that we must have devalued their friendship, damaging it irreparably, causing them to give up on us and walk away. Somehow, the worst possible probability always seems more likely to us than the sheer possibility that they might just be busy, distracted by their own lives at the moment.
When our boyfriends or girlfriends, husbands or wives do not respond to us with absolute elation or passion, we start to wonder whether they are falling out of love with us. We dwell over how much of a handful we have always been in the relationship, whether real or imaginary. We wonder whether they’ve stumbled onto someone else they mesh with better and we honestly could not blame them if it were to happen because we know how horrible we can be. No matter how much or how often they tell us they love us and they cannot imagine their lives without us, our anxiety leaves us with an overwhelming sense of insecurity that convinces us that anyone else in the world would be a better choice than we are for them.
If something goes wrong at school or at work, we automatically assume we must be to blame and seek out how we must be ultimately responsible. Even if we know for a fact we had nothing to do with a situation happening, we look for areas where our intervention may have prevented the mishap and blame ourselves for our inaction. We feel as if we’re damned if we do and damned if we don’t, but either way, we’re still to blame.
If something breaks or stops working, we trace back to our last time using it, considering every irresponsible action we have done that may have contributed to its demise. Somewhere in our heads, we rationalize that forgetting to shut off a machine when we were done using it once 6 months ago must have ultimately caused a chain reaction that led to its deterioration and destruction. It doesn’t matter if a dozen other people have each done a dozen different things since then to contribute to the situation at hand. In our minds, our mistakes are so glaringly horrendous that we cannot fathom any other explanation being more likely. It doesn’t matter if an item was past its prime or threadbare and past due to be replaced. Our anxiety tells us it would still be usable if not for us.
We internalize everything. We assume that the chaos within ourselves is constantly leaking out into the world around us, seeping into everything we come in contact with, making everything ultimately worse. Our minds race straight for the absolute worst possible scenario, making a pit stop at every other negative possibility along the way. Our anxiety tends to blind us to the positive possibilities or even to the simple likelihood of coincidences or happenstance. It discards any randomness, always looking for a definitive answer and cause. There must ALWAYS be a reason why, must ALWAYS be someone to blame, and our minds have designated us to be the sacrificial lamb.
We do not do this intentionally. It isn’t that we’re just being a Negative Nancy, refusing to listen to reason or see the positive side of things. When we blame ourselves, we are not having a pity party, expecting others to feel bad for us, too.  We genuinely feel responsible whenever anything goes wrong.  Part of having an anxiety disorder is having a brain that is constantly, consistently, working in overdrive, looking to connect and explain everything around us, whether those connections are real or imaginary. Even if those links seem ludicrous to others looking in, when our minds make those connections, they feel genuine to us. Our brains are often on autopilot, with us just along for the ride. Whenever the rational side of our mind tries to speak up, speak out, to even suggest we might be overreacting or making something out of nothing, that voice is drowned out by a hundred other voices, a thousand other possibilities, of ways and reasons that we might be, must be, wrong.
If we have ever had a friend in the past who have distanced themselves because they felt we were too much of a handful, part of us assume other friends will follow suit and discard us, as well. If we’ve ever had a partner fall out of love with us or cheat with someone else, part of us braces ourselves for the next time it will happen, leaving us abandoned and alone. Because of this, we have trouble letting people in, trouble trusting others and allowing ourselves to be vulnerable.  We are terrified of being hurt, of putting ourselves in that position again.  As much as part of us knows that our current friends and partners are not those people who hurt us in our past, our brains keep pushing to link everything together, to make connections even where none truly exist. Even worse, when we are faced with pain or abandonment from others, we still question ourselves, looking to take personal responsibility for the choices and actions of everyone else.
Perhaps even worse than the initial blame game we play with ourselves is the way our minds will keep building and compounding our theories upon themselves, escalating them to unfathomable proportions. We build these fragile houses of cards in our minds, adding new card after card until we’ve created a precarious tower of self-loathing and blame. We tear into ourselves with a never-ending monologue that continuously harps that if we had just tried harder, just been better, not been so broken, been more responsible, none of would have happened. Our minds taunt us, telling us we should have known better than to even try, reminding us that everything we do, everything else we try, will fail, too, in time. We tell ourselves the lie that we are destined to be alone, that sooner or later everyone always leaves, then push everyone away, creating a self-fulfilling prophecy.  We allow our anxiety to convince us that failure and loneliness is an inevitable part of our lives and that we don’t deserve any better. We sincerely believe that it’s just what we do, just how our lives go, that you cannot fight the inevitable.
Even if it eventually comes to light that we were not to blame, even if the situation had a simple explanation that has nothing to do with us, it does not quell our anxiety. Instead, we tell ourselves, “it might not have been us THIS TIME..” as we begin to mentally brace ourselves for the next time we actually will be at fault. We chalk it up to sheer luck and we don’t see ourselves as ever truly lucky so we consider it a rare free pass, unlikely to ever happen again.
I often catch myself travelling down that anxiety-ridden path, needlessly panicking before I even know all the facts. I find myself looking to rest all the blame on myself even before I fully understand the situation or its underlying cause. I often find myself taking any distance from family and friends personally, without considering that their lives are busy, too and that life happens to us all.  I feel like I have to be ever-vigilant, ever self-aware, so I have even the slightest chance to rationalize with myself before the inevitable self-blame-game begins. Even then, it is a struggle within myself because my body automatically reacts to the anxiety festering in my mind. Even if the logical part of my brain is able to determine I am not at fault, there’s always that kernel of doubt bouncing around in my head, asking “..but how do you know for sure?”
Years ago, I had a friend that used to jokingly tell me, “Beth.. get off the cross. We need the wood”. It’s a sentiment I’ve come to relate heavily to my own anxiety. After all, I have been needlessly carrying the burden, real or imaginary, of everything going on around me for my entire life. I am slowly learning to differentiate between the rational and irrational, taking ownership of my own actions and decisions without carrying the weight of the rest of the world on my shoulders. While I cannot will away my anxiety disorder with mind over matter, being able to catch myself and separate what is probable from what is unlikely is a good start.  I may have to live with this anxiety monster on my back, but I don’t need to keep feeding it.

Republished on The Mighty on 6/22/18.