It Isn’t All About You: The Selfish Side Of Depression

 

I am a selfless person. I always put others needs ahead of my own to the extent that I ignore my body and brain’s signals that I am not well. I want people to be happy… my family, my friends, my coworkers. I want the world to be happy ahead of me. I live to please others. Ask anyone I know, and the word selfish would never be used to describe me.

But two weeks ago I was reminded that there is always a part of you that is selfish, even when you don’t realize it.

I was going through a bit of a rough patch since my business trip early last month as usual whenever I travel. After I arrived home, I was met with several days of heightened Anxiety and even a Panic Attack. This was followed by 8 days of a Depressive state. I felt empty and alone. There were a couple of days I forced myself out of bed and many days I struggled to find anything enjoyable in my life. I knew if this lasted a few more days I would be headed to another diagnosed episode of Depression. Of course, in my mind, I was already there.

Within these 8 days I felt increasingly isolated, not from my family, but from social interactions with friends. I internally blamed myself as anxious Depressives often do. I was the reason my friends were ignoring me (so I thought). Was I talking about my Mental Illnesses too much? Was I too socially awkward for them? Did I say something? Did I do something? Was I acting too weird?

And then I got a text message from one of these friends asking me about something I have considerable knowledge on… psychiatrists. She then proceeded to tell me it was for her. There was some shock when I found out. In almost 6 years of knowing her, she never mentioned a need for a psychiatrist. I became worried and asked her what was wrong. She then requested a time we could talk face-to-face.

I went to her house last weekend where she told me why she has been so absent this last year (her story to tell, not mine). Never in my hysterical thinking did it ever occur to me that one of my close friends was going through a major life change. A mutual friend of ours was there too. She explained that she shared the same thinking I had, that we did or said something wrong. And then she said something that struck me…

“Although normal, it is such a selfish way of thinking.”

Ah ha! Light bulb moment!

And there it was, the selfish side of me, my Depression. Every question concerned only me, myself and I. I started to analyze my past Depressive episodes and the questions I always asked myself and there was one cohesive theme… I, I, I! How my life sucked. How no one wanted to hang out with me. How I was worthless. So many I’s and Me’s. It never occurred to me that my friends and family might see me differently, that they needed me, that they might be struggling. The thought of anyone else in my life having a rough time never passed through my mind. It was always about me.

Lies Depression Tells: “You Have No Friends… And Don’t Deserve Any!”

There is singing in my head, one song, on a continuous loop… “All By Myself” by Eric Carmen later remade by Celine Dion:

“…I think of all the friends I’ve known, but when I dial the telephone, nobody’s home…”

I hear laughter in the background as the song is being sung by a melancholy vocalist, myself:

“… Sometimes I feel so insecure, and love is so distant and obscure, remains the cure…”

Then I can visually see myself break out into the chorus with tears gliding down my cheeks:

“All by myself, don’t want to be, all by myself anymore…”

The laughing is growing and I am shrinking down into the fetal position on the floor, slinking my way into a corner. The source of my laughing, Depression, my friend, my foe, my constant companion.

It arrived back from its vacation a little over a week ago. Not wanting to stay quiet and play with Anxiety in the background, it has taken over my body. It has put all those ‘lovely’ negative thoughts back in my head that I worked so hard to get rid of… worthlessness, hopelessness, loneliness. I’ve tried to fight back, telling it that it will not take over me and every morning it is the personality trait that is dominant.

“You have no friends!” it echoes. There is a brief pause before it cackles, “And you don’t deserve any.”

This is a normal feeling that comes in waves throughout the year. For the most part, I can tell Depression to shut up, but this time, this time I can’t. I am silenced. I am not quite sure of the main cause of this Depressive state as it has been going on for over a week but I do know a few factors that have contributed:

My Business Trip: I love traveling for my job. I get to see new places, try local cuisine. This time I even met a friend for dinner. But traveling disturbs my routine and while I enjoy it, these trips are so jammed packed with work that I am constantly moving and never really decompress.

No Vacation: My husband, daughter and I took a vacation in April 2016 and will not be going on another vacation until October 2018. Yes, 2 1/2 years. We tried planning a long weekend this year but there were other commitments. So once again, no decompression.

Socialization: My therapist recommends I get out more with my friends. Easier said than actually done. Everyone is so busy except during the week. Even though it is summer, I work during the week.

It’s this last point that has been eating away at my happiness and refueling my Depression.

There was a group of friends of mine, close friends, close enough to call each other ‘Bestie’. Over the last year and a half there has been distance, mainly because our daughters no longer take dance. My instincts tell me there is more and I will sit and analyze this to no avail. My thoughts tell me I did something wrong or said something wrong. There were birthday parties my daughter wasn’t invited to. I blame myself for this. What did I do? Did I say something? I know, they are sick of dealing with me. There are photos of fun weekday pool gatherings. Stephanie, you work, you can’t go. There has been effort on my part earlier this year but now, now I am just so drained I have no more strength to try anymore. I know this is only hurting myself, and my daughter since she misses out on playing with her friends.

I feel alone, so, so, alone.

When I am lucid and logical I realize the falseness of this. “We’re all busy,” I tell myself, “Weekends are usually family time.” I mean, how can I deny the latter? That is when my husband, daughter and I can do something. I constantly tell myself that you have friends that you go out with. I just went out to see a musical with one of them. I have my best friend in the whole world living with me, my husband. I have family.

And yet, there is something missing.

Something about this group of friends and me. Something that is eating away at me. They don’t get it and at times, I don’t think they want to try anymore. They don’t get what living with Depression is like. They don’t understand how a Depressive thinks. I can’t blame them for this. My brain is not easy to understand. My husband, after knowing me for almost 21 years, still has times where my mind confuses him. Hell, my mind confuses me. And at times, those rare occasions where I do get to meet up with the ‘Besties’, I tend to feel uncomfortable because I constantly feel like I am being seen only as my illness. I know this is my Depression speaking. Sometimes it is just hard to separate my logical mind from my sick mind.

I have friends that get it. Friends that I met because we share Depression and Anxiety diagnosis’. I enjoy their company. I don’t feel like any topic is off limits. When my friend and I went to the musical, we discussed hospitalizations. They fulfill my socialization need. Then why the funk… why the constant loneliness, why the “You have no friends, and you don’t deserve any”?

I wish I knew.

Lies Depression tells us.

What Happens When A Dream Turns Into A Triggering Nightmare


Suddenly, I was back there.  That place, both a saving grace and a hell.  I was walking down the hall.  Bare concrete block walls.  Gray, solemn, just like the people that dwelled inside.  Doorways on both sides leading to rooms with aging office waiting room furniture that was once comfortable but now forlorn like their occupants.  I was one of them again.  An empty void, emaciated, internally crying for help.  Tempered glass and a counter to my left held those that treated us.  Their faces ranged from a gentle smile to a stare as if asking, “What is this person doing?  Am I safe?”  Slowly, I walked toward the end of the hallway where a window was.  Large, a glimpse to the outside world.  If only it was not right across the street from a cemetery.  

My eyes were welling up with tears.

Why was I back here?  There was no reason to be.  I have been doing well mentally and emotionally.  If this was the case, why was I, without warning, plunged into the short term psychiatric ward once again?  I was dreaming and being triggered.  Being both on the outside looking in and on the inside dying to get out.  

I have a love-hate relationship with the hospital’s psych ward.  When I was first there over ten years ago, I wondered why I was there.  I never thought I was experiencing the same problems as the other residents at the time.  I thought I was normal.  Ha, ha, good one Steph!  When I went back over two years ago, I begged for it.  I know being there would help me.


There are things I would rather forget about the hospital aside from the bare walls and gloomy atmosphere:  


The bed checks every 15 minutes… even if I was deep asleep, like clockwork I was awakened to a flashlight shining into the small glass panel in the door.  


The psychiatrists… although there to help, none of them appeared like they cared to help you. I spent all of five minutes a week day (they did not work on weekends or holidays) talking with them while their eyes looked elsewhere as if saying “You’re wasting my time.”


The wake-up time and routine… it was a bit rough waking up at 7am with all the medications I was given and then to go through the process of waiting in line to get weighed and our blood pressure taken.  


Lack of outdoor time… depending on your mental and physical state that day, you may be allowed to go for a short walk circumnavigating the hospital building viewing the nearby cemetery and emergency room.


But, where there is bad, there is also good.  As I mentioned, I knew I needed to be hospitalized again.  For some reason, I felt safe there.  I was only responsible for myself.  I could focus on my much-needed self-care and work on getting better even if it took a psychotic break to get me there.  I knew I would get the medications necessary to sedate me, stop my brain from its incessant thinking… you’re worthless, helpless, not worthy of love.  These medications would also stop my hysterical, borderline delusional, thoughts… take that screw, just jam it in your head, who cares if it kills you?!


Although the psychiatrists were lacking in care, there were some nurses that were a pleasant gift.  They would talk with you about your life focusing in on your face, treating you like a human being.  They remembered things you told them and asked you about it days later.  They were concerned about your care.  Sometimes they even sat and watched TV with us.


Aside from two very special nurses (1 each hospitalization), I made connections with fellow residents.  We talked about our experiences, gave each other advice, was there as a person who knew what it felt like.  I still, from time to time, communicate with my last roommate.


And yet, this dream triggered me.  I awoke with rapid breaths, scared, worried, panicked.  What did it all mean and why was it affecting me so badly?  I was somber the whole day.  Was this a prelude of another hospitalization to come?  Because of my Anxiety diagnosis, of course, here I am jumping to the worst conclusion instead of calmly thinking this through.  And if it is a premonition, why am I so fearful?  The hospital helped me.  Ultimately, I think I will have to consult my therapist on this.

When False Information On A Meme Makes You Angry…

Originally posted on Stigmama on Tuesday, June 20th:

The other day on Facebook I came across a meme… actually calling it a meme is too nice. I came across a shitty ad that basically told me and others that are Mentally Ill and medicated that we are now drug addicts. While addiction is a Mental Illness, I have not been diagnosed with it. I am a long time Depressive and Anxiety-ridden Mom that will fully disclose any part of my history because people need to know what it is really like to be Mentally Ill.

When I saw this, I was outraged, furious, and this was at 10am on a weekday morning in my cubicle at work:

What made this worse, was this was the pinned post in this group ‘The Free Thought Project’. My blood was boiling. I wanted to break something. Instead I decided to use this as an oppurtunity to educate.

I have seen many versions of this ad before (see below) consciously telling people that medication is evil and while I find them offensive, it didn’t hit me as hard as saying I now have a “lifelong addiction”:

                                        

Is medication shit… well I will flat out admit I wish I didn’t have to take it but comparing it to the stuff that would be on my daughter’s diaper years and years ago is a bit much.

Nature as an antidepressant… I agree wholeheartedly that nature is very rewarding.  I am an avid walker and hiker (and snowshoe-er in the cold winter months).  I love being outside.  After a hike, I usually find myself rejuvenated, feeling alive and most importantly happy.  A hike or a walk outside at lunch can ‘turn my frown upside down’.  There are just a couple of things wrong with this statement:  Nature does not have the same effect on everyone and when you are severely Depressed, it ain’t going to work, trust me, I’ve been there.

Being an Alpha personality, a control freak, a perfectionist, I will fully admit that I hated being on meds.  I couldn’t fathom the idea that a little pill (or four) controlled me.  I was only ‘normal’ because of them.  I thought I could get better without them.  I was wrong… very very wrong.

The first time I was prescribed medication was shortly after my 18th birthday.  It came in the form of a half white and half aqua capsule known as Prozac.  I was quickly told not to tell anyone I was taking it.  This was after I held a case cutter I stole from work to my wrist debating whether I should live or die.  This event, I was also told, to not speak of.  Ah, you got to love the stigma associated with being Mentally Ill.  Because of this, I thought medication was wrong, bad, sinful.  How stupid of me.

It wasn’t until my recent episode of Major Depressive Disorder and Severe Anxiety almost three years ago, that while getting better I finally said “Screw it!”  I didn’t care who knew.  If I had a megaphone, I would probably be screaming it.  There is nothing wrong with being medicated.  I really should create (or order if it exists) a shirt that reads: “Medicated & Proud Of It”.

These people that create these offensive and naïve memes have no idea what it is really like to live with these conditions.  Because it is invisible it doesn’t actually exist.  Because there is no official blood test or genetic test, we all must be making it up.  It is all in our heads… why yes, it is.  Because of a lack of Serotonin, something produced in my brain (i.e. my head) I live daily with two severe illnesses.  I am not making it up.  Who would make up paying monthly for medications, weekly psychiatrist & therapy appointments, being hospitalized, becoming severely delusional, considering hurting or killing yourself?!  Yes, I totally want all of this!

But we live in a society that believes Mental Illness is not on the same level as a Physical Illness.  It is okay if you take lifelong medications for illnesses such as Diabetes, Multiple Sclerosis, Lupus, and Cancer and that is not seen as an addiction.  Why is it okay for them but not for people like me?  Why am I considered ‘an addict’?  Why am I ‘faking it’?  I wonder if there was a real test that proved a Mental Illness diagnosis if these views would change.

I have weaned off medications a handful of times.  It can happen.  I lived 4 years med free before I entered into my 6th Major Depressive Episode.  Once on medication again, I took a hard look at my husband, my daughter, and my parents and told myself I didn’t want to see them suffer anymore.  I didn’t want to suffer anymore.  I decided then and there to never ever go off my antidepressant.  Lexapro and I will remain the best of friends.  I am not ashamed of my med.  Without it, I would be in a very dark place or not here at all.

To ‘The Free Thought Project’, research more on what is truth and what is fiction.  I don’t care if you lean liberal or conservative.  The Mentally Ill are a large population and by posting this, you are making us want to hide more.  Because of this, many people will stay silent.  Because of this, many people will not get the help they need.  Because of this thinking, more deaths by suicide will occur.  Remember that old adage “Stop and think before you speak”?  It would have come in handy here.

To all my fellow people with Mental Illness, please do not hide.  Do not believe a word of this absurdity.  There is help.  A walk in the woods can help, but it is not a cure.  It will not help as much as therapy and medication.  Remember:

 

When I Learned To Accept My Depression Diagnosis

I am not a woman who hides her age.  I will admit it, I am 37.  I don’t look it and that is probably why I will fully cop to my actual age.  I have a young (very young) face and I am short (incredibly short).  Throw these two traits together and I might as well be 20.  I still get gawkers and non-believers when I correct people on my age.  I am 37 and for the last 23 years, I have been a sufferer and survivor of Depression.



My first diagnosis was at age 14.  With all the rapid firing, teenage emotions, who would’ve known that Depression was there too.  I certainly did not.  I just blamed normal teenage angst.  The signs were there though… crying uncontrollably, hating myself, hating others, wanting to run away, wanting to remove myself from this crazy world (although not by suicide… that would come a few years later).  Once my parents realized there was something not quite right with me, I was brought to a therapist where I received my diagnosis and then to group therapy with other troubled teens.  Major Depressive Disorder.  I was angry.  I was so angry.  Why me?  Why couldn’t I just be ‘normal’?  And then there is the infamous stigma.  Back in the early 1990s, being labeled with a Mental Illness had people envisioning you in a strait jacket, talking to yourself and banging your head against walls.



I could not accept this diagnosis.  Being a teenager, I fought it like I fought everything else.  I barely paid attention at group therapy.  I still was mad at my parents.  No, nope, I would not be a Depressive.



A few years later, almost 18 and a legal adult, my 2nd episode with Major Depressive Disorder hit.  This time I was suicidal.  Group therapy was a thing of the past.  I was now seeing a therapist one-on-one.  I was deeply immersed into CBT (Cognitive Behavioral Therapy).  Even with wanting to die, holding a case cutter to my wrist, and seeing a professional, I could not accept living a life with Depression.  Nope, not for me.  I didn’t want it.  Someone please, for the love of God, take it from me.



My 4th bout of MDD was one of my worst, it was my battle with Severe Postpartum Depression and Anxiety, an illness so taboo in the mid-2000s.  I felt so alone.  I knew no one.  I became hospitalized.  Now, Stephanie, now would be the time to accept your circumstances and push past the trauma to live a fulfilling life.  Nope!  In the fight or flight aspect of Anxiety, I was and will always be a fighter.  I couldn’t understand why I had to go through this… hating my daughter, the panic attacks, crying spells, being an empty void for almost a year.  I couldn’t accept that I would never experience a typical postpartum and be the doting new mother.  I missed so much of my daughter’s first year of life, it just wasn’t fair.



My latest episode, brought on by taking care of and eventually having to give back my former foster son, was probably the worst.  I grieved for the loss of him for a good year and a half.  I was struck by several panic attacks, another hospitalization, and the realization that I was meant to only mother one child.  I lost myself, hopes and dreams I had for myself.  It brought back the trauma of my postpartum experience and ultimately gave me a PTSD diagnosis.  While dwelling so much in the past with the “Why me?”, “It’s not fair”, “I miss him”, I once again missed out on a big chunk of my daughter’s life, the child I did have.



It’s interesting though. I think we begin to learn acceptance with age.  After all, we are not as young and virile as we used to be.  I accept that I cannot run as fast I could before.  I accept that I can’t eat the foods I could eat before and maintain my weight.  I accept that my hair grays quicker after each coloring appointment.  So why couldn’t I accept my Depression diagnosis?  I have been living with it for over 2 decades.



Yes, I will never get that first year of my daughter’s life back.  I have so many pictures of my robot self from then, bad memories of myself caught on a piece of photo paper.    I will never get that year and a half of her life back from grieving the little boy who left our house.  I sat with this, after a year of EMDR therapy, and it came to me.  A light bulb literally appeared in my head and turned on.  By torturing myself with fighting my Depression, I was missing out on so much in life.  I took hold of a phrase my EMDR therapist would tell me:



“Invite your Depression in for a cup of tea.”



This time, after decades of being at war with my brain, I took his advice.  When I would find myself in pain over the past or self-loathing, I sat back and talked with my Depression, letting it consume me for that moment.  In time, I have learned to live in that moment, whether with my Depression or with my Anxiety, inviting it in for tea, and after a short time let it go.  My Depression no longer devours me.  The lies it tells me, no longer control me.  I have finally learned to live with this illness.



Twenty-plus years later, I have learned acceptance.


What My Daughter Knows

My daughter knows I hated her just two weeks after she was born. Pure hatred, where using the actual word ‘hate’ is valid and not taboo. She knows I wanted to leave her and never ever see her again. She knows I wanted to turn back time and never have her, completely obliterate her existence.

My daughter knows what suicide is. She learned this at age 8 because she overheard something on the radio. She knows that I have thought about committing suicide a handful of times and that one of those times I came very close to slitting my wrist with a case cutter I stole from work (and still have). She knows I was a teenager then, almost 18, a legal adult, only 8 years older than she is now. She knows that these ideations have blown into my mind like a breeze and have quickly left several times in the last twenty years.

My daughter knows I am sick. She has seen me at my worst, a vision I never wanted her to lay eyes on. She has seen me shaking, rocking back and forth, nails digging into my head spewing delusions out of my mouth left and right. She has seen the tears, witnessed the dry-heaving runs to the toilet, heard my self-loathing.

My daughter knows I have been hospitalized, twice. She accompanied my parents this latest time when they visited me, being forced to stay in the cafeteria with my father because she was deemed ‘too young’ for the short term psychiatric ward. The hospital feared the patients there would hurt or scare her by saying or doing something. This means they feared I would hurt or scare her too. She knows the emotional pain one feels when the only communication we had was through a phone… a phone that would cut you off if you moved wrong, a phone so desperate in need of replacement. She understands that the hospital is my safe place, when our home is unable to be just that.

My daughter knows she is an Only child because of me. She knows I was barely able to raise her in the beginning due to Severe Postpartum Depression and Anxiety. She knows at times I have been unable to care for her in the episodes of Major Depressive Disorder since. She knows that she lost her little brother, my beloved former foster son, because my illnesses prevented me from being able to function, let alone parent. I became a third child for my husband then, a childlike creature in an adult body that my daughter started to take care of, becoming a Mommy to her own mother.

What I didn’t expect for  this wonderful, kind, and loving child to learn was acceptance. Every time I had to explain these things, every time I hurt her, I expected anger and rage in return. I expected her to ignore me, shout “I hate you Mommy”, rotating the knife deeper into my back.  I expected extreme tears over losing her brother, many more than she shed (and she cried quite a bit).

Instead, she shocked me by becoming my protector of sorts, a role I never asked her to take and tell her now she can relinquish.  She truly cares if something will affect me, triggering me back to those dark dismal days.  She has true compassion and empathy, two traits I am happy she learned, although I wish she learned them with something other than me as the subject.  She is the Wise Fairy that her name, Sophia Faye, connotes.

There are so many things she has had to learn at the tender age of 8, 9 and now 10.  These things I would have liked to have postponed.  I have been called out by a select few saying she was too young for these strong topics.  Yes, I know.  But, I have to say, if by telling her about being mentally ill, suicidal & hospitalized has made her into the awesome kid that she is today, I am happy she knows.  I am happy she knows, because she won’t have to live in the shame and stigma of it if it happens to her.  She knows she has a loving mother who has been through hell and back that can help her.  And she knows that although at one point I hated her, wanting to leave, I couldn’t bare to live without her now.  She is my heart, my strength, my love, my Sophia Faye.

Can I Call Myself An Author?

I have always dreamt of being a published Author.  Writing has always been a huge part of who I am.  I remember writing imagination filled stories since elementary school.  In junior high, I expanded to poetry, the easiest form of writing to express myself.  I was even in the Creative Writing talent as my school was for the ‘Gifted & Talented’.  In college, I took a poetry class and threw in some laughter on a poem about bowling that symbolized sex (might post that one day).  I’ve been published in school anthologies with both stories and poetry.

But, can I label myself an author if I haven’t actually published a book of my own?

Dictionary.com defines “Author” as:

  1. a person who writes a novel, poem, essay, etc.; the composer of a literary work, as distinguished from a compiler, translator, editor, or copyist.
  2. the literary production or productions of a writer:
    to find a passage in an author.
  3. the maker of anything; creator; originator:
    the author of a new tax plan.
  4. Computers. the writer of a software program, especially a hypertext or multimedia application.

I definitely fit the mold of #1, yet calling myself “Author” doesn’t feel right.  I guess it stems from learning all those years ago, that to be a real Author, you had to be published.  Published.  What constitutes ‘being published’?  As stated before, I was ‘published’ in anthologies put out by the Creative Writing talent at my junior high.  I was ‘published’ in an anthology in high school.  Do these count?  Only a marginal amount of people will ever read them.  And while I still possess all of these works, I highly doubt they exist beyond my possession anymore.

I write this blog.  Starting in 2015, I created my blog, Rising From The Ashes, and still keep it active (although switching platforms from Blogger to WordPress).  I bought my own website to make it official.  I try to publish a post at least once a week.  I have contributed to other blogs, sharing my work several times with The Mighty, Stigma Fighters & Postpartum Progress.

I have been published as a Contributing Author (note my use of the word Contributing as I was one of many) in Stigma Fighters Anthology II and A Dark Secret… both books helping to tear down the stigma associated with Mental Illness and Maternal Mental Illness.

But I haven’t published a book of my own yet and now I am questioning if I want to anymore.

I want to share my life with the world to help others like me.  I want men, women, and teens to know they are not alone in there Mental Health struggles. I want to give them a voice. And while I have started my memoir, my book, to do this, I’m beginning to wonder if I have to complete it because…

Am I not doing this already?  Advocating for those who feel they need to remain silent.  Have I not been sharing my story piece by piece through this blog, on The Mighty and on Stigma Fighters? Was it not published in 2 compilations of stigma breaking books?

It comes down to time.  I just don’t have the time to finish this book right now or in the near future.  I don’t have time to actively contribute to The Mighty and Stigma Fighters if I even attempt to finish my book.  Time is something I cannot buy extra of.  Working full time, being active on my daughter’s school’s PTO, advocating.  Nightly, I am left deciding if I have time to breathe or read my book for 20 minutes (the book usually wins out).

If I do not finish my book, am I still an Author?

Have I still made a longtime dream of mine come true?

I think the answer may lie in the grin on my face below.

I am Stephanie Paige, Author & Advocate.

Mommy’s Sick… Does Anyone Care?!

A few days ago I stayed home sick.  No, I didn’t actually have a fever, but my nose was constantly draining as if someone forgot to turn the shower off and my body was achy everywhere.  I was involuntarily stretching because of these aches and knew that I would accomplish nothing, zero, zilch, nada at work.  I was lightheaded and nauseas.  From the moment I woke up, I knew I was doomed.  I texted my boss and informed him I would be out apologizing because I have a project deadline approaching.  I then crawled up the stairs and informed my husband that he would have to drive our daughter to school.

“I’m sick.  Can you please drive Sophia to school?” I voiced weakly, “I’m dizzy, achy, and my nose needs to be permanently attached to tissues.”

I should’ve known what his response would be, after all I have been married to the man for over 12 years and with him for over 20, but I was still a bit awe stricken…

“Ugh, do I have to?!” he whined.

Really?!

I love my husband, really I do.  He really is my rock.  So many times my Depression and Anxiety have told him to leave, that he would be better off without me.  But he never did.  He stepped in as primary parent and let me get the help I needed whether in the form of visits to my therapist or psychiatrist, a phone call to my parents or even a couple of hospitalizations.  He truly is my best friend and an awesome man with exception to this one thing.

During my hospitalization for Severe Postpartum Depression and Anxiety 10 years ago, I finally learned I am not Wonder Woman, I cannot do it all.  I mean ALL is a considerable amount.  The media will have you believe that mothers can do everything.  I haven’t met a mother yet that does everything and those that come close usually have large quantities of coffee or wine in hand.  Once I arrived home from this hospitalization, I put the phrase, “I need help” to use.  I mean, I honestly needed help.

“Jimmy, can you help me with this?” I asked my husband.  For awhile, he did (remember, this was a decade ago).  Then he would get whiny.  Once he started to get whiny, I stopped asking for help.  Without asking for help, my Mental Illnesses got worse, but I kept them relatively under control.  After all, I was forever in debt to him for being hospitalized and leaving him with a newborn to take care of for 12 days… at least I thought I was.  Then, I was hospitalized again and once released, he and my daughter questioned me how they could help me.

Ah, finally, they were asking how they could help, not waiting for me to beg them.  This, unfortunately, didn’t last.  I was once again asking them for help, not a lot, and I was using “please” and “thank you”.  They are the magic words you know.  My daughter usually obeyed, but lately, with prepubescence, it is becoming more difficult.  My husband…

And we’re back to… “Ugh, do I have to?!”

I tried not to get angry by this response.  I was completely drained anyway, but inside I was beginning to boil.

“Yes.  Thank you.”

He proceeded to do as asked.  I then called him at work around noon, after a nap and forcing some food into me, to make sure he was going to pick her up from school.

“You’re picking Sophia up from school, right?” I inquired.

“What? Me? Why me?  You’re home.  You pick her up.”

“I’m sick.  I’m not leaving the house.”

And once again… “Ugh, do I have to?!”

When this is a response you constantly receive, it makes it hard to ever ask for help.

Then, he added, “What are you making for dinner?”

What?!  Yes, I know I am home, but really, I don’t even have a desire to eat.  After explaining if he would like his food with snot on it (because, hello, drippy nose), I hoped he would understand that dinner making was not happening from me.  That wasn’t the end of it though… somehow he did guilt me into marinating the steaks I wasn’t going to eat.  With tissues stuck in both nostrils and my hands lathered in antibacterial gel, I got the steaks marinating.

It didn’t end there.  When these two people I love to infinity and beyond arrived home, their understanding of Mommy being unwell left the house.  I was constantly needed for something.  I don’t understand… the two of them functioned fine when I was away on business a couple of weeks ago.  But somehow they can’t understand the idea of me becoming sick.  To them, if I am present in the house, I should be able to function at 100%.  This, too, was the case 3 years ago when I had the flu.  They both couldn’t fathom why I wasn’t cooking and cleaning the whole house since I was home.  At that time, I put myself in quarantine… for 3 days all I did was sleep, go to the bathroom, and munch on toast.

And now, the tables are turned.

Hubby left work early 2 days ago feeling icky, deep into a case of the ‘Man Cold’ with the symptoms I had.  For those who are questioning what the heck ‘Man Cold’ is, I am pleased to tell you.  ‘Man Cold’ is the common cold when it presents itself in male humans.  Instead of acknowledging that they have a cold, they think they are dying.  They believe their sneezes and coughs are much more than a common everyday germ.  They somehow get the idea that this germ, the germ us females have just had, has mutated into a superbug.  They will continuously whine about how awful they feel and try to make you believe that they deserve to sit on the sofa and binge watch Star Trek and Mythbusters.

He stayed home yesterday to nurse said ‘Man Cold’ and mainly because school was canceled due to a couple of inches of slushy snow and ice.  He questioned why I wasn’t staying home too so I could take care of him and our daughter. I just looked at him oddly.  Home all day and he didn’t even salt the walkway, driveway and sidewalk.  Made for quite a theatrical performance for me getting to my front door last night after work.

This is the same person that only a few days ago was having me drive my child to school, make dinner, clean, pick up the child from school and wanted to know why I couldn’t go to work.  But I don’t whine when he asks for help.  Why?  Because I am Mommy.  I am the caretaker and my heart aches when those that I love are ill.  I just want to help them feel better.

I am sure there are men out there that do not act like they are on their death bed, that do not suffer from the dreaded ‘Man Cold’.  But, I haven’t met one yet.  Anyone who is married or with one of this special men, hold onto them tightly.  They are a rare species.

I’ve Always Wanted To Be An Architect… And Other Shit 

I remember my first Lego set.  I was six and my family had just gotten back to my Aunt & Uncle’s house from the mall.  I am not sure why I wanted this set so badly, but I begged, I pleaded, and now it was lying on the floor of the bedroom I was sitting in.  It was a medieval boat that came with two men in helmets.  I stared at it in awe.  Could I build this?  At six?

I worked hard on it but sure enough, I completed it.  I stared at it in amazement thinking, Wow, I built this!

This teeny-tiny itty-bitty Lego set started it all.  I wanted to become an Architect.  I made a major life decision at the respectable age of 6.

Through the years, I challenged myself.  The sets got bigger and my time to build them got shorter.  I would follow the directions, quickly erect the Lego building, look at it with pure elation and then take it apart.  At this point, I would be my own creations.  I was, after all, a budding Architect!

As I became a teen, I shifted from Legos to hand drawings.  I would draw floor plans just for fun.  Soon, I developed into drawing the front elevations of houses.  I received several home plan books and computer programs for my birthday and holidays.  I even received a drafting table.  Yes, this is definitely what I wanted to do.

In the fall of 1998, I started the 4 year Bachelor of Science in Architecture degree at the University of Maryland.  I was on my way.  For the next few years, I lived in the Architecture building, taking a particular interest in my Architectural History courses.  I became fascinated with buildings, mainly homes, from the Colonial and Federal time periods.  I graduated in May of 2002 and after a month started my career in Architecture.

But, I was far from my desire to be a licensed Architect.  I kept my work records and when the time came, I began to study for the exams.  7 exams at over $200 each.  I took my first exam when my daughter was 2.  I anxiously waited for my results.  The day finally came…

…FAIL.

I was heartbroken.  I was also in the midst of my 5th episode with Major Depressive Disorder.  I decided to take a break and wait for my daughter to get a bit older.  After all, the 5 year rolling clock didn’t start until you passed one of the exams.

1 year after I failed the first exam, I took a different one.  I felt confident going in.  I felt happy when I left.  I felt defeated when the results came…

…FAIL.

The word ‘fail’ and the fact that I am an Alpha with perfectionist tendencies, didn’t ease this situation.  I decided then and there, I was done taking exams until I had the money to pay for the review courses and the exams.

Years went by.  My job growth continued, although minimally.  I began to really think about my career.  Would being licensed make a difference?  At that point, no.  My pay would not increase.  My responsibilities would not increase.  Why spend the money?  Just so I could put ‘Architect’ after my name?

A few years ago, I was struggling with my career.  Where I was working was affecting my Mental Health greatly.  It was not a healthy place for me anymore.  So I once again thought about the question:

What do you want to be when you grow up?

Suddenly, the answer was no longer Architect.  I had become increasingly interested in hiking and nature.  Being outside rejuvenates my soul.  Researching, I realized that maybe a career in Forestry, like becoming a Park Ranger would be for me.  Lacking funds to go get a degree in it, I decided to start small and take a Certificate Course in Forest & Wildlife Conservation.  Most of the material intrigued me.  And then reality set in… there were very little, if any, paying positions in the Northeast, and we were not moving.

Next up in line, a Groupon became available to become a Certified Personal Trainer.  I studied and miraculously passed the exam (an exam that most of its material was not covered in the books the course came with).  To this day, I am still certified.  To this day, I have not used it.

Why?  I changed jobs.  I found a job that still uses my knowledge in Architecture that I enjoy.  Is it my passion?…

…No.

I feel like we stress deciding a career so early in life.  Of course, I made the decision even earlier than necessary.  I graduated college when I was 22, but one had to declare a major by the end of sophomore year.  I look at my daughter now, and can’t even believe that in less than 10 years, she will have to decide what she wants to do with the rest of her life.  How can we decide so young with so little knowledge and experience on what life really is?  She is already starting to decide.  So far she has narrowed it down to Fashion Designer, Illustrator, and Teacher  (Fashionista dropped off the list a couple of years ago).  These are her current passions, but when she is my age (a few years shy of the big 4-0) will she still feel that way?  I don’t.

If I could turn back time (someone send me a Time Turner from the Harry Potter world), I would change my major, knowing what I would endure in the years to come.  Becoming an Architect would fade away.  After suffering severely with Postpartum Depression and Anxiety and with Major Depressive Disorder and Generalized Anxiety Disorder, advocacy is my new passion.  I only want to help others to not suffer the way I have and to get better.  I want others to know they are not alone.  I want to be one of the many people to break down the stigma wall, block by block.  If money were not an issue, I would go back to school now.  I would get a degree in Mental Health Counseling.  I would become a Mental Health Counselor.  Since money does not grow on trees, I will do what I can, maybe one day going back to school.

For now, I am an Architectural Project Manager who advocates for Mental Health and Maternal Mental Health through my writing. And, I am content this way.

A Depressive’s Day Of Feeling Depressed… And What It Means…

Everyone has days where they feel sad, hopeless, empty.  A day here and there when nothing seems to be going right. A day where getting out of bed is a struggle you don’t mind losing.  The good news is most people, typical people, wake up the next morning and are ready to take on the world.  They woke up on the “correct side of the bed”.  They can easily carry out their normal routines and enjoy things.

This, unfortunately, is not the case of a diagnosed Depressive.

I’ve been unwell for so much of my life, that sometimes I am unsure if I am actually better, if I have overcome the latest bout with Severe Depression and her sister, Severe Anxiety.  I can easily tell when I have clawed my way out from the quicksand, my head finally above the surface, but the last few inches seems like an eternity to rise from.  Living with these two, even when well, is a constant battle and a huge drain on my battery.

I fear mornings when I wake up and know I’m off.  I feel the melancholy taking over.  My heart is a void, all emotion down it’s drain.  I don’t want to move.  I want to remain in my bed.  Soft, yet firm mattress.  Warm blankets.  A cozy cocoon.  If I stay there, I will feel safe.  I know though, that I can’t.  Years of therapy and battles has taught me I need to force myself out of bed.

So I rise.

I walk, slow, feeling the weight of my body all pushed down to my feet.  It’s an extreme struggle to take a step, but I push onward.  Dragging myself to the kitchen, I carry out my routine starting with feeding the cat.  After, I climb the steps trying really hard not to crawl up them and enter the bathroom.  I plug my flat iron in and start it and brush my teeth.  The routine is killing me on the inside.  As I gaze at myself in the mirror, those horrible negative thoughts come back:

“Why get ready?  Why go to work?  They will be just fine without your worthless self”

“You’re look horrible”

“You don’t deserve love.  You don’t deserve your husband, your daughter, your family, your friends.”

I hold back tears, repeatedly telling myself that this is my Inner Bitch talking, not the real me, the real Stephanie, ultimately failing at convincing myself.

Somehow I manage to get dressed and somewhat care about my appearance for work, hiding my inner dialogue and turmoil from those around me with the elusive faux smile.  In 20+ years, I have become an expert at it.

I get to work, still sporting the fake grin, but once in my cubicle, it is shed away.  I become quiet, a recluse.  I do not want to leave the cubicle.  I do not want to interact with anyone for fear that they may see what is going on with me.  I just desire to sit in my chair all day.  On and off, I will fight back tears.  Sometimes a few will make their way down my cheeks.  I don’t care if the sun is out, if the weather is beautiful, I want to stay hidden, be invisible.

When I get home, I am exhausted.  Heart still empty.  Body still drained.  Mind still double-crossing me.  I permanently erase the smile as I walk through the door.  At this point, my 10-year-old daughter instantly notices and says to her father who is in the kitchen preparing dinner, “Mommy is having a Depression day.”  Yes, baby, Mommy is.

Dinner is spent with me looking down.  I play with my food.  Some of it makes it into my mouth.  I am not hungry.  I just want to go into my room and hide.  I have no desire to watch TV, read, pay games on the Kindle.  Even scrolling through my Facebook feed doesn’t appeal to me.  I just want to be alone, alone with my hopeless self.  When I finally am, at the end of the day, tears fall… and every negative thought I have or action I’ve done feeds them.

I take a deep breath, swallow my pills, and eventually fall asleep hoping that tomorrow will be “normal”.

A day that most people have once in a while, but I am not the typical person.  Most times, I do not wake up the next morning feeling better.  It can take me a week or more to wake up “normal”.  This frightens me.  Experts (Psychiatrists & Therapists) say that after two or three weeks of feeling like this, that you are entering a Depressive state, that you are clinical.  I am already clinical, so what is the big deal, right?  I am scared of another episode with the Severe sisters, Depression & Anxiety.  My episodes have only gotten worse as I get older.  This last one took just about 2 years to get through.  What would episode #7 do?  Would I survive episode #7?

This most recently happened to me in December (one of the reasons there were no new posts from me).  For over a week, ten days, I woke up likes this.  Over a week, I didn’t exercise.  I didn’t even take my daily walks at lunch that I love so much.  I was getting worried.  I saw my therapist during this time.  Even he looked a little worried.  He assured me that I could contact him whenever, day or night, if I needed to.

Then on the morning of day 11, I woke up fine.