Blog for Mental Health 2013 Badge Voting

The voting for the Blog For Mental Health 2013 Badge Voting is coming to an end. Tomorrow, I will tally up the votes and the badges will be decided. Cast your vote now!

Sunny With a Chance Of Armageddon

The new year of 2013 is coming upon us, and quickly.  Last year, I started Blog for Mental Health 2012.  For those that are unaware of what Blog for Mental Health 2012 was, I’ll fill you in quickly:
Many people who suffer from mental health disorders do so in silence.  And prior to many of our own blogs, we may have done just the same.  By taking the pledge to Blog for Mental Health in the year of 2012, we celebrate our own voices that speak up in our own unique ways.  We pledge that not only do we blog about mental health topics for ourselves, but for the inspiration of others to raise their voices and tell their own stories of their own personal experiences with mental health disorders.

For more information about Blog for Mental Health 2012, visit the page.

I fully intend on continuing this…

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Just Snap Out of It

Society has developed some seriously bad attitudes toward mental illness.  It’s no surprise.  We see it attached to the stigma of it.  We’re treated like lepers, as if this were a terribly contagious thing.

Depression is no exception.  Today, a lot of people have been discussing the topic of the “Just Snap Out of It” phenomenon that occurs out there.  Honestly, there is a saying out there about how if a person hasn’t experienced it, then they can never truly know.  A person who hasn’t experienced clinical depression, either in the form of MDD or BP depression can never truly know it’s depth and breadth.  It is an all encompassing monster that claims every last bit of life and any possible joy that can come from it.

Having Bipolar Disorder, I am a person who naturally experiences some sometimes pretty obvious mood swings.  And the attitudes toward it are so completely off.  I have never had a person treat me poorly while I was in a manic episode.  Not one.  Not even when the plainly awful behaviors were showing.  Each person seemed to find it charming, amusing, or interesting.  Even when there were moments where I was so out of control that I was scared out of my wits, not a single person around me seemed to notice that there was something absolutely wrong with it.

No, my energy and spirits were high.  I would act impulsively, and people would take it as spontaneity.  I’d be overly, annoyingly chatty, and rudely interrupting others, but they took it as being outgoing.  Everyone seemed to think that was a sign that I wasn’t depressed anymore.  They seemed to think that it was some kind of miraculous recovery from “being like that”.

People only seem to take notice when I am depressed or mixed, like it’s some kind of disease that I choose to be afflicted with.  And the comments are absolutely endless, because everyone seems to have their own opinion about it.  It’s as if they consider themselves to be the authority on depression, anxiety and sadness in general. I will constantly hear phrases like, “Get over it” and “Get a grip” as if just snapping out of it were an option for me.

Meanwhile, people without mental health diagnoses start flinging clinical terms around, like they had some true application to their fleeting, shallow emotion.  For instance, “Oh, I’m so *bipolar* today”, instead of just saying that they are moody, or women arbitrarily making a comparison between PMS and Bipolar Disorder.   Or “I’ve just been so depressed lately”, to reference a little bit of discontent or sadness.

It’s not cute. It’s not funny. No one with those diagnoses thinks that it’s witty that someone is taking a serious clinical term with so much guilt and stigma that it could bring down a religion, and applying it to their BS, frivolous emotions!

It does everything it can to minimize those conditions.  It puts it in a light that we have some kind of real control over it.  As if it were something that a person can just “snap out of”.  It implies that a person chooses to be disordered.  It also puts a shameful connotation of attention seeking behavior.

Yeah, it’s the life, let me tell you. If I were doing anything for attention, it wouldn’t be this. It would probably be something more hilarious, like plastering myself with an obscenely worded banner and rollerblading through Downtown. Depression isn’t newsworthy, but that sure is.  Or maybe I’d be doing something a little more productive or noteworthy, like finding a cure for cancer.  But no, my depression is just that interesting that I would choose to gain that much needed attention from people I don’t even know or care about.

I have to wonder if the general public has to be so naive that they would actually be jealous over it.  So much emphasis is put on the “just get over it” ideals, as if that were possible. If I could will myself out of this state, don’t you think I would do it already? It would be more logical to think that I want to reclaim my life and be a productive person.  But no, according to others who are ignorant enough of mental illness, I am perfectly content to have disordered behaviors.   Sure, who doesn’t love ignoring their kid because the voices just got too loud? Personally, I love gripping my ears and screaming, “SHUT UP! SHUT UP! SHUT UP!!!!”

And as a result of this blatant ignorance, I am really starting to believe that some are just plain jealous.  Because, they seem to think that those with disorder aren’t being responsible for their emotions and behaviors that result.  I certainly have quarrels with wanting to thrust a sense of selfishness and entitlement out there, because it’s what I have to do to take care of myself and my own in this world.  It’s those same people that shove themselves and their ideals down other people’s throats, only to make them feel bad. Misery loves company, and we’re perfect targets, right?

The point is this.  If a person is out there reading this and getting offended, it’s time to take a step back and think hard.  Is it so fair to be so judgmental?  Isn’t it about time to take a look from another perspective?  Does a person with a congenital disorder choose to be symptomatic?  It would be an entirely different story if I were refusing treatment, but like anyone else, I am keeping my appointments and taking my medication according to doctors orders.  We don’t blame someone for their symptoms when they have a seizure.  Why should this be any different?

Let me assure everyone.  If could have snapped out of this disorder and been a “normal” person, I may have done it, instead of living this ongoing nightmare.

A Writer or a Hack? : 30 Days of Truth

Day 11 : Something people seem to compliment you the most on.

(Note:  I started writing this two months ago)

This prompt could not have come at a better possible time.

In my real life, there isn’t much I get complimented on. In fact, I just asked my husband his thoughts on this prompt. His response? A poor joke, followed by a, “I don’t know.” CoF, seriously, I think C.S. needs some husband boot camp.

All of the little girls at work love my hair. An elder creeper, insisting to talk to me despite me clearly wearing earphone and typing on WordPress for Blackberry, told me that I had pretty eyes. I was pretty glad the bus pulled up to the curb moments later.

Otherwise, I get quite the opposite of compliments. It’s okay, I’m used to it.

Here on WordPress, and especially everyone involved with the dialogue happening here on Pendulum, and on our local mental health blog A Canvas of the Minds, compliments are plentiful. I will spare details, mostly because I am embarrassed to talk about myself. And secondly, because I’m not sure I can completely believe it. I sit here and think, “If you only knew me.”

I find that I am most complimented on my writing.  Believe me, I am ambivalent to share that for a number of reasons.  First, I know that once a person reveals what appears to be a strength, it is preyed upon.  In my youth, I was eager to display my intelligence and talents.  There was always at least one person who was eager to take me down, either out of jealousy or just to prove a point of fallibility.  Next, I am often unsure of how much truth there is in identifying a strength or talent.  There is always some doubt and question of the validity of such a claim.  What is the measure?  Is it a popular opinion?

And finally, there is the self-doubt / humility aspect.  I do not make any claim that I am better than anyone else.  I am by no means a brilliant writer, and clearly not in the league of literary greats.  Hardly by the standard of journalist and even fellow blog authors.  I am not making an attempt to solicit compliments by saying these things.  I am only stating that I have serious doubts as to the claims made of any talent I possess.  However, I will not refute any opinion, favorable or unfavorable.

However, if there is one literary strength I have, I do know of it.  I have always possessed an uncanny ability to find a verbal expression for emotions, thoughts, and experiences.  Most often, I have had people approach me and say, “You grabbed it right out of my head, as if you lived in there with me.”  Some ask, “How do you find the words?”  To which I reply, “I really don’t know.  It just comes out.”

The answer is absolutely honest when I provide it.  I am unable to identify the mechanisms that produce the detailed emotions and internal experience.  Imagination?  Experience with the experience / emotion / thought itself?  Education?  Really, it is just something that was always there.  But, I will admit that it is a craft that I’ve unconsciously refined throughout the years, just by practicing what has been just a hobby throughout my life.

I’ve mentioned this before.  My poor eyesight has always been kind of a handicap for me.  Back in my youth, my family could not afford to provide me with glasses more than once a year, or once every other year.  Often times, I would have to wear an outdated prescription for an extended period of time, as my eyesight deteriorated.  Sometimes, I would break a pair by accident, and I wouldn’t be able to get a new pair for upwards of a year.  I learned to see and identify things by shape and color, rather than fine detail.  I could identify people by voice alone.  And one of the only hobbies I could really do without any difficulty was reading and writing, because I could only see about as far as my hand could go in front of my face.  (Note:  My vision has deteriorated so badly now that I can’t even see my hand as far as my face.  In fact, I can’t even see a book at a normal distance.  But, I have the means to correct my vision on my own now.)

I suppose I could consider it a talent, although I’m not sure how I stack up.  I guess I should worry less about a basis for comparison and just do what I do, the best way I know how.

Finally, I’d like to thank the readers for their encouragement to write.  Sometimes, it’s just a matter of necessity for my mental health.  There are other times, like these projects, where it is a matter of a pleasurable hobby.  And other times, most of the time, it is a way for me to get my message out and have a sense of purpose when it comes to my own mental health.  I do not want to feel as if my suffering is in vain.  I do not want anyone to ever have the feeling that they are alone in their own struggle with mental health.  That is the worst feeling in the world, the loneliness, isolation, and fear that accompanies it.

Thanks for giving me a place to do this, encouragement to keep on, and an audience to hear me.

Blog for Mental Health 2012 : Official Blogroll Summons

Hey mental health bloggers!

So, I figured out how to put a blogroll together, finally.  I’m about to put the Blog for Mental Health 2012 Official Blogroll together, and I need to know who has pledged so far.  I know there are a number of people.  Some of you may not be aware of Blog for Mental Health 2012, because maybe you’re newer.  Click the link, or peep the badge on Pendulum’s site.

Don’t be fooled by this badge:

That one doesn’t belong to us.  In fact, as you can see by the date, this badge came well after our New Years pledge to blog for mental health for the entire year, instead of just one day.

No, our badge is different and shows a commitment to blog for mental health awareness throughout an entire year, faithfully.

This is the badge that belongs to us.  If you want to participate, I’m officially sponsoring you right now.  Click the image to go to the blog page for Blog for Mental Health 2012’s rules and terms of use.  I’m more than happy to spread mental health awareness by lending my support to other bloggers and inspiring others to come forward.

I am proud of all of the bloggers that have already taken the pledge, and am more than happy to invite others to take it as well.  It’s still 2012; you can still join!

So, if you want on the blogroll, leave me a comment below, something to the effect of, “I have the badge” and “I made the post” or “I want in”.  Whatever, just something to know that you’re in on it.

Thanks!

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Invitations to Narnia : 30 Days of Truth

Day 05 : Something you hope to do in your life.

As it stands, one can find me within the wardrobe amongst the coats, between the real world and my Narnia. This is not the Narnia as others know it. It is the absolutely surreal, ever shifting landscape, containing both horrific monsters and beautiful, majestic creatures. All of that world is tucked away, within a wardrobe, in an innocuous cranny of my home. Many unsuspecting people could stroll up to it, jam their coat in, and never give this unassuming wardrobe another thought.

Lunaria

But, this world is not meant to exist tucked away.  This world lives inside of me, wrapped up in an old world map, tied with a satin ribbon.  It waits to unfurl for all of the world to see.

Snapshots of this map are contained within every word, in each piece that I carefully create.  Some have been privy to view them, scanning the terrain, gazing upon the horrors and magesty.  Others have been lucky enough to set foot on the Terra Amici, The Land of Friends, specifically set aside to welcome guests who have braved the Sea of Aliquim.  And others, those closest to me, have journeyed through the deepest, darkest places of Lunaria.

I dream of the day that I allow Lunaria to emerge from the wardrobe.  This is the day that the earth will quake around me to birth Lunaria from within.  I will invite others to explore at will, without the requirement of the confines to Terra Amici.  To brave the fiery mountains, volcanoes spewing molten rock,shifting and shaping the landscape daily.  The mountains grow higher, only to be whittled away by the erosion.  Bask in Bad Wolf Bay.  Peer deeply into Mare Demersi, but still fear to tread too closely.  Lose themselves in Vac Saltus, and navigate the sullen, sunken lands of Val Mergullado.

All of this, one day will be accessible to all.  Lunaria will rise.  I can openly narrate the tales and history of Lunaria without fear of persecution and ostracism.  I hope to accomplish my quest of bringing this all out of the wardrobe.  I want others to see what my world, one world of a woman with Bipolar Disorder looks like.  It possibly connects to other places, to weave a global patchwork of personal worlds, connecting us all, to encompass every single person who has been hiding their own Narnia.

I hope to have a voice that can bring this all to the world.  And I hope to build the strength to do it.

Not Your Usual Serving Of Canvas

As some of you might not be well aware, and you’d probably be correct at this point at any point in confusion, I am a co-founder with Ruby Tuesday and a writer for A Canvas of the Minds. The following is a post on Canvas that request every mental health bloggers help for Mental Health Awareness.

via Not Your Usual Serving Of Canvas.

Thank you for your support in advance.  I would guess that everyone who is involved with Blog for Mental Health 2012 would be interested in joining Canvas and participating with us in our time of need of your support!!!

Every New Beginning . . .

. . . Starts with some other beginning’s end.

Yeah.

Here it is.  The original pilot for my blogging.  And I’ve invited it to take over as my flagship.

I was talking with some dear friends about the direction Pendulum had started taking.  It started out with a simple premise.  Many people with mental health disorders do so in silence.  Pendulum, for me, was a way of breaking that silence.  Not only for myself, but in order to help others who might be suffering in their own silence.

It had started to greatly deviate from the original idea.  Sure, I had maintained my monologues.  But, as I described it someone dear to me, “Pendulum has become more of a bitch blog than a mental health focus blog.  I have never, never wanted a blog like that.” I was not relating my stories.  I was just detailing them like some kind of rag sheet.  I lost focus.

It had also become a sore point of disclosure in my relationships with others.  While I might be comfortable divulging my dirty secrets to the entire world as a means of confession and release, others were simply beyond uncomfortable with it.  Pendulum had become something that violated a certain sanctity, and became a serious communication block.  While I have always left it public for anyone to look at, it sucked the intimacy out of having those tender conversations with those that I love around me.

Yes, Pendulum was created as a means of building up the support network that I was sorely lacking.  However, I became too reliant on that support network, and completely lost focus on building the network around myself.  It became a means to isolate myself from others who are supposed to be those closest to me.

So, here it is.  Sunny with a Chance of Armageddon.  Relating my emotions and disorder(s) that surround them from one end of the spectrum to the other, and allowing for everything in between.  Because that is another thing that had began to impress itself deeply into me.  I lost sight of all of the grey area, attempting to tidy my confusing world by putting things in nice black and white labeled bins.  It doesn’t work like that.  All of the colors of the world exist, and should continue to exist in my world.

The premise of this blog is simple.  For the ladies out there, they’ll understand the analogy.  Carrie wrote Sex in the Cityrelating events in her life to a bigger picture and asking the big questions.  When applied to mental health, the premise is the same.  I am going to focus on writing about more of the general, practicing reflection, and only detailing what is necessary.

I hope everyone enjoys this blog as much as they did Pendulum.  I will not be taking Pendulum down, as it will continue to serve as my archive.  However, I will no longer be writing it.  I have pulled several of my most read pieces from Pendulum here for easy reference.

The Bipolar Language

How do you describe bipolar disorder to others who do not have it?

Most of the population experiencing bipolar disorder have heralded it as something “people can’t fully understand unless they have been through it.”  Being a member of that group, I can wholeheartedly agree. In my personal attempts to convey the complexity of bipolar disorder to a non-Dx person, I have found myself at a loss for words that would do it justice. Describing emotions is putting the intangible into context.

And so much more.

Even when I am successful at touching upon the idea, I am largely incapable of even scratching the surface. The intensity, duration, debilitation, and so many other aspects seem to get lost in translation. Non-Dx people are mystified. “I feel those things, too.” Every human being has emotions akin to those that are experienced within the spectrum of bipolar disorder. Non-Dx people cannot wrap their heads around the magnitude of what creates the dysfunction. “I can control them. Why can’t you?”

Frustration ensues. Such miscommunication is an extreme aggravation. Tempers may flare. “It’s not the same thing!” It’s the same animal of a different color. In essence, similarities can be drawn, but a fault line exists between the two.

I am empathetic to the plight of a person who suffers with bipolar disorder. I have experienced the rage that boils when I feel as if I a being dismissed or preemptively judged against an unjust standard. The words above send me into elevations, like a volcano spitting lava high into the sky. At this precise moment, communications break down entirely. All hope is lost. If the villagers don’t evacuate now, total destruction is eminent.

On the other hand, using descriptive language devoid of passion fails to drive the point home. To a non-Dx person, it is any regular conversation. Words are words. It does not have the demonstrative power of action. However, action is often misinterpreted more so than words. Too many questions arise. Why? Now, we’re right back where we started.

And extreme action is likely to be met with animosity or apathy. It is ironic that when a person has a severe bipolar episode, others often fall short of providing the appropriate responses. I’ve often encountered loved ones who laid certain claims; “I am not going to tolerate this behavior.” – “Get a grip.” – “I refuse to talk to you when you’re like this.” – “Get over it.” – “Are we going to go through this, again?” Resentment. That is what perpetuates throughout repeated episodes.

The schism between people with bipolar disorder an non-Dx people grows in breadth and depth. Communication is endangered, if not completely extinct. Isolation begins, and episodes worsen. Without a support system, a non-Dx person is likely to crumble. A support system that is non-existent in the life of a person with bipolar disorder is the quickest route to utter annihilation of oneself.

I have been there. Then, I managed to navigate my way back again.

Back to the original question. How do you describe bipolar disorder to a person that doesn’t have it?

In my experience, I have worked it out. Non-Dx people do have strong emotions. These are in response to serious situations. To them, they are overwhelming; to me, it would knock me flat.

I allow the non-Dx person to draw the comparison between emotions. It is a good jumping point, although it is likely meant as a retort coming from their end. “This is not an argument. This is a discussion,” I remind myself repeatedly when tempers start to flare. I continue with the following points:

My brain chemistry is unique in the way that I become particularly reactive. That is one of many facets of bipolar disorder. Extreme sensitivity to situations that provoke strong emotion.

This may be met with a usual, “Grow a thicker skin.” or “Let it slide.”

I continue:

Recall a situation where you felt strongly about something. Like, when someone very close to you died. Or, you lost your job. Or, you found out that the love of your life cheated on you.

Okay.

Weren’t you very distraught? Even extremely sad?

Yes.

Imagine having those feelings arise without cause. Then, consider what it would be like to live months like that.

That is how I relate depression. Extreme feelings of worthlessness, sadness, and despair for long periods of time.

For hypomania, I continue like this:

Now, remember a time where you felt the best you ever did. You got a promotion or bought your first car or house. Maybe the day your spouse said yes to your proposal or the day you got married.

Yeah, those were some great times.

Now, think of what it would be like to feel that way for a long time.

That sounds awesome!

Sure, but think of a time where you were the most angry you could ever be. Someone you love lied to you or stole from you. A co-worker betrayed you and threw you under the bus. Your boss unjustly blamed you. Think of a time where you just wanted to scream and break things.

That’s the other side of the feeling good. It is being really irritable or angry constantly for a long time.

Oh, that’s not good.

No. But that’s not all. What would it be like to never really know for sure how you’re going to feel? Pretty scary, maybe? And worse, you may never know how long you’re going to feel that way.

That’s part of living life with bipolar disorder. Did you ever have a time that you did or said something you regret because you lost control for a minute?

Of course!

That’s what an episode is like. Struggling for control, every single day, because you can’t help the way you feel.

It puts the person in your shoes for a second. It helps them cultivate an understanding of the intensity and duration of human emotion that creates the dysfunction. This dysfunction has a name. It’s called bipolar disorder.

Now, I want to know. How have you gone about relating your disorder to others? It doesn’t have to limited to bipolar disorder. Non-Dx people and people of different Dx’s all have trouble relating to disorders. How do you explain what you experience?

Blog for Mental Health 2012

Blog for Mental Health 2012 Project
Clearly, I am a mental health blogger. I have been dedicated to sharing my experiences with bipolar disorder for nearly seven months now. That is my primary focus, though I have a tendency to get a little off topic from time to time.  Not only is this therapeutic for me, but I hope that is can be an inspiration for others who suffer with mental health issues.  This is especially the ones who do so in silence.  Every voice is important, as it collects and makes our community’s voice stronger.

This is the premise for Pendulum, as written in the About This Blog page:

Many people suffering from Bipolar Disorder do so in silence. Prior to this blog, I could have included myself. This blog is meant for others to experience living with this disorder the way I, and many others, do. It is also for others to find their voice here and to know that they are not alone in their struggle. Lastly, it is to encourage dialogue and community between bipolar bloggers.

Sometimes it’s interesting. Sometimes it’s sad and at other times it sounds crazy. Grab the pendulum, and hold on for dear life. Otherwise, you just might end up in the pit.

This morning, I found myself interested in an official blogging project to raise awareness for mental health education. I sifted through Google for awhile, unable to find anything like it. And I thought, “Why don’t I start one?” It would be easy! All I would need to do is produce a graphic and some instructions.

The badge above is featured on Pendulum’s homepage, because I am dedicated to continue blogging throughout 2012 for mental health. So, here are the rules.

1.) Take the pledge by copy and pasting the following into a post featuring “Blog for Mental Health 2012″.

I pledge my commitment to the Blog for Mental Health 2012 Project. I will blog about mental health topics not only for myself, but for others. By displaying this badge, I show my pride, dedication, and acceptance for mental health. I use this to promote mental health education in the struggle to erase stigma.

2.) Link back to the person who pledged you.

3.) Write a short biography of your mental health, and what this means to you.

I have been symptomatic of Bipolar Disorder and Anxiety for most of my life. I was incorrectly diagnosed with MDD in my teens, and suffered in silence. After my son was born in 2008, I went on to experience a severe relapse in symptoms considered to be postpartum psychosis. Several months later, I sought treatment and was diagnosed with Bipolar Disorder II.

That was almost three years ago now. Today, I am experiencing the longest stable state I’ve ever had, going on three months now. I am still hesitant to say that I am in remission.

This pledge is my opportunity to commit to mental health awareness. I can publicly display this badge to instantly tell my audience what this is all about. And, I can encourage others within the mental health community that have a Dx to do the same.

4.) Pledge five others.

I am pledging give of my fellow bloggers who have stood with me, and have proven their medal in my eyes as mental health bloggers.

  1. Ruby – I Was Just Thinking…
  2. FracturedAngel – The Mirth of Despair
  3. Monday – Manic Monday
  4. Vivien – Manic Muses
  5. Sarah – bi[polar] Curious

If you happen upon this without being pledged, I still pledge you. Feel free to take the pledge! Promote awareness!