Mandala

Mandala

Monday, April 21, 2014

Call me crazy, apparently that is still okay

So, my education is in psychology probably because understanding people is something that has always been interesting to me.  I have found that the internet is a great way for me to study my favorite subject.  Recently, I have thought a lot about conversations about acceptance and rights for all groups of people.  There is a group of marginalized people often left out of this conversation because let's be honest, we have to have some group to make fun of.  I am a part of this group, so perhaps I am hyper-vigilant about the language that gets used.  This is not a post about poor me, your words hurt me, because I generally let words just be words.  However, I hope it does serve as some food for thought.

I am a person who is living with Bipolar Disorder sprinkled with a good dab of crippling anxiety here and there.  This is not a badge I wear, it is just a fact, and I try to be as honest and vocal about it as seems appropriate because most people think that I am pretty "normal", and I want the stigma to go away.  That's where we get into trouble though.  You see, I wear the normal mask well.  I've done it most of my life, and I have good coping skills (with a healthy dose of pills), that keep me in the mainstream.  So people do not filter themselves around me.  People who know me know my story, but it is not how I introduce myself to new folks.  So I hear a lot of ignorant stuff.  

I have two lives that I have lived.  The first is pre-diagnosis, the second is post-diagnosis.  So in theory I am five years old in this second existence.  And being in a group of THEM is interesting.  I get ouchy about these words, attitudes, and general misunderstanding not for myself, but for my fellow mental health sufferers who do not have support systems in place, are homeless, are embarrassed, feel worthless, and do not know that it is okay for us to advocate for ourselves.  There are millions of people with mental health issues who are not managing as well as I am.  Perhaps my education in Psychology has helped me, perhaps I am more resilient, I do not know, and I guess that it is not all that important.  So I sometimes feel compelled to speak for the ones without a voice.  And so here is what all you "normal" folks should know.


  • Referring to someone as nuts or crazy or schizophrenic or bipolar is really not okay.  I mean you could call me Bipolar I guess because that is part of who I am.  But your boss having a mood swing does not make her bipolar.  Stop it.
  • If you are going to throw out a diagnosis for someone because of their behavior and because your degree in physics clearly makes you that type of expert, at least have a basic understanding of the diagnosis.  Schizophrenia does not really mean what you think it means.  Do some research.
  • You do not want anyone to use the word gay or retard or any of the words that we use to disparage another on racial identity, but crazy?  Go for it.  
  • Remember that mental illness is largely a silent disease.  Most people do not go around advertising it, so watch what you say to anyone in this regard.  You know not to tell a racist joke in certain circles because a person's skin color is usually pretty obvious.  Mental illness is trickier than that.  And the truth is, your boss may really be bipolar, and when she hears that you were joking about it, it could get uncomfortable.
  • Know that there are 10 million people in this country struggling with what the National Institute of Mental Health calls "serious mental illness".  I would argue that most MI is pretty serious, but I will not get into an argument of semantics here.  In any case, this designation means that the mental illness causes a severe impairment in the ability to "do life" the way that others expect us to get it done.
  • The above statistic refers to those cases that are known.  My experience would lead me to believe that is a lower number than the realily. Probably because so many people are scared to get help or seek treatment because it really does change the way the world looks at us.
Oh hell, I could go on and on, but I want to make sure that you finish reading this and you get the gist.  In January of 2009, my entire world turned on its ear.  I had a job that I rocked at most of the time, I had a one year old baby boy, I had a great relationship.  And then it all changed in the matter of a 24 hour period.  Everyone wants to know when I first suspected that I was crazy...can I steal the LGBTQ answer that I was born this way?  Because here is the thing.  If mental illness was due to life experiences like abuse or drug use, or any of the other ways the uninformed seem to think that mental illness happens, then I would not have one.  Now we could argue all day about genetics and why am I sick and my brother is not, but no one really knows.  I like to think of it as a time bomb.  Like it was always there...I was always a little nervous, I always worried more than most kids.  But when I track my symptoms, I generally think of my college years.  I went to an academically rigorous institution.  It was really stressful.  Sometimes I think that I had the stuff needed in my brain to make it happen, and stress was the lighter of the fuse.

I did lots of self medicating over the years to deal with all of the stuff my brain was doing to me.  And I learned to wear the mask. I worked in the field for crying out loud...allowing myself to admit a problem would have been calamitous both internally and externally.  Because the truth is that admitting to yourself or to others openly that you have a mental health issue makes a difference.  People lose jobs, lose respect, are questioned about their parenting ability, and so on.  I am not trying to argue that MI is in some way comparable or as bad as being in some other marginalized group.  But it still totally sucks.  And it sucks a lot worse for people who are not hooked up with quality treatment.

Mental illness often looks like drug addiction, or homelessness, wrecklessness and a host of other behaviors that make our friends and family mad.  We get told all sorts of ridiculous stuff about exercising more, thinking happy thoughts, pulling ourselves up by our bootstraps etc.  Yeah that's helpful.  I get that people do not know the "right" thing to say when I mention my illness.  So just judiciously keep your mouth shut, hug me, love me, offer to babysit my kid for a few hours.  But do not tell me oh yeah, my great uncle on my mother's side committed suicide.  That's horrible for you, but has nothing to do with my experience.  

I am asking you to do your part to change the culture so that it becomes okay for mentally ill folks to ask for help.  Educate yourself some so that you might be able to recognize when a friend or family member are screaming silently for help.  According to the website here there is a death by suicide somewhere on the globe every 40 seconds.  Almost 2% of deaths internationally are suicides.  That's some sobering shit.  My guess is that there are many reading this who know someone no matter how distantly who has committed suicide.  And the terrible thing is that it is 100% preventable.  

It is a systematic problem that is not going to be solved quickly, I get that.  But when we consciously change our language, we begin to think about individuals and when we think about individuals we think about their problems.  When we think about their problems, some of us feel compelled to do something about it.  That's all I am going for here.  Educate yourself.  Choose reliable websites.  I find that .org and .edu are good places to start.  I cannot be explained on Wikipedia.  Don't look there.  

When we use "crazy" words to describe behaviors that we find annoying, offensive or out there, the message is sent that mental illness is still not okay.  It is a weakness, it is the fault of the ill, we chose this for ourselves.  Our brains are attacking us on a minute by minute basis.  It is exhausting.  Be gentle, be understanding, it's not like we want to be out of the ordinary, it just is.

Some Helpful Links:

Good articles and online support group for the mentally ill and their caregivers

6 comments:

  1. Thank you, a beautiful and powerful reflection. I tend to refer to myself as "crazy" sometimes, and I don't think I will do that anymore.

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  2. I don't know that we can ever totally get rid of that one. It's pretty embedded in our language and has lots of different meanings. I use it sometimes in a self-deprecating way, and that's never any good, so it is something for me to work on as well. I particularly find it disturbing when people use actual mental health diagnoses like bipolar, shizophrenic, or borderline, which seem to be the main choices to label someone in a derogatory way. That's what really gets my lizard brain into a frenzy. We often say "it was like he had Tourette's, or that guy is OCD". In almost every instance, this is not used in any sort of flattering way. It is a group that is still okay to use hurtful language with and to have discriminatory attitudes toward. The stigma is crippling to the goal of having people get treatment. If you are lucid enough to realize the attitudes that people have toward it, you figure that it is smarter to just grit your teeth and muscle through. Eventually, the dam breaks. It always does in one way or another. Mine ended up necessitating a 10 day hospital experience. No matter how functioning you think that you are, going inpatient is a humbling experience. Will probably blog on that next. Thanks for reading and for the comment.

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  3. Hard for me to understand the stigma that comes with MI. Just seems common sense to me. If i break my arm, i go see a bone DR. If i break my brain, i go see a brain Dr. Simple right.
    My most recent visit w/my therapist was due to a particularly stressful divorce (aren't they all). But something really weird was going on with me. Felt REALLY out of sorts & disconnected w/people & at some level "reality". I had recently started a blog (helps me quiet my mind that never EVER stops) & i postulated that i had anti-aspergers syndrome (i felt that people didn't get me). As the disconnection intensified i educated myself on aspergers (at least enough to know i didn't have it) & self-diagnosed myself w/Schizoid Personality Disorder. Which as bad as it is, at least it was identified now how to deal with it.
    Made appointment w/therapist and she asks: "Why do you want to have a Personality Disorder?"
    I replied: "I don't 'want' to have one, but something is wrong & i need help."
    I had recently watched "The Kings Speech" & made the connection that if i could identify the problem (whatever it may be) that i could then learn coping strategies to deal with it. I expressed to her my real concern that i was (or was possibly going crazy) & that it scared me. She let me know i didn't have Schizoid Personality Disorder (if i did, i wouldn't have sought help as i would of thought i was just fine, everybody else had the problem). She then asked me if i had ever heard of the Myers-Briggs Personality test. Surprisingly as much as i have been intrigued by psychology & the fact that in high school i had become infatuated w/ Jung i was unaware of it.
    So long story slightly less long, i took the test. Found out that i am indeed different (arent' we all). That as an INTP i was a small percentage of people (1-5%). Good news was i could now study (which luckily is what this type LOVES to do) what it was about & figure out strategies for how to get around my weaknesses for dealing with people (one of which ironically is the internet, because being an INTROVERT big time, it is easier for me to find like minded individuals with which i can bond with.
    So, in conclusion. If anyone that is reading this ever feels out of sorts, do NOT hesitate to seek help. I speak freely among family & friends (both of them) about the fact that i have a therapist. It is important to me to remove the stigma that exists.

    Apologies for the length, but thanks for the article.

    @DaveGrigger

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  4. Hi Dave, I get the brain that never shuts off thing. I have the same issue. Insomnia is often a result. Thanks for sharing your experience and insights. I love people talking about it and not being afraid to put it out there. My heart aches for the people in my community who are not able to get treatment, or who have to settle on Medicaid accepting treatment which can be subpar in a lot of cases. We definitely need to do better. I have been reading a lot about veterans who are coming back and struggling so much but are worried to seek treatment. The numbers are staggering. Many thanks for your perspective and willingness to share it.

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  5. Replies
    1. Wow! thanks for that. interesting stuff, us humans & how we work.

      @DaveGrigger

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