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the Light and the Dark

Sometimes I can’t believe that I actually made it through college.  It has nothing to do with myself as a student.  I actually made the dean’s list semester after semester, eventually graduating with honors.
The reason I can’t believe I graduated or even went to college at all is my damning, irrational fear of contamination.  It was unbelievably difficult for me to move about the campus with literally thousands of other people.
I tried living in the dorms.  It worked successfully at my second university, the one I transferred to sophomore year, for about a semester.  My roommate was great.  She was a kind, intelligent, and very clean girl and I didn’t mind her at all.  It was when I heard girls down the hall talking about everyone getting sick, the illness seemingly spreading from one dorm room to the next that I finally decided dorm life was and never would be for me.  I moved out Christmas break and have been living with my boyfriend, in a quaint, yet impeccably kept apartment ever since.
There were days that I struggled to get myself motivated to go to class.  It was the fear, rather than laziness or sleepiness that kept me away.  I couldn’t make myself face the unseen demon: contamination.
Going to class was in itself an ordeal.  There was never a time that I was late, when I went, which was honestly not as often as I would have liked.  I had to make sure that I got MY seat.  MY seat was usually the one on one of the extremes of the room and always at the end, never in the middle.  I had to be sure that I could make a quick getaway if anyone was to become “ill” in class or if I became too overwhelmed, which was difficult because I was overwhelmed as soon as I walked through the doors.
I used and still use several coping mechanisms to deal with those times when I cannot avoid being near potentially contagious people.  I find that hiding behind my hair, head slightly bent down works well to create a feeling of escape, for a few moments at least.  My mouth usually becomes tightly sealed, making it a chore breathing solely through my nose.  While walking anywhere, I feel the need to wear a coat or a jacket because the compulsion to tightly clench my fists, embedding my nails into my palms is just too strong.  I don’t want people to see me doing this; hence I hide them in coat or jacket pockets.  I indulged in these routines to extreme degrees when I went to class.  I was far too tense the entire time and usually came home sore, weak, and with a headache.
My daily walk to campus usually took me by the counseling services center.  I looked at it daily, somewhat longingly, somewhat fearful, and for some stupid reason, embarrassingly.  I didn’t want there to be anything “wrong” with me, but I knew the things I was feeling just weren’t right.  Everyone around me at least seemed happy and carefree and seemed to care less if they got sick.  I, however, had these ridiculous and irrational thoughts of contamination on my mind nonstop.  It got to the point where it was ruining my life.
After one particularly terrifying, life-altering episode involving my potential exposure to a “stomach virus,” I made a phone call to the counseling services center and scheduled an appointment with a therapist.
Holy cow was I nervous for that first appointment!  I had never met a psychologist before in my life and was honestly terrified of the whole experience, but as soon as I stepped into her office, my fears subsided.  She was a friendly woman, who genuinely cared for my needs.  She asked me several, personal questions that I answered with no problem.  When it came to describing my fear, however, I had to write it on a piece of paper.  I can’t even say the word.  I fear that if I say it or even see it written that it will become a part of my life.  For the sake of understanding this blog, I will write the word: vomit.
It is my biggest fear.  I fear this normal, bodily function more than anything in the world, even more than death.   In fact, I even told this to the psychologist.  It seems that the things I told her must have been especially troublesome because she immediately had me schedule an appointment with the psychiatrist because she didn’t feel qualified to help me.
Weeks later, I met for the first time with a psychiatrist.  He was also very kind and knowledgeable.   He asked me questions too.  He made many puzzling faces throughout, but finally, he smiled. “Megan, do you sometimes feel the need to perform a behavior that you can’t explain the reasoning behind?”  I didn’t know what he was referring to at first, but he continued.  “I have heard people saying that they breathe a certain way, or touch their hair in a certain way as a means for relieving some of these intense urges, compulsions.”  It hit me then.  He’s describing me!  I told him that yes, I did and I told him some of these routines that I performed daily, such as intense hand washing, taking a shower immediately when I return home, and never eating anything with my hands, fist clenching, and symmetrical touching.
The session came to an end and he told me that he strongly felt he knew where my symptoms came from: OCD.  He told me all about the disorder, the symptoms, what can be done to relieve them, and the biological components of the disorder.  I shook his hand, left, and made a second appointment at the front desk.  The second appointment would be my introduction into therapy and medication.
I remember leaving the center after that appointment quite well.  Almost as soon as I left through the heavy, metal doors, the sun warming the top of my golden hair, I began to cry.  I was not sad.  Quite the opposite in fact!  I was absolutely elated at the diagnosis.  Finally, there was a name for why I did the things I did.  A lifetime of intense stress and worry was relieved a bit because of those three words: Obsessive Compulsive Disorder.  For the first time in a long time, I unclenched my lips in a public place and just breathed.
Best,
Megan from The War in My Brain

About 메간

I am just an average, American girl living with OCD. I share my struggles, but also the good things in life. Please feel free to share your experiences with me :) I love having visitors!

33 Comments on “the Light and the Dark

  1. Lucky Wreck
    February 20, 2013

    Awesome post, Megan! Your courage to write about this is really inspiring! REALLY!

    • Megan메간
      February 20, 2013

      Thank you so much :) I genuinely appreciate that.

  2. Honie Briggs
    February 20, 2013

    This is truly an inspiring story and it’s so wonderful that you shared it.

  3. "HE WHO"
    February 20, 2013

    Good for you, Megan. It’s great you’re getting some relief!

  4. Janet (ocdtalk)
    February 20, 2013

    Great post, Megan, and I’m sure it was a relief to put a name to what was going on with you. Now you know you are certainly not alone. Thanks so much for sharing.

    • Megan메간
      February 21, 2013

      It definitely was. I’m amazed by how much support strangers have given me :)

  5. jeanjames26
    February 20, 2013

    This was a really great post. I’m sure it will help others. Thanks for sharing something so personal.

    • Megan메간
      February 21, 2013

      I appreciate that. I can only hope that others get something from it. I wrote it for myself, but that’s always a plus :)

  6. sortaginger
    February 20, 2013

    Thank you for sharing this.

  7. Kylie
    February 20, 2013

    It can really help to have a diagnosis, because that can mean having a strategy. And also, not feeling so lost and alone. Thanks for sharing this.

    • Megan메간
      February 21, 2013

      My thoughts exactly. Otherwise it’s like walking around without glasses on :)

      • Kylie
        February 21, 2013

        And THAT is no fun. No fun at all.

  8. Lyssapants
    February 20, 2013

    I am so glad that the mental health treatment you got was compassionate and met your needs!

    • Megan메간
      February 21, 2013

      Me too. This isn’t always the case, so I’m thankful every day.

  9. philosophermouseofthehedge
    February 20, 2013

    YEA you! Hope things are brighter now. You aren’t alone.

    • Megan메간
      February 21, 2013

      Thank you so much for sending that support my way :)

  10. The Bumble Filese
    February 20, 2013

    Megan, I can see why you would be relieved at the diagnosis. I can see why it would drive you mad. Finally, some help. Good for you!

  11. Elyse
    February 21, 2013

    Well done, Megan. I’m so glad you found your reasons and got help with a solution. A close friend of mine has a daughter with OCD and it is a challenge for them all.

    • Megan메간
      February 21, 2013

      Thank you for that :) All I can recommend is giving your friend and his/her daughter as much support as you can because I’m sure they’ll be needing it.

  12. The Hook
    February 22, 2013

    You’re a brave soul, Megan.
    Thank you for sharing your private war.

  13. faithhopechocolate
    February 22, 2013

    Thank you for sharing, Megan. I hope and pray that your journey through this continues to be positive for you.

  14. Val
    February 22, 2013

    While mine’s nowhere near as bad as yours, I do have bits of OCD myself – particularly the obsessional part of it as once I do something I do it til I’m ill (stuff online particularly). And I had – but now have very little – the same fear as you of the you-know-what word and thing (I’ll avoid saying it in case you still find it a trigger). That’s mostly gone now.

    I hope things continue to improve for you and thank you for your courage in writing about it.

    • Megan메간
      February 23, 2013

      Any struggle is difficult and I commend you for opening up to me. I can relate. I clean until I make myself nauseated and/or get a headache. I hate that about myself.
      Thank you for the lovely comment :)

  15. theravenloon
    February 23, 2013

    I am so glad you walked in that door for help! Too many people don’t, and the consequences can be immense. I also have OCD, but not anything with germs. Mine is repeating a sequence of numbers and letters, forwards and back – until it’s perfect … which it never is. I also have an immense fear of the collapse of society, and am fanatic about survival supplies and skills. It gets to be exhausting.
    Just know you aren’t alone. I have it, my son has it, my husband has it; lots of people know what you’re going through. Stick with it, and keep the word out there. You are capable of great things.

    • Megan메간
      February 23, 2013

      And I’m so glad I did :) I have to persevere like anyone else and it’s comforting to hear from someone else who struggles with this too. Thank you for the encouragement.

  16. She's a Maineiac
    February 23, 2013

    Just having a name for what’s going must be such a huge relief for you. You should feel proud of how far you’ve come with your OCD and for going to see that psychiatrist. My husband had suffered from it in the past, but is much better than he used to be.Best wishes to you.

    • Megan메간
      February 23, 2013

      Thank you for sharing. I hope to come to a point in my life too where I can say that it’s not that bad :)

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This entry was posted on February 20, 2013 by in Guest Blogger and tagged , , , , , , .
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