
Thanks to both Larry Parker, who now has a blog, and Lilit Marcus for directing me toward Liz Spikol’s mental health blog, "The Trouble With Spikol." I have so enjoyed following her blog because (not totally unlike me) she is brutally honest. A woman who tells it like it is … that’s Liz. And I love that about her.
Liz is senior contributing editor of "Philadelphia Weekly." She writes the award-winning column "The Trouble With Spikol," which began as a chronicle of her struggle with mental illness, and has since expanded into humorous musings on everything from graphic novels to how to use a mop. She also writes the paper's book review column, Lit Gloss. Her blog -- named one of the Top 10 Bipolar Blogs of 2007 by PsychCentral -- is about mental illness policy, news, personal journeys and more.
You can check out Liz’s video blogs by clicking here.
1) For your Nov. 21, 2005 post, you wrote:
I write a column called "The Trouble With Spikol" for Philadelphia Weekly. It's often about my struggles with mental illness, specifically bipolar disorder and OCD. I was also diagnosed with dissociative disorder N.O.S.--which means I suffer from intermittent depersonalization and derealization. Blah, blah, blah--check the DSM-IV for more.Here are the meds I take: Seroquel, Lamictal, Ativan, plus Melatonin for sleep. The meds have saved my life, though I need to add an antidepressant to the mix soon.
I want to write here in a quirky and penetrating way about what's going on with mental health in this country: medication issues, insurance coverage, stigma, prejudice, stereotypes, substance abuse, co-occuring disorders, diagnosis problems, legislation, psychiatry vs. psychology, electric shock therapy, new treatment options, and more. I'll also chronicle my own experience.
How did you arrive at that mission? Anger? Frustration? Desperation? What gave you the courage to “come out” publicly. I know from personal experience it’s not easy, especially when you’re surrounded by Tom Cruisish friends and family trying to persuade you that your meds are toxic. Was there one moment that you said to yourself, "the hell with it, I’m going to tell it the way it is."
It was inadvertent, really. I was working part-time as a proofreader at "Philadelphia Weekly," trying to do something to get back into the working world after having been on disability. While there, I was given an opportunity to write a teeny little blurb about having an Easy Bake oven as a kid. The editor of the paper, Tim Whitaker, loved the blurb. He thought it showed great promise, even though it was about 150 words. He asked if I wanted to write a column. Every week. About myself. Um, okay. Give it a try, he said. Write about Liz. The life of Liz. Little did he know the life of Liz was seriously pathetic at that time.
So I wrote a bunch of samples that had nothing to do with the real me but that nicely obscured the fact that I’d been struggling with a mental illness for the past seven years or so. I brought the samples with me to coffee with Sara Kelly, Philadelphia Weekly’s executive editor, and she was lukewarm about them.
Finally, I just told her the truth. "The reason I don’t have anything to write about it is because I’ve been struggling with a mental illness for the past few years and haven’t had a life. So I don’t even know where to begin in terms of being a normal person." Sara said, "That’s your column, right there."
And thus "The Trouble With Spikol" was born, as a newspaper column. (The blog came several years later.) I was lucky in that my parents were very supportive. They always told me to write my life as I knew it, as honestly as I could. My dad was a writer and editor when I was growing up, so it was the family trade. My parents were thrilled, and they never ask me to censor anything.
2) In my humble opinion, I think what makes your blog top-notch is the combination of valuable resources you give your readers, your commentary on pop culture regarding mental illness and its stigma in this country and around the world, and your own very dramatic and interesting personal experience. Plus, of course, your writing skills. But few people who have been as disabled by a mood disorder as you have—eventually seeking relief in ECT—can function so well on a professional level. I’m amazed. What’s your secret? (Not that this is “Parade” magazine.) If you had to name three things that you remember or do everyday to keep you out of the hospital, what would they be?
1. Take my meds.
2. Take my meds.
3. Take my meds.
Le me elaborate. Every person is different, so it’s unfair to say that taking medication is the answer for everyone. For me, the medication is the foundation of my sanity. Without the medication, everything else falls apart. But let’s say we’re taking the medication for granted. Here are the additional things that keep me out of the hospital:
1. See my psychiatrist every two weeks.
2. Never drink alcohol or use recreational drugs.
3. Get enough sleep.
4. Stick close to a daily routine that involves seeing other people who are expecting to see me, so I feel like I exist.
Oops – that’s four. But what’s number 5? Be nice to myself, and forgiving!
3) I’m also curious as to how you and your psychiatrist decided on ECT (electroconvulsive therapy). I almost went that route after 22 medication combinations failed. Luckily for me, the 23rd was the ticket! How many medication combinations did you try before ending up on the gurney? Or were you so suicidal that you didn’t have time to wait to see if the next combination would work?
Ah, the med-combo roulette. Lovely, isn’t it? I never stopped to count, but it was years and years. I had tried everything.
I was so suicidal for so long, I simply couldn’t bear it any longer. I was ready to die. I had been in and out of the hospital, had attempted suicide, had been officially labeled "treatment-resistant," which after a few years felt the same as having “hopeless” stamped on my forehead. I was desperate. I told my mother I’d kill myself if I couldn’t try ECT. She had no choice but to agree. ECT was misrepresented as a sort of last-resort treatment, which suggested it might work for more than, say, four weeks. It didn’t. Oh, and no one mentioned my memory would be shot, and I’d lose cognitive functioning.
Later, when I was writing an article about ECT, I called the doctor who’d performed the procedure on me years before. I called him as a journalist, not as a former patient. I asked, “What happens to a patient with dissociative symptoms who gets ECT?” He said, "A patient with dissociative symptoms should never be given ECT." I said, "But I got it, even though I had those symptoms." He quickly ended our phone call. Suffice to say, ECT wasn’t a positive experience for me. But I know for others, it’s been life-saving. I just wish people knew more about before they went into it.
4) I’ve watched a few of your video blogs and you look so comfortable in front of a camera. Move over "Lonely Girl." Personally I’ve struggled a bit with video blogs because they have been one more level of self-disclosure. As you know, it feels a bit like stripping in front of your readers (not that I have experience stripping). How has it been for you? Is it more challenging and time-consuming than writing? Why did you decide to do it?
I’ve always been a bit of a ham. I was one of those kids who loved to be in plays in musicals in school, starting in kindergarten. If I could be onstage, I would. It didn’t matter if I was just playing the triangle, I wanted to be up there. I’ve always felt more comfortable doing public speaking than chatting one on one at a party. Give me a lecture hall with 300 people and I’m completely at ease, even if I’m talking about very personal things. Self-disclosure doesn’t scare me. Hiding scares me. I hid what was wrong and ugly about myself for so long, and it almost killed me to be alone with all that pain. I want to live in the light now. How can people help you and love you if they don’t know you?
5) One of your videos was on weight gain. And you raised some excellent points. At the time you taped that segment (a year ago, I think?), you were feeling really depressed but you didn’t want to go up on your Effexor because of weight gain. I can empathize. I, too, was on Zyprexa for a month and managed to gain 20 pounds in that time. I said to my psychiatrist that, as a person with an eating disorder in her past, I’d take suicidal thoughts over the fifty additional pounds I was about to gain. It’s such a fine line. Any words of wisdom to the depressive who has packed on the pounds to stay sane?
If you ask me, this is the worst thing about dealing with psych illnesses (other than the madness itself): the weight gain. Zyprexa? Oh my god. I gained so much weight on Zyprexa. Right now I’m on Topomax to bring my appetite under control because I did have to increase the Effexor. I mean, ultimately, it’s impossible to live with suicidal depression. It’s easier—though just barely—to live with extra weight. But I have no words of wisdom. I struggle with this every day. It makes me angry and miserable. I play the piano and that’s very important to me. Yet if you told me that, for one pinkie finger, I could stay at a perfect weight for the rest of my life and never have to worry, I would not hesitate. Isn’t that twisted? So yeah, no wisdom here.
6) One more question. What’s gives you the most joy in your life? I realize that I sound like Oprah here. But seriously, what motivates you to get out of bed on the hard days?
Cute Overload.com. If nothing else, I have to see what the daily cuteness is on that website.


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Comments
In reference to asking Liz to name three things that she remembers or do everyday to keep you out of the hospital, what would they be?
1. Take my meds.
2. Take my meds.
3. Take my meds.
I appreciate her emphasis on this issue.
I read a sidebar on another bloggers philophy on Depression, etc.
One bullet point was -
"Be careful! Medication can have lasting side-effects."
and I'd like to add to that, Suicide can have permanent ones.
For me, without meds to this point, I would have committed suicide either overtly or as a by-product of "self-medicating" with excessive amounts of alcohol or other substances.
I do not enjoy or relish taking meds. It was not a goal of mine as a teenager, looking off to the future as part of my life. Gee, I hope I develop a severe mental illness and require a difficult journey of medication. It just is, and I suppose in all of the imperfectness in the "hunt and peck" process for any of us seeking help with a physical illness involving different types on the spectrum of mental illness, along with unwelcome side effects, it is a better alternative than trying to overcome what was "tougher" than me and fight me to the finish of my death without some "backup".
I realize this is not everyone's experience. Some people's level of depression or type thereof is simple enough or short term in nature where behavior modification and cognitive thought reframing, exercise and food changes are enough to heal. Wonderful. Those are the blessed creatures.
I am also blessed, as I have these imperfect medications, which I've already taken this morning, which allow me to read and write, be an worker and hopefully a contributor of goodness in life; along with being a wife and mother. I know my children's life experience would be forever altered should I choose to eliminate meds. I would ultimately wind up driking alcohol to slow or stop my brain, and if not institutionalized, would probably become an old term of "wet brain" or most likely dead.
I know my own history and patterns, and the saying "Insanity is doing the same thing over and over and expecting different results". That would be the true insanity for me. I don't look at myself as insane or nuts or crazy or less than because my being currently requires assistance in the category of psychiatric meds. The same as I look at any meds I currently need for other illnesses.
I am no pill-popping lover of being a victim or slave to pharmaceuticals. Nor did I embrace a number of other illnesses in my life and the medicines and their side effects. However, in this area, I resisted for longer than I should have. I think back to generations where people didn't even have the choice of medication. Many were the relatives that were put away; never to be seen or heard from again. Today, although far from perfect, as are we, there are choices. I know what a living hell it is to find a workable solution (not pefect, workable), which can decide to not cooperate with our body chemistry after a period of time, but I guess up to this point, I wan't to live more than I want to die, as I keep trying.
I have the following scripture above my computer on my bulletin board in my office - Isa. 40:31
For those who wait on the Lord
Shall renew their strength;
They shall mount up with wings like eagles.
They shall run and not be weary,
They shall walk and not faint.
Well - while I'm waiting, I'm doing my part. Some days I do it better than others, and some days I no longer want to wait. I do get weary and can bearly walk, let alone run. I cannot lift my arms above my head, let alone mount up with wings like eagles.
That's where faith, hope, trust in the process comes in. The Lord's Prayer - "Give us this day our daily bread". I am provided with the guidance, strength and direction just for this one day. It's all I've got. When I stay in the day and not jump into the fear of the future, I have a chance of having a decent day. Even when it's not decent, and I feel as though I have not been "given my daily bread", I pause, I pray, and yes, sometimes I just downright cry from the magnitude of it all.
So my wish is that we all have a peace-filled day; from the simple things to the larger tasks at hand (Larry - may God hold you in the palm of his hand on your transition today - keep you safe and feel the comfort of his care); that we may all come back to this sacred place of Therese's "Beyond Blue" to share our experience, strength and hope, and lift each other up and along our way.
Posted by: Nancy | November 3, 2007 9:46 AM
Nancy, I wanted to thank you publicly for your kind wishes.
I also sent you a private message sharing my gratitude as well.
Posted by: Larry Parker | November 4, 2007 1:00 AM
Therese...... i tried to sign up to receive your blog in my inbox....I dont want to miss even one of them!! i was directed to Feedburner to fill in a group of letters of the alphabet which i did. but each time i filled in one set another set appeared....and there seemed to be an infinite amout of them and there was no end to them. what do i do next?
Posted by: Kay | November 4, 2007 4:54 AM
re: So my wish is that we all have a peace-filled day; from the simple things to the larger tasks at hand (Larry - may God hold you in the palm of his hand on your transition today - keep you safe and feel the comfort of his care); that we may all come back to this sacred place of Therese's "Beyond Blue" to share our experience, strength and hope, and lift each other up and along our way.
Posted by: Nancy | November 3, 2007 9:46 AM
Yes! We never know who will hear/read what we say or how it will affect them... like that saying goes - To the world you may be just one person, but to someone you are the world.
Posted by: Cully | November 4, 2007 10:17 AM
Wow! I myself having been diagnosed with a varying array of "illnesses" (I don't choose to call it an illness, it's too much a part of me)that range from bipolar disorder, severe BPD, schizo affective disorder, and anxiety disorder, I have actually found that talking openly and honestly about it has helped me tremendously. My older sister also has pretty much the same diagnosis, with a few extra things thrown in for fun, but hers is quite a bit worse. Makes mine look like a day in the park. I'm glad that there's someone out there who is struggling with sanity and sharing it with people. For those that don't have and illness, it can give them a window into what it's like and maybe give them some understanding. For those struggling everyday to keep our heads above water, it can give hope. I was married before, and even though his mother was severely Manic/depressive bipolar and was supposed to take Lithium, he was totally lost when it came to dealing with me. A newsletter like this would have helped, but then again he was hopeless anyway. It's difficult for people who have either never dealt with it from a family member or they themselves fallen prey to it, have no idea how to separate the person from the disease. Although that can be difficult task when we're unreasonable or can't crawl out of bed, but we're still human, we still have names, and our personalities are in there, somewhere. Thank you, thank you, thank you, for having the courage to write about yourself so candidly. It will give many hope I think.
Posted by: Misty | November 4, 2007 5:30 PM
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