Have Faith in Yourself

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One may expect nothing good coming from completely losing one’s mind to madness, and dealing with the aftermath. I often heard the cliches about how I would be a stronger person as a result and I would learn so much through these experiences. However, looking back, those words of encouragement only spoke of the beginning of what I gained resulting from embarking on the recovery process.

I did a little bit of reflecting in my journal this evening about what I have lost and gained over the past fourteen years, since I was diagnosed with bipolar I following a psychotic break.

Here’s a small list of profound losses I experienced within the past fourteen years:

  • My physical health and good looks
  • My religion, which was a foundation of my life
  • My spirituality
  • My sense of identity
  • My sharp intellect and ability to learn new things went into remission
  • At a couple points, I lost my mind completely
  • My ability to adequately care for myself and my environment

I still struggle hard with my physical health and my ability to adequately care for myself. However, in the past fourteen years, I’ve regained much about the other items on the list.

So, not only have I gained back most of the above list of losses, I’ve found the following:

  • I’ve broken free from the institution of religion
  • I’ve broken the generational cycle of madness
  • I understand family and friends better
  • I’ve learned who I am and what I need to explore about myself
  • I’ve embarked on the road to recovery from severe verbal abuse and isolation growing up
  • I’ve discovered some things never go away, such as my analytic mind
  • I’ve confirmed my passion for writing
  • I’ve found wisdom and a new way of seeing the world
  • I can explore a rich spiritual identity and experiences

During recovery, there are seasons and there are trends. It was pitch black for many years of my life. I had therapy nearly every week for 9 months after my first episode, often focusing on the reasons why I shouldn’t commit suicide. All seasons of recovery present their challenges. Over time, the light becomes brighter, and during the seasons, this light will fluctuate.

However, just know that the deeper my pain, the deeper my loss, the more constitutive my loss… the deeper character I gain, the more I find, and the more cohesive I become as a result of these experiences. I’ve reached a point where I have become someone that is beyond my wildest dreams or imaginations, compared to fourteen years ago.

I’m at a brightly blossoming point in my road to recovery. I still have a ways to go, but I’m making progress faster than I have ever before. The truth is… those cliche encouragements did help a little bit when I took them in good faith. The darker the valley, the harder it is to climb out and the longer it takes to climb out. I had faith in myself that I could get through when I was unable to call on God for help and no one could be there for me.

One thing is always true: have faith in yourself. No matter how bad it is, you can overcome.

-theothersid3

photo credit: Stuck in Customs Aurora Over The Valley via photopin (license)

“Satan’s Industry of Death”

An extremist Christian group called “The Watchman’s Report” put out this video entitled “Satan’s Industry of Death” about psychiatry a year ago. However, their title is a self-fulfilling prophecy about what they are unknowingly encouraging, the idea that we should throw psychiatry out the window. Personally, I see them as Satan’s hand in this whole scenario.

The “documentary” is correct in that the roots of psychiatry are dark, indeed. However, so it was in all fields of medicine. Just as medicine improved with scientific discovery, anesthesia, and antibiotics, so did psychiatry improve with time. The Watchman’s Report claims psychiatry is evil, destructive, and Satan’s hand in diagnosing and drugging the masses in order to make money. The video claims that psychiatrists have no right to play God with peoples’ minds, while I say other doctors do the same thing in other fields with peoples’ bodies. Furthermore, God works through people to bring about healing.

I don’t think I’ve ever seen a documentary so skewed and taken out of context in a long time. Unfortunately, they are preaching to the choir of many who share the same beliefs. Without psychiatry, I would be a dead man. Do not be a poison to society and spread skewed lies that psychiatry does not work. You could end up convincing some of this and kill them or a loved one of theirs or make them suffer needlessly, b/c they refused psychiatric treatment after reading through rubbish such as your “documentary.” I also thought you had a nice touch with putting ()’s in to indicate what the imagery of the Bible should be interpreted as.

Bravo! And stop making a bad name for Christians!

“I Am Mental Illness” Vs. “I Have Mental Illness”

To be bipolar is to be controlled by my illness. To have bipolar is to have control over my illness. The subtleties of language have great differences in meaning. I imagine to be diagnosed with any mental illness, the initial tendency is to slap the label on myself, saying I am ADHD, anxiety, depression, bipolar, BPD, schizophrenic, <insert mental illness diagnosis here>. Likewise, the initial tendency for a person not educated about mental illness is to label those people who have it according to their illnesses.

I suspect this is the case because mental illness has an effect on the mind, which is very near to our core being. When it spins out of control, it is magnified and shows up prevalently in the forefront of that person. In order to become diagnosed, this must often happen. In my case, I couldn’t help but look out through a looking glass shaped by bipolar, interpreting a lot of the turmoils I was experiencing along with my past according to what bipolar is and does. My family did the same thing.

However, just like someone who has diabetes doesn’t say he is diabetes, or AIDS, GERD, irritable bowel syndrome, cancer, COPD, whatever illness you can conjure up, he HAS that illness. It’s something he becomes educated about, receives treatment for, and he learns how to manage and cope with it.

Mental illnesses are no different. I imagine them to be more challenging than many physical illnesses as they are much more abstract and hard to understand. For John, his recent diagnosis of bipolar may feel like bipolar is him at first, right at the core of his being, but it isn’t. It’s simply got a grip on him.

So please, keep that in mind. To label mental illness as not an illness is incredibly destructive, and so is labeling the afflicted as the illness. In time he or she will take ownership of it, manage it, and cope with it just like someone who has type 1 diabetes, say. Help him or her along by referring to the illness as something he or she has, instead. If you have been diagnosed with a mental illness, tell yourself you have it, not that you are it!

Bi-polarized Perceptions Part 3: Rapid Cycling

A follow up to part 2 of “Bi-polarized Perceptions.” I remember especially right before my first break, after a manic episode had been revving up for 5 months and I was running on 2 hours a sleep per night for months, I experienced rapid changes in my perceptions of things. For 15 seconds, I felt like I was on top of the world, ready to change it, and then for 15 seconds all I could think about was cutting myself or worse, just to get rid of this unbearable pain.

My moods flipped back and forth rapidly: 2, 3, 4 times per minute: really manic, really depressed, really manic, really depressed. I forced myself to keep going. Often, talking to people such as the chaplain in my school helped me out and set my mood back up for a little while, before it crashed again. Still, it was some relief.

Along with my moods about things in general, specific things were stolen away with my mood shifts wherever they went. I’d love my mom, hate my mom, really love my mom, really hate my mom. I’d sense demons were there to overpower me, angels come and relieve me of my battle, then the demons would come back after the angels left, and so on.

I could make it through this calculus class, there’s no way I can do this class right now, I’ll finish my homework in about 5 minutes for calculus, I don’t understand anything that’s going on right now. Colors would become incredibly vibrant, then fade into almost gray tones; food became an amazing, delectable treat, then a cupcake tasted like cardboard after I chewed on it for a bit, and my mood plummeted again.

This phenomenon is called “rapid cycling” bipolar, and it’s a nightmare. I lost my reference points pretty quickly when I experienced it. Soon afterwards, around Christmas 2003, a family Christmas vacation made me snap when I couldn’t sleep for about 4 days straight. Mind you, I was not on medication nor was I diagnosed at the time.

Future parts may follow to “Bi-polarized Perceptions.”

Bi-polarized Perceptions Part 1: Other People

Bipolar can have a fundamental effect on my perceptions of other people. One reason why bipolar is called bi-polar, is that the person with this disorder can view a person as ALL good or ALL bad – one end of the pole or the polar opposite. This was especially true for me after my first manic/psychotic episode and diagnosis. My perceptions were fundamentally distorted.

I viewed my dad an angel, my mom as vile, myself largely despicable, a girl I was obsessed with as perfect, my aunt as a betrayer… There may have been a small piece of truth in my perceptions, but bipolar caused me to magnify these fragments of perceptions to the point that small piece was all I saw in that person. It WAS the big picture – missing the forest through the trees, so to speak. The reality is that all these people are good, not perfect, and that I wasn’t innocent, either.

It’s hard to have healthy, balanced perceptions when my mind wants to focus on one small take of somebody. It’s also very hard on other loved ones when this happens. It’s toxic to relationships. It destroys my self-image and self-perspectives.

Cognitive-behavioral-therapy (CBT), medications, and education about bipolar all helped me overcome this problem. The steps I took in the CBT I received were:

1. Draw something abstract about someone that seems distorted – say, what I feel and think when I see that girl

2. Process thoughts and feelings in writing using my picture(s) as inspiration

3. Write down a list of thoughts and feelings balanced

4. Make it a habit to think of the balanced picture of the person.

When I thought about that girl, for instance, my mind wanted to race about how wonderful and perfect she was. Instead, I “changed the train tracks” of my thinking by flipping a switch and forced myself to have healthy and accurate perceptions about her that I spent a long time processing in writings and drawings before. When she comes up, my mind can rest.

Flipping the switch that changes my mind’s train tracks is a hard skill to develop, and it starts small. Once  I could do that, changing the train tracks of my thinking became easier, and avoided a lot of train wrecks in my thinking and decisions I made.

Knowing my Bipolar

A big part of recovery was getting to know my bipolar.

Part of it is learning about bipolar in general, part of it learning about my specific diagnosis (Bipolar I). The more I educate myself, the better I am equipped for doing other important things in my treatment and recovery process. A cheap way to find resources is at your public library for the cost of a library card. Also, therapists often have books to recommend, or even handouts to give. Be careful about the internet, as always.

So, why get to know my bipolar diagnosis and what it is? Without it, I’m lacking the reference point I need to know what bipolar is and what normal is. One necessary skill that require a knowledge of bipolar is monitoring my moods so I can anticipate a mood swing. Then, I can do something early before it happens.

Since I have bipolar, I must always keep my mind in check. I need to monitor it. When I have friends or family who are also educated about bipolar, it helps them help me as well. Noticing unusual thoughts, decisions, and behaviors is a sign things aren’t normal. I value their insights and that helps me manage my bipolar.

Eventually, monitoring my moods has become second nature to me. There’s a certain euphoric, wired feeling that can emerge, and when it does, I immediately suspect mania approaching. At that point, I have a plan of action, one of which is to make sure I take a sleep aid and get plenty of sleep.

When I’m aware I’m starting to get manic, I can do something about it. Knowing what to do comes with time and experience, trial and error. I always call my doctor if after two to three days it doesn’t go away, or if it starts getting worse. Knowing when to call your doctor is an important discernment (good taste and judgment) to have.

An excellent tool for monitoring whether or not your manic or depressed, or both, is the Goldberg Depression Scale (And Mania Scale).

The Goldberg Depression Scale can be found online:

http://www.mentalhelp.net/poc/view_doc.php?type=doc&id=973&cn=5

The Mania Scale here:

http://www.mentalhelp.net/poc/view_doc.php?type=doc&id=975&cn=4

Each one has a set of questions with answers that add a certain number of points to your score. Just read the question and go with your gut answer if you can – try not to think about it too much.

I took those tests every week or two for a while after I was diagnosed to monitor what my mood was, and wrote down my emotions, thoughts, and feelings were. Over time, looking back on all those entries, I could start to connect the dots and create a list of my symptoms of my moods. I could also figure out what external things might cause shifts. I learned my chemistry shifts cannot be controlled, and they happen sometimes and trigger a mood swing.

I do say, though, the medications made this process extremely hard, as it made my thinking very sluggish, dark, cloudy, and sticky!

My biggest trigger for mania is irresponsible sleep cycles. Even if I get enough sleep, if I don’t do it on a consistent time, it can really mess me up badly. I always have to work towards good sleep.

All this being said, bipolar is an irreducibly complex problem that takes a long time to manage. Meds, relationships around you, living situations, job, school, eating well, exercise, friendships made and lost, or trying to start something new, finding a good doctor, a good therapist, knowing who I am and what my bipolar is, and even more impossible: learning how me and my bipolar interact, learning to separate them and make bipolar be a small piece of who I am…. IT’S BEEN A CONFUSING JOURNEY!

But I’m in the light for the most part.

If you’re bipolar, or especially just diagnosed recently, my heart goes out to you.

I always welcome comments and suggestions, especially requests, so please drop me a line any time.

What Is A Psychotic Break Like? My Experience Follows

Psychotic Face

I’m shifting between two worlds. I call one the “evil world,” the other the “good world.” The evil world is what I knew in my old life as everyday existence. Transitioning into the good world is the rapture, where the universe cosmically contradicts itself and I walk blamelessly in heaven on earth. It is a peaceful place, thriving in universal harmony, and evil is a forgiven distant past, but not forgotten. They are parallel worlds that intersect, intertwine, and collide. Yet it’s much more complicated than that. There is a grave price for walking in heaven too soon while you’re still alive.

I arrive at the hospital, and get out of the van with my parents. While my mom goes in to start my admission process, I have a few cigarettes, sitting next to my dad on a rough wooden bench outside the hospital, probably the last ones I’d have for a long time. He puts his arm around me and rubs my back. The stars are bright tonight. A nice lady in a white coat appears in front of me and takes my smokes from me. Inside, I sign the lengthy forms they present, knowing the drill as I voluntarily admit myself.

Then I’m in another simple room with my parents, who are terrified but full of love. I’m blessed to have such support in my life. A lady in dark purple scrubs, tapping away on the computer keyboard, asks me lots of boring questions. She loses my attention quickly as my mind doesn’t just wander, but begins to cross over into the good world again. It draws me in – not just mind, heart and soul, but something else – ME.  I leave my body and I watch from the upper corner of the room down on myself as she activates the automatic blood pressure cuff, and I feel the sensation of it collapsing on my upper arm, but nothing’s there. I’m someplace else.

The night sky fades into the forefront of my eyesight a little. The device gives an error readout. The lady in scrubs taps away and voices a remark about the readout, which both echo in that small room from a long ways away as if I were in a giant cave. Stuck in limbo and floating in the corner of the hospital intake room, I watch myself for a few moments, before she resumes with more interesting questions than before.

My attention suddenly snaps me back to reality again. I see through my eyes as she tries the cuff a second time and feel it squeezing hard against my flesh, instead of trying to engulf the vacuum of my empty body before. Time resumes, and I’m 131/72; I knew it would work that time.

Next thing I know, I’m in my room, excited to see no roommate this time. There, I begin to transition to an eternal, peaceful place. I’m suspended in the entanglement connections of the quantum realm. My vision becomes foggy and breaks the barriers between the seen and the unseen. I gradually arrive in what seems to be a world of infinite possibilities. Every part of me, including my new body, and vaguely my old body, is in this realm – strings of my mind, extension, and emotions all someplace else yet there at the same time. The skeleton of my room falls far away, along with the hospital. I look around me and see the naked spectacle of the universe from space.

Contradictions ensue as that infinite world draws me in. The hospital is here and I’m in my room, yet it’s not here and I’m certainly not in my room. Nothing is finite, and there are no locations mathematically or otherwise. I peek in the hallways, and the rooms extend forever on either side. When I observe, each of the hospital wings form a perceptive fractal. Then they break up into waves of fractal possibilities and connections to people in there, to pure abstraction. My instincts tell me there are two normal hallways, but that feels more like my subconscious barely speaking to me about it. I’m in a special part of the universe, far away from the Milky Way right now, yet part of it, feeling near at the same time. I try to instinctively snap back, focusing on that “near” feeling.

Right away, I notice the lights outside – and the light on the smoke detector, particularly – flickering and turning on and off. The flickers are connected to my thoughts and intention, and the lights blink according to surrounding factors I can feel at other times. I lie down in my hospital bed and enjoy the spectacles – in a place of infinite possibilities, everything feels possible. I distinctly feel my heart dancing, racing, dreaming, poking everything and watching the fractals of existence vibrate, form, and multiply. It’s exhilarating! I start laughing uncontrollably in joy and pleasure at this spectacle, for I don’t know how long in the distant evil world.

However, the night nurse traumatically flashes before my eyes in the evil world, and screams that I need to learn some discipline, and then disappears from nowhere. I slowly enter a black hole and darkness envelops me, distorts me. I realize I’m completely and utterly alone. No God, no spirit, no one else; I’m the only being. I have not thought, let alone acknowledged, that I am. Everything runs in a formless loop.

A sharp pain devours me, of cold loneliness and agony, soaking everything. I go back, far, far, far back, to what seems the inception of consciousness itself… It sucks most of my own consciousness away. I am a… dying fetus without a body… I… can still feel pain… trying to flail my… nonexistent arms… and with a struggling… inner voice… scream… silently… in tortured agony:

How? Why? Is there?… a way?… to make a?…. connection?… somehow, in a?… place?… that has no?… connections? What is?… all of this? WHAT… AM?… I? There must be a?… connection somewhere?… So…. alone? Must find?… somebody?… somewhere? But there is?… no one?… and nowhere?… in this realm? How can I?… communicate? What am?… what am?… d-d-d-do-ing……. ……..

Here I am, only able to writhe silently alone, my unborn self there forever, barely having an inner voice. My thoughts are growing and multiplying as an early zygote does. I can’t seem to snap back to. I am lost and alone, scraping off my tiny fingernails on the walls to change that. What is time? What is space? Do they even exist? Everything is going nowhere. What does it mean to “measure?” How do you measure anything? There is no answer, but there has to be! I’ve thought it! Someone wrote the book because I can say these things! Someone wrote the alphabet! I WILL FIND A CONNECTION, SOMEWHERE, SOMEHOW! I BELIEVE THAT I AM NOT ALONE HERE!
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This is a summary of my experience being admitted in 2009. I leave on the note of what I call experiencing wisdom’s loneliness and suffering while being forced to witness the inception of existence. I consider it a treasure even though it was the greatest anguish I ever conceived of, which I don’t expect one to understand. It is so wonderful to see the birth pains of our universe and see that somehow, someone survived it by a group collective effort that we all are a part of.

Wisdom later comforted me in that episode and I could smell her presence in the literal sense. Wisdom’s scent is that of fertile desire, all types of love, the naked spectacle of the universe from space, and everything that’s good on earth. The scent was overpowering. I still miss that. As time goes on, I go back to these difficult experiences and learn more each time. They were my greatest curses, and now my greatest gifts.

I later read my chart, and during these experiences, my empty vessel of a body went to activities, saw doctors, wrote a lot, made crafts, and attended therapy. My parents visited me. I don’t remember any of it but flashes and brief thoughts. During the beginning of my admission, I remember touching base with reality a few times in the form of brief flashes of memory. But reality was in my subconscious, and the brief flashes were much like a lagged out video call catching up really quickly in a flash before my eyes. Most felt disconnected. I suspect the strange memory of my parents’ visit was of two distorted people in the visiting room that looked all at once like a combination of my grandparents and others I didn’t recognize. I felt something for them, though. Memories of reality were few and far between in the first period of my stay.

I was awake and asleep at the same time.

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Photo Credit:

http://www.flickr.com/photos/andresthor/3857180095/

Two Months after Diagnosed Bipolar, Mixed State (Highlights)

What follows are highlights of a rather long journal entry I made 10 years ago approximately 2 months after I was diagnosed bipolar and hospitalized. I was 17 at the time, and it was after a psychotic episode I had that revved up over the preceding six months or so and triggered by 4 days with no sleep at all.

Part of my treatment was in a crisis stabilization unit out of state on our family Christmas vacation, and the other portion was partial hospitalization in my home town because we couldn’t afford full hospitalization. I was on Risperdal right after my inpatient treatment, which dulled everything. I couldn’t handle it, so I begged my psychiatrist to reduce my dose. I became more unstable shortly after, my depression and mania magnified both at the same time, while allowing me to write more freely. I tried to stay positive, but I was in the middle of a storm at the same time. Here are highlights of this moment.

3-28-2004

-Feelings Journal Entry: exhausted, confused, guilty, angry, frustrated, sad, confident, happy, ashamed, depressed, overwhelmed.

– I woke up this morning wanting to kill myself to end the pain, and now I feel pretty good. Craziness.

-I’m writing now because my emotions are swirling in my head, and I don’t know how to express myself. I just want to throw up somewhere, and I’ll just do it here in writing.

– I wonder if I’m just being weak and lazy.

-Then I have bipolar thrown into the equation. And this word “equation” kills me – I am trying to calculate where all this is coming from – my past, present, illness, medication, or lack of will power. I’m sick of it. What’s me? My therapist showed me that I can keep the things that I like about myself, and reject and fight the disease that takes my strengths to the extreme – high or low.

-But yesterday and today, I woke up and didn’t feel like getting out of bed at all. Anything that requires effort seems to me no point in doing. It’s like I’m stuck in a rut and there’s no point in pulling myself out or making the effort even to grab someone else’s helping hand because I don’t experience the pleasure for long and I just slump back down. I don’t feel like doing anything productive, getting out of bed, doing research and homework, fixing food, playing guitar, taking a shower, going out with friends, planning events, going for a walk, maintaining relationships.

– I hope that this is not normal, and bipolar is involved – but I don’t want to use this as a crutch, and aren’t the meds supposed to take care of it?

-But there’s still this remnant left. One moment, I’m alone in my room or taking a walk and all I can think about is suicide. I just get more depressed and I feel exhausted over anything that requires effort, and I just want it to stop and just go away forever into heaven.

-But I’m suicidal one moment and I make an effort to get up, and I engage in activities, and the feelings of joy do return, and it’s little things. Little things are magnified throughout my days and I feel them fluctuate. This not only plays into my moods but in my concentration as well. I have a harder time concentrating and I tend to do things quite slowly.

-There’s something about her that really attracts me, how loving, and caring she is to people, and she knows what to say to give comfort. God used her picture there [in the crisis unit] to prevent me from slitting my own wrists.

-I’m still low on the self-confidence issue. First, there’s my body image. My gut is starting to sag, and I’m not eating healthily. I don’t have the drive to exercise like I used to. I went nuts, and my body and other peoples’ reactions show it. Eating is now a comfort for me to deal with my problems.

-I’m shy around people, and I don’t know how to handle conversations; did my bipolar have an effect on this? Am I social or am I not? I’m so confused.

-I’m also having a lot of problems with cognition. Things seem to always go in one ear and out the other, or if it stays in my head, I have a hard time finding it, let alone think about it. That is, compared to what I was like before I was on all these meds, particularly Risperdal.

– I still remember in the crisis unit when I got my first dose of Abilify. I was supposed to write a paragraph about why I was on the unit and after the medicine started kicking in, the thoughts and connections in my head started to become numb, one by one, along with all desires. It slowly started to paralyze me, till I couldn’t tell what I was thinking and I could write nothing down.

– Maybe the decrease in Risperdal will let me feel more normal. I’m worried about being in charge of anything, in general. Before, I was used to being the driven one and took on leadership roles. Now, the drive is not there, and I cannot keep track of many things let alone my own homework assignments.

– It’s awful for me to make the first few marks on the paper in art, to improvise in jazz, to follow conversations. I wish I were more spontaneous and loose. Oh, dancing is another good example of what I mean, but this one always was. I simply can’t dance. If somebody asks me what the music feels or looks like, I stand there like a rod. It seems like my ability to do art and conversation is fading to the point of my inability to dance.

-My therapist says this is important for me in relation to my bipolar, as life can throw earthquakes at times, but I don’t understand this yet. I don’t know how the role of being released in tough situations plays with bipolar, yet, because I haven’t had any quakes thrown at me yet with me being consciously aware of my disorder.

-I’m also reliving some of the experiences in the hospitals – both in and out of state.

-I wish these spells of thinking about inviting suicide would go away. Mom wonders if they’re spiritual attacks.

-I’m so glad that I’m not writing too furiously like I was when I was manic, believing that I have the revolutionary book that will change society. Sorry, that was kind of random.

-Mom, grandma, and aunt Bell are still not on speaking terms. It is partly my job to mop up the mess I created in the family the past few months. I dunno what to say. I wish my head was a little more clear.

-As far as the disease of bipolar vs. who I am is concerned, I wish I could keep all the good things, but sometimes my disorder enables me to be the good things or prevents me from being the good things. I wish I could control it.

Psychotropics (Mind-Altering Medications) and Bipolar

There is hope that the agonies associated with the psychotropics journey all people with bipolar undergo fade away.

The journey involves finding the medications that work and patiently discarding the ones that didn’t after giving them a fair chance. It is a mind-numbing process in the most literal sense, as many bipolar meds end up taking away cognition, drive, and emotional capacity to promote normal functioning. It was incredibly frustrating when I discovered a medication was useless for me as it felt like a wasted effort at times.

Then I find a med regime that works, and adjustments to make when bad things happen.

Then those “side effects” start to dissipate, and I begin to feel normal most of the time.

After that, I reach a point where I start to reduce my meds with my doctor’s blessing, which is a joyful, profoundly baffling experience. I know I’ll always need medication, but I get pieces of me back which I forget about by reducing them and eliminating some.

The worst thing I did was to stop my meds without my doctor’s blessing: bipolar then proceeded to stab me in the back. The last time I stopped my meds for two months I ended up in the hospital for over a month with a severe break on my hands to recover from.

Have any of you stopped your meds? What happened, why did you stop them, and how long did you stop them? What are psychotropics doing for you now – good and bad?

Now and Then

I just want to put it out there that bipolar I is not who I am… It’s something I have. When I live out my day, I don’t tell most people I’m bipolar, nor do I think about bipolar. It’s become a small part of me, but I choose to reflect on it so I can write about it for others who struggle with all of this.

When I was first diagnosed, bipolar was the biggest part of who I was, and at times it was me. When I lived out my days, I’d tell most people I met that I’m bipolar, and couldn’t stop thinking about bipolar. It became all of who I was, and I couldn’t stop writing about it and thinking about it to figure out what the heck was going on. I vented to friends and family a lot about it, burning many people out.

I still remember the moment I was diagnosed, that the doctor said I would lead a relatively normal life. He was right, as much as in the past I wanted to slap him in the face for what he said as it seemed impossible. It’s taken over ten years for normality to become reality, and it’s worth all the hard work, no questions asked.

Do you know any people who are mental illness survivors?