Tag Archives: bipolar disorder

Challenging stereotypes of mental illnesses – when to let it slide

I am very open about the fact that I have bipolar disorder. I was sure that revealing this to most people would help them understand me and my situation better. Unfortunately, that is not always true. I am usually also the first one to make a noise if someone describes a mental illness incorrectly, uses stereotypes or make fun of mental illness. Turns out people also don’t really like to be corrected, or being told their joke is not funny at all but actually ableist. Most of the time I don’t really care if people get pissed with me; it is my duty to educate; but occasionally it can cause trouble for me. I’ve had to learn the hard way that like most things in life, there is a time and a place. And WORK is not the right place.

I have a client who’s husband is a psychiatrist. The other day we chatted about her life. her family, how her husband is always on call, and naturally about psychiatric patients. She tells me, “Yes, some people are really incredibly depressed they can’t do anything! But you know who’s the worse? The bipolar patients! They seem to be constantly changing their minds, calling for a doctor and then telling him not to come.” Or something like that. Honestly, I wasn’t really listening anymore, because my mind was racing back and forth, ‘do I tell her, don’t I tell her?’ You probably won’t understand what a victory it was for me to say nothing, but it was. ‘Oh really? How interesting!’ was basically my response, while thinking ‘I wish I could tell you the truth and see how you react.’ It just proves again how ridiculous it is when people say things like ‘You have depression?! But you look so happy!’ (I actually got that while IN A PSYCHIATRIC CLINIC) Like my diagnosis is stuck to my forehead. So I did not correct my client. She pays money for my services and so I kept my mouth shut, even though I was ready to give her a half hour lecture.

People are ignorant and often not interested to learn, but I guess before I was diagnosed I didn’t know much about mental illness either because it just wasn’t part of my life. Not everyone is trying to be an offensive idiot, and sometimes letting it slide, even if it is hard, is the right thing to do.

 

Dealing with loss AND bipolar disorder

I’ve been meaning to write this post for a while now, but I didn’t really know how. I wanted to write something that would be relatable, but not just a story of what I’ve been going through. Something that makes to others and hopefully prepare them a little bit. I apologise if I didn’t achieve this, but I’m sure you’ll bear with me.

Today, four weeks ago, a very dear friend of mine passed away at the age of 32. She died from natural causes, but in unnatural circumstances. She still had all this potential to unleash on the world, and now she’s gone. We’d been friends since university days, but it was only really in the last 2 or 3 years, where both of us went through some very unpleasant life experiences that we grew really close. And when I say really close, I mean talk on the phone every 2 or 3 days for at least an hour, and sending texts almost every day in between. I still spoke to her on the Monday, and when I wanted to text her about something we had spoken about on the Thursday, I thought that I would wait until the evening before sending it because she had an important day at work. I didn’t know she was already dead.

Most of us know about the stages of grief: denial, anger, bargaining, depression and acceptance. I have lost loved ones before, I’ve been through them. But it being a person so young, with whom I shared so much with, somehow makes it very different. The good news, if there can be good news in a situation like this, is that I have not completely fallen apart. I’m devastated, I cry basically every night, reality hits me in the face over and over again when I don’t expect it. And yes, I was more or less unable to do anything productive for about five days, but somehow I’ve gone on with my life. At first it felt like a massive betrayal, moving on without her. But then the reality of ‘if I don’t work, I don’t get paid’ set in, and I had to get moving. I cycle between denial, anger and depression (I’ve never really understood the bargaining part), but I manage to come up for air every now and then. It’s true though, you don’t get over losing someone. You just learn how to live with it. I’m definitely not there yet, but I want to share what has helped me in the meantime.

Suffering from bipolar disorder, my first thought was that this was going to completely derail me and be a huge setback. I knew that I couldn’t deal with that too. I didn’t want to make this about me, and I think I managed to achieve this more or less:

  1. Be with people. I found this to be very important. Because I don’t live near the city, I couldn’t be with any of my friends who were also grieving, but I moved back to my home town exactly for a situation like this. I immediately packed my bags and went to stay with my parents until after the funeral. I didn’t necessarily interact with them, but it was good to have people around to distract me, to just check up on me and to make sure that I at least ate.
  2. Withstand the urge to numb the pain. Not surprisingly the first thing we want to do when we get sad news like this is reach for the bottle, or take a pill to numb the pain. I know from experience that drinking makes me more depressed, so when I did have a drink, it was just one glass. Another advantage of staying with my parents during that time; I didn’t exactly want to get completely trashed in front of them. I was also relieved that I didn’t have any benzos left, and felt to awkward to ask my new psych, so in the end I left it. It was a kind of bitter sweet, I almost didn’t make it through the memorial service, but I’m glad I didn’t numb myself. I also owed it to my friend to really feel my loss.
  3. Don’t go it alone. Whether it is making arrangements or going to the service or whatever you need to face, don’t go it alone. A friend of mine drove me to the memorial and back, handed me tissues, held my hand and just generally checked that I kept breathing. She knew the friend who passed from university also, but they weren’t really friends and she was much less emotional and more rational than I was at that point. There were so many old, familiar faces and so much emotion, it really helped to have my own little beacon who was there just for me.
  4. Share stories. The first week or so I was terrified that everything about our bond was going to fade away and that I would completely forget the small little things and moments that made her who she was. I post stories, memories and photos on social media. Whether it’s the ‘right’ way to do it or not, I don’t really know. But other people have commented that they appreciate it and that it keeps her memory alive. Some may feel and prefer to keep their grief private. In that case, write stuff down. I don’t think there really is a right or wrong way to do it. It just helps to keep the memories alive.
  5. Try sticking to your routine and med regime. This is a ‘basic bipolar rule’, but even more applicable when you are dealing with a loss. I forgot to fill prescriptions or just couldn’t bother getting myself to a pharmacy (not sticking to routine), so I missed more than one dose of more than one medication at different times, and it really isn’t ideal. It just causes side effects and more of an emotional roller coaster. I did take something to help me sleep (25mg Seroquel) for about 2 weeks which I don’t do anymore, but I check it with my doctor and realised I really needed it. My sleep was okay-ish after 2 weeks.
  6. Sleep as much as you need if you can. This isn’t exactly something ‘prescribed’ for bipolar, but necessary under the circumstances. Once the dust had settled, I realised that I was (am) extremely tired ALL the time. I’m busy with a big project so I can’t exactly afford to sleep a lot, but luckily I make my own hours. I basically work until I can’t anymore, power nap, rinse and repeat. I spoke to a few people who have also lost loved ones and they reassured me that it wasn’t my body giving in, but that grieving is hard work and so you have to rest as much as you can.

 

I’ve been feeling like I’ll never NOT be sad in my life ever again. At least the sadness has become a bit less intense, but I will always miss my friend terribly. So often I want to tell her something and can’t. I’ve become slightly obsessed with finding every photo, text, email, anything that we shared in the past 10 years. It is incredible and also ridiculous what reminds me of her. Silly things will spark a memory and have me in tears. But I am very grateful that I’ve somehow managed to focus on my loss without my bipolar interfering. I definitely wouldn’t have been able to deal with both.

 

If you have any advice, please share. I will take any help I can get!

Prescription medication vs herbal remedies

I’m almost a little scared to write about this, because it seems like these to very distinctive camps simply cannot agree. But in this post I don’t want to discuss which one is better than the other, or what I prefer. I just want to bring some facts to everyone’s attention, and hopefully give some insight. I’ll do my best to keep my personal opinion to myself.

Most people who prefer to uses herbal stuff are all-natural, free range, organic kind of people. The whole thing, as I understand it, is about not putting anything that the earth didn’t produce itself, into your body. I think. I respect that. The prescription drugs we take to keep our brains under control can have nasty side-effects and while they are good for your brain, they’re not always so good for your body. But is herbal remedies really that much better, just because it is only made from plants and things?

My major problem (and hopefully the last of my opinions) with herbal remedies is that it leaves waaaaay too much room to be swindled out of your money with nothing to show for it. A quick google search shows you that you can use anything from lavender to kava to a whole lot of unpronounceable herbs to ‘cure’ your depression. And these drugs are not tested by the FDA. Often, or dare I say most of the time, no studies were performed on these remedies, or the sample size was very tiny. So we can’t even know what the side-effects are most of the time, until we experience it. If you take a remedy with say hibiscus, your whole oral cavity can swell up and you wouldn’t have known that it would happen. At least when I took anti-convulsants, I knew of the possibility that a rash could develop.

The other major problem is that herbal remedies aren’t usually tested to find out how they interact with other herbal remedies, or western medicine. Maybe someone can help me with this one (honest question because I really don’t know): I’ve never used St. John’s Wart, mostly because the leaflets in my medicine boxes says it can cause a bad reaction. My question is if St. John’s Wart comes with the same warning label? How about its interaction with ibuprofen, paracetamol, codeine etc? Is it safe?

I understand why someone would want to use herbal remedies instead of medication for things like insomnia, anxiety, depression, energy etc. Heck, I used to use them for anxiety and insomnia. They aren’t addictive, for one. And maybe some of them actually work and are safer. I didn’t experience any side-effects from the ones I tried. But then again I didn’t experience any effects at all!

So here’s what I’m saying: Don’t dis western prescription medication. They have been tried and tested and refined. Sure, they can be bad for you, but there is at least some science behind them. You can talk to various specialists and while they won’t agree 100%, they will agree on the principles. And don’t start the ‘big pharma’ debate where I can hear you. If it wasn’t for medication I wouldn’t be typing here, I’d be dead by my own hand.

If you prefer herbal remedies, that is your prerogative, and if you have found something that has been proven safe AND effective, please let me know so I can check it out. But before you stick anything into your mouth, whether herbal or not, DO YOUR RESEARCH. And that’s not just checking the first site you can find on google. Find at least three corroborating  sources. TALK TO AN EXPERT, whether traditional alternative therapy practitioners, or western trained doctors, and make sure you find out about possible side-effects and interactions. MONITOR CHANGES TO YOUR BODY, just like you would with anything else you take. DON’T GRAB THE FIRST THING YOU SEE, because more expensive is not necessarily better. CHECK THAT THE MANUFACTURER IS CREDIBLE.

Don’t be a sheep and don’t be taken for a fool either. No matter what you choose to treat yourself with, be sure to check the facts and get your bang for your buck.

How mental illness is good for the environment

Let’s face it, in recent years, and maybe not so recent, us humans have been abusing and destroying our beautiful planet. My country is classified as a ‘developing’ one, and our government is incompetent at best. So when it comes to all things environmental, despite having brilliant scientists, I would say that we are generally a bit behind.

So when we had electricity shortages a few years ago, and then again a few years after that, no one was prepared. And when we went into a massive drought, where some areas have now been declared as disaster areas, no one was prepared. ‘Yeah, so what?’ I hear you thinking. ‘What has this got to do with bipolar or mental health?’

It’s simple. In trying to be more vigilant by finding ways I can save resources, I have found that due to my mental illness, I already do! Let’s look at saving water, for example: when I’m depressed I save loads of water from not showering or washing my hair. I’m not proud of this, but if you’ve been depressed you’d know that personal hygiene is really too much of an effort. I mostly just swap one pair of pajamas for another pair, so I very rarely have to do laundry. And even when I do, I just don’t. I certainly don’t touch the dishes (if I even eat), and my mushy brain completely forgets to water my few pot plants. The only water I really use, is for drinking, brushing my teeth (the one thing I always do) and flushing the toilet.

As for electricity, no need to turn the lights on when you’re sleeping most of the time. I don’t use much hot water, or big appliances. My food intake is normally restricted to pizza delivery, ramen noodles, bread and cheese or a meal replacement shake. And lots of chocolate. So no using stoves and ovens here!

And my carbon footprint? Well as we know many people with mental illness are unemployed or work from home. I now fall in the second category, which means I might leave the house once a day to buy groceries or see family (I would love to add ‘and go to the gym’ but that’s not exactly happening right now, or when I’m depressed).

So there you go. If your depression, anxiety, medication side-effects or whatever your brain problem is makes you behave in a similar way that I do, always remind yourself that even though you feel like trash, you are helping mother earth to survive. Who knows, maybe that is our collective goal as the mentally ill. When the planet is in trouble, we get sick so lighten its burden and help it get better, if that makes sense. That’s what I’m going to tell myself the next time I’m horribly depressed, anyway: The planet needs me!

 

*This post is meant to be a bit tongue in the cheek-ish, so if you are an environmentalist reading here, please don’t be mean and bury me under links to piles of scientific research. I might have a panic attack and slip into a deep depression. Or get mad and go into bipolar rage, and you really wouldn’t want that.*

Am I being bipolar, ‘normal’ or just lazy?

From the forums, other blogs and articles I read, I think many a bipolar diagnosed person asks themselves this question. I certainly do, every bloody day. Since all the major changes in my life happened, it’s like I can’t quite seem to pull myself together.

The first month or so after my move it didn’t really matter, because I was okay financially, and I was happy to take the time I needed to recuperate, sort out my living arrangements and set up my business. My deadline was 2 May, because we had a lot of public and school holidays here in April. Until then I wouldn’t really care sleeping until noon (or past it) and just doing a little bit of work every day. And now, after the deadline came and went?

I gave up my 50mg Seroquel for sleep a few weeks ago and while sleeping was obviously hard in the beginning, now I don’t struggle so much and I can actually wake up at 8:00 or so. The problem is, I don’t WANT to. It’s way past noon on a Thursday and I am actually embarrassed to admit that I am still in my pyjamas. I have to start actively promoting my business which means handing out flyers and phoning people, but I just can’t do it. I am completely overwhelmed by the idea of interacting with strangers. Yet, on the other hand I am freaking out because I kind of need to start making money soon.

I’m pretty sure that the ‘oh crap what if this fails and I lose everything?’ part is ‘normal’. I’m sure that, for an introvert, anxiety about putting yourself out there and talking to strangers is ‘normal’ too. But what about the complete mental block? And feeling like I can’t breathe at the mere thought? What about the refusal each morning to wake up, shower and leave my house? Despite the fact that I (think) I WANT to work and stop feeling like I’m a lazy, unambitious, blob of a person doing nothing and going nowhere in life?

And the guilt, OH the guilt! I do nothing, yet I feeling incredibly guilty about it, so I totally beat myself up about being lazy, but it doesn’t make me get up and moving. So do I cut myself some slack and spend the day in bed without feeling guilty, or do I pick myself up by my bootstraps and just freakin get over it?

Am I being bipolar or lazy? That is forever the question.

Big wave, little wave

*trigger warning* This post contains mentions of suicide.

Greetings  blogosphere and interwebs in general. I’ve delayed writing a bit because you see, a lot can happen in a year. Also because bipolar folk are notoriously unreliable when we hit an episode. It’s really not our fault.

As for me, I won’t share all the details because it will be much too long and I don’t think it will necessarily be helpful to anyone. So just in short, in the past roughly 10 months, I did a stint in clinic because I was suicidal, then thought I was fine. Then, mostly unbeknown to myself, depression became a mixed episode and my life and my brain became all kinds of fucked-up (I will gladly share details if someone wants to PM me), then I did actually try to commit suicide, failed/was stopped, spent 5 days in ICU, went through the aftermath with the people in my life (this was by far worse than anything else). If you want to kill yourself you better make damn sure you die. That being said, now I’m kinda glad I didn’t. Most of the time.

Anyway, then my life fell apart. I had to take unpaid leave from work and left the city to stay with my parents in my home town and receive intense therapy. My doc also put me, and here is the important part of the post, Lithium. It took some time and a whole lot of blood tests to get the dose right, but it pulled me out of my very deep hole. I won’t lie, Lithium has its stigma for a reason and its side effects are horrendous. Apart from the common shakes and dry mouth, there is hair loss, stomach cramps, vertigo, unbearable thirst, acne, possibility of kidney and thyroid problems and probably some others. But how does it look on a practical level? It means if I don’t carry water with me all the time, I get incredibly agitated from thirst. I can’t apply eyeliner or do any detailed kind of work with my hands. My writing is even worse than it was. Some days my stomach cramps so much or I get such bad vertigo that I have to lie down. No matter what I do, my skin looks terrible. But to me the worse is probably the hair loss. I have thick and long hair and it’s EVERYWHERE. I shed worse than my cats and it frustrates me to no end. These side effects make me feel very sorry for myself.

So why take it if it’s so horrible? Because the 1 pro far outweighs the many cons: It keeps me from wanting to kill myself. It’s as simple as that, and the no. 1 reasons doctors prescribe Lithium despite its side effects. I’m still not on ‘normal’ between hypomanic and depressed, but I’ve only have little waves, not big waves. And this has been with a whole bunch of crap happening in between. I quit my job, left the city to move back home, had to find my own place, my father passed away and I’m starting my own business. It hasn’t always been easy, and there has been plenty of days spent in bed or in front of the TV, but I’m managing.

While most of this is largely thanks to Lithium, I am also on Wellbutrin, Venlor and a very small dose of Seroquel. I’ve also basically stopped drinking and have a good exercise routine. I’m not under big city stress (like traffic), and I am not in an extremely deadline driven industry. I try to at least do one big task/errand a day. All these things help too. I still need to get into a better routine and do something about my diet (currently I have only bread, cheese and a bunch of sauces in my fridge).

I curse the fact that I have to live with these side-effects every single day. I get very angry that people don’t see it and therefore don’t know what I’m going through. I feel embarrassed when someone sees my food fall off my fork because my tremour is so bad. But then I get over it and remember where I could have been. How I almost drowned in the storm of my own mind. And I ride my little waves, that no one even sees, like a pro.

 

*If you or someone you know need support, please call the suicide prevention hotline in your area immediately, or reach out to someone you trust. Threats of suicide should ALWAYS be take seriously.*

Picture the sun

After a year I think I am ready and in the mood (ha) this blog up again. Maybe for no other reason than that I need to. I need to write about my experiences and about what is going on in my head. I need to not care what people think when they read it, and focus on the good it can do myself and potentially other. An I miss writing, to be honest. Even if the only thing I’m writing about is myself and my mental illness.

But before I launch into what you’ve missed over the past year, here is the tattoo that I finally got that was originally inspired by when I started this this blog and chose it’s title. Isn’t it the most beautiful thing you’ve ever seen?!tattoo

Getting over it and back: The first (practical) signs of depression

Happy belated new year to the troopers actually still willing to read my sporadic ramblings.

For me it’s mostly been a good one. I’ve realised that blogging, for me, is like praying (which is wrong on so many levels); when life is good, there really isn’t much to say (except for the occasional ‘thank you’), but it’s when things start going pear shaped that we (I) feel the need to reach out, express what I’m feeling or not feeling, look for understanding and kindness and someone to say that it will all be okay.

The last two weeks of December I found myself in a remote location on holiday with no working electronics to speak of, and no electricity for the most part. This recharged me like I couldn’t have imagined. It really put life into perspective and brought about peace that I had not felt in a long time. But then we get back to reality and have to face the world and we fall back into old habits and hangups.

As I mentioned in my last post, my psychiatrist told me to just ‘get over’ this little, ‘mild’ bipolar problem of mine. So I decided, skrew you, I will do exactly that. Which also means that I won’t see you again and not that it really matters, but you will lose my money so HA. I did give it an actual try though. My meds were working in their higher doses and I felt fine. So I decided no psychiatrists, support groups, blogs, forums, no nothing. Just taking my pills morning and night without thinking about it. And it actually worked, sort of. I really wasn’t giving much thought to this little ‘like high blood pressure’ problem of mine. I would talk about it freely with those who asked, but in a detached manner, like it was just something part of my past.

So I was almost two months in with this and it worked pretty well. In the meantime I met a very nice man, who it then didn’t work out with (men hey…). But shame, it’s not his fault that I’m depressed now. Maybe just a little bit. But I think it started a week or so before we broke up. Today I was extremely irritated and even a bit bitchy. I had one of those days where you just want to lash out and scream. And while I was lying in the bath tonight, while I was actually suppose to be at a dance lesson, it hit me. I am depressed. Not suicidally depressed, but it’s definitely there lurking underneath the surface. And I realised it’s been 3 to 4 weeks. And I wasn’t surprised as it seems like my period of calm is two months. It never lasts longer than that. Being older and wiser and being better at recognising things for what they are, instead of thinking it’s all in my head, I can now see some of my early signs of depression, which I will gladly share with y’alls.

The conversations in my head sound roughly like this:

  • ‘I am so bored. My work is so totally unstimulating, I can do it in my sleep.’ Followed by job searches.
  • ‘Once <insert event here> is over, I’m going to start tapering off my meds. I don’t FEEL anything anymore’.
  • ‘I have become such a boring person. Where is my sense of humour?’ (misses hypomania)
  • ‘Why bother getting up early when no one even cares if I’m an hour late for work.’
  • ‘There is a fat man standing on my chest.’
  • ‘I know it’s not really true but today it feels like life isn’t worth living’.
  • ‘Chocolate! I need chocolate!’
  • ‘I’m so fat!’
  • ‘Fuck I hate pms! This is the worse in my entire life!’ Followed by the realisation that I will only be having pms in a week or two.
  • ‘Take me back to the clinic where I can sleep all day and people feed me.’ Followed by looking at the clinic’s website and reminiscing.

Other signs include:

  • Easily sleeping 12 hours, being awake for about 7, and then sleeping another 12.
  • Drinking to get drunk.
  • Throwing all my good quit smoking resolutions out the door.
  • Being permanently irritated with my colleagues (but in my defense, some of them are chronically annoying)
  • Spending most of my time either watching series or staring at the roof.
  • Feeling like I have achieved nothing in my life and that I will die alone.
  • Guiltily stuffing my face, in a way that feels like I’m punishing myself.
  • Not showering over weekends.
  • Having unreasonable fits of rage or feeling like a friend/family member is out to get me or hurting me on purpose.
  • Obsessively worrying about something or someone.
  • Being totally unreasonable in general.

You get all those websites that list a bunch of symptoms about sleep and appetite and not enjoying things, but what I have listed above is what it FEELS like. The practicalities of it.

Luckily I have caught myself before things got out of hand. As always when I go through some kind of mood episode, I’m almost crippled by the thought that it isn’t the first and it won’t be the last. And frustrated that the medication that worked so well a few weeks ago has seemingly stopped working. And of course the horror of imagining riding out a depressive episode.

But chin up! This is still quite manageable. I compiled a shortlist of psychiatrists to research and luckily there is a support group next week. I don’t feel it, because I feel nothing but dread and horror, but cognitively I know that I can be proud of myself for spotting the signs early.

A history of the Madhouse documentary

I watched this BBC documentary today called A history of the Madhouse. Be warned that it is not for the sensitive viewer and if you don’t know much about the history of asylums and the treatments they performed, you might be quite shocked and horrified. I was, even with my limited knowledge. Dorms with 32 beds, every inch of the place locked up, padded sound proof cells, abuse by nurses, early forms of ECTs with no anesthesia, insulin treatment, lobotomies. The poor crazies (and actually not so crazies) at the time really got it in the 30s to 50s especially. Some went in for one week of observation and only left 5 years, 20, 30 years later. Locked up and isolated from the world. Most of these people weren’t even mentally ill, just unwanted or problematic. Patients were not seen as people but as research projects. Many died from lobotomies and insulin treatment that sent them into comas to ‘reset’ their brains. We look back on these treatments and regard them as barbaric. Others, like a more refined form of ECT and Lithium, are still used today. Some of us owe our lives to the poor people who were subjected to these atrocities year after year.

I think of the private clinic that I frequented and cannot even imagine how it must have been to be locked up in an asylum. Margaret Thatcher can be thanked for them finally being closed in Britain. Problem was, the community care everyone was raving about didn’t really work since most of these poor people didn’t have a vocation or basic life skills. Many of them ended up on the streets or at the Salvation Army, which I suppose is better than the streets at least. Thatcher’s plan was to destigmatise mental illness, to have society view it as illness rather than madness. How she must be turning in her grave to see that these prejudices still exist world wide.

The documentary made me wonder, will some of the treatments that we are subjected to today also be viewed as barbaric 50, 70 years from now? Will people be appalled about how we’ve been medicating our lives away just to function within society’s norms? Or will what is done now be considered as ground breaking, pathing the the way for more specific and sophisticated treatment? I know that some research is being done at the Mayo Clinic about isolating genes and then determining your exact bipolar type so that treatment can be tailored for you needs. But how long is this going to take? Another 50 years? We can only hope that it’s sooner, since those of us with mental health issues are not having such a bloody good time of it.

There is hope, I suppose, one never knows. In the meantime I am extremely grateful to the people who had to subjected to life threatening and debilitating treatment like lab rats, so that I can sleep a bit sounder, or function a bit better.

The bipolar roller coaster

A friend of mine who also suffers from bipolar disorder recently got an absolutely gorgeous tattoo of a roller coaster on her back (of which I am extremely jealous). (She also writes a blog definitely worth reading and much more eloquent and witty than my own) I just realised again today what an appropriate symbol of bipolar disorder a roller coaster is. Just three days ago, and for two or three weeks before that, I was in a completely state of self destruction and hysteria, mixed up with some calm for blissful half hours here and there. I honestly didn’t know how I was going to make it out the other side. The walls around me were not caving in, I was actually pushing them out, and I didn’t know how to stop myself.

What had brought me there? Switching anti-psychotics? Family drama? Recovering from my grandfather’s death? Work pressure? Romantic disappointment?  Probably all of the above to some degree. Especially since it all happened more or less at the same time. And today, not three days after a long series of gut wrenching mini-meltdowns, barely picking myself up each time, I seem to have turned a corner. I had a beautiful calm day, hanging out with friends, going to the beach with the dogs and having pizza and wine. I’m chilled. It was a good day. I didn’t even have to take an Alzam (for anxiety).

So what brought about this turning point in the epic roller coaster that is my bipolar life? The higher doses of Geodon (anti-psychotic) and Epitec (mood stabiliser) kicking in? The calming effect that the Alzams have had on me over the last few days? Getting a good 12 hours of chemically induced sleep last night? Reevaluating my life and realising things were getting out of hand? Having people pray for me? Trying to channel my energy constructively instead of destructively (I even wrote a song!)? Probably all of the above to some degree.

That’s what makes it so tough, isn’t it? Trying to isolate the variables is useless. There is no real knowing what causes what and what different things will trigger or what will bring you back from the edge. When I went off Seroquel and onto Geodon I was extremely hypomanic for about a week. I went away with friends and they kept saying that they’d never seen me that happy. It was true, I was having the weekend of my life. The weekend after that, I had a family weekend and stayed up until dawn two nights in a row. But what goes up most come down (except for Jesus, as my Sunday school teacher friend pointed out), or sideways, or upside down, or through a tunnel, or to some extreme state, if your roller coaster is a bipolar one.

I’ve always known that I just have to ride it out. It becomes the difference between yourself and suicide, the knowledge that it will pass eventually. What I’ve learned this time is that I CAN ride it out, with the right medication, rest, and support from people who understand and/or who care about me. People who just let me be a pretty fucked up version of myself without judging me. I don’t think it will ever be easy. It’s an illness after all, and a pretty terrible one, lets be real. It’s not suppose to be easy. But what I realise when I go through this ever so often is that I am stronger than I even know. I could probably rule a small country by myself. Be it by the grace of God or sheer willpower, I am a ninja, and every time I come back and kick life’s ass, I can confidently give it the finger and say ‘there, you lost again sucker!’ That doesn’t mean that it won’t take some time for me to nurse my wounds and recover emotionally from this ride to the depths of darkness and back. My soul, and my pride, is a bit bruised. After all, I hate roller coasters.