Moving On From A Haunted Past of Home and The Inner Caverns of Self Hatred

As a child I moved a lot. Sometimes once a year, sometimes within 6 months of settling we were moving again. We didn’t stay in the same area either. We lived all over the south half of the country. When it came to going to high school my parents decided it was time to try to stay in one place. For the duration of those eight years I didn’t live in the same house the whole time: that would be a ridiculous expectation to have from my parents. I did however stay in the same town at least. I also managed to stay at the same high school from year 7 to 13. Unfortunately it turned out that the only school I stayed at happened to be the one I hated the most. It was perhaps the most damaging school I’ve ever been to in terms of self belief, self-esteem and building yourself during your teenage years. I don’t think the role of high school is to destroy you from the inwards out, but it seems to have that impact on many teenagers.

I remember walking up the hill from the bus park and one of my friends stated, ‘these are supposed to be the best years of our lives’ as if some wisdom of hindsight and insight had been bestowed upon her from the future. I hoped she was wrong when she said it. I know she was wrong 10 years later. School was not any of the best years of my life. Not at all. Not by any stretch of the imagination. Never.

When I was in high school I started to develop my first signs and symptoms of mental illness. This quickly turned into a long battle with bulimia, and consequently eating disorders and all the shenanigans that erupted at 21. I didn’t feel supported at school. I wasn’t supported at home, although my parents did somehow get me referred to CAMHs via my GP and this is where the one constant figure of hope and support came into my life. I would see her at the outpatients department of the hospital, which I would walk to most weeks. I was very much left on my own in this journey with CAMHs but I wouldn’t have had it any other way.

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During those years, mainly 2005-2009 I would haunt around the city streets and parks on my own. I spent a lot of time on my own, struggling to maintain friends and my illness in any form of harmony, such as mental illness goes. I would eat in strange places and vomit in even stranger places. The country lanes where I lived for the most part of time in my home town were haunted with my running and cycling endeavours in a constant bid to lose weight, disappear, punish myself and repeat after me, ‘nothing is more important than losing weight. Nothing is more important than losing weight’.

If I cast my mind back to this period of time it is shrouded in a mass of thick black smog. I couldn’t see my way clearly at all back then. I struggle to see through it without the inner of my emotive self construing into tangles of excruciating pain. Yes, this place is technically my home town because I spent the most time growing up here but it was never home. Where we lived was never home. I felt outcasted, strange and extremely alone in my own dark world of writing in coffee shops, puking in public toilets, hedges and woodland, and trying to muddle through school at the same time.

I did have some good times, mainly whilst drunk. Often these weren’t even good times though because drinking on an empty stomach is a bad idea any time, but drinking on a stomach that hasn’t seen any form of solid food for 3 or 5 days is just a recipe for an involuntary puking disaster. Surprisingly I remember many of these moments well, puking in the gutter outside my friend’s house, collapsing in a field as the vodka spins took over and I could move, curling up in a hay bail in a barn completely disconnected from the music or people around me. Even my year 13 prom ended with me being traipsed home from throwing up in the hotels toilets for an amount of time that no one has any idea of. No one knows how long I had been in there puking and passed out.

Making connections with people was very difficult for me. It always has been. I put this down to moving house a lot and my impending shyness that creeps into each corner of my life. There was nothing healthy about these years. There was nothing positive to come from my life other than it could only get better once I moved away. It did for a while and even during my times of being very unwell in London I wouldn’t say they were as dark as my time growing up. I lived 4 of my 8 years waiting to leave. This hope is the only thing that kept me going and things did get better in my final year. I went to art school and had one of the best years of my life. Finally there was a crowd that accepted my quirkiness and invited me out anyway. Finally I had friends who I could actually relate to and I was old enough to drink my way through all of my problems without needing to sneak around, climb over fences into clubs and get creative in my ways of obtaining alcohol. Looking back, it really is remarkable that I survived those years as in tact as I did. To this day, I don’t know how I did it.

When I left home to move to London for university it very much felt like a second chance at life. It felt like a clean slate to move away from my demons, move away from the turmoil of my home life as a teenager and make my own way. It didn’t go quite to plan but here I found a home. Since I moved to London 8 years ago I have lived here for as long as I’ve lived anywhere and I’ve been to my home town 3 times. The last time was this year. Before that I went home for one christmas in which I was reminded very much how much it didn’t feel like home to be home, and how much it never really had felt like home. I went back a few years later, then left it a few more years before going back again.

The town felt haunted to me. Seeing my old school as I went by on the train sent a great discomfort through my body. Seeing the old hospital I used to walk to each week, sometimes multiple times a week, swamped me with all the emotion tied up in that experience at once. Seeing the old streets upon which I would wonder alone and drunk in a bid to escape my reality filled me with sadness at how alone I really felt at home. The first time I went home I realised how much I actually hated it. I cried and although I didn’t plan to not return for so long it felt necessary.

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The next time I went home it was slightly lesser of a haunting experience but still it felt strange. It was odd and nostalgic in the most unpleasant way in which nostalgia can stir up old feelings and experiences to churn them over into a curdled mass of sour substance within your stomach. This time I went home, it was a last-minute decision. I was hypomanic and struggling with it. It had become uncomfortable for me and I spoke to my Dad. He said he’d pick me up that night and drive me down.

He has moved house a few times since I left home. He has finally settled in one home which oddly feels more like a home than any of the buildings he has occupied previously. With is having been so long since I left and started to build my own life in London, London is my home. London is the place I’ve been more able to be myself, received more intense help for my mental health problems and met people who are ‘my people’. Sometimes they come and they go but being able to come clean about my mental health illness and still be accepted as a friend to people is something I never experienced growing up. My illnesses being met with compassion and support in my education settings since I’ve started studying up here is something else that has been new. Finally, an education institution with support services and compassion and the belief that you can succeed rather than being surprised when you don’t fail is a place I can learn the thrive.

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My experience of life in London has been very different to the one I knew before. It hasn’t always been easy or good by any stretch of well wishing, it has however taught me a lot and encouraged me to grow. I haven’t been suppressed, I haven’t been dismissed in the way I was at school or home growing up, I have been encouraged out of my dark cavern of self-hatred that I had grown to call my comfort zone. I left home more comfortable hating myself and actively acting on it. I am now in a place where that cavern is becoming a place of the past – and because I’ve managed to move forwards in my life, because i’ve made and had so many new experiences that i chose, because i made a home for myself with what I had even when that meant a back shed with slugs, mice and leaky rooftops it was home. It was the first home i had really experienced. All of this nurturing i have experienced from myself, my partner and friends through these years has shuffled me along to a place where I can go back to my home town when I’m unwell and find it a helpful respite from the chaotic surroundings I create for myself when I am unwell.

Life in London hasn’t been perfect but it has eventually gotten better than where I came from. This allows me to go home and appreciate the nature and beauty of the countryside with fresh untainted eyes. It allows for me to go home and sit in a pub with an old school friend and enjoy their company, fully present rather than drinking until I can barely stand any more.

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I have grown since then. I continue to grow and within that growth there is a strength to face those past memories in a less tangled, less curdling to sourness light. I can be. I can enjoy the place for what it is, a nice seaside town, then I can come home refreshed rather than stressed about my history with the place, and finally, my home town doesn’t haunt me, taunt me or internally destroy me ever so slightly more with each day that I spend there. I am also able to remember the good times from that period of my life.

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Rules To Live By In Numbers 

I am on holiday. Some people they may ask, ‘from what?’; I don’t work but I do study, part-time. I have been off from university for 2 months now, surely that counts as a holiday? I’m going to say no, not really. Firstly, I spent  ~a month of that time being unwell with the dysphoric hurricane of hypomania. I went in hospital and had my meds increased. I have since spent time trying to find my feet.

Although I’m not having a holiday from working, I am having a holiday, but what from?  I am having a holiday from being surrounded by mental illness. I live in a specialist supported accommodation which means there is no escaping mental illness at home because someone is always unwell, everyone is on meds and we talk about it amongst ourselves. There are no awkward questions about mental health because we all live there for a similar category of reasons. Also you’re constantly having to answer questions and attend assessments for how well, or not you are doing. Whilst here I have to keep taking my meds twice a day, and I need to use DBT skills to keep my emotional expressions proportional, and I have to take care in the heat because of my meds – there is no holiday from yourself after all – I am kind of taking a holiday from mental illness.

I am taking a holiday from appointments, seeing my social worker, psychiatrist and support workers. Whilst they provide me with a lot of support and access to specialist mental health care, it’s nice to not be talking about symptoms, side effects and how am I really so much of the time. I am taking a holiday away from the bubble I live my life in at home. I am exposing myself to new and unfamiliar territory. At the same time I’m staring anxiety in the face as I gain confidence with new experiences.


I’m taking a holiday from living well within the borderlands of self-imposed restrictions. I am taking a holiday from documenting habit trackers and mood charts. I could stop forever at any time but they are an important tool for my overall well-being, awareness and insight. Taking a week out to just be, live and experience is quite the luxury and a welcome break. This can only be done when I am relatively well and stable: which I am at the moment. This is as much of a break from myself I think it is possible to fathom.

Finally, I am taking a holiday from numbers. Numbers have played a significant role in my life for over a decade: calories in and out, body weight, body fat %, muscle mass, weighing food portions and the numerical data from my FitBit that I try to make perfect: steps, calories burned, hours slept, minutes of restlessness and wakefulness during sleep, heart rate, minutes of activity and exercise. My FitBit data doesn’t just quantify my existence, it quantifies the goals of my existence: calorie goals, BMI goals, body fat % goals, sleep hygiene goals, number of days active goals, heart rate goals, step goals – literally any way of quantifying my life via a watch that you could possibly want for under £200, it does. If I had blood sugar and blood pressure monitors, I would record that too. I shit not, I have previously looked into buying them – all in an effort to feel in control and achieve a way to be perfect.

 

I realise now that I treat myself more like a machine, rejecting how anything feels in order to try to obtain numerical perfection. It’s a great watch and that is what I bought it for but it can be tiring and distracting from the bigger picture. It seems this focus on numbers has become a replacement for my eating disorder behaviour. It is healthier and less destructive but that doesn’t mean it is healthy and not destructive. More numbers can be obtained to quantify my existence further with a premium subscription to FitBit. I have so far managed to resist.

When I left for the airport I saw my analogue watch, ticking away in it’s box from having been rooting for something else in the same drawer. I spontaneously, (get me being spontaneous) decided to switch it up. My analogue watch, get this, doesn’t even have any numbers on it. Not a single one. I need to have access to the time, I don’t like not knowing and can become disoriented with myself without a watch. I don’t think this is mental health related, I’ve been like this since I first got a watch and learned the time as a nipper. With this analogue watch I don’t know the time to the exact minute – which is why I haven’t worn it for the last 3 years it’s been sat in it’s box for. How could I possibly tell the time without knowing the exact minute of the hour? In answer, based on this week, just fine. Vaguely knowing the time of day and hour it turns out is enough.

My holiday from numbers includes not stressing about getting enough steps, enough sleep and enough activity to hit goals that equate to perfection. I have been able to let go a little this week. In my world, this small freedom equivelates letting my hair down, wild child I know.  On the way back from the hiking day to the Gorropu Canyon I wondered how many steps I had done that day, as if I needed to know the number as it would validate my experience and tiredness. Then I answered myself in my mind, it doesn’t matter; that day wasn’t about steps or minutes of activity. The day was about the experience, the memories and the nature I saw in numerous various forms. The number of steps wasn’t important to the experience in any way – and I recited this in a forced way in my mind, as if repeating fake it til you make it to myself.  The amount of calories burned was not important. The amount of time spent at fat burn, resting and cardio heart rates was not important. What was important was that my heart is strong enough to adapt to demand and by doing so allowing me to have days such as that one hiking through the mountains.

I feel quite liberated since cutting back on the permanent numbers game I’ve ben playing. I do find numbers calming, it is a form of coping mechanism for me which crops up more, naturally, during times of stress. Having said that, I feel like I do not need so many numbers in my life. They have evolved from a calming coping mechanism that allures a sense of control, to a controlling cage that traps me in trying to achieve the perfect set of figures across all platforms of my life: diet, weight, sleeping habits, heart rate, blood pressure…the lists goes on. Sounds familiar huh?

It is in this way that I have been giving numbers too much power over my life, letting them govern how I feel I ought to live my life and what I think is the right amount of everything. It initially manifested in an eating disorder, morphed into another eating disorder and now this. I’m a walking project of equations and sums. My experience is invalid without numbers in my opinion. I also know this to not be true.

 

I have had a desire to be clockwork and machine like for a long time, again, this was initially achieved by having an eating disorder. More recently it has been achieved by wearing my FitBit. The purpose is to not feel and to function impeccably. I want to do and power through life and for the whole while that my digits remain imperfect i have work to do. It hasn’t always been a helpful approach and has held me back in many ways in addition to always having work to do because I am human. I am an animal not a computer. Ironically, for want of a lack of feeling and human nature, this makes me upset sometimes. Most of us are familiar with not being what we want to be: a marathon runner, a CEO, rich, living in paradise but I have turned one impossible goal for another: being weightless for being numerically perfect in other ways. By doing so I have been choosing numbers over intuition and listening to my body or mind for what it really is.

Using numbers to control and restrict my life is not healthy. I don’t feel like I can preach balance when I am living my life so purposefully out of balance. Balance is not achieving perfection in any way be it weight, hours slept or heart rate. Perfection is not possible and life needn’t be constantly quantified in order to be living well – I am human. I am not a machine of equally spaced cogs designed to work like clockwork. Balance is less balance in the numbers of life and more adapting to the essence of change found in living. Evidently I have some way to go.

I Have a Big Mind, So I Can Keep Dreaming

I have a very big mind. I don’t know if you can quantify the size of a mind seeing as it is abstract. What I mean when I say I have a big mind is that it wanders. I have high ambitions for myself, and sometimes believe in them. I think I’m going to become an award-winning author, a Nobel prize receiving nutritionist (has that ever even happened?). I’m going to run marathons and go on to running ultra’s. I want to play instruments and dance like Darcey Bussell

I don’t just want to do all of this stuff. I strive to do it all. However, one obstacle keeps getting in my way. My mental health. I can be very disabling for me. Sometimes, when I am unwell, I can’t even cook or eat properly. I can’t wash. Going to the toilet feels like a chore. Understanding and depicting between reality and fantasy can be a challenge.

I think a lot. I use mindfulness to tame my thinking – and often my mind may be empty, and still I think a lot. I can switch off, but this doesn’t mean that I don’t want all of these things for myself, along with a fantastic relationship, and friends, and above all – learning to manage my mental health.

One thing I still struggle with a lot is knowing how much I can do. I often feel like I want every waking moment of my days to be achieving something – be that studying, learning, writing, reading, running, climbing, art. Perhaps I expect too much of myself. I’m not sure.

When I’m depressed though, something I always struggle with is my inability to do very much at all – and learning to reign in my ideals of how I want to live my life. Accepting the limitations placed on me by my illnesses is something I have not fully accepted. I have accepted it more than I could a few years ago: it is a process. At the same time, I don’t want to not live my life because of my illnesses. I don’t want to sell myself short. I think most people can relate to wanting to be the best version of themselves, and to wanting to live their life as the best version of themselves.

So accepting that I can only read a paragraph at a time, accepting that I can’t go out or leave the house, accepting that I can’t run 4 times a week because quite simply, I am too unwell is difficult to adapt to each time I get unwell. Unfortunately, for me, getting unwell is still a frequent part of my life and I wonder if ever I will be as well as I hope to be. I expected to be a fully functioning member of society with a brilliant job after being off work for 6 months. That was 6 years ago. Evidently, these hopes and desires didn’t quite pan out.

There are times when I wish I was someone else. There are more than numerous times when I wish I didn’t have my illnesses. In fact, I wish this most days that I’m affected negatively by them. I think that is natural, right? So here, on that point right there I need to do some more acceptance work. By that I don’t mean stop fighting and give in. By that I mean learn when to pull the reigns in and accept that for a period of time I probably can’t do everything I want to do or wish for.

The difficulty of this acceptance I think is compounded by the highs I experience. During these times, life is bloody wonderful and I’m functioning at 200%. I’m productive beyond measure, goal orientated like a world champion athlete chasing after an Olympic Gold. I’m talented. I’m brilliant. I’m capable of anything and everything I set myself to. This is called hypomania – and the part that gets me the most is the comparison.

When I am hypomanic, experiencing myself at 200% and loving it, producing grand plans and ideas of how I’m going to become successful in every sense of the word makes the contrast between this state and being so low I cannot leave my bed a more bitter pill to swallow – and in swallowing my meds, I am to an extent, forfeiting these periods of my best self.

Overall, I know it is worth it because I get severely depressed much more than I get hypomanic – yet the contrast of the, “but I’m so brilliant” during those times is a difficult price to pay for stability. Over the years I have refused medications and not taken my medication. Slowly I have learned that this is in fact the worst thing I can do because 90% I will go down, down, down. I have learned the importance of taking my meds, and the importance of self-care in terms of sleep hygiene, and keeping calm in my overall performance, because what is the use of functioning and being my best self at 200% for a few weeks once a year or so, compared to a functioning level between 60-70% for the majority of the time? It is an equation of better odds in longevity.

But I have a big mind and I despise not being capable. I despise not being independent 100% of the time. I resent the fact that I am resigned to not working full-time, perhaps ever. At times it eats me up inside that I may never reach my full best self due to my illness – and actively accepting that going to the shop for some milk and watching Netflix is as good as it’s going to get for a few weeks is a painful realisation to find yourself in when you have such a big mind.

I know that I need to tame my mind. I may not be able to be brilliant all the time, much to my disappointment – but I can be above good for most of the time when I’m well? Is that a fair price to pay for being 5% of myself, and totally disabled by my mental illness? No. I don’t think so. Is it reality though? Is that just how mental illness goes? Yes. I suppose it is. Do I want to accept that? Not at all. Do I need to accept that? Most definitely.

Many brilliant minds in the public eye are tortured by mental illness, yet they manage to be really quite remarkable. Stephen Fry. Ruby Wax. Catherine Zeta Jones. Demi Lovato. When I see how successful they are, I find myself thinking, why not me? There is an element of self belief required, but the truth is, these people are exceptions. Exceptional minds and personalities with mental illness. They do not represent the majority of people with mental illness. I think society forgets that and that help me to also forget that.

I see a lot of people where I live, and amongst the services and hospitals I’ve been to who experience severe mental illness, and for them, just living in supported accommodation or volunteering 4 hours a week is as good as it’s going to get. Yet I don’t see myself amongst that population. I don’t see myself as higher or better, but I see my mind as bigger. I don’t identify with the people in my living complex who spend all day every day staring into space smoking and drinking – I see myself in the Stephen Fry’s and the Demi Lovato’s: but I just can’t sustain my abilities at a high enough level – and that is something I suppose I need to learn to accept. That is something I need to learn to live with, without thinking I may as well kill myself at the same time. That is something I am sure many of us struggle with, mental illness or not.

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I just wish I could be my 200% for 100% of the time. I can dream. We all can. If I keep dreaming, and keep trying, it might become reality – until then, I need to reign in my expectations of myself again – and the heart wrenching reality of my illness hits me hard in the gut, in my soul, at my very core of what I consider to be my being. This is why I don’t work. This is why many people with mental illness don’t work and that’s OK – I just wish every person understood that without judgement. Maybe one day I too will work full-time, maybe I won’t.  Like I said though, I can dream right?

The Panic Proliferation Situation

When anxiety gets a grip on you it becomes very difficult to reason with the impending doom that feels like you have no choice to think about and feel in response to it. Lately I have been experiencing perhaps one of the worst bouts of anxiety I have had in a very long time. So much so that I am not always containing my anxious thoughts and feelings – and find myself acting on them in retrospectively and admittedly, extreme ways.

Last week my partner didn’t answer the phone. She stopped texting me and through a certain method of steps I took to analyse the situation I became convinced she was dead. So convinced was I that I managed to convince the ambulance service to dispatch an ambulance to her address because it was too late and I lived too far away to get there in time, you know, just incase she was on the brink of death rather than dead. She finally responded, all of 2 hours later to tell me she had fallen asleep. Of course, that makes complete sense. I cancelled the ambulance. Unfortunately, they didn’t receive the message to the vehicle and wound up arriving at her house. The guilt of having used and called an ambulance, perhaps away from another emergency ate me up for days of guilt.

At the time though, there was no reasoning. I was convinced. For the following days I kept getting the thought that she was dead or dying, and needed me – but I was unable to contact her. After a few days of “I’m fine” texts, I have realised this is an irrational anxiety thought so have stopped responding to it. Which means it has gone where? I’m not certain. I think a lot of it I am suppressing, whilst trying to ride out the smallest of the waves of emotion that are coming up for me lately as, I presume, a side effect of the stress I am currently experiencing.

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The anxiety has returned to focus on myself since then. I keep getting extremely anxious that people around me are talking about me, laughing at me and judging me to be a walking disgrace. I pretty much scarpered out of uni today as soon as I could in order to escape the lecture room full of people talking about and laughing at me. I thought it was just uni maybe. Maybe I had done something weird and not realised. However, it followed me all the way home to my room where I tried to relax and calm down from the ordeal of having to go out in public when I felt this way.

Cue the weekly fire drill. Normally I am able to ignore the alarm as it sirens throughout the building and my room. It goes off frequently, due to drills and I assume, the bad cooking of my neighbours. Normally I sit through it and it passes. Today though, the siren was piercing and I snapped. I entered into a panic attack of tears running through the building begging them to turn it off. The whole day I had been avoiding using medication to calm myself, but at that point I succumbed to the ease of popping a pill to calm myself down.

I know that lately my baseline is significantly raised due to stress. However, for as many DBT skills that I use I just can’t seem to get it under control. I have the insight. I know what is happening. Some mental health professionals equate this insight into the ability to control it. No, not at all, and to be honest, I am out of answers for dealing with this right now.

I spoke to my care coordinator about it on Friday, but her advice was to accept the emotion is happening and let it run it’s course. I thought I had been doing this already – but I suppose not because my response behaviours are still getting the better of me. I wonder if anyone has mastered their anxiety better than I have mine, what they would say to me about managing it?

How can I not let it get the better of me? How can I realise my response behaviour is not fitting to the situation? How do I reality check without reality checking with my anxious thoughts as a reality? How do I avoid a panic attack without having to take a benzo – because we all know relying on benzos isn’t the answer. Additionally, it is very easy when in a real state of anxiety/panic/upset to take too many because they take a while to kick in and wind up overmedicating.

I don’t know the answers. If you don’t know the answers, but still have suggestions that would be helpful too.

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A Crisis, A Sandwich and The Small Wins

I just ate a sandwich and I am drinking a cup of tea. I am in a public place and although I’m not talking to anyone around me, I just ate a sandwich. I don’t have an eating disorder anymore. I don’t have a digestive disorder. There is nothing physically stopping me from eating, but that sandwich I just ate? That feels like a small win in the realm of my mental health battles lately.
I’m not so sure on calling my difficulties mental health battles, but I’m also unsure about how I feel comfortable labelling these difficulties for myself, about myself or to myself. Mental well being wars? I’m not sure on that either. Either way, the point is my mental health difficulties lately have been on somewhat of a flare up. I don’t like to say I’m in a war with myself, however, when fighting against your mind every day you essentially are at war with a part of you every moment of every day of every waking moment. I repeat every in that sentence on purpose, just to hit home at how “every” my illnesses are in my daily life.

For a short while at the end of December to early January everything was great. My days were not very short of what I would call perfect. I was cooking most meals from scratch. I was running again regularly. I was chasing social engagement. I was acing life how I think life ought to be aced and it was pretty fantastic – not so fucking fantastic that I was skipping on sunshine, but pretty fantastic all the same. Then a freight train came choo chooing through my life at 100mph, knocked me sideways, spun my world upside down and paralysed me for a short while.

To escape, I engaged in maladaptive coping behaviour which resulted in not being very aware of anything for a few days and a night in general hospital. Physically, I have recovered. Mentally, it’s an ongoing journey on what currently feels like an uphill trail run.


For me, I am lucky and I realise that now in that I have people to support me professionally and personally. I am lucky to be loved and cared about – and maybe I need to write this in big bold capitals somewhere I see it every day to keep this reality conscious in the forefront of my mind.

As for right now? I am dressed, I am out of my home borough comfort zone, and I just ate a sandwich on my own, without being told to, without being encouraged and without recoiling into the comfort of not eating and letting the anxiety nausea get the better of me. Today, I am winning a slight win. I had help and that is ok because I am winning at today.

Coming Out of Hospital After 4 Weeks In

From the end of April to late May I spent 4 weeks in a psychiatric hospital, hence my absence. It was a difficult admission and still now I am struggling to quite get my head around what happened, what’s happening, and what I went through. I am also struggling to get back to every day life. Having spent 4 weeks in an NHS institution with nothing to do but sit and talk crap with other patients, sleep and eat I have struggled with going out, with my desire to leave my room, with socialising, with public transport and with getting up in the morning amongst other things.

I am still, after almost 2 weeks out, trying to pick myself up and get going with my life again. It’s been a hard ol’ slog. At the moment I am focusing on getting up and dressed in the a.m and trying to spend my days doing more than staring at the TV until I’m sleepy again. I haven’t managed to start exercising again yet – for some reason I’m really scared to go for a run, or get on my bike. I think this is going to be a long process that seems to be moving at a glacial pace.

I am however, trying to implement skills and tactics in order to get going again, and in order to cope with my new found freedom, in addition to coping in healthier ways than those I employed prior to my admission which landed me in hospital for 4 weeks. My journey from public place, to police van, to 136 suite and then to hospital was quite a surreal one. I did write a lot whilst I was in hospital about what I was going through, some of which I plan to share over the coming days in order to explore my experience. It kind of illustrates my journey with my experience.

After 4 weeks of doing very little, and becoming accustomed to sleeping the days away in order to pass time and be perceived ad the “good quiet” patient, I am slowly getting used to getting up and dressed, as I barely dressed or washed whilst I was in hospital. In fact, every time I have showered since coming out (2-3 times) I have lost the knack of keeping soap out of my eyes and mouth in the shower – this is also something I am currently grappling to re-learn.

So what am I doing to get myself back on track?

1.Set an alarm for 8:30 and 9am to try and get  up and out of bed in a decent time.
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2. I decided from today to not watch TV before 3pm, otherwise I will sit there and watch it all day at the moment. This isn’t usually something I struggle with but it has cropped up since I have come home.
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3. Making plans on sites like Meet Up to go out with people, socialise and become slightly active again.
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4. Making daily To Do lists to try and do something productive with my day and to get chores done.
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5. Trying to go out and acclimatise to using public transport again.
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6. Planning fun things to look forward to.
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7. Keeping a functioning and mood reflective diary.
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What Happens When You Don’t Get Along With Your Therapist?

We don’t get along with everyone in life. Unfortunately, there are just some people who rub us up the wrong way, infuriate us with their breathing habits or perhaps it’s just the mere fact that they exist. These are just some of the challenges we have to cross in our life times, and navigating people seems to be a pretty big challenge for some, especially those like myself who have a multitude of MH problems, some of which include getting along or rather not getting along with people as a symptom.

P.S. I’m not a massive asshole by the way, I just struggle with interactions sometimes.

What makes it worse is when we have to trust this person, and they are supposed to be an important person in your life that helps you, i.e. they’ve been appointed by the NHS as your therapist. Then, it’s even more challenging and difficult to get along when quite frankly, you don’t. So here’s how I responded to not getting along with my therapist and what I perhaps could have done better:

I argued with her.
I hold on the the notion that I had a valid point in each circumstance. Sometimes it can help to argue with your therapist if you don’t agree with their analysis of you, or what they’re saying about you. In fact most therapists are open to being corrected should they get something wrong – my problem with arguing with this particular therapist is that she doesn’t take well to being corrected just like I don’t take well to being analysed incorrectly and having said analysis affect my care.

I cried about it. 
Only slightly as I managed to hold it together more than in the past which suggests progress but I let it go and shed a tear here and there. Sometimes it is healthy to shed tears and cry a little bit. Apparently it releases hormones that make you feel good and a good sense of relief so that I wouldn’t change. In fact, if I could cry more and shorten the grieving process then I would.

I considered suicide over it. 
Now this is an over reaction. I’m glad I didn’t act on it but instead I spoke about it briefly with people because what she was saying made me think “what’s the point?” and “There’s no use trying anymore”. This I would change but I’m thankful I managed to not act.

I spoke about it.
In fact I’ll correct this, I bitched and I bitched and I bitched some more to anyone who would listen to and entertain my pain. I needed to talk about it as I needed to vent, but I would change just how much I needed to talk about it and to how many people because let’s face it, bitching isn’t the most healthy or positive of behaviours for other people to be exposed to all the time.

In conjunction to bitching, I laughed about it. 
This helped a lot. The source of humour was on occasion, perhaps a bit mean but it helped to laugh about it and make a joke of it.

I spoke to other members of my team about it. 
I think this was healthy and helpful because it let my team members know about our clash and gave me a productive avenue in which to vent and work through my difficulties with my therapist.

Thankfully for me, she’s leaving just as this clash came to a head, so I don’t know what the process to changing a therapist in the NHS would have been as I didn’t have to travel that road. In this case I was lucky. However, I think overall how I coped with this scenario since a difficult and painful conversation with said therapist on Wednesday was quite good so I have few regrets over how I managed this situation. I could have done some things better, but no pain or damage has been caused by my coping skills therefore this is an improvement on the past.