Tag: hallucinations

I hate the girl in the mirror

 

The Ladies’ facilities at work have mirrors all along the walls right above the sinks. Inescapable. Two more full length mirrors in the locker rooms, one of them again inescapably right by the door out to the shop floor.

I hate what I have to see in the mirror.

Fat first of all.  Fat, ugly, just Too Big. Too Much. Ugly, wrong.

Nothing matches up and I don’t fit together.

Hate. Look at yourself. Hate. Fat, bulging, disgusting. Foul, no wonder they don’t want you, no wonder, who’d want you?

Remember they’re watching. Remember they know. Everyone knows really. You’re a fake. You’re a liar. They all know how weird you are and what a nasty little thing you are. Listen –

No. Stop, please. I don’t want to hear it again. I wish I could cut the evil out. (Go on, purge, get it all out.) I wish I could go back. Disappear. No more demands of my disgusting body.

Rationally I know these thoughts are always strongest when I’m unstable for a long period. But it still hits me every time I have to look in the mirror and hate.

I’m scared

I’m scared. I’m scared of the memories and scared of the hallucinations. I’m scared of what SHE did to me and the thought she got pleasure in it and what she accused my father of…

I’m scared of what I hear and see and remember and I don’t want it and I’m trying to block it out with the TV always on. I only know after that it’s not real and after I’ve been so scared.

Am I going to stop knowing they aren’t real?  

The 1000th last straw

[TRIGGER warning for mention of self harm, overdose and suicidal thoughts, and childhood sexual abuse;  and for anger, i am really angry and hurt writing this.  I am not meaning people to worry about me. When i say I’ve given up i mean on therapy and the doctors and everyone i trusted, not that I’m immediately suicidal.]

I am so far beyond angry. Hurting. They can decide I don’t get help. But it does come to a point I can’t just keep going one day more and being told the bad things are temporary.

In group and after I desperately needed to talk about the abuse and trauma and the decision I’ve now got to make whether to make a full statement to the police. I needed help when I told them I was really high, right on the edge, really unstable, not safe. Nobody heard.

I’d dared to ask a friend for help and to help me talk through some of what I have to decide about the police. She’s cancelled and changed arrangements so many times we’ve had to meet. I doubt she really wants to anymore. She keeps meetings to the most difficult and shortest times. She knows I’m ill, she knows I’m desperate, she surely knows how difficult it is to talk about abuse! She agreed to meet in the middle of the day at her work. Obviously I needed to talk in private but if that was all the time she had then I was thankful for it. I was at my wits end today after group. She changed the time and place back and forth through the morning today. She knows this puts me right on edge if I have no idea what’s happening. She told me she only had 30 minutes, then that she had work to do and hadn’t finished, then couldn’t I wait an hour and a half later, then asking where I was, 2 hours earlier,  when she knew I was still at my hospital appointment. When I finally pinned her down to a time she still came 20 minutes late without even letting me know and we had to meet in a crowded cafe where I obviously couldn’t talk about a thing – what did she expect me to do?! “How’s your cappuccino? Oh yes and by the way, I’m not quite sure how I’m going to cope when I tell the police about my mother sticking things up me when I was 7, any thoughts?” I don’t think so!

Then she told me I ask too much, it would be impossible to do what I ask (really? Is it so very hard to agree to meet a friend, stick to the arrangement and turn up?) And she doesn’t believe i wanted to meet in private because I thanked her for agreeing to meet in the middle of the day (well just because I thanked her and was grateful doesn’t mean I was happy or it was what I needed, I was just grateful for any help – or what I thought was help). She said she didn’t know we needed to meet in private (really? Is she that stupid she doesn’t know if you have to talk about abuse you won’t do it in the middle of a cafe? I don’t think so).

I was in bits and in so much pain as well  – and yet again the last hope of getting help or to talk to anyone was snatched away. It’s not just today. It’s every single time. I’ve had it now after this is just repeated – every one i should be able to trust,  every place i should get help. They don’t hear. They don’t believe me. They don’t help. It’s some sick joke or someone’s plan to find out when I break, to laugh at me, to test if I want help enough. Well I’m screaming and nobody can hear. I can’t scream louder. They can choose to keep up this game. Well I guess they’ve won. I can’t shout louder. I can’t make them believe. I can’t make it so that I deserve or am allowed help. I can stop trying anymore because it does just hurt too much. That one’s down to me. It’s not really a choice because it simply now is too painful. But I can choose not to let anyone near me again so they can’t trick me, so they can’t decide to keep a distance because I’m not allowed help and cut me down again because I’d just started to trust and go forward believing they’d be there, so they can’t disappear and show me how they don’t really want me around and it isn’t a friendship and they won’t be there.

(Funny. She’ll threaten to call an ambulance – and if I do go to a&e I just talk to someone then get bounced back out after a few hours and I’m alone again – but she won’t come to see me when I’m not safe, understand how hard it is, sit with me when I’m terrified, come to see me when I was in hospital – every time I was in I was the only person on the ward who didn’t get a single visitor -or hug me when I’m crying. Why is it so hard to do any of that? The doctors don’t care and don’t help me and the only friend I have nearby doesn’t want me around and says go to the emergency services. So I’m not allowed medical help and not allowed friends.)

I’m not allowed any help. I need a friend and I need someone with me and I need to trust someone but every single thing I trust gets taken. It’s not just today it’s every time and I’ve had enough. Oh, you must keep going to work, they say. You’ll feel worse if you have nothing to do. No, I won’t. All I want is it to stop. I don’t want to go out. I want to sleep. I want drugs to stop me feeling.

Oh it won’t help you if you have anyone with you it won’t help you get better you have to be independent. Why is it for her to decide what I need? She’s not my doctor! She doesn’t know what it’s like! I need help. I need someone with me. I want a friend. I want someone to help me. I want someone to care. I want someone to be there when I can’t cope. Not only when I can say everything is fine. Not only when it suits them. Not only because they’ve decided I have to learn to be independent. I’ve always been independent. Nobody has ever been there when I needed them. Now I Can’t cope anymore. It’s even more cruel that every time I’m most desperate I have to be deceived into thinking someone’s there then left alone.

If you’re friends with someone, if you care for them, you are there when they need help. You don’t decide what they need or that something else is best for them or they have to learn something. You don’t see them sometimes then walk off when they’re ill. You don’t constantly change every arrangement. You don’t only allow them in certain situations and certain parts of your life. If they need you you’re there for them. If they’re sick you help them and care for them. You don’t just disappear because it isn’t convenient. That’s just utterly basic friendship and actually basic morality. I’d do it and do do it for anyone.

Is it really so terribly much to ask? Every other person in therapy has family, a carer or a spouse with them. I’m the only person who doesn’t, who lives totally alone. Is it really so terribly awful to want someone to be with me when I’m in crisis, to hug me when I’ve been crying for hours, someone to stick to a commitment, someone to be a friend, someone to help me when I’m cutting as soon as I’m alone, when I’m terrified of the hallucinations?

And the doctors know and they don’t care. They don’t help me. My friend says call them if I’m not safe. She says persist. I’ve been persisting for years. I’ve been accepting nobody wants me. I’ve told them in not safe. I’ve told them I’m cutting and overdosing and when I was planning to end it. They didn’t help me. I don’t want some stupid phone number for a few minutes of so called support. That doesn’t keep me safe or get me help or a friend or anyone with me. I’m on my own again. Left to just go back to the same cutting and overdosing. There’s no other way to cope. They tell me just keep going is temporary. I don’t care if it’s temporary. I can’t right now.

After years of making sure never to say what I needed and always to do weekday I’m meant to, I’ve had it. I’m a disgusting selfish b*tch and a baby and I’m screaming and I need help now and nobody can hear me. I’m not allowed help and I know I’m not but every time it’s proved the kick hurts even harder. I know it’s selfish and disgusting but actually the need and the hurt has taken over. Nobody wants me. Nobody wants me really, not what’s really me.

 

 

Snowballing. Not the white fluffy kind.

It feels like breaking over and over at the moment. I hang onto something then it gets taken away. I don’t know why I’m quite so stupid and childish that I keep hanging on to things and people. Last week it was trying to get my tax credits sorted, so things wouldn’t be so tight. Resistance and obstructions all the way. Then it was trying to negotiate a payment plan for my rent arrears. No response (again) to my phone call and letters, so another letter to write. Then trying to get the harassment and discrimination at my last employer investigated. Dismissed without any consideration whatsoever by the regulator. Another complaint to write and my case to be presented again. Then plans with a friend – cancelled. Then hanging on until my appointment with my CPN on Friday – cancelled, because he has to go on training. I can absolutely understand he has to do the training, but I so needed that. Last month’s appointment was cancelled too. Letters I can’t understand about my Housing Benefit and yet another form to fill out to claim for a Discretionary Payment…terrified I’ll lose my home and so my job….

Snowballing, snowballing, problems everywhere there should be help.

Only able to carry on one day more, then one day more, and only by cutting and taking more pills than I should to knock myself out so at least then I can’t take even more and end it.

Hallucinations and flashbacks shaking me too much to breathe.

Hating myself for being so so weak and so childish and for hanging on to things I should by now have learned well not to count on. Hating myself for needing to be cared for and needing help and not being a proper adult, just a burden.

It is very hard not to become bitter and not to give up. I can only try to think, God is teaching me to trust in nothing and no-one except Him alone. “God alone suffices,” St Teresa of Avila wrote. It is right, of course. His Love is all we need and all we cannot lose. But it is very hard not to be angry, bitter, childish and wrapped in my own hurt.

Ginny xx

What do you do “out of hours”?

I really needed crisis support on Friday but didn’t get it. After therapy group I was spiraling down and out of control, then a number of bad events came snowballing, knocking me further down. I had a brief conversation with the duty line at the hospital and was supposed to get to speak to them again later in the afternoon but they didn’t have time. I was in pieces, cut and was on the edge of the very dangerous place I cannot take a single step more and decide to end it. Thanks be to God I didn’t but I took a higher dose of my tablets than I should to knock me out and stop the hurt (not really an overdose as it wasn’t over the maximum dose of anything, but I took more than I’m prescribed and everything together).

I’ve been fighting through this weekend as I’m working. What I want is numb, stay at home, stay under a blanket, no more feeling, no more thinking, no more hallucinations, no more noise in my head, never have to speak again, never do more harm, someone to hold me, to go to the dissociated place, forget everything I have to fight through and just stop and be allowed to need it to be no more, stop, sleep.

What do you do when you feel this and you can’t get help? It’s the weekend and/or evening. I couldn’t get help from the hospital on Friday. There will be nobody available until Monday and who knows if they will have time then to see or call me.

I could go to A&E but I wasn’t sure what they’d do, and it’s not really an emergency and there isn’t an instant solution. I need more help day to day. I could call 111 the NHS out of hours line, but they tend to tell you to go to A&E if you admit to self harming or being suicidal. They’d probably take my tablets away too. When I’ve been put in touch with a community crisis team before I’ve actually found it really unhelpful. They did not (in my uneducated opinion) understand BPD. What they said piled on the guilt and made me closer to ending my life and they were determined to show me I didn’t need (or deserve,  I feel) any help and Iwasn’t genuine. If i got that right now I would go through with ending it.

Part of the problem needing help out of hours is having to try to explain your whole story – trauma, abuse,  flashbacks, hallucinations, voices, BPD, hurt, fear, desperation and needing to end it – to someone who doesn’t know you or the therapy you’re having. It’s too frightening to do and the cost of being misunderstood too great.

I promised a friend that if it got to the worst I’d go to A&E before I did anything. I would,  I’d keep that promise.  I made it only because she would be more worried about me and stressed if she thought I wouldn’t. I would go at that point, out of honesty to her. Even though having reached that point I’d not want to be stopped.

What do you do when you need support out of hours and can’t see your GP or your usual clinic / hospital team? I’d be interested to know what others do.

I know a lot of it may involve other coping strategies not going to someone else for help. But what about when it’s bad enough they don’t work?

Ginny xx

Hurting tonight

It hasn’t been a great week.

Hurting with physical pain from gynae problems and joint problems.

Going between guilt for worrying and burdening my family and not being able to do what I should, and feeling cut up that I’m “in the way” to them and need to be compartmentalised so I don’t intrude on their life – the part of it they actually want not just feel obligated to do.

Seeing far too many things. ..scary things. ..that aren’t there… that are hallucinations from memories that grip me and shake me.

Wishing someone would hold me and tell me it would be alright even when the flashbacks come.

Working through water or a fog each day and knowing I’m getting it wrong and doing wrong and so so tired.

I slept about 4 hours tonight if that. Tomorrow is group therapy again. I am so scared to go. I will go because I mace this commitment to everyone in the group, the therapists, and to trying to get better, to God, and I won’t throw away what I’ve been given. But I’m scared. I don’t know where we are, I don’t know how to be, I don’t know who to trust, and I can’t trust what I did trust or where I thought we were before. Everything unraveled last week. I wish I need not speak. I wish I could just sleep and stop it all.

I will try to go forward thankful. I will ask thankfulness for another day, to learn to thank our God for revealing His loving kindness in the tiny little helps of each day and pray to notice and see them not just the mess in my head. I will try to work to make something beautiful – even just draw, colour, sew, write to my family and my closest friends who mean so much to me simply by still somehow being here.

Somehow this moment will pass but good will remain. I’m trying to believe.

What if I don’t trust them?

I’m still struggling to process what I’m feeling after therapy group on Friday. Tomorrow I have my 1:1 appointment and I know we will be talking about it. It is going to be so hard to go and even harder to go back to group when it comes around this Friday.

Just when I’d dared to start to think it’s okay, it isn’t. Just when I’d started to think group might be a safe place, somewhere that you can dare to speak about things that are otherwise forbidden, it isn’t.

Just when I’d started to let my guard down a little and trust, it turns out I’ve hurt everyone and didn’t even know. How did I not know? Usually I can feel it right away and know it’s my fault and this time I didn’t. I so so needed to trust them there and now I can’t. I couldn’t understand what I was feeling then last night the thought hit me – what if actually I’m angry and hurting because I feel I can’t trust them? I did the wrong and I caused the hurt but what if I’m angry because I feel people didn’t say what was really happening?

What if I’m angry because I feel I can trust or speak anymore?

What if I’m angry because I really needed to trust and yet again it all breaks down, just as usual, every other time? I know and felt so so strongly they hate me, they are angry, they don’t want me there, they hate me, they’re angry, and they’re angry for each other too because I’ve done wrong and got it wrong and they think I’m nasty, a fake, no right to be there, they just want me to go away and just put up with me because they had to. What if that made me angry as well as guilty because I can never know where I am and know I must never ever let anyone close but so desperately need people?

Does anyone else ever just wish they could never have to speak again?

The hallucinations are multiplying as my thoughts spiral through all these things.

Ginny xxx

A closing drawbridge and a silent cry – Eating Disorders and Personality Disorder – #2

A closing drawbridge and a silent cry – Eating Disorders and Personality Disorder – #2

Protection in emptiness

Eating Disorders and Personality Disorder

Chapter 2 – My History, 1 of 2 : ages 3 – 16

In this chapter, I’m going to tell you a bit about the history of my own eating difficulties, as an overview. I am not going to go into detail of my feelings and the reasons I started to restrict or overeat at each stage, as I will go on to that in subsequent chapters.

I have done my best not to go into any detailed description of the techniques I used to eat less or conceal how little I was eating and so on, as I understand that this can be triggering for people who are unwell with eating difficulties.

It has proved much more difficult to write this “history” than I anticipated. I think what lies behind each of the periods of my life is more raw than I had admitted to myself.

Although I probably did not meet clinical criteria for an eating disorder until I was about 15, my relationship with food and my body was distorted throughout my life from preschool age.

I first knew I was “fat” when I was 3 years old. I remember vividly sitting on the stairs. It was shortly after Easter. On Easter Sunday I had been given a chocolate Easter egg with my name iced on it, and some other chocolate treats. As a typical child, I guess, I delighted in the egg. I shared it with my Nana and my parents but probably not very generously! (Typically, again, for a 3 year old.) I remember that on that Easter Sunday, I was praised for sharing. But then that day on the stairs (I don’t know how long after Easter), my mother was calling me “greedy” and shouting at me for how I had stuffed my face with chocolate and everyone else just had a crumb. I remember so clearly and it hurts even now. I remember knowing I was greedy and bad, and FAT. How exactly I knew to make that link, I am not sure, but I knew it meant FAT, and BIG, and that was bad. Perhaps I had already absorbed some of my mother’s preoccupation with food and body size.

My mother began weighing me in secret around this time, and keeping the fact hidden from my dad. (My dad recalls this and has told me about it. I myself recalled it from when I was a little older, maybe 5 years old.) When my dad found out what she was doing, he told her to stop, and she agreed, but actually continued with increased frequency and forbade me to tell my dad.

From the age of around 6, she would regularly tell me that I looked “too plump” and would send me to weigh myself and report back to her my weight. She would not believe the figure I told her and would then have me get the scales, bring them to her bedroom or the upstairs landing and weigh myself in front of her. Then she would stand me, often undressed, in front of the long mirror in her bedroom and point out the bits of my body that were too plump and too fat. Then I had to go on a diet until she considered I had lost enough weight. She did not want my father to know so I still ate the main course of the evening meal, but the diet meant no snacks or biscuits (most of the range of sweets and chocolates children ate were banned in any case) and something like lettuce and rice crackers or a small amount of plain pasta for lunch. Not the most extreme by any means, but I didn’t like it. When I got older, it meant exercise in the living room as well, sometimes with exercise videos and tapes.

I did dance classes from the age of 3 or 4; two or three classes twice or three times a week. This was about the only contact I had with other children and the outside world (my mother taught me at home until secondary school age and almost completely restricted any contact with friends or wider family members). In my classes, I knew that I was bigger than the other girls. I think partly I actually was rather a fat child and partly I was very tall for my age and so of a larger build than the other girls. In any case, candy pink leotards and tights or white ankle socks were not the most flattering outfit, to say the least!

I wanted to be little, thin and tiny. I wanted to be the smallest, not the biggest. From as soon as I could start to read (which was early, around 5 or 6 years old), I would go through my mother’s Prima magazines whilst she was asleep (there was a big stack of back issues beside her bedroom mirror).  I’d look at the pictures of the women there and, as I got older, read the diet features where you were supposed to live on grapes, yoghurt and hard boiled eggs. I remember in particular, one picture of a woman in a sparkly red dress. This was the late 80s when the extremely thin, emaciated look of models was popular, perhaps even more than it is today. I had pretty much uncensored access to these magazines whilst my mother slept. (My dad would go to work but my mother frequently would not get up until a good 2 – 3 hours or more later, during which time I’d play by myself or read books and magazines that I could find lying around.)

My mother, meanwhile, was very concerned with her own weight. She was convinced that she was fat (she was not). Her morning toiletry and beauty routine took an incredibly long time. She would spend a long time on extremely precise application of a lot of make up, then in front of the mirror looking at her body. One of her delusions with her schizophrenia was that she was being bitten by insects or that there was poison under her skin, which she would try to scratch out in front of the mirror. Her eating patterns were very irregular. She would eat nothing at all during the day and instead smoke a vast amount and drink coffee and later, wine. She would then eat an evening meal (except during the terrible arguments, when she might not even eat this). I thought that was how grown up women ate and waited for it to happen to me that I didn’t want to eat any more during the day. I didn’t have enough contact with anyone other than my mother to know that this wasn’t normal. I thought something was wrong with me that I still ate breakfast and lunch.

Food was also a big focus of my mother’s ill thoughts and actions. Arguments often started during the evening meal. If the argument (her shouting, crying, threatening and so on) had already gone on all the day until she suddenly went away to bed, it would resume over dinner on my father’s return from work. When I was older and had been out to school during the day or, rarely, elsewhere, dinner was the time for her cross-examinations about what I had done, what marks I had got, who I had seen, what conversations I had had, what I had said and what the other person had said, usually followed by a rehearsal of why that was not good enough and exactly what I had to say the next time and what the  other person would say in response.

During dinner she would watch me intently, observing in minute detail how I held cutlery and crockery, commenting and criticising and even accusing me that particular mannerisms or movements were done to punish her or because I was “pretending to be a little girl” and knew it would upset her. My father and I had to give effusive praise of every part of the meal if she had cooked it. She had a rotation of elaborate dishes. Not liking something was not acceptable. Other times she would completely stop cooking at all for months on end. The food had to be set out in dishes in a particular arrangement on the dinner table. She would eat with particular precisely repetitive actions that on top of everything else, just raised the tension to absolute boiling point. If she was eating yoghurt from a bowl (it had to be decanted into a bowl, never eaten from the pot), she would circle her spoon twice clockwise and twice anti-clockwise round the bowl, then tap it three times on the top of the bowl, before taking each mouthful. As a result, she ate incredibly slowly. My father and I had to sit still until she had finished. (Even writing this my anger is boiling!) If she was angry, or going to accuse me of punishing her in some way, her actions became more elaborate and pantomime-like. It was frightening and the spring that lived in my stomach around those years coiled tighter and tighter waiting for the explosion that came no matter what I did, anyway.

By the time I went to secondary school aged 11, having been taught at home by my mother from 4 – 11 years old, I was probably a completely average weight. I was still tall although not quite as extremely so as when I was younger. I was not particularly slim but I was not fat either.

At school, able to choose what I wanted for lunch and with some spending money for break time, suddenly I was away from my mother’s intense scrutiny of my food intake. She would always watch me extremely intently if she was sitting with me when I ate. At dinner time I hated the feeling of her intense gaze. It was strange. In other ways she almost ignored my food – for example, I got my own breakfast (unless my dad did before he went to work) and lunch from the age of around 6 years old. After her hospital admissions started I often cooked all or part of the family evening meal, when I was around 8 years old. But when she was present, she watched intently, worrying and judging and controlling.

So with this new-found freedom at school, I wanted to try all the foods my friends were eating which I had not been allowed. I wanted to eat sweets when they had them. I was hungry with the busy school schedule. The result was I did definitely have too much candy and sweet food in my diet. I ate it in secret from her, fearful of what her reaction would be.

Unfortunately, when I was around 12, my physical health problems started, first from an ankle injury and then a serious knee injury, following which I was on crutches for a long time. I have a mild form of joint hypermobility which did not help.

Not able to continue my dance classes or to join in sports or move around so much whilst I was on crutches, my weight started to go up. I yo yo’ed for a while, restricting severely when I was on a diet (drinking only fizzy drinks during the day at school and eating nothing) and at other times eating far too much sweet food. My physical health problems did not really get any better from this age and I was in constant pain in my legs and back (apart from a brief period when I was about 14).

By this stage, my mother was going into hospital with increasing frequency. When she was at home, she seemed the more angry with me. I was starting to challenge more her world that was wrapped up in the schizophrenia and closed in at home, I guess. She became angrier with me for my weight. The weighing had become less frequent but she would still call me to stand in front of the mirror and undress for her to show me what was wrong with my body. I was plenty old enough now that I did not want to do this in front of her.

Nevertheless, I did want to lose weight. I still wanted to be the thinnest, the smallest, the youngest. Over the summer I was 14, turning 15, I started to diet in earnest and this was probably the start of the longest period I had yet spent on a diet. I also started cycling into the next town, swimming, then cycling home. I had gone from being fairly inactive to doing a lot of activity. My stamina had increased and I pushed and pushed myself. I would swim 30 – 50 lengths of the 50 metre pool and cycle 5 miles there an back. Though I hated my body at this time, looking back I can see I was strong and fit for perhaps the first time. All I saw was fat, and my mother ensured that it stayed that way and commented constantly on my food combinations and portion sizes and if I went down a clothes size, would say it was ridiculous and I could not be that size, the clothes were sized wrong and I was much bigger. Nevertheless I enjoyed my swimming and cycling. It gave me some freedom to get away from my mother and out of the tiny village where I grew up. I was free of her whilst I was cycling and swimming and it was something she couldn’t take over.

When I went back to school that autumn, I was pleased with the comments on my weight loss. I continued to further restrict my food intake and fill up on fizzy drinks. I would skip breakfast, hiding it from my dad, and eat only vegetables sometimes with a tiny bit of potato or pasta at lunch time. I was in a musical production with my school, which I also loved (plus more time staying at school for rehearsals equalled more time escaping my mother). I was losing weight very rapidly now and by the time the performance came, the costumes that had been ordered to fit to me a few weeks earlier were hanging loose and had to be pinned in. I collapsed from exhaustion on one day and was so very cold and could not get warm. Although nobody appeared to notice at the time, and I certainly did not acknowledge it, I was probably entering the underweight range at this point.

I then took my dieting further and further and could not stop. My memory of this time is really not at all clear so it is hard to write about. People started to express concern – teachers and even other children at my school who normally hardly paid me any attention at all. I hated the concern and attention and was angry inside. I didn’t want anyone to notice me. I didn’t want anyone to stop me. I was fine. They should leave me alone, I thought. Nothing was wrong and what right did they have to try to reach me. They didn’t understand.

I kept on going swimming in this time, but my energy was now wearing out fast and the distances that I could swim were reducing. It was as if a switch flicked. For weeks I was able to push myself on, swimming 50 or 60 lengths of the pool despite being underweight, determined to go further and further and wishing I could keep going forever. That was safe and everything else stopped. But then within a couple of days, the power had entirely gone. I was so, so cold in the water. It was hard to move. I was being dragged down and it was so so very cold. Everything was pain and not being able to breathe. Even getting changed and getting into the pool took longer and longer and I could see the teachers watching me now. Suddenly it wasn’t where everything stopped anymore – I was being watched there too. I can still remember the last day I went swimming and the cold I felt then somehow seemed to get right inside me and I could not warm up and the feeling did not leave me for years.

I was still dropping weight and by now experiencing physical effects. Downy hair grew over my arms. I was shattered all the time. I caught a cold and cough that I could not shake and would cough over and over in the mornings waking up. It hurt. My skin cracked and split and didn’t heal. I was freezing cold and even basic things like washing and changing became painful because I could not bear taking my clothes off – partly from hatred of my body but a big part of it was the intense cold. I bruised easily. I injured my toes in a fall and the bruising did not clear up for months. I started losing bladder control, often barely making it to the toilet in time. Moving anywhere was such an immense effort and I walked more and more slowly.

Somehow this did not stop me or shock me. I brushed everything off. Nothing mattered because it was all obscured by the need to become smaller and disappear and shrink. The drive not to eat was overpowering. It was a desperate, driven, angry need.

My parents were late to express their concerns. I had done quite a good job of hiding from them what was actually going on and how much food I wasn’t eating. The illness made me nasty and devious. I did not tend to wear revealing clothes anyway and wearing more and more layers against the cold hid how thin I was.

When they did express concern I was furious. It was probably the one occasion on which they both, eventually, when I was severely anorexic, expressed unified concern for me. This stunned me. I hated inside that I was hurting and worrying them. Yet, starvation was stronger.

It was my dad who got me to admit to having a problem with my weight. He spoke to me one morning before my mother had got up and there was something in the distress in his eyes that finally shocked and scared me. I admitted that morning that I had a problem. I was 15 years old.

There were still many months before I actually began to regain the weight. During this time I suffered a serious back injury from which I still have disc damage. I was painfully helpless and I think this made me start to hate the disorder. I was walking with crutches and could not get up from a chair or out of the bath without help. The starvation which had previously protected me now threw me into far more intimate dependency on my mother than I could stand.

Nevertheless, I received very little medical input or help. My memory around this time is again very very poor. It was a really distressing time and I can remember arguments I could not cope with and immense sadness and fear and anger. I know now I was causing my parents a massive amount of hurt and pain and I feel terrible guilt for this.

My mother, in her illness, was adamant that I should not have help from the GP or specialists. My GP wanted me to attend a centre nearby for children and teenagers with eating disorders and to go to therapy and group sessions there. My mother did not want me to have this. She told me what to say to the doctor and what to hide so that I would not be sent to this centre. As she had done with the threats of her, my dad or I being sent away when I was younger, she made the idea that I might be sent away to a hospital into a terrifying thing that would destroy her and mean I was sent away from the family permanently.  She coached and rehearsed me on exactly what to say. She said that she had to be in complete control of my food.

For some reason, her power over me was so great that I went along with what she wanted me to say. For some reason, the doctor believed it. For some reason, my father did not know what was really going on.

So I didn’t get the referral. I didn’t see any specialist. I saw the GP for monitoring a few times, where I’d be weighed and spout the rehearsed sentences that would make it clear that I did not need any help and supposedly was completely in control.

What realised a few years ago, when I was working in an eating disorder service, is that at this time at the age of 15, my BMI was about 13 (I will not share my weight as I know that this may be sensitive and triggering to anyone in the midst of struggling with anorexia). I had Anorexia Nervosa so severe as to be considered life threatening.

When I realised just how unwell I was when my mother had done all she could to prevent me from getting help, my view of her started to change. I believe now that she prevented me from getting help from a specialist because she knew that if I was seen by a psychiatrist, the abuse she was subjecting my dad and I to might be discovered.

A physiotherapist I was seeing for my back injury realised exactly what was going on, I think. My mother hated her. The physiotherapist urged me to try to get more help. I was too much wrapped in my mother’s constructed world to understand what was happening to me. I could not speak outside of what she had told me to say and pretend was true.

I started to gain weight and I could walk again, but just as she said, she got complete control of me again.

This is the first time I have written about this period in my life. It is very very hard and it feels incredibly shameful. I am not ashamed of having had an eating disorder and/or still having eating difficulties. I don’t know exactly what it is. Somehow telling the story seems scary, unreal and I think part of the problem is knowing it won’t just be hidden inside anymore now that I’ve written it.  It hurts much more than I thought it would. However, I think it needs to be said. It’s almost as if the purpose the starvation served is lessened as I tell it. That probably doesn’t make sense right now but in my later chapters I hope it will.

Scared of imagining

My imaginary world used to be safe. My escape and my protection. I’d call it up at first and hide myself in it.

Later it came unbidden, with an invitation to slip through the ‘door’ to safety.

Later still, I just suddenly find myself there. Protected and dissociated. I’m safe and maybe others are too. Usually I know I’ve gone there and can hold on to an imaginary line and fight my way back into the present world.

But lately I dissociate into a place I don’t like where there’s anger and hurt and uncontrolled expressions of needs left wide, raw and empty.

And another where I’m the scared and frightened child and I’m back THERE again.

The latter two I can’t choose to leave. I have to wait til they eventually chuck me back out. I am terrified of who I am in them and how they hold me.

The lines between the worlds are blurring with more and more of my hallucinations and flashbacks. The scared child world is flashing into the present.

Knowing that as a child I could enter, at will and without will, the alternative worlds, I’m scared that other things are also false. That things I thought were in the present world then, are actually not true. That this means the awful frightening things – the abuse – things my mother did and said – did not really happen. What if I’ve somehow imagined it happened? And it didn’t really and I’ve invented it? What if I was a horrible sick evil child? Or what if I was psychotic?

So much that happened when my mother and I were alone means it can’t be corroborated.

What about the things I’m sure happened when my father was there or that I told him? And that he now says he didn’t know?

I do not know what the answer is I just know it could mean I’ve done something terrible I can never make up or make right or hurt myself enough to punish myself for.

How ever do I get an answer?

 

 

 

Psychosis… trying to process that word…

I saw a psychiatrist at the personality disorder service yesterday. I’d asked if I could have a medication review and talk to someone about my fears about my hallucinations (because of the focus of MBT therapy we don’t really talk about them at length in group or regular 1:1 sessions).

I was scared why are the hallucinations getting worse and why it seemed to be getting harder to know they aren’t real. They used to be voices inside my head. Now they’re often outside and at the time they’re totally real. Only after can I work out they couldn’t have been. And I’m seeing things too.

My mother had hallucinations and I’m just a year younger than she was when she gave birth to me and after that things got really bad for her. So I was scared is the same thing happening to me at the same age?

The psychiatrist was really nice,  understood me, understood my terror, understood the frightening experiences of my childhood and she took more interest in this background than I’d expected. Which was important because it allowed me to tell her about unusual, possibly hallucinatory (is that a word?!) visual experiences as a child and the very strong imaginary world I created to escape into, away from the bizarre experiences day to day caused by my mother’s weird beliefs and behaviour. I told her about feeling I dissociate into different personalities and worlds.

Then we talked about psychosis and schizophrenia. The psychiatrist used the words psychosis and psychotic symptoms for what I was describing. I asked if she thought I had Psychosis as another illness separate from my Borderline PD. She said it is hard to separate because having unusual external experiences is part of Borderline and I could be at a more extreme end of that, worsened by stress and perhaps as therapy is opening things up. Also she thinks I had a sort of ‘propensity’ towards it as a child – I can’t remember the word she used – and this interacted with my mother’s schizophrenic behavior and the abuse to make things worse.

I knew I have hallucinations. I was scared of Psychosis. One of the drugs I take is actually anti psychotic though I didn’t realise that.

It’s still scary that the word psychosis and psychotic symptoms is used for what I have. Partly, I think this is because I fear I’m going to lose all knowledge these things aren’t real and lose contact with the world and become as my mother did. Partly, it’s saying for sure I’m experiencing things that aren’t real. And I’ve so many fears about what’s real and what’s not real. Partly I don’t know yet.

I’m holding on to what the psychiatrist said, that if you keep taking the medication you do not tend to lose the knowledge that the hallucinations aren’t real. They might even go away.

So she’s writing to my GP for changes in my medication and higher dose of the anti psychotic meds.

I don’t know what to think right now. There seems a lot to get my head round again.

Ginny xx