Tag: therapy

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

Walking this Borderland – You’re not going THAT way

Walking this Borderland – You’re not going THAT way

Don’t look back.

You’re not going that way.

I don’t think we should never look back. Sometimes it can be helpful to look back, analytically, or in gratitude, or recognising how things have changed or how far we have come.

Yet, I like this quotation because it reminds me that, no matter how terrible things have been and are, we try to have courage to face each day hope-fully, and to trust that even if we don’t know where we are going, each day we struggle is a day we are going on, and that God promises us “plans for prosperity and not disaster; plans to give you a future and a hope.”

Ginny xx

I know they’re angry

Guilt. Guilt, unease, fear, trepidation of what will come.

Therapy group was painful today. My mind was spiraling with so many thoughts of what I desperately needed to say but couldn’t communicate. Everyone had so much they were feeling and so much that had happened.

I just know I’ve hurt and upset everyone. I know they’re all thinking you’re nasty, stupid, weird, fraud, go away, angry with me, hurt because of me. Cold and away and just wanted me to go and didn’t want to speak to me anymore and didn’t want me there… and I think someone left because of me and I’m scared what she’ll do and what have I done?

And I really really needed this group so much.

I’d just started to trust and now I’ve hurt everyone and they’re frustrated and angry and I can’t give what they need and it’s wrong and why why ever did I start trusting or thinking it would be okay? Why did I let my guard down and not see the hurt I was causing? Why haven’t i learnt that if I think something will be alright and start to trust that’s right when I cause harm?

I can’t put the details of what happened or what we talked about here because it would break confidentiality for other people.

It will be very hard to go back next week. It will be very hard to go to my 1:1 therapy on Monday too. I can tell they don’t want me now. I’d really started to need them. I’ve messed it all up like every other time.

Ginny xx

A closing drawbridge and a silent cry – Eating Disorders and Personality Disorder – #4

 

Protection in emptiness

Eating Disorders and Personality Disorder

Chapter 4 – Frozen

So, this is the first chapter of several in which I want to explore some of the things my eating disorders “provided” to me as a way of coping.

Please note a lot of the thoughts in this post are from my eating disorder and my psychosis and BPD – they are not ways in which I’m advocating thinking and I’m not saying that starvation is a good thing even though it did have a purpose for me. I’m in therapy partly to find other ways to cope rather than turning to methods that hurt me.

Emotions are frightening. Feeling is frightening. Feeling with such intensity is deeply painful and more suffocating and gripping than I can stand. Needing is not allowed, greedy, out of control, dangerous. My body and my longing centre that wants all these things (love, comfort, that I am good enough, that I can be safe, understanding, a parent, security, home, someone there…) is despised and resented. Inside me is evil, bad and ugly and it might get out. I want and I hurt and I do harm, I’m a liar and a fraud and I punish and it all comes out when I don’t even know.

If i dont feel it’ll be alright. If I don’t feel then I can walk one day more. If only the pain of knowing everyone around me feels so much will go away. If I can stop hurting them. If I can get away, because I so need to get away and shut off and sleep. I need the thoughts and the voices to stop. I need out and away from the terrible things I can feel all the time, that hit me and grip me and tell me I’ve caused hurt yet again.

There’s one thing that stops it. Don’t eat. Go on. Just a little bit longer. Stick to the plan of what you’ll eat. Count the tiny crackers out. Slow as you can take the tiniest pieces. Stick to it all and you’ll be rewarded with wonderful emptiness. Even go longer than you planned before you eat, by the minute then the hour. .. and the emptiness will grow and the high will rush through your body leading and lifting you to a higher and whiter and emptier place.

Keep going. You can keep going now. The starvation opens the door to aclosed off, frozen place. It’s good there. The thoughts and the needing and wanting and feeling stop. All you need is empty and all you feel is cold and numb and closed away.

It’s your place alone. You’re alone and safe. The voices are silent for now and you needn’t engage with anything your body or heart demands because you’re separated from those disgusting needy screams. In your frozen place the pain has dimmed and everyone else is safe too because you’ve gone well away.

Starvation created that empty place, as though it carved it away in your mind and it’s a sure retreat for you alone. Stick to rules and emptiness and no temptation and you will stay safe there. However frozen cold it is there and however much you feel your energy slipping away and your heart pounding and your muscles weakening, it is too dangerous to leave it. The feeling and needing (yours and others’) and consuming demands are just too dangerous. The emptiness and starvation has carved out this safe place and consumes more and more of your mind, like a cave in rock that becomes bigger and bigger, empty but consuming its surroundings with the very emptiness, so that it becomes harder and harder to leave.

To recover you are drawn slowly from this place or something throws you out of it forcibly and it is taken from you.

However much I am thankful to be recovered from the terrible physical effects of anorexia and the destruction it caused to the lives of those who care for me, a big part of me still wishes that this frozen place hadn’t disappeared. In my recovery I consciously said goodbye to this place as I knew I had to leave it. I cried for it. It hurt me and my loved ones badly yet also it had protected me.

Now without my eating disorder the terror of all the feeling and consuming is around me and there isn’t any escape. And added to it is knowing that I “should” be fine,  better, out of danger. Out of physical danger, yes, but ironically into pain beyond what I know how to stand, although I also know how very weak I am not to be able to stand what others deal with day to day, and that adds still more to guilt and longing for escape.

Perhaps my therapy will show me how to walk through these out of control feelings and how to continue when there is no escape and no freezing out.

Ginny xx

 

 

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.

A closing drawbridge and a silent cry – Eating Disorders and Personality Disorder – #1

A closing drawbridge and a silent cry – Eating Disorders and Personality Disorder – #1

Protection in emptiness

Eating Disorders and Personality Disorder

Chapter 1 – Introduction

I’ve been talking with a couple of people recently about eating disorders, eating difficulties and weight. Also, a kind reader commented that it was of interest to read a previous post in which I discussed some of the ways in which eating / not eating was (and at times still is) a coping strategy for me – a harmful one, but nevertheless a way of coping with something even more terrible to me than the eating disorder itself. I’d been planning to write more on this at some point and these comments have encouraged me to post on this topic now.

There are a couple of points I wish to make clear in this introductory chapter and I would be very thankful if readers would visit here before reading any of the other chapters in this Series.

Firstly, I want to make it explicit that my intention in this post (indeed any post on this blog) is not to promote eating disorders, food restriction, purging or any of the actions or thought processes that form part of them. This post and this blog are not “pro-ana”, “pro-mia” or for “thinspiration”. These terms are painful to me to write because I know just a little of the raw emotions and suffering that go along with them, for those struggling and their loved ones. I hope that there is nothing in this post that would come across as promoting starvation. Though it is something we may use to try to cope, it does immense physiological and psychological harm to us and I really, really hope that readers suffering in this way are able to get regular, face to face, professional medical and psychological help and support. I know how hard it can be to access that, both because of how hard it is to ask for help and because there may be so little specialist treatment available, with such limited criteria to access it. This is really painful and it’s a topic I will write on during the course of this Series.

In these posts I discuss and share my personal past and current experiences and feelings. Almost certainly they are not the same as those of the next person who has/had eating difficulties (although some of the themes I’ll explore I have heard other people with eating disorders talk about as well). I think it is important not to be afraid to discuss the reality of eating disorders and how they affect someone across their life – that is, across all areas of their life and often across many years as well. I think part of not being afraid and being able to find a way to recover from disordered eating is acknowledging this impact and the factors which may have been involved in the disorder taking hold and continuing.

Part of this process, for me at least, involved admitting that not eating, purging and so on and the state I attained through these things, did serve a purpose. Perhaps that is horrible and shocking. Possibly it is no longer as horrible and shocking to me as it might otherwise be, because I have gone through years of difficulties with eating, weight and body shape myself and I have also known many people with severe eating disorders.  However, I do know, and share the feeling in myself, that it is a very sensitive topic.

I hope that acknowledging the purpose and even “need” for something that the disorder gives in a sufferer’s life, is a way to begin to understand the person and what will help them best to heal and walk the path of recovery. I believe that unless we find another way of reaching what the eating disordered state provided, or an alternative means of living, it is completely impossible to break out of the disorder to continue to exist without it.

The second thing I want to make explicit at this stage is that by talking about a “need” for something the disorder gives, I do not wish to imply any blame on the sufferer (or anyone else) or that it is anyone’s fault or choice to be ill. I state vehemently that it is my belief that nobody with an eating disorder chooses to be ill or should be blamed for it. I believe we are incredibly hurt in a way even deeper and harder than the disorder itself shows.

It is cruelly true that whilst there is no choice or fault in the illness, great strength is needed in the sufferer to contemplate breaking out of it and reaching for another way of living.

I am not yet sure quite how long this Series will be and I am open to any questions or comments readers may have. I would love to hear from you. Especially as this is so sensitive a topic, I would really appreciate you asking any questions on things that are not clear or you sharing your own experience and thoughts, which likely will be very different from mine.

Please do leave messages or questions in the “Comments” section. Sometimes I am slow to respond to comments because I have poor internet access and I am very sorry for this. I am not deliberately ignoring you when it seems that I take a long time to approve a comment or reply. I do read all you say and I am very thankful that you take the time to visit this blog and to write. I hope that soon in the New Year I will be able to set up better internet access and thus reduce these delays.

As always, thank you for reading.

Ginny xx

P.S. The title of this series was inspired by The Killers’ song “Dustland Fairytale”. I In the final chapter I will explain the meaning I intended behind the title.

Walking this Borderland #4 : 5 more minutes

 

please read the Introduction to Walking this Borderland before this or any other post in this Series. Thank you.

 

When I feel the compulsion to do something to hurt myself I find it very hard to resist and do something else to cope with the feeling or the desperate need to obey the voices in my head telling me to punish myself.

On the occasions I have a little bit of control, I sometimes say to myself,  “Wait 5 minutes. You can do it, but not yet – just wait 5 minutes. ” If I can force myself to wait 5 minutes then when I do harm myself, then sometimes a little of the initial force of feeling has passed and I do it less viciously.  I’m hoping eventually I’ll be able to wait longer, little by little,  and then eventually sometimes not to self-harm.

I got the idea when I worked with people with eating disorders. One technique that may help people who struggle with purging after eating, is as a first step to delay a few minutes after eating before purging rather than doing it straight away. Then you can try to make the gap longer and longer and in this time, with support of a therapist or carer, try techniques for acknowledging and coping with the awful feelings and thoughts that are contributing to the compulsion to purge.

I’m new to doing this technique to delay self-harming. I think it’s working a little bit.

Ginny xx

 

Walking this Borderland #1: Introduction to the “Walking…” series

Walking this Borderland #1: Introduction to the “Walking…” series

I’ve decided to start a new series which I’ve called “Walking this Borderland”. I’m going to try to make each post in this series short and readable. My idea is that each will share an idea, skill, or thought that I find helpful in coping with an aspect of the symptoms of my Borderline Personality Disorder. Some of these are things that have been suggested to me by health professionals. Some are ideas a friend (perhaps who also has BPD) has given me permission to share. Some I have come up with or encountered myself in my path living with BPD.

I am sharing these in the hope others may find them interesting or helpful. Perhaps if you suffer with BPD or another Personality Disorder or know someone who does, you may find they are things you can identify with or are relevant or helpful to you. Perhaps they might equally be helpful to people who struggle with other mental health conditions – or even to anyone curious about emotions. Perhaps as a reader you would like to share your own experiences and ideas that help you, in the comments. I’d love it if you did want to do that.

As I have said many times before on this blog, what I’m sharing is personal and every person is very different in what is helpful to them or how they experience emotions. I really hope there is nothing I post in this “Walking…” series that would be unhelpful to anyone reading but please bear in mind that I am only sharing from my experience. Though I have worked in many mental health treatment settings and had some non-clinical training, and receive therapy myself, I am not a doctor, I am not clinically trained, I am not medically qualified to provide support or help to people with a mental health condition. So whilst I hope that this series is going to be useful, I very much urge you to please please access and rely on support from clinicians who are trained to help you.

Ginny xx

Another year ended (Perhaps, just for a minute, I can believe.)

Another year ended (Perhaps, just for a minute, I can believe.)

Today in my church we celebrate the Feast of Christ the King, the last Sunday of the church calendar year. Next Sunday will be the First Sunday of Advent.

Time passes too quickly.

It’s easy to regret, at this time of year.

Advent is a time of joyful waiting and hope in darkness – for me in my faith, preparing to receive in our heart’s God’s gift of love, and placing all our hope in a God who comes into our darkness just as He came as a helpless little baby to Bethlehem that first Christmas. He does not fear to enter our need, confusion and darkness and we need not fear our darkness and confusion because He delights to come to us.

This time of year is one of heightened scary emotions too. It can feel like being pulled back into too intense memories of the past, of past events and tensions, past failures to make things what I should have. We talked about the emotion of regret in my therapy group and I said, trying to give hope to someone else who said she felt regret, that the idea of regret implies perhaps that we know some way in which we would have liked things to have been different. Perhaps we can build on that.

Right now I don’t think I know how to make things different. Looking back this year or so has been terrible on the face of it with loss after loss. Loss of two jobs. Loss of a very close friend (former partner) when our relationship finally was dashed away completely. Leaving two temporary homes. Loss of the ability to carry on or hold it together. Loss of my job and loss of the ability to work full time; with it loss of stability, colleagues, confidence to be able to do anything at all good. I have been in hospital three times for a length of time as an inpatient and at least twice more for a period of hours when I was suicidal.

There is constant news of so much suffering, fear and terror (in all senses of the word) in the world and more and more hurt that cannot be stemmed. What do we do faced with this? What can we do that is good? What is going to win out in the end? I hurt so much too for people close to me who are ill or struggling or suffering and feel their pain to a point I cannot breathe. I wish I could be any good to them.

Is my grip on reality slipping further and further away? The voices, seeing things, explosive emotions, longing not to be alone…. trying to keep going seems more of a fake and more of an act, more exhausting and harder to keep up. Asking for help fills me with fears of unworthiness, having lied, being a fraud and my intense inner evil that I can’t purge.

Yet a couple of people close to me have said that they see a change in me and something getting better that wasn’t there before. I cannot see it yet but they can.

I have a flat of “my own” rather than just one room as a lodger. I can make it home.

I have discovered friends who do not abandon me even when to myself I am totally repulsive and when I cannot believe that anyone would choose me or want to be around me and when I feel I can be no good to them.

I got to work with someone I truly trusted and respected and learnt from him, not only specific skills and knowledge, but how to be fair and calm and how to give generously and work always in a dedicated manner, yet still keeping boundaries and structure and still holding on to a sense of one’s worth when everything around is screaming the opposite and deriding you. I cannot in any way hold that myself yet, but I watched and learnt and it stays with me somewhere. I hope we may stay in touch.

The Lord has treated me tenderly and shown me He is with me and in a moment of the most impossible despairing distress, showed me that at the deepest point and longing of our heart, there is love and there is Jesus, and just for a few minutes I could believe.

I have a therapist. I have one to one and group therapy. I can go to a support group sometimes. I can ask for help when I need it from a specialist PD service, which is a blessing and luxury in the NHS that such a thing is available in my geographical area.

I can join in a therapy which explores emotions and thoughts and reveals something to me every week. It hurts and shakes me but I have to trust that this can somehow lead me to coping and living better and being able to reach the same plane as everyone else in some way. I don’t think my BPD will ever suddenly disappear like with a magic curative pill but I do think I will learn to feel and live better and learn to let the good things ground me rather than the terror. The darkness will not grip so hard.

It’s the end of another year and Christmas is coming (and everything that means in my head, my heart, my family and out in the world). It’s a scary and shaken year and it has passed so fast.

Still, just for a few minutes, perhaps I can believe.

Ginny xx