Category: The emotional and the physical

Hitting when you’re already down…

I really don’t want to talk as if I think the state or the world owes me something. It owes me nothing. However it does hurt when it seems that the systems that are supposed to help you actually hit you down hardest when you most need help.  On its own it shouldn’t be a big thing but when it seems to be the norm it gets too much on top of being ill already.

Recently I claimed for tax credits (for readers from abroad or who otherwise don’t know, this is a small benefit paid to those who are working but on a low income, have children, or have disabilities).

I had first claimed in Spring last year and my claim was rejected before they had even gathered all the information needed. I was so ill at the time I just let it go. I claimed again since starting my new job in November, because I am working part time on a very low salary. The first step is to fill out a form online to request a claim form, then to wait up to 2 weeks to receive the actual claim form.

Monday, I received an email saying that I am already in receipt of tax credits and if I believe this is not true, call this (expensive) number. I called this number and asked to be called back as the call was so expensive for me since I had no landline (can’t afford more bills) so had to call from a mobile. They refused and said they have no facility in the building to make outgoing calls, which I found very hard to believe.

I explained that I am not in receipt of tax credits. I was told that I do have a tax credits award and the award is nil. Right, so I’m not in receipt of tax credits. Yes, you have a tax credits award and the award is nil. Sigh….this could go on for a while. .. eventually I persuaded them to take the details of my change in circumstances. Then the operator’s computer froze so he transferred me to another operator without explaining any of the background and I had to repeat the entire process again. By this time I’d been on the call for about 30 minutes.  They repeatedly asked the same questions and did not listen to my answers. I repeatedly told them I couldn’t afford this call and needed to be called back. I have a few pounds a day to live on and the call had taken just about all my food money for the week. The operator actually told me that because my phone bill does not arrive for a week or two they hadn’t cost me anything! At this point even I could not quite believe their determination to prove they had no responsibility for anything.

Then came to trying to claim for the disability element of tax credits.  I was told that I wasn’t entitled unless I was already in receipt of PIP. I knew this was wrong – that is only one of the qualifying conditions. Online and paper documentation I had when I made my claim made this clear. The operator refused to budge. I insisted to speak to a manager. 5 minutes on hold. …

The manager immediately contradicted what the previous operator had said. But still insisted they would not consider the disability element unless I was in receipt of PIP. I pointed out that he, his colleague, the online and paper documentation each said something totally different, so I needed to know which was the case. He threatened to terminate the call and told me I was making things very difficult.

I suspect I was making it very difficult for him to continue reading from his script without listening to what I was actually asking…. :/ 😦

Then I had to insist that he give me a straightforward answer – was it essential to be in receipt of PIP as he was saying, or was the written information around having a disability which puts you at a substantial disadvantage getting work, correct?  He refused to answer and put me on hold. When he came back on the line he read a lengthy script about the qualifying conditions which confirmed that all the information I’d been given up to that point was wrong. Had I not insisted to this point, I would have been assessed incorrectly for the benefit. I still believe I will be assessed incorrectly because when I tried to tell him the reasons I qualified for the disability element and to ask what proof they needed of this, he talked and shouted over me and forbade me to speak otherwise he would terminate the call. 

By the end of this process I had been on the phone 55 minutes to a cost to me of £25. I still had not been able to get an answer as to how to submit the documentation that would support my claim (and that would have supported the claim I had been rejected for last year, had I only been given the opportunity to provide it). I had been given different information about eligibility from each person I spoke to and from all the written information I had.

By the end of the call I was so distressed, panicked, angry, for seeing yet more financial problems …. this was the very last straw this week and I couldn’t cope anymore. I went home, cut and took a handful of pills, not enough to try to end it, though that was what I wanted at that time, but in order to make it stop and knock me out. All through the next day I didn’t leave the sofa and took more pills to sleep.

Stupid and childish not to be able to cope I know but there really comes a point you can’t go anymore and when you meet obstruction even where you should be able to get help you’re entitled to, sometimes you just crumble.

Ginny xx

 

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 – #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

 

 

Can’t you see they’re in so much pain?

NB this post refers to the films The Green Mile and The Perks of Being a Wallflower. This post is about BPD and experiences of others’ emotions however:

Slight movie “spoilers” alert if you haven’t seen the films and are planning to 🙂 ! Also, whilst both films were interesting and I definitely identified with characters, the first contains a few highly disturbing scenes and themes and part of the second was triggering to me at the time I watched it, though I think only through similarity with my personal experiences. Therefore to be on the safe side, I’d advise caution if you do decide to watch the films.

 

“Mostly I’m tired of people being ugly to each other. Tired of all the pain I feel and hear in the world every day. There’s too much of it. It’s like pieces of glass in my head all the time.” – John Coffey in Stephen King’s The Green Mile

Someone shared this quote with me today. It was years ago I saw the film “The Green Mile”. It is not the kind of film I normally go for;  it was watched as someone else’s choice. It was thought provoking and also deeply disturbing. I would not watch it again now as it’s too harrowing but it has a lot to say about our judgement of good and evil in ourselves and others and how this affects how we treat our peers, those we work for and those in our charge.

“The Green Mile” is set on death row in the USA. John Coffey is a black American prisoner who has been sentenced to death accused of the murder of the two children of the plantation owner for whom he worked. If i remember right he was sentenced because he was found at the scene. In fact he was not the killer; he was trying to save the children. Coffey has a super-normal (supernatural or spiritual?) power to heal people. He touches them and draws the illness out of them through his own body and then “breathes” it out and away. Coffey knew the children had been lured away and attacked and he was at the scene of the crime because he was trying to save them. During the film, Coffey seems unbelievably calmly accepting of the horror that he will be executed and shows astounding compassion to his guards and other prisoners.

In the horror of death row the introduction of this super healing power seems somewhat jarring. Perhaps that’s part of Stephen King’s intention. When we watched it my friend wondered wouldn’t it have been better if it were totally realistic without the introduction of the supernatural realm. I can see her point. Then again I think King integrates it powerfully into the story. In a place of utter despair and darkness on death row, good cannot be extinguished. Compassion and healing still exists through one poor man who continues to do good through being utterly judged, rejected, broken and condemned. No matter how weakened he is, he can still do good and he’s a channel for healing.

He is in the broken and condemned state he’s in precisely because of his desire to help, to heal, to do good even when people judge him wrongly, and because of how much he knows other people’s pain and hurt and needs. Had he not recognised the children were in danger, searched and tried so hard to save them, he would not have been found at the crime scene and would not have been accused…. through the film we see other examples of how Coffee’s compassion and feeling for others overrides his own needs or his own pain.

The quote I started this post with expresses some of the cost to Coffey of feeling so much other people’s pain and needs. I those of us with personality disorders and post traumatic stress disorders, or who have suffered abuse or traumatising relationships,  can struggle just the same.

We feel so very much what others feel. It goes beyond empathy. It goes beyond wanting to help. It is a mental and bodily sensation. We actually feel what the other person feels. Sometimes we feel it more suddenly, more clearly or more overwhelmingly than our own emotions and needs. It can be a shocking or crushing wave or grip. We can’t breathe or we tense and jump as though we’ve been hit. We feel something in us twist painfully and connect to the other person’s hurt and we feel more than a need to take it from them – perhaps a longing, draining need to take it, rather as if we could do as Coffey does in the film.

It can be too much to bear. Too much to be around anyone and so very tiring. After social situations we may need time to rest and recover and go away to some quieter, colder, more numb place in our mind. Or we need something desperately to distract us and this may be dangerous impulsivity, self harm, drink, drugs and so on, because we need anything at all to get away from the knowledge of such hurt and pain in the world that we can’t draw out.

For some reason it’s the feelings ofhurt and need or pain or anger that overwhelm us and fill us more powerfully than good feelings in others such as joy or excitement. I don’t entirely know why.

There’s another film that spoke to me about this too, “The Perks of Being a Wallflower”. The main character has suffered childhood abuse and at the end of the film, he asks the doctor treating him, “can’t you see that they’re in so much pain? ” – can’t you see that everyone around is in so much pain, because he can see it and doesn’t know what to do. I can see it and feel it and take it all on and I don’t know what to do. It can be so impossible to carry on through that feeling and so tiring, that we withdraw totally to protect ourselves. Then we seem cold and that we aren’t making any effort to help anyone and thinking only of ourselves – when actually we ate feeling so very much and so much wishing we could heal others’ pain.

In “The Green Mile”, despite being judged and condemned, Coffey continues to feel everyone’s pain and continues to heal people. He is utterly misunderstood. His power for good is hidden to almost everyone. But even there in death row it can’t be stopped.

Even if we are utterly weakened and broken, even if nobody understands, even if we can’t tell anyone yet what is really happening,  the good we can do will still remain. Even if we feel we’ve totally failed, there is good in us, even if it’s hidden from us too just now. Not seeing it doesn’t mean it isn’t there. Paradoxically, though our ability to feel so much has a great cost to us in pain, in being drained and spent and hurting, it may not be a bad thing. It may become something that enables us in the end to help and actually even connect to people.

I think learning to believe good in ourselves lasts even in weakness and apparent failure is a big part of getting there. So is finding a way to stand experiencing what we feel of others’ emotions and our own, so that we can use these feelings beyond empathy to be able to help people rather than having to withdraw because we cannot stand it. So far I really don’t know what the answer to this is, as yet.

Ginny xx

A closing drawbridge and a silent cry – Eating Disorders and Personality Disorder – #3

A closing drawbridge and a silent cry – Eating Disorders and Personality Disorder – #3

Protection in emptiness

Eating Disorders and Personality Disorder

Chapter 3 – My History, 2 of 2 : 16+ years – adulthood

From the summer I turned 16 I started slowly and painfully to gain weight. It was frightening and felt out of control but at the same time it was about the one time I was cared for by my mother.

Even so it was tightly controlled by her. If I couldn’t keep to my lowest, most broken weight, I did want to please her by the way I gained weight back. Sounds weird, I know.

But it wasn’t long before she flipped again into her hatred of me. As I was “recovering”, she made my emotions – rising rapidly to greater extremes as I lost the perceived safety of the anorexia – all unacceptable and to be dismissed because, she said, it was all because of the eating disorder. I had to realise what I was putting the family through and how impossible I was to be around.

Then as I continued to gain, the “fat” talk returned. Now she even claimed that my father agreed with her. “You’ve got too much fat on you.” “Daddy was saying last night how he is very worried about the amount of fat you’ve got on you.” “You need to eat fewer carbohydrates and stick to protein. You’re getting far too much fat.” I know now that this was when I had only by a few pounds left the anorexic weight range, to enter the underweight range.

My weight was still going up. I was eating now but knew I was out of control. I tried to stick to what I thought was healthy eating during the day, but at night it was as if the compulsion to eat took over. I couldn’t stop. After dinner when I was doing my homework I’d go back and forth to the kitchen. Even though my parents could see, I couldn’t stop. It was as if something was inside me demanding more and more to eat and it was never enough. I longed for the control of anorexia to be back. But somehow I’d lost it. I was utterly repulsed and disgusted at myself that I could not stop eating. I longed to go back to starving but where had the energy to do it disappeared to?

If I didn’t eat, I couldn’t concentrate on my work. And I was driven to do the very best I could at my schoolwork. It was what my mother needed. Perhaps I was terrified she’d accuse me of “pretending” again and punishing her if I did not do excellently. Her grandiose beliefs about my intelligence increased about this time and she thought I was a “genius” and that “nobody could cope with my intelligence”. I longed just to be normal. Not to have to achieve amazing things and with no superb powers. I knew the grandiose things she said were not real but it frightened me a lot.

Equally she continued to pressure me to diet, to eat only salad during the day, she’d look at me hard and tell me how ugly I was, she’d watch me with a look of utter scorn whilst I was eating, she did not allow me to buy any clothes apart from my school uniform and anything I had needed to cover up how fat I was… she’d tell other people how fat I was… if anyone said anything complimentary to me in her hearing, she’d tell me afterwards how it was very nice of them to say it but I had to remember that they were only saying it to be kind or because they were worried that I might get an eating disorder again, and I must be clear that really I was very fat.

Throughout sixth form, my weight increased, and by the time I began university I was objectively fat. I was binge-eating in secret by this time and furious with myself for it. All the while I was longing for anorexia again but saw myself as a complete fraud and disgusting pig. Why couldn’t I just stop eating again? Every day I’d promise I wouldn’t eat but I’d get through a few hours, then binge.

In the spring term of my first year, my relationship with my mother was breaking down completely and I felt I was drowning in a feeling of emptiness, sadness and I was going through a religious struggle as well, believing in God but terrified of Him as well. Physically I was exhausted and following glandular fever was ill with ME and fibromyalgia which were not yet diagnosed.

Somehow, the pain enabled me to stop eating again. Over a couple of weeks, I reduced what I was eating very fast. I stopped eating solid food and survived on slimline Cuppa-Soups and diet hot chocolate. For 8 weeks, this was all that I consumed. I lost a substantial amount of weight. My friends concerns and discovery of my “eating” patterns led me to start eating again out of guilt that I was hurting them. But I continued to restrict and was sure never to go over 1000 kcal per day.

The next year or so continued like this. My ability to restrict food was still not as strong as I wanted and I lapsed into bingeing. Now I had discovered purging as well. I am not sure how. I started to take laxatives after binges, or try to go running (which I couldn’t because of the post-viral exhaustion). I would overdose daily on laxatives and not care that they made me too ill to do my coursework.

Still I was utterly repulsed by my body. It represented everything foul and uncontrolled I believed was in me.

When I worked in a department store over the summer between my second and final years at university, the physical activity helped me lose weight and some of the anorexic mindset returned. I reduced and reduced my food during my final year and my weight plummeted again. I had stopped the laxatives because they made me too sick to go to my classes and do my work, but if I did binge I would make myself vomit afterwards. Soon it became a compulsion to do it if I ate any more than salad. Doing it until I could tell myself I was sure I had got rid of everything and punished myself enough (ie until I saw bile and blood and could no longer stand up by myself) was “safe” I thought, and I was addicted to the pain and emptiness and the “high” that came afterwards.

Although my weight didn’t drop quite as low this time as it had when I was 15 or 16, mentally I was even further into the clutches of the disorder. It was the best way I knew to punish and weaken myself. I think I did realise I looked ill and realised that I was too thin. Nevertheless, eating, consuming, meant that I was disgusting and I was terrified that I would go out of all control. I did fear fat but even more I feared everything it meant to me and feared not hurting myself.

Around this time, just after I finished university, I was received into the Catholic Church. I was learning not to fear my God and perhaps on some level to understand that he did not think that I was dangerous and that my relationship with Him did not mean punishing myself enough for the badness I thought was in me, before I came to Him. The “God” I had invented in my head during my childhood (before I understood anything of the Christian faith or any more than snippets of the Gospels) was very much a judging, watching, God and to whom I had to atone for all the bad things that I had done.

Shortly after this, I started to want to recover. I was still disgusted at myself but on some level I did want to get to be “normal” and to not be dominated by the disorder. I started eating again. I was very ill physically with ME and a back problem and could not walk without crutches. As my weight went up I got scared again and, without a job at this time, I turned back to the laxatives and overdosed worse than before.

It is hard to really understand or remember quite how I got out of this stage. Perhaps the ability to restrict slipped away again. Perhaps in my struggle to eat normally I did start to win a bit. Perhaps as I got further from the extreme starvation state, my body did not have the drive to binge-eat as much food as possible whilst food appeared to be available, and my control of my appetite returned. Perhaps I just got better at resisting the hunger when I felt the urge to binge (or at replacing food with coffee!). A doctor once told me that most people who recover from anorexia go on to develop binge-eating disorder, because of the physiological and psychological effects of such starvation and being so underweight.

By my mid-20s, I was not underweight and by all external appearances, was recovered. I have to admit that I had taken steps out of the “safety” of anorexia or the temporary “comfort” of bingeing, to more normal, regular eating and an acceptable weight.

The problem was what this left me with. What I discovered lay beneath, which I could no longer conceal and suppress. When these things are too terrible, punishing myself with food / no food, with the distress of purging, is still a compulsion that I have to fight – and give in to at times. An extra struggle at the moment is that I take several medications which slow the metabolism and cause weight gain, and that physical disabilities prevent me from any exercise but walking. Poor finances also mean that I cannot eat as healthy food as I would like and the cheaper options are often higher calorie density. My weight feeling out of control is highly distressing because inside, wishing to be small and tiny is still very much there. That’s the safe thing but it’s now a safe thing I can’t seem to reach to.

I am very thankful that I have recovered to the point I have and I realise the terrible health consequences of staying at a starvation weight or purging regularly. I know the upset it causes to people who care (no matter how much I should wish to be invisible or wish nobody would be hurt but me!). I don’t want to do this to anyone. I know the physical effects prevented me from working (vomiting and stomach upsets from overdoses, heart palpitations, collapsing, debilitating weakness, cramps, regularly catching viruses and infections, poor concentration and memory, and so on) and it would be irresponsible to do something that meant I could not work. I don’t want to be anorexic again but in the dark times, I do in some way think that I wish I could go back there, at least to the place in my head that it opened.

In my following Chapters I’m going to try to describe what that place was, what terrible things I had to admit did lie beneath, and what the eating disorder meant in my life.

Again, I am sorry that this Chapter is not very well written. There is a lot that I am not sure how to explain and the memories are emotive. I’ve also tried not to go too far into my thought processes at this stage because I wanted to give an overview of my eating disorder history here, then in the next Chapters I will go on to say more about the reasons I didn’t eat, purged or binged.

We’re applying to evict you… Happy Christmas!

Since I lost / was forced to leave my secretarial job at the end of October, financially things have been terrible. Not only had I lost my income for the future, I lost expected income – I was paid only SSP for the time I had been signed off, rather than my wage, and was not told this until afterwards; I was not paid all the holiday pay I believe was due to me; I was given neither a notice period as specified in my contract, nor paid the notice period salary, so I was left without a month’s salary. In the end this left me down about £2,000.

I have taken steps against my former employer, reporting to them to the regulator for how I and several other colleagues were treated, however I have no hope of seeing this money. I can’t afford court proceedings and would have little hope to win.

I was very fortunate to find my current job at a department store but it is fewer hours (this is all I can now manage around my hospital appointments and with the state of my mental and physical health at the moment) and much lower pay. I thank the Lord that I have any job at all. It could have been much worse.

I have to apply for several benefits and the process takes weeks at best before any money comes through.

I had problems paying my rent in November, whilst I was waiting for my Housing and Council Tax benefit to be calculated and to receive any money. I was paid very little in November from my new job, because the finance department’s cut-off dates meant that though I had worked nearly a month, I received only one week’s pay. I phoned up the housing association from which I rent and told them about my situation and they were apparently very helpful. They agreed that whilst I was awaiting the Housing Benefit, I should just pay what I could.

I rang them several times and had several conversations with them, as did the council who needed to confirm some details for my benefit claim. Each time I spoke to them I asked to arrange a payment plan to deal with the arrears of rent and each time I was told that I couldn’t do this and should wait until the Housing Benefit had come through.

Then on 23rd December, I came home from work to find a letter from the housing association saying that they were applying to the Court for possession of my flat!! I would be evicted and would be liable for their Court fees.

This tipped me over the edge. It was absolutely more than I could cope with. By providence I was on the phone to a friend when I opened the letter. I still went completely to pieces and was literally about to take an overdose. If my friend had not talked to me for a long time I believe that I would have gone through with it. Thankfully after speaking on the phone to my friend at length, I was then absolutely overwhelmed with exhaustion and slept til the morning, which probably again saved me from doing anything.

The next day I phoned the housing association first thing. They told me that it was not a notice of eviction that I had received and that “it might be possible to avoid going to Court”!! Why would I be taken to Court, I asked. They claimed that I had not contacted them since the end of October. They claimed that I had not asked to make a payment plan. They said that it was my fault, when actually I had done everything that they told me to do. I had asked to make the payment plan and they had told me that I could not. If I had made a payment plan, this would not have happened, they said. So why did they tell me I could not make a payment plan, when I asked to do it? They claimed they did not know I had physical or mental health problems, when the reason I was housed with them was because of my health problems, when the tenancy support worker who helped me at the start of my tenancy had discussed them with them, when I had declared them on the forms I had to fill in at the start of my tenancy, and when I had discussed my situation in full on all the occasions I had phoned them since I lost my job (which they claimed to have no knowledge of).

I told them that the letter I had received – a day before Christmas, basically – had caused me so much distress that I had been about to take an overdose. “Oh dear,” they said….

Yes, oh dear! And a bit more.

After a long conversation they agreed to suspend action until mid January and I now have to write to them with all the dates I contacted them and what was arranged each time. And I will certainly be sending a letter of complaint.

How is it possible for them to claim they have no record or knowledge of any of the conversations I have had with them? How is it possible for them to claim they did not know my health problems? I will certainly conduct all future correspondence with them by letter sent by signed for delivery, so that they cannot deny I have made contact with them. How could they take no responsibility whatsoever for having not recorded any of the conversations I had with them, and not sharing information within their organisation? They lady I spoke to on Christmas Eve just said over and over, “well, I didn’t know any of this, you’ve never spoken to me”.

This really was almost more than I could cope with. I now feel that it’s a immediate possibility that I will lose my home.

I felt so angry once the first terror had passed. I had just got myself out of debt when I lost my job and now I am out of control and thrown straight back in again. I know it is only my responsibility to resolve it but I do not know how I can get out of this. Everything else mentally is worse because this constant anxiety is bubbling and rising in the background. I so needed my home to be safe for once. It’s like I’m not allowed to be safe and secure because as soon as something improves for a little while, it’s taken away and crashes again.

It’s too easy to resent when I feel like this. I need to be able to keep hoping, keep doing all I can to sort this out, apply for benefits, keep working, keep praying. God does not test us more than we can stand. But I don’t see that I can stand.

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.

Not that far from Bethlehem

Underneath the stars, just a simple man and wife,

Somewhere in the dark, his words cut the silent night –

“Take my hand, for the Child that you carry is God’s own,

And though it seems the road is long,

We’re not that far from Bethlehem.”

(Hopefully the above link works. It’s supposed to link to a video for the Christmas carol “Not that far from Bethlehem” by Point of Grace – see the footnote!)

It’s just a week til Christmas. I have very confused feelings around this time of year. Advent has passed so very quickly. It’s a time I really wish everything would slow down. I struggle all the more with relationships, especially in the family, and the knowledge that I am not what I should be is all the more painful. This must be normal for everyone, to some extent, I think. I think the more expectations there are, the more distance and emptiness hurts.

Feeling so weak, though it’s one of the most (if not the most) abundant times of hope and grace. It’s the time that Our Lord Jesus came to us, to love and heal and forgive us. It’s the root of our faith. Yet, this time of year it’s harder day to day and I feel all the more that I’m failing precisely because of my fear and emptiness.

Prayer and hope can seem nearly impossible and just as I feel a terrible darkness that seems to black out everything else when I’m distressed about interpersonal relationships, losses and so on, in the same way I can enter this state if I start to fear my God. The faith that at other times sustains me becomes a source of utter pain, “knowing” that I’m bad and can never be “enough” or with Him.

I start to make my God a sort of compilation of all the terrors and obsessional thoughts in my head, making God a punishing judge, who is angry with me and knows I am evil inside and cannot wait to punish and reject me for it.

This is so very dangerous. God is not the sum of my fears. My relationship with God does not depend on my thoughts, fears, hallucinations and sickness. When I read God’s Word in the Bible, He tells me that “perfect Love casts out fear”. He does not say we must be enough, but only “come to Me”. He does not say we must perfect ourselves to earn His love, but “you did not choose me but I [Jesus] have chosen you” and that we love because He loved us first and lifted us up in His arms.

So, this time of year, I try to answer His gentle voice, “come”. In prayer, I meditate upon drawing close to Jesus, Mary and Joseph at the stable in Bethlehem that first Christmas. Jesus Christ, who is all Love, is come to us as a helpless little baby, to share with us every joy, every suffering, every need, every feeling. He chose a young and poor woman, to be his Mother and to answer “yes” to God’s call, and through her “yes” and through her body, He came into the world. He was born in the “stable so bare” as the carol says, laid in a manger. He did not ask riches or a palace or great astounding things. He asked only love and a place in our hearts.

As Christ was born in that poor empty stable at Bethlehem, so He will come into our poor empty hearts. It does not matter if my heart is empty – there is the more space there for him to fill. It does not matter that I feel I have nothing to give him. A baby asks nothing but love and to be with us always. So does the Christ Child. He will fill my heart and He will be everything I am not. No amount of pain that I may feel can change that.

So I say yes, and in prayer and meditation I kneel close to the manger, and I wait and watch and hope and rejoice, with Mary and St Joseph. There we gather united with everyone who struggles, longs and hopes. However dark it seems, however long this road is, even in the midst of this most awful pain, we can never be far from Bethlehem.

 

We’re not that far from Bethlehem, where all our hope and joy began

For in our arms we’ll cherish Him,

No we’re not that far from Bethlehem.

Lyrics and score by Point of Grace – film extracts from “The Nativity” – with thanks to Crisen de Guzman for the video – all rights belong to the respective artists

 

 

 

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