Tag: psychosis

They’ve found her

My mother has been found. My abuser has been found.

It has been a little over a year since I first reported to the police the abuse done to me by my mother in my childhood and early adulthood.

Since I made my statement, the police had been searching for my mother to question her. It had come to the point that with her not being found for so long, part of me felt perhaps she never would be. Had she chosen to disappear? She had gone from her last known address, disappeared and ceased contact with the hospital that was treating her, no information about her whereabouts was known by the very few former friends and similar, and none of the few leads I could think of helped (a relative she might have had contact with, a place she worked a very long time ago and so on). Even the police’s searches of records held by places like the DWP or tax office yielded nothing (very strange since she must surely be claiming a Benefit, or a pension, or working). The police had even searched the death and marriages registers and were talking about the possibility she may have passed away. It was in my mind whether the time would come that I might have to accept that, though bizarrely without ever really knowing what happened to her.

Then at the weekend I got the news that the police have found her.

Shock. I was stunned.

So, now I am to meet with the DC who is working on my case, the same person who took my statement. He has spoken to my mother. I don’t know if he has interviewed her. I expect he must have. He has things he needs to tell me but felt we need to meet face to face to talk about it.

I’m in a sort of suspense til our conversation. There are so many questions and uncertainties and fears. Where was she? Probably the DC won’t be allowed to tell me. How did they find her? Perhaps he will be able to tell me how. What state is her health in? She was not in good physical health when I last saw her and her mental health conditions are severe; she never believed she was ill though. Has that changed? I doubt it – but perhaps that’s too much of an assumption. No, actually, it isn’t; given the years and years history anything else would be astonishing. What has happened to her since our contact ceased? She disappeared from contact with the hospital team – not surprising, sadly – so has she had no treatment since? What’s she doing? What danger is she in? And what danger is she to others, that’s in my mind too, because of what she did to me, and because of her violence when she is ill.

For me, what now? If she’s been questionned, what happened? What did she say? What do we do now? I can imagine what she will have said to the police about me. I’m trying not to imagine too much in general about this, as it can lead to no good. There is no point in imagining scenarios until I meet the DC. A big issue will be her mental state now, I think, and whether she has capacity to understand proceedings. I think another big issue will be how will there be any evidence of what I went through? So much happened when I was alone and isolated with her. The lack of evidence gives the voices in my head power and I’m stifled and paralysed quickly with the flashbacks on the one hand, the voices telling me liar, disgusting, your fault, you wanted it….

The last 2 days dissociative episodes have taken hold scarily often. I’m fighting them, sometimes. But often that makes me break too much or I’m too far in.

If I have to make some decisions over what happens next, how can I choose for good?

Ginny xxx

The wrong voices calling

The voices are very bad at the moment. My emotions are soaring and plummeting at the moment since my last group therapy and discharge on Friday. So it is not surprising the voices are worse. They often are when I’m emotional and stressed.

It’s as if now this stage of therapy is completed and I’m trying to hang on to the good and the real, the voices are getting louder (stronger?) trying to pull me back to the blackest darkness and terror where “reality” was my abuser’s words and threats. All morning I’ve heard her calling out to me. Sometimes just my name. Sometimes the things she’d say – mocking, detesting, making me an animal, less than human, threatening, confirming my evil and the terrible things that would happen (unless I gave in and gave her total control). I hear her. And it is terrifyingly real. It is totally outside, not an echo in my head. I turn towards the voice and dread grips me. It stays totally real to me even as I try to repeat my safety statement.

I am Ginny. I am 32 years old. Today is January 30th 2017. She is far away. I am safe now. I trust in God. …He created me for good not evil.

These aren’t the only voices I have but they are some of the most frightening and separate me most from reality. I don’t know how or if there is any way to stop or change the voices. If there is I haven’t found it in the therapy I’ve had so far. If I can’t change them can I lessen their power?

I try to remember,although the world created by my abuser was my reality – the only reality for 11 years and the most of it for another 14 or so – it is not the truth. The voice is not trying to do anything, or pulling me anywhere. It is a hallucination. It is a memory. It is not a person (now). A hallucination does not have a will or an aim. A hallucination is not physical so cannot pull or drag me. So why does it have power to cause me terror, to return me into the frightened child, to make it impossible to believe in my freedom or any goodness in me?

Several other people I’ve met who have personality disorders have shared having experiences of voices. In my 18 month MBT therapy, we talked about hearing voices in the group sessions. Sometimes for example, I’d share that I was struggling to stay present in the room because the voices were loud and scary and I was constantly being pulled away from reality. But in therapy we didn’t get to explore the experience of voices or how to cope with them, how they may interact with what you’re feeling and what is happening in reality, how they affect interactions… in therapy the focus was on using grounding techniques to move away from them and be present in the group and able to focus on others. Sometimes we talked a little about how the voices may affect our thoughts about ourselves and about others, for instance when we’re interacting with someone, leading to assumptions (they think I’m evil, the know I’m bad, that’s what the voices are saying) rather than curiosity about the other person’s thoughts.

However we didn’t talk about how to cope with them. We didn’t talk about their emotional effect on us, the way they pull us with them, the control they have even though it makes no sense, how they bring traumas right back, how what they tell us and make us feel is more gripping than our current experiences, if there is any way we can respond to lessen their power…

There is a place for using grounding techniques to cope and this is valuable. There is great worth in learning to be able to stay present for others here and now. Probably a value to staying present in the moment for ourselves. Yet I wish there were more than grounding techniques because there’s always next time the voices come. Their apparent power stays the same.

Perhaps I’ll look to see if there are any books that explore voices and how to cope. I’ve pretty much been told that the voices won’t go away but if I keep taking my medication, I won’t lose my grip on understanding they aren’t real. I feel I need to find more than that.

I would be very interested to hear about experiences of voices that anyone would like to share.

Ginny xxx

World Mental Health Day – William, Kate & Harry

World Mental Health Day – William, Kate & Harry

I’ve been impressed by the work the Duke and Duchess of Cambridge and Prince Harry are doing to de-stigmatise mental health conditions and raise awareness of the importance of being able to access the help we need. You can read about what they have been doing today here.

To my recollection their work and their discussion of their own personal experiences (for example, following Princess Diana’s death) is the first time I’ve heard  a member of the Royal Family openly discussing mental health and wellbeing and the importance of responding with compassion not judgement and stigma. It’s encouraging to me to see this change. Recently, many friends of mine have met with really painful and dangerous discrimination and absence of help when they were really in need (as I have I too in the past).

I’m putting in an application for an opportunity through a service user involvement network to speak, from a service user / patient’s perspective, to medical students about mental health, discrimination and support. I’m happy students recognise the need to learn about it. I don’t know quite how this will progress or if I’ll be chosen but I’ll let you know.

Ginny xxx

Image thanks to http://www.aol.co.uk

Fear, tears, pain, joy, guilt, thankful, anger, strength, shaken…

The emotions are crashing over me now. They stayed temporarily a little distant in the activity of yesterday afternoon and today. Now the activity has stopped. The rush of mixed experiences of the past week is temporarily still. I am physically utterly exhausted, shaky and hurting and it’s all I can do to get across the room. Sitting I feel like I’m being crushed. I’m cold and my chest aches deeply. I’m curled up in my dressing gown and blanket, needing all the comfort and grounding I can get. I feel childish and guilty for saying that, because I have no right to – what have I been through that’s so bad? – but it is true.

There’s so much to take in right now.

Intense waves of scary emotions jolted me through the week, especially fear and anxiety I cannot attribute to a logical cause that was there at the time. On reflection perhaps it was an emotional flashback to earlier times and threats, both distant (childhood) and more recent.

The hallucinations strengthened – auditory, visual, sensory – and scared me more.

My escape imaginary world was closer than ever and its pull stronger than ever.

Anger is raging and rising uncontrollably in me against my stepmother. All at once I feel huge guilt, fear, hurt, rage, the need to express what I feel and the impossibility and danger of ever actually doing so.

It’s feeding anger against my dad again; then against both of them together.

More memories of specific painful derogatory, demeaning, restricting, humiliating things my abuser did have been coming to the fore, along with memories of how her abusive power was perpetuated, and then in turn, more thoughts of how it feels – and this is so scary to write – similar patterns still repeat in my family. I need to get away from that.

It was goodbye to a friend in my therapy group for whom I care very very much. I’m still crying for her.

Another member of my therapy group to whom I also feel a particular connection, has suffered an unimaginable avalanche of hurts, struggles and illnesses. Now, he has been diagnosed with cancer which is likely to be late stage. The end of his life could be close. I’m crying for him.

Today was a special day. I had a little coffee morning to fundraise for Macmillan Cancer Support (part of the “World’s Biggest Coffee Morning” Macmillan run nationally). It is the first time I have ever done an event like this at home (following on from the courage I gained from having had some close friends over for my birthday earlier in the year). My anxiety was huge. I put as much as I could into the preparations. Good things happened today. My guests’ care and kindness was wonderful. This fills me up with gratitude.

So here I am now, afterwards, with this whole mix of soaring emotions. All of them I need to face and there is a lot of work for me to do. My individual therapy is tomorrow and I’m so glad. When the emotions are too much, every so often, I’m going to try to return to the thankfulness for today and remember everyone’s enjoyment and generosity. Somehow, this just a little restorative.

Ginny xxx

Not my GP

I’m very fortunate to have been able to consistently see the same GP most of the time over the past two years and to have a mostly good rapport with him. I know this is a help that lots of people don’t have. My Surgery recognises the importance of seeing the same person if you have to attend regularly and have ongoing health problems. I find it helps so much practically, in not having to constantly go over your history every time and the cost on time and your emotions that this incurs, as well as gaining confidence in someone. I don’t find it easy to trust new people and the effect of the voices and hallucinations can be worse when I’m meeting with someone new and afterwards.

Tomorrow I have to see a different GP. The Surgery called me this morning and explained that very sadly, my usual GP has suffered a family bereavement and will be off for many weeks at least. I am sorry and sad for him, all the more as I think he is a really good person, so I feel all the more empathy with him in this loss. It’s very sad.

Tomorrow I am seeing a GP who I have not seen face to face before but I have spoken with on the phone. The conversation and trying to get help has almost never gone well. She has been what felt very dismissive to me. I don’t think she believes me. She has told me that I’m making nasty threats when I’ve been feeling suicidal and self-harming and trying to get help, absolutely at the most desperate I’ve been. She’s hung up on me. I’ve ended up getting very angry and distressed in response. It was after speaking with this GP that I completely lost it at the Surgery a few months ago. They called the police and I know that I scared people by being so angry and losing control and that they were worried about me. When the police came I was sure they needed to arrest me and begged them to take me away because I was so afraid I was going to hurt someone and was terrified of my loss of control.

I’m scared of losing it again and also scared of not being believed. Things haven’t been good this past week but I’m scared of talking about anything in case she interprets it as me making threats or thinks I’m lying. I’m sure already she’ll think I’m lying and that she hates me. I was sure of that as soon as I spoke to her last time and I’m even more sure now after how badly I behaved when I lost control. I need to get my medical certificate renewed but I don’t know what she’ll do – she has not seen me before and doesn’t know me – and I’m scared she won’t agree to do it. For some reason I’ve already convinced myself she’ll think I’m lying and she’ll say nothing’s wrong with me. She’ll think I’m a fraud and don’t deserve any help.

The voices are screaming at me in my head about what she thinks of me and all the evil, fraud, liar kind of accusations, telling me what to do to hurt myself, telling me all the terrible things I’ll do if I don’t, horrible images behind my eyes that disgust me.

There was no other GP I could see tomorrow. I didn’t feel I could say I didn’t want to see this GP or explain why because it would be rude and I feel so guilty for how I lost it before and how I upset people. I’ve booked in next week with another GP I know and trust and I know that will help and that it will mean however tomorrow goes, I still have this appointment next week with someone I am comfortable with. So that’s a help.

I’m already so anxious thinking about it and having panic attacks. I am so tempted to just cancel the appointment tomorrow. But I know I need to talk to someone and I do need to try to get the certificate renewed. I’m getting triggered so quickly by feeling I am not believed, which is ironic because I struggle to believe myself as the voices rarely give me rest from their suggestions (sometimes slowly increasing doubts, sometimes overwhelming screams) about how I’ve deceived people or how the evil inside me will be exposed. The emotions associated with the past abuse are so uncontrollable and coming back to me separate from the memory of specific instances of abuse and it’s really hard to understand what’s happening.

At least after the GP appointment I see my support worker, who is someone I trust, so that will help me to stay a bit safer.

Ginny xxx

Walking this Borderland #13: Tangled!

(For an explanation of the intention of this series please click HERE. )

In learning to sit with different emotional states, I’ve discovered that tactile, sensory experiences are important for me. I find warmth, softness, different textures, tastes and so on soothing and a major way of soothing and coping with anxiety and distress. Creativity and surrounding myself with an environment that feels safe and contains pleasant sensory experiences is a necessary part of staying stable and well for me. 

It’s not surprising then that I find certain objects are good for aiding self-soothing. One habit I fall into when I’m anxious, upset or emotionally uncomfortable is scratching and pulling at the skin on my arms, hands and sometimes face. Often, until it starts to bleed this is an unconscious thing, though it can also be something I’m aware of but irresistibly compelled to do in response to psychotic thoughts about evil inside me or mental images of having to cut things out of me.

Meet my new toy – it’s a Tangle.

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The Tangle is a bendy, twisty, small plastic form, made of lots of smaller sections connected together so it can be stretched out, bunched up, wrapped round and twisted into different shapes between your fingers. It has a smooth, pleasing texture. It’s very light and little, easily fitting in your pocket or bag. I’ve started carrying this with me and in times I’m likely to start scratching – when I’m waiting for something or when I’m nervous, for example – I hold the Tangle and fiddle with it. So far it has worked well to reduce the unconscious scratching.

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I’m sure no end of other objects would also serve this purpose and I also use a special pebble and a tiny stuffed animal toy for similar purposes.

Now, on the subject of Tangled, here’s another kind of “Tangled” – one of my goddaughter’s favorite Disney songs (from the movie of that name) which I have to admit is quite uplifting, for all it may be cheesy. We all need a bit of happiness sometimes and this scene is quite magical.

Ginny xxx

“At last I’ve seen the light” from Disney’s musical “Tangled” sung by  Mandy Moore and Zachary Levi.

A Very Hungry Caterpillar finds a home

I found this little guy when I was sweeping my patio. I thought he’d prefer a nice leaf to curl up on, rather than the paving stones.

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I am trying to tidy up my patio garden. It isn’t big at all – I have a patio door that opens onto a very small paved area and then a small flower bed beyond. I haven’t given this little space the attention I should since I moved in, largely as my physical challenges make gardening tiring and painful. Plus I’ve never particularly enjoyed it!

This week I’ve made the promise to start caring for it better. It is a blessing that I have this little outside space. I didn’t expect it at all and living in a flat it’s a privilege to have any garden. It’s a help for everything from being able to hang out washing to getting to sit outside, breathe, pray, ground myself in all the sensations of outdoors, and feel less isolated when I’m not well enough to walk far – I don’t have to stay totally indoors.

So I want to behave more thankfully for my little garden and take care of it and find ways in which, just maybe, I can create something pretty. It can be part of learning to give some time to creating a permanent and stable home, which I’m really not used to having, as until I came to this flat I was living between different kinds of shared and temporary accommodation where most of the time I stayed shut away in my one room, too scared of interacting with other people and too locked into my obsessional thoughts and hallucinations to leave it unless I could fulfil my compulsive behaviors and unless I could be sure I’d see no-one. I’ve had to leave so many places when I lost jobs, couldn’t make the rent, broke down mentally and was so disturbed I’d be asked to leave by the people I was living with.

Some level of security (though I’m not without financial problems) is a new thing for me and it’s hard to build on it. Any home I have, I expect to lose. Actually, for some strange reason i haven’t figured out yet, having a home and taking responsibility for it frequently fills me with panic. I feel like I’m losing control or can’t manage it, I’m out of control with everything I’d want to be in order (paperwork or cleaning etc) or other times I’m not sure what I’m scared of; something to do with I’m not allowed my safety, knowing it’ll be taken away, fears of being attacked or watched by my abuser and flashbacks associated to particular places in my flat. Having said that, I can feel safe in my home and I even have a place within my home where I surround myself with comforting and grounding things that help me stay safe when I’m dissociating, having flashbacks, the emotions are too much, and the like. I thank God for that. It’s so important for me to learn how to build on this otherwise I ignore the goodness of everything I have. Giving myself permission to trust in having security and knowing how to create an ordered home that I care for and give thanks for, is a new thing to me. I’m trying to take some little steps towards it, with my garden and trying gradually to bring more order to each room in my home.

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(Thanks so much to Cathy and her lovely blog at  https://cathylynnbrooks.com/ for reminding me how nice it is hanging out washing in the sunshine 🙂 – and as ever encouraging me so much to appreciate the beauty of the present moment in the little things. )

Ginny xxx

Crashing

This is a hard post to write.

I have not been coping physically with my job for a long time. I have really tried to ignore this. Since I started it made my pain levels worse and ever since they have kept increasing. I kept hoping it would at least stop getting worse and maybe that I’d get better at coping with it. I wanted to be able to do it. Be some kind of normal. My job sometimes helps me mentally, engaging in something creative and focusing on helping customers and giving the best service I can. It takes my focus outward which I’ve long believed is really important in staying well. The tactile aspects of my work, handling the different fabrics and trying to create attractive displays, can in themselves be grounding and soothing. Additionally, it’s an area where I can try`to do some good and not feel useless. (I know that’s something I need to work on, how connected my sense of worth is with others’ outward perception of me, but I can’t deny it helps for the time being.)

Now I’ve come to the point of crashing completely. In the last 3 months in particular my pain and physical weakness has increased faster. Since around the time of my operation I guess marked a real down-turn physically and it was to be expected really that  my fibromyalgia symptoms will be worse for a while afterwards. Everything is worse really, my back problems (I had a slipped disc years ago), arthritis…

I know I haven’t really talked about it so maybe this sounds weird. Whenever I talk about my physical health I worry it all sounds stupid, nobody would believe me, I’m a fake and I should just get on with it and everything’s my fault. (There’s a lot I have to work on there too, I know.)

I feel like I’ve crashed suddenly. Gradually it has got harder and harder to – move, to put it bluntly…  Getting harder to get through the day….harder to be able to get home, having to sit and rest, and crumpling as soon as I get in, lying down most of the evening… Today I have had to spend most of the day lying down. Pain and shakiness in my legs makes any standing and walking really hard. My legs are cramping and jerking out of the blue. I can’t feel in my right foot normally and at the same time the pain is really bad through my lower back and hips, worst on the right… I’ve had all this before although not as bad, but I am very scared right now. I feel scared and shaky and lost and so tired. I slept a lot today too. My support worker came this morning and I was so tired I was struggling to literally get words out.

So I find myself admitting again that I am probably going to have to leave this job. The physical deterioration from trying to meet its demands is too much. I have tried to look into reducing my hours but it does not look as though this will be possible. I;d have to massively reduce them in any case. My manager has been kind and understanding in her approach but has to follow the sickness absence procedures set down by the company. Since I have been off sick 4 times within a 6 month period, this is flagged as a problem. I can well understand that it is not fair to colleagues to be off too frequently and I know myself that I am struggling more and more with daily tasks, which is increasing my anxiety and in turn my psychotic thoughts and my fears about what colleagues are saying and thinking about me and making it harder to cope with the hallucinations and all the mental struggles of every day.

Outside of work the effect is great too. Not only are the pain and mobility problems an issue, but I have no energy or coping resources left to manage day to day tasks like keeping my house clean, keeping in touch with people, doing positive things to bring a balance to life outside work, or perhaps most importantly right now, giving the energy to therapy and recovery that I need to. The months I have left with the PD service are precious and working on making use of my individual and group sessions is demanding. I want to be mentally “present” for it, not shut off protecting myself because I’m desperately trying to cope with pain and utter exhaustion.

I’m going to be referred to Occupational Health so I await to see what they will suggest.

ergonomic occ health

I also have to follow my doctors’ and my support worker’s advice. I believe they would all prefer me to reduce my hours. My support worker definitely thinks so.

The one thing that ironically, in a twisted way makes this situation possibly not quite so bad, is that I may actually not be worse off financially working fewer hours or not working at all. I want to talk about this more in a separate post shortly. It’s a bizarre situation that doesn’t sit well with me. At the moment I am struggling in pain and making myself physically worse every day, working part-time, earning just above the minimum hourly wage.  I receive less than £10 per week help towards my rent, I am not entitled to any help at all with things like council tax*, and although I was initially assessed as eligible for a small amount of tax credits, this decision has now been changed and I have been told that I am not entitled to any.  Now, I strongly believe that it is morally right to work as much as I can and not to expect to receive handouts when I could be earning myself. However, what I cannot get away from is that on my current earnings whilst I am working as many hours as I can (well, I have to admit now, more than I can) I cannot live. I do not have enough to cover basic bills and simple living costs and I would not be getting by if it were not for regular help from my family and even occasionally my very good friend who has lent me money for grocery shopping when money has been tightest.

Not only can this situation not go on – I am over 30 now and I simply cannot go on needing financial help from my dad; I have to support myself – but the cost of this job physically is just too much to go through to still not be able to live. It is painfully ironic that because if I were not working or were working fewer hours, for example for a few months or so whilst I complete my therapy, my financial situation would actually be more stable because of the greater help I would get towards rent and living costs. That makes me really really uncomfortable and it isn’t right. Yet I have to be able to live.

It isn’t the main factor that has led me to this point. If I were coping physically I would keep going and if I could I would see if I can increase my hours. But I’m forced to accept that just isn’t so and physically things are not good right now.

I feel really worn out and vulnerable right now. The last time I was so low physically, about 7 years ago, I didn’t feel so afraid or sad. I wonder why that change has come. Perhaps I feel more responsible now. Perhaps I am sadder about potentially leaving my job because there are aspects of it that I genuinely like this time. Perhaps I feel more of a failure that this has happened again.

I need to focus on the good things that could come out of it if I do have to leave. My health problems are not life threatening or anything that serious and so many people are going through much worse, much more medically severe, perhaps without friends to help them and understanding doctors. In moments I can see that there can be ways that in the next few months I can try to turn things around.

I don’t want anyone to feel bad for me. Tonight I just needed to get all this out and admit that I’m scared.

Thank you for listening. I can’t imagine where I would be right now without this blog and the support of you lovely people who read and care and comment. There’s so much more I should say on that. I hope you know how much you mean to me. Hugs xxx

Ginny xxx

(*apart from the 25% single person occupancy discount. For non-UK readers, council tax is a roughly monthly fee payable towards local government spending like policing and other emergency services, refuse collection, some elements of care for vulnerable people, etc. Most working adults pay council tax. The amount payable depends on the value of the property you live in.)

Image not mine, sourced on the ever useful Google – I am afraid I do not know the artist (it says in the top left I believe but I was not able to expand it to read it.

So much I can’t get out

This hasn’t been a great week. There’s so much I want to write but can’t get down. Two really important relationships have turned out not to be at all what I thought they were. The two people who ever made me feel a little bit like I might not be all bad inside, told me what they thought of our relationship and of me. .. and these only relationships and only people told me I was a drain, resented, to be run from, too much, dominating everything,  nothing, not wanted, nothing had ever been shared.

I want to write but the words spiral through my head and get lost and I feel as if I’m spiraling too, falling uncontrollably away from my last hope of belonging or doing good, full of pain and doing only wrong, or dissociating and watching numb actions from a distance. I try to give my feelings a name but somewhere between the hurt, the fear, the spiraling thoughts and the words, it all gets lost. In any case,  I’m scared to talk to anyone and do not want to even step outside but at the same time I’m desperate for someone to hold me.

What do you do when you find out the most important things you thought you shared with those you cared about most,  were not shared? When the people who gave you hope tell you what harm you’ve done? When you trusted someone enough to tell them the most shameful, painful parts of your story- then they leave,  or tell you you had no close bond at all? And they walk away and you never do, ever.

xxx

A closing drawbridge and a silent cry: too much; too big

 

A closing drawbridge and a silent cry

Eating disorders and personality disorder

My body becoming too much

WARNING: this post contains potentially triggering content on the topic of eating disorders, weight, body image and emotions. Please proceed with caution. Please note that in this post I express my distressed thoughts about my body and the relationship between my body, needs, emotions and relationships. I’m aware that a lot of these thoughts are part of my personality disorder and historic eating disorders. I am not advocating or encouraging these perceptions and feelings but describing what the process of trying to live with my body and face emotions is like. I think the stage of therapy I’m going through is bringing a lot of this distress to the surface. 

My body is changing. It’s out of my control (or so it feels, though the angry punishing eating disordered voice in my head says it’s me that’s out of control – disgusting fat b*tch – and my own disgusting failure).

I have gained so much weight in the past 2 years. I have tried hard in the last few weeks to lose and done all the things that used to be my trusted go-to solutions, with the exception of using illicit medications. I have failed and no matter that I succeeded in restriction, my weight has hardly dropped. If anything, now I feel more out of control. Sometimes I wonder if any of it is to do with being in my 30s now (quarter aged spread instead of middle aged spread?!) and my mobility being poorer with so much physical pain just now.  But that does nothing to justify the gain or calm me. Many people taking the medications I take report weight gain as a side effect even when restricting.  I think it increases my appetite but I know so does my need for comfort and my lonely emptiness and my…feeling. Feeling that’s dangerous and unchecked and explosive.

Anorexia meant I was never alone. I was cold and numb and empty and hurting, but needs and unbearable feeling stayed where they belonged and I dissociated, living somewhere whiter, higher, safer, always with the twisted pleasure of bitter success in my spiral to greater protection and greater weakness. Anorexia was my companion, that reassured me all would be well if I did not deviate from this path,  spurring me on with wild energy to control and deprive and make dangerous need and demands unreachable. Soon enough I would detach and dissociate totally then maybe disappear.

Anorexia left me. Abandoned me. I failed yet again. Just like my friends, even my family, my protector and guide left me. Found out I was a vile disgusting greedy failure, undeserving of that whiter place. Anorexia too abandoned me, and sped away to a place I can no longer reach, now that it is proved yet again that really the evil inside consumes and demands and if anyone else thinks differently, it’s only that I’ve tricked them into staying and caring. They’ll leave soon, when they find out.

I could take it if it were only for my protection that I needed my friend anorexia. But the thing is, it was to protect everyone else, first and foremost, from the danger and “too much” “too big”that I am. Without my friend I hurt beyond control and I hurt others beyond control.

I look in the mirror and I’m frightened and recoil from what I see. I wish I could rip myself away from the “too much” in the presence that I see, hating every part of the space I occupy, the weight, the body that absolutely does not seem to fit together right and screams too much, too much. I cannot escape. I cannot get rid of this body and these needs. I cannot stop what it contains, the out of control, the demanding, aching. … alone without my friend to starve and cut and numb and leave this place, I cannot stop the damage I will cause to everyone I so care for and so wish to save, protect and love.

Ginny xxx