Tag: PTSD

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.

Slipping through our fingers

There have been several cases in the news recently, in particular two this week, of children suffering unfathomable cruelty at the hands of their parents / caregivers. Much has and will be made of the failings on the part of social services and social workers. How could the horrors and suffering go unnoticed and why were concerns not followed up, staff nor taking a more joined up approach, so the children could slip through the net?

I don’t doubt that there certainly were failings in the services. I’m not denying that. I can’t imagine the guilt the workers involved in those two cases are feeling right now. I’ve suffered myself and so did my mother and so have several other people I care about, because of failings in the organisations that should give support and protection, which let us fall through the net without intervention in times of crisis and without promised follow up or communication across different services. Sometimes the services involved have seem totally unaware of the harm this causes and unwilling to take responsibility. That hurts even more. Fortunately I have never suffered anything approaching what the children in this week’s cases did.

I’m not trying to deny that there were failings and I don’t want to hurt anyone who has been through similar experiences. However I think the somewhat understandable jump to publicise the blame attributed to the social workers and agencies masks some important points.

First, the perpetrators of the terrible abuse the children suffered were their mothers, father’s and family members. That’s the greatest horror. It is terrifying that as humans we are capable of inflicting such suffering on another, let alone on one of our own family or our own child. It’s particularly horrific that a mother can do this to her own child. It so negates every good and nurturing thing a mother is. It means no relationship and no home is immune to evil actions and absence of love.

Secondly, that is such a frightening fact and we want to know why. How and why can a person do that? What does that mean about what’s possible? About our human race? That sounds like an overly broad concept really. But I think it shakes us. Can we conceive that our world is one where what should be the safest and most protective relationship, mother and child,  is used to inflict fear and hurt and pain?  We don’t want to. We at least need some explanation. It’s easier to label the failing of a particular social worker or agency, because that we can understand. That we can name. What brought the abusers to use their own children that way, we can’t.

Thirdly – and this is something that’s hard to explain but significant to me as a survivor of childhood abuse – these horrific abuses can and do happen in secret and undetected. Trying to come to terms with what happened to me and questioning over and over whether the things I can remember done to me are true, I’ve often doubted myself and told myself it must have been my fault or I must be mad and inventing it all, because at the time nobody else realised what was going on and nobody intervened and people thought my family was normal (er okay maybe not but they didn’t often suspect the full truth). These two tragic cases in this week’s news show the awful fact that abuse much worse than what I suffered can indeed continue in secret. Therein lies the abuser’s power to control, manipulate and deny.

Fourthly, no more resources are coming for social workers and care and protection teams at the moment. The little glimpses I’ve seen from my work in hospitals, psychiatric services, care teams and so on has shown me loud and clear that there simply are not enough hours in the day and not enough people on the ground to have the contact and communication and time to spend directly with children, families, patients in need,  as well as following the ever more extensive proformas and completing paperwork that is required to meet the rules and regulations (which are supposed to ensure good care is happening but at the same time take you away from doing it).

This is no new or ground breaking feeling. I think most people in nursing or caring services have been saying this for years. But it’s still frighteningly swept under the carpet and denied by those in power. When I worked in a service that supported teenagers and young adults with mental health needs and social support needs, I would take the minutes of clinical team meetings. In one such meeting, changes to documentation for care planning and recording were being introduced, which would require nursing staff to (a) spend much longer away from patients, sitting at computers completing databases and reports and (b) in many cases require nursing staff to spend already limited professional development time on training in IT packages, not in patient care.  Of course, the aim of all these whizz new care planning systems was supposed to be a magical improvement in compliance with regulations about good care. However, nobody could answer who was going to be delivering the care during the time that the already over stretched nurses were completing the compliance paperwork. I wonder whether there’s a box in the risk assessment screen to record the increased risk caused by the fact the nurses and carers are filling in the [expletive deleted] risk screen instead of assessing the patients? 😉 Time and time again there was no answer to this impossibility. In that meeting, one or two nurses directly asked, how in the same shift with the same staff,  were they to fit in their work with their patients, as well as completing the new compliance activities being introduced. How could they do both? Which was to go when the time ran out? In my eyes the response was appalling. The nurses were told that was an unacceptable attitude to display and there was simply no choice and the compliance work was to be done. This came from a senior clinician who I had greatly respected and her response was totally at odds with her usual very reflective approach. Of course I don’t know the history with that particular member of staff who asked the questions and perhaps there was more to it than that, but there seemed a forced denial of the impossibility of continuing to provide good care and the level of presence on the ground with those we are caring for,  which is so important if we are to prevent tragedies like the children who slip through the net where abuse and suffering goes undetected.

I left the service I mentioned because more and more changes were taking clinicians, and support staff like myself, away from being able to maintain the personal contact with patients.  (I’ve since regretted leaving, I’ll admit.) Clinicians left too, at least in part due to stress and sadness around similar issues. They were a great loss to their patients, in my opinion.

A little later I worked a temp cover role as a secretary for the legal team that supported my local county council’s child protection services. Round about this time I thought about training as a social worker. I didn’t in the end. I thought I’d find far too many situations where my hands were tied and too many times bureaucracy stopped me doing the good that was needed.

….

I cry for the children that suffered and for those who so want to be present on the ground to help those at risk but who are taken away and whose voices are silenced when they highlight the lack of resources and impossibility of meeting the demands of keeping children safe in the field, and complying with everything that’s supposed to be ensuring children’s safety. One thing is sure and that’s that it is far too easy to be silenced – again both in the case of the victims and the carers pointing out the shortage of resources to help them. Let’s keep on speaking out.

Ginny xxx

Not my day off

Today has been demanding. It’s one of those days that seems too much to have been only one day. I got big stuff done but also I’m losing time in unsettling ways and I know I was dissociating a lot between the different tasks and meetings I had to do, slipping out of being engaged with what’s going on and what I’m feeling and struggling to come back. Nevertheless I got through quite a few challenges.

Last night I knew I needed to tidy and clean my flat. My support worker was coming today. Also I hadn’t been on top of the housework since my operation and it was bothering me more and more. Recently I’ve started to find a greater sense of order and calmness if I don’t have too many things disorganised around me. This is interesting because til now, I’ve tended towards accumulating things I don’t need and not being able to keep my house ordered, not exactly hoarding but not being able to face items and paperwork and household tasks without going into panic.

Yesterday I was very anxious about today but put some of the physical drive from the anxiety into cleaning and then went on to clearing out some of my cupboards. By late evening I’d cleared 7 big bags (between rubbish and charity shop) and set 3 more big bags of things to try to sell at a car boot sale. The fact I don’t have a car for the boot element of that plan is potentially problematic 🙂 but there are the odd few table-top, largely indoor, sales in community centres / church halls here in the summer and I’m hoping I can find one to join in.

Today was a struggle to get up. Everything hurt. Still, I got together the papers I needed to show my new support worker (more on this tomorrow), then it was off to my care coordination appointment with my CPN. This wasn’t easy to go to because, although my last appointment was okay, in the two previous appointments I’d been really distressed and felt I didn’t get heard when I was desperate and at risk. Today’s appointment was actually really good. We looked at some DBT skills and we did a review which was overdue (every 6 months or so is a review appointment). I’ve not yet felt able to discuss with my care coordinator exactly what went wrong in the difficult appointments earlier this year when everything was going to pieces. I’m scared I’d lose control and the feelings of anger and not being believed would return and I’d do bad things and be back where I was. However my care coordinator and I have managed to move forwards having 2 positive appointments. I was scared after what I’d done – how upset and angry I’d got – he wouldn’t believe me or want me anymore and they’d know how bad I am and that I didn’t deserve help. That hasn’t happened. That’s something that I don’t usually get to experience.

Straight after my care coordination I met my support worker, H., who is from a housing support charity I was referred to recently. He is going to help me sort out my benefits like Housing & Council Tax Benefit, Tax Credits and disability benefits,  as well as liaising with my landlord about the rent arrears that I got into when I lost my job last year. It was a long appointment. We went through the background to how I’d got here, financially and in terms of my health, and we looked at lots of documentation, my income and my benefit and Council Tax notices. This took a lot out of me and I came so close inside to panic and losing it and emotions shooting too high. H. was very calm and non judgemental, which helped a lot. (More on this in the next couple of days.)

Then I had to rush to my GP appointment, which was the first since I’d been very distressed and angry at the surgery a couple of weeks ago;  also the first since my operation and finding out endometriosis isn’t actually the explanation for my pain and gynae issues. I’m still working through what happened in today’s appointment. I was dreading going into the surgery because I’m still terrified of what I did and how much I lost it. I was ashamed and embarrased and knew that they probably didn’t want me around again. I knew I’d really upset and inconvenienced and disturbed people. I’d scared people. That’s the worst thing,  the harm I caused, the bad I’ve always feared getting out of me. Talking to the GP  and discussing what happened and then also talking about my physical health was really emotionally charged.  It’s hard trying to deal with a lot of uncertainties about my physical symptoms. I know not having endometriosis is a really good thing but not having any explanation for all the things I thought it explained, and the fact the doctor isn’t really interested any more in investigating what may be wrong – well, that’s hard and triggers all my fears that it’s all in my head, I’ve made it up or I’m mad, it’s my fault. …

After the GP it was off to the pharmacy with my prescription, then finally home.

It’s been quite a day. I had a soothing bath tonight. Today was the first day I could have a bath since the operation (don’t worry I promise I did still wash 😉 !). The doctor sealed the wound with dissolvable stitches so it was important not to soak them in water too soon or they could have come undone. Also it was not safe to try to get in and out of the bath whilst my mobility was further reduced with post op effects. Falling is a risk for me anyway because of the problems the fibromyalgia and arthritis cause in my legs. So, tonight was a good little relaxation and refreshment. The little things do help!

How has your day been?

Ginny xxx

 

Walking this Borderland #11: ice and lemon?

[Warning: the last 2 paragraphs under the *** contain discussion of self harm]

I know I’ve banged on about this technique elsewhere  in this blog but I just realised it may be a useful tip to add to the collection of coping strategies I’m trying to build up  in this Borderland series. Also, last week I learnt another similar very effective tip which I’d like to share. Thank you for bearing with me through the first two paragraphs if you’ve read my previous posts mentioning this topic.

In Borderline, regulation of emotions is difficult. States of emotional arousal shift quickly. Emotions and the intensity with which they are experienced can change rapidly and yet quickly become all consuming. The instability doesn’t make the emotions less real. Emotions may rise more quickly than they do in people without Borderline PD and stay at the higher level for longer. Equally, those of us with Borderline may suddenly enter emotionally numb or cut off states.

Both extremes can be dangerous, in my experience. Both can quickly tip into dangerous impulsivity, recklessbehaviour and decisions, self harm, suicidal intentions, explosive emotions and higher and higher states of distress. In either state we can’t explore our feelings and thoughts or other people’s feelings and intentions. Most coping strategies or systems of value that keep us strong, or protective factors like caring about other people, or religious faith or other beliefs that give us hope, become inaccessible in these states.

We need something that changes or emotional state so that we are able to reach again for these strengths and beliefs and strategies. One thing that can do this is giving the body a (non harmful) shock or surprise. We can only experience a certain number of sensations at once. A sudden strong physical sensation can serve enough to slightly bring our emotions away from the extreme. Once our emotions are coming away from the extreme, and only then, can we access other thought processes and coping strategies such as self soothing or the rescue box.

My top two ways to create this shift are as follows:

  • Lemon juice: lemon juice is a sharp sour taste. Take a couple of mouthfuls of neat lemon juice. You can even keep a small container of lemon juice in your bag when you’re out (easily available in supermarkets, eg the plastic “Jif” lemons).
  • Instant ice packs: I just discovered these! A really helpful nurse have me one when I was getting panicky in hospital last week after my op. I find this more effective and more practical than holding ice cubes, which is another alternative. Instant ice packs are really small and light, containing little crystals which activate to become cold when you squeeze and shake the packet. The tactile aspect is another helpful distraction too. I’m going to try to get some more. They appear to be available online from about 50p each, though I haven’t tried and tested any sources yet.

It sounds crazy, but the sudden ice and lemon shock does work. (Note to self, don’t follow the ice and lemon with the gin every time 😉 ! Remember to stick to Cola. Joke. No offence intended.)

Other potential ways of achieving the same effect include chewing small pieces of chilli (not too much and make sure you aren’t allergic first!), putting mustard on your tongue, or putting your head under a cold shower. The lemon and the ice are just the ones that work best for me and that I find most practical. I can use them even when I’m out or away from home.

This isn’t intended to be a long term solution but a short term way to keep safe and regain some stability. After you’ve used one of these techniques, you may then find you’re in a position to use other coping strategies once your level of distress is reduced (self soothing or mentalisation, for instance).

****

Incidentally, I wonder if there’s ever a link between why these techniques work and the drive to self harm. I say this with caution because it’s a sensitive and painful thing and what drives someone to self harm will be different for each person. For me, sometimes there’s pain, loss, need, anger, or self hate, or needing to hurt myself so I don’t hurt anyone else, or needing the physical pain to numb and quiet the noise in my head and voices, or to know what the physical pain will almost faithfully be as it stills some of the much more unbearable mental pain for just a little while. For the next person it’ll be different.

One CPN I talked to describes the ice pack and lemon type techniques as safe self-harm. It’s a shock, a not pleasant, over powering physical sensation. Personally I don’t see it as similar to self harm or at all a way of self harming safely. Nor do I think it has in itself directly reduced my self harming. I don’t think it’s yet something I could do to avoid self harming once I’m at the point I’m about to self harm, although perhaps it does stop me reaching that point in the first place. However I think perhaps I see some of the point the nurse was making, in that the ice or lemon shock serves to still and control the emotion a little bit. Maybe part of why I started to self harm was needing to control unbearable emotion.

Anyhow.  When life gives you lemons, as the saying goes. …

Ginny xxx

 

Losing her

Warning: this post contains one very brief mention of suicidal thoughts and overdose.

(Also I’ve a feeling it’s a load of rambling junk. Sorry.)

I’ve lost my friend. It really feels like a loss and hurts like she’s gone away, disappeared, except it’s worse because it’s entirely because of me that she’s chosen to go. She doesn’t want to be close anymore, she said; not close like she says she tried to be or like she says I wanted us to be. My personality disorder, me, my thoughts and needs, have made our relationship something stressful she doesn’t want.

I really care for her, I still do. My feelings for her haven’t changed. I still love her as a friend, want to thank her for all the times she has been there, want to do something to make right the hurt I caused, want to be able to be there for her when she wants or needs me – except she didn’t and doesn’t.

I don’t know exactly how long she’d been feeling she didn’t want to be close anymore before she told me. I’d suspected it for a long time. I really hate what I’ve done to her and that I’ve stressed her and been no good to her. I hate that my illness, essentially, me (my thought, my feelings, my needs, my actions) have been too much. Another person has gone away. Another relationship has gone. I’ve hurt someone else.

You can read a bit morehere (around paragraphs 5, 6, 7) and  here and here about some of the history of what happened with N. Our contact had been strained for several months.

After another period of not hearing from her following my last letter, call and texts, last week before my operation I decided to be more open than usual. I sent N an email, thanking her for forgiving me and explaining I was still really worried about the hurt and upset if caused her, and saying that as I wasn’t hearing from her and she hadn’t said anything beyond that she forgave me,  I was not sure if she wanted to stay in touch. The way I see it, N forgiving me for the hurt I caused did not have to mean she wanted to have contact with me going forward. I directly said I wasn’t sure what she wanted, and asked her.

Also, I took quite a risk and explained to her some of the thought process I talked about in my last post on this topic. I explained how when I don’t hear back from someone I really care about, when they stop communicating, or cancel plans, or don’t show without making any contact,  my thoughts are instantly either: that this proves how they can’t possibly want me around really (who would?) and as soon as I start trusting they leave because all along they knew I’m an evil fake really;  or that they are seriously hurt, or ill,  or got in an accident, and it’s my fault. Often both one after the other. Usually I never admit to these thoughts. I know it’s crazy. I know it’s weird. I know it doesn’t make sense I have these thoughts then get angry with people. I don’t want my friends to feel obliged to take into consideration my weird ill thought processes and make allowances for them in what they do. For example, I don’t want them to feel they have to be more careful what they say to me or to keep in touch more regularly with me than they would with another friend. (Paradoxically I don’t know if, in the way I think and what I need, I do require of people an abnormal level of contact. I’m diagnosed Borderline but I think I have features of dependent personality disorder too!) However things had reached such a point with N that I felt I had to be explicit about what I was feeling and why I had found it so hard to cope when over a few months she stopped keeping in touch and seemed to be restricting contact and canceled or altered several plans to meet (this was one of the things we first fell out over a few weeks ago).

I explained all this as well, as my hesitancy to explain it because I didn’t want to pressure her. I said I know that I make it too complicated and I need too much and my illness makes it too hard to be friends. That I really wanted to be there for her but it was clear I totally failed at that and it’s my fault there’s nothing good for her in the relationship. I said I’d rather know straight if it would be better for her not to be in touch with me.

I’ve never been that open with someone about my thought processes about my relationship with them, outside of my therapy group.

N wrote back a few days later. She was empathic – she said she is sorry there is so much distress going on for me. She said she doesn’t keep in touch regularly across the board when she’s busy. She said it’s stressful for both of us to communicate, when there is so much meaning for me in each interaction. She thinks it’s too distressing for me to cope with the likelihood of her changing plans. She said she can’t be as close a friend as she tried to be or as I want her to be. She offered that we can still meet sometimes or email – which surprised me, actually.

I know it isn’t a total end of the relationship. I’m hoping we can in some way keep in touch and I can remember she doesn’t want to be as close. I hope I can do that and not need too much. But I always need too much. Maybe this whole thing wouldn’t be so bad if I didn’t. Never would have happened if I didn’t.

One of the things that hurts the most is that I can never now make right the hurt I’ve caused N. I have made her and needed her to be closer than she wanted to be. I have made her stressed and upset when she’s done so much for me. It has been as I feared. I was too much, yet again;  I needed too much, asked too much, my thoughts and my behaviour made everything too much for the other person.

I told N some of that briefly too, and I thanked her for telling me honestly. I tried to tell her I’m sorry and thank you. I fear it appears it has little meaning now. I really meant it. I need to thank her for so much over the years I’ve known her. I don’t know if she knows. It seems to me all I’ve done is stress her. I don’t know exactly how long I’ve been making her be closer than she wanted. She doesn’t know it but she has possibly literally saved my life. One night I was on the brink of a massive overdose. She happened to call me at that time and as we spoke, she and her husband gave me some hope back and pulled me back from the edge. She knew I was distressed but not how close to ending it I was. I didn’t tell her explicitly at the time or afterwards, because I didn’t want to scare her or make her feel responsible for keeping me safe from that in the future if she knew how unstable I was and the potential influence ordinarily insignificant interactions and events could have on me. Now I wish I had told her.

Some while ago someone I care about told me, “look at what your friends do for you, why isn’t it enough for you? It’s nobody else’s responsibility to make you feel better,” and they told me I have to be more together so my emotions don’t dominate everything. Yet again I’ve acted on the basis of my weird thoughts, I’ve needed other people to do more than they wanted to, more than normal, and I’ve needed them to make it better.

I’m going to stop now. This post is a mess. I’m feeling so empty, hurting for losing N, hurting and angry for the harm I’ve done her, desperate because of how my PD and just …me….wrecks relationships and makes me too much.

Ginny xxx

 

I’m sorry —

I don’t know what to do about the hurt I’ve caused.

A few weeks ago I posted about how I’d fallen out with my good friend N. I have been wanting to apologise to her. I don’t feel I can ask her to forgive me. I know I hurt her. I know I spoke when I was angry and distraught and I caused her a lot of pain.

I was hurt too. I was desperate and unstable and in crisis and I did really need help, need someone; I was going to pieces. But this doesn’t mean I had the right to demand things from her or that she had to be there for me when she couldn’t. I acted ungrateful and angry. I lost sight of all the care she’d given me.

Then there’s the knowledge that she had found me a burden and my certainty I was an annoyance and inconvenience and angered her and she saw seeing me as a duty and there was nothing good for her in the relationship and she didn’t want to be around me anymore. Who would. She was clear she thought nobody would stay with me when I was in the state I was in. That was true and it was also true I needed someone but that didn’t mean it had to be her.

I know I’ve caused her a huge amount of upset and hurt and been very childish and selfish and needed too much. I know I’ve probably angered and hurt her in ways I don’t know yet or understand. She told me I had.

I don’t know what to do. I wanted to tell her I’m so sorry. I wrote to her so many times and tore it up because each time it seemed so stupid and self centred and a rubbish apology. I wrote several letters that I didn’t tear up. I went to her place to see her and took the letters. If she was in, I’d see if I could speak to her face to face if she’d let me. Then I’d go. If she wasn’t I’d post the letters through the door. I went and she was not in so I posted the letters through the door.

I didn’t ask for us to start meeting up again. I think that might not be good for her because I’m still so unstable. I’m still going from crisis to crisis and needing too much help and so upset and angry at times it wouldn’t be fair to her or anyone to try to be meeting up. That said I miss her and care for her a lot and really really really wish I could be there for her and thank her and support her when she needs it. (But I’m not the one she goes to when she needs anything, much as I’ve tried to be there.) I can’t ask her to meet again but I wish I could tell her I’m sorry. And know if she hears it or accepts it.

I haven’t heard anything from her since I dropped off the letter. It was 2 weeks ago. I wondered if she might be away but at this time of year it isn’t likely and the car was “home” when I left the letter. I am worrying if she could be ill. This turned into panicky, extended worrying that she is ill because of me, or worse. That’s what I worry about if I’ve upset someone.

I think she is so hurt and angry and disgusted with me she wants no more contact. I deserve that. Yet I wasn’t prepared for silence. I was prepared for her furious anger and hurt and her to tell me never to contact her again. Or for her to tell me how she felt about what I said and did. I did not expect and am not asking forgiveness. I wish I could know something I could do to make her know I really really am sorry and how much she matters to me and how wrong I was. I wish that even though I don’t think she can forgive me could she accept that I am sorry?

However needing to know that she hears and accepts that I am sorry is a very selfish part of apologising, when I think about it. It’s something that would stabilise the horror I feel at what I said and did and ease my own hurt.  I should accept not having it.

The amount I’ve hurt her is really raw and I’m really scared at what I’ve done. I’m sad and hurting for losing N. as well. It’s my fault but I’m still missing her and scared at what I’ve done. What I’ve done to the relationship and what I’ve done to her.

Ginny xxx

Selling star maps to the sun – disconnecting behind the front

Camera One closes in, the soundtrack starts, the scene begins- you’re playing you now…

on the corner of a street, in a lawn chair in the heat, sightseers see what they want, you’re selling star maps to the sun…

(Josh Jopin – Camera One)

The disconnection between what’s going on inside me and what I have to be on the outside is scaring me. I’m getting worse at it. Out of control emotions are scaring me, especially explosive rage. I’m losing control. It feels as if everything I feared might happen if I stopped self harming is now unfolding rapidly and I’m losing it.

I’m faking being alright whilst I’m dissociating inside, until a dream-state traps me and I can’t function or speak,  or until for no good reason at all the anger explodes.

I have to take responsibility and I desperately don’t want to run away from this but I have no control in those times. I’ve been taken over by a dangerous angry screaming force that can only hurt, or a needing, crying child. Afterwards for days it’s as if I’m just watching myself playing a part.

I don’t know how to break out of it.

Ginny xxx

One of the most dangerous ways to react to someone with BPD who is asking for help when they are suicidal or self-harming

 

 

TRIGGER WARNING: fairly massive warning on this one that this post discusses suicide and self harm and issues around getting care in crisis…

Yesterday I was met with one of the most punitive, ignorant and dangerous reactions I have had from a medical professional. I wonder if people who react like this actually do not realise the genuine danger patients are in and how much further into danger this kind of reaction pushes us.

As I write this post I want to be clear that I am now safe and have received help and I am not posting this to alarm or worry readers about me. I’ve been seen in emergency services and eventually had very supportive care, which I will post about in due course. Please don’t panic about me. I am now safe and have had help. I just think what I experienced earlier is a massively dangerous issue that needs to be highlighted.

Yesterday I was absolutely unable to cope. The pressure of my housing situation, financial problems, threat of losing my flat, trying to discuss things with my landlord, my physical help, repeated errors from benefits services and other supposed sources of support, the lack of help over the past 5 months or so when I’ve been at my lowest points, the voices and flashbacks and nightmares – everything boiled over and again I was in the place where the pain and emotions and loss and guilt blocked out any ability to carry on.

I lost it and I was at the point of trying to end my life. I knew how I was going to do it. I had tried and tried but had nothing left.

I spoke on the phone to the GP Surgery. Somewhere, I guess some part of me was still wanting some kind of help or at least daring to tell someone. (They had called me over issues with a mess up over the prescription i should have had; I’d again been left without my medication. ) I admitted what I was feeling. I begged to see someone. I don’t know what made me do that, ask for help when the decision was already made in my mind that this was it now and I’d come to the end. But I did.

I admitted that I wanted to end my life and that I was self harming. I admitted that I had the tablets to overdose. I asked to be seen and that I needed help now, could they see me or get the crisis team? I said how all the mess ups with my prescriptions and benefits and no help in crisis were piling things onto me and making it more and more impossible to cope. I was having hallucinations and flashbacks. I had been asking for help for months. Now I could not go on anymore, I was going to end it. I needed help.

The GP spoke over me from the start. She told me that “you have to be extremely careful about how you are coming across” if I expected to get any medication. She then told me repeatedly, in response to me admitting that I was suicidal and self harming, that “that is not a fair threat to make to people” that “you will find I do not respond to threats” and that I am a responsible adult able to make my own decisions and there is no reason that I should take an overdose. She then announced that she was going to end the call and hung up on me whilst I was begging her to help me.

If Someone with Borderline, or any other mental health problem, admits to suicidal thoughts, plans or intentions, or self-harm, it is the most incredibly ignorant and dangerous reaction to treat them as though they are making threats in order to manipulate and must be punished accordingly. The stereotype that people with personality disorders or any mental health problem are manipulative, or that being suicidal or struggling with self-harming  is attention seeking,  are extremely dangerous. It is all the more dangerous when it is trusted healthcare professionals acting on the basis of these stereotypes when their patients have dared to ask for help, meaning that when we are in immediate danger we are dismissed, punished and rejected.

Experiencing suicidal thoughts is not attention seeking. Self harming is not to create drama or cry for attention. Admitting that you are in danger and want to end your life, that you are absolutely at the end of the road and can’t go on, that everything being piled on you is pushing you nearer and nearer the edge, is not making threats. The attitude shown by the GP today makes it impossible to ask for help when we are most in danger. I now know that if I admit to the terrible thoughts and feelings, I’ll be treated as though I’m manipulating people and will be rejected. If patients are treated like this, suicide and self harm is made something that must never be admitted to or talked about and for which help can never be sought. If patients are treated like this, all the feelings and events that have brought them to the point of suicide are dismissed in an instant, as our position is made out to be manipulative fabricated threats rather than complete brokenness.

Yes, I am an adult. Yes, I am responsible for my actions. If I self harm or attempt suicide, it is my action alone. If I cause myself harm that is done by me alone. That does not mean that the experiences and emotions behind my actions are not real, that I am not in danger,  that I am fake. No longer being able to carry on doesn’t mean I am manipulative. Asking for help and admitting to the horrible things in my head doesn’t mean I am making threats. Asking for help doesn’t mean the feelings that make me want to end it aren’t real. The fact that if I do something to hurt myself, it’s my action, doesn’t mean I’m not in danger and don’t need help.

I’m terrified of manipulating or hurting people I care about. That’s why I hide my self harm and did not tell anyone for years, why I usually don’t ask for help after overdoses… I’m scared that people may feel responsible for saving me… and the self-harm itself started in order to punish myself and hurt myself to turn it all in and not let the horrible things in me hurt anyone else, and overdosing  is sometimes about utter pain and sometimes utter rage and loathing at myself and fear of who I’ve hurt.

People who are self harming and/or on the point of attempting suicide are not nasty manipulative frauds, they are in massive pain and massive immediate danger. They do not need punishment and dismissal. They need a place of safety and compassion and they need desperately for the hurt and the danger they are in to be believed.

It is terrifying to admit to things like how close you are to suicide or that you’re overdosing. I never say it to friends (though two friends have sometimes guessed) because I do not want to make them feel responsible to keep me safe or worried I’ll do it again. That’s one thing.  But it has to be possible to admit it to healthcare professionals, if there is to be any way to get help.

Yesterday, my life was saved by a police officer who recognised the danger I was in, and by the emergency team who assessed me when he took me to them, and by the mental health workers at the safe haven I was taken to. I owe them my life. Thanks be to God.

The safe haven is a new organisation that has been running for just two weeks in my local area and I think massive good is going to come of it. I’ll post more on that going forward. Please God can that be the support other people find when they are in the state I was in yesterday, not reactions like the one I got from my GP. Sadly I think I’m not alone in what I encountered. And this isn’t the first time. I’ve encountered similar and worse lack of recognition or response to the danger I was in, and accusations of making threats or being manipulative,  from within the personality disorder service and in crisis teams.  If i am ever recovered enough to be able to somehow try to help other sufferers or explain to people what BPD is like and how to help someone in crisis, tackling this would be a massive priority for me.

Ginny xxx

It just doesn’t stretch, whatever I do

I’m scared I’m so close to everything falling apart. Financially. But it feels like everything.

I got an automated voicemail message from my landlord telling me I’m to call them urgently to discuss “ways we can help you to pay your rent”. They had closed by the time I finished work so I have to wait til tomorrow to call them and find out exactly what it’s about but I know it will be about my rent arrears. I doubt they will be “helping” me pay, somehow! I know the fact of having to call them doesn’t instantly change anything but I’m really panicking.

I was struggling already today, feeling very sad after a difficult 1:1 therapy session on Monday, a friendship having broken down and a few other things. After getting this message I just wanted to crawl under my duvet, cry, shut off, everything and nothing…and the urge to cut is very strong but I’m trying to resist.

Nothing is working out. I got into arrears last year when I lost my job, wasn’t paid notice and holiday pay as expected, and my housing benefit didn’t come through for 10 weeks. Working part time I’ve been entitled to some housing benefit but my claim has been messed up, suspended, altered back and forth from start to finish and I’ve had more periods of weeks with no money coming in. I’ve been paying my rent, with great difficulty, but not able to clear the arrears.

Now they have stopped my housing benefit because my salary has increased by a few pence per hour. This leaves me unable to meet even the tightest budget. I do not have enough money to cover the bare minimun of rent, council tax, bills like electricity, telephone, prescriptions, travel to the hospital, some access to the internet and food (let alone any other expenses like buying clothes when needed, any longer distance travel, or socialising). I’ve cut back as much as I can, especially on food. I don’t make proper meals, just toast, cereal and cheap snacks. It makes me feel awful (plenty of guilt for bad fattening food) but I can’t afford anything else.

I know the arrears are my responsibility and I have to pay. I feel panic and guilt every day over them. I know that in the past when very unwell I made poor financial decisions and was irresponsible with money, which has contributed to why I don’t have savings. So has the fact that I’ve been too ill physically to work full time at several points in the last 10 years.

Part of what is so upsetting is that I am now doing all I can but I still can’t stretch to cover the tightest budget or see any way to change things. I am pushing myself as hard as I can to keep going to work. It’s very difficult mentally – and I’m sad that it is so hard to do it but that is the situation I have to accept right now. It’s very difficult physically too. The pain I’m in from the fibromyalgia, arthritis and so on has been increasing since I started and each day it gets harder to do certain things (going up and down stairs, staying on my feet for lengths of time, etc) and if it carries on it’ll get to a point the pain is too much or I can’t stand long enough or something like that. I hoped if I kept pushing I’d get better at dealing with it but that isn’t happening and instead everything is flaring up.

I really want to keep working. I’m blessed with kind and happy colleagues, a caring employer, a creative environment, varied days, lots to learn and so many good things. Psychologically this job is so much less stressful than the legal secretarial work I couldn’t cope with. There’s so much that should be positive that I don’t want to waste.

However I’m in a situation that I just can’t cover day to day living going forward let alone clear the arrears I owe. It shouldn’t be a reason to give up but when things seem to be falling apart anyway, it’s harder to keep pushing through the physical pain and mental struggle to keep working.

I feel really trapped because with the rent situation alone I think I’m going to end up losing my flat. I know the landlord, being a housing association, has given me more time with the arrears than many other landlords would. A private landlord would have thrown me out ages ago. I know that’s another way I’m fortunate. It’s my responsibility but I don’t know how I can or will be able to pay.

Even if I could clear the arrears  I don’t know how I’d pay the rent going forward. If I can’t,  I don’t know where I’d live because I have no money for a deposit to rent privately. If I went back to renting a room as a lodger my mental health would crash downhill but at this point I would have to be grateful for anything. If I lose this place and end up homeless I’d lose my job. I might anyway if my physical health keeps going down.

It’s horrible thinking even if I get evicted and lose my flat, I don’t know how I’ll change my situation. It’s horrible that trying as hard as I can to do the work I can, I’m not able to live on what I earn and I’m assessed not to be entitled to any benefits despite this. I want to work as much as I can but I’m actually in a worse situation, it appears, than if I were not working at all signed off sick. My rent and council tax would then be covered by benefits. Not that that would help with the arrears but it would at least cover rent going forward. The system says it shouldn’t happen that you are worse off working than not, but it does. I’m actually put into a situation where doing the most work I can means I’m left with not enough to live.

I was referred well over two weeks ago to an organisation that would help me sort all this out and talk to my landlord. I was supposed to have been seen by them within two weeks. I chased up as I hadn’t heard, only to find out they said they had not received my referral from the support worker. It had got lost in the secure email system somewhere,  ironically. It has been sent to them again but now they are not likely to see me til after my operation.

I have no idea what to do. There are so many “if”s and a spiraling whirl of consequences that make it feel that everything’s already falling apart.

I don’t want to make out I have it harder than the next person. I know so many people are in this situation. I know I have to deal with it. It’s a time I wish someone could catch me when I’m falling like this but I know that’s nobody’s responsibility. I’m scared and everything’s already unravelling inside.i suppose I have to try not to listen to the spirals in my head until at least after I’ve spoken to my landlord tomorrow.

Ginny xxx

My rescue box – update

A while ago I posted about making up a “rescue box” as a tool to help me cope in times of crisis. You can read more about the principle and how the box helps here and I’d strongly recommend reading that before reading this post. In brief, the Box is a way of putting together in one place, easily visible and quickly accessible, the things that will help you cope when you are feeling bad. For me feeling bad tends to mean very upset, crying, struggling with voices and other hallucinations, and re-experiencing traumatic memories. The Box is not a cure for how you are feeling and is not meant to make the emotions go away. It isn’t intended to be a way to suppress them. Having said that, it is to some extent distraction, and a way to access tools to lower your very heightened emotional state so that you can then be more able to cope, to think, or to avoid impulsive actions that may be harmful to you. The CPN who explained the idea to me recommends it as a tool for BPD sufferers. I would imagine it could help people dealing with a variety of other situations / conditions too.

I promised an update about my box once I had put it together, so here goes. I’m new to this technique and I’m sharing updates as I go along.

I made my Box by covering a cardboard packaging box in gift wrap. I’ve started to stick some pretty things to the outside of it as well – a flower, some Hello Kitty stickers because they make me smile, a few little snippets of encouraging text – and I’ve put a little plastic pouch on top with a pretty card and a message from a dear friend. I’ll continue decorating the box with more sensory, pretty, attractive things and things that have a meaning for me and remind me of good times. I think this increases the likelihood the Box will be in my mind and be an appealing thing. (Half the problem with coping strategies, I find, is remembering to use them when the hard times come – often the distress can be so consuming I just don’t think of how to access helpful tools and techniques! Anything that helps me call them to mind has to be a plus!)

rescuebox

The contents of the Box is very much a personal thing, of course, as different things will be important to each of us. In case it’s of interest, here are some of the things I keep in mine (you can see them in the picture).

  • A couple of little stuffed animals – I’ll freely admit I am very childish! 🙂 I find them comforting and have quite a collection. To be honest, Bunny is usually next to me on the sofa, not in the box 🙂 and I collect “ty” Beanie owls and my-little-ponies. I guess stuffed toys also give a soothing tactile experience when you hold them, which can be useful for BPD sufferers. As a soothing sensation increases, the unpleasant sensation of very heightened emotion may reduce (again, I explain this better in my earlier post).
  • For similar reasons, a little bottle of scent. It’s soothing and distracting and if you are trying to control your breathing, the pleasant aroma can help you be aware of exhaling and inhaling.
  • A coaster, to remind me – make a soothing cup of tea! Drink it really focussing on the warmth and taste.
  • A special smooth, flat pebble from the beach, which is calming to hold (feeling the cool, polished surface) and which reminds me of the happy day on which I collected it.
  • A CD – at the moment it’s a CD I like with songs that lift my mood. This is a new one for me to try and I’m not sure which way it will go. When I am not in crisis, I enjoy listening to music. Putting on particular kinds of music and even dancing to it (well okay that’s a strong word – bouncing, at least!) can really pick me up. I’m not sure what kind of effect listening to upbeat music when I feel absolutely dreadful will have, but I’ll give it a go! It’s a way of trying to take an “opposite action” i.e. forcing yourself to do something “happy” or good for you when you are feeling sad and bad about yourself. The idea is this may in turn lift your thoughts. So listening to happy music and making myself move around to it might help lift my thoughts and feelings. Equally, at times music that expresses some of the anger or sadness I’m feeling can help as a way of “letting it out”.  I think I am going to trial both and then put together a playlist of favourite tracks specially for times I’m feeling down. Good job I live alone so there’s nobody to suffer for the fact that if I sing along I sound like a mouse with a particularly bad chest cold 😉
  • A favourite book I know well, which encourages me at the very hardest times, and some prayer cards with very short prayers. I can read over passages of the book, or say the prayers in my head, to repeat a hopeful and loving message to take the place of spiralling panicky thoughts, or the voices I hear telling me that I’m evil.
  • A few cards and a pen, to remind me – could I write a note to a friend? I.E., something nice to take me “out of” my own mixed up head, to force myself to do something positive, thus acting against the negative thoughts in my head, and making somebody else happy too?
  • A ball of wool – could I do something creative? Make pom poms? Do some cross stitch embroidery? Colouring?

I’ve tried to include a mixture of things that are happy and soothing of themselves (eg the stuffed animals, the scent) and things to encourage me to do something positive (eg the cards or the music). I’m also going to add to the box some pictures of my family and my close friends and my godchildren, basically people that matter to me, as a reminder of reasons to keep going and all the good things and good times that I can be thankful for – all things that can so easily be eclipsed in times of extreme distress.

So, that’s my Box! I hope perhaps this might be of interest…. I’m new to this and I will post another update about whether / how I find that it helps me.

Do you use any kind of toolkit like this to help you in the hard times? What would you put in your rescue box?

Ginny xxx