Tag: Borderline Personality Disorder

Walking this Borderland #9: My rescue box

Eee, it’s been a long time since I’ve added to this Series.

My CPN and I talked about the following idea today. I’ve been meaning to put this together for a while.

All the other ideas / coping techniques I’ve written about so far in this Borderland series are things I’ve tried or do use currently myself. This post is a bit different because this idea is new to me and I’m going to be trying it out for the first time, so I can’t yet say how helpful I’ve found it. (Updates will follow and I’d love to hear from you if you use something like this!)

I’m going to make a “rescue box”. I’m not quite sure if that’s what I want to call it but for now, it’s what I’ve named it. Apparently some people call it a suicide box because it’s a box full of things to turn to when you’re feeling absolutely at your worst. I didn’t want to call it that because it emphasises the terrible feelings more than the good I’m trying to climb towards.

The basic idea is to make up a box filled with things that help you to cope in times of extreme distress. This works well, I’m told, if like me, you find sensory or tactile things helpful and grounding. As I think I’ve mentioned earlier in this series, in personality disorder when emotions are overwhelming, introducing other, soothing sensations can help bring the emotions down. You can also put things in the box that remind you of good times or reasons that you do keep going every day, or anything that triggers positive memories and thoughts in the hope that in the long run making more and more positive memories makes these stronger than bad memories or obsessional thoughts.

I’m new to this. I’ve been trying to think of things I could put in my box. Here are a few things I came up with:

  • A special smooth pebble that I collected on the beach one good day, which I find very soothing and grounding to touch. It also reminds me of the sea. Walking along the coastline and watching the sea always assures me of the presence of creation and love far greater than ourselves.
  • A small stuffed animal – yes I may be an adult (perhaps 😉 ) but I still find soft toys comforting.
  • A particular book that never fails to encourage me (more on that in another post).
  • Photos of my godchildren whom I love very much; seeing them always brings me joy.
  • A list of people I care about whom I can pray for or do something nice for – maybe write a letter or a card. This reminds me I’m not alone and helps me focus outwards on other people rather than my own problems.

That’s what I’ve come up with so far. I’ll post some pictures as I make up the box.

I have the feeling that the hard thing is going to be remembering it is there and being able to use it when I really need to. I can have coping strategies but being able to turn to them rather than a destructive “coping mechanism” is the hardest thing.

Do you use a box like this or anything similar? How do you remember to use it in the hardest times? Does it help when you’re distressed as well as when you’re feeling okay?

Ginny xxx

What do you do to stay safe?

Today I’m going to the hospital again for another meeting with the CPN. I’m very scared of going after I lost it there on Tuesday. I think I’m scared what will happen, scared of losing it again, ashamed about what happened and still feeling very out of it, although not in the way I usually am when I dissociate. That gives some kind of protection. This is raw at the same time as shaken and disconnected.

Also I’ve got an inescapable question that has been in my mind for several weeks. I’m not at all stable or safe at the moment. I want to continue with therapy. I committed to the group that I’d do it and not give up. I promised to God and Mother Mary in prayer. I’ve made quite a few sacrifices for it – I don’t think I’d have had to leave my last job if it weren’t, at least in part, for my therapy appointments (though my last employer were definitely at fault too, in my opinion). I’ve seen the therapy as the only hope of learning how to get better and manage my condition. I’m privileged to live somewhere MBT is actually available (there aren’t specific PD services in all areas of the UK). I really don’t want to have to stop therapy.

However, at the moment I’m actually more unstable, at least in part because of the therapy and the emotions, memories and questions that it raises. This isn’t necessarily a bad thing. Other people tell me they can see positive changes in me, for example communicating more clearly about emotions and things that happened to me in my childhood, none of which I can yet see for myself. However I trust the people who tell me this and think it has to be a good thing. It’s another thing I don’t want to waste.

So the big question is, what to do.  I can’t keep myself safe at the moment. For example I’m “coping” by cutting, taking overdoses or higher than prescribed doses of medication, drinking* (and this really isn’t me, I do not enjoy drinking in this way), escaping from daily life by ignoring letters, calls, etc and not able to keep on top of the basics of looking after my home and myself (cleaning, cooking etc). I’m more unstable in my moods, especially anger, and I’m struggling more to hide everything to try to participate in daily life by eg going to work. Things like hallucinations or paranoid thoughts or feeling dissociated are pushing their way more into the working day.

I don’t know what to do to change this.

I’ve some hope that medication changes could help and I’m seeing the psychiatrist on Friday. But I doubt that’s going to be the only answer. I’ve tried to exhaustion (both daily and when in crisis moments like the extreme distress or wanting to end everything) the techniques I know like distraction and grounding and self care / self soothing (this latter is very hard for me to do when I feel as I do about myself). It isn’t working. And I feel that the things other people could do to keep me safe, many of which are on my crisis plan, are not happening or not working either. I’m experiencing more and more let downs where xyz help is promised then doesn’t materialise (appointments canceled, calls not returned, planned sources of support withdrawn, mistake after mistake, discharge plan not followed). Or I’m told that the help I want to keep safe doesn’t exist or I don’t qualify. What is offered – and don’t get me wrong I’m grateful that it is offered and I know it’s more than many other services provide – is not enough to keep me safe. For example when I’m suicidal a 5 minute telephone call may calm me a bit for a few minutes but an hour later in usually feeling worse than before and – this is key I think – still on my own trying to cope.

What do I do in this position? Are there other techniques I can learn to cope better? Are there other or higher doses of medications? When I so so much feel I am not safe on my own and really need someone with me (especially when I’m really distressed but also day to day because the slightest thing, as little as a letter that makes me panic or a canceled appointment,  can thrown me into extreme distress, self harm etc) what can I do? The PD service are adamant I mustn’t be admitted and don’t qualify for any carer help and ongoing support in person isn’t possible. I haven’t any other way of getting that kind of support. I live alone, my dad and step mum live hours away and I don’t have friends very locally or whom I see regularly.

So how do I do my therapy and stay safe as well? How do I either answer this need not to be on my own when I’m so much at risk and unstable, or what solution do I have to learn instead?

What do you do to stay safe between therapy appointments or between times you can access support?

I know this probably sounds silly and I do get a lot more support than most people and all I’m talking about coping with is simple daily life. Right now this is where I am.

Ginny xxx

*just to be clear, I’m not diagnosed with any alcohol problem and I’m not comparing my struggle with that of someone who is struggling with alcohol or other substance use. That is a much more painful place. I sometimes use what is probably an objectively average amount of alcohol taken with my tablets to make myself fall asleep when I can’t cope. Not a great thing to do but I’m not trying to compare the two.

I lost it.

I lost it today. And I wasn’t on my own this time. I went to an appointment with one of the CPNs. I was shaky before I got there, anger rising in the waiting room as two other patients and I were talking about how let down they felt by services, and in my appointment everything I said it felt like it was minimised or dismissed, I think. I can’t remember what we talked about or what we said.

I snapped. I screamed and screamed and then I can’t remember. Pain. Then I was on the floor screaming and then I couldn’t breathe and I was crying and couldn’t stop. I thought I’d hurt the CPN and took a long time to believe I hadn’t. Then I couldn’t speak and somehow nearly an hour had passed with all this, though I couldn’t understand it. I was so tired.

I’ve never flipped out like that in front of anyone. I cut so I don’t get there. Now it isn’t working. Usually it just happens on my own usually at night. Now they’ve seen the worst of me. Now I’ve lost control. I want to take responsibility but I’m losing it more and more. Nothing is working.

I’m home now. On the way home I felt out of my body but unable to get away from everything being shaken. Tea and blankets and NCIS tonight, my usual escape. But I have to face it.

Fat, and hot, and horrible.

The hardest thing about the quetiapine (and venlafaxine maybe, though I attribute it more to the quetiapine) and clonazepam is what it’s done to my body, or rather what I’ve let happen.

Fat. Disgusting. Sweating and hot (that’s the pain meds too I guess). Conscious of my expanded body. I have gained so much weight in the last couple of years. And I’ve let it happen. It’s true the drugs make you gain weight and increase your appetite, but I’ve failed. I haven’t stopped it.

I’m repulsed when I pass a mirror and see the foul reflection, bigger and bigger; when I feel the flab around my stomach and waist, the one thing I used to be able to keep flat and small even if I did have chunky thighs I hid under skirts. It’s everywhere. Crawling disgusting flesh and fat.

Why did I let it? Why? Why did I return to this demanding sick big disgusting body? I want to rip and claw and cut. It’s out of control. It’s all wrong. Growing and needing and hungry and hurting inside and out, aching within, stabbing in my stomach, darts and shooting burning pains as my feet touch the ground and my joints feel like they’ve been smashed and bruised.

Failure. Why. Hate. Hate hate hate this growing sick too big too present body. Even in my dreams I’m fat fat fat, running and clawing to get out of my body. My mother is there, shouting and mocking and threatening and I wake up drenched in sweat and shaking because the nightmare is real now. I couldn’t save her and the foul thing I am stares back at me out of every mirror.

And I cry.

I’m sorry for being rubbish this week

I’m sorry for being rubbish this week

I’m sorry for being rubbish this week. I’m sorry for being so slow to reply to comments and not being there enough for you (lovely readers / bloggers) as well as other people important to me in my life. I have been so shattered and sinking and though that’s true and consuming, I hate yet again using that as an excuse. Someone I was close to told me a little while ago that at first maybe you can hope people will understand but not after it’s gone on for years. Certainly “it” has gone on for years for me. Whilst it hurt when she said that I can also sort of see that you cannot expect endless understanding and it feels like asking more and more the longer I am not there and not well.

It is only very special and very empathic people who continue to understand and to be there. I am very very thankful for you. I care about you and I am so sorry for the times I fail to show it when I cannot write or say or otherwise show the love and support I wish I could. You mean so much to me. Thank you.

***

Also, in the past few days I have been trying to put together something in writing, a kind of open letter, about how I feel about my current care and how I have been treated by different services in my struggle to get help. I’m going to finish this tonight in preparation for, hopefully, meetings with a nurse practitioner and the Psychiatrist at the hospital this week. I think I may share some of it on here because I don’t think I’m the only person fighting the failings that have pushed me nearer the edge.

Ginny xx

Silly post, but just to hold myself to it!

This is a pretty silly post but I’m writing it here in order to hold myself to it, because if I write it here I’ve made the commitment to all of you (lovely readers) as well as myself.

I went to group this morning. I’m so boiling with feelings and hurt and loss and anger (not with group or anyone in it but with the whole PD Service). I desperately need to shut off and the best ways I know without help are things that hurt me. And it’s very possible I could just go home and do that and dissociate or literally knock myself out. I am going to try to make myself take another action instead.

I commit that this afternoon I will write a card to send something to my step-sister that she needs. Then I will clean in every room in my flat. It is in a complete state as i have not cleaned or cared for it in the state I’ve been in in the last two weeks. I may not finish all of it but I will vacuum everywhere and I will clean at least three things in every room (it’s a small flat!).

And to keep going in the promises I made in my commitment to getting better, 5 things I’m thankful for today are:

  • I have a flat of my own to live in (well I say my own; it’s rented but it’s home and I’m blessed to have my place and my safe space).
  • I went to therapy today and talked about horrible feelings and the other members of the group listened and didn’t treat me like a freak. They actually seemed to understand.
  • I saw an old friend yesterday who I have not met in years. She seemed happy and well and she’s having a baby very soon.
  • My step-sister and I are getting in contact with each other more.
  • Um… I didn’t have to wait ages for the bus back to town after therapy, does that count 🙂 ?!

I’m wishing for something good to happen to you today.

Ginny xxx

Group and no more trust

Tomorrow is MBT (mentalisation based therapy) group. I don’t know whether to go.

All trust I had in the service has gone. It’s been completely wiped out by the lies and let downs of the past months, the proofs they don’t believe me, the tricks, the cuts that open me more and more vulnerable then leave me with nothing and noone.

I don’t really want anything to do with a service that does this, but I’m desperate and have nowhere else to go. I’m desperate for help but it’s denied, it’s promised then withdrawn, or I’m deemed not in need or not believed. I want to do the therapy but I can no longer go forward safely with it. I cannot cope between sessions except by overdosing to black everything out and self harming to punish myself, temporarily quiet the voices, temporarily be something other than the utter pain. I’m not allowed any of the things that would keep me safe between sessions.

If I go tomorrow, I will be so angry. I can’t say I’ll keep it under control in the session. I can’t say I’ll stay “stable”. Nothing keeps it in anymore. I can’t mentalise like this and really I don’t want to. These things just are as they are. There’s nothing to be “curious” about or explore my feelings or someone else’s thoughts. Their thoughts have been made totally clear – they don’t believe me, I’m not allowed help, they’re tricking me, they’re cutting me open then leaving me and finding more and more ways to do it. My feelings are exploding and total. Fury. Hurt. Trapped. Over the edge. Liar. Fake. Fraud. Pain. Screaming.

If I go to group I can’t avoid it being clear I have no hope and no trust left. If everyone or anyone else does trust the service and does believe they’ll help them, then maybe that gets them through and helps them and is a lifeline for them. I don’t want to destroy that.If I say what’s happened to me, even in the last couple of days, I could destroy it.

I could go and just try not to talk about anything to do with me and just be there for other people and listen to them and try to mentalise about what other people bring. But I’m so far gone over the edge I don’t think I can trust myself not to explode.

When the group started committed to do it all. I committed to not leaving. I committed it to everyone in the group – not out loud, we didn’t do that, but in my head I did. I promised to God and Mother Mary too. If i leave I break my commitment to everyone, not just the service. I really don’t want to do that.

Yet at the moment I’m just ending up in more and more danger. It seems as if I should just accept this’ll never end, dissociate as much as possible, hope for something sometimes bearable…. but I think I’m too far gone for that. I wish I’d never trusted them.

Time to pack it in and leave, I think

So the last couple of hours have brought me absolutely beyond all hope.

I’ve been led on a cruel dance by all the so called emergency out of hours lines.

The PD service secretary refused to even phone any of the clinicians. She told me all kind of rubbish and lies, like that she couldn’t put me through to anyone else in the hospital, she didn’t have a telephone number for any of the clinicians or anyone else in the service, she refused to get me help, she pretended the crisis team didn’t exist, she shouted over me. I called 111 the out of hours service, since it was after 5. They refused to get me an appointment face to face or telephone. They said my own gp still needed to see me. They were not responsible til 6.30. They refused to make me an appointment after 6.30 or refer me to the crisis team. My own gp put me through to the duty doctor. She refused to visit me because it was too late in the day. She refused to refer me to the crisis team because they wouldn’t accept a referral without her seeing me which she’d refused to do. She then hung up on me whilst I was speaking.  The so called emergency out of hours mental health line went to answerphone 3 times. I finally got through. They had none of my messages. They talked over me constantly and said nobody world come to see me and just go to a&e. I’m too ill to go out of the house and what’s the point of going to a&e? They just send you back out a few hours later. What was the point of the line then if they don’t offer help? If I wanted to go to a&e I’d have gone. The woman actually agreed yes it’s fairly pointless, she just tells people to go to a&e.

I am desperate. I have done everything I’m told to. I have jumped through every &*$/€(# hoop. I even trusted them. What do I have to do to get help? Every single thing gets taken away. How much sicker do I have to be before they’ll help me? Before they stop talking about building my resilience? They’ve taken every bit of my resilience away and finally pushed me over the edge.

I’ve been thinking for some time about just packing up and going away somewhere else. Going off to the other end of the country. Somewhere else I can live hidden, preferably under a different name, nobody else knowing all this $#@/!&£* inside me, nobody pulling me apart and cutting and cutting deeper, nobody tricking me, and it’ll be numb but it’ll be some pretence of normal, it’ll be numb and fake but I’ve seen what trusting gets you, nobody will come near to me again, the real and the screaming and the desperation and hurt, I’ve been shown what that deserves, I’ve had it. I think I should just choose the numb.

Punished for hope

Go on then. Smash me into the ground and kick me as hard as you can.

That’s what they do to me.

I was promised “victim support” when I went to the police about the abuse. I was promised support from the victim support team’s specialist CPN and to finally get help with the trauma, flashbacks and PTSD. A phonecall with the CPN was booked in for today by the support team. The police officer who took my statement knew.

I got the call from the CPN who told me she is employed by the same mental health trust as the hospital I’m seen at for my personality disorder. Oh good,  I thought, that should help, shouldn’t it? She’ll know my mental health background and have my records. Wrong! She said that she’d organise support for people who aren’t currently seen in the mental health trust and get them therapy to help them deal with the trauma of what they’d had done to them but because I’m seen in the personality disorder service I’m “already in the most appropriate pathway” and she can’t help me.

But the personality disorder service specifically don’t address trauma and PTSD. The therapy I have there doesn’t deal with flashbacks, memories, hallucinations etc.  It deals with here and now. Which is great and important but leaves all the trauma untouched. I need help with that.

Why am I not allowed that because I have personality disorder, when a victim who does not have personality disorder, would be allowed to access it? Why am I denied help with one condition because I also have another diagnosis? You wouldn’t say to someone who had been in a car accident and fractured their leg as well as aggravating a pre existing back injury, “oh sorry we aren’t going to get a surgeon to set your leg to heal because you’re already being seen in the spine clinic.” So why is it deemed okay to deny me victim support because I have BPD?

The CPN said I should make a list of all my unmet needs and take it to my appointment with the psychiatrist next week. Oh my days have I not already begged for help with all the “unmet needs”! She just didn’t seem to grasp that the personality disorder service simply do not address the PTSD area. Which in itself is fair enough, it’s a specialist PD service – but it’s not okay if you’re denied access to other specialist services!

Why was I promised psychological help from this victim support team and this CPN if this is the outcome?! Everyone knew I am being seen in the PD service.

Then the CPN said oh they just don’t offer this help in the community teams. Yes and don’t you think I know, after fighting for 15 years plus. … and that’s why it’s speed to be coming from her!

This is yet another kick and yet another betrayal. Yet another thing I held on to snatched away. Yet another desperate hope gone. Yet another trick, this time effectively from the police, it feels like, though it isn’t the officer’s fault, he was nothing but supportive and this victim support team is separate…. but this is the last hope of people believing me and allowing me any help. And it’s now gone.

It’s absolutely proved everything my mother threatened. People would think the fault was hers, if they ever found out, and they’d take her away. Nobody would imagine a child could do all this. But really she’d know and I’d know that it was my fault all along, and what I’d done (and how evil I am, the voices add). I told. They found out. They think the fault is hers. But I must remember, the voices say, really it’s me all along, really I don’t deserve anything because I’m so evil. It’s confirmed it. 

It’s the hardest kick and tightest grip of the terror and memories again.

I was promised support when I went ahead to make the statement. Now I’m left and left more raw than before. I don’t regret doing it but can’t cope and I’m not okay and I’m not safe.

To top it all off I called the personality disorder service to be told there are no calls back today because the team have gone on an away day. Shame the voices and flashbacks haven’t gone on an away day. Shame the planning for how much hurt I can cause myself hasn’t.

 

“It’s all grand and it’s all green…”

“It’s all grand and it’s all green…”

I’m trying to give myself permission to eat better foods. When I’m filled with self loathing thoughts it’s very difficult for me to allow myself to eat proper prepared food and meals, partly because of thoughts that I’m too disgusting to deserve it and partly because I’m just so tired I have no energy left for cooking after getting through the day.

Yesterday I decided to get some nice fruits and greens and I got my juicer out, which I haven’t used for months. As you can see, the result was a somewhat alarming colour and might have fitted in well in Oz*. However, it actually tasted very nice.

It’s a small start. 

[*Title from “One Short Day in the Emerald City” from the musical “Wicked”.]