Tag: BPD

What would you like to read in my revamped blog?

Some big changes are coming here at intothisbreakinglight, including a new name. See my previous post, Changes Ahead .

What would you like me to incorporate in my revamped blog? I want to help, as well as sharing my journey, so I’d love to know what you’d be interested to read.

Here are some elements I’m considering including:

– A specific section collating suggestions and resources for living with PTSD and complex trauma; what has and hasn’t helped me. I need to find out how to create this. Sifting through chronological posts is just not accessible for readers in my opinion, especially if the reader is exhausted or distressed.

– Similar specific sections regarding Borderline Personality Disorder and eating disorders / body image.

– A regular “question time” where I write a post in response to a reader’s question. Maybe once per month at first.

– A weekly journal-style entry to share what has been happening in my life and plans for the near future.

– A regular posting schedule. I don’t know yet what frequency I’ll choose. I will also post outside this schedule but I think it would be good to have a regular schedule I always stick to (even if I start with just one weekly journal and one other weekly post).

– I meet with medical students and researchers to share my experience of living with mental and physical health conditions. Loads of interesting questions get asked in these sessions. I think I may start writing some posts expanding on these questions (of course, not breaking any confidentiality).

These are just some of my plans. What do you think? Are they any good? What else would you like to see?

Ginny xxx

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Changes ahead

Changes ahead

I’m going to make some big changes to this blog over the next week.

It has been many weeks since I’ve posted regularly. My husband has been coming through major surgery for cancer. Another family member has been through severe trauma. We have been struggling through a heavy load of financial issues since last autumn. My PTSD symptoms are worse. I’m not coping with day to day basics as I want and expect myself to. I could go on.

However a big reason I want to make changes in this blog is that my posts have been too sporadic and too distressed and distressing. I don’t want this site to be just me venting and screaming about how hurt I am. That doesn’t help anyone.

Yes, I want to be totally honest in what I post. Totally real. I don’t want to turn the blog into a falsely cheerful, superficially positive story. After all I’m talking about very present and painful trauma, illnesses and struggles. I am not going to pretend that I have all the answers or that I’m “over it” and nothing can touch me.

Yet I am more than the damage done to me and the hurt of every day. I want to try to find that. I want to write about that. I want to be thankful for all of me and all of every day. Also, I want to incorporate more focus on what helps me cope and even heal.

I want to have a regular posting schedule and more defined sections on this site so I can share what’s happening in my life week to week, but also share information about what helps me and may help readers, answer readers’ questions, post in response to reflection about what’s happened to me in the past, how I tried to cope and why. I want this blog to be helpful to readers, partly through reflecting what living with PTSD and borderline personality disorder is like, partly through sharing resources and information.

Big changes are coming up. Please watch this space! Thank you!

Ginny xxx

I want to make changes in this blog

I want to make changes in this blog

I want to make some changes to how I write this blog.

A lot of everyday life feels @&)!%*€ awful at the moment. My husband has cancer and is having major stomach surgery next month. He has 3 other operations due and that’s assuming there aren’t complications of the March surgery. It has been horrendous since November trying to sort out our state Benefits and just when it seemed it was sorted, I was told I had to have a reassessment of my disabilities for one of my Benefits and had to complete a 25 page form and send around another 20 pages of evidence in with it. I have a face to face assessment 9 days before my husband’s surgery. This brings with it the worry my Benefits will be stopped or reduced if they decide against me. My disabilities are all worse than when I was last assessed but you hear nothing but horror stories about Benefits assessments. Our money could get cut off whilst my husband is in ICU after the operation. We have other financial worries as well. We have had a whole series of let downs from people that should be helping us, including doctors and nurses and support workers. We’ve been brushed aside and labelled as worriers or nutcases because we have mental health problems – when in actuality my husband has multiple tumours in his body. When I have severely painful disc damage and degeneration in my spine. We have complex and deteriorating family relationships to work through and little support.

I could go on.

I want to scream. I don’t know if I’m crumbling or exploding but I feel I’m on the brink of going to pieces. I don’t know when I last slept through the night. The nasty angry dangerous version of me is getting out more and more as dissociation takes over. Right when I need to help my husband.

I need to make this blog different. I have become more and more sporadic in posting. When I’ve posted at all it has been sad and angry, as the result of an overflow of emotion or a need for an outlet of some kind. Having that “let out” is important but I don’t want it to be all this blog is. When I started writing I wanted to be able to express myself and also to be honest about what living through mental and physical health conditions is like. A lot of that is difficult, but there are good times and strengths too, and I want to reflect that. I want to reflect learning and gratitude too. I want to try to explore different aspects of my conditions and what helps. I want to post regularly, with more structure.

I need to make plans for how to change.

Ginny xxx

Waiting and feeling like a fraud

I had to come to hospital this afternoon for an urgent MRI scan. I’m in a room off A&E waiting for the results. The GP told me I had to come in because my back pain, numbness in my legs and incontinence have got rapidly worse than usual and he was concerned I may have nerve compression. I feel sure the scan will show nothing or at least nothing new. Waiting and waiting it’s getting worse. I feel a total fraud. I feel sure they will tell me nothing is wrong. That I’m crazy. That I’m stupid. That nothing is wrong and there’s no reason for the pain. I feel panic and sick and dizzy thinking of it. I want to go home. My mind is spiralling thinking how angry my GP will be an how my relative who has found out I’m here, who doesn’t believe I’m ill in the first place, will use this to show how “it’s all in my head”.

I feel like I’m such a fake.

I want to go home to bed.

I’m so tired of pain and tired of hospital. Everything I’m trying to do, which the pain clinic tells me is meant to help, is making the pain worse. Or it’s getting worse despite it.

My head aches and my stomach feels like something clawing it and twisting from the inside out.

I don’t want to bring only despair

I am sorry I have not written in many weeks.

I am shattered.

There seems to be no end to the pain and suffering my husband and others I care about are going through. No end to how many times we are brushed off or turned away by all those who should support us. My husband is seriously ill physically and mentally and we are utterly overwhelmed by what he is dealing with and the fear of what’s to come and the frustration of being passed from department to department in the hospital, ultimately left to cope alone.

It feels like fighting and screaming for help in a massive black hole I’m at the bottom of whilst the people I would have depended on stand way above me at the edge of the pit and sneer and laugh at me. And it’s so many times worse because I’m crying for people I love to be heard and helped and understood, not for me.

I’m exhausted. I’m in a huge amount of pain. I’m struggling to do more as I’m “supposed” to but the pain is worse and worse and I don’t know how much more I can take. Physically, so many small things are now really difficult. So many things I want to help my husband with, I’m physically unable to. I’ve been going through a very bad time with family realising how the abuse I suffered is actually not over and people whose behaviour I excused, actually perpetrated abuse; how control and manipulation is still happening in my family and hurting vulnerable people.

Worse still, family members refuse to hear me when I speak out about what’s happening, precisely because I’ve been abused – they use this to say that the problem is me and that I’m the one with a sick view of the world.

This negativity and exhaustion and despair is not what I want to bring to this blog. I want it to be honest but I don’t want to write time and again about hurt and loss. When I started this blog I wanted it to be about hope. Holding on to hope is very hard right now. Lots of days I can’t write at all. I desperately want to share good things and desperately need to be more thankful. When I’m so low all I can do is try to walk through the day and I have no words left.

I need to figure out what changes I can make to shape this blog differently; to still be honest but write more consistently and change the balance of what I post about.

Ginny xxx

Panic in BPD and dissociative episodes – spilling over and used up at the same time

My mind won’t stop. Yet at the same time I can’t process anything. There is constant clamour; panic and fear rolling round my head, gathering speed and swirling til there is nothing else in my head. I cannot hear properly. What I do hear is senseless, clanging, distressing sound with no words or meaning.

Remember a feeling can never be bigger than you, my psychologist said. But this feeling is. It’s boiling and spinning and pouring and rushing, and once it had taken every space in my mind it rushed outwards and spun round my head, like a hurricane or a tornado, slower but heavy, making a colourless, invisible, but impenetrable barrier between my mind, my eyes, my heart and the outside world.

I’m full but drained. In my heart it’s like only the dregs of me are left.

The panic has sucked everything out of me, draining away like water down the plug hole. Nothing is left but exhaustion, emptiness, and emotion that has no route to be expressed, so it just feeds back somehow into an explosion of pain and anxiety. The barrier round me gets stronger. Panic locks it tighter in place.

I need to cry and scream and I need to be silent. Silent inside and silent outside. I need to stop, so very much, but my mind is unable to stop spinning because of the panic force driving it on.

I need to be held, I need to be safe, I need everything that I have no right to in the adult world, because the only part of me left after this tide of fear is done with me is a screaming toddler, overwhelmed by the world. A little child who needs to be carried and protected. Adult me is lost in the panic, feeling forces she doesn’t understand, and little me comes out all alone.

***

Pain after pain, trauma after trauma, repetitions of past abuse, are all happening to people I love the most. I don’t know what to do. I don’t know how to help. I feel so empty and I don’t know how to protect them. There is so much I need to give them and I can’t because the panic has emptied me already and that’s so selfish and stupid.

I’m exhausted and afraid of these exploding emotions that I don’t know how to control. I feel I’m barrelling on towards disaster. I feel failure. I feel the losses and longings and guilt and dread of terrified little me, alone after the abuse. Not knowing what to do or say when I see my loved ones suffer it too.

Xxx

A beautiful day

Today was amazing. I don’t know why but we were both full of hope for the future. It wasn’t that the many obstacles in our way at the moment had been moved. Yet we both felt lifted up by God’s grace. The magic and beauty seemed to be stirring in our hearts and giving an energy Ive never felt before. This evening I’m buzzing and high even though I’m exhausted physically and mentally. The voices are telling me this happiness and goodness isn’t for me and doesn’t happen to me; they are trying to fill me with the dread and guilt I always feel after any brief elation.

No. I choose Jesus. I choose my life by grace with Him and in the love of my fiance R. We are richly blessed. We are created for good.

Thank you Dear Jesus.

Ginny xxx

God whispers and the world is loud

I stumbled across this quotation today.

It’s apt for me. I need to rest and listen for God’s “still small voice of calm”. Amid anxiety, distress, confusion and an awful lot of dishonesty around me right now, His voice guides and assures and gives hope for now and the future; His voice is always there if I allow myself to hear Him. I know He is with me working out His plans. Where I am right now, He needs me to be and needs me to serve Him.

I don’t know who drew the beautiful illumination in the quotation or who wrote it, but I found it thanks to the Facebook page Contemplative Monk.

Ginny xxx

On the move

Its a few weeks until the wedding but I am getting ready to move house, packing boxes to go over to our new flat. It feels as though I’ve been trying to get to this point for months and not making progress, through a combination of my exhaustion, my physical disabilities and mentally being unable to make decisions or forward plan. At last we are making progress! Thanks be to God!

The approaching deadline of our wedding is certainly a motivating factor. So is the fact that we are putting our home together in the new place (my fiancée has moved there already). We are blessed that our financial situation is better than it was and this means for the first time – first time ever for me and first time for years for my fiancé – we can actually choose some furniture we like and pieces which all match or coordinate, to make a calm and restful environment for us both. It’s somewhere we both want to be and feel thankful to be. For the first time it’s not a move that’s fleeing something, escaping somewhere, or because of a loss (death, broken relationship, having no money to live, for example). We are moving to start our married life together and that’s wonderful. That helps me keep going.

It has been very hard for me to tolerate the mess and chaos of packing. My threshold for feeling overwhelmed and having a meltdown is lower than usual. I’m trying to recognise that and actively spend mental time focusing on the good we have achieved so far and the good to come. Actively thinking about the good is much more effective for me than saying “just don’t think about it [the things panicking me]” “just push it away” “just don’t worry about that” “you just have to keep it simple and be positive”. (What exactly does that last one mean, anyway?). I can’t “just” stop a thought or feeling by choice, and the fact I can’t do that when other people require it is likely to make me feel even worse. But I can dedicate time to thinking of a positive future, however imaginary it may seem, or to counting tasks I’m thankful we have achieved.

Yesterday a friend of mine in the parish took lots of my surplus kitchen things and clothes to give to a poor family and some refugees arrived in the parish. They will be able to use some of my furniture as well, if we can find a way to transport it.

Tomorrow a lovely charity are coming to take away all kinds of other things I can donate or that need to be disposed of, and to help me pack because I can’t physically do it myself. This is amazing.

My cat doesn’t think it’s so amazing and is walking around with a very suspicious look on her face. She doesn’t like a lot of bustle or things being moved round the room. She’s alternately ever so affectionate, then moody and trying to scratch. I think she has lived in so many different homes before I adopted her that she thinks she will be left again – that the signs of moving mean I’m going to go away and abandon her. Poor puddy cat has attachment problems just like me! 🤣

We shall have to see if her mood improves once she realises there will be lots of cardboard boxes to hide in…

Ginny xxx

Picture by memecenter.com

I told him what I see. He explained it away.

I told my dad today about my concerns over how he’s being treated by my step mum. I told him I’m worried for him. I told him about how she’s treating me and other people in the family. He denied it is happening. He denied any possibility that he may be being treated very badly and that he may not realise because he has had so many previous years of emotional abuse. He says there is no problem for him. He put my experience and my concerns for him down to the fact that I had harmful experiences when I was abused when I was younger and that means I perceive interactions now as a repeat of what was done to me back then when actually nothing is wrong / there is no similarity, and that my “world view” may not be a good one because of what was done to me then. Basically I am wrong, I am the problem, and there is nothing wrong at all in how my step mum behaves to him or me or others. He denied events that have happened, denied things that have been said, and bought totally into my step mum’s view of me as a failure, a let down, spoiled, the problem, unwelcome, at fault… he even upheld her emotional attacks on me as being fine and my feelings essentially as being because I have problems.

It was pretty much what I had expected would happen but he had a much deeper rooted explanation than I was ready for, for why things are not really as I have experienced them to be. At least he did not deny my experience. But he explained it away in such a manner that it secures my step mum’s casting of me as the difficulty and her as the perfect spouse and mother figure.

My concern was primarily for him and how he is being treated but she has cast me in such a role that no concern I raise, no event I try to discuss will have weight with him.

It is rather as my mother did, drawing my dad in to such an extent that he would not hear when I told him multiple times about her emotional, physical and sexual abuse. She could invasively abuse me pretty much in his presence, emotionally taunt and threaten me for hours on end partly in his presence. At the time he supported her, joined her in her emotional attacks on me, often continuing himself afterwards; somehow he ignored her physical actions to me… and then later when at long last he listened to me (when I was an adult, hospitalised) he claimed no memory of any of the events. He was that drawn into her world.

His blindness now both traps me again and leaves me alone. Traps me where I cannot reach him to warn him what is happening as he just won’t hear me. Leaves me alone because it feels universally declared that I’m mad, I’m wrong, I’m the problem; what I’m experiencing and seeing isn’t real. It feels like all the power has been handed back to my step mum. I feel as I did when I was a child; alone and my sense of reality torn to shreds.

Xxx