Tag Archives: Depression

Rebooting Is Hard To Do

Posted by What It Takes To Be Me in Being Alive, Communication, Expressing Emotion, Family, Writing and tagged with , , , , , , , , , , , , ,

So, as you may have noticed, there has been a gap in my blogging. A big one. I mean, I’ve written tons of blog posts in my head, but actually putting pen to paper – or finger to tablet, as it were, – not so much. I just couldn’t seem to get around to it. Everything felt too.. uphill.

I have been wanting to get a laptop for a long long time, in part to make blogging that little bit easier, or at least to remove some of the obstacles that made writing that little bit harder to do. But, money isn’t exactly on tap in my house, and this was a pretty darn big investment for me. So, I went back and forth for nearer to a year on which laptop to actually get. You know the dance; get the current 12” FruitBook, maybe a refurbished one, or wait for the next FruitBook Pro, suffering severe FOMO in case there was a massive spec bump, or – crazy thought – step outside of the FruitLoop altogether and save some dosh by getting something just as functional, less pricey, but also far less sexy, even though I knew what my heart truly desired? And, seriously, should I even be spending that money? What if? What if? What if? And then, late-ish last year, I was given a handwritten card from all of my Most Special People and it said: ‘It’s your birthday and we love you. We are so blessed to have you in our lives. You are Special to us, so we want you to have something Special. Stop fretting. Stop thinking. Get the new Fruity one that you know you really want!’

So I did. I got Mumin. [Or Moomin, if you want to be international about her.] She’s the loveliest laptop in the world, and she has the power to remind me that I am Special and that I am Loved. Every single day.

 

20161223_231456139_iOS

Meet Mumin                                                – the Loveliest Laptop in the World!

This wonderful gift should by rights have lead to an instant reboot of my blog. After all, that was a big reason for wanting a tappety-tap laptop in the first place. But, somehow, it just didn’t. Somehow, despite this amazing gift which reminds me that I am truly loved every time I start her up, I was still me. I was still as caught up in the throes of my everyday struggles as I had ever been, and I still couldn’t find a calm enough space inside to to sit down and write about my life. To share what was going on with you all. I absolutely wanted to. But I just couldn’t. The energy simply wasn’t there; or rather, what little there was needed to be reserved for breathing in and out all day long. And the blog laid barren and desolate, void of new content.

Then, in the last two and a bit weeks I received – I kid you not – fifty-three emails from various people around the world, people who I have never met in person, but who have in one way or another come across my blog and have been wanting to know not only where the heck I’ve disappeared to, or why the self-same heck I’ve not been updating my blog, but, have expressed a genuine and heartfelt concern about my well-being, wanting to know if I am OK, letting me know that I have been on their minds. On top of this, these people have sent tons of positive energy my way. And you all, each and every one of you, have my eternal gratitude, because those emails (and blog comments!) have really meant a lot to me. I may not have been able to reply to all of you – in fact, I know I haven’t – but just knowing that people who have never even met me, who don’t even know my name, have been wondering how I am, have been thinking of me, well, it’s kind of an amazing thing. It restores my faith in humanity. And I feel so very grateful to you. And it is time to repay you by getting back to blogging.

I know that this particular post hasn’t exactly been laden with emotion or posed any serious philosophical or life altering questions – it is certainly a far cry to my usual offerings – but; it is a start. I do have a lot of ideas of what to write about, some stemming from things people have written to me about, and I hope that I will be able to return soon with another post.

In the meantime; do be kind to your Selfs.

All my love and gratitude,

xx

Slow Progress and Power Ups

Posted by What It Takes To Be Me in Acceptance, Creativity, Depression, Expression Through Art, Flashbacks, Illness, Personal Growth, Psychology, PTSD/Extreme Emotional Stress Disorder, Sef-Awareness, Suicide, Uncategorized and tagged with , , , , , , , , , , ,

“Sunrise” – a drawing I made to illustrate how I felt one particular morning

It’s been a few weeks now, and I thought it was probably time to post something on here to avoid dust settling on my domain, if nothing else.

Things have been reasonably OK-ish lately. Physically I am doing a lot better, which is a real relief. Had another few rounds of tests over the last couple of weeks and in the end the good doc declared that I’d reached “not perfect, but certainly acceptable levels”, adding that I may just have to accept that it takes time for a body to recover, and that until then I may be more tired than usual. In essence, it’s one of those scenarios where “slow progress” will have to do. 

Now, I’m not the most active person at the best of times, in part owing to general depression – meaning that I can’t seem to find the motivation to drag myself out of bed unless I have an appointment that I have to get to, and in part owing to the fact that I suffer from a huge amount of flashbacks, more often than not making it far too dangerous for me to venture outside. [It has been less than a year since that particular point was quite literally rammed home; I was hit by a car, because I had a flashback and didn’t notice that I was walking into oncoming traffic]. So, being fairly used to a state of houseboundness, it really shouldn’t have made much of a difference being too physically weak to go out. But, somehow, it did. It’s one of those “I don’t want to run a marathon, I have no intention of ever doing it, but I’d like to think that I could” kind of things, I suppose. No, I wasn’t likely to go for daily walks – owing to the above stated reasons – but the fact that I physically couldn’t still somehow messed with my mind, made me feel even more a prisoner of my circumstances than usual. So, yes, I am very thankful to be officially NHS-doc-certified on the mend.

I have noticed a definite change in myself since I came out of hospital, in that I am very aware of all the things I would have missed out on, had I not survived my most recent self-poisoning. Every time I bump into a friend or get a text consisting of nothing but emoticons from one of my sisters’ too-young-to-write-actual-words children, I find myself mentally pausing to marvel at the fact that I got to have that precious moment, that I didn’t miss out on it. Because I so easily could have.

I have a friend who killed himself. It has been many years now, and while it isn’t acutely painful in the way it once was to think of him, I do often still think to myself ‘I can’t believe W. missed out this’ when something happens which I know he would have appreciated and enjoyed. And, I guess what I am experiencing at the moment is something similar to that, but in reverse.

I have been in this situation more than once [having survived a serious suicide attempt], but as I wrote in a previous post, this time I felt immediately grateful to have made it through. And as much as I am still struggling with all of the things I was struggling with before [yup, every single one of them], being able to take notice of the little things does help. It’s like one of those video games where you pick up a gem and it gives you a Power Up. Yes, it is temporary, and I may well get frustrated and bored with the game again – but while my little avatar is in Power Up mode (think Mario Kart blinking star mode), I feel GREAT.

And it’s been a looooong old time since I’ve felt that way, so, “slow progress with the occasional Power Up” – heck, yes, I’ll take it!

:)

Do be kind to your Selfs,

xx

“Moonlight” – making a small adjustment to express how I was feeling at the end of the same day

A Much Delayed Update

Posted by What It Takes To Be Me in Being Alive, Coping Strategies, Defence Mechanisms, Depression, Dissociation, Expressing Emotion, Family, Illness, Personal Growth, Psychology, Psychotherapy, Psychotherapy Breaks, Psychotherapy with P, PTSD/Extreme Emotional Stress Disorder, Sef-Awareness, Self-Harm, Sexual Abuse, Suicidal Ideation, Suicide and tagged with , , , , , , , , , , , , , , , , ,

It has been such a very long time since I last posted anything on here, it feels all but impossible to try to catch you all up. And maybe it’s not really the most important thing in the world that I do? If you’ve been following this blog for a little while, you’ll probably already have some idea of what sorts of ups and downs you might have missed in the last few months. After all, there is nothing new under the sun. And if you have only just arrived on my site, well, feel free to hop on board as you are.

So, I’ll just begin with where I am at now. Literally.

I am at home, very slowly trying to allow my body to recover from the hell I have recently put it through. I suppose you could say that I had been on a slippery slope to nowhere for a long time, and a number of weeks ago, my therapist started a referral for me to go to Drayton Park. I was already with the crisis resolution team at this point, struggling enormously with trying to keep myself safe. Being at a very low point, the only way I could really manage was by taking sleeping tablets. Paradoxically not to kill myself, but to stop myself from doing so. Perhaps not the best way to manage, but it was all I could do at the time. The referral to Drayton Park took longer than usual for a number of reasons that I won’t bore you with, and being asleep most of the time while I was waiting was the only way I could think of to stay safe. After all, if I was knocked out there was no way I could actually act on my suicidal impulses. Right?

A little over a week later I was finally given a place at Drayton Park, and that felt like such a relief. But it wasn’t all smooth and simple. The depression and the suicidal ideation, the flashbacks and the urges to self-harm came with me. And, although I have stayed at Drayton Park about a million times [OK, maybe not a million, but certainly enough times to feel at home there] this time felt like a distinct travel back in time. You see, the only room available was the one room I have always dreaded being put back in; the room I stayed in during my very first time at Drayton Park. Yes, I have stayed in other rooms there more than once with no problem, but this one holds some particularly bad memories for me; this is the room I died in. And this time it isn’t an exaggeration – I was found lifeless in that room, and while I have no actual memory of it, I was told by the doctors in ICU that I had been clinically dead for a number of minutes by the time the managed to bring me back.

The reason I was found lifeless in that room all those years ago was my own. I had brought a substance into the place that I shouldn’t have, and being the kind of person who – owing to deep seated psychological issues – is far more afraid of being found to have broken The Rules than to tell staff that I was afraid of what I might do, and that I needed help, proceeded to ingest said substance. So, this time around, being back in that room, I was overcome by memories of standing in front of the mirror in the bathroom swigging pure poison from a bottle, quickly followed by a handful of Smarties to mask the bitter taste, looking at myself, hoping to die.

This time around I used my one-to-one sessions at Drayton to talk about these memories, about the sense of being thrust back in time and the feelings evoked, and I was immediately and repeatedly offered to switch rooms. But, me being me, I thought there might be some therapeutic value in being able to stay in the same room, look at myself in the same mirror, but having a different outcome. I thought that the feelings brought out by staying in this particular room might be used for healing, for psychological growth, even. Sadly, I seem to have completely forgotten that the reason I was back at Drayton in the first place, was that magnetic lure of release from life – and that I wasn’t strong or stable enough to do this kind of work at this particular time. And it proved to be a costly miscalculation on my part.

Prior to admission to Drayton Park I had purchased another bottle of a similar but far more lethal poison, and it was still sitting at home, waiting for me. Thus, part of the objective of my stay this time was to get me to a place where I would be stable enough to be able to safely go back to my flat and pick up the bottle to hand it in to staff, without having the urge to down its contents on the way back. I was working very closely with both P. and staff at Drayton to get to this place, we talked about my feelings, about the reasons for those feelings and how best to keep me safe – we really were doing everything possible to get me out of this perilous place I had been perched at when I first arrived.

Admittedly, at first there was a fair bit of pressure for me to bring the bottle back at the earliest possible opportunity, but this plan was thankfully changed, when I – with the help of P. and staff who have known me for a long time – were able to to explain that bringing back the Bottle before I was ready to do so wouldn’t necessarily make me any safer; I’d just order another one online, or I’d feel pushed to act out in some other equally dangerous way. [Having a severe nut allergy means that I am never further than a chocolate bar away from having the means to end my life]. Instead we planned trial runs to my flat where I would go into my flat but not into my bedroom [where the bottle of Poison was kept]. I’d pick up post or a change of clothes, but there was no expectation that I bring the poison back. This worked. Twice. In fact, during one of my visits home I managed to – relieved of any pressure to perform, so to speak – bring back the anti-sickness tablets that were also part of my suicide plan. It was hard going back to the flat; in spite of our best efforts to have strong safety plans in place and in spite of never staying longer than ten minutes, I never quite felt safe.

Partway through my stay P. went on leave, as did K. This meant that most of my usual safety net was no longer available to me. And that, too, was hard. Destabilising, is the word that comes to mind. I knew that I would not be able to stay at Drayton until they were back from their respective leaves, and that didn’t feel good at all. So, fear of going home – having still not been able to hand in the Bottle – intensified. Towards the end of week two I was asked to make a Week Plan, to add structure to my stay, which I did. Knowing how hard it had been the two previous times going back to the flat, I only planned visits home for every other day, so as to not overwhelm myself.

But on the very first day of following my Week Plan I knew I wasn’t stable enough to be able to go home, even for a short visit. It was one of those very bad days with lots of flashbacks and thoughts of how much better things would be if I were dead, so, I switched days on my planner, did my Tuesday plan on the Monday. And it would have worked out fine, except the next day was just as iffy as the previous one, safety-wise. I wanted so badly to be able to stick to the plan, though, since otherwise there would be fewer opportunities to go home before actually being discharged. And I knew discharge would be coming, whether or not I had brought the Bottle back.

I want to pause here to make something perfectly clear: there was absolutely no pressure from staff for me to go home that day – none, zero, ziltch – and that is really important to understand – they were all working hard to keep me safe. All pressure to go home that day came from me, and me alone. But, in the end I did decide to push on through. And that turned out to be a near fatal mistake.

When I first got to the flat on that third trial run I felt anxious, but sort of within the realm of what I could manage. So, before entering I rang Drayton to say that. All was good, I sat in the kitchen for a bit, I even wrote an angry note to my flatmates about the washing machine not having been fixed during my two week absence. Everything felt normal.

And then suddenly it didn’t.

I know that I went and took a sleeping tablet in desperation. At the time I really thought it was just the one, so, that is what I told staff when I called them in panic. They stayed on the phone with me until I was out of the flat and I got a taxi back to Drayton. I saw my main worker when I got back, and prepared to go to bed [after all it was a sleeping pill I’d taken]. We agreed that they would check on me every hour, just to make sure I could be woken up, since I have a history of taking overdoses in a state of dissociation, and I couldn’t say with 100 per cent certainty that I hadn’t done so this time, too. [Entering a dissociated state is actually far more common than you might think, especially for people who have suffered severe abuse and have used dissociation as a coping mechanism all their lives]. About quarter of an hour later I knew that I must have done more than just taking a single pill, because I was feeling nauseas and drunk and was losing control over speech and movement. So, I went straight to the staff office and knocked on the door. [This is, incidentally, the exact opposite of what I did that very first time at Drayton]. The last thing I remember is lying on the sofa in The Quiet Room with a member of staff next to me, being told that an ambulance was on its way.

I woke up in hospital. I knew immediately that I was in hospital, because nowhere else on earth are you met with those cold harsh lights, and those ugly tiles in the ceiling. That is my first memory. My second one isn’t so much a memory as a feeling, a feeling of immense relief that I was alive, that I had in fact woken up. And I knew that was a big deal. Every other time I’ve woken up in hospital I have felt nothing but sheer anger that I hadn’t died, wondering what I had done wrong, thinking about when I could do it again.

I spent a number of days in hospital being given antidote every twelve hours. And that was one of the most scary experiences ever. The relief of being alive soon wore off, and the fear of not knowing whether or not I would actually live – and what that life might be – took over. I knew that things were bad, really bad – not just from the vast number of tubes coming out of my body or the urgent frequency with which blood tests were taken day and night – but by the fact that when I tried to ask doctors and nurses would I be OK, they avoided eye contact and would generally mumble something along the lines of Let’s not worry about that right now, sweetie.

It wasn’t until the very last day, the day I was due for discharge, that I finally found out the truth of just how close it had got. I didn’t ask the doctors or nurses this time because I didn’t trust that I could deal with what they might have to tell me, instead I reached for the journal folder at the foot of my bed. And there it was in black and white. Multiple organ failure. Prognosis: poor.

Of course, by the time I read those journal notes, I was out of immediate danger, but it was still a shock to see it. This was what I had done to myself.. I had put kidneys, heart and respiration at serious risk. When the first tox screen came in they didn’t think I’d live, and if I did I’d likely have reduced function of at least some of those organs.

I have now been at home for about two and a half weeks. I am extremely fatigued and am sleeping most of the time. Any little thing exhausts me. I have had follow up tests and the results are not great. They aren’t anywhere near as bad as they could so easily have been, but I am also not recovering at the rate the doctors would have hoped. So there will be more tests to come. In short, I still don’t know the full extent of the damage I have done to myself.

But, I am alive.

And I have a lot of feelings about that.

 

I hope that I will be able to write more about those feelings soon. –ish.

xx

 

 PS. I want to make a special mention that I have chosen not to share what has happened with my immediate family, in an effort to spare them pain and worry. At least until I know for sure what I am dealing with. So, should you be someone who knows me in person – and knows my family  – please make sure to keep this information to yourself. This blog is semi-anonymous, not for my sake, but for the sake of those close to me. It is also a place where I can safely share my feelings, and that means a lot to me.

 

 

Every Part Of You Needs Therapy : Baby S.’s Story

Posted by What It Takes To Be Me in Abandonment Issues, Attachment, Communication, Coping Strategies, Depression, Drawing, Expressing Emotion, Expression Through Art, Identity, Inner Conflict, Memories, Personal Growth, Psychology, Psychotherapy, Psychotherapy with P and tagged with , , , , , , , , , , , , , , , , , , , , , , ,
impossible shapes

“Looking Back At My Younger Self” – An ‘impossible’ drawing I did, inspired by Reuterswärd, Escher and Penrose

Whenever I think about who I am, I always reach the conclusion that there is more than one answer to that question. I have written about the concept of every person having different parts to them before [the baby self, the child self, the inner teenager, the adult etc], but I have been wanting to write more about each individual part for a while now, so that is what I am planning to do in the next few posts. [Emphasis on planning here – no promises, plans sometimes don’t pan out]. I have no idea how interesting this will be to anyone else, but as it is something P. and I do a lot of in our therapy [exploring, defining, trying to understand the different parts and how they work – and sometimes don’t work – together in my internal system], I know that it will be a useful exercise for me. So, I am going to be a selfish blogger for a little while. And I use the word ‘selfish’ here in the purely positive sense of allowing myself and my needs to come first. That said, I know from the emails I have been receiving from you over the years, that many of you share similar stories to mine, and I hope that you, too, will get something from this exercise – maybe even take a little time to think about your own internal system?

I am going to start with Baby S., because that is where the person I am now begun. Baby S. is simultaneously the very oldest and the very youngest part of me. She is the part of me who was there from the beginning, the tiny pre-verbal part of myself. She is the one who was around when I was living at the Indian orphanage in the first seven months of my life, she is the one who first experienced being abandoned, first experienced loss. When this happened, I don’t know, because I don’t know if I was born at the orphanage or if I was brought there. And if I wasn’t born at the orphanage, then I don’t know whether a stranger found me somewhere on the streets of Calcutta and handed me in, or if my birth parent made the decision to take me there themselves, because it was what they believed would be best for me. In fact, I don’t even know if my separation from my birth parents was forced upon them or if it was a choice they made. All I know is that at a very early age I experienced the extreme trauma of being abandoned. 

Baby S. is also the part of me who for the first seven months of my life experienced a serious lack of human-to-human [or rather adult-to-child] contact and care. This I do know for a fact. I know this, not from having a conscious memory of this lack of close contact, but because I have been back to the orphanage I came from, and I have seen the little metal cots shared between two or three babies [hence correcting myself earlier; there was most certainly human-to-human contact, but not adequate adult-to-child care]. This inadequacy was not because I came from a particularly bad orphanage, it is simply down to the fact that I come from an exceptionally busy and over-crowded one. [Actually, scratch ‘exceptionally‘ – it is probably no more busy or over-crowded than any given orphanage in India]. The nuns working at this orphanage no doubt tirelessly do so because they care very deeply about all these abandoned babies and children, and are passionately wanting to do what they can to provide for their tiny little charges, but there are simply not enough of them going around, and – sadly – their job becomes never ending rounds of nappy changes and bottle feeds – conveyor belt style – to ensure that no child is missed. So, in spite of these heroic efforts, precious little time is spent with each individual child, and the opportunity to form any kind of meaningful attachment is virtually nil. 
I was ten years old when I went back to visits the orphanage I came from, and even as a child of that age I was acutely aware of the Baby S.-part inside, and I didn’t need an adult to explain to me how lonely and frightening it must have been for me as a baby to be in that environment. It is hot, crowded and noisy, with little colour or comfort. No toys, no safety blankets, no dummies [that’s British for pacifiers], no cuddly teddy bears.. Bleak, bare and loud, with hardly any Big People to care for you; a very sad environment for anyone to be in, no matter what the age. Needless to say, visiting that orphanage had a big impact on me, and it has played a huge part in why I have always been so much more interested in understanding the effects of starting out in an environment like that – void of significant caregivers to form attachments to – than wanting to find my birth parents. 

Anyone who has been adopted will be more than familiar with Everyone Else’s two compulsive-intrusive questions: “Do you know who your real parents are?” and “Would you like to find your real parents?” My answer is invariably: “Of course I know who my real parents are – I grew up with them, and, no, I’m not hugely interested in finding my birth parents.” An answer, which is more often than not, met with disappointment. It is as if, being adopted, one ought to have a strong desire to trace one’s biological roots, and if you haven’t got that desire, well, you must be lying to yourself. I genuinely don’t feel I am lying to myself; I just haven’t a strong desire to trace those roots. That isn’t to say that I won’t ever feel that desire, merely that – as of now – it’s not played a big part in my life. Yes, of course I have at times wondered about them, but – somehow – I have always had a really strong sense of who my parents were and what they were like – even though I couldn’t possibly have any conscious memory of them. Maybe it is a biological imprint that we are born with..? I don’t know. All I know is that I’ve always been far more interested in understanding how my early life experiences have shaped me, than finding out who the people I came from were. So, let’s go back to exploring that: 

Apart from being abandoned, Baby S. is also the one who had to deal with the most extreme life change out of all of the parts that make up my internal system. At seven months old her whole life was turned upside down and inside out when she was brought from the orphanage in the loud and crowded city of Calcutta, to a tiny coastal town in the very north of Sweden. I don’t think the climate or cultural change could have been greater. This was a new life, in a whole new world, with strange new smells and sounds and ways of doing things. And a whole new set of people. A mother and a father and two older brothers, one of whom was also a deeply traumatised young child [2.5 years old on the papers, in reality closer to four] brought over from an entirely different part of India, at the same time. 

One of the things that is always said about me as a baby, post adoption, is that I was “such a good little baby”, meaning that I was a very quiet baby; I rarely fussed and I slept more than most. I was also out of nappies before I was a year old. Every time another story gets retold for the umpteenth time of what a good baby I were, I always have an urge to scream that “Of course I didn’t fuss! Why would I?” and I can feel that it is the Baby S. part of me having this reaction. By the time I was seven months old and came to Sweden I had already learned that there was no point in crying if I needed something, whether it be food, a new nappy or a cuddle, because no one would come, no matter how desperately I cried.. I simply had to wait my turn, whether I understood the concept of waiting or not. So, I stopped crying, stopped fussing, stopped trying to get the attention, care, and love that I so desperately needed. Because I knew that it was pointless. And the sleeping? Well, I’m no expert – but it sounds to me like either a stress relieving coping mechanism kicking in, or early depression. Or, more than likely, both.  

Because of Baby S. inside of me, I experience intense anger whenever I hear people asking new parents “Is he a good baby?”. What’s the answer to that? “No, she’s an absolutely terrible baby, she demands feeding and changing and she won’t let us sleep for more than half an hour at a time!” To me, good does not equal quiet – and I know that my sensitivity to this kind of talk is really Baby S. having an emotional respons. She can’t help but to kick off when someone starts talking in those terms. Which is great – finally she is able to express herself, be it through emotions rather than words. 

That brings us to one of the challenges of allowing Baby S. space in our therapy. Baby S. is pre-verbal, she doesn’t have language – or rather, she hasn’t got words. So, how can she be part of the therapy? I haven’t got a definitive answer to that. I mean how do you get a pre-verbal part to speak? My solution so far is to work on getting Adult Me to become more attuned to Baby S.’s emotional signals, so that she can verbalise on Baby S.’s behalf. It’s not an ideal solution, because dressing a baby’s emotional world in adult vocabulary requires translation, but it is a starting point in terms involving Baby S. in our therapy. The first step to giving Baby S. a voice in the outside world is to listen for it. So, I try to get Adult Me to actively listen to what Baby S. is communicating. It’s sometimes – often, actually – rather a difficult thing to do, especially if what Baby S. is desperately wanting to say, happens to be the exact same thing that Adult Me is wanting to hide from, and still needs to defend agains.

I believe that Baby S. only ever communicates truths – she has not learned that truth can be manipulated to suit one’s needs – and conflict can occur when Adult Me is not yet ready to face that truth. Still, it is work in progress. Through Adult Me’s active listening, and through her translation into spoken word, Baby S.’s feelings can be brought into the open in the space I share with P., and together we can work with it. 

And there is a lot of stuff to work with. Trust me. 

There is an excellent blog called Everyone Needs Therapy – a sentiment I share. Only I would take it one step further and say that Every Part Of You Needs Therapy.



Take good care of your Selfs,

xx 

I Solemnly Swear Never To Be Suicidal Again? – An Entry About Fears, Promises & Honesty

Posted by What It Takes To Be Me in Anxiety, Attachment, Boundaries, Counselling with D, Countertransference, Depression, Expressing Emotion, Psychology, Psychotherapy, Psychotherapy with A, Rejection, Suicidal Ideation, Suicide, The Therapeutic Relationship, Transference and tagged with , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,

When I uploaded the previous post twenty days ago, I was fully intent on posting the next one the following day. As you can see, this didn’t happen. Instead I have been telling myself every day since then that ‘You really must get around to writing That Post today’, each day finding conscious and unconscious reasons not to do so.

I’m not always good with feelings, with dealing with them, I mean. Especially pain. I have a tendency to shut down, to frantically try and get away from anything that may make me experience emotional pain. And I do this even more so if I perceive that the pain is being inflicted by someone I respect and care about. In some ways I suppose this behaviour makes perfect sense. Who wants to feel pain? Who wants to feel hurt by someone they hold important in their lives? And, yet, looking at it from another angle, it is sort of strange, particularly from someone who has spent so much time doing therapy, where much of the work centres around exploring and examining pain, past and present, often inflicted by those we find hardest to blame.

So.. this will be a hard one to write. But, I felt that I owed it to myself to be brave, to not hold back, to be honest and let it all out. After all, that is why I have this blog..

The week I had been discharged from Drayton Park I arrived for my usual Friday session with A. I had a very specific question on my mind, one which had been eating at me for a while, and I felt I really needed to pluck up the courage to ask A. about it, in light of what had been going on both with me separately and in our mutual relationship lately. I never got a chance to ask the question, because once I had sat down, A. turned to me and said ‘There is something I need to say to you.’ Alarm bells went off all around my body. Last time she started a session that way was when she told me she was pregnant, and I could tell that this time it would be something possibly even harder to deal with.

‘I can’t work with you under the threat of suicide.’

Ten words. Like bullets to my heart.

I must have sat quiet for ten minutes, my world stopping in its tracks. I felt cold, nauseous, struggling to breathe. Thoughts were spinning in my head so fast it was impossible for me to grasp any of them for what seemed like forever. For a second I contemplated just getting up and leaving, something I have never done in my life, to anyone. But, the pain was excruciating, and I felt that I couldn’t take it.

When I finally spoke, the words that came out, as I was trying to blink away tears that weren’t even there, were a mere whisper; ‘I guess that makes one more person who can’t cope with me, one more person who I’ve become too much for, who I have pushed too far’. I couldn’t look at A. as I said it, because I was too scared of the force of my own emotions.

This fear of becoming too much for people, it’s been central to my therapy from day one. It’s been a ridiculously regularly recurring theme, something many hours have been spent turning inside out. I know where it stems from: that pivotal moment when I was seven and told my mother about what my brother was making me do, when I broke her, when I discovered that there was no one who could help, no one I could tell without running the risk of breaking. And ever since then, that fear has remained, has evolved into this enormous ball of anxiety that now encompasses a million different things that I believe I do, which ultimately drive people away.

Having said that first thing, suddenly there were lots of other things I wanted to say, thoughts I wanted to share, because apart from fear and pain a plethora of other emotions were descending on me at breakneck speed. I took a minute or two to try to pick them out, to separate them. The most urgent one was the feeling that this was incredibly unfair, because in the past several months I had more than once felt unsure of whether or not A. could truly cope with what I was bringing to session, and more than once had I openly asked her if she could. And each time she had opted not to answer. So I said exactly that, adding that it felt like she was going from zero to a hundred with no steps in between. Silence, silence, silence and then ‘I can’t work with you’.

After a few more moments of silence, from both of us, I asked her how she had imagined I might respond to what she had just told me. A. said that she didn’t know how I would respond. In frustration I said that that wasn’t what I asked, I asked how she had imagined I might respond, because in my mind, she is an intelligent person, and it didn’t seem that far-fetched that she might have pictured me hearing what she said as a form of rejection and as further proof that there is no-one who can cope with me, and that it would take me down the path of ‘If even my therapist can’t cope with me, then what hope is there..?’

Later she said, in her very gentlest voice ‘I’m giving you a choice’ and because I wanted to be fair to her and to the reality of the situation, I said that I could see that, and that I can absolutely understand that it must be incredibly difficult – frightening, even – to work with me when I am suicidal. Especially in light of what had happened only a few short weeks ago. And, yet, at the same time I couldn’t help thinking ‘How is this a choice?’ She was saying that she couldn’t work with me under the threat of suicide, but how could I possibly promise to not be suicidal? It’s not something which can be switched on and off with the push of a button. It felt more like an ultimatum; ‘Either you stop being suicidal, or therapy stops’. I was going through the options in my head, thinking that I would be willing to say almost anything – even if it was a lie – if only she would carry on working with me. But, I also knew that I really didn’t want to have to go down that road, because it’s perilous in nature; one which would inevitable and seriously impact whatever work we might do in the future.

I said to A. that if I did make a promise like that, wouldn’t that by default make the whole subject of suicide and suicidal feelings taboo? Because, how could I ever trust that I wouldn’t accidentally step over the line of what A. felt was too much, now that she had shown me that such a line did exist, not only in the realm of my fears, but tangibly right there in that room? Wasn’t it exceedingly likely to have the effect that if things got to the stage where suicide felt like an option, I might not be honest with her, might not share these feelings, for fear of what the consequences might be for my therapy? To this A. said that of course I would also need to think about whether or not I could work with her. This may have been meant to make me feel that this was a two-way street, but it only left me with the feeling that perhaps she was hoping that I would come to the conclusion that I couldn’t, thereby giving her an ‘out’. So, I said exactly what I was thinking: ‘I feel like I am being pushed towards terminating this therapy. And that is not what I want.’ To which A. said that I may need to take some time to think about all of this.

I was silent for a while, trying to come up with something – anything – that may be used to bridge the gap between what I felt A. was asking of me and where I felt I was truly at, and suddenly I remembered something D. – the counsellor I worked with before I started seeing A. – and I used to do when things were very difficult. We would make an agreement that I wouldn’t act out in any way between sessions, that I would always come to the next session to talk things through with her. And, because I had a huge amount of respect for her, I knew that if I did make that promise, there was no way I would break it. It’s just how I am. And, if I felt that I couldn’t make an honest promise, it wasn’t a case of ‘Well, then I can’t work with you’ but we would instead find some sort of middle ground, acceptable to both, and which, crucially, didn’t entail making false promises. I might admit that I felt unable to promise that I wouldn’t act out, but that I could promise that before acting out I would do X, Y and Z (ie call the Samaritans, speak to three different friends, do my nails, make a painting, write a chapter on my book, contact the crisis team etc).

Having explained this set-up to A. she initially wanted to know how that had made me feel and I told her that it made me feel contained, that it was a positive thing, this process of coming to a reasonable agreement, because it made me feel that I had some control. And also, that not only did I know that I wouldn’t break a promise I had made to D., I also felt confident that she knew I wouldn’t.

After a short pause A. said that she felt she had made her position very clear and that any promise would have to be for as long as we worked together, however long that may be.

It felt like she was pulling the rug from under my feet, like she was responding to my tentative suggestion of a possible solution, by immediately raising the bar, to make it impossible for me to make the promise she was after.

So, I left that session in a daze, feeling unsure if that was it, if that was the end of the road for our work together, not at all knowing whether her earlier ‘You may need to take some time to think about this’ extended only to this particular session, if she was expecting me to show up for session the following Wednesday, or if she wanted me to do my thinking at home, so she wouldn’t have to deal with my suicidality, which clearly could not be dissolved from one session to the next.

*

I am not meaning to make this storyline of my life into any sort of cliff-hanger, but I am exhausted and I need a break. There is a lot more to say about what has been going on in my relationship with A. and what has happened since this session, and I hope that in the next few days, I will be able to post an update of some sort.

Until then,

Be kind to your Selves,

xx

Post Trip September Babyland Depression Begins

Posted by What It Takes To Be Me in Depression, Family, Family Dynamics, Psychotherapy with A, Sadness and tagged with , , , , , , , , , , , , , ,

I’m back!
Not just here on my blog, but in the country.
Got back on Monday. Feels like I’ve never been away; you know how it goes.

Except, of course, this trip does appear to have had an effect on me..

The main reason for going on this trip was so that I could meet my two newest nephews. Nope, not twins. My youngest brother and his wife had a little boy in mid-July, and my sister gave birth to another little fella on the same day I flew out there.

It’s been a good but challenging trip, once again coming face to face with the fear of never getting to have children of my own and wanting them so very desperately. The first week and a half I spent at my sister’s, with the rest of her family. As I mentioned, her little boy was born on the same day I got there, so he was only a few hours old when I met him. [My sister gave birth at 4 am, and checked herself out of hospital at noon(!)]

There is something very special about newborn babies. I mean, all babies are special, but with someone who is completely new in this world, well, it’s just different. They are so tiny – even the big ones – and so terribly fragile. So completely dependent on those around them. And holding my nephew that first day brought out all sorts of feelings, most of which I am still processing.

I spent many hours holding my nephew during my stay there. I’d just sit with him and look at him. Feel the weight and warmth of his little body, his special baby smell.. I also played with his older brother a lot – don’t worry, he was in no way neglected – and while I was still there it was pretty darn fantastic. [The older one has only just got into role/script-playing, so there was a lot of pretend play, which I absolutely love!]

But, as great as it was, when the time came for me to leave [I was flying across to stay at my father’s, to meet my other new nephew].. well.. it was hard. Really really hard. I don’t think I can quite put it into words just how hard it was. All I know is that when I arrived at my father’s, all I was feeling was that I was missing my sister’s little boys. Wanted to be back with them.

Prior to going, I had been worried about what it might be like to meet my new nephews, and had predicted that it would be, in many ways, harder to be with my brother’s little boy than to spend time with my sister’s kids, because, with my sister – even if it had felt really difficult to be around the boys – well, our relationship is such that I could have talked about it. With my brother, and – by extension – my family – that’s not really the case, and I knew even before going that there was a definite risk that, should it feel very hard to be there, I would fall back on old patterns of pretending to be OK, no matter what.

As it turns out, while I was there, it was actually fairly OK. Being with the baby, I mean. I always feel like something of an outsider around my family, like I don’t quite belong, but at least with the baby it was OK. I guess it’s that sort of thing where, with the kids in the family, well.. it’s not their fault that they were born into what is an exceptionally complex situation, is it?

But now that I’m back here, back at my place.. well, those feelings that were surely already bubbling under the surface are beginning to come out in a big way. And it’s hard. Really really hard. I’ve talked a little about it in therapy [only had one session since being back], but in these last few days, it feels like it’s starting to push through more and more. It’s nothing to do with the actual kids; I still love them to bits. But that doesn’t meant that the feelings they bring out can’t still be incredibly difficult and painful to deal with.

As much as I love being an auntie.. I just really want to be a mother. It’s the only thing I want.

So, post-trip, the truth is that I’m not doing too good right now.
Spent most of this week in bed, most of last night on the phone with the Samaritans, feeling frighteningly low and increasingly desperate.

It’s not a nice place to be.
Nor is it a safe place.

xx

Self-Harm & Self-Piercing

Posted by What It Takes To Be Me in Conversion, Coping Strategies, Depression, Faith, Judaism, Psychotherapy, Psychotherapy Breaks, Sef-Awareness, Self-Harm and tagged with , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,

Not very long until A. is back now.

Looking back at this break I can honestly say that there were definitely times when I didn’t think I would be around to see her return to work. I had some very very low points, where it felt entirely impossible to think that I could make it through. As you know, early on during this break, I did accidentally on purpose overdose, and even though this may sound weird, that wasn’t even the lowest point I got to. In fact it wasn’t even near to being the lowest point.

Then I had a bit of a breather, where I went to spend time with my sisters, where I reconnected with my faith, where I felt a little less frightened. Went back to only having the normal amount of flashbacks. And that was nice. And much needed. I count my blessings that I do have those times when things are a little easier. I try to take notice of the good in life, I really do. I know that reading this blog, it may seem that I only focus on the hard times, but I really do try to balance it out, to see the bigger picture.

I have to admit, however, that these last few weeks it has felt a little as if I am starting to slip again. I’m not sure if that is perhaps because, knowing that this therapy break is nearing its end, I am allowing myself to feel a little bit more than I have during the majority of this time. It’s possible. People keen to criticise my choice of therapy and therapist will, I’m sure, draw the conclusion that going back to therapy is what is making me worse; that therapy is itself the culprit. Needless to say, I disagree. Strongly.

Still, I do have to take these dips seriously; I am very well aware of my tendency to sink hard and fast, and to try to waive it off as nothing would be decidedly unwise. So, I’ve reached out. I’ve talked to my sisters, my friends, the Samaritans, just to make sure that I don’t plummet.

I did have a night last week which was particularly bad, where I felt very very tempted to get the scalpels out again, to release the tension, to get away from the bad feelings surging through my whole system. I resisted. Sort of. I had them out. I looked at them. Held them in my hand. Then I put them down. Put them away. Decided it was a bad option. Thought some more, and decided that there was something else I could do, which was a little less destructive, a little more spiritually meaningful. Something which I had been thinking about doing for some time.

The end result is a freshly pierced nose.

I know, to some, this seems little better than cutting myself, but to me, there is a big difference. Self-harming through cutting is a way of making my body look worse, it’s almost like physically punishing myself, not just through the pain inflicted while cutting, but also in the way the scars will always be there [and, trust me, I have plenty]. They only serve to make me feel bad, because they make me think of how I was unable to control my impulse to cut. Make me feel weak. And I don’t like feeling weak.

A piercing to me is different.

Whilst people may have varying views on the aesthetics of body piercings, or religious reasons for opposing them, to me, they are pretty – plain and simple: I like them – and my interpretation of religious text does not cause me to see them as forbidden. And so, in my mind, choosing not to slash my skin in destructive desperation, but deciding to do something different [albeit similar]; it makes me feel that I can control my impulses, I can convert destructive energy to something much more positive:

A sparkling reminder, right in front of my nose, that even bad nights do pass.

I feel I need to write a little something here about self-piercing: I am not an advocate of it, despite having done it more than once myself. Each time I’ve done it, it has been done as responsibly as possible. No dirty safety pins, no pound shop jewellery. Always clean hands and/or using gloves, always clean work surfaces, always proper after-care. Never without thinking it through, and never without, in my opinion, a genuinely valid reason for doing it myself.

You can read a detailed piece I wrote about my first self-piercing and my reasons for doing it myself here. Some of the things I say there are not quite how I see things now; it’s been four years. But the key is that it was a thought-through and reasoned decision. Not an in-the-moment act. In contrast to self-harming.

Even this latest piercing wasn’t something I did lightly. The reason I had the appropriate equipment in the first place was that I had been thinking about doing it for some time. And by thinking about it I don’t mean in the middle of the night in a moment of feeling very low, but during the day, consciously weighing the pros and cons. I made the decision to do it that night, because I wanted to – perhaps even needed to – prove to myself that I could do something other than cut, something which for me had meaning, something which wasn’t a destructive and impulsive form of self-punishment.

If you do choose to DIY pierce; do the research. Then think again. Think about why you are wanting to self-pierce and the risks involved. Also, think about where you want your piercing. Not all places are ideal for self-piercing. In fact, most aren’t. [In hindsight, I would have to admit that the nose definitely isn’t particularly ideal for self-piercing. And it was darn painful!] Also, just because something can be done, doesn’t mean it should be.

If the reason you’re considering not going to a studio to have it done is that you’re underage, get your parents to come with you to give their consent. Or wait until you are legally able to give consent. If you want it that badly, you’ll still want it in a year or two. From a religious point of view, getting your parents’ consent also matters in terms of honouring your mother and father through not choosing to do something your parents directly oppose. I’m not meaning to be preachy, I’m merely pointing this aspect out. [For me this was always a non-issue, as my mother sports a sparkling lip piercing of her own.]

For most people, people who just want a piercing because it looks good, my advice will always be: Go to a professional piercer! You won’t end up accidentally mis-aiming and come out with a wonky piercing in a place you hadn’t meant to have one. Seriously. Going to a professional piercer will generally be a much better experience; quicker, more than likely less painful and much much simpler all round.

First and foremost;

remember to be kind to yourselves.

xx

PS. I do realise I am displaying an astonishing amount of double-standards when it comes to self-piercing, but in my defence: I am an adult, I had a valid reason to do it myself and it was a thought through decision. And, as I wrote earlier, looking through a rear view mirror: I wouldn’t recommend piercing your own nose to anyone. Anyone. That includes my future self.

An Uneasy Dwelling – Delayed Reflections On Living In A Therapeutic Community

Posted by What It Takes To Be Me in Boundaries, Community, Diagnosis, Expressing Emotion, Family, Friends, Group Dynamics, Home, Illness, Psychotherapy, Reading and tagged with , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,

It’s been a year now since I moved out of the therapeutic community I used to live in. And I’m still processing it. The ups and the downs, pondering what I took from my time there, what more I could have got from it, what I’m glad to have left behind.

I can say without hesitation that I don’t regret moving in there. I can also say that it is the most stressful living situation I’ve every voluntarily put myself in. With three group meetings a week [on top of my individual therapy sessions outside of the house] it’s a pretty full on experience. Even though I often made the decision to stand on the sidelines, to keep myself at a distance, it was a pretty intense way of living.

Would I have got more out of living there, had I been more invested in it? I don’t know. Maybe. I don’t rule it out. Certainly it made a difference to the sense of community within the house that I chose to not engage as much as I could have, to not push for communal meals, to not easily join in with the household. Yet, at the same time, it just never made sense to me to bring my worries and desperation to the house meetings, to be looked at by people, who – although I liked many of them – didn’t feel particularly safe with. [This, incidentally, is solely a reflection on me, – not on them.] To me, it always seemed like the natural thing to do, to turn to my sisters and the friends I have always been fortunate to have when things got tough, to turn to them for extra support. And for the things I felt I couldn’t necessarily share with them [for whatever reason], well, I had my individual therapy with A. for that. Bringing it to the group sessions, it just seemed a bit odd.

That is not to say that I never shared anything in the meetings. I did. But not on a regular basis. It tended to be only when things were really really bad and I just couldn’t hold my tears back.

So, what was it that I found stressful? Well, in part what I have just written about; the expectation to involve myself, to engage and to share, and the feelings brought up by the fact that it was an expectation which I always felt I would never be able to live up to. Part of that was, as I said before, down to the fact that it didn’t quite make sense to me to share difficult things in a group of people I didn’t really know that well. But, of course, there were more deep rooted trust issues at work, holding me back. Other people, who may also have had friends and family they were close to, didn’t feel the same level of reluctance to take the plunge in the group meetings, and were much better able to let others see their vulnerability.

Another thing that was probably more stressful than I even realised at the time, was the constant stream of visitors to the house. Visitors who came to our meetings with a view to possibly join our household. This was a part of life in the house that I never got used to and always felt distinctly uncomfortable with. It was one of those things that made the place feel a lot less like it was my home as opposed to only being the place where I happened to be living.

People would come, share their story, share of themselves, [or in some cases not share] and we were, I suppose, meant to get a feel for whether or not this was a person who could fit into our house, who might benefit from moving in. It probably doesn’t sound particularly stressful, but it really was. Especially the decision making process, where – in theory – residents were said to have a big say in whether or not someone was invited to join, but which in reality often felt like a humongous and never-ending pressure to get new people in. Often at a time when all you really wanted was to find some headspace for yourself, to settle in the group you were already living with. I remember more than one meeting where one of the house therapists would say something along the lines of the process being about all of us reaching some sort of consensus about whether or not a person was suitable for our house, and in the next breath would not-so-casually mention how we needed to be X number of people living in the house for it to be financially viable. No pressure, right. :þ Also, I always took issue with the fact that the question “Is this someone I can live with?” seemed to be second priority to “Could this person gain something from moving in?”, which, it could be argued, sent the message that the gain of a person joining far outweighed the potential rise in stress level of those already in the house.

Clearly, there were times when the reluctance to accept new housemates were motivated less by worries about how a new person might impact the household negatively, and more about a strong wish to hold on to what was familiar. But, then, is that so strange? For a person to build a home, there arguably needs to be a level of familiarity and stability. A stream of new introductions allows little space for that.

Stressful was also the particular mix of people in the house at any given time. Without going into detail about any one individual, the people staying in the house – at least for most of my stay there – could be broadly grouped into either dealing with depressive and/or anxiety related issues, or difficulties which fell somewhere along the more psychotic end of the mental health spectrum. And, as housemates were supposed to support one another [rather than relying on the house therapists – who only come to the house for the meetings – to sort things out] it at points felt very much like the first group was responsible for the latter group.

It isn’t easy walking through the door, never knowing what you might be walking in to. I’m not going to say that I was in any way the person who most often ended up keeping track of others – I wasn’t – but, there were absolutely times when I had to drop what I was doing in order to help settle a very agitated housemate or, once or twice, call the police because someone had taken off, stating they were going to kill themselves. And I think this way of always being on the ready to put fires out, to some degree stopped me from being able to explore my own issues more. [Not the only reason for this, of course, but one of them.]

One of the really invaluable, yet hard bought, lessons from my time in the house, was having to seriously think and feel through what boundaries meant to me. Which ones were important to me, which ones did I feel able to be more flexible about? I had to work at asserting myself, when I felt the boundaries were being stretched beyond what was OK for me. Regular readers will remember that my decisions to ultimately leave the community came down to – in part – feeling that I needed to make a stand for myself, to not just go along with boundaries being pushed, but to recognise that what I feel OK with, or not, is important and worth holding on to. But of course, this was an ongoing battle, this getting a feel for when it was important to hold on to my way of living my life, yet at the same time question my reasons and motivations for doing so. When was there a valid reason, and when was I simply being stubborn and resisting change? When was it a case of me being the rebellious teenager I never got to be in my own family, when was it the adult me refusing to see things from another person’s perspective?

While I was staying at the house, one of the house therapists published a book about the community houses run by the Philadelphia Association. I made the conscious decision at the time not to read it while I was still living there.

Having now lived away from the house for nearly a year, I have read it, and I have to say that it’s a book well worth reading. I found it very interesting to read about the history of the houses [which I had some idea of, even before moving in, but, again had chosen to not explore too extensively], and how the philosophy behind the houses has altered and varied at different points.

I think it’s an honest book, even though I at times found myself smiling at the discrepancy between the idea of the community houses and the reality of them. At least from my point of view.

Anyway, if you are interested in reading the book for yourself, click the link or picture below.

If you would like to read about my time in The House: entries written between January 2009 and July 2011 were written while I was staying in The House. The first post I wrote having moved in is called “On My Own – An Entry About Finding New Ways To Cope“.

xx

An Uneasy Dwelling by Paul Gordon

An Uneasy Dwelling
by Paul Gordon

Sisters, Study-Avoidance & Melting Crayons

Posted by What It Takes To Be Me in Creativity, Depression, Expression Through Art, Family, Flashbacks, Psychology, Psychotherapy Breaks, Psychotherapy with A, Reading, Studying, Writing and tagged with , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,

So I’m back from my trip to Sweden, and at the moment it feels like it has done me a world of good. It was simply great to spend a whole week with my sisters and their little families and just enjoy being alive. The weather was great and although we all took turns taking ill, all in all it was just really nice to hang out. We basically ate, watched my youngest nephew run around and ate some more. That is, that’s what my sisters and I did. The boys were busy digging in the garden, planting a hedge around it. And in between that we managed to watch a film, teach my sister’s dog to go on the slippery-dip and get my youngest sister and her man to understand how to solve the first two layers of the Rubik’s cube intuitively.

Oh, and my sisters and brothers-in-law gave me the super-awesomest prezzie ever; the new iPad [which I am, incidentally, using as we speak, in conjunction with my bluetooth keyboard].

I feel that this trip has really helped to reset my brain. I feel so much happier than I have in the past several months, and although I am still having flashbacks it’s nowhere near as bad as it was, pre-trip.

Since I’ve been back I’ve started a new course, and – true to form – I’ve excelled at the art of study-avoidance. I am feeling a bit unhappy about having chosen the course I have; a very basic psychology course about stuff I pretty much already know, but just want to get on paper that I do in fact know it. It’s very hard to motivate oneself to read material about stuff you already know, when the main focus ends up being trying to remember sources for future reference, rather than actually learning. That said, of course anything psychology related will always push your little grey cells into action, and you’ll realise you have thoughts and ideas you might not have had when you originally read about a specific study. In short; once I actually open the book, I do get quite into what I’m reading.. it’s just getting to that point of opening the book, which holds me back. There are always a million other things I feel I need to read; blogs, news, tweets, facebook updates.. You know how it goes.. And that’s before I’ve even got to the various iPlayer programs I simply must catch up on, not to mention the millions of YouTube clips I feel will enrich my life to no end..

I do slightly regret that I didn’t decide to do the course on the autistic spectrum which was also on offer. I would really have liked to have been reading that right now. But, I’m trying to use it as a carrot of sorts. If I manage to get through this course [ie find a way to utilise good days of fewer flashbacks, days when I have a reasonable level of concentration] then I’ll be allowed to do the autistic spectrum one after.

So, I suppose that’s all good. Especially the part where I am actually, actively, looking ahead, into the future. The last few months have been so rough, it’s been very hard to think like that, to imagine a time when things feel different, but right now things seems to have swung around for me a bit.

Also, since I’ve been back, I’ve been feeling a lot more creative. I have been working on my book, which is ever so slowly taking shape, and I find myself curious to find out where the characters will take me. And that’s always a good sign.

On top of that very specific writing, my sister and I also hatched an idea about setting up a collaborative writing site online, the idea being that you could go to the site, read something someone has posted and then take over the writing, or join in. I for one have several writing projects which I have started, but which are now mainly collecting dust on my harddrive. What you could do on this new site is to upload what you have written and invite others to complete it, or to co-write it with you. Or you might want to be someone else for a day [come on, we all have those days].. Well, you could go onto the site as a character and join in some playwriting, adding lines on behalf of your character. This is all still in its infancy, but, I only posted the idea late last night on another blog, and I’ve already had people contact me to say they would be interested in joining or starting writing projects.

Observant readers will have noticed that while I have written about how great it was to be with my sisters and how that’s really helped resetting the serotonin levels I’ve omitted to talk about seeing my father the first time in over two years. This is, of course, not by chance. In short, it was actually really lovely seeing him and his boyfriend, and spending time with them. But, knowing me, I tend to only begin processing these kind of encounters a while after getting back to the UK. So, keep an eye out and there will more than likely be an update on this particular part of my trip to Sweden.

In terms of not having therapy, well, there is no getting around it – that is still really hard. I miss my space to voice my thoughts. Of course I talk to my friends and I do my writing and all of that, but there just isn’t a substitute for therapy. Therapists definitely should not be allowed to have children! [..says the Therapist’s Daughter..] July – or whenever A. in reality decides to go back to work – feels very very far away indeed..

Anyway, me and my new iPad and bluetooth keyboard need to get to the library now, so I’ll leave you here for now.

Do be kind to yourself, and enjoy the utterly ESSENTIAL YouTube video below..

All the very best and more,

xx

I really need to try this, but maybe on a black or gray canvas, 
and just letting the crayons melt organically in the sun..

When You Have No Voice – Making A Decision To Communicate

Posted by What It Takes To Be Me in Community, Coping Strategies, Depression, Expressing Emotion, Faith, Family, Flashbacks, Friends, Illness, Judaism, Medication, Psychology, PTSD/Extreme Emotional Stress Disorder, Sexual Abuse, Suicidal Ideation and tagged with , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,

It’s been a long time, I know, but I’ll try to put you all back in the picture, as I know you will have all been eagerly awaiting my next update. [What? No?]

In the last few weeks I have been dealing with one of those much dreaded periods of flashbacks, and things have often felt completely and utterly hopeless. The flashbacks have by no means gone, but there have been a few days every once in a while when there have been fewer, and I’ve been able to find at least a little breathing space in between. When things are bad, that’s the time to focus on small blessings.

At the beginning of last week I had to go into hospital for a whole battery of tests and examinations. Part of these was a gynaecological exam, which for me is essentially an equivalent to psychological torture through physical means. I always try to prepare whoever is doing the exam by explaining that I come from a background of having been sexually abused as a child, and that these exams are pretty much garanteed to trigger off flashbacks; in short that they may need to brace themselves for my emotional response. They then usually say something along the lines of “Don’t worry, darling, I’ve seen it all before”, which is of course very kind and much appreciated, but it generally tends to become apparent that this is not really the case. When they’re faced with the sobbing heap these exams turn me into, it’s often clear that I react worse than most people they’ve examined. This then spirals into this odd cycle of them feeling sorry for me, and me feeling sorry for them having to carry out the exam on me..

So, not nice at all.

This particular nurse was absolutely fantastic, though, I have to say. It was very obvious that she was affected by my reaction to what she was doing, but because she was very open about that, I found that somehow reassuring and it in many ways it helped bring me out of the flashbacks and back into the here and now where we both were.

Concurrent with the flashbacks and general depression I have this week come down with some seriously nasty bug. This bug, by the way, is completely unrelated to the hospital thing, unless I have really lucked out and managed to contract MRSA while I was there..

At first I thought it was just hay fever, as this is the season when I usually have to stay indoors with my inhaler close to hand at all times. Had a very painful throat – not sore – painful, something I don’t usually get with my hay fever, but initially I just assumed that my body had decided to take my allergies to the next level. As it turns out this wasn’t it. Came down with a 39C temperature [that’s 102F, if you’re so inclined] in the middle of the week, and it’s been going ever since. So, what with the painful throat and the fever I’ve essentially had to be on paracetamol non-stop. It’s not great, Ibuprofen tends to be more effective, but for various reasons I am currently banned from taking that particular pain reliever, so there you go.

Feeling miserable on all levels is not a great place to exist and things have been unbelievably difficult. I know my last entry was pretty dire, and from there I suppose you could say things went south. Having no therapy has been really challenging, it feels like years until A. returns from maternity leave. But, I am still around, still fighting – even if the evidence of this has not been posted on my blog.

This Friday I had been invited to two sedarim – the special meal eaten by Jews on the first night of Pesach, but instead I spent the evening in bed, fighting flashbacks and this blasted bug. Last night I had booked a place at the communal 2nd night seder at my shul together with many of my friends. I did make it there, in fact even went for a pre-seder drink with one of my friends, but didn’t make it through the meal. Was feeling incredibly rough and then began having flashbacks, and I had to make the decision that I needed to make sure I could make it home safely before things got even worse. Hated having to leave, but as it turns out it was probably a wise choice.

This morning I woke up having absolutely no voice.

I have lost my voice in the past, but never quite this completely, and it’s kind of an interesting thing; the second you discover you have no voice [in my case when I began recording a voice message for my sister] you realise how much you rely on it.

I don’t usually use my phone or computer on Shabbat or during religious festivals. This is not so much because it’s biblically and/or rabbinically decreed that one should not use iPads or Blackberrys during festivals, as much as – being a modern reform Jew – I’ve made the informed decision that for me stepping away from all my techie gadgets and disconnecting for a bit makes those times different to other times. I am normally contactable at any given moment, day or night, be it through texts, Facebook updates or tweets, and so I like to make Shabbat and festivals different and special to other days, through unplugging in this way. Admittedly, most of my friends think this is completely bonkers, but hey, it’s just the way I roll.

However, since that accidental-on-purpose over-dose the other week, I decided that it’s actually a lot more life-embracing to temporarily break that self-imposed rule than to keep it. Which is why you are seeing this update today, during a week I would normally steer clear of modern technology.

To help me through particularly rough patches over these past few weeks I have often sought support over the telephone from my sisters, my friends and the Samaritans, regardless of whether or not this has been on Shabbat. Being able to talk about what’s going on, both physically and psychologically, makes me feel less like I’m on my own in this.

So, as you can imagine, waking up this morning, with no voice at all, has come as a bit of a shock, and has left me feeling very vulnerable. Which is why I’m sitting here now, writing this..

I guess that even when you haven’t got an audible voice, you can still find ways of making yourself heard.

Do be kind to yourselves,

xx