The January Post, or, ‘Hello I’m Still Alive’

Why oh why is it so darn hard to sit down and write updates for this blog? I have a million and three ideas flying around in my head at any given moment for things I’d like to write about, posts I’d like to upload – in fact one of them has been mentally written in my head since October last year [Harry Potter and The Mental Health Issue], but I’ve just not been able to make myself sit down and focus for long enough to actually write and arrange things into a cyber publishable format.

I suppose that part of the issue lies in the very nature of this blog – it’s not just about psychotherapy and mental health in general, it’s about my mental health, my journey. It’s about the PTSD, the depression, the suicidal ideation I struggle with, all of which severely impact my ability to focus, to knuckle down and just do things. Even when I really really want to write a post, when I am sitting there with an absolutely brilliant idea for a post, I often simply can’t write it.

In the last few years, because I’ve struggled so much with my mental health and the aforementioned difficulty in being able to concentrate I’ve had to make a switch from writing – something I have been doing my whole entire life in order to make sense of myself and my world – to drawing and painting. For years and years writing was What I Did to express myself, to explore what was going on, to give my imagination and creativity a chance to run wild. And then, somewhat suddenly, with the entrance of PTSD in my life, that was no longer an outlet I could count on. It’s hellahard working on a book, or even just part of a dialogue when you are constantly interrupted by traumatic memories in the form of PTSD flashbacks. So, I had to find another medium, one that wasn’t quite so badly affected by interruptions as writing is, and the medium that came to me most naturally, was art. So, that’s what I’ve been doing: I’ve been art-ing. Sometimes alone, sometimes with friends, I’ve been art-ing and art-ing and art-ing. Some of the drawings or paintings I’ve incorporated into random posts on this very blog, but for the most part I have been posting privately to friends and family on closed[-ish] social media. It was only in October last year that I finally got around to starting a public Instagram account. Shameless plug: If anyone is interested you can find me here. I’d love to have another follower or two. [SPOILER ALERT: the drawings that were supposed to go with that blessed Harry Potter post are on there].

One final reason [read: Exceedingly Lame Excuse] for my severely dwindling number of posts in the last few years is the very fact that I’m in therapy. I see the Greatest Therapist In The Known Universe [sorry you missed out, folks!] three times a week. On top of that I see my care coordinator every three weeks and my social worker about as often. Plus, I am blessed with the most amazing, insightful and supportive friends in the world. So, between the professionals [Team Scout, as I like to call them] and my friends I do a lot of talking and reflecting on what is going on for me. In fact, one of my sisters recently raised a concern that I wasn’t talking to her and my other sister about how I am doing. She was worried that maybe I was either trying to protect them, or that I somehow didn’t feel ‘allowed’ to tell them about the more difficult aspects of my life, when in reality it’s just that I’ve already got plenty of space to let the difficult feelings out. It’s not about wanting to – or feeling that I have to – shut anyone out, it’s just that sometimes – even when I’m really really struggling – I get a bit talked out. I’ve filled my need for expressing myself, I have felt heard and seen and cared for – so by the time I get to talk to my sisters I’m ready to just have a laugh. And, I think something similar has been going on with this blog.

You know how I said “one final reason” in the paragraph above, as if it was going to be the last reason given..? Well, if I’m honest with myself, there is one more very obvious reason for why you, my lovely lovely readers, have been left so badly neglected; I am an Expert Procrastinator. With everything. If I can put off doing something, I will. In my world, things get done as close to the deadline as humanly possible. And when there is no deadline..? Well, quite often things don’t get done at all.

Towards the end of last year, just around the time when I had to finally accept that that ruddy Harry Potter post wasn’t going to happen that side of the new year, I made a promise to myself [I hesitate to call it a new year’s resolution, because those are clearly made to be broken, right?]; that I would manage to upload one post a month in 2018. So, here I am, at just gone 6 a.m. on a Wednesday in the second to last week of January, writing something to kick the year off.

I know this hasn’t been the most inspired or thought provoking post, but, it’s a start.
And, hey – February is just around the corner!

Although, knowing me, you can probably expect the next update on or around the 28th….. And that’s only because this isn’t a leap year. ;)

Anyway, until then – loyal followers and new arrivals alike;

Be Kind to Your Selfs

xx

Rebooting Is Hard To Do

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.

 

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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

A Much Delayed Update

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

 

 PSI 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.

 

 

From Swan Lake to Daft Punk – A Post About Psychotherapy Breaks

Every time I upload a new post I do so with the intention of posting another update soon thereafter, but it just never seems to happen that way.. I suppose I will have to own that this happens in part because I slightly lack the discipline to stick to a set publishing schedule, but, also, it happens because – well – life happens. I’m sure you know what I mean. It is hard to write about your life at the same time as you are experiencing it. Especially when the going is tough.

So, what has been going on in my life since my last post? Quite a lot, it feels like, and at the same it is rather a lot of the same that is pretty much always going on; flashbacks, crises, therapy breaks, family stuff.
I’ve been under the care of the crisis resolution team six or seven times already this year and had one stay at Drayton Park. That’s a lot, considering we are only in the eight month of the year.. And I have a feeling that another stay at Drayton Park may be on the cards in the near future. I am actually seeing the crisis resolution team later today, and my guess is that they will suggest to start a referral for some residential care. To keep me safe from myself. Without going into too much detail, the going has been exceptionally tough this year in general, and recently in particular.

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P. has been on annual leave for about two weeks now, with another two still to go. I know that I have written about therapy breaks many many times in the past, but it is for good reason: they really are that difficult to cope with.

And I know for a fact that I am not the only one who experiences breaks in therapy as major triggers for all manner of extreme abandonment, attachment and separation issues. A quick look at the stats for how people find this blog tells me that some of the most commonly used search terms are variations on the theme of How To Cope During Therapy Breaks. This is also a topic that people frequently email me about. [Much appreciated, and – as always – apologies if I’ve not been able to respond to your email yet]. 

So, this is clearly not something I alone struggle with.  

I think part of the reason why it is so hard to manage while one’s therapist is away is that Everyone Else [friends, workmates, family, even mental health workers] find it seemingly impossible to grasp just how important and intimate a therapeutic relationship is, and what huge emotional waves the absence of your therapy partner sets in motion. So, we are left feeling that the pain we experience because of our therapist’s absence goes unheard, thus redoubling the pain.

I have some absolutely wonderful friends, I am very very close to my sisters [by golly I love them more than I could ever express!] and I really wouldn’t describe myself as a lonely person per se [although I do perhaps crave more alone time than most] – but my relationship with P. is different to every single one of my other relationships, no matter how good, close and meaningful they are, and it takes up a huge amount of emotional spacetime in my day-to-day life. Even on the days between sessions. 

So, when P. goes away for any length of time, that is going to be hard to cope with. I am used to being able to voice thoughts I don’t share with anyone else three times a week. I have 150 solid minutes every week that are there for only me, to express whatever I want to or need to. 9,000 seconds a week to experience being heard and seen by a pseudo-parent who genuinely wants to understand and help find ways to ease the pain. And that’s not even counting the email and text contact P. is encouraging me to maintain in between sessions and over weekends. So, of course her absence is going to be massively felt.

It isn’t a case of my being needier than most, it is simply that this is a big change to the structure of my week – and I think that most anyone who had that kind of drastic change to their life [even if it is temporary], would find it quite challenging to get used to. 

And – of course – we are none of us in therapy for the sheer fun of it. Something has brought us there. There are Issues to be worked through. Usually more than one, and hardly ever the easy-to-resolve variety. [If, indeed, such a variety exists.. I have my doubts..]

During a break the therapeutic process gets put on hold. Or – perhaps more accurately – the format of the therapeutic process changes during a break. Of course we don’t go into a period of zero growth during a therapist’s absence [in fact, in my experience breaks more often than not bring growth in its wake, both for me personally and in my relationship with P.], but the rhythm is upset. There are no two ways about it. It’s like listening to Swan Lake for a solid month and then suddenly having that musical loop switched to Daft Punk. It’s not bad for us [I would never call Daft Punk bad!], but it IS vastly different. And even if we know that the switch is going to happen [having bravely attempted to talk about the upcoming break and the feelings it brings to surface], going from Swan Lake to Daft Punk is going to affect us. Different feelings will be stirred up, often difficult, deep-seated ones. And we will be on our own to cope with them. 

Or, as in my case, you’ll end up working with the crisis resolution team for the umpteenth time.. ;)
So, that’s where I am at right now.

Getting used to Daft Punk. 

xx

When God Smiles At You

So, I took the steroids for four days and I completely flipped out, disappointing a lot of people along the way. All for nothing. There was no chance that taking the medication for only a few days would do anything at all to reverse my self-inflicted hearing loss, considering even with the full course the odds of a measurable positive outcome was slim in the extreme. It was a complete failure.

Except when I went to the audiologist to have moulds made for my future hearing aids about two weeks after the steroid drama, a final hearing test was done and to everyone’s amazement it turned out that there had been some improvement. Not in both ears – there was no change at all in my left – but hearing in my right ear was almost exactly back to where it had been back in May! It’s impossible to say if this was down to the steroids or some sort of freak natural reversal, but the tests were clear. Yes, my hearing loss was still severe enough to warrant some serious hearing aids [none of those tiny, invisible, in-the-canal domes for me], but this regain of hearing in my right ear means that a cochlear implant may not become necessary.

I felt as if God was smiling at me!
[My far wiser friends have since reminded me that God is always smiling at me; I’m just not always all that receptive to it].

About a month later – three weeks ago today, actually – I went back to the audiology department to pick up my brand new hearing aids. The audiologist popped them into my ears, did a bit of fancy-schmanzy computer twiddling and, finally, switched them on. I took a deep breath, mentally recited the shehecheyanu and BANG! – just like that I had Spiderman-like hearing. The most emotional part was hearing the sound of my own voice again. I wasn’t born deaf, so I’ve obviously heard it in the past, but it’s been quite a long time since I’ve been able to hear it. For a long time I’ve only really been able to feel the vibrations of my voice when I speak rather than actually hear it, and it was a pretty overwhelming sensation to hear myself again. It was something of a shock to discover that it didn’t sound at all as I remembered it. It sounded tinny and harsh and extremely loud, reminding me of how it sounded when I as a child would hook my father’s microphones up to the stereo and speak into them. Every time the audiologist asked me a question I had a Cheshire grin on my face, because it was so completely rocking that I was able to actually hear him – even when he was turned away from me! – and every time I answered his questions I jumped at the loudness of my own voice. The audiologist did a bit more twiddling and tested my reaction to him opening and closing doors and windows etc, to see that it wouldn’t be painfully loud. As he put it: ‘It will be annoyingly loud, but it shouldn’t be painful’. There are so many sounds that my brain has not picked up for a very long time, and to the brain any new sound is automatically processed as ‘important – needs to be actively listened to’. I have been told that it will take possibly upwards of three months for my brain to retrain and figure out which sounds are important and which sounds are merely ignorable background noise, because it is in essence rebuilding the sound filtration system from scratch.

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– My New Best Friends –
I call them Watson and Mycroft

 

I won’t lie – having the hearing aids is both totally amazing and incredibly difficult. It’s super cool to be able to hear things, but it is also quite disorienting when people walking past my house sound as if they are in my room [not great for someone with PTSD who is already on permanent high alert], and it can be quite tiring when just brushing something off my clothes sounds like a major earthquake.

In the first two weeks I found it quite overwhelming and confusing to hear my own voice, because it was still sounding tinny and foreign to me – as if someone else was speaking my thoughts, and I really missed not feeling the vibrations anymore [I suppose by brain was too busy processing the sound of it, to also allow me to experience the physical sensation of it], but now – three weeks into wearing my hearing aids I’ve got used to what my voice sounds like – it no longer sounds distorted – and I can once again feel it in my throat and chest, which is reassuring.
A lot of sounds are still very loud: refrigerators, traffic, people coming and going, but I suppose that eventually those sounds will fade into the background. When I first stepped out of the hospital I felt as if the world was assaulting me with its sheer loudness, but, in the midst of sirens and buses and people talking on their mobiles I picked out a sound I hadn’t heard in a very long time: the sound of a bird chirping.

I suppose you have to listen out for the really good stuff, in the same way that you have to actively tune in to sense God’s smile..

And the other week, when visiting my sisters, I had ample opportunity to practice this; as annoying as the sound of my sisters’ kids rummaging through boxes of Lego and train tracks was, being able to hear their little voices when they excitedly called out for me made it totally worth it! It was ace!

The journey is of course far from over, I’ll have a re-tune of my hearing aids in a few weeks where the volume will be turned up even louder, but all in all, I am really glad that I finally made the decision to do something about my hearing.

xx

Surviving An Ending: Starting Over

Finishing with A. was always going to be immensely painful and would inevitably leave me with a whole host of scary feelings, and nowhere to put them. So, in a bid to keep myself from harm’s way I decided to give myself a time-out immediately after The Ending.

Chickening out of allowing any kind of time or space for those Scary Feelings to rear their ugly heads, I made sure to book a seat on the first morning flight available after The Ending – and – looking back, I think that was a wise choice, indeed; getting through even just an afternoon and evening after my final session with A. was a momentous task, and didn’t feel like something I could have coped with safely for any length of time at all, to be perfectly honest. Far safer to spend time with sisters and nephews and brothers-in-law, all of whom provide sufficient distraction, and help me find some balance between being hit at full force by the painful loss of my relationship with A. and shutting down altogether. In short, I made a conscious choice to be around people who I knew I would feel OK to not be OK around, if that makes sense.

But, now I’m back. And – fearing that reality is about to strike – I have purposely thrown myself into all things Olympic in order to buy myself some more time and shelter myself from the whirlwind of emotion which is sure to soon come sweeping across my soul.

*

I had my first two sessions with The New Therapist this week, and that was both absolutely emotionally draining and a huge relief. The New Therapist – who I have decided to call P. [as that was the letter that immediately came to me the very first time I met her, at the initial consultation], is very different to A. Although she is a psychoanalytic psychotherapist, just as A. is, she is also attachment-based. And that is a whole new ballgame for me. It’s all very relational, very direct and very open. Even at our first meeting I noticed that she actively wants to make eye-contact with me, and seeks to engage in a completely different way. And that will take some getting used to. As much as I have often found myself frustrated with what I have experienced as a certain lack of closeness or intimacy with A., now that it is being served to me in this way, it is quite a scary thing, because in that slight distance between A. and I, there was also safety: for better or for worse I could opt to hide in that space if I needed to, and I have a feeling that is something that will be a whole lot harder to do with P. There is something about this open invitation to attach that leaves me feeling vulnerable and somewhat exposed. And allowing myself to enter into a relationship in that way feels strange and more than just a little scary.

I will say that, instinctively, I rather like P., and I think that – once I get more used to this new way of relating to The Therapist, this could be quite fruitful. But, at the same time, I do have a lot of ambivalence: I find myself going back and forth between ‘Go on, dare to trust. Everything you have seen of P. so far points towards you being in safe hands. Try to not hold back so much’ and ‘Don’t do it. Don’t let her in. You’ve been wrong about people in the past, and ultimately you’ll be let down, and you’ll end up being hurt’.

*

As I am writing this post, I suddenly feel very aware that with every difference I note between A. and P., the realisation that I won’t be seeing A. anymore knocks on the door – makes my eyes tear up – and I am also struck by the feeling that I am somehow being disloyal to A. in writing about anything even remotely hopeful about P.  Almost as if I am cheating on her with another therapist. I remember feeling something very similar when I started seeing A., having learnt so much from my work with D., and worrying that in one way or another moving on to a new therapist meant that I didn’t value what D. had offered or the hard work she had done with me. I know that these feelings will eventually subside, and I also know that in some ways I had outgrown A. – or perhaps we had both outgrown our relationship – and the time to part ways had come. But for now, each reminder that things have come to an end in my relationship with A. hurts. Because I really miss her.

I suppose that in a way, ending with A. – and the fact that I really won’t be seeing her again – is a bit like dealing with a death, and I suspect that over the next several months I will be going through all the different stages of grief.

But, hopefully, I won’t be doing it on my own.

xx

Ps. To those of you who know about my trip to Sweden: I know that I am missing out two absolutely massive things about my time there, both of which deserve some proper analysing; I will return to those things in a later post, but for now, I am choosing to leave it out. *hangs the STILL PROCESSING sign on the door*

Being Safe vs. Feeling Safe – The Power Of The Past

Ever since my run-in with M. last week, I have been on extremely high alert. Like many people suffering from post-traumatic stress disorder I am hyper vigilant at the best of times, but in the last week I have been a million times more nervous than usual, any sound I’m not expecting making me jump. From Monday when it happened until Wednesday night I didn’t sleep. Not as in I’ve barely slept a wink, but I literally didn’t sleep, at all. In fact, getting to A.’s place on the Wednesday afternoon was a real challenge as I was battling the symptoms of sleep deprivation, being confused, nauseas and very unsteady on my feet.

I used both my Wednesday and Friday session with A. to talk about what happened when I saw M. and how it’s really affected me quite badly. In the Wednesday session I was close to tears, just thinking about it, because I felt like any sense of security I had been able to create for myself had been totally and utterly shattered. My jitteriness was so bad that even the sound of A.’s voice made me jump more than once in session. [My relief upon realising it was A. and not someone else each time, on the other hand, was immense].

I have been trying really hard to calm myself, to tell myself that although I don’t feel safe, I am safe. Only it seems to make no difference whatsoever. My feelings out-power my intellect with frightening ease, in complete contrast to how I normally deal with any extreme emotions by rationalising them away. Also, one could argue that the reality of being safe holds very little, if any, value if you don’t feel safe.

Needless to say, my anxiety level has been on a steep upward curve every day since last Monday, doubling again and again the closer I got to my next session with Z.

Z. telephoned me on the morning of my session, just to reassure me that she would definitely be there to meet me at the reception, to let me know that I didn’t have to worry about having to walk through the building on my own. So, I picked up whatever fragments of courage I could find and set out. I had to stop several times on the way, because I was so anxious my legs didn’t seem to want to carry me. I kept looking nervously around, to see if he might be there.

And then it happened. Only fifty metres from the relative safety of the reception I spotted him. He was on the other side of the street, slightly behind me, accompanied by a woman, talking and laughing as if the world was a beautiful place to be. I stopped being the grown woman that I am in that instant and turned into 8-year-old me, hiding behind a tree as he walked past on the other side of the street. I went from Adult Me to Little S in seconds flat.

I hung back, watching him enter the building, not really knowing what to do. It was time to meet Z., but I just couldn’t go into the reception, in case he stopped to talk to someone there. So, I waited a while – I’m not sure how long – and then, on unsteady feet, made my way across the parking lot. As I cautiously approached the door, hoping to take a peek through the glass panes to make sure that M. had left the reception, a man came out through it, holding the door politely open for me. Ready or not, I had no choice but to enter.

I collapsed on one of the chairs immediately inside the door, bending forward, hiding my head in my hands, forcing myself to keep breathing. Z. came up to me right away; I guess she may have been sitting behind the receptionist desk, looking out for me – I wouldn’t know, because I never looked around when I entered.

I somehow managed to get it out that I knew M. was there, because I had seen him go in, and there was no way I could walk through the dining hall, even with Z. by my side. Z. thought for a moment and then told me to wait while she went back into the reception to ask another member of staff to open the fire exit for us, so we could enter the building that way; the only way you can get to the stairs leading to Z.’s room, without having to go through the dining hall.

I made it up to Z.’s room on shaky legs, and as soon as I was in there, I sat down on the chair. I didn’t do any of the things I usually do: put my backpack down, set my Rubik’s cube aside, take my shoes off. I just resumed the position I had had in the reception, head buried in my arms, bending over, sobbing violently without tears. It took me a good while before I was able to get back to myself enough to do those things, to bring myself back to where I was, and even then I left my shoes in such a position that I would be able to just step into them, should I need to flee.

I explained all of this to Z. That, even though she was there and I had made it to the room safely, I was ready to run, to jump through the window if need be. I just wasn’t at all able to catch hold of the fear or rein myself in. Throughout the session that feeling never left. At one point I could hear male voices in the hallway outside the room, and in panic realised that I might not be able to recognise his voice, as he would be speaking in English, and that might not at all sound like the very distinct way he spoke Swedish, with a strong Arabic accent.

That is something that has been playing in my mind almost on repeat during the last few days: the way he spoke. In particular, the way he used to say my name. He never used the short form of my name like everyone else, but would always call me by my full name, only his accent caused him to mispronounce it slightly.

It turned out to be a good session, all things considered. We spent time trying to explore the fear, and also talking about the circumstances surrounding M. coming to live with us. How we had a family meeting, talking about taking this badly psychologically damaged teenager in, and how, at first it had all been very exciting. He had three different foster families to choose from, but – much to our delight – decided on our family. He later said that the reason he chose our family over the other two was ‘because there were children’, and I couldn’t even begin to express the chills that sends down my spine thinking of it now, knowing what he went on to do.

We talked about changes that was made in my home prior to M. moving in: all toy guns, including water pistols, were banned – as M. was a refugee from the Lebanon and had seen war up close. The lock in the family bathroom was fixed, having never been in working order for as long as I could remember. I have a particularly vividly memory of my mother telling me that I was not to walk around in a towel after a bath or shower, as that wouldn’t be something he was used to, since it was something women from his culture didn’t do. It has stuck with me, that conversation with my mother, because even though I had never been someone who did that [always being very careful to cover up, never leaving my room without either being fully dressed or wearing pyjamas buttoned to the very top], I felt that there was some sort of indirect implication that were I to walk around in a state of semi-undress M. could not be held responsible for his actions. That it was somehow down to me to make sure nothing untoward happened.

We also talked a little about something else that I even now find difficult to deal with: the fact that while my parents have never outright said that I am lying about what happened with M., they have both categorically and repeatedly said that “it couldn’t have happened”. The reason they have given for this is that they were acutely aware, taking him in, that he was volatile and somewhat mentally unstable, and couldn’t necessarily be trusted as there was a violent and unpredictable side to him, and – according to them – they consequently made an agreement to ‘make sure that us children were never alone with him’. This – the idea that we were never left on our own with him – is of course highly implausible and falls to pieces at first look: my father was working full time and my mother, while being a stay-at-home mother at the time, certainly wasn’t ever someone who would be keeping her children in her sight at all times. We had always been allowed to roam free, and her own bipolar ups and downs would have had her sufficiently preoccupied to often not know where we were, or who we were with. And I know for a fact that I was regularly sent over to the guest house [where M. was staying] to fetch him. I know this because M. would often pretend that the intercom system wasn’t working when I rang to let him know dinner was ready, and my mother would tell me to not be so lazy and to just go over there and tell him myself..

Z. made a comment about this, about my parents deciding to take someone in who they apparently knew not to be safe, in spite of having three fairly young children at home. She wanted me to talk about how I felt about this, but, while I do have a lot of feelings about it, I simply didn’t feel quite able to, or – perhaps more accurately – didn’t feel quite ready – to express them.

I am not sure why my parents – who have no problem believing that their own son sexually abused me for more than twelve years – are so adamant that the abuse M. subjected me to could not have happened. Maybe the thought of having twice missed something like that is simply too much? Maybe the knowledge that he wasn’t safe, and the subsequent sense of guilt at not having protected me, stops them from being able to acknowledge – even to themselves – that it did happen? People often defend the hardest against the things that cause them the most pain, and I don’t think my parents are all that different in that respect. I have a few additional theories about their reasons for flatly denying what happened, all of them excruciatingly painful for all involved.. but, for now, I think I will keep the more probable ones to myself, as I don’t feel ready to deal with them just yet. I have on occasion talked to A. about it, but I feel that this blog is perhaps not the most appropriate place for me to explore it further. At least not for the time being.

After session, Z. walked me all the way through the building and across the parking lot outside, only saying goodbye when we got to the street, having first asked me how I was going to get home. It gave me the sense that it really mattered to her, all the things that have happened to me, all the fear I am carrying with me.

And that felt very special to me; very different to anything I have experienced before.

xx

Sharp eyed readers will have noticed that I have made no commented in this post as to whether or not the person I met really is M., or just someone who looks like him. The reason for this is that in so many ways it doesn’t matter whether it is really him or not. In my head it is him, and that’s what I am reacting to, so that’s what I have chosen to write about: my experience of what is going on. Whether the threat is real or not, the fear certainly is..

New Year, New Hopes – A Tiny Update

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Don’t worry, I’ve not gone crazy.. At least not in the traditional sense..
Tonight at sun down is the Jewish new year, Rosh HaShanah, and I have to admit that I am kind of excited about it. I know that a date is just a date, really, and it’s what we do with each day that matters, but, there is still something about starting anew that always makes me feel positive and hopeful. It’s that delicious feeling of opening up a brand new journal, 300 buttery white pages, there for me to fill. I kind of know that as much as I’ll try to use only my very neatest handwriting, sooner or later I will fall back into old habits, switching to my sloppiest, most illegible, journal writing style, almost without noticing. But, until I do – man, does it feel good!

So, what am I hoping for in the new year?

Motherhood. Always at the very top of my wish list. Comes as no surprise to anyone who knows me. But other than that? Well, a little bit of relief from the drama of the last few months would be nice. I remember my youngest sister concluding a number of years ago that I always have a serious dip in September, but knowing what the last few months have been like, I’d like to think that this time the dip came early, and hopefully I am on my way back up now.

I hope that creativity will flow. Both in terms of writing, and in terms of artistic endeavours, whether it be painting, drawing, carving or whatever other quirky ideas I may come up with. My latest project, as you can see above, is hand painting canvas shoes. Hopefully this will continue to offer me an alternative way to express myself and provide a safe haven to go to, a place where I can disconnect, if only for a moment, from mundane day-to-day stresses.

I hope that my therapy and my relationship with A. will continue to both challenge me and bring deeper understanding, and that I will find the courage to carry on expressing my feelings. I hope that the work I am doing with Z. will help prove to myself that I can do it [talk about the abuse without breaking either myself or the person who is listening to me], and that it will ultimately lead to a decrease in the amount of flashbacks I experience on a daily basis.

Stepping away from purely therapeutic/professional relationships, I also feel a lot more ready to be in a romantic relationship with someone. I have been single ever since Dev and I separated after five years together. That is now almost five years ago, and I have to admit that in those years, I have always felt ridiculously comfortable with my single status. A. has more than once hinted at the possibility of me being somewhat fearful of entering into a new intimate relationship, but I genuinely don’t feel that’s the case. I mean, yes, there are absolutely things that frighten me about letting another person in, but not on a level where it would stop me from forming a relationship with someone; I’ve just felt very strongly that I needed this time to deal with my own issues, to have emotional time and space to explore who I am, to get to know myself better. I still don’t feel particularly desperate to find someone, nor do I feel burdened by loneliness; it simply just feels like it would be nice to have someone to share my life with, to settle down. To Set This Circus Down, to use a McGraw-ism. I don’t think I’m about to [re-]join a dating site or start going on the prowl or anything like that, it’s not really my style. I would love it if Prince or Princess Charming found their way into my life, but I feel no need to go on a hunt to find my perfect match today [or even tomorrow]. Rather than an intense hunger for breaking free of singlehood, I suppose you could say that I have more of a relaxed ‘if it happens, it happens’ attitude towards it. But, as I said earlier, it would be nice if it did happen.

Anyway, I think I’ll end my ‘update lite’ here, and – whether you are Jewish or not – I would like to wish you all a very good and sweet year to come.

שנה טובה ומתוקה

~ Shanah Tova Umetukah ~

Have a marvellous 5774!

Much love,

xx

(For Lillsessan..)

Set This Circus Down © 2000 Bill Luther and Josh Kear

Identity – Being Adopted & Missing Pieces

Dayan Zhanchi, Void Cube & Core(also Dayan seen through the Void)

Dayan Zhanchi, Void Cube & Core
(also Dayan seen through the Void)

You may be wondering what the above picture has to do with identity and being adopted, you may even fear that this will be an entry entirely about cubing, rather than my usual musings about life’s twists and turns. Don’t worry. It shall all become clear. Or at least I hope so.

[By the way, if you are a ‘cuber’ and happen upon this post, what will follow are metaphors, so absolute minute accuracy isn’t what I’m aiming for. Feel free to refrain from correcting me on technicalities. ;) ].

Anyway, earlier today I decided to bring the above ‘props’ with me to my therapy session. But it wasn’t just for the fun of it, therapy isn’t fun and games; there was some thought behind it. As you may know I’ve recently had pneumonia, and being stuck in bed, I’ve consequently had even more time on my hands than I usually do, and this time has largely been spent solving my various cubes and Thinking About Things. [I find that the two go very naturally hand in hand.]

It started in an ordinary enough way, just randomly solving cube puzzles and thinking about which ones I like better. The regular 3x3x3 [commonly referred to as the “Rubik’s cube”] was a given, but the other puzzle that stood out for me was the funky one you can see in the picture above, the one with a hole in it; the Void cube. I then started thinking about why I liked that puzzle in particular and eventually came to realise that I in a somewhat odd way identify with it.

Now, to make the philosophy which is to follow make sense, I need to explain a little about the regular 3x3x3 cube. One of the keys to this cube is that the centres are fixed, meaning that no matter how much you mix it up, just by looking at the piece in the centre you will know what colour that side will be. Thus, if a side has an orange centre, that will always be the orange side, once the cube is solved.

Now, the Void cube has no centres, and so once it’s scrambled you have no way of knowing what colour any given side is going to be. In short, you are left to guess and hope for the best. And this is the reason why I feel I can relate to this cube.

You see, most people can look at themselves in the mirror and say “Oh, look! I’ve got brown eyes, just like my father” or “Those dimples definitely came from grandma.” Just like the centre square of the Rubik’s cube gives a clue as to why that specific side is a certain colour, you may be able to identify why you look the way you do. At least to some extent.

But, me, I was adopted, so just like the Void cube, I have no clues as to why I look the way I do. Of course, it’s not chance for me, any more than it is for anyone else; we all get our DNA from our parents, but because I don’t know who my birth parents were, I don’t know what they looked like, or in what ways I am similar – or indeed different – to them. I simply have nothing to go on. When I go to the doctor, and she asks “Have you got a family history of diabetes?” I usually joke that “Yes, my mother is diabetic, but that’s nothing to do with me!”, before I explain that my mum is diabetic, but I was adopted, and I simply don’t know what my biological background is.

Taking the cube metaphore one step further, something else that makes me more like the Void cube than the Rubik’s cube is this: if you were to take a Rubik’s cube apart, you would see that all the little pieces are supported by what is known as a core, and no matter how much you mix them up they always swivel around this core. As you can see in the picture above, all the centre pieces – the clues to what colours go where – are firmly attached to this core, hanging at the end of the different branches, much like pictures of family members on a family tree. This is again something, I – and the Void cube – lack. There is no central core, no known family tree to hang pictures on, nothing for all the other pieces to revolve around.

To compensate for this lack of an obvious central core, I had to develop a whole different strategy for holding my pieces together. Rather than relying on a central core to support the pieces that I am made up of, they are instead held together by one another. One might think that would make it prone to easily coming apart, but in fact, it is the exact opposite. Whereas a Rubik’s cube is both easy to take apart and put back together [because of that internal family tree], the pieces of the Void are tightly held together in a way that is very very hard to prise apart, almost as if it is defending against the possibility of falling to pieces, knowing that it will be a real challenge to put it back together again. And that is how I sometimes feel, too; there is a very real fear inside of me that were I to take a few pieces of myself out to look at, as helpful as that may be, there is always a risk that I mightn’t be able to put myself neatly back together again. And this can sometimes cause me to hold back in therapy.

Of course, with therapy and cubes alike, the main object isn’t to take it apart piece from piece, but rather to scramble it, so that you get to see things from a different angle, and can then look for a natural way to get the different pieces back into place; to temporarily mix things up, so that you ultimately get some sort of understanding of why they go together in the way they do.

But even when you just scramble the Void, you have no set starting point, and as a consequence it is that little bit harder to figure out, because if you make an incorrect assumption about those missing pieces at the centres, things simply won’t turn out the way you had expected; when you think you’ve done it, when you only have a few more pieces to go, you will discover that the side you though was meant to be orange, is really meant to be blue, and you’ll have to go back and try again.

Now, of course I know that people, myself included, are not cubes; it’s not as black and white [or orange and blue!] as that; there are people who can trace their family back hundreds of years, who are just as lost, and just as frightened as I am, of mixing things up. Whether we have a known family tree or not, the core of who we are is made up of much more than just that. And, of course, it isn’t just people who were adopted who have missing pieces and blind spots; everyone does. Also, whatever our internal structure looks like, there is something there that holds us together, despite those missing pieces.

And most importantly, for us humans there simply is no permanent ‘solved state’. We are forever scrambling and un-scrambling, and having to sometimes go back a few steps to in order to better understand something about ourselves, really isn’t such a bad thing. And although we often wish we could solve the puzzle really quickly, in reality, we have our whole lives to do it.

So, be kind to your Selves; get a Rubik’s cube.

.. or a Dayan..
.. or a Fangshi..

:)

xx

Being Unwell And Feeling Cared For

Cure For The Ill

Cure For The Ill

I’ve been unwell. Still am, actually. Pneumonia. It’s a bit of a long-winded story, but in short it involves leaving a psychotherapy session early for the first time ever, thinking I was better when I wasn’t, and ultimately on Friday having to go see the doc urgently.

I had just left a session, and on the train home I suddenly had this terrible pain in my chest. And it was a pain I had felt before; two years ago I had a pneumonia, and this was what it felt like.

Anyway, once I got to the doctor’s, she had a good listen to my chest, took my medical history and told me she felt confident that what I had the previous week was more than likely a flu virus, but that I had milder symptoms than most, since I’d had the flu jab, and that despite this my immune system was compromised enough for me to develop a pneumonia. [Ironically, the reason I have the jab every year in the first place is so as to make sure I don’t come down with secondary complications, such as this..] Since I have a history of pneumonia, starting in exactly the same way [top right lobe a week after having had another illness] and because my asthma was kicking off like crazy, she decided that she’d rather start me on antibiotics straight away, than wait for test results to come through.

So, home I went, antibiotics in hand. Crashed into bed, and this is where I’ve been stuck up until just now. I have to say, antibiotics are a wonderful thing once they kick in. You really do feel so much better, very quickly. Of course there was always a chance that the pneumonia I had was viral rather than bacterial, in which case the antibiotics would have done nothing for me, but ‘thankfully’ it turns out that it must have been bacterial.

While in bed I have been thinking about being unwell. It’s something I have a fair amount of experience with. You see, I have a really poor immune system, and so whenever something’s going ‘round, I tend to catch it. I mean, I had swine flu long before it became fashionable. But, also – as I have mentioned in previous posts – I am prone to what I call psychosomatic fevers. Other people get upset tummies when they are stressed out; I get a temperature. And this is what’s been on my mind, these last few days; the relationship between having a genuinely poor immune system and getting psychosomatic illnesses.

You see, I don’t think it is entirely chance that I get ill very easily, weak immune system aside. When I was little I was always seen as someone who could look after myself, someone who was responsible and dependable and able, far beyond my years. My parents tended to assume I’d be OK on my own, and mostly I was. I’m sure it was sometimes hard for my parents, this fierce independence I had; not so easy parenting a child like that. But, at the same time, they were very busy people; three other kids, one of whom really rinsed them clean of any energy they may have had. So, as confusing as it may have been for them, I’m guessing it was also something of a relief that I didn’t seem to need much looking after, that in fact, I was perfectly able to look after myself as well as anyone else.

But, when I was unwell, it was almost as if my parents’ parenting instincts suddenly kicked in, as if this was the kind of parenting they could understand, could relate to. After all, they are both trained in healthcare professions. This was something they knew what to do with. And so, as a consequence, when I was unwell, those were times when I truly felt like a child, like they were my parents and I was in their care.

At all other times I always felt equal to my parents. I always felt like I was an adult, just like them. And to a large degree, I think that’s how they and other adults around me saw me, too. But when I was sick, well, I could allow myself to be the child I really was.

So, is it so strange that I am prone to getting ill? Even now, as an adult, when I am ill, both of my parents will call me, will want to know how I am, will maybe even worry a little. This in contrast to other times, when I am nearly always the one to call them, nearly always the one to ask what’s going on for them.

Of course, something like pneumonia is a very real illness, it’s not psychosomatic, not imagined, not exaggerated, but in the midst of feeling so terribly poorly, I also do feel cared for, in that very special way.
Just like I did back then.

Psychology..
It’s interesting stuff.

xx

How I’ve kept myself busy. The Square-1 cube puzzle. It’s a fair challenge, getting it back into a cube shape, and then getting all the colours right.

Square-1

Square-1