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I don’t fit, or at least if I do, I don’t know where. This feeling is nothing new to me; I’ve never fitted, always felt different. I suppose I should be grateful that at least now I know why?

I didn’t think I had a problem with being different, in fact I’m still not sure I do after all I can’t imagine I’d enjoy being normal. Just a quick reminder to anyone even thinking of saying or even just thinking “oh but what is normal anyway?” I don’t know, but I know what it isn’t. That question rates even higher up the irritation scale than any of the wanky platitudes, don’t do it.

When I went mental, I started to feel a bit like I wasn’t different anymore; I was the same as all the other mentals. But that’s just it, I am the same

as

all

the

other

mentals….

I have a lot in common with the depressed, the manic, the obsessive compulsives, the voice hearers, the eating disordered, the self-harmers, the suicidal, the psychotic, the delusional, the gender confused, the insomniacs, the narcissists, the anxious, the attachment disordered, the selective mutes, the substance abusers, the paranoid- I could go on…..

I can identify with everyone; I’ve been there, am often there and will no doubt be there again at some point. I suppose if we’re looking at transferable skills at least I can rest easy, safe in the knowledge that I have a promising future career in writing leaflets about mental illness?

I left a comment on a blog last week; it took me some 4 days of writing and deleting to actually click ‘submit’. My comment wasn’t anything controversial or even particularly interesting or important but it was different. The topic of the blog piece was labels- what we mentals call ourselves and are called by services. I’m a firm believer in self-definition but of course, for me this means selves-definition. My comment reflected this

I cut the comment short, I define myself in numerous different ways but I was feeling incredibly self-conscious about what I’d said.

So I feel different from other people like me, other mentals

I don’t fully understand why I felt so self-conscious, I’m not ashamed of having DID, I’m happy to talk about it. You may have noticed.

I feel like I ought to say “my illness doesn’t define me” but it’s simply not true. When your illness makes you believe you are more than one “me” it does tend to dictate how you operate.

I’ve felt uncomfortable within the Madosphere for a while, I don’t read many blogs at the moment and I comment on very few. Whilst I have something in common with everyone and can offer advice, sympathy and understanding in all and any situation, I shy away from doing so. I don’t feel unwelcome, far from it but I do feel very different and quite alone. The ultimate paradox of sharing your head/body/life with [number I will never reveal] people is that it can be incredibly lonely.

I know there are several people out there with DID, I read some of their blogs; I don’t even feel like I fit there. Why? What makes me so special? What makes me think I’m different from all the other multiples out there?

On paper, nothing. Whilst all multiples are unique, there’s a sameness about us too, we share similar experiences and face similar struggles. There are a few tangible things I can point to that make me feel out of place within the online DID community.

Other DID bloggers use different terminology to me, I can’t discuss this further as it’s triggering, therefore other DID blogs can be triggering for me. So I’m like the meanie of the madosphere, I have no blogroll and generally don’t follow blogs. I have some in my reader as then I can carefully choose when to read them. I tend to avoid using terminology at all, I slip in the odd technical description but my story-telling approach to blogging often doesn’t call for it.

Other DID bloggers share names, I nearly fled Starbucks in terror last time I went and they asked for a name to put on my drink (why do they do that?!). I can’t work out if my reluctance to share names is symptomatic of the denial that we had any for so long or indicative of my overall secretiveness. I’m happy, for the most part to hide behind the collective noun, it feels safer that way.

Other DID bloggers share system information, I am like the MI5 of the multiple world when it comes to sharing information. I think it would make me feel incredibly vulnerable and unsafe to detail parts of my system.

Other DID bloggers talk about therapy; I allude to it but can never imagine retelling a session. I’m not ashamed about what happens in session, I often don’t know and am in no doubt that it’s always overtly mental but I think that therapy is for me, whoever I may be on the day and the <?> therapist.

Other DID bloggers talk about trauma. I have no trauma. I know that’s the typical multiple response but I genuinely have no memory of trauma. Sure my childhood was less than perfect and I can remember a lot of the less than perfect bits- which suggests they don’t count as trauma, but more unhelpful additions to a psyche that was already teetering. I can’t imagine if I ever uncover any trauma *clings to denial* I’d want to share it outwith therapy though.

So I feel different from other people like me, other people with DID

I’ve done the sums and if I’ve correctly identified ANPs (apparently normal parts) and EPs (emotional parts) I am 63% normal or apparently normal anyway. So the majority of the time, I’m technically, apparently normal. Twenty minutes in a room with me however and it becomes glaringly obvious that in spite of the mathematical evidence, I’m not normal. In fact, you don’t even need to be in the same room as me, anyone who’s ever received an email from me will know that bits of apparent normality do not compound into something totally normal, indeed it has the rather opposite effect. Those of you who’ve been lucky enough to receive hand-written correspondence from me (always unsigned but you can tell it’s from me as you recognise the handwritings) will appreciate that whilst there’s no doubt I can be normal and often am, all the normal together or even just a few of the normals together at the same time makes something completely abnormal.

So I feel different from other people like me, normal people

I think I feel different because I feel different and have always felt different. It’s causing me some angst it’s fair to say, especially as I think I’d be equally angst ridden to find out I was just the same as everyone else.

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Two years ago today I wrote this blog post

Ever wish you hadn’t asked?

Some time last year that post was edited and the link within changed- the link was originally to the Wikipedia entry on DID (which incidentally I think is rubbish). I know why it was changed and for the purposes of this post it doesn’t really matter. What does matter is that for two years I’ve known I had DID, the nature of DID means that I didn’t always know I had it and often didn’t think I had it- but I do and I’ve known for a very long time.

This post is dedicated to all the psychiatrists, psychologists, nurses & doctors (and there have been many) that have met me and treated me in those two years; I know many of them read the blog (though strangely they never leave comments). Even if you’ve never had the privilege of being involved in my ‘care’ if your profession brings you into contact with human beings, you may learn something too so please read on.

I can’t believe you all missed it, it was hardly subtle and I did, very kindly point it out on a number of occassions. You all need to learn about dissociation and dissociative disorders, you all need to find the courage, humility and confidence to do what’s right for those in your care. If you don’t know what you’re doing- admit it and find someone else who does. Listen to your patients, accept what is true for them, however distasteful, frightening and anxiety provoking it is for you. Put your egos to one side; ignore the flawed politics of the system you represent, stop damaging people who have been damaged enough, admit you got it wrong. If your manager/colleagues/profession are unsupportive- call them out on it, stand-up for yourselves, stand-up for your patients.

It’s too late for me, the damage caused by your mistakes is huge- but there will be others and you owe it to them, to your profession and to yourselves to ensure you don’t do to them what you did to me.

Don’t make anyone else have to fight the way I had to fight to get the correct diagnosis, care and treatment- for that fight was very damaging. Don’t assume that you know more than your patients, for all your qualifications it is the person sitting opposite you who is the expert on their own mind. Listen, believe and accept, if you can’t or won’t, have the decency to find someone who can and will. I hope every one of you has learned something from me and I hope some of you will go on to learn more in order that you can do your job and do it well.

You hold peoples lives in your hands, you have great power- but always remember what Spiderman said……. or Voltaire if that’s your bag, he said it too but Spiderman says it better.

A multiple never forgets

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I think this may be one of those posts on depression I talked about, I’m not sure, I’ll just write and see what happens.

It’s been a funny day- as in not at all amusing in any way shape or form and in fact nothing funny has happened so I’m not sure I can qualify that summing-up. It just feels funny. I’m sure there are many pathological explanations for this- a shift in mood state, the inevitable come-down after a period of elevation, the fact I stopped taking the dreaded lithium on Sunday night? It’s not my area of expertise so I’ll stop speculating.

I’ve had a hard week, again, nothing particularly difficult has happened (especially when you contrast this week with the past 3) and I haven’t actually done anything or been anywhere.

Monday- a social worker from the local children and families team came to carry out an assessment in light of the 3 “child at risk concerns” from the police following my behaviour over recent weeks and contact from the ninja CPN. The assessment was a gruelling affair and ultimately felt like a lynching. I had it all under control for around 45 minutes until the ninja CPN arrived (45 minutes late) and in my words “painted me as a total loony” in her words “told the truth”. Either way the assessment went on too long and I lost it towards the end, partly due to nicotine withdrawal, partly due to being talked about as though I wasn’t in the room and partly due to the social workers insistence on informing me that there may have to be a child protection investigation.

The social worker herself was patronising and clearly had little understanding of mental health. I know I’m not the best mother in the world and I know I don’t always try my hardest but to have to sit and listen to a complete stranger tell me just how badly I was failing was very difficult indeed.

Of course maybe she never implied that at all? I have noticed this week that every interaction I have had with the ninja CPN where I mention something someone else has said, she insists on me recounting it verbatim so that she can point out where I am misinterpreting things, employing magical thinking or just fabricating things. I can’t even trust my own thoughts and impressions any more. I feel stupid, childish and powerless.

I am not surprised or ashamed that my family has come to the attention of social services; I’d be more surprised if we hadn’t. My argument against their involvement is simply that they have nothing appropriate to offer. I was also more than a little annoyed that suddenly they were intruding on our lives when in all the time the 17 year old lived here and his autism wreaked heartbreak and havoc on us all they never offered a service, in spite of being asked. What my family needs in order to function properly is for me to be well- thinly veiled threats about child protection measures aren’t going to help me achieve this. The social worker wants to come back- well at least I think she does, I received a letter addressed to me and the 6 year old, making an appointment to visit the 6 year old and someone else who doesn’t even exist. Clearly just an admin error and my rage over it is no doubt my own fault for being difficult and misinterpreting things but it pissed me off anyway.

I assume the appointment is to see the 6 year old and the 14 year old again. The 14 year old is largely unimpressed with the social worker, her opening gambit of “I know it’s not easy being different, well some people like to be different- like Lady Gaga” sealed her fate with the 14 year old. The 14 year old is a wonderful creature, intelligent, engaging and probably the funniest person I know. She may be a little “old for her years” at times but she can spot a patronising bastard a mile away. I don’t disagree that the 14 year old would benefit from some emotional support, after all if I had cancer others would be falling over themselves to ensure she was ok, I’m just not sure that social services are equipped to offer her the kind of support she needs.

So the intervention of social services has me hell-bent on proving that their services are no longer required, maybe that’s the way it works?

Tuesday- the Fab Therapist visited me at home, she was impressed by my apparent fineness given the horror stories she had been told by other “team members” since our last interaction some 6 weeks ago. I don’t think we talked about much, I’m not really sure but we can’t have done as I don’t recall having a meltdown after she left. It was kind of her to circumnavigate my avoidance by visiting me at home and I expect our next appointment in 4 weeks will only have me moderately filled with dread and fear as opposed to having dread and fear seep out of every pore like usual.

This brings me to the realisation I’ve been generating this week- mental health professionals cannot make me better. I have a great “team” (that makes me want to vomit) an Awesome Psychiatrist, Fab Therapist, Wonderful GP, Lovely Dietitian, Fantastic ninja CPN and even an ok-ish community based psychiatrist (promoted from “dickhead” after he didn’t put up a fight against my discharge from the local bin last Thursday). They are all very knowledgeable, compassionate people that work very hard but there are no magic wands.

At the end of every appointment, at the end of every day, I am alone with the mental.

Part of my problem is I don’t know where I am or what I should be doing. Am I ill? Am I recovering? Am I all better now? Should I be taking it easy? Should I be trying harder? I simply don’t know. The last few weeks have been a kind of perpetual crisis and I knew what I had to do then, I had to fight, fight against the horror that is admission to the psych ward, fight against the intrinsic death that is psychotropic medication. I won both of those fights- my prize?

I’m still mental.

This evening I find myself back to struggling to find the will to live. I am aware I have very few coping strategies for times of “distress” (that also makes me want to vomit) so I’ve had a quick look on some websites to find out how other people do it. I’m still none the wiser. Yes sure I can sit here, in my corner and name all the colours I can see but that won’t help sort out the mess that is tax credits, it won’t help me be able to put up with the simultaneous noise from the TV, the DS and the 6 year old when he is here, it won’t help me be able to sit and enjoy a film and some mother-daughter bonding time with the 14 year old, it won’t get the school uniforms washed, dried and ironed in time for school on Monday, it won’t help me get back to work, it won’t pay the mortgage, it won’t cut the grass or fix the bathroom…..I could go on. When your life is a catastrophe, it’s very easy to catastrophise.

Wednesday- I have no idea what, if anything happened on Wednesday- oh yes, I wrote my last blog post and sure enough as I said in reply to one comment I am still as lost and clueless as I was when I wrote it.

Thursday- again, nothing happened that I can recall but in truth it’s therefore not impossible that there was a zombie apocalypse or a plague of sharks or something, my recall of events is sketchy at best.

Friday- AKA today. Well I think I’ve outlined above where I am today, I’m not sure even if I read it back I will have any idea. I think I’m back at the “must get a grip” stage, I have a to-do list for tomorrow- it has one item on it-

Get washed and dressed

 

In all honesty that will be a major achievement, wish me luck.

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As I write it’s Wednesday 14th of September 2011, just after 8.30pm. My day has been unspectacular, especially by my own standards of late. I woke before 4,30am, on the sofa in the same clothes I had worn and slept in since Monday.

That paragraph sounds much like the beginning of one of those posts on depression I am so loathe to write, it’s not.

My mood remains “elevated” but it’s not the colouring-in, book writing elevation that we all like so much. This elevation can be fun, it gets me through the long days, the kids love “manic breakfasts” (bacon and pancakes- sometimes real sometimes imaginary), laundry gets washed and occasionally dried on the same day, I am (I like to think) funny, fun and engaging for my twitter audience. My energy levels are high and more than ever I miss my stupid car (it’s still in Newcastle) as there are so many places I want to go- usually to buy stuff- usually stationery. Mostly I just want to run away.

However this kind of elevation also brings with it a mix of anger, fear, rage, irritability, distractibility and anxiety that turns most days into a waking nightmare. I can’t concentrate on anything; basic conversation is beyond me and anything anyone says winds me up to a point I can’t hear them over the noise in my head. Writing this is a huge struggle and I’m not even sure what to say.

I am consumed with anger and rage at the slightest stimulus, be this political or personal. I get so overwhelmed by these feelings I end up going mental in some of its most basic forms- laughter, crying, a mixture of the two, fixating on rhyming words, taking risky walks in the dark alone, rocking back and forth, pacing or becoming completely immobile. All the while my thoughts are fast, jumbled and largely useless. I am easily confused and inclined to forget things, going out presents the ever-present danger of getting lost

We’ve been having the fine/ill debate regarding my mental health on twitter for some time now; for the most part I insist I am fine with fleeting moments where I confess I feel less than well. Many others have told me I’m not very well and haven’t been for sometime. I have had some advice to the contrary, the kind of advice that suggests I’m being somewhat self-indulgent and need to simply “stop” doing what I am doing. I can’t even comment on that advice right now except to say, maybe those who say that are right?

Every health professional I’ve encountered recently has gone to great lengths to tell me that they are “concerned” about me and that I am “very concerning”. This concern makes me feel guilty and I am going to extraordinary lengths to no longer be a “concern”. My attempts are superficial however and mainly involve lying about my mental health and telling people what they want to hear. I feel vindicated in doing this as I very quickly discovered “concern” never mutated into anything useful for me.

I don’t want to be a concern, I want to be fine.

I don’t think I am fine but I’m not entirely sure what to do with this revelation. I think  the part of me that surfaced over the last few weeks and tried to destroy me is on her way back (I still argue that starving my body kept her quiet) and I’m not entirely sure what to do (early signs are the drugs inventory and purchase of new razor blades). I am currently safe though it’s through conscious choice at the moment. I still don’t really know what happened over the last few weeks but I know I very quickly got to a point where I had very little say in my own safety. How do you keep yourself safe from part of yourself, a part of which you have little awareness until you see the cuts on your body or have to talk your way out of yet another MHA?

I don’t know where I’m going with this, I’ve just read it, it’s not one of my better pieces, (actually it’s shit) but it’s going up on the blog as I think it may be a cry for help whilst I am still able to do so.

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So I took my first dose of lithium last night, it was a traumatic affair. Today I feel poisoned, vacant, drowsy and unwell. I agreed to take the lithium in order to get me out of hospital (this was hospital number 4) after a somewhat tumultuous week.

Those of you who follow me on twitter, are members of the local constabulary, ambulance crew, health profession, journalists, social workers, air ambulance crew or one of those poor unfortunate people I have picked on to be friends or family will know just how frankly mental and unwell I have been recently.

I have scared myself, I am carrying the buckets of shame that often come after an episode and I have caused more worry and disruption to more people than I care to quantify. I am very sorry.

I don’t have the words or the desire to blog properly; I am barely managing to drink tea today. I have a lot to fix and I don’t even know where to start, the extent of my activity today has been lying under a blanket feeling ill.

I met a new blog fan this week, it’s always nice to meet a fan and thank you for your kind words but I still can’t believe you let me convince you to let me leave that hospital on Tuesday night, out of my face on a modest overdose of benzos, covered in my own blood, wearing a hospital gown, in a taxi. Given that I had no recollection of getting to the hospital and it was in a fucking helicopter you’d think someone would’ve noticed something was amiss. I clearly come across rather well when faced with the possibility of detention under the mental health act. It’s a gift.

And they say I’m mental.

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As I mentioned in my previous post I am considering taking lithium again. This was not my idea, in fact it comes way down on my list of ideas somewhere after “stick pins in my eyes”, “swim in a crocodile infested pond”, “go to a Miranda Hart gig” “listen to Demi Lovato”, “eat offal”, “take up card making as a hobby”….you get the picture.

Lithium is the idea of my Awesome Psychiatrist, a gentleman I was very lucky to be referred to and even luckier that he found me “interesting” enough for him to continue reviewing my diagnosis (diagnoses?) and treatment. It is not surprising that in light of recent events he thinks it might be time to try and introduce some sort of chemical stability into my chaotic life.

I trust the Awesome Psychiatrists completely, I did instantly, I have no idea why, I usually make mental health professionals work very hard indeed to earn my trust. The Awesome Psychiatrist is very skilled and very experienced he is a “designated national specialist” according to one website, I’m not actually sure what this means but he’s a nice guy, very funny, gives me tea during appointments and laughs at my jokes, all good qualities as far as I’m concerned.

In spite of this I am still in a quandary over taking lithium again, for reasons I will explain, some perfectly rational, some possibly less rational but no less pertinent for me.

I have taken many psychotropic medications in the past, so many I’m not sure if I can remember them all but I will try- bearing in mind I only came to the attention of the psychiatric profession (this time around) in January 2010 this is quite a list-

Fluoxetine

Venlafaxine

Olanzapine

Quetiapine

Aripiprazole

Carbamazepine

Lithium

Agomelatine

Sodium Valproate

Duloxetine

Various benzodiazepines

Various hypnotics

I took propranolol in an attempt to counter the tremor lithium gave me- it made me almost blind

I was also once prescribed Risperidone for about 20 minutes but never took it

These drugs were in various dosages, in various combinations at various times, I stopped taking anything on the 19th of January 2011. I started taking Agomelatine on the 16th of  March and stopped taking it some 8 weeks ago for reasons that will probably soon become clear. I could write a blog post on each one and the reasons I hated it but this post is about lithium.

So I’ll start with the rational reasons I don’t want to take lithium again.

Lithium has many nasty physical side-effects; in my experience it causes agonising leg cramps, nausea, dizziness, constant fatigue, headaches, disabling whole body tremor, constant thirst, an insatiable hunger and accompanying rapid, uncontrollable weight gain. I don’t cope well with physical ailments, I tend to ignore most physical symptoms, preferring to ignore the fact I actually have a body at all. Feeling ill all the time forces me to acknowledge I have a body that is more than just somewhere to apply pyjamas. It makes me very uncomfortable. When I look back at diaries or blog posts I am reminded of just how dreadful I felt whilst taking medication. I accept I was over medicated, poorly medicated and poorly monitored but I have no confidence this won’t happen again. I would be mad to volunteer to make myself physically ill again.

Drug-induced weight-gain is tortuous, for anybody, for someone who likes to be in control of food as much as I do it’s even worse. I have managed to crawl to quite a sound footing in terms of eating disorder recovery, most days I eat three proper meals a day, snacks in between and have managed to make it through a whole month without any self-induced vomiting. No mean feat for someone who appeared hell-bent on starving herself to death a short time ago. I remember the incredible lithium hunger so well, I would be drop-down-dead starving almost all day, it never went away. I can’t help but think introducing a drug that messes with my metabolism would be self-sabotage at this stage.

Lithium is a mood-stabiliser, yes it helps prevent extremes of mood but it also has a tendency to cancel out all the ones in between as well. I functioned on lithium but I was without thoughts, ideas, feelings or reactions. I was empty; I am in danger of straying into the less rational reasons for not taking lithium so I will direct you to this post written by a much loved friend on the subject, she explains it better than I ever could.

So those are my experience-based, rational, understandable reasons for being reluctant to take lithium again. If I have the words and the courage I will try and explain the other reasons. I would appreciate anyone reading to let me know that they nodded and said “uh-huh” throughout this next bit as opposed to laughing aloud or further questioning my sanity, I have awareness that my beliefs are a little skew-whiff but this does not stop me believing them.

I often joke about being “poisoned by the medical profession” in fact during my first consultation with the Awesome Psychiatrist I made him promise not to poison me, I make it sound funny- I am deadly serious. I believe the medical profession want to poison me and make me something/somebody I am not. This belief  has some basis in fact, after my diagnosis there was a tendency to attach pathological labels to all my past behaviour. All the things I did, all the things I achieved were painted with bipolar, taken away from me, turned in to symptoms as opposed to qualities.  I believe that the psychiatric profession do not like me being who I am (or perhaps rather who I can be when not hooped-up on mentalism?) I am tempted to self-censor here as I know that what I’m about to say merely supports my diagnosis but I will go ahead. The psychiatric profession want me to be the same as everyone else, they want me to conform, be normal, be boring. I haven’t quite made up my mind if “they” (ie- everyone else other than me in the whole world) feel envious, threatened or just don’t like me, either way I know they want to drug the Zoë out of me.

The way I feel about this is paradoxical to my general feelings of self-loathing and I can’t really explain that other than perhaps by referring to that shameful symptom of bipolar- grandiosity. It is my understanding that grandiosity is a symptom of a manic state though and high or low I feel exactly the same way about lithium and exactly the same way about what “they” want to do to me. Even when I am crushingly low I would rather be dead than take lithium.

Simply thinking about taking lithium again makes me panic, it gives me the fear I shake and sweat, my heart races and I start scurrying around inside my own head. I have got as far as allowing the Awesome Psychiatrist to start the process, I am still in control, at this stage I have no intention of taking it.

I believe that in voluntarily taking those tablets I would essentially be killing a part of me. This sounds like a standard case of “missing the highs” and maybe it is, it feels much scarier and final than that though.

Lithium mutes the Zoë in me, it leaves behind a fat, trembling body inhabited by functioning parts, things get done but we don’t “do stuff” (“stuff” being a handy catch-all word to describe the stuff  Zoë does). Having re-read that (very long) sentence I am aware I am possibly making little sense, except perhaps to myself. It’s 3am I should probably stop and have a milky drink.

I don’t know what to do about this situation, I clearly cannot continue the way I am, I am just not safe- in either mood state and I accept that I am unwell (though I am willing to argue as to just how unwell I am). However I know that if I take lithium, the author of this blog will die and I suspect she’ll take the twitter account holder with her, I will still exist in some form but I won’t be living.

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Again so much I could write here, I’d have no idea where to start with an account of the time since I last blogged. Those of you who know me will know there is an awful lot I could write about. To sum up, in handy list format-

The stupid car is 157 miles away

I’ve been in two different hospitals in two different countries in a week

I didn’t get sectioned (three times)

I don’t think I am very well

I could recount all the gory details but to be honest I don’t remember that much of them, there are “highlights”, again in handy list format-

 Having to get all my appointments with my entire team rearranged as I had “discharged myself” from mental health services.

 Almost puking my own skeleton up during a 20 hour Parvolex infusion (a fitting punishment for my abject stupidity).

 Meeting my newest psychiatrist and being told a hot milky drink was the cure for that chronic, severe insomnia I talked about.

other hot milky drinks are available

The Fantastic CPN becoming the “ninja CPN” after she appeared, unseen, unexpectedly, unannounced and played the pivotal role in ensuring my most recent “episode” didn’t end in disaster.

9 hours or so in A&E (157 miles away) practising my dinosaur impressions, pacing, being stalked by security and getting into completely unwinnable, protracted arguments with mental health professionals.

I have been a monstrous consumer of resources of late, again a list-

      Ambulances

      Doctors

      Nurses

      Police

      Social workers

      Psychiatrists

      CPNs (both ninja and non-ninja)

      Hospital beds

So I haven’t exactly covered myself in glory recently. If I do a little CBT reframing of the past week or so I can come up with the following list-

 I’m still alive (in all honesty undecided if this is a positive but feel obliged to say it)

I didn’t get detained under the Mental Health Act or the Mental Health (care and treatment) (Scotland) Act.

I was again reminded that a lot of people care very much about me and will go to great lengths to help me. (thank you all for everything)

 The children appear well and happy (though I am aware I am raising the next generation of mental health service users).

So what’s next? In all honesty I don’t know, there are a lot of unknowns at the moment. I could make some predictions based on my knowledge to date but for fear of any of them becoming self-fulfilling prophecies I’ll resist.

I am considering re-starting Lithium therapy, this decision deserves its own post and it will get one. I had that MRI I was agonising over in my previous post, no results yet but am now also awaiting an appointment with a neurologist, these tests are mainly to rule things out, just a case (no doubt previously unheard of) of a psychiatrist being thorough. I have an appointment with the Fab Psychologist on the 13th of September, I will agonise over that nearer the time.

So yeah, I’m still here and again if rapid-cycling was an Olympic sport, I could be a real contender for the gold.

So a short post, covering a short time where an awful lot has happened, there’s a lot missing, follow me on twitter for the minute by minute account of the pantomime that is my life.

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There is so much preamble I could put here, but I’m not going to. I’m so relieved that I got this project out of my head and onto paper before “that” feeling was gone, it’s taken almost 23 hours of almost solid work. So lots of colouring in, very little sleep, very sore hands, some scanning, lots of little niggling imperfections but here is is, my latest project. Please leave comments- I will reply- probably up until around Thursday or Friday when I will no doubt slide into my pit of black sludge again………

All images and in fact everything on this blog subject to copyright, don’t steal my shit.

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>Art?

>Since my illness hit I have created many pieces, in many different ways, most are safely locked away but here is an example from today. I have the feeling it may be a prolific day art wise!

This one uses acrylics, pencil, pva glue and Hama beads stolen from the children (actually Pyssla cheap IKEA equavilant of Hama beads!)

It’s called

Bursting out, Seeping in
I’d like to say it’s not one of the finest examples of my work but the standard is pretty typical!

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