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Out to Lunch

(Redux- my first version of this disappeared for no reason!)

Right, I deleted my grumpy posts about losing my passport and having to waste money because I couldn’t get my flights and to shell money I don’t have on now getting an 11 hour journey home by ferry. Grr. I had been planning this visit home for ages and was furious that it all fucked up at the last minute due to quite extreme forgetfulness. (Fun fact: I took my passport out of my bag and then put it in a cool little travel wallet I had. Then I triumphantly declared I would put it somewhere safe, somewhere so safe that even tearing the house apart didn’t reveal its whereabouts). Robert is lovingly missing his flight to Belfast on Saturday to get the ferry with me later so that I don’t go mad and nut a Glaswegian in their beautiful face. Oh how I hate being cooped up on trains.

Boils down to: I will be away in Belfast for the next nine days or more, and not contactable by email since my mum lives in a household with no internet. Yes, they exist, but it’s Ireland so we’re lucky to have electricity EH. Have yet to book a return back to London as I’m not sure I’ll try chancing it with a shitload of birth certificates and stuff with Easyjet or if I’ll have to get the ferry back by myself. So! That’s it.

In mood news for a rare relevant post, for the past few weeks have been rather jittery, very anxious, imbued with the raging horn (oh yes), buggered for concentration, sleeping about two nights a week, talking bollocks, and, I guess, slighhtly hypomanic (which Robert was openly bemused at when we went to Tesco the other day and I was gabbling to myself about all the things I was putting in my basket while running up and down the aisles deciding I needed this and that) which is one reason I’ve been struggling with long entries. I’m okay, except that in the hassle to sort out getting home on extremely short notice, I forgot to pick up my prescription and will not have any medication until get back, which, at this point, is in question. That might spell trouble. So, if I come back in a week raving about being the next queen of France (which would be ridiculous, France doesn’t have a monarchy so expect further delusions of, “THEY’RE COMING TO GET ME WITH THE GUILLOTINE! MERDE!”) then do point and laugh. I also find it amazingly funny when I do take my medication and see someone- case in point, the therapy woman on Wednesday. I was still slightly drugged but also quite jittery so I was all over the place, rambling, pacing around then half-slumped. On the way back, the haze mostly lifted but I was almost FOILED by what I thought was half a polo mint in my pocket actually being half a 200mg Seroquel. I popped it in my mouth then spat, but bitter was my disappointment. But I smoked a menthol cigarette so all was well.

I shall leave you with some photos From My Real World and Everything to prove that I have a life, that I’ve taken recently, just to make this entry less of a waste of…internet.

Take care chaps.

Rob, my lovely ex boyfriend, with David, my lovely Scottish friend, playing with his band The New Royal Family at Ant Lib

Robert kissing Jack after kicking a ball into his face on Hallowe'en

We didn't just kidnap a child, that's Robert's stepson, and our pumpkin

 

 

 

Cheerio!  x

Blogs, forums and resources on ECT

Hello!   Do any of you know of write/moderate/recommend good blogs, forums or resources on Electroconvulsive Therapy?  I’d really like to compile a list and since my computer fried up last week (woe, had to reinstall the operating system), I have lost every single bookmark (fecking loads),  documents et al that I had concerning it.  Or if you’ve had ECT and have any personal experiences you’d be able to share, that would be appreciated too.  I can’t even find my own post on it.

Thank you muchly in advance.  Thanks also for commenting on my previous sad wee post- funny few weeks really to round off a strange year!  I feel like Egbert’s been at my head with a whisk.

EDIT:  This post isn’t about me, I’m not having ECT or anything.

On or around the 2nd of December 2009

Feck

I am embarrassed to be writing this but I need to talk.

(Talk of imaginary spiders and ranting, cut for boringness and embarrassment)

Read more »

Hypocrite

I know the vast majority of people with mental illnesses- like the vast majority of people without- aren’t going to stab me.  So I am feeling quite guilty that this morning, while in the reception area of my local CMHT, I seriously thought I was going to get knifed by someone sitting opposite me. They were staring at me very intently with an air of hostility, and the intensity of the stare frightened me.  I found myself busying myself in a boring way, to show how uninteresting and also unthreatening I was.  I nibbled a bit of the Tesco fruit salad I had in my bag. (I ended up not sleeping.  Thought fruit would perk me up). I pulled my hat down over my ears.  Sauntering up to the desk I forced myself to look cool and unbothered. Then I legged it.

Of course I wasn’t in any danger.  And they could have been staring at me because I looked like an idiot (I did).  And I’ve been the starer in the past.  I’m used to strange behaviour.  I’m often a strange behavee.   I’m wondering if this is a case of Mentally Ill Dominos, in which a circle of people with mental health problems act in ways which are innocuous but which feed into the mentalism of the other people in the room.  In this case, my ever-present paranoia.  Would I have felt the same in ANY waiting room?  Or am I indeed just a stinking hypocrite who’s afraid of people with mental illness?  Or am I just afraid of everyone?

Edit: Aha, showing your own prejudices there!  It was a woman.

Thank you Psych Central! and therapy things

Hello, this entry is sponsored by parenthesis (signifying an aside so you don’t have to).  And tiredness.

I’m in Robert’s new digs in South London, where he was born and grew up.  He is currently in pyjama bottoms exercising with a giant pumpkin.

Edit:

Thanks Robert!

First of all,  THANK YOU! to Psych Central for giving this blog first place in their 2009 Top 10 Bipolar Blogs!  It was second last year so I was happy (and surprised, since I don’t feel I’ve posted much of interest lately) to be first this year.  Here is what they say:

1. The Secret Life of a Manic Depressive
Do’s and Don’ts for the Mentally Interesting was a BBC Radio play based on Seaneen’s blog produced last May and just nominated for a Mind Mental Health Media Award. Always a compelling and honest read, it was no fluke or sympathy vote that caused us to place this blog near the top of our list last year – it deserves many accolades. Well done.

I feel awkward at this kind of thing so will just say thank you for the loveliness. Well done to everybody, especially Bipolar Chica and Patient Anonymous, whose blogs I love.  I’m glad to see that this year includes a lot of newcomers, and not just old timers like me, Spikol et al.  And hooray for the madosphere!  Aceness abounds.

Life, as usual, continues at my undazzling end. I’ve seen not one but two of my Belfast friends of late, which is always lovely (and, for the photographically inclined, feel free to nosey at my October photos on Facebook).  Apparently I sound English to my countrymen’s ears, and Northern Irish to the English.  It’s no wonder my (Irish Republican) family only half-jokingly refer to me as “the traitor”.

It’s been a little bit of a strange month with my moods teetering to and fro.  I’m still feeling a bit weird so excuse me if I sound…er, weird.  I had the drying-out alcoholic shakes, so no sugar in the tea unless I was armed with a sponge at all times.  My mind had been racing a little bit too, with a slew of unsettling negative thoughts, which wasn’t good. Background noise was also turned up to eleven. I’d been on minimal medication for some time- my usual dose is 400mg but I’d cheekily lowered it to 100mg, then to 50mg, occasionally nothing, which, I have discovered, is a bad idea.  I know my reactions well enough to be able to do so fairly safely. Up the dose when hypomania strikes, lower it when depression does.  See-saw. So I upped the dose to 200mg, and the agitation has calmed down.  It had no choice but to, given the fact that I have pretty much spent the past three days asleep because of the extra 100mg.  It’s hard to shiver and shake in your slumber.  Downside is I’m exhausted, my concentration and memory are still shot and I have no idea how to help that.    I joke about my terrible concentration and my memory but it gets me down.  It buggers with two of my greatest joys- writing and reading.  I find it a huge struggle to write sometimes, I can rarely read anything more challenging than a magazine and I’m generally a forgetful, scatterbrained twat.   I need a tattoo pen to write stuff on my forehead but I’d probably forget what to write or get distracted halfway through.  Bollocks.

Last Thursday was my first (first! I thought there was only one!) therapy assessment.  I’d been a wee bit nervous about it as the therapist is an icicle of a woman.  She is beautiful.  That was my first impression of her when I met her last year.  In the olden days when people still cared about the possibilities of verse, many a thigh-rubbing poet heart would have been in an absolute frenzy about her hair, a waterfall cascading in sunlight, the golden silk with which god spun the sands…and so on.  You wouldn’t be able to hear yourself think above the din of quills scratching paper.

And she is cold. Her golden loveliness (even her name is lovely) makes her stiffness more striking.  She is expressionless, often toneless.  She is professional.  The impassive manner of therapists is the stuff of cliches but having had little to do with therapy, it’s something it’ll take me a little while to get used to.  I guess I’m more accustomed to the casual and friendly manner of my social worker.   Though I would much rather speak to someone who is professional than someone who isn’t, or who tries to be chummy and matey without knowing me.  I’m just not used to it.  And besides, we don’t know each other, even professionally.

(Urgh, professionally.  I realise sometimes that seeing me is someone’s job.  We’re not friends, and they might not actually give a toss outside that one hour a week.  It’s a disconcerting thought sometimes and makes me wonder about people’s sense of duty, not just professional people.  How would I feel if I didn’t have anybody, had never had anybody, who cared about me?  Even though I am unsure most of the time if I do, but I must do, because almost everyone does really.  I wonder how I’d feel about my appointments then.  I do, for the most part, look forward to them).

Anyway.  I was in a bit of a funny mood that day (aha).  And nervous, and a bit anxious about rambling and just sounding like a churlish, entitled brat and so on.  I wanted to be articulate, and to answer her questions.  Because these things can feel like the world’s strangest job interview.  (Especially when your social worker is sitting in on it.  But I was glad she was). Read more »

Hooray

I’m going to apply for this.

Addaction SmartScheme

Good idea?

“STATE-SANCTIONED MALINGERING IS THE BIRTISH DISEASE”

“Birtish”?

If this article can’t even be properly edited then why should I trust what they have to say?  Learn to spell.

The Daily Express is a horrendous little rag anyway, but here, for fun.

It is telling that more than1.1million incapacity claim- ants are not suffering from any physical disability at all, but get their handouts by moaning about problems like “stress” and “depression”.

Once again, the largesse of the welfare system provides perverse incentives for people to exaggerate their emotional suffering rather than demonstrate resilience; no wonder, then, that the number of people saying that they are “too stressed” to work has trebled during the 12 years of Labour rule.

By far the greatest outrage is the money dished out to more than 100,000 alcoholics and drug addicts. It is the height of lunacy and immorality for the state to pay people to continue with their dangerous habits. Awarding “disability” handouts to drug abusers makes a complete mockery of the law, given not only that narcotics are illegal but also that a  significant proportion of crime is committed by addicts.

These people deserve spells in prisons, not an easy lifetime on the dole (not sure what’s “easy” about living on £50 a week…). The incapacity benefits system has been disastrous for the moral fibre of our nation.

Ants claiming incapacity benefit is a new one.  But I can understand them being off work for stress.  Ants work really long hours.

I don’t trust any articles written about benefits that still call them “incapacity benefits”.  It is the Employment and Support Allowance now.  If someone can’t even use the correct name for the benefit, they have no authority to write in a national paper about it.

Anyway, there you go.  I am too knackered and pissed off today for much else.  But stop your moaning about potentially fatal illnesses like depression, eh.  Demonstrate more resilience.  Hang yourself from your good old Birtish stiff upper lip.

I am sick of this bullshit being published.  Swap places with someone incapacitated by schizophrenia for a week, you fucking idiots.

Edit: Going to add here, when I was sixteen/seventeen, before I got kicked out of college for being mental and manic, when people thought I’d be destined for Oxford, I used to lie in front of traffic, and think I was Jesus.

6am, awake

And tearful.  I miss my dad. I feel sad, in an almost nice way, because sometimes it’s good to sit in the early morning quietness and miss someone.

I’m going home next month for a week.  My family live in a different house now.  So he has never been there, and yet, I miss his presence.  This is what became of the house we lived in.

God knows what it’s like now.

I wonder if I become depressed and reflective in October because I’m sandwiched between my birthday and Christmas, and two times of my life that will never be the same again.  I think when you have your parents, in some way, even as you grow up- into your twenties, thirties, forties- you can still be a child.  Their child.  There will always be a moment of petulance in an unguarded moment, or someone to bat your wise adult hand away from the hot stove.  And then when a parent is gone, it’s not the same anymore. With Christmasses and birthdays now I don’t feel like my mum’s child but her equal.  Being the Grown Up, making sure she’s okay, and hiding it when I’m not.  No tantrums allowed, however seductive they seem.  I really miss arguing with my dad.  I miss screaming til my lungs are raw and slamming doors so hard the wood splits.  I genuinely miss it.  I miss Christmas day fights too.  It doesn’t feel the same now.

I try to nurture my sense of childishness at Christmastime, by myself, enjoying the lights, being excited by the weather reports, entranced by the midis of carols that would be charmless in July.  I don’t want to lose that.  I don’t want to be cynical and find that part of me is gone.

I become sad when I think of some of the more horrible birthdays and Christmasses we had- the birthday my dad rang up to tell me he wanted to top himself, when I went home for my eighteenth birthday and didn’t even get a card, and a few particularly brutal Christmasses.  There is no way to even up the tally now.  At least the last Christmas, my last one with Paul Molloy being my father, was happy.  He stayed sober for three days or so.  The last I saw of him- as an alive, animated person, not a yellowing sarcophagus, dying- was paying for my taxi to the airport, and, as he got out and headed to the off-licence, he was happy.

Ah, I should just go to bed.

Hooray, I’m not dead!

Tongue in cheek but …

Happy one year anniversary of me not succeeding in topping myself! And three year anniversary of being diagnosed with the mentals!

Shame, my flat’s a bit of a mess right now.  Maybe I should find some more pills for the sequel and get it cleaned again.

It’s been a very strange year indeed.  Changeable, surprising, painful, joyful, somewhat unproductive and downright fecking weird!   When I don’t feel so delicate, I’ll go into detail.

In 2009 I seem to have mastered the art of forcing myself to carry on living with a glimmer of confidence it might actually be worth it.  I went mental from April-July and didn’t realise how mental (manic, mostly) I’d been until I was chewing my fist off in August and howling, “OH MY GOD WHAT THE FUCK WAS I THINKING?!”  Swings and WOO-HOO! roundabouts, though.   I went through the heartbreaking end of a relationship with someone hugely important to me that I probably wouldn’t be here without and who I love(d) very much that was complicated with-and partly caused by- madness, which made me (and makes me, and scares me because I don’t want the same thing to happen again, to take people for granted, to make the same mistakes) sad and angry, but survived and coped with it like a “normal” person, i.e crying an awful lot. And began a new relationship with someone who taught me what love was when I was fourteen, which, to be honest, is sometimes very surreal.

I haven’t escaped a year without a fairly severe wobble since my mid-teens, so if I make it to 2010 lesser-scarred (and hopefully not mentally scarring those close to me, like I did this time last year), it’ll be a bit of an achievement.  Self fulfilling prophesies may not be us after all. I do have nightmares sometimes about the events last year.  It was fairly traumatic, but hey ho.  More traumatic for everybody else who saw my boobs that day though.

If I’d expired in my own vomit last year my Radio 4 play would have ended on a bit of a downer.  And I’d never have met Michael Palin.  Did I tell you I met Michael Palin? LOOK I MET MICHAEL PALIN!

That’s him considering the marriage proposal I’d scribbled in the inside of the book.  It was accompanied by a line drawing of my breasts.

Point is, it’s a year on and I don’t feel that way anymore, which I couldn’t imagine back then.

Anyway, hooray for me not being dead!  Cut yourself a slice of cake, but do hide the knife.

Edit: Robert sneaked out in secret and bought me a lovely coffee walnut cake with three candles.  It was bloody delicious and the other half has gone into hiding lest I scoff it down immediately. All a bit silly, but there’s nothing wrong with taking one day a year to go pat yourself on the back with some cake.  Or to let someone else do it for you.

Big old pile of toss

I feel like shite today. How are you?

My body the hand grenade

Because this blog is the only place I feel free to moan.  This isn’t a blog about eating disorders and body dysmorphic disorder but I still have both (to use the names of the terms, shorthand) and they are making me fucking miserable.

Read more »

Is there any debate on this?

I have to rush out to go to a wedding reception so apologies for this post being short and rubbish but quickly, here’s a story on the Daily Mail website about a twenty six year old woman who swallowed anti-freeze and arrived at hospital with a note requesting her wish to die.  Which was honoured.

It has the usual hysterical Daily Mail title of,

What kind of country have we become if doctors and lawyers allow a disturbed young woman to die?

The coroner’s verdict was unequivocal. Dr Alexander Heaton, he said, ‘went over and above what was required of him’ when Kerrie Wooltorton was admitted to the Norfolk and Norwich University Hospital.

She had swallowed anti-freeze, but insisted she didn’t want to be saved. In her hand was a note which began: ‘To whom it may concern, if I come into hospital regarding taking an overdose or any attempt on my life, I would like for NO lifesaving treatment to be given.

‘I would appreciate if you could continue to give medicines to help relieve my discomfort, painkillers, oxygen etc. I would hope these wishes will be carried out.’

Kerrie Wooltorton who died at the Norfolk and Norwich University hospital after drinking anti freeze and leaving written instructions not to revive her
Kerrie Wooltorton, pictured with her godson George Miller, died at the Norfolk and Norwich University hospital after drinking anti freeze and leaving written instructions not to revive her

Those wishes were eventually carried out, to the letter – throughout the 37 agonising hours it took for Kerrie to slip away. But, initially, a second opinion about Kerrie’s mental state was sought by Dr Heaton as to what he should do: in other words, should he save this young woman’s life or not?

The medical director of the hospital was contacted. The hospital lawyer was consulted. Then, and only then, was the decision not to treat Kerrie taken, the Greater Norfolk Coroner William Armstrong told me this week.

In other words, as far as Dr Heaton and his colleagues were concerned, all the boxes had been ticked. Legally, anyway.

Had he and his team not respected Kerrie’s wishes, Dr Heaton argued, they could have opened themselves up to charges of assault. That’s the law, apparently – one which, to all intents and purposes, has now resulted in lawyers sitting in judgment on life-and-death cases in A&E departments.

Such cataclysmic developments should give us all cause for concern, and this special investigation into the circumstances surrounding Kerrie’s death will do little to allay the fears of those who believe a culture of ‘medicine by lawyer’ is beginning to prevail.

The case has provoked fears that ‘civilised’ Britain is moving insidiously into an era of euthanasia on demand. All but forgotten, it seems, by those at the centre of this tragedy is the central principle of the Hippocratic oath, which has guided doctors for the past 2,000 years. It is: ‘Never do harm to anyone.’

She requested pain-killing treatment and explained she had called an ambulance because she didn’t want to die at home alone.

The problem here is that she was young and physically healthy and her illness was a mental one.  There is a prevailing attitude that anybody with a mental illness who is suicidal isn’t in their right mind.  In fact, having a mental illness at all- which invariably clouds your judgment (as does pain in the case of terminal illness, but that’s different because death is imminent)- means that their wish to die shouldn’t be respected.  That people are always treated, always eventually saved, will always look back and say, “I’m so glad I didn’t end my life then”.

But that isn’t always the case and sometimes, ending your life is the rational decision you take, not the irrational one.  And as far as someone can demonstrate that they know what they’re doing, then their wishes should be respected.

The Hippocratic Oath is the tenet of practice in modern medicine but medical intervention can just be a sticking plaster prolonging the process of life without any consideration as to which quality of life the person has.  It’s the whole, “sanctity of life” idea, that, “Hey, at least you’re alive!”, without thinking if that life is worth living to that person.  Not everyone would choose life over death.  If they had intervened in this case, Kerrie might have just been on dialysis for the rest of her life, and possibly would have made another suicide attempt.

I know it’s all well and good saying, “might have been”, by the way. Likewise, you could argue she might have been okay, might have been happy. But she wanted to die, the doctors honoured her wishes and they shouldn’t be attacked for it as harbingers of moral doom.  It is far more respectful to actually give a thought to the individual person’s desires than to just treat them with the vague, hypothetical, “first do no harm”. And I think it’s everyone’s right to end their own life if they want.  It is their life, after all.

Anyway, excuse the lack of proper intelligent commentary here but I mostly just wanted to bring this story to your attention- what do you think?  Should the doctors have intervened and tried to save her life?  Should suicidal people be allowed to die if you can’t prove that they’re in their “right mind”?

Workshy scroungers redux

Hypomania is calming down. I am a little bit disappointed by the relative quietness in my head. This typing sounds like thunderclaps.

Anyway, hooray for the Conservatives, the new-New Labour.  First we find out that DLA is in danger and now they want to cut incapacity benefits and boot people onto JSA, which is already a criminally low amount of money.   Given the idiosyncratic and very-much-geared-at-physical-illness criteria for ESA in deciding who’s “fit for work”, let’s enjoy our final few months hating ourselves for being too mental to hold down a full time job so we can hate ourselves for being even poorer.

The Conservatives say they would pay for their £600m plan to “get Britain working” by cutting the incapacity benefit bill.

People on employment support allowance who are deemed fit to work would be put on the jobseeker’s allowance, reducing their benefits by £25 a week.

All incapacity benefit claimants would be assessed to see if they could work.

Robert noticed my worried face as I read this story and said, “It’s ages away and anyway, it won’t be for people like you, who have real illnesses and have the doctors and nurses helping you”, but it is for people like me, and for people like you, not just the famed, “dodgy backs” of Britain.  (Speaking of which, as I write this, I have a completely buggered neck I can barely move.  GIVE ME MONEY).  It’s not the first time someone has said, “Ah, but YOU deserve it”.  They can only say that because they know me well enough to know and see first hand how severely my illness affects my life.  I’m still judged unfit to work by the DWP but I’ll eventually be assessed and probably booted onto JSA.  I can walk, after all.  And people who do bullshit, like a certain someone I know who does the double (works and claims benefits) and who faked a panic attack at an assessment, should be pulled (and in her case, kicked up the hole although there are many people who are in such poverty that they claim benefits for the much-needed extra income, which is seemingly never addressed).  But the process for judging who is and who isn’t “deserving” isn’t just a medical one, it’s becoming a moral and social one.  The system is hugely flawed.  Have a read of the Benefits and Work forum to see actual examples of the judged “dodgy backs” who find themselves utterly fucked because of it.

I am aspiring to be in part time work by mid-next year.  Nobody, including myself, believes me well enough for it yet,  but I try to routinely do something (even if it’s just writing something by a deadline) to test myself and to keep busy.  I am meeting the therapist for an assessment on the 22nd so that might help, too.  But it’s besides the point.  There is a sour attitude towards people who are ill in Britain right now.  I feel like human flotsam, guilty for every single penny I spend, even though I worked and paid my taxes since I was seventeen.  Just force people into shitty, badly paid jobs and cut benefits to the point where there’s no financial gain to be had on them. I don’t even have the energy or the impetus to write about it.  “Benefit reform” by both Labour and the Conservatives have long since ceased to pretend to be humanitarian.

(P.S:  I should say that I am embarrassed to be writing this as I know some people reading will be thinking, “Get to work! There’s nothing wrong with  you!  You can type this, you have a life!”  which is a little internal prejudice against myself I hold also because my problems are mental and I am often ashamed of them.  Which I think says quite a lot about what “real” illness allegedly is

Lydia just pointed out how much she hates the, “what do you do?” question from people.  Ah, yes, me too).

Dos and Don’ts was nominated for a Mind Mental Health Media Award. Hooray!

Cheers, MHM!

Leading mental health charity Mind today announces the shortlist for this year’s Mental Health Media Awards, sponsored by Comic Relief and Shift.Terry Pratchett, Fiona Phillips and Alastair Campbell are among those competing for the full length television documentary prize, and the BBC and Channel 4 go head to head in many of the categories, with top rated soaps Eastenders and Hollyoaks battling it out for the soaps and continuing TV drama award.

This is the first year the prestigious event, which celebrates the best portrayals of mental distress and reporting of mental health in broadcast media, will be managed by Mind following its merger with Mental Health Media earlier this year.

Radio Drama

  • (BBC Radio 4)
  • Dos and Don’ts for the Mentally Interesting
    Uplifting factual drama based on 23-year old Seaneen Molloy’s acclaimed blog about learning to live – and love – with bipolar disorder.

Yay!

I am proud, though feel somewhat fraudulent (and I do find it tricky listening because of this) as the play was partly based on a relationship with Rob that is no longer (though it’s no-longer-ness does not negate its loveliness and immensely life changing importance when it was an is.  And he is still my much loved friend).  But!- it’s very very lovely that people consider the play to have raised awareness of mental illness.  I hope it did in some way. I never really know what to say about it because its existence at all is highly surreal! But I was very happy and proud to be involved.

So, well done to the lovely Louise Ramsden, who adapted the play, and Fiona Kelcher, the equally lovely  producer!  (And squeak! Jimmy McGovern is one of the judges!  Quake!)  I have no idea if we’ll win anything but it’s still rather nice to be nominated for something (last prize I ever got a plastic parrot that had been wronged by nature).

Also on the shortlist:

EastEnders (BBC One)
One of EastEnders’ most loved characters, Stacey Branning comes to terms with the prospect that she may have bipolar disorder, the same condition that her mother has had for many years.

Eastenders fans, what do you make of this portrayal?  A spiteful text was sent to Robert about it about the episode in which she was diagnosed. Watch it! I hadn’t watched it in years, but the texter clearly thought such a portrayal would, er, somehow unmask my own monstrosity and his lunacy at being with someone like me.  (You can read Robert’s not-entirely-serious ramblings at The Trap Box and decide who is the real lunatic. The answer is, as usual, neither).

What from I’ve seen, it’s been handled rather well.  The discussion with the psychiatrist raised both a wry smile and inspired a somewhat uncomfortable shifting in the chair from me.  TV drama tends to go a little overboard when trying to convey bipolar disorder.  The characters are usually jumping up and down and waving their arms frantically, or leaden with depressive paralysis.  But Stacey was agitated- that skin crawling, can’t sit still, can’t hold a coherent thought agitation that’s very familiar to me.  And her terror, having seen her mother go through it, and her denial, was quite an important point to get across.  Now she’s descending into psychosis.

I was a little bit pissed that the histrionic, “promiscuous” (I hate that word, I hate what it implies, I don’t believe in it, but it’s what Eastenders were scripting her as) character was the one who became mentally ill, and thought it might have been more effective if someone less stereotypically “mental” became so, but I guess it did illustrate the descent, the gradient, the tremors.

Anyway, what are your thoughts?

I’d like MHM to introduce a web category for outstanding websites and blogs about mental health.  I imagine it would be a somewhat impossible task to be representative, but a cursory look over —————–> shows that there’s more than enough to warrant such a thing.  (And on a side note, how pissed off does the woman on the banner look?  GERROF MY WEBSITE!)

And to say I have bloggers’ block right now is an understatement.  I might join the ranks of the uber-Web2.0 Facepeople and do a video post next time, providing I can somehow brush my hair over my face and talk from beneath the curtains like the Wizard of Oz.  I may be struggling with writing, but christ, I can talk. (Though cannot promise to be coherent or interesting since I have slept not-much of late and I am a tiny bit high and have been admittedly somewhat unstable lately.  I am managing though, just not very good at concentrating for long, or short, periods of time! So, er, probably not a video but I can try).

(P.S:  I got an indefinite award from DLA, which I’m guessing is due to the, well, obvious.  It’s been three years since my diagnosis and here I still am. Anyway, no sooner had I found out the happy news of not having to do the renewal form in two years, I discover that they’re thinking of scrapping the fecking thing! You gits!)

(P.P.S:  The Mentally Interesting community still lives at Ning! Go frolic! Or as best you can do on antipsychotics! Go forth and stumble!)

ARRRRRRRRRRRRRRRGH

-DELIVERANCE!  Literally.  DLA forms have turned up!

So, er, panic averted.  Anyone got anything nice to talk about? Read more »

A note

I habitually private/delete posts here that I consider too personal/too whingey/too directionless (on a blog like this, the criteria is rather… loose).  So if something you comment on goes missing, it’s not you, it’s me.

I got a few emails with my last into-the-ether post asking if they’d personally pissed me off.  No, and no-one ever has ever pissed me off enough for me to delete the post in a hissy fit.  So never fear!

So, some moaning to get out of the way:

I haven’t felt like writing in general lately so forgive my sporadicness.  It’s been like that for months, so.   I’m struggling so stupidly with writing that I keep finding that, when I do, I miss out words, spell things wrong and generally fail to find a flow.  I don’t feel like a good writer anymore, and I don’t feel like I have any of worth to say in this blog.  I’m so far unsuccessfully trying to boot my arse back into the habit.  That I am having such trouble with it has saddened me.  Blogs are often a good starting post to clear the blocks but this one, not so much.  I keep it deliberately focused on mental health and because I’ve been in a funk- both mentally and “creatively”- I haven’t really felt like writing about it.  There aren’t many ways to say it, unless I just post a picture of tumbleweed, like this:

That’s pretty much it.  I’m going to start a new, general blog in the hope of helping me regularly write again, and about subjects other than a) mental health and b) myself.  I could sit down with a Word document open but unfortunately it never seems to encourage that, “MUST DESTROY THE LOVELY SNOW WITH MY FOOTPRINTS!” feeling that I wish it did.  I might go through the comments on this post for inspiration.

I’m not unhappy.  I’m just a bit lost.

I’m still muddling through the changes of the past few months.  I haven’t felt like publicly talking about any of it.  A load of good things have happened too, but I am a screamy-tantrumy-child when it comes to change.  I need to think of the future, and I’m…well, yes, a bit lost.  Not entirely sure where I’m going in my life in general.  Vortexy, confusing.  And another reason I haven’t been writing here or in general is Life Stuff- I’m doing the Life Thing, living it, rather than blogging it.

Hope everyone out there is okay.  Once again apologies for not keeping up with people and being terrible at replying to e-mails.  I haven’t really felt like I’ve much insight to offer for some time now.

It has been a strange and difficult year.

BBC Ouch on disability

Hello!  Here is another article from me on BBC Ouch.  It’s about what I discussed here recently; feeling like a fraud in terms of “disability”.

Here’s an excerpt from it:

One night at the pub, I was emptying my pockets looking for my keys when it fell out. It lives in a distinctive orange wallet and has the words ‘FREEDOM PASS’ emblazoned across it. An acquaintance picked it up for me and cocked an eyebrow. “How come you get one of these?” he asked. I cocked an eyebrow right back.

“Because I’m disabled”, I responded. With a barely concealed smirk, he replied, in the laborious tone of disbelief, “But you’re not disabled”. And, although my social worker, the Department of Work and Pensions and Islington council, beg to differ, a part of me agreed.

Disability is defined as, “a physical or mental impairment that substantially limits one or more major life activities”.  Having a mental illness does “substantially limit” my life. There are times in which I barely function on any meaningful level. No one would look at me and guess that sometimes I need help bathing myself, or that there are times I can’t cook a meal. But I do, and there are.

And yet, even though I’m speaking to you from Britain’s best disability website (oh yes), I feel like a total fraud. I felt like a fraud when I was filling in my Disability Living allowance forms, I felt like a fraud when I was staring blankly ahead for the passport photo I needed to get my Freedom Pass and I felt like a fraud when I retorted to my friend. I just have a mental illness, and some people don’t even believe that mental illness exists. Though I live with one, even I question whether I’m ill or just weak. And when it comes to mental disabilities, many people may question whether mental illness counts as a disability at all. Why should I get a Freedom Pass? What do I know about genuine disability?

The rest lives here.

Sorry I haven’t written in here for almost a fortnight.  It’s been a busy one, although most of it has been taken up with carking Lemsip in a bid to fight off the ills.   I’ve been busy in the social sense of staying sober and sleeping in the sitting room trying to stop coughing,  but absolutely unproductive in every other sense.  I haven’t written anything in two weeks.  I need to get back into the habit of writing regularly before I surrender myself to utter uselessness.

In terms of mood, I’m going through one of those strange emotionless, spaced out phases which are neither noteworthy, nor easy, to write about.

Before I go, a relevant post on therapy

Hello!  Occasionally some posts, like this one, will be illustrated by the lovely Prozacville, so go and visit him and give him praise as you would a deity.

I am sick of having “issues”.  But here is a post moaning about them!  Delicious irony.

But ooh.  I had forgotten the (free and fixed) Macbook had Photobooth.  Here I am relaxing in my sitting room.  Not pictured are my chandelier, maid, cigar and rent boy.

Except I’m clearly not relaxing in my sitting room, as only maniacs can relax when a lens is on them, and I have in fact turned the Macbook upside down and that’s not a relaxing pose.  I also have silly hair.  I dyed it red and blue, which apparently means orange and green.  I like to think I look like I’m sporting beguiling autumnal plumage, and not that I just look like a twat that’s been left out in the rain too long.

Ah, an illuminating appointment with my social worker today, so, thought I’d write about it.  Long, self obsessed and introspective- you could say it’s a Classic Secret Life… post.  (And a caveat here: remember this is a blog exclusively about mental health.   Some people seem to forget that.  I do not go through my day to day life going, “ARGGGGGGGGGGGGGGGGGGH”.  I have other, more cheerful topics of conversation).

I’ve never really gone into detail about my now twice-monthly (or, as the kids say, “fortnightly”) appointments with my social worker.  They are mostly a bit of a chat, commentary on mood and someone for me to talk to.  She’s a lovely woman, quite clearly no-nonsense, which is sometimes appreciated and sometimes not (who doesn’t occasionally want a bit of, “Ah, there, there” and to just moan into your sleeve) and I like her.  The appointments are usually conducted in a small room with one window, and today there was the smell of cat piss emanating from…something.  I suspect it was me, since I’m not entirely convinced that Girl Cat hasn’t weed on the cords I’m wearing.  Then again, I didn’t really care this morning when I got dressed.  A cheeky sniff almost clears my name, but I have a bit of a cold so I may well infact stink of her waters.  My social worker insisted it was somewhere else in the room as, being a residential area, cats sometimes become cat burglars (a term which used to confuse me greatly) and pee all over the place before they’re shooed away.

She helps me with practical matters, and carried on my old CPN’s work in terms of benefits and housing.  But I can mostly do these things alone.  Okay, it takes me about three and half millenia to get round to doing it,  but I am fairly independent, as far as people within mental health services go.  She has been trying to sort out direct payments for me to study something, with both of us agreeing I need more structure in my life.  I keep- genuinely- forgetting to ring up, but I will tomorrow.  To be quite honest with you, I don’t particularly feel up to a lot right now, but I’d regret not trying, and it may well be good for me, especially with Robert going to university in October.  We could compare notes.

Today we discussed therapy, and why the person who makes the assessment had been unwilling to make an appointment with me.

I had therapy was last year, and it was CBT for body image problems (BDD).  I spent most of 2008 in a depressive stupor, indeed, I don’t particularly recall much of it.  Therapy started off okay, but I was already rather depressed, and as it progressed, I began to feel worse.  By the time of the fourth or so appointment, I was so depressed that I didn’t actually give a toss about my appearance, so it was difficult to engage with it.  What had seemed greatly important no longer felt important, along with everything else in my life.  So, the therapy ended.

It was assumed that the trials of therapy had worsened my depression.  The stress of looking inward and so on.  To this day, I still don’t think that was the case, but maybe there was something subconscious.  Either way, in September (or possibly October), I was prescribed Effexor, went loony, took a huge overdose and there you go.

So.  The Therapy Lady didn’t want an appointment for that reason, and also another reason, which is that she didn’t think I saw some of my problems as being part of my personality and that I only saw my problems as part of a chemical imbalance.  Ergo, therapy would not be helpful.

It is true that I have tended to be overly clinical about myself.  I am increasingly seeing myself as a whole person, with other problems, but for a long time, I was quite clinical about everything.  I saw my moods etc etc as being outside myself.  Which puts me in a helpless position, no?  Not entirely.  I have made the appropriate “lifestyle changes” to manage my illness- I didn’t drink for ages and am not doing so again, don’t take drugs, try to sleep, try to eat, avoid stress etc etc etc.  But…

Being diagnosed with bipolar disorder was a kick in the bollocks for me.  Who in their right mind (FNAR!) wants to be diagnosed with a serious mental illness?  It sucks.  It’s crap.  It makes you feel as though you have, “REJECT” stamped across your forehead.  The only way I felt able to cope with it was to see it in a medical sense, as an illness, as something outside myself.  Because if I thought that I bought this on myself, that it was my fault, that I was flawed and fucked up (which I do often think), I could not cope.  I would simply just not be able to face it.  Giving myself distance, writing about it, even sometimes coldly analyzing, was what I needed to do for a few years.  And I was rather, “Ah.  Well.  That explains an awful lot”.  And I should have been relieved, but I was devastated.

It was easier for me to see it that way.  I would not have come this far without that perspective.  It’s unhelpful for therapists, but I needed to face up to and deal with the other stuff in my own time.  I do consider bipolar disorder to be a chemical thing, by the way.  The chemical basis, if you will.

I have other diagnosed problems, namely body dysmorphia, bulimia and self harm.  My social worker mentioned that those things in tamden with bipolar disorder are not that common, due to the shifts in self perception and weight that comes with bipolar.  This is true,  but it still stands, although in terms of bulimia, I’d consider myself better.

That’s enough for me- I don’t really want more fecking problems, more diagnosis. I have trouble enough agreeing with the existence of the others.  I don’t want to be pathologised.  And, although maybe once I did see these things in isolation to bipolar disorder, I don’t think I do anymore.  As time has gone on, I’ve moved further and further away from defining by diagnosis, and thinking in terms of diagnosis at all.

Then she said the dreaded words- “personality disorder”.  My arse clenched right up.  You couldn’t have fit an atom up there.  Because I knew what was heading towards me, with the stinging predictability of a slap from a raised hand.  Borderline personality disorder.

Diagnose me with shit if it’s accurate.  Don’t diagnose me with inaccurate shit just because I’m a woman who self harms and has rapid cycling.  Borderline is one of those things nobody really wants to be diagnosed with because it is the equivalent of your doctor saying, “Fuck knows”.  I don’t want to be diagnosed with it, either, because I think it’s wrong. I was told I had “borderline traits” after an hour long appointment with a doctor in Haringey a week or so after I left hospital.  That isn’t a diagnosis, but I even disagree with traits. Read more »

24

Right, enough self pity for now! I need a self pity break.  I have one scheduled in my calender.  (This is not true.  The only calender I have in my vicinity is the Ramadan Countdown Calender.  It has chocolates.  It was a worthy purchase).

Tomorrow I am 24!  Or I could be 24 today, because nobody knows for sure when I was born.  You think my mother would remember me crawling out of her vagina, but apparently she doesn’t.  And I didn’t really crawl, I just kind of fell out.  On maybe the third or fourth of September, I was born in a lift.  Which gives me HILARIOUS ammunition when people chastise me for not shutting doors behind me.  Oh yes.

Anyway, for my birthday I got a ticket to Offset, in which I shall break my festival hymen.  (This post seems all about the vagina today.  Let’s see how many more references I can slip in).  So, that’s where I shall be this weekend. Before I go, I will clean my sofa cover as, due to an unfortunate incident with a bowl of cereal, it looks like I have pissed myself.

So, I’ll see you in a few days or so.  Have a good weekend chaps!  I’ll leave you, as usual, with an attempt to force my tastes down your throat.