Tag Archives: mental illness

Cauliflower

You don’t have to understand. I understand that you want to but you don’t have to.

It’s OK not to understand. It’s ok to be totally at sea and bewildered and confused and just totally fucking ignorant to it all ok?

I am.

You don’t need to understand to care or to support or to squeeze my hand or to push back my hair to look me in the eyes and tell me that really it will all be alright.

It’s because it’s emotional isn’t it?

It’s made of the same things that ask what do you mean you’re scared of clowns? What do you see in him? Why are you crying about that film? How can you not like kittens?

If something is a made of emotion it is so often assumed that we have a choice, as if we wake up one day and think, yeah, I’m going to be properly shit scared of yellow flowers, just because I feel like it.

You can’t help who you fall in love with and you don’t decide to hate cauliflower or love the smell of cut grass or that you’re gay or straight or just not really bothered. These aren’t decisions but things that are engrained into our selves. They go by, for the majority I hope (because sure, there are some people who perhaps have slightly bigoted views out there) unassuming and unnoticed and unquestioned.

Because no one, on learning that the person sitting opposite them cannot stand cauliflower, leaps from their chair sending cutlery flying through the air to exclaim oh holy shit. This…this isn’t going to work. This…we…we can’t do this anymore. I mean, I just don’t understand. It’s cauliflower dude. What…how…I mean, cauliflower. How can you not like it? Why. Why have you made a choice to have these feelings and emotions and how can I overcome all of my misunderstandings so that I can still look you in the eye.

There’s a lot in life that I don’t understand. A lot. Like how I lived with a boy at university when I was a teenager and he had a ridiculous Tasmanian Devil towel and I ironed his shirts (even then) and he taught me to play poker while we watched the Lion King on DVD in my cupboard sized bedroom – that boy and I somehow managed to create and subsequently sustain human life. I’m shaking my head in disbelief because, I mean…

The same goes for why I love pineapple so much or why my little toes curl rebelliously making my feet wide or exactly why one eyebrow is millimetres higher than the other naturally but even with all the will in the world (because I like the snark) I can not make it raise independently to the other.

Who gives a fuck right?

Who cares why so and so doesn’t like biscuits or loves the feel of cotton wool, who cares?

There are people in my life who I have seen transform from healthy to nothingness. I have seen the effects of illness and disease and the devastation that it brings in its wake.

There are others who I watch live their lives with something, some ailment or illness that they have to manage or control or simply try to push firmly into the background and use all their energy to give real life it’s rightful place in the spotlight.

All of the above are crap. You would wish suffering on no one. But I don’t understand it. I don’t understand why that bit is wrong with this bit and those tablets do this so that this bit can keep working…

I don’t understand and I don’t need to because not understanding doesn’t stop me from being able to talk or laugh or cry or hold or, well, anything really.

So why the fuck do people feel such a need to understand mental illness?

It’s not a choice, it’s an illness – that is literally the beginning and end of it and all the information that you ever need to know in order to continue to associate with someone unlucky enough to suffer.

Maybe I’m naive, lucky that I have never seen someone close to me suffer badly from any illness. Maybe if someone I loved dearly was desperately ill I would feel that I needed to understand as much as I could so that I could deal with it better, I really don’t know.

All I know is that although I have never, ever had to explain myself to my family – although I often try to and want to explain how I feel – I certainly have had to justify my illness to others.

If you were told that a friend or an acquaintance or the son or daughter of that nice bloke you bump into at the chip shop every Friday evening while you wait for your cod to fry had a broken leg or any physical illness you would never, ever act in the same way as if it was a mental illness.

If you don’t understand, it really, really doesn’t matter. Can you honestly say that you understand the common cold from genetic make up to transmission to the way the germs interact with the antibodies in the blood and how and why because I really, really bet that you can’t. But does that stop you buying oranges and magazines and cuddling someone you care about through their snotty sneezes and as it sounds like they are making a valiant attempt to cough up a small country? No, right?

No one decides to catch a cold or the flu or break their neck or develop diabetes or arthritis and no one decides to get mentally ill, just for a laugh/attention/to be cool/something to do.

I promise.

An illness is an illness and no one suffering really wants your understanding, your reassurance and your presence is all that’s needed.

Hold their hand, don’t make them justify the unjustifiable.

Damn Well Unique

When I was in my early teens I was all Tippexed nails and Impulse body spray and blue mascara and the Rachel cut. I loved Art and I hated Geography and I huddled close to friends for warmth behind the library building during cross country that I never ran. I was in love with a boy who wasn’t in love with me and the best day of my life was the one when he wrote his phone number in the margin of my maths workbook.

I was naive and innocent and bright and normal until something took over. I was on Prozac before I turned sixteen. At the time I genuinely didn’t understand what was happening to me. I was trapped in a heavy misery in a heavy body that wouldn’t move thinking thoughts that I couldn’t articulate and barely seeing through the darkness. I had no idea what was wrong. I was fifteen and I had never kissed a boy and I couldn’t get out of bed or find a better way than self harming to release the pain I felt from nowhere.

And that’s where memories that are hazy become blank and suddenly I’m a year older and the Rachel cut is grown out and dyed black to match my nails and I’m wearing flared sleeves and baggy jeans and skater trainers to college where I make friends and laugh and kiss a boy.

I had a little moan about this yesterday and when writing that post and browsing YouTube I found this video. Please watch it, it really is brilliant. Brave, inspiring and something I probably couldn’t do now, let alone all of those years ago.

Thanks for letting me share your vlog Emma :)

Problem

problem dictionary definition

In life there are many problems, sometimes they seem to fall from the sky and sprout from the ground and divide and multiply until they cover everything in a big problem-y tangle. We all have those days or weeks or years when everything seems to go a bit wrong and no matter how many solutions you dream up the problem remains, steadfast and mocking.

The days when you realise you have run out of nappies at the exact same second that one is ceremoniously filled, when you spill red wine on your new top or miss the bus or forget to send an important email or the boiler breaks. All pain in the ass, tooth grinding problems, thankfully all with solutions of some kind.

Last night as I snuggled under the blanket in front of One Born Every Minute my pertinent problem was that I couldn’t write the post that I had planned to because my camera batteries have run out, and, erm, no one tell the husband, but the charger may be broken. Thanks to my newly discovered ‘no problem’ attitude I threw my blogging plans to the wind and ate chocolate and welled up at all the labours and births and tiny babies.

When the final advert break rolled my problem was that I couldn’t be bothered to move as far as the kitchen to get a cup of tea. So I didn’t bother. One advert made me pay attention, mainly because there was an absence of the usual whoompwhoompwhoomp bass line thud and bright, flashy colours that normally flood the room when people try to sell us stuff.

Ah, I thought, the new Time To Change advert. One I’ve managed to miss since it aired for the first time the other day – which is shocking really, given my vested interest and the fact that I am known to zone out come 7:30pm and spend my evenings lit by the warm, flickering glow of the TV.

The whole Time To Change ethos is something that I wholeheartedly agree with although not necessarily something that I purport to know all that much about. From what I do know, they exist to make efforts to break down the stigma or taboo or whatever you want to call it that surrounds mental illness in a very big and very real way.

Mental illness should be spoken about, I think, it shouldn’t be something that sufferers have to squirrel away and pretend isn’t real. It’s an area that needs to be brought out into the public domain in a positive way – if there is such a thing – to bred understanding and support from the fear and misconceptions that exist.

I like to think of myself as pretty open and honest, I would always be happy to talk to anyone about my experiences with my own mental illness if I was asked to, but saying that I would never introduce myself all ‘Hi, I’m Clara. I like Party Rings and I’m a bit maaaaaaaaaaaad’ firstly because I hate (hatehatehate) the use of the word mad (or crazy or insane or doolally or bonkers or mental or…) but most importantly because I am not an illness, I’m a person and a personality and hopes and dreams and dislikes and interests far bigger than any illness could ever be.

So yeah, lets talk and lets be open in the hope that more and more will understand and care will improve and discrimination will end and all the rest of it. For this ambition, I am whooping and cheering all the way for Time To Change.

But…

I might be wrong here but I imagine that anything, absolutely anything, released into the public arena by any charity or organisation working to change the perception of mental illness is scrupulously checked and double checked and rewritten and reworked and tonnes of other things so that by the time the finished product reaches our blanket wrapped, TV zombified selves it in no way accidentally portrays an image of wooohooo guys we’re all flipping crazy but it’s ok, you can still talk to us, we don’t bite. And for the most part, it does. But I have one little problem.

…when I found out that my son had a mental health problem

…my daughter had a mental health problem

…my friend had a mental health problem

What is wrong with mental illness? Does that not do the job perfectly in summing up what is, in fact, an illness?

It’s funny – the husband and I were watching the news earlier and in a(nother) piece about the snow a reporter was talking to the son of a elderly woman who was snowed in. This man suffered from a heart attack on Friday. Friday! It’s Wednesday lunch time and he’s sat at his kitchen table sipping a cup of tea and wearing a nice jumper. Until fairly recently a heart attack was fatal, people who suffer from a heart attack are not usually brewing up and having a chat in their chintzy kitchen a mere five days later.

Similarly cancer is no longer what it used to be. The research and the improvements and the advancements mean that so many cancers can be treatable now. All this is just amazing and both of these things are big, scary illnesses that are not uncommon, not unheard of and very much out there in the public arena.

But you’d never hear anyone say ‘I have a cancer problem’ or ‘I had a bit of a heart attack problem last Friday but I’m right as rain now…another tea?’ would you?

So why coin the phrase mental health problem? The opposite of health is ill health illness – tomayto tohmahto – doesn’t that do?

I honestly don’t think that I have a problem with my mental health. I know that I have a mental illness. Can’t we just call it what it is? Or is this just my problem?

Everything

I wrote down what I wanted to say because I knew it would get lost once opinions and information flew around the room and because if it was written down I would have to speak it, a promise to myself.

My head was in my phone as I waited to be called out of the pink glow of the waiting room. I read and checked and double checked what I wanted to say even though I had it committed to memory word for word and bullet point by bullet point.

I have lived with this for nearly two years. I have spent every day trying, just trying. I know where the illness ends and I begin even when it takes over and the only bit of myself left is hovering above my prone body, floating to the ceiling and looking down on what I look like when it threatens to take me over.

I talk myself through panic attacks and guilt and the impulses to drag something cold and deliciously sharp across my hot, soft skin. I understand. How could I not after more than twenty months of trying?

I do want help I really do. I want support and guidance and someone who can coax me back out of my shell and stand close as I pick myself up, battered and bruised but with all my thoughts ordered, rationalised.

I have my own coping mechanisms and they are why and how I have come through all these months without a single physical scar, they are the reason I managed to avoid hospital and avoid worse.

What I want now, what I need, is to go back to the beginning and actually say out loud all the things that I never did at the time. I need the distance that verbalising things gives, I need to say the words and hear myself as I do. I need someone to help me understand them so that I can learn that it’s ok and this is why and maybe next time…

Suddenly a hand is being proffered in introduction and I rise and the fake leather cushion creaks and squeaks as it expands back into shape as I am lead into the windowless room with the forms and the tissues. There’s always tissues. I never cry.

I settle into the chair against the back wall. It’s blue and it’s scratchy and one of the front legs is loose. I kick it idly with my heel while my psychologist clicks her mouse until my details fill the screen. I peer out of the corner of my eye and try to read what it says.

June. It was June when I first made the call? I count the months in time with the thud of my Converse on metal.

Thud.

Thud.

Thud.

Thud.

The leg moves half an inch and I grip the seat to steady myself. Feet firmly on the carpet I register that it has taken four months to get to this point.

I look at my palms and I think while eyes locked on her monitor the psychologist scrolls and scrolls and outside a car drives past and crunches into gear. I have appointment palms, pink and hot and covered in the sheen of my own sweat that tries to compensate for my dry mouth when I feel under pressure to say the right things.

I go over and over my bullet points in my head until I can see them so clearly it’s as if they’re scrawled in ink down my fingers. And then I realise something. Suddenly it’s really obvious when I feel the most shit. The times when I’m a bit slower to pick myself back up again, a bit more anxious than usual.

It’s this.

It’s the constant asking and begging and pleading for help. I have asked and asked and asked but every time, every single time, I have been put on hold or redirected or turned down or overruled.

And it kills me.

Harder than almost anything else is siting in a box like room sharing stale air across a table with a stranger who has boxes to tick and risks to assess and I just don’t quite fit and they just don’t quite understand.

Because its not just about boxes as ticks and scores and totals and whatever the preferred method of treatment is in that given month. It’s personal and varied and emotional and there isn’t anywhere on the forms for that.

I have to answer whether I think people would be better off without me, whether I’d be better of dead.

Dark.

I answer honestly. I answer yes.

Do I know how I would do it?

No. I have no plan that I would follow or processes in place. It’s not like that for me and as much as I think I’m not worthy to be a mother sometimes I would never ever take myself out of my childs life, just like that.

But these two boxes don’t tally. If you have thoughts then you must have plans because that’s what the official form says and I guess training doesn’t cover any what ifs outside of that. Grown ups shouldn’t colour outside the lines. I try to explain but it comes out jumbled because frankly I find discussing the fact that sometimes it hurts so much that I want to die is pretty…ugh.

I explain how I have made it this far. I explain the revelation that came to me. Is it a revelation? I ask. In a room lit by strip lights and filled with the buzz of a 1990s computer and the stare of this woman who is there only to judge exactly how broken I am my conviction feels just as likely to collapse underneath me as my chair.

When I was pregnant I had everything that I ever wanted; a husband who is gorgeous has a wicked smile, brilliant sense of humour and kisses that make me melt, a baby in my belly, a lovely house in a lovely town, Cath Kidson wallpaper, two cats…everything.

And then there was all of that and a baby and that should have (could have?) just been the most amazing thing in the world. I had it all, the girl with everything.

Only my hormones went a bit mental and sent me a bit mental and made me think that I didn’t love my own baby and that I was going to throw her down the stairs and drown myself in the bath.

Every night for the first twelve weeks of her life as she lay on the husbands chest and learned to hold her tiny new head a little bit steadier on her neck or flex her little pink fingers around the corner of the blanket that cocooned her against her daddy I lay in a hot lavender oil bath. A bath I had been told to have daily by the midwives to help me heal after the birth, a bath that the husband made sure that I had because it was doctors orders.

A bath that I would sob into, hot tears rolling down my cheeks and splashing into the water that lapped at my chin.

I would lay there for a long time just staring at the tiles on the wall opposite me while my skin reddened and wrinkled and life carried on outside the locked door. If the baby cried I turned the taps on so that I couldn’t hear. I would slide down the smooth plastic behind my back until I was submerged, looking up at the blurred ceiling from underneath rippling water.

I didn’t want to come up. I had to stay there.

Every night.

And then there would be a noise or movement or something and time suddenly sped up and I pushed my way up to air and coughed and gasped and took hungry lungfuls of steam filled air and pushed the hair from my face. What the fuck? I don’t want this. I have to get out of here. I rip the plug out on its chain and clamber over the edge of the bath dripping all over the floor and my discarded clothes and some magazines and a forgotten dummy. I rub my hair aggressively with a towel before hanging it across my shoulders so that I can pick my way across the floor and click open the lock. I can’t be here. I have to go.

I leave wet footprints behind me all the way up the stairs in my hurry to get dry and shake the feeling that’s hanging over me. A feeling and a pressure and something outside of me, bigger than me, telling me I should have stayed under water.

Five minutes later, avoiding the damp shadow of my hurried path up, I walk shakily down stairs and into my family asleep on the sofa. The room smells of baby and the husband and the congratulations on your beautiful little girl flowers. I stand leaning against the door frame and watch the rise and fall of their chests in the half light, listen to their snuffled sleep sighs. I feel jealous. Empty. Nothing.

But I’m ok. They’re ok.

I had everything but something had made it sour, made me ill.

And now? Now we have a council house that is still unsafe after more than nine weeks of graft, debt, no job so no income…we lost it all but we are finding each other. Which is such a fucking cliche it makes me itch but its true.

I have a husband who has been my rock and we have a daughter who does love me and who I do love back.

When I was well and life was lovely and wrapped in Cath Kidston print and money and ease I was fine and then I wasn’t. But now look at all that has happened in the time since. The husband left his job, we lost our home and our money and our cats. He lost his wife and she lost herself. We left the lovely town and we fought and battled for housing until we got a total dive…

But we made it though. I made it through. Just how strong must I be to have done all of that while I was empty and shattered and broken and our world was falling apart?

She’s not taking notes anymore, her pen rests in the spine of the notebook and her head rests on her hand. She blinks. I take a breath and shuffle in my seat. I’ve more than said my piece.

Five slow seconds tick by. A dog barks outside. Someone comes and goes in the room next door. The screensaver starts up on the computer (it’s the fish one).

She ticks another box.

‘In our meeting we decided that something called behavioural activation would be best for you. It’s the step below CBT if you like. It’s all about getting you back into doing things slowly by planning on a time table. For example, on Monday you could try to wash up. That would do for a week. And then I will call you in two weeks and we can discuss your readiness to move towards more tasks until you’re functioning normally…’

Are you joking? How…wha…How can a timetable and chores see me beat this?

She carries on. In that room I managed to say more than I planned to and I saw it all more clearly than I ever have before.

Isn’t that more important than continuing the battle for some counselling? All I want is some counselling.

I washed up on Monday night. And then I cuddled my baby and tickled her to make her laugh so she would curl up with delight and nestle in tighter to my chest so I could bury my nose in her hair and smell her smell. I promised the husband that I can do this and we’ll be ok and I’ll be ok while I wrapped my fingers around his and rested my head on his shoulder.

Everything will be ok. It’s my family that will continue to see me through, nothing else.

C7: Where The Mentals Are

My old psychology lecture room. I walked the same floors as I did ten years ago, to the same room that I sat in doodling while studies and theories seeped out of the tutor’s mouth and bounced off the walls. The hot afternoon sun beat in through the open windows casting long shadows as the marker squeaked across the whiteboard and I planned my weekend. It was also the room that housed my exam results one August a decade ago. I was scared to go in and then scared to look and then ohmygoodnessIdidok!

Everything is the same but different as I walk in after all this time. The chairs all face the opposite wall, the whiteboard has been moved but cobwebs still cling to high corners and sway gently in the breeze, the sun still pours in through the windows. No longer a room where I would study psychologists and daydream about seeing friends and boys and boyfriends on Saturday, it had become what I desperately needed to be a glimmer of hope, of help, and a way to access treatment.

I jumped through all the compulsory hoops (again); I filled in the forms, scored my mood out of eight and ticked the relevant boxes to get here. The next step. The place where I would decide what treatment would be right for me to help me to recover. It struck me as odd that the best way to do this would be to assemble the mentals sufferers of anxiety, depression, panic disorders, phobias and similar in an enclosed space, close proximity, away from home and extremely publicly.

I feel far from comfortable about being in a room full of people with various mental illnesses of varying degrees of severity. In no other aspect of my life would I ever smile at someone I had never met before and, holding out my hand in greeting, divulge that I have a mental illness before I have introduced myself.

A PowerPoint presentation begins; every cliché, stereotype and misnomer about depression and anxiety presented in 72 point comic sans as each slide is read aloud for emphasis.

Stress.

Low mood.

Stress.

Common.

Change.

We all have to deal with stress, the projected slides tell the room, sometimes we don’t deal with it correctly and it becomes a vicious cycle. You, yes you, can learn to change that vicious cycle. We will give you workbooks and homework and group meetings where we will explain to you in fine detail all of the mistakes that you are making in life and how to put them right. And then if you work really hard you won’t be stressed anymore.

Shit, I’m in the wrong room. Did my feet carry me here because it’s a path that they were so used to treading? I should really put my hand up or something. Or just leave…A quick glance at the sign stuck with blu-tac at a jaunty angle on the inside of the door tells me that I am in the right room. Oh.

And then I want to leave. Are you telling me that this is a choice that I have consciously made for myself? I have been living this for nearly eighteen months, if I could have changed it I would, it’s taken everything from me. It’s taken me.

Break flashes up onto the wall, projected in looming letters (I hate comic sans) and bends and distorts around the woman who moves forward to tell those who want to stretch their legs to be sure to return in five minutes. I want to go. I want to sulk and flounce and close the door behind me on my way out. This isn’t what I need to hear or anything close to what could help me. I soak in my own private pity party on my chair in my old psychology room in my old college missing my old life. The last thirty minutes told me that I can choose not to be this way, but they also told me that depression makes you cry all the time. Over nothing. I want to cry; nothing.

The slides start up again. Not one person left the room. More animated bullet points about stress and its vicious cycle. The pity drains away and leaves anger in its wake. Slide after slide after slide of information about workbooks and healthy eating and exercise and homework and courses and spider diagrams and flow charts.

A person who feels a little low may put things off, for example, they may keep putting off washing their hair because of lack of motivation.

What about looking after a newborn baby? What if I can’t even look after my own child? I didn’t choose this. Fuck washing my hair. I want help. I want to be a mum.

My inner voice screams.

I have just ticked a box to say that I think about self-harm, that I think things would be better for everyone if I wasn’t around. How is any of this relevant and why should I give a shit?

Ten minutes later we are dismissed. I float out of the room, outwardly blank but internally screeching.

Cuckoo Cuckoo Cuckoo

Writing about my PND helps me. Most of the time. Sometimes the simple act of emptying my mind out through the keyboard is enough to make me feel more settled. Sometimes, if I’m lucky, my thoughts find order in themselves in the translation from brain to screen, sometimes an insightful or lovely comment will shed some light on everything.

But, and here’s the shitter, depression is extremely hard to put into words. Thoughts and feelings all seem to exist in a transient, abstract way that makes them hard to grasp for long enough to make sense out of them.

It’s exhausting just trying.

Having one thought rattling around in your brain all day, poking and poking and poking at your consciousness is hard. Poking and poking and poking and dragging you down down down.

Not all but some of these thoughts need to be de-scrambled in order to be pushed aside. For example: you can’t cope, you’re a terrible mum.

Why? Why do I think that, allow it the space in my head to affect every move that I make?

Only when I can reach out with a sure enough hand to grasp a train of thought am I able to try to dissolve it with some level of rationality.

I have coped. I have done it before, there’s no reason I can’t cope today. I’m not a terrible mum, I’m the best mum that I know how to be right now. And that’s all I can do.

Isn’t it?

Left unchecked the thoughts echo and bounce their day away inside my head, with a firm hold they can be blurred around the edges and made quieter.

That’s just one thought. One lonely sentence that pops up like a vengeful cuckoo in a clock every fifteen minutes or so, but there are others. I’d say I have enough mental destruction going on to account for every waking minute of the day.

So that’s part of the reason that I write. Because it brings rationality, sense and order to something so fucked.

But it is hard, and as much as I wait for the inspiration to smack me in the face I have never been able to put together an articulate enough collection of words to summarise everything neatly.

Yesterday I read this. A single sentence nuzzled in between some powerful paragraphs written by a very clever man indeed:

“I don’t feel able to feel a feeling without feeling that feeling isn’t actually feeling that feeling.”

It resonated. It made sense. It’s often what I have been trying to say without realising that it was my point all along.

Thank you, it’s horrible but it helps when someone unknowingly reaches into your mind and unknots everything that you have in there.

[Shameless plea: The MAD (mum and dad) blog awards are open for nominations and if you want to make me squeal with delight it will only take a minute. You can nominate your favorite blogs here.]

Irresponsible

I’ve been away, again, for a week now. The week started with me being literally pinned to the bed, unable to move or blink because of the crippling weight of my depression. Tremors or panic attacks would break up the endless hours.

I couldn’t eat, couldn’t drink, couldn’t go on.

Now I am managing to force a slice of toast into my dry mouth once a day. I can’t stand for the time it takes the kettle to boil because I feel so weak and dizzy. My heart constantly pounds and is exacerbated by too much movement, making catching my breath hard work.

At the beginning of the week I couldn’t even speak to the husband on the phone. It made me too anxious. I have been trying to work out why, what it is that makes me want to hide. Total lack of self worth? Probably. Fear of responsibility? Definitely.

Coming away has relinquished me of all responsibility. I don’t need to worry about what to make for dinner or whether the washing needs doing. I don’t have to put on a happy face for Beans or reassure the husband that I’m ok. Frankly I’m too weak to deal with any responsibility right now.

The husband and Beans might come to see me tomorrow. I miss them both desperately. I so want the husband to wrap his arms around me and tell me it’s all going to be ok. I so want to scoop Beans up and cover her in kisses.

But I’m terrified.

Will I be able to cope? Will it be too much for me and leave me sprawled in bed, shaking and pinned to the mattress?

I keep trying to tell myself that I am doing the right thing by being away. That I need to concentrate on me, to get to a level where I can function again before I am any use to anyone, let alone an extremely active toddler.

But my head swims with thoughts; what kind of person ever thinks that they don’t want to see their baby? How can I even think things like that?

I wish there was an easy answer. I wish I knew what to do.

Thump

THUMP THUMP THUMP.

My heart pounds hard and fast as I gasp for breath, my body shakes violently causing all of my muscles to cramp and ache.

Maybe I had it wrong, all this time I have said that the medication isn’t working, was my depression just getting worse and worse all along? Now I have to start all over again.

I can’t calm down. For the first time the last strand of reality that I have held onto finally snapped under the strain.

THUMP THUMP THUMP.

I’m dying. This is it.

THUMP THUMP THUMP.

For all of this time I’ve wanted to escape myself. For all of this time home has kept me safe, my comfort blanket when everything heightened my anxiety.

Home is gone, I don’t feel safe there anymore. This has come at the worst possible time and I can’t cope.

THUMP THUMP THUMP.

We call the emergency doctor after being told by my therapist that if I don’t calm down they will be able to prescribe me something. Anything. I can’t do this anymore.

THUMP THUMP THUMP.

The doctor tells me to do some online CBT to learn how to control my panic. I breathlessly try to explain that I can’t, I can’t move, I can’t breathe. I’ve gone beyond deep breaths and calming thoughts.

THUMP THUMP THUMP.

Once again I am half carried half bundled into the car to be taken away, back to my parents, back where I can calm down.

THUMP THUMP THUMP.

Day four of new medication and it’s messing with my head. I’m not rational anymore. I’m panicked and paranoid and detached.

The husband is going to leave me, Beans won’t remember me. Worst of all, I don’t even care. I can’t even bring myself to call home, the guilt and the paranoia and the fear of everything has made me mute.

THUMP THUMP THUMP.

I can’t eat. I force myself to drink. My parents drift in and out begging me to have some food, their faces contorted with worry.

I can’t move.

F*ck You PND

Today is a good day and god does it feel nice. Every good day I have seems to enable me to get my head a little bit further above the water. Every good day I have makes everything just a tiny bit clearer to me.

Good days come and go, and I know I have a long battle ahead of me. But I know more and more that I have to take control of this, I can’t let it control me. I need to find my way through.

But, I didn’t come here to moan (I know, right?!) I came to be positive and happy and say fuck you post natal depression, you fucking suck. Continue reading

Missing Memories

Taking medication for PND is a bit of a catch 22 for me. Boo was around eight weeks old when I went to the doctors and made my plea for help. I was given anti-depressants straight away. It took about four weeks before I stopped feeling the side effects (dizziness, nausea, headaches, sleeplessness, mood swings, and heightened anxiety – all lots of fun) and they started to work properly. It goes without saying that without them I would be a total mess, probably incapable of even the smallest of tasks.

But with them isn’t easy either. Yes, they take the edge off my depression, they dull my feelings just enough to mean I can at worst crawl through a good day with fairly good functionality. The tablets affect my sleep, either I hardly sleep at all or if I do I have the foulest vivid dreams that leave me a bit shaken for the following day. Continue reading