Category Archives: Borderline Peronsality Disorder

Can I have a do-over?

Or at least that’s what I text my friend the other day.

These last….six months have been relentless. I haven’t been able to catch my breath from one moment to the next. And that has been exhausting.

For someone who requires stability and routine in order to function from one day to the next….the last few months have left me spinning. My very own waltzers have been increasing in momentum….my homing beacon isn’t only just switched off…it’s in a different universe from what I can tell…my swans wings have been flapping almost as hard as my feet have been paddling and still…..the war of attrition has sucked me back in.

I’ve changed jobs, to one that whilst…requires less hours…it requires much more head space and much more mask wearing. I’m on my own for great swathes of the day. That’s a long time to be with my own thoughts.

My very own Everest has beaten me for now. I could see the summit…and then I slipped back too far to reach it this year.

Childcare has been a nightmare, I get that having kids and going to work was my choice. And I did it for all the right reasons. But its a minefield. And mines are detonating everywhere I turn.

There’s been a bereavement…which I found out about…by accident it would appear. Actually there is no appear about it. That’s exactly how I found out.

I’ve had to meet loads of new people. In fact its a prerequisite of my job – forming relationships. The irony of someone like me having to form and build relationships for a job. That’s hilarious.

And perhaps most concerning….I’ve come off my antidepressant.

Not my anti psychotic. We increased the dose of that and removed the antidepressant. At first it was accidentally. In the maelstrom of changing jobs and all the drama that ensued with the big green kitchen company….I forgot to take it. My sleep didn’t change, I woke up in a good mood….so I ran with it…..

The first month was amazing. Everything was fantastic. No withdrawal….no sleep issues…I was happier and more content…awesome right?

Then the second month happened…the nightmares came back, the insomnia came back. I was so tired I cried in a car park because someone snapped at me…I felt physically ill with exhaustion. My bones hurt. I was so tired….but I just couldn’t sleep….and when I did sleep….back to the beginning…back to the violence of past relationships, back to seeing my girls die before my eyes….back to waking up screaming and drenched in sweat…there was just no respite.

Then the third month came….the nightmares are less. I still dream. I still have exhausting dreams, but the antipsychs are keeping me….well sane I guess. My sleep pattern is some bizarre version of fucked up. I’ll sleep for 10 hours one night and not at all two nights later. I’m assuming it’s just my body trying to work out its own thing….I’ll ride it out. I don’t want to go back on the anti depressants.

Not because I have anything against them….but because…the benefits of not being on them are now outweighing the benefits of taking them. And thats part of taking control of my own health….learning when I need the boost and when I can manage on my own….

But in saying this….it’s not been all bad.

It’s kept me on my voyage of learning who I am.

I swapped jobs to another role within an international company…and I love it. It pushes me, it engages me…this could be a career. So I’m passionate about it….the big green company job is another post entirely. And one I will be writing, and one I will tag them in. Because that was a soulless,destroying company and hell will rain down on the heads of the management before I’m through with them…..

I’ve maintained some good relationships with people I thought I’d lose over the natural course of time. But now it’s like, because we don’t have work binding us together…we have to make the effort….and that’s nice. It’s reinforcing the lack of scarlet in me at the moment.

The bereavement…I genuinely…I don’t care. And thats not my BPD. It sounds horrible, but the woman who died….she hadn’t engaged with me for years prior to that, and her son – my father, well he was no better. So finding out by accident was a bit cruel, but hey….so what?

 

So overall, no I don’t want a do over. I’ve learnt lots about myself in the last 6 months. I’ve learnt how resillient I am. How strong I am. How I can adapt as needed.

I’ve learnt that actually, I really am in control of my BPD. And that, that’s amazing. Thats real progress. I really love some aspects of my mental health illness… I still love the empathy I have because of it. I really love how it means I can help people. I love the way I see sounds and taste words. I’m fascinated by the way my mind works.

 

I hate the way I don’t have that much control over my emotions. So I’ve taught myself to control how I react to my emotions. Thats a life skill, even neurotypical people struggle with.

 

So fuck it, overall…I’m still winning this battle. Or at least…I’m keeping from being overthrown. And for now. That’ll do.

This kid’s not alright.

So young. Sat on a bench, her short legs just hanging there listlessly, unable to reach the ground. But without engergy enough to swing. Her scuffed shoes just there. 

All encompassing, pervading every facet of my being. Darker than the blackest black. The stuff emo kids can only dream off. So thick it’s a relative forcefield around me. Ironically the one thing keeping me together was the same thing that was destroying me.

Loneliness.

Not the kind that a text from a friend, or a smile from a stranger can help stave off. But the kind where you know you’ll never be free of it. The type where you’re surrounded by people, quite literally, but no one can reach you and, most crucially, you can’t reach any one.

It’s only now, in my stronger self, with my new learnt techniques and medication, that I can look back on my darker times and start pinpointing what the emotions I had were.  I can identify fear well now, that was an emotion I only really felt in my mid to late teens, other periods of my  life seem to be conspicuous in the absence of fear. Sadness, I was never sad, I was always…..melancholy. Sad implies a cause and therefore a solution. Acceptance, not from people, or even myself, but acceptance of the way I was/am (interchangeable at times). Etcetera…I felt happy at times…like on journeys with my step dad to watch the football, or getting a good mark on a piece of work I’d really worked on, or when I completed prose that I felt told the story….

I’m painting the picture of a very unhappy child, but I wasn’t. I was certainly grumpy or crabby or mardy. Now it’s pretty obvious that actually it could have all been avoided pretty easily.

No, I wasn’t unhappy. That darkness I was speaking of? That’s loneliness.

It is only with time and hindsight I have learnt that. It’s still something I battle with now. Which is tedious given the fact from the minute I wake til the minute I sleep I’m with people. And even when asleep, I’m not alone. I’ve got the good old night mares to keep me company.

We all know my back story, I’m 27, had 5 different psychiatrists, 6 different counsellors, 3 psychologists, 2 overdoses, 5 different anti-depressants, 2 anti-anxiety drugs, and now a lovely cocktail of happy pills and none crazy pills, 4 diagnosis’ (Depression, General Anxiety Disorder, Chronic  Anxiety and now Borderline Personality disorder with an addition of dissociative and schizophrenia behaviours thrown in for good measure).

So what does that have to do with the price of fish?

Simple really. As a child, I couldn’t name my emotions. I didn’t understand them. Even now as an adult, I have to focus to see what the cause behind the emotion is. I mean, happiness is easy to determine, as is melancholy. But anything beyond those two, well thats harder. I feel anger, immense anger. But only temporarily, very fleetingly. The only emotions that seem to take hold and stay are loneliness and melancholy.

But admitting to that, isn’t allowed. How can I be lonely when I’m married and surrounded by friends?

Well I’ve figured it out now.

How can you not be lonely, when you don’t like being alone?

Which sounds absurd, because I love alone time. But never silence. I can’t sit in silence. Which is difficult, because too much noise overstimulates me and makes me cranky. But when I’m alone, I have to have music. Always music. It acts as a dampener to my thoughts. I can’t think too much when I’m concentrating on lyrics can I?

I know I’m not the only one who struggles with this. Loads of people can identify with the feeling of being alone when at a party.

My problem is, I can’t take being alone for what it is.

I have to over analyse. I have to over think. The ball of neuroris that is my brain can’t tolerate too long without input from other sources. Otherwise it takes off at a tangent and colours everything green.

Remember, everything has a taste, colour or sound. Thursdays taste of bacon, my teeth itch, lonliness is green.

Back to that kid. That young girl on the bench in her playground. She was eight. Eight. One year younger than my eldest is now. I still remember it. Clearly. As if it was frozen in time, an image I get to replay every day. That young kid. She wanted it all to stop. All to go away.  Her heart hurt, her brain hurt. All she wanted was for it to stop. To stop and end for ever ever.

See, I’ve been battling this for longer than I can’t remember.

I’m okay now. But acutely aware of the fact I’m still in this war of attrition. Knowing that I’m only okay because my medication stop me being anything else. Knowing that too long without the tablets and it all comes back. Knowing that I still don’t have the energy to fight it again. Not yet. I don’t think I ever will.

I don’t have the energy to fight and still be a good mother. To fight and still be a good friend. A good wife. A good person.

But that’s fine. At least I’m honest about my crutch. I’m honest that I need the pills. I’m all talked out. All lessons learnt. All opposing thoughts done. I’ve done the years of therapy, and psychiatry. Time served. I’ve spent over half my life in therapy. Therapy can’t change who I am.

And I am that neurotic mess who hides behind a face of makeup, hard walls, sarcasm and apathy. I am that person who will say something cutting just because she can. I am that person who will always be there for my friends. I am that person who will burst into tears because her hot bread has been toasted too much. I am that person who will learn, learn and learn some more. I will set myself unachievable targets and hate myself for failing. I will always be my harshest critic. I will always be battling my own brain.

Because I have no choice. I can’t be anything but who I am. I can’t be that happy, easy going person I want to be. I can’t wake up in a good mood when I’m coming round from a drug induced sleep. I can’t be that person who always has a kind word. I can’t be that person that other people gravitate to, because she makes them feel good.

 

I’ll forever be that person, that makes most people feel slightly uncomfortable, despite them not even knowing why. I’ll forever be that person who’s more spikey than cuddly. I’ll always be that person, who people think is joking because no one can be that mean.

But, I’ll also always be that person, who is the first to help. The first to offer solace and comfort. The first to empathise. The first, and last, to stop caring.

Me and my resting bitch face, may be unapproachable. We may make people feel uncomfortable.

 

But, something I’ve learnt over the years? That’s usually because in me, they see parts of themselves they don’t like. They see in me, the chance of the battle they will have to face. And no one likes that. No one wants to admit that mental health illness can, and will, attack anyone. They want to think its only the weak. It’s only the lazy.

.

And in me, they see that unfortunately, its indiscriminate. It will take anyone it desires. It will render even the strongest, warmest, move loving of people. And turn them into a shell. It will make them feel that lonliness I live with. It will make them feel like no one around them wants them or needs them. It will twist your own brain so much you can’t trust it. So by extension, you don’t trust anyone.

 

 

Oh. And I’m a total bitch…..

BPD and me…my new realisations.

I appear to be writing more frequently about my BPD at the minute. I’m not having a relapse, but I am acutely aware of it at the moment.

I’m tentatively telling people about it again. Mainly because I’ve been seeing flashes of the scarlet me coming through. But also, because every so often I gain a new level of insight. It’s like all the time my subconscious is working on it, trying to unravel the thread and help me. Help me to know just exactly what is going on inside my head.

Recently I became aware of how even missing a single dose of quetiapine will spark my absurd behaviours and brain whimsy.

My BPD causes me to suffer with dissociation. This means that I have a constant “out of body” experience on my life. Like I’m looking down on whats going on, but I’m not really there. The quetiapine and mirtazpine mean that for the last 18 months that hasn’t happened. Well. Not as bad as it was. See, I have great swathes of my life that I don’t really remember. The mundane things, the day trips to castles, the grocery shopping, passing my driving test….these things happened through a curtain. I could see, smell and taste. But I couldn’t engage properly. It means my recollection of these things is hazy. It’s why I’m in the habit of documenting life through photographs.

My grasp on what I actually look like hasn’t improved. I’m still surprised when I look in the mirror. I still see my self as that ugly sewer rat. I’m sure other people do too. I know, logically, that I’m perfectly average looking. But I can’t believe that. So I cover up the insecurity and low self esteem with makeup and bravado. It’s a tool in my armoury that gets me through.

My paranoia is at an all time low. Unless I miss a dose of the Quetiapine. Luckily, I have a close friend I can rely on to give it to me straight. She soon tells me if my reaction to a situation is within normal parameters or not.

My control over my emotions…well. I’m there. I’ve grasped it sort of. I know how to present a neutral face. I’m still the swan paddling furiously, serene to everyone but hectic underneath, and I still don’t have a homing beacon. But I’ve learnt to put a facade on. “If it’s not okay, it’s not the end”. I get described as “cold”. Which I’m fine with. I’m not. I’m about the most loving, spirited person I know. I’m legitimately batshit mental, I laugh so hard I cry, I get so angry I can’t see, I love so hard my heart hurts. But each, and every single time. “Are you ok” or variations there of, always, without fail get answered with “yeah I’m good thanks”. Because, not only do people not want the legitimate answer, but I don’t know how to give it. How do you respond to “are you ok” with “I’m seeing and tasting words, my thoughts are too loud and I’m over stimulated” which is what my “Im good thanks” translates to. You can’t. You can’t give people that answer.

Which brings me nicely to … yes, I still see words. I still taste them. I see sounds…not in the cool way with colours, but in shapes and patterns. Remember old alacetel phones? The ring tones on them were little red cuboids with rounded corners. Thursday still tastes of bacon.

My self esteem is largely the same. I still use bluff and bluster to get me through most situations. I have a telephone voice I use with nearly everyone. I still ignore most phonecalls. And most social situations. Unless it’s a random spur of the thing. I just can’t handle it.

So have I really come that far in two years? If I still avoid situations? If I still wake up screaming in the night? If I still feel like I’m on the waltzers and want to get off? If I still question everything…why did they say that, why did they look at me like that, are they laughing at me, what do they want from me? I still lie in bed and feel like the words in my thoughts are too loud  and too bright…like I’m hurtling head first into the back of a truck.

I have. I’ve come a long way. I’ve had a job for the last 18months, I’ve maintained a couple of friendships, I’ve helped people. I’ve been good and kind, just because I can. Not because I know it’s the normal thing to do. I’ve stopped getting stuck in the memories that I wish I could rip out of my mind and pour bleach onto.

But I’ve also become quite numb. Things that should devastate me…well I can switch off to them. That’s brilliant. I don’t obsess over the negative now. I’ve learnt that my emotions are fleeting. And something that hurts in that second, well, in the next second I’ll probably have moved on from it. Because thats what I do. Ultimately, afterall, BPD is defined by being unable to regulate emotions. Now I’ve learnt thats why I can’t…I’ve stopped hating myself for it. And instead I’ve educated myself on suitable responses to normal , everyday situations.

Have I forgiven the people that have contributed to making me this way? No. I never will. Have I forgotten them? No. Does it consume me still? No.

 

And thats that. That’s why whilst it doesn’t seem like I’ve come far…I have. I’ve come miles. I’m still on a journey with no destination….but now the journey isn’t horrible

 

 

If it’s not the dreams it’s the reality.

Screams rent the stillness of the night. Blackness surrounds, a crushing weight lays on her chest. Wrapped in a prison of sheets, her legs kick as the sweat trickles down her back. The screams stop, the panting begins….on her feet looking for her nearest exit…her mouth tastes of pre-vomit acid, her stomach roiling against the images her mind conjures for her. Memories, half embellished, half true to life…horror movies playing relentlessly whenever she sleeps.
At night, the fears and anxieties she manages to gloss over during the day: they fight back. Whilst she lies sleeping, her conscious mind switches off….none of her defences are there. The armed guards have stood down for the duration. The deflective humour, the scathing sarcasm, the self-deprecation…is all gone. All that is left is her imagination…an imagination that appears to be determined to do what her illness couldn’t: send her insane.
For her dreams, some: they’re just memories. 1080P HD images of her worst times, on an endless loop. Other times; well they’re tricks her own brain plays on her. Her own brain becomes her tormentor (not unlike it is during the day). It plays terrifying fiction videos of half buried bodies down the side of the mountain, each face being someone she loves…Pup 1 …Pup 2….Mum….Sister…and on and on….all the way to the bottom where she’s greeted by a masked man ….. or sometimes, perhaps worse…the dreams….they’re so real she can taste them…and it’s just fear after fear being realised. How many times must she watch her children die?
See, even when I’m sleeping my BPD is against me. Right now, surrounded by trigger after trigger….I’m wondering how I manage to get through it. How I manage to stay one step ahead of the battle and one step ahead of my own mind that is working tirelessly, relentlessly against me. It’s like I’m in a whole other world where I can smell the food….but can’t touch the silver wear.
I fight all the time, especially at the moment…the weather…work…university…everything seems like an uphill fight. I’ll win. I always do. But I can see my behaviours starting to manifest again…keeping exits to my back, or standing in the corner, making hot drinks just for something to occupy my hands, black humour, procrastination…all my little coping mechanisms. And sure they make me odd…but they do something to stem the tide of noise and sensory overload.
Do you know what it’s like to lay in bed with your eyes closed, waiting for sleep and suddenly feel dizzyingly sick as in your mind’s eye your rushing into the back of an articulated lorry and you’ve no way to stop? An adrenaline rush as I lay there doing nothing more than practising mindfulness?
It’s funny really. All my plates are still spinning, yet I can hear them crashing to the ground. The panic is raw in my throat, the blood pounding in my ears…yet still…I’m fine. I’m always fine. Like a swan gliding effortlessly on the surface, beneath it…my feet are paddling madly and my internal GPS system is switched off. I have no homing beacon, so I’ll keep paddling away aimlessly until I happen upon where I’m meant to be. And when I reach there; I’ll take a breath. I’ll stop. I’ll stop to smell the roses.
But in the meantime, my resting bitch face is in situe, I’ll be quiet around people I don’t know, and exuberant with people I do. But all the while my mind is like the waltzers that have been spinning too long and too fast. I’m dizzy and I want to get off.
But as ever this is a journey I’ll never finish, an end I’ll never see. And whilst most of the time, it’s fun and exciting, because hey! Who doesn’t like to be surprised by themselves? At the moment, I’m wading through mud in flip flops.

Why I am who I am and not who I’m not.

It’s been a while since I posted. As ever, life took over. University, work, children….all take over and I get caught playing catch up with little time to think of posting or anything else.

But recently, I’ve felt more and more compelled to. I fought the urge for a while, wanting to be able to define where the desire to write about my mental health was coming from. Now I think I know.

Recently, I’ve watched two close friends struggle with their mental health. Quite run of the mill disorders (not saying they aren’t as bad, just emphasising for a reason). Both of them resisted treatment and help.

As usual my trusted line came out. You’d go to to the doctor for an ear infection, why not a mental health problem? Both of them went. And I’ve full faith that both of them will recover and become well again. I’ve talked with them, one at length, about how important self care is. How we need to put plans in place to help us recover, and remain recovered. Explaining that I see mental health like cancer, you’re in remission, but it’s never truly gone.

My own mental health is holding up strongly. The medication is keeping me nice and even and my moods are stable.

So why am I here now? Because I want to explain why I’m proud of myself. Why I allow my BPD to define me.

 

See, for years I struggled with my illness, before it was diagnosed and after. I felt ashamed. Like I had a big secret, that people would turn against me for. Then I stood up, squared my shoulders and took control.

BPD, causes extreme ranges in emotion, massive insecurity, paranoia, to name but a few things. Without my medication I can’t trust my own brain. I become my own worst enemy, and hurt people around me and systematically and wholly destroy who I am. The scarlet shows through the beige.

So now, every night before bed. I take three little pills. Sleep soundly and know I’m probably going to be crabby when I wake up. A small price to pay to keep me in remission.

 

I’m proud of where I am, of how much I’ve achieved. Even now I still want to cut my losses and run. I want to throw in the towel with university, thinking I’ll expose myself as a fraud. I’m just not intelligent enough for a degree. Thats my biggest thing. It’s the biggest thing I’ve ever attempted. It’s my Everest. I won’t quit. I’ll keep going. Keep plugging away. Keep studying too late, and pushing myself harder and harder until I’ve done it though. It’s becoming integral to my well-being. If I fail at this…..well then I hope my coping mechanisms are strong enough to keep me well…

My BPD is on my shoulder and in my ear though, whispering lunatic ramblings about how I’m not good enough, how I’m just winging it, how everyone is laughing behind their hands at “poor old Beth, thinks she can actually do it”. I ignore her you know. I ignore the bitch on my shoulder.

 

So why do I let it define me? Because it IS me. I don’t know who I am without it. And I don’t want to. Because BPD also brings me empathy, understanding, compassion. It brings me loyalty. Even in my darkest of times she’s been there. Ironically, she’s put me there to begin with after all.

BPD is my longest standing friend and enemy. She colours my thoughts, my tastes, my words. She clouds my outlook, which pushes me to look deeper in to things. Pushes me to further my knowledge.

 

Also, because it’s lead me to this point. After years of struggling, it’s given me the experience and tools I need to help others. It’s driven me into studying a subject that will get me to be able to professionaly help people. It’s gotten me to a stage where my friends can open up to me.

Which, from my own experience. I know is invaluable. When I needed someone, no one was around that could understand my random witterings, my catastrophising. No one could understand why I woke up screaming in the night. Or why I’d watch the same show or film on repeat for 12 hours at a time.

 

But it allows me to be there for people and to help them in the way I need it.

 

So yes. BPD defines me. It’s a massive part of me. So fuck you to the people that don’t understand me. And to anyone that needs a helping hand, a sympathising ear….I’m here. Help is out there.

 

You’re not alone now, and never will you be.

B.P.D; a journey without a destination.

1 year on from my first diagnosis. Not of my life, prior to this correct diagnosis I’ve been given: Depressed, General Anxiety Disorder, Attention Seeking, Crazy, Nut Job, Over sensitive, Loser…..Most of which any one on the journey of mental health improvement have probably been given themselves.

So one year on, a lot happens in a year.

I detoxed off Venlafaxine (I’ll describe this in detail!), changed my medication, increased my medication, attended work shops, and the most important thing? I’ve educated myself and accepted it.

So, detoxing from Venlafaxine…..easily the hardest thing I have ever done. My first obstacle was trying to convince my first psychiatrist that it does have withdrawal effects. Over the course of time of my being on Venlafaxine, 2 years (I finally made it to this horror of a medication after playing with Fluoxetine – HAYLO crazy dreams and insomnia! Sertraline, gee thanks for the hives, Citalopram, useless and I just slept constantly, amitryptaline can’t say I took it long enough to notice any significant benefits) I learnt to never miss a dose. I always knew I had when the dizziness started, a not the kind of dizzy you get from spinning in circles, more a slow motion dizzy, I’d move my eyes from something and two seconds later my mind would adjust to what I was seeing. But as time went on, I was having to take my doses earlier and earlier, and I was on the full, maximum dose of the stuff, but the withdrawal was starting within 12 hours, then 11, then 10……Pharmacists and doctors laughed me out the room when I tried asking for help, I remember sitting in my doctors room crying because of how awful I felt and he just said “that’s not possible”) Well thanks to google I soon learnt that I wasn’t abnormal, this was happening to thousands of people across the world. In November 2014, I went cold turkey….my doctor refused to prescribe me it, and I didn’t see my psychiatrist for another 4 days when I ran out….

Day one.

The dizziness started. It felt like my eyes were moving too quick for my mind to keep up, and eveything was sliding into place in stead of clicking. I got irritable, and shaky. Nausea started. I was over emotional, crying at almost everything. And the ranges in my temperature were amazing.

Day two.

New symptoms met the existing ones. Static shocks to my brain, the only way I can describe that periodic zap that went over my brain, sometimes it even made me wince with pain. The nausea got worse. Heart palpitations. Constantly cold. Week as a kitten, could barely walk. I have literally never felt so ill. I think at this point my husband got really worried for my mental health. I dont remember any thing apart from the symptoms. Not what I was wearing, what I did. I tried to counteract the worst of the symptoms by taking a citrizine based anti-histamine as recommended by fellow sufferers. It worked slightly, I could keep food down.

Day three.

The current side effects weren’t enough apparently. Lets add agonising pain and noticeable random twitching. I wish that was a joke, I’d sit there watching t.v. or talking to a friend and randomly twitch, and it wasn’t small, I scalded myself with tea twice. My brain became so foggy, articulation was difficult and upsetting. My heart was hammering that hard in my chest I thought I’d be sick. It actually hurt. I cried and begged for relief. It was … beyond horrible. I really wouldn’t wish that on my worst enemy.

Day four.

I saw my psychiatrist for my new medication. I literally curled into a ball in the bucket seat as they spoke to me. The look of horror on the face of the consultant psychiatrist, registrar psychiatrist and counsellor were plain to see when I said I’d been cold turkey…..the psychiatrist wrote his own letter of complaint to my doctors about them stopping the medication. He put me back on 150mg to wean to zero over six weeks. I was glad. Another day like that and I genuinely don’t know how it would have ended. Hospitalization probably, I was a danger to myself. Thank god for good friends who helped me mother my children.

So when I finally detoxed, after the six week course of ever decreasing doses, it still wasn’t easy. It was still one of the hardest few days of my life…..but I was damn glad I’d done it. I’d rather be sectioned than ever have to put that detestable “medication” in my body again.

Then came the new medication. Having tried to manage my condition by myself in earlier years and it not being very successful (two overdose attempts – serious not cry for help) years of self harm, so bad it had become habitual, I know medication is the only way I’ll ever manage this. So to help with my sleep, anxiety, racing thoughts, dis associative tendencies and the whole shebang I was given a new antidepressant, an SSRI instead of an SNRI (I’ve also been on tri-cyclic) and an anti-psychotic, to help stabilise my moods.

2 months on, I can say that they seem to be better. My memory is back, I’m not having those horrendous dreams I used to have, I also practised immersion therapy to help with this, I can feel a range of emotions again, I laugh and feel happy, my vision is clearer, I had perfect eye sight (wahoo! go me!) but everything sees brighter and clearer now, I can focus on one thing at a time, I feel more connected to the world. But I’m also more irritable and cranky, and paranoid (of bizarre things, like my phone being tracked and hacked). Symptoms of my illness, and also just who I am, I’ll discuss this with my psychiatrist, becuase there is scope to increase my medication further, and I know that if it is then those awful parts will go and I’ll be a nicer person again. I’ve also regained my wit, sarcasm, and judgement. I’m no longer in this quagmire of life, just plugging away.

A year on from my diagnosis I can actively engage again, caused the loss of a few “friendships”  because I finally saw them for what they were, acceptance of my illness, and I’m no longer looking for a way to “cure” myself. I finally accept that it’s who I am, without it I wouldn’t be…me. And I’ve lived with it that long (I first remember the desire for my life to end at 8) I don’t know who I am without it, it’s a core part of who I am. And that’s fine. What isn’t fine, is allowing the negative side of it to overpower the positive. Which is what was happening. It’s okay to be ill ya know, but it’s not okay to not seek help. One year on I’m happier, more confident, more accepting, generally a better person than I’ve ever been. My uni work is excelling my own expectations, my brain is firing on all cylinders, I’m proactive in my health and fitness, I’m hungry again. Not for food (well yes that too, cheers quietepine! and my need for sweet stuff lol), but for experience, and knowledge. I can’t learn enough now, or pass that knowledge on. My love of cooking is back, and playing with my children. The best parts of me are back.

So this is probably the last time I’ll talk about my illness. Perhaps not, I might have a relapse, and might have dark times again. But hopefully this is the last time.

But I want everyone to know that mental health illness, isn’t the end of life. Whilst with my particular one there is no cure, no end to it, it’s always there on the fringes, or “in remission”, it’s no longer my ruler, my controller. I now control it. And everyone else can theirs. There is always help there for those who need it. There is always recovery as an option. And one, two, three etc, relapses don’t mean you’re beaten. You’re down but you’re not out.

So if you’re struggling at the moment, remember talk to your support team, that’s your friends, family and doctors. If you’ve not sorted a support team yet? Then do it now. Not tomorrow. Now. Because without them, you won’t and can’t succeed, but with? Hell yeah, nothing can stop you.

Thanks for being here for me, I’m glad I’ve got this far, and I know, without a doubt, that I have the ability to control this, regardless of what life throws at me.

BPD; A journey without a destination. The truest words I’ve said about it. There is no destination, no end to it, but it’s a journey I’m on, and engaged with, and instead of being a passenger on this journey. I’m the driver.

And it feels good.