Mental

Is Suicide Selfish?

/ bornwithoutmarbles / 26 Comments

Whenever the topic of suicide is discussed, several adjectives will magically appear depending on the speaker’s opinion on the issue. Over the years I have heard it described as “tragic”, an act of “desperation”, something “incomprehensible” to those surrounding the victim, something “unexpected”, and all of these are valid words to use. One of the adjectives that I hear come up that I strongly disagree with however, is the idea that suicide, and thus the people who “commit” suicide, are selfish.

Obviously I cannot speak for everyone who has ever struggled with suicidal thoughts, attempted or committed suicide, but for me, when I am feeling suicidal, it is actually the idea of continuing to live that feels like the selfish option (I am not saying that this idea is right and that therefore people should start killing themselves all over the place…DON’T DO THAT…I am just being honest and saying how it feels.)

Depending on how well you know me, whether you are a casual blog peruser, an online pal or friend/family member in real life, you may or may not be aware that I am currently in what all the professional psychology people around me may call, “in crisis”, although I personally prefer the term “in one hell of a pickle”. “In crisis” might be more professional and accurate a term, but if I am going to be in the state I am currently in, I would at least like the silver lining of naming it something a little less frightening than “in crisis”, and a little more related to the process of preserving some kind of food by anaerobic fermentation in brine or vinegar. As you can see I am all about finding the fun where I can/describing myself in ways that make people think of cheese sandwiches.

I don’t want to freak anyone out or make anyone panic by what I am going to say in this post and I want to reassure everyone that I have a hell of a lot of people on my pickle like case at the moment. Professional people keep phoning me (not that I answer because I am terrified of phones but they try anyway), I am having appointments all over the place, meetings are being held, I am never left alone and my mum has even been sleeping in my bed a lot to keep me safe on the really bad nights where I am really out of control. Therefore whatever I say in this post, please REMAIN CALM AND KEEP YOUR ARMS AND LEGS INSIDE THE VEHICLE AT ALL TIMES.

So, I don’t really know what exactly has sparked off my predicament and has caused things to get worse than they already were (it isn’t just the recent appendix thing…I actually wrote this blog post before all that and am editing this bit in now…hello!), but truth be told, a lot of the time I have been feeling like an outsider watching my own life and my actions in it.

You know when you have been reading a book for a really long time, flicking through the pages without really noticing until you suddenly stop and realise that you only have one chapter left. When you read that last chapter it sort of feels different to all the chapters that came before it because you know that this is the end. It doesn’t matter how many cliffhangers or revelations are being whipped out by the author, you are holding the book and you can see there are only a few pages left. It doesn’t matter if there are still mysteries to solve, if the monster hasn’t been vanquished yet, you know it is the end because you can FEEL it and see it just as you can see the handful of pages that is left.

That is how I feel when I look at my life. I feel like a reader on the outside of my story knowing that of all the mental health crises I have had before, this is the last one, the one the story is going to end on. No matter how hard I look, I cannot see any pages past this, any way around it, this time it is all too much, the pain is just too intense. Sometimes when I have been in difficult situations and have been extremely suicidal in the past I have been able to see it as something that I will eventually get through, I might know that it is impossible to feel that any emotion is forever, yet somehow this time it feels different. I feel different.

I am having a dramatic breakdown practically every day and rely on medication most nights just to keep me safe. Being conscious is currently so unbearable and overwhelming that I have been napping for hours each day just to get through them, the small tasks I set myself for the day have mainly been reduced to “just try to keep breathing” rather than anything productive on top of a task that most people take as fairly mandatory. Even that task however is getting harder by the day, and to be blunt, I physically cannot do “this” much longer.

I am putting all of my effort in and trying so hard, but there is only so much effort, only so much that one person can physically take before they crumble. Every time you drive over a bridge there will be a road sign telling you how much weight that bridge can take to warn you that if your vehicle is over that limit you might want to find an alternative route. It isn’t because the bridge gives up or isn’t trying when something that heavy passes over it, it is because it physically can only withstand so much.
Due to all of this, my family, friends and professionals are putting a LOT of effort in to try and help me through it and I appreciate it more than I can say. I can hand on heart say that I would not be here if it weren’t for the insane amount of support I am getting from the people around me, yet that is what is prompting me to think that actually the unselfish thing would be to just get on with it, end things and stop them having to put in so much of their time.

Even if they love me, even if they want to help, in concrete, factual and unemotional terms, it would be a lot easier for everyone if I wasn’t here anymore, and rather than suicide feeling like the selfish option, it is forcing people to carry on putting all their efforts in to keep me alive that feels selfish. When I am struggling with suicidal thoughts and the feeling that that is the only option as I am now, I am not thinking “screw everyone else I am in pain and I am going to end it whether they like it or not”, I am thinking “I really think this is the only option. The best thing to do for ALL of us.”

Like I said I am so incredibly grateful for all of the love and support I have been receiving lately, but at the same time I can’t help but feel incredibly guilty. My parents are constantly on tenterhooks (I don’t know what a tenterhook actually is but they are certainly on them), they are scared to ever leave me in a room by myself and they are called into my room increasingly frequently by me screaming in my sleep due to some nightmare. My therapy team are having to make extra appointments, extra meetings to make sure everyone is on the same page, texting me, phoning me, and generally suffering under an increased work load simply because I am unable to manage right now.

I have amazing and wonderful friends taking the time to visit me at my house when I do not feel able to leave it, they read my texts at 4am, tell me they love me when all I can see is hatred, they send me letters in the post, cards, even parcels containing amazingly wonderful things like books about penguins who have a tendency to worry a lot (if you have never heard of the “Worried Arthur” books then good God you need to look into them because they are FABULOUS), cuddly penguins and a myriad of other wonderful things that I am so grateful for and touched by, that saying thank you doesn’t do justice to what I think.

Think of how much effort that is for people to be worrying in the middle of the night, reassuring some lunatic who will only worry about the thing they are being reassured about again in half an hour even after great advice, spending money on presents and letters. DO YOU HAVE ANY IDEA HOW EXPENSIVE POSTAGE IS? A FIRST CLASS STAMP IS 65p…AND THAT IS JUST FOR A LETTER. For a parcel you are talking £5.70 and again, that is only if the parcel comes from within England! If it is from another country it is even more than that! You can’t just whack a crown on your head, snap a selfie, print it and stick it to a letter pretending to be a stamp, (trust me that doesn’t work…not that I have tried it myself…ahem…*removes crown and smiles sheepishly*), you have to pay if you want the postman to carry your parcel to someone, and that is then more effort for the postal service! I AM FORCING THE GOOD HONEST WORKERS OF THE ROYAL MAIL TO CARRY PARCELS OF PENGUINS TO MY HOUSE. They could be at home with their families! And £5.70 for a parcel stamp? You could get six two litre tubs of vanilla ice cream for that price and you would have 18p left! You could get 1120g of chocolate buttons and still have 30p left jangling in your purse! I AM DEPRIVING PEOPLE OF ICE CREAM AND CHOCOLATE BUTTONS. DEAR GOD I AM A MONSTER.

As you can see then, rightly or wrongly, when suicide is the only option I can see, the only way out of this utter hell of a brain situation, it is not because I am selfish and don’t care about how that might affect other people. Indeed it is the benefit my disappearance would be to everyone, that is actually one of the arguments my mind throws at me in the middle of the night when everyone else is asleep and I am too afraid to close my eyes incase I see the things that make me scream.

Like I said, I am not saying in any way that I think it is selfish to not kill yourself and I am NOT ADVOCATING SUICIDE IN ANY WAY AND WOULD ADVISE ANYONE WHO IS IN A SIMILAR SITUATION TO REACH OUT FOR HELP. If you do not have a therapy team and family around you I will put a link below to some of the charities out there who can help you, I am just writing this post to try to explain to the people who may think that people who commit suicide are selfish how it feels for some people who really are struggling with suicidal thoughts.

If you are one of the people who is currently supporting me I thank you from the bottom of my heart and I am really sorry that I am putting you through all of this stress, worry and effort. I promise I am trying. I promise I am looking for pages that could make a next chapter. I really hope that I find them. I wish I could be better for all of you. You deserve so much more.

I love you all so very much.

Take care everyone x

SelfishSuicide

Phone Helplines:

Samaritans – National freephone number: 116 123. They are open 24 hours a day, 365 days a year.

SANEline –  National number is 0300 304 7000. They are open 6pm–11pm, 365 days a year.

The Silver Line – If you are over the age of 55, this service is open 24 hours a day 365 days a year and their number that you can call from anywhere in the UK is 0800 4 70 80 90 (freephone).

CALM – Helpline for men experiencing distressing thoughts and emotions. Their national number is 0800 58 58 58. Open from 5pm–midnight, 365 days a year.

 

How Physical Health Problems Can Trigger Mental Health Problems

/ bornwithoutmarbles / 17 Comments

Last week I talked about a recent incident where my mental health, more specifically my eating disorder’s obsession with drinking a lot of water, had a detrimental affect on my physical health and in a hilarious twist of fate and example of bizarre symmetry (and by hilarious I mean literally the most unamusing thing to happen ever), this week I am talking about how the opposite can also be true, and how physical health conditions can end up triggering or making a pre existing mental health problem worse.

So when we last left off, I had explained how I had been admitted to hospital for water intoxication and was being treated for this problem via a strict fluid restriction plan to get all of my electrolytes back to acceptable levels (it is at times like this when I wish I had one of those “previously on” video clips that they show before episodes of various TV dramas…I should really look into that…ooh and a theme tune! I do love a good theme tune!)
Now, after a few days, the fluid restriction, whilst being incredibly annoying for me, seemed to be working, and my sodium levels kept improving until they were back to normal. Really, that should be the end of the story, the problem was solved so I should have been packing my bags and making my merry way home, but alas the story did not end there and developed into what I like to think of as an epic novel of utter ridiculousness.

You see whilst my sodium levels were improving, I wasn’t feeling any better which didn’t make much sense. I had been admitted for a problem that was being successfully treated yet bizarrely, as the days went on, I became more unwell with a pain in my stomach. The doctors couldn’t really make sense of this and before long I was in so much pain that I couldn’t stand or lift my head off the pillow and was in need of all the morphine I could get. A few tests were run but no answers were revealed so a surgeon was sent to have a look at me.

After thumping me in the abdomen with an iron mallet a few times (she said she was only going to “press gently” but trust me from the pain I am pretty sure that woman had a mallet and a vendetta against my stomach region), it was concluded that I might have a swollen appendix. I was told that normally the surgeons would book me in for an operation to whip it out just incase, however due to my already poor physical health from my eating disorder, they wanted to avoid taking me to theatre (alas the operating one and not the version where you get to watch The Sound of Music on stage whilst eating a little pot of ice cream with a spoon that is basically just a mini plank of wood with no resemblance to a spoon whatsoever), because they weren’t sure I would survive an anaesthetic.

Thus it was decided that they would only operate if they were absolutely certain that such a thing was necessary and therefore some more tests were scheduled to try and clear up what was going on. The problem with this was that by leaving time for tests, we were also leaving time for things to go downhill which they did fairly rapidly. Again the surgeon visited and again an operation was suggested but also feared so I was sent to yet another test in the form of a CT scan where I was basically shoved in and out of a tube a few times whilst doctors took photos of my insides (I really hope that my organs put on their best clothes and posed nicely for the occasion…it isn’t every day someone wants to photograph your intestines).

After the CT scan was complete it was around 1am and I was finally allowed to have some more morphine and attempt a snooze, whilst my sister, who had been sitting beside my bed for the past few days, went home. That was until 4am when another surgeon woke me up, to tell me that the scan had shown that things were rather serious and I was scheduled for emergency surgery immediately, my sister being called back in by the nurses having only just left. The next little bit of time is somewhat of a blur but from what I remember I was pumped with anaesthetic and taken to theatre (again, the operating one. I didn’t get so much as a lick of ice cream and I saw no children dancing in curtains. Livid.)
I was so knocked out that it was about 24 hours before I woke up from the procedure, dazed and confused with a tube coming out of my stomach and leading to a bag of some unidentified liquid.

It was then that I was informed that my appendix, in being left for so long, had ended up exploding. (The surgeon told me that I shouldn’t say that it “exploded” because in technical terms you should say that it “ruptured” but damn it I went through a hell of a lot of pain and nonsense because of what happened so if I want to say that my appendix literally exploded like a firework on the 5th of November then I will jolly well do so!)
Consequently my body had been filled with poison, hence the tube and bag scenario coming out of my stomach after the appendix had been removed, to drain the poison out (the poison being the funny liquid in that bag.)

Since then the job has basically been to free my body of poison, recover from the surgery and try to build my body back up after its internal beating, a job that isn’t going too well at the moment because this whole physical health problem extravaganza has triggered the life out of my mental health problems, more specifically my eating disorder.

Admittedly I haven’t been doing particularly well for a while now, but I have been clinging on to some sense of stability by rigidly carrying out the same routine meal plan via some form of repetitive autopilot action. Unfortunately, this event has utterly destroyed my autopilot “just do what you did yesterday” routine.

I think when you have an eating disorder, eating your meals is kind of like a recovering alcoholic avoiding the pub.
If you force yourself to eat the same meal plan every day, you get into a sort of rhythm, a rather bumpy and unpleasant rhythm that you can’t lead a good conga to, but a rhythm all the same. Missing one meal however is like an alcoholic downing one mouthful of vodka after a few months sober and then suddenly finding it impossible to stop.

Knowing that missing one meal will always make the next one harder is the reason that I fight so hard to complete my meal plan even on the bad days because I know that not doing so will make it harder for me in the long run, but in this whole “my organs are exploding” situation, missing a meal wasn’t something I had any control over.
For the first day of the hospital admission, eating was mentally impossible because I was in a different place with different foods. This problem was somewhat solved when family and friends hauled bags upon bags of my safe foods to my bedside, but by that point I was physically in too much pain to lift my head let alone grab a spoon to chomp down on some cornflakes. During all of these pain days I was also constantly being wheeled in and out of various tests that doctors were telling me I wasn’t allowed to eat before, and incase I was going to need emergency surgery after some of these tests, my stomach also had to be kept empty on the off chance that people would be whipping the scalpels out (apparently it is significantly harder to operate when one has just demolished a peanut butter sandwich…or any kind of sandwich…not that there is any other sandwich worth mentioning).

Post surgery I was finally allowed and encouraged to eat to regain my strength and I genuinely tried, but again there were hurdles. Firstly the combination of anaesthetic/poison/million medications made me extremely nauseas, and I was being sick multiple times a day. My taste buds had also suddenly gone haywire and for some reason I could not tolerate sweet foods which for someone who always picks sweet over savoury and who lives off sweet things like porridge and cereal, this was somewhat of a problem. Even the flavour in toothpaste made me throw up (all over my toothbrush I might add…suffice it to say my breath was not minty fresh), and shock of all shocks, I started to be repulsed by peanut butter. Me. Repulsed by peanut butter aka the food that was previously the holiest substance on earth? Who am I? I think I am going through some kind of identity crisis. You might as well start calling me Malcolm.

Therefore I was trying to find new foods that I could both mentally and physically tolerate, family and friends bringing in new groceries every day (including my parents who had had to cut their holiday short and catch an emergency flight back to the UK with fears that they might not get “back in time”…safe to say their relaxing trip to Malaysia was somewhat of a disaster this year..).

Excitingly, a new safe food that I could physically and mentally tolerate was discovered in the form of mashed potato, but by this point it had been so long since I had eaten properly even that was a struggle. I felt sick at every meal time and I could never be sure why. On one hand it could have been the “genuinely physically ill with poison and anaesthetic” sick that I shouldn’t have forced myself to fight as nothing I ate would be kept down anyway, or it could have been the simply sick with anxiety and fear of food sick that I really should have been challenging to prevent it getting any worse. Sometimes food would arrive and I would feel so ill that I wouldn’t risk a mouthful only for the food to be taken away, the sickness to go and me to realise that all that nausea had been anxiety as apposed to anything related to physical complications.

After multiple meetings with my eating disorder services who visited me a lot on the medical ward, it was decided that I would be discharged home incase eating became easier there due to familiar surroundings. Armed with a ridiculous amount of mashed potato, I really tried but a few days in found that I was struggling to swallow. Again I assumed this must be that whole “throat closing up with anxiety” thing, so I persevered, but then after finding some weird white nonsense all over my tongue and throat and a trip to the doctor, it was discovered that life had thrown yet another curve ball and in my weakened post surgery state, had given me tonsillitis and oral thrush, conditions that make swallowing rather difficult and would therefore interfere with anyone’s ability to eat…Oral thrush? I didn’t even know that was a thing? WHAT THE HELL IS GOING ON WITH MY BODY.

Now I am three weeks post surgery (happy no appendix anniversary to me!) and in positive news, the nausea from anaesthetic and poison is practically gone. Having started another lot of antibiotics and some weird throat drops I have also regained the ability to swallow but after so many physical preventions to eating, I am now mentally more terrified than ever at the prospect. I have been to my eating disorder unit and the scales say that I have lost weight yet somehow I feel bigger.
Doctors are telling me that I have to get back to my old meal plan immediately so that we can add new things in to regain all that I have lost but it feels impossible. I cannot comprehend how the hell I was managing to eat before, despite the fact I was doing it only a few weeks ago, because now such an ability has become alien and frightening. I am tied up in a bundle of fear over food, throwing up, weight gain, trying to eat whilst being laid up in bed unable to carry out my usual exercise routines and consequently recovery from surgery isn’t going very well because I don’t have the energy to recover. Both the physical affects and mental health problems are feeding off each other like my body is an all you can eat buffet, and ironically the one person not getting fed in this situation is me. I have been on the edge of collapse for months now, clinging to the edge of stability with all the strength I can muster, but this has thrown me. I have fallen off the cliff. I am spiralling.

…And on that jolly note, that is pretty much my explanation of how a physical illness can go on to affect/cause/trigger a relapse in a pre existing mental illness. As with a lot of my blog posts, it hasn’t been a particular barrel of laughs as far as topics go, but it is the honest truth, and as always, that is what I am determined to put out there in terms of raising awareness of mental health problems.
Now after all this typing, I think I am very much in need of a nap and then maybe I will give some more mashed potato another go. Eating food is the last thing I want to do right now and my stomach is already full from terror, but I promise, I really am trying.

Take care everyone x

AppendixExplode

The Dangers Of Drinking Too Much Water When You Have An Eating Disorder

/ bornwithoutmarbles / 16 Comments

So in last week’s blog, I talked about a recent lesson I had learnt about the importance of familiar surroundings when you struggle with OCD, and funnily enough I have learnt something else in the past week too.
I am learning a lot of things lately. It is like being back in pre-school only Daniel Jones hasn’t stolen my green crayon (if you are reading this Daniel then yes I know it was you and I still want it back), and the topics of these recent lessons have been far more focused on mental health and less on how messy one can get whilst finger painting/what noise a cow makes (hint: it is moo).

In life, we are constantly being told to drink more water. If you have ever sat in a doctors’ waiting room you will have no doubt seen several posters about how drinking a lot of water is very important, how kidneys love the stuff, how dangerous it is to get dehydrated, and from all of these posters and health warnings you may assume that the more water you drink the healthier you are, which…well… isn’t exactly true, especially if you are someone who is struggling with an eating disorder.

Drinking too much fluid is by no means something common to all people with eating disorders however, and in my years of experience getting to know fellow sufferers, there seem to be three camps of people and how their disorders manage fluids.
In one camp we have the people with eating disorders who struggle to drink enough water and end up extremely dehydrated, then there is a second camp of people who could drink a whole swimming pool if they had a big enough straw, and then finally in the third camp there are the people with eating disorders who do not have a problem with maintaining safe fluid levels and would therefore like to leave the camp I have just put them in and go back home to a habitat that is slightly less tent like.

As it happens, I am in the second aforementioned camp (ours has a lovely log fire and on Saturdays we roast marshmallows), and I struggle with drinking too much water even if I am not at all thirsty.
It is odd because I have always known that drinking too much liquid isn’t good for you, but when it comes down to it, me gulping down glass after glass of water is like some uncontrollable compulsion, a kind of outer body experience.
Many a time I have been pouring myself another litre and in my head have been thinking “NO. STOP! THIS IS DANGEROUS NOW” but my body won’t listen and carries on filling up my glass anyway. It doesn’t matter how ill I feel, drinking the water feels like an urgent and necessary task as if I need to dowse a fireball that is burning somewhere in my stomach, no matter how much water it takes.

Even in the camp of people with eating disorders who struggle with drinking too much water, it is likely that everyone will do so for a variety of reasons and it is rare for two sufferers with the same disordered behaviours to have the same reasons for carrying them out.
When it comes to me though, my compulsion to drink a lot of fluid is partly because of posters I used to see at my local gym telling me that if I didn’t drink enough my body would hold onto water (leading me to fear that the number on the scales would go higher), but mainly it is because no matter how many doctors or dieticians talk to me about the science of the intestine, I am convinced that if I do not drink ridiculous amounts, any food I eat will get stuck in me forever.

Technically I know all about stomach acids and the body’s ability to break down solid foods via various muscle contractions and other clever things that go on behind one’s belly button, but in my head, eating anything solid conjures up an image of that solid thing getting stuck in a tube. Say for example I eat an apple, it doesn’t matter how much I chew it, when it is in my stomach I still picture it as a big red cartoon like shiny apple with the stalk attached, a lump that will stay there unless I am able to create enough waves to erode and wash it away.

For this reason, to try and keep my drinking under some form of control, I have been on a fluid chart for years where I write down everything I drink to try and keep an eye on things so that it doesn’t get out of hand. If I don’t write my fluids down my brain tends to trick me and convince me that I haven’t had a mouthful of water in days (even if I am surrounded by empty bottles of Evian and have been peeing every five seconds), so it is safer for me to keep a record of it so that when the compulsion to drink a lot comes, I can remind myself that I have already drunk more than enough and need to distract myself elsewhere. Last week however, this fluid chart thing went a little bit off plan with the disappearance of my parents on holiday.

I have had several people message me asking what on earth happened after the mass break down described last week, whether my parents ended up cancelling the holiday or whether we gave it a go despite plan A being a rather sizeable fail.

Well, after people had realised that I couldn’t stay at my parents’ friends’ house for the duration of the holiday, the immediate conclusion was that the holiday would be cancelled, but eventually we managed to come up with an alternative plan wherein mum and dad would go off to Malaysia as planned and I would stay at home with my sister and my most legendary friend of all time alternating sleeping over to try and help me stay safe.

It was going rather well for the first few days (or at least better than the disaster that had been plan A), but as time went on I started to get more and more anxious about my parents being away and consequently the urge to drink increased in order to wash all of that anxiety and stress away. I know it sounds pathetic but without my mum there to verify how much I was drinking and suddenly in total control of my fluid intake myself, things started to get out of hand. People who stayed over would be able to support me in the day time but when up late at night I couldn’t help but manically gulp glass after glass of water over the sink. All the people who write those “yay kidneys like water, stay hydrated” posters would probably be thinking that is great but as with most things in life, moderation is key and you can have too much of a “good thing”.
Drinking too much water can cause problems for anyone who has been hitting it hard on the old H20 because your kidneys cannot process it and consequently the water stays in you where it can dilute the salt/sodium level in your blood and cause a condition called hyponatremia, which doesn’t sound particularly exciting but in general language this is known as water intoxication, and I am pretty sure that phrases containing the word “toxic” are never good phrases to hear describe someones physical health.

In healthy adults eating and maintaining a healthy diet, a few extra glasses of water will not cause this kind of thing, but the risks when it comes to people with eating disorders is often greater purely because they may not have been consuming enough salt/sodium in the first place, and essentially there is a risk of drowning your cells on the inside. This then leads to things like heart problems, fainting, water on the brain, seizures, psychotic episodes, death, and basically a lot of things that mean you “aren’t very well” which is exactly what happened to me a few days after my parents flew off to Malaysia and is exactly why my poor sleepy friend had to call an ambulance at 2am on a Saturday morning having been woken by me banging around, generally delirious and spouting nonsense (and a little bit of water. I was like a living water feature. Delightful).

The reason I stayed in hospital for so long however is a slightly more complicated story which I will have to get around to next week, just so that we are all up to date and clear as to why I was so rude as miss a blog post two Mondays ago (Oh the shame. And I was raised in a house with such good manners!), but as an initial explanation, the problem was that I was hospitalised for drinking too much water, and it is now after some severe tellings off from several health professionals that I feel the need to write this post about it so that people realise just how dangerous drinking too much water can be when you have an eating disorder, in case it is something other people struggle with themselves and seriously need to seek support for. If you are one of those people who struggles with drinking too much water I know you are probably doing what I used to do upon hearing these kind of things, the whole “surely it can’t be that bad” and “it would never happen to me” but trust me when I say that water intoxication is extremely dangerous and potentially fatal so if you struggle with it, even if your head tells you “you will be fine”, it is vital you get regular blood tests to check your sodium balance.

Luckily after a few days of being on a water restriction in hospital (good lord was I thirsty), my sodium levels returned to a more acceptable level…it is just that other things started to go wrong after that but again, patience dear friends! All in good time!

Now what I don’t want is for someone who already struggles with drinking enough to read this blog and suddenly panic and start restricting their fluids more than they already were because that is NOT what I am saying you should do and that is dangerous for a different bunch of reasons all on their own. I am just saying it is dangerous to go ridiculously overboard when it comes to fluid consumption even if your eating disorder tries to force you in that direction, and that instead of not drinking anything, just do it all in moderation. Water isn’t dangerous, everyone loves a good paddle or dip in the swimming pool, you just have to keep it at a safe level and be careful not to drown.

Take care everyone x

Kidney

P.s I am sorry if this blog is a little bit all over the place. Physically I am still not in the best place right now and my ability to write is somewhat affected but please bear with me! I am sure recovery will hurry up soon!

Why Familiar Surroundings Are Important When You Suffer With OCD

/ bornwithoutmarbles / 2 Comments

The original title of the blog I was planning to write today was “Tips on staying away from home when you have mental health problems”. You see, my parents were jetting off to Malaysia and seeing as I am not well enough to manage by myself at the moment, the plan was for me to go and stay with their friends in this lovely little house out in the countryside.
We have been planning it for months, I had visited the house and felt OK about it seeing how nice my bedroom, personal office AND personal bathroom were going to be. There was even a cat called Pingu. A cat. Named after my favourite childhood penguin. Ideal right?

Well I thought so, but was still worried about managing my mental health with new carers who do not know me as well as my parents, so I came up with a list of coping strategies and ways to manage it. Consequently I decided to write a blog sharing my oh so helpful tips incase anyone else out there was in a similar situation, but then…well…I went to the house where I was due to stay for two weeks, lasted approximately four hours and then was driven home in hysterics at midnight with my parents due to fly the next day despite having still not packed so much as a flip flop, because we have been spending weeks packing for me to go away (if you want to imagine how many things and bags it was, think of the average stuffed car that people often drive off to uni in, double it and chuck a penguin on top for good measure. Oh and a Christmas elf. One must never travel without one’s cuddly Christmas elf. Oh there we go! I did give a travel tip! YAY ME.)

Clearly then, I am in no place to be giving tips about staying away from home right now BUT over the course of this traumatic experience, I have been reminded of a valuable lesson about mental health problems, so I thought I would share that with you today instead.

Having been mentally ill and having been in therapy for over a decade, I would say I understand my conditions and myself rather well, which is why I felt that I could make a plan about an approaching situation in advance without running into any unforeseen issues.
Trying to do my same rituals in a different place however, really reminded me of something a lot of people might not realise: that being that sometimes with OCD, it is not just about carrying out a specific behaviour like a shower routine, it is about carrying out a very specific shower routine in a very specific shower.

I always knew that because of OCD and anorexia, I have a LOT of routines, rituals and specific ways of doing things. I eat out of certain bowls with a certain spoon, I drink tea out of a certain mug at certain times of the day and I wash my hands, shower and get dressed in very specific ways. As rigid as these and a number of different actions in my day are, logically you could assume that I could carry them out in a different place so long as I had the correct equipment. There was a shower where I was going to stay so of course I could do my shower routine, there was a sink so of course I could wash my hands and I was taking all of my cutlery/crockery so obviously I would be able to eat all in my usual ways.

Even I can admit that years ago, though still having OCD, I was able to do these fixed ritual things in other places with other sinks and showers. I have been on holiday since my diagnoses, have stayed in a hospital and went to university (kind of…), always carrying out the same actions just in different locations. Therefore I tried to do that this time going to a strange house but, with things how they are at the moment, as hard as I tried and as good as my intentions were at the time I attempted it, it isn’t possible (at least to a manageable realistic degree that doesn’t involve hysterics 24/7 for a fortnight which is less “a good challenge” and more cruel torture. I am all for accepting challenges and trying things out of my comfort zone but sometimes you need to eat a few mini muffins before you are up to demolishing an entire five tier wedding cake by yourself).

I was truly shocked as I sort of hadn’t realised how bad things have got again.
The descent has been a gradual process, little slips that in the end add up to a sky diver height of a fall. It is like what they say about if you put a frog in boiling hot water it will hop out but if you put it in warm water and gradually turn the heat up it will boil to death before it realises (that is what they say isn’t it? Who are these people? Please dear readers, do not go putting frogs in boiling water. If you really want to see some green bubbling in a pan just whack in a bag of frozen peas, far more humane AND one of your five a day).

When we pulled up at the house I fully intended on staying for the next two weeks (obviously I did, I had my penguin and my cuddly Christmas elf, I was committed to this trip). Even though I was anxious, by using multiple packets of anti bacterial wipes and with support from my parents, I got through the unpacking and after two hours my room, bathroom and office all looked really nice, filled with familiar things, a comfortable home from home.

It was when I tried to shower that things went so horribly wrong. First there was the issue that the shower was a stand in shower cubicle with a door. At my house our shower head is hanging above the bath, so when I am getting all lathered I can stand out of the flow of water to reach the required bubbliness (I know that this is not the most environmentally friendly way to live my life and that I could just turn the shower off but just know that I am unable to do that at the moment and to be honest when you are focusing on just keeping yourself alive your carbon footprint is not a top priority. At least I am not flying across the globe in an aeroplane to Malaysia like SOME people…).
With this stand in shower however, I was unable to reach the desired bubbliness needed to get through all of my thought routines because before I had time to count to the required numbers the suds had all been washed away.
Then there was a problem that I had to put my soaps in a basket so my lemon shower gel for feet was too close to my banana shower gel for body and far too close to a wall that I couldn’t touch, and the way you turned on the shower made my usual vitally important life saving way impossible.

I took so long to shower that all the hot water ran out and after a while of forcing myself to stand under the cold ice like hail pelting me in the face, I got out though I still didn’t feel clean. I was in a bit of a state but I didn’t want to give up so I persevered and tried to get on regardless but it was one thing after another. I couldn’t wash my hands in the sink because the tap distance to the back of the sink meant holding my arm at 135 degrees rather than 90, I couldn’t step off the towel I had laid on the floor because my bare feet couldn’t touch the tiles and I couldn’t put on the socks that I had brought into the bathroom with me without direct access to trousers and slippers. “You should have taken slippers in and trousers too” I hear you cry but I had thought of that already and couldn’t because there was nowhere safe in the bathroom to put those things at an acceptable distance away from each other. I found myself standing stranded on this towel shivering and blue with cold, so I naturally did what any other person would do in that situation. I cried uncontrollably and screamed in terror for my mother.

Luckily my parents were still there because the unpacking had taken such a long time that they had ended up staying for dinner whilst I showered.
Seafood rice was cooked and eaten and a homemade rhubarb crumble was just being served when the screaming happened and mum came running. She tried to help by offering solutions, one being the ideal “I can go and get the trousers and not let them touch anything”, but I didn’t want to do that. Yes it would have been safe, but I wanted to solve the problem by myself somehow with support.
Mum could have easily gotten my trousers and I could have left the bathroom but what the hell would I do the next day when she was on a beach somewhere in Malaysia? Around this point my “in a bit of a state” descended into full on “out of control don’t know what I am doing dangerous risky chaotic hysterics and panic” and from there things are a bit of a blur. All I know is that I cried for several hours (I tried to talk too but was at that hiccuping crying point so “I don’t know how to manage I want to disappear” came out more like “Hic gasp gulp hic scream”), and my parents and friends frantically tried to decide what to do.
When I was able to talk and sob at the same time I made it clear that I felt it was a challenge too many and that rather than tackling the “parents away and totally different location for all rituals for two weeks” I wanted to attempt the “parents aka usual carers away, in a familiar place” challenge. Losing both was like losing both of my homes, a tortoise rudely ripped from his semi detached terrace house and his shell in the same day leaving a cold naked slug unable to survive in its place.

There were then more hours of discussion before we realised that this really was not a feasible option and then after two hours of packing all of my things back into the bags we had unpacked them from (we didn’t have to pack my elf. He went and got himself back in the car the second he heard the first bout of screaming. He knows me well), we were back in the car driving home in the dark, leaving the abandoned now cold homemade crumble on the dining table. It is a big shame. My parents love rhubarb crumble.

So it was that I ended up back home after my much shorter than planned and somewhat failed “stay away from home with mental health problems”. On the plus side I did manage to get to the house and unpack…I just left two weeks too early.

Clearly then, I think I have proved my point and raised awareness to all the people who might not understand OCD, that when it comes to OCD and other mental health problems with ritualistic behaviours, it isn’t just the rituals that are important to a sufferer but the specific location and circumstances under which those rituals are carried out.

Take care everyone x

Bubbly

The Frustratingly Illogical Existence Of Life With An Eating Disorder

/ bornwithoutmarbles / 10 Comments

A few days ago, I met up with a friend who I have not seen for 15 years. It was a friend I have known since the tender age of zero after we stumbled across each other at an antenatal class our parents had been attending in the hopes of learning what the hell to do with the new humans they were about to produce and were expected to raise without any prior knowledge of how to do such a thing.
We may have only been newborns but our connection was instant, we bonded over Thomas the Tank Engine and have been friends ever since (although like I said, we haven’t seen each other for fifteen years because when you get to senior school and puberty a lot of nonsense gets thrown at you and there isn’t any time left to discuss the wonderful intricacies of your favourite blue tank engine…senior school is cruel.)

Recently however, after reconnecting over the 21st century miracle that is “social media”, we decided to meet up, and thus it was that I found myself sitting opposite my oldest friend in a coffee shop several days ago.
I think when you meet up with anyone, either new to you or as old a friend as your life itself, there is always a tendency to compare yourself to that other person in some way. Frustratingly, even though I know that appearance and weight are the least important of all things, my eating disorder automatically compares my body to those around me and without fail will always manage to convince me that I am an inferior disgrace who should go home and hang their head in shame. Like I said, I know weight doesn’t mean anything and I quite frankly don’t care what other people weigh. The number of pounds shown up on someone’s bathroom scales does not matter to me in the slightest, nor does it affect my opinion of them, yet for some reason when it comes to me specifically and my body, weight is of the highest significance and summarises my self worth as a person.

When I saw my friend standing there then, I felt really embarrassed and had it not been for the desperation to see her after such a long time, I probably would have run out of the coffee shop and would still be hiding in a bin somewhere.
Eloise Unicorn McGlitterface (I may have added the “Unicorn McGlitterface” myself just for fun…she really likes unicorns…and glitter…), looked fabulous, and I wished I could look like her.
Immediately my eating disorder was triggered and the thoughts telling me to lose weight struck up their familiar bellowing.
I didn’t want to be thinking about these things at all, as I left I wanted to be thinking about how lovely it had been to see my friend, but as I got in the car to go home, my head was screaming at me to lose weight, and here is where I get confused.

I know for a fact, that my friend Eloise Unicorn McGlitterface, on paper, is a healthy weight, and even though I don’t believe the “facts” my psychologists tell me about me being “underweight”, I understand them, sort of like someone understanding the theory behind someone’s religion without believing in that religion themselves. Logically then, according to doctors and science, most people would conclude that in order for me to look as fabulous as my friend, I would need to gain weight. On paper and if talking to anyone else, I would easily be able to agree with this argument yet somehow, when it comes to me, even though I cannot explain the science behind it myself, I am convinced that the only way for me to look like someone who weighs more than me…is that I need to lose weight. WHAT KIND OF LOGIC IS THAT.
When I tried to explain this to my mum I couldn’t. Naturally she thought that I sounded irrational and like a lunatic (she would have a point), yet despite my inability to explain the science behind my thoughts, I remain utterly convinced of their truth without really understanding them…
I even thought that if I tried to write this blog post and tried to explain my theory I would realise how ridiculous I sound, how my thoughts make no sense and therefore cannot be true, yet still here I sit, unable to explain how my body defies science and needs to lose weight to look like someone who weighs more than me, yet utterly convinced that this is the case.

There are a lot of things I believe that make no sense to other people when it comes to my eating disorder, but at least I can see the logic behind them. I know it doesn’t make rational sense that I cannot eat unless my hair is tied up in a very specific way at a very specific angle, but I understand where that belief/behaviour comes from and the rationale behind it according to previous experiences. I know it doesn’t make sense that I cannot eat with forks, knives or plates and am only able to use spoons and bowls, but again I understand the reason I feel this way. There is no science behind it, but it makes sense to me and I could explain it to people.

This however, I do not understand, yet like I said, this doesn’t make it any less compelling. I guess going back to the religious comparison, it is like being a devoutly religious person who can hear all the arguments against their beliefs but believes nonetheless and is convinced in their heart by pure faith. I don’t want to insinuate that my eating disorder is at all some kind of religious movement, it is a murdering mental illness that destroys lives, but I think this example goes to show that when you have an eating disorder your belief in your thoughts are held and driven mainly by a faith that you cannot explain the logic behind. In my experience at university studying theology and when talking to religious friends, if you ask them to explain “why” they hold their beliefs, any explanation will be secondary to the feeling they hold inside them. They can say “why” but when it comes down to it the thing that convinces them is a faith, an indescribable feeling that they have which means that they “know” what they believe to be true even though they can hear people arguing about why they might be wrong.

I don’t wholeheartedly believe my eating disordered thoughts because I am stupid and don’t understand science, somehow I believe them in spite of that understanding. This whole “to look like my healthy friend I need to lose more weight” thing is exactly like my obsession with green tea. I hate the stuff and over the years hundreds of people have told me that it makes no difference to your weight, I have read the studies and I know they are true and more scientific/rational than any thoughts I get from my eating disorder…yet somehow I am still convinced that if I don’t drink a certain number of millilitres of green tea I will gain several stone overnight. Consequently I drink that green nasty fluid that I am horrified is held in the same category as all other teas. WHERE IS THE LOGIC HERE EATING DISORDER? HMM?

I think what this really proves is the fact that eating disorders make no sense and that even if their thoughts don’t have a reason behind them, they are nevertheless believable. People with eating disorders aren’t stupid people who don’t understand how bodies work, they understand all of those things, often better than most, yet still the disordered thoughts are so strong and so compelling that they are convinced to follow them without being able to say why. Eating disorders have the power to make science sound ridiculous and nonsense sound like fact. I guess this example also proves the fact that eating disorders are flipping stupid and will always manage to convince you and tell you that you need to lose weight no matter what the facts of any situation.
Usually when I write blogs about eating disorders I do it to try and explain the reasoning behind
them to people who don’t understand, but clearly, sometimes life with an eating disorder is about not understanding a damn thing about your thoughts yourself and just basking in a frustrating confusion.

Take care everyone x

NonsenseBin

Being Afraid Of Your Own Brain When You Have Mental Health Problems

/ bornwithoutmarbles / 19 Comments

I feel like there is someone in my brain who is trying to kill me. It feels like I am being stalked by something, like a lion stalks a gazelle, but I can’t see how close or far away they are because when I turn around there is nobody there. Nobody else can see them either, they are in my head and unfortunately my eyes are positioned in a way that I can only see the outside world rather than what is going on internally (sort it out evolution for goodness sake, you gave us opposable thumbs now can you please work on swivelling eyes…And whilst you are at it can you please take this appendix away because it is taking up valuable storage room).
I am scared that this thing in my head is going to succeed in trying to kill me and I am also scared that it will fail. I don’t like being chased and sometimes I just want the thing to catch up and get whatever it is planning over with.

You might be wondering how on earth it is possible for someone to be afraid of their own brain because surely if the brain belongs to me, I am in control of it and what it decides to do. You don’t go round worrying that your own fist is going to punch you in the face because if your fist were to ever get such an idea it is likely you would tell it that you would rather not be punched in the face and could it maybe do something more helpful like make you a cup of tea.
That’s the thing though. I don’t feel in control of my brain and I don’t feel like I know what it is going to do at any given moment anymore. I always thought that if I owned my brain and my brain was me, then I would know my way around it. I would know every lobe, every memory, every thought and every desire because…well…they are supposed to be mine. If I have a secret that I keep from other people I tuck it away in my secret brain cupboard so they won’t be able to find it, but lately it has felt like my brain has a whole separate section where it is keeping its own secrets in its own secret cupboard that I cannot access.

“Maybe it is a nice secret” I hear you cry, “maybe your brain is preparing you a surprise party” but I don’t think that is the case, partly because it doesn’t feel like a nice secret and partly because I know for a fact that my brain hasn’t been balloon shopping recently and as I have said many a time on this blog, one cannot have a party unless there is at least one balloon present. If there is something magical in this secret cupboard, I know that it is not Narnia and is more likely to be a direct doorway to the White Witch.

I am worried that I am not making any sense and that I am being confusing in this post but if I am I guess that would be an accurate representation as to how things feel with my mental health right now, confusing and making little sense.

The Depression and BPD are still there, the OCD, and anorexia still have their claws in and dictate every one of my actions, yet still it feels like there is something different, something weird going on. I am more out of control than ever and half the time I don’t know who I am or what is going on.
I keep seeing things and I can’t tell if they are real or if I am imagining them. It started off as spiders, not the most pleasant things to imagine crawling around you and I would far rather imagine waddles of penguins approaching if I have to imagine anything, but I don’t think I have much of a choice in the matter. I started seeing spiders out of the corner of my eyes yet I was able to turn to face the place I thought I saw a spider and I could see that there was nothing there. Now though the spiders are bigger and they have tails. They also have fur and have lost four of their legs. They are rats now. Even when I know I am alone in a room I can feel people standing behind the curtains or crouching just outside beyond the window sill. I don’t know what they are doing there and it must be incredibly stuffy wrapped up in a curtain for hours every day (I can confirm this after years of playing hide and seek as a child), but they stand there anyway.

I am scared that I am actually “going mad”. More often than not I have been having to wake my mum up in the middle of the night to come in and sleep in my room because I don’t feel safe from my brain. It is as though, if I close my eyes and go to sleep for a minute, I am leaving myself unguarded and it will be able to sneak an attack in whilst I am busy being unconscious. I don’t understand the logic behind this fear as surely if I am asleep, my brain is asleep too, yet still I feel so disconnected from it these days that I can’t be sure what it is up to when I am not looking. It is clearly doing something underhand during my snoozing of late because I keep waking up screaming and often have no idea why.

I stay awake all night to keep myself safe and I also have stay awake all night to guard the house, because if I go to sleep ,not only will my brain start wreaking havoc but the people outside below the window sill will also find a way in somehow. It is ridiculous, if there ever was an intruder in reality I highly doubt my presence would be the thing to deter them (a point my psychologist pointed out last week…I think she was trying to be helpful but to be honest I took it as rather rude because clearly rather than assuring me of my safety she is actually implying that I don’t look as terrifyingly strong and powerful as I clearly am and I take the insinuation that I could not intimidate a burglar very offensively.) Still, logical or not, sense or nonsense aside, the feeling that I must guard the house is always there.

It is just a difficult situation to be in because I know that I should be responsible for my own mental health and therefore should be responsible and keep myself safe. I am 25 years old, certainly old enough by society’s standards to look after myself but I don’t feel responsible or in control and consequently I don’t feel certain I can keep myself safe. I have been disassociating for days on end (I will do a post soon explaining exactly what that is because it is an important mental health topic I somehow haven’t discussed yet…FOR SHAME!), but basically it means that there are a lot of days where I am not really “present” and therefore I have a lot of blank spots in my memory. It is all so frustrating I could scream, yet I don’t think that would make any difference. All that would mean was I was scared and could hear myself screaming and I would rather have the former without the latter if I have to have the former at all.

Like I said before, I am worried that this post won’t make any sense as I am not sure I understand it either, but still I wanted to write about how this feels. To try and explain or raise awareness of this side of mental health problems, the side where your brain is so mixed up all over the place that you are frightened of it, just incase there is anyone else out there experiencing the same thing and feeling as scared and alone as I do right now. Sometimes my mental health problems involve being depressed, being suicidal, or self harming. A lot of the time they focus on being afraid of germs, being afraid of food, and now, apparently they involve being afraid of myself.

Take care everyone x

ScaryBrain

“I Wish I Had The Self Control To Be Anorexic”

/ bornwithoutmarbles / 2 Comments

Several times in my life I have heard the phrase “I wish I had the self control to be anorexic” and, considering I am now writing this blog post about this phrase, you can safely assume that I have a lot to say about it.
You may be thinking “Katie, you already wrote a post about people wanting anorexia and how silly that is, why are you repeating yourself?” (a post you can find at the link here: A Message To All The People Out There Who Are “Pro-Ana”), but please hold that thought as I actually think that the problem with this phrase is not about people wanting eating disorders.
Indeed, unlike people who are “pro-Ana”, in my experience, people who say this are not actually craving the bulging rib cage and hip bone images promoted on “pro-Ana” websites. The mistake these people make is not that of idolising a mental illness, rather it is of completely misunderstanding what an eating disorder actually is and what it is like to suffer from one.

I think when it comes to illnesses such as anorexia, there is a misconception that when people with the illness don’t eat, it is because of their will power or an extreme superhuman ability for self-control. They assume that sufferers feel hungry and want to eat but powerfully override the primal urge to seek food because they are strong, yet in my experience, it is the total opposite, and it is in the times that I am unable to follow this primal urge that I feel the weakest that I have ever felt in my entire life (even weaker than the time I was beaten in an arm wrestle by an rather arrogant and ambitious sloth I met drinking tequila in a bar a few years ago…that was a BAD evening.)

Whenever I miss a meal or don’t eat a free sample handed to me in a supermarket, it isn’t because I implement my ability to make decisions/affect my actions as the word “control” implies. Instead, it is because I am not in control at all, a point I think is easier to explain if we take a trip down memory lane and travel back in time to any birthday I have had over the course of the last decade.

Most years, when it gets near to my birthday, if I am out shopping in a supermarket with my mum, when we walk past the birthday cake section, she will look at the birthday cakes and sigh. Following this signal, we may have a wander over to look at all the intricately decorated creations topped with thick white icing and pictures of various Disney characters (I don’t look at the plain old boring cakes for “adults” that simply say “Happy Birthday”. Seriously who wants one of those when you can have an sponge shaped like a minion or a giant chocolate caterpillar with a cheeky grin?!), and then after five minutes of eye wandering my mum will turn to me and ask the question “can I get you a birthday cake this year?”.
Now, if I had any degree of “self-control” when it comes to food and my ability to nourish myself, I can honestly say I would turn to my mother in these moments and say something along the lines of:

“Can you buy me a birthday cake? Why of course! There is no question regarding such a matter! It is my birthday in two weeks and I simply cannot celebrate the occasion without a cake! Quick! Let’s go around all the supermarkets and bakeries in the area to try and find the biggest penguin shaped chocolate cake available. I want nothing more than to share such a delight with all of my nearest and dearest friends! Ooh can I please reserve the chocolate beak for me because it is my birthday? I do love a chocolate beak! Hurry mother, let us away to the automobile and get started on this quest immediately!”.
I would probably then insist we head to the candle area to pick the most garish, brightly coloured candles on offer to adorn my perfect penguin centrepiece, poised and ready for the moment when I am ready to blow out the flames and make a wish that Helena Bonham Carter hurries up and marries me already.

That is the response of a Katie who is in control. Unfortunately though, we haven’t seen “In Control Katie” around much lately. That Katie popped out for bread about ten years ago leaving an out of control mess in place, and since then we haven’t heard anything (better be picking up some damn good bread is all I can say…I’m talking a good quality ciabatta or we are going to have issues).
Therefore, with “In Control Katie” otherwise engaged on a mission to find a tasty source of carbohydrates, it is the “out of control” one that turns to Mum year on year with a dejected look and says: “I wish. Maybe next time”, at which point we agree to try again next year before repeating the annual routine in roughly 365 days time.
I know it would mean the world to my mum to buy me a giant penguin birthday cake to share with her/the family, and I desperately want to accept her offer each time mainly because I want to see her reaction. I want to see her face light up with the brightness of a birthday cake candle, filled with hope that for once she can do something that normal mothers do rather than having to come up with some kind of eating disorder friendly replacement for her neurotic offspring (e.g. the act of sticking a candle in a pink lady…the kind of apple I mean…not an unsuspecting blushing female who doesn’t know what’s coming).
When I do not accept the offer of a proper birthday cake then, it is not because I don’t want to, it is because my mind throws up barriers that make me feel that I physically can’t.
It is like a “normal” person standing in front of a bonfire and wanting to put their hand in it to retrieve a particularly nice log. They can look into those flames and want to put their hand in to get the log (this person really likes logs), but no matter what, they can’t. Of course they are physically capable of moving their arm into the vicinity of the fire, but the fear of pain stops them (no matter how much they like logs).
Saying “I wish I had the self-control to be anorexic” then, is basically like saying “I wish I had the self-control not to put my hand on a bonfire”. Of course eating and setting yourself aflame aren’t the same thing, one is vital for life whilst the other is downright ridiculous and not something I advise anyone to try at home or anywhere else for that matter, but the similarity exists in the sense that both the person who doesn’t put their hand in the fire and the person with the eating disorder do not carry out their actions because of self-control, rather it is because they are both scared and fear the pain that could result from their actions.

Whenever you hear yourself or anyone wishing they had the “self-control” and “will power” to eat like someone with an eating disorder then, please know that when it comes to eating disorders, self-control has absolutely nothing to do with any of it. When someone is unable to keep themselves healthy by eating enough, it is because they are not in control, and because the reins of decision are actually being held hostage by an evil dictator in their head who is trying to kill them.
If I had self-control and willpower over my life I could write a list of about a million things I would use it for. The ability to fill my mother’s eyes with disappointment, to refuse sharing a dessert with a friend or turn down the offer of a birthday cake would not be on there.

Take care everyone x

ControllingPea

Why It Can Be Scary To Take Medication For Mental Health Problems

/ bornwithoutmarbles / 8 Comments

Recently, my psychiatrist prescribed me a new medication to help me with some of my mental health problems. I am on various medications already with a variety of different purposes and have been for some time, but in terms of what these new tablets are “supposed to do”, the aim is for them to reduce some more of the anxiety that my current medications are allowing to linger long after they have done their jobs. Ironically though, despite having had this packet of anti anxiety medication on the kitchen worktop for over a month, I am too anxious to take them.

I think being scared of taking medication for a mental health problem is extremely common and to be fair it would be weird if people weren’t a little afraid of whatever tablet their doctor has recommended them to take. A big reason for this is of course the long list of side effects that comes in any box of medication from Calpol to Morphine, although when you think about it there are no medications that have side effects, there are only effects.
Tablets do a lot of different things and it is the scientists/elves (I am not sure who makes medicine these days but I am sure it is one of the two) who decide which effects to put in the “Purpose of tablet” column and which go in the “side effects” column, aka the effects that are harder to advertise. For example, for some people Paracetamol can have the effect of giving them yellow skin so that effect is categorised as a side effect because that effect is less easy to advertise than the more attractive “this will help take your head ache away” effect (unless of course you are dealing with someone who wants yellow skin so that they can look like a Simpson, in which case I suggest body paint which is probably a lot safer).

I think mental health medication is scarier to take than “normal” body medication though, because there is a fear that it will fundamentally change you as a person, your characteristics, interests and identity. When you take a physical medication that may turn your skin the colour of a freshly picked banana, there is a separation there between you and the skin. Ok the skin is your skin, but aside from holding all your body parts together your skin doesn’t affect who YOU are and no matter what the colour of your skin, you will be the same person you were before and will be able to react and interact with friends and family in the same way as you did prior to your sudden transformation into a Simpson. The skin is just the irrelevant wrapping paper on the more important gift. If you wrap a new video game in white paper and then colour it yellow, you will still have the same present inside.
With mental health medications however, they are designed to interfere with how your brain works and the side effects of that can feel more personal. By changing your mind, it feels that they are changing an integral part of you, so that one second you could be a lover of Julie Andrews dancing round your kitchen belting out “the hills are alive” and the next you are on some uncontrollable rampage to burn every copy of the Sound of Music and Mary Poppins
I think we can all agree it is infinitely less stressful to take a tablet that might change the colour of our wrapping paper rather than one that risks turning the games console under the Christmas tree you have been waiting months for, into a sardine which in comparison is about as much fun as…well…a soggy sardine.

Indeed, I know from experience that medications can change fundamental parts of my personality. When I was a teenager there was one medication that practically turned me into the incredible hulk. I was filled with rage all the time, a rage without reason, and I became violent and out of control. I am really ashamed of a lot of things I did during that time of constant fury, as it changed my character so dramatically that I ended up doing a lot of things I wouldn’t normally do like kicking through a glass door.
As well as medications that have changed my character, I have experienced medications that have simply had mental side effects that were unpleasant such as one tablet that pretty much knocked me out and left me sleeping twenty four hours a day. I guess it did its job of reducing the number of OCD rituals I was carrying out, but that was only because I was a comatose zombie who could barely lift a duvet let alone shower for several hours.
I have also been on a medication that gave me hallucinations (if the police are reading this I would like to make it clear that these tablets were prescribed to me by a medical professional and were not in any way purchased in a dark alley from someone in a rather large coat). This was yet another unpleasant side effect, and every day I found it even harder to tell the difference between what was real and what wasn’t, what had happened in reality, and what was just a figment of my imagination. Luckily, during this time I was in hospital so there were nurses around constantly to help me distinguish between the two or sit with me through the scary ones, and though a lot of that time is a blur, looking back I find it easier to separate events that actually happened during that time from the more fantastical fictions written by my dodgy brain chemistry, based on what things are most likely to be true. For example nowadays I reason that it was most likely a hallucination when one of the nurses danced around my bed waving an assortment of Hawaiian shirts but obviously real life when I was awarded the Nobel prize for literature and rode around the country on an ostrich…I just wish I could find the prize money…and the ostrich…

It is also scary to take a mental health medication because the same medication can affect two people in completely different ways so it is impossible to hear of someone else’s experience with a particular tablet and know what to expect when you swallow it yourself, so you sort of go into it blind like some medication Russian roulette. Will you continue dancing around the kitchen singing “supercalifragilisticexpialidocious” or will you wake up next day to a smouldering pile of ashes in which you can vaguely make out the image of Julie Andrews dressed as a nun.
Indeed I have friends who have taken the same tablets as I have but with completely different results, and the medication that turned me into the Incredible Hulk (a medication I was swiftly removed from), is the same medication as the one that my friend has been taking for years because for her, the effect is far more calming than the urge to kick through the conservatory door.

With this medication I have been prescribed most recently though, the fear I have isn’t actually one that is related to the fear that it will change my brain chemistry and me as a person. To be honest things are so difficult at the moment that I wouldn’t give a curtain wrapped Von Trapp child if the medication changed me as a person (please forgive me Julie Andrews).
No, this time, the fear is more about the physical side effects listed in the instruction manual, most specifically the one that says “possible weight gain”. I know that whenever medications put this as a side effect it generally means that the tablets may increase a person’s appetite, consequently leading them to eat more food and gain weight because of that, rather than directly from the medication itself, so as someone with an eating disorder who eats the exact same rigid meal plan and amount every day without taking heed of hunger cues, that reason for weight gain would not happen to me. However again, as someone with an eating disorder, the fear of risking a random weight increase because of a tablet, even if I don’t change my diet, is terrifying. If that were to happen I would feel totally out of control, more anxious and likely to restrict my diet more than I already do. It is a difficult thing to balance, on one hand I could take this new medication and it could help me with anxiety, and on the other it could simply make things worse.

I know that medication is not always the answer, neither does it solve all your problems (a topic I really want to come back to sometime if you are willing to stick around as a reader of my blog…I will give you cookies…), but right now I do think that I need to give this medication a go considering the fact my brain isn’t responding to any of the other therapies/attempts to sort it out. In a few weeks time my psychiatrist will ask me how the new medication I have been taking for the past few months is going and at the moment I will have nothing to tell him because all I have done is look at it and I can wholeheartedly confirm that staring at the tablet has had no therapeutic benefit to me whatsoever. I really am determined to try it…at some point…possibly…definitely…I think…It is just the case of taking the first one and getting over that hurdle, cracking out a pot of maple syrup – going with the grand advice that a spoonful of sugar will make the medicine go down and not my weight go up…Good lord, where is Mary Poppins when you need her eh?

Take care everyone x

WheelOfFortune

Mental Health Problems In The LGBTQ+ Community

/ bornwithoutmarbles / 10 Comments

This is just a little note to say that this post mentions incidents involving self harm so if that would trigger you, I thank you very much for joining us today but maybe go and treat yourself to a good cup of tea and biscuits instead. Safety first pals!

I once had a psychologist who, during a talk about my mental health and how broken my brain is, asked me if I thought any of my issues “were because of being gay”. I was appalled.

“How dare you!” I replied. “What homophobic nonsense is this? I am deeply offended! You think people who are gay must also be mad because nobody with common sense would be queer? For-shame! A plague unto you and your ancestors! Watch me flounce out of this room waving my rainbow flag in a fury! Watch me flounce I say!” (please note that this was what I replied in my head…in reality I think I just squinted my eyes a bit and formed a quizzical expression).

At the time I didn’t see what being a member of the LGBTQ+ club, had to do with my mental health at all, but after a little bit of discussion, research, and no actual flouncing, I realised that this psychologist was on to something.
Turns out, rainbow folk in general show higher levels of anxiety, depression and suicidal thoughts than heterosexuals, so seeing as it is Pride month in the UK this month, I thought I would use this post to think about why that might be. It’s like that old saying, “if you are gay and you have mental health problems, it is your duty to mush those experiences together and write a blog about it.”

In my experience,I wouldn’t say that for me personally, being a member of the LGBTQ+ community has been THE trigger that led to all of my personal mental health problems, although I know that for some people, it can be.
Often I think it can be things like homophobic bullying and external discrimination that are the reason people who are LGBTQ+ might go on to suffer problems, and in that respect, I have been very lucky.
I have never been bullied for my sexuality, my family have always been very accepting (my mum to the point where she is basically a walking gay pride parade all year round and always gets very excited/becomes a fan every time any celebrity comes out as a homosexual), and I live in a country/time period where it is safe for me to be “out” without fearing arrest.
The only discrimination I have ever had has been the odd homophobic slur shouted out of a car window at me as I was walking down the street, but this has never really bothered me as I don’t have that much respect for the opinions of people who shout abuse out of car windows… I might admire their ability to project with their vocal chords out of a moving vehicle, but when it comes to their judgements on who I fall in love with, frankly, I don’t give a damn.

However being LGBTQ+ has certainly affected me because of discrimination, it is just that all of that discrimination came from my own head and in the early days of my queerness, led me to feeling very ashamed.
Nobody in my external surroundings was telling me I was weird or shouldn’t be gay, but my head was, and consequently I was scared to tell anyone about it incase they felt the same. Indeed I decided that rather than tell anyone, I would start a grand “make Katie straight” mission so that nobody would ever have to find out. You may wonder how on earth one goes about “de-gaying themselves” as surely to do so is impossible, and in that assumption, you would be right. Little old me however, was convinced otherwise.

The idea came to me whilst watching a television program which funnily enough, was about a straight woman seeing if she could undergo treatment to turn her gay…Good lord they show some weird things on TV these days…
Anyway, in the program, this woman was told by some mad scientist to use this machine that would give her electric shocks every time she thought something heterosexual in an attempt to recondition the brain to stop thinking those things. The theory was that if your brain experiences an electric shock every time you think about something, it will stop thinking about that thing (either that or your hair will stick out all over the place forevermore and you will run up one hell of an electricity bill).
Unfortunately, I did not have an electric shock machine. I did however, have access to a lot of sharp things around my household, and I think you can guess how things went from there without me providing any more detail. As part of my “make Katie straight” plan, I set about trying to literally cut the gay part away from me, a futile pursuit considering “gayness” is not an extra body part or a long fingernail you can clip away at until it is gone. Unsurprisingly, that plan didn’t work, but it did get me into a cycle of self harm that I couldn’t get away from and still struggle with to this day.

Admittedly, my struggle with self harm is not about being gay anymore, but the whole situation introduced the idea of self harm as a punishment, a coping mechanism to try and remove guilt or shame I was feeling about anything in life.
Rather than being a punishment for being gay, it has become a punishment for things like bad marks on a test at school, or saying something mean in an argument, and I actually used to keep a little notebook in my pocket throughout the day to keep track of my “crimes” so I knew how many “punishments” I deserved later.
At first I was only doing a few things “wrong” a day, but because I was scared to talk to any of my psychologists about it as that would involve telling them how self harm started, and though I was ok with being gay, I didn’t expect everyone else to be. Consequently the notebook of punishments escalated and got so out of hand that after a few months, every action was considered a crime deserving of punishment, from using a “large blob of toothpaste” (which would use up the family tube sooner and lead to money needing to be spent on a new one), to “not smiling well enough at my friend in the corridor at school”.

It wasn’t until my mum found some blood soaked clothing in my bag which I had been trying to smuggle into school to wash in the school sink before she could see it in the laundry, that the whole self harm as punishment thing came out, and even then I wouldn’t tell people how it had started.
By the time I did tell people that I was gay, I had already been in therapy for 8 years or so and had been through two admissions to psychiatric hospitals, always keeping that part of my identity hidden. Like I said, being gay has never been a cornerstone in the almighty Jenga tower of my insanity so I don’t think that keeping that part of me a secret severely hindered my treatment. I was still able to talk openly and honestly about the depression, OCD, BPD related problems and anorexia in therapy, yet although it isn’t the source of my mental health problems, when I finally came out to professionals it did serve as some kind of relief. Whether it had been important to OCD or not, I always had to watch what I said in sessions incase I accidentally let a possible clue slip like “I LOVE HELENA BONHAM CARTER AND I WANT TO MARRY HER IN A BIG GAY WEDDING WITH A BIG RAINBOW CAKE BECAUSE I AM A BIG GAY MYSELF”. Being able to talk openly without worrying about that certainly made a difference and made me feel more connected to my therapists, because I think if you are ever keeping a secret from anyone, you are automatically reserved around people even when that secret isn’t being discussed.

As you can see then, compared to some members of the LGBTQ+ community with mental health problems, being queer hasn’t had anywhere near the impact on me that it has on other people. In essence, being gay is the vanilla extract in my giant cake of insanity rather than the flour of which the majority of the cake comprises.
That said there are a lot of LGBTQ+ folk out there who struggle so much with their identity either due to judgement from outside sources or internal judgement on themselves, that being LGBTQ+ can be a direct cause of certain conditions like depression or anxiety and it is for these people that we need to talk more about this kind of thing in the hopes that they will be able to seek help themselves. If shame about your identity leads you to having mental health problems, it is likely that shame will prevent you from seeking help for them, and as we all know that is just going to make things worse.

In this post I do not want to do a shoutout to all the LGBTQ+ people out there who are hiding in the bushes and tell them to run about telling everyone about their identity, because I understand that for some people in certain families or countries, that might not be safe for them.
All I want to say is that if you are struggling and feeling like there is nobody to turn to, you are not alone and I can promise you that there are people out there who understand (I am one of them. Hello, it is nice to meet you. My name is Katie and if you bring me penguins we can be best friends). If being LGBTQ+ is causing mental health problems and it is not safe for you to speak to people around you, there are hundreds of LGBTQ+ mental health charities out there for every country (I will link a page recommending some existing in the UK below), and if you can, I would encourage you to reach out to them for support.
I am not going to demand you just get a rainbow flag and feel proud because it is pride month, as I understand it is not as easy as that, but I do hope to offer some sense of reassurance that being LGBTQ+ is NOT something anyone needs to to be ashamed of or punished for, no matter what that voice in your head tells you.

Take care everyone x

RainbowBlog

https://www.mind.org.uk/information-support/guides-to-support-and-services/lgbtq-mental-health/useful-contacts/#.WV0XKlKZPVo