Tag: mental illness

Mental Health Awareness Week: The Medication Debate

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Medication is a huge debate whether you have a mental illness or not. It’s something that definitely needs to be spoken about more, in fact I think it’s one of the biggest reasons that people are reluctant to talk about mental illness. There are some people that are of the opinion that those who take medication are taking the ‘easy way out’ or mean that people don’t want to try, as someone with experience neither of these are true. The other extreme belief is that all medication turns you into a zombie, someone who can’t think or do anything for themselves, again an image of simply giving up.

From my own personal experience and the experience of every single person I’ve spoken to about medication it is definitely NOT the easiest solution. While it’s right to say that medication is not for everyone  and some people don’t want to take them, that’s fine. For me I’d tried so many other things counselling being the main route, trying to sleep properly, nothing was working. I was emotionally and physically exhausted when a doctor asked me if I just wanted to try and see how it goes, because I looked completely at the end of my teather. That was the first time and I freaked out about the stigma surrounding them and I just quit, I was done. Then a while later I got at a low stage again and decided to give it a go, the side effects were horrendous. I didn’t sleep for three days, I felt sick all the time, I was sick, I called my doctor to ask if this was normal (it was my first experience of insomnia) who said give it a few more days and see. Luckily this time I carried on, after a few adjustments, reviews and such I eventually settled.

There are a lot of horror stories and it’s rare for someone to go on medication and it be right for them instantly. There’s usually a lot of adjustments, a lot of change. A lot of people ask me why, why put this in your body? For a long time I struggled, who was I, why did my stupid body need these tablets? I really beat myself up constantly. I didn’t want to be someone who relied on medication to function, I didn’t feel normal. That said I could see changed after about a month, it’s hard to describe online, hell it’s even hard to describe in person. It’s like for a long time I was walking around with this fog in my head, everything I did felt wrong, heavy and even when I was happy there was something in me that constantly tugged at my happiness. When the medication worked I wasn’t fixed, but the fog cleared and I could finally think and see things clearer. After I took my medication I started to go back to who I was before the depression took hold of me and I started trusting myself again.

It took a long time but my mentor reminded me of this quote:

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I wasn’t scared of the medication, it helped me after years of just feeling like I was drowning I had some calmness. No one would ever dream of telling a diabetic not to take insulin because of the fact ‘it changes their body’ well, yeah that’s the point. While there are some negative aspects of medication and again, it’s not for everyone BUT it can help. Who has the right to dictate whether or not someone should take something if it does make them feel better, if it enables them to tackle the day or makes the tough days a little bit easier.

It’s the same for me with anything medical, if it’s not your body then you can’t really dictate anything. I truly believe that unless you’ve been through something you can’t judge someone else. Stigma related to taking a medication that makes you well doesn’t really make any sense to me. Like I said, it’s not the easy way out, a quick fix or anything like that without going to see a mentor once a week for a long time my medication wouldn’t have been very effective. People need to work through their problems or the root cause of their depression, sometimes medication makes it a little clearer and a little easier to talk about.

I refuse to be ashamed of treatment for a health condition, neither should you.

 

As always let me know your comments, questions and just generally chat below!

 

Today’s MH Update: Felt a little overwhelmed today and did have a bit of a crumble BUT now feeling very positive and happier!

 

Images from Pinterest

Mental Health Awareness Week 2016 on chloemetzger.com

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This week is Mental Health Awareness Week, as my regular readers know I’m really big on promoting awareness, sharing my own experiences with mental health and just generally getting mental health in every day conversation. Whether we like it or not there’s still a stigma attached to mental health issues and it’s not the way it should be BUT with weeks like this we can end the stigma sooner rather than later.

This week I’ve decided to relate all my posts to raising awareness of mental health. I’ve got posts planned around my experience, opinions, books related to mental health, motivation – it’s all going to be going on over here! As always I’d love to hear for you in the comments, on Twitter. I’ve found that when I’m really not doing well Twitter is one of the places I can talk to people to understand and generally be in a better mood.

I also want to do an honest mood update each day, because sometimes I can go a few weeks of feeling fine and then it’ll go downhill, it’s the ways of having Depression. For today I’ve been really sleep deprived so my mood hasn’t been the best, I’m at a really overwhelming point in my life and everything’s changing so I think that’s to be expected.

I can’t wait to write this week and raise as much awareness as possible! As always leave comments and questions below!

Book Review: Sane New World: Taming the Mind – Ruby Wax

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As this week is Depression Awareness Week I decided to add this weeks book review into the theme and have picked Ruby Wax’s first book about Mental Health and Mindfulness. The choice behind this was because Ruby was coming to visit my university and I wanted to know more about her views on Mental Health. Unfortunately I couldn’t go to the talk because I just had too much work to get on with and finish BUT I did manage to work my way through Ruby’s first book.I will say before I start this is not what I would class as a memoir, although there are snippets into Wax’s life it more of a big jumble of personal opinion, science and illustrations . Not what I expected, but not bad either.

Although Ruby Wax is a known entertainer she also studied the brain at Oxford University in an attempt to better understand her own mind and the problems she has. Through the book wax tries to simplify the complex nature of the brain into something that anyone with an interest can understand. Apart from the diagrams and scientific names for all parts of the brain, Wax also tries to engage with the practice of Mindfulness and how it can be used in our busy everyday lives. It is because of this that the four sections of the book don’t seem to fit as well as they possibly could have, while I admire Wax for trying to speak about these incredibly complex scientific matters, it does at time feel like too much information that isn’t resolved. For example the second half of the book is focused on Mindfulness and techniques, exercises and stories of the use, leaving the science pretty much forgotten (in my case at least). It almost felt as if this would have worked much better as two books, or even one much bigger book because both seem like they need more time and space to be fully understood.

I think the way to describe her opinion and how it is portrayed is very marmite, you either love it or hate it. Unfortunately I was not a fan of some of Wax’s opinions, I feel like she could come across as slightly rude or even ignorant of other people. There is a heavy presence of wanting to prove herself to people in her past, and while there is nothing wrong with that the sections about her mother in particular seem to be misplaced in the book, almost as if it was a haha look at how far I’ve come. While Wax is incredibly honest about her experiences, it can leave people feeling slightly negative, there are some instances where Wax has tried to make jokes and in the process can come across as quite mean or rude to whole scores of people. This is one of the main problems with the book, it appears that Wax still has a great deal to learn about the people behind the statistics and the lives of others. She may be incredibly open about her own experiences but it comes across that she only see’s others as the numbers and reports she saw at Oxford, rather than the people behind them.

I will say though that the exercises that are in the book are great and a good way to start looking into Mindfulness. It’s definitely something that I want to look into further after reading Wax’s suggestions, thoughts and experiences. That said, I did find her very dismissive of the practice of Cognitive Behavioural Therapy (CBT), something I myself use. Again Wax quotes statistics to back up her point, but this was another instance where I felt that she didn’t see it through the eyes of someone who does get a great deal of help from CBT.

Overall I gave Wax’s first book 3 stars (***), while I appreciate the topic and the fact that it opened conversations it felt really all over the place as a book. It was almost as if Wax couldn’t decide whether she wanted the book to be science based, opinion based or technique based and so all three have been kind of thrown together in a few hundred pages. It’s not that I didn’t enjoy reading, I did, but I found the narrative and some of the comments to really put me off of reading and so it took me a long time to sit and get myself through it.

As always I’d love to hear your comments, what do you think of this book, of CBT? Leave me a message down below!

 

 

Depression Awareness Week: What You Don’t See

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This week it’s Depression Awareness Week, and of course I’ll take any opportunity I can to get involved and spread more awareness about the mental health condition I’ve been living with for about six years. Of course, for this blog, writing about Mental Health is nothing new, I frequently write about my own experiences, struggles and triumphs so that other people can see that they’re not alone, because that’s what I felt for a really long time.

Every single person reading this blog knows or had known someone with a mental illness, in the UK 1 in 4 people have a diagnosed mental illness, and those are the people willing to talk about it. It can be a really huge and scary thing to think about, let alone talk about. It took me a really long time after my diagnoses at 18 to be able to say the words ‘I have Depression’ out loud. For some reason, somewhere along the line mental illness was percieved as a person being weak, which is definitely not the case.

This year along with #sicknotweak, people have been sharing their stories of what you don’t see. We’re at a point in time where we share our lives online all the time BUT we often forget that these are edited. It’s rare for someone to share a picture of themselves at their lowest points, we create something that people want to look at, and most of the time that isn’t pain or suffering. SO, as a social media addict I thought it would be good to share 10 of my experiences of what isn’t seen when dealing with my illness.

What You Don’t See… is my mind going into overdrive while I’m trying to sleep and I’m tossing and turning.

What You Don’t See… is the days when I can’t get out of bed, because even having a shower is a mammoth task.

What You Don’t See… Tears, all the bloody tears sometimes for no reason, sometimes for a list of reasons.

What You Don’t See… The exhaustion is real, especially in low points.

What You Don’t See… Is the lack of motivation before going to the gym and taking those selfies.

What You Don’t See… My life when I’m physically sick and can’t take my medication for a few days…not pretty.

What You Don’t See… is the struggle to write day to day when my head is buzzing.

What You Don’t See… when I have an anxiety attack about things that I cannot control.

What You Don’t See… is the scenarios that my brain creates to induce me into another panic attack/ anxiety attack, over situations that will probably never happen.

What You Don’t See… what I don’t want you to see.

Who’s going to hire me? -Embracing your past

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I didn’t expect to be laying in my  wide awake at 4am this morning, followed by wandering aimlessly around my flat. To say my sleep pattern is messed up at the moment is an understatement, my days and nights kind of blur together if I don’t have anything to leave the flat for, I’m in a constant state of write, study, read and possibly eat at some point. I found myself thinking and worrying this morning about getting a job at stupid o’clock in the morning. What if they read about the problems I’ve had this year and don’t want me? What if they do secretly discriminate against me because of my mental health? What if was a prominent theme of the torture my sleepless brain put me through. But, it’s not because I’m dramatic.

I’ve been filling in a few job applications here and there, currently only for roles that I really want and could see myself working in and then there is the box that asks if you have a disability. While I myself don’t like being called disabled because it’s a crappy label, I know that to get help I need to tick it, lately though I’ve found myself  not wanting to tick that box, to hide a part of myself and my past out of fear more than anything. Like many other third years, I’m scared of the unknown and I know that the odds aren’t in my favor. Talking to Ali about it tonight he reminded me that there is so much proof that I can do so much more than a label, and I already have done so much more.

I’ve never been embarrassed or ashamed, and I’m not but I do know there is still a lot of people who are uneducated about my condition, but I’ve managed to educate people through telling my story before. With that in mind, why should I be scared of doing that again? When I saw this quote on Pinterest it made me take a breath, because what’s the point in trying to hide a part of my life or the hardships I’ve faced in the past? There is none. If anything that takes away from what would make me a great employee. I work hard, I persevere. Yes there may be times where my illness kicks my ass and I need a day to get myself better but I’m not a quitter. I got through my final year at university with a healing spine, a ‘broken’ mind and sickness and I think I’ve still done pretty damn great and have never let it affect my two jobs.

Why am I writing this? It’s not to brag. It’s because I know that sometimes you need to see someone else lay everything out. All the good times and all the shit times too and just remember that actually, you may not be ‘normal’, whatever the hell that means, but it doesn’t mean you don’t have a story to tell. To some people I’m an ‘inspirational’ person, which I’ll take but to me it’s just my everyday life, carrying on no matter what because I will not let a label or a box define me. I am so much more than that.

Back to the Routine

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When you’re in a depressed cycle, getting back into routine after a string of bad days can feel like a mammoth task. This morning I wanted to go back to bed as soon as I woke up, I didn’t want to face going to uni, being around people and facing up to my responsibilities now I’m back from being sick. Urgh. My mentor said she was really proud of me for trying to get back into the swing of things, even though I felt so overwhelmed this morning and just wanted to pull the duvet over my head and cry. From being sick and my body being so exhausted I’d fallen into my depression again and it wanted to pull me down and strangle me.

For someone who doesn’t know much about living with depression and anxiety it might seem like I’m being melodramatic or a giant cliché and I hate that. I hate that there is this sense that I have to defend myself when I’m feeling back enough, so I’ve stopped. I’ve decided to be honest with people and then just see how things go because, frankly, I’m exhausted. I can’t use my energy trying to make myself feel better because other people don’t or don’t want to understand. I’m lucky that I have got a lot of people around me who do support me when I’m struggling, but that doesn’t stop me feeling alone sometimes.

It’s going to be harder to keep routine now that most of my classes have ended and it might not be as strict, but being down has reminded me how important it is. I know that I have some big challenges for me in terms of my illness coming up, I’m going to have to deal with a lot of uncertainty and a lot of change. Am I scared? Absolutely. It’s like my own personal nightmare, leaving somewhere I’ve laid down roots, become the person I wanted to be and feel safe. No one here knows the old me and the way I used to be, the thought of returning to a town where a lot of people know the old me is terrifying, because I don’t want to go back to being that sad and terrified young girl I was. So I’m trying to learn now, get a toolbox of things that make me feel better and the knowledge I need to be able to fight my fears head on and getting back into routine is just the start.

 

 

Stressed, Depressed, but well dressed?

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When I was in Brighton a few weeks ago I saw a jumper with the slogan ‘Stressed, Depressed but well dressed’ across the front. I’ve seen these shirts before and they’ve become popular, before this it was the slogan ‘more issues than Vogue’. I’ve always felt conflicted with these shirts. For me, someone who does have issues and does get severely stressed and depressed because of my illness, it can be funny to wear these shirts, it’s me laughing at myself. With that in mind though, there is a bigger issue.

There’s been a lot of talk about making mental illness fashionable and there’s definitely been a surge of people claiming they’re ‘super anxious’ or ‘feel really depressed’ or that someone is ‘so OCD’ because they like things clean. These are things I can’t stand because these illnesses are so complex and damn hard to live with. A few years back there was controversy when two t-shirt were released by Urban Outfitters.

Now, I’m all for raising awareness and the ‘stressed but well dressed’ shirt isn’t outright offensive like the Urban Outfitters ones, but it is problematic. For people who have little information and are the type to throw around these words around and claim illnesses that can, if we’re being frank, kill people. People do die of these illnesses.

So do I think I’m going to buy one of these shirts? Probably not. While I can laugh at myself and say yes this is so me on some of my bad days, it’s not usually the reality. I can tell you that when you’re super stressed you don’t want to get dressed, particularly well dressed. Right now I am really sick with stress, so much so it landed me in hospital. Everything is an effort, getting out of bed, putting on clothes and as for makeup? You can forget it, unless I really have to I can’t be bothered. I think designers have to be mindful of what it’s really like for real people. You wouldn’t make a shirt about cancer because people know just how horrible it can be and how ill people get, and mental illness should be treated the same.

Maybe life’s not fair..

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When we’re young we get told life isn’t fair and as we grow older we realise this. there are things that we can’t control that we wish we could, illness is one of those things. You can help with some to prevent it or sooth symptoms but there are others you can’t, and mental illness is the same. I’ve learnt a lot in the last few years about myself and the illness that I have. I’ve thrown myself into research to learn more about the science behind it, recent research and theories to try and have a handle on something that I didn’t choose to have.

Ask a group of people with a mental illness and none of them would have asked to have it. It interrupts life and sometimes for some of our friends it takes theirs. I’ve thought a lot recently about this, about health. As much as I try and treat my body right with certain foods and getting fit and healthy I can’t do much for my mind. Sure I can surround myself with positive people and listed to my mind and my body but other than that if I’m having a low there are a lot of times where I have to wait it out, live with my depression or the anxiety attacks I sometimes have.

That said, ask that same group of people if they could flick a switch and it would have never happened and it will never happen again, it would be a much harder decision. Don’t get me wrong, in the last 6-7 years my illness has made my life hell and has taken things away from me, but it’s also given me things too. I’ve had depression since I was a teenager, so I don’t know what it’s like being an adult without it so sometimes I wonder, would I be as empathetic if I’d never had it, would I be as passionate and would I be so grateful for the little things in life. I don’t know. But I do know, because of my illness, that I have the best possible people in my life who pick me up and who know when I need the day or when I need a kick up the ass. Through lows and highs I’ve got great writing ideas or lyrics I wouldn’t have necessarily thought of, I’ve connected with amazing people and can be blissfully happy by the tiniest of things like waking up in the morning and feeling ok and other things too.

Why am I writing this? For a few reasons, one because I didn’t feel so great in my mentoring session today and we talked for a long time about depression, how I feel about it and the fears I have. There is fear, fear that I might go back to a dark place like I was at school but my mentor pointed something out to me. At 15/16 I had no experience, I hadn’t been diagnosed and I didn’t have a good medical team. I didn’t have a lot of information or ways to recognise my feelings and try and combat them before they got too bad, I had unhealthy ways of dealing with my feelings. In the last 3 years especially I’ve done well to get as far as I have and while the fear won’t go away, if I take note I’m in a better position than I was when I was 15/16. I have a voice and I have you guys too, who can cheer me up on Twitter to no end.

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Taken on my 15th birthday, I was happy here and hadn’t really experienced bad depression yet. 

People may call me names like a nut job, loon, or make snide remarks about being unstable and therefore unable. I’m getting to the point where I’m starting not to care and their hate makes me more driven. This illness may never go away but that doesn’t mean people will always be ignorant, which is why I write things like this to educate, to explain. I’ve written before about my story (the short version, maybe one day I’ll write it in detail) before and I’ve always been open on here about my highs and lows. I think it’s important to remember, for anyone who has an illness, that this is just a part of you, it does not define you. 

So no, life might not be fair and there are thousands of people in the world who live with my illness every day, but we aren’t alone. We might feel like it when depression grabs us and drags us under for a few days but at the end of the day there are so many others out there who are at all different stages of their illness and recovery. Don’t be scared of being you.

I’m not ready for 2016

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2016 is supposed to be an exciting year for me. Graduation for a lot of people is something to celebrate but with graduation comes a minefield of uncertainty and basically leaving me on the verge of panic attack central. As the days creep closer to the new year I feel like I’m digging my heels in and just saying no, no, no, no.

I’m not feeling happy or confident about graduating. I don’t like not having a plan and knowing what I’m going to do. I don’t know what I’ll graduate with, I don’t know if I can get a job or if I’ll get the one I want, I don’t know if my MA will run or if I’ll be able to afford it. Where will I live? Will I be able to deal with doing my MA and working at the same time? All these questions are running around my head and my anxiety is attacking me like a laser.

I’m hoping I’ll calm down and take it day by day, month by month but you do get asked a lot of questions. Everyone is interested in a kind way but it’s still stressful. Knowing that in a few months people will be coming to view mine and Ali’s home for the past few years and that I’ll have to start boxing things up again…To say that all this makes me emotional is an understatement and this is all probably a lot work because I’m tired and generally emotional at the moment.

It isn’t all doom and gloom. Some nights I think about exciting things and plans I have and ideas for the blog or the book I’ve always wanted to write. I guess it’s all ups and downs. I’ll try and go into 2016 with a day by day attitude because there are going to be a lot of changes coming my way and I am really anxious. I’m hoping I can work on my techniques and keep fighting the anxiety because I really do want to enjoy what I have left of my undergraduate degree and hopefully there will be good things to come in 2016.

 

 

Picture from Pinterest

Living with a mental health condition at Christmas

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Ah mental illness, you little pest, of course you want to pop your head up for the holidays. I’ve been thinking a lot about mental illness and christmas time, I say thinking and I mean getting anxious about it. I’ve wanted to write this post for a long time but almost couldn’t find the words for what I wanted to say.

For most people Christmas equals joy and happiness, right? For some of us though our mental health threatens the celebrations every year whether we like it or not. Not only is it hard for the person dealing with the illness, but also the people around them and so I’m going to be frank. One day of the year doesn’t make a mental illness magically disappear, it doesn’t work that way.

In the past I’ve been ill on birthdays and ill on Christmas day and it sucks. I’d probably call it one of my absolute worst points of the illness. I was 16 and even though I loved all the gifts that I’d gotten and my family I was on a low and it wouldn’t shake no matter how hard I tried. So my family got a ‘meh’ response, I cried, my Mum got upset and my Dad was confused. It was Christmas, why was I upset?!? This was long before any diagnoses or medication and I felt like I was drowning. I hated myself for not being excitable like I normally was. A phone call changed everything though. I spoke to my Gramps on the phone and we talked, I cried again and he said not to worry Christmas can be an overwhelming time. We spoke more and by the time we ended the conversation I felt better and hugged my Mum to tell her it wasn’t anything she’d done at all.

Thankfully the further I’ve gotten into my recovery the better Christmas has been. Last year I woke up before my little sister and woke her up in our matching onesies. This year after assignments I was finally excited, singing christmas songs and getting excited about presents. Am I anxious about lows? Sure. Right now though I’m doing things to combat it, I’m getting as much sleep as I can, eating healthier and will be exercising this week at home.

I have to point out I’m at a stage in my illness where this is all possible. 16 year old me was too absorbed by it to do anything. So I guess what I’m trying to say is if you live with someone with a mental health condition they’re not doing this because they hate christmas, because they want to ‘make things difficult’ or because they’re not trying. They doing it because it’s a part of the illness. So if someone is depressed, anxious or struggling with their food just let them deal with it the way they can. If someone with an eating disorder needs to have something else at the dinner table, don’t make a fuss or judge. If someone needs half an hour of alone time because things get too much then let them. Basically they need to do what they need to do to get well.

As a message to the others who are anxious about the holidays. It’s one day ofthe year, it may seem like the biggest thing but next year there will be another christmas. The most important thing is taking every day one by one and that is what you will do. I’ve been there, when you feel like you’re going to ruin everything and people would be better off without you but that’s not you speaking, that’s the illness I promise.

So as I travel home for Christmas today, I just want to tell people to be kind. Love no matter what this Christmas and remember a hug can mean more than a million words. I hope everyone has a Merry Christmas before we hurtle into 2016!

Chloe

P.S I’ll still be blogging every day over Christmas! Don’t think you’ve gotten away from me that easy!