BPD As Described By Claudia Boleyn

Trigger Warning: frequent mentions of self harm, suicidal thoughts, and suicidal behaviour. If this is something that you will find triggering or upsetting, please don’t read ahead. Please always put your mental health first.

Given that it’s Borderline Personality Disorder (BPD) Awareness Month, I felt I should write at least one post about BPD, although one is all I have time for at the moment, what with my uni workload. This is one of the videos I watched pretty early on after my BPD  diagnosis and it really, really helped me. It’s such a good, informative video, completely free of the stigma that is often attached to this diagnosis.

I really recommend watching the whole thing but I want to talk about some of the points Claudia makes, as well as adding some of my own thoughts.

Borderline Personality Disorder (also known as Emotionally Unstable Personality Disorder) is a type of personality disorder, a type of mental health problem where your attitudes, beliefs, and behaviours cause you longstanding problems in your life, that impact your life daily. Struggling with how you think and feel about yourself and others – and that causing problems in your life – can lead to an investigation into whether you might have BPD. Having said this, many clinicians are reluctant to diagnose it as there is such stigma attached to it, with many in the health sector seeing those diagnosed with BPD as ‘difficult’ and ‘attention seeking’ (x). Personally, I have been told on numerous occasions that I should consider abandoning the diagnosis to avoid negative assumptions from doctors, a suggestion I find deeply offensive and have ignored. It explains things about me that I can’t otherwise explain and I’m not going to give that up because of other people’s ignorance.

Considering how many misunderstandings and how much stigma there is around BPD, Claudia uses the framework of the diagnostic criteria, as detailed by the Mind website (as of 2016, although the diagnostic criteria listed has not changed), to describe the symptoms of BPD and how she experiences them.

Fear of Abandonment

  • She talks briefly about her parents separating when she was a child and how, while it wasn’t an actual abandonment, it could be perceived that way, especially in the mind of a young child.
  • “I think I do struggle with that feeling that people are gonna leave, that people are gonna leave me.”

I definitely relate to this. I’ve had several people abandon me, intentionally or not, and so I have serious anxiety about people leaving me.

  • “[I’ve struggled with] that feeling of being not good enough and that when people know the real you, they’re not gonna want to stick around and stay with you. I really have struggled with that.”

I also relate to this, although my fear usually stems from feeling like a burden and that one day, the people in my life will feel like I’m just too much of a burden and walk away.

On Feeling Emotions Strongly

  • “I do have very, very strong, very, very intense emotions and I have done since I was younger.”

I most definitely have very strong emotions, sometimes overwhelmingly so.

  • “I don’t seem to have a middle point, for emotions at all. I don’t have a happy setting. I know that sounds odd but I don’t have a happy setting. My happy setting is feeling calm and I rarely manage to feel calm. I either feel very excited, very happy or very agitated or I feel anxious, and depressed, and low, and suicidal. I don’t have that relaxed place.”

This is very true for me too. My emotions tend to be at the extreme ends of the scale with very little middle ground. 

  • “It’s exhausting because everyday I’m going through these hundreds of emotions and I’m feeling the full force of them as if big things are happening when really hardly anything is and it exhausts me. It’s really tiring and it’s really hard to deal with day to day when your emotions can be so easily triggered like that. It says, ‘you can go from feeling very happy and confident in the morning to low and sad in the afternoon,’ and that is so me because I’ll wake up in the morning some days and feel great and… I don’t know… It happens so quickly and suddenly I’m suicidal… Most people assume that something big must’ve happened to make you get that low but with BPD it doesn’t need to be a big thing… I get really big ups and downs and there’s no middle ground for me.”

It can be scary and as Claudia says, exhausting, to have such big emotions that ricochet around inside you, changing every time they collide with something. If that makes sense. When they’re so big and they change so quickly and dramatically that it’s like the ground is constantly rocking until your feet; nothing feels stable or reliable.

  • “I do get really big ups and downs and there’s no middle ground for me emotionally. There is no centre.”

On Having Unstable Sense of Self

  • “I’ve had to develop a sense of who I am because, I think with BPD – just from my experience – I feel very empty and very blank canvas-y and I do struggle with understanding who I am: ‘Am I a good person or a bad person? What do I think about things?’ Sometimes I feel like I’m not even here, everything’s too much, and I just think… ‘What am I? What is this? What’s going on?'”

I really relate to this, to feeling empty, to feeling like I don’t truly know who I am. I know little things, that my favourite chocolate is milk chocolate and that thunderstorms make me feel alive. But the answers to the big questions about myself continue to elude me: Am I a good person or a selfish person? What do I really think about this issue or that issue? Am I actually good at the things I think I’m good at? What are my strengths? My weaknesses? It’s very confusing.

  • “You might notice I use the name ‘Claudia Boleyn’… It’s not my birth name anyway and I think what I’ve tried to do because of the issues I’ve had with feeling so empty and confused about this kind of thing is I’ve tried to form an identity based on people I admire… Some people think it’s like copying. It’s not necessarily copying; it’s trying to deal with that empty, confused thing. There are things I like and things I don’t like and I can tell you the things I enjoy and the things I don’t enjoy but I couldn’t tell you about me as a person because it changes so much. I couldn’t tell you if I was an introvert or an extrovert… it’s just a million things. I couldn’t describe myself. Or if I were to describe myself, you could ask me the next day or an hour later and it would entirely change… I do change a lot. Fictional characters are important to me and historical characters are important to me because they help me ground myself a little bit. It’s hard because, with BPD, people who don’t have it find it very difficult to understand that. So with the Anne Boleyn thing for me, she represents a lot of what I find admirable and I want to replicate some of those qualities but at the same time I want to be myself. It’s a really hard balance to strike. It’s not that people with BPD don’t have that personality, it’s that they feel so much so much of the time and they can change so often that it gets confusing, you know? What is my stable identity? What is that? It’s really hard to figure out when it’s changing all the time.”

I can definitely understand taking the best of our favourite people or fictional characters and building an identity and personality using those traits. I’ve absolutely done it. When I was younger, I would accidentally take on the whole person with both the traits helpful and unhelpful to me; I’d end up making decisions that weren’t what I wanted at all but were what the person I was emulating would do, which got me into some complicated situations. But now that I’m older and I understand that this is something I do, sometimes unintentionally, I’m better able to use it to strengthen me, rather than completely change me.

On Finding It Hard to Make and Keep Stable Relationships

  • “I haven’t had a super serious romantic relationship… I actually am petrified – I tell you, PETRIFIED – of being in a serious, serious, like, forever relationship because, when you have something like BPD and you have that mindset, everything is very all-or-nothing so I do worry about the state of my emotions when being in love, and being in that sort of intense relationship because just the normal things for people with BPD can be overwhelming so with something like love, which ‘normal people’ find absolutely out there, for someone with BPD, that’s a lot. That’s a lot to deal with. I think I want to be in a really stable place for that.”

This definitely resonates with me. Romantic relationships scare the crap out of me. The only relationship I’d consider significant was late in my teens, before I had my diagnoses of BPD (as well as ASD, depression, anxiety, etc) and it ended very traumatically. While that will always be on the other person, I did really struggle throughout the time we knew each other, especially with the big emotions and fear of abandonment curtesy of the BPD, as well as the social difficulties of ASD. And with no explanation for why I operated that way, it was probably doomed from the start. Still, the other person didn’t need to be such a cruel, manipulative human being…

  • “It’s a lot to deal with if you have BPD. Maintaining those relationships is hard because it means so much to you. It means a lot. That being said, it’s not that I find it hard to keep stable relationships, or maybe I’ve just got lucky with the ones I’ve got… I do a thing where… (*see point below)… because of the BPD, where I do not talk to someone for a very long time and I don’t know why this is but I find it really hard to keep contact with people. So my closest friends are those people who are very understanding and very patient.”

I really relate to what she says about relationships being complicated because of how much you care. I’ve been devastated by the ending of friendships, relationships, etc and that does make maintaining relationships of any type very stressful at times: the idea of saying or doing the wrong thing and that damaging the relationship irreparably (even relationships that, in theory, aren’t so fragile that one mistake would ruin them) is terrifying and that in itself can lead to making bad decisions, saying or doing things, etc that aren’t true to who you are, that could damage the relationship. If that makes any sense.

I also relate to what she says about not being great at continuous contact. For me at least, I think it’s about exhaustion: communication is so loaded and requires so much energy, social energy, emotional energy, etc. Sometimes it all just becomes too much and I have to retreat for a while to recover.

  • *”Can I just say… if you’re a friend of mine and you’ve been a friend of mine once, I consider you a friend for my whole life. I just wanna put that out there.”

This is definitely a trait of mine. If you’re a friend once, you’re a friend forever (barring a serious falling out). It’s one of the things that I find very confusing in other people: when they don’t feel the same way about friendships. It just doesn’t make sense to me.

On Acting Impulsively

  • She explains that, with BPD, acting impulsively often involves doing harmful, dangerous, and risky behaviours, anything from shoplifting to taking drugs.
  • She, understandably, doesn’t want to discuss her personal risky behaviours on the internet but does elaborate on the feelings involved.
  • “The impulse control is bad with me. With BPD, because of the high emotions and feeling everything so intensely, obviously you feel so out of control and it can be really hard to control your impulses sometimes.”

I don’t consider myself a particularly impulsive person. In fact, I’ve always been terrified of not being in control of myself or making thoughtless decision. That’s probably partly why I’m such an overthinker. 

On Suicidal Thoughts and Self Harming Behaviour

  • “I am constantly suicidal and I have been as long as I can remember. Now that sounds odd. I don’t mean in the sense that I’m going to actively go out and do it constantly 24/7. I just mean that there is a constant undercurrent with me… I think it’s called suicidal ideation, it’s sort of being passively suicidal. It’s that feeling of, even when you’re at your best, thinking, ‘well, I’m not going to do it but if a car hit me right now, I wouldn’t complain.’ It’s hard to exist like that. I think it’s hard for people who don’t understand that [to get it].”

I’ve been meaning to write a post about being passively suicidal for ages; I just haven’t had the time that I would want to dedicate to it, given how important it is. But I’ve definitely experienced this and continue to have phases of feeling this way, some that last for days and some that last for months.

  • “I think it’s to do with the huge emotions and the exhaustion and being so confused and things can feel like so much and there is a lot of pain that comes with BPD because being so emotional, reacting  to stuff so strongly can make you feel like you’ve got no skin. It’s like you’ve got no emotional skin, nothing to protect you, and it’s painful and it’s hard and it’s tiring and it’s exhausting and it leaves you with this, for me, this undercurrent of suicidal ideation.”

The ‘no emotional skin’ leapt out at me immediately. I really relate to that. Sometimes everything is just so overwhelming and painful; it can all feel like just too much to cope with, to survive, to live a life that isn’t unbearably painful.

  • She briefly mentions two suicide attempts but again, completely understandably, doesn’t want to share the details with the internet.
  • “I’ve been a self harmer since I was about twelve years old. I began self harming before I knew what self harming was… It just came as a sort of reaction to me. I used to scratch my thumb with a safety pin because I felt so upset and angry and when I felt a big emotion, I would just scratch until my thumb bled. I didn’t know self harm was a thing. It was a response to the emotions and feeling too much and feeling completely trapped in my body and not knowing what to do.”

I’ve self harmed on and off since I was about thirteen. To be honest, I never really thought about it as self harm – not for a long time at least: I didn’t think of it as harm myself because that wasn’t the primary motivation for doing it. I did it (and sometimes still do it) when I got so overwhelmed, so full of feeling that I had to get it out of me. I didn’t know how I would survive if I didn’t do it; it was a coping mechanism, like a pressure valve that helped me regulate the intensity of my emotions. I’m obviously aware now that it is self harm but after much discussion with my therapist, we’re not worried about it on it’s own. If it’s a coping mechanism (and one that I use relatively rarely), then the best use of our time is working on helping me to regulate my emotions so I don’t need to do it rather than stop me from using the only coping mechanism I currently have.

Feeling Empty and Lonely A Lot of the Time

  • “I do feel very empty and this sounds incredibly emo and angsty but it’s just a default setting for me, as it can be for other people with BPD. I just feel very empty and alone and just scared really. I think, living with BPD, you’re in a constant state of low fear, you know… terror sometimes and you get so used to it that it’s just there and it’s only when you come to think about it, you think, ‘wow, I’m living with this in me all the time.’ It’s quite hard to think about actually but it also makes me feel proud of myself for still being here and fighting through and getting the help that I needed and sorting myself out.”

I can absolutely understand the feeling of emptiness; I relate to it a lot. Sometimes I wonder if the emotions in me and around me are just so big and so overwhelming that that part of my brain just shuts down to keep me from being constantly overwhelmed, to keep all the fuses in my brain from blowing. Maybe empty is safe. I don’t know. But ‘feeling empty’ is definitely something that resonates with me. 

  • “I do have a constant sense of emptiness and just feeling like nothing is ever enough. Everything is too much for me and yet it’s simultaneously never enough for me, it’s never enough to fill that empty feeling.”

‘Everything is too much for me and yet it’s simultaneously never enough for me’ is a phrase that could sum up my relationship with my emotions. My emotions are so big that they’re overwhelming but they also don’t feel quite enough. I can’t really explain it; I don’t know if there are words for it. It’s so deeply emotional that I’m not sure it would translate. I guess it’s kind of like sucking in so much air you feel sick but none of it is actually getting to your lungs. Maybe? I think that’s the best analogy I’ve got. Right now, at least.

Getting Angry and Struggling to Control Anger

  • “Yeah, I’ve had some issues with anger… [but] I’m not a violent person at all. Whenever I get the extreme upset and anger, I’ve always taken it out on myself. I’m a self harmer. I can be truly cruel to myself sometimes and when I feel that intense anger, I’ve always acted more inwardly.”

I don’t often get angry. I don’t think I ever even felt angry until I was twenty. I always just jumped straight to sad. So anger is a strange and confusing emotion for me. I only ever really let it out when in the midst of an autistic meltdown. As I’ve already talked about, I have a lot of fear around saying or doing the wrong thing and the chances of that happening, in the heat of an angry moment, make that a lot more likely to happen. Plus I really hate confrontation. I can do it but I hate it.

Paranoia, Psychotic Experiences, or Feeling Numb When Anxious

  • She talks about having had psychotic experiences and that they’re triggered either by feeling really low or by very intense emotion.
  • “I’ve had some very scary things happen before because of psychosis.”
  • She talks about a period of time where she genuinely believed that there would be a school shooting.
  • She goes on to talk about how, after talking about it with her psychologist, she learned that it was her brain’s response to extreme stress and “thankfully, [her] life is different now” so she hasn’t been experiencing that level of stress and the resulting psychotic episodes.

Fortunately, I’ve never experienced a psychotic episode and hopefully my mental health never reaches that point. They sound incredibly scary and I feel for anyone who has them.

  • “I get depersonalisation and derealisation, where I don’t feel like I’m a real person and I feel like the world is not real. Sometimes I get that when I’m getting towards psychosis because I feel like nothing is real and I’m not convinced… sometimes it feels like this is all some virtual reality or something and I’m not sure what’s real and what’s not and ‘Am I alive? Am I imagining this?’ and it can get really  scary and it spirals out of control quite fast. But yeah, I do get very numb and checked out and when I get ‘bad,’ sometimes I will sit down for a while and lose a huge chunk of time…”

I’ve definitely experienced periods of feeling like I’m not really here or like I’m really far away from everything and everyone, separated by something intangible but powerful. I’ve struggled to believe that I’m real and that the world is real. It’s confusing and difficult and lonely. I usually only experience it when I’m deeply depressed but it does appear on other occasions. 

She talks about the stigma similarly to the way I described it at the top of this post but says that she wanted to share her experience with it in the hopes that it will help people and lessen that stigma. She also talks about the impact that her mental illness has had on her life: she’s studying for a degree at home because that’s the path most conducive to her mental health and that’s something she’s proud of because she’s still working to achieve the things she wants to achieve, even if she has to go about it in a less than traditional way.

“I really am working on structuring my life now; like how some people structure healthy eating in their lives and they think about what they’re gonna eat in their diet, I think about myself emotionally and giving myself time and all these kind of weird emotional things that I have to think about, like that. But yeah, having my diagnosis was a huge weight off my shoulders because it feels real and you feel very validated… And like I said, some people don’t like a diagnosis and that’s fine. That’s up to them but for me, it felt validating and I’m not ashamed of it. At all.”

Many of the things I’ve talked about personally are very much inline with Quiet BPD, a less well known presentation of the disorder – sometimes people don’t initially believe me when I say I have BPD because I don’t fit neatly into the classic presentation. I read about it before my diagnosis and after investigating it with my psychiatrist, it’s always been accepted that this is the form that my BPD takes. I really want to write a longer, more personal piece on BPD and on my experience of Quiet BPD but I just haven’t got the time at the moment, being in the home stretch of my Masters. It’s also something that I feel is so important to get right and I just haven’t felt like I’ve been in the right space to do it justice. But these days I do feel more confident in my experience and, maybe when the stress of the Masters is over, I’ll feel able to write that post.

The DSA Process For My Masters Degree

Since the academic year is starting up again, I thought I’d write about my experience with getting support for my Masters Degree as a disabled student. The DSA (Disabled Student Allowance) process can be very difficult so, having been through it twice now, I thought I’d share my experience. I don’t know if I’ve had a good, bad, or typical experience but I thought that simply putting the experience out there might be helpful to anyone at the beginning of this process, to give them an idea of what may happen down the line. As I’ve already said, it’s difficult and tiring but that’s not to say that I would discourage someone from applying. I was just very naive going into it the first time and was blindsided by how complicated and stressful it was; I’m lucky to have had help going through this both times. Having support from sources such as DSA can be hugely beneficial but I wouldn’t want anyone going into the application process unaware so I thought I’d share my experience as I haven’t seen many accounts of the whole process…

I wrote about my first assessment in great detail here, so I suggest reading that but I’ll also sum it up here to make sure I’m sharing the full experience in one place. So… That first assessment was a complete disaster. The assessor was perfectly nice but when we got to discussing what support DSA was willing to offer me, it went downhill fast. They would offer me a laptop, but not one with an operating system required to run the programs I needed for my course because apparently that was a course specific need rather than a disability specific need despite the fact that I – a disabled student – needed them to do my course. They wouldn’t offer me any travel support towards commuting because I’d ‘chosen’ to live at home when I actually had to live at home because of my disabilities. And they have no direct contact with the universities themselves so they couldn’t offer any support through them. So, essentially, they weren’t going to offer me anything because my needs didn’t fit their guidelines, because my disability didn’t fit with their idea of disability. It was hugely frustrating and distressing and I left in tears. I felt completely let down and abandoned.

By the end of the assessment, I was so utterly distressed that the assessor told us that we could appeal, which we did. The second assessment was with a different person, a really lovely woman called Rebecca, and was much longer and in much more depth. We went through everything again in minute detail: from the necessary computer specifications to the exact details of an average university day’s travel. She went through all the possibilities and all the potential outcomes, as well as the potential roadblocks and the reasonings behind them. It was a lot of information but I did leave feeling more hopeful; I really felt like she was on the case, like she was really committed to helping me get as much support as possible. Her report went through several different people before reaching a senior SFE (Student Finance England). It was initially rejected but then, when we provided them with documentation proving I receive PIP (Personal Independence Payment), they changed their minds and granted me a new laptop, software and apps to help with my lectures, independent study, and mental health, and mentoring through the National Autistic Society (although it seems that, due to the pandemic, this service no longer exists). I didn’t get any support for the travel but I’m grateful for what I did get, plus the travel costs haven’t exactly been an issue over the last few months… From that second assessment, it was four months before I received the support I was awarded.

In my experience, the whole DSA process is very slow. It was slow when I went through it during my Bachelor’s Degree and it’s been even slower this time, presumably due to the pandemic. I started this process in January – much later than intended but my mental health was so bad that I couldn’t handle the in person assessment – and didn’t get the equipment until June. Then the laptop that arrived wasn’t the right one and so we had to spend another two weeks – and a somewhat ridiculous amount of emails proving that it was in fact the wrong one – organising the swap, insuring that I got the one that my DSA assessment had determined I needed. A couple of weeks later, the new laptop arrived but setting it up took much longer than it should have. This was due to how the people who’d previously worked on my laptop had set it up, making the transfer of all my files much more complicated and messy. It’s still not as sorted as I would like it to be but it is functional.

Factoring in all of this, had I been doing my Masters in one year rather than two, I would’ve had this equipment for less than a semester before I finished the course. Yes, this was affected by the pandemic, problems with the university Autism support person, and the late start in pursuing DSA but that was due to the reasons I was in need of support so it’s not the most efficient system in that regard: what happens if you’re too disabled by your disability to seek help?

The laptop and software that DSA have provided me with has been invaluable, especially since my laptop was dying a slow death around the time I received the new one. We didn’t get everything we were hoping for but it’s definitely better to have it than to not. So, having now been through this twice, I thought I’d offer some tips that would’ve been helpful to me before going through the process…

  • If you disagree with part or all of the final assessment, ask to talk to someone else – It’s not something you’re necessarily made aware of when you have the assessment but I was so distressed by the end of the assessment that the assessor told us we could appeal. My second assessment yielded quite different results than the first one so it’s definitely worth asking if you feel that you haven’t been heard or fully supported.
  • Ask what kind of documents act as proof of a need for support – The earlier you find out what paperwork might help your case, the quicker the process will go. We, unfortunately, didn’t know that the PIP documentation was helpful and the whole thing may not have taken so long if we had.
  • Take someone with you as it can be overwhelming and tiring – These assessments can go on for hours and there’s a lot of information to both give and receive. Plus, it can be a pretty emotional experience so having someone with you can make the whole thing easier; you have someone to lean on and two pairs of ears to take everything in.
  • Ask for everything that you would find helpful – You might not get it all but you definitely won’t get it if you don’t ask and hopefully you’ll get some of it. It’s also always worth asking what you’re potentially entitled to because there may be things you aren’t aware of that could be helpful.
  • If you’re told something isn’t possible, ask why – The assessors can’t know every relevant question to ask and you can’t know every relevant piece of information to give so if they tell you something isn’t possible or available, it’s worth asking why because you may have some information or some paperwork that changes the situation and what support you can get.

I hope this post is helpful for anyone considering or going through the process. I hope I haven’t made it sound too scary. I really do recommend it but I wouldn’t want anyone to be unaware of how difficult and stressful it can be. You deserve to get the support you need and I only want to make that easier, if only by arming you with information and advice. So, if you’re going through it, I wish you the best of luck and I’m rooting for you.

Claudia Boleyn on BPD and Obsessions

EDIT: Since writing this post, I’ve learned a lot about the language around mental health and I no longer think that the word ‘obsession’ is necessarily a helpful one. I think something like ‘subject of intense interest’ or ‘specialised interest,’ not dissimilar to language used when describing ‘special interests’ in Autism. Having said that, I’m reluctant to change the language in this post because it’s the language that Claudia uses and because I think it’s potentially important to leave the post in its original form. Also, the negative connotations of the word ‘obsession’ are potentially relevant in the context of BPD as it’s a condition that can have unhealthy (a word often linked to obsession) and damaging behaviours for both the person living with it and the people who surround them (and I say this as someone who struggles with BPD).

I’ve written about Claudia Boleyn’s videos before but this is another great one that I think really clearly explains something that happens with Borderline Personality Disorder (also becoming known as Emotional Intensity Disorder) and various other mental health problems. I really recommend watching it.

In this video, Claudia talks about how, when you’re struggling with your mental health, you can develop obsessions with certain things, particularly fandom related things: fictional characters, books, TV shows, etc. These special interests can overlap with autistic special interests but they can also come about as a coping mechanism; they can become an escape from the difficulties of the real world.

She talks about how she can categorise her life by her obsessions, including Emmerdale and Anne Boleyn and certain areas of art history. She talks in particular about her obsession with Anne Boleyn, how it strengthens her and gets her through the really tough times. She even uses Boleyn as a surname: “I use it to exist in the world.” She talks about how she uses this obsession and others to understand herself. All of this makes those obsessions really special and important. I can definitely relate to this. My life can be divided up by my obsessions: animals but particularly horses – I obsessively read the Animal Ark and Saddle Club book series – Harry Potter, crime dramas, Taylor Swift, certain youtubers, anything superhero related…

“My identity and my life is sort of filled up with the stories of other people rather than stories of my own.”

With BPD, there’s the extra layer of struggling with your identity and your sense of self. Claudia talks about how she would go to school dressed as her favourite characters and how a teacher once asked her, ‘When will you come to school dressed as yourself?’ But that’s really hard when you don’t know who you are. I’ve always found it very easy to lose myself in fandoms or characters because I don’t know who I am to begin with and I’ve had a couple of experiences where I’ve done things I didn’t actually want to do because I thought that’s what a character would do, i.e. what I should do to embody those good characteristics.

“I’ve never felt like I have a proper identity in myself so I’ve sort of constructed one in a way based on what I admire and what I want to be and what will make me as good a person as I can be and what will make me contribute to the world but it’s really tough.”

It can be a good, helpful strategy – until it starts to dictate your emotional state.

“I think this isn’t spoken about enough with BPD, especially because we can struggle with identity and who we are and what sort of people we are. I think we often construct ourselves based around fiction and around those characters we admire and I think it matters a lot to us. It feels like it becomes a part of our identity in a way, so when it goes wrong, it feels like we’re falling apart. Yeah, it’s difficult.”

Another problem in BPD is that of regulating your emotions. Small things – day to day things – can have massive impacts on your mood. It can be exhausting and stressful to go through such ups and downs and it’s constant; there’s a lot of fear and uncertainty involved. So escaping into an obsession or fandom can be helpful and soothing but then, when something goes wrong in or around that fandom, for example, it can cause really negative emotions because your escape, your safe place, has been threatened. It might seem extreme from the outside but it’s very real and personal if you’re going through it.

I really relate to this video and I’m really grateful to Claudia for putting it out into the world. We need to talk about all parts of living with mental health, not just the relatively straightforward ones.