Posted on January 1, 2024
TW: Discussion of depression, self harm, and suicidal thoughts and ideation.
Much like last year, I have no idea how to sum up this year. I don’t think I have it in me to write a long post that involves such intense emotions and I think that, if I wait until I do, we might all be waiting a very long time so I’m just going to write until I can’t anymore and that’ll be that. It’s just too hard.
While there have been good moments (some of which can be seen in the collage below), it’s been a fucking painful year and it’s now the third New Year’s Eve that I’ve spent crippled by depression, suicidal thoughts, and overwhelming fear and dread around the future. I’m pretty sure I’m in full autistic burnout and I feel like I’m living in a fog. Last year, I think I described my depression as a drought but, this year, I think the better metaphor is drowning: I feel like I’m drowning in this depression and I have so little energy left that staying afloat is feeling more and more impossible. I’m so tired. I’m tired of trying so hard, of feeling like I’m not trying hard enough; I’m tired of feeling this way, of feeling like things will never get better, like there’s no point in even trying to feel better because there’s nothing worth feeling better for. It just feels like there’s so much bad in the world, so much agony, that it isn’t a world I want to live in. I feel broken; I feel like a prime example of a defective human being. There have been good things, like I said, but it seems like they can never just be good things: there’s always so much bad or hard twisted up in them that enjoying them isn’t as straightforward as it sounds. I miss feeling safe. I miss feeling safe to feel things.
A big, hard part of this year has been that I started taking Phenelzine again, for the third time. I didn’t want to and I felt coerced by the circumstances to take it. I was so angry about it all that I made potentially my most dramatic, self destructive move so far: I cut my face and then, when it got infected, I was so reluctant to treat it that I’ve ended up with a fairly visible scar. The most confusing part of it was that, even though I didn’t want anyone to bring it up, I was surprised that no one did; it seemed like the kind of thing that would trigger some alarm. Just as I imagined voicing consistent suicidal would but no one’s really commented on that either. It only makes the experience more isolating and lonely. But back to the Phenelzine: while it helped me get out of bed and go out now and then, it hasn’t had the same impact that it’s previously had on my mood, even on the higher dose. And that means that I’ve officially run out of medication options. I’ve been going to therapy consistently, for the most part, but I feel like it’s getting harder and harder; there have been sessions where I’ve left feeling traumatised. We’ll be trying something different in the new year but I’m struggling to feel hopeful, but that’s not specific to just therapy.
I look at the collage I made for this year and although I remember each of these moments, I feel disconnected from them; the emotions feel dulled. A lot has happened, somewhat to my surprise…

I went to multiple small shows; I went to hydrotherapy religiously and started physiotherapy; I got adopted by a puppy and then had my heart broken when she was taken away; I went to Nashville for Tin Pan South; my application for an Autism Service Dog was successful; I released my single, ‘House on Fire,’ as well as creating all of the visuals for it; I was diagnosed with Fibromyalgia; I went to art exhibitions (and even helped to build my favourite art piece, Breathing Room); I hung out with friends, online and in real life; I travelled to Germany for the wedding of one of my best friends and was reunited with multiple friends that I hadn’t seen in years; I got to hang out with some of my American friends when they performed here; I fought for Taylor Swift tickets; I had my heart broken again when the rescue puppy we applied for was homed with someone else; I went to some amazing concerts; I met Amanda Tapping again and she’s still one of the most wonderful people I’ve ever known; I started performing again; I read books and watched movies and TV shows that are now among my favourites; I adopted a puppy (which still doesn’t sound real to me); I swam 5km for Mind, raising over £600; I went to multiple Maisie Peters shows and got to meet her too; one of my cats got very sick and we had to nurse her back to health; my aunt died; I changed heart medications; and I worked on lots of different musical and academic work. I know all of these things happened; I remember them clearly but it’s like watching them play on a screen. I know these memories are mine but they don’t feel like mine. It’s weird and sad.
I’m so tired. I’m tired of masking but I don’t know how to stop. I feel broken – physically, mentally, and emotionally – but as hard as I try, it never feels like enough. Over ten years later, it should be getting better not worse, right?
I don’t know what else to say. Life feels increasingly scary, internally and externally, and I just feel too broken to manage. I don’t know how people walk around without all of the fear and grief and anxiety that I do, that I see as such an intrinsic part of being human. As I wrote last year, “I don’t know what tomorrow brings. I don’t know what I want it to. I didn’t want this year. I didn’t expect to still be here and I’m not happy or pleased or grateful for that. I feel pathetic and stupid and cowardly; I feel broken beyond repair. I feel frozen, overwhelmed by all of these big feelings. If feelings could kill you, I think these would have.“
Category: animals, anxiety, autism, chronic fatigue, chronic pain, death, depression, diagnosis, emotions, event, family, favourites, heds, hydrotherapy, medication, mental health, pots, self harm, suicide, therapy, treatment Tagged: 2023, actuallyautistic, amanda tapping, antidepressants, asd, autism, autism spectrum disorder, autistic, autistic burnout, autistic singersongwriter, charity, dbt, depression, dialectical behaviour therapy, ehlers danlos syndrome, family, fibromyalgia, heds, hydrotherapy, hypermobile ehlers danlos syndrome, maisie peters, maois, medication, mental health, mental illness, monoamine oxidase inhibitors, new year, new years eve, phenelzine, physiotherapy, radically open dialectical behaviour therapy, rodbt, self esteem, self harm, self injury, self loathing, singersongwriter, songwriter, suicidal ideation, suicidal thoughts, taylor swift, therapy, treatment resistant depression, trigger, trigger warning, year in review
Posted on October 21, 2023
TW: Mentions of being suicidal.
Year two of dealing with chronic pain. Since it’s Bone and Joint Week, I thought it seemed timely to update this series, although hEDS isn’t bone related. But whatever. I needed to post this at some point and my joints hurt so this seemed as good a time as ever.
Unfortunately, very little changed during the second year. I was incredibly depressed, to the point where I was periods of being consistently suicidal, so I wasn’t capable of much. But we were also waiting for the Pain Clinic to get in touch as they’d promised to.
This post spans from April 2022 to March 2023.
OCTOBER 2022
After finally getting the referral to the NHS Hydrotherapy Department in December 2021, I tried to work that into my routine to get some exercise, strengthen my painful joints, and just improve my quality of living. It was pretty hit and miss for a while (as my post about it reflects) but around August, I found a pool that allowed me to do all of the assigned exercises and managed to work out a schedule. From that point on, I was going at least twice a week, if not more, and I could really feel the difference.

I wasn’t pain-free by any stretch of the imagination though; I was in enough pain to significantly disrupt my life at least 50% of the time (and a lot of the time it was still there, even if it wasn’t upsetting my day-to-day life). I was getting stronger, with more stability, but still with no word from the Pain Clinic on how to manage or, dear god, get rid of the pain.
Into 2023 and we still hadn’t heard anything. I was working hard at hydro and I could feel the difference – I was stronger and I enjoyed the exercise – but I was still in pain a lot of the time. We’d asked my GP to chase up the Pain Clinic but not heard anything from either of them.
Category: chronic pain, depression, emotions, exercise, heds, hydrotherapy, mental health, suicide Tagged: chronic pain, depressed, depression, eds, ehlers danlos syndrome, exercise, gp, heds, hydrotherapy, hydrotherapy referral, hypermobile ehlers danlos syndrome, hypermobility, joint pain, major depressive disorder, mental health, mental illness, nhs, pain, pain clinic, suicidal, suicidal ideation, suicidal thoughts, suicidal urges, trd, treatment resistant disorder, trigger, trigger warning, tw
Posted on September 10, 2023
TW: Discussions of suicidal thoughts, suicidal urges, self harm, and irrational thinking. PLEASE think carefully before reading further if these things may trigger you or cause you distress. Please always put yourself and your mental health first.
This, I think, is the first time I’ve written directly about my experience with suicidal thoughts and urges. I’ve mentioned it in relation to the side effects of medication and written around the edges of it but I don’t think I’ve ever talked about it in such detail. I have omitted certain moments and details since it’s been proven that sharing about plans and methods can lead to further suicides but this is as honest as I can manage, even though it terrifies me. But as hard as it is, I’m sharing these experiences because I think it’s so deeply important for people to understand what it’s like to feel this way, to live in so much pain, to feel so desperate. Keeping these stories in the dark only increases the shame and stigma so, even though it’s difficult and uncomfortable and scary, we need to talk about them. It’s the only way the world will get better at supporting people who are struggling.
I’ve experienced suicidal thoughts on and off since I was a teenager but for a long time, they were passive. Walking to school, I’d cross the road and, dreading the day ahead, I’d imagine getting hit by a car. But the thought would leave as quickly as it arrived. I thought it was normal. To quote Ned Vizzini, “Who hasn’t thought about killing themselves, as a kid? How can you grow up in this world and not think about it?” (I may have hated that book but that line really resonated with me.) This was before I was diagnosed as autistic* and I thought everyone felt as overwhelmed by their emotions, by their anxieties, as I did – as I do – but were just better at managing it.
*Autistic individuals, especially autistic women, are at a much higher risk of suicide than the general population; the factors include mental health problems (especially if they go untreated), the impact of a late diagnosis, challenging life events such as bullying and ableism, the burden of masking, isolation, and cognitive inflexibility, which can lead to difficulty in seeing any option but suicide. (x)
(Left: During secondary school // Right: During sixth form college)
I continued to experience passive suicidal thoughts and then, during my second year of sixth form college, I started to struggle with depression and my ever-present anxiety reached all-new heights (although, in comparison to what I experience now, I’d happily go back to it). Almost a decade, multiple diagnoses, and more than twenty medications later, my depression is the worst it’s ever been and I’ve been actively suicidal for almost two years. There have been short periods over the years (always in concert with the times I tried medications other than Phenelzine) where I’ve struggled with suicidal thoughts but, for the last two years, they have been almost constant.
They began in earnest when I started taking Xaggatin for my ADHD (and had to stop taking Phenelzine because my ADHD clinician was insistent that the side effects were unsustainable – I disagreed for multiple reasons but this isn’t the post for that story). I thought the intensity of the thoughts – and their slow, scary manifestation into urges and intentions and plans – was a side effect but it wasn’t long before my depression crept back in, sucking me down. Between that and the other awful side effects, my psychiatrist switched me to another medication, Bupropion, an antidepressant that’s supposed to help with ADHD but it only made things worse: I was so anxious, depressed, and suicidal that I couldn’t function. I tried a few more antidepressants, was traumatised by several more doctors, and had the crisis team called out (although they didn’t do anything, including the things they’d said they’d do). I quit treatment entirely for a while, unable to mentally handle it; I basically retreated to my bed and stayed there. I couldn’t engage with the world: it just hurt too much. But without treatment (I didn’t even have a therapist at this point, another thing that had spun my life out of control), the claws of my depression dug deeper and deeper. I remember one day where I had the sickening realisation that I wasn’t doing anything worthwhile with my life, that I had wasted my time and my education, that I was a complete waste of space. There was another day when I realised that something had broken inside me, something that could never be fixed, and I was no longer the person I had been and would only ever be a defective, inferior version of her. I avoided mirrors for months. On New Year’s Eve of 2021, I stared at the fairy lights in my living room and thought about how I had no desire to survive even the next 365 days. It wasn’t a resolution but I felt it with a quiet certainty. I thought about it everyday but then somehow that dreaded day arrived and I was still here, despite that certainty, despite my plans. I hated myself for it, feeling like a pathetic, weak-willed coward. It was a terrible night, not that I remember much of it given the distress I was in.
Somehow I ended up on Phenelzine again, despite my revulsion at the thought; I still don’t really know how it happened and I still find myself so angry about it that it feels like it might consume me. But, for a while, the chronic suicidality was relocated to the side burner: it was all still there but it wasn’t the only thing in my brain anymore. I could ignore it for sometimes days at a time. But after a while, my depression seemed to billow back in, like ink in water. The suicidal thoughts and urges became – and still are – the constant undertow to my thoughts and sometimes it’s all so overwhelming that I can barely breathe. Self harming has long stopped being an effective coping strategy as it just makes me feel pathetic for not doing more damage. I don’t know why I haven’t acted on these thoughts. I don’t know why I’m still here. If asked, I’d probably say, “because I’m a coward,” even though I know that I’d likely get a verbal thrashing from anyone I voiced that feeling too. I can practically hear my therapist (yes, I’m back in therapy) encouraging me to dissect that feeling. I know it’s not a healthy, rational thought but it is a real one. It’s a weird state to live in and the conflict of planning for a future I don’t particularly want to exist in is disorientating and miserable. It’s exhausting. But I know what my fate is, whether it comes sooner or later, and I have for years.
Following a slightly different train of thought, it’s very strange to me that people can’t seem to tell, just because it’s such an overwhelming experience for me. I feel like I have a massive neon sign over my head: “SUICIDAL.” But then I wouldn’t be surprised if people just don’t comment because they don’t know what to say. The last time I self-harmed, I cut my face because I needed to look as broken as I felt (or inasmuch as I could physically manage, which wasn’t enough – more shame and self-hatred) and almost nobody even mentioned it. (Not that that was the point but it did surprise me. Most of the time I avoided the question. I only lied once: I was in a weird headspace already and the question took me off guard and I just didn’t have the emotional energy to explain.) The cut got infected and took weeks to heal. I’m glad it left a scar but I resent it for not being bigger: the disfigurement doesn’t accurately reflect the feelings, not by a long shot.
(Left: The dressing on my face after I self harmed // Right: The scar after it finally healed, having got infected.)
In some ways, I feel like I’m already disappearing: I struggle to make sense of my face in the mirror and, while I don’t know about this year, there are fewer than ten photos of me in 2022; my autistic masking is so ingrained that the real, brutally honest me who is struggling and suffering (who so desperately needs to be seen) gets locked away so tightly that she might as well not exist, while a socially acceptable and palatable projection of me – the only version of me that people could want, says the voice in my head – takes over my body, acting almost without my permission; I feel like no one knows the real me any more, not after months in bed, besieged by suicidal thoughts and impulses. I feel permanently damaged by it but people are still treating me as who I used to be and not who I am now (not that I think it’s their fault – while the damage feels so deeply clear to me, I know that it’s not visible to anyone else). I remember the old me. I remember the person who could be proud of being different and who advocated for acceptance, even though she still felt broken. It was a balancing act but there was balance. Now the broken feeling has broken the scale. I feel unrecognisable. I noted down somewhere – last year at some point, I think – that feeling like this feels like one elongated near death experience. Almost every day for more than eighteen months, I’ve been so close to death that I can feel it’s presence in the air when I breathe in; I can feel it in my lungs. One decision – one split second – away. Maybe it’s just dying in slow motion. Feeling this way… I don’t know how it doesn’t change you.
I was reading various articles as I both researched and procrastinated this post and, in one of them, the author had written this: “Because depression, as we all know, is almost always treatable.” The statistics vary, depending on where you look, but a high percentage of people (this page claims between 80% and 90%) do eventually respond well to treatment. After ten years, over twenty medications, and more hours in multiple therapies than I can count, I’ve only ever managed periods of being mentally well. The longest period was, I think, two and a half years at the most. Only one medication actually helps and I’ve run out of new ones to try. The other options, according to a consultant in another very distressing appointment, would be the Ketamine trials or Electroconvulsive Therapy, neither of which doctors fully understand (the same could be said for antidepressants). Given how abnormally I respond to multiple medications, I’m terrified of how these treatments might affect me. I’m terrified of how Phenelzine is affecting me. With all of that in mind, I can’t help but wonder – and have wondered for a long time – if I’m included in that small percentage that doesn’t respond to treatment. And if that’s the case, it means that this is forever and that is an unbearable thought.
I’ve spent a lot of time talking with my therapist about this – and no doubt this post will spark multiple new discussions – and we did talk briefly about what I could write for this post, what would feel actually helpful to someone reading (I never figured that out, by the way, so I have no idea if this is helpful or not). She said that the most important thing is to talk about it and that it’s much more dangerous not to talk about it. I agree with the latter part but I’m not convinced that talking about it is helping me; I often feel like I’m just going around in circles and exhausting myself. She asked me what I would say to someone I loved if they expressed all of this to me and the truth is that I honestly don’t know. I don’t know because I’ve never heard anything that’s helped me. I think we all have the knee-jerk reaction to say, “Please stay. I love you and I’d miss you.” It’s true and it’s heartfelt but is it fair to ask someone to live in agony, in unbearable misery, because you’d miss them? We want to say, “Things will get better.” But we don’t know that. We can’t promise that. We want to say, “How can I help?” But it’s unlikely that there’s any one thing a person can do to help, although that one is more specific to the individual person. If someone asked me that, I couldn’t give them an answer because there is nothing they can do to help. It’s so much bigger than one person, than them or than me. Maybe these help some people. For me, none of these things change the reasons I’m suicidal and they’ve only added unhelpful pressure and stress. I’d hate to do that to someone else. I’m not saying the right words aren’t out there. I’ve just never heard them. Or discovered them.
Obviously I haven’t shared everything. As I said, I didn’t want to share things that have been proven to push people passed their limits (although I hope everyone read the warning and acted accordingly and prioritised their mental health) but there are also certain things that are too hard to share, too raw, too loaded. But I wanted to share my experience today, not just because it’s an overwhelming aspect of my life, but because sharing our experiences and our feelings is, as I said in my introduction, one of the few ways (and possibly the most powerful way) that the world gets better at helping people. People can only do that if they understand the battles being fought and the support that’s needed. I hope that sharing my story can help with that, even if it’s just a drop in the ocean.
RESOURCES:
Category: adhd, anxiety, autism, death, depression, diagnosis, emotions, medication, mental health, school, self harm, suicide, therapy, treatment Tagged: adhd, antidepressants, asd, attention deficit hyperactivity disorder, autism, autism spectrum condition, autism spectrum disorder, autistic, bupropion, content warning, cw, depression, disfigurement, ect, electroconvulsive therapy, it's kind of a funny story, ketamine, ketamine trial, masking, medical trauma, medication, medication change, ned vizzini, passive suicidal ideation, phenelzine, psychotherapy, quote, secondary school, self esteem, self harm, self hatred, self injury, sixth form, sixth form college, suicidal, suicidal ideation, suicidal thoughts, suicidal urges, suicide, therapy, treatment, treatment resistant depression, trigger, trigger warning, tw, world suicide prevention day, world suicide prevention day 2023, wspd, wspd 2023, xaggitin, xaggitin xl

Hi! I’m Lauren Alex Hooper. Welcome to my little blog! I write about living with Autism Spectrum Disorder, ADHD, OCD, CPTSD, depression, and anxiety, as well as other health issues including hEDS and POTS.
I’m an alt-pop singer-songwriter (it’s my biggest special interest and I have both a BA and MA in songwriting) and my most recent EP, Too Much And Not Enough, Vol. 1, is available on all music platforms and is the first in the series of works based on my experiences as an autistic person.
Finding Hope