Tag: disability

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05/10, Ĉano – Part II (TBA Readalong)

Hello! We’re reading The Butterfly Assassin together, following the calendar of the book, and discussing the worldbuilding and writing process. Jump to 17/09, Eraro to start from the beginning, or join us wherever you like!

On the 5th of October, Isabel continues to have a shitty day. She’s sufficiently unwell – and visibly so – that Ashvin sends her home rather than let her do her paper round, and she doesn’t make it to school. While she’s trying to remember how to think in a straight line, Daragh calls her, and gives her the results of her latest blood tests. They’re not good. You always know it’s not good when doctors start using words like “prognosis” and “palliative care”. But Isabel hasn’t given up, and she asks Daragh for Grace’s number.

It’s another brief one – though we get about a page and a half today, rather than yesterday’s scant handful of lines – and the focus is still on pain and illness. Some reviewers aren’t fans of that, finding it frustrating that Isabel spends so much of the book suffering. To which I can say two things: first, trust me, this was even more pronounced in the early drafts, and second, yeah, being in pain all the time sucks and is boring, I agree.

Sorry, did that sound bitter? If it is, it’s not because I’m annoyed at the reviewers (they’re well within their rights to dislike the book for any and all reasons they might mention, and it is in fact none of my business unless they tag me in it! Although sometimes they do tag me in it. Alas). The bitterness is because chronic illness and pain do suck… but also because it’s so rare to find characters who have those experiences and, in part, it’s because there’s a belief (perhaps justified) that nobody wants to read about being in pain all the time. For those of us for whom this is our lives, though, this basically just tells us we’ll never be the  main characters of our own stories, and that’s… kind of a bummer?

In a previous draft, the AMM rewrite, this scene was another in-person appointment with Daragh, and Emma had come with Isabel for moral support, so it was Emma who gave Isabel Grace’s number:

“I’m sorry,” Daragh says, “but this is bad.” And what she hears is, You’re losing.

But she will not die like this. Nor will she go to her father and beg him to save her, which seems to be the only rope anyone can throw her as she drowns day by day in the encroaching blackness of the poison. Never mind that he’s missing, that she might not be able to find him even if she tries – she will not try. She refuses to give him the satisfaction of seeing her come crawling back to him.

And she won’t go begging at Ronan’s door, either.

She looks from Daragh to Emma and back at the test results on the doctor’s desk. “Emma,” she says, “do you have Grace’s number?”

As with many of the changes to this middle section of the book, it was largely for pacing reasons that I cut this appointment, combined several days into a single chapter, and made this a phonecall. And, of course, in the earliest drafts, Isabel would have been in hospital by then. Although she suggested they asked Grace for help, it wasn’t an active decision that she made as part of her attempts to solve this herself – it was, instead, part of her relying on others to fix things. I was very keen to push Isabel to be as active a participant in the plot as possible, and that was one of the main changes in the AMM rewrite: Isabel tries to save herself, and asking Grace for help is part of that.

We’ll see more of that in tomorrow’s post, in which you’ll get to learn about the chapter that required the most research of anything in the book. In the meantime, I want to hear your thoughts – anything and everything evoked by this chapter. Drop them in the comments and I’ll see you tomorrow!

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02/10, Kulpo (TBA Readalong)

On the 2nd of October, Grace gives Isabel the antidote to the memory suppressant. They talk a little about Mortimer, and whether or not he poses a threat, and Isabel wonders exactly how deep in Grace’s debt she’s going to be.

Since the previous chapter didn’t exist in any of the early drafts, neither did this scene, although Isabel did, at one point in the first draft, discuss Mortimer with Graham:

“Mortimer’s more perceptive than most people.”

“Yeah, he is.”

“You shouldn’t trust him.”

“I don’t. I don’t trust you either. That doesn’t mean I won’t accept your help.”

(A classic taste of how much of the first draft was pure dialogue with no dialogue tags. This is often the case with my first drafts, but when you take a scene out of context, it makes it very hard to figure out who is speaking. This one is Graham – Isabel – Graham – Isabel, ftr.)

There’s a slightly more readable version of this in Draft IV:

“Oh.” Warily, Isabel allows Grace to take her arm again, and they make slow progress down the corridor towards the medical room. “Mortimer knows about you, you know.”

“You told him?”

“He already knew. He says you’re bad at hiding it.”

“Mortimer’s more perceptive than most people.” A moment of silence. “You shouldn’t trust him.”

“I don’t.”

She thinks Grace probably smiles at that, but she can’t see her face from this angle. “I’m sorry this has happened to you, Isabel,” says the librarian eventually, and Isabel has no idea how to respond to that.

We can see that Grace and Mortimer are on friendlier terms in the late drafts than they were earlier on, but that’s mostly because I gave them actual characterisation, and also because Grace is no longer affiliated with Hummingbird the way that Graham was. Mortimer isn’t aware that Grace is a freelance poisoner, but if he was, the fact that she specialises in antidotes and nonlethals would probably reconcile him to that information, even if it would initially be a shock. On the whole, though, he’d struggle to be friendly with a guild member – Isabel becoming a notable exception to that. His suspicion that Grace was/had been a poisoner in the early drafts was a big part of the tension between the pair of them.

Come Draft VI, Grace was a poisoner, Mortimer didn’t know but suspected, and we were creeping towards a recognisable version of this scene, but we still didn’t have my favourite moment, a version of which showed up in 2020:

“He doesn’t know I’ve been poisoned. Or that I was trained as a child. But the rest…” She shrugs, trying to hide her discomfort. “I don’t know what he’ll do with that information. I don’t think he’s planning to do anything yet, but I can’t be sure.”

“Want me to poison him for you?” says Grace.

Isabel looks up, shocked. “No,” she says instantly. “No, of course not, that would – wait, was that a joke?”

The librarian pulls a face. “Not exactly. I mean, I’d rather not. Despite his many flaws, I do actually like Mortimer. But if you’d asked, I’d have considered it. Something nasty but nonlethal.”

Want me to poison him for you? I love Grace in this moment. This is the moment we realise she’s switched from a threat to Isabel to a genuine ally: somebody who will protect her. And Isabel has few enough of those.

There’s not much else to discuss in this chapter, so I’m going to be slightly cheeky and slip into the 3rd October, because I have a couple of sections to cover there. Since the first of them happens at 04:23am, it’s still kind of the 2nd, especially as it’s not quite dawn.

In this scene, Isabel wakes from a dream, triggered by the memory suppressant breaking down, in which she remembers creating the poison for her father. She wakes before she can remember the formula, horrified to realise she’s been, in part, the architect of her own suffering. Michael, suffering his own nightmares, calls her, and the two have a late-night call, solidarity in the face of mutual trauma.

There are two things I want to say about this section.

Firstly, that it was important to me that Isabel was at least partially implicated in her own suffering. It’s pretty clear that the poison wasn’t her idea, and nobody else would hold her responsible for creating it, or think that she deserved to suffer as a result – but Isabel does, to a certain extent, see it that way. She doesn’t consider herself blameless, and this moment creates ambiguity (to her) about the extent to which she’s a victim.

When I temporarily lost the use of my hands at seventeen, a lot of it wasn’t my fault. I didn’t design my own genetics and give myself hypermobility syndrome. I wasn’t the one who gave me bad medical advice and worsened what might otherwise have been a smaller issue. I didn’t create the school system that pushed me to try and overachieve.

I did, however, write 700,000 words of fiction in eight months while doing my AS Levels, writing for three blogs, preparing for grade eight flute and violin, and playing in half a dozen musical ensembles. Repetitive Strain Injury was, as it seemed everybody wanted to tell me at the beginning, my fault.

For most people, RSI would have been temporary, if possibly recurring; for me, I became disabled, at first quite significantly. And it was my fault. I believed that. I’d overdone it, I hadn’t listened to warnings, I’d had bad posture, I’d pushed too hard, I’d done this to myself and therefore I deserved it. Did this mindset contribute to the pain sensitisation that trapped me in a cycle of chronic pain? I don’t know. But it sure didn’t help, because believing I deserved it also meant, on a deep subconscious level, that I didn’t truly believe I deserved to get better. Or that I was allowed to get better.

And then, when I got diagnosed with coeliac disease, it was after a year in which I had more or less exclusively lived on bread and pasta. (I was a first-year undergrad with limited kitchen facilities; it happens.) In other words, I’d spent a year poisoning myself. Did I know? No, of course I didn’t know. Did it make it worse? In the long term, probably not; in the short term, yes, it was the reason my antibody count was through the roof and my general health was so poor.

What mattered, though, at the time, was that I was not the blameless disabled person who had done everything right and still got sick, and was therefore worthy of sympathy. I had done everything wrong, and I had made myself sick.

In the years since then, I’ve learned two things: first, it doesn’t matter if you do everything right. This is an awful thing to have to learn, because it makes you realise that no matter how hard you try, you can’t actually protect yourself from illness, because illness is not a moral punishment and sometimes it Just Happens. Yes, even if you were good, even if you took all of your vitamins, even if you exercised, even if you rested – we are not, in the end, in control of our health, and we cannot protect ourselves from illness and injury and pain. And recognising that also doesn’t wholly take away the guilt and sense of responsibility. But it helps a little.

The second thing I learned is that it wouldn’t matter if I was fully, 100% responsible for all of my health issues: I still deserved help. I still deserved to get better.

That is, frequently, the point I am making here. Isabel is not blameless – in so many ways, she has been the cause of suffering. She is not perfect, not innocent, not untouched by her parents’ teachings. She still deserves better. She still deserves help, she still deserves to be safe, she still deserves medicine and care and friends. Because those are not conditional.

I said I wasn’t going to over-explain my motivations and thematic intentions because I want the book to stand alone, but I couldn’t help myself with this one, because this matters to me. It matters to me that Isabel isn’t innocent, and it matters to me that she still deserves better – and this is the first chapter where we really get a sense of that.

The second thing I want to say about this chapter is, you’ll be pleased to know, a little lighter in tone.

When Isabel is on the phone with Michael, he tells her that he can’t sleep because one of his roommates in the hostel where he’s staying is snoring like a rowing machine. This is drawn directly from my own personal experiences of staying in a hostel in Leeds in 2018, on my way to a job interview with the British Library in Boston Spa. Somebody in my dorm snored exactly like this: a long, noisy drag in, and then a sudden whoosh out. I had Green Day playing at top volume through my headphones and I could still hear them.

I may have hit them with a pillow. More than once. You can’t prove it. I’ll deny everything.

By the time I woke up at 7am to catch the bus out to my interview, I had not slept very much, and I was not very happy. I was also wildly unqualified for the job and, frankly, I don’t know why they interviewed me; needless to say, it didn’t work out, which is why I still live in Cambridge with its extortionate house prices, and not in Yorkshire, where less of my monthly income would go on rent. But the experience taught me something vital, and that is that some people snore like rowing machines.

I’m sorry, Michael. Nobody deserves to go through that.

Again, I have to say, I have a soft spot for the Michael we meet in this chapter. It’s clear he understands Isabel in a way that nobody else does; they’re alike, and they have shared experiences that nobody else has. This scene was another late addition to the book (really, this whole section was) – it showed up in 2020, and then almost got cut again in my autumn edits that year, but I decided the character moment was worth keeping. I’m glad I did. I think it was worth it.

What about you? Any thoughts on this chapter? How did it make you feel to realise that Isabel had helped make the poison – did it change how you viewed her and her illness? And, to keep things light, who’s the worst snorer you’ve ever had the misfortune to share a room with?

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22/09, Doloro (TBA Readalong)

You will be relieved to know that this is a short post and you get a day off tomorrow, since nothing in The Butterfly Assassin takes place on 23rd September. (For Isabel, it’s a Sunday, so a quiet day amidst a school-based schedule.)

On the 22nd September, however, Isabel wakes up in the middle of the night, in severe pain, and wonders what to do next. This is the first couple of pages of Chapter 7, for those keeping track. For the first time in this scene, Isabel attributes her symptoms to the probability of poison, and not to anxiety or general sickness, and we begin to get a sense of where the plot is going…

There is no wound, no knife, and there are no weapons that can protect her from an enemy that’s inside her.

Poison has always been a plot point in this book, even back in the earliest drafts, but it’s changed significantly over time, in terms of the nature of the poison and the symptoms it causes, as well as its purpose within the plot. When I wrote the first draft back in 2014, I had never knowingly been poisoned. By the time it was published, I was describing it jokily as “OwnVoices for poisoning”. What changed?

Well, in 2015, I got diagnosed with coeliac disease, an autoimmune condition which means I can’t eat gluten.

Some coeliacs are largely asymptomatic. They don’t experience noticeable symptoms when accidentally ingesting gluten, although that doesn’t mean there’s no damage: it can cause nutrient deficiencies and malnutrition, and increase the risk of bowel cancer. Many are diagnosed because of persistent, severe anaemia due to malabsorption of iron, which was also true for me – I complained of fatigue, said I thought my anaemia was probably returning, and mentioned that I’d stopped taking iron supplements due to stomachaches. The doctor ran a routine test for coeliac antibodies just in case, and discovered my immune system was halfway through setting itself on fire, with an antibody count of 216. (Around 20-30 would’ve been enough to suggest coeliac disease.)

But I hadn’t had significant symptoms before then, so it was a surprise, the first time I accidentally ate gluten after diagnosis and a couple of months of a strict gluten-free diet, to find myself in the bathroom wishing for death.

It turns out, when your immune system is on fire at all times, you don’t notice the reaction when somebody throws a bit of extra fuel on the pyre. But once you’ve got the fire under control… yeah, after that, the smallest thing sets it off like a flamethrower.

These days, I have to avoid all traces of gluten. “May contain wheat” is enough to mean I can’t eat something, just in case. I have to have a separate toaster to avoid crumbs touching my bread, because they would make me sick. I have separate utensils, especially wooden spoons which are hard to clean thoroughly, and I essentially travel with the kitchen sink to make sure I can safely prepare food when I’m away from home. I have an extensive list of additional dietary restrictions, which makes things extra complicated, but it’s only the gluten where the tiniest trace will make me sick.

I don’t get glutened often, because I’m very careful. But when I do… it sucks. And I drew on that experience for Isabel.

There are no weapons that can protect her from an enemy that’s inside her. Writing as someone with a couple of autoimmune conditions and chronic illnesses, plus chronic pain and fatigue… this, here, is one of the main things the book is about. That terrifying loss of control that comes from realising your body is turning on you.

OwnVoices for poisoning.

I know that this loss of – and fight for – control over your own body has been something that’s resonated with disabled and chronically ill readers, because they’ve told me so. But it probably wasn’t clear from this first glimpse of the poison that that was going to be such a major focus of the book, so I’d like to know how youse reacted to this scene. Did you think, “Oh, she’ll be fine, YA books never kill off main characters”? (lol) Or did you think, “Oh, shit, how’s she going to get out of this one?”

Leave your answers, or any other remarks, in the comments, and I’ll see you back here in a couple of days for the rest of this chapter.

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Control And Recovery

You would think, after eight years in a perpetual yo-yo of decline and recovery, that I would know how to write about recovery. I don’t. On this occasion, recovering from top surgery and a knee injury and pandemic-induced inactivity simultaneously, there’s plenty of material. But some of it’s gross, and some of it’s boring. Some of it is a story of anxiety (“Is this healing correctly? Should it look like that?”), and some of it is a story of determination (daily walks getting slowly longer as I test my ability to walk without a cane). Sometimes, it’s staring into a mirror wondering whether I’ve always been this wonky, or whether I need to go back to the osteopath because my spine’s gone twisty again. None of it makes for a tidy narrative or an inspirational story.

Here’s the part that’s a story: three years on the NHS gender clinic waiting list and no sign of a first appointment, so I went private for top surgery, because selling The Butterfly Assassin gave me the money to do it. And that’s narratively significant and tidy, because The Butterfly Assassin is a story about struggling for control over your body and your life, and this was a form of taking back some of that control. It’s also a book I first wrote during the summer of 2014, around the same time I was having my initial gender crisis. These facts are probably not a coincidence.

The rest is messier. The rest is about balancing my squeamishness, my fear of being visibly trans in an increasingly hostile world, and the fact that surgery cost two-thirds of my yearly income with the fact that I needed to feel at home in my own skin, in an urgent way that wasn’t compatible with the absurd NHS waiting lists. The rest is private: my choices, my anxiety, my body. No matter how the media likes to pretend that trans lives must be endlessly subjected to public debate and examination.

The knee injury, though, I can talk about that. I hurt it in October, and since then my walking has been limited to what I can manage with a cane. My reliance on it has gradually reduced — initially I could hardly walk at all — but I was still using the cane when I travelled for surgery, and my inability to lean on it without aggravating my chest afterwards forced me to focus on rehabilitating the knee. There’s a lot of that, when you have hypermobile joints that perpetually injure themselves. Decline and recovery, decline and recovery, a constant process of rebuilding and relearning and reshaping.

So I’ve been going for walks, because they’re the only exercise I can manage. The unseasonably warm spring weather has helped, making it easier to motivate myself to leave the house, although there are still days where I’m tempted to stay in bed all day. But I force myself out. Sometimes, the walks are short: up the park, a quick circuit of the Pokéstops, taking over the gyms again if somebody’s kicked me out, and then home to recover. Sometimes they’re longer, not always intentionally, as I go a street or two beyond my usual circuit and then drawn further afield by curiosity to see what I’ll find.

Two things have made these walks bearable, even at the beginning when they were brief and slow and required frequent rest-breaks. The first is that I’m living in a new area, and so even a circuit of the streets will bring me sights I’ve never seen before, rather than the dreary familiarity of an area where I’ve lived for years. Novelty creates excitement, even when the novelty is just a different block of flats and row of shops. Since I’m due to move again next month (I’ve begun to feel like I will never not be moving house), there won’t be time for this area to become drearily familiar, and instead I have a sense of urgency, like I need to make the most of it while I’m here.

The other is Pokémon Go. I know: it’s 2022, not 2016. But in 2016, downloading Pokémon Go did wonders for my fitness, prompting me to take that extra digression on the way home just to loop in a couple of extra Pokéstops, rather than always taking the shortest route. It helped me build my stamina and strength, something that’s essential to managing my hypermobility. I stopped playing a while back, but last year downloaded it again to try and motivate myself to leave the house more often. It didn’t work very well then — it helped a little, but then I hurt my knee, so I couldn’t go out — but now it’s coming into its own.

Walking slowly, pausing often, and sticking only to familiar routes where I won’t accidentally find myself too far from home are boring limitations on an ordinary walk. But Pokémon Go makes them easier to bear. I walk slowly, so that gives me time to catch the Pokémon I pass. I’ll pause at a gym to reclaim control of it, giving myself a chance to rest and lower my heartrate before I continue. And I’m always looking at a map of the area, so it’s easier to find my way back when I stray off course.

It has become — in a strange kind of way — an accessibility aid. This game, which was not designed for me, and which favours those who can walk significant distances and regularly, is helping me to manage my disabilities and rehabilitate an injury that has plagued me for months. It makes it worth putting my shoes on just to manage a 15-minute walk, because at least that’ll help maintain my streak of visiting Pokéstops. It has, unexpectedly, gamified recovery.

The game has its challenges and problems. The repetitive movements aren’t great for my hands, and staring down at my phone probably isn’t doing great things for my neck either. But my knee is improving. The other day, I managed to walk for ninety minutes, which I haven’t done in months. My mind feels clearer for it, too: an hour each day away from Twitter and the endless news cycle of doom and despair, the rising cost of living and the spread of virulent transphobia and the war in Ukraine and the perpetually growing COVID figures…

It’s frustrating, when people turn out to be right that fresh air and exercise help. Partly because I’m a creature of the indoors at the best of times, and partly because I don’t always have a choice about my ability to experience those things. For months my knee has kept me trapped, unable to walk further than 10 minutes from home in case I can’t get back again, and no matter how much I wanted to go out and exercise, I couldn’t. Anxiety quickly begins to close in when you feel you’ve lost all sense of control over how you manage it.

But now the winter is coming to an end. The days are getting longer, and the air is getting warmer, and I, like the flowers, am slowly coming back to life again. Slowly getting some colour back, and raising my head to the sun. One gentle walk at a time.

I’m beginning to feel hopeful now that when I’m allowed to dance again, once the post-surgery restriction on cardio has been lifted, I might actually be able to. I’m beginning to look forward to choreographing, to having space to dance in a way that I haven’t since the start of the pandemic. Getting my rhythm back. Expressing myself in a way that doesn’t need words. This time, without having to strap myself into a painful, over-tight sports bra before I start.

With every day that passes, as I get stronger and as my chest heals, I begin to feel that little bit more at home in my own skin. And it’s not body positivity per se. My body and I will always have our wars, particularly over its inability to digest anything I might actually want to eat. But it’s body neutrality. It’s recognition of the self. It’s glancing in the mirror and going, “Oh, yeah, that’s me.” Flaws and all. Rather than feeling caught in a trap, caged in by something I don’t have control over and can’t relate to.

The Butterfly Assassin is a book about struggling for control over your body and your life. About wanting autonomy when you’re losing even the ability to function on a day-to-day basis. About trying to find a balance between surrender and stubbornness: when to ask for help, and when to go it alone. In the eight years since I first drafted it, I’ve lived that over and over, through different periods of decline and their subsequent eras of recovery, and I know that recovery will never be ‘final’, but always an ongoing process. That’s what chronic means. It’s never just one injury, one surgery: it’s a dozen small things and all their effects.

Still, I feel hopeful now that when the book comes out, in two months, it’ll be a much stronger version of me who is there to greet it. Not the hermit-like winter me, kept trapped by pain, but the version of me that takes a slightly longer walk every day, and feels my body remembering what it feels like to do what I want it to do.

Maybe I’ve learned to write about recovery after all. Or maybe it’s the kind of thing you relearn every time, the way I relearn how to walk, the way I regain my strength. An endless cycle. A perpetual process of becoming myself, and claiming my own body.

The Butterfly Assassin will be released on the 26th of May. You can pre-order it now.

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Letters From The Past

The first email I got this year was from myself.

I’d written it in July 2012, addressed to the Me of 2022, and scheduled it to arrive in the future. It didn’t come as a complete surprise: I knew I’d written the letter, because I’d been wondering, recently, where I’d saved it. There were a few of them in total, written between 2012 and 2015, all to be read in 2022 (because it was ten years after the first, not because the year was special). But I wasn’t expecting the email, and I suppose on that front, my past self is lucky that I never deactivated my old email addresses despite changing my name.

In this first letter, my sixteen-year-old self speculated about what I might have done in the past ten years, and also tried to give me some advice. This had the weird effect of feeling like I was being patronised by myself, although at least younger me was self-aware enough to know that there was no way I’d be taking any advice from a teenage version of myself. Still, it was a snapshot of my expectations for my future, and one that managed to surprise me despite thinking I knew my past self quite well.

It was funny to see the kind of things I wasn’t sure if I’d remember. I made a reference to Brave New World, then wondered if I’d get it, and supposed that if I did, it was either because I hadn’t read many more books, or because I’d reread it recently. Well, I’ve probably read well over a thousand books since I wrote that letter, and I absolutely couldn’t tell you when I last read Brave New World, but I still remember the helicopters, so sixteen-year-old me needn’t have worried on that front.

Some of my teenage self’s expectations were predictable. “Published? I really hope so. If not, I wonder what happened. Did you stop writing? Give up on your dreams?” I want to say: not yet, give me a few months, come back to me in June and I’ll have a different answer for you, I never stopped, I didn’t give up. I want to tell my younger self that sometimes things take much, much longer than you were expecting. I had high expectations for myself as a teen writer; I was convinced I’d be published before I was twenty, or at least not long afterwards. (You can imagine the crisis I had on my twentieth birthday when I realised that definitely wasn’t going to happen.)

Then my younger self gives me some advice that reminds me exactly how young sixteen really is. “You know, scrapping teenage fantasy doesn’t mean giving up on everything you ever wanted to do, it just means being realistic about it. If you’re still writing, but you have a day job and you’re struggling to find the time, remember – if you really want something, really really, then you’ll get it. Eventually.”

If only the world actually worked like that. If only wanting was all you needed to ensure success. I know what I meant: I know I was trying to encourage myself not to give up, even if things didn’t take the path I was hoping they would. But I was writing this from the point of view of a mostly able-bodied, mentally stable teenager. Becoming disabled and grappling with my mental health has left me with a very different perspective — that sometimes it doesn’t matter how much you want something or how hard you work, because it will be taken from you. The hardest lesson I ever learned as a teenager was that determination and willpower aren’t enough and you can’t actually overcome every barrier in life just by trying hard enough.

The same naivety is visible later in the letter: “I hope you’re still writing. And dancing. Whether or not you’re a dancer or a dance teacher – and if you’re not, DON’T think of that as failure! – I hope you’re still using that gift somehow.” It’s funny: my sixteen-year-old self had such high expectations for me as a dancer, despite the fact that I’d only recently returned to classes. I really thought I might be able to do vocational training one day, or become a teacher. These days, I’m trying to gradually rebuild enough strength to even do a barre, after being kept out of the studio for the best part of two years by the pandemic and a cascading series of injuries.

And hey, I’m not supposed to think of it as a failure that I didn’t achieve my dreams in that regard. Which, well, I wasn’t, but I appreciate the reassurance anyway — and maybe my younger self would have been proud of some of the performances I’ve done in the intervening years, even if they wouldn’t quite be able to fathom how it feels to have a left knee determined to stop me dancing. I know they can’t imagine that, because of the way sixteen-year-old me went on to tell me I couldn’t give it up now, and should start classes again if I’d quit. Again with the assumption that all anything requires is determination.

It’s strange, to be reminded that once upon a time I trusted my body to still be able to do what I wanted it to in the future. It never even occurred to me in 2012 that it might be my health, not my choices, that changed my plans.

At least there’s one regard in which I wouldn’t have disappointed my past self: “I wonder what you did at uni. Was it ASNaC? Or did you go a bit more normal and do, like, English or something? Please don’t say you did something normal. I’m disappointed in you if you did.” With a BA in Anglo-Saxon, Norse and Celtic and an MA in Early and Medieval Irish, I can definitely promise my younger self that I didn’t do something normal at university.

This anxiety about abandoning my teenage weirdness pervades these letters. Letters plural, because although I did go looking for the file containing the others, I didn’t need to: the 2013 letter showed up in my inbox this morning.

The 2013 letter is an interesting one, written maybe two weeks before I injured my wrists and temporarily lost the use of my hands, developing chronic pain that still plagues me to this day. I’m much harder on myself in that one: rather than simply wondering whether I’d managed to get anything published yet, I told myself, “I’m disappointed if you haven’t made it to successful author status yet. You better have published a few novels though. I mean, I’m seventeen and I’ve completed 12 first drafts and written Watching nine times, so you legitimately have no excuse for not doing anything. You can just dig them out and edit them, right?”

Harsh. But I get it, I really do. Seventeen-year-old me had spent the year writing intensively, averaging about 90k a month. I never stopped. Every time I finished a book I’d start another one, barely resting in between, and I had half a dozen more lined up in my head to work on. It was like I couldn’t stop, until the moment my hands went caput and I was forced to. Of course I wanted to know it was worth something, that it went somewhere, that I wasn’t wasting my time. I was sacrificing my time — and my health — at the altar of writing, and I wanted an answer.

This letter, written two weeks before my injury, shows again that hubris of able-bodied youth: “you legitimately have no excuse”. Would I have said the same if I knew I was going to spend the next year using voice recognition because I couldn’t type? That I would be having to reconstruct my entire sense of self because I lost a huge chunk of my personality, social life, and dreams when I lost the ability to play music?

No excuse. What a letter to leave for your future self. Again, I leap to defensiveness: come back to me in a few months, I’m trying, I didn’t give up. But I know it isn’t this me that past me is talking to, really. It’s that me. It’s the version of me that I was pushing and pushing until the moment I snapped.

Throughout the letter, there are references to fandom and nerdiness (I was really into Hannibal at the time, apparently), bookended by speculation about whether I’d get the references, whether I’d know what I was talking about. It’s like I thought nine years would be long enough to forget everything about my adolescence. And that’s what I mean about the anxiety about losing my weirdness. I think the fact that most of the adults I knew weren’t interested in these things made me think that as an adult, I wouldn’t be either.

I was seventeen, and at seventeen you’re in this weird, nebulous, liminal state where nobody can decide whether to treat you like a child or an adult. You’re an adult when they want you to make choices and take responsibility; a child when they don’t want to have to listen to you. In this letter, I can see those pressures weighing on me, this fear that if I wanted to be ‘grown up’ I would have to let go of all the things that made me, well, me. The bizarre hopes and dreams, the niche interests, the nonconformity… I was even worried whether future me would still be queer, or whether that would genuinely have turned out to be a phase.

(It has not.)

“Please tell me you followed through with SOMETHING you wanted to do as a teenager,” I begged my future self, because apparently nothing scared me like the idea of becoming a “straight, married, normal person with an office job”. And while in hindsight it is hilarious that both of these letters, 2012 and 2013, wonder if 2022!me is married, I can’t help but feel sad for my younger self, who didn’t have a roadmap for their future. I didn’t know how to imagine me as an Adult Who Stayed Weird, because I didn’t know anyone like me. Just as I didn’t really know what a queer future would look like, because I didn’t know any older queer people who might offer me alternative paths to follow.

Both of these emails were scheduled on the same day, in early July 2013, which means I don’t think my 2014 and 2015 letters will be showing up in my inbox over the next couple of days. But I dug them out anyway, and the mood there is very different.

The 2014 letter was written in January of that year, so it’s only a few months later. Still, that version of me feels much older. Much sadder, too: midway through one of the hardest years of my life, grappling with pain and new limitations on my body and my hopes for the future. Maybe that’s what made my eighteen-year-old self so much kinder than their younger counterpart. Eighteen-year-old me had learned that the pressure to live up to your younger self’s expectations could be crushing, and they didn’t want that for me.

They wrote, “I think what I want really though is for you to be you. I’ve spent a lot of time clinging on to dreams that were broken and worthless instead of finding new ones and I don’t want you to do the same thing so, if you can, just be you. Write books if that’s what you do (and I hope it is), but don’t feel like you have to because your eighteen-year-old self would be disappointed if you didn’t.”

Eighteen-year-old me had learned that you can’t keep clinging to something that’s no longer what you want, just because you wanted it for a very long time in the past. They’d learned that sometimes plans change, and it’s not within your control, but if you keep trying to stick to the original map once the road has been redirected, you’re going to end up stuck in a bog somewhere.

Eighteen-year-old me was also less focused only on what I might personally have achieved. They were thinking about the world: “I hope the world is a better place for you. I hope there’s a better Minister for Education than Gove, and not everything is about straight white dudebros, and that the world isn’t so cissexist and heteronormative…” It’s interesting to see these glimpses of my political concerns from early 2014, but it’s tough to imagine writing back to my younger self and telling them how much worse so many things have got.

Not everything is about straight white dudebros, at least: books especially are far, far more diverse than they were in 2014, particularly in YA, and my current self has access to stories than 2014!me couldn’t even imagine picking up from a mainstream bookshop. But the world is a darker place, overshadowed by the pandemic and the government’s perpetual mixture of incompetence and corruption, dogged by climate change, and punctuated by widespread mainstream transphobia in the media. How can I tell my eighteen-year-old self that? How can I take away their hope that the future would be a better place?

I can’t, of course, but it’s a sobering thought.

And finally, we come to my last letter. 2015. “I’m Finn, sometimes, you know,” it begins, because nineteen-year-old me wasn’t sure how to address the letter or how to sign it off, caught in the grips of an ongoing identity crisis. It goes on to wonder why I’m writing, when I have enough journal entries and poems to give my future self a pretty good picture of who I used to be, but then says, “I still kind of want to write these letters. I always think about who I’m going to be. I think it’s because I’m not so sure about who I am now.”

I can understand that. I know myself better in 2022 than I did in 2015, and certainly better than in 2012, but I still perpetually wonder about my future self. If I sat down to write a similar letter to me in 2032, what would I say? I can’t fathom a version of me who is in their mid-30s. It seems impossible. Absurd, even, and any letter I write now would surely feel as childish and far removed from myself in 2032 as the letter from 2012 does now. I know people who have 3-year, 5-year, 10-year plans for their futures, but I don’t have a strong enough sense of what I want to do that: I can’t work towards a goal I can’t visualise.

That’s something I have in common with my nineteen-year-old self, I suppose, but not with my seventeen-year-old self, who thought the biggest risk to my dreams was me abandoning them, and not life getting in the way.

When I wrote this letter in 2015, I had just been told I might have coeliac disease, and was grappling with the idea of yet another health issue to work around. I hoped future me would “beat” my disabilities, but I said I’d understand if I didn’t. If it all got too much, and I took to my bed. Well, I haven’t given up on anything much. But I do spend a lot of time in my bed, and I guess at nineteen I understood that. The fatigue was beginning to close in already.

There’s one thing, however, that really stands out from that letter: “I’m working on the Moth Trilogy at the moment. Book one is proving more difficult than ever, but I drew a new map of Espera today, and I’m pretty proud of it. I hope you’ve done something with these books, because they are taking up a lot of my thought power and energy. If you haven’t, though, I can only hope it’s because you’ve found something else worthwhile to work on.”

The Moth Trilogy became The Butterfly Assassin. The professionally-designed map that will be in the final book is based on the one I drew the day I wrote this letter. Book one may have been “proving more difficult than ever”, and it may have taken another six years to wrangle it into shape, but I got there.

I got there, I want to write back, it was worth the thought power and energy, it was worth the time, it was worth all the other books I wrote and abandoned, you were right.

2015 is the last of these letters, and the one most open to the possibility of changing. I was a self in flux, and I knew I would continue to change. I asked myself whether I’d ever followed through on some of my plans. If I hadn’t, was it because I was too scared, or because I’d found a different path that made me happier? It echoed the post I wrote a few weeks ago, about trying to make my choices based on love, not fear. It seems I’ve understood this tension for longer than I realised — and that I knew sometimes I need a reminder to consider why I’m actually doing or avoiding something.

From my sixteen-year-old self, who couldn’t really imagine giving up on any of my current writing projects, to my nineteen-year-old self, who had accepted that I might move on but really hoped they’d go somewhere, I can see a shift in how my teenage selves perceived future me, and what that says about how they perceived themselves.

Two weeks after writing 2013’s letter, I was forced to face the fact that we cannot predict our future. That sometimes our bodies let us down, and our plans become impossible, and it doesn’t matter how much we want it, that doesn’t mean we can have it. 2014 and 2015’s letters reflect that knowledge. They make fewer demands of my future, but they offer soft hopes: that I won’t have given up or abandoned my dreams, but found better ones. That I’ll have moved on, rather than walked away.

What I learned between sixteen and nineteen was that you don’t always get a choice about which of your dreams you’re able to keep pursuing. Sometimes, things fall by the wayside because of circumstances outside of your control. But sometimes, you move on because you’ve found something better. You set aside an old dream, and create a new one; you shelve a book, and write another. And that’s okay. Good, even. Because you can’t always be trying to live up to the expectations of your younger self, who didn’t know what you know now, who wasn’t who you are now.

But sometimes, your younger self really is the foundation on whom your adult self is built. And all of them, all these past selves, were hoping I would keep writing, and that I would be published by the time I read their letters. January 2022 still sees me in the pre-publication void, but I’m close. So close. By July, the ten-year anniversary of writing the first of these letters, I’ll be able to honestly say, Yes. I did it. I did what you wanted. I did what we wanted.

Even despite the year spent dictating because my hands didn’t work. Even despite abandoning all the novels my teenage self had high hopes for. Even despite not “beating” my health issues. Even despite the challenges of the publishing industry being greater than I ever imagined.

I did it. It’s my debut year. The Butterfly Assassin comes out in May.

I’m pretty proud of it, said nineteen-year-old me, and honestly? So am I.

Add The Butterfly Assassin on Goodreads, or pre-order it now.

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Dancer In Recovery

I am trying to remember how my body works.

No, that’s not quite right. I know how it works. I know the stiffness of my knees in the morning, the strain of that early cycle into work. I know the clicks and clunks of my spine as I shift in an uncomfortable chair, the way my head feels too heavy for my spine, the threat of a headache that will linger for weeks.

But ballet… ballet feels like pouring myself back into an old mould, trying to inhabit the shape of it again. Tracing familiar paths, looking for the routes I remember. It’s familiar; I haven’t been gone so long. It’s unknowable; it is a thousand years since I have spoken this language and the words of it are lost to me.

Pliés are fine, though soundtracked by clicking joints, with the occasional throb of the left foot where I might have a stress fracture. (More likely, it’s a tendon problem. I’m to have an x-ray on Wednesday, just to be sure.) And I am remembering the rhythm of tendus, feeling the stretch of every fondu in calves strung tight by Irish dance, drawing up into a developpé supported by muscles honed more often by cycling than by dance.

It is attitude that poses the problem. Not mine — the step. Raised leg, bent at the knee, body making spirals from the floor on up and up. The hip injury that kept me from Irish dance all of last term makes itself known, reminding me that while I may have redirected some of my focus for the moment, these two disciplines are not so different that ballet is a place where I can escape from my injuries.

Of course I can’t escape from them; letting go of pain has always been my body’s problem. It insists on clinging to it, sounding alarms long after the fire has been put out. More than a quarter of my life has been soundtracked by those alarms, the ache in my hands still a barrier, if a smaller one than it was six and a half years ago.

My hips are tight, that’s the trouble with these attitudes. I am not currently capable of keeping my hips turned out the way they need to be, because after months of not being allowed to stretch, not being able to push too far, not being able to use them, the muscles around my hips are like a tight cage, trying to protect the fragile area.

I have been reading a book about pain, about how to tame it, because this is something I need to learn how to do. The book told me that a dancer who suffers from a foot injury will feel pain more intensely than an office worker with the exact same injury. For the dancer, this injury is a risk to their livelihood, their career, their passion — and so their brain processes the threat as much larger than the officeworker’s brain. And because the brain recognises a threat, it rings the alarm bells louder.

Brains are only trying to protect us, but sometimes, they are so bad at it.

My hip throbs. Except that’s not really what it feels like. It’s more of an… itching, underneath the skin. A scratchy kind of pain, like a low-level electrical current, or steel wool where there should be soft cotton. And with it comes a predictable cycle of thoughts.

You’ve injured your hip again, my brain tells me. You shouldn’t have gone back to dance. You should have waited longer. Now you’re going to have to take more time out. You should drop out of the show. How can you tell them that you have to drop out? You have a soloist role, you’re going to screw everything up for everyone. This isn’t going to go away. You could take the whole term out and as soon as you dance again it will come back. It’s never going to heal fully. You’re going to lose dance the way you lost music. You’re going to have go through all of it again.

Those last two thoughts worm their way beneath my skin, itchy as tendon damage. You’re going to lose dance. It’s a vicious whisper. You’re going to have to go through it all again.

Our brains know our worst fears. How best to frighten us into compliance. My brain remembers 2013, the overwhelming despair of losing the use of my hands, the profound depression when I didn’t know if I would ever write again. My brain remembers feeling like I barely weathered that storm.

My brain knows I’m afraid that if that happened again, I would not survive it.

The book I am reading about pain is very keen on stopping these spirals before they get to that point. It is, after all, very hard to deal with them once they already have, especially when they have such potent fuel as ‘past trauma’ and ‘legitimate anecdotal evidence’ to fan the flames. My brain processes the sensation of pain in my hip, draws its own conclusions based on several months unable to dance last year, compares that to the older injury and subsequent chronic pain and everything that I lost because of it, and concludes that this is the threat level it needs to process.

It says: you are going to lose dance.

The pain intensifies.

In an ideal world, or as ideal a world as one could find where I would still be experiencing the pain in the first place, I would stop my thoughts in their tracks almost immediately.

There is a pain in my hip, says my brain, in this not-quite-ideal world.

I can feel that, I would say in return. That doesn’t mean another injury. I must have overworked it a little today. I need to rest it. Perhaps a heat pack or a hot bath will soothe the muscles, and I can take some painkillers and go to bed. In the morning, it will have eased off. I’ll have to remember that pushing my turnout like that can trigger the pain, and take it slower in the future.

And my brain would say, Okay. I just wanted to make sure you knew about it, and I wouldn’t have an anxiety attack while cycling home, and the pain would lessen.

The things brains do to protect us are sometimes not as helpful as they should be, especially when they learned how to ‘help’ from a traumatic experience that has left them with a skewed understanding of the body. I am learning to acknowledge that. I am learning not to berate my brain for it, but to gently remind it that maybe it is reacting based on instinct, not evidence, and that perhaps this is closer to a PTSD episode than an objective assessment. Not all pain is life-changing, life-ruining, neverending.

But it is hard, when those are the tracks I have walked for so long. More than a quarter of my life. It feels unfathomable. If my seventeen-year-old self had known what my twenty-four-year-old self would be living with, what effect would that have on me? It is better, I’m certain, that I didn’t know. Hope is the only thing that kept me going.

I am not going to lose dance. These days it is less about hope and more about stubbornness. Even if my participation doesn’t always look like this, I have to believe that I will not lose dance. I refuse to consider the possibility of losing it. I have already lost too much, and the grief of that is feeding my fear now. I cannot give it any more fuel.

As I stand at the barre and assess my posture, perhaps it’s not that I need to remember how my body works. It is that I need to teach it all over again. I need to relearn the muscles and the joints, remapping my brain’s understanding until it no longer automatically associates my right hip with pain even in my imagination. I need to start again, from the beginning.

One hand on the barre, first position. Demi-plié. And rise.

Christ’s College Chapel, 20th December 2019

The pain management book I’m reading is A Practical Guide to Chronic Pain Management by David Walton. [NB: This is an affiliate link.]

To support me as a dancer (and, potentially, in getting therapy to deal with all the pain stuff), please consider dropping a couple of quid into my tip jar.

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Dear Younger Me, from the Future

I thought about writing a regular post summing up the past year and the decade before it, but that seemed like a cliché, so I decided instead to write a letter to my younger self — the person I was as the year turned from 2009 to 2010.

Dear younger me,

It’s hard to know how to start a letter like this. You’ll hate me if I gush about how young you are, because you’ve always hated being patronised. I don’t mean it like that. I just mean… well, you’re not me yet, are you? You’re hardly even you. You’re a half-formed thing, much as you like to think otherwise.

A selfie of me wearing an elaborate Venetian mask with feathers at the top.
Venice, Summer 2009.

But the groundwork’s there. The skeleton of who I’d end up being. Actually, as I stare down my twenty-fourth birthday I look a lot more like you, almost fourteen, than some of the selves I’ve been in between. I do Irish dance again, for a start, just like you do. I compete in preliminary championships and I’ve taken masterclasses with Ciara Sexton. I can practically see you freaking out from here, and you don’t know the half of it.

I quit, though, for a long time. That seems absurd to you — you’re still in love with it, still in the honeymoon period. In about a year and a quarter, you’re going to walk away from it. You’re going to do ballet instead — another thing you can’t imagine right now. You won’t go back to Irish dance until you’re 21. It’s what you need, or at least, it felt like it was at the time, but that doesn’t mean it’s going to be an easy decision when it happens.

Then there’s the music. I’m trying to remember exactly where you’re at right now. 2009… oh! Of course. You just joined the wind band. They were playing the title piece from Riverdance and you being an Irish dance nerd, you wanted to be a part of it. It was a great concert, wasn’t it? I remember the high of it. You took up the piccolo this year as well, I think, but I don’t exactly remember where you were at with the violin.

You’re going to lose that.

Sorry. It sounds blunt when I put it like that. It was blunt when it happened. You’ve got about three more years, and then you’re going to injure your wrists, and develop debilitating chronic pain. They’ll tell you you’ll be playing again in a few months and then six years down the line you still won’t be able to hold a fiddle for more than about fifteen minutes before the pain kicks in. You’ll lose your entire social life — this is what happens when you put all your eggs in the orchestra basket. It’s going to suck.

A photo of me with long dark hair, playing the flute in a mostly-empty band room.
September 2011.

It’s going to shape most of the rest of the decade, too. Your entire identity is going to end up moulded by this, which is what I mean when I say that you’re not me yet. You’re still able to trust your own body, trust that you’ll be able to do whatever you like without triggering pain that will leave you unable to write for days on end, or too fatigued to move. You don’t even have any real food intolerances yet, though you’re going to lose the ability to eat fruit some time in the next year or two (trust me, that’s the tip of the iceberg…).

You’re going to lose so much, and it’s going to be so hard, for so long, and there’s nothing I can do to protect you, no warnings I can give that will prevent it. Your body is a time bomb. You could spend your whole life being careful and eventually it would still go off.

You have no idea what’s coming. And for that, I’m sorry. I wish I could tell you now to make the most of it — especially music, which you’ll lose more completely than anything else. I also wish I could tell you to install and get used to voice recognition software before you lose the use of your hands entirely for a few months, because that would really help me down the line, but… I can’t.

Let’s talk about writing instead. Another thing you’ll almost lose — but don’t worry, at least you get that one back. You’re only just beginning to realise how important it is to you. You’ve got two short, crappy novels under your belt (I hope you don’t mind me calling them crappy. I’m pretty sure you’d describe at least one of them that way, and … just trust me on the other one, please), but you’re going to write, like, seventeen more before this decade’s out. Some of them you’ll rewrite half a dozen times. Some of them will be bad, some of them will be good, some of them have potential but they’re not there yet.

You’ll self-publish three poetry collections. Have your poetry appear in a couple of small magazines. Write literally hundreds of thousands of words in blog posts (and then delete all of them). You and Charley (yes, you’re going to stay friends) will help co-write a boarding school mystery. You’ll write YA and adult and fantasy and contemporary and everything in between. Most of it’s going to be at least a little bit gay.

(Oh yeah, spoiler alert: you’re not straight. You’re not even a girl. You have a lot of identity crises coming, younger me, and none of them are going to be easy, and I’m closing off this decade still not having the answers to a lot of seemingly simple questions. Good luck with that.)

A photo of me sitting on a milecastle at Hadrian's Wall, with short fluffy hair and a plaid shirt.
Hadrian’s Wall, August 2014.

It’s going to feel like everything’s taking forever, and you’re going to be struggling to find direction or the courage to take the plunge and just send your work out into the world. Eventually, you’re going to enter something called Author Mentor Match, and you’ll get in. You’ll team up with a more experienced writer (if I tell you it’s Rory Power, author of Wilder Girls, it’ll mean nothing to you, but I promise you it’ll mean something a decade down the line), and she’ll give you the support you need to tear your book apart and rebuild it from the ground up. You’ll make friends, too, with the other mentees — a writing community you haven’t had since Protagonize shut down, and which you desperately needed.

Oh, yeah, right. Protagonize shut down. It’s okay, though. You had a good few years of it, made some lasting friends, caught that writing bug for life, and really, in the long run, it’s probably a good thing that all of your writing from 2009 and 2010 isn’t still floating around online. I know you’ll be annoyed at me for saying that, but I don’t mean it to put you down. If anything, it’s an encouragement. You’re going to get so much better at this.

I guess while we’re on the subject of Protagonize, we should talk about right now. New Year’s Eve 2009/10. You’re about to lie to a moderator who caught you making a sock puppet account to boost your own ratings because you’re way more insecure than you’ll ever admit to being, and you’re going to get banned from the site for a month. I don’t think you’ve had that conversation yet (I think it’ll happen tonight), but… it’s coming.

You’re an idiot, younger me. An idiot for making the fake account in the first place, and even more of one for lying to a moderator about it and then arguing with them when they (rightfully) made you face some consequences for it. I’m pleased to report that you’re going to grow out of that, at least; ten years down the line I’m not as honest a person as I’d like to be, but I’m working on it, and I never did anything like that again.

So. You’re going to start this decade banned from the site. Unable to access or continue any of your existing stories, you’re going to start something new. Write the first few chapters of it and then abandon it until, oh, around April, when you’ll rediscover it and keep going.

That book’s going to go through nine drafts and then you’re going to shelve it. You thought it was a standalone at first, then the first book in a trilogy. In a few years you’ll realise it’s actually a much later installment in a larger series. Then, eventually, you’ll realise that virtually nothing of that original book will survive, but for some version of a few of the characters.

But those first wisps of characters that you began to develop during that month of creative isolation are still going to live in your head in ten years time. Alex Kian Robson? He’s right here. I call the series Death and Fairies, which was a joke that stuck. Alex isn’t the main character any more (he got demoted), but he’s very much there. So is Jennie. You didn’t know what kind of story you were trying to tell yet, but you laid the first stones of it anyway.

So it’s not a waste of a month. It just feels like one. It’s your own fault, but cheer up — things can only improve from here.

A selfie of me holding a pencil, with short hair and glasses.
Cambridge, October 2016.

And they will, in writing terms. I cannot understate how much you’re going to improve in ten years. And finally, right at the end of the decade, you’re going to keep your promises to yourself and you’re going to start querying — properly, this time. It’s a book you haven’t even thought about starting yet, though you’re only a couple of years away from creating the bare bones of its protagonist, Isabel. I think you’d like it. It’s sad and violent and there’s no kissing at all.

It would take too long to tell you everything that happened in the past decade. Some things I think you’re going to have to find out for yourself. You’re going to face… pretty much everything for the first time, I think. You haven’t really experienced much yet. You’re going to lose your grandparents, and that’s going to suck, and your brother’s going to move to Canada (you’ll miss him more than you’ll admit). You’re going to have some pretty dark moments and sometimes it’s going to feel like you’ll never drag yourself out of the hole that you’re in.

But there’ll be brighter days too. You’ll go to Ireland, just as you’ve been dreaming of doing for years already. Multiple times, in fact! You’ll meet Kate Thompson. Maggie Stiefvater, too. You’ll do a degree in Anglo-Saxon, Norse and Celtic, and get really, weirdly into medieval Irish literature. You’ll start learning Irish, properly this time. You’ll get a job as a trainee librarian and move to Cambridge. You’ll go to conferences, turn your dissertation into an academic article, and start thinking about doing a master’s. You’ll become a Quaker (you don’t even know what a Quaker is yet), after years of struggling with and losing your faith. You’ll love and be loved and there will be people who understand you, eventually.

Right now, you can’t see any of that coming. But I promise that it is.

A photo of me looking back over my shoulder, wearing a gown and hood, with King's College Chapel in the background.
Graduation. Cambridge, June 2018.

And no, you won’t be published before you’re eighteen, or even before the end of the decade. And a lot of what you thought might happen won’t happen. In fact, the vast majority of what went down in the past ten years isn’t what you might be expecting. (Did I mention the fact that you’re queer? You’re… super queer.)

Will you have regrets? Absolutely. Will you mourn missed turnings, abandoned paths, lost opportunities? Of course. Will you find yourself wishing you could turn back time and go back to who you were at the start of the decade?

No.

You’re not me yet. You’re not even you yet. And I’m not sure I’m me now, but I’m a lot closer to it than when I was standing where you are. These ten years haven’t always been kind, but we’ve grown up, younger me, and we’re almost ourselves now. I don’t know who we’ll be in ten years time, but at least nowadays I’m confident I want to stick around to find out.

So hang in there, younger me. You’ve got a long decade ahead of you, but the only way out is through.

With love and in friendship,

Finn*

A selfie of me with a gleeful expression, accompanied by a very fluffy black and white cat.
Boxing Day 2019, with my sister’s cat, Tyler.

*Oh yeah, you’re going to change your name. It’s a short form of delorfinde, so really, it’s not so strange to you; you’ve yet to start using your legal name online. Anyway hi. This is me. You. Us. <3 Wait ’til you find out about pronouns…

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Fear and the Future

In the aftermath of the election, it’s hard to know what to say.

Maybe it’s easier to say nothing, to let it pass unremarked as so many things do on this blog these days, but that feels dishonest. I have so much I want to say; it’s articulating it that’s the hard part. I’ve started writing this post three times already. Everything I say sounds either melodramatic or untrue, and I can’t get past that.

How about this:

I didn’t think I had been allowing myself to hope for a different result, until the exit poll was announced and I found myself sobbing.

Or what about:

Ever since I started hanging out with Quakers, I’ve heard a lot of people talking about ‘God’ as meaning ‘the innate goodness of people’, but sometimes it feels like that’s as hard to believe in as a childhood conception of God as a bearded man in the sky.

Maybe just:

I’m scared.

I’m scared about what this means for the future. I’m scared of the country I live in, where I cannot trust people to look out for their vulnerable neighbours, where xenophobia and racism are on the rise, where racist rhetoric wins hearts and votes. I’m scared of the inevitable fallout when Brexit happens — a fear I’ve been living for three years already and will continue to live with until the worst happens and there is nothing left to be afraid of because it has already happened.

A blue IKEA shark propped up in a chair holds a Labour Party election pamphlet. It is wearing two red badges. One reads, "Kick out the Tories". The other has a heart with the EU flag and Union flag on it, and says "Better Together".
Láeg mac Blåhaj may be blue but his heart is not. He couldn’t drag himself out of bed yesterday to face reality, but today his expression says it all…

I’m young. I’m trans. I’m disabled. This government doesn’t care about me. It has already killed disabled people with cuts to benefits and the NHS, and it will kill more of us. If the NHS goes under, I have friends who will die. You see what I mean about the melodrama? I try and state it like the bald fact that it is, try not to let the emotions creep in, but it still sounds dramatic: this is a matter of life and death.

But it is. I don’t know how else to say it.

I wouldn’t think of myself as a single issue voter — I care about so many things. I care about the environment, I care about peace, I care about equality, I care about creating a system that doesn’t work people into the ground just so that they can survive. I care about education and the arts and the idea that everyone should have the chance to thrive, not merely to keep breathing. There are dozens of things that matter to me.

If there were to be a single issue, though, it would be the NHS.

I’m lucky, so far, in that none of my lifelong health conditions are the variety that have to be continuously medicated or they become fatal. I rely on the NHS for those frequent blood tests, the B12 injections, the extra vaccinations to support my immunocompromised system. Without them I would suffer. Without low-cost access to medication I would struggle. But others? Others would die.

Others have already died, abandoned by a benefits system that will leave them with an unplugged fridge and no insulin, or declared fit to work while terminally ill.

And yes, I have complained about NHS waiting lists and I will probably complain again. I’m currently on three, the longest of which is approximately two years, the shortest of which was a minimum of three months and I’ve yet to hear from them. But I know that those waiting lists are the result of cuts and deficits and strain imposed by the quiet privatisation of different services. By the lack of proper governmental support for mental health services. By this country’s rampant and growing transphobia, and the lack of funding for healthcare to support trans people.

(The rise in vocal, vicious transphobia in this country is another fear I live with constantly, but there’s nothing I can do about it. I suspect it will get worse. I can’t do anything about that, either.)

A black satchel covered in pin badges. Slogans include "trans rights are human rights", "avenge Oscar Wilde", "kick out the Tories" and "Quakers oppose all wars".
Books and politics — and a little bit of Ogham. Perhaps this bag is meant to symbolise this blog.

I see my friends in the US crowdfunding to afford medication they need to live. I see people bankrupted by medical debt while dealing with the grief of losing family members. And I can’t fathom how anybody could look at that and think it was something to emulate, but I’m afraid that some of the politicians our country has just elected think exactly that.

I hope that my fear is unfounded. I hope that the people who say, “They’re not going to sell off the NHS,” are right, just as I hope their promises to fund it aren’t yet more lies spouted by spineless, heartless cowards who will say whatever they have to say to convince people.

I hope that I am wrong.

I can’t express how much I hope that.

I hope that Brexit doesn’t destroy this country. I hope that it doesn’t send food prices through the roof, make it impossible to obtain certain medications, or result in a huge deficit of medical professionals. I hope that it doesn’t destroy our relationship with Ireland. I hope that those who have made their home in Britain are allowed to stay, made welcome rather than treated with suspicion and bureaucracy.

I hope all of these things. That doesn’t mean I believe in them. Hope can be a ruinous thing. We cling to it until it shatters and the shards of it slice our hands to pieces. Hope isn’t enough; to thrive in the face of something like this takes work.

I wish I could promise to put that work in, to fight for all of us, to agitate for change, to be an activist and a pillar of the community and a support to those around me… but I’m so tired. Some days it takes all of my energy just to get out of bed. Fatigue is a full-time job, and that scares me, too: the knowledge that I don’t have the strength to stand up for myself and my friends. I admire those who have it in them to be an activist, but I know that I’m not one of them. Not at the moment. Not when I’m barely coping as it is.

My method instead is avoidance, and perhaps that’s cowardly, to pretend none of it is happening, but sometimes all you can do is distract yourself as a way of barricading your mind against the constant fear. Yesterday, I finally finished writing the gay werewolf novel I was working on for NaNoWriMo, because it was a distraction that I needed. I’m not sure what I will work on next, but I have a dozen small projects that I can lose myself in. Perhaps that’s the easy way out, to refuse to face up to reality until it forces itself on me, but I know that my powerlessness and anxiety will break me if I allow them to be my focus, so I have to look elsewhere.

I have to find peace where I can.

Yesterday, I spent half of my lunch hour in the college chapel, seeking silence, somewhere to hide from the world and the screaming headlines and the fear burning electric through the inside of my head. I found a kind of peace there that quieted my mind a little. Oh still small voice of calm. This world is so loud, especially at the moment. It seems harder and harder to seek that quietness, and part of me feels guilty for trying, when it feels like I should be out on the streets with a placard and a chant.

But all of us can only do what we can, and for me, at the moment, it feels as though existing is all the resistance I can offer. Continuing to be me, refusing to apologise for all the things that I am: queer, nonbinary, pacifist, creative, exhausted, loving, helpless, disabled. Continuing to exist in a world that only offers boxes I don’t fit in. Allowing myself the shocking luxury of unapologetic rest.

I am afraid of what the next five years will bring. I’m afraid of my own helplessness. I’m afraid of my country and I’m afraid for my country and I’m afraid for myself and I’m afraid for everyone more vulnerable than me, who don’t have the privilege of safety nets.

But I hope — desperately — that I’m wrong.