Be Yourself! But Not Like That!

A while ago, I tweeted something like this:

“Cis society: Be yourself!
Trans people: Yes, okay
Cis society: No, not like that!”
It’s been running through my head a lot since. I figured it deserves a blog post.

I see this as a sibling post to my often shared post about the pressure I feel as a bi person to “choose” to “be straight”… Because I feel a similar pressure to “choose” to be cis.

There is a very strong message that often comes from within trans communities as well as from cis society that says that being trans is so, so intrinsically awful that nobody would (or *should*) be trans if they could possibly avoid it. Indeed, many people spend months or years trying to convince themselves that they don’t want to transition when they actually do because of this very prevalent idea.

And just as with sexuality where most people will concede that some people can’t choose not to be gay, it’s understood that some people can’t be cis but it is frequently suggested that some people do have a choice – and that the “correct” choice is to be cis if at all possible.

I would be rich if I had a quid for every time someone tried to convince me that I should be able to live as a cis woman instead of as a trans man.
People told me (as if I somehow didn’t know) that women can dress in men’s clothes, that women can do and be anything men can, that it’s okay to be a lesbian, that it’s okay to be butch, that women can be androgynous and still be women… And I don’t disagree with any of these things! They just aren’t reasons why I should be someone I’m not.

I also frequently get told that I’d be “prettier” as a woman, that more men would be attracted to me if I lived as a woman, that more women would be attracted to me… And I don’t believe that. Authenticity is much more attractive than forced cisnormativity ever could be and even if it weren’t, I wasn’t born to be attractive I was born to be my best self.

The ways people have tried to convince me to stop being a man say a lot about why they think trans people transition. I’m not trying to become more attractive, I’m not looking at the clothes I want to wear and trying to make my identity “match” the side of the shop I find my clothes in. I don’t think that men are any better than women and I’m not trying to avoid homophobia. I know that women can be butch or androgynous – I’m not trying to escape one set of restrictive gender roles by fitting myself into another set.

I am, quite simply, trying to be myself.

While pretending to be a girl / woman made me deeply unhappy and caused me mental pain and anguish, that isn’t even really the reason I live as a man. I live as a man because THAT IS WHO I AM. There is no good reason why I should try to “be” anyone else but me.

Think about it, especially if you aren’t trans. Can you really imagine people telling you that who you are is wrong and you should be someone else instead? Imagine for a minute being told to act like someone else for the rest of your life and being told that the other made up, false “you” was actually more real than anything you thought or felt about who you are. Like going undercover or acting, say, but forever. It’d be doable, sure, but could you be happy? Could you be even satisfied with a lifetime of being someone else, even someone almost but not-quite like you? Or would the not-right-ness wear you down? Would the pressure of hiding anything that might blow your cover eat away at you? Would you be tempted to call it quits and just be yourself and hang the consequences?

I could, in theory at least, live as though I were a cis woman. But why on earth would I trade my integrity and authenticity for a thin veneer of cis privilege?

If you feel like you’re pretending to be someone else and you want to try being yourself, you don’t need to wait for the facade to be killing you to be “allowed” to drop it. Whether that’s a gender, a sexuality, a religion, a relationship, a career or something as simple as having a name that isn’t working for you, you don’t have to wait for things to feel completely intolerable to make a change. You deserve to be your self, with integrity and authenticity, right now.

I don’t need to earn the right to be myself or to suffer through every possible attempt to find a way to me kinda like myself but not trans before I can be the trans man that I am. No one should have to exhaust every other option before being who they are just because who they are is trans.

To expect otherwise (and many people do expect otherwise) is to insist that being cis or appearing to be cis is innately better than being trans. It’s not.

We all deserve to be ourselves. So don’t you dare tell me it’d be better if I was someone else instead.

Actually, yes, I DO have a job…

It’s not a surprise to any of my frequent readers that my income is (and looks set to remain) almost exclusively from social security payments (or “benefits” as most of the UK press call them). I get paid by the government because I am too severely ill an disabled to be fairly expected to look for, find and manage full time work. Should be simple enough, right? I got ill, I can’t look for work, I get paid until such a time as I can do (even though that time is likely to be “never”).

However what both the public and many politicians and media people who should know better have managed to twist this into is: “Liam doesn’t work and the government is taking money from people who do work and just handing it to him for nothing!” That’s not what’s going on. But the idea reveals what various people think it is that I and other sick and disabled people do with ourselves – they think we do nothing and especially that nothing we do is “work”.

Well, you know what, I DO work.

My job is staying alive with a malfunctioning body, nonstandard brain and a damaged mind while living in a broken system. My job is maintaining a decent quality of life. My job is the upkeep of my relationships. My job is being the best human being I can be during my one life.

If that’s not enough for you, let me break it down.
Per month I do:
16+ hours of therapy, processing, meditation and planned exposure to things that scare me.
4 or so hours talking myself out of self-destructive urges.
8 hours written and email correspondence with my care agency/social services
5 hours getting to and from medical appointments
2 hours attending planned and unplanned medical appointments (other than aforementioned therapy)
2 – 4 hours collecting and collating pieces of paper that can be used as “proof” that I’m ill, disabled and poor
12 hours researching aids, appliances and services that might help me live (more) independently and trying to work out how/when/if I can afford them
3+ hours emailing places / events I want to go to trying to find out necessary access information
3+ hours arranging for other people to do things like phone calls and planning travel arrangements for me
8 – 24+ hours lying on the bed resting because I’m too exhausted to do anything else no matter how badly I want to
3 hours writing emails apologising for missing stuff / not replying sooner because I was too ill to do so
1 – 2 hours writing emails requesting copies of documents about me be sent to me in a font size I can read
4 hours trying to order groceries online because I can’t drive or carry more than one bag of shopping or go shopping every day
3 hours waiting around in pharmacies
2+ hours getting hopelessly lost in places I know well and have on googlemaps on my phone

…. plus hundreds of hours of pain , dozens of hours of nightmares, taking twice as long as my peers to do most things and all the time that takes up…
Oh and plus all the things non-disabled people do like meeting up with friends, going on dates, talking to family, eating etc
But you get the idea. That list of things above is what I’m doing instead of working in a month when the DWP isn’t harassing me into spending multiple hours a day trying to fill in their forms and photocopy them all the evidence they want and understand their latest demands. It’s a month in which I don’t have any huge crises or get acutely ill with anything. It’s a bare minimum of what illness and disability gives me to deal with in any four week stretch.
And at the crux of it, that is my JOB. I work full time at managing my illnesses and conditions and the way they interact with a structurally disablist society.

I also happen to volunteer but not as much as I would if I didn’t have all of this going in the background.

A lot of people want you to believe that those of us who get benefits spend our time “do nothing” and while I don’t actually see much of a problem with people doing nothing if they want to, that’s not what we actually do. Having a chronic illness or a severe disability is a full time job in itself.

(If you think you that you / people who talk about benefit scroungers “doing nothing” don’t mean people like me, you’re sadly mistaken and this will be the topic of my next post.)

Third Blog-iversary!

Readers, I have now been writing and publishing this blog for three whole years. This February just gone is the first month I’ve missed – though I have several mostly written posts that I wrote during February. They should be up soon!

Writing Yetanotherlefty is a huge achievement and each year I feel very proud of myself for keeping this up. My mental health has not been so great lately and knowing that I can write about it here and people will empathise and understand is really helpful.

I hope that my writing has helped some of you this year.

I’m not going anywhere. More posts will be up soon.