Tag: people

Employability first, disability later

Employability first, disability later

by elizabethmdouglas ♥ 0 Leave a Comment

Since moving to London last month, I’ve applied for part-time jobs which will allow me to have enough money to live, whilst also leaving room for me to pursue a career in radio and broadcasting. And during these job applications and subsequent interviews, I’ve been repeatedly faced with society’s favourite question about disability: how does your condition affect you on a day-to-day basis?

Everyone loves this question; it offers neat and comfortable parameters within which a disability can be defined and the methods for ‘dealing with it’ clearly laid out. Yet, every single time a person asks me this question all I ever feel like doing is laughing, because even though their intentions are probably good, the question makes literally zero sense.

On the surface, what’s being asked is how my Spina Bifida will impact my ability to work – or, if the government is the one asking, then it’s more about how it will impact general life. But the problem is that this seemingly simple question doesn’t have a simple answer, because it assumes that disability is this one fixed condition, which has these fixed symptoms, which impact everyone who has this specific disability in these fixed ways. Such an organised experience of disability would be nice – trust me – but it’s about as likely as pigs flying tomorrow morning.

Each time I apply for a job, I’ve carefully considered whether I think the role is something I can physically manage, so I don’t feel it necessary to tell the employer I’m physically disabled at that point because I’d prefer to be judged in the same ways as all the other applicants. Plus, at this stage, I don’t think that my medical history is anyone else’s business. However, when I get to an interview and the employer asks if I have any questions, that’s when I’m explicit about my needs – basically, I just need to be able to sit down regularly to relieve the pressure off of my feet for a bit. But by then, I’m 90% sure it’s wouldn’t disrupt my ability to do the job and it’s something the employer could sort out pretty easily. If the employer agrees (which, more often than not, they do) then we start filling out all the HR forms so I can be put on rotas.

This is where it can get a bit sticky because I always have to send over my medical information to prove my disability so the company can do a risk assessment, but that mountain of paperwork paints my condition as a ticking time bomb because all that’s mentioned are my operations, blisters and infections. But, as I explained to the lovely lady who recently gave me one of my jobs, the government (a.k.a. who the paperwork is written for) only cares about when the Spina Bifida has been at its worst; there’s no room in the notes for the million and one ways I take precautions every day to ensure that I’m fine.

So why is it a bit silly to ask me how my disability affects me on a day-to-day basis? Well, because I don’t know which days you mean. I could tell you the days when my foot is in a good condition, but how far are you asking me to walk? Are my shoes new? Is it hot outside? Am I walking uphill, downhill, or on a straight road? Can I drive part of the distance? Am I tired?.. Is there a correct answer to this question?

Obviously, I know that in the context of employment, companies have to cover their own backs and make sure that they’ve got the correct provisions in place to look after me. But the point I’m trying to make is that even though life with a disability can’t be explained as neatly as we might all wish it could, I still want and need to work, and ‘catering’ to the needs of disabled people in the workplace actually isn’t that hard when you listen to the person with the condition. I’ve worked all around the world in shops, and schools, as a summer camp counsellor, in radio stations and in car dealerships, and if I ever had a problem with my feet whilst employed, I communicated with my boss and I dealt with it just like everyone deals with random problems in life.

So, I don’t have an issue with employers asking a person how a disability affects their daily life, I just hope that they’re not surprised when they don’t get a simple answer. Also, I hope that there’s an acknowledgement that the person with the condition has probably put a lot of time and mental energy into deciding whether they can do the job before they even applied, and thus if they’re qualified in every other way for the role, then it’s no one else’s right to tell them what they can and can’t do.

Well that was a bit silly of me

Well that was a bit silly of me

by elizabethmdouglas ♥ 0 Leave a Comment

Okay but, why is it that whenever I get bored, lonely, or horny (or heaven forbid a combination of all three), I think it wise to make some stupid decisions? Something happens in my head where I think that for some reason, a lad who I’m definitely not that interested in not only requires my attention, but he also deserves my stress and occasionally even my tears. I swear to you, if I had a pound for every time I’ve gotten irritated over some romantic situation, where, if I actually took a step back and thought about it, I’d decide I was really not that invested anyway, then I would be a very rich woman right now.

And I know that everyone says this but I promise you, pinky swear and lock it in, I don’t enjoy the unsaid games which happen before you’re in a relationship with someone. I can’t be bothered to wait for ages to text someone back, I don’t care about how long they take to text me back – unless it becomes clear that they’re playing the game, then that does irritate me – but more than anything, I hate how being involved in the game makes me overthink EVERYTHING. And yet, I still do it! Often with people I don’t even like that much! I’m also incredibly picky and very very rarely say yes to going on a date with someone. So am I part of my own problem? Possibly.

I think that part of it is that if you actually sit and think about the efforts a person would have to take to not think, speak about, or see romantic relationships in everyday life then you come to realise that it’s kind of impossible. Every time you turn the television on, it doesn’t matter if it’s reality tv or a drama, odds are there’s a hefty section devoted to finding a relationship, being in one, or leaving one. Then you walk down the street and someone’s being cute with their partner, or there are advertisements suggesting what you should do with your partner, or what you should buy them. Plus, you’re judged if you go out and do things on your own, let alone the lame fact that it’s kind of unsafe for a woman to fly solo in towns and cities once the sun has gone down, so even if you wanted to go for a drink on your own, there’s that little voice in your head wondering whether it’s worth the potential hassle.

Therefore, we’re encouraged to be lonely, we get bored, and if those two weren’t enough, the sex drive comes along to make us momentarily ignore that part of our brains which tells us that something is probably not a great idea. Because maybe it is a good idea for the near future. And it’s not that deep anyway! And they’re interested in me! Or they seem to be… And it’ll make for a fun story to tell everyone tomorrow morning.

I try not to waste time regretting my actions, since I know that if I were put in the situation again, I’d probs do the same thing anyway, but sometimes the embarrassment does find its way into my internal monologues and when it does, you’ve got to flush that shit away like a spider in the bath.

But second-hand embarrassment aside, at least I try to treat people the way I’d like to be treated so it’s not as if I’m out here being a massive cow when I’m making questionable decisions. However, this isn’t the part where I promise never to text someone who I know is only going to play some game and then irritate me by doing that, because ladies and gentlemen, I am silly at times. Buuuutttt, I will congratulate myself for finally being decent at knowing when enough is enough and just deleting the conversation thread. That’s some solid character progression right there. Go me.

Making London moves

Making London moves

by elizabethmdouglas ♥ 0 Leave a Comment

I’ve never been a person who’s particularly scared of change, especially when that comes to living in a new place. In fact, once I finished secondary school I worked three jobs so I’d have enough money to go travelling before I started my university degree. Then when it came to moving to university, I definitely cried when saying goodbye to my parents but that’s just because they’re both so much fun to be around; I don’t think that I was actually that daunted by moving away from home. But last week, with the help of my parents, I moved all of my things to London and even though I’ve lived in a lot of new places over the past six years, this time the first couple of days in my new home didn’t fill me with excitement; all I could feel was terror.

When I’ve travelled to different countries, I’ve always only been there for a certain amount of time. Therefore, even if I was living in a massive metropolis like Seoul or New York City, I could square all the walking distances and activities in my head because I knew that once I got home I’d be able to go to the same doctor who’d been seeing me since the age of three, she could treat me, and if I had done too much walking then it’d be fine because I could stay at home and rest for a couple of weeks before I went onto the next country or back to university.

So my utter panic at now living in London was/is that this is now my every day and I don’t have an opportunity to overdo it and then rest for a few weeks if the condition of my feet does worsen, because if I get the blister then I can’t go to work and if I can’t go to work then I can’t make my rent. Not to mention the fact that I now have to rely on totally new doctors who don’t know the nature of my disability and thus, may not be able to help me in the way someone who’s seen me through all the operations and every type of blister could. Plus, I don’t have a job yet because working in the broadcasting and radio industry requires you to 1) be in the place where it all happens, 2) be able to network your way into the buildings and then 3) work from the bottom to the top, if the bosses judge that you have the ability to make it up there. So, I have to find a part-time job in order to make my bills and give me enough time to put my graft into radio and broadcasting – that part sounds easy though, doesn’t it? “Just pick up some shifts at a bar, restaurant, or cafe!” I hear you say! Only, I physically can’t be on my feet all day and the hundreds of other people also looking for part-time work can, so my chances of getting the work are slimmer and waaayyy more stressful than when living in a smaller city.

Thus, I’m not frightened of this move because I think that I can’t do it; I’ve always been a total grafter. Nor am I frightened because I’m scared to live in a new place, far away from my family. The overwhelming panic that I’m trying not to think about comes from a fear that this ridiculously inaccessible world will stop me from being everything I know I can be, just because I can’t walk far or stand for long.

But it’s not helpful for me to wallow in this fear, because if I did, then I never would’ve gone travelling or anywhere further than twenty minutes down the road. So you have to push it aside and focus on controlling what you can, rather than catastrophising all the ways the risk you’ve taken could end in disaster.

Once I’d moved a couple of things into my new room my parents asked me how I felt, and I tried my best not to let the nerves show because I didn’t want them to drive away feeling worried about me, but they, and my closest friends, all assured me that it’s totally fine to be frightened of this; being scared doesn’t make you weak or foolish. Living in this city with a physical disability is no small feat and I’m bound to have a bit of a moment every now and then, so the best thing to do is to quite literally take everything one step at a time. Then, once I know how to look after my feet in the big city, I can explore!!!

Get your kit off!

Get your kit off!

by elizabethmdouglas ♥ 0 Leave a Comment

Last week I was sitting with one of my best friends and I asked her how often she looks at herself naked. (Bit of an intense way to start a blog, I know, but I didn’t know how else to kick this topic off lol). I asked her this because we’re all well aware of the level of scrutiny our bodies are under in regards to what size they should be, what shape, what colour, what texture, et cetera et cetera. So, I guess I was just curious about how often my friend stands in front of a mirror and has a look, to then compare it to how often I do the same, especially since the act of looking at your naked skin in broad daylight is one of the most vulnerable things you can do. After all, we might not always like what’s reflected back to us.

My friend’s a total queen though; her response was ‘all the time’ and I said the same – buuuut, I did go on to explain that I don’t spend too many seconds looking at my Spina Bifida lump or my legs in the mirror, so I’ve got room for improvement.

I think that in general, as women, we’re not encouraged to stand with ourselves and get familiar without being critical, so it can be quite unusual to see a woman who is totally comfortable with her naked body. However, I would like to clarify here that by ‘totally comfortable’, I’m not suggesting that there aren’t things you dislike, or would prefer to not look a certain way some days because we’re going for honesty here, not idealism.

One of the best things I ever did for getting comfortable with my own skin was starting to sleep naked every night. I wouldn’t say that before doing that I was ever particularly uncomfortable with my body, but sleeping naked just forces you to see and feel yourself exactly as you are: you get used to your boobs falling in every direction depending on how you’re sitting; you see all the stretch marks and ‘imperfections’ highlighted by the sun when you wake up, and you stop getting a little startled by the image of your naked body first thing in the morning. But overall, sleeping naked allows your skin to breathe and everything feels better after that.

Quick sidenote: I do realise that a lot of my words and descriptions here lean very close to the topic of masturbation, and whilst I’m not really going to go into that much today, I will say: for god’s sake, masturbate! Especially you ladies! It’s good for you! (Literally.) :)))

Many people (especially (British) women) would rather die than speak about topics such as this one, but after being lucky enough to have known women of all shapes and sizes who are so comfortable in their own bodies that they’ll take their kit off at any given opportunity, I’ve never underestimated the power of being proactive in loving your body. Every clothing campaign badgers on about it nowadays – some in a very live laugh love sort of a way (*puke*) – but the human body is truly a remarkably beautiful thing, and even though we’re never going to love ourselves entirely every single minute of every day, making sure that we at least accept ourselves every day does wonders.

Regardless of how we each feel about our own bodies though, we should be careful to never (!) shame another person for being confident in their body just because you wouldn’t do the same. I like to sit/hang around my house in a towel, or my underwear and I’ll put the bin out with ‘just’ a big t-shirt and knickers on; you not doing the same doesn’t mean you love your body any less than I love mine, but it also doesn’t leave room for my body to be sexualised or criticised when all I’m doing is watching TV or putting the recycling out. After all, if you can’t wear as much or as little as you want in your own house, then where can you?

Cover those callipers!

Cover those callipers!

by elizabethmdouglas ♥ 0 Leave a Comment

I was seventeen the first time somebody complimented my shoes. I remember, I was walking up the stairs in the secondary school I’d been attending for seven years already, when a new member of staff who I didn’t recognise came in the opposite direction, took one look at my callipers, and said ‘I like your shoes’. I stopped dead on those stairs feeling a mixture of shock, outrage, and confusion because I thought that he was taking the piss and I wasn’t exactly sure how to react to a teacher being blatantly cruel to me, but then I looked at his face I realised that this compliment was genuine; it didn’t come from a place of pity and it wasn’t him trying to wind me up. So I gave him a stunned look, said ‘thank you’, and went to tell my friends about what had just happened.

It’s strange because I know that my reaction to this type of situation implies that I’m insecure about my shoes, but I think to draw that conclusion is too easy. The fact is, that I know I’m physically disabled, I know I have to wear these callipers to correct the positioning of my feet, but wearing these shoes wasn’t a choice I ever got to make; I don’t particularly like the way they look, they mess with the silhouette of my outfits, they draw people’s attention to a part of my body I’d rather not be stared at, and the sight of them can make me be treated very differently. Yet, regardless of how I feel about them, there is absolutely nothing I can do to change whether I wear them. So, it’s not that I’m insecure about my callipers and my disability, it’s that I don’t necessarily enjoy the judgements people make of me when they see them – and I can’t really fathom them looking stylish…

Now I know what many of you might be thinking: if someone judges you because of two metal bars on each of your legs then that’s just their ignorance, it shouldn’t be something which you allow to bother you. Fair point, well made. But what I’ve noticed when speaking to people about this kind of thing, and then going out and existing in the world, is that individuals have absolutely no idea of the difference in how the able-bodied world treats me when they can see my callipers, versus when they can’t.

Let’s take going to the airport for example, since I was at JFK last week. I always wear trousers which cover my shoes when I go to the airport because it’s a place where you’re guaranteed to see a lot of people, you might be tired (maybe a bit stressed), and for me, I always know I’m going to get searched because my shoes will set the metal detector off, so I don’t want my callipers to draw any more attention to me than I’m already going to get. However, this then causes me problems when I ask for disability assistance because without those metal bars, nobody can understand how I could possibly be physically disabled enough to not be able to stand in a queue for 25 minutes; people take one look at me and they assume I’m trying to unjustly weasel my way into a shortcut. So, what do I do? I wear an outfit which shows my callipers just to avoid that hassle, even though I know it’ll mean seeing loads of people staring at them when I’m in precisely the wrong mood? Why should I have to do that?

This feels like a perfect point in the discussion to use the term many of us have seen knocking about on signs next to disabled toilets since the pandemic, and preach that ‘not all disabilities are visible’. But what I find hilarious, is that my disability IS visible! It doesn’t matter what I’m wearing, you can still see the glint of the metal bars at the base of my shoes – god knows people still give any centimetre of calliper a good stare – so I’m not sure that it’s even about how much of my shoes the world can see. I think there’s a problem that people either expect to see disability as consuming the appearance of a person, or not there at all, but if you’re the former then you’re too disabled to be anything other than that, and if you’re the latter, then you’re exaggerating and you’re not disabled enough.

I sit somewhere in between both of those ideas, and it means that a lot of the time, I’ve got no idea what I am so I just do what makes the most sense to me in a given situation. I wear outfits which show my callipers whenever I want and I switch off to the staring, but in the moments when I’d rather everything else about me take precedence over the disability, then I’ll cover them up, even if that comes with expecting to get some shit off of someone at some point – it doesn’t always happen, but it’s highly likely if I’ve covered them and then have to ask someone of authority for a bit of disability assistance. Also, you probably won’t see me going on a date, or meeting new people in an outfit which shows my shoes.

But before I leave you, I want to emphasise that these acts of hiding my callipers aren’t because I’m ashamed of them – I might not actively like how they look, but shame has nothing to do with it – it’s because having a visible physical disability encourages people to focus on it for longer than you might like them to. So even though I have nothing to hide, I hide it to take control of the situation and encourage you to look at and listen to me like you would anyone else, and then you can notice the Spina Bifida later. It’s a double-edged sword though because if I now need to ask for help, if you can’t see my shoes, then you might not believe me…

Tricky, isn’t it?

Consistency is key

Consistency is key

by elizabethmdouglas ♥ 0 Leave a Comment

No matter how much I post about my disability on the internet, I am not, and never have been, very good at asking for help with it. I can do my own TedTalk in a room full of strangers about how ‘it impacts my life’, or overshare on the internet, but internally, I still wince from embarrassment each time I have to ask someone to alter their actions to accommodate my disability.

As a little girl, I had six operations which caused me to spend prolonged periods of time in a wheelchair and at hospital appointments, but I still don’t remember ever feeling ‘different’ because of that – shout-out to some top-tier parenting from Mr and Mrs Douglas there. Obviously, there were times when I was confused and frightened by it all; I mean, I remember the fever when an operation on my left foot got infected so the bone could be seen from the outside, I remember bawling my eyes out every time my parents told me I had to go in my wheelchair, and I still physically cringe when I think about getting stitches taken out of my feet after operations. But in and amongst all of that, I climbed as many hills as my able-bodied brother whenever we went camping, and I have no memories of feeling lesser than my peers or my siblings because I was ‘disabled’. However, I’ve come to realise that this was largely due to the fact that until I was in my mid-to-late teens, my disability wasn’t my own; it was my parents’. This Spina Bifida that everyone told me about was something I knew I had, but the dealing with it was something my parents did; like any six-year-old, I just went wherever I was told with a smile on my face and a Cinderella dress on.

Stuff started to get a bit sticky when I was a young teenager though, because by this point my friends and I were old enough to go into town on our own. So, instead of having the luxury of being lifted onto my Dad’s or my oldest brothers’ backs when the walking distances started to get a bit too far, I had to rely on my 14-year-old friends being emotionally aware enough to know the limits of my disability, even though I’ve always been too embarrassed and too stubborn to bring it up. Inevitably, this didn’t go very well and there were a lot of angry tears at the kitchen table.

Then in my late teens, I did really try to quieten my ego in favour of being responsible with my feet. But that’s indescribably difficult to do when not a single person around you is having to do the same – not to mention the fact that I’ve also got a naturally adventurous, ‘go on then!’ attitude which makes me want to do things I probs shouldn’t. So I effectively had to go through a period where I mourned the fact that I was too old to ignore my disability now; I had to grow up a bit. But thankfully, the wallowing didn’t last very long since crying over not being able to run a marathon or go on a hike for four hours wasn’t going to change anything. Plus, I can do plenty of other stuff anyway.

Sometimes I do still feel the loss though, like when I’m walking through town with my friends and they’re walking faster than me, my legs are getting tired, and I’m getting out of breath trying to keep up. Or, when another person in a Council or Security uniform tells me I can’t park here, that there aren’t any disabled spaces, and that they don’t know where I can go. Or at the thought of going on a date with someone I’ve just met, them wanting to walk around, me not being able to, and having to talk about my disability before I get to say anything else about myself.

Basically, I find asking for help with my disability humiliating and exposing, and I’ve been disappointed by a lot of people before, so it’s likely that if you do offer to help me out, even though I’ll obviously really appreciate it, it’ll take me a minute before I trust that you’re not going to forget next time. I know that that can be annoying if you’re intentions are sincere, but I can’t help it.

If you do want to be supportive of someone with a disability, I think the best piece of advice I can give you is to be as subtle and consistent with your actions as you can. I might speak very publicly about disability, but even I don’t want it to be brought up in every conversation – in fact, the best-case scenario for me if I’m out and about, is you being the one to suggest sitting down or getting an uber because you’re tired. That way, my legs are looked after and I don’t feel guilty or embarrassed for making you do something you wouldn’t normally have to.

Graduation, but then what?

Graduation, but then what?

by elizabethmdouglas ♥ 0 Leave a Comment

In my head, I think that I’m pretty good at hiding my emotions…but then every time I’m even slightly upset or angry, it usually takes my friends, family, or colleagues about 0.5 seconds to notice. So clearly, I’m slightly deluded. However, whilst it may be true that my overall mood is very easy for others to discern, I am that person who takes on a lot of things and eventually snaps when all of those things have piled up in my head. Then it’s in the moments when I’m close to snapping that my mood goes down, I’m tired, and I’m likely to burst into an ugly cry if anyone hits me with the ‘are you okay?’.

Don’t worry, I’m not about to confess to the internet that I’m in the middle of having an existential crisis…Though I will say that I’ve had a pretty intense last few months which have gifted me both good and bad stress, resulting in a few days when my mood hasn’t been as chirpy as it is normally. And one of these stresses has been something that I know many of my peers are overthinking right now: what the hell are we going to do after graduation?

For me, my graduation from university mostly brings a sense of relief. The last 3 years have been a lot of fun in parts but I’d be lying if I said that I don’t feel ready to leave; I’m tired of being confronted by the same annoying problems brought to me by Durham University, and I ache to leave the education system behind for a second. I mean, I’ve been in it for 17 years! That’s a long time. Granted, I had a year out before university but I did work in 2 schools for 6 months of that…then I taught in 3 of the 4 countries I visited…So no matter how much I know I’ll continue to study something for the rest of my life, I think I’d like to give formal education a rest for now.

It’s scary though. I can see it in my friends’ faces when we actually sit for a minute and talk about what we each want to do after uni: everyone masks the apprehension at being thrust into the adult world with talking about ‘panic masters’, internships, job placements, and the classically vague ‘maybe I’ll go travelling’ statements. The fact is that many of us have absolutely no clue what’s next or where we’ll end up, and it’s stressing a lot of young people out that they’re expected to have their whole life mapped out when just a couple of weeks ago we were sitting our exams.

I’m a lucky one in that I do know what I want to do, and I have made moves towards that, but even I feel like I haven’t had a second to breathe before I have to sort the rest of my life out. Also, there’s a stigma against the graduates who choose a different route from the traditional ones. For example, I know I’m moving to a new city and I know what I want to do there, but a career as a radio presenter doesn’t exactly have a cushty grad scheme for me to apply for, so whenever I tell people my plans, they inevitably sound half-baked, and that makes me self-conscious. Even though, we don’t all have to work in an office straight after university if we don’t want to…

Sometimes everything feels like it moves so quickly that there’s no way you can keep up, then other days it’s easy – occasionally, even a bit boring. I’m definitely not qualified to be giving advice on what to do in these situations given that I’m part of those going through the experience, but what I have said to my friends when we’ve been in the car or in a living room, stressing about the future, is that the best approach to have is to do whatever makes you happiest. That might be another year of university, working abroad and travelling, moving to a new city to start a new job, or having absolutely no clue and needing a couple of months of nothing to figure yourself out. Obviously, money is a factor in this and it’s not always easy to do exactly what you’d ideally want to do, still, try not to put so much pressure on yourself to have everything mapped out right now; take a minute to breathe.

Truly, there is no rush.

A Big Weekend for Accessibility

A Big Weekend for Accessibility

by elizabethmdouglas ♥ 0 Leave a Comment

Just over a week ago, I went to BBC Radio 1’s Big Weekend in Coventry with my friend. I’d won the tickets because a few weeks before the festival, I’d been to the Student Radio Association’s conference where during a talk on how to put on a live event, I’d asked the speakers how they were trying to make festivals like Big Weekend more accessible to disabled people. Originally, I wasn’t going to ask the question at all because frankly, no matter how much I share with the internet, I do still feel incredibly lame every time I bring up disability in front of a crowd. So, sitting there, in a room full of strangers – many of whom, I was trying to impress – my instinct was to avoid the topic for fear of tokenising myself. But then again, as my Mum and Dad say: if I’m going to do this disability representation thing, then there will be times when I have to fight my ego, and just ask the question.

I’d never been to a music festival before. That wasn’t because I’d never wanted to, it was just not something that I thought I’d be able to do, given that the two main taglines for my Spina Bifida are that I can’t stand for long, or walk far. So, I just learnt to compartmentalise the jealousy I felt when I saw friends posting photographs of each other covered in glitter in the middle of a crowd, dancing to the tunes of some of my favourite artists, in the same way that I’ve accepted I’m never going to go ice skating. But, as many disabled people are likely to tell you, I’m excluded from experiences such as these not by my ‘condition’, but by society not really bothering to try and get me involved. However, there are plenty of people who want to change that and it’s not always useful to base the conversation around accessibility on all the things the able-bodied world does wrong.

Obviously, I completely loved Big Weekend: I danced for hours until my legs ached, I pushed my way to the front to see an artist I’m not even that fussed about, I ate greasy food from a burger van, and I got a bit emotional at the beauty of sharing all those experiences with strangers in a field. But, I’m disabled, so it was unsurprising that I also had some not very nice moments during the weekend.

The festival had lots of things put in place to try and make it accessible, and when it came to the company and the people working within it, I have my hand on my heart when I say that I felt like they were sincere in wanting to make everyone feel welcome. However, individual people work these events, and it was the individual’s understanding of disability which created issues for me. For example, on the first day of the weekend, I wore trousers which covered my callipers – something I know makes people totally unaware of my disability. On that day, because I don’t look ‘disabled’, each time I asked to cut through barriers so that I wouldn’t have to walk all the way round or if I could please be directed to the accessibility exit closest to me, I was consistently doubted and questioned – even after saying it was because I’m disabled. Whereas the second day when I wore a dress so my callipers were on full display, I didn’t even need to finish my sentence before barriers were lifted, no questions asked.

This kind of experience wasn’t unique to BBC Radio 1’s Big Weekend, though. I get this everywhere I go, whether that be in an airport asking for disability assistance from one terminal to the next, or simply driving into a disabled space outside the shop. I’ve had people tut at me, roll their eyes, knock on my car window to ask me what I think I’m doing; people have told me ‘no’, accused me of ‘stopping people who need this help from getting it’, and I’ve even had my name removed from accessibility lists because someone took one look at me and assumed that it must’ve been a mistake.

So yes, I love love loved BBC Radio 1’s Big Weekend and it did make me feel for the first time like I’m also invited to music festivals, and I do trust that the BBC has every intention of improving the accessibility of its events and internal structures. But when I speak about accessibility and disability inclusion, I’m going for more of a paradigm shift: I want everyone to change the way they understand and perceive disability. It’s a hefty task, it’ll take a hot minute, and it’s as much the responsibility of the individual as it is of the institutions, but I’m an optimist, so I think it’s possible.

This is about individuals engaging with their preconceptions of disability and how they react to situations – both passively and actively. How do you see me? How should I look? Why do you think I’m lying? These are the questions we need to ask each other because organisations can put provisions in place, but those provisions are useless if the people with the power to let me access them are going to make me beg.

So,you think you’re a sl**

So,you think you’re a sl**

by elizabethmdouglas ♥ 0 Leave a Comment

At this age, lots of us like to sit with our friends and rip into each other for all the times someone has been a liiiittle questionable when it comes to their romantic relationships – whether those relationships be purely sexual, on the road to something stronger, or somewhere in between. Maybe you’re the prolific dater, maybe you’re the type to get with someone then change your mind the second they start to like you, maybe you really enjoy flirting with people but you’re too picky (*cough* scared *cough*) to commit to something serious. Or, maybe you’re like me and you’re a combination of a few… 🙂 ! Well, whatever you are, as long as you’re not being awful to people, then I don’t see much harm in it. And, the chaos does make for a good drinking game.

I’ve posted enough blogs by now for you to know that I’ve never been in a relationship, and that the lads I attract tend to be a whole lot of talk and very little walk…HoWeVeR, I have been the third wheel for enough relationships (and been involved in enough situationships) by now to be able to say something about how we’re treating each other. And the main thing that I’ve noticed is that people are so terrified of being on their own, that they stay or get themselves into situations simply because it’s comfortable, and/or because out here in the single world most people are screwing each over left right and centre. I mean, the sheer lack of respect I’ve heard (and seen) demonstrated by some single people when they’re talking to or getting with someone on a night out is ridiculous. And there’s just no need for it!

I’m not saying that we can all come out of every experience looking like the good guy, because no matter how hard each of us might try, there’s always going to be a few moments when we’ve messed up and we just have to swallow that. That doesn’t mean that you shouldn’t at least try to not be a d*ck, though. Yes, this age is probably the best and most convenient age to get with as many different types of people, in as many different situations as your heart desires because it’s a time when we’re free to put effort into figuring out who we are and what we want, but be aware of what you’re doing as you do it pls.

I’m a big believer in the power of surrounding yourself with sex-positive people who don’t feel the need to apologise for their sexualities because as much as I’m also very sex-positive, there are times when I can fall victim to the voice in my head that likes to give me a cheeky slut shame when I’m hungover. And it’s never about how many people you get with because I know lasses who feel rubbish about the 1 or 2 people they’ve slept with or texted again when they shouldn’t have. It’s about the fact that lots of us aren’t allowing ourselves and others to just have a little bit of fun.

Personally, I’ve not been hurt by a lad in quite a long time now but that’s just because I got bored of being disappointed and making all the moves, so I’m leaving it up to the lads to have the balls from now on. But me having that perspective right now, doesn’t make it inevitable that I’m going to start being rude to a lad who I kiss in a bar by ignoring his texts or playing with his emotions. It also doesn’t mean that I wake up the next day and tell myself off for kissing someone I don’t intend to date. And finally, it most certainly does NOT give me an excuse to judge and shame my friends for having a different approach to romance than me.

So if you’re going to take anything from this week’s ramblings, let it be the acknowledgement that even though it’d be impossible to never be the bad guy in relationships, that isn’t an invitation to always forget about respect. Ask out who you want to ask out, kiss them if you’re both into it, try and be nice about it if you’re not, and go on, have a bit of a FLIRT!

Something’s wrong with my face today

Something’s wrong with my face today

by elizabethmdouglas ♥ 0 Leave a Comment

Do you ever have those days where for some reason none of your clothes seem to fit you the way they did the last time you tried them on? You’re getting ready for the day, or for a night out, and your face just doesn’t face the way it should, you’re clothes don’t look right, your hair won’t do what it’s told, and the time is starting to run away; you’re going to be late to whatever you’re supposed to get to, so you start to get a bit hysterical and self-critical until you just wish you could crawl back into bed, hit a reset button, and try again tomorrow when everything hopefully does what it’s supposed to.

Just me?..

I’ve written before about how people shouldn’t let their insecurities control them, and I wondered whether I should write about this topic again when I could just reshare an entry I’d written a couple of years ago. Except, my body, and a whole lot of other stuff, has changed since then and I don’t really see this as a problem that can be fixed by a few hundred words.

So I’m going to give you a few hundred more! Yay!

We each know the power which comes with feeling confident, but like many other feelings, confidence is unfortunately very brittle. Just the other day, I’d woken up feeling pretty good about myself but it only took a few silly things happening throughout the day to leave me with a mind full of self-criticism by the time I was getting into bed for the night. And the frustrating thing is, that the moments which chipped away at my confidence were so minor it was stupid: I saw my reflection in a full-length mirror and I didn’t like the way my legs in my callipers looked, then a friend took a photograph of me and another friend and I thought my arms looked fat, and finally, the hot weather made me tired and subsequently self-conscious about how obvious my Spina Bifida was whilst walking through town.

Not one of these things is important, nor are they anything anyone else would take any notice of, let alone care about. But that’s what insecurity is: getting stuck inside your head about silly things which in the grand scheme of things, do not matter. Only, they matter to you and sometimes they matter so much that you torture yourself over thinking about them.

I’m lucky enough to be able to keep my insecurities at bay most of the time. But the times when I can’t – which do tend to be either when I’m drunk drunk, or experiencing the boozer’s blues the day after drinking – in those moments, I can’t do much except let myself just sit in it. I eat loads of snacks, or I cry to my friend, or I watch a film, or I stare at the wall whilst listening to my sad playlist. And I know that if a psychologist were to read those coping mechanisms, they’d probably say that they’re all really unhealthy – disclaimer: I’m definitely not about to make a case for you to do exactly what I do. However, I do think that my generation tries to psycho-analyse themselves far too much and that we need to just feel whatever it is we’re feeling for a second, without self-diagnosing. Obviously, there are limits and lines where a person needs help but it’s also okay to feel naff for an afternoon. In fact, surely it’d be worrying if we didn’t feel like rubbish once in a while?

I’m not going to patronise you now by listing all the reasons why we should be kinder to ourselves because I’m not a motivational speaker (shocking, I know), but also because we all know this already and knowing that I shouldn’t criticise myself, unfortunately, doesn’t mean that I won’t from time to time. It’s about being able to strike that balance where you allow yourself to feel what you need to, whilst also making moves to pick yourself up out of any ruts you encounter – it’s not always easy, and I’m not a pro, but we do our best.

So if you do wake up and your face isn’t facing, or your body isn’t bodying, and although you know it’s just in your head you’re still feeling meh, then that’s alright! As our lord and saviour Hannah Montana once said: everybody has those days.