Social Robot

My name is Dave, and I am a social robot.

What I mean by that is, as much as I hate to admit it, I rely heavily on words and phrases that I've picked up from other people, TV, YouTube videos etc. My day job is to help customers via online webchat, and in the webchat world this kind of phrases are called canned answers or canned responses. I've always felt that I don't really have an opinion on most things, but I'm starting to realise that it's more that I do have opinions and feelings, but I don't always have the words to express them. Either that, or I don't care enough to have an opinion. Sometimes when I hear people talking about a certain topic I'll take a word or a phrase that I've heard them say that most closely matches what I feel and either repeat it back to them in the conversation to show that I agree with them, or I'll use it next time I'm talking to somebody about that topic. I think politics is probably the main topic that I've done this with because until a few years ago I really didn't have a clue about it. Not that I know what I'm talking about when it comes to politics these days, but I definitely understand more than I did.

This use and recycling of social canned responses is part of autistic masking, but it's also a way to learn about things for me. It gets me involved in the conversation (or what little conversation I generally take part in...) and helps me to pick things up and learn that way. And I guess the fact that most people don't share a lot of my interests probably helps with the masking side of things in that they don't know that it came from a game or a film or something like that.

Not all of my canned responses came from other places. I came up with some of them myself (although they were usually short) and I have been picked up on using the same words and phrases a lot in the past. One that I remember when I was a kid was that I used to "Yeah, fine" a lot and my dad joked that I should have a button to press so that it says it for me. Looking back it probably sounded a bit dismissive but it was the quickest and easiest way for me to express that whatever we were talking about was ok. I never was one for talking lots.

The term "social robot" itself came from a book I read probably around 10 or 15 years ago about how to meet women. The writer used it to compare the performance of meeting people and obeying social rules of "popularity" to how you would normally be in every day life. I feel that being a social robot is better suited to autistics in reference to masking for survival and to get through social encounters with neurotypicals. A lot of us have actively spent time studying social rules and observing neurotypical behaviour so that we can learn the behaviours and communication methods that we can then perform rigidly in our robot state to pass as neurotypical. I personally haven't done a lot of conscious studying of people, although I do definitely pick up bits and pieces as I go through life and they sometimes become so ingrained in me that I can't always remember where they came from, or that it even came from somewhere else in the first place. This is similar to (or maybe part of) how many autistics including myself have confessed that they don't know where the mask ends and where they begin. I would go into masking in more details but it's not something I've really got my head around yet in terms of how/when I do it, so I've asked somebody for a guest post about it from their point of view which should be coming up soon.

In the meantime, as always, please hit the Follow button in the side bar and follow me on social media. I'm on Twitter, Facebook, Instagram, Pinterest, and you can buy me a coffee at my Ko-Fi account here.

[Image description: Black silhouette of a toy humanoid robot on a white background. Under the silhouette is the word "Autism" in rainbow colours, and under that is "Social Robot" in black.]

Autism As A Label

Autism is something that's often considered by neurotypicals as "just a label" and not something you should be putting on yourself. Despite this, the autistic community take a very different stance on it, and that includes those members of the community who are self-diagnosed. As someone with lived experience of being told "it's just a label" prior to diagnosis, and then seeing and fully appreciating the value that said diagnosis brought, I thought this would be an important topic for me to discuss here.

After my first autism assessment concluded that my only issue was a lack of confidence it left me unsupported and without the closure I was seeking as both me and my wife knew there was more to it than the assessors had decided. That's why when I moved back to York I decided to go for a second opinion. The first GP that I saw in York was of an older generation who clearly didn't believe in mental health issues, which was shown by how she dealt with other family members seeking help by pretty much rejecting them and telling them they were over reacting. Anyway, in my particular case she asked why I want to label myself with something like that, she told me I didn't need it and then gave me the details of another mental health service that wrongly sent me to a couple of months' worth of CBT sessions for social anxiety. I soon realised the CBT wasn't working and arranged an appointment with a different doctor who then set the ball rolling for me to get assessed in York (my previous assessment was in Leeds).

Fast forwarding to over 18 months later I finally got my autism diagnosis, but not before I had difficulty at work in requesting reasonable adjustments because my role had changed. I think I explained in a previous post about the issues I had at work so I won't go into it here, but the long and short of it is that I had to fight for months to get any adjustments put in place throwing all sorts of law and regulations at them before I finally got the adjustments I needed, but even then it was on a temporary basis until I got officially diagnosed. My diagnosis came just as the temporary period was about to end and it made sure that it was made permanent. So that's one way in which being "labeled" by a diagnosis would have helped me much sooner when it comes to the world of work.

On a personal level though, the uncertainty of "am I/aren't I?" was unbearable and the acknowledgment that my diagnosis brought gave me so much closure and relief. I felt like I could finally be open about being autistic and discuss it more publicly than just in the online autism community. A fellow autistic online (can't remember who it was, but if I remember I'll edit this to credit them) once said that labels in the sense of food packaging are helpful because they give so much information about the food, nutritional information, allergens and so on, and basically said that an autism diagnosis is the same in that yes it is a label, but it's one that helps others understand that you might not thrive in social situations, or that you might be sensitive to loud noises, or that you might really, really enjoy trains or wrestling or anime or psychology or literally anything else. It's a much quicker, easier and more painless way of communicating your needs and your reasoning. Imagine if someone questions what you're doing when you're flapping your hands. If you answer along the lines that you're self-stimulating to soothe yourself because you're feeling overloaded they're likely to think you're a bit of an oddball, whereas if you answer with "I'm autistic," their reaction will probably be closer to "Oh, I get it now." At least, I like to think so anyway.

Autism diagnosis or a self-diagnosis isn't JUST a label. To many of us it's validation, it's acceptance, it's acknowledgement, it's understanding, it's a weight off our shoulders, it's a word that we can give to society to explain who we are. This is why we should be congratulated when we receive a diagnosis in adulthood instead of commiserated. I like to think that the same congratulations should apply to a family whose child has been diagnosed because it means they've been given a greater understanding of what exactly they may have been struggling with (if struggling at all - each family will be different) and what they need to do to help both their autistic child and themselves as a family. But in reality a lot of parents let their lack of understanding manifest in grief, and/or taking the wrong route in an effort to support their child (such as ABA for example). I guess being late diagnosed may have saved me from something like that in my childhood, but on the other hand there are things that I really would have benefited from had I been diagnosed in childhood.

I was bullied at lot at school and I would hope that having a diagnosis would have helped with that. I think it would have been another target for the bullies to get at me for, but I really, really hope that if I had been diagnosed my school would have done a hell of a lot more about it than what they actually did, which theoretically would have counteracted the bullying.

I've never been good at making or keeping friends and I believe firmly that if I knew I was autistic I would have received much more understanding from my peers as well as possibly known my own limitations and set boundaries for social situations.

Tying into that is my eternal struggle (until I met my wife) with romantic relationships. Each of my 3 previous relationships was shorter than the last, and the first 2 ended primarily because I was a lot more interested in them than they were in me. It's only in the last couple of months that I've discovered this is a very common autistic trait and the person we're dating can become a sort of special interest. Again, I think knowing I'm autistic and being able to explain that to my partners at the time would have theoretically made them a bit more patient and understanding of how I am. Either that, or it could have put them off completely and made them not enter a relationship with me in the first place. If I'm honest I don't know which route would have been better.

And finally, I think it would have benefited me in a professional capacity as well to have known I'm autistic. I've had more jobs than I think most people have, and I left a lot of them on bad terms. I know I've said it a lot here but it all comes down to understanding as I could have explained my needs and my employers could potentially have been more accommodating of them if we knew I was autistic. Don't get me wrong, there were non-autism-related issues that came up with some jobs (like when I was 20 or 21 I would show up to work hung over more often than I should have), but overall it was mostly issues that could have been addressed and dealt with had I been diagnosed autistic earlier on in life.

So there you have it. That's my take on the "label" of autism, and how it can be an extremely helpful thing for an autistic person to have in life. This is just my personal experience though, and I'm sure that there are infinite other benefits that autistic people have/would have experienced from it depending on when they were diagnosed. Please hit the Follow button in the side bar and follow me on social media. I'm on Twitter, Facebook, Instagram, Pinterest, and you can buy me a coffee at my Ko-Fi account here.

[Image description: A red and white name badge that says "Hi, I am" in a digital font, and then "Autistic" in a font that resembles handwriting. This is on a white background with "Autism" written at the bottom in rainbow colours, and under that is "As a Label" in black.]

Social Hangover

Being diagnosed autistic later in life is weird in a way. There are some things that even now, 18 months after diagnosis, I'm still working out about myself and my past even though in reality they should have been clear signs that I'm autistic. The thing that dawned on my most recently was that whenever I went on a night out I would always feel hungover the next morning, even if I didn't drink. There was a period of about 6 months in my early 20's where I couldn't drink because of the medication I was on, and there were other times here and there where I chose not to drink for different reasons, but every non-drinking night out still left me with what felt like a hangover the next morning. Granted, a less intense hangover than if I had been drinking, but other than intensity it felt pretty much the same. I never knew what it was until it randomly occurred to me the other day.

Now that I'm armed with the knowledge that I'm autistic I've put it down to being worn out by social interactions. I would wake up feeling nauseous, which is known to be a common thing in neurodivergents. When you feel anxious or worried for example, you feel it in your stomach which is why a lot of autistics develop stomach issues or other digestive issues. Growing up autistic (especially if you don't know it) is a stressful experience so it makes a lot of sense that my stomach would be sensitive the following day. I also used to feel physically over-sensitive after a night out, which does happen when I'm tired. I don't think that's just due to staying out late because at the time I was largely struggling to find work so I slept in a lot due to having nothing to really get up for. So the tiredness must have been mostly from trying to be sociable and exhausting myself. I sometimes had a headache in the morning as well, although that wasn't as frequent as the other symptoms. They are all signs of tiredness and/or stress which makes a lot of sense if I'd been putting a lot of effort into masking.

Masking isn't something that I've ever been aware of doing, but looking back I must have masked in some way or another through my childhood and up to around my mid-20's for nobody to have realised I might be autistic. It's a common thing for autistics to not know where the mask ends and where they begin so it's not surprising that I've never knowingly done it.

It's just a quick one this week because I just wanted to share that sudden realisation that when I used to go out but didn't drink I got social hangovers. To be honest, I'm not even sure if "social hangover" is the right term for it, or if there's even a term for it at all so I'd be interested to hear what you call it in the comments or on social media. Also let me know if you get social hangovers whether it feels the same or different for you. Please hit the Follow button in the side bar and follow me on social media. I'm on Twitter, Facebook, Instagram, Pinterest, and you can buy me a coffee at my Ko-Fi account here.

[Image description: Black silhouette of a human holding their head with both hands and lightning bolt-like symbols near the head to show distress. Below that is "Autism" in rainbow colours, and under that is "Social hangover" in black.] 

Guest Post: Autism In Women

I've got another guest post for you this week. This time it's by Vicky of Actually Aspling who is a brilliant and very active autism advocate, a fellow northerner, and has a Vaporeon tattoo on her arm which I love! You'll find her own blog here, and she's ActuallyAspling on both Twitter and Instagram. I realised that one of the biggest areas I haven't discussed yet is autism in women so I asked Vicky to write a piece on it for me since I'm not really qualified to talk about it properly due to being a man. So here we go with Vicky's thoughts:

I honestly can’t remember much from my childhood, only what I’ve been told from my parents, things are quite blurry in that sense. From what I know I was quite passive as a small child, and didn’t have many friends, and to be honest that hasn’t changed much.

I’d say being a girl definitely heightened my experiences in some ways, and for that reason I went undiagnosed for many years. Our understanding of Autistic women and girls is ever-growing, its evolving, and we are learning every day, but sadly it came too late for me.
High school for me was a nightmare, everything went wrong, and I stood out for all the wrong reasons. You could say I was a typical Autie girl. I clung to all my friends, I copied their behaviours, hoping I could survive the school day. It didn’t work. As a result, I camouflaged even more, changed my interests and created a whole new persona, something which many young Autistic girls feel they have to do to pass as Neurotypical. The issue is, we shouldn’t be pressuring Autistic individuals to do so, we should be teaching them, giving them the skills to be themselves, and allowing them to unmask.

Honestly, I think one of the reasons I was undiagnosed for so long is because of this mask, I had created a person who could fit in, who could pass as neurotypical, I appeared ‘normal’ or ‘high functioning’ to some. But the thing is, every Autistic woman is different, just like every Autistic person is diverse, its not one size fits all. I also think the understanding of trait presentation was lacking, especially in medical services.

I remember the first time I went to my doctor, I told her I think I could be Autistic, and I could tell by her face that she didn’t believe me already. So, what did she do? She printed off a biased, probably outdated questionnaire from her computer and proceeded to ask me a set of questions. One of which is ‘do you have friends?’ to which I said yes, and that I did like to go out with said friends. And of course, that meant I couldn’t possibly be Autistic, because we all know Autistic people cannot possibly have friends. I came across as quite social, again like the typical autie woman.

Eventually I sought a different opinion, and I was referred straight away for an assessment. This was fantastic, the only downside? My assessment was completed using the Autism Diagnostic Observation Schedule (ADOS), an outdated tool which lacks empirical sensitivity, it is biased and its methods do not reflect traits which are often displayed in women and girls. It’s a tool which follows stereotypical ‘male’ traits. However, I eventually did receive a diagnosis, after years of camouflaging and comments that ‘women can’t have autism’.

So many young girls are going both undiagnosed and misdiagnosed due to outdated tools, a lack of sensitivity and an absence of knowledge. Its about time that things change, we need a new perspective on Autism, but hey, I’m working on it!

[Image description: Vicky sat in her garden cross-legged holding a blue mug with both hands. She has short-ish light brown hair and is wearing a blue t-shirt, blue Christmassy trousers and white socks.]

Guest Post: Am I Autistic?

This week is my blog's very first guest post, so it's something I've been excited about sharing. It's by my online friend Kayleigh Hyland of Kayleigh And Her Friends. Kayleigh focuses on a range of subjects, most notably body positivity and sharing inspirational and positive stories from many others who she meets online. You can check out her own blog here, and also find her on Twitter and Instagram as kayleighann88 and kayleighandherfriends respectively. Of course you can find me in all the usual places online, but this post isn't about me so without further ado, I'll let Kayleigh take it away:

Am I Autistic?

I’ve asked myself this question since I found out what Autism was. There are traits that I see in myself which mirror the traits that put you on ‘The spectrum’.

I struggle with breaking routine and like things to have an order, I also have anxious and obsessive compulsive behaviours. Though in themselves these disorders are not typical of people with Autism, they are more common than in the average person. I can also struggle to concentrate when there is a lot going on at the same time and if I’m into something, like a TV program for example, I will talk/think about it a lot until I replace it with something else.

However, I do not struggle with social cues, in fact I have a better understanding of body language than most people.

I maintain good eye contact and I can differentiate between when someone is being ironic and when they are serious.

I think this is why there is a spectrum as a lot of us will find that we relate to a number of the behaviours even though we are not diagnosed as Autistic.

x

Skill Tree

I was watching a YouTube video earlier today about how to explain autism to people who don't understand it. While watching that I had my own idea of an analogy that could help explain autism to people, so I wanted to post it here and see what people think. One of my biggest self care activities is playing video games, and I'm a fan of video games like Horizon Zero Dawn and Assassin's Creed where you build up your character by earning skill points that can be exchanged for skill from a skill tree. Obviously you'll be stronger and have more abilities and tactics at your disposal with each skill that you unlock, but each given one tends to be optional.

So I came up that this skill tree analogy, where we imagine life as the game that we're playing with a largely neurotypical society being the setting for the game's events. There's an image near the bottom of this post to help explain the analogy, but in this scenario neurotypicals naturally have most - if not all - of the skills shown in the skill tree image. Conversely, autistics tend to naturally grasp few - if any - of these skills although it's not unheard of for autistics to study, learn and achieve some of the skills. If we look at the example image, we can take the example of small talk that neurotypicals tend to naturally be good at and comfortable with. I on the other hand, can't do small talk to save my life. I myself have never taken the time to do some people-watching to study social interactions and try to learn how they work, but there are certainly other autistics who have, and had success with it to the point of being able to effectively "fake" small talk. With that said, how comfortable they may or may not be at the time is a completely different issue.

Empathy is also something that autistics stereotypically struggle with. The reality is that yes, some autistics (myself included) do absolutely struggle to feel empathy, although many other autistics do feel empathy but either express it differently or don't know how to express it at all. Sometimes, an autistic person can feel so much empathy for a person that it overwhelms them and the outwardly become what neurotypicals would deem to be overly emotional. I've never been one to feel or express a lot of empathy in face to face situations, although my empathy has really improved at work where I deal with customers over webchat instead, so the only contact I have with other humans is through a computer screen via instant message. Even then, it took a long time and a lot of work for me to learn when I should show empathy and what I should do to show it properly. If I'm completely honest the empathy is entirely fake, but it's the way that it comes across that's important in a job like mine, rather than whether you mean it.

This will make sense to fellow gamers like myself, but I hope I've explained it well enough for non-gamers to understand as well. Obviously everybody is different whether neurotypical or neurodivergent so each neurotype could have any combination of skills and abilities, but as a generalisation, neurotypicals will have many more of these skills than autistics. It's also worth pointing out that the skills shown in this skill tree image I made are by no means exhaustive as I made it purely for the purposes of example and demonstration.

Let me know what you think of this analogy. As far as I'm aware it's completely original and I hope it proves to be a helpful way to explain how autism works to people. Please remember to click Subscribe at the top of the page and follow me on social media. I'm @DepictDave on Twitter, Facebook, Instagram, Pinterest, and you can buy me a coffee at my Ko-Fi account here.

Theory Of Mind

I thought I'd do something a bit different this week. Every now and then when I'm catching up on the autism conversation I hear about theory of mind. It's something I've looked into before but only very briefly so I'm not really sure what it is. What I thought I'd do for this post then is research what theory of mind is and report my findings here. Please feel free to sound off on whether I've got it right in the comments or on social media.

So here we go... Theory of mind is basically how you understand and anticipate other people's reactions and behaviours. Despite being called theory of mind it's not so much a theory in the sense of a wider known philosophy, instead it's your own theory about the way other people's minds work and their mental state. So for example, if you give somebody some news you'll usually try to predict how they'll react. That's your theory of how their mind is regardless of whether your prediction is right or wrong

Theory of mind wasn't something that was discovered until people started researching autism. Although it's not exclusively an autistic trait (it can be seen in all neurotypes) it seems to be most prevalent in autistics. A child's theory of mind starts to develop around the age of 4 or 5, which would explain why my nearly-3-year-old doesn't seem to grasp that things affect other people quite as much as her 4 year-old brother does. If you're good at putting yourself in other people's shoes that would indicate that you've got a good theory of mind, whereas if you struggle to understand other people's points of view that would indicate that you've got a poor/lack of theory of mind.

So long story short, theory of mind is really the understanding that other people have different thoughts, different feelings and different experiences than you. It sounds like something very simple that anybody should be able to grasp, but in reality it's not that easy for people like me. I remember one point in my teens not long after I left school a friend was talking to me about his complicated love life while we were hanging out one day. I was quite happily listening to him when he mentioned that he doesn't think I understand what he's talking about. I 100% understood the events that he was explaining to me, but I think what he was getting at is the emotional side of it and what affect things had on him. I had completely missed that whole part of what he was telling me because he didn't specifically say it with words, which would definitely be explained as a lack of theory of mind now that I know a bit more about it. In this way theory of mind has also been liked to empathy, and everyone knows the stereotype that autistic people don't have empathy at all. If we go back to purely theory of mind in itself though, there have always been little hints in my personality that my theory of mind isn't very good. I've always struggled to understand how some people don't like wrestling or don't like Nightwish (my favourite band of about 10 years or more). When I'm upset or angry I also seem to automatically think that people will know why even if they've had no involvement in the situation. This isn't helped by my alexithymia meaning I struggle to put words to my emotions.

There is a common theory of mind test that psychologists use on children when assessing for autism. It's called the Sally Anne test and consists of showing the child 2 dolls (called Sally and Anne, hence the name). One doll has a basket and the other has a box. The assessors will then put a marble in Sally's basket, Sally will go away for a bit, and Anne will take the marble and put it in her box. When Sally comes back the assessors ask the child where Sally will look first for the marble. The idea being that children with a good theory of mind will understand that Sally hasn't seen the marble being moved so she'll look straight in the basket where she first saw it. Those with poor theory of mind tend to believe that because they know the marble has been moved it means everybody including Sally knows that the marble has been moved, and they will usually say she'll look in the box because that's where it actually is. I wasn't given the Sally Anne test during my diagnostic assessment, but now that I know about it I'm starting to understand more about certain parts of my assessment and why the assessors did certain things.

For me, learning about theory of mind is one of those light bulb moments when you look back at yourself and think "That's me!" The same kind of moment happened when I learned that alexithymia is a thing, and I hope that by doing posts like this it helps other autistics understand themselves better, as well as helping neurotypicals understand us better. If you've enjoyed this post please click Subscribe at the top of the page and follow me on social media. I'm @DepictDave on Twitter, Facebook, Instagram, Pinterest, and you can buy me a coffee at my Ko-Fi account here.

[Image description: Black silhouette of a male head on a white background with rainbow-coloured cogs in the brain area. At the bottom of the image is "Autism" in rainbow colours and "Theory of Mind" in black.]

Friendships

As an autistic person I've always struggled to make friends. That's not to say I've never had friends because I absolutely have, but the few friendships I somehow managed to make were mostly temporary and often circumstantial. I had a couple of friends at college but as soon as we graduated we pretty much stopped talking to each other. When I was at school I had a couple of friends who I spent pretty much all my time with, but didn't make friends with anyone outside of our little group of 3 until much later on in the final year of school. Looking back now they weren't all they were cracked up to be as friends, but I enjoyed what I had.

I think one of the reasons that I've never found it easy to make friends is because my special interests have never matched up with what anybody else was interested in so I didn't have anything to talk about. I've always found it hard to know what to say to other people, especially if I don't know them. Similarly, if I see anybody I haven't seen in ages I struggle to know what to say there too, which is why I don't like meeting up with people I haven't seen in years. It's like my head reverts back to them being complete strangers and I start getting anxious, even though I'm a lot more comfortable with those exact same people if I see or hear from them on a regular basis. I wouldn't go as far as saying it makes me more socially competent, but it makes me more comfortable if nothing else.

I think my definition of friendship has changed as well as I've grown older. When I was younger I used to define a friend as somebody I would be happy to go out to a pub with for example. I once explained to some colleagues at one of my old work places that there are lots of people working there who I like and get one with, but nobody I would consider a friend. There were only a handful of people at the time who I would have happy gone on a night out with, and there are even less of them these days. Nothing against most of the people I knew or work/ed with, it's just that I don't value most people's company as much as spending some quiet time on my own in peace.

Nowadays I've come to realise that I wouldn't even necessarily want to go on a night out with a friend. For example, my current team leader at work is probably the closest thing in-work that I've got to a friend. I help her with a few work bits and she's really been there for me when I needed her, brought me out of my shell and massively helped me raise my game at work. I'll be sad to lose her as my team leader when things at work change over the next couple of months, but we'll still be around to see each other which I'm glad about but that doesn't mean I'd want to go on a night out with her. I feel more comfortable going out as a team so that there are at least a few other people there meaning I can fade into the background when I need to. Just as another quick example, there's my friend Emma who I met on Twitter (you can check out her mental health blog here). We've never met in person and I can't say I'm overly keen to change that, but we've got a couple of things in common and we've tried to be there for each other when we needed it so I consider her a friend even though we don't talk online that much.

Going back to my friendships being circumstantial for a minute, almost all of my nights out when I was single had a purpose. That was to get me out and about and hopefully meet someone to start a romantic relationship with. Of course it never worked until I met my wife when I wasn't even trying to (I had bigger things to worry about that night), and it's not that I didn't like being around my friends and have fun because I really did, but for me the centre of every night out was putting myself out there to find love. Looking back, my friends did put up with a lot from me and I appreciate them being there because the search for love in itself became somewhat of an autistic special interest consuming almost every part of my life - which ironically is probably a reason it didn't work! I met my wife one night when I was doing stand-up comedy and was too preoccupied with my set and how badly it failed to worry about meeting anyone, but I did. My comedy group was another set of friends who I almost immediately fell out of touch with as soon as I started working full time and got together with Sarah so I didn't have the time to commit to the actual comedy any more like I used to.

I guess at the core of what I'm trying to say is that I don't gain anything from sociable interaction. It could either be because I'm autistic, or because I'd learned due to bullying etc that I'm better off staying reasonably isolated, or it could be a mix of both. I often wonder what neurotypicals get out of socialising with each other, and especially from small talk. To me, talking to people is a way to get information. I really don't believe that I need or want 90% of the information that people seem to give and take from each other but for some reason that I'll never understand they enjoy it. A perfect conversation for me is if one of us asks for information or an outcome, the other one gives it, and that's the end of it, we both go about our day. I feel very similarly about reading as well. It's rare that I'll ready anything for the enjoyment of it, but if it's something I want or need to know then I'll end up reading everything that I can find about it.

So that's how my autistic mind is with friendships. I'm sure a lot of autistics will likely agree with me, and so I hope it's given you an interesting insight into how we - or at least I - tick. If so, please click Subscribe at the top of the page and follow me on social media. I'm @DepictDave on Twitter, Facebook, Instagram, Pinterest, and you can buy me a coffee at my Ko-Fi account here.

[Image description: A handshake between a black hand and a white hand. The image is on a white background with "Autism" towards the bottom in rainbow colours, and "Friendships" under that in black.]

Autism Advocacy

It's World Autism Awareness Week so I thought it would be an ideal time to discuss what autism advocacy means to me and why I do it.

I started this blog just over a year ago in the run up to last year's World Autism Awareness Week partly because I wanted to raise money by doing a 10 mile walk with the blog being a way to spread the word of what I was doing, and also to raise autism awareness in general. After I did the walk I carried on blogging once a week because with my busy schedule of work and parenting it's all I've got time to do in terms of advocacy. I wanted to make sure I was at least doing something.

So what is autism advocacy? It's a way for people (usually autistics themselves) to actively engage in the conversation around autism as a condition and to ultimately aid society's understanding and acceptance of us as people. I sometimes see debates online where people argue that we need to focus on autism acceptance rather than autism awareness, and therefore they disagree with things like World Autism Awareness Week. While I do agree that acceptance is the ultimate goal, I also think they go hand in hand. In my opinion, to achieve autism acceptance people need to understand autism, and the way to understand autism is by advocates such as myself explaining it - i.e. raising autism awareness. Autism awareness is about more than just letting people know that autism exists. I don't believe that you can have one without the other, so for that reason I think World Autism Awareness Week is a great thing despite the fact that in an ideal world we shouldn't need to dedicate a specific day or week to it, it should just be the norm. But obviously not much in this world is ideal.

I do wish I could do more for the cause, but my hours at work will be changing very soon so maybe that'll give me a bit more time to dedicate to advocacy in the future. World Autism Awareness Week is 30th March to 5th April.

For now though, I'll just remind you to please click Subscribe at the top of the page and follow me on social media. I'm @DepictDave on Twitter, Facebook, Instagram, Pinterest, and you can buy me a coffee at my Ko-Fi account here.

[Image description: The word "Autism" in rainbow colours on a white background. Directly underneath it are the words "Awareness", "Accessibility" and "Acceptance", all in smaller black text. Towards the bottom of the image are the hashtags #ActuallyAutistic and #Asking Autistics. This is the image used on my Instagram to promote this post.]