Tag Archives: health

Wasted years: Autism and Depression

I have not blogged much over the last few years, and most of my posts in the past year have been along the lines of “Here is why I have not been writing”. In those posts I have talked about my plans to write more and projects I wished to work on, and yet as you can tell by looking at the recent posts on this blog, that has not happened. Why is that? There are a few reasons. As I have written about these issues before I debated whether I should write about them again, but I believe it’s still worth talking about due to those blogs having been written sometime ago, and things having moved on from where I was at that time.

Around four years ago – not long before my first book was published – my family went through some personal issues: bereavement, illness etc. I had struggled with depression for a while before this, and always had the issues that come with autism to deal with, for example sensory overload and anxiety. But after this point my depression became worse and worse until it reached a point where it was hard to even get a shower or watch a film. I believe I also went though an autistic crash around this time (for those of you who do not know an autistic crash is when you become so overloaded from having to do the things you need to do to get through each day, e.g. mask, deal with sensory overload, that you crash. You just stop being able to do those things.) What I mean by this is that I stopped being able to cope with the overload and anxiety. Once I was overloaded I could not do anything to bring myself out of it. Between 2015 and 2019 there were periods of weeks on end where I could not go out, write, read, or even pick something to watch. Days when I would do nothing at all, just pace around the house getting more and more stressed due to how bad I felt, and my inability to do anything about it until the stress would erupt in an outburst. I stopped working out and began to eat more. I began to see the impact of that; not only did I put on weight, I lost a lot of my strength, my skin got worse and I began to feel more and more ill day to day. Part of how bad I was feeling physically was also down to how little I was getting out. I hardly left the house at all. Everything I used to do: uni, volunteering part time in a shop, or going to the cinema fell by the wayside. Sometimes weeks would go by without me leaving the house. I hardly even went in my garden for four years. This took its toll on my physical health in the form of constant colds, headaches, and general feeling of sickness and lethargy. I found myself at times feeling as if I was under house arrest; unable to go out, and unable to take my mind off things by doing anything within the house. What made this all the more frustrating was knowing it was not something anyone was doing to me, it was something within my own mind that was putting me in the situation I was in. The days seemed to drag on; when you’re home all day, every day with no work to do it’s hard to fill the time even if you’re still capable of feeling enthusiastic for the things you normally enjoy. If not the time seems to stretch on forever with no end in sight. You would think that I would have been sleeping a lot, but in fact that was not the case. For about three years I hardly once got to bed before two in the morning. Not that I was doing much at night, but by that time of day I had got so much in to the swing of trying to pass the time that I just kind of carried on doing it without thinking “You could go to bed now”. Needless to say this did not help matters. I got bags under my eyes, could not stop yawning, and found it hard to focus on films/books even when I was able to try watching or reading them. Plus I was almost constantly grumpy, as you would be if you had been getting to bed at that time for months on end.

I say “was” not because I am fine now, but because this year so far has been better than the ones that came before. It’s not been perfect, not by a long shot, but it’s been better. I have still got to bed late more often than I would like, but I have also got to bed early on more nights in the past two and a half months than I have in all of 2017/18. I am on track to read more books and watch more films than I have in any of the past three years. For the past few weeks I have been going for a small walk twice a day; it’s not a lot, but it’s me out in the fresh air, and helps to stop my mood slipping back down to where it was. I have not been on a strict diet, but I have been eating much less unhealthy food than I was last year, or the year before. In short things are not where they need to be yet, but they are better than they have been in a long time.

So what now? Well it might be a cliché but its one step at a time. I have learnt now that you can’t always change things over night. Things take time, and even though you want everything fixed right away and one slip up can feel like all your hard work was for nothing, that’s not how the real world works. Things take time. They change slowly, but they do change. The first three months of this year have not been perfect by any stretch of the imagination, but I can safely say they have been better, more productive, and more healthy than any three months out of 2016/17/ or 18.

That’s a positive way to look at things and what’s more it’s the right way, but it’s not always easy to keep that outlook. Sometimes I will start to think about the years I have wasted, being in the house, the weeks, months and years of doing nothing, and begin to feel low all over again. I think of all I could have read, learned or written in that time. Could I have had another book or two published? If I had been working-out that whole time what kind of shape would I be in? What could I have done with this blog in that time? Could I have sold more books, or done more talks?The answer to all those questions is yes, of course I would have done a lot more. When I start to dwell on that it can make me feel as if I have not just wasted a few years, but wasted my life; as if somehow the time to do those things has been and gone. When I begin to feel like that I have to remind myself I have only just turned 24. You never know how long you have left of course, we could all die at anytime, but you can’t account for that. In theory I could have another sixty years of life left. That’s a long time, a lot longer than the four years I have wasted. I can’t say, and nor would I want to, that I am going to throw myself in to my work, write three books by the end of the year, get in to film-making, and never waste another second of my life. That won’t happen. But what I can say is that for the first time in quite a few years things are starting to slowly get better rather than stagnating, or actively getting worse. Yes I might not have done much for the last four years, but I have still read some great novels, watched some classic films, found new music to love, and learnt a lot more about depression and autism. While I might still feel sad about the time I have wasted it’s important to keep in mind that even in another four years I will have only just turned 28. I can honestly say that I do not think the next four years will be anything like the last four. The mere fact that I got the urge to write this blog, wrote it in one go, and put it out there is a sign of that!

You can find my new book here: http://www.jkp.com/uk/communicating-better-with-people-on-the-autism-spectrum-34251.html

If you need any help or advice abut Asperger`s/Autism or simply want to talk about it check out our free help and advice service ASK-PERGERS?

Twitter https://twitter.com/ASKPERGERS

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And have a look at our books (at the time published under pseudonyms, but we did write them trust us on that!)  http://www.jkp.com/catalogue/author/1762

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Beneath the Mask lies …. who?

In November 2014, when I was forty eight years old, I was diagnosed with autism. Since then I have been trying to write something about being diagnosed so late on in life, but I seem to have a complete block these days when it comes to writing, even though writing is something I have done all my life. My adult autistic son keeps asking me to write something for his blog, and I have tried so many times, but I just seem to blurb out a load of nonsense and not have the energy to edit or try to make it make sense in any way, and so there is never anything for the blog from me.
I have not had time to process what an autism diagnosis means for me – if it is a good or a bad thing – and do I feel better or worse for having this diagnosis? I thought it would it be a good thing, and give some meaning, some explanation for my past, and that I could use it to move forward in my life, armed with the knowledge that I am not broken, or a failure, or that life is wasted on me as I have always thought, but that I am autistic, and that is who I am, what I am, what I have always been, and that I finally know and understand who and what I am. That I could claim autism, being autistic, as my identity.
But nothing could be further from the truth.
In all honesty the one thing that has become clear to me since being diagnosed as autistic is that I have no idea who I am, what I am, or where, or even if I fit in to the world.
Every day it is becoming clearer and clearer to me that I have masked and faked my way through my life, and that no one really knows me, and I don`t even know myself. I feel as though I don`t exist outside of what I do for other people.
This is not to say that I have not had genuine feelings for people, that I didn`t care about them or love them, and the things I have done for them didn`t mean anything to me. That`s not what I am trying to say.
I`ll try to explain, but I am not sure I can.
It`s like from a really young age, probably four or five, I just didn`t know what to do, how to be. It`s like I read the hand-book on how to be a good daughter, sister, friend, partner, Mum, human-being, and I followed it to the letter with no veering from it, no time to think about myself or my own needs. I think I have always been, or tried my damndest to be, exactly what my parents needed me to be, exactly what my siblings needed me to be, exactly what my ex-partner needed me to be, and the perfect Mum. I have always given a hundred percent to every person in my life, every job, every action, with no room for error, no room for mistakes, no room for me.
It is like putting make-up on each day before you can face the world, afraid to let the world see you, who you really are, what you really look like, because you don`t really know who you are, but you know that you can never measure up to other people. And to be honest you don`t know what the fuck you should be doing, or how you should be doing it, so you watch, you observe, you learn, you copy and you do, just to fit in. But you can`t copy and do everything your peers do, at whatever age and period in your life you happen to be, because you can`t get it wrong. Mistakes are not ok. You have to be the perfect daughter. You can never put your own needs, or feelings, or wants above what your parents need from you. And you have to be the perfect sister. You can`t be selfish or think of your own needs, and no matter how overwhelming or exhausting or damaging it is, you have to do what your siblings need you to do. And friends? Well you have to be there for them constantly don`t you? You have to follow their ideas, do what they want to do, put off what is important to you and ignore your own wants and needs and prioritise theirs don`t you? And in a relationship? Well you can`t argue or shout or hurt someone`s feelings. You have to absorb all the shit, but never dish any out. And being a Mum? There`s no room for mistakes, you have to be completely selfless and give everything you have got, and never, ever put your own needs above those of your child. And society at large? Well you always have to be polite, and kind, and caring and put yourself out, even for complete strangers. And when people: family, friends, partners, work colleagues, people in general treat you like dirt, well you just have to take it and never, ever retaliate because the idea or hurting someone`s feelings – even if they hurt yours on a daily basis – is just unbearable. And they are the un-written rules of the metaphorical `hand-book` on how to be a good human-being, except, they are not. They are the rules I imposed on myself because I didn`t know how to be me, how to look after me, as well as being a good daughter, sister etc. I didn`t know how to be a real person, what I was supposed to do, so I subconsciously developed a persona of trying to be the perfect everything to everyone, to make sure everyone else`s needs are met. I still do it. I don`t know how to not do it.
Am I making any sense? I guess what I am trying to say is that because I was so confused and bewildered by life, all my life, I kind of learned how to be the perfect daughter, sister, friend, partner, Mum, employee, student, citizen, always trying to do the right thing by everyone else, that I never really learned anything about who I am? And somehow I have reached the age of 52 feeling as bewildered and confused by life as I did when I was five. And somehow I have blundered through to reach this age without ever really doing anything I have wanted to do (or I`ve had short bursts of trying but never really succeeded with anything) and I have never really known or understood me, who I am, what I want. And I don`t think that anyone else knows me at all, apart from my son. I think my parents knew me pretty well as their testament to how I was as a child went pretty far to me being diagnosed as autistic. I have always been extremely close to my parents, but even with them I had to put on a front a lot of the time when they needed me to help my siblings, and I couldn`t say no. I could never say no to my parents, or `what about me?` I always did exactly what they needed me to do to support my siblings, and I never once complained, or told them how hard it was for me to push myself to do the things they needed me to do.
I know I am not painting a very good picture of myself here, but I just don`t know how else to explain it. I am not the perfect anything, but I have nearly killed myself trying to be.
I keep seeing hashtags about `taking the mask off ` on Twitter, and being your true, authentic, autistic self, but I have many masks, for many different situations, and although I feel they are slowly destroying me, if I take them off what then? How will I go to the shop to ask for something? Make a phone call? Have an electrician or a plumber in the house? Order a taxi? Get my haircut? Interact with my family, neighbours, and society in general? Make sure my son`s needs are met?
Without the masks I can`t function, and if I don`t function I can`t support my son, or even do anything.
I am all for autistic people getting on with being autistic, and not having to go through the stress of trying to fit in to society, not having to `mask`, but if I don`t have my masks then what do I have to present to the world? I can`t present `Me` because I have no idea who that is ….

Jane Donlan

You can find my  sons book here: http://www.jkp.com/uk/communicating-better-with-people-on-the-autism-spectrum-34251.html

If you need any help or advice abut Asperger`s/Autism or simply want to talk about it check out our free help and advice service ASK-PERGERS?

Twitter https://twitter.com/ASKPERGERS

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And have a look at our books (at the time published under pseudonyms, but we did write them trust us on that!)  http://www.jkp.com/catalogue/author/1762

Is this illness or stress?

Autistic people tend to get quite stressed with sensory issues, changes in routine, the need to plan, anxiety build-up, and social communication all playing a part. Stress can and often will have a physical impact: this might be stomach pains, headaches, sickness and more extreme symptoms. I have found this out myself on more that one occasion. Headaches, feeling sick or having pains in my stomach is far from uncommon, and I know by now that they are all signs of an overload. When I was around five or six, before I was home-educated, I would have awful pains in my stomach and feel as if I were going to throw-up knowing that I would have to go to school the next morning. If anyone had seen me they would have thought I was ill, but this was something I felt every night and every morning before school. It was not an illness, it was stress and anxiety brought on by my hatred of school. In more recent years there have been two times when after a big event, for example, a talk or my book launch I have found myself racked with stomach cramps that have led to me being unable to anything, but lie down and wait for them to pass. These have not come on an hour or two after though; the first lot came the night after my book launch, and the second lot came the morning after my talk. I have not had anything like them at any other time, and despite how bad my stomach can get, this was much worse. The first time this came on after my book launch I knew I was going to be sick; it was around eight when I first started feeling the pain, and I was up till after four in the morning, throwing up four times. The next morning I was fine – they were gone as soon as they’d arrived. The second time I was not sick, but again the pain started when I woke up and I could do nothing but ride it out. By the end of the day I was almost back to normal.

It is my belief that these pains and the sickness were brought on by the build-up of anxiety and stress that led up to each event. Add to that the social pressure and sensory impact of the two events, and you can see why the stress and overload might be so great it has a physical impact on my body.

In fact sometimes it can be all too easy to put something down to stress or anxiety or overload. On Monday night I started to feel pain in my side and stomach again, not as bad as the two times talked about before, but the same kind of pain. I had been to two quite stressful and overwhelming appointments in the week leading up to this after months of not doing much at all, so I put it down to that. I had been trying to get back to normal after a long time of not doing anything and I had been doing well, but now my body was telling me not to push it. So when I woke up the next morning and the pain was still there I cancelled the appointment I had for that day, and decided to rest. In fact the pain lasted most of the week. I am free of it today, but it’s been there to greater or lesser degrees since Monday.

On one hand the fact that I was able to see when things were too much, and take a step back with out pushing myself too far is a good thing. In the past I have not always been able to do this, and although I was in pain this time there was no throwing-up, and the pain was not anywhere near as bad as it has been in the past. But it made me think; as soon as I felt that pain and the feeling of sickness that came with it in the first day or two my mind instantly said “stress and overload”. On the third day I thought about the idea that it might be a strain of some kind, but that would not make sense as I felt it in two places, and as I say it also came with a feeling of sickness. But I do wonder how do you tell normal pain and feelings of sickness from pain and sickness brought on by stress? I knew what I had been doing in the week leading up to getting the pain for the first time so I guess it makes sense that my mind would jump to that. But in doing so I run the risk of ignoring a real physical illness that could get worse the longer it’s left. It’s a hard call to make; you do not want to go running of to the doctors every time you have a bit of pain, and it is often good to let things resolve themselves on their own, but even if leaving something will not cause any harm and it does fix itself, I am still left with the question – am I feeling pain as a result of stress, or is there something else wrong?

The pain induced by stress can come in all forms, and sometimes last for days so at what point do I say there might be something else going on? When you add to that my high pain threshold, and the way I tend to get used to feeling a certain way it’s hard to find that point. When I talk about getting used to feelings what I mean is (and this might apply to other autistic people) I mean that I find myself getting used to feeling a certain way very quickly. This has often led to things going unnoticed for a long time in the past. I have talked in blogs before about the infection I got in my foot at one point. When I first began to feel the pain I brought it up, but then within days I was just used to feeling pain in that toe, to wincing every time it touched my bed covers, or I had to put my shoes on. As strange as it might sound I did not think about the pain in-between those moments; I was aware of it and aware that it had not always been that way, but it was weeks or perhaps even a month after first bringing it up that I thought to tell anyone that it was still causing me a lot of pain. Now of course that was nothing to do with stress, and I did not think for one moment at the time that it was. But you can see how it might lead to issues at some point; a pain starts and I put it down to stress, it stays for a few days but stress pains can do that so I leave it, and it would be easy for me to just adapt and not think too much about it from that point. I do know that this might not make any sense at all to some of you, but perhaps some other autistic people might understand what I am talking about.

I have no idea when I start to feel pain if I have hurt myself some how, if there is something else going on, or if it’s due to stress. So I have a day or two of relaxing to try and de-stress and the pain goes away, but who knows, perhaps that is just coincidence? Anyone could feel stress-related pains from time to time, but when you are autistic they happen – at least in my case – quite a lot, and to make things more complicated they do not always feel the same. Sometimes it’s feeling sick, sometimes it’s headaches, and sometimes it’s feeling dizzy or faint, and much more. In the worst case scenario this could lead to me putting something down to stress that is in fact a symptom of something physical. But even if that never happens it is still very irritating to never know the source of any pain that I might feel, to have to make a guess and hope that it is right.

Does anyone else find this hard? Do you know when something is down to stress, and when it’s physical?

You can find my new book here: http://www.jkp.com/uk/communicating-better-with-people-on-the-autism-spectrum-34251.html

If you need any help or advice abut Asperger`s/Autism or simply want to talk about it check out our free help and advice service ASK-PERGERS?

Twitter https://twitter.com/ASKPERGERS

Facebook https://www.facebook.com/ASKPERGERS?ref=hl

And have a look at our books (at the time published under pseudonyms, but we did write them trust us on that!)  http://www.jkp.com/catalogue/author/1762

Why my anxiety levels rise when people come to do work in the house.

Over the past few weeks we have had to have quite a few jobs done around the house. As these are jobs we cant do ourselves this has meant having to have tradespeople around such as joiners,and electricians. You might think that having people in the house and the noise they make when working would be the worst part of this, and for some autistic people it might well be, but for myself – and I am sure for some other autistic people – the worst part by far is waiting for them to come. I don’t just mean waiting for a few hours for them to arrive on the day either. Let me explain what I mean.

In my mind when I make a plan it’s a set thing; if I have to be somewhere I want to know the day and the time I need to be there, and the chances are I will be early. If I can’t make it I will get in touch and give as much notice as I can. You might put that down to my autism and you may well be right, but I also think it’s just basic courtesy. If you are going around to someone’s house you should at least tell them when you plan to arrive! Yet this basic information is almost impossible to prise from most people who do come around; want someone to come around and do a basic job in the house? They will be with you some time early next week. Well what day is that? Monday, Tuesday at the latest? Unless they get busy with something else then it might be Wednesday. OK, and would that be morning or afternoon? Morning, unless they run late then, afternoon.

Ah, OK, cool, just let me put three days aside for a half hour job then. Due to my autism it is almost impossible for me to focus on doing anything if I know I have someone coming to the house. As strange as it might sound to non-autistic people on a day when I have workmen around even though I am doing nothing, and they are doing all the work just having them come around and do the job takes up all my energy for that day. The waiting in, the knowing I will have to have some level of social contact, the not knowing how long the work will go on for, the noise, the disruption of having people in my house and what that does to my routine. Having to set one day aside to deal with this is bad enough, but it must be done in order to get things done around the house. But if this goes on for three or four days as it will if people are not clear on when they are coming, then you can end up wasting half the week being sat round feeling anxious not knowing if someone is coming around or not!

I am not quite sure why people find it so hard to look at a diary and see what day they are free before making plans instead of putting aside big blocks of time where they may or may not come around if they feel like it. It means instead of the anxiety building up over one day, and then being able to get back in to the swing of my routine the next day, you end up having two or three days of build up and if you’re lucky then having someone come to do a job. Which brings me on to the next issue…..

If you commit to being somewhere at a set date and time and you can’t make it you have to get in touch and explain that right? I think we can all – autistic or not – agree on that. But if you just say you might be somewhere that seems to be some kind of get-out clause. If you said you might come around at six and you realise you can’t you don’t have to ring up and tell the people whose anxiety has been building up all day because you only said you might be there. Never mind the fact that they may well have changed plans for you, changed their routine, waited in and are going to be on edge for the evening in case you turn up. It takes a few seconds to send a text saying “Can’t make it, call tomorrow to rearrange.” And yet the amount of times someone has just not turned up without any form of contact is, for me at least, shocking. Again this is not just about the impact on my autism, though that can be huge. Waiting in all day unable to do anything only for the person not to turn up without any contact to let us know of this change of plans does add to my levels of stress and anxiety, but it also means the day ends with me knowing I have to do it all again. Not only do I have to do it all again, but when I do there will be even more anxiety because now who ever it is has a track-record of not turning up. So I will half expect them not to turn up again which just adds a whole new level to things. But as I say it’s not just that. Again it goes back to common place courtesy: make a plan, make it clear and then stick to it. If you can’t then have the decency to let who ever you made the plan with know.

And when I say make a plan I don’t mean text the night before and ask if you can come around and do a job. The answer will always be no. I need notice, not a few hours notice, but a few days notice at least. This should not be too hard to understand or to give. I do understand that for most non-autistic people this would not be as big a deal as it is for me, but still people have work or university; they do things with their lives’s so you would think that a few days notice would be important for most people. Again it comes back to the fact that making a real plan, showing that you will take the time to plan things out, and then stick to them is always better than doing things on the spur of the moment.

It is hard to get someone who is not autistic to fully understand how disruptive and stressful having someone come to the house to do jobs can be. The levels of anxiety and the change in routine make it very hard, but I honestly believe that if it were more clear and well arranged the stress would not be half what it is. If I knew someone was coming at seven on a Wednesday evening then yes it would still be hard to focus that day, yes I might still feel overloaded once they had gone, but at least it would then be over. A plan would have been made, I would have be able to make plans for that day knowing that work was going to be happening, and how that would make me feel and from the next morning I could be back to my routine.

But if I have to put aside two or three days in case someone comes around only for them not to come around, and then I have to go through the same act the next week just to get one small job done I can lose the best part of two weeks just for an hours work. As well as driving my stress levels up this makes it much harder to get the jobs done on the house that need doing. If it takes two weeks of stress to get one job done I want the next few weeks to catch up on work I missed due to the change in my routine, plus the last thing I want to think about is trying to make more plans to get jobs done. This means other jobs that need doing get left because I just can’t put up with another two or three weeks of messing around just to get someone to come round and do them.

I understand that not everyone knows about autism and even if they do they don’t know I am autistic, but again I think what I am saying should be true in most cases. No one wants to wait three days to find out if someone is coming only for them not to turn up, no one wants to be told someone will be there some time between ten and seven, and no one wants someone to cancel or change plans without notice. The difference is for most people it’s a minor irritation, but for myself and other autistic people it can be a massive disruption and cause of stress/anxiety; something that takes an already stressful event and makes it ten times harder than it needs to be. I can do work around dealing with the stress of knowing someone is coming, and I can try and get myself to a point where I can do other things instead of just wait. But it can’t all be me, at some point I need people to meet me half-way, and at least let me know what day it is I will have to prepare myself for!

You can find my new book here: http://www.jkp.com/uk/communicating-better-with-people-on-the-autism-spectrum-34251.html

If you need any help or advice abut Asperger`s/Autism or simply want to talk about it check out our free help and advice service ASK-PERGERS?

Twitter https://twitter.com/ASKPERGERS

Facebook https://www.facebook.com/ASKPERGERS?ref=hl

And have a look at our books (at the time published under pseudonyms, but we did write them trust us on that!)  http://www.jkp.com/catalogue/author/1762

The transition in to January: Why it can be so hard and what can help with it.

I have written quite a bit about how hard Christmas and New Year can be for autistic people, but it’s also worth saying how hard January can be. December is full of change and we all know how hard that can be, but by the time you have started to get used to it, it all changes back again. What you eat, what time you go to bed, your routine, the decorations everything goes back to normal pretty quickly. Because it’s going back to normal it might not seem like as big a change, but it is, and it can in fact be even worse. At least with Christmas you get time off or nice food – the change might be hard, but for a lot of people it at least comes with positives. But January is an almost universally hated month to begin with; nothing much happens in it for most people, the fun of the holidays is over, and everything changes back to normal within a day or two.

For autistic people there is also the fact that January can be spent dealing with the build-up of sensory overload that can come with Christmas. It’s not uncommon for a meltdown to occur days, or even weeks after the event that trigged it. There have been times where I have become overloaded due to going out, but have seemed to be doing quite well for three or four days after only to have a meltdown the next week. In December you have a month full of change and things that can lead to a build-up of overload, and the knock-on effect of that can be felt well in to January.

So when you put those things together you have a month that can be pretty dull and grim anyway, starts with a big change all of its own, and is more than likely still being impacted by the events of December.

What can you do about this?

The first and most important thing is just to be aware of it. That might sound strange or not specific enough, but it is extremely easy to forget all about how hard January can be. December is over and that is the month that draws attention to itself; the changes are very clear, and it’s easy to see what impact they might have. But everything changes back so fast it’s easy to forget how long that impact can last, and also to forget that the change back to normal life is a huge change all on its own. Add that to the fact that the year is literally changing, and you can see why you should be aware of how hard January can be, but also why it often gets forgotten about. Just being aware of the issues that might arise will help. If you’re feeling overloaded or stressed-out remember why that might be, and perhaps be on the look-out for signs of a meltdown, or just keep in mind that just because the year changes the build-up of overload will not go away.

Another idea might be writing down how things will change, and if these changes will be good or bad. This is something worth doing at the start of December too, and it might be that you do it all in one go – talking about how things will change for Christmas and New Year, and how they will change back. Or you might do another chart for January talking about how things will change back, how this makes you feel and what the impact will be, for example less time around the house, different food, and the fact that that might make you feel more stressed or overloaded. (If you want to find out more about our strategies for dealing with transition check out our book on the topic https://www.jkp.com/uk/helping-children-with-autism-spectrum-conditions-through-everyday-transitions.html )

If you can you might also ease yourself back in to things slowly. So plan things out: What day are you taking your decorations down? When are you going to change your diet? Perhaps don’t plan one day to switch everything back, spread it out over the first week or so of the year so that it is not so overwhelming. If you have work or school then you will have a set day you need to be back at that, but perhaps don’t change everything on that date. So you could take you decorations down the day before or the day after so that the change does not happen all at once.

It might also be worth planning a few nice things to do in January. It’s a month most people dislike and it can be made better by having something positive in it. This will not work for everyone as making plans to do things outside the norm can sometimes just create more stress and change. For me a positive plan might be to try and get out for a few walks in the park. So nothing with any real social interaction or travelling, just something to help ease the tension in a house containing two overloaded, autistic people!

It might be that your plans are small and specific like mine, or it might be than having a few bigger plans works for you. Nothing will work for everyone, and everyone is different so just find what works for you and stick with it.

December and January can be hard months – fun at times, but also hard – and one key thing that you have to bear in mind is some, not all but some, of the change you can opt out of. You don’t have any control over school, college being closed, but perhaps if there are shifts on at work you could take them. You can’t stop everyone else putting up Christmas decorations, going out or having a party for New Years, but you don’t have to make a fuss about any of it. You don’t have to change what you eat, what time you go to bed, you don’t have to stay up till midnight, and if you work from home you don’t have to stop working or change your routine over the holidays. I am not suggesting that you don’t get in to the holiday spirit as lots of autistic people (like myself) love doing so even if it comes with some challenges. But what I am saying is that for some people not making those changes, and therefore having less to change back in January, might make this time of year a bit easier. And if that’s the case then my point is that you should do what works best for you regardless of any pressure from family, or society as a whole. That might be more of a tip for the coming December, but I just thought it was worth putting in.

With all that being said I don’t want to sound like I am being wholly negative about this time of year. It can be nice to start a new year and look forward to the year ahead. It’s just that I know from my own experience that it can also be a hard time of year. Hopefully you all had a good Christmas and New Year, and January is not proving to be too difficult for you.

You can find my new book here: http://www.jkp.com/uk/communicating-better-with-people-on-the-autism-spectrum-34251.html

If you need any help or advice abut Asperger`s/Autism or simply want to talk about it check out our free help and advice service ASK-PERGERS?

Twitter https://twitter.com/ASKPERGERS

Facebook https://www.facebook.com/ASKPERGERS?ref=hl

And have a look at our books (at the time published under pseudonyms, but we did write them trust us on that!)  http://www.jkp.com/catalogue/author/1762

Why the frustration of planning for Christmas is worth it for autistic people.

For most people the idea of getting time off school, work, or college for Christmas is a good thing, and something to look forward to, but for some autistic people that is not the case. Change of any kind can be hard to deal with, and Christmas is a very strange time of year how ever you look at it. It’s a huge change of routine; breaking up for Christmas is in itself a big change as the normal day- to-day routine no longer applies. You are not going to the same place each day, or doing the same things, and that might mean having to put aside a routine you have spent months working on, and getting used to. Added to that is all the other changes that come with this time of year – some bad and some good, but all change. Places look different if they are done up for Christmas, the food you eat will be different, what’s on TV will change, you might have to spend more time with family, and of course there will be the buying and receiving of gifts. It’s worth pointing out that just because you are autistic does not mean you can’t enjoy Christmas, it just means that all the change might lead to things like overload or outbursts related to sensory overload and meltdowns, it definitely has for me in the past.

That can sometimes be the most difficult part of planning for an event like Christmas – balancing the feelings of looking forward to it with the practicalities of having to plan for it. Ways of planning for the changes that come with Christmas are talked about in more detail in some of my other blogs (which I will be posting links to in the coming weeks) but I just wanted to use this blog to talk about how strange/hard it can be sometimes to put them in to place.

It might be that you love Christmas, that it’s your favourite time of year, and you start looking forward to it months in advance. You might love the changes that come with it: time off school, different food, and presents. But that does not mean that all the change of routine won’t lead to overload and outbursts, and yet even if you know that on a practical level thinking about it might still feel like it’s making Christmas more serious and negative than it needs to be. If you have to draw up charts, and sit and talk/plan everything fun, for example holidays, Christmas or going out then it’s easy to grow frustrated, and to feel like doing that is stopping you from being able to relax and enjoy yourself. It’s hard enough sometimes to have to plan for things you don’t want to do, but having to remind yourself that even fun things can come at a cost can be even harder. But that being said it’s worth keeping in mind that however hard it might be, or however frustrated you feel at having to plan and prepare again, anything that helps prevent outbursts or meltdowns ahead of time is worth persisting with. It might be that you find yourself at a point where you have to make decisions about what you do over Christmas based on past experience, and that might lead to you cutting out things you enjoy. For example you might like the idea of staying up late, but realise that in the past if you didn’t stick to your bedtime routine you tended to have outbursts and be left feeling worse. So you might have to make the call of not doing something you enjoy in order to try and prevent overload and outbursts. Again this might not feel good, and you might end up resenting having to do that, but it’s worth recalling how bad overload and the aftermath of an outburst/meltdown feel. Having to face up to your own limitations is never an easy thing to do, but I have found that at times it is necessary. After all, even though that might sound like quite a serious thing it’s really just about trying to make sure you have a good time, and not doing things that are going to bring you down in the long run.

The other side of this are people who hate Christmas and the holidays, and just try their best to stick to their normal lives, and not get drawn in to it. That’s fine to a point, but it can also be hard to do. If you work you might be able to work over Christmas, but if you are at school/college you will have time off whether you want it or not. You might not decorate your house for Christmas, but you won’t be able to stop everywhere else looking festive; in short you can only block it out and stick to your normal routine up to a point. So even if you don’t want to engage with Christmas, and plan not to think about it too much you might still find that if you don’t plan for it then it will leave you overloaded. Just because you don’t want to be part of a change does not mean you can stop change happening, so it would be worth planning for it anyway – perhaps it would be worth drawing up a chart looking at how things will change, and when they will start to change back. Working out in advance anything you might be doing in terms of going out, and thinking about how where you are going might be different than it normally is, and how this might impact on you.

Whether you enjoy Christmas or not there are two things that can not be denied: one, Christmas is a big change from our normal lives and routines, and two, despite how fun it can be it can also be a very overwhelming time for autistic people. That’s why it’s always worth taking the time to plan for. There are numerous reasons why you might not want to sit down and plan for Christmas, be it that you are worried about taking the joy out of it or that you would rather just ignore it, but in the end it is always best to be prepared, and to try and head-off overloads and meltdowns before they happen. Taking the time to plan and prepare might not make everything perfect, and prevent all overloads or outbursts, but it will go some way to making Christmas time that little bit easier.

You can find my new book here: http://www.jkp.com/uk/communicating-better-with-people-on-the-autism-spectrum-34251.html

If you need any help or advice abut Asperger`s/Autism or simply want to talk about it check out our free help and advice service ASK-PERGERS?

Twitter https://twitter.com/ASKPERGERS

Facebook https://www.facebook.com/ASKPERGERS?ref=hl

And have a look at our books (at the time published under pseudonyms, but we did write them trust us on that!)  http://www.jkp.com/catalogue/author/1762

Why I have not been writing.

As you might have noticed I have not been blogging much over the last few months. I did write a post about this a while ago talking about why I had not been writing, how low my mood was and saying I was going to try my best to get back in to writing and blogging, but as you can see things have not quite gone to plan. There is no point going over those issues again too much, but I thought it worth addressing as I am trying once more to start blogging.

As you will know if you have been keeping up to date with my blog I have been finding it hard to write, or in fact hard to do much of anything for quite a while now. This has been due to a mix of overload, depression and family issues. Back in August when I first wrote about these issues I did mean to start blogging again, once a week if I was able, but it did not work out that way. I have been finding it hard to get rid of my overload, and have been overloaded almost constantly, to the point of not being able to do anything. I will write about this as an issue on its own as it’s still on-going, and there is quite a lot to be said about it. But I am sure you can understand that if I am so overloaded I cannot even think straight, or sit down to relax, that writing,editing and posting a blog has been beyond me for quite sometime.

It is something of a vicious circle as not being able to write has only added to my low mood. For years I was sure that I wanted to be a writer, that writing was something I enjoyed and would always want to do. But when my mood dipped, and I was so overloaded I could not even think about trying to write without feeling worn-out, and fuzzy-headed, some of that belief started to leave me. It’s hard to make a living out of writing. I don’t do that now and I never have done, but my hope has always been to one day be able to make enough money from my writing to live off. Even though that’s hard when you are getting up early every morning and writing two thousand words a day, posting blogs every week, editing one novel while writing another, and having articles published in newspapers and magazines, it is easier to imagine. When you get to the point where you are hardly writing, you are not posting your work, and you are not even thinking of good ideas – or if you do think of an idea you do nothing with it – then it becomes harder and harder to think that you will ever make a living off it.

When I decided not to go back to university it was so that I would have more time to write. At the time it was a good idea; after all, I wanted to be a writer so what was the point in using the time I could be writing to do something else? But then when I became unable to write confusion set in; if I was not using this time to write had I made the right call? I had made a choice, uni or work, and I had chosen work only to find I was not doing either! Now on a logical level I can say to myself that knowing the way I have been feeling the past year or so that university would not have worked for me. As I say I have been too overloaded and depressed to even pick up a book or watch a film a lot of days, let alone go to university. So whatever I had chosen I would not have ended up doing due to my mood.

But even so doubt starts to set in. The more I think about it every job I would want to do involves writing, and I have been writing in some form or another since I was six years old. I have a book published, have co-written two other published books, and have written over one hundred articles so most of my life – certainly any part of it involving work – has been centred around writing, and being a writer. So when I suddenly stop being able to write what am I meant to put in its place? What am I meant to work on? To aim for? It puts me in a place of uncertainty, and casts doubt on plans I have been working on for years. And we all know that change and uncertainty are not good for autistic people. That’s not the only impact – writing is like everything else; if you want to be good at it you have to work at it and do so often. You can not just write once every few months, and expect what you write to be good. Even looking at my writing here I can tell it’s not my best. That being said I do not judge myself too much on my writing in blogs. I feel they are less formal and I tend to worry less about the style of my writing. But the point still stands – if you want to be good at something, at anything, you have to do it as much as you can. Taking breaks for months at a time is never going to have a good impact on your writing skills.

So I can’t write because of my low mood and the less I write the worse I feel.

I have been working on lifting my mood and cutting down on my overload quite a bit over the past few weeks, and I will write more about how I have been doing that, and how it has been helping. You can see of course that what I have been trying has been working somewhat as I am writing this now. Although it is only one blog that in some ways is just going over issues I have already blogged about, or setting up blogs I plan on writing, but have not written yet, I am still glad that I was able to sit here and type it out. It might not be a lot when compared to what I used to do, but compared to what I have been doing most days for, well for most of this year, which is absolutely nothing, it is a lot. But how ever much it is I am just happy I have been able to write something, and I plan on keeping it going. My aim now is to write something, even if it’s only a few lines every day, from now until the end of the year, and then take stock in the New Year and see where I go from there. Things are still hard in lots of ways, but I feel more upbeat about them now than I have done for the last few months.

You can find my new book here: http://www.jkp.com/uk/communicating-better-with-people-on-the-autism-spectrum-34251.html

If you need any help or advice abut Asperger`s/Autism or simply want to talk about it check out our free help and advice service ASK-PERGERS?

Twitter https://twitter.com/ASKPERGERS

Facebook https://www.facebook.com/ASKPERGERS?ref=hl

And have a look at our books (at the time published under pseudonyms, but we did write them trust us on that!)  http://www.jkp.com/catalogue/author/1762

Autism, and how routine is helping my low mood.

Lately I have been finding it hard to get things done. I have had low energy and a low mood, but it’s been hard to pinpoint just what the cause of this might be. I have tried my best to get on with things, but a lot of days I just end up falling asleep in the afternoon, and not even being able to decide which film to watch. Even the things I enjoy doing like watching films and reading have suffered. I was finding myself unsure of what to do most days, even though I had a lot of stuff I could do, or wanted to do I could not decide what I should be doing, and that made everything feel much more overwhelming than it really was. This meant that whole days were going by where I did almost nothing, and the things I needed/wanted to do just built up and up.

After talking to my Mum about this she offered to help me come up with a new routine to try and put some more structure in to my day. I did used to have a routine, but due to various family issues it has become disrupted.

We started the routine on Thursday night and I found it worked. On Thursday and Friday I was much more productive, and also found time to get the things I enjoy done. Knowing what I was doing, when, and for how long helped me. Having it written down and being able to tick off each thing as I did it was also a help as it allowed me to see what I had coming up next, and become used to the routine more quickly.

I am sure that I don’t need to go in to how important routine can be for autistic people as that has been talked about so much. As a child I worked on routines all the time. I can recall how hard it was when there was even a slight change to one. But I have to admit it did surprise me how much I still need a strict routine in my life.

Even as an adult if I don’t plan out what I am going to do I get nothing done. Let me give you an example that will show just how important a routine can be, and what a difference it can make.

On the first day of my new routine I was up at six, I did a work-out, showered, sat down and worked till lunch time. After lunch I watched a film, did some more work, and then spent the evening reading. It might not sound like a lot, but I had spent weeks worrying about how to fit all those things in to one day, but not actually doing any of them – that is despite the fact I am at home all day. But just knowing when I was going to do each thing and having it planned out for me meant I got it all done with ease. Not only did I get stuff done, but I ended the day feeling less tired and feeling better about myself.

Then let’s look at the weekend. The one fault with our new plan is that it does not cover the weekend. So I know what you might be thinking – why could you not just get up and do it anyway? Well I don’t know. But I found Saturday just drifting away. The truth is I am not even sure what I did – and I don’t mean that in a relaxed sense. I did not read, did not watch anything or do anything that I can think of. The day just seemed to pass, and then be over. Sunday was a bit better, but by that time it had become clear to both me and my Mum that just having the weekend as free time was not going to cut it. We needed to make at least a basic plan.

Because that’s the thing a lot of people don’t get about autism and planning; I don’t just need to plan when and how I work, I need to plan when and how I relax too. I can have all the free time in the world, but unless I have some structure and a plan nothing, or next to nothing, will get done. When I say I did nothing on Saturday I mean it; I did not have fun, or relax, I just drifted round unsure of what to do. The less structure there is the worse I feel, and the more worn-out I get. But just by putting a good routine in place and sticking to it all that can change. This morning I stuck to my weekly routine: I got up, worked out, went to the field with the dogs and wrote this blog by 09:17 in the morning.

The past few days have been a reminder to me how key routine is, and how despite not being a child any more having a good routine and structure to my day is just as important, and useful now as it ever was.

You can find my new book here: http://www.jkp.com/uk/communicating-better-with-people-on-the-autism-spectrum-34251.html

If you need any help or advice abut Asperger`s/Autism or simply want to talk about it check out our free help and advice service ASK-PERGERS?

Twitter https://twitter.com/ASKPERGERS

Facebook https://www.facebook.com/ASKPERGERS?ref=hl

And have a look at our books (at the time published under pseudonyms, but we did write them trust us on that!)  http://www.jkp.com/catalogue/author/1762

Why research in to autism needs to be led by autistic people.

In my last blog I talked about an article put out in the Daily Mail linking autism to radicalisation. (  https://askpergers.wordpress.com/2017/06/29/are-autistic-people-at-a-greater-risk-of-being-radicalised-my-response/ )I explained why the ideas put forward in this article are wrong, and why I think the idea behind the article itself is dangerous. I am far from the only autistic person to take issue with the article; in fact I have yet to come across an autistic person who does think positively about it. One of the issues that came up the most when I was talking to other autistic people on twitter about this article, is the lack of autistic-led research around autism.

More often than not if someone is planning a research project around autism, wants to decide which projects will get the most funding, or wants to talk to the press about autism research, that person is not autistic. Often autistic people are not even consulted in these matters. If you look at the autism and radicalstion article the team behind that admitted on twitter that they had not worked with autistic people on the idea before they published it in the press. The article came out, and met with a strong reaction from the autistic community that you imagine would have been wholley predictable had the authors just talked to a few autistic people before-hand. In fact if they had spoken to autistic people they might have decided that the research they were planning to do would not be the most helpful – or at least focusing it on terrorism would not be. Perhaps it would have ended up being a wider piece of research looking at how autistic people can often fall victim to things like so called `mate crime` where they trust someone to the point of thinking they are still friends even after that person has hurt them, or tried to push them in to doing something they know to be wrong. This is something that can impact on a growing number of autistic people, and knowing more about it, and working with the police to help them understand, might genuinely help some autistic people. But as it was we got a poorly researched article that did little more than drum up fear around an issue autistic people had not even asked anyone to look in to. I am not trying to say that non-autistic people can`t do good work around autism – they can. But if you really want to know what you`re talking about, and be taken seriously then at some point you have to talk to the real experts – autistic people.

I am not alone in thinking that if professionals and researchers would take more time to listen to what autistic people are saying, and work with us instead of trying to do what they think is best, it would be better for all involved. We see a lot of studies coming out saying things like “Making eye contact can be painful for autistic people”, to which most autistic people reply “Well yes. We have been saying this for years.”

There is a sense that autistic people can say something for years, and it not be taken seriously until a non-autistic professional says it too. As if we can’t really be trusted to know or understand how our own minds work. And at the same time if a piece of research comes out that we don’t agree with we are meant to just take it at face-value, and accept things about ourselves that we know not to be true. While research by non-autsitic people does play a part in helping us all to understand autism – and I would not want to downplay that, or make it sound as if only autistic people should be working on understanding more about autism – I do think autistic people are well within our rights to reject some findings, or directions of research. We can look back to papers published by highly respected researchers in the 1940s and 1950s that blamed `cold and unfeeling Mothers` for causing their children’s autism, and see that at times it would be silly to accept something just because it’s written in a book by a so-called `expert.`

When things like this happen it often takes professionals years to admit they got it wrong, and all this does is deepen the divide between autistic people and the non-autistic professionals, leading to a situation where time and money is being directed at arguing a case that autistic people already know is silly, just to avoid having to back down. For a more recent example of this look at how the professional world has reacted to the idea of females being autistic. For years they said females could not be, but now – even after countless women and girls have been diagnosed – some (not all) professionals are still clinging to the idea that these females must somehow be super-manly on the inside, or else how could they be autistic? Instead of just admitting they got it wrong, and trying to look at why that might be, they still cling to the idea that autism is a male thing, even when the autistic person is female. Understandably this approach does not earn those professionals a lot of respect in the autistic community

Autism is a way of thinking, a way of feeling and a way of seeing the world, and the truth is autistic people are the real experts. I am not trying to say that non-autistic people don’t have a part to play in understanding autism, and thinking of ways to help autistic people with some of the things that we do find more challenging, but I am saying this needs to be done hand-in-hand with autistic people.

Perhaps if all research around autism were to be led by autistic people – or at least take the time to talk to us and find out what we want, and how we feel about things – there would be less conflict between the autism community and professionals. And autistic people might start to feel that our voices are being listened to. Much more could be achieved if autistic people and professionals were able to work with each other instead of clashing. But for that to happen autistic people need to be given a greater role in leading research, and studies around autism.

You can find my new book here: http://www.jkp.com/uk/communicating-better-with-people-on-the-autism-spectrum-34251.html

If you need any help or advice abut Asperger`s/Autism or simply want to talk about it check out our free help and advice service ASK-PERGERS?

Twitter https://twitter.com/ASKPERGERS

Facebook https://www.facebook.com/ASKPERGERS?ref=hl

And have a look at our books (at the time published under pseudonyms, but we did write them trust us on that!)  http://www.jkp.com/catalogue/author/1762

Autism and the stress of a simple walk

I have written a lot about sensory overload, and the impact this has on me and other autistic people, but there might be an idea that to get this overload I have to go somewhere busy, or noisy. This is not the case. In fact just the act of walking my dogs in the streets for fifteen minutes can be full of so much sensory and social stress that I become overloaded by the time I get back home. I would like to use this blog to explain how even something that sounds so small can be so full of stress. So let’s use the idea of walking the dogs as an example for now – the point being that I don’t have to go anywhere; I am not going shopping or to a meeting at the end of the walk, in fact I am just walking around and and then going home. So why is that stressful?

  1. Build up: There is still the build-up to going out even if I am only going on a small walk. I have to decide when to go, plan for it, get myself ready, and know that I will have to deal with all the stress that I encounter when I am out there. For some things you might be able to go out early in the morning, and get them over with, but other times you might have to wait and the longer you wait the more the anxiety about having to go at all builds up. It can get to a point, for me at least, where if I am not able to go out until the early evening – even if it’s for something I want to do and something I know will hardly take any time at all – I have had so long for the anxiety to build up that I would do almost anything not to have to go.
  2. Noise: The outside world is noisy: be it birds, cars, planes or people, almost anywhere you live someone or something is making noise. These are just the background noises of life, but sometimes, depending on how I feel, even they can be too much. In the course of walking down one road with my dogs I might have to contend with the sound of drilling, of a plane going over head, of people walking by talking, of music coming from cars and the sound of the cars themselves passing by. Because for non-autistic people these sounds just fade in to the background I think it’s easy for them to forget just how much noise there is outside on a normal day, and how quickly that can build up in terms of sensory input. It’s worth pointing out here that a lot of autistic people deal with this by using headphones, with or with out music playing.
  3. Crossing the roads: I have not had the chance to talk to a lot of other autistic people about this one, but I know that it is a real issue for me. Over the years I have known some autistic people who did not feel a sense of danger, and would just run out in to the road (some of whom have even been hit by cars/buses) but that is not what I want to talk about here. I want to talk about the awkwardness of crossing a road. When I get to a road no longer can I walk with my head down, not looking at anyone. I can’t stay lost in my own thoughts, blocking out the world around me. No, I have to come fully back in to reality. I have to look up and be aware, stop blocking things out, look around me and try and pick out the sounds of cars approaching from the noise all around me. I have to think and make decisions on the spot; do I cross now or do I wait? But it’s not just making that call, it’s all the things going on around me as I make it. There might be other people waiting alongside me; are they crossing? No? Why not? Is it wrong of me to try and cross now? Yes, they are crossing? Should I go too, or wait here? Should I have gone then? If the road is busy do I just stand here and wait, or keep walking and cross later? What should I be doing now? Am I doing the right thing or not? OK, you might say that is being silly, that none of it matters, and that if you’re unsure what to do just wait till there are no cars and cross – staying safe is all that matters. Fine, but that’s not so easy when you have a brain that will overthink everything without giving you much say in the matter. Then when you do get to the point of crossing the road there is the interaction with the drivers. Cars come to a stop and you have to look at the driver and work out what they are trying to communicate to you. It’s hard enough to read what someone is saying via non-verbal communication when your face to face and have the time to think about it, but trying to do it from a few feet away through a pain of glass when you`re in a situation where you are expected to move quickly (at least by the waiting driver!) it becomes even harder. You have to work out if they are slowing down to let you go or not. Are you waiting too long when they are letting you go? Are you misreading what they mean and stepping out when you should not be? Again the main question for me is am I doing something wrong here? And again the answer comes back, who cares? It’s not like the interaction with the driver means anything; it comes and goes and everyone moves on with their lives. I don’t care in the long run what the people in the cars think of me, and I know that even if they did think anything it would be forgotten in the space of seconds. But that’s the point, it’s not what I know to be true in my head that has the impact, it’s the way my brain over thinks that brings on stress from even these seemingly meaningless interactions. Overthinking brings on more stress and anxiety, so much so that it can get to the point where the worry about crossing the road sets in before I even get to them, no matter how much I know on logical level that it is a silly thing to worry about.
  4. Walking past people: Another point that relates to overthinking is when you pass someone in the street. There is little to no interaction with them; perhaps they might smile or say hello as they pass, but that’s about it. But if like me your anxiety makes you over-think things you will find that as soon as you see someone walking down the road in your direction you will start to worry about what to do. Should you look at them? Will that seem as if you are staring at them? If you look away will it look as if you are avoiding looking at them? As if you think there is something wrong with them, or are passing some kind of judgement? If you look away then look back up will it look strange? At what point do you step aside to let them pass if need be? Does any of this matter? The answer to that last question at least is a simple one. No. The chances are if someone walking down the street notices you at all they think nothing of you, and if they do it’s not like you would ever know or be able to guess. But again I must go back to the fact that just understanding this on a logical level does not do anything to lessen the impact that it has. It’s all about what’s in your head, and the fact is that unlike noise from the outside world, you can’t do anything to shut it off.

I hope that the points listed above give you some insight in to why even a short work with no big social interactions such as going to the shops, or going to work can be a stressful and anxiety provoking experience for autistic people. It’s not to say every walk will be like that, or that every autistic person feels the same things I do, but it might be that some of you out there understand how I feel. For me what can be so hard about the whole thing is knowing that apart from the noise, the rest of it is in my head. People are not judging me as I walk down the street or try to cross a road, and even if they were I would never know. But when your brain is pushing you in to thinking certain things and feeling anxiety and stress it can feel like there is not much you can do about it. When you add that to the noise that surrounds you as you walk down the street, and the stress and anxiety that is a part of the build-up to going out you can see how even a small walk can lead to a sensory and emotional overload.

It’s worth keeping in mind that an autistic person does not have to be in a room packed with people talking at the top of their voices to become overloaded. Something as small as walking the dog can be so full of anxiety and stress, and lead to so much overthinking that it can bring about an overload that might come as a surprise to the autistic person, and those around them. And yet when you break down what goes in to even a small trip outside you start to see that for a lot of autistic people it is not so small after all.

Let me know what you think in the comments, as how ever much I try, I can only really speak for myself.

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