Naturally we include the obligatory autism reference to a piece of jigsaw puzzle!

Because obviously we're the forgotten about pieces of puzzle that go under the sofa yet without us, the jigsaw is incomplete.

Jigsaw
Because you know, its a website about autism so there's got to be the obligatory jigsaw reference!
Showing posts with label employment. Show all posts
Showing posts with label employment. Show all posts

Saturday, 18 March 2017

Autism only applies to children

"It's Asperger's and Autism Awareness month! In honor of all children who struggle every day!!"

Every now and again I see similar things appear on my Facebook newsfeed from well-intentioned people trying to 'raise awareness' of the suffering that autistic children face. Inevitably with World Autism Awareness Week (27th March - 2nd April 2017) coming up, I expect to see more of those kinds of social media posts. 

There's a few things that irritate:

Firstly they claim to raise awareness and provide no education, no quick facts or anything that we can learn. If you want to raise awareness, actually provide some meaningful and useful content might be a starting point, yes?! When is Asperger's and Autism Awareness month anyway?!

This notion of universal daily struggling or suffering kinda grates on me. Actually some days as an autistic person I couldn't actually say I struggle. I've had issues all my life but I am not sure if it's just manageable (ish!) because this is all I have known or if in the grand scheme of things, I am generally okay? I avoid stuff that upsets me and that's my coping mechanism. I know certain social activities and career paths would upset me so I don't do it. Simple, right?!
Okay, I get sensory overload and yes it's unpleasant but it's not constantly upsetting me. I am one of the fortunate ones who can generally extract myself from situations before they get to the point of a meltdown. I realise too that not all autistic people can do that and perhaps I am on the end of the scale where I have fewer undesirable autism related aspects about myself than many others.
Autism doesn't impact on my mobility either so I think myself lucky that I can do lots of things for myself. 
When I think of suffering, I think of someone with chronic pain and challenges that impact their lives so greatly that a large chunk of it is utterly miserable. Maybe I am an ablest amongst the autistic demographic but I have never put myself in a category of where I feel I suffer daily. I won't apologise for that either. My lens is how I view the world and I can't pretend to fully know or understand everyone's view but I can try (despite supposedly autistic people being void of empathy - yeah, right!). Sure, life can be struggle at times but autistic people don't have a monopoly on that. 

The whole "in honour of" thing...
Are autistic people in need of celebrating or having our challenges, differences and similarities respected via a little Facebook post? We didn't pick to be like this. We didn't earn this cognitive style. It makes as much sense to me as celebrating people with blue eyes. 
WELL DONE all you lot with the eyes the colour of the sky. You worked so hard just being yourself. 
This is how we are and I think most of us, like the rest of the planet, generally get on with it the best we can?! 
It's all a bit patronising for me.

Finally.... 
There is some notion that within these copy and paste crap that autistic adults are off the radar. 
Do only autistic children count? Now you're 18, the Facebook concerned no longer bother about us. Or maybe they think we have a terminal disease called autism whereby we don't actually reach adulthood. Incidentally, I am exceeding all lifespan predictions being in my 30s... Or perhaps one of my autism super powers is cheating death by using complex mathematics?!
Hmmmm or maybe by the time one leaves childhood, we have magically grown out of our cognitive style and become fully signed up members of the "Normal Club"?! Here we have lost our sense of systemising, become extremely empathic and gained wonderful social skills to become an artful host within high society. 
Or more likely, we just get on with it. We perfect our coping mechanisms in time, we learn how to pretend we're okay, understand more about ourselves to avoid things in life that upset us and perhaps care a little less about what others think. It's not that we have cognitively changed in our essence but many intellectually higher functioning autistic people probably have adapted from where they were in early childhood.

So when I see such Facebook posts, don't be surprised if I remind the person about the existence of autistic adults. It's not to be pedantic (ok, yes a touch!) but because it's attitudes like that which reinforce the view that only those in education and young people are entitled to autism related support. This is because I often feel like the existence of autistic adults is denied unless they have comorbidities and require social care and institutionalisation. Us autistics who seem okay on the surface are often forgotten. Time and time again, I think back to my experiences of working in education and my life and seeing support in schools and colleges but it almost disappears overnight once one has left their educational institution.

So please, let's not make sweeping statements that do nothing to help anyone, spread generalisations and misinformation but also ignore a sizeable demographic with autism. I'm not sure we need your kind of sympathy...

Now, if you like, you can return to your fake news, click bait websites and videos of extremely daft people doing very daft things! 

Sunday, 12 March 2017

The importance of the right work environment

This article was first written for the website: aspergermanagement.com about a decade ago, so 2007 ish! The article can be found here, as told to the founder of the site, Malcolm Johnson: http://www.aspergermanagement.com/case-studies/work-environment/ but I have included it below.

Malcolm not only runs this interesting website full of resources for professional people with autism but has a book out too, entitled Managing with Asperger Syndrome: A Practical Guide for White Collar Professionals

----

Background

Caroline is 26 and in the process of receiving a diagnosis for Asperger Syndrome.

She has a degree in Political Science and a Master’s in Computing but has found building a career a struggle. Central to this has been finding a Work Environment that suits her needs.

Initially she worked for a large telecommunication company in computing after A Levels and turned down the opportunity to train as a religious studies teacher. Finding it difficult at work, she left to gain the degree in Political Science two years later.

Confusion continued however with what career path to follow and so she studied for a Masters.

She now works for a secondary school maintaining computers and hopes to pursue a career in teaching in ICT and, also, part-time, building her own web design business. By learning about the environment and culture she believes that her career and work objectives be much more achievable.

Exact details in this case study have been changed for confidentiality reasons. The views expressed are personal, for illustrative purposes only and should not be related, or automatically applied to, other situations or scenarios.

Case Study

When I came to initially decide on a career, I gave little thought to the type of environment that I would need, i.e. culture, ergonomics or colleagues. But then, as now, I had not been diagnosed with Asperger Syndrome, (AS).

My initial career choice was therefore difficult and somewhat confused. I had a choice between a place to train as an RE primary teacher or an apprenticeship in the telecommunication industry. I enjoyed computing as a hobby, so hoped to work using computers, but I also enjoyed RE at school. It was the chance to earn money straight from school that led me to taking an ICT apprenticeship.

It was during the two years at that telco company that I became self-aware that I had problems adjusting from a school environment to a work environment. As someone who hadn’t been diagnosed with Asperger’s, it became clear that there was a problem with the way I interacted with people and the way I was learning in the workplace.

Most team communications were conducted through email, and I was particularly pleased that I did not have to talk to the person sitting next to me as email communication was the norm. However, it was slow and cumbersome and often people would not reply.

My line manager said it would be more effective to go talk to people, but I felt awkward interrupting their work whilst hanging around their desk. What I really needed were clear explanations of what was required of me in terms of task and work objectives.

I would also accidentally make inappropriate comments to work colleagues and felt out of place amongst them. I put this it down to being a lot younger than the others and because I was working in a male dominated industry. Everyone else had Masters’ degrees in engineering, whilst I had social science A Levels – that, for me, explained why I was different!

Consequently, I felt uncertain, out of my depth amongst IT specialists and awkward about asking questions about things that they would regard as basic concepts. I suspected they felt I should know about them already. As a result, I tended to not bother asking and remained confused if I could not find the answers on the Internet. I lacked focus and felt overwhelmed and, as a result, my work was not up to the standard expected of me.

When my line manager suggested I work things out for myself and be a bit more proactive in order to complete tasks, I would panic as I found this too hard. I was expected to maintain computers with unfamiliar operating systems, but I had no idea where to begin so I started to feel like a failure and my confidence started to decline. I also doubted my intelligence even though I was well qualified. Every task within my job role seemed so vague and unstructured. I never thought that my line manager might have not been meeting my specific needs or that I should ask him.

At the same time, my driving instructor became increasingly frustrated with me for similar reasons and suggested I might have dyspraxia. I did nothing about this for many years and ignored the possibility of having a problem.

I did though speak to my line manager about having dyspraxia. He did not dismiss it, but it was not something that was investigated fully. He did however attempt to break down tasks into more detail and put them into emails after he realised my progression was slow. This helped greatly, but by then my morale had fallen. It felt too little too late, and I was thinking of quitting the job to escape the anxiety. With hindsight what I should have done is explained things and asked for assistance earlier.

I did not give my company or manager a chance to help me. However, I needed a change to avoid some sort of meltdown. I was succeeding well with my NVQs and BTEC HNC, but I could not comprehend why I was under-performing elsewhere. For someone who always thought herself to be strong academically, this was quite a shock.

When I was told I could not study for a third year to gain an HND due to financial constraints, and not ‘being good enough at my job to deserve it’, I knew I had to leave. The motivation I once had disappeared and it was compounded by the worries that managers had about redundancies and profit.

I became depressed because I felt I was not achieving what I should have or was capable of, so my company sent me to occupational health to access my cognitive well-being. The doctor dismissed the possibility of dyspraxia and seemed to think all I needed was some medication or a career change. Perhaps I did not explain myself properly, but he failed to understand the seriousness of how I was feeling.

I put the thought of having dyspraxia behind me and decided to do a political science degree to change direction in the hope that a different career might be more suitable. I knew I had to get away from the job I was doing, and going to university seemed the easiest way out at the time.

I thrived at university. I was comfortable and felt at home because the environment was structured. I knew when the essays were due, their titles and the reading lists for each lecture. It was well organised and I knew exactly what I needed to do. Although I did not go out much, I had friends. I mixed mostly with the mature foreign students and this probably helped me to fit in as I had more in common with them.

I enjoyed the subject and thought about becoming a teacher again, but realised political science was not taught often in schools; I picked the subject as it looked interesting rather than as a way of getting employment. However, I did not have the drive to push myself into that career and decided to do a Masters degree in computing to put off getting a job and, perhaps, find a different branch of computing I might enjoy.

I changed university, and it was during this time I got an official diagnosis for dyspraxia. I had always been clumsy and lacked coordination, so felt it needed further investigation. I was diagnosed with dyspraxia, though mild, and was told I should investigate further the possibility of having AS. However, the doctor was unable to confirm it properly as she did not specialise in AS diagnosis.

A year had nearly past since I first became aware of my potentially having AS. I saw my GP who was convinced I was affected and referred me to a specialist to get a complete diagnosis. He was very helpful and acknowledged that this would help me to understand myself and give me legal protection in the workplace.

The Masters degree was near completion and I started work in a school maintaining computer resources. I chose this work because the environment was structured as at University, and also, familiar. I had after all, felt secure in education before.

However, whilst working in the school, I started to feel that the previous problems were re-appearing again that I encountered before I went to university. I found tasks a struggle if they were not clearly explained and I became frustrated with my inability to problem solve quickly. After a heated argument with my manager at the school about how my work was not always of the required standard, we jointly discovered what the problem was and a way forward.

I had informed my employer of having both dyspraxia and AS when I started the job, but, unfortunately, they did not understand the full implications of how it manifests itself in an adult. As a result, people did not understand me or how to satisfy my personal work requirements.

Although there were many children in the school with AS, it was not obvious to members of staff how AS could appear in an adult. I felt the condition was undermined with people saying: “you seem alright to me”, but I knew this was not so as I internalised much of my anguish and would hide when things got too much for me. I had no qualms about divulging my AS, as the school was quite supportive and sympathetic to people’s problems. Once my manager knew how I worked best, our relationship improved and was good.

It was the children’s noise though that was particularly challenging and put me consistently on edge when I first started the job. The environment did not offer the solace I needed to work effectively. I found it difficult also to confront bad behaviour in the children, whilst, at the same time, not allowing myself to appear a pushover. This was the same with dominant members of staff, so I avoided them as I was not assertive.

Since working in a school, I have felt it much of a blessing that I became aware of having AS, as an adult. However, I would still not necessarily divulge my condition to anyone who did not need to know as doing so may mean I am targeted or viewed as different (and therefore less capable).

Many children who have been diagnosed seem to be treated as different and special. Although it is good that their problems are being addressed, I feel fortunate that I have had to cope alone because, once out of education, the support can be limited. As a result, I have had to learn to fit in so initially my problems are not apparent. It is not obvious to me how I have done this except by copying how other people react and behave in a particular situation.

I am now moving my career in a different direction whilst taking on board the lessons I have learnt. Central to this has been locating a more appropriate work environment. I have been privileged to meet a wonderful man who has been helping me develop the skills to have my own website design business as an aside to my school work. This has provided me with a supporting mentor, and I believe it is important to have someone to guide me within a work context. I seek this now to provide support and make me feel more confident in my own abilities.

Working at home after my day job to create websites in my own time, affords me the flexibility to manage my personal requirements. Sometimes I have meltdowns, but I can come back to my work when I have calmed down and still get to complete deadlines.

It is the structure and formality of the working day that I still find challenging. I am still drawn to wanting to teach because of this, but right now I am not geared up to secondary teaching. I have considered lecturing to avoid the sensory overload that accompanies a boisterous adolescent environment.

AS is not necessarily a barrier to succeed, but for myself, I have no desire to work up a career ladder in a prescribed setting. I don’t like the rigidity of rules within the work place that can stifle creativeness. Doing what I do now, and the work context I operate in, means that I have my own space.

In addition, my work colleagues understand my limitations and talents. I have been given the opportunity to grow into the job and progress. I believe without supportive and understanding work colleagues, this would have been much harder. The stress levels have dropped right down since I have been relocated to my own office at the school as personalised working space is essential; I cannot hear the children as much as before. I am now able to focus and concentrate on my work, something I did not have whilst working at the telecommunications company previously. If I did not disclose my condition, I doubt this accommodation would have been made.

I feel at this stage that working in education is not what I would like to do long term because it will not support me financially. However, by not being the only person affected by AS in the school, albeit only alongside students, it has helped me to transfer from university to the workplace where people understand the condition to some extent. I have also learnt that my problems are not unique and many students will be feeling they are no different to everyone else.

I have come a long way from when I first was told I had AS and my frustrations have subsided greatly. I am slowly becoming happier with who I am, knowing that I will be able to build my own successful business with the support of my partner having identified the working environment and conditions that I need.

Looking back, I think I could have worked well in the telecommunication industry if my problems were identified earlier and required adjustments made. I did not dislike the work when I understood it, but as it was an apprenticeship whose learning style did not suit me. Vague on the job training or directives like ‘go figure things out for yourself’ was something I found it all too hard.

I realise now that my work should engage me in order to motivate- but not overwhelm – me. I need – and like – a work environment that keeps me busy, one where I do not have time to think too much or procrastinate. Tasks should be broken down into manageable pieces and it has been incredibly useful for me since the school has implemented a computerised help desk system. Providing technical support to computer users has given me the organisation and structure I need and, as a result, I have felt much happier in myself. Seeing small results has also increased my confidence and self-worth.

Although I am still waiting to see a specialist to formally diagnose AS, my employer is treating me as if I do have it and is making all the reasonable adjustments regardless of the legal requirement to do so. I appreciate this and it has made my working life a lot easier. Whether I have AS or not, I feel I am able to work effectively much more than I was before.

However, importantly, I have also made fundamentally changes personally. I don’t automatically blame others for my behaviour and I accept my own responsibility. I realise now that I can say and do inappropriate things, but I have become more humble, accept my shortcomings and am willing to apologise if need be. I try to be more considered by thinking how my actions would be received if someone did it to me.

Although I do slip up, it has helped me to fit in and overcome my social deficits and, in turn, help me be better in the workplace by being in the right environment for me.

Tuesday, 28 February 2017

Dealing with lots going on at work: how to get organised

Some weeks I feel quite content because I don't have lots of things going on. I may have big things but not a long list of stuff and I don't like long lists...

It's when my to do list becomes the length of the weekly shopping list that I become panicky and I don't know what thing to do first. I get mentally overloaded by everything I need to do so I sometimes ignore things, hoping they'll magically go away. I end up burying my head in the sand because I am so overwhelmed by what I have in front of me. When deadlines approach, my utter hatred of failure and messing up puts me into overdrive and I meticulously work through the most urgent of items at the last hour.

But this approach put a lot of stress on me. I find that it triggers migraines and makes things all the more unproductive. I don't like it so I do what I can to avoid things stacking up in the first place. I believe that prevention is the best way to avoid a lot of the autistic meltdown/shut down reactions, if that is at all possible!

Yesterday I felt like it was getting too much at work. I had tasks coming in from one manager and another lot from another manager. All the tasks felt urgent and my head was swimming with so much to do and not a lot of clarity. So I decided I would be methodical and spend a bit of time to work out what I had to do so I could work with a bold aim in mind.

I use Microsoft Outlook for my work e-mail and I use the flag tool (follow-up) to help me identify work I have been given and I can set myself a reminder attached to the e-mail so that Outlook automatically reminds me when things need to be done. The idea is that e-mails can be "flagged" with reminders and I can colour code them with categories as well based on the type of work I have been set for my categories (also brilliant in highlighting events in my calendar). Microsoft have helpfully provided web pages to show us how to use the follow-up tool in Microsoft Outlook and how to use colour categories in Microsoft Outlook. The follow-up tool then builds a to-do list and marks what needs to be looked at in order of the dates I have set for reminders. This then helps me see at a glance what I need to do first and I can work through things in order and add to it as new things come in.

I try to keep the to do list short or the sheer length of it makes my brain hurt. I remember from my web design days of reading about the psychology of web design. The idea was that the human brain rarely can process more than seven things at a time so a website with a menu of over seven items will be hard for the end user to browse through. I take the same design concepts into my lists. Its why I have to scan each item of the shopping list to find the item to check it off since I can't easily glance at the whole thing (where it is long) and see an item quickly. Its important that my to do lists don't grow to unmanageable lengths. So my list is a reminder to me to keep flagging my e-mails so I remember to go back to them and so things aren't lost. I ensure I keep my task list not too long or else it will make me overwhelmed and I will run away until I come back with fresh and less stressed eyes.

There's often talk about reasonable adjustments and the onus being on the employer to provide the support and workplace chances but I believe we need to also help ourselves if they aren't suggesting the right things. The one way is to maximise the benefits of the tools we might already have in our workplace.

As a former ICT lecturer and IT trainer, I think that not enough time is given to staff to learn how to use their computing tools. It is assumed that we somehow just figure it out on our own. We don't. If we don't know a function is there, we won't be magically looking for it unless we have that curious disposition. Many IT users are scared of doing something wrong. Its understandable.

I have trained people to organise their e-mails so they automatically go into different folders based on the contents and who its come from. At the end of the session I see real impact to these IT users because they are no longer faced with such an unmanageable wall of information but that it is sifted by topics and senders automatically into clearly labelled folders. It reduces the stress and helps aid productivity.

I know that creating e-mail sorting rules in Microsoft Outlook or flagging and categorising isn't the only solution to information overload but its a start, right?

Reference:
McCracken, DD. & Wolfe, RJ., (2003) User-centered Website Development: A Human-Computer Interaction Approach, Prentice Hall

Friday, 17 February 2017

A medical solution to a not very medical problem - occupational health

I decided that I would be proactive at work and request that HR refer me to occupational health.
What I wanted was to have my autistic needs formally recognised in terms of my seating arrangements when we move to a new site later in the year.
What I was seeking to avoid was to be placed in a large open-plan office surrounded by noise, lots of people and near a high traffic area. The last thing I would need is to sit nearby to the printers! That kind of working environment would see my productivity fall, my stress levels rise and I could be penalised in my appraisals if I wasn't meeting my potential.
Alas, to get the clout needed to mobilise various people and departments to take my needs seriously and lead to a satisfactory result, the only way I could think of was through occupational health.
So I visited this occupational health place. It was on a business park not at all accessible for those who don't drive and the lack of easy car parking was worrying (cars blocking in other cars in parking bays). I saw no evidence of disabled parking. I hope that the less able bodied would perhaps be visited at home or at other more suitable premises.
So on the day I was stressed. I didn't know the area well and finding the site was challenging to say the least since the provided map and instructions made little sense. I got there early and was glad that I had looked on Google Street Maps to visualise the turnings and road layouts. It removes some of the mystery of driving around the unknown.
What bothered me the most was the way one gets into the reception. I don't understand how intercoms work in that they seem to each have their own operating methods and the procedure of what to say into it. I often found this process utterly confusing. Some systems remotely unlock the door; others don't. I appreciate the need for security but none of it of what to do was transparent and I think a sentence or two on the instructions about finding the place would have been useful. I felt a little surprised that the door couldn't be unlocked remotely and it was so irrelevant to my day but it still bothered me that someone had to press what looked like a door bell to open it.
The doctor was pleasant enough. I won't be critiquing him but I was somewhat amused when he told me he was familiar with Asperger's Syndrome. Familiar. It made me think he'd encountered it at some point in an hour CPD session but it was clear he was no expert. To be fair, I wasn't expecting him to be. He's a generalist I suspect, who when not seeing me, would to be working with those with mental illness and stress and those who have physical difficulties that require perhaps a different kind of support in the workplace from what I was seeking.
I felt like I had to tell him what I needed. It would have been refreshing if he was leading it because he knows high functioning autism in women but I felt it was really me speaking up about what I found difficult. Sometimes I get so tired of being my own advocate. It would make a change if more people just "got it". When I meet those kinds of people, I really value their insight and experience. It's incredible to feel normal again.
Here's the thing I find odd: it takes a doctor to write a report to HR that I need a quieter working environment. The solution is very much non-medical. Anyone who knows about autism would know the kinds of solutions I am looking for. It doesn't take a doctor to know this. Teachers (those with ASC experience). Carers. Autism researchers/academics. Parents of autistic children. Autistic people themselves. Lots of other people with much more meaningful experience. And yet because these such people aren't clinicians, their expertise and experience counts for nothing in the eyes of HR.
This is what makes things so irritating because I have to get a doctor involved when I am still grappling with the idea of whether autism is even a medical thing.
I get it. The Equality Act 2010 talks about disability as one of the nine protected characteristics. This legislates about discrimination and requires businesses and so on to provide 'reasonable adjustments' in the workplace to disabled people. It also defines disability as having a physical or mental impairment that has a ‘substantial’ and ‘long-term’ negative effect on one's ability to do normal daily activities. Autism is covered by this law.
Disabilities are often seen in terms of the medical definition and the doctors are supposedly good at understanding the whole clinical side. They can diagnose such things. It makes sense.
And here's the difficulty for me: I am disabled because my autism has a ‘substantial’ and ‘long-term’ negative effect on my ability to do normal daily activities.
Well, kinda. I make reasonable adjustments for myself all the time through my coping mechanisms. If I can't stand the sound of my work colleague munching through a pot of carrot sticks, I'll make the team their tea and coffee. I win brownie points for being nice and we all chuckle that I have hit my record of making five cups without spilling it. My dyspraxia rather makes carrying hot drinks tricky so I am rather pleased that one of the ladies got a high sided tray that'll fit five cups in it. I am happy to do shuttle runs between the kitchen and office as it rests my eyes from the computer monitor.
By the time I am back with the last cup the carrot muncher has finished.
And also since HR has now listened to the doctor (I am hoping!), my new desk location will not cause me any substantial or negative issues within my working environment.
Perhaps too my husband and child and other people in my life will understand how I operate and change their behaviour in such a way that they don't put me through unnecessary upset. It comes through understanding autism and me speaking up when something is upsetting.
With all these informal and formal adjustments in place, I wonder if actually I now would be considered disabled under the EA2010?!! And yet if I wasn't legally recognised as disabled, I wouldn't then be able to have reasonable adjustments in the workplace.
Whoa... Seems a paradox?!

Monday, 21 November 2016

To declare or not to declare...

I was recently asked by a mother whether her daughter, who was starting to look for employment, should declare her autism on her job application form.

I can see this situation from many angles.

Firstly, I am autistic who is currently employed but has also experienced long-term unemployment too. I've done my fair share of job interviews; some have resulted in jobs, others not.

Secondly, I am my trade union's equality rep at my place of work. I am familiar with British law in regard to the Equality Act 2010 and reasonable adjustments in terms of the employer enabling an autistic person to fit into a workplace.

I wanted to be able to get all excited about the Equality Act and tell this mother that if her daughter is able to do the job, she could be a great candidate. Her autism would be no different to someone with a heart condition (for an office role) in terms of it not holding her back.

But you see, I emmmed and ahhhhed. I wanted to be realistic and not suggest that the Equality Act has somehow removed that barrier to employment. We probably know autism and our potential but can we say the same about the HR department and managers we might encounter on an interview panel?

Let's give an example. I was working in a school a decade ago and busy getting my head around my diagnosis. I was talking to a teacher and she asked if I had light therapy. Well, I was nearly foaming at the mouth!! I was thinking bloody hell: I have a degree (completing my dissertation for my MSc at the time), drove, lived independently and all sorts. Light therapy indeed!!! But this is the thing, if a teacher who may well come into contact with intellectually high functioning autistic students thinks that, what could an HR person think?!
To be fair to the teacher, she wouldn't have necessarily had any autistic training. I never had any when I did my further education teacher training either. It's all on the job 'work it out for yourself with Mr Google' and a brief chat with Student Support.

If we can't trust the recruiters to understand the basics of autism, what should I suggest to this mother?

I felt that it depended on many factors:
The first is the size of the organisation. A large organisation may be accustomed to reasonable adjustments much more readily than a small business. A large supermarket chain looking for cashiers has a large HR department and will be dealing with things across their stores. (Probably a bad example as supermarkets are laden with nightmarish sensory overload 'opportunities')!
Bob's Plumbing services looking for an admin may not have those resources and knowledge to support an application from an autistic person.

But there's no hard and fast rules.
The supermarket may have disability recruitment targets and may be keen to hire. But Bob himself may be a family man who has personal experience of autism with a relative. He may appreciate the sorts of skills an enthusiastic autistic person may give to his business.

So I said all this to the mother and she nodded. And I felt like I didn't answer the question with a definite answer.

And then the situation became murkier.
It's a very neuro typical thing to meet with a bunch of people and be asked theoretical questions on one's ability to do a job.

"Look. I'm not wanting to make friends. I am not interested in work to primarily expand my social circle. I want to earn money in a manner that keeps me engaged. Getting on with people just facilitates that end goal. And yet, the interview panel asks a wide range of stupid questions..."

Tell me three positive characteristics your friends would say about you...

"Whooooa! Hang on... Why ask me?! Isn't that what the personal reference is about?! How the heck do I know what my friends think about me?! Ask them! Oh, and it's a very neuro typical assumption to assume I have friends. Maybe I don't and I thought the job interview was to find out if I fit the organisation, not a test of if I have mates. Notice the statement assumes multiple chums... "

And so the stupid questions go on and some moron might think it's trendy to ask a lateral question too.
It wasn't so long ago I was asked about whether a Jaffa cake was a biscuit or a cake. It's actually got a technical answer to do with tax. Let's not bring my knowledge of VAT case law into a job interview for an IT job...

Then for the higher level jobs, one might have to deliver a presentation on a laptop one has never seen before. Oh, anxiety is seriously spiking now...

So what I said in the end to the mother is thus:
Understand the organisation in which you want to apply to. Figure out if they may be are autistic friendly in their recruitment process. It might just be a wild guess.
If you need reasonable adjustments for the interview, request it. See what happens. It might be an act that puts one's name in the rejection bin (it's wrong but let's not be naive) but don't forget an interview is two-sided. We as job seekers often forget that we are interviewing the employer too. Will we fit in? Will we find the lack of interest in fulfilling reasonable adjustments a nightmare? Do we want to work there?
And of course, if you do not feel like you need reasonable adjustments in the interview process but will do later, you can declare the autism after the contract is signed.

Alas, I am a cynical person and one still must get through probation. It's dead easy to get shot of someone during that time. My view  and it's just that, is that a declaration at least offers some explanation if one fails to meet probation targets. The employer is in a position of strength with getting rid of new employees but at least the diagnosis is documented. And it's discrimination to sack someone on disability grounds regardless of their length of service in the job.
But try proving it... And employment tribunals are not a cheap or a pain free way to go.

Ultimately, finding a job can be hard for anyone. Just be prepared for lots of rejections (often the case for anyone!) and don't give up. There's a good reason why there's a low percentage of autistic people in employment.
BUT: There will be a great employer out there. It may take time but don't give up...!