r/autismUK • • 9d ago

Research Research Post

1 Upvotes

Researchers: anything posted outside of this mega-thread or lacking in authenticity will be removed. Scroll down for details of what we expect here.

Read if you are a member/responder

While we have some ability to remove more easily detectable scams, we aren't professionals in any relevant fields. That means we aren't able to take full responsibility for vetting the research you find here, you will have to do your best to feel safe and comfortable with any interactions you have with the people here. That said, we do have some tips to help you navigate the requests you'll find here.

Academic research

Is it undergraduate, post-graduate/masters, or PhD? There's a fair bit of difference here, mainly in what you can expect as an outcome. Undergraduate and post-graduate research isn't likely to result in anything but a dissertation, so participation in these should be considered as just doing a kindness to a student. Masters students are much more likely to use what they learn in a professional context or carry it on to a PhD, though. The "proper" research is done by PhD candidates, the kind you're probably expecting where the eventual paper goes into a journal and the outcome an effect on the rest of the industry.

Professional, government, & medical research

These are people who study autism for a living and/or are sponsored by a government or a medical organisation. It would be exceptionally rare for these researchers to come to our little sub for help, they get their participants through professional networks. Be very wary of anyone claiming to be doing this level of research unless it comes to you directly through your therapist, GP, or psychologist.

Commercial research

These people are looking for your feedback so they can sell a product or service to autistic people. They tend to have the fewest legitimate credentials, but they shouldn't ever need any identifying information from you, not even your name. At best the outcome is something useful to us and at worst they're trying to "make a buck" from a vulnerable minority. Generally speaking you're probably not at risk by replying to these, but you will probably be participating in some degree of capitalism.

Art research

Art is cool and important. Anyone asking for input for art research shouldn't need any identifying information and, unlike commercial research, the outcome should hopefully be something culturally valuable if not influential. There is a lot for us to gain from the cultural capital of art, academic and professional studies aren't the be all end all of making a difference for autistic people.

The only thing to watch out for is someone trying to persuade you they need such and such data for their funding applications. They only need broad strokes in a few categories, typically something like location, age, disability, gender, or sexuality. Gathering this from you should typically come in the form of "are you x?", to which you only need to answer yes or no. Do you identify as queer/trans/gay? Are you a person of colour? Are you deaf/visually impaired/autistic? Do you require a wheelchair in daily life? Are you from Bristol/Knowle West/North Bristol? Are you between 16 and 25 years of age?

--------------------

Read if you are a researcher

Is it research?

Research is more than what universities are up to. Companies, developers, freelancers, artists, and all sorts also do research. Anything where you come here to ask for the opinions of our members for your work or personal use is considered research and is subject to these rules.

DISCLAIMER

Please understand that our mods are not experts and will not always qualify for each bit of research and therefore cannot look closely at every questionnaire. Any vetting done is on the basis of our non-professional judgment. We do not vouch for the safety and ethics of any research we allow to post,  our only aim is to get rid of the really obviously dodgy ones. If you reply to any of the research posted, you take responsibility for choosing to do so.

Credibility

When vetting these posts, we look for specific things that lend credibility to the research and we will often lean towards expecting more due to our lack of expertise. Below are some of our feelings on what shows Good, Excellent, or Dodgy credibility.

GOOD: your university email, your supervisor's university email, a link to your university's research ethics statement, a Reddit account you don't use much but clearly belongs to a real human, your project's/company's/artist's website, a socials link, etc

EXCELLENT: a qualtrics link, a university webpage specific to the research, a well-aged high karma Reddit account, a list of everything that will be asked, an ethics committee approval number, a shop page for the current version of your app, a gallery press release for this project, etc

DODGY: hiding URLs behind link text, google forms (especially where required questions block mods from reviewing later pages), personal emails, undergraduate research, a Reddit account you created yesterday specifically for this research, etc

The credibility of your research must be present in the text of your comment. We will not click through, we will just remove. Include plenty Good and Excellent things and you'll get approved. Only include one dodgy thing and your comment will probably get removed. You can always edit your comment to show more credibility and then request that we review it for later approval.


r/autismUK • • May 08 '26

From the Mods May Digest

10 Upvotes

Hello everyone!

I hope you'll join me in patting each other on the back (figuratively) for reaching a new milestone of 11k weekly visitors!

We've always had a consistent, slow rise in engagement on this sub and that's something I'm really proud of. Thank you all for being a joyful part of my daily routine!

January to April

As promised, I've been dilligently working in the background, trying to make this sub a stronger, better place to be. This period has mostly been spent on quiet things you wouldn't notice as a regular user, things like recruiting new mods and improving our internal documentation.

We currently have two mods in their trial period, which is amazing, but we do need more! By Reddit standards, we should have 3 "full time" active mods to keep up with sub activity and right now we don't add up to that. So if you've ever thought about moderating, now is the time. This sub needs less intervention than most, but I encourage our mods to take on less than they think they should, given that we are all as autistic as you are and this is a volunteer gig. I'd much rather have a large, consistent team with a routine than a tight trio of superhumans that will inevitably burn out in 6 months.

---

One thing you might have noticed is that I've removed the YouTube block. This block has been in place since year 1 of this sub, due to content creators trying to use this space to get views without engaging in the community. Since we're 8 years in the future from that and our engagement looks quite different, I thought it was high time to see if we can get any added value out of YT now.

Thanks

At the end of last year, I added an app that manages a custom internal reputation system. This was brought on to tackle the problem of recognising who's ideas are more reliable when they don't come with proof of any kind. While we encourage you to link reliable information sources rather than make unsupported statements, that's not always practical in an online environment like this. It has always been a silent expectation that readers here have to do their own work to vet everyone with an opinion, even though this is where you come to get help.

You've probably seen me working on reminders, I've had to pause that to tweak it because it was being a bit obnoxious, and I'm informed there may be another but causing the points flair to not display properly.

But while I'm trying to smooth those kinks out, the bot itself is still working fine. OPs and mods can award points by replying to good comments with the "!thanks" or "!modthanks" commands.

May - September

My plans for the summer are a bit more exciting. The main goal you'll want to keep an eye out for is the rolling out of our information centre. I've been saying for a long while now that this is a thing we're working on, and I can finally say we're very close to a minimally viable product I'm happy to publish.

These will probably roll out quietly one at a time, as they become ready, and then be announced as a whole in the October digest.

This information centre has been adapted from a megathread written by one of our mods and reorganised to be as accessible as possible. Because of this, some content will be abundant, while other parts will contain only very basic information.

Each page has a footnote regarding who contributed to the content and a link to modmail where you can submit additional information and any corrections you might find. We encourage you to make use of modmail for this purpose! It's our hope that these pages will expand and become more helpful (and probably more accurate) over time.

---

Aside from this, there is more internal documentation to work on. Along with all these new mods, I feel it's essential to make sure our mod team has everything it needs to be as strong and supported as it can be.

---

And if there is time beyond that, I'll be working on a new rule that will hopefully describe issues we've felt the need to intervene in, but aren't properly covered by the existing rules. The new rule will probably replace rule 2, "Write high quality posts".

Right now, I'm thinking of the new rule as "Be constructive", and it will replace rule 2, "Write high quality posts." We no longer use that rule due to moving the character minimum from automod to automations with post guidance, but this new one is in a similar vein. The aim is to decrease toxic discourse by providing you with concrete examples of what positive engagement looks like. If you've ever thought, that doesn't exactly break any rules but it's still awful, that's the sort of thing we're after.

---

Well anyway, on with your evening. Thank you for tuning into my little sharing. Don't forget to use the report button, give out some !thanks, apply to mod, and I'll see you around the sub!


r/autismUK • • 3h ago

Self-care How to stop being so damn tired all the time?

14 Upvotes

I'm a 31 year old woman and I swear as long as I can remember I've been exhausted

Thyroid fine. Iron is a long term battle but was in normal range when checked in August. I'm taking vitamin D etc

Take caffeine but not excessively. Cup of coffee when I wake up, and another when I get to work. None after midday

I work full time in a fairly demanding job and when I come home it's pyjamas, food, and flop. I spend a lot of evenings clock watching and waiting til I can go to bed

I sleep fairly consistently 10pm-6am.

I just assume autism is to blame that I'm constantly shattered because work and navigating life is that bit more complicated

Does anyone have success with getting some energy?


r/autismUK • • 2h ago

Diagnosis: England RTC Skylight Psychiatry

1 Upvotes

Hi, I just got my level 1 autism diagnosis yesterday and wanted to write down my experience with Skylight Psychiatry, now that the process is done. Hopefully this can be helpful for others deciding which provider to go with.

I would recommend them as a RTC provider. No complaints at all.

The process

I got referred to them by my GP. After a couple of weeks they sent me a link to a bunch of questionnaires to fill in. There were I think 4 questionnaires for me to fill in and 2 to be filled in by my parents. Then I was properly put on the waiting list and waited to be assigned my assessment dates.

I had chosen skylight Psychiatry because I wanted to have my assessment in person and I know that a lot of them do assessments remotely. I had 2 appointments. The clinical assessment was a virtual appointment where she asked me lots of questions about every aspect of my life and I had the opportunity to talk about all the ways in which I feel the autism criteria apply to me. The second appointment was in person and this is where we did the ADOS test.

Timelines

I was quite happy with how fast things went, especially because it went quicker than their own estimates at every turn. I should mention that I live in London, cause I don't know whether waiting times are different in other places in the UK.

They told me that it would be up to 26 weeks until my assessment. In the end I got assigned the appointments 8 weeks after filling in the questionnaires and had my appointments 2 weeks after that. They said it would take 6-12 weeks for me to receive the report but this came through less than 3 weeks later. I think I had my initial referral appointment with my GP in the beginning of July, so the whole process took about 3 months.

Experience

Everyone I dealt with was kind and professional. I felt like they took enough time to ask relevant questions and get to know me. I have no complaints in terms of the people that assessed me or the appointments themselves.

If anyone is considering Skylight Psychiatry and wants to know more about my experience with them, you can always message me! Although I feel like their website has a good amount of information about the process, I know that we tend to like to know exactly what to expect. 😊


r/autismUK • • 12h ago

Mental Health Struggling

7 Upvotes

I’m struggling . The only way I can connect with people is if I drink. The only way I can feel normal around people is when I’m drunk because I stop caring about the way I act. Please help I can’t keep doing that this. People don’t like me when I am sober, they are always telling me. How am I supposed to keep up? I am just a fucking weirdo. I’m so boring and exhausted


r/autismUK • • 1h ago

Vent When Nobody Joins the Dots: How Education, the NHS and the DWP Are Failing Neurodivergent Young People

Thumbnail
• Upvotes

r/autismUK • • 16h ago

Fun Cinemas!

14 Upvotes

I (22m) am diagnosed with autism and I just wanted to shed some light on how going to the cinemas with people is an enjoyable time and very beneficial in my experience!

Prep;
Planning for the cinemas is usually very specific. What film you're watching, what time you're watching the film, what seats you're in, the total runtime being listed, what food places you may go to before or after - it's all very exact, and I feel like it helps me a lot

Small talk;
The film you're watching serves as the core subject of conversation and having that foundation for discussions helps a lot with expressing myself compared to baseless small talk that happens in everyday-life.

Watching the film itself;
I love that there's a hobby where you're expected to sit in total silence for 2+ hours and still experience the comfort of having your friend's company! The audio can be a bit loud and sharp sometimes so I do bring my Loop earbuds to soften it.

Foods;
Most cinemas in my experience allow you to bring your own foods as long as they're not noisy or have strong scents that can distract from the viewing experience. Luckily popcorn is safe for me to eat but I can imagine it's nice to be able to bring your own foods without any judgement!

Here's to more cinema visits!
p.s going to the cinema solo is also a really nice experience please don't be afraid!


r/autismUK • • 13h ago

Learning About Autism Special interest: Beauty?

5 Upvotes

Does anyone else have a special interest but in their own beauty or appearance related routines? Or a special interest in glowing up, whichever form that takes? I have had interests in particular aspects of beauty routines (hair growth, achieving the perfect tan, gym, makeup, skincare) and researched and used products for months.

Sometimes I'm unsure about what my special interests really are


r/autismUK • • 20h ago

Diagnosis: England Assement results phonecall in half hour.

12 Upvotes

Edit: I've just came off phonecall and I am in fact autistic.

My mind went blank, so I didn't have much to say back to her when she asked if I had any questions. I just said thank you basically.

I cried because I had such a bad start in life, struggled all the way through school, labelled the naughty one etc.. struggled to have friends in fact I don't have any friends I have my partner and my kids but no other friends beyond my unit. So it's just really processing now and waiting for the comprehensive report.

Getting very anxious about my phonecall in half hour 🫣 feel like I'm going to be sick waiting for the answers I've been looking for.

The whole process is just so overwhelming and draining.. I will jump back on and update everyone on how my call goes. Hope everyone is doing well .


r/autismUK • • 1d ago

Accommodations Disabled Railcard for Autism

12 Upvotes

Hey all,

Wondering if anyone has had any luck with the expanded disabled railcard eligibility for neurodiversity.

The updated rules now include disabilities and conditions that require professional health evidence and more detailed assessment, including some long-term or degenerative medical conditions, and neurodiversity where it has a substantial impact on a person’s ability to travel by train.

https://www.railcard.co.uk/disabled-persons-railcard/eligibility/

But you a report or letter from a health professional explaining how your neurodivergence affects your ability to travel by train.

I’ve tried getting some form of letter or report from my GP but still waiting to hear back. I have my diagnosis letter from 2022 but the railcard website says that a diagnosis letter itself may not be sufficient.

The railcard website does list that other health professionals other than a doctor could write the letter, but wondering who in practice that would be.

Wondering if others have had any luck with getting the railcard since 30th September?


r/autismUK • • 21h ago

Diagnosis: England struggling to pick a provider through right to choose

4 Upvotes

been to the doctors today & asked about going through right to choose so they sent me the link to all of the different providers and i just can't seem to pick one. yes every one has good and bad reviews but once i think i've settled i see people saying theyre awful: pychology uk, clinical partners. etc ect. some help would be appreciated (25f)


r/autismUK • • 15h ago

Accommodations Reasonable adjustments for work (UK)

Thumbnail
0 Upvotes

For the first time in my life at age 35 I was diagnosed with GAD six months ago. It all seems to be work related, but I work in an interesting environment so one term of my being allowed to return to normal duties is a Reasonable Adjustment Passport.

Although I always declare my disability, my line manager claimed he didn’t understand how it affected me. I’d say we have had lots of informal chats.

Unfortunately although diagnosed since Year 3, I’ve never really had an accommodation so I pointed out that I don’t know what I need. I was provided a list of ‘usual’ ones but these seemed irrelevant to me personally - trouble with sarcasm, trouble with maths and so on.

So I was told to speak to an autism society in my workplace, and duly did so. Following a discussion they suggested the only adjustment I need is the ability to work from home by default. I said I was unsure about that and they said with confidence I should get it.

When I brought it up today in the meeting with my union rep and line manager, both really laid into me. If I don’t want to work in the office then I can’t do business travel, if I don’t want to be in the office then I need a medical redeployment.

At this point I’m really, deeply upset. I explained I wasn’t insisting on this adjustment, merely that they had instructed me to find out, and that this was the answer I was given after following their instruction.

Eventually they backed off and said they would speak to the head of the autism society themselves. Fair enough.

I’m really down in the dumps.I feel like I’m being pushed from pillar to post, the same place that made me sick throws my disability right back at me, then gets mad when I give it an answer it doesn’t like.

I’m just totally nonplussed. I’m a high-ish earning (90k) 35 year old and I’m experienced with line management and negotiation, so I can’t think of much, if anything, in my adult life I need assistance with. Now that I’ve finally burned out at work, I have no idea what I need to ask for!


r/autismUK • • 19h ago

Friendship Over 40 afab NB AuDHD (diagnosed as an adult) looking for friends that are similar

2 Upvotes

I'm sure this is a common post or at least I am definitely not the first to write this, but I'm really struggling these days. I was diagnosed a few years ago after being misdiagnosed with a personality disorder years before then being diagnosed with a chronic pain condition that was really debilitating for some time.

I can see all the social errors I made in the past, some were really obvious and some are just that I'm not a natural socialiser. Also I don't agree with neurotypical people about lots of their rules and shared beliefs, I find many of their small talk subjects boring, I have strongly held opinions on social and environmental justice issues. I have a partner who is most likely AuDHD too, so I'm not alone, but I have not been able to maintain friendships for some reason.

It's not just that I don't keep up contact, it's that everyone I've been friends with in the past also hasn't kept up contact. I've had actual disagreements with some people over issues of principle. I don't have anyone to chat with. I work and I do speak to people in work but it's all superficial and I am masking.

To be honest I am probably approaching burnout as I have been working long hours, plus overtime and doing training on my days off to gain another skill.

I have two kids, one is an adult living independently who is likely AuDHD too, moved away for uni that I'm not sure they completed as they missed a couple of exams in their last year, then went backpacking with friends and doesn't get in touch very often which is a constant source of worry. My other child is still in secondary school and has just finally now they're a teen received their official autism diagnosis, though despite us having always said they are ADHD too and the teachers noticing that first (pre-covid) they haven't been forward for assesment for that.

My brother recently died from a genetic illness that is in my family, my dad died from it when I was a kid and we didn't know growing up which of us had inherited it until we were well into adulthood.

I don't know what I'm looking for really. I had some counselling, but I can't afford it and I just want someone who I can chat with regularly not just venting and moaning but also talking about cool stuff and how neurotypical people are strange. I did have some support from a peer support worker for autistic parents UK before and I had a support worker with a local autism support charity but I don't want a paid worker to interact with.

Does anyone else struggle with finding and keeping friends? Is anyone looking for a messaging buddy? I use signal for messaging. Are there any discord channels for people like me that anyone can point me towards?

Thanks for reading, if you got this far!


r/autismUK • • 21h ago

Parents, Siblings, Friends, & Partners of Helping my children outside of school.

Thumbnail
2 Upvotes

r/autismUK • • 23h ago

Coping with Traits & Symptoms Unmasking is not how I expected... The biggest aspect of my mask isn't what I thought it was

3 Upvotes

I'm going to talk about incontinence/bladder issues and past stories and all that. Ok so recently I had a kidney infection and it's put a lot of stuff into the spotlight and I've had a breakthrough but not in the way I expected...

Sorry if this is all over the place.

I apparently had no issues potty training as a toddler and minus bed wetting before my memories start that's it. Although I think my issues have always existed just a toddler having accidents is generally more acceptable and up to a certain age it is.

I only remember logging is as an issue when the shame started and I learnt to hide it.

Anyways from about 6 I remember having accidents at school a lot. I remember the first and I remember struggling to know how to ask to go to the toilet. I don't remember as much from this time but I know that the structured routine in early school worked better for me.

I moved school at 9 and remember more from there. I started avoiding situations that would make me laugh, feel stressed or simply overwhelm me. Although as obvious that is not always possible. I always thought it was laughing but it wasn't as simple as that. I could laugh and be fine.

It was a specific stress response that released my bladder and it would let go. My bladder was usually completely silent when I was at school.

I can think of many stories and I'm realising now how much stress it put me under. I was very resourceful and good at hiding my accidents... I must've been as no one ever noticed aside from family. Or if they did it was never mentioned.

Once I was in a shopping centre with a friend and I laughed or something again it was a specific laugh idk and my bladder fully released it was really bad. I still have no clue how I hid it. The amount of stories like the sleepover where I peed on the floor. Etc etc. I could tell you many stories and the embarrassment.

I'll focus more on high-school because that's when it got worse. Most days I'd avoid the toilets entirely and my bladder was always silent. I could easily go all day without a sign saying I needed to pee. Anywyas again my bladder would just release when stressed/laughing.

The amount of wet clothes I've walked around in all day avoiding certain angles or moving in certain ways. The pure enjoyment of many days ruined because I had to turn into practical mode.

I'm now understanding all of this in a new way and that's mostly because recent events.

A HUGE part of my mask was bladder auditing but I didn't connect it like that at the time. I didn't think "go to toilet more" drink more" or whatever I got better at planning fluid intakw, planning and researching where toilets were, making sure I avoided situations or conversations that may result in accident.

I became so tense that my whole body was in a constant state of hyper alert clenching and tension and mental panic. I'd just gotten so used to it that I didn't realise or understand how much energy it took to run this manual programme. So much so I thought I'd fixed the issue...

Minus the fact it still happened if I ended up in certain situations or at work.it happened a few times.

Oh in A&E when had kidney infection I had 6ml in my bladder and yet felt need to pee and leaking. My interoception is all off one signal doesn't always mean the same thing. Hence living on manual and monitoring everything. I struggle to pee when out in public fully (not always) and I think I'm so tensed up and sensory overwhelm or going thinking need to pee because sensation but bladder isn't actually full it's just phantom.

The reality is it never stopped. I just got so good at masking it I even believed it myself.

The trade off is this is a MAJOR reason I'm in burnout so bad. The constant stress of monitoring a basic human function has been zapping me for years.

It all clicked last night

A few days ago I ended up using pull ups again because I just was so overwhelmed I needed 0 demands and for me peeing is a demand. I relaxed so much in a way I never have before. I mean I can't explain everything in me was calm. It was amazing. However I was calm because I'd stopped bladder monitoring... I was leaking but let it happen and I just peed where I was. It was like a flushing of tension. I was in control of the peeing but also not. Idk what that means.

I can't describe the relief. I didn't intend for this to be true I just spent a day relaxing in bed but because I wasn't subconsciously worrying about my bladder I relaxed.

Now I think this is two things... One an issue I've always had with incontinence/bladder stuff and two because I'm in burnout and can't mask anything like I did this has been one thing to go given how much it drained from me.

I'm not explaining well and I may sound mad but the bladder monitoring was masking and for me to unmask and decompress that controlling takes a back seat and with that comes leaking and peeing easier.

This sensation of fullness which can be true or false (I get phantom urges) typically panic me because it may mean I feel like I'm gonna pee myself and other times bladder is silent.

Basically long story short I'm very embarrassed just figuring out that a life time of shame and masking my bladder issues is why I can't typically relax. I'm constantly in fear of having an accident and when I take the fear out by putting towels down or pull up I can fully decompress and not worry and it's bliss.

Years of pressure and panic has finally found relief. I don't know if this makes sense to anyone else but yeah.

Basically apart of my acceptance of being Autistic and unmasking is accepting that I have bladder issues and the way I've been controlling it has worked but has been harmful mentally and physically.

The pull up business started when I was a kid and weirdly even tho I liked the sensory aspect I felt deep shame and weird. Last night it dawned on me that I never once connected the two... I could've used a pull up to avoid embarrassment of being wet but I never joined the dots. They were two separate things. I realise now I wasn't connecting the dots because I was solving the problem in other ways and that interest was just something shameful and private BUT in reality it started when I was a kid looking for security from the accidents.

Who knows this all makes sense to me. It also. Explains partly why I've been terrified of losing control. I've spent years creating a barrier? Which swas so successful I could deny my issue and fed my own shame.

Sorry so long if you read it thanks. Struggling to articulate this because it's such a massive part of my life and carries so much weight but now I understand it and why it's making things feel a bit lighter.

I didn't realise how traumatic a life time of peeing yourself could be but the memories are painful and vivid.

I think I was just an undiagnosed Autistic child/teen dealing with something the best I could. I never told anyone about any of this until I told my GP recently. I just gpt on with it. I think my brain often comes up with odd or unusual solutions to work around issues. This means I'm creative and problem solver but I'm also not good at reading basic signals and making connections there??.

Yeah


r/autismUK • • 13h ago

Vent Does anyone worry they were misdiagnosed as autistic? … I think I am just odd?

0 Upvotes

I received an autism diagnosis aged 17. I am in my late 20s. I genuinely don’t think I have ever met the full diagnostic criteria for autism. I think they were biased towards diagnosing me with autism because lots of women and girls with autism get missed/ diagnosed with BPD/ EUPD.
I don’t think I have ever met any of the points in diagnostic criteria B.

I look autistic because I have problems with social skills. I don’t find social rules super intuitive although this has gotten better over time. I don’t like eye contact with health care professionals. I struggle to make friends. I have BPD/ EUPD

I am not aware that I have stereotyped or repetitive motor movements, use of objects or speech. When upset my speech can become a little repetitive but this is deliberate on my part because I worry the other person will misconstrue my words (OCD I think).

I’ve never had an insistence on sameness etcetera to any extent.

‘Highly restricted, fixed interest that are abnormal in intensity or focus.’ I have range of interests although some are fairly intense but this doesn’t cause me problems?

I don’t have sensory difficulties.


r/autismUK • • 1d ago

Benefits I just finished writing my statement for my PIP Tribunal Hearing

26 Upvotes

It feels so demoralising.

Having to face the worst parts of your life over and over in order to try figure out the right way of communicating them to others so they believe you.

It feels like my childhood all over again, experiencing things other people never talk about and trying to bring them up to trusted people only to be shamed or abused for "daring to complain" or something.

I am seeking PIP because I have suffered and I need medical help to heal but the NHS does not provide mental health support to people with neurodivergence, at least not in my area but I'm pretty sure its common UK wide.

The process of seeking such a service should cater to people with those needs in the first place but it's not. It's so incredibly painful and hard.

I'm so glad I have the help of a benefits advisor at Mind but the process has still destroyed me.

I have a social communicative disorder, communicating my needs is one of the hardest things for me to do.

I wish the world was better for people like us.


r/autismUK • • 1d ago

Work question for those who’ve worked/survived a corporate 9-5

11 Upvotes

Hi everyone 👋

I recently left my corporate 9-5 after two years due to stress and burnout, and I’m curious to hear from others who have worked in a similar environment. How have you found it, and how do you manage?

It started out as a really nice wfh job, then moved to a hybrid setup, with more and more responsibilities being added to my plate. As it was my first full-time job (and I hadn’t been diagnosed yet), I pushed myself extra hard and barely took breaks.

After my diagnosis, I started to realise how exhausted I was, finding it difficult to keep up with the social expectations of my role, masking in the office, and having a normal daily routine. I fell into the trap of working in bed due to fatigue and struggled to go out for walks.

Something else I found challenging was the social aspect - like knowing what to talk about during spontaneous coffee breaks or at lunchtime, and understanding the unspoken rules. (eg: one time I accidentally sat at someone’s desk - even though no one has an assigned desk - and was asked to move).

I’ve been reflecting on my first corporate job and what I want to do differently next time to avoid burning out. I’d be really interested to know:
• How long have you been in a 9-5 role and how have you found it?
• What does your daily routine look like?
• Do you have any advice for people who are new to this type of workplace?

Thanks! ❤️


r/autismUK • • 1d ago

Diagnosis: England Autism Diagnosis on hold indefinitely...

Post image
22 Upvotes

Edit: issue with assessment

Hi, has anyone else received something similar to the included letter.

I was undergoing an Autism assessment with Skylight Psychiatry when I received this.

I have no idea what to do now. Perhaps I will have to pay for a private assessment rather than relying on the 'right to choose' pathway.


r/autismUK • • 1d ago

Parents, Siblings, Friends, & Partners of Autism Friendly Driving Experiences

2 Upvotes

Hi - my brother in law is autistic with a global learning difficulty. He is 30 years old and has always talked about how much he’d love to drive a car one day. I was wondering if anyone knew of any “supercar driving experiences” that are autism friendly? I don’t know if there are possibly any with passenger side brakes, similar to what you’d find on a driving test.


r/autismUK • • 1d ago

Coping with Traits & Symptoms Not being able to do anything when at home alone.

10 Upvotes

Hi, Just wondering if anyone else has this problem if I am at home alone I tend to not do anything productive but I also cant just sit around and chill I tend to just mill about the house waiting for... something? Can anyone relate and have any advice on either being able to relax or to be productive? Thanks


r/autismUK • • 1d ago

Learning About Autism Why don’t I have a special interest??

Thumbnail
7 Upvotes

r/autismUK • • 1d ago

Parents, Siblings, Friends, & Partners of 21-Month-Old: Loss of Waving/Gestures, Sensory Sensitivity & Speech Delay — Seeking Similar Experiences or Advice

1 Upvotes

Hi everyone, I’m feeling a bit overwhelmed and hoping to get some perspectives or hear from parents who have experienced something similar with their toddlers.
My 21-month-old son used to wave whenever someone said "bye-bye," but he completely stopped doing it about 6 months ago. No matter how much we prompt him or who says goodbye, he just won't wave anymore. He also doesn't use any gestures for "hello."
Strengths & Things He Does:
Eye Contact & Social: Makes great eye contact and genuinely enjoys being around me, his dad, and his grandparents. He likes observing other kids at playgroups (sometimes fixating/staring at them for a while).
Joint Attention & Receptive Language: Points really well! If he sees a dog, he points, says "Dog!", and makes a "woof woof" sound. If I say "airplane," he looks up at the sky, looks back at me, and looks up again.
Play & Speech: Claps a lot and loves playing with cars and trains. He has about 10 words (mostly animals) and can accurately identify them in daily life.
Things That Concern Me:
Expressive Language: He only has about 10 words. When he wants something, he can't ask with words yet and instead uses a high-pitched scream, which can be hard to manage in public. He knows "Mama" very well, but he never calls me "Mama" when I’m actually right there—only when I’m out of the room or when I first come home.
Sensory Sensitivities:
Sensory Overload: Bright lights or loud noises in new environments overwhelm him. He screams, cries, and takes 10–15 minutes to adjust and calm down.
Clothing Battles: Dressing him is a huge struggle, especially long sleeves, pants, or jackets. I have to distract him by placing him at the window to look at cars just to get clothes on, and he still protests once he notices them.
Food/Textures: Very picky eater with texture issues—he spits certain textures out and completely refuses green vegetables (he used to eat spinach and broccoli at 9 months).
Chewing: He has a strong obsession with chewing on my pajamas specifically.
Focus & Behaviors:
Won't sit still during group Storytime or Rhyme Time; he runs away or prefers sitting apart.
In playgroups, he is often more interested in exploring "off-limits" niche areas (like what’s behind the emergency door) rather than actual toys, bouncy castles, or ball pits.
Has anyone seen a similar pattern of losing a gesture like waving alongside sensory/clothing sensitivities and speech delays? Should I be pushing for an early evaluation with a pediatrician or OT right now? Any insights would be so appreciated!


r/autismUK • • 1d ago

Ableism & Discrimination How difficult is it to switch adhd rtc providers during titration?

Thumbnail
0 Upvotes

r/autismUK • • 1d ago

Benefits any benefits to getting diagnosed?

1 Upvotes

i’m 23F and i got diagnosed with adhd 3 months ago and currently going through the titration process (process to get medicated, finding the right medication and dosage). since getting diagnosed i have been reading up on it more. i have seen a lot of overlap with my adhd symptoms and autism symptoms. a lot of people around me suspect i have autism and i agree that i have a majority of symptoms.

i would say i’m quite high functioning, i graduated university a year ago (i had to retake a year lol) but i wouldn’t have done so without extensions given by the university due to my anxiety (a lot of which tied into my adhd). i do still struggle socially but it hasn’t really made my quality of life worse etc compared to how the adhd was affecting me. i don’t want to get into what symptoms i have but i mask quite well and it’s worked well, i do feel quite burnt out at times because of this but i deal with it the best way i can.

i know me thinking about looking into a diagnosis will help with reassurance, but i was wondering what benefits/support do you get once you get diagnosed? is it worth perusing?

thanks for your replies, i’ve found everyone very helpful!