University attendance monitoring apps spark controversy amid surveillance and deportation fears
Concerns are growing across UK university campuses that mobile phone apps used to record attendance could be used in surveillance and to potentially even wrongfully deport international students.
Since Covid, universities have increasingly adopted mobile phone software that students must download, allow to track their location, and use to mark their own attendance by entering a one-time code when they arrive at class.
One of the main reasons that universities introduce these digital check-in apps is to prove to the Home Office that international students are at university, and to report people to immigration authorities if they are not.
Some students and staff at universities that have adopted these apps are worried that they could put international students at risk of wrongful deportation.
Dr Lucy Mayblin, a political sociologist at the University of Sheffield and expert on UK migration, said: “International students are in an Orwellian situation. The idea that these apps are impervious to human flaws is a complete myth. The apps are just a faceless computer. Students are getting trapped in the system which doesn’t care and is oriented to deporting them.”
Student deportations based on bad data have happened before. After a BBC Panorama documentary in 2014 which revealed cheating by some international students in English language tests, thousands of them were wrongfully accused and forced to leave the country. There are fears it could happen again.
“The stakes are really high for international students,” said Dr Mayblin.
The pressure is also intense on universities to provide data to the Home Office, because they risk losing their visa license to sponsor international students if they fail to keep up with Home Office requirements. The consequences of losing sponsorship status would be dire for universities, who are financially dependent on international tuition to balance the books.
The University of Sheffield is one of the many schools that have started using an attendance app to streamline their reporting to the Home Office.
Andy Winter, Director of Student Support Services at the University of Sheffield, said: “We launched a digital check-in tool to make recording student attendance faster, easier and more consistent across the University.”
Universities say that these apps also make it easier to identify students who may be struggling with their coursework and might need extra support.
In January, the university started requiring both UK and international students to check-in to class on iSheffield, an app which uses software licensed from Israeli company Ex Libris.
If location tracking on students' phones is set to 'always', Ex Libris is able record and store data on the whereabouts of them everywhere they go. Ex Libris operates attendance apps for at least 11 UK universities, and is only one of several companies providing similar services across the country.
For some international students, the new app is making them feel even less welcome in the country than they already do.
“I don’t feel like a human being, I feel like a number. Why can I be tracked 24/7 by my university?” said Jonas, an international student at the University of Sheffield. Jonas, who is gay and from the Middle East, asked to use a pseudonym for protection from anti-LGBT discrimination in his home country.
He said: “The fact that my university, who is supposed to help students find their voices, is instead tracking us… That says a lot.”
Student activists at the University of Bristol and Goldsmiths, University of London, have recently staged boycotts against the check-in apps at their schools. “The controlling and monitoring of our locations is fundamentally an affront to our freedom of movement as well as a threat to our privacy,” said Student Action Bristol.
The University of Sheffield has told staff that it will not use the geolocation data for anything other than check-in verification. Rachel Scheer, a spokesperson for Clarivate, the parent company of Ex Libris, said: "All Clarivate products operate strict data security protocols and the data within our apps is only available to the university or institution who licensed the app.”
Some staff, however, continue to question if this is the case for international students. Dr Annapurna Menon, an associate lecturer in Politics and International Relations, said: “We don’t want to be complicit in deporting our own students. We haven’t gotten any assurance from the university that if the Home Office demands specific location data, will the university refuse? We are educators, we are not the police.”
A wide variety of technical issues are also causing distress for international students struggling to get their attendance recorded accurately. Like many students at the university, Jonas regularly struggles with technical problems: “What if my phone is dead and I turned up to lecture? Multiple times I would be in a building with no service and I wouldn’t be able to check in.
“The reports that we’ve gotten from students is that the app is really fallible,” said Colombian international student Maria Jose Lourido, education officer at the University of Sheffield Students Union.
“A lot of students say that lecturers are not putting up the attendance codes, that the app is not properly tracking them when they’re in the room, that the codes are not working, that the app is slow. The university cannot come in and make sure the internet across campus is excellent, so where the internet is not strong, it will fail.”
Mr Winter said the university is attempting to resolve the issues: “The option to be checked-in by a lecturer also remains for anyone who experiences any difficulties or cannot access the app.”
Ms Jose Lourido says that isn’t a solution: “When the university tells international students that they have to register their attendance or they’ll have immigration problems, the students have to spend 15 minutes, when they have class, saying to the lecturer 'please, I’m trying to log on but it’s not working’.”
Despite the issues with the attendance taking app, teachers and students interviewed for this article all agreed that some form of attendance taking is a good thing.
Imad Tak, an international master’s student studying data analytics, sees benefits to the app: “People are forced to come to the classes, and it’s good to have students in lectures.”
Many suggested alternative ways to take attendance. Most of the people interviewed for this article prefer a system where students would scan their ID cards at card readers installed in classrooms, which would reduce technical issues and prevent universities from giving location data to outside companies. “We have university ID cards – why are we not using ID cards when we already have them?” said Ms Jose Lourido.
Dr Menon, who teaches classes in the politics department said: “We already were able to catch if students were falling through the cracks with our earlier attendance system when teachers recorded attendance manually. We could go back to that.”
The Home Office’s student visa sponsorship guidelines do not actually require universities to report attendance, only to prove that they have a “a single academic engagement policy that applies consistently” to all students. This could include data showing any combination of proof that students are submitting coursework, doing research or laboratory work, and attending classes.
Mr Tak suggested a big rethink for universities trying to maintain their visa sponsorship status: “Rather than focusing on student attendance, universities could focus on our grades.”
Labour to hold Mosborough, says source
Labour source says Tony Downing has kept his seat in Mosborough, a ward the party was very anxious about losing, which was very closely contested last time and they were worried the area would swing to the Liberal Democrats.
National snapshot
As we await first result from Sheffield and Barnsley, here's a quick look at the national picture.
38 out of 107 councils have been declared so far.
- Conservative: 125 seats, -142
- Labour: 351 seats, +65
- Liberal Democrats: 127 seats, +21
- Green: 28 seats, +15
- Independents: 67 seats, +41
Female footballers risking injury due to inadequate footwear
By James Harrop & Jack Roberts
A lack of female-specific football boots are forcing players to wear footwear designed for men and children, putting them at increased risk of serious injury.
Research has shown women on the pitch are between two to six times more likely to suffer ACL injures than male players and over 80 per cent of female footballers suffer discomfort on a regular basis, according to a study conducted for the European Club Association.
Ellie Doyle, who plays forward for Tranmere Rovers Women, in the North West Women's Regional League, injured her Anterior Cruciate Ligament (ACL) earlier this season.
She said: "I have to wear the kid's version of men's boots because they don't sell my size. They are probably not the best for my feet with the amount of times I wear them a week."
This week, 'Project ACL', a three-year research campaign, partly funded by the PFA and Nike, was launched. It aims to better understand the prominence of the injury in the women's game.
The study will focus on players in the Women's Super League, with the aim of reducing the number of ACL injures, which caused 37 players to miss the 2023 Women's World Cup, including England captain Leah Williamson.
Nim Fenton, who play for Hemsworth Miners Welfare Ladies FC, said: "It's quite expensive to buy women's boots.
"When it comes to women's kit there could be a better range, including football boots. You will only find certain boots from certain brands."
Some major football brands, such as Adidas and New Balance, currently do not sell boots specifically designed for women.
When contacted, Adidas said: "All our boots are tested to the highest standard with parity between men and women... and this ultimately means we are delivering boots that support all players on-pitch to play to the best of their ability."
Likewise, New Balance admitted to not currently producing football boots specifically for women.
Traditionally, all football boots are based on the dimensions of a generic white male foot, not accommodating for the subtle differences of women's feet, which have a higher arch and different heel shape.
IDA launched the first football boot designed exclusively for women in 2020, just before the COVID-19 pandemic temporarily halted sport across the world.
Evie Driscoll-King, defender for Peterborough United Women, said: "I have always just opted for men's boots because of the lack of choice in women's.
"I may wear them in the future, but they are very niche and very limited. Because of the nicheness of them they are very expensive."
IDA currently have five pairs of boots available, and these cost between £74.99 and £134.99.
“I had to translate for my parents at five-years-old”: the unique experience of children with deaf parents
Roanna Van Os can still remember the dread she felt as a little girl when she was asked to act as an interpreter for her deaf parents. It made her feel different from her friends and stand out, at a time when she was desperate to fit in. "School was dreadful," she says. "They always forgot to hire an interpreter for parents' evening. They would trust me to translate everything and all the kids in my year would stare at me. I'd feel embarrassed and then guilty for feeling embarrassed.”
The daughter of two deaf parents, Roanna, 23, from Bury, Manchester, was forced to start interpreting for her parents when she was five-years-old. “My parents made me feel loved and supported, it was my other peers that made my life more difficult. It was always conversations I didn’t understand and my dad would get upset that people wouldn’t give him enough respect by simply writing it down or making eye contact. In most situations, I had to translate because the person my parents were trying to speak to would just look at me and ask me to translate because they were uncomfortable. My dad would then get really upset and was often called aggressive,” she says.
“When I was younger, people would demand to speak on the phone and they didn’t like to hire interpreters a lot of the time. To this day, I still have phone anxiety."
It wasn't just interpreting that made Roanna stand out. As a child of deaf parents, she was not used to regulating her voice, so would often get told she was too loud. “At sleepovers my friends parents would say ‘tell Roanna we’re not deaf like her parents'.”
The graphic designer believes the lack of understanding of the deaf community contributes to the ignorance people with hearing loss face. British Sign Language (BSL), is a language in its own right, but differs in sentence structure compared to English, and has its own grammar, syntax and lexicons, explains Sign Health.
“English is not a first language for my parents, BSL is, so like many deaf people they struggle with reading and writing. My sister Megan, and I, have to look over texts, emails and letters for our parents,” says Roanna.
Josefa Mackinnon also has deaf parents and explained she too had far more responsibilities as a child which resulted in her feeling isolated from her peers and forced to grow up very quickly.
“From the age of seven, having to call the bank or call the doctors, has a huge impact on how you're brought up," she says. 'You're involved in adult worlds before you really should too. I remember feeling, at the age of 11, that I was kind of older than my parents; that I had to be responsible for them.”
Although Roanna, grew up feeling as if she was a carer for her parents, she says her unique childhood had many positive elements to it too. “I love being a child of a deaf adult (CODA) and I’m proud to have deaf parents. My dad is highly respected within the deaf community. He speaks publicly a lot, something I can’t even do and he does it so well. He knows two different kinds of sign language and has a lot of charisma.
“My mum has a gentleness and taught me and my sister, Megan, to always be empathetic, something that I think does come with her disability. They both taught us to love everyone when growing up. I feel lucky to have grown up as a CODA because I don’t think I’d have the same emotional understanding otherwise.
“My communication skills are definitely better, especially when I go on holiday. Sign language teaches you body language and it makes it easier speaking to people,” she explains.
Both Roanna and Megan attended a CODA camp, run by an organisation, which was set up 13 years ago, offering support, refuge and a network for children with deaf parents. It hosts an annual camp for seven to 17-year-olds where children can participate in fun activities with other children with similar lived experiences.
“Coda camp really changed my life," says Roanna. "At the time, I think I was 14 and I remember thinking 'Oh my God why are they making me do this as a teenager', but I had the most amazing time. I felt normal.”
Matthew Shrine, 34, CODA camp director, said: “It is the only national organisation representing solely children of deaf parents, where people can meet others with a shared experience.
“As a coda, you often have to filter yourself and as a kid you can feel misunderstood. I was called loud and abrasive growing up. But events like CODA allow me to be exactly that, and I realised oh wait I’m not odd.”
Mr Shrine, a therapist, also runs a CODA-specific therapy service to help those who find it difficult to share personal experiences with someone who doesn’t understand.
To find out more information about CODA go to https://www.codaukireland.co.uk/coda-camps
Turnout data for Barnsley
Total votes cast: 44967
Postal votes: 24129
Postal turnout: 53.6%
Total turnout: 24.14%
Compared to last year: down from last year by 0.56%
Last year votes: 45569
Total eligible electorate: 186249
Women less likely to be diagnosed due to ‘male bias’ of autism screening
Women with autism are finding it harder to get a diagnosis due to a male bias in the methods used, according to a psychology expert.
The ratio of autistic males to females is estimated at 3:1, but a "big gender disparity" and “disproportionate research funding” is causing problems with female diagnosis, says Dr Gray Atherton, a psychology researcher at the University of Plymouth.
There are 50 questions or statements in the Autism Spectrum Quotient (AQ) for adults which is used in screening and published by the Autism Research Centre in Cambridge. These include 'I am fascinated by numbers' and 'I don’t particularly enjoy reading fiction'. In the Autism Spectrum Screening Questionnaire for children, one question asks if you 'lack empathy'.
Yiqing Zhong, 27, a postgraduate student at University College London who got her autism diagnosis last year, believes the Autism Spectrum Quotient makes it more difficult for women to get a diagnosis.
She explained: “People will assume that autistic people are very sensitive to numbers or maths, but I’m not. I’m super insensitive to that. For a lot of autistic females, they may be more interested in art or literature.”
Ms Zhong added that she has relatively good social mimicry skills and strong empathy ability. She said: “So I was worried before I went to my GP. I was afraid that they wouldn’t believe me and wouldn’t refer me because I don't show the typical symptoms associated with autism or anything like that. I even made slides about my traits to convince them.”
“It's just so hard for women to get a diagnosis. Females and males present very differently in terms of autism, but autism scale development is actually still based on males, which women can’t fit into. This leads to more invisible autism in females.
“It is highly possible for women, especially women like me, who can find a job, who can succeed in their degree and who look like a normal person, to get refused by their GPs because they would think you’re not serious enough to get referred.
"This made it more difficult for autistic females to be understood and to be seen by society. Thus, it would make women feel more ashamed to express themselves and to justify their autism.”
'Standardised on largely male samples'
Dr Atherton suggested that many of the instruments used to diagnose autistic people were "standardised on largely male samples”.
She said: “There's a big gender disparity that a lot of people know about in autism. Males are much more likely to receive a diagnosis."
Dr Atherton believes that, in general, males are less likely to mask, and thus it is easier for them to be noticed and diagnosed with autism. Females are more likely to be taught from a very early age to mask their autistic traits.
“I was always told to be polite, be kind, be nice and be all of these very pro-social things as a little girl, that might make me hide certain aspects of myself that might not be accepted. Because of this disparity in the socialisation of males and females, people like parents, teachers and medical professionals are less likely to associate autism with females,” she said.
Dr Atherton also suggested that women who were diagnosed later in life reported higher levels of autistic traits based on her research.
“It was a lot harder for women to get diagnosed late in life because they didn't get that recognition earlier in their life. I think it has a tremendous impact on women. When they are missed for a diagnosis, it leads to a lot of stress, insecurity, and an increased risk of masking and camouflaging. These are really pressing issues.”
Disproportionate research funding in gender bias
The latest report from NHS announced that Small Business Research Initiative (SBRI) Healthcare has invested over £900,000 in research about autism and learning disability, but Dr Atherton suggested that there is not enough research funding for studying gender bias in autism.
She said: “In my experience as an autism researcher and being familiar with the funding landscape, I don’t think enough money goes to topics like this (gender disparity).
“I think that when you are competing for funding, and you present a topic like this (gender bias), it is a bit harder to get funding. In a sense, a lot of autism research money goes to other things."
Dr Atherton suggested that a significant amount of funding would go into topics like the genetic or biological basis of autism.
She added: “Considering what we do know about the proportion of money that goes to different topics within autism, not enough funding is going towards gender bias.”
“I think that we need to divert a lot more funding and research resources towards reducing the gender disparity in autism...including providing extracurricular opportunities for specifically autistic females," Dr Atherton added.
Labour seem “quietly assured” in Sheffield
Tom Hunt and Ben Miskell have been spotted at the count in Sheffield and seem to be "quietly assured", according to reporter Peter Spriggs.
Some wards have begun verify their results while the count continues throughout the day.
As the count continues, Labour is hoping to increase their hold over Sheffield.
Labour Group Organiser “hopeful”
Darfield councillor and Labour Group organiser Kevin Osborne told Sheffield Wire he is "hopeful" regarding today's results.
"There's always hope. Certainly what we're hearing on the doorstep is that there's a great regard for the 'new-style' Labour Party that we're seeing nationally.
"Before in previous elections, there was reference to the previous leader of the Labour Party and that detracts a little bit from local government.
"Thanks to what's happening nationally, we're getting a little bit of feedback locally."
Cllr Osborne won 50% of the vote in 2021.
‘The government doesn’t take it seriously’ says student waiting 660 days for autism diagnosis
A university student who asked his GP for an autism diagnosis two years ago is still waiting for a reply - despite an official target of people being seen by a specialist within 13 weeks.
Tony, 20, a second-year undergraduate animation student at Falmouth University, who asked Sheffield Wire not to use his surname, called his doctor in June 2022 but has not heard anything back.
He said: "I phoned them up, and explained why I thought that I should get done. But they just said we'll put you on the list without really asking any questions, and then they just hung up."
Tony had been wondering if he was autistic since he was 16 years old, after experiencing various autism traits.
He explained: “I'm really bad at keeping a regular healthy schedule. Because of how strongly motivated by mental stimulation I am, if I’m engrossed in something I find engaging. It can be difficult for me to stop, even to feed myself or sleep, which can be detrimental to my health."
Tony said he tried to eat two meals a day and sleep a decent amount of hours, but he found it “especially difficult to do so consistently”.
He said: “I often end up falling asleep between 4am and 6am on average. It is especially hard for me to try and have a healthy sleep schedule because unlike food I don’t really enjoy sleeping at all, which I don’t want to do. I’ve been without sleep for more than 39 hours.
“Because of my autism, I’m hyposensitive to a lot of physical sensations like hunger or tiredness, which means I can pretty easily stay awake and functional for 30 hours, or at least having slept only one or two hours or so, without using stimulants at all. This makes having an unhealthy sleep schedule exceedingly easy.”
While Tony was waiting, he developed a form of insomnia and missed several classes. His problems were also exacerbated due to living in student accommodation.
He said: “Being autistic makes a lot of social things really exhausting.
"The noise and parties also made it harder to try and sleep at a good time, and I would find it difficult to motivate myself to use my shared kitchen until late at night. I found trying to use it at the same time as my flatmates on a regular basis very distracting and sometimes stressful, which meant that I would eat very late, which would then cause me to sleep very late, and then I’d end up waking up later and later until I was waking up at around 7pm on average every day and missing all of my classes and I just couldn’t stop."
Tony failed the first year of his degree because of this.
He said: “I didn’t get much sunlight or talk to anyone in person for days and on occasion a week at a time. I would also not be able to buy groceries because everything would be shut by the time I was ready to leave my flat, so I would sometimes basically starve alone in my room for days which made doing my work even harder.”
After speaking to a counsellor last year, it was suggested he could be autistic. However, Tony said he could only afford the counselling for a few months because it cost £60 a week. He could also not afford to pay if he wanted to get a private autism assessment.
Tony said: “If I manage to get a diagnosis through the NHS, I can get free if I wait long enough, theoretically. If I had a diagnosis, I would be able to actually prove that I actually do have a reason for various things I struggle with, instead of just being incompetent, which is what people will assume if they don't know you.”
The newest data from the NHS revealed that 172,022 people were waiting for an autism assessment in December 2023 in England, which marks a 47% increase in the number of patients waiting compared to the previous year. Also, only 766 patients received a diagnosis in September 2023. This shows a 27.62% decrease in the number of patients receiving an autism diagnosis, compared to September 2022.
Tony said that the government should give more funding and more priority for autism.
He said: “I think they don't take it seriously, which is the case with most things to do with mental health.”
Data from the NHS shows that only 5.9% of patients can access the first appointment, while NICE (National Institute for Health and Care Excellence) suggests that patients should wait no longer than 13 weeks.
A spokesperson from the Department of Health and Social Care said: "We want every area to meet NICE guidance and the recommended waiting times but recognise that some people are waiting a long time for an assessment.
"We know it's vital to have a timely diagnosis of autism and we are taking action to reduce assessment delays. We’ve made £4.2 million available this year to improve care for autistic children and young people, including autism assessment services."
“Am I going mad?” – The misunderstanding for autistic people during the menopause
When Rose Matthews woke up in a police cell, they couldn't understand how they had got there and why their life felt as though it was spiralling out of control. After what they could only describe as a 'meltdown', Rose had been locked up and left to feel like a criminal, but unbeknown to them, their experience, as an autistic person, going through the perimenopause wasn't unusual.
A recent study co-authored by Rose, who is now a researcher specialising in autism, believe their unique profound and experiences going through the menopause, isn't experienced by non-autistic people. The report also revealed a lack of information and support, leading to a downward spiral of difficulty and distress leaving autistic people feeling like they couldn't cope.
Outwardly, Rose’s life had all the hallmarks of success. They were academically gifted as a child, had excelled at university, got married and had children but a different story lay behind these milestones. “I had to change jobs frequently," they say. "I was exhausted, confused and quite often abused. I burnt myself out doing a PhD, working two jobs and struggled with the demands of motherhood. My life became very disorderly, unpredictable. But somehow, against the odds, I managed to keep afloat, to keep working. I managed to survive.”
They now understand whey they were experiencing were autistic meltdowns - an intense response to an overwhelming situation when someone temporarily loses control of their behaviour. They can be expressed both verbally through shouting, screaming, crying or physically by kicking, lashing out, or biting.
Rose, now 64, from the North East, had an outburst two years before their diagnosis. They had warned their partner about the possibility, but when it happened it was a shock. “In not knowing what to do he did exactly the wrong thing, which was to try and get hold of me," says Rose.
“Afterwards he went and spoke to somebody who decided it could potentially be domestic abuse. He found himself being interviewed by the police as a potential victim, which he didn't feel he was, but that was the protocol. I was then arrested.”
Fortunately for Rose, the ordeal didn’t lead to anything more serious but it did make them book an appointment with their GP to try and understand why everything was out of control. The GP thought they were stressed from juggling a demanding job and prescribed antidepressants. It wasn’t until later when a former colleague was diagnosed with autism Rose realised the similarities.
“I'd always ruled out autism because stereotypical media portrayals didn't match me," says Rose. "I didn't see many adult women with an autism diagnosis or read anything about how it had affected their life. But, just before my 59th birthday, I found out I am in fact autistic. Contrary again to the sort of popular myth, I'm not just slightly autistic because it didn't get spotted. I'm 100% autistic. It's just I had learnt to adapt, accommodate, blend in, copy and use various other strategies to get by.”
Dr Rachel Moseley, 37, is principal academic in Psychology at Bournemouth University and co-authored the research alongside Rose and other academics. She says: “People are finding their worlds are absolutely rocked by menopause. Many of them don't have an autism diagnosis and what they're experiencing at menopause is so dramatic they can't read a description of normal menopause, they can't identify with that.
"So they're wondering what's wrong with me? Do I have some terrible disease? They're experiencing things that are dramatic and what we've seen across those studies is menopause seems to really exacerbate features of autism and ADHD.”
This means if you have difficulty regulating emotions or sensory sensitivity, as an autistic person, these can be exacerbated. Experts believe autistic people will have problems controlling their attention, with organisation and simply coping with everyday life. However, research shows each person's experience is different. People going through menopause now are also of a generation where it is unlikely they will have been diagnosed as children especially if assigned female at birth. Both Dr Moseley and Rose were diagnosed later in life as were the majority of participants in their study.
Despite more awareness, the Autistic Girls Network highlighted 80% of autistic girls remain undiagnosed at age 18. Until recently research has mostly focused on boys and Cathy Wassell, CEO of the charity, explained that assessment tools can still be very biased. “We think of behaviours such as lining up cars and trains, which is a generalisation of the ways boys play," she says.
“For girls, things like special interests and repetitive behaviours tend to be more as their peers would do. So they tend not to stick out as much. They tend to be more typical girl interests like art or horses, Harry Potter or K-pop, any of those kinds of things, it's just they're more intense."
Receiving a diagnosis has helped many autistic people but it is not the end of the journey by far. "I think there is a myth that you can have a production line, wheel people through, diagnose them and then they'll be fine," says Rose. "Well, actually, the real work starts after you get your diagnosis. It's a bit of an existential crisis to discover you've lived most of your life not knowing who you really were.
"Some people experience an awful lot of grief because they have missed out on opportunities they now recognize they might have had. I was fortunate in the sense I'd been married, I'd had children, I'd had a career, and I hadn't really been prevented from doing things I wanted to do. I often think had I got to the point of a diagnosis and those things haven't happened, how much harder it would have been to accept."
Dr Moseley emphasised there are many undiagnosed people with autism and ADHD. "They are likely to have difficulties flaring up at biopsychosocial transition points like menopause and puberty," she says. "So those are the times where undiagnosed neurodivergent people are going to be more visible.
"I think it's important for healthcare workers, if they have someone who struggles at menopause, and maybe they have a history of struggling in life, then it's really important to consider a possible diagnosis."
A website has been created for the research study mentioned and Dr Moseley has created a website which has information on autism and menopause. Additionally The Autistic Girls Network has lots of resources that can be accessed online.
The outlook in Sheffield
Here's the latest from Sheffield Wire reporter Peter Spriggs:
The count is underway in Sheffield and the ballot papers for the 28 contested wards are rapidly firing across the counting benches.
On what is already shaping up to be a triumphant round at the polls for Labour across the country, taking control of Sheffield council would be a huge political scalp for them and a formidable statement of intent to the Tories for the upcoming general election.
However, Labour have had the most seats in Sheffield for a while now, despite not having overall control. Resentments among the electorate over local issues such as the proposed traveller site in Beighton will have the Lib Dems fancying their chances to challenge Labour seats as the most likely rivals for control of Sheffield council.