
Symposium: Are we over-diagnosing mental health conditions?
Clockwise from top left: Lade Smith, Suzanne O'Sullivan, Minesh Patel, Joanna Moncrieff, Brian Dow
Britain is in the grip of a mental health reckoning. Once taboo, the language of anxiety, depression, trauma and neurodivergence is now part of everyday conversation. Public campaigns have encouraged us to speak openly about mental well-being. But as awareness has surged, so too has a thornier question: are we diagnosing too much, too readily?
In March, Health Secretary Wes Streeting argued that we are. 'Not every feeling of sadness is depression, not every feeling of worry is anxiety,' he said, warning that Britain is at risk of 'over-diagnosing' mental health conditions, especially in young people. His comments sparked fierce debate. Is the surge in diagnoses a long-overdue recognition of hidden suffering? Or are we at risk of medicalising life's ordinary struggles?
The numbers are striking. Demand for NHS mental health services has more than doubled since 2017. Yet questions are growing over whether those services – already overwhelmed – are being diverted from those in greatest need. Are we mistaking everyday emotions for clinical disorders? Or does broader diagnosis simply reflect how far we've come in confronting mental illness?
This is not just a clinical debate – it is a political one. The way we define and diagnose mental illness shapes the policies and resources that follow: whether that's school counselling budgets, workplace well-being schemes, GP referral pathways, or access to talking therapies. Over-diagnosis risks diluting resources and excessive medicalisation; under-diagnosing leaves silent suffering unaddressed. While one finds a range of views, even among our experts, there is one clear consensus: the system itself is in dire need of support.
Dr Lade Smith CBE, President, Royal College of Psychiatrists
It is no surprise that there has been an increase in mental illness diagnoses. Risk factors associated with mental ill-health – financial, housing and food insecurity, loneliness and isolation – have increased over the past decade.
We have seen a 20 per cent increase in the number of people classified as disabled because of anxiety and depression – both eminently treatable conditions, both driven by social determinants.
Subscribe to The New Statesman today from only £8.99 per month Subscribe
With earlier intervention and assertive treatment, anxiety and depression can get better within months – long before a person's condition deteriorates into disability. However, the number of people waiting for mental healthcare has grown by 29 per cent in the last two years and now stands at 1.6 million.
Moreover, severe mental illnesses, such as bipolar disorder and schizophrenia, are under-diagnosed or diagnosed far too late. This is particularly important for younger people, because 75 per cent of all mental health conditions arise before the age of 24.
With illnesses like bipolar disorder or schizophrenia, it can take up to ten years before people receive a diagnosis and treatment, significantly impacting them achieving their potential.
During this time of no diagnosis, their illness is likely to curtail their ability to complete education, function at work and form healthy relationships. They may even become homeless or come into contact with the criminal justice system.
It is essential that people with mental illness have access to an evidence-based comprehensive assessment from a trained psychiatrist or qualified mental health professional, which formulates their problem, clarifies their diagnosis and provides a package of care and treatment to enable that person to recover and have the best quality of life they can.
When misdiagnosis does occur, it is largely driven by people being left to diagnose themselves or being assessed by those with no or inadequate specialist skills and training. We must be careful not to encourage stigma and discrimination. People with mental illness are not 'fake sick'; the UK's productivity has not been undermined by over-diagnosis, but by poor access to timely and effective care.
The Darzi investigation noted that mental illness is 20 per cent of the disease burden in the UK but receives 10 per cent of health funding. The treatment gap created by chronic under-resourcing results in a failure to quickly ascertain who is ill and who is not, and to assertively treat those who actually need it.
Over-diagnosis is far less of an issue than lack of access to good-quality timely assessment and treatment by well-qualified mental health staff.
Dr Suzanne O'Sullivan, Consultant neurologist, University College London
Any discussion about over-diagnosis needs to start with a clarification of the meaning of the term. Over-diagnosis should never be read to imply a person is not struggling or in need of support. It simply asks if medicalising that suffering is the best way forward for them.
Mental health conditions don't come with biological markers, so nobody can truly identify the point at which psychological distress moves from being part of the normal human experience into being a medical concern. Therefore, over-diagnosis can only be recognised by looking at how the growing number of people with a mental health diagnosis are benefitting in the long term. If the diagnoses are appropriate, they should lead somewhere positive and allow an easier progression through life.
With that definition in mind, it feels impossible to say that mental health conditions are not over-diagnosed. Consider how the prevalence of autism has grown from affecting one in 2,500 children decades ago to more than one in 100 children today.
More inclusive diagnosis promised to improve long-term mental health and well-being for young people. And yet, mental health diagnoses in adults, particularly young adults, are also steadily growing. This is the very definition of over-diagnosis — more early diagnosis, but no downstream improvement in well-being. Worse, these statistics suggest that the growing population of young people diagnosed as neurodivergent may actually be faring worse in adulthood than any population that has gone before.
A medical label is not inert. It has a power all of its own to make people sick. When you tell a child that they have a neurodevelopmental condition, you risk encouraging that child to focus on what they cannot do. It could create the impression that the difficulties that child is experiencing cannot be overcome. You lower others' expectations for that child. The diagnosis can impact identity formation and become a self-fulfilling prophecy.
Diagnostic labels make social and psychological struggles seem set in stone, which gets in the way of an examination of life that might have a more lasting positive impact on well-being. A thirst for finding mental health diagnoses in milder forms and the growing number of mental health awareness campaigns risk pathologising ordinary differences and encouraging people to worry unduly about the natural highs and lows of mood.
We need to learn how to recognise and support struggling people, and children in particular, without medical labels because the current system is not working. Better lives for children, social change, is how you create healthier, happier adults.
Suzanne O'Sullivan is the author of 'The Age of Diagnosis: Sickness, Health and Why Medicine Has Gone Too Far'
Minesh Patel, Associate director, Mind
It's hard to imagine that if the rates of cancer screening and diagnosis went up through public campaigns encouraging people to be aware of symptoms, to not suffer in silence and to seek support, it would not be a cause for celebration.
But when it comes to mental health, that's where we are. And for many, it's treated as evidence that 'mental health culture has gone too far'. This is despite the fact that the threshold for a diagnosis hasn't changed.
Several senior politicians from across the spectrum have made the argument about over-diagnosis or self-diagnosis, or a variation of it, in the last year. But I think, especially when it comes to the interventions of politicians, it's important to consider the context in which the debate is taking place.
We are talking about a time of tight public finances, a rising welfare bill, and increasing numbers of people unable to work due to mental health problems. We are living in the shadow of a once-in-a-generation pandemic and cost-of-living crisis, both of which we know, from the people we speak to every day, have been substantial drivers of mental health problems.
There are 1.6 million people on mental health waiting lists, with those on low incomes experiencing some of the worst health outcomes. While it has become convenient, or in some cases politically expedient, to deny that the scale of rising mental health problems is real, such denials inevitably lead to policymakers not pursuing a proper appreciation of what might be driving such rises. This increases the burden on both the healthcare system and patients, as the earlier the intervention, the more treatable these issues become.
Our starting point has to be one of understanding the factors behind increasing levels of poor mental health and addressing the delays in people getting support. The solution certainly does not lie in making claims about over-diagnosis, which have little evidence to support them. This is especially the case when many of the people experiencing poor mental health are already facing the sharpest impacts of poverty and will be those hit hardest by proposed welfare cuts.
It's clear we still have a long way to go when it comes to equal treatment of physical and mental health, a point made more real by the proportion of the NHS budget going to mental health falling next year. What's needed now is a conversation that is careful not to stigmatise people's real experiences and does not undermine the expertise of medical professionals. It must instead focus on how we can best create a mentally healthier society – one where fewer people experience poor mental health in the first place.
Joanna Moncrieff, Professor of critical and social psychiatry, UCL, and NHS psychiatrist
With the increasing diagnosis of mental health problems, we are medicalising a variety of human situations that are not medical problems. This has negative consequences for individuals and for society.
Diagnosis is a medical activity. It implies that people have an underlying biological abnormality that is the cause of their symptoms. This is not the case with mental health problems. When someone is diagnosed with depression, anxiety or ADHD, this is simply a description of their problems. It is a label. It is not an explanation. It does not mean there is an underlying biological deficiency.
The widespread belief that depression is due to a chemical imbalance has never been demonstrated, for example, and biological mechanisms have not been established for any other mental health condition. As a result, the process of making a mental health diagnosis is highly subjective. It depends on the beliefs and circumstances of the individual doctor and patient, and it is influenced by general social and economic conditions.
Yet, giving people a mental health diagnosis creates the impression that there is an underlying biological problem. This is harmful because it results in people feeling pessimistic and powerless to change anything. It can lead people to limit themselves. It also results in unnecessary exposure to medical interventions, such as antidepressants. Despite being widely used, there is little evidence that antidepressants are helpful, and plenty of evidence that they can have serious adverse effects.
Moreover, giving people a diagnosis risks overlooking the real problems. It focuses everyone's attention on the symptoms of the condition, rather than the problems that caused them originally. Overwhelmingly, these problems are social, such as poverty, unemployment, relationship problems, loneliness and lack of meaning.
Diagnosing the understandable consequences of these features of our society as medical conditions inhibits social change. It enables politicians to ignore the inequality, insecurity and social fragmentation that have resulted from neoliberal political and economic policies, and which cause so much misery and stress.
In the short term, medicalisation provides financial security for some through the benefits system, but this could be (and in some cases is) done differently, on the basis of need. In the long term, medicalisation perpetuates the system that is causing our mental health crisis in the first place.
Joanna Moncrieff is the author of 'Chemically Imbalanced: The Making and Unmaking of the Serotonin Myth'
Brian Dow, Deputy chief executive, Rethink Mental Illness
There is lots of talk about the over-diagnosis of mental health conditions. But for most people living with mental illness, the reality is often a struggle for a timely diagnosis and access to the right treatment.
Our charity's research found the majority don't receive support quickly enough, with four in five experiencing a deterioration in their mental health while they waited. The consequences are serious: crisis, suicide attempts and lost livelihoods.
Of course, as in any area of medicine, misdiagnoses do occur. Some people in recovery may come to feel that a diagnosis no longer serves them. And yes, we should be doing much more to prevent people from falling out of education or work, rather than simply writing them off.
On the other hand, a diagnosis is often the only way to access life-saving support. And we don't suggest that cancer awareness-raising campaigns are problematic because most people who get checked won't have cancer. Quite the opposite: we encourage people to seek help, knowing that early intervention saves lives. So why discourage the same approach for mental illness, when the effects can be just as devastating?
This is a complex issue that requires nuance, not oversimplification. Right now, there's no compelling evidence of over-diagnosis, but there is ample evidence of a rising tide of mental distress and under-resourced services failing to meet demand. Recent research from the Institute for Fiscal Studies shows that mental health difficulties, particularly among young people, are increasing.
Mental illness has never reached parity with physical health in either investment or priority. Our analysis of NHS data shows someone is eight times more likely to wait over 18 months for mental health treatment than for physical healthcare. The government's target for 92 per cent of patients to start treatment within 18 weeks does not currently include any commitment to tackling waits for mental health services. Against this backdrop, we must be extremely cautious we don't deter people from seeking help. We also need to do more to tackle the drivers of poor mental health, especially given that mental illness often begins young and becomes entrenched without support. That means investing in school-based support, housing, tackling poverty and reducing isolation. This is not soft policy; it's a pragmatic way to reduce pressure on an already overburdened system.
While different conditions require different responses, all mental illness, from mild to severe, is distressing to the individual. What matters is delivering the right support, in the right place, at the right time.
The question isn't whether we're over-diagnosing. It's whether we're doing enough to help.
Related

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Daily Record
an hour ago
- Daily Record
Rutherglen MSP welcomes £6.6 million of funding to reduce waiting times in Lanarkshire
This investment is part of the Scottish Government's £200 million commitment in the Programme for Government to increase NHS capacity, reduce delayed discharge, and improve the flow of patients through hospitals. Rutherglen MSP Clare Haughey has welcomed the Scottish Government's announcement of £6.6 million of targeted funding to reduce waiting times in Lanarkshire, as part of £106 million new investment across NHS Scotland. This investment is part of the Scottish Government's £200 million commitment in the Programme for Government to increase NHS capacity, reduce delayed discharge, and improve the flow of patients through hospitals. Ms Haughey said: 'This is another clear example of our SNP Government delivering for our NHS, with real action to cut waiting times and get patients in South Lanarkshire the care they need faster. 'By focusing funding where it's needed most, like orthopaedics, cancer, and diagnostics, we're helping tackle the longest delays head-on. 'This will mean quicker, diagnoses, more procedures, and better outcomes for people in South Lanarkshire. 'South Lanarkshire communities deserve timely access to care, and this SNP Government is making the investment to deliver that. While we know some people have to wait too long for treatment, the SNP is getting on with the job of driving improvements for patients.' *Don't miss the latest headlines from around Lanarkshire. Sign up to our newsletters here.


The Independent
2 hours ago
- The Independent
What we know about the new NHS cervical screening guidelines
New NHS guidelines in England will invite women aged 25-49 with negative HPV tests to cervical screenings every five years instead of every three, starting next month. The change follows recommendations from the UK National Screening Committee and aligns England's screening intervals with those of Wales and Scotland. Analysis from King's College London indicates that extending the screening interval to five years for HPV-negative women maintains a similar rate of cancer detection as the current three-year interval. Health Minister Ashley Dalton stated the change aims to increase testing opportunities for women with HPV while extending screening intervals for those with negative tests, emphasising early detection and treatment. Experts encourage women to attend screenings when invited, with the NHS implementing measures like phone reminders to improve participation, while Cancer Research UK highlights the impact of screening and HPV vaccination on reducing cervical cancer rates.


Daily Mirror
2 hours ago
- Daily Mirror
‘People thought I was nine months pregnant - it was a giant ovarian cyst'
WARNING: DISTRESSING CONTENT Robyn McGhee, 28, went to the doctors after people mistakenly thought she was pregnant - and discovered she had a giant ovarian cyst that made it hard for her to walk In February 2024, Robyn McGhee noticed that she was gaining weight. However, with Christmas and New Year 's just gone, she put it down to overindulging over the festive period and resolved to hit the gym and cut back. 'I spent a few months eating healthy and trying to lose weight but the weight wasn't shifting, I was actually getting bigger,' she said. 'I could physically see it, it wasn't all in my head.' Then the tiredness came, and the pressure she felt to lose the weight intensified - worsened by the fact that strangers on the street were asking her when she was due to give birth. The 28-year-old from Glasgow told The Mirror: 'I just had to say 'no I'm not pregnant' and just leave so they didn't feel awkward. It kind of highlighted how extreme my stomach actually looked.' Looking back at the pictures now, Robyn said, it's hard to feel angry at the people who presumed she was pregnant. 'I looked about eight or nine months pregnant, the weight had shot up. But I couldn't eat at all, I'd lost my appetite." At one point, despite knowing she wasn't, Robyn thought: 'Maybe I am pregnant, maybe that's what is going on and I just don't have the usual symptoms that you would expect.' None of her clothes would fit, she couldn't go out, and was struggling to walk. After returning from a holiday in June during which she didn't feel like herself, Robyn decided it was time to see a doctor. 'At that point, I could feel a ball in my stomach and it was causing a lot of pain. I went to the doctor and explained my symptoms and they off the bat said 'are you pregnant',' she said. 'I knew I wasn't, I'd taken a few pregnancy tests.' Robyn added: 'I felt like I was getting dismissed by the doctor, I explained my symptoms and said I was worried it was something more than weight gain and they said 'like what?' I thought, 'I don't know, that's why I'm here'.' After getting a second opinion, Robyn was referred for urgent CT scans and blood work, which was when they found the cyst. It was about 25cm and weighed more than a stone. The NHS describes an ovarian cyst as a fluid-filled sac that develops on an ovary. Symptoms can include pelvic pain, heavy or irregular periods, a swollen tummy, pain during sex, a frequent need to urinate, and feeling full after only eating a little. Despite knowing an operation was imminent, Robyn felt that she could finally breathe. 'I was relieved, because I had an answer for why I was feeling this way. It was confirming that it wasn't all in my head, it was actually happening to me.' In September, Robyn underwent a three-hour operation. While keyhole surgery is usually used for cysts, the size of Robyn's meant that open surgery was the only option for her, and she now has a large scar down the centre of her stomach. But there was another surprise in store when surgeons found that she had endometriosis as well - which is a disease in which tissue on the inside of the uterus grows outside of it. According to Endometriosis UK, 10% of women (176 million) worldwide have endometriosis, which can cause severe period pain, heavy periods, and pain when going to the toilet. 'I thought my period symptoms were normal, the pains and cramps I had were the type that everybody had,' she said. Doctors removed the cyst, along with one of Robyn's ovaries and fallopian tubes, and her appendix. The recovery took about 12 weeks and the first part was 'really tough' with 'ridiculous' amounts of pain. 'I also felt a lot lighter, obviously,' she said. Taking her experience to social media was her next step, and the decision to open up came from the lack of stories or resources on the topic out there, she said. 'I was trying to research the type of surgery I was getting online and on TikTok but there wasn't that much about it. I thought 'I don't have any reference point of anybody going through a similar situation to what I am'.' Since posting her story on her TikTok page (@_robynmcghee), Robyn has had messages from people all over the world. 'It's been wild, I feel like I have helped people', she explained. While the operation was 'absolutely terrifying', she insists to others going through the same thing that it was 'better than any other outcome'.