Unlocking the 5%: A Strategy to get Britain Moving
George Holt |
Published 21 January 2026
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George Holt |
Published 21 January 2026
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Columns are the author’s own opinion and do not necessarily reflect the views of Onward.
Wasted potential is a phrase often used about the state of the UK. Sadly, it also applies to many of our students and working-age adults.
At the heart of our social contract is an understanding that if people put in the effort – in the classroom, in the workplace, and in their communities, society will give them the chance to succeed. Too often, that promise is not kept. For those with Attention Deficit Hyperactivity Disorder (ADHD), the gap between potential and opportunity is especially stark.
Attention Deficit Hyperactivity Disorder (ADHD) is thought to affect around 5% of children and between 3-4% of adults in this country. Yet, because diagnosis varies so much depending on where you live, the real figure is hard to pin down. This paper looks at how ADHD has been understood over time, how it is recognised today, recent political developments, the rise of self-diagnosis, and the debate over recognition. It also sets out a national ADHD Strategy with practical policy measures. The aim is simple: if we tackle ADHD earlier and more effectively, and focus on giving people a hand up rather than a hand-out, we can unlock huge amounts of educational, economic and social potential.
Although ADHD has been recognised here for more than two decades, public understanding still falls short. For years, children and adults showing signs of ADHD were dismissed as lazy or disruptive, which left them stigmatised and without proper support. Those old misconceptions are one of the reasons the condition remains so underdiagnosed.
In recent years, there has been a sharp rise in ADHD diagnoses, especially among adults. Greater awareness and reduced stigma around mental health have both played a part. The downside is that demand for assessments has outstripped the NHS’s capacity, leading to long waits and patchy access across different regions. Politically, there is a case for building on existing frameworks, such as the Autism Act, so that ADHD and other neurodiverse conditions are properly covered and supported.
The rise in diagnoses has also triggered debate. Some worry that the criteria are being stretched so far that everyday behaviour risks being medicalised. Others argue the figures show that a condition neglected for too long is finally being taken seriously. Either way you choose to look at it, accurate identification and tailored support remain vital.
Concerns have also been raised about private ADHD clinics, some of which offer snap diagnoses after brief online assessments. These practices exploit vulnerable people and damage the credibility of all diagnoses, making robust regulation essential.
Social media has added a layer of complexity. On one hand, people sharing their experiences online has helped encourage others to seek help. On the other hand, it has fuelled self-diagnosis based on half-truths. While personal stories can be powerful, they are no substitute for professional expertise. If left unchecked, this trend will trivialise ADHD and pile extra pressure onto challenged services.
For all the obstacles, people with ADHD bring remarkable strengths. Their creativity, drive and fresh perspectives can be invaluable in classrooms, workplaces and communities alike. Yet time and again, those talents go to waste because of the barriers built into our systems and attitudes. If we are serious about honouring the social contract, making sure effort and ability are matched by opportunity. Then we cannot afford to leave this potential untapped. Giving neurodiverse people the tools to thrive would not only make society fairer, but it would also help get the UK economy moving by putting their skills to work where they are needed most.
In the early 20th century, what we now call ADHD was barely understood. Children who struggled to sit still, focus, or control their impulses were too often dismissed as troublemakers. Teachers complained, parents were blamed, and the children themselves carried the weight of being seen as lazy or unruly.
Nobody thought to look deeper.
Doctors weren’t much different. For decades, there was doubt, even within medicine, over whether ADHD was a real condition at all. This scepticism meant countless people went without the help they needed. Many left school with few qualifications, struggled to hold down work, and ended up on the margins of society. A wasted generation – not through lack of talent, but through lack of understanding.
Things began to change at the turn of the millennium. In 2000, NICE (National Institute for Health and Care Excellence) published its first guidelines confirming ADHD as a genuine medical condition. Eight years later, those guidelines were extended to adults, underlining that ADHD doesn’t just disappear when childhood ends. Schools followed suit, adding ADHD to the list of recognised special educational needs. Teachers received training, and children were offered support. Yet too often that support was framed around what they couldn’t do, rather than what their condition might enable them to achieve.
Outside government, progress was pushed by individuals and charities. Dr Geoffrey Kewley raised awareness in clinics, while campaign groups gave parents somewhere to turn when the system fell short. Over time, public attitudes shifted. Awareness campaigns, media coverage, and later social media all played their part. Stories from real people cut through stereotypes and showed that ADHD could affect anyone – not just “naughty boys” in the classroom.
But new problems came with this visibility. TikTok and other platforms have made ADHD a trend, with quick-fire videos encouraging people to self-diagnose on shaky evidence. While some are nudged towards proper help, others convince themselves they have the condition without ever seeing a professional. That risks trivialising ADHD and adds pressure to a system already stretched.
And stretched it is. NHS waiting lists for ADHD assessments run into years in some parts of the country. Many turn to private clinics, but standards there vary wildly. A BBC Panorama investigation found cases where people were diagnosed after online calls lasting less than an hour. One reporter, with no ADHD symptoms, received three separate diagnoses and was offered medication each time. That kind of practice not only exploits vulnerable people, but it also undermines confidence in genuine diagnoses.
The bigger picture is this: Britain cannot afford to keep sidelining people with ADHD. When our social contract works, it is simple – those who want to contribute should be given a fair chance to do so. Right now, too many with ADHD are locked out of education, shut out of work, or left dependent on benefits.
That isn’t just unfair to them, it’s a drag on the economy.
We need people in jobs, not parked on waiting lists or written off as NEETs. With the right support, those with ADHD can be innovative, creative and highly productive. Unlocking that potential would strengthen the workforce, reduce dependency on welfare, and give the UK economy a boost it desperately needs.
In the last few years, more and more people have been diagnosing themselves with ADHD. Part of the reason is frustration with NHS waiting lists, but the other part is the sheer amount of content available online. Anyone can take a short quiz or watch a few videos and be sure they “must” have ADHD with just a few clicks. For some, this is when they start looking for real help. But for a lot of other people, it’s the end of the road, and that’s where the danger lies.
The problem is that these online tests and videos focus on broad and very human traits, such as having trouble concentrating, feeling restless, and having trouble meeting deadlines. Who doesn’t go through these things?
It’s easy to see how a teen who watches TikTok could see themselves in a sixty-second video and think they have a problem. But without a proper medical evaluation, it’s just a guess.
This trend is most obvious among teens and young adults. TikTok, Instagram, and YouTube all make short, eye-catching videos that show ADHD as a set of strange but relatable habits. Algorithms then show viewers more of the same, making echo chambers where doubts are drowned out and subtlety is lost. What starts as raising awareness quickly turns into false information. The more one watches, the more one thinks they “fit the mould.”
The results are not small. Some teens and young adults stop engaging with education and the workplace because they think their “ADHD” makes it pointless. Some people leave the job market before they even get there, believing that a label – often one they give themselves and can’t prove – explains and excuses their lack of success. This is a worrying trend in a country that already has a lot of NEETs and people who have been dependent on welfare for a considerable time. People feel validated in their struggles, but society loses out when their potential contribution is never realised.
There is now a profitable business based on this trend of self-diagnosis. Online clinics give quick evaluations, sometimes in less than an hour, and give out labels and medication without much thought. People who need clarity or a sense of belonging end up paying the price, both in money and in their personal lives. Even worse, these actions make people less sure of real diagnoses and make people who have gone through the right channels look suspicious.
There are also real risks to your health. If you say you have ADHD when you really have depression, anxiety, autism, or something else, you might miss it. Some people use stimulants that aren’t prescribed to them to “treat” a disorder they might not even have. Instead of making it easier for people to get jobs and go to school, this cycle can keep them dependent, making the problems they were trying to explain even worse.
It’s good that people are becoming more aware of ADHD, since stigma has kept too many people from getting help for too long. But awareness without accuracy is a false economy. If the UK really wants to help people keep their end of the social contract, public campaigns need to change their focus. They should promote accurate clinical evaluation, emphasise the dangers of self-diagnosis, and clarify that ADHD does not merely signify common distraction.
This is important for more than just health outcomes. The goal is to get people into jobs, training, and roles where they can help instead of just watching. It’s not about letting people off the hook for their long-term dependence on benefits. Most importantly, it’s about making sure that people who really have ADHD get the help they need and keeping others from being misled by false information. We need to cut through the noise on social media if we want to rebuild trust in our health system and get Britain working again.
Over the past 20 years, ADHD has gained more recognition in UK health and education policies. ADHD is increasingly being covered under Special Educational Needs and Disabilities (SEND) provisions, with schools taking the lead in this development. Individualised support for children with ADHD must be provided by schools, including classroom modifications and the creation of Individual Education Plans (IEPs). Although there has been noticeable progress, regional variations in implementation remain. Some schools lack the tools and expertise necessary to offer successful interventions.
In order to bring about political change for ADHD, advocacy groups have been crucial. battling stigma and advocating for legislative changes. Their work has demonstrated the need to increase funding for mental health support, facilitate access to diagnostic services, and discuss ADHD as part of a broader disability rights discourse.
The effects of ADHD have drawn the attention of all of the UK’s major political parties, but their approaches to solving the problem differ. Although everyone agrees that ADHD needs to be addressed, no concrete steps have been taken to make this happen. Conflicting priorities, misunderstandings, or disinterest frequently halt progress because of the way UK politics operate. not providing a clear legal path for those with ADHD.
For those with ADHD in the UK who require assistance, not being able to obtain a diagnosis is a major issue. The NHS’s diagnostic pathways for ADHD are plagued by lengthy wait times. For an evaluation, some patients must wait years. In addition to harming children during critical developmental stages, this delay also affects adults who are seeking a late diagnosis after living with a condition that may have gone untreated for a long time.
The void has been filled by private diagnostic services, but issues with quality and equity have been brought up by their exorbitant prices and dubious methods. Lack of funding is not limited to diagnosis. There are insufficient treatment options available in many places, such as behavioural therapies, counselling, and medication access.
The way that the UK incorporates ADHD into its mental health policies hasn’t always been consistent. Although the government has pledged to treat mental and physical health equally, laws pertaining to mental health and disability rights frequently overlook ADHD. Despite having a significant impact on individuals and families, it is occasionally overshadowed by disorders like autism and depression.
Although it is a good thing to include ADHD in SEND frameworks and disability rights laws, implementation is still inconsistent. In order to ensure that ADHD is addressed alongside other conditions in public health strategies, workplace policies, and educational frameworks, an integrated approach is required. Without this, people with ADHD will still struggle to get the support they require.
People with ADHD’s strengths are often overlooked at work. Employers either don’t know how to make the small changes that would help neurodiverse employees do their best, or they don’t think to. A little more flexibility with hours, clear and structured feedback, or a stable work environment can make all the difference between someone who is struggling and someone who is driving innovation and productivity.
This begins long before you get a job. Schools are the first place where kids with ADHD can get the help they need to do well. Problems can get worse if you don’t get help early, get personalised instruction, and have teachers who know what they’re going through. If you do things right in the classroom, you can cut down on suspensions, get better results, and most importantly, get kids ready for jobs and training.
If you don’t do it right, you will have more NEETs, more people who depend on welfare, and more wasted potential.
It is not enough to just raise awareness of ADHD; we need to do it if we want to make the most of all of Britain’s talent. Bigger public information campaigns should help get rid of the myths and stigma that still surround the condition. The more correct information there is, the less room there is for false information and stereotypes that spread so quickly on social media.
Workplaces can set an example. Employers can set the tone for society by being open about showing what can be done with the right support. Government and charities can help with this by running awareness campaigns. This way, people will understand that ADHD is not an excuse for not doing well, but rather a condition that can lead to amazing results when it is treated properly.
This change in culture needs to be supported by changes in policy. Adding ADHD to the Autism Act would make it clear that the government needs to come up with a national ADHD strategy instead of letting families fight over who gets what. It should also be easier and faster to get a diagnosis. Kids shouldn’t be left without a name until they’re teens, and adults shouldn’t have to wait years for NHS tests. It will take work and money, but the long-term savings – both in terms of less reliance on welfare and more productivity – more than make up for it.
The only way to make real change is through a coordinated national effort. That means:
• Making the production of a national strategy for ADHD a legal duty for the Government by adding it to the Autism Act.
• Enhanced training for Primary School teachers to spot ADHD, to enable them to notify parents/guardians
• By 2030, the NHS should be able to cut the time it takes to get an ADHD diagnosis to no more than six months.
• Making it easier to get work with clear ADHD-specific instructions.
• Stopping abuse by regulating private clinics.
• Starting a national campaign to combat false information.
If we choose to do nothing, the cost will be great. People who have undiagnosed ADHD are less productive, use the NHS more, and even get involved with the criminal justice system more. It is also over-represented among people who get Universal Credit. That should make us all worry. We can reduce reliance on benefits and create pathways to meaningful employment by enhancing support. Finding problems early can stop students from being kicked out of school, keep them in regular classes, and help them do better in school. All of this makes the economy stronger and lessens the need for the state in the long run.
This is not only a moral argument – it is also an argument about money and the economy. If Britain wants to grow, and if we want to see more people working and fewer people stuck on benefits, then we need to deal with ADHD the right way. The social contract is all about helping people make a difference, and right now, we’re not doing that.
George decided to write this paper after encountering conflicting reports in the press, some suggesting ADHD is widely underdiagnosed, while others claim it is already overdiagnosed. Growing up in Kent, George faced challenges in the education system, being suspended from school at 15 before finding his footing through an apprenticeship that better suited his learning needs.
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