
It is time to call care workers like me skilled – and pay us properly for all that we do
At work, I am part psychologist, nurse, bereavement counsellor, occupational therapist, mental health advocate, group therapist and palliative care expert. What am I? The answer, of course, is a care worker. And yet this week, the message from the government was that I – and thousands like me – are 'low-skilled'. Tell that to the people we look after and the families who love them.
When Labour announced plans on Monday to scrap a visa scheme for overseas social care recruitment in a drive to bring down 'low-skilled' migration, it was just the latest in a long line of negative messages about the sector I work in. The irony, though, is that we need to value caring now more than ever because the industry is in crisis, and what's keeping it afloat is the goodwill of workers – mostly women.
Around 80 per cent of carers are female – their work is critically undervalued financially, but also socially. Wages are low, we're constantly being told we have no skills, and it's leaving many of us feeling unappreciated and invisible. But after working in social care for more than three decades, I know from experience how complex the work we do is and why we have to recognise its worth more than ever.
I started working as a carer when I was 26 after training as a nurse and developing an interest in community care. Today, I work as a manager at a medium-sized family-run home called the Alexander Care Home in Morley, Leeds, and I'm lucky to be part of a team that feels like a family. But there's no doubt that caring is tougher now than when I started out because a lot of the people who would once have had specialist nursing care are now being looked after in the community.
It means cases are increasingly complicated and carers need everything from physical to mental skills to manage them. You need resilience, patience and tenacity for a start, as well as practical and technical knowledge, physical fitness, and most essentially empathy and the emotional intelligence to be able to connect with people.
And ironically, it is this emotional skill needed that is, I believe, a key part of why caring is so chronically undervalued. It's no coincidence that traditionally male, practical jobs like plumbing or electrics are seen as highly skilled and often well paid, while the 'softer' skills needed to be a carer are just seen as an extension of what women do for our families every day and are not financially rewarded. But these are skills that you can't measure on paper.
Caring professionally for people who aren't relatives requires a whole different skill set on top of that. You have to be able to quickly adapt because no two days are the same, project manage and balance short-term decisions with a long-term view. The patient who is too weak to move into a chair today may develop pressure sores tomorrow. Our work is a constant stream of tiny but critical assessments of everything from physical state to mood.
While some people come into it with few academic qualifications, everyone has to undergo intense training in everything from health and safety to wound management once they start. I've often seen, however, that even when carers develop huge competence at work, they lack the confidence to see what they are worth, and they don't see those skills as transferable. I work with so many incredible women, with a lot of skills, who have no idea of just how good they are.
Every area of social care has different challenges. Those working with people affected by neurodevelopmental issues, for instance, might have to develop a lot of skills to deal with complex identity and independence issues. In elderly care, we are working with those who've usually experienced significant loss – whether it's a partner or a home – and we have to work through their grief, convince them that their new life, or that of a partner, is not an end, it's just the start of something new.
Yet despite this important work, many colleagues don't like to admit publicly that they're a care worker because it's not seen as an achievement, and they're often judged. The only time we got an uplift in public perception was during Covid, but I still feel that what carers went through then has not been recognised in the same way that the contribution of those working in the NHS was.
Then, I was asking young women to come into work, often being paid just above minimum wage, to be on the frontline of the pandemic with no protection because all the PPE was diverted elsewhere. I was overwhelmed by the number of them who chose to work even when they were facing true trauma. People walked through the door every day knowing they could take Covid home to their family, and it was the time when all the many levels of our collective expertise and knowledge were really proven. And yet we are still considered low-skilled workers. What other job asks so much for so little in return?
There needs to be a shift in our value system about what is socially and financially rewarded. Work as anything from a train driver to a lawyer, and you'll be valued in different ways. Not so for carers, despite the incredibly important work we do. Most of us know we could earn the same working in a supermarket or fast-food chain, but we want to make a difference, make others feel comfortable and safe. We respect elderly people who have contributed and now need looking after. It's about a value system that we believe in, our capacity to care for our most vulnerable people. It is valuable work that should be equally valued. The pandemic showed what happens when that system breaks down.
What we do is a form of intelligence; it's all about human skills that not everyone has. It's time that, at the very least, the government started to respect those skills. Because, as carers, we don't just look after individuals, we look after whole families and society too.
As told to Megan Lloyd-Davies
Hashtags

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


Daily Mail
an hour ago
- Daily Mail
Katie Price gives update on son Harvey's course of Ozempic-style weight-loss jabs after revealing he now weighs almost 30st
Katie Price has given an update on her son Harvey's weight loss treatment, as she revealed he was due to start a course of Ozempic -style jabs next week. The former glamour model, 47, previously revealed the 23-year-old son was going on the weight-loss injections in a bid to help improve his life, after his weight reached almost 30 stone. Harvey is blind, autistic, has septo-optic dysplasia, and is one of the 2,000 people in the UK with Prader-Willi syndrome, a genetic disorder. A recognised symptom of his Prader-Willi syndrome is constant hunger, leaving Katie fearful for Harvey's health without further intervention, after already trying a number of different weight loss strategies over the years. Speaking on her podcast, The Katie Price Show, with her sister Sophie, the mother-of-five gave fans an update on her eldest child. From A-list scandals and red carpet mishaps to exclusive pictures and viral moments, subscribe to the DailyMail's new Showbiz newsletter to stay in the loop. She explained that she set to perform at Portsmouth Pride this week and that Harvey was joining her on the trip. While Katie then added: 'Hopefully Harvey starts his Mounjaro this week, but we'll talk about that next week and I'll go through all of what's happening about that.' Mounjaro is the brand name for the drug tirzepatide, and has been hailed as the 'King Kong' of slimming jabs - more effective for shifting the pounds than similar drugs like Ozempic. In April, Katie said she was 'heartbroken' by Harvey's weight increase, as she explained how it had left him struggling to walk and at risk of a heart attack. She took to her Snapchat to explain how she wanted him to start Mounjaro as soon as possible, to improve his quality of life. She said: 'I'm so heartbroken and gutted that his weight is just going up. I just googled it in stones, 188kg is just a few kg of being 30 stone. 'It's so bad now, I'm still waiting for the doctors to get back to me starting on the Mounjaro and his journey to a healthy life.' She went on to say how difficult it was watching Harvey's ongoing fight, but vowed she would get him through it. Katie said: 'It's so sad his quality of life at the moment where he's so big, he just can't really do much. 'It's just another thing I have to deal with because he's at high risk of having a heart attack, he struggles to put his trainers or struggles to walk anywhere but I love him and I'm going to help him through this. 'So sad, obesity and his condition is sad, it's sad to see someone go through it and he doesn't understand.' Katie first revealed her intention to for Harvey to start using weight loss jabs in February, after consulting with his doctors. Speaking to The Sun to raise awareness, she explained that his medical professionals advised he may be taking the jabs for up to two years. She said: 'It's really, really serious and life-changing for Harvey. He's at risk of a heart attack, and because of his condition, he's not getting any smaller. 'He's putting on weight. It doesn't matter what we do. So the doctors are doing it to give him a better, longer life, and for his health.' The TV personality added: 'The good thing about starting him on the drug is, if it has any effect, you can stop it because you do it weekly. We've tried food, he's had dieticians, it's just the way he is. 'They want to try him on it for at least one or two years, which is a long time, but they'll control what level he needs then up it as they assess it.' It comes only a week after Katie shared a loving tribute to Harvey to mark his 23rd birthday, with series of throwback snaps of them together. Among them was a smiling selfie of her and Harvey together on the beach and another picture of her son planting a kiss on her cheek. In a caption, she gushed over her 'forever love' for her son and shared her excitement over spending Harvey's birthday with him. Harvey's biological father is former footballer Dwight York, who briefly dated Katie in 2001, breaking up soon after Katie fell pregnant with her eldest child. The ex premier league star denied he was the father, until a DNA test proved his paternity. Katie previously claimed that Dwight has barely seen Harvey since he was born, saying: 'I think he's seen Harvey about nine times in his life.' She claimed: 'I don't think he liked it that I was with Pete [Andre] before adding: 'I don't know whether it's because he couldn't have me or Harv, to this day I don't know. 'I've tried to send him pictures of Harvey on Instagram, Harvey playing the piano, he just ignores everything. He doesn't want to know. But the door is always open, always.' WHAT IS PRADER-WILLI SYNDROME? Prader-Willi syndrome is a rare genetic condition that causes problems including constant urges to eat food, restricted growth and reduced muscle tone. Other potential issues include learning difficulties, lack of sexual development and behavioral problems such as tantrums or stubbornness. The rare condition, which affects one in every 15,000 children born in England, is caused by a defect on chromosome number 15 - and happens by chance. Because there is no cure, treatment aims to manage the symptoms – with parents of sufferers urged to get their children to stick to a healthy, balanced diet. Children with the syndrome can eat up to six times more than children of the same age – and still feel hungry. It was first described in 1956 by Swiss doctors A Prader, A Labhart and H Willi.


Daily Mail
an hour ago
- Daily Mail
EXCLUSIVE My entire body went numb and I couldn't walk after taking common ADHD drug prescribed to millions
Hannah Schweickert never thought a common medication for ADHD would leave her numb from her face to her toes, at times unable to walk. Schweickert, from Indiana, has had attention deficit hyperactivity disorder since she was young. Doctors had prescribed her the popular drug Adderall, a stimulant taken by 16million Americans known to improve focus, attention, and impulse control. She started on a low dose, standard practice doctors follow to minimize side effects, which can include insomnia, increased heart rate, anxiety, mood swings, and jitteriness. When she showed no improvement, doctors increased the dosage, first to 15mg, then to 20mg, 30mg, and, finally, 40mg, her highest dose. Schweickert, 25, took a 40mg tablet every day for about two months with little incident. But when she went on a family vacation, she began experiencing troubling symptoms she didn't immediately connect to the prescription stimulant. 'I was scratching my neck and I couldn't feel anything. My neck had no feeling,' she said. That numbness spread from her neck to her fingertips, and a week later, to her cheeks, eventually taking over her whole body. Back at college one night, alone in her room and unable to feel her bed underneath her, she panicked. 'I thought I was dying,' she said, describing a destabilizing panic attack. 'I immediately shot up, couldn't breathe, my heart was beating out of my chest. 'I didn't know what a panic attack was, but that's definitely what was happening.' Schweickert laid in a state of panic for an hour before a friend was able to get to her. She calmed herself, but it was far from the last panic attack that would strike. She said in a TikTok: 'Then that started happening every day. The worst one probably lasted about two hours. 'I couldn't walk. My friends had to carry me to pee.' She went on to say she had gone to the emergency room for her panic attacks, a common response people have to the sense of chest-tightening panic that mimics a heart attack, four times over the next few months, but doctors were stumped. Her mom then suggested something that had not occurred to Schweikert previously: stop taking Adderall. 'At this point, I had no feeling in my entire body,' Schweickert said. 'It had been 22 days with no feeling. So all my nerves, something was wrong with them.' Doctors would test her ability to feel touch on her arms, head, and legs, and according to them, everything seemed normal. She said they were not concerned and let her leave without any answers. So she took it upon herself to figure out what was going on. Schweickert stopped taking her Adderall for a week, something doctors do not generally recommend because the withdrawal symptoms can be intense, causing depression, anxiety, headaches, muscle aches, and sleep disruptions. But some of her numbness subsided in that time. She continued her research, having seen a study that found rats given Adderall at high doses experienced considerable changes in their brains. The 2017 study, published in the journal Neuroscience Letters, studied rats given 10mg of amphetamine (a key component of Adderall) and an antidepressant called desipramine, which extends the stimulant's effects. The rats' dopamine levels plummeted and stayed low for seven days after a single dose. In addition to producing feelings of motivation and reward, dopamine can regulate pain and sensory signals. But the researchers also found evidence of other neurotoxic effects in rats that could potentially explain Schweickert's reaction. The medicine starved the rats' brain cells of their energy source within an hour, making it impossible for nerve cells to send signals. This could lead to Schweiker's initial feelings of having a dead limb or tingling. The medicine then overstimulated their brain cells by flooding the brain with glutamate, a chemical that can be toxic in high amounts. In humans, this could lead to hyperexcited nerves burning out, causing paralysis or numbness. The drug also caused a chemical 'explosion' in the brain that wiped out the brain's natural defenses against antioxidants. In humans, the destruction of the chemical in the brain that acts as a fire extinguisher against harmful substances called free radicals can cause nerve pain and numbness, particularly in the arms and legs. 'That's the only thing that I found on the internet in a study that I was like, actually this could be what's happening to me,' she said. She said she had never heard of someone having 'allergic or neurotoxic effects' from Adderall, but added, 'there must be someone in the world who's also experienced this.' The feeling in Schweickert's body did not return completely, even after six months without taking the medication. '[I got] really nervous that my feeling would never return,' she said. 'Now I can say that it has.' There are few studies that delve into the potential brain-poisoning effects of stimulants, including Adderall and Ritalin. Maria Ingalla, an Arizona-based nurse practitioner of psychiatry, told if Schweikert had taken other drugs recreationally, their effects could have compounded Adderall's tendency to constrict blood vessels, thereby reducing blood flow and causing numbness. Ingalla said: 'If she tried this med recently after a psychedelic or other drugs, it wouldn't be an unusual reaction because of additive effects those drugs can have on vasoconstriction and the sensory systems of the brain.' Schweickert did not say in the video whether she had been taking any other medication or drug at that time. Figures for the number of children taking Adderall or other ADHD medications are hard to pin down due to differences in prescription databases, changing trends over time (due to the Adderall shortage in 2022, for instance), state-by-state variations in reporting, and the rise of telehealth prescriptions. But current estimates say that around 10 percent of American children, aged two to 17, have been diagnosed with ADHD, and 62 percent of them are being treated with medications, translating to about 4.5 million children.


Telegraph
2 hours ago
- Telegraph
Rape victims can challenge dropped cases after sexsomnia fiasco
Victims of rape and serious sexual assaults will get the right to challenge prosecutors' decisions to drop their cases. Labour is to pilot a scheme in which rape victims can secure an independent review if prosecutors are planning to abandon their case because they believe there is insufficient evidence. Under the current system, criminal cases can be stopped at any point if a prosecutor decides there is no longer a realistic prospect of conviction. Under changes announced on Thursday, victims of rape or serious sexual abuse will be offered the right for a different independent prosecutor to review the evidence before any final decisions are made. If that prosecutor determines there is enough evidence, the case will continue. The move follows a campaign by Jade Blue McCrossen-Nethercott, 32, after her rape case was dropped amid claims that she could have had an episode of 'sexsomnia'. An 'important first step' Ms McCrossen-Nethercott received £35,000 in compensation and an apology from the Crown Prosecution Service (CPS) for its decision to drop the case before the evidence had been tested in court. She contacted police in 2017 because she thought she had been raped while asleep. She said she had woken up half-naked, finding her necklace broken on the floor. But charges were dropped by the CPS days before a trial was scheduled to begin after lawyers for the alleged perpetrator claimed Ms McCrossen-Nethercott had sexsomnia – a medically recognised, but rare, sleep disorder that causes a person to engage in sexual acts while asleep. She welcomed the pilot scheme to be run in the West Midlands as an 'important first step'. 'It can't undo the harm already done to victims like me, but it's real, tangible progress, and I hope it marks the beginning of a fairer system, one where victims' voices are not just heard, but acted on,' said Ms McCrossen-Nethercott. Victims already have the right to challenge a decision not to charge suspects once it has been taken, but the pilot scheme will extend that right to before prosecutors decide to drop a case. 'Make Britain's streets safer' Lucy Rigby, Labour MP and Solicitor General, wrote in an article for The Telegraph: 'The existing scheme is already an important tool in delivering justice, but this new commitment from the CPS will extend that right, so that victims are further empowered to question decisions made in their cases, resulting in fewer cases falling through the cracks and more offenders brought to justice. 'Beginning on Friday, the pilot will become operational in the West Midlands. If it is a success, we will look to extend this across the country to support all victims of rape and serious sexual assaults. 'We know there is much to do to fix the justice system. But this is a vital step towards building the system that victims deserve and ultimately make Britain's streets safer.' Just one in 40 (2.6 per cent) rape offences resulted in a charge in the year ending March 2024, up from 2.1 per cent in the previous year, but a fraction of the 12 per cent charge rate in 2014. Labour has committed to halving violence against women and girls and will publish its strategy on how to achieve that this summer. The plan has inherited a series of initiatives by the last government and police, including an overhaul to focus investigations on perpetrators rather than testing the credibility of victims. Police chiefs have pledged to apply the same investigative and disruptive tactics to rapists as they do to organised crime bosses, where they are pursued by police even if victims withdraw their complaints. We can't leave victims to go on suffering Our broken criminal justice system is in dire need of repair, which is why our pilot scheme aims to empower victims of rape and sexual assault to question decisions made in their cases, writes Lucy Rigby KC MP. Too often, victims of violence against women and girls are let down by our criminal justice system, compounding what is already a traumatic experience. I have strong views on the reasons why. Chief among them: 14 years of governments whose approach was nothing short of negligent. This resulted in too few bobbies on the beat, overflowing prisons and a record backlog in our courts, leaving victims of very serious crimes waiting years to see perpetrators in court. In short, a broken criminal justice system in desperate need of repair. The impact on victims and public trust in the justice system was significant. A creaking criminal justice system undermines one of the basic principles fundamental to our democracy: the rule of law. That is to say the law applies to everyone equally and all must have access to justice. This happened despite the work of thousands of dedicated public servants to protect us all. I've met many of them – including the prosecutors from across the country that dedicate their careers to sifting through evidence, often in harrowing crimes, to build a case and pursue justice on behalf of victims. Empowering rape victims This Government has begun the difficult task of fixing our criminal justice system as part of the Plan for Change, in which we pledge to halve violence against women and girls in a decade. To achieve this, we are putting domestic abuse specialists into 999 control rooms, introducing new Domestic Abuse Protection Orders, doing more to effectively tackle spiking, stalking and coercive behaviour. That means better support in place for victims and giving them the confidence that specialists are helping them. These changes will also see more police on our streets, locking up abusers, but importantly – getting quicker justice and support for those suffering at the hands of perpetrators of these horrific crimes. As Solicitor General, I've heard heart-wrenching accounts of women's experience of the criminal justice system – sometimes lasting years – which have seriously impacted their mental health, wellbeing and relationships. We cannot let this go on, which is why we are ensuring that adult victims of rape and serious sexual offences will have access to a dedicated victim liaison officer, as well as pre-trial meetings, so that they feel more prepared for court. The right to question But we have to do more. In particular, it is vital that our criminal justice system further empowers victims to best navigate it. It was Prime Minister Keir Starmer who, as the director of public prosecutions, launched the Victims' Right to Review Scheme in 2013, to give victims and bereaved families the right to challenge decisions not to charge suspects or drop cases. Leading victims' rights voices, like Jade Blue McCrossen-Nethercott, the Centre for Women's Justice, Dame Vera Baird and Claire Waxman OBE, the Victims' Commissioner, have recognised the success of this scheme and that is why we are extending it to better support more victims. A new pilot launched this week will give survivors of rape and serious sexual assault the right to have their case reviewed before CPS makes any final decisions. Currently, criminal cases can be stopped at any point if a prosecutor decides there is no longer a realistic prospect of conviction. For the first time, survivors of rape or serious sexual abuse will be offered the right to request a review by a different prosecutor before their case is dropped. Where a review finds that the initial decision was wrong, the case against the accused will continue. A system victims deserve The existing scheme is already an important tool in delivering justice, but this new commitment from the CPS will extend that right, so that victims are further empowered to question decisions made in their cases, resulting in fewer cases falling through the cracks and more offenders brought to justice. Beginning on Friday, the pilot will become operational in the West Midlands. If it is a success, we will look to extend this across the country to support all victims of rape and serious sexual assaults. We know there is much to do to fix the justice system. But this is a vital step towards building the system that victims deserve and ultimately make Britain's streets safer.