
Retiring NHS England boss says cancer treatment on ‘cusp of golden era'
In his final interview before retiring, Sir Stephen, 64, told The Times: 'We are at the cusp of a golden era in terms of the way we treat a range of cancers.
'For many cancers now, people should be confident that it's not a death sentence and that more treatments will become available.'
He said the rise in people living longer and surviving cancers would continue, alongside cures for some forms of the disease.
'Our understanding of the genetics of cancer, of the way we can target cancers with particular drugs, and how we can use the body's own immune system to target cancers itself, is being revolutionised,' he said.
He compared the progress made in treating cancer with the success in developing HIV/Aids treatments since he qualified as a doctor 40 years ago.
He also said an increased focus on prevention will help eliminate certain types of cancer.
🧵Today is my last day working at NHS England. It has been an honour to serve as National Medical Director for the last seven and a half years. Thank you to everybody who has supported and encouraged me over the years.
— Professor Stephen Powis (@NHSEnglandNMD) July 10, 2025
'We can't prevent all cancers, but there are cancers that we can certainly prevent,' he said, adding that he hopes lung cancers will become 'a lot rarer'.
Cancer treatment, he said, would be 'driven by genetics' to become more individualised with the increased ability to pinpoint mutations in cells.
His comments come as experts warned of a 'postcode lottery' in cancer services that focus on improving patients' quality of life and providing urgent care for people with the disease.
The Royal College of Physicians (RCP), the Royal College of Radiologists (RCR), the UK Association of Supportive Care in Cancer (UKASCC) and the Association for Palliative Medicine (APM) have called for urgent investment in supportive and acute oncology.
Sir Stephen warned the biggest challenge facing the NHS was the rise in elderly people and the economic pressure that is putting on the younger generation and the economy.
Last week, Sir Stephen warned the British Medical Association (BMA) to 'think really hard' about whether industrial action by resident doctors – formerly junior doctors – planned for later this month is justified.
He told The Times the walkout would cause 'tens of thousands of appointments and procedures' to be cancelled.
The kidney specialist has served as national medical director since January 2018 and held the role throughout the Covid pandemic.

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North Wales Live
an hour ago
- North Wales Live
Covid cancellation of routine check up and singing helped save nurse's life
A senior nurse reveals how singing in a choir saved her life after two cancer diagnoses - and the pandemic cancelling a check-up may have also helped keep her alive. Her body was fixed by the NHS yet her mind was broken after two gruelling cancer recoveries but now she feels her life is back on track. As a busy ward manager for a North Wales hospital, Christine Plant knew perhaps more than most about the signs and symptoms of cancer. When she noticed blood in her poo occasionally, she knew the best thing to do was to get an appointment with her GP, and a follow up consultation for a colonoscopy. As a full-time nurse, married with two teenage boys, a very busy and demanding job, Christine, 54, of Conwy, still believed that the demands of her job, perhaps were at the heart of her problems. 'I thought I eat healthy food I had a good BMI, and I don't drink much at all, so I would be ok. But I was told I had rectal cancer, commonly known as bowel cancer and that I would need surgery, a stoma and chemotherapy. "I was 46 and hadn't expected to hear I had cancer, it was a frightening time and my sons who were age 13 and 16 at the time and I felt for them.' Following surgery, chemotherapy and a stoma reversal, Christine went back to work and decided to switch jobs from being a ward manager to specialising as a breast cancer nurse in 2019. But just prior to the Covid pandemic in March 2020, Christine was called for her first routine mammogram. This was cancelled due to COVID. A few months later Christine felt a small pea-sized lump in one of her breasts. Life was busy and she didn't make an appointment at the time. But as the first routine check-up had been cancelled she was called back in the autumn. 'It was September 2020 and I was called for my first routine mammogram. Working as a breast cancer nurse, I knew the protocol - but then I had a recall to say they wanted to see me and it was then I was told then I had breast cancer. "I felt grateful in a way that I was seen in September rather than the March as it may not have been picked up six months earlier and it could have been a different story,' she says. 'Following surgery and radiotherapy to treat the breast cancer. I felt my body was fixed, but my mind wasn't. "I remember going into clinic one day and thinking, I can't do this, I need to change something, my mind wasn't fixed and that's when Tenovus Cancer Care changed everything.' Christine was scrolling through Facebook and came across an invitation for Sing with Us Choirs and that was to change the course of Christine's life. She explained: 'I got in contact with the choir master Andrew Roberts, and he asked me if I knew what type of singing voice I had? "I didn't have a clue! I wasn't even sure I could sing, but that didn't matter, as the main thing was I felt welcomed as soon as I came through the door on that Tuesday night in Llandudno.' 'For the first six weeks of being in the choir I kept expecting someone to tap me on the shoulder and tell me to mime. Instead, I felt lifted in spirit and in my mind. I truly believe that singing in the Tenovus choir has probably saved my life." She added: 'I never thought that singing in a choir would have been on my bucket list, but it was, and If I missed a choir night, I could feel myself going downhill and getting slightly more depressed. 'Having got so much out of the choir, I knew I wanted to give something back and so I decided to volunteer in the Conwy Tenovus Cancer Care shop a morning a week and I love it, I meet so many amazing people.' And for Christine it didn't stop there, having chatted to Andrew about her feeling the need to give back, he suggested she join forces with the charity as a Community Engagement volunteer. Now Christine shares her story to groups, to encourage others that there is light and hope at the end of what can seem like a very dark tunnel. 'I always tell people how the choir made me feel whole again. I come out with a beaming smile every time I go. "Since joining three years ago I have sung in the Tenovus 80th birthday celebrations in St David's concert hall with 400 other choristers, done a firewalk, an abseil, organised a Tea for Ten event, held a dressage event, Canter for Cancer and now organising a fashion show, using clothes and accessories from our shops. "This is all done with the help of family and friends, old and new as we have a strong community here in North Wales.' Since going through two major cancer operations and treatments, Christine is now working as a gynaecology oncology nurse and working with cancer patients. She feels her experience means she can look at things in a different way to perhaps some of her colleagues. 'I listen to patients and If I feel they need help with their mental wellbeing, I do refer them to the choirs." * Christine has been recognised by Tenovus Cancer Care as part of the annual Volunteer Awards in the collaborative section for dedication and commitment to the work she does for the charity in her spare time.


Metro
15 hours ago
- Metro
I couldn't chew properly then my doctor said my life was at risk
It was lockdown, November 2020, and I'd treated myself to one of the only things that still brought me a bit of joy: A fancy dinner. After getting Covid and going through a break-up I'd been struggling with a lack of appetite for months, so I welcomed my renewed desire to eat and had picked up a boil-in-the-bag moules marinière. Ever since I'd been working from home I'd lived on soft foods like soups, couscous and hummus and I'd noticed that sometimes my face would get stiff when I tried to chew or swallow, but I'd always brushed it off. As I worked a mussel around my mouth that November evening, however, I suddenly felt my throat constrict and my mouth seize up. I couldn't swallow. Snorting and spluttering, I grabbed a napkin as salty, creamy sauce dripped out of my nose, stinging like hell. I was confused, in pain and alarm bells started to ring. That uneaten bowl of mussels was the last straw and I made an appointment to see a doctor. My GP referred me to an Ears, Nose and Throat specialist (ENT), but an initial consultation and blood tests couldn't find anything wrong. I pushed back as I'd noticed my mystery symptoms would come and go and often worsen at night. By the end of some days my face felt so tight I'd be slurring my words and I'd wake up feeling better, able to manage soft foods again. However, as these appointments were often in the morning I don't think doctors took me seriously. They put my symptoms down to stress, suggesting I take a holiday that Christmas to relax. That New Year I travelled to Dubai, which was allowed under the government's traffic light system at the time, to see a friend. And then I caught Covid, which only made my symptoms worse. I video-called my consultant on January 2, by which time I was slurring my words and my eyelids had drooped – I thought I was having a stroke. 'I know exactly what this is,' she told me. 'Your life is at risk – you need to come home now .' She then referred me to a neurologist who diagnosed a rare autoimmune condition called myasthenia gravis (MG) – a condition that causes the body to attack itself and had resulted in muscle weakness in my face, throat and chest. Worst case scenario: My diaphragm might stop working and I wouldn't be able to breathe. Immediately the neurologist prescribed medication called Pyridostigmine, which worked like magic. I went from not being able to move my mouth to speak, to eating a KFC an hour later. Problem solved – or so I thought. As MG is often triggered by issues with the thymus – a gland in the chest that's an important part of the lymphatic system, making special white blood cells called T-cells to help the immune system fight infection – the specialist wanted to investigate further. The results of my CT scan were devastating. 'You have a tumour called a thymoma in your thymus,' my consultant explained, pointing to an area beside my heart on the scan. At first, I couldn't even process what I was being told: The tumour on my thymus was 11.5cm – the size of an iPhone! – and there'd be no way of telling whether it had spread or wrapped itself around my organs until they took it out. It took a couple of hours to really sink in, and when it did, I felt utterly terrified. A week later, at the end of March, I underwent a six-hour operation at St George's Hospital in London. When I woke up in recovery, the first thing I groggily asked was: 'Did you get it?' 'We got all of it,' my consultant reassured me, but said it had to be sent to a lab to find out if it had metastasized. I spent four days in hospital before I was discharged and then all I could do was wait. That was by far the worst part – I couldn't settle physically or mentally. A fortnight later, I was well enough to take a short walk in my local park when my phone buzzed. 'The cancer was stage 2. We got it all – no further treatment needed,' my consultant told me. I was in bits, crying tears of relief right there in the park, so grateful not to need radiotherapy or chemotherapy. Unfortunately, because my autoimmune condition had already been triggered, I still have to live with MG and take medication, including Pyridostigmine and steroids, daily to manage my symptoms and stop it from flaring. And while that's not ideal, I'm embracing life. I never take a single day for granted, I'm so much closer to my family and I've moved from London back to my hometown in Devon and married my lovely husband Nick. More Trending I've also accessed support from Myaware – a charity that helps people with MG, including their online groups and forum – which makes me feel like I'm not alone, and in October 2021 I ran the London Marathon to raise money for Shine Cancer Support, a charity that supports young adult patients. There are some cancers that are really hard to detect and thymoma is one of them, but my body was telling me loud and clear that something was wrong. If you have unusual symptoms, always listen and see a doctor. View More » As told to Jade Beecroft Do you have a story you'd like to share? Get in touch by emailing Share your views in the comments below. MORE: I felt invisible in my 50s – my four-day-a-week hobby fixed that MORE: I tried to give Gran a hug – her reaction still haunts me MORE: My date showered me with compliments – until I turned down his request Your free newsletter guide to the best London has on offer, from drinks deals to restaurant reviews.


ITV News
a day ago
- ITV News
'No one deserves to be left waiting": The emotional toll of NHS waiting lists
Two women are urging others to advocate for themselves when trying to get treatment on the NHS after waiting years for surgeries. Michelle Turnock, from Merseyside, waited nearly three years for breast reconstruction surgery following cancer. The long wait took a serious toll on her mental health. The mum-of-two finally had her operation in May. 'The staff were amazing,' Michelle said. I first spoke to Michelle as she waited for surgery in 2024. Now recovering, she rewatched her original interview from before the surgery. When asked if she recognised herself, she replied: 'No, it was a scary time, I just didn't know whether I was coming or going, we were very much in limbo." Michelle's story is not unique. In the North West of England alone, more than one million people are waiting for NHS care, and over 40,000 of them have been waiting more than a year. Gail Wild from Melling also knows what it means to wait and to fight for the care that she needs. She reached out after seeing Michelle's story on the telly. With a family history of cancer and a positive BRCA2 gene result, Gail made the difficult decision to have preventative surgery, including a double mastectomy, so that she could be around longer for her sons. She said: "It was too emotionally upsetting waiting for results that you think, Is this the year I'm going to get cancer?" But when it came to reconstruction, she hit wall after wall. Her local hospital said no, while other hospitals turned her away too - some didn't even offer the surgery. Asked what that was like, Gail replied: 'Soul-destroying. I didn't know whether I was going to get the surgery. "People need the surgery for a valid reason, I'm very high risk. I don't want to get cancer, and I know if I did get cancer, I would cost the NHS an awful lot more money." Eventually, a hospital in Sheffield agreed to carry out the surgery. It changed her life. Prime Minister Keir Starmer said he acknowledges the long delays on the NHS and said his government is taking action. He said: "I am really pleased that we are making progress bringing the waiting lists down, but I don't want to diminish the experience of anyone in the North West who is on a waiting list. "All I can say is this, we are working as hard as we can, sleeves rolled up, and I have them in my mind's eye when I take the decisions that I do in relation to the NHS, we're determined to tackle this problem." There are signs of progress. At Warrington Hospital, a new 'super clinic' model allows patients to be seen, assessed, and booked for surgery in one visit. The Gynaecology Super Clinics, introduced by Warrington and Halton Teaching Hospitals in May 2024, have cleared the hospitals' Covid-19 backlog and are ensuring that patients receive appointments within weeks. Since the launch, the Super Clinics have seen more than 1,500 patients, with 80% starting or completing their treatment plan at the clinic. The Super Clinic is part of the national 'Further Faster 20' initiative. Warrington and Halton Teaching Hospitals are one of 20 trusts taking part in the initiative to transform patient pathways and improve access to treatment. Dr Anuradha Leburu, Senior Gynaecologist, said: "It has been a dream come true, actually we've been trying this for so many years. "It has come through actually for us and we are so pleased as clinicians were pleased and the patient, look at the feedback we get, they're very very happy." For Michelle and Gail, finally getting surgery gave them more than just physical healing. It gave them hope. Michelle now has a new job and is planning a holiday she has put off for three years. Gail, on the other hand, has been planning a wedding and looking forward to wearing her wedding dress. They want others to advocate for themselves, try different hospitals and push to be seen. They also want hospitals to do more to help their patients. A Department of Health and Social Care spokesperson said: 'We inherited a situation where too many people are waiting too long for care, but we are working at pace to turn this around. 'The latest figures show that NHS waiting lists fell in May for the first time in 17 years and have dropped by more than 260,000 since July 2024. 'This recovery through our Plan for Change is only just beginning, and we are working hard to improve access to services and bring down waits for treatments.'