
'I found a lump on my neck I thought was flu but it was cancer'
When Ezzy Pearson felt a lump on the side of her neck, she was not immediately worried. She has just started at university and put it down to "freshers' flu", a common sickness many new university students contract after meeting lots of new people.
However, what started as a runny nose, fatigue and a persistent cough turned out to be a form of cancer known as Hodgkin lymphoma. Ezzy, from Bristol, was just 18 when she received her diagnosis.
She said: "On the Wednesday of Freshers' Week, I noticed a lump on the side of my neck and just felt really rubbish. I was constantly carrying around a box of tissues and assumed it was just Freshers' Flu. But when it hadn't cleared up after a month, I went to the GP."
Following several blood tests, she was referred to an Ear, Nose and Throat (ENT) specialist. Following a biopsy on the unusual lump in her neck, she was given the diagnosis of Hodgkin lymphoma, a type of cancer originating from the body's lymphatic system, a crucial part of our immune defence.
Despite undergoing six months of chemotherapy, she sat all her first-year university exams, including one just hours after a treatment session. Fast forward nearly two decades, Ezzy, 37, is now cancer-free and participating in the Race for Life in honour of her mum, Jo, who tragically lost her battle with lung cancer at 64.
Ezzy - now holding the role of Commissions Editor at BBC Science Focus magazine - is vowing to support the research that gave her a second chance at life. Ezzy said: "If I'd been born 30 years earlier, that diagnosis could have been a death sentence. But thanks to advances in research - much of it funded by organisations like Cancer Research UK - I had access to treatment that saved my life."
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She was heartbroken when she lost her mum, saying: "I was devastated when my mum died. She was a smoker, and I know there's a lot of stigma around lung cancer because of that - but it's more complex than people realise. Everyone deserves compassion and support, no matter how their illness came about."
She remembers her mother as an inventive Scout leader, and feels her own creativity and writing talents are inherited from her. Now settled with her partner Sam, whom she met shortly after losing her mother, Ezzy continues looking forward.
Although Jo and Sam never got the chance to meet, Ezzy has discovered touching ways to bridge the gap. Ezzy will have the honour of setting off the start of this year's Bristol Cancer Research UK Race for Life wearing her late mother's engagement ring.
Ezzy said: "After my mum passed, I started wearing her engagement ring on my right hand. When Sam and I signed our mortgage together, I moved it to my left. It was my way of letting her know I planned on keeping him, even if I couldn't tell her in person."
The event will take place on Sunday, June 22, where Ezzy will trigger the starting horn for almost 2,000 runners bracing themselves for either the 5k or the 10k at The Downs in Stoke Road. They will all be rallying for Cancer Research UK's leading fundraising event in Bristol.
Ezzy continued: "I'm so excited and honoured to be starting Race for Life Bristol. It's a powerful reminder of how far we've come in cancer research - and how much more we can achieve together."
She urged others to join in, saying: "Race for Life is just a great experience. It's not about being the fastest or the best. It doesn't matter if you run, walk or hop like a bunny - it's about coming together and doing something fantastic for a great cause."
The upcoming weekend is full of fundraising activities, kicking off with Pretty Muddy and Pretty Muddy Kids obstacle races on Saturday, June 21. In the south west alone, around 37,300 individuals receive a cancer diagnosis each year.
The Race for Life, sponsored by Standard Life (a part of Phoenix Group), brings communities together through a variety of events such as 3k, 5k, 10k, Pretty Muddy, and Pretty Muddy Kids runs across the nation. The series gathers millions each year to raise crucial funds for cancer research. Cancer Research UK's spokesperson for the South West, Ruth Amies, said: "We're incredibly grateful to Ezzy for being our VIP starter at Race for Life Bristol."
She added: "No matter how cancer affects us, life is worth racing for. Sadly nearly 1 in 2 of us will get cancer in our lifetime but all of us can support the research that will beat it."
Talking about the event's success and its significant role, she said: "We're proud that Race for Life has had such a positive impact. Every pound raised supports our life-saving work, which has helped double cancer survival in the UK over the last 50 years."
Ruth added: "Our events are strictly non-competitive which means everyone can have a go- and love every minute. There's no pressure to finish in a certain time, just give it what you can. Lace up and join in.
"Whether people are living with cancer, taking part in honour of or in memory of a loved one with cancer, in it for the medals or just for the fun of fundraising, there is a place for everyone."
Since launching in 1994, Race for Life has welcomed more than 10 million participants who've raised copious amounts vital for research efforts.
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Telegraph
5 hours ago
- Telegraph
We'll use AI to spot more prostate cancer, says Science Secretary
Artificial Intelligence will be harnessed to find hidden cases of prostate cancer, the Science Secretary has said. Peter Kyle told The Telegraph that the Government is investing £168m on initiatives to use public data better and one major goal is to improve cancer screening on the NHS. A world-leading initiative led by Cancer Research UK has been given £10m in funding to improve cancer screening methods by identifying the most at-risk people and offering them personalised tests. The funding will 'develop AI-powered tools that can predict cancer risk', Mr Kyle said, and could save thousands of lives a year. The Telegraph has launched a campaign calling for a targeted national screening programme for prostate cancer, which focusses on men who are at the greatest risk. This includes men over 50, black men, whose risk is twice that of white men, and those with a family history of prostate cancer. Steve McQueen, Bob Willis and Chris Hoy are some of the high-profile British men to be recently diagnosed with the condition. Around 55,000 men are diagnosed with prostate cancer annually in England and around 33 men a day die from the condition. Writing for The Telegraph alongside Stian Westlake, the executive chairman of the Economic and Social Research Council, Mr Kyle said: 'This funding will support work on a project linking health records to demographics, family history and behaviour to identify those at higher risk of this devastating illness, so that it can be treated early – potentially saving thousands of lives every year.' The plan is to create flexible national screening programmes which can pick up more cases in individuals who may otherwise be missed and diagnosed only when the cancer was incurable. Officials are hoping to replicate the success of BRCA1 genetic screening. Around one in 400 people has faulty BRCA genes, which give women a 60 per cent chance of developing breast cancer. This received widespread attention and became known as the 'Angelina Jolie gene' after the Hollywood actress underwent a double mastectomy after finding out she was a carrier in 2013. The NHS now offers genetic tests to high-risk groups, such as Jewish women, to catch as many cases early as possible. Mr Kyle said: 'Just as BRCA gene screening, heroically brought to the fore by campaigners including Angelina Jolie, revolutionised how we understand and manage the risk of hereditary breast cancer, this next generation of data-driven screening could do the same for more cancers, including prostate cancer.' Scientists running the scheme hope it can enable the NHS to offer more frequent cancer screening sessions or screening at a younger age to those at higher risk, while those at lower risk could be spared unnecessary tests. People identified as higher risk could also be sent for cancer testing faster when they go to their GP with possible symptoms. The wider Administrative Data Partnership will last until 2031 and try to repurpose data that already exists to make improvements to the judicial service, education, health and other public sectors. Combining, standardising and interpreting different datasets simultaneously is a daunting challenge for scientists owing to decades of independent data collection and little crossover. However, the Government believes that vast data reserves, combined with the power of AI computing, could transform healthcare. The cancer screening project will build new models over the next five years to merge relevant data as well as creating algorithms which will process it and ensure the results are accurate and reliable. Antonis Antoniou, the programme director and professor of cancer risk prediction at the University of Cambridge, said: 'The UK's strengths in population-scale data resources, combined with advanced analytical tools like AI, offer tremendous opportunities to link disparate datasets and uncover clues that could lead to earlier detection, diagnosis, and prevention of more cancers.' Dr David Crosby, the head of prevention and early detection research at Cancer Research UK, told The Telegraph: 'The single most important thing we can do to beat cancer is to find it earlier, when treatment is more likely to be successful. 'With half a million cancer cases per year expected in the UK by 2040, we need a major shift towards more accurate diagnosis and detection of early cancer. 'The Cancer Data Driven Detection programme will link health data sources together and build the powerful new tools doctors need to identify those at highest risk of cancer and prioritise resources towards them. 'Moving towards a preventative approach to healthcare will not be easy and will take time. Cancer Research UK's investment in the programme is an investment in the future of cancer care.' Data is the key to changing lives for the better By Peter Kyle and Stian Westlake For much of our everyday lives, data is king – from digital maps getting us from A to B, to health apps keeping our fitness and sleep in check, to even streaming platforms suggesting the next drama we might want to get stuck into. For this government, making good use of data is the difference between successful policies that are rooted in evidence, and those that rely on hope, luck or intuition, which no minister, legislator or council leader wants to rely on. Ultimately data is the bedrock of decision-making, ensuring policies, programmes and funding are doing what they are intended to do – changing lives for the better. Linking data from across government to the national pupil database for example can help to really dig into the source of inequalities that trap too many Brits from childhood through to the labour market – helping us to take targeted action in boosting social mobility and shattering glass ceilings. Or by better applying it in the justice system, we can understand patterns of reoffending, stopping career criminals from inflicting more misery on the law-abiding majority. And it can forecast the impact that this government extending the national living wage has on younger workers, so that millions more who put the hours in take home the pay they deserve. What unites all of these examples is that they were all made possible by UKRI's administrative data research UK partnership. It works to connect, and make sense of, the huge wealth of data that is generated by government services, bringing it to our world class researchers securely and with the public's privacy at heart since 2018. In short it has been demonstrating the role data can play in improving lives in as many ways as we can imagine and more. But we know we can go further and too many social and economic researchers – many of the very best of whom are right here in the UK – simply can't access the data they need. It is fragmented and siloed, held in different datasets by different public organisations. That means too many rely instead on insights from abroad, which while offering much, simply can't tell the full story of life in Britain in 2025. Accessing the raw resource of all that data and translating it into a form that researchers can use is no easy task, and while we need to grow our data science expertise, we also need to build relationships and make the case to other organisations that secure data sharing has the power to change lives. That is why UKRI is investing a further £168m to continue ADR UK's programme of work through to 2031. This includes continuing our partnership with Cancer Research UK to develop AI-powered tools that can predict cancer risk based on health records, family history and behaviour. Just as BRCA gene screening, heroically brought to the fore by campaigners including Angelina Jolie, revolutionised how we understand and manage the risk of hereditary breast cancer, this next generation of data-driven screening could do the same for more cancers, including prostate cancer. This funding will support work with organisations and charities like Cancer Research UK for example, on a project linking health records to demographics, family history, and behaviour to identify those at higher risk of this devastating illness, so that it can be treated early – potentially saving thousands of lives every year. The ADR will also offer learnings for and help us shape our new national data library, a central government resource designed to bring together existing research programmes and make it easier for policymakers and public bodies to access and use data securely to improve public services. As the incredible opportunities and challenges of technology like AI advance at unprecedented speeds and as we grapple with the fate of our planet as our climate changes, using data to drive policy for the generations to come has never been more important. This government is driven by a plan for change that will transform the lives of the British people, from growing our economy so that our payslips go further, to unlocking opportunity for everyone regardless of background, and building an NHS that is fit for the future and makes the most of the opportunities in new technology. Data can play a huge part in getting that right and targeting government support where it is needed most.


The Independent
10 hours ago
- The Independent
Wanna get away? Sorry, there's no destination safe from seasonal allergies
There's no escape from it — pollen is in every U.S. state, ready to torment your nostrils. The seeds rain down from the trees in a strange yellow haze and ascends to the skies from the flowers and grasses. Even if you could easily pack up and move, nowhere is safe to avoid the dreaded, sniffling effects of seasonal allergies. 'It's a little bit like playing Russian Roulette,' Hannah Jaffee, the director of research at the Asthma and Allergy Foundation of America, told The Independent. 'If you already have allergies, you can be exposed to an entirely different set of allergens if you relocate.' 'Worst case scenario: you may live in a place and either not have allergy symptoms or have mild allergy symptoms. Then, you move somewhere else and start developing significant symptoms,' she added. Everyone is going to respond differently to a new location. 'If you already have allergies, you can be exposed to an entirely different set of allergens if you relocate. So, you might be trading some symptoms for others.' 'And then, in some cases, your symptoms might improve by relocating,' Jaffee said. More than 100 million Americans live with various types of allergies and over 81 million have seasonal pollen allergies. Some are genetically predisposed to develop allergies, which can factor into what they're allergic to and potentially how severe their symptoms would be. Many people develop allergies as they age and their immune system weakens. Seasonal allergies, which are also commonly known as 'allergic rhinitis' or hay fever, occur when people are exposed to pollen. The inflammatory response can cause sneezing, congestion, a runny nose, or red, watery, and itchy eyes. For people with asthma, it can lead to an asthma attack. For tens of thousands of people, it may even result in a trip to the emergency room. The severity of allergy symptoms also depends on where you live. There are three main types of pollen, including tree, grass, and weed. This year, the highest tree pollen levels were forecast across a wide swath stretching from the Pacific Northwest to the Southeast. The highest weed pollen levels were expected around the Plains states, the Carolinas, and along the Gulf Coast. The foundation also released what it named the nation's top 10 cities for seasonal allergies, with most located in the South and Southeast. Historically, the worst cities are in those regions, Jaffee noted. 'That's because these are climates that tend to be more humid and warmer, so they kind of favor that growth of pollen and mold,' she explained. Wichita, Kansas, led the rankings as the worst city for allergy sufferers. 'Since allergies are so different for everyone, you can thrive in the Southeast part of the U.S. and not have any allergies or still experience significant allergy symptoms elsewhere,' Jaffee said. 'It's kind of a mixed bag.' So, what do you do if you are moving — or want to? Generally, experts recommend that you visit the location for about two to four weeks ahead of time to get a sense of how your body responds, or to visit during different seasons. Talking to an allergist will also be useful for more personalized recommendations. Still, pollen seasons are getting longer and stronger for everyone. Human-caused climate change is resulting in earlier seasons, as well, with warmer temperature trapping heat around urban areas, increasing air pollution, and stimulating pollen production. The amount of pollen released by trees is higher and the strength of the allergic response to the tree pollen appears to be stronger. 'There's no question [that] as there's global warming, the pollen season is increasing,' Dr, Sanjiv Sur, director and professor of Allergy and Immunology at Baylor College of Medicine, said earlier this year. What may help ease the pain, if only for right now? Dr. Neelu Tummala, a clinical assistant professor of otolaryngology at NYU Langone Health, advises that people time taking medications so they are optimally effective, change clothes and take off shoes after spending time outside, and bathe pets. Jaffee recommends a pollen tracking app, in addition to personalized allergy testing. But, ultimately, there needs to be a wider response. 'Long-term, we should be looking at policy change to reduce the impact of climate change,' said the foundation's chief mission officer Melanie Carver.


Daily Mirror
16 hours ago
- Daily Mirror
Breast cancer warning issued to all women as common sign won't always appear
More difficult to notice and poorly understood, lobular breast cancer is finally coming under the spotlight but it's not as easy to spot the signs, especially one common one woman look for Lobular breast cancer, also known as invasive lobular carcinoma (ILC), is more common than ovarian and skin cancer yet there is little awareness of it. According to Cancer Research UK, one in seven women will be diagnosed with breast cancer in their lifetime and around 15% of those will have ILC. BBC presenter Victoria Derbyshire, 56, was diagnosed with the disease in 2015. ILC is different to the most common form of ductal breast cancer. Instead of starting in the breast ducts, it starts in the lobules, the glands that produce milk, and grows in a spider's web pattern. Cancer cells infect the tissue around the glands and rarely show in lumps, so it is harder to spot and likely to be diagnosed later. At least a fifth of ILC cases return years later. When this happens, the cancer becomes even harder to treat. And yet it's an under-diagnosed subtype of breast cancer that is underfunded and poorly understood. Kate Ford, a campaigner from the Lobular MoonShot Project (LMSP), says, 'The basic biology of this disease has never been studied and it has no specific treatment. ILC needs a moon shot approach – a fast injection of cash – to research funding.' On 24 June, 22 women led by LMSP Founder Dr Susan Michaelis, who sadly passed away from ILC on 9 July, held a vigil outside 10 Downing Street and delivered a petition backed by more than 350 MPs to the Prime Minister, calling for urgent funding for ILC research. Symptoms to watch out for Lobular breast cancer rarely forms lumps. Instead, the things to look out for include an area of thickening or swelling around the breast, a change in the nipple, for example it becoming inverted, or a change in the skin, such as dimpling, puckering or even a small new mark. Don't ignore other changes Cancer Research UK suggests people should also look out for pain and itching, a new lump in your breast or armpit, a change in the size, shape or feel of your breast, skin changes in the breast such as a rash or redness of the skin, fluid leaking from the nipple in a woman who isn't pregnant or breastfeeding and/or changes in the position of the nipple. If you see any of these symptoms you're advised to visit your doctor. Get a diagnosis Your GP will refer you to a clinic if they believe you might have ILC. They will examine your breasts and check for swollen lymph nodes. They may use a mammogram, an ultrasound if you're under 35, a biopsy or an MRI scan. MRI and biopsy are the most effective detection tools for ILC. Mammograms and ultrasound often fail to show the presence of the disease. How ILC is treated ILC is currently treated with chemotherapy, surgery and drugs to reduce the level of oestrogen, which cancer cells need to grow. Chemo works best on fast-dividing cells, but lobular breast cancer is not fast dividing, so the efficacy of chemo on ILC is not entirely understood. Depending on the size and abnormality, whether cells have receptors for drugs, your general health and age, a doctor will consider the best treatment, but generally it is the same as for the more common types of breast cancer. Hope for the future The Lobular Moon Shot Project is campaigning to raise £20min government funding to carry out vital research on ILC in partnership with the Manchester Breast Centre and led by breast biology expert Professor Rob Clarke.'With this funding, we could potentially develop a drug and begin testing it on patients within the next five years,' he says. "The fear of recurrence is always with me" Lobular Moon Shot Project campaigner, teacher and mum-of-three Katie Swinburne, 49, was diagnosed with ILC in 2023. 'Prior to my diagnosis, I was extremely fit and healthy, and took care with the food I ate. I remember the morning I found a lump very clearly. It appeared overnight after two years of other symptoms including pain and itching. It was extremely large, but in my ignorance I thought it was a cyst. 'I went to see my GP and was sent to have a mammogram, the nan ultrasound. The sonographer felt the lump but was confident there was nothing to worry about. He performed a biopsy to try and establish what the lump was. 'At my next appointment, a consultant came in, followed by a nurse. I was soon to learn the nurse was a Macmillan nurse. I was smiling and chatting away to the consultant, expecting to be sent on my way, when he said, 'We have the results – you have an invasive lobular carcinoma.' 'Hearing the words 'you have cancer' is like nothing else. My life, my body and my future were no longer assured. At the time of my diagnosis, my children were 10, 12 and 14. The thought of leaving them left me breathless. 'A whirlwind of appointments followed, including CT, MRI and DEXA scans. I had a double mastectomy and dose-dense chemotherapy, then radiotherapy. The nurses are angels. They hold your hand through it all. You find reserves you never knew you had. 'The fear of recurrence is always with me. I'm two years on from diagnosis and still too young for screening. Had that lump not appeared, my story might be very different. I think we need to start education and screening at a much younger age.' The Macmillan Support Line offers free, confidential support to people living with cancer and their loved ones. Call for free within the UK on 0808 808 0000