
‘I was raped. And my dreams were shattered' – Gina Miller on abuse, cancer and the toxic race for Cambridge chancellor
'I rarely have time for breakfast,' says Miller, who turned 60 this year. 'I'm only just able to drink coffee again after my chemotherapy treatment for breast cancer, which is amazing. As my dose has just been reduced, I was able to have the one cup I'm limited to today.'
The only outward clue that she is undergoing the treatment is a new Jean Seberg-style crop. She exudes energy and a zest for life.
'I was diagnosed in September last year,' she says, breezily. 'Actually, I should say 'self-diagnosed'. I knew something wasn't right with one of my breasts. The GP kept sending me away but after my fourth visit they agreed to a biopsy. I am so glad I listened to my inner voice that all was not well. It turned out that I had an aggressive form of the disease and had to have a very high dosage of chemotherapy from October to February. In March, I had a double mastectomy. I will be on the lower-dose chemo until December.'
Since the recurrence rates are so high, Miller has opted for further surgery to remove her ovaries and fallopian tubes in January. 'I don't want to keep looking over my shoulder to see if it's going to come back,' she says. 'I'm lucky; I've had my three kids so I don't need my female organs. If I get rid of everything, the prognosis is good.'
In February, in the midst of what must have been an exhausting and stressful period, Miller was approached by a group of Cambridge professors who asked if she might be interested in standing for chancellor. She initially said no, believing it was open only to Cambridge alumni, then learned that this was not a requirement. Still she demurred, but not because of her illness.
'I told them I wasn't interested in taking on a ceremonial role. I only want to do something that has a real impact because I think our country, and the world in fact, is at a particularly traumatic time in history. Cambridge has the resources, and the great, brilliant minds and standing as an institution, to contribute to the world and to us finding a more resilient and sustainable future.'
Researching what scope the chancellor actually has, she discovered that the role includes the power to ensure that university officers are performing as they should be, and to resolve disputes where solutions can't be found otherwise. 'I came to the conclusion that although it has previously been a figurehead role, that could change. The chancellor sits on the university council so could act as chair. I decided I would throw my hat in the ring.'
How did she find the energy to do that while undergoing chemotherapy? 'It's true, chemo is gruelling. It's not only the treatment, it's the emotional side of it. Your appearance changes. Losing your hair, your eyebrows, your eyelashes, it changes the way people treat you and judge you as a woman. But although I suffered terribly with nausea, I didn't stay in bed all day. I still tried to work for two to three hours a day and rested a lot, too.'
I tell her the new haircut looks elegant and she laughs. 'You never normally see the shape of your head. I think I have a weird double crown. But thank you.'
Miller made her name in 2016 in a landmark challenge to the government's right to trigger article 50, formalising the UK's exit from the EU, without a parliamentary vote, and then in 2019, successfully blocking a no-deal Brexit by fighting Johnson's attempt to prorogue parliament for five weeks. Although you may imagine that a freethinking, remainer-leaning academic hub such as Cambridge might welcome Miller with open arms, her appearance on the 10-strong candidate list has ruffled feathers.
For one thing, there has never been a female chancellor in the university's 800-year history. To give a sense of the type of individual the role attracts, the previous two incumbents were Prince Philip, who was succeeded in 2011 by Lord Sainsbury of Turville. Apart from Miller, the only other female candidate is the comedian Sandi Toksvig. Also in the running are the former BP head John Browne and the former Labour minister Chris Smith.
In his campaign statement, another candidate, the astrophysics professor Wyn Evans, wrote: 'If Cambridge needs a high-profile or celebrity chancellor to be noticed, we might as well give up and rebrand the university as a reality TV show: 'Keeping Up With the Cantabrigians'.'
Miller is unimpressed: 'Weirdly, the candidate who made the Kardashians comment is actually someone who is saying that the university needs to address its bullying and harassment issues.'
There have also been cries of foul play, with concerns over certain candidates spending money on PR and social media, bad-mouthing opponents and using the university insignia to promote themselves, which is against protocol.
In the run-up to the elections, Miller has been speaking to past and present students, professors, researchers and academics at the university. 'The word that keeps coming up is complacency. Cambridge really needs leadership. Its ranking has slipped [from fifth to sixth in the world], and it needs to resolve the issues it's facing. Behind the scenes there is disquiet, be it in terms of discrimination, short-term contracts, intergenerational unfairness and the coming austerity measures.'
She says that throughout her life, education has always been 'the anchor that has helped me to survive'. Her biggest inspiration was her father, Doodnauth Singh, who rose from being a petrol pump attendant in Guyana, studying law at night school, to become the country's attorney general. 'Education is what brought me to the UK, to a small boarding school in Eastbourne aged 11. Guyana was going through a dictatorship at the time and so I was sent to the UK to be safe. My parents were deeply passionate believers in the power of education.'
But beyond all these motivations, she has a more pressing reason to want to contribute to the university's future: 'It just so happens that the type of breast cancer I have is a very rare genetic mutation, PALB2, which affects only 1-2% of breast cancer patients. Some of the scientists who discovered it are based at Cambridge University and I've got to know them, talking about the astonishing work they are doing and the medical advancements going on there. So I do feel as if I have a debt to repay them.'
That the university needs strategic leadership is not in doubt. According to its internal watchdog, the university ran up a deficit of £53m for 2023/24 'with no clear understanding of what has happened or why'. It is expected to report a £47m deficit for 2024/25 and cuts of 5% have been instigated across the institution.
Cambridge has also been ranked the worst university in the country for the support it offers its disabled students, according to a recent study. 'That is not good, especially when you have so many neurodiverse individuals. We need to tap into that brilliance, but that has to come with care and support,' says Miller, whose eldest daughter, now 37, has severe special needs.
One of the biggest issues she is keen to address is wellbeing and safety support for students and staff. 'There is a lot of pressure on individuals to perform in a way that excels at every level. But not much focus on supporting people to get there.'
She says that she would advocate for each college having a properly trained psychotherapist and wellbeing support teams. 'This isn't just for students, it's for staff. I've spoken to lots of young female researchers, especially those from ethnic minority backgrounds, about microaggressions and misogyny that is going on. They need an independent person to talk to. All schools and corporate environments offer this. Why doesn't Cambridge University? It's a false economy to run away from this.'
Miller has very good reason to get behind this cause. In 1987, two months before she was due to sit her final exams for a law degree at the Polytechnic of East London, Miller was attacked by a group of four Asian men on campus.
Even 38 years on, she is still visibly upset recounting the events of that night. 'It happened on campus. It was cricket season and India had just played Pakistan. The Asian student societies were all celebrating. I had been studying in the library and when I left, I was intending to go to Mile End tube station. Four men spotted me. They had wrongly identified me as an Indian woman and accused me of dressing and behaving too western. They had seen me with Adrian, my white boyfriend. They attacked me.' She pauses, distressed. 'I was raped.' This is the first time Miller has described the incident as rape.
She did not report the crime, nor did she tell anybody. 'Like many cultures, in my community there is a lot of shame associated with crimes like this.'
She stopped attending lectures. 'I was completely broken and dysfunctional for at least seven months, probably a year. In my mind, I was going to go back to study when I felt better. My dream had always been to follow in my father's footsteps, to become the best goddamn criminal barrister there was. Or maybe I'd go into family law. But after the attack, my dreams were shattered. In the end, unsupported, I just couldn't face going back.'
Instead, she moved to Bristol to set up a photographic business with Adrian, who became her first husband and with whom she had a daughter when she was 23. Later, she went to study marketing at the University of North London. Ironically, 30 years after she left the Polytechnic of East London (which became the University of East London in 1992), it awarded her with an honorary doctorate of laws in 2017.
In her memoir, Rise, Miller describes feeling an acute sense of 'identity limbo' when she started law school. I wonder if this might explain the drive behind her hyperactive CV. She has campaigned on domestic violence, modern-day slavery and online abuse, as well as launching numerous business ventures. In 2024, she stood as a parliamentary candidate for Epsom and Ewell, representing her own political party, True and Fair, but lost her deposit.
'I've had a very eventful life,' she laughs. 'Education has always supported me, but life has educated me, too.' Along the way, she escaped a difficult second marriage, taking her eldest daughter with her and later marrying her third husband, Alan, with whom she has a son who is studying medicine and a daughter who has just sat her A-levels.
But since 2016, her life has been lived against a backdrop of horrendous abuse. At the height of the Brexit legal proceedings, her family were under the protection of the anti-terrorism squad. To this day, she is still at the sharp end of public vitriol. Why would she put her head above the parapet again? 'I've considered this role really carefully. I think I have the bandwidth to do it.' She does add, though, that she is done with politics. 'I discovered that it's not for me. I'm disillusioned with our political system.'
Before we finish, I ask Miller if she ever switches off, and she mentions her love of cooking, sharing with me a foolproof recipe for crispy aubergine, as well as dancing and music. Unexpectedly, she turns out to be an Iggy Pop fan. Was she a punk? 'No! But I did like Chrissie Hynde. As for Iggy, I just love Lust for Life. If you want to understand my take on life, that is the perfect song.'
Information and support for anyone affected by rape or sexual abuse issues is available from the following organisations. In the UK, Rape Crisis offers support on 0808 500 2222 in England and Wales, 0808 801 0302 in Scotland, or 0800 0246 991 in Northern Ireland. In the US, Rainn offers support on 800-656-4673. In Australia, support is available at 1800Respect (1800 737 732). Other international helplines can be found at ibiblio.org/rcip/internl.html
Hashtags

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


Scottish Sun
11 minutes ago
- Scottish Sun
Grandmother, 57, dies after ‘trapped nerve' mistakenly blamed for her back pain and headaches
Click to share on X/Twitter (Opens in new window) Click to share on Facebook (Opens in new window) A GRAN passed away after her back pain was initially dismissed as a 'trapped nerve'. Helen Arthur, 57, first became unwell on Good Friday in April 2019, experiencing persistent back pain and visual disturbances. Sign up for Scottish Sun newsletter Sign up 6 Helen Arthur with her grand-daughter Penny Credit: SWNS 6 Helen, pictured with her husband Brent, was initially told her back pain was caused by a trapped nerve Credit: SWNS 6 But she was later diagnosed with an aggressive brain tumour called glioblastoma Credit: SWNS Her GP put it down to a trapped nerve but Helen's condition didn't improve. After developing headaches, Helen had an eye test, and her optician thought she may have suffered a minor stroke, so sent her to hospital. A CT scan revealed a mass on Helen's brain and she was diagnosed with a glioblastoma, an aggressive and incurable brain tumour. In May 2019, Helen underwent surgery to remove the tumour, followed by six months of combined chemotherapy and radiotherapy. But a routine monitoring scan in 2021 showed the tumour had grown back and Helen underwent another course of combined radiotherapy and chemotherapy. Another MRI scan revealed Helen had multiple inoperable tumours and her condition deteriorated too quickly to treat. Helen, from Merthyr Tydfil, Wales, died in May 2022, three years after her initial surgery. Her husband Brent Arthur said: "We were told Helen had a brain tumour which was a complete shock. "The doctors said most people survive just two to three years. "Words left me, I was speechless. A mum dismissed her twitching eye as stress until discovering it was a rare brain tumour "We were told there would be a recurrence, but it took us by surprise, we thought we had more time." It comes after the NHS launched a new immunotherapy trial to treat glioblastoma and is seeking people to take part in it - after one patient saw his disease vanish. After Helen's first CT scan, at Prince Charles Hospital in Wales in Merthyr Tydfil, which revealed a mass, she was transferred to the University Hospital of Wales in Cardiff. Brent recalled getting the awful phone call from his son, revealing the devastating news in May 2019. He said: "I wasn't feeling well so I went to bed and expected our son Benjamin and Helen to be home within a couple of hours. 6 Helen with her grand-daughters Penny, on the left, and Nora Credit: SWNS 6 From the left, Emily, Benjamin, Brent and Helen - the gran spent lots of time with her family after her diagnosis Credit: SWNS "I got a call from Benjamin saying I needed to go to the hospital. "Confused as to what could be wrong, I went. "That was when our lives changed." Helen's initial surgery and six months of combined chemotherapy and radiotherapy were thought to have been a success. She was monitored with quarterly scans as she continued to live an active life, and spend time with her family and her grandchildren. In late 2021, one of these scans showed the cancer had come back. Helen underwent another course of combined radiotherapy and chemotherapy but an MRI scan in April 2022 revealed multiple inoperable tumours had developed. Just a week later, Helen's original pathology results showed she had a one-in-three million genetic mutation, which might respond to targeted medication. She never got to enjoy the role she was so excited for. All she ever wanted was to be a young nan, but this cruel disease robbed her of that Brent Arthur Sadly, by this point, Helen's condition had deteriorated, and treatment was not possible. Brent said: "We were all shocked and devastated. "We spent as much time together as possible, with the children and grandchildren. "Seeing Helen decline was difficult for us all." Helen is survived by husband Brent as well as children Emily, 35, and Benjamin, 33, and grandchildren Penny, six, Nora, four, Isaac, three, and Rhoda, one. Brent said: "Helen lived for her family. "She was looking forward to reducing her work hours so she could help care for our grandchildren. "That's what hurts the most, she never got to enjoy the role she was so excited for. "All she ever wanted was to be a young nan, but this cruel disease robbed her of that." Push for a cure Brent and his family have now raised more than £5,700 for Brain Tumour Research, enough to fund two days of research at one of the charity's Centres of Excellence. On Father's Day on June 15, Brent completed a 10,000-foot skydive in Helen's memory. Brent said: "Our family has been robbed of a wife, mother and grandmother, and more funding is desperately needed for research. "Without it, other families will continue to face the same heartbreak we've been going through." Each year in the UK, around 3,200 people are diagnosed with glioblastoma, yet just 160 will survive five years or more. What are the symptoms of glioblastoma and how soon do they show? Glioblastomas are the most common brain tumour in adults, while also being very aggressive and deadly. Brain Tumour Research says tumours increase pressure in the skull, causing headaches. Symptoms to look for are: Headaches Loss of appetite Nausea and vomiting Loss of balance Mood swings Problems speaking Problems with memory or concentration Seizures Impaired vision The symptoms can initially be quite non-specific, meaning they could be mistaken for lots of other conditions- even stress or a hangover. The brain controls so many different functions that symptoms can vary greatly depending on where in the brain the tumour is. Glioblastomas are very fast growing. Once found, experts can see them double within seven weeks. But, according to Dr Stephen Bagley, assistant professor of medicine at Penn Medicine, the first spark of glioblastoma in the brain remains something of a mystery to medical experts. One study concluded that a glioblastoma starts growing 330 days on average - almost a year - before a diagnosis. Another found that there are changes in immune function up to five years before a diagnosis, with markers in blood samples - but symptoms only occur three months prior. Glioblastoma accounts for one in three primary brain tumour diagnoses, and current treatment offers little in the way of long-term hope. Letty Greenfield, community development manager at Brain Tumour Research, said: "Helen's story is heartbreaking and all too common. "Glioblastoma is an aggressive brain cancer with limited treatment options and a devastating prognosis. "We are incredibly grateful to Brent and his family for honouring Helen's memory through their fundraising. "It's support like this that helps us push for better outcomes and ultimately a cure."


Telegraph
11 minutes ago
- Telegraph
I have helped more than 300 people reverse their diabetes – here's how
'The traditional view of type 2 diabetes is that it's chronic and progressive,' says registered dietitian Helen Gowers. This will be a recognisable characterisation of the condition for the 4.1 million people in the UK who have it and, upon diagnosis, were swiftly put on to a lifetime course of medication, typically metformin and then insulin, to keep their blood sugar levels at bay. 'However, our approach is to undo insulin resistance by removing the visceral fat that's clogging up key organs – the root cause of type 2 diabetes – so everything starts working normally again,' Gowers says. 'You can't achieve that with medication, it has to be done through weight loss and diet.' Doctors now recognise that reversing type 2 diabetes through diet is a very real possibility for many patients. A study, published in the journal BMJ Nutrition, Prevention & Health in 2023, showed a diet low in carbohydrates (found in bread, potatoes and pasta) helped 51 per cent of the 186 type 2 diabetes patients involved achieve remission within three years – meaning their blood sugar levels were below the type 2 diabetes range and they no longer needed medication. To spread this method to the masses, Gowers joined the charity Public Health Collaboration in 2021, offering an eight-week diet and lifestyle course called The Lifestyle Club (TLC) for type 2 diabetes and prediabetes patients to help them reverse the condition. So far, more than 1,340 people have completed the course, and based on a recent TLC service evaluation in collaboration with the University of Surrey, she estimates 308 of them will have achieved remission or reversed prediabetes. Their study found a 23 per cent remission rate for a TLC cohort in Guildford after six months, which will have reduced their risk of developing diabetes-related complications, such as heart attacks, strokes and kidney disease. What causes type 2 diabetes and how can it be reversed? Scientists are still trying to unpick the exact mechanism behind type 2 diabetes. However, it is known that a build-up of fat in the liver and pancreas are major contributors. We all have a personal threshold for being able to store body fat, Gowers says. 'Once you've reached that level, the only place you're going to be able to store extra calories is in your abdominal area as visceral fat, which surrounds the liver and pancreas.' Eventually, the liver and pancreas then become clogged up with fat, which contributes to insulin resistance, meaning that the cells stop responding to insulin – a hormone vital for bringing down blood sugar levels. 'The pancreas then churns out more and more insulin as the insulin resistance gets worse to try and overcome it, and it's only when it finally can't produce enough that blood sugar goes up and remains high,' Gowers explains. It is at this point that type 2 diabetes is diagnosed. 'Diabetes is literally just the end of the show.' While needing to pass urine frequently, being very thirsty and feeling very tired are all symptoms, a lot of people experience no symptoms. 'The body's so incredible in the way that it manages all of this quietly,' Gowers says. Is remission possible for everyone? When it comes to putting type 2 diabetes into remission, the goal is to drain the liver and pancreas of fat, so their function can return to normal, reversing insulin resistance – meaning that people can come off their medication. 'For people who have been diagnosed with type 2 diabetes within the last year, that remission rate shoots up to 77 per cent,' Gowers says. 'For prediabetes, it's 93 per cent. The earlier in the journey that you find people, the better.' However, there are cases of patients who had type 2 diabetes for decades being able to reverse it. Even if you're unable to hit remission, there are still benefits of following a low-carb diet in an attempt to reverse it, she notes. Weight loss is one of them. 'We've had people who have had diabetes for 20, 30 years and they make phenomenal progress,' she says. 'They'll reduce their medication, their blood pressure will come down, they'll lose a bit of weight, they'll feel more energetic. There will always be improvements, even if we don't call it remission, so it's definitely worth a go.' How to reverse type 2 diabetes Reduce your sugar and carb intake Cutting out sugar and dramatically reducing your intake of carbohydrates, both of which cause surges in blood glucose, are the main changes needed to reverse type 2 diabetes, Gowers explains. 'You want to reduce them as low as required to achieve your goals, and this varies from person to person,' she says. The reason is that these foods raise insulin levels, and when these are high, you can't lose body fat, Gowers says. A low-carbohydrate diet means having no more than 130g per day. When you do have carbs, it should be whole-grain varieties, such as brown rice, pasta or bread. In practice, this means cutting out food including white bread, rice, pasta, potatoes, crackers and cereal. Patients are advised to cut out added sugar – found in sweets, cakes, biscuits, chocolate and fizzy drinks – and avoid foods that are high in natural sugar, such as honey and certain fruit. While blueberries, strawberries and raspberries are allowed as they are lower in natural sugar, it's recommended not to have some tropical fruit, such as bananas, oranges, grapes, mangoes or pineapple, because their sugar content is very high. It's also key to ditch low-fat foods, which are typically high in sugar. 'Go for full-fat dairy, fish, meat and eggs,' Gowers says. 'The natural fat that comes with those foods is fine. It's turning the current dietary guidelines on their head, really.' Consider options such as coleslaw for a tasty, low-carb side, and cheese, avocado and mayonnaise can also be enjoyed, she notes. Breakfast is a good place to start, when it comes to adopting the low-carb diet. 'People tend to consume a lot of carbs at breakfast, whether it's bread, cereal or pastries,' Gowers says. 'The human body only needs one teaspoon of glucose in the bloodstream at any one time and if you're having toast, cereal and orange juice for breakfast, that's going to break down into about 16 teaspoons of sugar. 'Full-fat yogurt and berries or eggs won't cause spikes in blood glucose and they're really nutrient-dense, meaning they will fill you up for the rest of the morning.' Fasting, which can be done by pushing back your first meal of the day until lunchtime, can also be a helpful tool in sticking to the low-carb diet, Gowers notes. You don't need to be worried about skipping a meal, she says. 'You're not starving – your body is going to be using fat stores, which is great. Think of it in terms of, I can either fuel my body with food or I can use my own fat stores as fuel.' However, she recommends anyone taking medication to seek advice before changing their meal patterns. Rather than a quick fix, the idea is that low-carb and low or no sugar are diet principles that you carry forward for life, she says. 'Some people might go all out for eight weeks to reverse their diabetes and then think, 'There's no way they can be as strict in the long term,' so make concessions to keep their diabetes status within the range they're happy with,' Gowers notes. This may mean that they are able to reduce their medication or put themselves into the prediabetes category, rather than fully reversing it, she says. Base meals on 'real' foods If you begin cutting out carbohydrates and sugar, you may naturally find yourself gravitating towards whole foods, such as protein, vegetables and dairy, Gowers says. 'Make sure you have a good amount of veg to fill you up – it also offers lots of fibre,' she notes. A large portion of broccoli, courgette or green beans can substitute mash, pasta or rice – and they can still be covered with gravy, Bolognese or curry. Thinly sliced cabbage that has been lightly boiled is a great low-carb option instead of tagliatelle, she notes. 'The idea is that the fewer carbs you're eating, your body shifts to burning fat, so you're going to be able to utilise your stored fat to fuel your body, rather than the sugar you were eating before,' she explains. 'The note of caution is that you don't want to add loads of extra fat when you're trying to lose weight – but it will fill you up. It's just eating real food and the fat that comes with that food.' It's also recommended not to eat too much processed meat, which includes ham, bacon and sausages. Snacking is generally not recommended, though some crudités with full-fat hummus, a couple of squares of dark chocolate or a few plain nuts won't spike your blood sugar or leave you feeling hungry, she says. 'But people find that they don't need all of those extra snacks that they were used to having before.' Have enough water and salt In the early stages of following the low-carb diet, it's important to make sure you're drinking plenty of water and having enough salt, Gowers says. 'When you switch over from having a diet that's very high in carbohydrates to low-carb, you may initially become dehydrated and get headaches or constipation,' she says. 'Insulin disrupts the way you process salt so you're releasing a lot of the salt and water that your kidneys were holding on to,' she explains. 'One of the reasons that people lose weight quite quickly is because you're losing all of that water retention.' As a result, you need to make sure you're replacing the lost salt, which you can simply do by adding salt to your meals as you cook them or adding an extra stock cube to your meals, as these are high in salt, she says. 'Having sufficient water and salt means you're not going to be dehydrated and you're less likely to get headaches, cramps and feel a bit lethargic as you transition to using fat as your fuel.' Have a support network When overhauling your diet, it's vital to have a support network around you to help you stay on track, Gowers says. 'Long-term support is what makes the difference,' she notes. It's especially important that it's available when people feel like they've drifted off their diet and are trying to get back on it again. On the eight-week TLC course, there are weekly 90-minute Zoom sessions overseen by a health coach. Once the course is finished, people are invited to monthly catch-up meetings, where there are guest speakers, such as consultants and chefs. There are also Facebook and WhatsApp groups for people to chat to each other or suggest low-carb meal ideas, and some meet for coffee or go for walks together, she says. 'It's keeping the momentum going,' she says. If you don't join the course, you can enlist the help of friends and family to keep you on track. It's initial intensive support, as well as the long-term support after the course, that is vital to ensure patients stick to the healthy changes they've made, Gowers explains. 'People can dip in and dip out; it's not that everybody needs the support all the time but you've got to be there so that when someone needs it, you're there to help and get them back on track.' Prioritise diet over exercise While exercise is excellent for health, diet is the focus when it comes to reversing type 2 diabetes, according to Gowers. 'It's what's going to give you 70 per cent of the benefits,' she says. However, you're much more likely to maintain your dietary changes if you bring in some exercise as well, so it's important to be more active, even if it's not straight away when you first try the diet, she notes. 'Once you've regained some metabolic health, you've lost a bit of weight, you're feeling so much better, you are much more likely to want to do some exercise. 'Don't beat yourself up trying to go to the gym three times a week at the beginning; start with diet and naturally you will feel more like moving about as time goes on.'


The Sun
11 minutes ago
- The Sun
Grandmother, 57, dies after ‘trapped nerve' mistakenly blamed for her back pain and headaches
A GRAN passed away after her back pain was initially dismissed as a 'trapped nerve'. Helen Arthur, 57, first became unwell on Good Friday in April 2019, experiencing persistent back pain and visual disturbances. 6 6 6 Her GP put it down to a trapped nerve but Helen's condition didn't improve. After developing headaches, Helen had an eye test, and her optician thought she may have suffered a minor stroke, so sent her to hospital. A CT scan revealed a mass on Helen's brain and she was diagnosed with a glioblastoma, an aggressive and incurable brain tumour. In May 2019, Helen underwent surgery to remove the tumour, followed by six months of combined chemotherapy and radiotherapy. But a routine monitoring scan in 2021 showed the tumour had grown back and Helen underwent another course of combined radiotherapy and chemotherapy. Another MRI scan revealed Helen had multiple inoperable tumours and her condition deteriorated too quickly to treat. Helen, from Merthyr Tydfil, Wales, died in May 2022, three years after her initial surgery. Her husband Brent Arthur said: "We were told Helen had a brain tumour which was a complete shock. "The doctors said most people survive just two to three years. "Words left me, I was speechless. "We were told there would be a recurrence, but it took us by surprise, we thought we had more time." It comes after the NHS launched a new immunotherapy trial to treat glioblastoma and is seeking people to take part in it - after one patient saw his disease vanish. After Helen's first CT scan, at Prince Charles Hospital in Wales in Merthyr Tydfil, which revealed a mass, she was transferred to the University Hospital of Wales in Cardiff. Brent recalled getting the awful phone call from his son, revealing the devastating news in May 2019. He said: "I wasn't feeling well so I went to bed and expected our son Benjamin and Helen to be home within a couple of hours. 6 6 "I got a call from Benjamin saying I needed to go to the hospital. "Confused as to what could be wrong, I went. "That was when our lives changed." Helen's initial surgery and six months of combined chemotherapy and radiotherapy were thought to have been a success. She was monitored with quarterly scans as she continued to live an active life, and spend time with her family and her grandchildren. In late 2021, one of these scans showed the cancer had come back. Helen underwent another course of combined radiotherapy and chemotherapy but an MRI scan in April 2022 revealed multiple inoperable tumours had developed. Just a week later, Helen's original pathology results showed she had a one-in-three million genetic mutation, which might respond to targeted medication. She never got to enjoy the role she was so excited for. All she ever wanted was to be a young nan, but this cruel disease robbed her of that Brent Arthur Sadly, by this point, Helen's condition had deteriorated, and treatment was not possible. Brent said: "We were all shocked and devastated. "We spent as much time together as possible, with the children and grandchildren. "Seeing Helen decline was difficult for us all." Helen is survived by husband Brent as well as children Emily, 35, and Benjamin, 33, and grandchildren Penny, six, Nora, four, Isaac, three, and Rhoda, one. Brent said: "Helen lived for her family. "She was looking forward to reducing her work hours so she could help care for our grandchildren. "That's what hurts the most, she never got to enjoy the role she was so excited for. "All she ever wanted was to be a young nan, but this cruel disease robbed her of that." Push for a cure Brent and his family have now raised more than £5,700 for Brain Tumour Research, enough to fund two days of research at one of the charity 's Centres of Excellence. On Father's Day on June 15, Brent completed a 10,000-foot skydive in Helen's memory. Brent said: "Our family has been robbed of a wife, mother and grandmother, and more funding is desperately needed for research. "Without it, other families will continue to face the same heartbreak we've been going through." Each year in the UK, around 3,200 people are diagnosed with glioblastoma, yet just 160 will survive five years or more. What are the symptoms of glioblastoma and how soon do they show? Glioblastomas are the most common brain tumour in adults, while also being very aggressive and deadly. Brain Tumour Research says tumours increase pressure in the skull, causing headaches. Symptoms to look for are: Headaches Loss of appetite Nausea and vomiting Loss of balance Mood swings Problems speaking Problems with memory or concentration Seizures Impaired vision The symptoms can initially be quite non-specific, meaning they could be mistaken for lots of other conditions- even stress or a hangover. The brain controls so many different functions that symptoms can vary greatly depending on where in the brain the tumour is. Glioblastomas are very fast growing. Once found, experts can see them double within seven weeks. But, according to Dr Stephen Bagley, assistant professor of medicine at Penn Medicine, the first spark of glioblastoma in the brain remains something of a mystery to medical experts. One study concluded that a glioblastoma starts growing 330 days on average - almost a year - before a diagnosis. Another found that there are changes in immune function up to five years before a diagnosis, with markers in blood samples - but symptoms only occur three months prior. Glioblastoma accounts for one in three primary brain tumour diagnoses, and current treatment offers little in the way of long-term hope. Letty Greenfield, community development manager at Brain Tumour Research, said: "Helen's story is heartbreaking and all too common. "Glioblastoma is an aggressive brain cancer with limited treatment options and a devastating prognosis. "We are incredibly grateful to Brent and his family for honouring Helen's memory through their fundraising. "It's support like this that helps us push for better outcomes and ultimately a cure." 6