
Covid guru Devi: How my fight for NHS cancer care laid bare Scotland's waiting list crisis
A public health expert who advised the Scottish and UK governments has revealed how her own battle to access cancer treatment exposed chronic failures within the NHS.
Professor Devi Sridhar became a leading voice during the pandemic, when she counselled Nicola Sturgeon on the SNP 's COVID response and made regular appearances on television shows like Good Morning Britain and Channel 4 News.
But despite her significant expertise and government influence, the Oxford-educated academic was told she could face a six-month wait to learn whether the abnormal cells discovered in a smear test were cancerous.
Ms Sridhar said: 'I was calling three to four times a day to see if anything was available, saying I could come any time.
'It was scary and it was frustrating because I teach this stuff, right? So I know there's delays in the system and I also know the statistics on treatments. Each day I move forward [before] being treated, my chance goes down by 2 per cent.'
Like 280,000 other Scottish women each year, Sridhar had undergone a routine test to detect signs of HPV, a group of viruses responsible for 95 per cent of cervical cancer cases.
The health expert was shocked to receive a call explaining that 'possibly cancer' was present – but even less prepared for the prognosis of indefinite delays and administrative chaos that accompanied it.
Sridhar repeatedly begged for a date for a follow-up consultation, but was left 'waiting on a letter from the system where you're just a data point'.
Having lost her own father to cancer when he was just 49, the prospect of facing lengthy delays while simply hoping for the best was particularly galling.
She told The Sunday Times: 'Everyone did say, 'he's gonna be alright'. And he wasn't,'
Although the professor is sympathetic to the pressures on NHS staff, she admits that her struggle to beat the backlog reveals the extent of the crisis facing the health service.
She added: 'We're not meeting the targets for even those with an active cancer diagnosis … and that is why our survival outcomes are not as good as other countries.'
Ultimately, Ms Sridhar's persistence paid off and she was given a cancelled appointment slot after two months.
The abnormal cells were frozen to stop them from growing and Sridhar also received the HPV vaccine to increase her immune system's response to the virus.
But she advises that her own experience demonstrates how 'you have to be an active participant in your patient journey' to access timely care – a daunting challenge for those without the academic's medical expertise.
The warning comes after Public Health Scotland revealed that more than a quarter of patients referred with urgent suspicion of cancer are waiting longer than the 62-day target for their first treatment.
Cancer Research UK's public affairs manager in Scotland, Dr Sorcha Hume, criticised the waiting times as 'completely unacceptable'.
She said: 'NHS staff are doing their best but they're battling against under-investment alongside rising cancer cases.
'If we're to turn the tide on the anxiety faced by so many, we need to see adequate funding for staff and equipment.
'Innovative reform and rapid progress against Scotland's cancer strategy is also essential.'
While Ms Sridhar credits the NHS screening programme with protecting her health, she echoed CRUK's call for increased investment in public health initiatives.
She said: 'I don't understand sometimes why we think we're saving money by pulling back from screening programmes, prevention programmes, intervention programmes, when it ends up costing us more in the end.'

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Daily Mail
27 minutes ago
- Daily Mail
EXCLUSIVE I almost died after my chiropractor tore an artery while cracking my neck
When Carissa Klundt visited a chiropractor to fix her sore back she never expected the healing therapy to almost kill her. The mom-of-three from Las Vegas decided to start treatments after suffering back and chest pain as a result of a breast implant removal surgery four years prior. She had attended three appointments and had no issues before a substitute practitioner stepped in to perform her spinal adjustments on the fourth. Carissa, 41, was immediately concerned when she felt a sharp pain in her neck after the female chiropractor performed one particular cracking procedure. While she experienced pain after the appointment, Carissa brushed it off as a 'strained muscle' until her husband, Cassidy, insisted she visit the hospital when she began 'blacking out'. There, doctors confirmed that Carissa had suffered a tear in the inner lining of the vertebral artery - a condition known as a vertebral artery dissection (VAD) Vertebral artery dissection (VAD) is rare, with an estimated incidence of just one in 100,000 people annually. Doctors warn chiropractic neck manipulation heightens the risk of VAD, and it is estimated that one in 20,000 spinal manipulations results in the condition. The holistic practitioner was rushed to the intensive care unit at a specialist hospital as medics feared the VAD could trigger a stroke. After she was discharged, Carissa had a long road to recovery, facing constant pain, and mobility issues. While she didn't suffer a stroke, the mom says she was diagnosed with the communication disorder aphasia, due to reduced blood flow to the brain from the torn artery. The condition impairs a person's ability to express and understand language, whether spoken, written, or signed. Adamant her visit to the chiropractor in November 2022 nearly cost her her life, Carissa is warning others to be wary of the alternative medicine. Detailing what originally led her to visit a chiropractor, she said: 'I went to my chiropractor because I'd been having a lot of strain in my chest and my back and a friend had recommended one. 'I had breast implant illness (BII) and after my 'explant' all of my symptoms went away that year. 'My body had kind of protected me so my muscles got really tight. It was such a huge surgery, the muscles tightened, it was really painful.' After visiting a chiropractor to help relieve some of her symptoms, Carissa felt a sharp pang of pain in her neck during her fourth session. Carissa said: 'As soon as it happened, I knew something was wrong. You do hear a crack anyway when you get an adjustment but I knew something had gone wrong. 'There was a pain in my neck. I got home and felt like I was going to throw up. 'I had no idea a VAD could even happen. Because I work in health, fitness and wellness, I was active after [the appointment]. I was teaching classes, I went to a salon - I did everything wrong. 'A few weeks after seeing the chiropractor, I was seeing things and blacking out and my husband said 'we're taking you to the ER'.' After undergoing a CAT scan, doctors told Carissa that she had suffered a VAD and transferred her to an ICU at a specialist hospital. Carissa said: 'I knew straight away that it was from the chiropractor - that's where the pain all started from. 'They said I could've had a stroke. If I hadn't gone to hospital, I would've had a stroke. 'I could've so easily died. It traumatized my whole family. 'For the first month I was pretty much in bed. I was exhausted, sleeping for 17 hours a day. I needed help walking. I was in constant pain.' Carissa says her life was put on pause after suffering the artery tear and is now spreading awareness of the signs and symptoms of the life-threatening condition. Touching on her health status years on, she concludes: 'I still have lingering symptoms now - it's a whole lifestyle change. I'll never ski again, I'll never go on a rollercoaster, I'm not teaching classes anymore. 'There's still a residual fear of it happening again. I'm doing well now but it's been a long recovery process. 'My life was really put on pause. I absolutely regret going to the chiropractor. It's not about blaming anyone, it's just about spreading more awareness. 'I want people to understand what the symptoms are and that this is a life-threatening condition. 'I never thought anything like this could happen to me. I was healthy, active and deeply in tune with my body.'


Daily Mail
34 minutes ago
- Daily Mail
Rania has a life many dream of... But she's been hiding a devastating secret
At first glance, Rania Melhem seemed to have it all - she had just finished a university degree, landed her dream job and married the love of her life. But behind closed doors, the mum-of-two was hiding a devastating secret: she had been silently battling multiple sclerosis for years after being diagnosed at age 19. From the outside, Rania seemed perfectly fine - but she was suffering from nerve pain, muscle spasms, constant severe pins and needles, and blurred vision. Beneath her calm exterior, a silent storm raged inside her body - one she fought fiercely to keep hidden. The early signs were subtle, yet relentless. 'My blood pressure would drop, and then I would end up fainting. My vision would blur and I'd start to feel a tingling sense in my fingers,' Rania, now 35, told FEMAIL. The dizzy spells struck without warning, shaking the foundations of her everyday life. 'I was endlessly tired. It was my first year of university so I had a job - but I'd fall asleep on the train and miss my stop,' she explained. Before her diagnosis, the unpredictability of her symptoms forced her into isolation - and slowly, her world grew smaller. Despite her growing fears, getting answers was anything but straightforward. 'My GP refused to give me a brain scan because my sister had been diagnosed with multiple sclerosis (MS) years prior and he didn't believe it could happen twice in one family,' she recalled. But the truth was revealed after Rania's mother took her to another GP and pushed for a scan: she also had multiple sclerosis, a chronic neurological condition that would alter the course of her life. For many years, Rania kept her diagnosis to herself, sharing it only with her closest family and a few trusted friends. 'For probably the first five years, I didn't talk about it much,' she explained. At the time, she struggled to find the words to describe what she was going through. Though, no one would ever suspect she was struggling with an illness. She was attending university, working, and living a life that looked no different from any other young woman her age. But she was grappling with a daily reality that was far more complex and exhausting. During those early years, the mental and physical toll of the illness was at its most difficult. 'That was probably the time when, mentally, I was the worst,' Rania recalled. The fatigue was overwhelming, and her body often betrayed her in unpredictable ways - her blood pressure would drop suddenly, causing her to faint without warning. Navigating social situations was a challenge, especially when friends didn't understand what multiple sclerosis was or how to react when she became unwell. In those moments, Rania felt vulnerable and isolated. She relied heavily on her family for support and poured much of her energy into her studies, finding comfort and focus in academia. Looking back, Rania reflects on that period as one of her deepest personal struggles, - but also a time of profound introspection. The challenges she faced forced her to reconsider what truly mattered in life and to cherish the people who stood by her side. It was during this time she deepened her relationship with her now-husband - a connection that brought hope and stability amid uncertainty. Despite the hardships, she graduated among the top students in her state, a testament to her resilience and determination. Yet to the outside world, she was simply 'fine,' masking the invisible illness she fought every day. One of the hardest aspects of living with MS, Rania says, is the invisibility of the disease. 'You can look completely fine on the outside, and no one realises what's happening inside,' she said. The damage MS causes to the brain and spinal cord, along with the variety of symptoms it produces, often remain unseen by others. Over time, Rania learned to hide the pain and fatigue behind a practiced smile. 'You get really good at pretending everything is okay,' she explained. Even now, after nearly two decades, few people truly know how she feels beneath the surface. The turning point for Rania came after she married and moved out of her family home. For the first time, she faced the full weight of managing her condition independently. While living with her parents, much of the physical burden had been shared - from cooking and cleaning to practical everyday tasks - allowing her to conserve energy for work and recovery. But once she was responsible for running her own household, juggling a full-time job, and managing her symptoms alone, the exhaustion became overwhelming. It was then she realised she needed to ask for help. At 25, Rania reached out to MS Plus, an organisation offering support and services to people living with MS. Through them, she connected with an occupational therapist who assessed her needs and helped put practical measures in place. She was able to access cleaning services to reduce her fatigue, physiotherapy to manage pain, and ongoing emotional support. The therapist also encouraged her to use writing as a form of therapy, recognising how important it was for Rania to express her experience. What began as private journaling soon evolved into a blog, where Rania shared her journey under the alias 'Miss Anonymous.' Despite the challenges, Rania clings to the things that bring her joy. Music, once a passion she shared on stage, became a private refuge since MS affected her swallowing. 'I used to sing a lot, but the MS impacted my swallowing, and it was making me swallow a lot slower. So while I was singing, sometimes I would choke because I couldn't swallow and get the words out in time.' Though she stopped performing publicly, she still sings every day, finding comfort in the melodies that carry her through the hardest days. Her story is also one of family bonds - her older sister Marie was diagnosed with MS at 27, facing similar struggles at a time when understanding of the disease was far more limited. 'Back then, MS wasn't something many people knew about like it is now,' she said. Though they have undergone similar treatments, the illness manifests differently for each of the sisters. 'We both have different side effects and different symptoms,' Rania said. Looking back, Rania remembers the protective cocoon her parents created during those early years. 'I didn't really know what was going on because I was only 13, and I think our parents used to really try to protect us from anything bad that was happening,' she said. Today, Rania urges Aussies to offer practical and emotional support to those living with MS. 'Making them a meal, helping with the kids if they have them, taking them for a few hours so they can get something done, or have a rest. Helping them clean if they'll let you - I hate people cleaning my house, but it's definitely something that would be super helpful,' she said. She encourages friends and family to connect with MS Plus and participate in community events. 'It's a beautiful walk around Albert Park, and it's really good to reflect and be together as a community of people who have MS, their families, their carers, their kids, their loved ones, to really feel like you're in it together,' Rania said. Though MS remains a daily challenge, Rania credits her family for giving her the strength to keep going. 'We're lucky to have our mum and dad, who always taught us to be strong, and to get up every time you fall,' she said. Their love and resilience remain her guiding light through the uncertainty. In closing, Rania offers a heartfelt tribute: 'This is dedicated to my dad, who passed away recently. Thank you for always giving us the strength and the courage to keep going even when things were difficult.' Rania is an ambassador for MS Walk Run + Roll - the national fundraiser supporting those living with Multiple Sclerosis.


The Sun
39 minutes ago
- The Sun
Mounjaro is the best decision I've ever made & not because of the 4st I've lost – it's down to a surprising side effect
CLARE Butler struggled with her weight for most of her adult life. As an emotional eater, food was her go-to whenever she felt sad, happy, stressed, or angry. But after turning to fat jabs, the 48-year-old mum has seen many aspects of her life transformed - not just her waist. 5 5 5 Weighing 18st, 3lbs at her heaviest, Clare spent years trying every diet under the sun but found no long-term success. The trigger for her weight gain? Years of fertility struggles and a fibromyalagia diagnosis. Clare, from Manchester, shared: "I went through years of heartbreaking fertility struggles, including 19 miscarriages, and food became my comfort. "About nine years ago, I was diagnosed with fibromyalgia. That's when my movement slowed, and the weight started creeping on more and more." Clare turned to various diets - including SlimFast shakes, Weight Watchers, even the Rosemary Colney diet - but the problem she found was consistency. She revealed: "I'd do well for a couple of weeks, but then something would trigger a binge. "I'm an emotional eater - sad, happy, stressed, angry - food was always my go-to. "Every time I slipped, the guilt, shame, and self-hate would pile on. I couldn't understand why I couldn't just stop overeating. This cycled continued through her 30s and 40s and deeply affected her mental health. "I battled depression and panic attacks, and I missed so many moments with my children," she said. I lost 5st on Mounjaro - weird side effects are worth it, it's life-changing "I'd stay home while they went out with my husband, and when they came back full of stories and pictures, it broke my heart. "I felt like a burden, convinced they'd be better off without me." But it was January last year when a friend told her about Mounjaro. Mounjaro (tirzepatide) became available in the UK in February 2024, primarily for private use. But access to the weight loss jab through the NHS has gradually been rolled out. By activating GIP and GLP-1 receptors, Mounjaro slows down the emptying of the stomach, making you feel fuller for longer and reducing appetite. I spent months researching it, and in July 2024, I finally decided to take the plunge. It's the best decision I've ever made for myself Clare Butler This can lead to eating less food overall. Clare said: "A friend told me about Mounjaro and the amazing results they were having. "I spent months researching it, and in July 2024, I finally decided to take the plunge. "It's the best decision I've ever made for myself." "I had lots of questions and uncertainty at the start and I could never get hold of anyone at the pharmacy for advice and help. "That's when I started to research for a pharmacy that offered support and found Voy and I am so glad I did. What are the other side effects of weight loss jabs? Like any medication, weight loss jabs can have side effects. Common side effects of injections such as Ozempic include: Nausea: This is the most commonly reported side effect, especially when first starting the medication. It often decreases over time as your body adjusts. Vomiting: Can occur, often in conjunction with nausea. Diarrhea: Some people experience gastrointestinal upset. Constipation: Some individuals may also experience constipation. Stomach pain or discomfort: Some people may experience abdominal pain or discomfort. Reduced appetite: This is often a desired effect for people using Ozempic for weight loss. Indigestion: Can cause a feeling of bloating or discomfort after eating. Serious side effects can also include: Pancreatitis: In rare cases, Ozempic may increase the risk of inflammation of the pancreas, known as pancreatitis, which can cause severe stomach pain, nausea, and vomiting. Kidney problems: There have been reports of kidney issues, including kidney failure, though this is uncommon. Thyroid tumors: There's a potential increased risk of thyroid cancer, although this risk is based on animal studies. It is not confirmed in humans, but people with a history of thyroid cancer should avoid Ozempic. Vision problems: Rapid changes in blood sugar levels may affect vision, and some people have reported blurry vision when taking Ozempic. Hypoglycemia (low blood sugar): Especially if used with other medications like sulfonylureas or insulin. "Unlike most pharmacies they don't just send you your medication and leave you to figure it out on your own. They offer full support alongside it. "They give you 1:1 health coaching, and my coach has been incredible in helping me with my mindset around my emotional eating, something I would have struggled to deal with alone." Clare was nervous before taking her first injection, but once she did it, she said she barely felt a thing. She continued: "Within hours, the constant food noise in my head quieted down. "I stopped obsessing over what to eat next, and for the first time, I felt in control. "I started learning about nutrition, trying healthier foods, cooking new recipes, and most importantly, learning that no food is off-limits - it's about moderation. I remember going out with friends or family and wondering how they could leave food on their plates because they were 'full'. I never understood that feeling before. Now, I do Clare Butler "For the first time in my life, I can stop when I'm satisfied. "I remember going out with friends or family and wondering how they could leave food on their plates because they were 'full'. "I never understood that feeling before. Now, I do." While weight loss jabs have been known to cause extreme side effects in some people, Clare says her side effects have been minimal - dry mouth, some headaches, a little acid reflux, and occasional loose stools, which she adds are all manageable. Since starting the jabs in July, Clare has lost 4st 4 lb. She still wants to lose another 2.5 to 3 stone, but already feels better than she has in years. 5 5 Clare said: "My confidence is back, I'm enjoying life, and now when my husband and kids go out, I go with them. "We recently went on holiday to Crete, and for the first time, I didn't need a seat belt extender on the plane - I cried happy tears. "I even shared that moment on TikTok, and hundreds of people reached out to say they related." And weight loss jabs have had a positive impact on her mental health too. She explained: "My depression affected every aspect of my life. I barely left the house for fear of panic attacks. "Mounjaro didn't only quieten the food noise, but it helped to quieten the over thinking anxious thoughts that had consumed my life for so long. "My life is so different now to how it was a year ago. Do I still suffer with anxiety and panic attacks? Yes, but it isn't as severe and my confidence is slowly returning. "My mind feels quieter around everything, not just the food noise. I have still had panic attacks and I still suffer with days of low mood but it isn't as severe as it was." Clare gets her Mounjaro from a pharmacy called Voy. But she didn't actually start her weight loss jabs journey with them. She said: 'I used a couple of other pharmacies but they just were not good enough for me. 'I had lots of questions and uncertainty at the start and I could never get hold of anyone at the pharmacy for advice and help. 'That's when I started to research for a pharmacy that offered support and found Voy and I am so glad I did. 'Unlike most pharmacies they don't just send you your medication and leave you to figure it out on your own. They offer full support alongside it. 'They give you 1:1 health coaching, and my coach has been incredible in helping me with my mindset around my emotional eating, something I would have struggled to deal with alone.' Lifestyle changes like diet and exercise are crucial when taking weight loss jabs, especially for long-term weight management. Exercise is still tricky for Clare because of her fibromyalgia, but she's added gentle movement like walking on a walking pad at home. She said: 'As the weight comes off, my energy has gone up, and life feels good again – something I never thought I'd say. 'I'm still on Mounjaro and ball park figure I've spent so far is £1,500, but starting it has been the best decision I've ever made.' Latest guidance on fat jabs On June 5, 2025, the Medicines and Healthcare products Regulatory Agency (MHRA) issued new guidance warning women taking fat jabs to ensure they are also using effective contraception. While information is already contained in patient information leaflets, concerns have been raised over many women purchasing the drugs online, who may not be aware of the risks. Women taking Mounjaro should also use condoms if they're on oral contraception because the weight loss drug may reduce its effectiveness, said the MHRA. And glucagon-like peptide-1 receptor agonists (GLP-1 RAs) must not be taken during pregnancy, while trying to get pregnant, or during breastfeeding and anyone who gets pregnant should stop using them immediately. This is because there's currently not enough safety data to know whether taking the medicine could cause harm to the baby, the regulator added. In some cases, women are advised to continue using contraception for up to two months between stopping the medicine and trying to get pregnant. The MHRA has also reminded patients of the symptoms to look out for of acute pancreatitis - an uncommon but serious side effect of fat jabs. The main symptom is severe pain in the stomach that radiates to the back and doesn't go away. Anyone who experiences this should seek immediate medical help. Everything you need to know about fat jabs Weight loss jabs are all the rage as studies and patient stories reveal they help people shed flab at almost unbelievable rates, as well as appearing to reduce the risk of serious diseases. Wegovy – a modified version of type 2 diabetes drug Ozempic – and Mounjaro are the leading weight loss injections used in the UK. Wegovy, real name semaglutide, has been used on the NHS for years while Mounjaro (tirzepatide) is a newer and more powerful addition to the market. Mounjaro accounts for most private prescriptions for weight loss and is set to join Wegovy as an NHS staple this year. How do they work? The jabs work by suppressing your appetite, making you eat less so your body burns fat for energy instead and you lose weight. They do this my mimicking a hormone called GLP-1, which signals to the brain when the stomach is full, so the drugs are officially called GLP-1 receptor agonists. They slow down digestion and increase insulin production, lowering blood sugar, which is why they were first developed to treat type 2 diabetes in which patients' sugar levels are too high. Can I get them? NHS prescriptions of weight loss drugs, mainly Wegovy and an older version called Saxenda (chemical name liraglutide), are controlled through specialist weight loss clinics. Typically a patient will have to have a body mass index (BMI) of 30 or higher, classifying them as medically obese, and also have a weight-related health condition such as high blood pressure. GPs generally do not prescribe the drugs for weight loss. Private prescribers offer the jabs, most commonly Mounjaro, to anyone who is obese (BMI of 30+) or overweight (BMI 25-30) with a weight-related health risk. Private pharmacies have been rapped for handing them out too easily and video calls or face-to-face appointments are now mandatory to check a patient is being truthful about their size and health. Are there any risks? Yes – side effects are common but most are relatively mild. Around half of people taking the drug experience gut issues, including sickness, bloating, acid reflux, constipation and diarrhoea. Dr Sarah Jarvis, GP and clinical consultant at said: 'One of the more uncommon side effects is severe acute pancreatitis, which is extremely painful and happens to one in 500 people.' Other uncommon side effects include altered taste, kidney problems, allergic reactions, gallbladder problems and hypoglycemia. Evidence has so far been inconclusive about whether the injections are damaging to patients' mental health. Figures obtained by The Sun show that, up to January 2025, 85 patient deaths in the UK were suspected to be linked to the medicines.