
Paramedic's brain tumour missed five times by doctors
A paramedic has said her brain tumour was missed five times by doctors.
Hannah Lemanski, 24, thought she was experiencing symptoms of stress from shift work when she complained to medics about vomiting, headaches, and double vision.
She first visited her GP in February 2023 after experiencing headaches and vision problems for two months, but was sent home with no answer and told her symptoms would be passed on to another doctor.
On her fourth visit to the GP she was told she had a lazy eye.
After a fifth visit to the eye assessment clinic, an MRI scan diagnosed her with central neurocytoma – a rare brain tumour which grows in the ventricles of the brain.
She had 80 per cent of the tumour removed in surgery but two years on it is returning.
Doctors recommended gamma-knife radiosurgery to shrink the mass but this is not funded by NHS England for her specific tumour type.
The treatment is recognised by the NHS and used to treat various health conditions, including brain tumours, both benign and cancerous.
She is now fundraising to get the treatment privately.
Ms Lemanski, from Middlesborough, said she thought she was going to die when she was first told of her diagnosis.
Her wedding to her now-husband, Przemek Lemanski, 34, who was delivering invitations at the time of the diagnosis, had to be delayed.
She underwent surgery to remove 80 per cent of the tumour James Cook hospital in May 2023 and returned to work as a paramedic.
During a routine scan in March 2025, she was told her tumour is returning.
The NHS offers conventional radiotherapy, a destructive treatment which can lead to more cancer developing, but doctors told Hannah the most effective treatment is gamma-knife surgery – a non-invasive and highly targeted form of radiotherapy.
But Ms Lemanski was told by The National Centre for Stereotactic Radiosurgery in Sheffield's Royal Hallamshire Hospital that they don't offer this treatment for her condition – and said NHS England does not commission funds for this treatment and her specific tumour type.
She applied for individual funding, but this was rejected.
She said: 'It's quite upsetting. You pay your taxes every month and you expect to be looked after when you need it. How can you not look after one of your own?
'Maybe if I wasn't someone who worked for the NHS, I might have just accepted the conventional radiotherapy route, which I think for anyone of a young age without cancer puts them at so much higher risk, especially when there's more effective treatments out there.
'I think it's quite discriminatory really, because I don't understand why someone's brain tumour is better than mine.'
Her friend Becky Calpin, 32, has raised over £12,000 to help Ms Lemanski get private treatment, but it could cost up to £20,000.
Becky said: 'Hannah is more than a paramedic – she's a bright, healthy, active young woman, married to her best friend and dreaming of starting a family.
'She's the kind of person who lights up every room – always smiling, always giving, always ready to help.'
An NHS England spokesperson said: 'We understand the importance of making decisions quickly to avoid unnecessary distress and, where treatment isn't routinely funded, clinicians can submit an individual funding request if there are exceptional clinical reasons.
'The NHS funds specialist stereotactic radiosurgery and radiotherapy for some cancers where there is evidence of a clinical benefit over standard treatments, as part of the personalised care provided for patients.'
Hashtags

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


Daily Mail
an hour ago
- Daily Mail
Gardening expert reveals the very unexpected secret ingredient that could keep your plants thriving during the heatwave
As temperatures have been soaring recently, green-thumbed brits have become increasingly concerned about how the searing heat will be affecting their beloved plants. However, Waine Delaney, a mushroom specialist at Monotub, has suggested not all may may be lost. According to the expert, watering plants with the mushrooms mixed into the liquid could be the key to helping them survive the heat. Mushrooms are particularly useful in the garden as they are natural sponges meaning when they are submerged in water they act as a 'hydration pod'. Mushroom-infused water therefore infuses more slowly into the soil than ordinary water - and also evaporates far slower during the hottest times of the day. As well as keeping plants better hydrated, the infused water also nourishes them with micronutrients which are naturally found in the fungus. Mushrooms are packed with nutrients such as potassium, selenium, magnesium, and phosphorus, which are typically used up faster by plants in warmer temperatures. Feeding plants with this infused water is also far less harsh than using typical shop-bought feeds which can increase the risk of overfeeding. Opting for mushroom water over the hose pipe can also have long term positive impacts in the garden. Mushrooms grow from fungi which contain mycelium, a root-like network of fungal threads found within the soil. The infused water contains mycelial matter which, when poured on to flowerbeds, encourages fungal activity. Increasing the presence of this root network in soil means all the plants in that soil can improve their uptake of water, as the soil retains moisture for longer. Mushroom water can be made at home with any variety of the veggie, by simply soaking a chopped handful in tap water for 12-24 hours. Even better, the same mushrooms can be used up to 2-3 times before being composted. Similar to normal watering practices, the best results from using the infused water come when watering plants after the sun has set. Geoff Stonebanks, 71, has a multi-award winning garden in Seaford, East Sussex. He has also stressed the importance of keeping plants hydrated in the summer months. The gardener suggested using the reservoir method paired with watering plants less but for longer periods. He said: 'Try not to frequently water the garden - instead do it less but water for longer periods. 'Short bursts of watering can mean it doesn't have the opportunity to sink into the ground before being evaporated,' he pointed out. 'A heavy douse will ensure plant roots remain moist for longer.' Geoff then gave details on how to best hold and make use of excess water by creating a reservoir with tin foil at the base of plant pots. He said: 'How often do you go to water the pots on the wall and the water just runs straight through them, without giving the moisture chance to soak up into the compost and subsequently the plants? 'By creating an inner saucer, where excess water can flow over the side and through the hole at the base, you ensure some is retained to be able to be absorbed by the plants. 'It works well with all containers, not just wall pots. I've been successfully using the idea for many years.'


Telegraph
an hour ago
- Telegraph
Care delays putting people with glaucoma at risk of blindness
Care delays are putting people with glaucoma at risk of blindness, experts have warned. The Association of Optometrists (AOP) said the current approach to the condition in England is 'failing the public'. A survey by the organisation found more than half of high street optometrists have witnessed patients going blind from the condition because of late detection or delays in treatment. Glaucoma, which affects around 700,000 people in the UK, is caused by fluid building up in the front part of the eye, leading to the optic nerve, which connects the eye to the brain, becoming damaged. The condition does not usually cause any symptoms to begin with and can develop slowly over many years. A report by the Royal College of Ophthalmologists suggests cases could rise by 22 per cent by 2035. Adam Sampson, AOP chief executive, said: 'The current approach to glaucoma in England is failing the public. 'Each year, people are faced with the reality of permanent sight loss as a direct result of delays to care and inconsistencies in eye care provision. 'But glaucoma services led by optometrists show that it does not need to be this way.' According to the AOP, reforms in Wales in 2022 mean optometrists can offer glaucoma services on the high street, with schemes also running in Scotland and in some areas of England. It is now calling for the Government to commit to a national glaucoma pathway for England, working with high street opticians to ensure patients have equal access to treatment. The AOP found of 915 optometrists, 54 per cent had witnessed a patient with glaucoma permanently losing their sight in the past year. More than six in 10 optometrists believed most of their patients were unaware of the condition or its risk factors, which include age, ethnicity and some medical conditions such as diabetes. Mr Sampson added: 'The research we have conducted reveals a national glaucoma pathway in England could free up 300,000 hospital eye appointments and save the NHS over £12 million every year. 'We are calling on the Government to act now to overhaul health in England. 'We must ensure high street optometrists can protect the public by detecting, monitoring and treating glaucoma, and ease the burden on hospital eye services.' Matt Weale was diagnosed with glaucoma after a routine eye test in 2021 revealed dangerously high pressure in his left eye. The 54-year-old said: 'By the time I was finally offered a follow-up appointment my vision had already started to deteriorate. 'I felt like I was falling through the cracks. It was terrifying not knowing if I was going to lose my sight because the system was too stretched to see me. 'If I hadn't been able to pay for private care, I truly believe I would have gone blind in my left eye. I lost confidence, I had to give up my job, the things I loved like playing football and performing.'


The Guardian
an hour ago
- The Guardian
Is it true that … we're all a little bit intolerant to dairy?
Most of us aren't inherently dairy intolerant, but we can go through periods where we become more sensitive to lactose in our diet, says Amanda Avery, an associate professor in nutrition and dietetics at the University of Nottingham. She says that when people talk about being 'dairy intolerant', they're usually referring to lactose, the sugar found in milk and dairy products, such as milk, cheese and yoghurt. In most people, that sugar is broken down by an enzyme called lactase, which is found in our small intestine. It helps our bodies digest and absorb lactose without causing discomfort. 'We're born with plenty of lactase. But as our diets diversify, our lactase levels decline,' says Avery. 'If there is minimal milk in the dairy diet then lactase levels may be zero, thus people from some cultural backgrounds and countries where dairy intake is negligible may be intolerant.' People who don't produce enough lactase may find themselves having gastrointestinal symptoms such as abdominal pain, bloating and loose stools when they consume dairy. Some people can find their lactase activity is temporarily reduced when their gut function is disrupted by antibiotics or stress. This can lead to 'transient lactose intolerance' – a period where your body struggles to digest dairy even if you weren't previously sensitive. If people cut out dairy and then reintroduce it, they might also experience abdominal symptoms for a short period while their lactase activity is being restored, says Avery. But this doesn't necessarily mean you're permanently intolerant. It could just be your gut enzymes playing catchup. 'Good practice, even if you do think you are slightly intolerant, is to try to keep a little dairy in your diet – cheese or yoghurt should be OK. Cheese has very little lactose, and in yoghurt, much of the lactose is broken down by the bacteria. Even having a little bit of milk in your tea helps,' says Avery. So, is it true that we're all a little bit intolerant to dairy? No, but our ability to digest it can definitely fluctuate. For many, it's not a lifelong intolerance but a temporary reaction.