
How eating strawberries each day could help keep dementia at bay
The arrival of the first British strawberries of the year is always a treat.
But now scientists have shown that as well as satisfying our tastebuds, they could help to ward off dementia too.
Research has revealed that the fruit can boost the speed at which older people's brains process information.
Age-related decline in cognitive processing speed is known to be a symptom of dementia – a disease which affects nearly 900,000 in the UK.
The findings come as Britain prepares to enjoy one of its best strawberry crops in years. Shoppers have been told to expect giant berries twice the normal size after weeks of dry, sunny weather boosted growth.
This is welcome news for a country which consumes a whopping 168,000 tons a year.
Previous research has already shown that the chemicals known as flavonoids which strawberries contain can bolster heart health.
And in the latest study, a team from San Diego State University in the US recruited 35 men and women in their 70s to see if the same effects could be seen in the brain.
The scientists gave participants a freeze-dried strawberry powder, made with a handful of fresh berries, to mix in water and drink every day for eight weeks.
They then repeated the experiment with a fruit-flavoured powder which contained none of the health-boosting ingredients found in strawberries. Researchers then got the volunteers to perform cognitive tests.
They found a marked improvement in the brain's processing speed following consumption of the strawberry powder but little change with the fruit drink.
Although there was little improvement in scores for memory tests after consuming strawberries, researchers said the change in processing capacity was significant.
Slower processing speed is known to hamper people's driving skills and make financial decisions more difficult.
The strawberries also helped to lower blood pressure and led to increased levels of disease-fighting antioxidants in the blood, the results published in journal Nutrition, Metabolism and Cardiovascular Diseases showed.
The researchers said: 'Strawberry consumption may improve cognitive function and there is accumulating support for its effects on brain health.'
Hashtags

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


BBC News
32 minutes ago
- BBC News
Leeds woman's boxing class for people living with Parkinson's
A woman who was diagnosed with young-onset Parkinson's disease has set up a boxing class as a way to empower others and help them manage their Pearce, 58, said after experiencing the physical and emotional challenges of the condition first-hand, she discovered that boxing could significantly improve balance, strength, coordination and overall to find a class that matched her work commitments, she took the initiative to start her own at Trident Fitness in Morley, said: "I know by taking control and doing this exercise it helps me to feel as fit as I can for as long as I can." Parkinson's is a progressive disorder that affects the brain, nervous system, and muscle control. It is the fastest growing neurological condition in the world, with about 153,000 people in the UK living with the is currently no cure for it but treatments are available to help relieve the symptoms. 'A diagnosis I never wanted' Mrs Pearson was diagnosed three years ago, decades after her brother John was told he had the now experiences stiff joints, low mood and anxiety and struggles with insomnia, fatigue and her balance. "It wasn't a total shock, but it was a diagnosis I never wanted but I guess I knew would come one day," she by how her brother faced his diagnosis despite his health declining over the years, Mrs Pearce said she realised the importance of looking after she overheard someone say how boxing had helped them manage their symptoms, she began looking into it."It's hugely important to have the opportunity to access Parkinson's specific exercise classes," she said."It's almost as if exercise should be on prescription because it's the only thing known to slow down the progression." The classes at Trident, which take place Thursdays at 18:30 and Saturdays at 10:00, started in November and are partly funded by England Boxing and Parkinson's Pearce said the class was hugely popular and gave people a welcoming space to openly share their experiences."Everyone's Parkinson's journey is very individual," she said."Some people will have a tremor, some won't, some will have stiffness, some people's posture will be really challenged - no two people's journeys are the same."Mrs Pearce said she was grateful for the support she had received in setting up the also helps run Yorkshire and Humber Younger Person's Support Group which supports people under 67 living with Parkinson's."We try and uplift people as much as we can and lead by example," she said."Whilst we live with Parkinson's, we all live very full lives." Listen to highlights from West Yorkshire on BBC Sounds, catch up with the latest episode of Look North.


The Sun
39 minutes ago
- The Sun
It was worst pain of my life, says Kate Lawler after hospital dash on holiday in Greece uncovered health trauma
FOR five years, Kate Lawler battled debilitating stomach pain. But doctors repeatedly told the TV personality, 45, 'everything is fine', so she assumed it was nothing to worry about. 5 5 It wasn't until she was rushed to hospital while on holiday in Greece that she began to suspect something serious might be wrong. But even then, it took numerous scans back home in the UK and several misdiagnoses for her to discover the truth. Kate, who won Big Brother in 2002, tells Sun on Sunday Health: 'My symptoms started in December 2017. 'The abdominal pain was worse than any pain I've ever had. 'It was crippling - sometimes too unbearable to even get out of bed - and it felt even worse during menstruation and sexual intercourse. 'It was a sharp, stabbing pain that would last from 10 seconds to several hours. 'Then we were on holiday in 2018 and I thought I had a serious hernia or something was wrong with me, to the point that I went to hospital. 'But doctors thought I was just going mad. They just said, 'You're fine,' and left it at that. 'I was made to believe it was simply caused by my hormones, or ovulation.' The mum-of-one, from London, visited her GP twice and was told it might be a hernia, and she believed it could also be endometriosis, but she wasn't offered a referral. The 5 causes of pain in the pelvis all women should know Desperate for answers, she visited a private gynaecologist in November 2021. 'She did internal scans and all the tests and said, 'Absolutely everything is fine',' Kate says. 'All she could tell me was that everything was clear, which was a relief. 'But also, when you're told everything looks normal but you're still experiencing intense pain, you then start to think, 'Am I making this up in my head?' 'I didn't want to be a burden and keep going to the doctors, but I was so desperate to get it sorted. 'In the end I literally felt like I was going to have to live with the pain forever.' It was only during a chance conversation at a routine appointment for her varicose veins in August 2022 that she discovered she had pelvic congestion syndrome (PCS) - a little-known condition caused by hidden varicose veins around the ovaries and womb. It's most common in women aged 20 to 45 who have given birth more than once, as well as those with varicose veins, a family history of them, or polycystic ovary syndrome. Most patients experience dull, achy or heavy pain in their pelvis. It may feel worse at the end of the day, before or during your period, during or after sex, and when you stand or sit for long periods. Some people also need to use the toilet more urgently, or have pain when they pee. Most Brits have never heard of PCS, but it affects around 1.5million people in the UK. 'We're a very veiny family' Kate, who has appeared on Hole in the Wall, Celebrity Total Wipeout and Love Island, says: 'It was only when I went to see Professor Mark Whiteley at The Whiteley Clinic that I heard about PCS. 'I was getting the varicose veins on my legs treated and he started talking about PCS and I said, 'Sorry, what are you talking about? Because I can relate to all the symptoms you're saying.' 'I felt like that was exactly what I had. 'I had never linked my varicose veins to my pelvis but he offered to test me. 'My mum's got varicose veins, my grandparents had them, and my dad's got them all over his leg. We're a very veiny family. 'Eventually your varicose veins and your legs can cause pain and discomfort and you can end up having ulcers, which my grandma had. 'Varicose veins and PCS are often interlinked. And once I'd had the test, it transpired that I had both.' 5 The most common treatment for PCS is pelvic vein embolisation - a walk-in-walk-out procedure which involves placing tiny coils, thinner than human hair, inside the damaged veins under X-ray guidance. Kate says the procedure in November 2022 was 'uncomfortable but not painful' - and it has changed her life. 'Suffer in silence' 'I was holding a stress squeezer and cursed a few times, but once it was over it was amazing,' she says. 'I realised, 'God, I was in a lot of pain before'. I would wake up and immediately be in pain, and no amount of painkillers would get rid of it. 'I just learnt to live with it - though I didn't want to be on painkillers my whole life. 'I can't explain how much I've improved and how I no longer feel crippled by this pain that would strike at any time.' Like thousands of others, Kate is frustrated by the lack of awareness around the condition. She says: 'So many women go to the NHS or private doctors and they're just not given enough training when it comes to women's health, and that includes things like menopause, perimenopause and PCS. 'They get trained in a bit of everything, but unfortunately it's not enough. 'What Prof Whiteley is doing is incredible, and we just need to get the word out there. 'I want women to be able to find out exactly what's wrong with them if they're experiencing the same things I did, because most are misdiagnosed. 'I've spoken to many different people who have suffered from it, and most of them will go into hospital, have loads of scans, and then just be sent home. 'One woman was actually told to have a hysterectomy unnecessarily. The gynaecologist didn't know what was causing the pelvic pain so he thought, 'Oh, I'll take out your uterus.'' She adds: 'Women's health is so underfunded and doctors need to be more informed. 'There needs to be more money and awareness so that when a woman goes to the GP in pain, it's not brushed aside.' Despite the challenges, Kate is urging women not to be shy about asking for help or thinking they're making a fuss. 'No woman should suffer in silence,' she says. Dr Sophie Strong, consultant gynaecologist at The Whiteley Clinic, adds: 'A lot of the women we see will have been suffering from pelvic pain for many years but their conditions will remain undiagnosed. 'Our new Pelvic Pain Clinic is a place for women who have been told there's no hope and there's nothing that can be done for them. We can make a real difference.'


BBC News
2 hours ago
- BBC News
Protesters gather to demand hospice reopens and question funding
Campaigners have returned to a hospice inpatient unit in Liverpool a year after it was shut to stage another protest to demand the facility reopen as soon as possible. The 26-bed unit at Marie Curie in Woolton, Liverpool, closed in July 2024 because of a shortage of specialised nursing decision sparked immediate concern and a campaign group, Save our Hospice, formed to demand a u-turn. A Marie Curie spokesman said it was in talks with the NHS Cheshire & Merseyside Integrated Care Board (ICB), which commissions end-of-life care in Liverpool, to agree a "sustainable long-term plan" for the unit's future. A large group of campaigners gathered outside the unit on Saturday afternoon and held placards criticising Marie Curie for not "taking up our offer" to fundraise for the unit. Some wore yellow t-shirts with the slogans "Save our Hospice" and "Save our Ward". Independent Liverpool councillor Lucy Williams, who attended a protest at the unit on Saturday, told the BBC: "It's been a year since they closed their doors to the inpatient unit and it's been a year that they've continued to receive funding from the ICB."So we're here today to ask where has that money gone and why haven't they delivered that service that they're getting commissioned to provide."Williams worked at the hospice as a palliative care nurse for two years, and said: "People's relatives and loved ones have died here and a lot of them have committed their time to fundraising for this hospice."We found out over this year that money doesn't come to this hospice, it goes into a national pot - so throughout the closure this fundraising has continued and people haven't been aware that the inpatient unit in Liverpool has been closed." 'Get the ward open' Williams said an "easy" resolution was to immediately re-open the ward. She said: "They're receiving the funding to have the ward open, surely they can have one or two beds? That's better than none at all. "So get the ward open and if Marie Curie aren't competent to provide the service then the ICB need to commission someone who is."The Marie Curie spokesperson said the charity hoped to reach an agreement with the NHS integrated care board "as soon as possible".While admissions to the inpatient unit "had been paused", the hospice had remained open and was providing palliative and end of life care to "thousands of people in Liverpool in different ways", they added. The spokesperson said the ICB was aware its funding was being used to provide these services. Listen to the best of BBC Radio Merseyside on Sounds and follow BBC Merseyside on Facebook, X, and Instagram. You can also send story ideas via Whatsapp to 0808 100 2230.