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From hormones to lifting stones – studying complexities of strength training

From hormones to lifting stones – studying complexities of strength training

Irish Times2 days ago

Your PhD looked at how female athletes perform in elite sports – tell us more.
We have done a lot of research with female rugby players, looking at training performance and coaching styles as well as the impact of factors like menstruation and using the contraceptive pill. Historically, research on sports and training performance has been focused on men, and we wanted to see whether men and women need to train or exercise differently, and whether women need different resources and pathways to train and perform optimally.
What did you do to answer those questions?
We used lots of different methods. We analysed GPS data from Six Nations matches to track the demands of the games on female athletes, and we measured muscle gain and performance in female athletes over time. We also interviewed athletes and strength and conditioning coaches from around the world about their perceptions and experiences.
What did you find about training and performance schedules?
Research shows that, in relative terms, men and women gain muscle at the same rates with the same training schedules. The coaches told us, though, that while the technical training in the gym was the same for men and women, they often used different styles of coaching.
The women often benefited from more emphasis on lifting technique, as they may not have been taught at an early age, as the men often were. That points to the need for more supportive pathways for female athletes early on.
READ MORE
And what about menstruation and hormonal contraceptives?
We found that based on the current body of evidence, there's no reason to suggest that hormonal contraceptives affect how much muscle you gain when doing gym-based exercise. There's also no evidence to suggest that the menstrual cycle phase has an objective effect.
But our research with players showed their lived experience, that they perceive the menstrual cycle to have an impact on their performance. It could be that with the changes in hormones, it feels harder to produce the same force with our muscles, or the symptoms that go along with menstruation could also be playing a role here.
What are you working on now?
I'm a lecturer now in DCU School of Health and Human Performance, and I'm expanding the work on hormones and how they affect strength and health more generally. We are starting a project to look at the effects of testosterone replacement therapy.
This is not just for athletes, and it refers to therapy to help people who have symptoms of low levels of testosterone, such as low mood and fatigue. We will look at how the therapy can affect things like motivation to exercise and energy levels and muscle gain.
Are you an athlete yourself?
I'm always a massive advocate for strength training, and I regularly train in powerlifting. I also recently competed in a stone-lifting competition in Armagh.
Stone lifting?
Yes, it's an area I'm interested in from a lot of angles. I'm working with a sports historian to study the history of strength in Irish culture, and we have been looking at these large 'lifting stones' that are found in many parts of the country.
They are often near graveyards and ports and other places where people would congregate, and men would each try to lift the stones to the waist or chest, as a competition. It's a real link with our past, when you go to lift these stones, you are putting your hands in the same spots as people would have done maybe centuries ago. It's like reaching into the past.

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Letters to the Editor, June 14th: On young people in nursing homes, attacks on Iran and Greta Thunberg
Letters to the Editor, June 14th: On young people in nursing homes, attacks on Iran and Greta Thunberg

Irish Times

timean hour ago

  • Irish Times

Letters to the Editor, June 14th: On young people in nursing homes, attacks on Iran and Greta Thunberg

Sir, –The recent RTÉ Investigates exposé on Irish nursing homes made for harrowing viewing. But behind the headlines lies an even more invisible reality: the quiet, routine institutionalisation of younger people – including those with conditions like Early Onset Parkinson's – into facilities designed for people decades older. I'm not only the co-founder of Early Onset Parkinson's Disease Ireland, but someone who has lived with Parkinson's for 13 years. I've met too many people in their 30s, 40s and 50s with neurodegenerative conditions who have been placed in nursing homes simply because there is nowhere else for them to go. Today in Ireland, 1,249 people under 65 years live in nursing homes. One of them is a 47-year-old man with Early Onset Parkinson's, surrounded by residents three and four decades older than him. This isn't because he needs round-the-clock care – it's because our system has failed to develop any alternative. READ MORE This practice isn't just inappropriate; it's profoundly damaging. People with conditions like EOPD need tailored supports: physiotherapy, neurological care, and exercise programmes that are critical to slowing disease progression and preserving independence. Most nursing homes are not equipped to offer any of these. Instead, these individuals face isolation, accelerated decline, and the emotional toll of being removed from their peers, their communities, and their sense of self. The Ombudsman's 2021 Wasted Lives report exposed the systemic failures driving this crisis. It found that many younger people were placed in nursing homes without full consultation or understanding of the long-term implications, particularly under the Fair Deal scheme. One young man, Francis, was told his stay would be temporary; he's been there for nine years. Another, Alex, entered a home at 34 after a brain injury. He told investigators: 'If I thought it was for life, I would drive my chair off a bridge.' The 2024 update to Wasted Lives offered no comfort: every month, 32 more people under 65 are admitted to nursing homes – that's more than one person every day. We don't even have accurate data on how many of these people are living with Parkinson's. Without data, we can't quantify the problem, let alone solve it. This must change. We are calling on the Government to act now. It should collect and publish national data on younger people in nursing homes, their diagnoses and needs. It should develop age-appropriate, community-based supported living options; create clear pathways to transition out of inappropriate care and reform the Fair Deal scheme to ensure full, informed consent. In addition, the Government should guarantee access to multidisciplinary care and therapies tailored to younger adults. This is not just a healthcare issue; it is a human rights issue. These are not statistics. They are teachers, artists, musicians, parents – people with lives worth living. We must ask ourselves: what kind of care system do we want to be known for? One that hides people away or one that sees them, values them, and supports them to live with dignity? It's time for Ireland to choose. – Yours, etc, JOE CONDON, Director of Early Onset Parkinson's Disease Ireland, Dublin. Israel's attack on Iran Sir, – The Israeli government knows no limits in flouting international law . By attacking Iran's nuclear plants and facilities it has brought the Middle East to the brink of an all-out war in the region. It has shattered and undermined the ongoing diplomatic US-Iranian talks to end the Iranian nuclear build-up impasse and by its illegal actions has invited retaliatory action by Iran. This time the international community must act swiftly to bring the Israeli government to justice . – Yours, etc, BRENDAN BUTLER, Drumcondra, Dublin. 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It is sectarian and racist in nature and it is fed by certain politicians who gain leverage from simplistic sloganeering. It targets the vulnerable in the name of perverted jingoistic politics and it gains traction by defining unacceptable rituals as 'culture' where, for example, the burning of effigies is seen as a festive activity. This, for many of us, has always been unacceptable – the step from burning flags and posters to burning houses with people inside, is not a huge one – but in the present context of global politics with the growing influence of neo-fascistic elements on the far right, it is disturbing indeed. We need to call it out for what it is in essence – part of a continuum in a certain strand of the politics of Northern Ireland which is exclusive, uninterested in compromise and dependent on 19th-century notions of supremacy, privilege and power. 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Rather than belittle the efforts of Thunberg to bring attention to the climate and biodiversity crises, which are real things despite Ms McRedmond's delusions, she might be better placed using her journalistic nous to explore further the underlying motivations for Greta's pessimism. On that point Ms McRedmond might like to know that rate of extinction of species in the last 100 years, which has rapidly accelerated in recent decades as we destroy ecosystems for economic growth, is higher than those in most of the previous mass extinction events. Climate activists such as Just stop Oil see that lack of urgency and the lip service being paid to this crisis by governments and vested interests. They also see how the general population has been rendered apathetic by a tech-induced stupor so feel compelled to create impactful 'publicity stunts' in order to grab their attention. Ultimately, we are the consumers and the voters, and we can drive change but only if we are motivated. People like Greta Thunberg are prepared to take the vitriol of our online world to bring attention to existential crises and global injustice, while many commentators prefer to judge them based on their own prejudices. I know where my admiration lies. – Yours, etc, BARRY WALSH, Blackrock, Cork. Sir, –Would Finn McRedmond be commenting on Greta Thunberg using terms such as 'little to like, ghoulish, the enviable self-assurance', if Greta were of the male gender? Is this article not evidence that gender bias and stereotypes around female likeableness and confidence are still in practice in 2025. To my mind, Greta Thunberg demonstrates great courage in the face of unwarranted criticism based solely on her age and gender. – Yours, etc, MAUREEN O'SULLIVAN, Bantry, Co Cork. Sir, – Finn McRedmond's flippant article does your newspaper no service. With supporters like McRedmond, Thunberg doesn't need enemies. – Yours, etc, SHEA CARROLL, Dublin 8. 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Power cut cancels Wicklow school classes but Curiosity Cube saves day
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Irish Independent

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Power cut cancels Wicklow school classes but Curiosity Cube saves day

Students who were destined for a day of learning at home were able to become scientists for the day at the Curiosity Cube, which is designed to make science, technology, engineering and math (STEM) accessible. The retrofitted shipping container came to Gaelscoil an Inbhir Mhóir for the fourth year as part of a Europe-wide tour. The Life Sciences Volunteer team from Merck – the science and technology company driving the Curiosity Cube – reached out to the local community through WhatsApp and social media and invited other local schools, students, families and friends to work alongside Merck employees from Sigma-Aldrich Ltd, the primary centre for cGMP production of commercial and late-stage APIs and advanced intermediates. In total, 130 children from Gaelscoil an Inbhir Mhóir, their families and other local primary schools enjoyed an interactive day at the Curiosity Cube. Throughout the visit, students from Gaelscoil an Inbhir Mhóir and other local schools explored real-world science through three interactive experiments focused on the fundamentals of artificial intelligence (AI): image authenticity, pattern recognition and self-driving cars. These hands-on activities were designed to show students how STEM is all around them and to equip them with critical thinking skills needed for future careers. Site administrator for Merck's Sigma-Aldrich Ltd in Arklow, Sharon Kennedy, said: 'We love to have the Curiosity Cube back in Arklow every year, it means an awful lot to our local community and our colleagues that we are here every year visiting the schools. 'For four years and counting, the visit of the mobile science lab has always been making a big difference to not only us on site but also the students and the community in Arklow in general.' Despite the growing demand for STEM professionals, many students struggle to see themselves in these careers. A recent survey funded by Merck found that nearly half (48pc) of middle school students find it difficult to envision themselves as scientists, despite engaging in STEM-related activities every day. In 2024, the Curiosity Cube engaged more than 43,000 students across Europe and North America, visiting 14 countries and hosting 282 events. ADVERTISEMENT This year, the Curiosity Cube embarked on its fourth European tour, aiming to connect with 20,000 students via more than 130 events. Each stop on its tour is supported by employee volunteers who share their passion for science, providing students with real-world insights into STEM careers. 'Every student who walks into the Curiosity Cube walks away with a new way of looking at science,' Curiosity Cube coordinator Stefanie Rammer said. 'That spark of curiosity can make all the difference in shaping the scientists of tomorrow.'

The onerous cost of Crohn's disease: ‘It becomes a choice between paying for a utility bill or medication'
The onerous cost of Crohn's disease: ‘It becomes a choice between paying for a utility bill or medication'

Irish Times

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  • Irish Times

The onerous cost of Crohn's disease: ‘It becomes a choice between paying for a utility bill or medication'

People react in different ways to grief, but the day after the death of a close family member, Amy Dennis developed stomach cramps and diarrhoea. Just a teenager at the time, her GP put it down to being bereaved, but the symptoms persisted and the bouts of diarrhoea became a recurring issue that played havoc with her life. As time went on, and her situation didn't improve, it was thought that she could have had an intolerance to gluten – the protein found in grains – but it wasn't until she began to get 'properly sick' that a thorough investigation was undertaken. It was discovered that she had Crohn's disease – a chronic and debilitating digestive condition with lifelong consequences. The condition can require the need for surgery, hospitalisation, immuno-suppressing treatments and higher risks for some forms of digestive cancers. READ MORE 'At the start of 2021, during the second Covid lockdown, I began to lose extreme amounts of weight from both diarrhoea and vomiting,' says the now 23-year-old. 'I went from 84kg down to 48kg in under a year. I was hospitalised for an unrelated issue, but that is when I had more blood tests and a colonoscopy, which led to me being diagnosed with Crohn's disease in December 2022.' [ Inflammatory bowel disease: 'I remember being in primary school and thinking maybe if I skip breakfast, my stomach won't hurt' Opens in new window ] Once diagnosed, living well with this condition is possible, but it does come with a cost, as medication, new dietary requirements and other treatments add up. Crohn's disease and colitis, two types of inflammatory bowel disease (IBD), affect about 40,000 people in Ireland. Research published last month showed that 60 per cent of people living with IBD face 'financial difficulty' as a result of their condition. The report, launched by Crohn's and Colitis Ireland, showed that patients spend an average of €3,252 annually on managing their condition including treatment and dietary needs , while 47 per cent have avoided seeking necessary medical care due to cost. Figures showed 62 per cent reported that taking time off work due to their condition has negatively affected their financial situation 'to some or a great extent'. Costs associated with attending medical appointments also play a significant role. Some 85 per cent said that mileage and travel costs added to their financial burden, 83 per cent had issues with parking fees, 62 per cent with overnight stays for medical appointments, and 49 per cent cited childcare fees as taking a toll financially. Dr Orlaith Kelly, consultant gastroenterologist at Connolly Hospital in Dublin, says Crohn's disease can be diagnosed at any age, but commonly presents in people aged 15-35, with a second wave of diagnoses occurring at 50-60. Treatment is not curative, but can control the disease, which can have very debilitating symptoms. 'Given the age profile of patients, IBD can often impact people when they are ordinarily at the height of their working lives or entering work life or parenthood,' says Dr Kelly. She says that 60 per cent of people living with IBD face financial difficulty directly because of their condition, while almost half have avoided necessary medical care because of the cost. 'In a cost-of-living crisis, for some, often it becomes a choice between paying for school uniforms, a utility bill and maybe forgoing medication or missing an appointment to work to do so,' she says. 'And this has obvious impact on patients' wellbeing and health down the track, possibly resulting in an emergency visit or more hospitalisation when the disease flares or is out of control.' It would be good for us to be able to enrol in the long-term illness scheme, or at least lowering the cost of the drugs payment scheme for us — Amy Dennis Amy Kelly, chief operating officer at Crohn's & Colitis Ireland, urges the Government to 'listen to the needs of the community and to improve access to care in Ireland'. 'This includes including Crohn's disease and ulcerative colitis in the chronic disease management programme and expanding medical card eligibility, ensuring equitable access to essential medical care,' she says. 'This inclusion would provide free, structured care, potentially reducing patients' out-of-pocket healthcare expenses through fewer emergency room visits, hospital admissions and lower medication costs.' According to Dr Orlaith Kelly, care for patients should cover access to more IBD physicians and multidisciplinary team members such as specialist nurses, psychologists and surgeons in a more timely and uniform manner across the country. This also includes timely access to intestinal ultrasound, endoscopy and MRI scans when needed and to infusions and theatre slots. 'This requires joined-up thinking at national programme level, provision of adequate resources to assess current needs through accurate data capture and adequate resourcing of this area in hospital and national health budgets,' she says. 'The truth is this type of strategy will in fact save money along with countless improvements in quality of life for the patients by avoiding the long-term complications and [emergency department] visits, which inadequate care or lack of access can so often lead to.' Dennis says this would be a welcome relief for herself and others with IBD. 'It would be good for us to be able to enrol in the long-term illness scheme, or at least lowering the cost of the drugs payment scheme for us,' she says. 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