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'We just need a bed' - Baby with 'days to live' can't access lifesaving treatment
United Kingdom🏛️ PoliticsProgressiveOverlooked by conservatives8 hr. ago

'We just need a bed' - Baby with 'days to live' can't access lifesaving treatment

A three-month-old baby named Macs, diagnosed with dilated cardiomyopathy, is critically ill and requires a specialized treatment called the Berlin Heart to survive. His parents, Dylan and Catrin Green from Cardiff, report that their son has been in a specialist unit in Bristol for weeks without access to a suitable hospital bed for the critical treatment. The Berlin Heart is only available at two hospitals in the UK: Great Ormond Street Hospital in London and the Freeman Hospital in Newcastle. The family emphasizes that the treatment could allow Macs to lead a normal life despite needing prolonged hospitalization. They express frustration over the lack of available beds and urge greater awareness about organ donation, noting that less than five patients in Wales and England are currently using the Berlin Heart. The NHS Wales Joint Commissioning Committee acknowledged the emotional strain on the family but did not provide further details.

Nicky Hatton, a 59-year-old mother of two from Chatteris, Cambridgeshire, described her experience with the NHS waiting list as unbearable, leading her to travel to Lithuania for a hip replacement surgery. She said she felt as though she had “broken glass in my hip” due to prolonged pain caused by osteoarthritis. Her condition worsened to the point where she could no longer walk, prompting her to seek alternative options after being told she would have to wait more than a year for treatment within the NHS. Hatton’s journey began in September 2025 when an X-ray revealed her hip was “bone on bone.” Her general practitioner referred her for a hip replacement, but she faced a long wait. After four months of enduring severe pain, she was informed that she would likely not receive the operation for 12 to 18 months. During this period, she relied heavily on painkillers and became increasingly reliant on a walking stick. Eventually, she decided to look into private alternatives, finding a clinic in Lithuania offering the procedure for significantly less, £8,600 compared to £20,000 to £25,000 in the UK. In April 2026, Hatton traveled to Kaunas, the second-largest city in Lithuania, for the surgery. She described the recovery process as transformative, noting how her ability to move around improved dramatically. Just 13 weeks post-operation, she was already climbing stairs and moving freely, a contrast to her previous state of immobility. She emphasized the emotional impact of the delay, stating that the prolonged suffering had taken a toll on her mental well-being. The situation reflects broader challenges facing the NHS. Data released in July 2026 indicated that the elective waiting list in England had risen for the second consecutive month, reaching 7.3 million appointments. This marks a reversal of recent improvements, with officials attributing part of the strain to heatwaves, which they say are placing similar pressures on the system as winter. At the end of May, 7.28 million treatments remained pending, affecting 6.16 million patients, an increase from 7.22 million and 6.11 million recorded at the end of April. The rising demand for private healthcare services is also evident. According to the Private Healthcare Information Network (PHIN), 953,000 Britons paid for medical care in 2025, marking the fourth consecutive year of growth. Much of this increase is linked to employer-funded private medical insurance (PMI). While the number of private admissions increased slightly to 953,000 from 947,000 in 2024, the trend underscores growing dissatisfaction with NHS capacity and accessibility. Hatton’s case highlights the personal consequences of systemic delays. As a full-time carer for her disabled adult son, she struggled to maintain her daily responsibilities while dealing with chronic pain. She criticized the lack of resources within the NHS, citing insufficient staffing and funding as key barriers to timely care. “There are not enough doctors, not enough nurses, not enough money going into NHS hospitals,” she said. “They can't possibly facilitate all of the care to all of the people that need it because there's no infrastructure to do it.” Her decision to seek treatment abroad is part of a larger pattern. Recent statistics show that 523,000 UK residents traveled overseas for healthcare in 2024, a rise from 431,000 in 2023 and 348,000 in 2022. This trend suggests increasing frustration with the NHS’s ability to meet patient demands, particularly in areas such as orthopedic surgery. With the waiting list continuing to grow and public confidence waning, the pressure on both the NHS and private healthcare sectors is intensifying.

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3 reports

Daily Mirror logoDaily MirrorIndependentProgressiveFactual 85Objective 654 days ago
‘I flew to Lithuania for op as NHS delays left me feeling like I had glass in my hip’

Nicky Hatton, a 59-year-old woman from Cambridgeshire, traveled to Lithuania for a hip replacement surgery due to prolonged NHS waiting times in the UK. Diagnosed with severe osteoarthritis, she endured significant pain and mobility issues while awaiting treatment on the NHS, which delayed her surgery by over a year. Faced with limited options, she opted for a cheaper private procedure abroad, costing around £8,600. Her experience highlights growing concerns about NHS waiting times, which have recently increased despite previous improvements. Officials attribute the rising backlog to factors such as heatwaves impacting healthcare capacity.

Bias read (Progressive): The article frames the NHS waiting list issue as a systemic failure exacerbated by government mismanagement, emphasizing the personal hardship caused by bureaucratic delays. While it does not overtly criticize specific political parties, the narrative leans toward portraying the NHS as under-resourc

Why factuality (85): The article reports a personal account from Nicky Hatton, a real person who reportedly flew to Lithuania for a hip replacement due to NHS waiting times. While no primary source document is available, the claim aligns with broader public reporting on NHS waiting lists and the trend of patients seekin

Why objectivity (65): The article uses emotionally charged language such as 'glass in my hip' and 'swallowing co-codamol like' to convey the severity of Nicky's condition. This subjective description leans into emotional storytelling rather than presenting facts objectively. The focus on Nicky's personal struggle may pri

Daily Mirror logoDaily MirrorIndependentProgressiveFactual 75Objective 703 days ago
'Respect the wishes of organ donors' to save lives, says campaign mum

Becca Lambert, a mother whose daughter Poppy requires a heart transplant, is advocating for legal changes to ensure that individuals’ registered wishes regarding organ donation cannot be overridden by family members after their death. Poppy, born with a rare congenital heart defect, has undergone multiple surgeries and now requires a heart transplant. Becca argues that the current system allows families to reject donations despite a person’s clear intent, which she claims results in lost opportunities to save lives. She cites NHS data showing that approximately 84 to 101 potential donors are declined annually, leading to over 900 missed chances to save lives. Becca, who works in NHS blood donation, emphasizes the importance of respecting individual choices and urges families to honor registered donor decisions.

Bias read (Progressive): The article frames the issue as a matter of personal autonomy and ethical responsibility, emphasizing the importance of honoring individuals’ pre-registered wishes. It highlights the negative impact of allowing families to override these decisions, suggesting that such practices undermine democratic

Why factuality (75): The article provides specific statistics from the NHS regarding the number of deceased donors in 2024/25 and the percentage of times families override donor decisions. These figures appear consistent with general knowledge about UK organ donation rates. However, the exact numbers (e.g., 842 donors,

Why objectivity (70): The article presents the mother's perspective strongly, using emotive language such as 'crusade', 'chance of life', and 'Change the Law for Life campaign'. It frames the issue as an urgent need for legislative change based on personal experience rather than presenting multiple viewpoints or acknowle

BBC News (UK) logoBBC News (UK)State / PublicProgressive8 hr. ago
'We just need a bed' - Baby with 'days to live' can't access lifesaving treatment

A three-month-old baby named Macs, diagnosed with dilated cardiomyopathy, is critically ill and requires a specialized treatment called the Berlin Heart to survive. His parents, Dylan and Catrin Green from Cardiff, report that their son has been in a specialist unit in Bristol for weeks without access to a suitable hospital bed for the critical treatment. The Berlin Heart is only available at two hospitals in the UK: Great Ormond Street Hospital in London and the Freeman Hospital in Newcastle. The family emphasizes that the treatment could allow Macs to lead a normal life despite needing prolonged hospitalization. They express frustration over the lack of available beds and urge greater awareness about organ donation, noting that less than five patients in Wales and England are currently using the Berlin Heart. The NHS Wales Joint Commissioning Committee acknowledged the emotional strain on the family but did not provide further details.

Bias read (Progressive): The article frames the issue around systemic healthcare shortages and highlights the urgency of medical treatment, emphasizing the human cost of bureaucratic delays. While it does not overtly criticize specific political parties, the focus on institutional failure and the call for increased organ捐赠(

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