
Isle of Wight swimmer, 104, says 'sewage' stops him going in sea
The film featuring Mr Smith's comments is part of the charity's multi-million pound Solent Seascape Project to restore nature to the waters of the Solent."I look at the sea, how lovely it is, but regrettably I feel I won't be able to swim here again," Mr Smith said.
Explaining his concerns about pollution, he said: "That makes me more worried about swimming in the sea, it's worrying to think that pollution is there. The sea now is not what it used to be."Mr Smith, who was born in Bedwas, south Wales, first started swimming aged three and has attributed his long life to swimming and exercise in general.
A spokesperson for Southern Water said: "While huge progress has been made in creating healthier rivers and seas here over the decades, we are committed to working together with all Island partners to go further – reflecting the myriad of factors which can impact water quality, including farming, industrial and road run-off."
Kate Donlon of the Environment Agency said: "All of the Isle of Wight's 15 bathing waters are classed from 'Good' to 'Excellent' and we test the waters regularly between May and end of September to give swimmers like Mr Smith confidence in their bathing water of choice."
You can follow BBC Hampshire & Isle of Wight on Facebook, X (Twitter), or Instagram.
Hashtags

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


Reuters
15 minutes ago
- Reuters
UK scientists find genes linked with chronic fatigue syndrome
Aug 6 (Reuters) - Researchers at the University of Edinburgh said on Wednesday they have discovered differences in the DNA of people with chronic fatigue syndrome that should help dispel the notion that the debilitating condition is psychological or driven by laziness. Their study found eight areas of genetic code that are different in people with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) than in healthy volunteers. The finding provides 'the first robust evidence that genes contribute to a person's chance of developing the disease,' the researchers said in a statement. The key features of the condition include worsening of fatigue, pain and brain fog after even minor physical or mental activity. Very little has been known about the causes of ME/CFS, and there is no diagnostic test or cure. The condition is believed to affect around 67 million people worldwide, the researchers said. The DecodeME study analyzed DNA samples from 15,579 people who reported having chronic fatigue on a questionnaire and 259,909 people without it, all of European descent. Gene variants that were more common in people reporting ME/CFS were linked to the immune and nervous systems, according to a report of the study that has not yet been peer-reviewed. At least two of the gene regions relate to how the body responds to infection, which aligns with reports that the symptoms often start after an infectious illness, the researchers said. Another gene region has previously been identified in people with chronic pain, another common symptom of the condition. The findings 'align with decades of patients reporting on their experiences,' researcher Andy Devereux-Cooke said in a statement, adding that they "should prove game changing in the ME/CFS research field.' 'These results will not mean that a test or cure will be developed straight away, but they will lead to a greater understanding," he said. Scientists who were not involved in the study said using volunteers who self-reported chronic fatigue syndrome rather than restricting participation to those with a diagnosis from a medical professional somewhat weakened its conclusions. They called for larger studies to replicate the results. Substantial work will be necessary 'to translate these findings into new treatments," said Dr. Jackie Cliff, who studies infection and immunity in ME/CFS at Brunel University of London. "This will take considerable investment in academia and by industry.'


Times
19 minutes ago
- Times
My flat is damp and mouldy. Can I take action?
Q. I moved into a basement studio flat which became damp the first night I stayed. It has been deteriorating ever since. There is now mould on the walls. Under what legislation can I claim? A. Many housing conditions can expose tenants to damp and mould. They may feel unable to open windows because of security or noise concerns, their properties may suffer from poor or inadequate insulation or ventilation, and damp-proofing may be damaged or non-existent. Private and public sector landlords must comply with several pieces of legislation, including the Defective Premises Act 1972, the Landlord and Tenant Act 1985, the Homes (Fitness for Human Habitation) Act 2018, Minimum Level of Energy Efficiency standard (2018), the Housing Act 2004, the Environmental Protection Act 1990 and the Decent Homes Standard (2006). These fall into two categories. • Read more expert advice on property, interiors and home improvement First, there are the statutory rights tenants have against their landlords that supplement any obligations set out in their tenancy agreements. Of these the most important are landlords' obligations to repair the structure and exterior of rental properties under section 11 of the Landlord and Tenant Act 1985 and the obligation to ensure properties are fit for human habitation under the Homes (Fitness for Human Habitation) Act 2018. Also, landlords have duties to ensure tenants are reasonably safe from personal injury and damage under section 4 of the Defective Premises Act 1972. Tenants routinely bring county court claims for compensation under these provisions and obtain orders for specific performance requiring landlords to remedy damp. Second, there are the housing health and safety standards enforced by local housing authorities as part of their public health functions. If council officers inspect and find damp that poses a risk to tenants' health, they have a range of options. These include the service of Improvement Notices under the Housing Act 2004, more draconian prohibition orders and financial penalties (that is, fines). You can therefore take action yourself under the 1972 and 1985 acts or ask your council to enforce health and housing standards under the Housing Act 2004. Mark Loveday is a barrister with Tanfield Chambers. Email your questions to


Times
an hour ago
- Times
Breakthrough genetic study offers treatment hope for ME patients
Myalgic encephalomyelitis (ME) could have genetic roots, researchers have found, in the biggest scientific breakthrough yet into the disease. A team at the University of Edinburgh analysed DNA samples from people with ME, also known as chronic fatigue syndrome (CFS), in a hunt to uncover the biological roots of the illness. About 400,000 people in Britain have the disease, which leads to profound exhaustion and pain, but until now scientists knew 'next to nothing' about what causes it. The new study revealed eight 'signals' in genetic code where people with ME tended to have markedly different gene variants compared to the healthy population. It is the first robust evidence that genes predispose people to the disease and suggests that ME may be caused by processes in the immune and nervous systems.