Bexley GP surgery to get £360k to help reduce wait times
Bexley Council has confirmed it will give a grant of £359,196 to Crayford Town Surgery to implement work which will see the creation of two new clinic rooms.
The money was gathered from unallocated Section 106 (S106) contributions from the redevelopment of the former Electrobase site in Crayford.
S106 agreements between developers and local authorities are used to mitigate the negative impacts of a new development on the local community.
A total of 559 new homes will be built as part of the redevelopment of the brownfield Electrobase site, likely resulting in increased pressure on local infrastructure and in particular health services.
Bexley Council was approached by the NHS South East London ICB (integrated care board) with a request for the money to 'enable them to develop and implement a scheme to increase clinical capacity at Crayford Town Surgery in partnership with the practice' following confirmation that the residential development would be going ahead.
The ICB considers that the S106 funds will cover the entire project which aims to increase patient capacity 'through reconfiguration' and through the constitution of two new clinic rooms.
The ICB has welcomed the cash injection for the surgery. A Bexley spokesperson for the South East London ICB said: 'Investment received because of the Electrobase residential development Section 106 contributions, will allow Crayford Town Surgery to reconfigure and refurbish its current site.
'This will include two additional consulting rooms and a hot-desking room, for primary care colleagues from the wider neighbourhood team, to provide more joined-up care to patients.
'This investment will enable the surgery to increase its clinical capacity (GPs and multi-professional clinicians) and meet the health and care needs of the new population moving into the Electrobase residential development.
'NHS South East London Integrated Care Board has worked in partnership with the London Borough of Bexley and is supportive of this investment.'
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Yahoo
6 minutes ago
- Yahoo
West Midlands named worst for common travel-related illness and reason why
The West Midlands has been named the worst place for cases of a common travel-related sickness bug. The region recorded the highest number of travel-related gastrointestinal (GI) infections in England, according to the UK Health Security Agency (UKHSA). There were 477 cases in the West Midlands, representing 17.6% of the total cases in England. READ MORE: Tragedy as man's body found in West Bromwich canal Get breaking news on BirminghamLive WhatsApp, click the link to join The UKHSA said the main bugs causing these infections include cryptosporidium, giardia and salmonella – generally picked up from infected water and food. However the region also recorded the second highest rate of enteric fever (typhoid/paratyphoid) nationally, with 67 cases. These illnesses are caused by things like salmonella bacteria, which is more common in countries with less developed sanitary facilities. They can be spread through food and drink, including shellfish affected by sewage entering drinking water. However infections are preventable in all of these cases. Meanwhile, malaria also remains a significant risk for people travelling to endemic areas, with the West Midlands accounting for around 9% of UK cases in 2023 (181 out of 2,106), an increase of 27% on 2022. The reasons for travelling cited by UK cases were visiting friends and relatives (74%), travelling for holiday (20%) and travelling for work (6%). Elsewhere, travel-related measles cases have increased significantly since 2022, reflecting global trends of the disease and increasing levels of travel following the pandemic, with children under 10 most affected. Recent outbreaks have been seen in several other European countries including Romania, France, Belgium, Italy and the Netherlands. Katie Spence, UKHSA Regional Deputy Director West Midlands, said: "The West Midlands is a central transport hub and has a diverse population, so there is a lot of international travel, increasing risk of travel-related infections. "The main infections we are seeing in the region are gastrointestinal and enteric fever, which are preventable, with risk greatly reduced by practicing good hand hygiene and making sure fresh food is rinsed well in clean water. "Measles remains an ongoing risk, both in England and abroad, particularly for children, so it's important to make sure everyone is up to date with their MMR vaccines. "Certain countries also require specific vaccinations, so you should arrange these with your GP surgery in good time before travelling. "The Travel Health Pro website, has detailed country-specific information, including what vaccines to get, any important medication such as malaria tablets, and how to avoid traveller's diarrhoea and other serious gastrointestinal infections. "We want everyone in the West Midlands to enjoy a safe and healthy holiday season, whether at home or abroad. "So whether you're visiting family and friends, taking a mini-break, going somewhere you know well or a more exotic location, there are simple steps you can take before, during and after travel to reduce your risk of picking up an unwanted infection, ruining your trip and having to take time off work or school when you get back. "From vaccinations to basic hygiene, practising safe sex, and being aware of symptoms, there are easy ways to stay well."
Yahoo
34 minutes ago
- Yahoo
Living kidney donor 'will give our son a new life'
Amrit Paul was in the middle of his computer science exams when he was told by doctors he would need a kidney transplant. "It was a shock. I didn't really know how to handle it and, in all honesty, I went into a shell," he said. He was placed on the organ donation register almost five years ago, having been diagnosed with a chronic kidney disease aged four. Amrit undergoes nine hours of peritoneal dialysis each night, a method of blood purification used when kidneys fail. "People say I look fine, but under the hood there are a lot of problems," the 24-year-old said. Now he and his parents are appealing for a living kidney donor from the South Asian community to come forward. 'Debunk myths' "Feeling your body change as your organs start to decline is tough," added Amrit, who works remotely in software sales. "My family are my motivation, they've been so supportive." Amrit's mum Jatinder Paul is leading their campaign. Their poster reads: "Please, help us find an angel for Amrit." Their appeal comes as NHS Blood and Transplant reveals that a record number of people are waiting for a life-saving transplant in the UK. When Amrit's immediate family, who are Indian Punjabi, discovered they were unable to donate, they also became aware of the shortage of matching donors from global majority backgrounds. "As a parent, it's hard not being able to donate because of your own health issues," said Jatinder. "So you reach out to the wider community and ask if there's someone who can help give him his life back." Dr Rhys Evans, clinical lead for kidney transplantation at Royal Free London, where Amrit is receiving care, said ethnicity can play a significant role in how long a patient waits. "Unfortunately, for patients like Amrit who has blood group B, which is more common in South Asian and Black ethnic groups it often means a longer wait, because there are fewer donors from those communities," he said. As of 31 March 2025, more than 8,000 people were on the active transplant waiting list across the UK - the highest number ever recorded. Over 1,300 of those patients are based in London. In the capital, the number of deceased organ donors fell last year to 130, down from 154 the previous year. Fiona Loud, policy director at charity Kidney Care UK, said greater awareness and conversation within ethnic minority communities is vital. "Sadly, every day at least one person dies waiting for a transplant. This has to change," she said. "People from Black and South Asian communities are more likely to need a donor from the same background as them so that the organ is less likely to be rejected. "Talking about it and sharing your decision helps debunk myths and makes your wishes clear to loved ones." Funding for more black and Asian blood donors Lack of ethnic diversity among egg and sperm donors Couple donate stem cells in 'rare' double match Anthony Clarkson, director of organ and tissue donation and transplantation at NHS Blood and Transplant, is also urging people to register their wishes. "We are facing an incredibly concerning situation. More people than ever are waiting for transplants, but fewer donations are taking place," he said. "We need to act across all areas - modernising the Organ Donor Register, improving understanding of the law, and investing in technologies that preserve and treat organs." Despite the difficulties and uncertainty about whether a donor will come forward, the family say they remain hopeful. "We want to spread the word, bring awareness and find a match," said Jatinder. "He's focused on living a normal life, and that's what gives us the strength to keep going as a unit." Listen to the best of BBC Radio London on Sounds and follow BBC London on Facebook, X and Instagram. Send your story ideas to NHS: Become a living donor
Yahoo
an hour ago
- Yahoo
Living kidney donor 'will give our son a new life'
Amrit Paul was in the middle of his computer science exams when he was told by doctors he would need a kidney transplant. "It was a shock. I didn't really know how to handle it and, in all honesty, I went into a shell," he said. He was placed on the organ donation register almost five years ago, having been diagnosed with a chronic kidney disease aged four. Amrit undergoes nine hours of peritoneal dialysis each night, a method of blood purification used when kidneys fail. "People say I look fine, but under the hood there are a lot of problems," the 24-year-old said. Now he and his parents are appealing for a living kidney donor from the South Asian community to come forward. 'Debunk myths' "Feeling your body change as your organs start to decline is tough," added Amrit, who works remotely in software sales. "My family are my motivation, they've been so supportive." Amrit's mum Jatinder Paul is leading their campaign. Their poster reads: "Please, help us find an angel for Amrit." Their appeal comes as NHS Blood and Transplant reveals that a record number of people are waiting for a life-saving transplant in the UK. When Amrit's immediate family, who are Indian Punjabi, discovered they were unable to donate, they also became aware of the shortage of matching donors from global majority backgrounds. "As a parent, it's hard not being able to donate because of your own health issues," said Jatinder. "So you reach out to the wider community and ask if there's someone who can help give him his life back." Dr Rhys Evans, clinical lead for kidney transplantation at Royal Free London, where Amrit is receiving care, said ethnicity can play a significant role in how long a patient waits. "Unfortunately, for patients like Amrit who has blood group B, which is more common in South Asian and Black ethnic groups it often means a longer wait, because there are fewer donors from those communities," he said. As of 31 March 2025, more than 8,000 people were on the active transplant waiting list across the UK - the highest number ever recorded. Over 1,300 of those patients are based in London. In the capital, the number of deceased organ donors fell last year to 130, down from 154 the previous year. Fiona Loud, policy director at charity Kidney Care UK, said greater awareness and conversation within ethnic minority communities is vital. "Sadly, every day at least one person dies waiting for a transplant. This has to change," she said. "People from Black and South Asian communities are more likely to need a donor from the same background as them so that the organ is less likely to be rejected. "Talking about it and sharing your decision helps debunk myths and makes your wishes clear to loved ones." Funding for more black and Asian blood donors Lack of ethnic diversity among egg and sperm donors Couple donate stem cells in 'rare' double match Anthony Clarkson, director of organ and tissue donation and transplantation at NHS Blood and Transplant, is also urging people to register their wishes. "We are facing an incredibly concerning situation. More people than ever are waiting for transplants, but fewer donations are taking place," he said. "We need to act across all areas - modernising the Organ Donor Register, improving understanding of the law, and investing in technologies that preserve and treat organs." Despite the difficulties and uncertainty about whether a donor will come forward, the family say they remain hopeful. "We want to spread the word, bring awareness and find a match," said Jatinder. "He's focused on living a normal life, and that's what gives us the strength to keep going as a unit." Listen to the best of BBC Radio London on Sounds and follow BBC London on Facebook, X and Instagram. Send your story ideas to NHS: Become a living donor