
West Lothian bids invited as £15m mental health fund set to relaunch
A £15m programme described as a 'life saving' by West Lothian's Third Sector is set to open the purse strings for its latest round.
The fund, first launched at the height of the Covid pandemic, has so far delivered £2m to local volunteers who promote better mental health within communities.
Up to 150 grass roots organisations have been supported to help those most in need.
And, each year, West Lothian's share of the national pot- around £470,000- could have been spent three times over given the number of applications. Difficult decisions have to be taken.
For West Lothian this year, a further £470,000 will be made available. Applications to the Fund will open in September and around 80% of organisations will be considered for two years of funding to support their projects.
It is expected that the Scottish Government will make a similar level of funding available for 2026/27.
Alan McCloskey, the CEO of Voluntary Sector Gateway West Lothian (VSGWL) said: 'This funding saves lives.'
The head of the local Third Sector umbrella organisation added: 'Over the past four years, £2m from the Scottish Government`s Communities Mental Health and Well-being Fund has been provided to 150 small, grass roots grass roots organisations to support their initiatives.
'We know that the money helps organisations to support vulnerable adults across West Lothian from the impacts of social isolation, loneliness, poverty, and inequality. It is fantastic that we will be able to help projects with much needed additional funding over the coming two years as well.'
The fund has been heavily oversubscribed every year, with applications seeking around £1.3million annually.
Funding helps organisations with costs such as staffing, equipment, venue hire, training and volunteer expenses.
Projects have tackled social isolation, loneliness, mental health inequalities, and supported those most affected by the pandemic.
This includes projects supporting a range of at-risk groups, including women, particularly those experiencing gender based violence; people with a long-term health condition or disability and those from a minority ethnic background.
Volunteers who work with people affected by psychological trauma have also benefited from the fund since 2021, along with those who have experienced bereavement or with neurological conditions or learning disabilities.
West Calder and Harburn's Community Development Trust is one of the organisations which has benefited.
Good Connections supports people in the West Calder and Polbeth areas to access activities, services and opportunities that improve their lives.
It uses a Social Prescription model whereby a Well-being Link Worker offers 1-2-1 sessions to help identify what a client wants to get out of the service, what is available locally and then supports them to access those opportunities.
The project also provides activity groups where they are lacking in the area such as walking, yoga and arts & crafts for well-being.
Matt Pearce, the manager of West Calder and Harburn Community Development Trust, said: 'Good Connections has received funding from the Communities Mental Health Fund for three years now and it has enabled us to support so many people during hard times in their lives. The impact has been huge.'
'The project is run by West Calder & Harburn CDT and Polbeth Community Hub offering support across the communities including from our local Community Woods and Garden. It has helped hundreds of people find activities and groups to get involved in to improve their mental health and supported them to access additional services as well.'
Adele Prendergast, the manager of Polbeth's Community Hub said : '86% of people who accessed our project over the last two years have seen a meaningful improvement in their mental well-being and 100% of our regular group attendees said that the activities had had a positive effect on their mental health.
'They also all said they would recommend others join our groups. This is the impact funding like this has'.

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Daily Mail
3 hours ago
- Daily Mail
Our lives changed forever after my husband had the Covid jab...a stroke left him blind and paralysed - and the stress has broken our marriage
When Vicky O'Neill casts her mind back to life during the pandemic, one date remains forever etched in her memory. For it was on May 17, 2021, that husband John awaited his turn to have the newly-approved AstraZeneca Covid vaccine. The doting father-of-two from Althorne, Essex, was considered more at risk from Covid-19 because of his asthma and was optimistic the jab could offer a 'return to normality.' Still, moments before his appointment, the then 41-year-old turned to his wife and said he was worried about the possible side-effects. 'We were sitting in the car, just the two of us. And he said to me, "I'm going to go in and have AstraZeneca, and you're going to have the Pfizer. That means if there's any problems - because we don't know much about these vaccines - at least there is still one of us here for the kids." 'I told him not to be stupid. He went in, had his jab and didn't think anything of it.' But the IT contractor's words turned out to be a chilling foretelling of events that would forever change their lives. Within the next 10 days, John suffered a devastating stroke that would leave him blind in his left eye, paralysed down his right side and 60 per cent brain damaged, among other permanent disabilities. As he and his family would later discover, John had suffered an extremely rare reaction to the Covid jab that causes blood clots with a low platelet count. Known as VITT - vaccine-induced immune thrombocytopenia and thrombosis - medical experts said such a reaction would only happen to one in 50,000 people. Four years on, John and his loved ones acknowledge just how lucky he is to even be alive - but the repercussions continue. Now aged 46, John has been left a shadow of the man he once was, unable to work and needing full-time care. The financial impact on the family has also been immense - with John confessing they have been 'living on nothing', and their beloved four-bed detached home is now up for sale. Having received an 'inadequate' compensation payment from the Government, John fears he has become one of the 'forgotten' individuals whose lives changed immeasurably after they had the vaccine - and he has added his name to a 50-strong class action currently going through the courts. In the latest consequence of this tragedy, the tremendous stress endured by the couple has brought an end to John and Vicky's 16-year marriage, with the pair taking the difficult decision to divorce. It's a decision borne more out of necessity than desire, with both clearly devastated that events have turned out this way. But after 25 years together, both agree it is the right thing to do for their children and are determined to remain heavily involved in each other's life. 'As you can see, we get on but everything has changed. John's changed. I've had to change, and life is so very different,' said a tearful Vicky, who has cared for her husband full-time over the last four years. John, who still struggles with his speech in the aftermath of his stroke, simply nodded while dabbing away his tears. Looking around the lounge of their comfortable home, vibrant family photos point to an array of happier times in their life. Vicky had just turned 18 when she met John, an ambitious IT contractor who previously earned a six-figure salary. 'We were very lucky. John worked really hard and we had a good life, like we've never asked for anything. I was working as a graphic designer for an architect in London. 'We were both very career-minded, but we knew what we wanted. We bought a house together in Romford while we were still very young and we had our own cars. We done it all ourselves. You know, we had a good life.' The couple married in 2008, and four years later had their daughter, Freya, now aged 13, followed by their son, Mason, now eight. 'He's been diagnosed with autism and ADHD so he's 100 miles an hour, but the most amazing kid,' Vicky enthused. 'We had everything we wanted - life was good.' Five years ago, the couple decided to move from Romford to the more rural surrounds of Althorne to provide 'a better life for the kids'. They bought their current home and planned to renovate and extend the property, but plans were halted after the world was plunged into the Covid pandemic. Both John and Mason, who was aged just four at the time, suffered from severe asthma and out of caution the family shuttered themselves off from seeing anyone. 'We were extreme, we didn't want anyone to visit because they both had asthma and we worried about the virus. 'When this jab came out, we thought this is what we needed to get us back into the world again.' At first, none of John's initial concerns about the vaccine came to fruition. He experienced the typical flu-like symptoms reported by others after the first 24 hours, but otherwise seemed fine. But as the days went on, Vicky noted that John seemed 'extremely tired' and had experienced fleeting moments of feeling sick. Ten days after his vaccination, John awoke in the morning and complained of an intense pain in his left eye. After calling 111, he was advised by a doctor that he likely had a sinus infection and a prescription was issued over the phone. Vicky recalled that she left the house to go and pick up the medication, only to find John saying the pain was 'unbearable' when she returned. Within hours, he began saying there was something wrong with his jaw and decided to return to bed. But when he got up around 6pm, Vicky could see her husband was seriously unwell. 'He walked in here, and he was grey and clammy. He said his vision had gone in one eye and couldn't stop being sick. He pleaded with me to call an ambulance.' A first responder arrived within minutes and suspected John, who by now was also slurring his words, was having a heart attack or stroke. When the ambulance arrived, he was taken off to Broomfield Hospital in Chelmsford. Despite the severity of his symptoms, the doctors believed at first that John simply had a migraine. But overnight he suffered a major stroke, originating in his optic nerve, that damaged 60 per cent of his brain. Consultants then discovered his left carotid artery had become 'completely occluded'. John would need to be transferred to the Royal London Hospital for a life-saving procedure to insert a stent, with Vicky warned by medics 'he might not make it'. She was told hours later that despite an initial problem the stent had been successfully inserted, but when Vicky went to visit her husband the next day she found him 'in a state'. 'He had a temperature. His left eye was completely shut. He was thrashing around and kept pulling his left leg up and groaning.' Vicky had previously noted at Broomfield that John's leg had a strange 'mottling' around the ankle, but was reassured by doctors that this would be assessed after he was transferred to the Royal London. However, when she asked if this had been done, a doctor seemed to be unaware of the issue. 'I'd looked at his leg again and now he had these red blanches all the way up his skin. The doctor pulled the sheet back, and said "Oh my God. He's got a haematoma." He began shouting for the team and said John needed to be scanned quickly.' Within hours, Vicky was approached by a haematologist consultant, who delivered devastating news: John had developed a condition known as VITT as a result of the Covid vaccine, which had caused his blood to start clotting in all the main arteries of his body. The rash on his left leg was a major clot that had formed. Vicky was asked to make a choice between John having his leg amputated or to start anticoagulation treatment including a plasma transfusion, but both procedures were 'extremely life threatening.' 'John was already paralysed on the right side by the stroke. He could not move, he couldn't sit up, he couldn't do anything for himself. He couldn't even lift his own head. 'The only thing he could do was lift this leg - and now they might amputate it.' Devastated by such a decision, Vicky said she believed John would not want to go ahead with amputation but would be guided by the doctors. They agreed to go ahead with the plasma exchange, with John reacting well to the treatment. He remained in intensive care for weeks before finally being transferred back to Broomfield Hospital and a short rehabilitation stint at Homerton Hospital. In all, John spent four months in hospital before coming home - but life would never be the same again. He presently takes 17 tablets a day and remains 'under every consultant possible'. 'John struggles with his speech and has aphasia. He also has difficulties reading and writing and recognising numbers. He's blind in his left eye. His carotid artery is now completely blocked, so doctors have to monitor him constantly to ensure he has no issues there. 'The artery in his left leg is blocked. So he has no pulse below the left knee and that causes a lot of problems. If he walks even 10 metres he gets pins and needles because of the restricted blood flow. 'His right leg was affected by the stroke and is now his weak leg. 'He's also now on the border of heart failure as a result of the stroke and we are getting him assessed for possible dementia.' Lifting his right arm and hand, John shakes his head before letting it drop. 'That arm is nothing', he added, showing he had lost the use of his limb. With the benefit of hindsight, Vicky acknowledges that at the point John returned home in September 2021 - and she became his full-time carer - the challenges had only just begun. 'Mason was starting school, and then Freya went back for the first time since the pandemic began - and we had to just try and be normal. 'But when I look back now, I didn't ever have any downtime. I had gone from my husband nearly dying to having to come home to look after the children and get them to be understanding of what was going on. And in all of this, I was still learning what was going on with John.' There were also new concerns for Vicky around their finances. 'John had been the main breadwinner, and all of a sudden he wasn't there. We would be OK for a little while due to savings, but my husband has had a stroke and he's not going to get better. I kept thinking what are we going to do?' John has been eligible to claim Personal Independence Payment and Employment and Support Allowance, while Vicky has claimed Carer's Allowance and been able to work a few hours each week to supplement her income. 'But for a family of four, you just can't survive on that,' explained Vicky, who said they had struggled over the last four years and the couple have had no other option than to sell their home. John was found to fit the criteria for the Government's Vaccine Damage Payment Scheme (VDPS), which offers a one-off financial payment of £120,000 in the event that a vaccine likely caused at least 60 per cent disablement. In John's case, that figure was found to be 90 per cent - but that money alone will not be enough to financially secure the family for the years ahead. He has now joined a class action launched by Leigh Day solicitors against AstraZeneca, which was indemnified during the pandemic, and the Government, which would likely pay out if their claim is successful. Lawyers representing victims and families are suing AstraZeneca under the Consumer Protection Act 1987. They argue the vaccine was 'a defective product' that was 'not as safe as consumers generally were reasonably entitled to expect'. AstraZeneca has strongly denied these claims. Health officials first identified cases of VITT linked to AstraZeneca's jab in Europe as early as March 2021, just over two months after the vaccine was first deployed in the UK. On its website, Leigh Day stressed it was not an 'anti-vaccination' case. 'It is however a case about fairness – a case in which we are trying to secure fair compensation for those families who paid the ultimate personal price for agreeing to be vaccinated during the pandemic.' Vicky said if they were to be successful, the money would take away their financial stress - but tragically it would never bring back the life they once had. 'I was lucky that we didn't lose John, and our children were lucky that they didn't lose their dad, but they have lost him in a huge way, in every way possible. He is still here, but he's not the man he was. 'It worries me going forward, because John has lots of issues and we don't know how they are going to progress. 'Money can't buy happiness. It can make things stable, which is great, but it's not going to change what happened. It's not like having a broken arm that you can fix and go back to enjoying life, doing your job and taking the kids to the park. 'It's never going to happen for us. 'John has been robbed of his life, and he can try and make another life for himself, but it's always going to be limited because of what happened.' Vicky is keen to stress that she and her family are not against vaccinations, but feels saddened their lives were upended simply because they tried to 'do what was right'. 'We just wanted to do right by our family, our friends, the country. We just wanted to do our part in getting back to normal. 'But life is far from normal for us - and we just don't know what the future holds.' In a statement to MailOnline, Leigh Day partner Sarah Moore said: 'As a result of his injuries, John will never be able to work again, or be the husband and father that he once was for Vicky and their children. 'Presently the Government scheme provides them with a one-off payment of £120,000. That is less than John's annual earnings prior to his injuries and is wholly inadequate to provide him with the specialist care that he needs to live with his injuries let alone provide for his family. 'John stepped forward for vaccination at the Government's request, along with thousands of others, and yet when he needs the Government to stand with him and his family by providing meaningful financial support they are nowhere to be seen. 'John and others like him do not want to have to bring a legal claim, they want to put their energies into putting their lives back together. 'The fact that they are having to do so should be a cause of national shame, the pandemic was a period of national solidarity and yet, in the aftermath when the country has moved on, those injured like John have been forgotten.' Official data shows at least 81 Brits have died from blood clot complications apparently linked to the AstraZeneca jab, according to figures collected by the UK's drug watchdog, the Medicines and Healthcare products Regulatory Agency. A further unconfirmed number have been injured and/or disabled. Further Covid vaccine rollouts have either minimised use of the AstraZeneca jab and/or phased it out entirely in favour of mRNA alternatives like those made by rival pharma giants Pfizer and Moderna. However, AstraZeneca's jab is credited with saving some 6million lives globally during the Covid pandemic. AstraZeneca previously said in a statement: 'Our sympathy goes out to anyone who has lost loved ones or reported health problems. 'Patient safety is our highest priority, and regulatory authorities have clear and stringent standards to ensure the safe use of all medicines, including vaccines. 'From the body of evidence in clinical trials and real-world data, the AstraZeneca-Oxford vaccine has continuously been shown to have an acceptable safety profile and regulators around the world consistently state that the benefits of vaccination outweigh the risks of extremely rare potential side effects.'


South Wales Guardian
20 hours ago
- South Wales Guardian
First Minister meets Sir Chris Hoy to discuss prostate cancer testing
The champion cyclist was diagnosed with the disease last year before finding out it was terminal. He spoke to the First Minister – along with Health Secretary Neil Gray – in a roundtable at Mr Swinney's official residence Bute House in Edinburgh on Friday, along with his wife Lady Sarra Hoy and others who have experience of living with prostate cancer. The Olympic gold medallist has swapped the track for activism since his diagnosis was made public, pushing both the UK and Scottish governments to do more to fight the disease, and raising awareness among men of the signs of the condition. Earlier this year, Sir Chris urged ministers to change NHS guidance on the testing for prostate cancer. Currently, men over the age of 50 are considered to be at the highest risk, with the health service urging them to get tested. But Sir Chris has called for GPs to proactively contact men known to be at higher risk – for instance, due to a family history of prostate cancer – earlier to offer a test. 'I was diagnosed with stage four prostate cancer at 47. By this age, my prostate cancer was advanced and could have been progressing from when I was 45 or even younger,' he said. 'With prostate cancer, the earlier you find it, the easier it is to treat. We need the system to change to enable more men to get diagnosed earlier and stop them getting the news I got.' Speaking after the meeting, Laura Kerby, chief executive officer of Prostate Cancer UK, said the charity was 'delighted to be working with Sir Chris Hoy and the Scottish Government'. 'In the months after Sir Chris shared his story, we saw a huge increase in men using our online risk checker and the number of men in Scotland starting treatment for prostate cancer reached an all-time high,' she added. 'We're so grateful for the lifesaving impact he's making and continues to make with events like his upcoming Tour De Four cycling challenge. 'But, today, men in Scotland are still more likely to get a late prostate cancer diagnosis than anywhere else in the UK, so it's incredibly important that we do not take our feet off the pedals. 'We're grateful to the Scottish Government and First Minister John Swinney MSP for assembling such a talented group of experts and leaders in this space today to continue the vital work to change this unacceptable situation.' Alison Wright, chief executive officer of Prostate Scotland, said the meeting was an 'important first conversation'. 'We hope it leads to ongoing collaboration and concrete steps to close detection gaps, so no man at risk is left behind,' she said. 'Far too many men – especially those with a family history, black African or Caribbean heritage, or inherited genetic mutations – are diagnosed late because testing was only prompted by symptoms. 'We advise that clear prompts for GPs be introduced to consider PSA testing based on risk factors alone, not just symptoms. Acting early will save lives.'


STV News
21 hours ago
- STV News
First Minister meets Sir Chris Hoy to discuss prostate cancer testing
First Minister John Swinney has met with Sir Chris Hoy and his wife to discuss tackling prostate cancer. The champion cyclist was diagnosed with the disease last year, before finding out it was terminal. He spoke to the First Minister – along with health secretary Neil Gray – in a roundtable at Swinney's official residence Bute House in Edinburgh on Friday, along with his wife Lady Sarra Hoy and others who have experience of living with prostate cancer. The Olympic gold medallist has swapped the track for activism since his diagnosis was made public, pushing both the UK and Scottish governments to do more to fight the disease, and raising awareness among men of the signs of the condition. Earlier this year, Sir Chris urged ministers to change NHS guidance on the testing for prostate cancer. Currently, men over the age of 50 are considered to be at the highest risk, with the health service urging them to get tested. But Sir Chris has called for GPs to proactively contact men known to be at higher risk – for instance, due to a family history of prostate cancer – earlier to offer a test. 'I was diagnosed with stage four prostate cancer at 47. By this age, my prostate cancer was advanced and could have been progressing from when I was 45 or even younger,' he said. 'With prostate cancer, the earlier you find it, the easier it is to treat. We need the system to change to enable more men to get diagnosed earlier and stop them getting the news I got.' Speaking after the meeting, Laura Kerby, chief executive officer of Prostate Cancer UK, said the charity was 'delighted to be working with Sir Chris Hoy and the Scottish Government'. 'In the months after Sir Chris shared his story, we saw a huge increase in men using our online risk checker and the number of men in Scotland starting treatment for prostate cancer reached an all-time high,' she added. 'We're so grateful for the lifesaving impact he's making and continues to make with events like his upcoming Tour De Four cycling challenge. 'But, today, men in Scotland are still more likely to get a late prostate cancer diagnosis than anywhere else in the UK, so it's incredibly important that we do not take our feet off the pedals. 'We're grateful to the Scottish Government and First Minister John Swinney MSP for assembling such a talented group of experts and leaders in this space today to continue the vital work to change this unacceptable situation.' Alison Wright, chief executive officer of Prostate Scotland, said the meeting was an 'important first conversation'. 'We hope it leads to ongoing collaboration and concrete steps to close detection gaps, so no man at risk is left behind,' she said. 'Far too many men – especially those with a family history, black African or Caribbean heritage, or inherited genetic mutations – are diagnosed late because testing was only prompted by symptoms. 'We advise that clear prompts for GPs be introduced to consider PSA testing based on risk factors alone, not just symptoms. Acting early will save lives.' STV News is now on WhatsApp Get all the latest news from around the country Follow STV News