
Defibrillator installed at animal sanctuary in Wolvey in son's memory
A family-run charity has installed a defibrillator at an animal sanctuary in memory of their animal-loving son, who died of a cardiac arrest at the age of 18.Jamie Rees, from Wolvey in Warwickshire, collapsed and later died on New Year's Day in 2022. There was a defibrillator near the scene, but his friends soon realised it was locked inside a school, so they were unable to access it.Since then, the OurJay Foundation was set up by Jamie's family to fundraise and install defibrillators across Rugby, Warwickshire, and even further afield.This week, the charity installed a community defibrillator at the Nuneaton and Warwickshire Wildlife Sanctuary, on Oaston Road in Nuneaton.
Jamie's mother and the chair of the OurJay Foundation, Naomi Rees-Issitt, said she was thrilled to be able to combine the ability to help people with helping animals through the installation of the defibrillator at the sanctuary.Mrs Rees-Issitt said: "One of Jamie's biggest passions and loves when he was with us was animals. "He loved foxes - we used to live in a village, and he walked the lanes to try and see foxes. "He had a passion for any animal. He used to rescue them. If he ever saw one in distress, he'd be the first to pull over and try to help."When visiting the sanctuary for the installation, Mrs Rees-Issitt told her husband: "It's somewhere Jamie would have absolutely loved to visit."
Geoff Grewcock runs the sanctuary with his daughter, Emma Hudson.He said: "It is fantastic that two charities with saving lives at the heart of them can come together to provide something so crucial for the community."The process is simple. If the equipment is needed, just call 999 and read them the location on the box, and they will issue a code and instructions."Everyone in the town knows where the sanctuary is, so it couldn't be easier for people to access in the event of an emergency.""It was an absolute joy to work with Geoff and Emma," Mrs Rees-Issitt said. "We absolutely love to work with other charities. A lot wouldn't be able to afford to buy a defibrillator."
So far, the OurJay Foundation has installed 259 defibrillators that are accessible to the community 24/7, alongside 60 in Snap Fitness gyms and 61 portable pitch-side defibrillators at sports clubs.Mrs Rees-Issitt said that so far, they were aware of 16 lives that had been saved through their defibrillators, as well as one life saved through one of their bleed kits, which are kept alongside the defibrillators, after a stabbing in Coventry.On one occasion, she received a bouquet of flowers from a woman who said the defibrillator had saved her mum's life.
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Telegraph
28 minutes ago
- Telegraph
Brighton GP practice investigated for prescribing trans hormones to children
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Daily Mail
an hour ago
- Daily Mail
Woman, 21, forced to 'glue eyelids open' just so she can see due to rare condition - but doctors say there's no cure
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In severe cases sufferers may be unable to open their eyes due to excessive eyelid spasm. Doctors do not have a cure but are continuing to trial different volumes of Botox in her eyelids. 'I have the same level of sight as a visually impaired person but I've got nothing wrong with my eyesight,' Tia-Leigh, who was an aspiring trainee accountant, explained. 'I know it's neurological but they don't know what causes it which makes it worse for me, because if they could say it's caused from this, I think it would make me feel slightly less in the dark. 'To be told I've got this for the rest of my life and not know why is a hard thing to deal with.' She admitted she's 'not been coping very well' and was prescribed antidepressants half-way through the ordeal. 'I didn't get along with them,' she continued. 'I tried therapy, I've tried hypnotherapy but nothing was helping. 'The longer it's gone on I've gotten used to it but there are still days where I get really down about it. Especially as the Botox runs out.' Tia-Leigh added that the longer she grapples with the condition, the more her body will get used to the injections and 'it won't work anymore'. 'I have them done every eight to 10 weeks at the moment. It was 12 weeks. But I only get about three to five weeks where it actually takes any effect,' she remarked. 'The rest of the time I have to physically hold my eyelids open to be able to see anything. 'When I glue or tape them open I can't blink at all. The doctors have said the longer I do that for then I've got more chance of actually damaging my eyes and then possibly losing my sight, which I don't want to do.' Tia-Leigh has even had bruises on her eyelids from the tape before. 'It's hard,' she admitted. 'Because I've either got no sight or one hand essentially.' Tia-Leigh was training to become an accountant, but has had to stop working because of her condition - ruining the plans she had for her life. 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It added: 'Blepharospasm happens when the part of the brain that controls your eyelid muscles stops working correctly. 'Sometimes blepharospasm runs in families, and women ages 40 to 60 are more likely to develop it. But in most cases, doctors aren't sure what causes it.' Treatment options include Botox injections and in some cases a surgery called a myectomy - where muscle nerve tissue is removed from the eyelid - can be recommended to alleviate symptoms. The NEI recommends seeing an eye doctor if: Source: NEI 'It's the stress of it as well that makes it worse. Anytime I'm really stressed it will make my eyes closed and accounting, I found it really stressful.' For her, the biggest struggle is loss of freedom and independence. She can't go out by herself if her eyes are closed, unless someone can drop her off. Tia-Leigh avoids solo outings because she gets 'too anxious not being able to see it'. 'I'm basically inside most of the time,' she said. 'It stops me doing things I enjoy. 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She has been documenting her experiences on TikTok, where Tia-Leigh has more than 3,700 followers.


Daily Mail
an hour ago
- Daily Mail
Shock Covid warning: Ultra-catchy 'Nimbus' variant could trigger summer wave amid 97 per cent infection surge
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