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Manchester City boss Gareth Taylor wants improved communication between players and officials following Sunday’s controversial draw with Chelsea in which he felt the referee handed out bookings “like confetti”. City looked the brighter side and had taken a 1-0 lead via Chloe Kelly’s deflected seventh-minute strike, but late in the first half referee Emily Heaslip decided Alex Greenwood had been time-wasting after taking 26 seconds to take a free-kick and dismissed the bewildered captain with a second yellow. It was an encounter with potential title implications that ultimately saw 10 yellows issued, including a second to Lauren Hemp 15 minutes before Guro Reiten’s stoppage-time equaliser, with the decision against Greenwood in particular lambasted on social media and criticised by big names including Ian Wright and Beth Mead. Taylor, who himself was booked in the second half, said: “We submit a report which normally is fairly straightforward. “I think this one will be quite an interesting one, just in terms of some of the feedback I’ve had from the players as well, in terms of the communication back and forth from the officials. “Everyone makes mistakes. I think owning those mistakes at times is is much easier to handle, because we all do it, and I think it’s just a little bit easier if we get that communication between us, which is really important, so that we can create – not necessarily accountability – but we can create communication between us and go, we’re seeing it as this and you guys are seeing it slightly differently, who is right or wrong here? “It’s important we get the feedback. Let’s see what we hear back.” City, who also unsuccessfully appealed a three-match ban for Leila Ouahabi, sent off in their season opener, next travel to Everton on Wednesday to kick off their FA Cup campaign, a competition Taylor insisted “is not something to be sniffed at”. City are looking to qualify for Champions League football again after narrowly missing out with a fourth-place WSL finish last year, with success against top sides like Chelsea critical in the short 22-match season. The next thing you know, before you know it, they're handing them out like confetti Gareth Taylor While Taylor suggested Sunday’s decisions “went against us, it always seems to be against us and not Chelsea”, he conceded the first yellow of the game, shown to Blues forward Lauren James, was “harsh, and the next thing you know, before you know it, they’re handing them out like confetti”. He also brushed aside theories that his side were less disciplined than Hayes’, adding: “They always seem to talk around that their discipline is much higher, but I don’t think there was any ill discipline from us at all. “It was a real anomaly of the game and it forced us into a really, really difficult situation which the players coped with so well. “I’ve been so impressed with the players and the way they manage that. “To put four points on the board in both of those games, when you lose players, has been amazing.” Read More Dawid Malan thrilled to ‘keep silencing people’ with World Cup hundred FA chief Mark Bullingham: Critical the whole country feels involved in Euro 2028 Garry Cook vows to make Birmingham ‘a powerhouse’ amid Wayne Rooney reports Catalans win in Grand Final would ‘make huge noise around the world’ – McNamara A closer look at the UK and Ireland’s host venues for Euro 2028 A closer look at the UK and Ireland’s host venues for Euro 2028

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A woman who felt she was being “suffocated” by her cystic fibrosis – and was told she had been just two weeks away from dying – has climbed Snowdon and run a half marathon after receiving two lungs from a transplant donor. Georgie Cooper, 26, was diagnosed with cystic fibrosis (CF) – a genetic condition which causes sticky mucus to build up in the lungs and digestive system – when she was two. The complaints and compliance officer, who lives in Essex, took medication and used nebulisers – machines which allow you to breathe in medicine – every day. She managed to maintain a “steady” lung function between 70 and 80 per cent until her health started deteriorating in her late teenage years. Cooper said 2018 was “the worst year” because she could not breathe properly and spent four months in and out of hospital as her lung function had dropped to 30 per cent and then to just 9 per cent. She was prescribed Orkambi, followed by Symkevi, to manage the condition. She was told she needed oxygen therapy 24 hours a day, which meant she had “tubes hanging out (her) nose”, and had to use a wheelchair. “It felt like constant suffocation, like I was being suffocated every minute, every second of every day.” Just two weeks before Christmas 2018, when she was 20, Cooper was told she had “a maximum of two years to live” and should consider a double lung transplant. While she waited for a donor, Cooper was prescribed Kaftrio to treat her CF, which she believes kept her alive. Her mother, Lesley, who she described as her “rock”, became her full-time carer and, after three false alarms, Cooper finally received the call that “we’ve got a set of lungs for you”. The surgery in June 2021, at Harefield Hospital in London, was successful – and came just in time. Cooper was told after the operation that her lungs had looked like “pulled pork” due to the CF damage, and she would have only lived for around two more weeks without the transplant. Before her surgery, Cooper had experienced three false alarms about suitable donors, and had started to believe that “to die would be peace”. During this time, she planned her funeral and created a “dream” bucket list – including going abroad again – to look forward to should she survive. She said she tried to stay positive as she knew she only had “a short time left on this Earth”, but found it extremely difficult knowing she was dying. “I had actually written my goodbye letters to my mum, dad, brother, my nan and pa, in case it didn’t work out, or in case I died before my transplant,” she said. She is incredibly grateful that the fourth call from the transplant service was a success. She describes her donor, who cannot be identified, as her “hero”. In August 2022, and after recovering, Cooper climbed Snowdon – now also known as Yr Wyddf and the highest mountain in Wales. She also completed the Bath Half Marathon in October 2023. “Snowdon, at that point, was my greatest achievement,” she said. “I felt like that’s the closest I’m going to get to my donor for now, which was really emotional. Someone else has selflessly given something of theirs to save another life – it’s incredible. She is the greatest hero that I never knew.” Cooper was born with no health complications, but soon developed a persistent cough, which raised alarm bells for her parents. After being referred to the Royal Brompton Hospital when she was two years old, she received her CF diagnosis and started taking medication and using nebulisers and having physiotherapy. While this was “normal” for Cooper, during secondary school she said she was “outed” as having CF during science lessons and her classmates and teachers discussed symptoms and life expectancy. According to the charity Cystic Fibrosis Trust, the median age of death of someone with CF in 2022 was 33. While Cooper was aware of the statistics, she said her peers at school would regularly say: “Oh you’re going to die soon, you haven’t got long left, have you?” Cooper says she cannot believe what she has overcome and achieved since the surgery, having also secured her first job as well as her running and mountain-climbing exploits. She now plans to climb Ben Nevis in Scotland – the highest mountain in the UK. While she still has to take immunosuppressants and struggles with survivor’s guilt, Georgie says she feels she has been “reborn” and now “lives for two people every day”. She was told her donor’s favourite quote was “your mountain is waiting”, which inspired her Snowdon adventure, and she wants to encourage others to “live every day like it’s your last”. She said: “Life is full of tablets, but I’m not having any physio, no nebulisers, and it’s like being reborn – it’s a life I’ve not known and I’m making up for lost time. I owe my life to my donor. She is my hero, she’s the greatest hero I never knew. It’s a gift of life, and that’s the best gift I’ll ever be given.” For more information and support, visit Cystic Fibrosis Trust’s website at: cysticfibrosis.org.uk. For more lung transplant information, visit: cysticfibrosis.org.uk/what-is-cystic-fibrosis/cystic-fibrosis-care/transplant-information-and-resources.

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