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replica handbags online Seven online friends with cystic fibrosis finally meet in real life after life saving lung transplantsEXCLUSIVE: Pals met each other online and went through their health struggles together after they were all born with the condition that meant they eventually needed new organsSeven women who have battled cystic fibrosis and supported each other met up to celebrate their bravery for the first time (Image: PA Real Life)Get daily news updates directly to your inboxSubscribeSee our privacy noticeMore newslettersThank you for subscribingWe have more newslettersShow meSee replica bags joy our privacy noticeCould not subscribe, try again laterInvalid EmailThis could be seven ordinary women enjoying an afternoon of prosecco.But the photo is a true picture of courage as they became friends while waiting for lifesaving lung transplants.All born with cystic fibrosis, George Compton, 28, Ashley Harris Moore, 36, Libby Clare, 22, Holly van Geffen, 26, Sharon Brennan, 37, Charlotte Davies, 24 and Josie Stewart, 25, have had their lives saved by the kindness of anonymous donors.Diagnosed with the genetic condition as youngsters, they a few years of good health before declining to the point where they needed new organs.Woman, 29, with cystic fibrosis who gets out of breath rolling over in bed could die without lung transplantHolly, whose deterioration started aged 18 when a lung said: “You try to battle on as best you can and not let your condition hold you back.”But there does come a point when you see all your peers growing up, becoming more and doing all these adult replica bags louis vuitton things while you feel as if you’re regressing.”Although all had the support of family and friends, they found it was a great help to speak to somebody else who was weathering the storm of waiting for a transplant.Over time, they found each other through a Facebook support page, eventually setting up a WhatsApp group called Transplant Girls.Josie said: “We built up such a special bond.”But, due to strict cross infection rules, cystic fibrosis patients are normally told not to meet in person until after their operation.So for years their friendship existed only in the digital world, where they spoke every week.At least 10,400 people in the UK have the disease, which causes the lungs to become clogged with sticky mucus, making it difficult to breathe and leaving sufferers far more vulnerable to life threatening infections.One by one, the group began receiving with Charlotte having the first in October 2011, and Josie the last in July 2016.Those who had operations offered reassurance to those still waiting, and they all checked replica bags wholesale mumbai in with each other regularly determined to keep their spirits up and their bond strong.Then, having all recovered from their transplants and adjusted to their new normal, the group were finally able to meet in person for the first time in July 2018, toasting their health and friendship together over a bottle of fizz in London’s Chinatown.George said: “We chose London as that’s the easiest place for everyone to get to. A couple of us have met one on one over the years but we’ve never all been together as a group before.”It was so amazing to see them all there in person and to laugh, drink and life together.”In September 2014 her lungs began to give up again. Put on the transplant list, she got new lungs 11 months later.Her life changed instantly, as she was able to do all the little things that had once felt impossible, like blowing out birthday candles.. replica handbags online
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