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simply cut out the diseased part, so we were told the only way they could get rid of the cancer was by removing her windpipe, oesophagus and voice box – she’d never be able to speak again. For a girl who’d just turned 19, it was horrendous to hear those words. Kez didn’t want to lose her voice but if she didn’t have something done she would die. I didn’t even want to contemplate life without her, so desperate for advice I phoned Kez’s uncle, who lives in Italy and is a medical research translator. Incredibly, he’d heard about a surgeon who’d been researching windpipe transplants but hadn’t yet performed one. Looking at all Kez’s medical notes, the surgeon agreed to do the operation. Although scared, Kez couldn’t face losing her voice, so


after a lot of thought she decided to have the pioneering operation in the hope she’d be able to retain her voice. Eleven of us, including her older brother Chris and her boyfriend Joe, travelled to Italy in July last year when Kez had the transplant. When her diseased windpipe was removed, the tumour was about 6cm in length – far bigger than they had anticipated. It turned out the surgeon was able to remove all the cancer. We were delighted. It was an outcome we never expected! Since the operation, Kez has been in and out of hospital to repair a small hole that developed between her oesophagus and windpipe. Thankfully, because of Paul’s House, I’ve been able to stay by her side every time she’s had to go in. We are given our own room with a direct phone link to the ward, and the staff at the house are wonderful. The emotional support and advice they provide is invaluable. When your child’s in hospital it’s such an awful time, so not having to worry about travelling there at all hours or how much it will cost is a godsend. On her good days, Kez has even been able to walk over to the house and sit with me, which helps give her a change of scenery too. Kez is still recovering now and, amazingly, she got her


voice back this August. She’s is so incredibly resilient and focused on going back to hairdressing and leading a normal life again when she’s well enough. Of course I will always worry about what the future holds for Kez, especially as her type of cancer is one that tends to come back. Though she has the best prognosis because they removed it all, I know if she’s ever in hospital again I’ll be by her side, thanks to Paul’s House.


Clic Sargent formed in 2005 when charities Cancer and Leukaemia in Childhood (CLIC) and Sargent Cancer Care for Children merged. Around 5,500 children and their families are supported by Clic Sargent every year. It costs around £3,750 to support each young person. Specialist nurses care for children


CLIC SARGENT THE FACTS


with cancer at home and in hospital. The charity funds play specialists who help children to understand what will happen to them. A Home from Home service means families can stay nearby while their child is in hospital. They also provide free supported holidays for the family across the UK.


PROJECT UPDATE


The £13,524 raised in The Candis Big Give will pay for eight families to stay at Paul’s House throughout 2011, while their child is treated at University College Hospital or Great Ormond Street Hospital in London. Paul’s House provides free accommodation to reduce the strain cancer treatment can have on families. Opened in September 2010, it’s expected that 160 families will use it every year.


WWW.CANDIS.CO.UK | OCTOBER 2011 119


As told to Amy Salter Photo Teena Taylor


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