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Issue:- Saturday, 22 August 2015

Merseyside man takes on 15 challenges to beat Cystic Fibrosis

SEAN Chappell, 25, a Team Leader at the University of Liverpool from Neston, Merseyside is taking on 15 challenges this year to raise money for the Cystic Fibrosis Trust as he was diagnosed with cystic fibrosis at 6 months old.  Most people don't understand what cystic fibrosis is, or what it does, until someone close to them is affected by it. They soon discover it's a life shortening genetic condition; only ½ live to celebrate their 40th birthday. It causes the internal organs, especially the lungs and digestive system, to become clogged with thick sticky mucus, resulting in chronic infections and inflammation of the lungs.  Sean tries not to let his condition affect him too much, he says:- “I've had ups and downs, but I try not to let my cystic fibrosis affect me that much and if it does, try to make it positive. I use keeping well as a motivation for spending my time with people I love and doing things I love to. The good thing is I've always had an amazing group of people around me and not just family and friends. The team of doctors and nurses who looked after me at Arrowe Park Hospital, when I was younger and at Broadgreen Hospital since I turned 18 have been amazing.”

Sean set himself these 15 challenges because a lot of people have raised money in his name and he has always wanted to give something back. He explains:- “Inspired by people who take on mammoth tasks, I wanted to do something that would really get people's attention, not for my own ego, but for other people or families affected by CF. The challenges have been quite a lot tougher than I had imagined, but we did do a 100 mile bike ride 3 weeks after running a marathon!  Eating enough has been tough as well. Having cystic fibrosis means I need more than the normal amount of calories in a day anyway, but when it comes to exercising and burning more calories, there isn't enough time in the day to eat enough. My family think I'm mad. I've caused untold worry and stress by doing all of this and I think they'll be glad when it's over. In all seriousness though, they have been as supportive as they always have. Everyone's thrown themselves into it and they're all getting involved in as many challenges as they can do as well which is great. It really does seem to be promoting a positive attitude towards life with cystic fibrosis.”

Cystic Fibrosis Trust Community Development and Fundraising Manger, Serena Wilson, says:- “The task that Sean has set himself to complete 15 challenges demonstrates his amazing motivation and determination and he should be very proud of his achievements so far. We are very grateful for all the work he is putting in to train for and complete these challenges for us.  Money raised will enable the Cystic Fibrosis Trust to invest in cutting edge research to develop transformational treatments and life changing therapies. It will also provide support to those with cystic fibrosis and their families and help the Trust to drive up standards in medical care.”

Anyone wanting to sponsor Sean may do so online. Sean's challenges can be followed through his Facebook Page.

Get involved in Wear Yellow Day, a part of CysticFibrosis.Org.UK who are a registered as a charity in England and Wales (1079049) and in Scotland (SC040196). A company limited by guarantee, registered in England and Wales number 3880213.

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Deceased estates notice - Lilian May Jackam

Pursuant to the Trustee Act 1925, any persons having a claim against or an interest in the Estate of Lilian May Jackam (also known as Lillian May) Jackam (Deceased), late of Birch Abbey Rest Home, 55 Alexandra Road, Southport, Merseyside, PR9 9HD, UK, who died on 04/10/2018, are required to send particulars thereof in writing, to the undersigned Solicitors, on or before 24/05/2019, after which date the Estate will be distributed having regard only to claims and interests of which they have had notice. Churches Solicitors, 12 High Street, Fareham, Hampshire, PO16 7BL, UK. Ref:- 'T553015.'

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