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Dad joins run in aid of cystic fibrosis kids



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Published Date: 08 September 2008
Mike Jarrett knows just what it's like to face the possibility of losing a child to a life-threatening disease.
When Mr Jarrett's daughter was misdiagnosed with cystic fibrosis last year it struck fear in the family's hearts. So now the local dad is preparing for the challenge of the Great South Run to raise money for cystic fibrosis sufferers across the country.

Mr Jarrett, from Bishop's Waltham, will take part in the 10-mile race to raise vital funds for the Cystic Fibrosis Trust.

Mike, who is preparing for the run, said: 'My three-year-old daughter Isabel was diagnosed on her second birthday, last year.

'Thankfully, the diagnosis was made in error, but for 48 hours my wife and I had an all too real experience of what life is like for a child with cystic fibrosis.

'It was certainly a birthday we'll never forget and our brief insight into living with and fighting against cystic fibrosis has inspired me to try and do all that I can to help the trust.'

Cystic Fibrosis is the UK's most common, life-threatening inherited disease and claims three young lives a week in the UK.

Average life expectancy is just 31, although improvements in treatments mean a baby born today is expected to live longer.

Sponsorship money will help provide support, advice and appropriate clinical care to the 8,000 babies, children and adults with cystic fibrosis in the UK.

The Bupa Great South Run will be held in Portsmouth on Sunday, October 26.

To get involved contact the Cystic Fibrosis Trust events team on 0845 8591100. You can also sponsor Mike Jarrett at www.justgiving.com/mikejarrett_GreatSouthRun.

The full article contains 289 words and appears in The News newspaper.
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  • Last Updated: 08 September 2008 9:11 AM
  • Source: The News
  • Location: Portsmouth
 
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Tina Holm,

East Jordan, Michigan USA 08/09/2008 19:56:22
Thank you so much to david and his family for what he is doing for Cystic Fibrosis. I am a mother of 8 and 4 of our children have been diagnosed with Cystic Fibrosis. We are on the same page when it comes to raising money for the Cystic Fibrosis Foundation. These are my children and I want them to live long happy lives.

Thanks again,
Tina Holm
Please watch our video at
www.holmfamily1992.blogspot.com
www.cff.org/Great_Strides/TinaHolm5560
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