Tim Wotton
Tim Wotton, a Cystic Fibrosis sufferer, has been defying the odds for over 40 years and is sharing his life lessons and experiences. After counting down to the massive 40 milestone in 2011, he is now regularly sharing his trials and tribulations via this blog and his forthcoming book…
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- See which 'c word' offers the most hope for cystic fibrosis sufferers - timwotton.wordpress.com/2013/04/26/dar… 3 weeks ago
- See which 'c' word is so important for cystic fibrosis sufferers - timwotton.wordpress.com/2013/04/26/dar… 3 weeks ago
- How long are you prepared to wait for the most important thing in your life? Find out the answer in my CF blog - timwotton.wordpress.com/2013/04/26/dar… 3 weeks ago
- It's tough to exercise with cystic fibrosis... find out more in my latest survival blog 'Catching the bug' - timwotton.wordpress.com/2013/03/07/cat… 2 months ago
- I've been catching the right kind of bug recently... find out more in my latest CF survival blog 'Catching the bug' - timwotton.wordpress.com/2013/03/07/cat… 2 months ago
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Tag Archives: Tim Wotton
Dare to hope
Hope of a cure is crucial for anyone suffering with a life-threatening illness like cystic fibrosis (CF)*. My hopes have been raised and dashed in equal measure over the years. But is the outlook at last changing? Having just turned … Continue reading
Catching the bug
People with the life-threatening illness cystic fibrosis (CF)* are used to catching infections but the bug I’ve recently caught is proving to be more of a help than a hindrance… I’ve not been particularly happy with the state of my … Continue reading
Goodbye to all that
A candle was blown out at Christmas, when the life of a fellow cystic fibrosis (CF)* adult was cut horribly short. For me, this has always been the hardest part… He left a lasting impression on anyone that had the … Continue reading
Posted in Postcards from Earth
Tagged beating the odds, CF, Cystic Fibrosis, death and CF, death and cystic fibrosis, enduring, Goodbye to all that, hockey, inspire, leave a CF legacy, paul harvey, Postcards, Postcards from Earth, relentless, survival, The hardest part, Tim Wotton, Wotton
16 Comments
Introspective
The recent death of my father has given me fresh perspective on how I can and will keep battling the life-threatening illness, cystic fibrosis (CF).* People have kindly told me that my struggle with CF has given them perspective on … Continue reading
Cross to bear
Hide and not seek. This is the latest challenge for people with the life-threatening illness Cystic Fibrosis (CF)*… Under current medical guidelines CF patients have been advised to no longer spend time with each other. It’s all down to the … Continue reading
Race for life
The true Olympic ethos has it that ‘it’s not the winning but the taking part that counts.’ This is also true of my family and friends who have stepped up to fundraise for my illness, cystic fibrosis (CF)*. Perhaps prompted … Continue reading
Posted in Postcards from Earth
Tagged beating the odds, CF, CF and exercise, CF and Sport, CF fundraising, chariots of fire, Cystic Fibrosis, enduring, Eric Liddell, hockey, inspire, Isaiah chapter 40, Olympics and CF, positive thinking, Postcards, Postcards from Earth, pushing on, race for life, sporting life, survival, the show must go on, Tim Wotton, Wotton
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Into the blue
Leaving the grey of England for a recent family holiday to sunnier climes allowed me to take a break from my cystic fibrosis (CF)* and diabetes… or did it? In late June we went on holiday to Turkey. We had … Continue reading
Not alone
It’s not just the sufferer who’s affected by the diagnosis of a life-threatening illness, like cystic fibrosis (CF)*. Close family and friends have a crucial role to play as well… During the recent Jubilee holiday in the UK, I met … Continue reading
Breaking the mould
I’ve been celebrating this last week since my gorgeous son Felix turned five. Every parent takes delight in the milestones of their children, but there’s extra poignancy for me… Born in 1971 and diagnosed six months later with the chronic … Continue reading
Business as usual
For anyone suffering the daily grind of a life-threatening illness such as cystic fibrosis (CF)*, there’s no such thing as a normal working day. This is magnified when going away on business… As an internal communications consultant, every day while … Continue reading
