Last Friday saw Churchill College, University of Cambridge, host the Moving Mountains conference on how sport and exercise can benefit those with long-term health conditions, such as cystic fibrosis.
Our own, Paul Rymer, Head of Principal Involvement attended from the Trust and has given us a flavour of the informative, interesting and exciting events there
In the next year fitness and sport will be an increasing focus for the Trust. Last week I attended a conference highlighting the benefits of exercise, including better mental health, less reliance on drugs, and increased feelings of confidence and social inclusion.
Our own, Paul Rymer, Head of Principal Involvement attended from the Trust and has given us a flavour of the informative, interesting and exciting events there
In the next year fitness and sport will be an increasing focus for the Trust. Last week I attended a conference highlighting the benefits of exercise, including better mental health, less reliance on drugs, and increased feelings of confidence and social inclusion.
The event was organised by Dr Jonathan King, who has CF, in
partnership with others living with chronic conditions.
Jonathan used a slide presentation and props (bottles of
water) to engagingly describe lung function, his treatment regime, what
happened when things went badly wrong during a holiday, and then the months of
recovery. With persistence, and support from his care team, Jonathan managed to
avoid a lung transplant by gradually improving his lung function though
exercise. At first he could barely move, but over a period of months he
gradually increased his physical activity, from walking a few steps, to trying
a treadmill, to jogging and then to running 4K. Jonathan now uses regular exercise
to maintain his health. His next endeavour is to cycle 1,200 miles from London
to Barcelona in support of the
Cystic Fibrosis Trust.
Nick Talbot gave an extremely funny account first of his
experience as a young man with CF, including dating, relationships and work. He
then shared his experiences climbing mountains in the Himalayas, and the
challenges of doing that with cystic fibrosis. Where Jonathan’s story was one
of survival against the odds, Nick’s was an example of someone not accepting
the perceived limitations of cystic fibrosis. Nick is aiming to climb
Everest in support of the Trust in April–May.
Charlotte Wells, a specialist respiratory physiotherapist,
talked engagingly about her experience working with CF patients, and the
benefits of exercise from a clinical perspective.
Because of the risk of cross-infection, Jonathan spoke
before a break time, and stayed in one area of the large venue, while Nick
arrived later on, and aside from when he was speaking, remained at the back of
the audience. At one point they were both in the venue, but at the widest
possible distance (and it was a very large theatre). They then spoke through
microphones asking each other questions. This really brought home one of the
saddest aspects of living with cystic fibrosis – people unable to meet in
person and share ideas, jokes and experiences.
Following the conference there was a drinks reception with
special guest of honour Professor Stephen Hawking, who kindly posed with Nick
and a Trust banner. In a short speech, Professor Hawking said: “You have to
live life to the full. I am very aware of the preciousness of time, act now
however difficult life may be there is always something you can do, be brave
overcome the odds, it can be done.”.
Learn more about the
Moving Mountains conference.
If you have an interest in exercise, fitness or sport and
would like to join me in exploring how the Trust can do more in this area,
please email me at paul.rymer@cysticfibrosis.org.uk.
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