We use your sign-up to provide content in ways you’ve consented to and to improve our understanding of you. This may include adverts from us and 3rd parties based on our understanding. You can unsubscribe at any time. More info

Caitlin Rich, 25, is working with the Cystic Fibrosis Trust after noting that life in lockdown was similar to the precautions she has to take in her everyday life.

Caitlyn, of Hadfield, Derbyshire, said: “The idea came from a conversation with my nurse who called me before a hospital visit to check I didn’t have Covid-19.

“After the first question of ‘do you have a persistent cough?’ there was a pause. I’ve known this nurse for nearly a decade and have had a cough the whole time due to my cystic fibrosis.

“I said, ‘Of course! What do you think I’m coming in for?’

“We laughed, but unfortunately most people don’t find my cough as amusing.

“I quickly realised that we could draw on many more parallels between living in the pandemic and living with cystic fibrosis – social distancing from others with the condition, fear of catching a dangerous infection, restrictions on socialising and travelling.

“It has always been difficult to get people to understand what it is like to live with cystic fibrosis but this campaign might help by relating it to our universal experience of the pandemic.”

What is happening where you live? Find out by adding your postcode or visit InYourArea

The campaign – CF Truths – includes the slogan, “We were coughing before it went viral”.

An accompanying poll of more than 2,000 adults found that 86 percent did not know those with cystic fibrosis cannot meet each other in case they pass on deadly infections. Sufferers must also stay away from family and friends who are ill.

Cystic fibrosis is an incurable and life-limiting genetic condition that affects almost 11,000 people in the UK. It causes a build-up of thick, sticky mucus in the lungs, digestive system and other organs. The typical age of death is just 36.

David Ramsden, chief executive of the Cystic Fibrosis Trust, said: “We want to remind people that those with cystic fibrosis will still, every day, weigh up the risks of catching infections that could damage their lungs and lead to lengthy hospital stays.”

Source: Read Full Article