Stay up to date with notifications from The Independent

Notifications can be managed in browser preferences.

The guinea pig who hopes for reprieve from constant infection: Children would benefit most from genetic engineering technique that could be used to treat Britain's most common inherited disease

Tom Wilkie,Ann Barrett
Wednesday 25 August 1993 18:02 EDT
Comments

Your support helps us to tell the story

From reproductive rights to climate change to Big Tech, The Independent is on the ground when the story is developing. Whether it's investigating the financials of Elon Musk's pro-Trump PAC or producing our latest documentary, 'The A Word', which shines a light on the American women fighting for reproductive rights, we know how important it is to parse out the facts from the messaging.

At such a critical moment in US history, we need reporters on the ground. Your donation allows us to keep sending journalists to speak to both sides of the story.

The Independent is trusted by Americans across the entire political spectrum. And unlike many other quality news outlets, we choose not to lock Americans out of our reporting and analysis with paywalls. We believe quality journalism should be available to everyone, paid for by those who can afford it.

Your support makes all the difference.

PALE and slight, Darren Keen sat quietly beside the doctors and scientists, more troubled by the sight of the British media pack than by the prospect that he may be the first Briton to undergo gene therapy for cystic fibrosis, writes Ann Barrett.

In a quiet, husky voice (he has yet another painful lung infection), he made light of the physiotherapy he has to undergo to clear his lungs of mucus. 'My girlfriend beats me up twice a day and makes sure I take my tablets,' he said.

He has known Dawn Wooton for 14 months and she hopes to be a nurse if her exam results this week are good enough. She visits him daily to help, and has applied for an invalidity attendance allowance so that she can continue.

Now 23, Mr Keen lives in a flat on his own in Hemel Hempstead and has been unable to work for two years because of his illness. Since he was two, his life has been dominated by cystic fibrosis. He has to take 70 tablets a day to stop him getting chest infections, to improve his breathing, and to help him digest food. This is supplemented by nebulisers and surfactant, a lubricant for the surface of the lungs.

After many years of fighting lung infections, his breathing was laboured as he talked. Mr Keen has a tube into a vein in his arm for the high doses of antibiotics he needs.

When doctors at the National Heart and Lung Hospital in Kensington told him about five months ago about the possibility of the treatment, his reaction was: 'I'll be cured.' However, he said that now that he understood the therapy better, he did not expect a cure. 'But it might stop me getting an infection. I'm pleased to be able to help.'

The hospital has the largest clinic for treating cystic fibrosis in Europe. But neither doctors nor the nine volunteers will know until November, at the earliest, whether the technique has worked.

(Photograph omitted)

Join our commenting forum

Join thought-provoking conversations, follow other Independent readers and see their replies

Comments

Thank you for registering

Please refresh the page or navigate to another page on the site to be automatically logged inPlease refresh your browser to be logged in