Colin Farrell’s Dublin marathon bid raises thousands for friend with rare skin disorder

Emma Fogarty endures a constant battle against the most severe form of a rare, genetic disease

David Young
Monday 21 October 2024 11:01 BST
Actor Colin Farrell has thanked the public for backing his marathon run for his friend, Emma Fogarty, who has epidermolysis bullosa, after a joint TV appearance boosted donations (Andres Poveda/RTE/PA)
Actor Colin Farrell has thanked the public for backing his marathon run for his friend, Emma Fogarty, who has epidermolysis bullosa, after a joint TV appearance boosted donations (Andres Poveda/RTE/PA)

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Colin Farrell has thanked the public for backing his charity marathon run for a friend with an agonising skin condition after a joint TV appearance prompted more than 400,000 euros in donations.

The Hollywood A-lister and Emma Fogarty, who is Ireland’s longest-surviving person battling the genetic condition epidermolysis bullosa (EB), starred on RTE’s flagship Late, Late Show on Friday night.

The Penguin star is running next Sunday’s Irish Life Dublin Marathon to mark Ms Fogarty’s recent 40th birthday – a milestone she thought she might never see.

Colin Farrell and his friend Emma Fogarty at the Irish premiere of The Banshees of Inisherin (Mediaconsult/PA)
Colin Farrell and his friend Emma Fogarty at the Irish premiere of The Banshees of Inisherin (Mediaconsult/PA) (PA Media)

She will join him in a wheelchair for the final 4km of the course – with each kilometre representing a decade of her life.

Ms Fogarty, from Co Laois, endures a constant battle against the most severe form of the rare, genetic disease (recessive dystrophic EB), with sufferers currently given a life expectancy of around 30-35 years.

Born with no skin on her left foot and right arm, she experiences excruciating blisters on her skin from the slightest touch – the condition is also known as Butterfly Skin.

Her and Farrell’s “Run to 40” challenge has now raised more than 500,000 euro, with Friday’s appearance on the Late, Late Show alone pulling in 415,000 euro.

The funds will support the charity Debra, which helps 300 people in Ireland living with epidermolysis bullosa.

Dubliner Farrell hailed Ms Fogarty as a “legend”.

“There are four forms of the condition and Emma has the severest one,” he said backstage on Friday.

“She is the third person in Ireland with her type of EB to reach the age of 40 – she’s a miracle really, and a legend.”

Emma Fogarty celebrated her 40th birthday in June
Emma Fogarty celebrated her 40th birthday in June (PA Media)

Speaking to host Patrick Kielty during the show, Ms Fogarty highlighted the challenge the 4km distance will pose to her.

“Four kilometres sounds very little to a lot of people – there’s people here who probably run 10km every day or 5km or whatever,” she said.

“For me, that’s going to be a very long journey because potholes, ramps, even a pebble on the road – I will feel every one.”

Debra chief executive Jimmy Fearon said he is in a “state of shock and absolute excitement” at the public’s response to Friday’s show.

“I can’t believe that this has been achieved,” he said.

“Emma and Colin were outstanding and we are overjoyed with the funds raised – the good things we can do for families with EB is what this is all about.”

To support the fundraising initiative click here or call (00353) 01 902 3938.

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