Michael is the chairman of the Tipperary Branch of Cystic Fibrosis Ireland. Michael and his wife Bridie have been involved with the Tipperary branch of CFI for 47 years. Seamus Kelly heaped praise on ...

Despite new medication, cystic fibrosis often leads to permanent lung damage. Working with an international team, researchers from the Technical University of Munich (TUM) have discovered that the ...

The three studies demonstrated statistically significant reversal of liver fibrosis with leronlimab monotherapy (compared to an isotype IgG4 control arm with p-values across all 3 studies < 0.01).

Ireland will need to build 93,000 homes a year meet demand between now and 2031, according to a report by stockbroker Davy. The estimate is significantly higher than housebuilding targets included ...

OpenAI’s big rebranding effort brings a new logo and a new typeface, OpenAI sans. OpenAI’s big rebranding effort brings a new logo and a new typeface, OpenAI sans. Emma Roth is a news writer ...

Tickets available from Hawk’s Well Theatre. SALT FILM PREMIERE Sea Pea Films, in collaboration with Cystic Fibrosis Ireland (CFI) will premiere of the award-winning film Salt at The Model on ...

Sionna Therapeutics is eyeing a $156 million IPO as the cystic-fibrosis-focused biotech looks to take its lead candidate into phase 2. The Waltham, Massachusetts-based company already unveiled ...

Ireland’s Six Nations defence got off to a dream start as the reigning champions came from behind to record a 27-22 win over England in Dublin. Cadan Murley scored the opening try just minutes ...

Ireland coaches Andy Farrell and Simon Easterby alongside captain Caelan Doris and fly-half Sam Prendergast. Next up in our set of previews ahead of the 2025 Six Nations we examine the prospects of ...

for families of people with Cystic Fibrosis. Ireland has the highest rate of CF per capita in the world, with around 1,400 adults and children living with the condition. Julian Benson is one of them.

At least 1,000 Ukrainian men, women and children living in hotels across Ireland have received notifications in recent weeks that they are to be relocated to new accommodation by February.

Louise, and fellow parents in the group, are being supported by Cystic Fibrosis Ireland, and believes the only solution for people with CF like Aaron is for the EMA to reconsider their policies ...