Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 1,200 people in Ireland (70,000 worldwide). There is a high prevalence of CF in Europe, with the highest worldwide prevalence in Ireland, which is three times the average rate in other EU countries and the United States.
TLC4CF(Tipperary, Limerick & Clare for Cystic Fibrosis) is a regional branch of the Cystic Fibrosis Ireland dedicated to improving services and quality of life for people with Cystic Fibrosis living in the Mid-West of Ireland.
TLC4CF was founded by friends and family of People with Cystic Fibrosis (PWCF) in Tipperary, Limerick & Clare. TLC4CF work closely with the CF specialist team at the Mid-Western Regional Hospital Limerick, to give maximum assistance to both parents and children/adults living with Cystic Fibrosis.
We are supported by fundraising and voluntary contributions and are solely concerned with the well-being of people with Cystic Fibrosis
The 65 Roses events in Listowel raised €2,070 for TLC4CF!! Events included a flag day, a Superhero run and Raffle.
Special thanks to organiser Charlene Tydings, a huge team of volunteers and 65 local businesses who donated Raffle and spot prizes. Also thanks to Journalist and Publican Billy Keane for opening the run and for thanking supporters so eloquently. ... See MoreSee Less
The 6.5k Superhero Fun Walk/Jog/Run for CF will be held tomorrow Sunday 23rd April at 1pm in Listowel Town Park. All are welcome and you can register from noon. The event is in aid of TLC4CF to mark 65 Roses week.
Entry for adults is €10, students €5 or for a family of 4 is €20. Under 16's must be accompanied by an adult. Raffle tickets will also be on sale. There are some great spot prizes for the best costumes so come as your favourite superhero, cartoon, movie or disney character! ... See MoreSee Less
TLC4CF was founded by friends and family of People with Cystic Fibrosis in Tipperary, Limerick and Clare. We are a regional branch of the CFAI, dedicated to improving services for people with Cystic Fibrosis