Cystic Fibrosis Ireland

CFI is a voluntary organisation that was set up by parents in 1963 to improve the treatment and facilities for people with Cystic Fibrosis.

Health - Ireland
  • Transparency

2.8 / 10

2024 PLAN

€6,060

raised of €10,000 goal

2

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Projects

  1. CFI working with our branches and the generous support from the general public has provided €7.5m to improve CF centres throughout Ireland in 2014 and 2015>

    No result yet

  2. CFI continue to play and important role in ensuring access to new and innovative treatments for CF. Kalydeco (the first drug that treated the underlying cause of CF) was made available in 2013, suitable for around 11% of the CF population in Ireland. CFI are currently seeking additional access to this drug for 2-5 years and access to Orkambi, another new drug treating the underlying cause of CF, which could benefit another 50% of the CF population in Ireland.

    No result yet

  3. CFI are seeking the continued improvement in the rate of double lung transplants. The rate of transplants increased from 4 in 2012 to 19 in 2014 in Ireland. CFI is also supporting the Mater Hospital in terms of the resources required for Post -Transplant care

    No result yet

2024 PLAN

€6,060

raised of €10,000 goal

2

altruist

Create fundraising page

Donations made here are eligible for a charity to reclaim in tax paid in Ireland