Cystic Fibrosis Trust

Fran’s London Marathon Fundraiser

Francesca Falzon

Francesca Falzon

My Story

hey! My name is Fran, I'm a 24 year old Maltese CF sufferer who is attempting my first marathon! This charity is extremely close to my heart as without them and their research, I definitely would not be here today or at least as well and healthy as I am 🫶🏼💛

I would like to fundraise £5,000 for the CF Trust before the 26th April (big marathon day)! Would be so lovely to actually reach this goal AND finish the marathon in one piece 😅

Thank you for supporting 🙏☺️

Cystic fibrosis (CF) is a genetic condition which causes sticky mucus to build up in the lungs and digestive system. It affects more than 10,800 people in the UK. One in 25 of us carries the faulty gene that causes it, usually without knowing.

Cystic Fibrosis Trust is the charity uniting people to stop cystic fibrosis (CF). They fund vital research, improve care, speak out and race towards effective treatments for all. They won't stop until everyone with cystic fibrosis can live without limits.

 

Cystic Fibrosis Trust

Raising for:

Cystic Fibrosis Trust
156%

Funded

  • Target
    £5,000
  • Raised so far
    £7,791
  • Number of donors
    108

My Story

hey! My name is Fran, I'm a 24 year old Maltese CF sufferer who is attempting my first marathon! This charity is extremely close to my heart as without them and their research, I definitely would not be here today or at least as well and healthy as I am 🫶🏼💛

I would like to fundraise £5,000 for the CF Trust before the 26th April (big marathon day)! Would be so lovely to actually reach this goal AND finish the marathon in one piece 😅

Thank you for supporting 🙏☺️

Cystic fibrosis (CF) is a genetic condition which causes sticky mucus to build up in the lungs and digestive system. It affects more than 10,800 people in the UK. One in 25 of us carries the faulty gene that causes it, usually without knowing.

Cystic Fibrosis Trust is the charity uniting people to stop cystic fibrosis (CF). They fund vital research, improve care, speak out and race towards effective treatments for all. They won't stop until everyone with cystic fibrosis can live without limits.