Tough Mudder for Cystic Fibrosis

Hi everyone, its Mia, and at the end of November 2018  I was diagnosed with cystic fibrosis. To help raise some money for the Cystic Fibrosis Trust, my brother Alexander organised for him and a group of friends and family to take part in a 10 mile'Tough Mudder' in May 2019.  For those who don't know, CF is a genetic disease that affects more than 70,000 people worldwide and if you want to find out more you can visit the CF Trust's web page which I'll link below. Finding out that I have CF has altered my life massively, but thanks to the pioneering research of charities such as the Cystic Fibrosis Trust, I am able to live what you would call a normal life. With this said, there is still work to be done against CF, and so any donation you could make would mean the world. Thank you in advance to all who are taking part in the Tough Mudder and to anyone who makes a donation.  

More information about Cystic Fibrosis Trust: The Cystic Fibrosis Trust is the only UK-wide charity dedicated to fighting for a life unlimited by cystic fibrosis (CF) for everyone affected by the condition. Since we started in 1964 we have dedicated ourselves to promoting excellence in research and clinical care, as well as providing practical support and advice to people with CF and their families. Our mission is to create a world where being born with CF no longer means a life-long struggle.

https://www.cysticfibrosis.org.uk