Primary Ciliary Dyskinesia (PCD) Support UK

Katie's page

Katie Horton

Katie Horton

My Story

Have you ever had a chest infection? Imagine getting multiple chest infections every single year. What about needing to stay in hospital for weeks a time, multiple times a year? This is the reality for many living with Primary Ciliary Dyskinesia (PCD).

Despite the impact of this condition, there is no cure for PCD.

This is why we need your help. I am fundraising for PCD Support UK, the UK’s only charity dedicated to supporting those affected by PCD and championing research into this rare disease for over 30 years.

I’ll be riding 100 miles across London and the Essex countryside. It's been a while since I last rode my bike, so this will be a big challenge for me! 

Thank you for your support and generosity :) 

Find out more about PCD Support UK on their website https://pcdsupport.org.uk/

44%

Funded

  • Target
    £500
  • Raised so far
    £220
  • Number of donors
    10

My Story

Have you ever had a chest infection? Imagine getting multiple chest infections every single year. What about needing to stay in hospital for weeks a time, multiple times a year? This is the reality for many living with Primary Ciliary Dyskinesia (PCD).

Despite the impact of this condition, there is no cure for PCD.

This is why we need your help. I am fundraising for PCD Support UK, the UK’s only charity dedicated to supporting those affected by PCD and championing research into this rare disease for over 30 years.

I’ll be riding 100 miles across London and the Essex countryside. It's been a while since I last rode my bike, so this will be a big challenge for me! 

Thank you for your support and generosity :) 

Find out more about PCD Support UK on their website https://pcdsupport.org.uk/