Georges journey living with Cystic fibrosis

Do you want to join me in making a difference? I'm raising money in aid of Cystic Fibrosis Trust and every donation will help. Thank you in advance for your contribution to this cause that means so much to me.

I have set up this page for my son George who was born in June. He was diagnosed with Cystic fibrosis at 19 days old and when Me, my husband and family recieved the news our hearts just sunk. Cystic fibrosis is a life limiting condition, most people only live till their 30s to 40s with it, It affects several parts of the body the main ones being the lungs and the digestive system, unfortunately there is no cure but im hoping one day they will be. I have set up this page to try and help raise awareness about the condition I dont feel there is enough information out there about it. I have also set up the page to try and raise money for George's condition and eventually I will be doing events to raise money.