We hope that this website will provide you with an chance to see how a family live with an illness. Become a fan on Facebook-just search "www.hannahsbags.com." Look forward to talking to you!

We will try and keep it as up to date as possible! Hannah & her family would like to wish all the best to all PWCF & their families everywhere. All of the info in this website is entirely SUBJECTIVE and is in no way representative of the opinions or thoughts of any medical professional, medical establishment, charity (branches & sub-charities) and finally the People with Cystic Fibrosis and their families.