Cystic Fibrosis
Donation protected
**new update**
Raising money for not only my family member but all children and adults who suffer with this silent condition. CYSTIC FIBROSIS
Louie is only 4 months old and was diagnosed with cystic fibrosis by his 3rd week of life. Already being medicated up to 27 times a day. He also undergoes physio therapy twice a day where a pep mask is used to help expand his airways. Treatment is very expensive and as currently no cure exists I want to help raise awareness and funds to better support cystic fibrosis sufferers to BREATH with ease.
22.02.18 Louie is currently in hospital his return date home is currently unknown. Tiny warrior keep fighting. He’s still smiling, which is testament to how amazing his family are how amazing modern day medicine can be. Please support in anyway you can. Share, donate or talk about cystic fibrosis
#cysticfibrosis #louie
Please view our mini blog at http://docherty.co.uk
Raising money for not only my family member but all children and adults who suffer with this silent condition. CYSTIC FIBROSIS
Louie is only 4 months old and was diagnosed with cystic fibrosis by his 3rd week of life. Already being medicated up to 27 times a day. He also undergoes physio therapy twice a day where a pep mask is used to help expand his airways. Treatment is very expensive and as currently no cure exists I want to help raise awareness and funds to better support cystic fibrosis sufferers to BREATH with ease.
22.02.18 Louie is currently in hospital his return date home is currently unknown. Tiny warrior keep fighting. He’s still smiling, which is testament to how amazing his family are how amazing modern day medicine can be. Please support in anyway you can. Share, donate or talk about cystic fibrosis
#cysticfibrosis #louie
Please view our mini blog at http://docherty.co.uk
Organizer
Terri Owen
Organizer