Cystic Fibrosis

£229 of £2,500 goal

Raised by 18 people in 1 month
**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
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Sadly Louie is currently in hospital: How long he will stay in is not currently known. Breathing tends to comes so naturally to most of us but for those who are diagnosed with CF, well they rarely get the chance to feel that. Help donate and fund research, equipment, medicine plus so much more. If you can’t donate then knowing about CF is just as good. Share my post and lets make some noise and raise some money.

Thank you
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Thank you so much to everyone who has donated so far. Please share share share and help us raise awareness of cystic fibrosis and also raise money for the research of a cure.
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£229 of £2,500 goal

Raised by 18 people in 1 month
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Debra Newton
3 hours ago
Peter Cox
15 days ago
Ludek Smilek
23 days ago
Will Hodgson
27 days ago
Lee Harris
1 month ago
David Gardner
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Will Anderson
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