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WE DONE IT GUYS!!!!!! From the bottom of my heart I can not thank you all enough for all your support and donations towards Jayden's vest!!!! I have changed the limit of our goal because seeing how quick we raised that money for my son I want to help other CF children and adults too!!! As use know the government do not fund CF so we can't find a cure and they don't provide medical equipment.
LETS KEEP THIS SITE GOING!!!!!
every little helps xx
Jayden-James is 7 months old, he got diagnosed with cystic fibrosis at the age of 3 weeks. Cystic fibrosis is a genetic disease that primarily affects the lungs and digestive system. A defective gene leads to the creation of mucus, which is thicker and more sticky than usual. This mucus is difficult to cough out of the lungs due to these properties, and can hamper breathing and lead to severe lung infections. In the pancreas, the mucus interferes with digestion and prevents enzymes from breaking down food properly. This can lead to malnutrition. Cystic fibrosis is a serious condition. The symptoms that it causes are life threatening. The most common cause of death in people with CF is respiratory failure. jayden-James has been hospitalised for 5 months of the 7 months he's been born, he's fought and fought for his life and is such a strong little boy! hes on a LOT of medication throughout the day and also needs nebulisers plus physio therapy more than four times a day, this is no life a child or anyone should be living! ive made this page to kindly ask everyone if they could donate some money towards buying Jayden an airway clearance vest which is a replacement for me doing his physio manually! It would give him the independence and help him a lot with his breathing, it clears his chest and he can play with his toys whilst getting treatment. Jayden is not coping well with CF so we're trying to do everything we possibly can to make his life the happiest and healthiest we can! This is why we need you to donate and help up raise money for this physio vest! The NHS and government do not fund CF so we can't find a cure and can't get issues a vest.
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