Now, her determined parents, Tom Bliss and Faye Edginton, are

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cheap nfl jerseys Mother’s heartbreak as baby diagnosed with devastating condition at just nine days oldReeva Grace was just nine days old when she was diagnosed with Cystic Fibrosis following a routine heel prick test14:29, 13 JUN 2017Reeva Grace with her dad, Tom Bliss, mum Faye Edginton and sister Milla Rose cheap jerseys (Photo: Gloucester Live WS) Get daily updates directly to your inbox+ SubscribeThank you for subscribing!Could not subscribe, try again laterInvalid EmailLittle Reeva Grace Bliss is a smiling and happy baby.But behind her giggles, the youngster hides a devastating condition.Reeva Grace was just nine days old when she was diagnosed with Cystic Fibrosis following a routine heel prick test.Now, her determined parents, Tom Bliss and Faye Edginton, are hunting for ways their little girl can have as normal a life as possible.People with cystic fibrosis experience a build up of thick sticky mucus in the lungs, digestive system and other organs, causing a wide range https://www.gradeajerseys.net cheap nfl jerseys of challenging symptoms affecting the entire body.Desperately ill girl, 11, told she could die months ago has life cheap nfl jerseys cheap nfl jerseys saving surgery after last minute wholesale nfl jerseys donor was found(Photo: Gloucester Live WS)Mum Faye said: “She was nine days old when they said she had abnormalities in her blood, so she went to Bristol hospital the next day.”As a mother, I kind of knew because when she was first born, they thought she might have Down syndrome. But when they said she had CF, it was shock to find out.”At the moment, little Reeva Grace who lives in Cheltenham with her parents and sister Milla Rose has a hospital visit to Gloucestershire Royal every eight weeks.She also sees a health visitor and has physiotherapy appointments every few weeks, as well https://www.gradeajerseys.net/ as seeing a dietition, reports Gloucestershire Live.(Photo: Gloucester Live WS)Reeva Grace also has help from a Cystic Fibrosis specialist team, and her mum said that the support and care has been fantastic.One in 25 people carry the faulty gene that causes the condition, usually without even knowing.Mum Faye wants people to realise that it’s not just adults suffering from the condition. She said: “It’s something you’re born with, and the sooner it’s caught and people know about it, the better.”On a day to day basis, Reeva has antibiotics and vitamins, alongside two sessions of physiotherapy with her parents.. cheap nfl jerseys

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