When Eden was 7 weeks old she was diagnosed with Cystic Fibrosis. She wasn't gaining weight or growing as expected and her routine heel prick test had showed irregularities. From that day on our lives changed... Cystic Fibrosis is a life limiting genetic condition that affects both the lungs & digestive system. There is currently no cure! Fast forward 7 years and Eden is a gorgeous, clever, funny & talented little lady who takes all the medication, hospital appointments and daily phsiotherapy in her stride. She is now aware that, although she keeps very good health, many children with CF are not so lucky requiring long stays in hospital and much more rigorous treatments than she does. When the Leanne Fund helped Eden get some indoor physio equipment earlier this year she immediately said she wanted to do something to say thank you and to help others with this cruel condition! So here we are - she set herself the challenging target of raising £1000 by climbing Bennachie - we're now 6 sleeps away from our climb and almost at 200% of the target! Thank you all 😘

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