Very, very sadly Becky passed away on March 12th. Our beautiful daughter couldn't fight anymore. She tried so hard but became too weak and her kidneys gave up in the end.
There is a big hole in our lives which Becky filled with fun and laughter.
She was an inspiration to us and to many others. We have found out that she helped a lot of other CFers, giving advice to them and keeping their spirits up.
She was a wonderful daughter, grand daughter, sister, aunty and friend.
wished we had a celebration of her life here in Spain and her UK family held one over there for her too. Lots of friends came to pay their respects and to see photos and videos of Becky.
We are going to keep raising funds and awareness of Cystic Fibrosis
in Becky's name. Our son has designed a logo for us. We are hoping to start an association and the money raised will be sent to where we think it will be of the most use.
Breathe easy Angel. xxx