**Follow Charlotte And The Sixty-five Roses on Facebook! @CharlotteCF2016**



On the First of August 2016, at two weeks of age, our daughter Charlotte was diagnosed with Cystic Fibrosis, and so our lives changed forever all over again. 

Cystic Fibrosis is a life long and often limiting disease which affects over 10,800 people in the UK alone. A build up of thick sticky mucous in organs such as the lungs and pancreas, means that Cystic Fibrosis Fighters have to take a lot of medication and undergo hours of physical therapy everyday to keep healthy and live their lives to the max.

The Cystic Fibrosis Trust... The support that they provide is amazing and so important for such an isolating and complex disease. Whether you are the Cystic Fibrosis Fighter, the carers, a sibling, friend or a loved one, there is support or information there for you! The all important raising awareness and campaigning, along with research funding, all of your efforts are really appreciated!

The plan is to keep this page running all of 2017 to try to raise the maximum funds possible. Anyone will be able to participate in some way with the different events and obviously with how this site works, any donations are greatly appreciated, even if you do not wish to partake in events.

Also, if anyone has any fundraising ideas please share!! It would be amazing if we could reach the target and maybe even more!

Thanks for taking the time to visit my JustGiving page.

Donating through JustGiving is simple, fast and totally secure. Your details are safe with JustGiving - they'll never sell them on or send unwanted emails. Once you donate, they'll send your money directly to the charity. So it's the most efficient way to donate - saving time and cutting costs for the charity.