Some how I seem to have convinced to do a sky dive in May for the Cystic Fibrosis trust.  The jump is quite costly, so we need to raise as much money as possible.

As terrfying as it may be, what I face throwing myself out of an aircraft is nothing compared with what hundred of brave young souls face with CF every day, so please consider them and dig deep.

 

Cystic Fibrosis (CF) is the UK’s most common life-threatening inherited disease

Cystic Fibrosis affects the internal organs, especially the lungs and digestive system, by clogging them with thick, sticky mucus. This makes it hard to breathe and digest food.

Average life expectancy is around 31 years and, although improvements in treatments mean a baby born today could expect to live longer, there is no cure for CF and lung transplantation is often the only option. Most individuals with cystic fibrosis die young, many in their 20s and 30s from lung failure.

Each week, 3 YOUNG LIVES are lost to Cystic Fibrosis.

We are aiming to raise a lot of money to go to the Cystic Fibrosis Trust to help towards research and care for those suffering from CF, so please give generously.

 

 

Thank you so much in advance, and please cross you fingers for me!