Why Cystic Fibrosis ... as a mother to a 10 year old daughter with Cystic Fibrosis we all feel the challenges faced with the incurable disease. 

Phoebe looks a picture of health on the outside, but so much is going on on the inside that only she feels the consequences of.... the need for twice daily Physio , pills and more pills , nebulisers and exercise to the extreme is just a daily event to try and stay healthy, alive and reduce hospital admissions. 

As a close theatre team we are coming together as colleagues and with the help of friends we are going to walk the whole guild wheel, which in it's self is a challenge, let alone taking it on after a week at work 😜 

Please come along and join us for an 8am start at Avenham park near the Continental pub.  We aim To be back  at the Continental by 4pm ! So if your not walking get the refreshments in 🍻And your unwanted change in the CF bucket 😜

If you would like to join us please contact me , I need £5 donation as an entry fee and a tee shirt size 😀

Any contribution towards this amazing trust brings us ever closer to a cure. 

Phoebe has completed the Guild Wheel today ( 3rd June 2017.) in fact she cycled over 25 miles in just over 4 hours, she's is aged 10 ,  living with lungs that feel like your breathing through a straw and uses twice as much energy as a none cf person .. so come on friends and friends of friends please come and join us on this walk and help us find a cure for my amazing girl 👊🏻😀👍🏻 Please donate