We're a charity based in Worthing & Chichester. Providing support to children up to 18yrs old with Cystic Fibrosis & the immediate family living in Sussex.
#yelfie day! Let's see them people. Please wear yellow and support the #cftrust & #cfcommunity today πππ
Post your pics here, we would love to see them. Xxx
Wow, wow, wow! What a day yesterday was!
From the bottom of our hearts we would like to say a HUGE thank you to every single one of you for making the day a roaring success!
We don't have the words to do you all the honour you deserve but please know we are truly grateful.
Hoping you'll all have a go with our sweet tombola on Saturday. Some great jars and fab star prize up for grabs! Another great bit courtesy of my aunty & nan. Thank you both so much. Xxx
#sweets#tombola#sweettombola#sweettooth#ccffwc#cysticfibrosis
So the big day is nearly here! And to give you a small taste of what's to come...
A bouncy castle!
Courtesy of @Backyardbouncersllc who have been incredibly patient and accommodating! We highly recommend!
#backyardbouncersllc#funday#fundraiser#ccffwc#cysticfibrosis
Today we started putting together the goody bags! Send your cards/treats this way if you would like.
So far we have @theovenmagician & @cartsofdelight
@MissBettysBeauty will be putting some vouchers in with their cards so you'll want to come along to get your voucher π
Final game for the reserves and the long awaited trophy presentation.
Sadly the opposition could not raise a team so we have 22 man in house game involving all the lads who helped the ressies win the league in style.
Well done Pepp,Barlow & all the players.
Up the Barrowmen .
@s_cystic DR MARTIN BURKE AND GRAD STUDENTS
HAVE DISCOVERED A NEW USE FOR AN EXISTING DRUG [AMPHOTERICIN B] IN
THE TREATMENT OF CYSTIC FIBROSIS.
https://t.co/Qvhhp2fKJB
Good to see rare diseases getting the attention they deserve in the morning papers. My constituent Barbara McGovern and her son Archie showing again the injustice those with #PKU face.