#Kaftrio has been proven to change lives. Please don’t make our under 12’s wait, especially in times of so much uncertainty. Save our CF children 💛MHRAgovuk Cystic Fibrosis Trust

1,000’s of children are asking for 1 thing for a Xmas. The gift of a life unlimited by #CF MHRAgovuk pls stop dragging yr heels you were supposed to make things quicker! EU Medicines Agency hv approved #Kaftrio u just need to rubber stamp now.

Welcome to the new BREXIT Secretary! Wow 🤦🏼‍♀️ #nohope

Pls RT for #CFWeek and if able to pls consider a small donation⬇️ crowdfunder.co.uk/p/cf-drugs-for… So that all countries can benefit from modulator therapies #cysticfibrosis cf/Aware Cystic Fibrosis Aust Trikafta for Kiwis Robert McCarthy #CureCysticFibrosis Beth Finn Belle Raisers Liam Mc Hugh Natasha Robinson R&R CF Fighters @cystik101

Every person with #cysticfibrosis in every country should have access to #Trikafta - a life-saving drug Please sign & RT petition⬇️🙏 actionnetwork.org/forms/cf-drugs… Salty Dr Meghan McGarry Christine Noke CFF_Peoria CF Get Loud beth Vanstone Beth Finn kistikfibrozis Azad #cfaware

“Don’t wait to see cystic fibrosis” - I honestly couldn’t agree more, what a powerful message. Will you now follow through with this message and ensure that #trikafta is made available to ALL children and adults with CF from ALL countries? #VERTEXSAVEUS Vertex Pharmaceuticals

We have one very happy Megan Butternut Box…..she loves her advent calendar 🎄🐶♥️ #DogsDeserveChristmas

So proud of my beautiful friend!! Smashed it 😘 xxx

Petitions that get shared more often, get more signatures. If you know someone with CF please share this every day this week. Thanks. petition.parliament.uk/petitions/6337… cf/Aware CFAdultNewcastle Cystic Fibrosis Care @CF_Artists Gray Hair CF Club In The Buff @IanRElliot Nick Smith Beth Finn #cfaware

The Coronation propaganda at school has been full on, and last night my 6yo asked why I'm not excited about it. I try to be honest with my children so I told her I find it obscene that so much money is being spent on it when people are struggling to eat or have nowhere to live.

Nearly 4 years on from this and Isabelle’s life has improved dramatically. She is 1 of the lucky ones. We are still supporting Cystic Fibrosis Trust trying to raise funds to continue their amazing work in finding a treatment for all! Please read our story 💛 justgiving.com/page/andy-cole…

Please help support my dad…he is starting his fundraising challenge today for Cystic Fibrosis Trust #BusPass4CF 💛

TV presenter and former Pop Idol runner-up Mark Rhodes is advocating for all adult #cysticfibrosis patients to have free prescriptions in line with other chronic diseases. Pleases RT and sign/share this petition widely on all social media: PETITION ⬇️ petition.parliament.uk/petitions/6337…

Pls sign/RT Free prescriptions for CF adults In the 1960's #cysticfibrosis was excluded from the exemption list because most did not live to adulthood, now they do but adults with CF in England still pay for their prescriptions petition.parliament.uk/petitions/6337… Beth Finn Emma M Smith 💙

Unbearable, arrogant and deluded! #embarrassing #cringe

Urgent calling to our CF community, CF Voices Needs you! I can’t begin to tell u the difference #Kaftrio has made to my life & I want to be sure that future generations with CF r able to benefit in the same way. Pls join CF Voices now to keep up with developments & announcements

What a great piece in the paper today and £8,000 raised for Cystic Fibrosis Trust and Great Ormond Street Hospital Charity , what a way to remember Elle and her #elleswishes campaign! Thank you as ever Chris Riches and Daily Express #UK CF campaigner Sharon gemmaleighweir Beth Finn

Can’t believe this was 5 years ago Cystic Fibrosis Trust. How life has changed. Forever grateful 💛