🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

Please share. Children with CF need you ❤️ actionnetwork.org/forms/cf-drugs…

We are advocating for #CysticFibrosis patients EVERYWHERE, including the UK, where Vertex Pharmaceuticals’s prices are causing anxiety for many CF families. Our petition has surged and we will ensure that Vertex hears ALL your voices, loud & clear. Please sign: actionnetwork.org/forms/cf-drugs…

I’ll be live on BBC Wales News tonight at 6.30 talking to them about the blow the CF community has had this week 🎥

Josh will be on BBC Wales News tonight talking about the situation for CF families across the UK, following NICE's draft guidance published last week about the cost effectiveness of Kaftrio, Orkambi & Symkevi. Great to get some media attention in Wales on this issue! Vertex Pharmaceuticals

Please sign this petition & help #cysticfibrosis patients have continual access to life-changing modulator medication. Thank you! 😊 ♥️ #CFWarriors #cysticfibrosisawareness petition.parliament.uk/petitions/6506…

Pleased to join Mike Tipton in this important launch video for The Physiological Society launch of our new report Great _laurenclayton_ feature - showcasing her CF Warriors funded testing looking at responses in LTCs (#cysticfibrosis) who may be at increased risk in the heat

Fantastic to see _laurenclayton_ featured in this video, helping to raise awareness for the work that our charity is doing to improve the lives of those with #cysticfibrosis. This is such an important issue facing so many vulnerable groups around the world.🌍

Are you living with CF and interested in participating in our latest research study at the University of Portsmouth? We are investigating how individuals with CF respond to exercise in the heat? Please contact us for more information #cysticfibrosis #research #CFWarriors

📣Attention all CF Warriors📣 Please get in touch with the team at University of Portsmouth and help our research study on exercise in heat. Thanks in advance for your support! #CFWarriors #cysticfibrosis

Happy #Thanksgiving to all our friends, family & #CFWarriors across the pond. Wishing you a weekend filled with turkey, pie and American football! 🏈 #Thanksgiving2023

There's still time to get the last few tickets for next week's Christmas Concert at St Donats Castle for a night of food, fizz & entertainment with Emily Langford & friends, all in aid of CF Warriors! Contact Emily for tickets! 🥂🎄 📧 [email protected] #CFWarriors

💪#WednesdayWarrior💪 Archie is a 2yr/o that never stops! He loves biking with his grandpa & going over the big jumps in the forest, swimming & soft play, going to toddler football & trips to Hartlepool to support his daddy’s football team. Welcome to our team Archie #CFWarriors

A HUGE Thank You to Emily Langford and everyone involved in last night's #ChristmasConcert at St Donats Castle. It was such a fantastic evening and thanks to the generosity of guests at the event, we raised over £1,300 for the charity! #itsbeginningtolookalotlikechristmas

Happy New Year to all our friends, supporters, volunteers and people who have joined the community, and played a part in helping the charity in 2023. Here's hoping everyone has a happy and healthy 2024! Big Love to you all from #CFWarriors♥️ #happynewyear2024 #happymonday