Marc Cotterill's health was transformed by #Trikafta One of his best friend's Craig is talking about his reasons for taking part in the #crossingforCF to raise funds and awareness for the #RightToBreathe campaign Donate here: classy.org/team/454643 Please RT for #CFAwareness

Youseff from #Egypt has #CysticFibrosis, he has lost 3 siblings to CF & his family can’t imagine losing him too 😢. Youseff and children in LMICs around the world need access to #Trikafta now. They deserve to live. #Right2Breathe #NoOneLeftBehind

Join us for Africa’s leading conference on rare disease treatment and access, Rare-X proudly hosted by Rare Diseases South Africa Rare-X 2024 will take place from 14- 17 February in Johannesburg, South Africa! For more info visit rare-x.co.za #rare #rarex #conference

Join us in our #CysticFibrosis Advocacy! Legal researcher Baone explains the impact of compulsory licensing in our fight for better #access to CFTR modulator therapies. Let's make a difference and transform CF into a manageable condition for all! #AccessToMeds

Let's raise awareness about #CysticFibrosis and access to life-changing medicines like Trikafta. Learn about Compulsory Licensing and Cheri Nel's court application. SECTION27 is making a difference with amicus intervention for better medicine access. #AccessToMeds

Heartbreaking stories from Moms of child with CF without access to modulators Vertex Save Us please listen

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…

Congratulations! Well deserved indeed!

I stand with #CysticFibrosis patients worldwide in calling out Vertex Pharmaceuticals for their unacceptable profit-driven behaviour. Their lack of compassion & failure to make lifesaving treatments accessible is costing lives. Read more ⬇️ tinyurl.com/5fcjejje #RightToBreathe

💥💥URGENT CALL to South African #CysticFibrosis patients 💥💥 Join the landmark case to gain access to life-saving CF medication #Trikafta. Together we can win! Sign up to our webinar to find out more: bit.ly/SA-CF-case 🗓️ 29th February 🕖 7pm (SAST) #RightToBreathe

🌍A historic legal battle is underway in South Africa. #CysticFibrosis patients are challenging Vertex Pharmaceuticals's monopoly in court, to access to the lifesaving drug Trikafta - currently priced at $326k. Read our blog to find out more: righttobreathe.net/post/south-afr… #RightToBreathe

People living with cystic fibrosis in South Africa to band together against big pharma greed thecanary.co/global/world-a…

You are AWESOME! Acknowledge someone in this post because they are awesome - tag them, give them a call, heck - organise a coffee with them! ! ! ! Let's celebrate each other ! ! ! And don't forget to celebrate yourself...

Saturday | Thriving conversations | Let's hear what our beautiful families have to say about headless chickening... Could it be a superpower? Could it make the world a better place? Please remember to share! Have fun #thrivingdinners #myfamilyiscool

This photograph reminds me of pure power. Let's stand together and make sure all CF warriors have equal access to Trikafta. #nooneleftbehind