@SpotlightNSP And still @VertexPharma has this exhorbitant price tag for my country. It's really hard to see how my fellow CF warriors are suffering and dying. Adults battle with employment, and children battle to complete school, because we are in hospital or at a clinic so often.
@SpotlightNSP Approximately 5-7% of South African citizens are contributing to the personal income tax base. This relatively small percentage reflects several factors, including high levels of unemployment and widespread poverty. The South African Revenue Service (SARS)
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
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...
🌍A historic legal battle is underway in South Africa.
#CysticFibrosis patients are challenging @VertexPharma's monopoly in court, to access to the lifesaving drug Trikafta - currently priced at $326k.
Read our blog to find out more:
https://t.co/HnL4lxGrem #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: https://t.co/JcRRFdb6Y1
🗓️ 29th February
🕖 7pm (SAST)
#RightToBreathe
I stand with #CysticFibrosis patients worldwide in calling out @VertexPharma for their unacceptable profit-driven behaviour.
Their lack of compassion & failure to make lifesaving treatments accessible is costing lives.
Read more ⬇️
https://t.co/j8DRYXdZem #RightToBreathe
@SenSanders Thank you. As a patient dying because of pharma greed, it is encouraging to see that someone willing to take on the system. Please help to save thousands of children and adults! Vertex is a terrible company!
We are advocating for #CysticFibrosis patients EVERYWHERE, including the UK, where @VertexPharma’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:
https://t.co/PGx7P7uZYQ
Huge support in the room at #NACFC - the tide is turning against @VertexPharma.
It's time for them to listen to patients & clinicians around the world, drop their outrageous $326k price tag, and ensure global access for all!
Get involved 👇
https://t.co/gVHcpjlnn6
"We won't stop until everybody has access." ✊
Our Senior Organiser & @VertexSaveUs member @gayle_pledger making it clear that we will not stop speaking out and challenging @VertexPharma until every patient, everywhere has access to lifesaving treatment.
#NACFC#RightToBreathe
A vital presentation by Jonathan Guo on the challenges to access for patients worldwide.
"Elephant in the room is that cost remains the barrier to treatment. While inequalities in access are stark @VertexPharma is enjoying record profits."
$326k a year is unjustifiable! #NACFC
Hello from Phoenix, Arizona! 👋🇺🇸
We & @VertexSaveUs are here at #NACFC to speak about the #RightToBreathe campaign for global access to lifesaving #cysticfibrosis medicines! 🌍
Here's some highlights from day 1 so far...⬇
BREAKING: #CysticFibrosis families from @VertexSaveUs & advocates confront @VertexPharma at their head office in Boston.
"How many billions is enough?"
They are here to challenge the exorbitant $326k/year charge for life-saving CF meds, leaving only 25% of patients with access.
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