Supporting NHS patients exposed to Hepatitis C (HCV) from #contaminatedblood in the 1970s, 80s and 90s fight for truth and compensation. #infectedbloodinquiry
For the thousands who are suffering the effects of Hepatitis C from contaminated blood transfusions, life will never be the same. We are supporting victims to get the truth, finally obtain justice and secure meaningful compensation.
#InfectedBloodInquiry https://t.co/NNpHeB6DMr
Solicitor for victims of the contaminated blood scandal @EjonesEm has urged the government to ensure that those infected and affected are given sufficient time to input into the appointment of an independent reviewer https://t.co/zhoH1ACgko
Alan Vickers met his wife Sally in 2003. In 2004 she collapsed at home and was rushed to hospital. It wasn't until 2005 that she was diagnosed with Hepatitis C contracted from a contaminated blood transfusion received as a teenager in 1982. Sally's story: https://t.co/C2PNqjWado
Alan Vickers met his wife Sally in 2003. In 2004 she collapsed at home and was rushed to hospital. It wasn't until 2005 that she was diagnosed with Hepatitis C contracted from a contaminated blood transfusion received as a teenager in 1982. Sally's story: https://t.co/C2PNqjWado
Alan Vickers met his wife Sally in 2003. In 2004 she collapsed at home and was rushed to hospital. It wasn't until 2005 that she was diagnosed with Hepatitis C contracted from a contaminated blood transfusion received as a teenager in 1982. Sally's story: https://t.co/C2PNqjWado
Did you know? The number of people living with a rare disease is equivalent to the world’s 3rd largest country. Download, edit and adapt #RareDiseaseDay infographics from https://t.co/UzxORuTmDw. Share them on social media to spread the word about Rare Disease Day on 29 February!
Alan Vickers met his wife Sally in 2003. In 2004 she collapsed at home and was rushed to hospital. It wasn't until 2005 that she was diagnosed with Hepatitis C contracted from a contaminated blood transfusion received as a teenager in 1982. Sally's story: https://t.co/C2PNqjWado
🚨WE'VE JUST LAUNCHED A NEW REPORT🚨
We're celebrating the incredible impact of our peer work through our new report: 'Leave no one behind: Engaging and empowering people in hepatitis C care and treatment through peer and support'.
Read more here: https://t.co/BUsBpctlI5
The consequences of this episode are still unfolding: our helpline took 4150 calls in 2019, 1000 more than 2018. This increase is down to calls related to #InfectedBlood. Some are from people only just diagnosed who got #HepC from infected blood pre-1992
https://t.co/xe3biuUVoV
Great article from @JVLazarus: "Ultimately late presentation represents a failure of the health system to diagnose infected individuals when they are in greatest need."
We need to find the tens of thousands of people who have hepatitis C but are undiagnosed.
Otherwise, elimination will be impossible and more people will become infected.
Our manifesto shows how the next government can make sure we find and treat them: https://t.co/6DcOiFfrxp
We've published the last of our blogs on the @bloodinquiry for this year on our website. To conclude, Chair Sir Brian Langstaff said: "If there is criticism to be made, I shall make it, and I shall not hesitate to name names where it is appropriate."
https://t.co/VL41il97Ca