MENINGOCOCCAL INFECTION – JAAC’s STORY
aHUS patient Jaac and his mother Ria are from the UK. Ria spoke to Global Action about her son’s meningococcal infection…
aHUS patient Jaac and his mother Ria are from the UK. Ria spoke to Global Action about her son’s meningococcal infection…
If there is no cure for aHUS then remission is a disease free state which is possible for aHUS patients. Patients…
In September last year a group of aHUS patients and parent/carers met with FDA and told them about aHUS. A summary…
A cure for aHUS would mean an individual would be at no risk of the disease again. Patients ask Will there…
Some aHUS patients have ended up with end stage kidney failure and need to have a kidney transplant. Such a transplant…
It’s 2024. A New Year.This year around the world about 4000 people will newly onset with the primary form of aHUS.…
Thank You to all Participants! View the completed Rare Disease Day 2024 project here http://bit.ly/RDday2024aHUS While Rare Disease Day is marked…
Last year at this time Global Action published an article recording a conversation we had with ChatGPT ( an AI thing)…
The United States Thrombotic Microangiopathy (USTMA) Consortium was formed in 2014 as a collaborative initiative to organize research efforts in the…