aHUS Awareness Day 2018 – The Video
Once again, with the help of aHUS Patients and their families, the aHUS alliance has produced a video to spread the…
Once again, with the help of aHUS Patients and their families, the aHUS alliance has produced a video to spread the…
Looking for the latest 2017 facts and key research about the rare disease atypical hemolytic uremic syndrome (aHUS)? You’ve found…
So aHUS is a genetic disease caused by the aHUS gene. Many people talk about "the aHUS gene" as though it…
The aHUS alliance has put out its aHUS Awareness Day video for 2017. 72 patients, or family members, from 18…
Last month the aHUS alliance in partnership with Andrew Siedlecki , the USA National Coordinator for the aHUS Registry and other…
We welcome the aHUS community in Poland as the newest of aHUS patient organizations uniting with other nations under…
It is just 25 days to aHUS Awareness Day 2017 and patients and patients' organsations around the world will be making…
The 3rd international aHUS Awareness Day is just 2 months away. The world will join together on…
The aHUS Alliance, an international group of atypical HUS patient organizations and global advocates, announces its 3rd annual worldwide aHUS…