aHUS Day video- Thoughts for Doctors
The aHUS alliance has put out its aHUS Awareness Day video for 2017. 72 patients, or family members, from 18…
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…
Genetics is very important to aHUS patients. aHUS is a very rare genetic diseases. aHUS patients get to know and understand…
Patients sharing their rare disease journey help bring new levels of understanding to researchers, industry, and the general public. Whether…
Use the following link to see the work of aHUS patients, parents and carers from 17 countries around the world on…