“Good News” from talking about aHUS and Pregnancy
Earlier this year ,when the alliance was responding to the Rare Disease Day video questions , aHUS Patient Megan contacted the…
Earlier this year ,when the alliance was responding to the Rare Disease Day video questions , aHUS Patient Megan contacted the…
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…
Post-Event Update:Presentations were videotaped, and appear on ourAtypical HUS Clinical Channel as the key asset of 2017 aHUS Awareness Day (24…
Patients are at the heart of healthcare. Patients are the recipients of medical care, and the participants in research and clinical…
The 3rd international aHUS Awareness Day is just 2 months away. The world will join together on…
Earlier this year the website featured an article ( click here )about the nomenclature used to described aHUS. Clinical articles now…
Post-Event Update: Presentations were videotaped, and appear on YouTube on the aHUS Alliance Atypical HUS Clinical Channel .…
* To have genetic tests for all aHUS patients and families featured in the Rare Disease Day video ( see here).…