Life and legacy bonds for all with aHUS
In the reception area of Alexion's HQ in New Haven Connecticut there is a piece of conceptual art. ( see the…
In the reception area of Alexion's HQ in New Haven Connecticut there is a piece of conceptual art. ( see the…
Especially with very rare diseases such as atypical HUS, medical research and education efforts are keys to unlocking information that’s critical…
The previous blog illustrates the difficulty of diagnosing aHUS. From the basic information about some patients have a go at diagnosing…
Feeling sick is difficult enough without going to a doctor’s appointment and learning that the diagnosis might possibly be the…
A question ,which featured in the Rare Diseases Day video, will have resonated with many aHUS families as it was about…
Tomorrow, and the day after, a significant event is taking place in New Dehli which is of great importance to aHUS Patients…
Most who have had an encounter with aHUS will be familiar with the anxiety and uncertainty felt by Deborah in her…
Exploring your Questions, Rare Disease Day 2017 Children living with the rare disease atypical HUS are first and foremost children. Despite…
Like the "Rocky" films, the alliance Rare Disease Day video has a follow up version as more people from more countries…