Feeling sick is difficult enough without going to a doctor’s appointment and learning that the diagnosis might possibly be the rare disease atypical hemolytic uremic syndrome, also known as…
Like the "Rocky" films, the alliance Rare Disease Day video has a follow up version as more people from more countries have asked to be included since the video was…
It’s difficult for rare disease patients to find information about their condition and even more so for patients with medical conditions that affect very small numbers of people, like…
Patient engagement in research is a developing issue. For it to be successful there needs to be a mutual appreciation of the value that can be added by including patients…
An article entitled "An innovative and collaborative partnership between patients with rare disease and industry-supported registries: the Global aHUS Registry" has appeared in the Orphanet Journal of Rare Diseases in which the aHUS alliance has…
A key outcome from conferences like Kidney Week in Chicago ( American Society of Nephrologists.) is the sharing of knowledge from thousands of bits of research which together help close…
aHUS, or atypical Hemolytic Uremic Syndrome, is what is known to be the illness that affects a very few patients around the world. But it is also known as atypical…
The latest aHUS patient organisation to affiliate to the alliance is aHUS Kids Japan. They introduce themselves in their own words with English translations. aHUS kids Japan 患者会設立のお知らせ この度、小児非典型溶血性尿毒症症候群（aHUS）の患者やその家族を対象にした患者会を「aHUS…