Since the AKU Society was founded in 2003, it has grown rapidly, helping several sister arms to become established in other countries. These have been set up to raise awareness of AKU, provide support and information to patients and families and promote medical research. They are run by patients and patient representatives who really understand AKU and the impact the disease can have on patients’ life.
Hi! My name is Maria and I am currently a 2nd-year student at Royal Holloway University of L.. ...more
Today's blog is written by Nick Sireau the Chair and CEO of the AKU Society, It was in.. ...more
We are delighted to announce that all the data from the SONIA 2 clin.. ...more
My name is Alev Sen. I’m the main researcher on a study of treatment for AKU in UK hea.. ...more