Your journey of learning starts here
This website is intended for people and parents / carers of children who are being treated for atypical Haemolytic Uraemic Syndrome (aHUS).
It may be scary to find out that you or your loved ones are living with aHUS. You may have questions and concerns about the disease and how it affects your body.
Learning about aHUS is important and it can empower you to start taking control of it.