Kawasaki Disease Foundation Australia has partnered with Sanford Coordination of Rare Diseases (CoRDS) Registry.
This is an international and Central registry of individuals of any age who have been diagnosed with a rare disease. It was primarily developed to meet an unmet need for patient registries worldwide.
If you or a family member has been diagnosed with KD, you can help researchers see the whole picture.
To enrol in the CoRDS registry, or for more information, visit www.sanfordresearch.org/cords