Rare Disease Report is a website and weekly e-newsletter that offers an independent voice for the Rare Disease Community. It strives to bring together medical, scientific, investment, regulatory, and advocate professionals interested in rare diseases and orphan drugs. Recently the work done by cureCADASIL was spotlighted by RDR.  We are excited for this opportunity to share our programs with the rare disease community.

Spotlight on CureCADASIL

Ruth J Hickman, MD
Published Online: Saturday, Apr 23, 2016

“CureCADASIL (also known as CADASIL Association) is a nonprofit group dedicated to raising awareness of the rare disease cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Through the aims of communication, advocacy, research, and education, CureCADASIL is working to improve the lives of those affected by the disease.”