Connect. Cure. Share.
We are a registered, parent-led non-profit organisation based in the US but with a global reach. Co-founded by two parents of bright boys struggling with NURR1 deficiencies caused by ultra rare changes to the NR4A2 gene, together with a team of other parents, we represent a very small but growing community of children, adults and families.
Our sole and solution-oriented mission is to find a treatment or cure for NR4A2-related disorder and the diverse neurological, motor, behavioural and emotional symptoms that are caused by a deficiency of the important NURR1 protein that it encodes.
We seek to actively connect researchers, pharmaceutical companies and clinicians from around the world in order to facilitate research and accelerate access to novel therapeutics, whilst actively consulting with and advocating for patients and their families.
Contact Us
Get in touch if you are an individual with a NR4A2 (NURR1) genetic change, a parent or guardian, or a professional working in this area.
Fill out some info and we will keep you updated on the latest research and, in future, treatment possibilities. We are looking forward to hearing from you!