We’re delighted to launch our new website and hope that it provides a useful source of information and support to our members and for the wider public including healthcare professionals working with people who have Noonan Syndrome.
An important strand of our work at the NSA is awareness raising and along with providing useful medical and wellbeing information for individuals and families affected by Noonan Syndrome, we also celebrate our collective achievements – see our Member Stories and Events pages.
The Resource section will be added to shortly with a series of Factsheets, and we are continually adding to the FAQs as we receive and respond to queries. Please get in touch if you have a specific question.
