The Charity’s aims centre on Support, Research and Awareness and its activities are chiefly:

  • The provision of events, advice and support for individuals and families affected by Noonan Syndrome, their families, dependants and carers, including the families and dependants of those who have died from Noonan Syndrome and pregnant mothers where it is believed that their child may be born with Noonan Syndrome;
  • The facilitation, promotion and pump-priming of research into the causes, effects, diagnosis, treatment and relief of Noonan Syndrome with the useful results of the research being disseminated for the benefit of the individuals and families affected by Noonan Syndrome; and
  • By advancing the education of the public and professions providing services to individuals and families affected by the condition in relation to the effects of Noonan Syndrome by communicating reports and disseminating information by any means or media concerning research work and studies undertaken by or on behalf of the charity.