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Supporting Families
Established in 1985, RSAS aims to provide direct support to the families and carers of Rett girls and women in Scotland, the North of England and internationally. Healthcare Advice
RSAS works in partnership with a dedicated team of Medical Advisers, through whom we can offer healthcare advice to Rett carers. We fund research into the causes and implications of Rett Syndrome, headed by Dr Mark E.S. Bailey at Glasgow University and disseminate the findings of this and other research amongst the Rett community. Public Awareness Alongside regular newsletters, we offer a back-catalogue of Rett-related publications. We aim to facilitate a better public awareness of Rett Syndrome and can provide expert speakers to media and public organisations.
RSAS relies on a dedicated team of volunteers, headed by a committee of twelve:
Chairman: Graeme Dallachy Treasurer: Helen Wright Secretary: Caroline Wilson
Committee Members: Jan Hunter, Anne McLeod, David Jackson, Isabel McFarlane, Qmar Ali, Kate McMahon, Betty Barrons, Frances Binnie, Pauline McQuillan
RSAS is a Scottish Registered Charity No. SCO16645
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