RSAM is on a mission to improve and enhance the quality of life for all of those affected by Rett Syndrome in New England.   We achieve this by providing supportive services, resources, advocacy, education, awareness, and raising funds towards the advancement of Rett Syndrome research.


Co-Presidents: Larry Fallon and Maggie Wurm

Secretary: Irene Gladstone

Treasurer: Kathy Schoener

2020 Board Members
Michelle Boom

Bonnie Budd

Larry Fallon

Tracy Freeman

Irene Gladstone

Ariane McMahn

Kathy Schoener

Laura Tempesta

Maggie Wurm

Committee Members

Dr. Michela Fagiolini

Jessica Henry

Jane Joyce

Sibling Volunteers:

Caitlyn Wood

Sara and Michael Anastasia

Hannah Sweeney