One of the challenges the Society has set itself is to become the authoritative voice of people affected by MS and to take the lead in raising awareness about a condition that, as yet, has no identified cause or cure and impacts hugely on their lives. To achieve its aims in research, in support and information to those affected by MS, and in raising standards of care, the Society must continue to align even more closely with the individuals and groups who have the control and influence to help it achieve these aims, and to engage with them in positive and compelling ways.

Dave's youngest son was diagnosed with aggressive relapsing-remitting MS in December 2005 when aged 25.  His life and career-changing experiences continuously help to shape Dave's views about the key role the Society can fulfil and his belief about the part he can play.

Dave's work as a management consultant helping individuals and groups collaborate successfully on achieving their goals, together with experience as a trustee of a counselling charity and as a chair of school governors has, he believes, equipped with him with skills that can help the Society achieve its ambitious aims and long-term vision.  He is currently one of two vice chairs on the Board.