Our Strategy for the future
Our strategic goals represent our five year plan.
We have developed and refined them alongside people with MND, our trustees, our volunteers, health and social care professionals, the research community, our members and staff.
Goal 1: Advancing research
We will be a leading international contributor in identifying the causes of MND and understanding how it progresses. We will support the research community in turning this new knowledge into potential treatments and ultimately a cure.
Goal 2: Ensuring quality health and care
We will do all we can to ensure that people with MND, their carers and families can access the care, support and information they need, when and where they need it, reflecting their diverse needs.
Goal 3: Strengthening professionals’ ability to treat and care for people affected by MND
We will better understand the disease and clinical progression of MND. We will facilitate the sharing of knowledge, data and resources to improve outcomes relating to people’s diagnosis, prognosis and treatment.
Goal 4: Working together
We will achieve more for people with MND, their carers and families by working in partnership and collaboration with other organisations, and by being a credible and effective operator in the external environment.
Goal 5: Raising awareness
We will increase awareness and understanding of MND and raise the profile of the work of the Association to influence decision-makers and reduce the social isolation so often experienced by people with MND.
Goal 6: The difference we make
We will continue to affirm our place as the leading authority on MND by growing the MND community – that is, all those who share our vision – and continually improving how we run our organisation.
We will report back on our progress against this plan every year in our Impact Report. You can also take a look at our key activities for 2017.
This is a paper submitted to our Board of Trustees summarising progress made in the final year of our strategy running 2013-2016. Although this is a report written for the board, we are keen to make it available for all. Some of this information will also feature in our impact report which will be available early summer.
The Impact Report explains how the money you have raised has been spent on behalf of people living with MND and details our plans for the future.
Our Annual Report and Consolidated Financial Statements provides our Trustees report and full financial details for the Association.
For more information or to give us your views, email firstname.lastname@example.org.