So much has happened over the last 30 years to improve the care for people living with MND. Of course there is still much to do but with the support of the MND Association, our Care Centres, our Branch and Group network and our hundreds of committed volunteers, people living with MND can continue to live with dignity.
Through individual stories and accounts read how the care of people with MND has changed over the years and how the work of the MND Association continues to make a difference to people affected by the disease.
Janet McMillan, chair of the Leicestershire and Rutland MND Branch first came into contact with MND in 1985 following her father, Don Luckman's diagnosis.
Christine Hosgood-Jones was diagnosed with MND less than a year ago. Christine talks about the wide range of support she receives and how it has helped her live with MND.
Director of care development Heidi Macleod looks back over the last 30 years and the developing role of the MND Association.
The facts speak for themselves: read about the changes the Association has seen over the years.
