Janine Vince

“My husband had the familial form of MND and died in January 1993.  Since then I have been involved with the MND Association at branch level and also spent 7 years as a Trustee.  During my time as a Trustee I served on the Research Advisory Panel as a lay member and have always had an interest in research as we need to learn more about this disease.  I was invited to join the MND CSG as a lay member and have been involved now for ??? years.  Advancements since my husband’s death have encouraged me greatly that we will one day find a cure and more treatments for this awful disease”