Reading Time: 2 minutesKaren Pearce, the MND Association’s Director of Care, blogs about presenting the Association’s wheelchair project at the Allied Professionals Forum, which happened prior to the
Author: Kiran Goyal
I work as a Research Officer within the MND Association to help organise the International Symposium and communicating the latest updates of MND research across our social media platforms. I graduated with a master's degree in Neuroscience from Cardiff University in 2023. I have previously supported the awareness of Fragile X syndrome within the UK.
Reading Time: 3 minutesEvery day there are two sets of talks going on at the same time during the International Symposium. On Saturday morning there was a symmetry
Reading Time: 4 minutesA huge ‘atlas’ mapping the locations of motor neurone disease (MND) causing mutations within the genetic code has been collated. This has followed years of
Reading Time: 3 minutesYesterday at the International Symposium on ALS/MND Prof Ammar Al-Chalabi (Director of King’s Care Centre and Professor of Complex Genetics at King’s College London) cautioned
Reading Time: 3 minutesThe MND Association’s Director of Care (South), Karen Pearce, gives her thoughts on one of the clinical sessions on the first day of the Symposium.
Reading Time: 4 minutesCould there be a small number of people for whom there is a pause or a reversal in their disease progression? A talk at the
Reading Time: 3 minutesWhile muscle cramps are a very common symptom of motor neurone disease (MND) there is currently few effective ways of management and treatment. Even though
Reading Time: 3 minutesAdult onset condition, those with genetic mutations associated with the disease don’t get it until they’re adults, starts in one place and then it spreads,
Reading Time: 3 minutesUpdate (February 2017): All sites are now closed and not recruiting for participants. If you would like to be added to a waiting list for