Scientists from the University of Oxford have set up ‘Families for the Treatment of Hereditary MND’ (FaTHoM), an initiative to bring together the community of families affected by inherited forms of MND. Their first meeting will take place in Oxford on Tuesday 18th April.
Most people living with MND cannot identify a relative who has also had the condition. However, around 5% of people with MND will have a family history of the disease, which is known as inherited or familial MND. This happens when a single faulty gene is passed down from parents to their children across number of generations.
We thought we’d share this fantastic festive photo of (to our knowledge) the world’s first ‘gingerbread MRI scanner’, lovingly created by students at the Oxford Centre for Functional MRI of the Brain (FMRIB) and kindly sent to us by Dr Martin Turner, lead investigator on the BioMOx study.
Gingerbread MRI Scanner
Many thanks to everyone who has so enthusiastically participated in BioMOx and our other clinical research studies, which are helping to improve both our understanding of MND and future approaches to treatment. This research simply couldn’t happen without you!
With very best wishes for the Christmas period.
The MND Association’s Research Development Team
More information on BioMOx: