Every year, alongside Nikki Zimmerman and the Rare Dementia Support (RDS) team, we organise a support group meeting for families living with familial frontotemporal dementia (fFTD). This is a fantasti...
Covid-19 has changed the world for many of us. Much FTD research has had to be put on hold in recent months and the FTD talk team have all had to work from home since early March. However, although...
