I am posting this on behalf of mum . She is my dad's carer. He has been diagnosed with PSP about 4 years ago now and need help for feeding and brushing teeth ( among other things ...). She is trying to make him spit but this doesn't work and he usually ends up soaked or having water dribbling down his neck at the front. Anyone have any devices / props - aside a towel that would help?
thank you for any tips!