A new poster here.
Diagnosed 15 years ago but only recently felt effects of PPMS. Retired on medical grounds in December 18 after 35 years.
Mobility poor and can only manage a few paces with a frame. Stairlift now in place but house not suitable for wheelchair. Getting an extension with wet room and downstairs bedroom, but this is around 6 months away.
Feeling really down and depressed, wife suggests I try and speak to someone who can help. Any suggestions,?