previous post entitled NONE
I am feeling more positive tonight , I feel I am in the system and on the radar.
Today we went to our new surgery . Dr had never heard of PSP but before we left she had promised to look up the website of the psp association, write to social services and carers association, organise occupational therapy visit and refer my husband to a neuro physiotherapist and organise ocasional day respite to give me a break. A whole lot better than my previous GP who told me to get in touch when I could no longer manage. This positive response with all your helpful suggestions and supportful blogs will keep me onwards and up , my grateful thanks to you all .