Just to say that my main frustration with this disease has always been the lack of support from GPs, charities and social services. The people on this forum know way more about how to communicate with a person with anosognosia, (lack of insight) than the professionals.
For me personally, the disease allowed me to get closer to my mum than I was before, and I feel my care of her was the most important job of my life. So although there is lots of horrible stuff, there is some good stuff too.
For me personally, the disease allowed me to get closer to my mum than I was before, and I feel my care of her was the most important job of my life. So although there is lots of horrible stuff, there is some good stuff too.