This was good for many reasons including educating people what it is like to have Alzheimers/dementia, as some of us still have levels of autonomy and choice - although this will diminish over time I know. My current husband said it didnt give him any more clues how to cope with my foggy days and general problems, but it did increase his understanding of how it affects us all differently.
For my own part, I start a singing group for the brain in June and found the programme so reassuring as I have been worrying about my awful singing voice. I am now settled and secure in the knowledge it will help and stimulat my brain. I can no longer read music for some reason, but I get pleasure and joy from listening to music - preferably without words as I cannot remember them anyway.
My great sadness lay with the young family being robbed of years of family life. I was diagnosed this year, but was able to live a normal life until just before this. For that I am truly thankful.
I thank all those who are involved in research projects and those spearheading projects.