eg
Share experiences with people who may be having similar difficulties.
Be able to gain access to group therapy and exercise.
Have speakers who have relevant information for people with Parkinson’s, examples would be research, living aids exercise.
Or just a social place to meet and put less relevance on Parkinson’s.
1) Speakers with relevant info, positive news.
2) Info on clinical trials
3) Birds of a feather sharing.
Have speakers who have relevant information for people with Parkinson’s, examples would be research, living aids exercise.
Social place, new advancements, share experiences with others
Thank you. I think there all important too, but getting the balance right is difficult
MichaelSquire: Good point about location of support groups. Real problem for those that cant drive, meaning spouse/friend/relative must also participate. Not a bad idea, just hard to implement.