The Parkinson's You Don't See: Cognitive and Non-Motor Symptoms 

19 years post-diagnosis, this is still so helpful to hear. most of my symptoms are these type--not the usual obvious motor symptoms. this is a very good summary!! THANKS!

Wow! Every word was helpful and hopeful! You spoke to me as the caregiver and to my husband as the patient. Without knowing it, you even described our first-and less than competent-neurologist. Please keep these coming. Thank you for informational and encouraging words.

Thank you😊

Very well done! It's hard to find those words... I know.

Thank you so much for this -- and I will say, it's not just Parkinson's. I have MS and while I was diagnosed only five years ago, I have had symptoms for nearly thirty years (I'm 52) and almost all of them haven't been motor but cognitive and emotional and other non-motor physical symptoms. It took a motor symptom (a numb leg) after years of other issues and being told it was all in my head to finally get an MS diagnosis. And although I currently have excellent care and medical support from the best in the region, these top-end experts still don't really recognize anything beyond the motor symptoms. So thank you and please keep spreading the word.

Pretty much everything which largely eats up my time, besides just what all I need to get done. Whatever my body is doing interrupts me continuously. A larger problem to me seems to be a culturally developed set of unrealistic social expectations that are more and more off the rails every day, for just everyone whether they are chronically ill or not. The demands are more than 25 times as much in my estimation

Some say I have Parkinson some say MSA....all my test are on the fence .....how do I know....symptoms tell nothing I have the same for both evidently...... Anyone have any insight?