hope today has been better for you and that you are getting the support you need.
my husband has parkies, not me, but he doesn’t do much internetting and I can only speak from our experience over past 9 years.
Parkys brings good and bad days or hours, we know stress and anxiety has the biggest effect on him and can block the action of his meds. But we don’t let parkys stop us doing stuff tho sometimes it makes things trickier. Last year we found the European Parkinson’s therapy centre in Italy, we haven’t anywhere like it in the uk tho some areas have first steps programme for newly diagnosed and that contains some aspects of Italy’s work. It was enlightening, empowering and hard work but it did improve his symptoms and we went back recently for a top up/kick up the backside to do the exercises!
diagnosis is a shock and it takes time and Italy’s therapy is informative and positive, oh so positive, ran by a lovely guy with parkies.
Check them out and go if you possibly can, I wish we had found it years ago!
There are are few postings on here from folk that have been.
stay strong, stay positive, keep active.
all the best x