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Stress and Parkinson's symptoms
I think my symptoms are increased when I feel stressed.
We currently have visitors staying close by and the pressure I feel to think about their needs every day as well as our own seems to be making my symptoms worse.
I've noticed it also when I go for hospital visits.
Do others experience this?
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I understand. As of it isn't bad enough dealing with this disease, having to battle to get the care that you need and deserve is humiliating and draining. I hope that you have family and friends around you that will help you to navigate your way through it.
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1 ReactionAnd yes, I used to struggle with it when I was in the US and I'm sure that many others do as well.