My consultant has recently changed my diagnosis from Parkinson’s to MSA-P. I think many people also refer to this as Parkinson’s Plus.
I have found a few Forum threads on it, but they are all very old. I’ve also looked at the MSA Trust website.
However, it would be lovely to speak to anyone who has experience of MSA as there are so few of us and it’s a daunting diagnosis.
Hoping someone is out there and feels like contacting me!
Take care, all.