Atypical type of Parkinsonism, rare, no meds currently to treat, very progressive.
My wife is being placed under this PSP, primarily because she does not respond to normal medications used for Parkinson’s. Not a pretty picture as symptoms develope faster and more severe. Life expectancy is cut drastically. Can I get feedback from others that may be experiencing the same.
No but getting a DAT scan to see if I have MSA