When PSP is diagnosed, and cognitive decline is mentioned, how did the nuerologist explain it to you?
TLDR: How has cognitive decline looked for your loved one or you with PSP? I am trying to understand what to anticipate with my mom.
Context for why I’m asking: There have been some patterns with her speech. She sounds out of breath when I talk to her, but when I’ve done oxygen levels at her primary, her oxygen is in a good range and indicates no issues. Is this apart of PSP as well? When I find videos online, a couple people seem to be speaking in this spread out cadence that sounds of breath, with very few words. I’m worried if I should anticipate for dementia.