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Hello all,

Since my mom was just diagnosed last Spring and I am relatively

new to this site, I am really just beginning to learn about MSA. Mom

has a good neurologist and primary care physician. I am in regular

contact with her physician and I sometimes wonder how much she

knowledge she has on MSA. She regularly refers to my mom's

" Parkinson's " rather than calling it MSA- am I being too sensitive?

I am under the impression that people diagnosed simply with

Parkinson's disease don't have such acute and serious symptoms as

people with MSA. From what I've read, people with MSA may have a

shorter life expectancy and may need many more services/special

equipment than the average person living with Parkinson's.

Feel free to offer any words of wisdom on this subject (lay

terms rather than a heavy scientific explanation would be more

helpful for me at this point!).

Many thanks, Noreen S (myweller) in CT

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