KATHYJWHITE
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Living with MSA (Multiple System Atrophy)

Things Have Changed

5/12/2020

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Well, COVID-19 certainly has changed a lot of things.

My carefully-constructed "house of cards" has been blown to hell. Years of ideas and solutions... poof!

Managing the needs of a pandemic is challenging, especially in a wheelchair with limited fine motor skills.
​Even gloves/face masks and washing hands is difficult and time-consuming. Lots of good reasons to stay home...

Items may not be available, meaning a wasted trip or more deliveries. Both are hard on a limited budget.
Handibus is on essential service. Boy, that makes staying home easy.
Gym/pool is closed which means exercising at home.
FCSS support is cancelled. Very slowly clean, change bed, do dishes. Garbage piles up.
Library is closed. TV is re-run extraordinaire. Finding new ways to entertain myself.
Social media is dire, full of experts, wanna-be stars, scams and fix-everything cures
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    Kathy White was diagnosed with MSA-C in Jan 2005. The creator is not a doctor or health care professional. This site reflects her own opinions and experiences.

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