Open post
disability, expenses, long covid, POTS
being disabled is always expensive (I have to pay more for things I can use instead of being able to do it myself), but here's an example of a cost that might not be obvious:
I have POTS (postural orthostatic tachycardia syndrome), which means my heartrate spikes when not laying flat
one tool used to mitigate some of the effects is compression leggings (from my ankles to the bottom of my ribcage), which were $30~40 for a decent pair...
which now doesn't compress my butt and torso very well because I've lost so much of my musculature over the last year of being bedridden
I've been contemplating having to get a new pair that fits a bit better, but I'm also unsure how long that would last
#Disability #Covid #LongCovid #MECFS #POTS
p.s. if you're not disabled, I need you to take in this information, use it to fuel your empathy for disabled people (you will join us one day, as a note), and act on that empathy 
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