It is the first barrier to understanding. The ME alone almost nobody - i can’t count the doctors - recognizes or understands. And the CFS has so much diminishing stigma attached.

thank you this is so useful - both the individual anecdotal experience and the data. so important to remember if you have me/cfs - a medicine or treatment can always hurt more than it helps. thinking that way is not pessimism, it’s self preservation

now THIS is some company to be in!!

that says everything. *sighs and groans in woman*

this is beautiful! now i need to look up/ buy French Girl

also ME/CFS! was AFAIK the biggest trigger pre-covid. and reactivation with long covid…

thank you!!! screenshotting this and going to start playing

would love that! off to check if i have the most updated app…

yes, i have the apple pencil pro! do you have any favorite brushes you’d rec? i’ve just been choosing pencils and pens and paintbrushes at random

i do have an ipad! i’m still trying to figure out what presets to even begin with, how to get any kind of handle on line weight and pressure and also whether being a lefty has anything to do with my incompetence there

just checked your profile - your work is great!! i have only dipped the tiniest toe into digital art, am so intimidated by all the settings I don’t understand. Do you use procreate?

The biggest shocker? I haven’t been seeing in 3D. Hard to draw depth if you can’t see it! #mecfs #longcovid #dysautonomia

I got a migraine from trying to draw a maple leaf. Which led to the discovery of SEVERE binocular vision dysfunction. My eyes are now very misaligned, and my brain has been shutting one of them off.