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lavivianaleyva.bsky.social
@lavivianaleyva.bsky.social
Chronic illness. ME (Myalgic Encephalomyelitis) Dysautonomia.

And cats, always cats.
Thank you, I did. And thankfully it didn’t lower my baseline.

People have no idea what we go through
April 10, 2025 at 8:27 PM
Reposted
“Our collective spoons are our greatest asset!” We each are limited but together we have power👇. Do what you can, rest, pace, and stay focused, friends.

Y’all are awesome! Keep it up!👏👏👏
/end
March 28, 2025 at 4:22 PM
I understand completely
April 5, 2025 at 10:41 PM
Reposted
Rule of thumb for shooting at a protest, capture the crowd, not the people.
April 5, 2025 at 7:19 PM
For some of us it is hard. I absolutely agree with what you’re saying, and the need for Alt. Text, but saying it’s not hard is ignoring that many of us with brain fog and low spoons it can be. Just keep that in mind please.
I avoid posting pictures now when I can’t.
April 5, 2025 at 7:30 PM
Reposted
Thank you @scishow.bsky.social for putting this together.

#MECFS is probably the:

- most common (1 in 100)

- extremely disabling illness (worse quality of life than most conditions even cancer and chronic kidney disease)

- people know next to nothing about (only 6% of med schools teach it.)
Exercise Actually Makes Chronic Fatigue Syndrome Worse
YouTube video by SciShow
youtu.be
February 20, 2025 at 7:19 PM