Pray and Compose Poems! @vegypower.bsky.social

"Tyranny requires constant effort. It breaks, it leaks. Authority is brittle. Oppression is the mask of fear. Remember that."

Looking forward to seeing Jimmy back on the air.

I'm "Sewin'" Love with Sweet Gracie!😻🧵🪡

“People in the community who are bed-bound know that if they can’t mail in a ballot, they’re not voting. You’re basically depriving people of their citizenship rights.”

#MEAction board member @jenepgh.bsky.social shares in @juliametraux.bsky.social latest disability coverage for @motherjones.com.

Gracie on the prowl while I nurture a thirsty paper wasp with water and creamed honey.

The truth here is so ever relevant, is so simple and profound. I think I might pop it into my next book. Sharing yet again:

Strange interaction on BlueSky last week has me like...

My submission for 'Most Scenic Dual-Dumpster Location Across the Nation'

Despite the enormous disease burden ME/CFS and Long COVID present worldwide, afflicting 275+ million people, there is still no FDA-approved treatment. Finding effective therapies to relieve people’s suffering is critical. Heck, we don't even yet have molecular diagnostics. #MillionsMissing #Cat

Check out this essay by Violet Affleck - "A Chronically Ill Earth: COVID Organizing as a Model Climate Response in Los Angeles." Impressed with the understanding of ME.

yaleglobalhealthreview.com/2025/05/18/a...

#PwME #MECFS #MyalgicEncephalomyelitis #LongCovid #PublicHealth

#MEAction is sending an urgent letter to the newly appointed National Institutes of Health (NIH) Director, Dr. Jay Bhattacharya, calling for the NIH to allocate $50 million to fund the ME/CFS Research Roadmap. Sign & share: bit.ly/MEcfsRoadmap

#pwME #NIH #MyalgicE #MECFS

We are winding down our day of #MillionsMissing action but just starting a week focused on creating change! WOW! You are blowing us away with the amazing shares on social media and we are beyond grateful to all who showed up in person in DC and at actions around the world.

#DisabilitySOS

May 12th is Myalgic Encephalomyelitis Awareness Day. On this day, the millions of people with myalgic encephalomyelitis (#MillionsMissing) gather to demand recognition, research and clinical care for people with ME. #SolveME

Massive sit in/lay-in,
Berlin, Germany today, bringing awareness to the deadliness and lack of options currently available for treating or curing ME/CFS. #MillionsMissing #SolveME #OMF

www.meactions.org/millionsmiss...
I've been absent from career, hobbies, weddings, funerals, graduations, reunions, volunteer opportunities and everything else that adds meaning to our lives for more than five years.
I don't want your pity, I'd like your understanding.❤️‍🔥 #MillionsMissing #SolveME

@nateslongname.bsky.social