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Hourly comics day, part 1/4: My health is at a low ebb at the moment (part 2 | 3 | 4 | all)
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
🧵 Another excellent blog by Fred Rossi who is well worth following
"The Patient Who Isn’t Supposed to Exist"
I taught Cognitive Behavioral Therapy (CBT) before Long COVID made me a patient. WIRED got the story exactly backward.
Nominally on the recent, controversial WIRED article but the points are pretty general.
"So the community is not a mob protecting a story. It is a population that watched a treatment paradigm hurt its own members and now flinches when the same machinery rolls out under a new name. That flinch is learned, and it was learned the hard way."
I love how people with chronic pain can be at extreme levels of pain and just be like “My body is ouchie”
something truly wicked about a disease that punishes you for perceiving the world around you, for thinking, for moving your body. me/cfs is more like a magical curse than an illness. it's something a warlock would cast on you
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
URGENT MUTUAL AID REQUEST
I’m raising money for my soul sister Arlen, who is very sick and lives alone. She has severe ME, CCI, hEDS, and a multitude of conditions caused by complications. She can no longer tolerate food, and she relies on donations to sustain herself with oat milk.
She has an appt on March 21st where hopefully they will schedule port surgery to give her access to TPN!
THIS IS WHAT SHE NEEDS TO STAY ALIVE. Without it, she will die.
BUT we need $250 urgently to pay a month of insurance debt or the appt will be canceled.
We have been waiting for this for years! We can’t give up now!
Click this link for her amazon lists and gofundme:
SAVE-ARLEN.COM
Venmo: @ArlenDaza
PayPal/Zelle: [email protected]
Cashapp: $ArlenDaza
What would you do if you could buy more time? My name is Arlen and I am fighting to bu… Arlen Daza needs your support for Help Me Fight
Please donate, and share, share, share!
We need to break out of our echo chamber.🙏🏼
And follow Arlen at @mienfermedadinvisible!
Will you dobate $10 today? The race is on to raise enough before it’s too late. We have 4 days!
This is the instagram post we made, you can help by commenting, liking and sharing it!
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I've been struggling with my energy level lately. There are never enough spoons. But block carving is something that I find I can often do even when my energy is low.
Save our support systems, save our science, save our society! My chronic illness, ME/CFS, is the most underfunded disease by disease burden in the NIH, leading to under diagnoses even of severe cases and no existing FDA approved treatment.
Two things you can do to help are...
sign this letter urging the NIH director to prioritize ME/CFS research: airtable.com/appEwdLZCdtR...
and/or donate to MEAction's SOS fundraiser: www.meactions.org/millionsmiss...
I wish I had been able draw something nicer, but this is what my energy level and cognitive function are up to today, and with my parents out of town for a week now, taking care of more essential things have been the priority lately.
