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@magebastard
writing tag for pinned post srry

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hi! carey means needs help still - he's the voice actor for frylock in aqua teen hunger force! adult swim screwed him badly and pays no residuals and barely paid him during the show's run. he has heart failure and survives on con earnings, plushie sales, and donations while waiting for disability to get back to him. posts used to make the rounds for him, but haven't in a while, so i wanted to make a new post!
if you'd rather buy a plushie - here's the shop he and his wife run!
update: CAREY MEANS AND HIS WIFE ARE HOMELESS AS OF A FEW DAYS AGO
his wife also been in an accident and has been down and out due to illness and injury
ppal + gfm + site shop
whenever i complete chores i get an achievement banner pop up in my head dark souls style
Please, please, look at my donation campaign and help me. I have newborn children and my son Ahmed needs treatment. He is a heart patient and suffers from two holes in the heart. He needs help and treatment. We do not have money and we are stuck in Egypt because of the Gaza war. My wife and I lost my jobs and there is no source of income. I would like you to help. To care for my children and provide the necessary treatment for my child Ahmed, please donate even a little thing to save my child’s life
I write to you with a heavy heart 💔 My children and I are going through very difficult times, and no one is asking about us. My son needs treatment and medication, and he needs milk, diapers, and urgent care. Please don't leave us alone in these difficult circumstances. 😔
We need your help. The situation is extremely difficult. You are our last hope. Food, clothes, milk, rent—everything has become incredibly expensive. My son, Ahmed, needs heart surgery and eye surgery. Please help my son so he can complete his treatment and undergo the operations. In addition to my family in Gaza, my parents, brothers, and sisters are also living in dire circumstances. Please help me for the sake of my family.
My name is Sharif, and I suffer from a back injury. I need intensive treatment and physical therapy to recover. Unfortunately, we lost everything in Gaza; we have no income and cannot work. The situation is extremely difficult.
PLEASE HELP 🙏🏽 EVEN A SIMPLE REPOST AND COMMENTING CAN MAKE A DIFFERENCE!
Hello, I'm Sharif Al-Amoudi from Gaza. I'm married and have twins, Hussam and Ahmed, who are five months old. They were born after four atte
https://www.tumblr.com/sar-soor/800243879780761600?source=share
https://www.tumblr.com/nabulsi/777393943645208576?source=share
https://www.tumblr.com/90-ghost/768348012370100224?source=share
https://www.tumblr.com/a-shade-of-blue/777485404670656512/this-fundraiser-has-been-shared-by-nabulsi?source=share
Please donate to this family if you have the means to at all, anything you can give will make an impact and is absolutely worth it even if you can only afford to contribute a small amount, and be sure to reblog this post with tags so more people can see it and donations can keep being made consistently!
shariff had to restart the campaign from the beginning because gfm closed down his previous one, so please donate to the chuffed link.
Let's help the Al-Amoudi family out! Their campaign is at 2%
He was given artificial oxygen and needs special care, surgery, and numerous treatments at great expense. He now needs special milk and medi
Every reblog helps if you cannot donate!
Verifications:
@/90-ghost here (Old GFM)
@/a-shade-of-blue here
@/nabulsi here
@/virovac here
Every reblog helps if you cannot donate even a small amount. Do not let them feel unheard!
The campaign has slowed to 2,4% But we are gratful to those who have contributed since our last round. Thank you for your kindness!
I heard another video game is coming out soon
this has to stop

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I just ate one
You can lie when you name things
i’m really struggling lately! but i’m alive and i have yogurt
I will have a life beyond these bad days
We have started this GoFundMe to help support the family of Cyrus Carmack-Belton and … Todd Rutherford needs your support for Justice for Cy
the upcoming civil case is going to be his family's next chance at legal justice, but the legal feels are going to become TREMENDOUS
Lesbians are the only hope
Pride Parade, San Francisco, California, 1970s, by Judith Shane Hoth. (source)

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i coul dnever be the captain of a ship. everyday id be like third lieutenant ..... do a backflip lol
Long COVID patients can experience severe energy crashes after physical exertion. New research provides clear evidence that there's a biolog
Full Transcript at the link; 3-minute listen.
Quote:
By taking biopsies from long COVID patients before and after exercising, scientists in the Netherlands constructed a startling picture of widespread abnormalities in muscle tissue that may explain this severe reaction to physical activity.
Among the most striking findings were clear signs that the cellular power plants, the mitochondria, are compromised and the tissue starved for energy.
"We saw this immediately and it's very profound," says Braeden Charlton, one of the study's authors at Vrije University in Amsterdam.
The tissue samples from long COVID patients also revealed severe muscle damage, a disturbed immune response, and a buildup of microclots.
"This is a very real disease," says Charlton. "We see this at basically every parameter that we measure."
I feel insane seeing stuff like this because this research already exists for Myalgic Encephalomyelitis, a post viral condition caused by multiple types of viral infections that a LOT of people with "Long Covid" meet the diagnostic criteria for.
This article mentions that ME/CFS is a "similar complex condition" but that's DEEPLY underreporting the similarities. The phrase "post exertional malaise" (now researchers are trying to replace it but this article uses that phrase) was INVENTED for ME/CFS. It's the only known condition, before "long covid", that causes these kinds of symptoms after exertion!
It's good to know for sure that it's the same mechanisms at play when the inciting viral infection is Covid and not, for instance, Epstein-Barr or RSV, but half the time it doesn't seem like researchers are making comparisons at all, just reinventing the wheel and acting like "long covid" is a totally new phenomenon with no previous point of comparison. There are literally drugs in human trials to try to treat the mitochondrial dysfunction in ME, this dysfunction is well-established and fairly well understood and I feel insane when ppl report on long covid without mentioning that there is already a named and studied condition that accounts for this subset of symptoms!!
SOME researchers are drawing comparisons but they're largely ME researchers who everyone else is largely cignoring because of the widespread perception that ME is a fake disease for lazy women.
That same perception btw is why "graded exercise therapy" (GET), or exercise gradually increasing in intensity, cwas for years the go-to treatment despite MOUNTAINS of evidence that it makes ME patients sicker. Some end up permanently bedbound and unable to even eat or drink without a feeding tube/IV because the damage is so bad! The GET recommendation was finally changed only in the past few years in the US and the UK, and many doctors hate that they're not allowed to recommend it anymore, because they insist despite the evidence that ME/CFS is psychological and ME patients are just "deconditioned" and too lazy to do anything about it.
Now the same kind of "treatment" is being recommended for long covid patients despite evidence showing exercise is having the same kinds of cellular effects as it does in ME patients. "Taking PEM into account" sounds gentler but I'm deeply concerned about the reinvention of GET for patients who meet all the criteria for an illness that's been shown definitively to become permanently worse with GET. This mitochondrial damage is progressive in ME, and there's no reason to believe patients who meet all the criteria of ME after Covid won't experience the same progression if they force themselves past their energy envelope in such a systematic way.
The additional finding that T cells — part of the immune system's arsenal — had infiltrated the muscles of long COVID patients also caught Iwasaki's attention, possibly indicating "an autoimmune response within the muscle cells."
This autoimmune response is well-researched for ME. Every time you overexert, you're injuring your cells more and more. It's deeply worrying that rebranded GET is being recommended for long covid patients who meet the criteria for ME when research like this study keeps showing it's the same phenomenon.
I have three beverages advising me at all times
goodbye straight people
this is the vibe i bring to the party actually

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