Long term injury
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Love Begins
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@littleelectric
Long term injury
guys you gotta stop thinking of women in their 30s as elderly it’s just misogyny
you also gotta stop thinking about actual elderly women as lesser human beings. Youth is not a measure of one’s worth.
Another Makoami collection dump
MWAH
This month people have been tearing Flock cameras off their poles.
This month people have been tearing Flock cameras off their poles. Perched above public streets, they are birdlike things, weatherproof, and they photograph every passing car and file it in a searchable national database. Somebody cut two of them in half at Washington Avenue and Westcott in Houston, spray-painted the wreckage, and left an American flag on one of them. Police were notified on the morning of the Fourth of July. Somebody severed a camera in Rutherfordton, North Carolina. The police department posted the photograph itself and collected more than twenty thousand comments. “Not all heroes wear capes.” “Give them a medal.” Here is what the cameras do when nobody cuts them down. Cops use them to hunt immigrants and to follow ICE targets across state lines and to find women who ended pregnancies in states where that is a crime and to watch exes and to watch women they want, without a warrant and without a judge. A cop types a reason in a box and the box does not check. A man in Burleson, Texas, told deputies his girlfriend had taken abortion pills. He showed them the photographs, the FedEx envelope, the instructions. Deputies opened a death investigation into a non-viable fetus, and the district attorney told them the state could not charge her, and they searched anyway: 83,345 cameras across 6,809 networks, a month of everywhere she had been. The reason they typed was had an abortion, search for female. The search reached Illinois and Washington, where what she did was legal. They found her in Dallas. She came into the sheriff’s office a week later, and they thought she had come to explain the fetus, and she had come to report that the man who called them had put a gun to her head. A sheriff in Jerome County, Idaho ran his wife’s plate more than seven hundred times in three months. He typed the same reason every time. Test. The attorney general found nothing to charge him with. He retired in April. The Institute for Justice counts at least twenty-two officers who used the system to track people they were romantically interested in, and calls that almost certainly an undercount. And the cameras keep falling.
Become ungovernable.
#sfw #artfight | For rainsonder of Nuru 💚👙🏐
Ill render this at some point but for now take this cat
Some Amy sketches
Wayfaring stranger
oh brother
Little Bingqiu fluff comic from brainworms
hello EDS people. calling all EDS people. especially if you live in Victoria, Australia like me.
what is the process of evaluation like? what kinds of tests do they do?
I have been informed that I should discuss this with my GP and get a referral to a rheumatologist(?). I have been ignoring this possibility for years but given that I had an actual nurse informally assess me and on the basis of that tell me that I should get it formally assessed, I'm actually thinking of getting the process started with the assumption that it will take a long time.
also, not to be flippant, but what's the point? what will I gain by getting my fun joints assessed? why should I care?
and yes, while I was told to ask specifically about EDS, I do not have enough information currently to know either whether I would genuinely meet criteria for any kind of hypermobility, or whether Ehlers-Danlos is even the kind of hypermobility that would be relevant.
@thebibliosphere i think from memory you have EDS? sorry for the ping but I just want to be faintly prepared before I go to my GP next week.
funny fact: it was actually a crisis assessment team psych nurse who was doing a holistic initial assessment and when I mentioned both ASD and potential POTS immediately asked whether I was bendy or not, then asked me to demonstrate specific joints. she seemed more interested in my bendiness than the "psychotic symptoms"... which were the actual reason I'd been referred to the CATT in the first place after coming out of the psych ward a few days earlier. I find this amusing. anyway.
I can’t tell you what the process of evaluation will be like for the area you’re asking about, but to address your “what’s the point?” point:
Ehlers Danlos Syndrome—and many other connective tissue disorders— affect Every facet of your health. From dental care to vascular health, to which antibiotics are safe for your tendon health, to straight up needing different types of sutures, anesthesia, and recovery care after surgery.
And that doesn’t even begin to cover comorbidities like POTS, MCAS, fibro, etc and general quality of life.
It’s also important to determine which type of EDS you might have because it can help with preventative care for your future based on the specific subtype. There are some very specific health complications that can occur and knowing if you have EDS can help you take preventative steps, but also hopefully ensure you get the care you need more quickly in the event something does go wrong.
I have hEDS and while my joints are garbage, it’s my immune system that’s more heavily impacted, as well as my internal organs which have tried more than once to become external of their own volition. I also had my Achilles tendon rupture spontaneously after being given an antibiotic (ciprofloxacin), which can affect connective tissue, even in people without Ehlers Danlos Syndrome.
To put it bluntly: it’s not just your joints, it’s all of you. And all of you deserves care ❤️
thank you! I will bring it up with my GP next wednesday for sure then. everybody cross fingers and toes for me (but gently. please do not overextend.)
also, in the process, should I specifically mention that my dad is Highly Suspect also for various of these things and I am casting an eye at him too? my GP is also dad's, and I've told dad before that there are certain things he should bring up to the doctor (e.g. his funky reaction to local anaesthetics that mean he's happier to go without than to have to suffer the weeks of agony that follow an anaesthetic that doesn't even help him), but he always just goes 'oh well' about them because he doesn't care enough about certain aspects of his health that he has decided do not matter. I'm assuming family history of flexibility is at least moderately important to mention, but none of us have a diagnosis of anything that I'm aware of. ...maybe I drop that on the family chat just to double-check my bendy sister hasn't snuck off and got her a diagnosis of something though.
I would yes. Amusingly, my diagnosis led to my mother getting a “this is very likely what is wrong with you” comment from a plastic surgeon following her double mastectomy, when her wounds just refused to heal.
I was on the phone to my dad during the doctor rounds while they were talking about wound care and I was trying to be like, “hey did anyone tell them I just got diagnosed with EDS.”
And suddenly I could tell the plastic surgeon had crossed the room because his voice, which had been much further away, was suddenly right there and he said, “say that again.” And I explained I’d been diagnosed with hEDS a few months before and you could hear the unspoken “son of a bitch!” In his voice, because if he’d known there was a history of EDS in the family, he would have done her surgery differently to accommodate her wound care needs.
So, yeah. Bring up family even if they’re unwilling or unable to get a diagnosis. My mother constantly having premature babies in the third trimester was apparently an indicator of connective tissue issues not being supported that to this very day she still blames on herself for drinking too much caffeine.
Family history of Weird Stuff matters.
Have a Monday Mourning for pride!
🍃wip
Shizun can never say no to Bingpup
new ocs ref yay
today i have a study for you guys