@m-e-isannoying @liebelesbe
AnasAbdin
Xuebing Du
he wasn't even looking at me and he found me

Kaledo Art
Lint Roller? I Barely Know Her
occasionally subtle
Claire Keane

⁂
RMH
Sade Olutola

pixel skylines

JBB: An Artblog!

titsay
ojovivo

shark vs the universe

we're not kids anymore.
NASA
noise dept.

seen from Australia

seen from Türkiye

seen from T1

seen from Argentina
seen from United States
seen from United States
seen from Germany

seen from United States
seen from United States
seen from Switzerland
seen from Italy

seen from United States

seen from Germany

seen from United States

seen from Türkiye

seen from Malaysia

seen from Malaysia
seen from United States
seen from United States

seen from Australia
@neco117
@m-e-isannoying @liebelesbe

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Tom Hiddleston talks Teddypine on The Ankler
they really don't respect the time of disabled people. your application can take up to 12 weeks. the specialist waitlist is 3 years. your assessment will be any time within the next 6 months. let us know if you cannot attend this appointment you waited 7 weeks for and we'll reschedule next year. we've decided to assess you at this time and day and you have to be available or any support you dared to apply for is not going to happen. and in between these long bouts of waiting you have to survive the everyday
as the one and only surviving member of this fandom, here is one of about ten carry-on edits ive made this month because im coping with the fact that literally nobody actively cares about this movie anymore sadge
Das ist das erste Mal, dass es jemanden mit ME trifft, den ich persönlich kenne. Danke, Kim, für Alles 🖤
Das ist die 4. Todesnachricht aus der ME-Community in der vergangenen Woche. Viele dieser Tode wären durch ausreichende Versorgung und Aufklärung vermeidbar gewesen.
ME (Myalgische Enzephalomyelitis, unvorteilhaft auch ME/CFS genannt) ist eine schwere, chronische, neuroimmunologische Multisystemerkrankung, die zwar schon seit 1969 von der WHO klassifiziert ist, aber zu der wenig geforscht wurde und absolut keine Versorgungsstruktur existiert! Wir sind in Deutschland über 650.000 Betroffene (Stand 2024 - da ME vor allem durch eine Vireninfektion ausgelöst wird, sind die Betroffenenzahlen durch die Corona-Pandemie in die Höhe geschossen. Es kann also wirklich jede*n treffen) und es gibt keinerlei anerkannte Therapien und Medikamente. Es wird im Liegen demonstriert, um die Situation vieler Betroffenen sichtbar zu machen. Einige sind so schwer erkrankt, dass sie bettlägerig im dunklen Zimmer sind, kaum noch Nahrung zu sich nehmen können und auf 24/7 Pflege angewiesen sind. Das Kernsymptom von ME ist die post-exertionelle neuroimmune Entkräftung (PENE) - eine extreme Zustandsverschlechterung nach jeglicher Art von Belastung. Weitere Symptome sind Brain Fog, Muskelschwäche und Muskelschmerzen, Nervenschmerzen und Kopfschmerzen, Schlafstörungen, extreme Erschöpfung, extreme Reizempfindlichkeit und viele mehr... Mit ME ist dein Leben auf’s Kraft einteilen ausgelegt; wirklich alles dreht sich darum. Da ME aber immer noch sehr unbekannt ist, werden viele Menschen gefährlich fehlbehandelt und landen beispielsweise durch eine Reha in der Bettlägerigkeit. Durch Aufklärung könnte man dies verhindern. Training und Aktivierungstherapie ist Gift für Menschen mit ME!
Wir brauchen dringend flächendeckende Aufklärungskampagnen, Kompetenz- und Informationszentren in jedem (!) Bundesland, Forschungsgelder, Anerkennung von ME als extrem einschränkende, körperliche Erkrankung seitens der Krankenkasse und Behörden, niedrigschwellige Möglichkeiten für Diagnose und Betreuung, etc…

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Just some Stargate memes to brighten your day
nooo youre so sexy please don’t speak as though chronic fatigue and ME/CFS are the same entity. nooo please ur falling prey to a common misunderstanding. the generalised symptom of chronic fatigue can occur in anybody for many varied reasons from burnout to cancer to vitamin deficiency and is different to the distinct condition of ME/CFS which is a specific organic entity featuring the hallmark symptom of post-exertionsl malaise and complex additional symptoms and requires a totally different treatment approach compared to other types of chronic fatigue unless you want to risk causing long-term damage noooo lol
i’ve seen some people (both on here and ig) minimizing ME/CFS like it’s no big deal (like how fibromyalgia was and still is treated) and if you think that, sincerely fuck off. and to do that during ME/CFS awareness month? cruel. after a man with very severe ME/CFS DIED? horrid.
ME/CFS is an extremely debilitating systemic disease with lethal potential. pwME have an extremely low quality of life and no approved treatments. the majority of people never recover.
take it seriously. this isn’t the “i’m tired” disease.
tag transcription: #saw someone call it “very treatable recently #like what planet do you live on /End
this was one of the things i had in mind when i made this post. i would LOVE to live on whatever planet where it’s ‘very treatable’. instead i’m being evaluated for palliative care. it’s such a punch in the gut.
i’m used to doctors and abled people not caring about ME, but seeing other disabled people not take it seriously is disheartening.
the ME awareness slogan being Millions Missing, 25% of pwME being severe-very severe, mild ME being a 50% reduction in function, that sure implies ‘very treatable’ i guess. /sarcasm
ME/CFS has such a horrifying multitude of symptoms - calling it "chronic fatigue" or "just tired disease" is ... Wild.
Also what treatment? The meds that try and fail to keep at least a few of the symptoms under control? Or maybe the scams that try to press as much money out of us as we have?
James Moriarty + what to call Sherlock Holmes
WTF, WTF, WHAT THE ACTUAL FUCK!!!

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'For someone, finally, Teddy is enough. That's something really important. Teddy is never enough, not to himself, not to Roxy, not to Roper. He's always wanting more, reaching for more, until that moment when he realises he's just enough.'
'They realise very early on that they'll need each other. They become a mirror for each other. There's this mutual need and a mutual curiosity and a mutual fascination, but it’s coming from a soul connection that they don't fully understand yet.'
- Diego Calva and Tom Hiddleston for The Antler.
GAYS WHAT EVEN IS LIFE TODAY
here's where to find it on windows 10
Ugh, it was in mine. It's off now.
IT GETS WORSE
I had to turn this off, but it's something that allows Windows and anyone using your device to generate text/images.
LOBOTOMIZE YOUR MACHINES
AI is a freacking plague, I share this for any windows user.
#Pride Month Headcanons for Sherlock & Co:
Sherlock: he’s gay and ace, the kind that’s so obvious he doesn’t feel the need to explain it. He just expects people to already know. The only time he ever verbalized it was when John still hadn’t realized, and Sherlock got irritated by how slow he was.
John: He’s a late-bloomer bisexual in his 30s who, ironically, is having his bi awakening with his best friend’s brother. It’s not full-blown passion or anything, it’s more like yeah mate Mycroft is hot, tall, and attractive, we get it.
Mariana: She’s a very self-assured bisexual. She has A LOT of crushes on both men and women, but she’s not really interested in a serious relationship right now. She probably prefers something more casual. She has a thing for a few people at Scotland Yard (cough, Gwen? Tom? Lily?)
Mycroft: I could say he’s gay, but in this specific adaptation he gives off the vibe of a very promiscuous bisexual.
Moriarty: Gay. Capital G-A-Y. That ass belongs to a gay man in every universe.
Gwen: A butch lesbian, divorced, who keeps her relationships very private and discreet.
Stammo: A very supportive straight guy who used to kiss his guy friends at college parties sometimes.
There are still many characters missing, but these are the ones I can think of right now
superbat yay
airplane ears were my favourite thing to draw

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Seemed like a good way to cap my latest sharing of ShanksRants™️