Witchy 🔮
@witchurst
Guided by the moon, governed by karma. Armchair traveller, dreamer, nail artist, gamer and mum #pwME
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ME left me bedbound for nearly five years. A potted plant helped me rebuild my life theguardian.com/society/2024/o…
You could say this at literally anytime but now would be a GREAT time for Australia to have a bill of rights.
Australian petition. Please sign/share no matter where you are in the world. We need so many changes, including update of 21 year old med guidelines & removal of #GET/#CBT, Dr education, research $, specialist centres for patients with Very Severe #ME… change.org/p/harm-caused-…
Help us find new donors by sharing this post and asking your people to book an appointment at donateblood.page.link/q4JL #lifebloodau
Imagine If China Did To The US What The US Is Doing To China "Your brain would have to be made of soup not to look at that graphic and understand who the real aggressor is here." caitlinjohnstone.com/2023/02/19/ima…
Australians Aren't Allowed To Know If There Are American Nukes In Australia "It's assumed to be none of Australia's business whether there are foreign nuclear weapons in Australia." caitlinjohnstone.substack.com/p/australians-…
🔴 The Game On Cancer team is live playing Fall Guys and Rocket League to kick off the #HolidaySpectacular ! Join @Magic_Casts, @QueenMorgie_ and @juxti24 to raise funds for cancer research! Come say hi 🥰 twitch.tv/gameoncancer
A share of the responsibility for what has happened needs to land with the Australian government which passed laws during the height of the war on terror requiring telecos to police purchases and store copies of driver licences + passports when the consequences were obvious. /15
And it's 1 2 3, What are we fighting for? Don't ask me, I don't give a damn, Next stop is [anywhere]; And it's 5 6 7, Open up the pearly gates, Well there ain't no time to wonder why, Whoopee! We're all gonna die. #fuckwar
New video: What is ME/CFS? A brief overview of symptoms, diagnosis and treatment based on the 2021 NICE guideline. Its not being tired all the time, patients have an energy impairment that dramatically limits their activity.
Okay so, thread of ALP showing their true faces, because it's annoying trying to hunt down the same screenshots over and over to answer the same tired dribble over and over.
We just want our lives back, or something that resembles a life at the very least. Severe ME is a torturous living death. #MyalgicEncephalomyelitis #SevereME #severeMEAwarenessDay #MEcfs #LongCovid #LCME
An artwork I created a few years back expressing what #SevereME feels like to me. The ME you don't see... #pwME #MEcfs #LongCovid #LCME
12th May is #MEAwarenessDay all across the globe. For decades #pwME have been neglected & suffered gaslighting by many doctors & others in the medical field, the community at large, friends & even family. These are the ‘Facts about #ME in Australia’.👇 meaustralia.net/wp-content/upl…
This is massive. The govt is approving the destruction of habitat relied on by threatened wildlife at an increased pace, despite scientists warning of an escalating extinction crisis😥🍃 theguardian.com/environment/20…
The US Has Zero Moral Authority "To be a westerner is to be continuously inundated with made-up stories about evil tyrants who want to terrorize the world while living under a vast empire that is actually terrorizing the world." caitlinjohnstone.substack.com/p/the-us-has-z…
Managing Myalgic Encephalomyelitis is not doing nothing. People with ME make 100s of micro decisions every single day, striving to gain some freedom from limitations they don't control. #meawarenesshour
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