georgina (@geolouwill) 's Twitter Profile
georgina

@geolouwill

25• theatre maker • Disabled, neurodivergent & queer • ME/CFS and POTS since March 2020 • she/they

ID: 1080957173843275777

calendar_today03-01-2019 22:40:48

1,1K Tweet

717 Followers

451 Following

georgina (@geolouwill) 's Twitter Profile Photo

right-wing politics are so reactionary. something happens and they all scream and rage and build their entire personalities and policies around it, then a few days later, something else happens and they all move on. in a few days, they'll all have forgotten charlie kirk existed.

🇵🇸 (@nnnnnnxox) 's Twitter Profile Photo

If you've read this article, please share this link. This surrogate is being sued for the death of a baby and has immense legal fees. Please show up for this woman as you did when reading the article!!

If you've read this article, please share this link. This surrogate is being sued for the death of a baby and has immense legal fees.

Please show up for this woman as you did when reading the article!!
Disability News Service (@johnpringdns) 's Twitter Profile Photo

The proportion of working-age disabled people in England who are “economically inactive” is not “spiralling” and may even have fallen over the last nine years, new official government statistics suggest. #DWP disabilitynewsservice.com/government-rep…

BLACK STAR Ⓐ 🌍 (@blkstrmutualaid) 's Twitter Profile Photo

The cognitive dissonance is very real . I just went through a community health program this summer where nobody masked but me and we were talking about HIV and it was really wild to see the parallels between the aids crisis and now but see ppl in community health (1/2)

georgina (@geolouwill) 's Twitter Profile Photo

I was 19, now 25. I have a twin brother and in that time he has: - graduated university - got a girlfriend - got a good job - moved in with his girlfriend - (lost his job) - found another, better job - bought a house - adopted cats We are missing out on so much life.

Jack | amatica health (@jackhadfield14) 's Twitter Profile Photo

You never grasp just how sick someone can become until you witness severe ME/CFS. At my worst I spent a month blindfolded with ear defenders, lying still, able only to sip water and take small amounts of food when I could digest. And others endure way worse.

georgina (@geolouwill) 's Twitter Profile Photo

My uncle has had "flu" for 2 weeks. Only it wasn't flu, it was a haemorrhagic stroke and now he's in the ICU. Do not dismiss symptoms. All he had was severe fatigue, dizziness and headaches. His wife only took him to the doctor because he started becoming confused.

sarah 🚩 (@ratherbeinpisa) 's Twitter Profile Photo

where is the fucking outrage? this is the UC rate for the sickest most severely disabled people who are so ill they cannot work - they CANNOT make up the difference. i warn you, DO NOT get sick, DO NOT become disabled; Starmer's government will starve you.

where is the fucking outrage? this is the UC rate for the sickest most severely disabled people who are so ill they cannot work - they CANNOT make up the difference. i warn you, DO NOT get sick, DO NOT become disabled; Starmer's government will starve you.
DWP Spin Decoder (@leith1076) 's Twitter Profile Photo

There is no "moral case" for threatening and starving disabled people into jobs they are unable to do, that don't exist and that don't want them.

Amy (@alexandrite113) 's Twitter Profile Photo

Almost 6 years ago I caught COVID. I have spent the last half of my twenties bedbound. I need a wheelchair for occasional Dr appointments. My doctors have told me my quality of life is similar to that of an end stage cancer patient. We need treatments. #LongCovidAwarenessDay

Almost 6 years ago I caught COVID. I have spent the last half of my twenties bedbound. I need a wheelchair for occasional Dr appointments. My doctors have told me my quality of life is similar to that of an end stage cancer patient. We need treatments. #LongCovidAwarenessDay
Paul Whiteley (@paulwhiteleyphd) 's Twitter Profile Photo

And a reminder that stuff that says people can 'think their way out of' this devastating illness or that 'it's all just deconditioning' has served no-one well. ME is a biological illness and progress along those lines, although slow, is being made.