When I was 15 I had an urine infection for a week or so. 6 months later I was still exhausted and in pain all the time and was diagnosed with Chronic Fatigue Syndrome (as the NHS had just changed the name from Myalgic Encephalomyelitis, though now they're used interchangeably).
Video of Karen Gordon filmed on 8 Mar 2025 at Conquest Hospital Hastings UK. Please share with as many people as you can. Karen has very severe ME & has been in hospital for over a year. Please sign our petition to try to save Karen https://t.co/myZMK0Nolw
Karen Heather Michael
@TheSims While The Sims 3 will always hold the biggest space in my heart, my primary memory of The Sims was with the first game when one of my Sims starved to death by being trapped in a public bathroom due to a busker standing in the doorway. #TheSims25Giveaway
I'm giving away SEVERAL #TheSims4ForRent codes!
✨ Like, comment & retweet
✨ Follow me on Twitch, YouTube & TikTok
✨ Tune into Twitch on December 7 & 8
I'll be checking for your following proof at the time of drawing 😈
Good luck!
#SponsoredByEA#EACreatorNetwork
@zefrineTTV Unfortunately I miss a lot of your streams due to time differences and chronic illness, so not always able to 'tune in' on certain days. Doesn't help that twitch notifications don't work properly.
💜GIVEAWAY💜 Thanks to the #EACreatorNetwork I’m giving away one code for the Sims 4 For Rent Expansion Pack!
How to enter:
💜like & retweet this post
💜subscribe to https://t.co/LNpJ7XolcO and comment a pic
💜winner will be drawn on Dec 7th
PC/MAC only! 💜
#SponsoredbyEA
@WheelieGoodLife If he does have a child with additional needs I feel sorry for that child, as has to live, and probably depend on, someone who clearly thinks his stuff and convenience are more important than another human being's right to independence.
The rollout of new charging points for electric vehicles is stripping vital pavement space away from pedestrians and wheelchair-users, two campaigning organisations have warned the government.
#ElectricVehicles#ChargingPoints
https://t.co/H5kVzIwSpf
Mild ME is only ‘mild’ in comparison to moderate/severe ME. Mild ME in comparison to a healthy/non-disabled person is life-altering. I was mild when I had to stop working, it didn’t feel mild. Now that I’m severe, I look back and wish I was as mild as I was then. #MEAwarenessHour
Todays travel access fails:
- Refused access on a train because people had put suitcases or were standing in the wheelchair space
- No ramp so wheelchair was carried off the train with stranger transferring me
- Left not knowing what in the world was going on. Again.
@JustEatUK How would that possibly help with you including an option for plastic cutlery (as an extra, paid for if necessary) from the restaurant, rather your website stating you no longer allow it?
@JustEatUK I understand wanting to limit waste, but preventing us from requesting plastic cutlery means options become limited when someone doesn't have access to some (such as being on holiday, in the middle of moving, etc).
@adamfare1996 I no longer have the energy to care what other people think. No matter how I respond to being in pain 24/7, extreme fatigue, loneliness, etc, I can't win. And I have such little energy it needs to go into surviving til tomorrow.
The study showed that recommending people wear masks (not whether or not that wore the masks) didn't make a clear difference in symptom based Covid. Maybe fact check your studies before sharing them out of context. #WearAMask
https://t.co/3WMx5i5sHI
@CircleBackG1rl@Derek_a_Franks Thanks for sharing misinformation that makes you feel better about enforcing permenant lockdowns on disabled/chronically ill/vulnerable people such as cancer patients. https://t.co/ROOW2eiKvM If you have a legitimate medical reason not to wear a mask, that is different.