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Replying to @AOC
The President & Dem leaders can no longer get away with familiar tactics of “committees” and “studies” to avoid tackling our crises head-on anymore:
- Restrain judicial review
- Open clinics on federal lands
- Court expansion
- Expand Fed access/awareness of pill abortions
- etc
ME Amanda☮️ retweeted
Mysterious things are happening in 'Toby and the Silver Blood Witches', an award-winning, heartfelt story from Sally Doherty.
It's an ideal adventure for any 9-12 year old who loves tales filled with action, mystery and wonder.
#kidlit | #booktrailer by irontree.co.uk
ME Amanda☮️ retweeted
The #LongCovid & #MECFS community will protest at the White House TODAY at 12 pm ET to tell @POTUS that #CovidIsNotOver & to call on him to declare a #NationalEmergency. Activists are planning acts of civil disobedience to send a message. Livestreamed here. #MillionsMissing
ME Amanda☮️ retweeted
I would love to understand the pain I have where my arms and legs connect to my body.
It’s excruciating.
Feels like they’re being ripped from my body or something is gnawing at the joints.
Would also like to know what I can do about it. Any ideas?
ME Amanda☮️ retweeted
got an important question: For which viruses did you get tested In conjunction with ME/CFS, fibromyalgia , CCI?. I have a few and want to get more tests done. They cost money so I want to get the right ones done. thank you. Hugs to all who are fighting chronic viruses in body.
ME Amanda☮️ retweeted
#Birmingham, #Alabama, USA
Men ages 39-65 needed for research study involving #fibromyalgia +/or #chronicfatiguesyndrome
Participants earn up to $750 for the completion of this study
residency.peds.uab.edu/repor…
Jarred Younger study
#MyalgicE #Fibro #MEcfs #CFS #CFSME #FM #FMS
ME Amanda☮️ retweeted
What test would show enough blood not getting to head when upright?
I am supposed to have MRI ti check for hypoperfusion etc but I will be lying down and the concussed feeling is much worse when I try to sit or stand. #mecfs
ME Amanda☮️ retweeted
"Physical therapists have a lot to learn about post-viral fatigue in the wake of a “tsunami” of long COVID patients"
scienceline.org/2022/08/phys…
ME Amanda☮️ retweeted
Lovely #pwME, I need your help again!
My book has made it to the finals of the #WriteBlendAwards. It features a young carer whose mum has #MECFS. Please vote for Toby and the Silver Blood Witches if you can!
It would be amazing if a book about Severe ME won 🤞🤞
#SevereMEDay
Replying to @WriteBlendbooks
Middle Grade Finalists
Autumn Moonbeam Dance Magic @FinlaysonPalmer
Extraordinary Adventures of Alice Tonks @Emilie_London
Small! @MissDePlume
Toby and the Silver Blood Witches @Sally_writes
11%Alice Tonks
31%Autumn Moonbeam
21%Small!
37%Toby Silver Blood Witches
527 votes • Final results ME Amanda☮️ retweeted
Hey #pwME I'm making a mini doc on severe ME/CFS to raise money for OMF. I need pic's of a few brave bedbound folks to be featured in the vid. Could anyone help? DM if so, thanks. 👍🙏
ME Amanda☮️ retweeted
looking for lyme Doctor in Munich Germany. If anyone knows of one please DM. I am desperate.If possible one on the heakth service
ME Amanda☮️ retweeted
Stephen King's The Talisman could be a huge part of #StrangerThings 5 trib.al/FMeJrkD
ME Amanda☮️ retweeted
Any #pwME have experience with candesartan for migraine?
Feeling even more woozy and lightheaded than usual.
Universe, we need a win here!!!💫✨
Beto O'Rourke is raising more money than Greg Abbott in the race for Texas governor, and polls show a single-digit contest between them. Suddenly, improbably, perhaps unwisely, Texas Democrats are again daring to think that maybe this could be the year. nyti.ms/3J5OG0C
ME Amanda☮️ retweeted
As someone affected by #longcovid it still shocks me that #ME sufferers have been going through this experience for decades & still managing against all odds to keep going.
If LC has done one thing, it’s opened my eyes to the strength & enduring determination of these people ❤️
This quoted post is unavailable.
ME Amanda☮️ retweeted
I've never had a party trick or a talent.
Lying on the floor a lot with #ME I've mastered the ancient art of remote control and mobile phone balancing on the carpet.
Just broke my record - 1 hour and 12 minutes.
It's the simple things in life.
#MyalgicEncephalomyelitis #pwME
ME Amanda☮️ retweeted
🧵
USA: CDC: School-Based Active Surveillance (SBAS) of ME/CFS Among Schoolchildren, comments invited until 20th Sept 2022
federalregister.gov/document…
#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #CFIDS #PwME #YPwME #YPwMEs #YPwC #YPwCs #CFSME
Looks promising
1/
ME Amanda☮️ retweeted
Allergic people in the USA: anyone able to get hold of #nizatidine?I understand there’s a supply squeeze. Can’t tolerate famotidine. Any thoughts on alternatives, please? I’m on ketotifen, so not sure if #Cromolyn is possible? TY 🙏 #H2Blockers #MCAS #LongCovid






















