Also, come and join us for this at the brilliant @bridewell.bsky.social Will preview new season, answer some questions & stick around for some 🍺 📧 Email evertonbyline@gmail.com or DM us to reserve your place - thanks to those who have already! #EFC
Liz L
@elefebvre11.bsky.social
Everton 💙 toffeeliz.com she/her 📍Chicago Long Covid - ME/CFS Someone, anyone please talk about the CW’s Nancy Drew with me 🕵️♀️🦞👻
Perhaps a long shot! But does anyone know any of the people in these prints? I’d like to send them to them, as I have no use for keeping them. All photographed by me at Goodison Park 💙 Thank you 🙏🏻
Season Tickets to watch Everton Women at Goodison are now on sale. This includes all home Cup games, and the Women's Super League has now expanded to 14 teams, so lots of football for your money, with rewards, including open training sessions 💙 www.evertonfc.com/news/2026/ju...
1/ A proposed federal rule could let the government cancel active ME/CFS research mid-study when political priorities change. The public comment window closes July 13. Here's what you can do 🧵
Pretty much every word of this piece resonates with my experience of PEM. “Maybe it’s time we stopped asking people with PEM to make everyone else comfortable with their limitations. Maybe it’s time the people in our lives made the effort to understand what we’re actually dealing with.”
Why I Can’t Just Meet You for Dinner
The Reality of Post-Exertional Malaise
darthfoo.substack.com
Come on, come on... get down to Goodison Park 🎵 If you haven't been back to Glorious Goodison yet, Everton Women play their last WSL game of the season against Leicester on Saturday 16 May 1pm. Whoooo! www.evertonfc.com/news/2026/ma...
This blows, their content is great! Also not like chronic illness is skyrocketing due to long COVID or anything …
After Condé Nast's decision to close SELF, I spoke to chronically ill women about what the women's health site meant to them. "We have to acknowledge chronic illness as a politically, culturally, and socially marginalized category" Latest for @motherjones.com. www.motherjones.com/politics/202...
Anyone have a clip or gif of Ndiaye screaming WE BUILT THIS CITY ? 😔
Always read Brian Phillips; definitely always read Brian Phillips on Artemis & the moon!!
I wrote about Artemis II
Pre sale of my 3rd book, 'On The Banks' is now live! 👇 www.lauragatesphotography.co.uk/shop/p/onthe...
Louder for the people in the back 🗣️ The PWHL and Togethxr teamed up to create a T-shirt with a message just in time for our puck drop at the world’s most famous arena. ➡️ US pre-order: bit.ly/4vgEaeG ️➡️ CA pre-order: bit.ly/4vgEfz0%E2%8... ➡️ Shop in-venue at MSG and TD Garden
Today we celebrate Transgender Day of Visibility and the trans and non-binary individuals across our communities.
@quigley.house.gov ME/CFS research at the DoD has been a lifeline for patients and veterans. Please keep ME/CFS eligible in the Peer Reviewed Medical Research Program in FY27. #MEAwareness
@quigley.house.gov Congress directed NIH to develop an ME/CFS Research Roadmap. Please fund it with $50M in FY27 so we can finally move from plan to action on diagnostics and treatments. #MEAwareness
@quigley.house.gov 9M Americans including myself have ME/CFS. There are still no FDA-approved treatments. Please support $15.4M for the CDC ME/CFS Program in FY27. Funding has remained the same since 1996, despite COVID increasing the number of ME/CFS diagnoses #MECFS #AdvocacyWeek2026 #MEAwareness
@durbin.senate.gov ME/CFS research at the DoD has been a lifeline for patients and veterans. Please keep ME/CFS eligible in the Peer Reviewed Medical Research Program in FY27. #MEAwareness
@durbin.senate.gov Congress directed NIH to develop an ME/CFS Research Roadmap. Please fund it with $50M in FY27 so we can finally move from plan to action on diagnostics and treatments. #MEAwareness
@durbin.senate.gov 9M Americans including myself have ME/CFS and there are still no FDA-approved treatments. Please support $15.4M for the CDC ME/CFS Program in FY27. Funding has remained the same since 1996, despite COVID increasing ME/CFS diagnoses! #MECFS #AdvocacyWeek2026 #MEAwareness
@duckworth.senate.gov ME/CFS research at the DoD has been a lifeline for patients and veterans. Please keep ME/CFS eligible in the Peer Reviewed Medical Research Program in FY27. #MEAwareness
@duckworth.senate.gov Congress directed NIH to develop an ME/CFS Research Roadmap. Please fund it with $50M in FY27 so we can finally move from plan to action on diagnostics and treatments. #MEAwareness
@duckworth.senate.gov 9M Americans, myself included, have ME/CFS and there are still no FDA-approved treatments. Please support $15.4M for the CDC ME/CFS Program in FY27. Funding levels have not increased since 1996, despite COVID causing a rapid rise in cases. #MECFS #AdvocacyWeek2026 #MEAwareness
In less than three years, we’ve gone from a concept to sold-out arenas with a fan culture that’s unlike anything else in sports (thank you to all our fans from around the world!) We’re proud of the progress... and we're just getting started!
An exclusive look at the World's Most Innovative Companies
Check out the Most Innovative Companies in entertainment, media, sports, technology, and more.
bit.ly
Article is from 2024, and while I no longer have coworkers as long covid forced me out of full time employment, the information still applies to all people with long covid, not just your coworkers! A useful guide for empathetic convos! www.fastcompany.com/91245084/5-t...
5 things not to say to a coworker with long COVID-19
Here’s what you need to know to be more empathetic to those dealing with long COVID—or other chronic health conditions.
fastcompany.com
☑️ 70 degrees and sunny in Chicago 😎 ☑️ Liverpool lose ❌ ☑️ Everton 3-0 Chelsea 💙 (🤏 Everton women thisclose against ManU) Sing some blues and someone have a pint for me at the Denbigh!! 🍻💙
Yesterday James Garner was helping participants from Everton in the Community's social inclusion group build towers out of pasta and marshmallows. Today he's in the England squad. Absolutely delighted for him.