Sabrina Poirier
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sabrinapoirier.bsky.social
Sabrina Poirier
@sabrinapoirier.bsky.social
#CommunityEngagement Expert. Life sidelined by #MECFS #MCAS #POTS #Fibro #Gastroparesis +

#MECFS & #LongCovid #ResearchPartner & #Advocate • Chair of #MedicalEducation Group • #PwME #Disability

(Unceded) #Canada

https://linktr.ee/sabrinapoiriercanada
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Hey everyone. I have updated my starter pack of community leaders, advocates, researchers, clinicians, patients and carers from our #LongCOVID and #MyalgicEncephalomyelitis community.

Please check it out and feel free to share.

go.bsky.app/6R7bqc7
Reposted by Sabrina Poirier
I'm grateful to have been able to present preliminary findings at #ICanCME2025, and can't wait until it's a paper to show you.

Thanks to organizers and all who presented & will present today! Your work means a lot to us broadly, and a lot to me in particular. ❤️

We appreciate you!
November 6, 2025 at 4:32 PM
Reposted by Sabrina Poirier
--but pay a great deal for the fallout. And that a lot of people attending conferences may think, "People with lived experience seem bright, alert and focused. They look neat and tidy. How bad can it be?"

I don't feel like I'm fully crashed. I managed with lots of extra meds and got good rest.
November 6, 2025 at 4:32 PM
Reposted by Sabrina Poirier
Considering how flattened I am, I don't think I can cover the third day.

One thing I appreciated about the #ICanCME2025 conference opener was that the conference organizers talked about this: how people like me would look 'together' and 'on' while the conference was underway--
November 6, 2025 at 4:32 PM
Reposted by Sabrina Poirier
Thank you for sharing Sabrina
November 6, 2025 at 7:28 PM
Reposted by Sabrina Poirier
"Nothing About Us Without Us".
I've been thinking about the title of this meeting and asking myself, why don't we hold more scientific meetings like this? The public brings the questions for the scientists, and we show them what we are doing to address it. #ME #MECFS
#AcademicSky
October 8, 2025 at 9:39 PM
Reposted by Sabrina Poirier
Thank you so much @spichaksimon.bsky.social for your live tweeting the #ICanCME2025 conference today. 🙏

The energy and time you give to support our #MECFS community is so appreciated. 💙
November 5, 2025 at 4:57 AM
Reposted by Sabrina Poirier
Love that we are getting some poop visualizations. /gen

One of those things that even some doctors are squeamish about, but it's an important diagnostic!

Rebecca Ryan is discussing how #POTS affects digestive function re: hypovolemia, & #MCAS can affect what/whether ppl eat on a regular schedule.
November 5, 2025 at 9:22 PM
Reposted by Sabrina Poirier
Rebecca Ryan up now to discuss GI manifestations in ME #ICanCME2025
November 5, 2025 at 9:10 PM
Reposted by Sabrina Poirier
Very cool imagery in Sammie's presentation. A collage of dismissive statements teens have heard when they say they're sick, including " you would feel better if you didn't spend all day in bed", "you are looking really well", "it could be a lot worse" and "kids don't get Long COVID"

#ICanCME2025
November 5, 2025 at 9:09 PM
Reposted by Sabrina Poirier
Love the way Maitland frames mast cells as helpers who have lost their way 😂

And that there are a lot of potentially underlying causes and that it's best to look for autonomic and connective tissue issues for first mover

#ICanCME2025
November 5, 2025 at 8:51 PM
Reposted by Sabrina Poirier
The legendary Anne Maitland is here! Nearly every interesting paper on #MCAS has her as an author. #ICanCME
November 5, 2025 at 8:27 PM
Reposted by Sabrina Poirier
Just gave the talk!! (Whew.) Sabrina said "please go slowly for the interpreter" and that added five minutes, just goes to show how quickly I usually talk!
November 5, 2025 at 7:00 PM
Reposted by Sabrina Poirier
Getting ready for Day 2 at the #ICanCME2025 conference!

I'll be delivering a talk about neurodiversity in #pwME and IACCs in general. Hope to see you there!
November 5, 2025 at 5:25 PM
Reposted by Sabrina Poirier
Are you registered?

If so, please join us for our last day together! 💙
Today is the last day of the #ICanCME2025 Conference.

We will be talking research design today!

Common mistakes, gaps in knowledge, tools we need to create, opportunities for increased diversity and inclusion, hoe to increase accessibility in research, why patient partnership matters, and more!
November 6, 2025 at 1:06 PM
Today is the last day of the #ICanCME2025 Conference.

We will be talking research design today!

Common mistakes, gaps in knowledge, tools we need to create, opportunities for increased diversity and inclusion, hoe to increase accessibility in research, why patient partnership matters, and more!
November 6, 2025 at 1:04 PM
Reposted by Sabrina Poirier
Joining day 1 of the ICanCME Canadian Collaborative Conference on Myalgic Encephalomyelitis (ME).

Huge shout-out for the respect for lived experience! Wonderful start!

#ICanCME2025

#NothingAboutUsWithoutUs

@icancmeresearch.bsky.social, applause to planning team!
November 4, 2025 at 6:18 PM
Reposted by Sabrina Poirier
Yeah, I had to stop, folks! It was really good, though, and what I liked most about it was the wide-ranging series of topics so far. It hasn't felt like any other research conference I've attended.

#ICanCME2025 has a combination qual/quant vibe that's really appealing.
November 4, 2025 at 8:40 PM
Reposted by Sabrina Poirier
At the #ICanCME2025 conference today!

Sabrina Poirier & Maeghan Taverner's intros blew me away.

~Acknowledging labor from people with lived experience
~Setting out expectations
~Moment of silence for those we've lost

This is what a conference designed by people with lived experience looks like 🧪
November 4, 2025 at 6:23 PM
Reposted by Sabrina Poirier
November 4, 2025 at 7:16 PM
Reposted by Sabrina Poirier
Honored to be speaking about ME, gender bias in medicine, and women's "unexplained" chronic illness at the #ICanCME2025 conference this afternoon. Thanks @icancmeresearch.bsky.social! icancme.ca/research/202...
2025 ME Conference - ICanCME
icancme.ca
November 4, 2025 at 4:44 PM
#ICanCME2025 is happening this week!

This was an initiative driven by people with ME and their loved ones with the support of many along the way! We’re so thankful for everyone’s support so far.

And please be patient with us this week if we run into any issues. 🤞💙
November 3, 2025 at 3:51 PM
Reposted by Sabrina Poirier
Case report by @sunsopeningband.bsky.social et al. @workwellfoundation.bsky.social @wearlumia.bsky.social

This case report explored whether reduced blood flow to the head contributes to postexertional malaise (PEM) in myalgic encephalomyelitis (ME). Using a new in-ear device, researchers measured
journals.lww.com
October 30, 2025 at 12:51 PM
Please check your spam or junk folders for an email from ICanCME if you haven’t received your link yet for part 2 of the conference registration. :)

Also, we had some missing emails and some that were rejected for being written incorrectly (missing the @ sign for example).
October 30, 2025 at 11:34 AM
Reposted by Sabrina Poirier
Thanks for sharing this Solve.

We appreciate it.
Register today for the @icancmeresearch.bsky.social online conference Nov. 4-6. The event was designed by people w/ #MECFS and the theme is “Nothing About Us Without Us.”

icancme.ca/research/202...
2025 ME Conference - ICanCME
icancme.ca
October 13, 2025 at 4:40 PM