Sabrina Poirier (On Hiatus)
@sabrina_poirier
Community Builder / Passionate Collaborator / Chair - #MedicalEducation Group / #ResearchPartner / #MECFS #LongCovid Advocate / #PwME / #MCAS / #POTS / #Fibro
ID: 450773131
https://linktr.ee/sabrinapoiriercanada 30-12-2011 16:56:54
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NEW STORY from me for The Sick Times: A legal and political analysis of mask bans across the country. With a list of bans per state. Politicians tell us mask bans are about crime and antisemitism. What they’re not saying: Mask bans are about Covid. 1/ thesicktimes.org/2024/09/03/per…
What a mindfuck to be a disabled writer/artist -- artist residencies have no concept of accessibility beyond ♿️, and only one (iirc) allows disabled people to bring a caregiver. MacDowell Virginia Center for the Creative Arts Hedgebrook et al, you're excluded disabled people.
Are you a health researcher? Patients are the experts in patient engagement. Here's an easy opportunity to learn from them (next week!) Check PxP. 3 days with a wide range of time zones. Dr. Dawn Richards, PhD Hetty Mulhall CIHR-IMHA Community Dr. Christine Chambers
This LACK of protocol in our NHMESS hospitals for SEVERE M.E. is a murderous disgrace & I will NOT mince my words. Let’s get ME Foggy Dog letter ✉️ trending #meawarenesshour #MURDERinME SIGN ✍️ 🔻🔻🔻 organise.network/actions/petiti… #pwME
Can the ME Community help ME Foggy Dog get more signatures on this petition and get it trending during ME Awareness hour this evening? ow.ly/3yKp50TfbNS #MyalgicEncephalomyelitis #VerySevereME #SevereME
KarenLesliePhysio Wear pattern free dark clothes washed in fragrance free detergent/soap, rubber soled shoes, no perfume and no sparkling jewelry. Paper instead of screens. Do not let them let you overstay. Social interaction the hardest part for both of you. #ME life is so lonely. 💔
1/ Looking for 5 perspectives about the online learning modules developed by IMHA Patient Engagement Research Ambassadors. Can you help? Drop your quote in the comments below, or email us: [email protected]