A global network fighting for equality for Myalgic Encephalomyelitis. #MEAction #MillionsMissing linktr.ee/meactnet

Global
In honor of #SevereMEday, #MEAction is honored to share the Severe ME Artists Project 2026! Over 100 of you submitted photos, drawings, writing, and videos of your work! We are thrilled to share so many amazing and powerful pieces of artwork. meaction.net/post/honoring-s… #SevereME
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Have you checked out all the amazing things Pillow Writers has going on lately? So many options! pillowwriters.wordpress.com/ They are an international ME/CFS writing community, free and open to anyone with ME/CFS or Long Covid. We are honored to host this amazing group! #pwME #pwLC
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"There’s a long, dark history here, rooted in centuries of dismissal of predominantly female illnesses as “hysterical”, and amplified in recent decades by government attempts to reduce the benefits bill and insurers’ attempts to reduce payouts."
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"We need to ask why so many patients have been abandoned, why discredited and dangerous treatments continue to be prescribed and why ignorance and neglect still dominate, in the health system and beyond. In other words, there has seldom been a stronger case for a public inquiry."
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#MEAction Network retweeted
Whilst we know the average quality of life for ME/CFS patients is amongst the very worst for chronic diseases, I think in advocacy the true disaster that is severe / very severe ME has been significantly underplayed. New @wecrunchme visual on this topic 💙
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Registration is open for RECOVER-TLC’s 3rd annual workshop on Nov. 4-5, 2026. Virtual & in person options. web.cvent.com/event/e0be4010… "This two-day session includes keynote speakers, interactive panels, input from people with lived experience, and networking opportunities."
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Our Scientific Director, Jaime Seltzer, is reporting out from the NIH conference -From Mechanisms To Medicine: Rethinking the Discovery-to- Care Continuum in Multi- System Disorders. Reporting from home today & in person tomorrow. Follow along: bsky.app/profile/exceedhergr…
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Happy 1st day of fall! Changing seasons can be tough when you have ME. Can you even notice the change? I have learned that anything I can find any joy in is good to amplify. What do you find joy in? If this season is not one where you can find joy, sending you extra love!
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The ME/CFS Exchange Webinar Series launches next month! First in the series will focus on post-acute infection symptoms. October 8th from 1 pm to 3 pm ET via Zoom. Registration required: rtiorg.zoom.us/webinar/regis… Hosted by NINDS in partnership with MECFSnet. #NIH #PwME #MECFS
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Last #MedicaidMonday, we shared that CMS announced states may use a tier system to determine which Medicaid applicants qualify for the medical frailty exemption from new work requirements. Today, we are going to explain those tiers! #Medicaid #PwME #PwLC #disability
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Tier 3: Cases that cannot be resolved through available data would proceed to individualized review and potentially documentation. Self-attestation is allowed in most states for 2027, but will be much more limited starting in 2028.
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MEAction advocates are talking w/ multiple states, urging them to put ME, Long COVID and other IACCs on their lists of conditions eligible for medical frailty exemption. We are also advocating that ME/CFS - which always impairs a person’s ability to work - be included in Tier 1.
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Applications are open for the NextGen IACC Scholarship! Trainees create original research projects using a pre-existing chronic disease dataset in this funded, mentor-led research opportunity. MS, PhD, & MD/PhD trainees enrolled in Canadian uni can apply. meaction.net/scholars-progra…
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#MEAction Network retweeted
Last day to complete the Understanding Post-Exertional Symptom Worsening in ME/CFS survey. Your responses go directly into CTN Lite trial design — shaping the terminology, outcome measures, and how crashes are defined and measured. 👉 Take the Survey: ow.ly/pImY50ZITNr
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#MEAction Network retweeted
You’ve made a plan to vote, but now what? There’s more to do before Election Day! One thing we suggest is getting involved at the local level in your community. This can look like many things, so we’ve put together a list of three ways you can take action before Election Day. You can get involved with REV UP and find your local coalition: aapd.com/revup-join/. ID: Blue and red text on a cream background. Three ways to engage in collective action during Disability Voting Rights Week. REV UP has 27 coalitions in 26 states! Join or start one in your area. AAPD will help you! Sign up to be a poll worker! Advocate for laws that support accessible voting, and a more accessible democracy.
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The first ME/CFS CDC meeting since 2024 starts in less than an hour. #MyalgicEncephalomyelitis #MECFS #pwME
TOMORROW: The CDC ME/CFS Stakeholder Engagement and Communication (SEC) Conference Call is on Sept. 18th at 3:00 pm ET. Register: ow.ly/jMYn50ZLwsJ Guest speaker: Nancy Klimas, MD. Also featuring program updates from CDC's ME/CFS program staff and a Q&A. #pwME
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