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Read the latest in ME news and campaigns—never miss a beat!
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Our Community Needs Urgent Support
A $44,000 grant is waiting. Help us unlock it.
2 days ago2 min read


4,000 Voices Heard by HHS. Here's What Comes Next.
Nearly 4,000 of you signed our letter to Secretary Kennedy calling on HHS to protect Medicaid access for people with ME and Long COVID.
4 days ago2 min read


We Made Real Progress at #MillionsMissing — Here's What's Next
We built key relationships to protect Medicaid for ME and Long COVID. Now we need your help to keep going.
May 142 min read


How to Participate in #MillionsMissing 2026
ME awareness month is here. Here's how to show up (at whatever battery level you have).
May 12 min read


#MEAction Sends Letter to Dr. OZ Urging for Medicaid Protection
Join our fight to protect Medicaid for our community!
Apr 282 min read


This Is What We Are Up Against
Fury and hope can coexist. Here’s why we believe this is the year everything changes for people with ME.
Apr 233 min read


#MEAction to Meet with NIH Director during #MillionsMissing Week
#MEAction and NIH Director to Discuss Funding for ME/CFS Research Roadmap
Apr 142 min read


#MEAction Joins National Webinar: Impacts of H.R.1 on Disability Communities
Our year-long campaign to protect Medicaid for people with myalgic encephalomyelitis (ME) and Long COVID continues! We are pleased to share that our Advocacy Director, Ben HsuBorger, will be joining a national webinar to discuss how the H.R.1 funding bill passed by Congress last year (commonly known as the One Big Beautiful Bill) will affect disability communities. The Grassroots Project, which supports disability grassroots advocacy, networking, and leadership development,
Apr 102 min read


Celebrating A Big Senate Win
#MEAction has been working hard with #NotJustFatigue to advocate for the ME/CFS Research Roadmap and it has paid off! The Senate Appropriations Committee included the roadmap in their report!
Aug 1, 20251 min read


SOS: #MEAction Responds to Urgent Crisis – MN Long COVID Funding At Risk
We cannot allow our elected officials to harm chronically ill and disabled people with rampant cuts. This is yet another SOS moment for people in our community.
May 7, 20252 min read


Research Roadmap Petition
We reached 7,000 signatures on our last letter. This time, our goal is 10,000. Please sign the letter today and share it with your friends and family.
May 7, 20251 min read


Share This SOS Image On Your Socials
Share this message about #MillionsMissing with your own networks.
Apr 28, 20251 min read


Millions Missing Scotland 2025: Red alert for ME
#MEAction Scotland will be outside Scottish Parliament in Edinburgh on Wednesday 14th May, from 12–2pm, calling on the Scottish Government to act on its promises.
Apr 27, 20255 min read


#MEAction: Congress Is Hearing from Us
#MEAction has been hard at work connecting individuals to their elected officials to talk about the ME/CFS Research Roadmap, Medicaid, and telehealth.
Apr 23, 20252 min read


SOS: Save our Science
It’s time to send out our SOS signal if we want to have funded research.
Apr 11, 20256 min read


Why We’re Sending out an SOS this #MillionsMissing
On May 12th, we're sending out an SOS to Congress to Save our Support Systems, our Science, and our Society.
Apr 8, 20252 min read


#MillionsMissing 2025: Sending Out An SOS
For #MillionsMissing 2025, #MEAction is sending out an SOS.
Apr 2, 20252 min read


White House Halts Funding for Long COVID Grants
The White House has abruptly announced that it is terminating funding for NIH RECOVER grants studying Long COVID, effectively stopping 45 studies that were almost complete.
Mar 27, 20252 min read


Office of Long COVID at HHS Closing
Read the statement from Ian Simon, the head of the Long COVID Office at Department of Health and Human Services.
Mar 25, 20252 min read


#MEAction Celebrates Powerful Women
#MEAction acknowledges and celebrates the amazing women in our community.
Mar 5, 20255 min read
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