#MillionsMissing 2023: “Telling Your Story- In Under A Minute!” Training
April 11, 2023
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We will be holding a highly interactive 2-hour webinar to inspire you and help you hone your stories for advocacy.
Tag: #MillionsMissing
#MillionsMissing Press Hits are Rolling In!
September 20, 2022
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The press hits are rolling in! The media showed up in a big way yesterday to cover our #MillionsMissing protest in front of the White House. One day after President Biden declared the “pandemic is over,” our community was at the gates of the White House to send Biden a message that a pandemic of chronic
Protest at White House to Tell President Biden “Pandemic Is NOT Over”
September 19, 2022
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Protesters disabled by Long COVID and myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) lay down on the White House sidewalk today risking arrest to tell President Biden that the pandemic is not over, and that millions are being disabled from post-viral disease, including Long COVID and ME/CFS.
Americans Disabled By Long COVID and ME/CFS Protest Biden’s Claim that “Pandemic Is Over.”
September 19, 2022
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Protesters disabled by Long COVID and myalgic encephalomyelitis (ME/CFS) are protesting at the White House sidewalk TODAY at 12 p.m. ET to say that the “pandemic is not over,” and to call on President Biden to declare Long COVID and ME/CFS a national emergency.
Get ready for #MillionsMissing
April 8, 2021
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We are gearing up for #MillionsMissing 2021! This year will be a week long event, from May 9 to 15, of action and activities to strengthen our community, and fight for recognition, research and medical education for myalgic encephalomyelitis (ME). Check out our website for the #MillionsMissing timeline of events, grab your t-shirt, and plan a local event! We
Get ready for #MILLIONSMISSING 2021 – Purchase your t-shirt
April 7, 2021
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We are excited to announce that #MillionsMissing t-shirts are now available for purchase along with other items in our online stores! Shop U.S. Shop UK Shop AUS This is our 6th anniversary of #MillionsMissing to raise awareness and fight for recognition, education and research for people living with myalgic encephalomyelitis (ME or ME/CFS). Millions are
#MillionsMissing 2020 was powerful (full report)!
May 19, 2020
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*We added an update below. Videos like the “I got a virus” video from #MEAction UK and #MEAction Scotland were viewed over 90k times on multiple platforms. Better than originally reported! Dear Friends, You are amazing. You made #MillionsMissing impactful, powerful, and moving. This virtual year no doubt had it’s challenges, but it was beautiful
We Are Essential Campaign
April 9, 2020
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#MEAction is going to embark on a four week campaign, #WeAreEssential, asking Congress to recognize that the disability/chronic illness community is ESSENTIAL and must be included in the next Covid-19 packages.
We did it! This is what the #MillionsMissing Look Like.
May 14, 2019
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It has been a big week, with over 100 public and virtual events happening across the world! We are honored and grateful to be in this fight for health equality with you. We showed the world that we are the #MillionsMissing – that we will fight for the recognition, treatment, and compassion we deserve for
#MillionsMissing from ME: 2019 Stories
May 9, 2019
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We asked you, the #MillionsMissing from ME to tell us your stories. We are grateful for all that you’ve shared with us and each other. We are proud to publish your words. We won’t give up the fight. Here is the collection of your stories from 2019. *We tried our best to include all of