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#MillionsMissing 2023: Watch Livestream of Press Conference

The words 2023 #MillionsMissing May 12, 2023 in white over an image of a dark blue sky and the Washington Monument. The logos of #MEAction and Body Politic in the bottle right hand corner. On a red box, the words in black Watch Livestream of Press Conference
Hybrid Hybrid Event

May 12 @ 2:00 pm 3:00 pm EDT

LIVESTREAM NOTE: MEAction’s YouTube Live account will stream directly to this page during the event. If you don’t see it try refreshing the page. The embedded livestream may not work on all browsers. If you are experiencing technical issues please stream from one of MEAction’s social media accounts: YouTube, Twitter, Facebook.

Join #MEAction in partnership with Body Politic for #MillionsMissing 2023 held at the Washington Monument on the National Mall in Washington, DC on May 12th that will feature an art installation and press conference.

#MillionsMissing 2023 will demand bold, urgent governmental action for the millions of people living with myalgic encephalomyelitis (ME), Long COVID, and other infection-associated, complex- chronic diseases.

Our protest will be an art installation that will have rows and rows of cots to represent beds at the base of the national monument as a symbolic protest to illustrate that though the pandemic is deemed over—the ending of the Public Health Emergency by the federal government—it is not over for millions of Americans who have ME and Long COVID.

We will also have a press conference that will be livestreamed at 11am PT/2pm ET that you will be able to watch on our social media channels.

RSVP today to let us know if you plan to watch the livestream!

Here are the speakers at the press conference:

Jo Hsu wearing a black shirt and necklace.

Jo Hsu, Phd MFA
Jo Hsu, PhD MFA (They/Them) is a writer, educator, and scholar with ME/CFS. They are an assistant professor of Rhetoric & Writing at the University of Texas at Austin and the author of Constellating Home: Trans and Queer Asian American Rhetorics. They study storytelling as political strategy and their work appears in The Huffington Post, The Boston Globe, The Progressive, and many other news media, literary, and academic outlets. Their current research examines how cultural biases affect medical research and how diagnostic terms get distorted for political ends. You can access most of their work at www.vjohsu.com.

Dr. Gage wearing a pink headband, necklace, and head towards tilt with head in hand.

Dr. Gage 
Dr. Margot Gage (she/ her) is a social epidemiologist and a nationally recognized expert on patient experiences with Long Covid. Dr. Gage has spoken nationally and internationally on medical inequality experiences by women with Long Covid. Her work aims to inform women on how to advocate for themselves in medical settings. She also focuses her research on health disparities, medical cannabis, environmental and social issues. Dr. Gage is an associate professor at Lamar University. You can follow her work on Twitter and Instagram. 

Jaime is wearing a black jacket over a striped shirt. Jaime is wearing glasses and leaning on a wall.

Jaime Seltzer
Dir. Jaime Seltzer, MS (she / her)  is the Director of Scientific and Medical Outreach at #MEAction. She is responsible for fostering communication between research scientists, clinicians, and people with ME/CFS. She works with Stanford, Columbia, Mayo Clinic, and Project ECHO on post-infectious chronic complex diseases, including ME/CFS and Long COVID, and is running a survey-based study and small proteomics mass spectrometry project on these diseases.

This is a picture of me from the Bloomberg Law article. I was photographed while wearing a 10 day holster monitor. I was later diagnosed with Inappropriate Sinus Tachycardia.

Brooke Keaton
Brooke Keaton (she / her) is married to her college sweetheart, Jared, and a mother to two beautiful daughters, Jaren and Bria. Prior to having Covid in December 2020, Brooke was an Early Childhood Educator. Unable to return to work, she has taken on the role of an Advocate for Long Haulers like herself. Her Long Covid story has been featured on WCNC, Bloomberg Law, Raleigh News & Observer, NC Health News, Msn.com, and The Scientist Magazine. She’s also filmed two PSA’s for the NC Dept. of Health and Human Services. They are currently running on all major social media platforms as well as all NC network channels.

Gabriel is wearing a black shirt with long brown hair and is smiling.

Gabriel San Emeterio
Gabriel San Emeterio (she/he/them) is a queer activist raised in Mexico City and living in New York City for the past 23 years. They hold a BA of their own design in Unique and Interdisciplinary Studies from CUNY, focused on Gender Studies and Community Organizing. Following their commitment to social justice, Gabriel obtained his graduate degree with honors from the Silberman School of Social Work with Community Organizing as a method of practice and a certificate in Social Policy. Gabriel’s passion for liberatory community work guides her life efforts, which include advocacy and grassroots organizing around policies and issues that affect the LGBTQIA+ community, welfare rights, and people living with HIV, ME/CFS and other fatiguing illnesses such as Long COVID.

Morgan is wearing a red shirt, with a brown bob and smiling. Standing in front of a green grass and trees.

Morgan Stephens
Morgan Stephens is a journalist who has written for CNN Politics, CNN Business, The Daily Beast and HuffPost. After developing Long Covid in 2020, she wrote frankly about her traumatic experience in an essay for CNN Opinion. Since then, Stephens has appeared on KCAL, ABC Los Angeles, NPR, CNN+, Poynter, Columbia Journalism Review and a variety of podcasts discussing the issue. She is currently writing a memoir and poetry collection.

Mary is smiling with brown hair and bangs.

Mary Dimmock
Mary Dimmock (she / her) worked at Pfizer for 31 years in drug metabolism research, clinical trials management, R&D information systems development, and R&D business process improvement and integration. She retired in 2011 when her son became ill with ME. Since then, she has spearheaded a number of US and international advocacy initiatives to accelerate research and improve clinical care for people with ME. She has also participated on NIH’s Common Data Elements initiative and CDC’s ME/CFS Medical Education Roundtable and together with Dr. Lucinda Bateman of Bateman Horne Center, co-founded the US ME/CFS Clinician Coalition in 2018. Mary is the carer for her son and daughter-in-law, who has now developed ME following COVID-19.

Dr. Murphey is smiling with long brown hair. Dr. Murphey is wearing a  red lace shairt and gold hoop earings.

Dr. Dona Kim Murphey
Dr. Dona Kim Murphey (she / her) is a neurologist, neuroscientist, historian of science, and community organizer. She considers health as telescoping connections within and between individuals, families, communities, and society and frames all policy as health policy. Dona currently sits on the boards of Woori Juntos, Doctors In Politics, and the Race and Equity Leadership and Research Collective. She has also participated in patient-ledresearch and advocacy efforts in Long Covid. Dona is a former school board candidate in Texas who recently filed a Voting Rights Act lawsuit against Pearland Independent School District demanding single-member districts for representative local government.

Her latest endeavor is prognosUs, a public benefit company that delivers early dementia screening and culturally fluent and language-specific counsel to caregivers fromcommunities disproportionately impacted by this racialized disease. Dona received her B.A. in History and Science from Harvard College and an M.D. and Ph.D. in Neuroscience from Baylor College of Medicine.

Physical Event Location

The physical location of this event will be at the NE corner of the Washington monument at 15th st and Constitution Ave.

2 15th St NW
Washington, DC 20024
+ Google Map
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