Jaime Seltzer
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Jaime Seltzer is an American ME/CFS patient advocate and Scientific Director at The MEAction Network.[1] She is "responsible for fostering communication between research scientists, clinicians, and people with myalgic encephalomyelitis"(ME).[2] She was included in the TIME100 Health list in 2024 for her engagement with clinicians.[3]
MEAction and ME/CFS research resume[edit | edit source]
- Present Scientific Director, MEAction
- Scientific consultant on the ME/CFS project, Stanford University, PI Dr Ronald Davis
- Representative of healthcare advocacy organization #MEAction at Centers for Disease Control and Prevention (CDC), National Institutes of Health (NIH), Capitol Hill; author of solicited research documents (RFI) to the NIH and for researchers at Stanford University’s ME/CFS symposium, each with 75-100 citations assimilated
- Editor and consultant for Jen Brea’s TED talk on healthcare equality and groundbreaking, Sundance-award-winning health documentary Unrest
- Managing Editor for the online advocacy platform #MEAction, writing/curating 5–15 articles per week in advocacy and biomedical sciences while maintaining social media accounts and managing staff and volunteers[4]
Speeches[edit | edit source]
- May 14, 2018, Jaime's Speech (#MillionsMissing San Francisco 2018)[5]
Online presence[edit | edit source]
- e-mail: jaime@meaction.net
References[edit | edit source]
- ↑ "Welcome Jaime Seltzer to the #MEAction Team – Director of Scientific and Medical Outreach | #MEAction". The MEAction Network. Retrieved August 14, 2018.
- ↑ "Jaime Seltzer". LinkedIn.
- ↑ Ducharme, Jamie (May 2, 2024). "TIME100 Health: Jaime Seltzer".
- ↑ "Jaime Seltzer". LinkedIn.
- ↑ Seltzer, Jaime (May 14, 2018). "Jaime's Speech (#MillionsMissing San Francisco 2018)". YouTube. The ME Action Network.
