Jaime Seltzer
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
Jaime Seltzer is an American ME/CFS patient advocate and Director of Scientific and Medical Outreach at The MEAction Network.[1] She is "responsible for fostering communication between research scientists, clinicians, and people with myalgic encephalomyelitis." (ME)[2]
MEAction and ME/CFS research resume[edit | edit source]
- Present Director of Scientific and Medical Outreach, 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[3]
Speeches[edit | edit source]
- May 14, 2018, Jaime's Speech (#MillionsMissing San Francisco 2018)[4]
Online presence[edit | edit source]
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.
- ↑ "Jaime Seltzer". LinkedIn.
- ↑ Seltzer, Jaime (May 14, 2018). "Jaime's Speech (#MillionsMissing San Francisco 2018)". YouTube. The ME Action Network.