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]

Online presence[edit | edit source]

References[edit | edit source]