Jaime Seltzer

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.

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]

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[3]

Speeches[edit | edit source]

Online presence[edit | edit source]

References[edit | edit source]