Long-COVID Alliance

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
Image: ©︎https://longcovidalliance.org

The Long-COVID Alliance or The LC Alliance (LCA) was founded in 2021 by a group of organizations.[1][2]

Aims[edit | edit source]

Services[edit | edit source]

Founding partners[edit | edit source]

Core Steering Commitee[edit | edit source]

  • Body Politic
  • Dysautonomia International
  • Ehlers-Danlos Society
  • LONG HAUL covid fighters
  • The MEAction Network
  • National Health Council
  • Patient Led Research for Covid-19
  • PolyBio[1]

Notable people[edit | edit source]

Patrons[edit | edit source]

Medical advisors[edit | edit source]

Research/Notable studies[edit | edit source]

History[edit | edit source]

The LC Alliance was founded in 2021, in response to the many people who become ill after contacting the COVID-19 virus, but were not recovered.[1][2][3]

Funding[edit | edit source]

Interviews and articles[edit | edit source]

Online presence[edit | edit source]

See also[edit | edit source]

Learn more[edit | edit source]

References[edit | edit source]

  1. ↑ 1.0 1.1 1.2 1.3 "About". Long-COVID Alliance. Retrieved November 14, 2021.
  2. ↑ 2.0 2.1 "Long Covid Alliance (LCA)". Solve ME/CFS Initiative. February 25, 2021. Retrieved November 14, 2021.
  3. ↑ "Home". Long-COVID Alliance. Retrieved November 14, 2021.
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