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Long-COVID Alliance
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
 | This article is a stub. |
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]
- Covid-19 Longhauler Advocacy Project
- Global Pandemic Coalition
- Solve ME/CFS Initiative and the You + ME Registry[1]
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]
- Website
- Facebook page
- YouTube channel
See also[edit | edit source]
Learn more[edit | edit source]
References[edit | edit source]
- ↑ Jump up to: 1.0 1.1 1.2 1.3 "About". Long-COVID Alliance. Retrieved November 14, 2021.
- ↑ Jump up to: 2.0 2.1 "Long Covid Alliance (LCA)". Solve ME/CFS Initiative. February 25, 2021. Retrieved November 14, 2021.
- ↑ "Home". Long-COVID Alliance. Retrieved November 14, 2021.
