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Felicity Callard
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
 | This article is a stub. |
Felicity Callard became an advocate for people with Long COVID after she developed the illness in 2020.[1]
Open Letters[edit | edit source]
- Sep 24, 2020, Why the Patient-Made Term 'Long Covid' is needed
Articles[edit | edit source]
- May 8, 2020, Very, very mild: Covid-19 symptoms and illness classification[1] - (Full text)
- Oct 5, 2020, How and Why Patients Made Long Covid[2] - (Full text)
- Oct 1, 2020, Why we need to keep using the patient made term “Long Covid”[3]
Notable studies[edit | edit source]
Talks and interviews[edit | edit source]
Online presence[edit | edit source]
- Website/Blog
- YouTube
See also[edit | edit source]
Learn more[edit | edit source]
References[edit | edit source]
- ↑ Jump up to: 1.0 1.1 Callard, Felicity (May 8, 2020). "Very, very mild: Covid-19 symptoms and illness classification". Somatosphere. Retrieved November 7, 2020.
- ↑ Callard, Felicity; Perego, Elisa (October 7, 2020). "How and Why Patients Made Long Covid". Social Science & Medicine: 113426. doi:10.1016/j.socscimed.2020.113426. ISSN 0277-9536.
- ↑ Perego, Elisa; Callard, Felicity; Stras, Laurie; Melville-Jóhannesson, Barbara; Pope, Rachel; Alwan, Nisreen A (October 1, 2020). "Why we need to keep using the patient made term "Long Covid"". The BMJ. Retrieved October 11, 2020.
