Moved post
Not much information online but apparently Michael (Austrian neurologist who has been at the forefront of ME/CFS advocacy in Austria) published a book about ME. He says it doesn’t replace medical care and hopes it is helpful for those for whom the diagnosis is still unclear...
https://onlinelibrary.wiley.com/doi/full/10.1111/ene.70466
LETTER TO THE EDITOR
Open Access
Uncovering Hidden Profiles: From Pain-Centric to Multi-Symptom Small Fiber Neuropathy
Svetlana Blitshteyn, Michael Stingl, Jill R. Schofield
First published: 23 December 2025...
Abstract
Background/Objectives: Growing evidence suggests that mast cell activation (MCA) may contribute to Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), a debilitating disorder characterized by persistent fatigue and post-exertional malaise (PEM). Particularly in relation to...
A Practical Approach to Tailor the Term Long COVID for Diagnostics, Therapy and Epidemiological Research for Improved Long COVID Patient Care
Hoffmann, Kathryn; Stingl, Michael; O’Mahony, Liam; Untersmayr, Eva
The term long COVID (LC) effectively describes the broad long-term disease burden of...
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to our use of cookies.