Dysautonomia in ME/CFS and Long COVID

  Рет қаралды 5,010

Riksförbundet för ME-patienter

Riksförbundet för ME-patienter

Жыл бұрын

RME (The Swedish ME-Association) holds a yearly conference, inviting among others, scientist from all over the world to talk about their recent finding.
In this video Professor Peter Rowe,
Johns Hopkins University School of Medicine, Baltimore,
talks about dysautonomia in ME/CFS and Long COVID.

Пікірлер: 13
@cherylallis2458
@cherylallis2458 Жыл бұрын
Interesting that CBF is reduced even without measurable POTS symptoms. That explains why so many ME patients don't have less fatigue when POTS symptoms are reduced by medication.
@cherylallis2458
@cherylallis2458 Жыл бұрын
Thank you so much for posting this video. It re-enforces that it is beneficial to me to lie on the floor for several minutes with my feet up on a chair or couch after standing up to get dressed or shower or sitting up to eat. It would be interesting to know how that effects CBF.
@bridaw8557
@bridaw8557 Жыл бұрын
Doctors used to ridicule ME CFS sufferers. These sensitive people tend to have over reactive immune systems. Perhaps more women suffer from these conditions? They called them similar to hysterics. Now we know better. When psychological symptoms in response to the symptoms. The severe pain which doctors would say is psychogenic. We’ve all had past trauma but these kind of people are more sensitive from childhood so any environmental trauma during development. But it’s not an emotional or psychological problem that blames the sufferer and says they just need behavioral therapy. This kind of treatment is a trauma itself due to isolation, pain, invalidation and desperation Anyone who isnt passive and mellow is going to be in serious anxiety. And being more emotional is often something women’s biology creates . I always knew my best friend was telling the truth and stared going a little bunkers wondering what was happening to her and being shut down She’s better now but still has to be careful to get enough sleep. That’s the biggest issue. If you can improve sleep and actually try to relieve the pain long enough to relax. It took her 8 years to get better.
@Fiawordweaver
@Fiawordweaver Ай бұрын
Thank you for being such a loving friend and posting your observations.
The new (2021) NICE Guidelines for ME/CFS: Following the science
39:31
Riksförbundet för ME-patienter
Рет қаралды 2,6 М.
TWiV 1029: David Tuller on Long COVID and ME/CFS
1:01:06
MicrobeTV
Рет қаралды 10 М.
Зачем он туда залез?
00:25
Vlad Samokatchik
Рет қаралды 3,3 МЛН
Amazing weight loss transformation !! 😱😱
00:24
Tibo InShape
Рет қаралды 58 МЛН
Дарю Самокат Скейтеру !
00:42
Vlad Samokatchik
Рет қаралды 8 МЛН
Joint hypermobility/EDS and ME/CFS
30:23
Riksförbundet för ME-patienter
Рет қаралды 2,7 М.
Pathophysiology of Exercise Intolerance in Chronic Fatigue Syndrome
1:03:32
Osher Center for Integrative Medicine
Рет қаралды 26 М.
Defective energy metabolism in ME/CFS
35:24
Riksförbundet för ME-patienter
Рет қаралды 9 М.
Dr. Amy Proal: Persistent infection and viral reactivation: a driver of common ME/CFS and LongCovid
33:03
How long COVID ruined my life (and why it won't go away)
14:57
PhD, Dr. Bhupesh K. Prusty: Understanding infectious origin of ME/CFS
44:05
Riksförbundet för ME-patienter
Рет қаралды 1,7 М.
ME/CFS Research Roadmap Webinar - Circulation
3:45:50
NIHNINDS
Рет қаралды 793