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Questions in the Category: Oxygenation

Hyperbaric oxygen therapy – is it safe?

ME Essential Spring 2025

I know several people with ME who claim that hyperbaric oxygen therapy (HBOT) has been helpful. I’ve read your review of the evidence in a previous issue of ME Essential and have been following the interesting reports on the MEA website and Facebook page regarding the clinical trials that are now assessing its use in Long Covid. So, while I’m aware that this has to be regarded as a very experimental treatment, I would like to give it a try. But are there side effects that I need to be aware of?

Micro-clots

ME Essential Spring 2024

Has there been any progress with the research that has been looking at the presence of ‘micro-clots’ in Long Covid and possibly in ME/CFS as well?

I know that people are still travelling abroad to be treated with apheresis to remove these small clots at expensive private clinics. But I understand that no such treatment is available here in the UK – either privately or on the NHS.

Treatment: Hyperbaric Oxygen Therapy (HBOT)

ME Essential Summer 2023

Has there ever been a clinical trial to assess the use to hyperbaric oxygen (HBO) in ME?  I know that HBO is being used by people with multiple sclerosis as well as ME – so it seems that there are positive effects in the case of neurological diseases. I’ve also read that a clinical trial involving people with Long Covid has found some beneficial effects.

Treatment: Apheresis

ME Essential Summer 2022

Are you aware of a new treatment called apheresis that is being given to people with Long Covid? It is supposed to remove small blood clots that are involved in causing Long Covid. Some of the overseas clinics that are treating people with Long Covid are also offering apheresis to people with ME/CFS and I know of several people who have travelled abroad to have apheresis – with mixed results. So why isn’t apheresis also being made available to people with ME/CFS here in the UK?

Blood Flow: Oxygenation

ME Essential Summer 2018

I know there has been some interesting research involving neuroimaging studies and that this has demonstrated defects in blood flow to certain key parts of the brain. But does this research mean that people with ME/CFS have low levels of oxygen entering the brain? If so, does it also explain some of the key brain symptoms – cognitive dysfunction in particular? And could it lead to new forms of drug treatment?

Charles Shepherd
ME Essential magazine
ME Medical magazine
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