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Questions in the Category: Blood Vessels

Can nimodipine be used to treat ME/CFS?

ME Essential Winter 2025

I know that nimodipine, a drug that dilates blood vessels, has been used by some doctors in the past to treat ME but this no longer appears to be the case. In view of some of the recent research into both ME/CFS and Long Covid, which indicates that part of the problem may involve reduced blood supply to the brain, I wonder whether this is a drug that we should be looking at again.

I've mentioned this to my GP but he won't even consider prescribing this drug. If it's something that might just work, I don't understand why my GP won't even give it a try.

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.

Research: Post-Mortem

ME Essential Summer 2023

What is happening to post-mortem tissue research into ME/CFS at the moment? Is the ME Association still funding and carrying out any postmortem research? And have any significant abnormalities been found in the post-mortems that have been carried out so far?

Dysautonomia: Orthostatic Intolerance (OI) and Postural Orthostatic Tachycardia Syndrome (PoTS)

ME Essential Summer 2021

I keep reading about orthostatic intolerance, PoTS and postural hypotension and how they can all be symptoms of ME/CFS. But what do all these medical terms mean? What is going wrong? And are all these symptoms and syndromes related to each other?

Symptom: Low Temperature

ME Essential Summer 2020

Do people with ME have a low body temperature? My body temperature always seems to be slightly below normal when I check it with a thermometer and I’ve seen this being discussed on internet discussion forums. I’m also starting to feel the cold more than I used to do.

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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