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Questions in the Category: Chronic Pain

TENS machines for pain management

ME Essential Winter 2025

I've read that an electrical device called a TENS machine can sometimes be helpful in relieving muscle and joint pain. Is this a device that might help with pain in ME? And is it safe to use?

Allodynia – increased sensitivity to touch and movement

ME Essential Summer 2025

I have just been told that as part of ME I have a condition called allodynia which, as I understand it, affects the brain and nerves. As a result, my brain is detecting pain which is often caused by touch or sometimes movement. The painkillers that I'm currently taking – ibuprofen and paracetamol – don't really help. Is allodynia more common in people with ME? And are there any other drug treatments that I could try? I should add that I also suffer from occasional migraine-type headaches.

Neuropathic pain

ME Essential Winter 2024

Please could you explain what is meant by neuropathic pain? Is it different to ordinary pain? And is the treatment any different?

CBD oil for pain relief

ME Essential Autumn 2024

I keep reading about people with ME/CFS who are using cannabis oil (CBD oil) for pain relief – with varying degrees of benefit. My GP said that he isn’t allowed to prescribe cannabis oil for pain relief and he wasn’t convinced by the claims that are being made. So is there any evidence that CBD oil can help with pain relief? And given the link to cannabis is it safe to try if you have ME/CFS?

Bone pain and ME/CFS

ME Essential Autumn 2024

I have just been reading the new MEA information leaflet on pain management. This covers muscle, joint and nerve (neuropathic) pain ME/CFS. But why isn’t there any mention of bone pain? I have hip pain that was eventually diagnosed as being due to osteomalacia and vitamin D deficiency – which I understand is more common in ME. This is now being treated because my doctors felt I was at increased risk of having a fracture in the hip bone.

Alternative treatments: Flotation tank

ME Essential Winter 2023

A friend of mine who has a painful rheumatic disease has been using a local floatation tank to help relieve her pain. I have quite a lot of ME related joint and muscle pain and the drugs that have been prescribed are of very limited benefit.

Is this something that’s worth trying for pain in ME? Are there any potential side-effects?

Symptom: Nerve Pain

ME Essential Winter 2020

Like most people with ME/CFS, pain is a fairly constant and frustrating symptom. But this has become more persistent and severe over the past few months. My GP has prescribed various pain relieving drugs – including low doses of amitriptyline and gabapentin – none of which has had much effect. As well as the pain, which often has a burning quality to it, the areas around it sometimes feel numb and strange. I’m starting to feel quite depressed as a result – is there anything else that could be done to help?

Charles Shepherd
ME Essential magazine
ME Medical magazine
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