MEDICAL MATTERS

Search all questions

Choose a letter to see our categories

  • Show all
  • A
  • B
  • C
  • D
  • E
  • F
  • G
  • H
  • I
  • J
  • K
  • L
  • M
  • N
  • O
  • P
  • Q
  • R
  • S
  • T
  • U
  • V
  • W
  • Y

Questions in the Category: Parkinson’s disease

Caffeine-containing drinks – are they safe if you have ME?

ME Essential Autumn 2025

I know I probably drink far too much coffee – about 5 cups a day – but it helps me to ‘wake up' in the morning and stay more alert during the day. But what do we know about the effect of caffeine on the brain? Is it actually harmful or beneficial to people with ME/CFS?

Shakiness

ME Essential Summer 2025

I am hoping you can shed some light on two types of shakiness which I've had since a recent relapse of my ME.

Some days I start feeling shaky shortly after getting moving in the morning. It's like I've had a big dose of caffeine (which I definitely haven't) and at its worst my hands will be too shaky to do anything fiddly like sewing but resting is hard because I feel wired with it. It normally fades around the middle of the day. It's intermittent and there are no obvious triggers.

More difficult to describe is a sensation I get sometimes which is more disturbing. It's like an inner wobble, possibly centred around my abdomen. It comes and goes and tends to make me feel vaguely weak. It's possible that one trigger is doing too much but otherwise it's random and can disappear for weeks. I find it difficult because I don't know whether I should be resting more when I have this shakiness or trying to ignore it like a lot of other symptoms.

Eyelid twitching – Blepharospasm

ME Essential Autumn 2023

During the course of my illness I’ve experienced muscle twitching in my legs and sometimes in my arms. The twitching tends to occur when I’m not feeling well or tired. And while this can be annoying it doesn’t normally interfere with what I want to do. I’ve recently started having a similar problem with my eyelids. Is this common in ME/CFS? And is there any form of treatment?

Symptoms: Vision

ME Essential Spring 2022

I have ME/CFS and 2 years ago I had to move to varifocal glasses. I had my eyes tested in April and had to return those glasses as I needed a different prescription. I have had them retested today, and needed another prescription. The optician said that my prescription seems to change as my condition fluctuates. What is happening to eyesight as a result of ME/CFS and is there any research in this area? I get a lot of migraines and I think this is because of the problems I have with my vision.

Symptom: Tremor

ME Essential Spring 2018

I understand that a tremor, or shaking in the hands, sometimes occurs in ME/CFS. But it could also be a sign of Parkinson’s disease. I’m in my mid fifties and have had moderate ME/CFS for about five years. It is fairly stable but the tremor, which is in both hands and tends to be more noticeable when I’m fatigued, has only been present for a few weeks. Should I see my GP?

Neuroinflammation

ME Essential Spring 2017

I keep reading about what is called ‘neuroinflammation' in relation to research into ME/CFS. I assume this means inflammation in the nervous system. But is this the same as encephalomyelitis (the E in ME)? I know that encephalomyelitis is largely dismissed by many doctors and is the reason why some doctors refuse to even use the name ME/ myalgic encephalomyelitis.

Dr Charles Shepherd

Charles Shepherd
ME Essential magazine
ME Medical magazine
Shopping Basket
Scroll to Top