MEDICAL MATTERS

  • Medical Matters features questions asked by Members of the ME Association on health-related topics.
  • Dr Charles Shepherd and the ME Association's other advisers answer these questions by sharing their expert knowledge.
  • Medical Matters is based on the popular ‘Ask the Doctor’ series in ME Essential magazine.
  • It is a free resource that supplements the detailed information contained in the full range of literature that can be found in the website shop.

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Questions in the Category: Exercise

Treatments: Mestinon (Pyridostigmine)

ME Essential Winter 2022

I’ve read about a drug called Mestinon being helpful for some people with ME, especially if you also have postural orthostatic tachycardia syndrome (PoTS), and I would really like to try using it. I know it can cause unpleasant side-effects but I’m willing to take a risk. Do you have any advice on how I might be able to convince my GP to prescribe it? Or do you know of any private doctors that might be willing to prescribe it?

Post-Viral Fatigue Syndrome, Myalgic Encephalomyelitis or Encephalopathy, Chronic Fatigue Syndrome, and Long Covid

ME Essential Winter 2022

Please can you define what PVFS, ME/CFS, and Long Covid mean. I am having difficulty determining if they are the same disease or different. Thank you!

Management: Fitness

ME Essential Winter 2021

Can I ask what the advice is on heart health for people with ME? As most of us can’t exercise, how do we maintain a healthy cardiovascular system? Is a healthy diet enough?

The 2021 NICE Guideline ME/CFS: Regrets

ME Essential Autumn 2021

I know you feel that the new NICE guideline is a major improvement on the first one. So do I. But do you have any concerns, disappointments or disagreements on the content?

Cardiopulmonary Exercise Testing (CPET)

ME Essential Spring 2021

Why aren’t the oxygen levels of ME sufferers routinely checked?

Management: Swimming

ME Essential Autumn 2020

Like some people with ME/CFS I’ve made a significant degree of improvement over a number of years. I’m fairly stable, mobile, able go for longish walks, and manage to do some part-time work. A well-intentioned friend who goes wild water swimming has suggested that I ‘give it a try’. She claims it can have all kinds of health benefits, including “resetting body clocks that have gone wrong”. She even pointed me to some research about the benefits of cold water swimming for conditions such as arthritis. I’m very open-minded about trying anything that might work. But I’m concerned that this could actually make ME/CFS worse.

Symptoms: Muscle Cramps

ME Essential Summer 2017

Muscle pain has always been a significant part of my ME/CFS. But I've now developed painful episodes of muscle cramp — especially at night. My GP has prescribed quinine —which has helped a bit. Is there anything else you can recommend that might help?

Treatment: Hydrotherapy

ME Essential Spring 2017

My physiotherapist has suggested that I might like to use of the hydroils therapy pool at a local hospital.

I have been making fairly steady progress over the past year (with the occasional short relapses) and used to really enjoy swimming — something that I haven't done since becoming ill with ME three years ago.

The physio says that the changing facilities are good, the water is warm, the atmosphere is relaxed and nobody is encouraged to do anything that they do not feel comfortable with. So why not give it a try?

Charles Shepherd

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