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: Research
The DHSC Delivery Plan – Why won’t the government provide any funding for referral services or research?
I listened to the excellent speech from Tessa Munt in the House of Commons debate on ME/CFS. It’s perfectly clear that all the well-meaning words in the DHSC Delivery Plan are of very little use if there isn’t going to be any new money for either the specialist referral services or for research. Why is this?
Can nimodipine be used to treat ME/CFS?
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.
DecodeME results – Quick answers to four common questions
a) Have the researchers found a specific gene for ME?
b) Do the genetic markers that have been found cause ME?
c) Are people with ME born with these genetic markers?
d) Do these results mean that we can now find a drug treatment for the underlying disease process in ME/CFS – instead of just managing symptoms?
Does the MEA fund research that involves the use of Animals?
I understand that there may be some research into ME/CFS and Long Covid being undertaken or planned that involves the use of experiments that use mice. Does the MEA Ramsay Research Fund support or fund any research that involves the use of animals?
Low-dose naltrexone (LDN)
Having read a large number of reports from people who are taking LDN, I would like to give it a try. My GP says that he knows nothing about this drug being used in ME/CFS and has refused to prescribe it on the NHS. I also see a consultant rheumatologist privately and he won't issue a private prescription.
I know that there's a pharmacy in Scotland that supplies LDN but I want to use it under proper medical supervision. Why is it so difficult to just try taking a drug that may be of benefit?
Biomedical research
How can we ensure that important biomedical research information about the cause and treatment of ME/CFS is getting through to policy makers and health professionals so that people are treated correctly?
MEA Ramsay Research Fund –administration costs
I am considering making a large donation to help fund biomedical research into the cause or treatment of ME. I know that there are several ME charities both here and abroad that fund biomedical research into ME. But I only want my money to go direct to research. So please can you let me know how much of my donation would go to administration costs if it went to the MEA Ramsay Research Fund.
Post-mortem research – age restrictions
I was very pleased to read that the ME Association is once again going to be organising and funding post-mortem research – this time in conjunction with the Manchester Brain Bank. Please could you explain why the upper age limit for accepting post-mortem requests is set at 50.
Meeting my MP – what should I ask?
As we are heading for a general election later this year, I thought it would be useful to see if I could arrange a face to face meeting with my MP. To my surprise I have been given 15 minutes at his local ‘surgery’ in a few weeks time. What are the most important issues that I need to make my MP aware of?
Treatment: Hyperbaric Oxygen Therapy (HBOT)
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.
Dr Charles Shepherd
Dr Shepherd has been Trustee and Hon. Medical Adviser to the ME Association for more than 40 years. He is integral to the charity's activities and provides information and support based on his professional knowledge, personal experience as a doctor with ME/CFS, and the understanding gained from helping many thousands of people with the condition. He was a member of the comittee responsible for the 2021 NICE Clinical Guideline and is a recognised expert on ME/CFS in the UK. His knowledge extends to Post-Viral Fatigue Syndromes (PVFS), Myalgic Encephalopathy/Encephalomyelitis (ME), Chronic Fatigue Syndrome (CFS), and Post-Acute Sequelae of SARS-CoV-2 infection (PASC) or Long Covid.
If you have questions about ME/CFS or Long Covid, you can:
- Review the free information in the What is ME/CFS section of the website, and the free Covid-19 and Long Covid information in the website shop.
- Review the largest range of literature covering all aspects of living with ME/CFS. Download detailed information about symptoms, diagnosis, management, co-mordidities, employment, education, related health conditions, The 2021 NICE Clinical Guideline, welfare benefits etc.
- Join the ME Association as a member and you'll receive the highly-rated ME Essential magazine, and you can ask questions of the charity’s expert advisers including Dr Shepherd.
- Contact us via the ME Connect Telephone Helpline (open 365 days a year) and speak to one of the national team of fully-trained volunteers who waiting to provide information and support.
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Medical Matters is based on the popular ‘Ask the Doctor‘ series featured in the highly-regarded member’s magazine, ME Essential, and in the healthcare professional magazine, ME Medical. Both are produced by the ME Association and published as hard-copy magazines every 3 months and sent to members and healthcare professionals by post to home or business addresses.
If you are a Health Care Professional you can sign-up to receive ME Medical magazine (people with ME/CFS can also nominate their HCP by completing the sign-up form).