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.
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
- 5
- LFT's
- Lactic Acid
- Lactobacilli
- Legal Advice
- Lethargic
- Life Expectancy
- Ligaments
- Light Headedness
- Limbs
- Liver
- Liver Disease
- Liver Function Tests
- Lockjaw
- Long Covid
- Long Term Condition
- Low Glycaemic Index
- Low dose naltrexone
- Low mood
- Lupus
- Lustral
- Lyme Disease
- Lymph Glands
- Lymph Nodes
- Lymphadenopathy
- Lymphatic system
- Lymphoma
- Lyrica
Questions in the Category: Lyrica
Pregabalin (Lyrica)
I have been reading some disturbing newspaper reports about the misuse of pregabalin and it looks as though there may be further restriction on doctors about prescribing this drug. I know that some people with ME/CFS have had major problems with side effects. But there are others like myself who have found pregabalin to be very helpful for pain relief where other drugs have failed. Do you think that my GP will be able to continue prescribing it?
Treatment: Selective Serotonin Reuptake Inhibitors
My doctor has suggested that I might like to try using a drug called sertraline (trade name is Lustral). I know it’s normally used to treat depression but he says that it may be worth trying because ME can upset the levels of chemical transmitters in the brain and this drug can help to increase the level of one called serotonin. Is this drug safe? And is there any evidence that it can be used to treat ME?
Symptom: Nerve Pain
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?
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-mordities, 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.
- Contact us via email or social media: Facebook, Instagram, Twitter, LinkedIn.
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 an HCP you can sign-up here to receive ME Medical magazine (people with ME/CFS can also nominate their HCP by completing the sign-up form).
