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Questions in the Category: Insomnia

Daridorexant (Quviviq) for sleep disturbance

ME Essential Autumn 2026

I have been reading about an interesting new drug for treating insomnia called daridorexant. I thought it might be worth trying as I have difficulty getting off to sleep, wake up several times during the night and always wake up feeling completely unrefreshed. My GP said she didn’t have any experience of using this new drug and that it was also quite expensive. So she wasn’t willing to prescribe it.

Is there any evidence that this is a drug that could be helpful for people with ME/CFS? If so, should I go back to my GP?

Treatment: Modafinil

ME Essential Summer 2023

I have had PoTS and ME/CFS for over 10 years and now have Long Covid as well – if that’s even possible as perhaps they are the same thing anyway? My question is about a drug called Modafinil as I have been offered a trial of this treatment from my PoTS consultant to help with my fatigue. I have looked online and can’t find a lot regarding its use in patients with ME/CFS. Please could you point me in the right direction for any research on this or anyone with ME/CFS that has any experience of taking it. One of my main concerns is that it will create a false energy high, so that I will want to do more, then I will end up with worse PEM and crashing. Another potential problem is that I already have mental-health issues as some of the side-effects are mental-health related.

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!

Treatment: Low Dose Steroids

ME Essential Autumn 2022

I’m having joint problems at the moment and my consultant wants to inject a steroid into the joint to calm things down. I’m concerned that this could make my ME/CFS worse because I thought that people with ME/CFS should not take steroids. What do you suggest I do?

Mental Health: Depression

ME Essential Spring 2018

Like many other people with ME/CFS, I often feel fed up and frustrated by all the restrictions this illness imposes on my life. But I don’t feel depressed. I now have a new bright GP who thinks I am depressed and he wants me to try a course of antidepressants – to see if they make me feel happier! I know I would feel happier if I just felt well again. But I’m not convinced that I need antidepressants to do so!

Charles Shepherd
ME Essential magazine
ME Medical magazine
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