What we treat

Chronic Fatigue Treatment in Marylebone, London

Chronic fatigue syndrome, or ME/CFS, is disabling fatigue made worse by activity, with unrefreshing sleep, pain and difficulty thinking. The evidence for magnetic stimulation here is early and this page says so. One of our former patients has written publicly about his own course, and his account is one account rather than a typical outcome.

Chronic Fatigue

Understanding chronic fatigue

ME/CFS is a long-term condition whose central feature is fatigue that is new, persistent and not relieved by rest. Its defining sign is post-exertional symptom worsening: activity that used to be ordinary leaves you worse for days afterwards. Sleep does not refresh you. Thinking, holding attention and finding words all become harder. Pain, headaches and light-headedness on standing are common alongside it. NICE guideline NG206 sets out how it should be diagnosed and managed in the UK.

No single mechanism has been confirmed. A large proportion of cases begin with an infection. Autonomic dysregulation is measurable in many people, which is one reason heart rate variability is tracked continuously through a programme here. Non-restorative sleep sustains the fatigue once it has taken hold. Anyone who tells you the cause is settled is ahead of the evidence.

What we can do is assess you properly and then treat conservatively. Sessions are seated, brief and require no physical exertion, but repeated travel to Marylebone is a real load for someone with post-exertional worsening, so the schedule is planned around that rather than dropped on top of it.

Etienne Balland wrote about his own treatment here in The Telegraph on 16 March 2026, under his own name. His chronic fatigue syndrome began in March 2022 and he spent a year bed-bound with his parents as his carers. He had thirty sessions in his first course, fifteen to twenty minutes each, sometimes two or three in a day. He reported improvement within two weeks and a clear turning point by week three. He relapsed in June 2025, had a second course, and says he feels 90 per cent back to normal. He describes his illness as chronic fatigue syndrome and does not attribute it to Covid. He is now training as a practitioner.

Sceptical? You should be. One published account is not evidence of a typical outcome. The trial evidence for rTMS in ME/CFS is early and small, and NICE guideline NG206 does not recommend magnetic stimulation for this condition. Your clinician will tell you that at the free consultation, and will say plainly if a course is not a reasonable thing for you to spend money on.

What you do get is measurement. Grip strength, continuous heart rate variability and cognitive testing across twelve domains are taken before treatment and repeated during it, so a decision about continuing is made against your own numbers rather than against how you happen to feel on the day you are asked.

What causes chronic fatigue?

  • No single cause is established; NICE guideline NG206 describes ME/CFS as a condition without one confirmed mechanism

  • A triggering viral or other infection, which precedes onset in a large proportion of cases

  • Autonomic nervous system dysregulation, measurable as reduced heart rate variability

  • Altered central nervous system processing, which is one proposed driver of post-exertional worsening

  • Non-restorative sleep, which sustains the fatigue once it has started

  • A period of sustained physical or emotional stress before symptoms began

Common
questions

Is there real evidence for rTMS in ME/CFS?

Not much yet, and we will not pretend otherwise. The published work is early and small, and NICE guideline NG206 does not recommend magnetic stimulation for ME/CFS. What we can offer is careful assessment, a course delivered slowly, and measurement that tells you early whether it is doing anything.

Who is Etienne Balland?

A former patient who described his treatment here in The Telegraph in March 2026, under his own name. He had chronic fatigue syndrome from 2022 and was bed-bound for a year. He is now training as a practitioner. One published account is not evidence of a typical outcome.

Will a course make my post-exertional symptoms worse?

That is the right question to ask. Sessions are seated, brief and require no exertion, but travelling to Marylebone repeatedly is itself a load. We plan the schedule around that, start conservatively, and will slow or stop a course if your symptoms worsen rather than push through.

How many sessions did the patient in The Telegraph have?

He described thirty sessions in his first course, each fifteen to twenty minutes, sometimes two or three in a day. He reported improvement within two weeks and a clear turning point by week three. He relapsed in June 2025 and had a second course. Your own course may look nothing like that.

Do I need a diagnosis before you will see me?

Not for the free consultation. For a course, we need to know what we are treating, which means a diagnosis and a look at what has already been ruled out. NICE guideline NG206 sets out how ME/CFS should be diagnosed in the UK, and we work to it.

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Naya • 1 Orchard Street, London W1H 6HJ

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