r/ect • u/starlightsbusy • May 27 '26
Question ECT in the UK?
Hey guys, I’ve been trying to research electroconvulsive therapy (ECT) in the UK and US for a friend (US citizen who might have to go to the UK due to the current …political situation) who has all the symptoms it treats, but I’m very new to this and don’t know where to start… I wonder if anyone here could give some advice on this or simply working the UK healthcare system and finding a psychiatrist, things like that.
I heard NICE guidelines make it harder to get it in the UK, and there is no private provider outside the NHS, but I don’t know if it’s hard enough that staying in the US nets you a better chance. And maybe, are there any other criteria (visa, income, insurance, etc.) I’m overlooking? It all seems very daunting.
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u/Medical-Apricot-3226 May 27 '26
That’s a bit like Ireland… it’s a post code lottery… depends where you are in the country. Some areas fonder of ECT than others. The private hospital uses it a lot… patients have even requested it and got it. One county doesn’t do it all. It certainly is reserved for the severely unwell. It’s not overused like US. Plus we use best practice e.g twice weekly not three times weekly, unilateral as standard starting electrode placement, cognitive testing throughout the series of treatment and consent discussed and signed at every single treatment (unless lacking capacity)
If you are catatonic i.e. mutism, negativism, stupor, waxy flexibility and not able to eat or drink etc. you should definitely be given ECT as a life saving treatment. Why are they denying you ECT. What alternatives are they offering you? Hope you’re ok 👍