Does anyone know where to get radar keys from and the process? (Radar keys allow the user to access disabled toilets)

Also does anyone have any advice for claiming disability benefits for fibromyalgia sufferers?

I'm currently based in Crewe, UK

Hi lovelies, does anyone uk based have a round about timescale of how long a neurologist referral takes? Also what will happen at my appointment, letters not even here yet and im already nervous xx

Hi, Technically this is 2 questions but they are interlinked so I thought I'd ask them together x

I am already on P.I.P because of my Disc Degeneration, but now I've been diagnosed with FM as well, should I try to get my award updated or leave it till my review next year. (I don't want to end up losing what I already have)

Part 2 Has FM been classified yet in the UK as a long term disability? I know it has in America and Northern Ireland but not sure about here.

Thanks for your advice x

Has anyone tried this? Was given it on Wednesday to start for pain as its the new fibro medication apparently although my pain isn't fibro related at the moment but as nothing else is working and additive this is the best way forward.

Has anybody had a lyme disease test, since 2015 I have been steadily going down hill(mind and body) last year more rapidly and now walk with a stick.
Was diagnosed with fibromyalgia end of 2019 although I was convinced I had MS.
I recently had a lyme disease test that came back positive for borrelia, bartonella and babesia... I know alot of you have similar symptoms so it's worth getting checked