Lhermitte's?

Yes mine started just as I finished RT. It was never really bad. If it is it feels like electric shocks, really unpleasant. 
2 years on I still have it but it’s improved vastly and not even a minor inconvenience. 

Yes, same here. 

Like Dani, mine has vastly improved but still catches me out occasionally!

Linda x

Thanks both. That’s reassuring

Hi, yes I had it too after RT. Mine didn’t last long I’m pleased to say. Just another thing they don’t tell you might happen. 
Fi 

Yes I had/have this, was quite often but nearly 8 months out of treatment now and it’s getting less and not so intense

Yes I’ve also got Lhermitte’s. Mine started a couple of months after radiotherapy finished and felt like an electric shock down my spine, legs and feet. It was only when I mentioned it to my HNC nurse that he asked if it just happened when I bent my head towards my chin. Up until then I hadn’t realised that was what was triggering it. Classic signs of Lhermitte’s he said. Apparently it will go in time. 

Best wishes

Carol x

Strange nobody ever tells you about it. I learned here. Then did some research