Does anyone else find that during a flair up that symptoms are 100 times worse at night?
Flair: Does anyone else find that during a flair up... - NRAS
Flair
Yes most definitely . I also sweat terribly at night
Yes, I put it down to being under the bedclothes and heating up even more than normal !
It's more difficult to distract yourself from pain at night, especially if it is keeping you awake.
And I find I quite rapidly stiffen up as soon as I stop moving around.
So my main pain relief is taken at night and I have been known to take some more at 3am as well.
Yes worse at night definitely. If I want to move in bed it takes ages and I have horrible pain.
I stiffen up during the day as well if I stop moving for a few minutes.
I am in a full body flare now just want to call someone if I could have a steroid shot as had to stop Leflunomide a month ago and will start Otezla on the 5th March. That's when I have an appointment to see the nurse.
And the pain is worse at night definitely...
Yes definitely worse at night.
Pain is always worse at night because you don’t have any distractions
At night you're just within yourself. Not just pain, but the slightest itch seems to wander around the body with your mind chasing it. It's annoying. I get over it by meditating and focusing on my breathing. I start by counting from 1 to 20 and back in one of many foreign languages. That really focuses my mind and then I can concentrate on breathing.
Yes. My electric blanket is my friend at these times, well that and the news droning on for a bit kinda lulls me back to sleep for a bit! M x