I'm already on gabapentin for TN, its been a miracle drug for me.

I also had the paresthesias with the attack that got me my diagnosis. That's different than this though. With that, I would sit down on cold tile and it would feel like I just sat on a pit of lava. It was really weird. Thankfully that faded.

You're right, this seems completely unrelated to the environment. It seems perceptual, but then I sweat, shiver, etc. Who knows? It is just so irritating because its impacting my sleep. I'll layer up, fall asleep, and wake up in sweat. Take the layers off, go back to sleep, and wake up shivering. There's just no winning since its just swing from hot to cold to hot, and sometimes both at once! I could deal with it fine if I could just sleep through it. Sigh...

I have a long scheduled neuro appointment early next month. I'm definitely going to bring this up.

Maybe buy an electric blanket that you can put on a timer so it goes off and on? -- might be hard to coordinate with chills and sweats. Bit it's a thought!

When I first got MS I was constantly running low grade fevers all the time. They were confused because the docs didn't think that was a typical MS system. It was so unpleasant. My husband could immediately tell when I was running a fever because I just slowed down like molasses. That went on for a couple of years. But now they appear to be gone! Yeah!!

Natalie. me too. I still run low grade fevers, for no other apparent
reason. In the hospital, after my fall, the Nurses noted a LGF
almost every day.

OMG, I just thought my body was set on wacko! No, its just set on MS! My house can be set on 72 and Im freezing, later on I'll check the stat again because Im burning up and its 70, and Im like !! My hands and feet are constantly like Ive been keeping them in the freezer, even in the summer. Oh, lets not forget the tip of my nose, arctic cold, cant explain that, but my nose decided to get in on the fun. DH likes to make fun of that one, its my one freebee I give him

You are very funny but correct!

ANN