Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
Gentle hugs, Linda
I have it too! I get it in both my hands and feet in the shower, and just my feet in bed at night. I understand your saying it's hard to describe. I tried to describe it to my husband and he was looking at my like I had two heads or something, like I'd lost my mind. I'm with you sister!
Barrie
My fingers get it alot when my hands get really cold...feels like they are frostbit. but the burning you describe I get alot in my feet and my face....but Im almost positive it is numbness or in my face it happens before the TN hits or a migraine. Its like my warning signs that something more is about to happen. LOL
Good luck to you with this
PS if anyone tries the roll on Ban....let me know how that works, I just have deodorant sticks but will get some to keep on hand if it helps.
HUGS
Janel