Multiple Sclerosis (MS) Support Group

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Brain & Nervous System
/ Multiple Sclerosis (MS) Support Group

Burning (sunburn feeling) spreading

deleted_user
deleted_user
So I've had the burning pain (similar to a sunburn) across my shoulderblades since my second flare. But now after over a month on Copaxone, and increasing my Gabapentin dosage, the burning pain has extended beyond my shoulderblades to my arms, back, neck & legs. Is this a bad thing? -- Or is it just another fun part of the MS rollercoaster?
deleted_user
deleted_user
I call it "THE BURN". I have had some where it felt like a heart attack. Its a M.S. thing best thing to do is dont stress and stay cool. It will pass. MerryChristmas.
deleted_user
deleted_user
I get this too in all the places you describe--esp my left side face though :( and my NECK ouch!!!
Its constant and it doesn't go away ever for me. I'm assuming this is an MS joy I can cherish my whooole life *sarcasm*

HUG I feel your pain! I recommend ice packs too! And keep an eye on the inflammatory content of your meals! Once I cut down on inflammatory foods, I noticed the burn was less severe

Hope that helps some!
mmthlvr
mmthlvr
I've also had "THE BURN" in my chest & it scares me every time. I also get it when I sit back in a chair, it feels like I'm leaning on a heating pad. The burns suck, it always seems worse at night. Merry Christmas:)
deleted_user
deleted_user
I get it also. Just did the other day. Forearms and back, which is weird as it's usually neck and scalp. Hadn't had it for a while, and until this site..thought I was CRAZY....so thankful to read of others like myself. Sorry you experience it though =(

Heidi