This Is MS Multiple Sclerosis Knowledge & Support Community

Maybe I'm in what they call 'denial' lol. Testing positive on all 3 tests should be enough for me to be sure I have MS.

ya there's def ms-style crap wrong with me too, but whateves guys. denial is good for ya hehehe! and we know how to fix some of our probs associated with it right?

for instance arti, i'm going to look up if there's any research on the ms hug and magnesium. it would make sense to me if there is a connection. we already know magnesium has helped some of us here in a few different ways!

for me it's only been 2 and a half years and i have improved plenty with a variety of vitamins and minerals. still more work to do but getting better. i'm pretty sure even the laps i did in the pool yesterday didn't mess with me quite as bad as last year.

I think it's just a case now of... what caused the facial spasms I had last fall? Doctors looked and said "Kinda looks like Bells Palsy" (my mouth wasn't drooping however, it was being pulled up on the right side). I can still feel nerve pain slightly off and on (dull burn that I get in my face occasionally, more so my neck on the right around where my neck and shoulder meet). It could be the MS, but it could be something else... that's the bothersome part. Oh and this burning mouth, which I will say has gotten tons better, but I can feel a definite spot on the top of my tongue where it feels like nerve pain, and then I get the soreness in my right cheek, and sometimes around my gums.

oww! i should go back and read some older stuff before i ask you this next question about burning mouth! it's not sort of cyclical in a way these days at all is it?

Dude, chill out. We're here to support eachother, not compete.

Misdiagnosed wrote:I see why I never posted. This thread has been hijacked. Please use the private message option

Ouch that hurt

this is how we roll here mis-D, we're all just kinda sayin, ya, hear dat, i got some questions bout my dx too, and firin info back and forth.