This Is MS Multiple Sclerosis Knowledge & Support Community

I think that was only concern, the mri, this was so long ago haha! thanks!

Well, this year fell apart fast. Though I knew what MS was before, now I know for real. It attacked my spine and put me in the hospital/rehab for 2 months. Been in and out of a wheel chair all year. In and out of hospital all year as well. Symptoms keep popping up, new and old, symptoms I never even...

I was on LDN, then was on Rebif, now I start Tysabri on the 12th. I have also been raising money for a stem cell transplant haha.

Lol went by so fast... Yes, 22 now, well, 22.5? Lol....

Most people would say (though I am not talking from experience for several reasons) that you go on a few dates, get to know each other well and then IF it seems like things are clicking you bring it up but CASUALLY, "you know I just thought I should tell you, I do have a slight autoimmune issues, MS...

Yeah luckily have been on Prednisone for a while and since I react well to it I have not had to deal with fatigue for a bit but when I do it can get HORRIBLE, I hate it especially when my mind if not tired but my body is.

I will have to look him up and see if I can get him to join the group!

yes, disturbing and painful indeed. It feels really bad when you cant accomplish what you actually always wanted to, i had a craze for good physique build up was regular with it, years before diagnosis. But, now everytime i try to do some workout, it end up with another relapse, be it minor. I neve...

3:09 pm - "banged my head on wall edge, while putting my trimming machine in rack. All was sudden, involuntary, but reflex back was fast. :cry: " - sometimes, i've notied while sleeping my jaws are suddenly involutarily closed and back. Leading my inner cheek skin between them !! :oops: Yash :peace...

Yeah bit all they got to say is "hey, what up?" and that is better then nothing! I don't know, since I posted this my relationships with so many people have gone up down and everywhere in between until finally some of them has disappeared and to be honest I kind of like it this way now.

I don't try to hide MS anymore, its too had, I mean, I don't advertise it to everyone but if it comes up it comes up. If you add me on FB you can join my group and participate there just don't add anyone else because sometimes they have some MS logo on thei pictures and then your friends will be abl...

yes, will definitely visit your pages. Actually i'am visiting to calgary for few days i had thought even you were from that place, none of my frnds know this that i'am an Ms'er, they won't even understand. So, i just prefer rather not disclosing it, anyhow i'am about to get my MRI contrast done, wh...

Hi Matt !! even i'am 21 yr old, male !! I just couldn't find anyone of my age with this prob. So, its nice to meet you here the only diff. here is thsat i'am from India, a place where this problem arises rarely and you from canada, had read about you on net months back. Right now my left half of my...

Yeah at first I thought SPMS meant you had to be in really bad shape but thats not always the case, its just a matter f how the disease is actually progressing. I'm starting to think I might have it but it's WAY too soon for me to jump to conclusions haha...

Rusty: Thats good that you still have a pulse haha, hopefully you can get that taken care of soon, I'm sure it sucks! Bart: Funny, it seems like everything is like that! A negative means nothing but a positive means everything just like a spinal tap for MS man I hate that. So basically the test I ha...

Sounds more like Secondary or Primary Progressive MS which could cause those very problems without presenting actual flareups, just a slow progression of symptoms. I wrote about this a while ago, maybe it will help you. http://www.mattsms.com/2011/01/4-types-of-ms.html I too had pretty bad numbness ...