This Is MS Multiple Sclerosis Community: Knowledge & Support

Just passing through to introduce myself. :P

hi. I have been visiting (lurking, researching, exploring) this site since last summer in support of a v. dear friend who finds it all too much to absorb, think about, handle on her own. You have a fantastic site and group of people here and the stories and information you share has been incredibly helpful to both my friend and myself.

Right now I am researching what some options are as her RRMS shifts into ...

Hi everyone,

Stumbled across this site looking up LDN and the pro and cons as my neurologist is unsure of its findings ?

Anyway Iam Simon from London,England. 37 years old, married and 1 stepson. Finally diagnosed with MS last summer 2006 with a MRI scan after spending a week in St.Thomas' Hospital. Been a long journey looking for answers for at least 4 years, eventhough both my parents have MS and my fathers brother ...

HI :P MS FORUM MEMBERS. MY NAME IS SEEVA IAM NOW JOINT AS A MEMBER. I AM SUFFERING FROM PROGRESIVE MULTIPLE SCLEROSIS SINCE 1998. MY BALANCE IS NOT GOOD. I AM WARLKING WITH THE HELP OF CANE. MY MAINE MEDICATION IS LDN. MY NUROLOGY WAS NOT HAPPY TO PRISCRIPE THR LDN FOR ME OTHER MY MS FRIENDS. FINALY WITH THE HELP OF DR.BOBLAWERENCE WHO IS ALSO A ...

Hello All

My name is Brenda

I was dx'ed with clinical dx of ms in 1999 I have trouble walking and use
a cane as needed, sure wish someone wouild come up with a cure lolo

Just an introdution to all here.

As you prob konw my wif ehasn't been officially diagnosed yet, but the noises the neuro made tend for it to seem that she does. Still early stages and from what we know it looks like RRMS at the moment. The hospital did take a wad load of blood to test for, whatever they test for, to check for other causes of the symtoms she has.

However with ON, ...

Hello Everyone,

It's hard to know where to start except to say I need the support and advice of others who understand what it's like to deal with MS.

I'm 51, 'old' for MS to begin as one out of four of the neurologists I have seen told me. Never having been sick other than stuff my five kids brought home from school and hospitalization for childbirth, having to inject myself with Betaseron every other ...

Hello, I am a 40 year old female and native of Atlanta, GA. My first symptoms were in 2000 when I experienced episodes of dizziness and balance problems. Throughout the years my symptoms progressed and neurologist could not diagnose me. I received probable diagnose from Lupus, dystonia... and finaly, It's in my head. During this time I lost strength in bilateral UE/LE, right greater than left. My right hand is clawed. I also developed tachycardia, ...

Hello every body
I hope you will excuse my poor english language...
I just discover your site today
I discovered I have MS six months ago
I use Rebif since october 2007
I have made a blog about MS, it is in French but you can click to translate it
I'll come back to read you more
Pat

I'm 53, Male, newly diagnosed with RRMS, and more than a little scared and confused.

Are there any support groups in upstate NY or in Mid (Rutland area)Vermont? I'm working with Dartmouth Medical Center MS clinic in NH but it is 80+ miles due East. Albany, NY is also about 80 miles due South and they have support programs also. I know if nothing relatively close so far. I'm not on any treatment so far ...