This Is MS Multiple Sclerosis Community: Knowledge & Support

Anyone ever have a MS hug? This was one of the first symptoms of a flare up. It all started with a little numbness in the toes and feet. Then it moved up one leg. To the point that I could walk but wasn't sure were my feet where. Then it skipped over my waist line and went from my belly button to under my chest. Now when it got that far is when it ...

I'm 26 yrs old going on 27 w/in the month.

Just this past week I've had an MRI done as my neurologist suggested. Both brain and spinal MRI's were attained and I'm currently waiting to hear back from my Neurologist. I was wondering if people that have been diagnosed with MS can weigh in on my current condition (outlined below) to see if these were some of the early symptoms you've had before you were ...

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just a question.. how many of you, honestly, think that one day, hopefully in the not so distant future, there will be a cure for this disease? With all the research with stem cells, do you think that one day it will become the next, say, strep throat where one just takes some pills and is done with it? or am i just hoping for too much? I read an article about some stem cell ...

My nuerologist is sometimes in a wheelchair other times on crutches. This has offten time made me curious. He is a wonderful guy and I like him alot. He has never volunteered what his condition is to me. My question is would it be wrong of me to ask? This doesn't make a difference to me so maybe I shouldn't. It is just something that I have wondered about since my first visit almost two ...

I know this might sound crazy (ironic since I'm talking about Zoloft) but here goes anyway. I tried to stop taking my daily Zoloft pill. After about three or four days I began getting these strange sensations in my head. It felt like electrical zaps. After a few weeks I couldn't stand it anymore and started taking the Zoloft again. The zaps went away when I started taking the drug again. What's up with this? ...

This was a gotta-see-it-to-believe-it story. What can it do for an MS patient, if it could?......
http://news.bbc.co.uk/1/hi/health/7354458.stm

http://c.moreover.com/click/here.pl?j13 ... 6&w=464753

Is driving me crazy! This was almost completely gone during my steroids treatment and a bit after, but it's slowly come back.

Anyone else dealt with burning mouth before? It can be pure agony. I get the burning in the mouth, esp. on my top right side and my cheek feels like it's on fire (on the inside), my tongue feels like a million bees are stinging it, and my lips can feel a slight ...

Hi guys

I just wanted to ask if anyone has found anything which helps with this. Mine seems to be getting worse.

My neuro said it's normal for ms patients, but apart from neuropathic pain killers (gabapentin etc), which have some terrible side effects, nothing else was offered.


Thanks

J.