In fact my symptoms of convulsing on my right side continued after my EEG test and were becoming so bad that I began to have them in my sleep.  I would wake up with my muscles in spasms on my right side.  This time I went to see a Physician's Assistant at my neurologist's office.  I told her about my recent EEG and the results and she told me a story.  One of the nurses there was showing signs of having seizures so she sent the nurse to get an EEG.  When it was found normal she was then sent to get an MRI where they found lesions and subsequently diagnosed her with MS.  The Physician's Assistant told me, "Yeah she was jerking and flailing about and I thought for sure this was a seizure but I was wrong." 

This made me feel better (and my friend too who had originally suggested that I should get an EEG) that these MS symptoms can sometimes mimic other disorders. 

I am glad I got the EEG, just for peace of mind.  And I never thought I would say this but I am grateful it was just my MS.  I still wonder about some of my MS symptoms as they seem so unusual but this seems to be the nature of the disease.  One thing you can say about Multiple Sclerosis is that you never have a dull moment. 

So tell us about your experience.  Have you ever had an EEG?  Does anyone out there have a seizure disorder and MS?  Have your MS symptoms ever mimicked other health problems?  Tell us all about it, we want to know.  You help others when you share your story here.