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Q: Symptoms of MS?
asked by: jendi75 on August 18th, 2008
New User
Hi,
I started experiencing possible symptoms of MS about 6 months ago. To begin with, my father has had MS for at least 10 years. My first incident was somewhat mild, since it lasted less than 24 hours. However, it did cause some concern so I went to a neurologist. My first symtom was a shocking feeling that ran up and down the back on my right leg. Any time I touched the back of my leg, it caused the shocking feeling. This lasted about 24 hours. The next day the schocking went away, but then I experienced a buring feeling on the front of my leg. Almost like I was sunburned. This went away after 24 hours.
I saw a neurologist and he reccomended getting an MRI of my brain, given my family history. The results came back with multiple white spots, but according to my doctor they were small and not located in the parts of the brain that could signify MS. However, he did say that he could be wrong and wanted me to get a 2nd opinion with an MS specialist, who apparently is one of the best in the country.
I saw him about 2 weeks ago, and he didn't seem to have an opinion one way or the other. He didn't say that he did not think it was MS, all he could say was to do a follow up mri in a few months and also an emg. He also said that one of the white spots were considerably bigger than all of the rest.

I was completely fine dealing with all of the above, until the past week. The numbness in my legs and arms has gotten worse. I am feeling it off and on during the day, and it is a lot worse at night. For the past week I have had trouble sleeping, because I wake up and both of my arms are completely numb. I am also getting feelings of pins and needles, and occasional stinging in my toes. Kind of like it feels like someone took a staple and stapled my big toe.
Today has been the worst. I feel very shaky, almost like it is anxiety. But, I am not depressed/worried or anxious enough to feel like it is from anxiety.
I'm now worried, but I guess the only thing I can do is play the waiting game for the next few months until I go for my next mri and emg.

Has anyone else experienced the same? Any feedback from anyone would be greatly appreciated. Thanks.
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zigemyster
replied on September 1st, 2008
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Yes I have experienced the same symptoms as you. Your neurologist is on the right track...in order to obtain a definate dx of MS certain criteria must be met and some do the let's wait and see game (that was my situation which was yes, then no, then maybe a 10% chance the yes).

The fact that you have white lesions on your brain is significant and the EMG is a good start, interesting test, and your neuro wanting to do an MRI in a few months is also a good step. As well as monitor you for new symptoms, how long they last, etc. It is best to keep a journal

You said that your father also has MS so you are probably familiar with these types of tests and the waiting game, etc.

~Zig
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