Temporary paralysis - ten second flashes
Posted: Sun Jul 06, 2008 11:46 am
Hi to all,
I have a question. For about a month I'm getting partial temporary paralysis to my left hand and parts of my face - mostly lips, chin and the right eye. It happens every few (15 or so) minutes for about 10 seconds - I can't use my left hand, can't speak, I kind of freeze. After 10 seconds or so I get well again.
It's a strange feeling during the "flash" - like having local anaesthesia. I can move my hand though, but the strength is very limited and I hardly have any control. The sensority is almost gone at the time. For example, I can't open a bottle at the time. Even worse, i've dropped plenty of things when it happened, like a cell phone.
Let me mention that I have MS diagnosis for more than 4 years. I'm not on any meds for now even though I've had a fair share of exacerbations - sometimes 5 a year, sometimes none for more than a year. I can still run and ride a bike though, for example. My exacerbations are usually very "slow" (few months) and the remission is never complete. I have had 14 or so lesions on the last MRI.
I also believe that MS is a consequence, not a cause itself. I'm looking at my cause and this may have something to do with it. I'm wondering: has anyone had similar symptoms? What could they mean? Any suggestions? I'm about to call my GP and neuro this week or so since this doesn't get better.
Thank you for your answers.
P.S.: just an anecdote. A friend (who was working in USA) got MS. It was progressing very fast, even faster when she got on Copaxone. She was a biotech post-graduate student (she's PHD now). She was on a wheelchair in few years or even less. She was very much interested in her condition and did not believe that she has MS. She convinced the doctors and together they found the cause for her "MS". As I know she had an operation (don't ask me what exactly was wrong because I don't know) and she recovered completely. She works in Sweden as I know, I didn't hear from her since she got well.
Just some hope. If she wasn't so curious and determined she would probably be dead today - of MS ofifcially. I believe there's a cause for each of our MSes but nobody will come to us and help us - we have to help ourselves and each other. And forums like this can help (I also have a forum for MSers in my country, for 4 years).
I have a question. For about a month I'm getting partial temporary paralysis to my left hand and parts of my face - mostly lips, chin and the right eye. It happens every few (15 or so) minutes for about 10 seconds - I can't use my left hand, can't speak, I kind of freeze. After 10 seconds or so I get well again.
It's a strange feeling during the "flash" - like having local anaesthesia. I can move my hand though, but the strength is very limited and I hardly have any control. The sensority is almost gone at the time. For example, I can't open a bottle at the time. Even worse, i've dropped plenty of things when it happened, like a cell phone.
Let me mention that I have MS diagnosis for more than 4 years. I'm not on any meds for now even though I've had a fair share of exacerbations - sometimes 5 a year, sometimes none for more than a year. I can still run and ride a bike though, for example. My exacerbations are usually very "slow" (few months) and the remission is never complete. I have had 14 or so lesions on the last MRI.
I also believe that MS is a consequence, not a cause itself. I'm looking at my cause and this may have something to do with it. I'm wondering: has anyone had similar symptoms? What could they mean? Any suggestions? I'm about to call my GP and neuro this week or so since this doesn't get better.
Thank you for your answers.
P.S.: just an anecdote. A friend (who was working in USA) got MS. It was progressing very fast, even faster when she got on Copaxone. She was a biotech post-graduate student (she's PHD now). She was on a wheelchair in few years or even less. She was very much interested in her condition and did not believe that she has MS. She convinced the doctors and together they found the cause for her "MS". As I know she had an operation (don't ask me what exactly was wrong because I don't know) and she recovered completely. She works in Sweden as I know, I didn't hear from her since she got well.
Just some hope. If she wasn't so curious and determined she would probably be dead today - of MS ofifcially. I believe there's a cause for each of our MSes but nobody will come to us and help us - we have to help ourselves and each other. And forums like this can help (I also have a forum for MSers in my country, for 4 years).