<< Subj: Re: Buzzzzzzzzzy legs
Date: 11/19/98 3:09:53 PM Atlantic Standard Time
From: <A HREF="mailto:N Mack92">N Mack92</A>
To: <A HREF="mailto:MTripimcca">MTripimcca</A>, <A HREF="mailto:tmic-
list(AT)eskimo.com">tmic-list(AT)eskimo.com</A>
In a message dated 98-11-19 00:47:18 EST, you write:
<< Nancy,
I have noticed more tingly feeling in my legs the last couple of months now
and have just put it off the the herniated disk at C 5-6 messing with my
system. I mentioned it to my "new" neuro and he didn't blink an eye on Monday.
I am interested in what everyone else has to say to this also.
By tingling I mean they tingle for a bit then go numb. wonder if it is the
TM or disk.
Please explain what you mean by buzz more to me? When I think of buzz, I
think of a bee buzzing. So buzz to me means a sound. I want to understand what
you mean.
And yes please do join in. I actually picked it up from Erroll in
Queensland, Australia where it is summer time.
Maria in Tonawanda where it is getting down in the 20's tonight but now snow
Mary, HA! >>
Maria,
I will feel the pins and needles in my legs, but they rarely really go numb.
When the pins and needles gets bad, they will ache or hurt. If I overdo it,
or walk hard and fast for a short time, they feel almost like there was
something electric or vibrating inside of them. You know how it feels if you
put your hand on something vibrating really fast? Sort of like that. Maybe
it is like the pins and needles times one-hundred. Does that help?
Nancy, where the sky is bright a >>
Nancy,
I understand exactly what you are saying now. I used to have the same feeling
but now my legs go numb when I sit, especially if I put pressure on my
tailbone or cocyccx area. Then they will go numb at a quicker rate. If I walk
too much my lower back gets very sore and my legs loose mobility. I cannot be
of much help here except to say, and this I learned only from these fine
people here on the list, that the messages are getting screwed up. Am I
remembering this right Bob and Gunny?
The neuro in the ER had told me my symptoms don't make sense. My GP said that
he thinks it is due to my TM and thinks that the neuros are full of you know
what!
Not much help, but just to let you know you are not alone!
Maria in Tonawanda, NY where the neuro's don't know there head from a hole in
the ground :)