FOR ME IT HAS BEEN WORSE AT TIME BUT LIKE WALKING ON TENNIS BALLS. WHEN tm 
FIRST STARTED,I WORE BOOTS TO WORK AND i THOUGHT THERE WAS SOMETHING WRONG WITH 
MY BOOT.LIKE IT HAD GOTTEN WET AND BUNCHED UP RIGHT AROUND MY TOES AND 
THEY DIDN'T FIT RIGHT.
EEPS CAPS ON
took a couple of times checking to notice it was my foot and boot was fine.
but that bunched up feeling soon went back further than my toes and made it 
hard to walk on,not for pain but my in my mind i thought i was steping on 
things but there was nothing there.
lol,,,,my mind was messed up enough without all this!

--- On Wed, 4/13/11, kevin weilacher <hwyfli...@yahoo.com> wrote:

From: kevin weilacher <hwyfli...@yahoo.com>
Subject: Re: [TMIC] enough!
To: "PAMELA S" <subers...@msn.com>, jcs...@yahoo.com, "TMC Group" 
<tmic-list@eskimo.com>
Date: Wednesday, April 13, 2011, 8:47 AM

I understand the sensations...A few months ago, I started getting the sensation 
that my socks were bunched up inside my shoes....
When it first started, I was continually sitting down and taking my shoes off 
to check...and everytime, my socks were fine...not bunched up at all.
Now, I know it's happening so I just try to ignore it.

I brought this up to my neuro and he said that it was typical to have those 
type of sensations...very common in neurological disorders and unfortunately 
not too much that can be done about it.

Kevin
N.E. Ohio (Canton)

From: PAMELA S <subers...@msn.com>
To: jcs...@yahoo.com; TMC Group <tmic-list@eskimo.com>
Sent: Wed, April 13, 2011 12:09:29 AM
Subject: RE: [TMIC] enough!


 




Okay, it's my hands and my feet and my legs!!!!!But, I got so sick of being 
called crazy when I tried to describe it.  20 years later it still drives me 
nuts, and I don't drink, I'm not using morphine etc. etc. etc.  I Do wish 
caregivers had to experience just one hour of it.  FYI...if you ever have to 
have a psych exam just to get a neurologist to take you seriously....make sure 
you keep the record, or 7 years later you'll see the shrink again just to get 
the new resident whatever to take you seriously.   I learned that the hard 
way.  Wasting hard earned money to get someone to sign a paper saying those 
spiders ARE NOT in your head!  Perhaps raid in the neurologist coffee:)  (That 
is a joke, not a threat just in case someone should think otherwise)  But, 
anyone who has lived with these sensations knows what I mean.
 



Date: Tue, 12 Apr 2011 14:13:56 -0700
From: jcs...@yahoo.com
Subject: RE: [TMIC] enough!
To: vgor...@twmi.rr.com
CC: tmic-list@eskimo.com





even knowing whats going on I'm always rubbing and looking.

--- On Tue, 4/12/11, vernon <vgor...@twmi.rr.com> wrote:


From: vernon <vgor...@twmi.rr.com>
Subject: RE: [TMIC] enough!
To: "'john snodgrass'" <jcs...@yahoo.com>
Date: Tuesday, April 12, 2011, 5:10 PM




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That’s the way my hands feel
 

From: john snodgrass [mailto:jcs...@yahoo.com] 
Sent: Tuesday, April 12, 2011 3:43 PM
To: transverse myelitis
Subject: [TMIC] enough!

 





my legs are creping me out today ,one feels like it has spider webs on it and 
the other feels like bugs are crawling on it!


 


TM,,,,,gotta love it,,


 


 


 


NOT!

 



                                          
 






      


      

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