Kim,
I feel so bad for you  that you can't wear socks or anything on your feet.  
Mine tingle and the  toes are broken on my right foot so they hurt, but I 
can still keep my feet warm  with socks and leg warmers.
 
Jude,
Michigan.
 
 
In a message dated 1/24/2013 10:14:48 P.M. Eastern Standard Time,  
[email protected] writes:

 
My wish is for  someday to be able to wear sock or shoes.. and winter is a 
pain barefoot, but  the pain of anything touching my feet is unbearable.. 


 
____________________________________
 From: "[email protected]"  <[email protected]>
To: [email protected]
Cc: [email protected]
Sent: Thu, January 24, 2013 9:08:56  PM
Subject: Re: [TMIC] Re:  Subscribe

I am wearing socks  and leg warmers right now along with my TED boots that 
hold my feet up in  bed.  Plus, I have a sheet and two blankets on, and a 
quilt when I go to  bed.
 
Jude
Michigan
 
 
In a message dated 1/24/2013 4:46:29 P.M. Eastern Standard Time,  
[email protected] writes:

My feet are cold most of the time.   I am  assuming that is natural for TM  
-  anyone else?
Janice
 
 
 

 
From: _Kim Harrison_ (mailto:[email protected])  
Sent: Wednesday, January 23, 2013 6:29 PM
To: [email protected]_ (mailto:[email protected])  ; 
[email protected]_ (mailto:[email protected])  
Cc: [email protected]_ (mailto:[email protected])  
Subject: Re: [TMIC] Re: Subscribe


 

 
 
Thank you Jude.. our Cheerleader !!
How is the cold effecting ya'all.. I HATE it... everything stings and  
hurts more and worse is I can not wear sholes for socks so TM legs stick and  
feet are freezing...  anyone else?



  
____________________________________
 From: "[email protected]"  <[email protected]>
To: [email protected]
Cc: [email protected]
Sent: Wed, January 23, 2013 7:24:07  PM
Subject: Re: [TMIC] Re:  Subscribe

I'm happy that you guys are glad to see us  active again.  I am working my 
========= off to keep us up and  running.  Neither Jim Lubin or Sam Siegel 
are interested in doing  anything with us anymore so it is just me trying 
like hell to keep things  interesting.  However, I am running out of ideas to 
talk about and need  your help.  I just got an email today from a lady who is 
interested in  joining us, so I sent her the info.  Help!
 
Jude
 
 
In a message dated 1/23/2013 5:51:24 P.M. Eastern Standard Time,  
[email protected] writes:

 
i wollowed with why and how and the thought came to me,,it  doesnt matter 
how or why,,,, if i knew,,it would still hurt.
 
 
 
  
____________________________________
 From: Robert Pall  <[email protected]>
To: [email protected];  [email protected] 
Cc:  [email protected] 
Sent: Wednesday, January 23, 2013  1:56 PM
Subject: Re:  [TMIC] Re: Subscribe


There is a ton of information and personal stories,pictures  etc at the 
T.M.I.C. Internet Club. The reason I  like this site is that we talk about TM 
and the medicines and conditiions  we have. I am not looking to make friends 
(although that is a plus). I  just want to share information that  may help 
us cope with this awful condition. As for me I have always  believed that 
the cause of my TM was excess stress which  probably caused my immune system 
to overreact to some minor illness like a summer cold.....that being said no 
doctor can  say what caused any of us to have TM....I myself decided it was 
stress....everyone one of us thinks he knows the cause of TM  ...but none of 
us do!

All the best and  happy to see this site in action once again!
Rob in New  Jersey



-----Original  Message-----
From: Heyjude48458 <[email protected]>
To:  i.whiddett <[email protected]>
Cc: tmic-list  <[email protected]>
Sent: Wed, Jan 23, 2013 1:41  pm
Subject: [TMIC] Re: Subscribe


Thanks Iris, I am so happy you are  writing.  I am really punishing myself 
to find topics for us to talk  about.  What can you think of that is 
pertinent  toTM?
 
Love you,
Jude
 
 
In a message dated 1/23/2013 7:20:44 A.M. Eastern Standard Time, 
[email protected]_ (mailto:[email protected])  writes:

Hi  Jude  
I've always wondered if I somehow snuk in under the radar of  TMIC.  When I 
was diagnosed with TM 3 1/2 yrs ago it was all new  and very frightening 
and I had very little help or info from the  doctors.  While looking for help 
on the Internet, I was lucky  enough to find the group and finally began to 
understand what had  happened but, like most us, not why it had happened!  
So, thanks  for taking on board what seems to be a lone voice from the UK and 
for  all the kind words of encouragement and advice.  Just to be sure I  am 
a "proper" member, my details are:-
 
Iris Whiddett
98  Eastwood Road
Rayleigh
Essex    England                     Tel: 01268 771642
 
Regards
Iris UK  






















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