I have the burning and/or freezing problem so sometimes I play mind games. When 
my feet  burn so bad I want to cry, die, say good-bye to them, I try to 
convince myself they're freezing .  When they are freezing, I ask myself if 
they are really burning. Either way they hurt, but it gives me a feeling of 
being in control. 

Patti -  Michigan

On Jan 24, 2013, at 10:14 PM, Kim Harrison <[email protected]> wrote:

> 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
> Sent: Wednesday, January 23, 2013 6:29 PM
> To: [email protected] ; [email protected]
> Cc: [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] 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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