Wow, that's a lot of breaks. Do you also have brittle bone disease like I do? What did you do for the 5 months with a walking boot on it. I have one for my broken leg, but it leaves me with sores on my leg where it rubs on it. Hugs, Jude In a message dated 1/25/2013 12:55:50 A.M. Eastern Standard Time, [email protected] writes:
I fell last year and broke my leg, ankle, heel and foot. because I can't take anything on my feet lucky for me orthor knew about TM and in place of surgery he put a "walking boot on it) funny still could not walk LOL had to wear it for 5 months but when the TM burning started up I could take it off for a little while ____________________________________ From: "[email protected]" <[email protected]> To: [email protected] Cc: [email protected] Sent: Thu, January 24, 2013 10:19:14 PM Subject: Re: [TMIC] Re: Subscribe 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
