I was able to upload a picture also.
Candy K.
- Original Message -
From: Kevin Wolfthal
To: [EMAIL PROTECTED];Tmic-list@eskimo.com
Sent: 5/15/2007 7:55:34 PM
Subject: Re: [TMIC] Re: Who's got what?/ Photos
I also was able to upload a picture, view at your own risk. ;-)
Kevin
Patti,
My doctors told me that someone with TM will only have a re-occurrence if
they had underlying illness such as, MS, Sarcoidosis or some other autoimmune
disease. I can't imagine going back through what I went through(total
paralysis from neck down). It was hard enough to survive the
Dido here, we don't want anyone to go anywhere!
Larry Throne, MSW
From: [EMAIL PROTECTED]To: [EMAIL PROTECTED], tmic-list@eskimo.comSubject: Re: [TMIC] Re: Who's got what?Date: Tue, 15 May 2007 09:28:10 EDT
No need for a vote -- we're not that kind of a club. :) Of course no one wants you to l
For about my first year of having TM, it always seemed as though I was
smelling burnt wood. At first, I thought it was the atmosphere in the
hospital,
but I went into a nursing facility, and it smells the same there. After the
nursing facility came home, and for a brief time, I smelled it
Hi Bobby Jim and Everyone,
A neurologist I saw in 2005, who herself has MS, told me that TM is now
considered under the "umbrella" of diseases covered by the MS foundation.
So, guess we are all in the same family now.
Natalie
On 5/15/07, bobby jim hijar <[EMAIL PROTECTED]> wrote:
As long as th
Just read this:
http://news.yahoo.com/s/ap/20070516/ap_on_he_me/vitamins_prostate_6;_ylt=Ao78ytODfcLhRYyZfipBrNwE1vAI
Kevin
Tracey,
Does this mean we are all going to be covered by your insurance company?
Larry Throne, MSW
Tracey L. BlackCertified Insurance Service RepresentativeHockley & O'Donnell Insurance AgencyPhone - 717-334-6741, x 29Fax - 717-334-3414Thank you for providing information to us. Please beware that
As long as there are conflicting opinions on what is TM, what is MS, what is a
CNS affliction,
what is anything as long as there is all that out there, there will
be confusion, upset folks, unhappy sufferers, angry malcontents, et cetera.
Hang in there, y'all.. we are all here
The prevailing knowledge is that indeed, TM will attack and then settle down
and that MS attacks and attacks and attacks, ergo the name MULTIPLE sclerosis,
TM being a SINGLE sclerosis event, and in progressive MS, those afflicted do
indeed get worse over time.
In remitting-relapsing MS, the p
Neither do I.Must be an Apple exclusive, the pikkies, that is. Bobberino
From: [EMAIL PROTECTED]To: [EMAIL PROTECTED]Cc: tmic-list@eskimo.com
Sent: Tuesday, May 15, 2007 7:50 AM Subject: Re: [TMIC] Re: Who's got what?
No, I don't see any picture of you or even a header in
I also was able to upload a picture, view at your own risk. ;-)
Kevin
[EMAIL PROTECTED] wrote:
*I WAS ALSO ABLE TO UPLOAD A PICTURE. I WILL ADD MORE LATER.*
**
*PRISCILLA IN TN*
See what's free at AOL.com
<
I WAS ALSO ABLE TO UPLOAD A PICTURE. I WILL ADD MORE LATER.
PRISCILLA IN TN
** See what's free at http://www.aol.com.
I went today and added my photo and had no problem but it wouldn't work if I
used upper & lower case letters, I used all upper case
Ella
** See what's free at http://www.aol.com.
Hi Barbara,
If I go to _http://www.myelitis.org/_ (http://www.myelitis.org/) and click
on "support groups", it leads me to an error page. That's what I was trying
to get at about the site. This may or may not be something going on with my
puter, but I thought it should be looked at by
Thumbs up from out here too.
Heather in Calgary
- Original Message -
From: <[EMAIL PROTECTED]>
To: <[EMAIL PROTECTED]>; <[EMAIL PROTECTED]>;
Sent: Tuesday, May 15, 2007 9:53 AM
Subject: Re: [TMIC] Re: Who's got what?
Why don't you all take a vote and
decide whether or not you wou
I don't see any pictures either.
Heather in Calgary
- Original Message -
From: [EMAIL PROTECTED]
To: [EMAIL PROTECTED]
Cc: tmic-list@eskimo.com
Sent: Tuesday, May 15, 2007 5:50 AM
Subject: Re: [TMIC] Re: Who's got what?
No, I don't see any picture of you or even a head
Why don't you all take a vote and
> decide whether or not you would like to see me leave this list.
ONE BIG THUMB UP
Let her stay!!
F
The reason there are so many responses when one of us blunders and says
something inside-out is because we each respond as soon as we read the email
without waiting to see if the originator apologized for the blunder. We should
wait until we have read a few more postings before we start our own
This is how my neuro explained TM to me also. He said that TM is usually a
one-time occurrence and I should have already seen its worse affects on me.
He didn't give me any false hopes of further healing, but I also don't fear
getting worse. He called it status-quo.
Patti
"Tracey L. B
I agree with Barbara. I think that Jude has beat himself up enough about this.
No one wants to see you leave. Just give yourself 50 whips with a wet noodle
and then lets all put this to rest. I don't think we want to be the kind of
club where people can't talk witout fear of retrogression. Jude
Barbara's absolutely right.. and Jude you don't need any more stress added
to your life. It's over you have apologized. Don't agonize about it anymore.
We're a family. remember that. Now have a great day!
Trudy
Virginia where it's getting hotter and hotter
BTW I live right outside Washington, D
A friend of ours developed MS for no particular reason. He didn't have
any injuries, etc. He just woke up one morning and was blind. The
blindness lasted about 2 weeks and during that time frame they found out
he had MS. He was fine for about a year and then all of a sudden, he
woke up blind again.
No need for a vote -- we're not that kind of a club. :) Of course no one
wants you to leave.
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/)
In a message dated 5/14/2007 10:10:33 PM Eastern Daylight Time,
[EMAIL PROTECTED] writes:
I seem to get into trouble
I was told there was a 20% chance me TM could turn into MS. After 11 years I
would guess that is not likely to happen -- I hope, anyway! But the number
of TMers here who have gone on the MS have reassured me that it is
handle-able, so that has taken a lot of the scariness away for me.
My
There's an article on candida here:
_http://www.emedicinehealth.com/candidiasis_yeast_infection/article_em.htm_
(http://www.emedicinehealth.com/candidiasis_yeast_infection/article_em.htm)
I would think the ankle would be an unlikely place to get it because you
usually get it in moist places
I can't imagine that anyone on this list would want you to leave! I
have gotten lots of information on here. I don't think you need to
apologize any more, you have apologized and explained the confusion.
Please let it go and continue to send emails to help the rest of us out
here dealing with t
We were told that TM could very easily turn to MS later in life. I don't
know remember what the % was but I think it was about 14% of people who
have TM go on later to be diagnosed with MS. My understanding is that TM
works backwards compared to MS. TM starts bad and gets better, MS starts
slow and
If you go to the photo gallery page at
_http://www.myelitis.org/gallery/index.php?cat=2_
(http://www.myelitis.org/gallery/index.php?cat=2) up at the top
it says "Register" or "Log in." If you've never used the page before to send
photos, you have to register with a user name and password.
Both the Members Photos link and the Members Activity, Recreation, and
Travel links from the TMIC site at _http://www.myelitis.org/tmic/_
(http://www.myelitis.org/tmic/) work for me -- the link for the support
groups from the TMA
page at _http://www.myelitis.org/ _ (http://www.myelitis.org/
You're welcome. :)
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/)
In a message dated 5/14/2007 9:21:20 PM Eastern Daylight Time,
[EMAIL PROTECTED] writes:
I did not know about the Member;s Activity, Recreation, & Travel
section. Thank you, Barbara.
Alto
No, I don't see any picture of you or even a header in e-mails.
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/)
In a message dated 5/14/2007 9:28:58 PM Eastern Daylight Time,
[EMAIL PROTECTED] writes:
> I would love to see pictures of everyone [with the emai
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