I'm not sure why the list address would
work as forwards and CCs but not as regular e-mailing? But then I'm not very
technically literate. Hope somebody with more expertise can
help.
Barbara H.
In a message dated 10/12/2005 2:26:47 PM Eastern Standard Time,
[EMAIL PROTECTED] writes:
I AM NOT SURE WHY ANYONE THAT HAS TM IS MORE SUSCEPTIBLE TO COMING DOWN WITH
MS,
I did not know that the chances of getting MS if you have TM are increased.
I just want to let everyone know that I wwas going to answer this yesterday.
TM is an auto-immune event. The damage is only done
Hi again,
another question for medication
I was prescribed Amantadine to help with the fatigue. Does anyone take this
med and those it help?
Chantal
in Ontario
I HAVE NOT SEEN MY NEURO IN YEARS, AND HAVE AD TM SINCE 1994, CONFINED TO A
WHEELCHAIR AND COMPLETELY PARALYZED FROM THE NIPPLE LINE DOWN SINCE THEN.
WHAT CAN HE/SHE DO FOR ME? NO CURE YET, I TOLERATE THE PAIN AND SPASES,
HAVE TRAINED MY BOWELS - SOMETIMES, AND SEE MY GP FOR OTHER MALAYS AND
Unhindered MovementGetting Out Of Your Own Way
When you find yourself facing obstacles that appear
to be blocking you from your goals, it is important to try not to
get
Well, then me missus must have a phantom MS
as her lesions are both on her spine.
Innn teresting ggg.
Bobberino
From: ROBERT
COOK To: Diane
Cc: Sally Wilkinson ; tmic-list@eskimo.com
Sent: Wednesday, October 12, 2005 9:33 PM
Subject: Re: [TMIC] Hello
AS I WROTE THAT, I THOUGHT
Well, dah'lin', I'd say that you're one of
the lucky ones.
Bobberino
From: [EMAIL PROTECTED]
To: tmic-list@eskimo.com
Sent: Thursday, October 13, 2005 4:31 PM
Subject: [TMIC] neuro visits
Hi Everyone ,
I haven't seen a neuro
doc in years . I also have not had any MRI's , CT scans ,
Welcome my friend, Leta. So glad you joined us! Although we have
different diseases, disorders or whatever you want to call this stuff, a
lot of what we go through is the same...fatigue, inability to walk much,
if at all, etc.
Any questions or issues...fire away! That's what we are here for.
Mary
In a message dated 10/13/2005 12:47:28 PM Central Standard Time,
[EMAIL PROTECTED] writes:
thanks
frank, i do sort of feel like i'm out of duct tape.
sue
Hi Sue,
I have a brand new mega-roll of duct tape you can use
until you replace yours. Let's stick together...
Peace,
Jude
I'm with you Cheryl. I also have
not had an appointment with my neuro for three years. There is nothing
that can be done for me. At this time, there is no medical cure and my PC
provides me with all of the pertinent medications to keep me as comfortable as I
am going to get. I do worry
My 2 cents - my neuro has me dx'd as probable MS but says that the odds
are that because of my age (63) and the age of onset (57), I'm unlikely
to have another serious neurological occurence. Somethin' to hang
on to.
Diane in Canada
BobbyJim wrote:
Well,
from what I've read here and there, age
My baclofen pump dosage level has not yet accomplished its raison d'etre.
The violent leg jerks are gone, but I still have excess tone in the affected
lower leg.
I have had 36 or more increases in the dosage level; I've gone from 50
ug/day to 1125. And my toes still twitch and crawl [but that is
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