John no need to apologize. Questioning is how we learn.
Patti
On Sat, Jan 14, 2012 at 9:18 PM, john snodgrass jcs...@yahoo.com wrote:
I apologize for any inconvenience I have caused in the questioning of
anything concerning TM and the brain.
it really doesn't matter if I am right or wrong
I have had TM for more than 14 years and I have gone to the best Doctors (Dr.
Kerr). In this group as well as some of the other facebook groups there seems
to be a preoccupation with trying to find the cause that brought TM into our
lives. I certainly understand the importance of medical
I have been saying this same thing since I got DX-ed two years ago.
My only concern is that there are medications or treatments available to me
to reduce the pain and give me some time each day during which I can be
useful to others. I never bothered worrying even about what I had! The Drs
Rob, I agree with you 100%. I admit I am really curious as to the “why” of
it, but am getting used to my new life and am adjusting to most of it. All
we can do, at this point, is treat the symptoms
and share successes with the other TM’ers.Who knows, it just might help
someone else -
Dalton, I hate that this is a part of your TM.It seems that most of us have
a problem that seems separate from TM, but I wonder if it is really.Doctors
will give you the symptoms of TM,
then tell you what you can expect as time passes.You can feel you are
making progress, then
While I agree, for the most part, about getting on with our lives with what
we have, I also have a desire to know 'the cause' for the following reasons.
Since contracting TM almost 6 years ago and discovering it is an auto-immune
condition, my sister has been diagnosed with two different
I realize that I am not the one that has TM but joined this support group
because of my mom, you all have been amazing for me!
Mom was just diagnosed with sleep apnea and myanethia gravis as well!
These auto immune diseases are so devastating and very devastating to to me to
watch my mom go
Vernon
I reckon thats why the neuro has us fill out the medicle history of sorts each
time we visit,,to see what if anything that they may do that would give us some
relief.
From: Janice Nichols jan...@centurytel.net
To: Dalton Garis malugss...@gmail.com; john
thats is a good case to wonder.
in a way I wonder if we minded our mitochondria like the Dr lady done in the
video with MS, would it make any difference at all because it seams as if our
immune system was more of a bandit,,,not having good instructions,when we were
attacked.
then again it may
if i were to advise i would say help when you can, be patient when you
can't,,and be very prone to listen.
love is the most important thing in this mess.
From: Tracy Lea Bell tracyleab...@yahoo.com
To: Elizabeth Clark xbeecla...@gmail.com
Cc: Janice Nichols
I was told I had TM on April 26, 1998 although I had been feeling numb and
tingly in my leg and trunk since October. It was a slow onset. It is
almost 14 years! Don't know why my immune system attacked me, but it did. I
have had 6 episodes where I felt numb and tingly and the doctor put
Remove me from mailing list..too many emailsOdile Connor
From: celr...@aol.com [mailto:celr...@aol.com]
Sent: Sunday, January 15, 2012 2:19 PM
To: robthe...@aol.com; tmic-list@eskimo.com
Subject: Re: [TMIC] Is it really so important to know?
I was told I had TM on April 26,
i am one handed, recovering nicely from carpal tunnel surgery.
i am strongly considering the mitochondria diet..
fascinating
i,too.believe our immuine systems are the bandits.
susan,phx,az
On Jan 15, 2012, at 1:12 PM, john snodgrass wrote:
thats is a good case to wonder.
in a way I wonder
I have had TM for 5 years and one of the first questions I asked my doctors was
the possibility of our daughter “inheriting” this disease.I was told that
they think it is not inherited,
but I know they don’t know a lot about TM.I do think the majority of us
have not had it passed on to
Jane,
This is really new to me - the fact that you have had so many
episodes/attacks of TM, and then you are back to normal.I don’t know
anything about your other disease, but I am sure
you have checked it out. Hope someone will pop up here to talk to you about
it and can empathize.
Susan, tell me about this diet and why it would be good for us.
janice
From: Susan Kleinz
Sent: Sunday, January 15, 2012 6:02 PM
To: john snodgrass
Cc: Elizabeth Clark ; 'Janice Nichols' ; tmic-list@eskimo.com ; 'Robert Pall'
Subject: Re: [TMIC] Is it really so important to know?
i am
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