Re: [TMIC] Sjogren's (Amended)

2010-01-08 Thread Grace M.
*Hi Linda,  *
**
*Sjogrens was one of the diseases considered whenever I was still in the
diagnostic process, before they had received the results of my NMO IgG
test.  MS was not considered as a possibility at that time, the reason being
that my paralysis and optic nerve involvement was bilateral, which is not
typical for MS attacks.  This also allowed them to quickly eliminate the
possibility of stroke.  Diseases considered included Sjogren's, Lupus, ADEM
(Quickly eliminated because there was not yet any brain involvement.),
Sarcoid, and Vasculitis.  Once all of my clinical results were complete,
including the NMO IgG, it was a done deal.*
**
*As an aside, my neuro opth thinks that I have now developed Sjogrens in
addition to NMO, though I had a negative SS-A, Ro, SS-B and La with no
Rheumatic Factor.  My eyes are so dry right now, that I have scratches on
the cornea.  Same deal going on with the mouth.  I have to see her every six
months for a complete workup due to NMO, so I'll no doubt find out more at
that visit.  *
**
*Stay warm!*
*Gracie   *


  Grace, thanks for posting this Sjogrens site.  I have to say, of all the
 info I have read, this is the ONLY place that has actually mentioned
 Transverse Myelitis - up to 1% with Sjogrens!  My doctor explained it to me
 when I got TM, but I had no idea what he was talking about - still sitting
 there in a fog with a totally numb body.  I kind of feel like the doctor
 explained it to me again today, except today I actually know what he was
 talking about!  I don't know, maybe ignorance was bliss at that time...

 Regina, did you read the articles and were you a bit surprised?

 Linda

 - Original Message -

 *From:* Grace M. grace...@gmail.com
 *To:* regina...@sbcglobal.net
 *Cc:* tmic-list@eskimo.com
 *Sent:* Thursday, January 07, 2010 4:23 PM
 *Subject:* Fwd: [TMIC] Sjogren's (Amended)

  *Hi Regina,  *
 **
 *They've actually identified the autoimmune antibody that is a marker for
 Devic's NMO.  Although one can have a concurrent diagnosis of NMO AND
 Sjogren's (Which is extremely rare.), I don't think that they are related
 with the exception that both are autoimmune diseases, at leat I have not yet
 read anything to that effect in the literature.  *
 **
 *No Regina, the optic damage that occurs in Devic's NMO is limited to the
 optic nerve and disk.  It is much more destructive that the ON which is
 encountered in MS, and permanent blindness is a relatively common
 occurence. *
 **
 *Did your doctor not explain to you that Sjogren's can affect parts of the
 body other than the eyes?*
 **
 *
 Sjogren's Subtypes Primary Sjogren's Disease VS Sjogren's Syndrome

 Apr 24, 2006 http://www.suite101.com/daily.cfm/2006-04-24 Elaine 
 Moorehttp://www.suite101.com/profile.cfm/daisyelaine
This article describes the clinical and diagnostic differences between
 primary and secondary Sjogren's syndrome.

  Sjogren's disease is a chronic autoimmune disease that occurs as a
 localized syndrome primarily causing mouth and eye dryness (sicca syndrome)
 or as a systemic disease affecting multiple organs. Sjogren's is suspected
 of affecting about 2-3 million Americans, 90 percent of them women.
 Frequently, the condition remains unrecognized and untreated, and when
 treated, the average diagnosis is reported to take 3.5 years. Women in their
 fourth decade of life are most likely to be affected. The complaint most
 often listed at the time of diagnosis is mouth dryness. In Sjogren's
 syndrome, white blood cells known as lymphocytes invade the exocrine glands.
 The exocrine glands produce needed moisture for lubricating and bathing the
 body's organs.

 Continued at:

 http://autoimmunedisease.suite101.com/article.cfm/sjogrenssubtypes
 Grace


  *




[TMIC] Linda---More Resources/Research papers re: Sjogren's and TM.

2010-01-08 Thread Grace M.
*Hi Irish,  *
**
*I dug these out of my files for you.  There's a lot of info re:  Sjorgen's
and TM.  Hope they're helpful.  If you want any more, let me know.  I've got
a ton of papers stashed away in this old computer.  If you would like to
research further, just search for Sjogren's and TM using boolean search.
(And, not, or, but, near, or the +  (and) and - (not) symbols.  You'll pull
up a lot more information that way.)  *
**
*XOXO*
*Gracie*

http://jnnp.bmj.com/content/77/6/780.extract

http://www.myelitis.org/newsletters/journal-1-07.htm

http://archneur.ama-assn.org/cgi/content/full/58/5/815

http://www.sjogrensworld.org/mandel.htm

http://www.ingentaconnect.com/content/adis/dgs/2004/0064/0002/art1

http://emedicine.medscape.com/article/1066649-overview


[TMIC] sympom check question

2010-01-08 Thread randy rankin

 I would like to know if any of you have had the following symptom(s)
 
I try to read everything people write and this might have already been 
addressed 
 
Yesterday, I had a power electric shock to my entire right arm to the tip of my 
fingers.  It wasn't a moving sensation.  The entire arm just felt like I just 
grabed an electric wire. 
 
The only motion that I made before it happened was to raise my RIGHT arm up to 
write on a board. I think I raised my head upwards to look at the board.
 
less than two hours later the same even happened to my RIGHT arm except I 
looked down, from a seated position, and reach to get my cell phone.  The 
second that I touched the phone and just started to curl my fingers around it a 
more powerful electrical shock hit my entire right arm. It hurt and frightened 
me. 
 
Has anyone exprienced this?
 
The back of my neck has been hurting.  It does NOT hurt to move my neck except 
to look down.  I can't stand that.  


  

RE: [TMIC] symptom check question

2010-01-08 Thread Butcher, Bernie (SFS)
Yes, I get electric shocks from my left armpit down to my fingers
sometimes. I have isolated it to my ring finger - if I twist it or bang
it, I get the shocks. Then it will go away for months (?) 

 

Bernie



From: randy rankin [mailto:rj_ran...@yahoo.com] 
Sent: Friday, January 08, 2010 3:39 PM
To: tmic-list@eskimo.com
Cc: tmic-list@eskimo.com
Subject: [TMIC] sympom check question

 

 I would like to know if any of you have had the following
symptom(s)

 

I try to read everything people write and this might have
already been addressed 

 

Yesterday, I had a power electric shock to my entire right arm
to the tip of my fingers.  It wasn't a moving sensation.  The entire arm
just felt like I just grabed an electric wire. 

 

The only motion that I made before it happened was to raise my
RIGHT arm up to write on a board. I think I raised my head upwards to
look at the board.

 

less than two hours later the same even happened to my RIGHT arm
except I looked down, from a seated position, and reach to get my cell
phone.  The second that I touched the phone and just started to curl my
fingers around it a more powerful electrical shock hit my entire right
arm. It hurt and frightened me. 

 

Has anyone exprienced this?

 

The back of my neck has been hurting.  It does NOT hurt to move
my neck except to look down.  I can't stand that.  

 



Re: [TMIC] sympom check question

2010-01-08 Thread pjv1234
Yes.  My lesion was at C4-c6.  I sometimes get exactly that feeling when I 
reach with my right hand.  It feels like I have grasped a live wire and makes 
me think twice about what I had just done.  (Did I just stick a fork in an 
electrical outlet?)

I do not have (LeHermittes -sp?) tingling when I bend chin to chest.  However, 
I get a shock feeling, tingling, or loss of balance if I bend my neck 
backwards.  I had lots of muscle spasms in my neck prior to TM.

Patti - Michigan
 randy rankin rj_ran...@yahoo.com wrote: 
 
  I would like to know if any of you have had the following symptom(s)
  
 I try to read everything people write and this might have already been 
 addressed 
  
 Yesterday, I had a power electric shock to my entire right arm to the tip of 
 my fingers.  It wasn't a moving sensation.  The entire arm just felt like I 
 just grabed an electric wire. 
  
 The only motion that I made before it happened was to raise my RIGHT arm up 
 to write on a board. I think I raised my head upwards to look at the board.
  
 less than two hours later the same even happened to my RIGHT arm except I 
 looked down, from a seated position, and reach to get my cell phone.  The 
 second that I touched the phone and just started to curl my fingers around it 
 a more powerful electrical shock hit my entire right arm. It hurt and 
 frightened me. 
  
 Has anyone exprienced this?
  
 The back of my neck has been hurting.  It does NOT hurt to move my neck 
 except to look down.  I can't stand that.  






[TMIC] Shampoo shower caps

2010-01-08 Thread Alle111
Hello everyone (and happy new year). I was talking with Dan  Montz (Pam's 
husband) and he wanted if I used them and asked if I'd pass the  info to you. 
It does seem like a good thing. Have a good  one...Ella
 



 
In a message dated 1/7/2010 8:28:52 P.M. Eastern Standard Time, MontzMagic  
writes:

 TMIC GROUP ABOUT THEM--OK -HERE IS THE INFO ---SAGE  PRODUCTS  
INC--1-800-323-2220---3909 THREE OAKS ROAD--CARY OL. 60013---REORDER IS   
NUMBER IS 
#7909
 
COMFORT SHAMPOO CAP--ALL-IN-ONE--RINSE FREE SHAMPOO ANS CONDITIONER -1  CAP 
PER BAG --- I THINK PAM WOULD LIKE FOR THEM TO KNOW ABOUT HIS IF THEY DO  
NOT  ALREADY??





[TMIC] cold feet, good socks

2010-01-08 Thread kale_...@netzero.net
Hi Everyone,
I seems like a couple of years ago someone wrote about some warm socks that 
really helped.  At the time I didn't live in really cold weather, but have 
since moved and find the cold not only affects how my feet feel, but the 
spacticity and my ability to function.
I've been looking at some NuWool toe socks by injinji on Amazon.  But they're 
about $16 + shipping and thought it might be worth it to ask for some feedback 
first, just in case someone has some better ideas.  I've got a couple of pairs 
of toe socks that go to my knees and they make a difference in how I feel.  I 
bought them when I lived in warmer weather, but haven't been able to find them 
now that I live in cold!  I find short ones that only go to my calves, but all 
the way up to my knees is better.   
Any Suggestions?
The toe socks help because the tight muscles all the way down my leg, on my 
right side (where the original paralysis was) have caused my 3 middle right 
toes to curve under like hammer toes and the extra fabric around each 
individual toe helps to keep them a little straighter, as well as warmer.  Does 
anyone else have this problem?
Sally

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Re: [TMIC] sympom check question

2010-01-08 Thread Mindy King
24/7 since March 1 2007 from the chest down and google Lhermittes  
sign, I have that too.

Mindy the Artisan



On Jan 8, 2010, at 3:39 PM, randy rankin wrote:


 I would like to know if any of you have had the following symptom(s)

I try to read everything people write and this might have already  
been addressed


Yesterday, I had a power electric shock to my entire right arm to  
the tip of my fingers.  It wasn't a moving sensation.  The entire  
arm just felt like I just grabed an electric wire.


The only motion that I made before it happened was to raise my  
RIGHT arm up to write on a board. I think I raised my head upwards  
to look at the board.


less than two hours later the same even happened to my RIGHT arm  
except I looked down, from a seated position, and reach to get my  
cell phone.  The second that I touched the phone and just started  
to curl my fingers around it a more powerful electrical shock hit  
my entire right arm. It hurt and frightened me.


Has anyone exprienced this?

The back of my neck has been hurting.  It does NOT hurt to move my  
neck except to look down.  I can't stand that.