RE: [TMIC] leg and foot comfort in bed

2009-04-19 Thread Patricia Cooley
I, TOO, AM FORTUNATE THAT I DON'T HAVE ANY SKIN SENSITIVITY.  I ALSO DON'T
HAVE THE PAIN SO MANY OF US HAVE.  I DO HAVE A SPASMS IN MY LEFT LEG ONCE IN
A WHILE.  IN FACT, I CAN CAUSE A SPASM BY TURNING MY LEFT FOOT TO THE LEFT
AND ALL OF A SUDDEN I CAN FEEL A SPASM.   WHEN I GOT TM AND WAS IN THE
HOSPITAL I WAS UNABLE TO TURN OVER AND HAD TO SLEEP ON MY BACK WHICH WAS
ALSO SO UNCOMFORTABLE BEFORE.  I FOUND THE HOSPITAL BED PROVIDED SOME RELIEF
AS I COULD RAISE THE HEAD OF THE BED SO I WASN'T SO FLAT ON MY BACK.  I WAS
EVEN NOT ABLE TO LIFT MY LEGS UP IF THEY SLID OFF THE SIDE OF THE BAD AND
HAD TO RING FOR A NURSE.   I HAVE A STRONG RAILING ON THE SIDE OF MY BED
WHICH MADE IT POSSIBLE FOR ME TO FINALLY TURN OVER.  I HAVE IMPROVED
TREMDOUSLY AND AM ABLE TO TURN OVER WITHOUT MUCH ASSISTANCE.  ONE OF MY
PROBLEMS THIS PAST WINTER WAS I WAS ALWAYS SO COLD???  I SLEPT IN FLANNEL
NIGHTGOWNS AND AT LEAST 3-4 BLANKETS.  IT WAS THE ONLY PLACE I COULD GET
WARM.  WITH WARMER TEMPS I AM NOW ABLE TO SWITCH TO SUMMER SLEEPWEAR.  AS
MUCH AS I FEEL SORRY FOR MYSELF AT TIMES, I KNOW HOW VERY LUCKY I AM THAT I
DON'T SUFFER MANY OF THE PROBLEMS A LOT OF TM'ERS DO.  MY MENTAL OUTLOOK HAS
IMPROVED TREMDOUSLY, WHICH I THINK IS BECAUSE OF ALL THE SUPPORT FROM ALL OF
YOU ON THIS WEB SITE.

 

PATTI IN WISCONSIN

 

From: Janice [mailto:jan...@centurytel.net] 
Sent: Saturday, April 18, 2009 11:34 PM
To: tmic-list@eskimo.com; balmat...@aol.com
Subject: Re: [TMIC] leg and foot comfort in bed

 

I am s fortunate that I don't have the skin sensitivity that so many of
you talk about.If I pull up something really soft, like my gown or robe,
I will spasm for a minute, but I don't really have pain, just discomfort and
only for a minute.   I would think that

the cotton knit would be a blessing.   I like 100% cotton to sleep in for
summer - it helps keep me cool.

Janice

- Original Message - 

From: balmat...@aol.com 

To: tmic-list@eskimo.com 

Sent: Thursday, April 16, 2009 12:20 AM

Subject: Re: [TMIC] leg and foot comfort in bed

 

I am such a happy camper with my cotton knit.  Such a miraculous fiber.
Isn't it great when we find something that works for us, most of the
time  It's just amazing!  It's definately a game of trial and error,
that's for sure.  Life is so much fun when you have TM. 

The majority of my sensitivity is in the evening and during the night.
There are times when I cannot even stand skin to skin contact.  That's why I
sleep on my back with my knees bent many nights. 

Take care everyone!

Hugs, Barbara A








-Original Message-
From: Janice jan...@centurytel.net
To: tmic-list@eskimo.com; balmat...@aol.com
Sent: Wed, 15 Apr 2009 8:30 pm
Subject: Re: [TMIC] leg and foot comfort in bed

I have the sensitivity of cloth rubbing (or barely touching) my legs too.
But, I have no problem with sheets and blankets on

me at nite.   I sleep with a pillow between my knees and that takes care of
any problems I guess.  I have slept with a summer

gown all winter, otherwise I get too hot. Janice

- Original Message - 

From: balmat...@aol.com 

To: tmic-list@eskimo.com 

Sent: Wednesday, April 15, 2009 12:23 AM

Subject: [TMIC] leg and foot comfort in bed

 

I think that this is something that most of us suffer from at some point
during our TM lives, skin sensitivity against fabric, and it's the worst
when we are trying to get some much needed sleep.

I have purchased so many sets of sheets and blankets over my TM years (T
8-10, 6/1/99), and I have had this sensitivity for most of that time.  It
started as sensitivity and is so often PAIN.  I've gone from egyptian
cotton, very good quality flannel, jersey (like T-shirt material) and all
sorts of thread counts of cotton.  In sheets, I think that most of the time,
my most comfortable sheet happens to be the jersey.  I'm not saying that I
can always have my legs against them, because I cannot, I lay on my back
many nights with my knees bent so nothing touches my legs.  Blankets are
much worse, so you need to get the most comfortable sheet you can near your
skin.  If you have any old pajama bottoms, those are also some of the most
comfortable, or I wear the short ones.  

I've bought some microfiber plush pants this year from OldNavy.com and they
have been warm on my legs and haven't irritated them.  I am very much
looking forward to warmer weather when I can wear short pants all the time
and not being uncomfortable.

Hugs to all, Barbara A in CA 

 


  _  


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  _  


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[TMIC] transverse myelitis

2009-04-19 Thread Betty Shaffer
I'm a new subscriber to the TM internet club and find the messages
interesting.
I was diagnosed with T.M. ( Cl and C 2 level) in 2004 at the age of 77.
Numb from my toes up to and inclucing my neck, I rar3ly feel pain but have
much discomfort from the banding, especially in my torso and neck.  I walk
well with a walker, but need my eyes to tell me where my feet ( and seat)
are.  Without the walker , balance is a problem.

Anybody have problems similiar to those ?  I live in a retirement home where
I'm able to walk and to exercise 5 days a week, and I know this helps.
There is no support group in the area

Betty in Oregon


RE: [TMIC] leg and foot comfort in bed

2009-04-19 Thread jrushton
I just remembered that when I first came home and lay in bed I had the
sensation that my legs were both in mid air, about a foot off of the bed. 
Now, 4 years later, my right leg feels like the leg is bent and only the
knee is up.  Isn't that strange or another normal/abnormal for us TMer's?? 
Jeanne

---Original Message---
 
From: Patricia Cooley
Date: 4/19/2009 10:50:57 AM
To: 'Janice';  tmic-list@eskimo.com;  balmat...@aol.com
Subject: RE: [TMIC] leg and foot comfort in bed
 
I, TOO, AM FORTUNATE THAT I DON’T HAVE ANY SKIN SENSITIVITY.  I ALSO DON’T
HAVE THE PAIN SO MANY OF US HAVE.  I DO HAVE A SPASMS IN MY LEFT LEG ONCE IN
A WHILE.  IN FACT, I CAN CAUSE A SPASM BY TURNING MY LEFT FOOT TO THE LEFT
AND ALL OF A SUDDEN I CAN FEEL A SPASM.   WHEN I GOT TM AND WAS IN THE
HOSPITAL I WAS UNABLE TO TURN OVER AND HAD TO SLEEP ON MY BACK WHICH WAS
ALSO SO UNCOMFORTABLE BEFORE.  I FOUND THE HOSPITAL BED PROVIDED SOME RELIEF
AS I COULD RAISE THE HEAD OF THE BED SO I WASN’T SO FLAT ON MY BACK.  I WAS
EVEN NOT ABLE TO LIFT MY LEGS UP IF THEY SLID OFF THE SIDE OF THE BAD AND
HAD TO RING FOR A NURSE.   I HAVE A STRONG RAILING ON THE SIDE OF MY BED
WHICH MADE IT POSSIBLE FOR ME TO FINALLY TURN OVER.  I HAVE IMPROVED
TREMDOUSLY AND AM ABLE TO TURN OVER WITHOUT MUCH ASSISTANCE.  ONE OF MY
PROBLEMS THIS PAST WINTER WAS I WAS ALWAYS SO COLD???  I SLEPT IN FLANNEL
NIGHTGOWNS AND AT LEAST 3-4 BLANKETS.  IT WAS THE ONLY PLACE I COULD GET
WARM.  WITH WARMER TEMPS I AM NOW ABLE TO SWITCH TO SUMMER SLEEPWEAR.  AS
MUCH AS I FEEL SORRY FOR MYSELF AT TIMES, I KNOW HOW VERY LUCKY I AM THAT I
DON’T SUFFER MANY OF THE PROBLEMS A LOT OF TM’ERS DO.  MY MENTAL OUTLOOK HAS
IMPROVED TREMDOUSLY, WHICH I THINK IS BECAUSE OF ALL THE SUPPORT FROM ALL OF
YOU ON THIS WEB SITE.
 
PATTI IN WISCONSIN
 
From: Janice [mailto:jan...@centurytel.net] 
Sent: Saturday, April 18, 2009 11:34 PM
To: tmic-list@eskimo.com; balmat...@aol.com
Subject: Re: [TMIC] leg and foot comfort in bed
 
I am s fortunate that I don't have the skin sensitivity that so many of
you talk about.If I pull up something really soft, like my gown or robe,
I will spasm for a minute, but I don't really have pain, just discomfort and
only for a minute.   I would think that
the cotton knit would be a blessing.   I like 100% cotton to sleep in for
summer - it helps keep me cool.
Janice
- Original Message - 
From: balmat...@aol.com 
To: tmic-list@eskimo.com 
Sent: Thursday, April 16, 2009 12:20 AM
Subject: Re: [TMIC] leg and foot comfort in bed
 
I am such a happy camper with my cotton knit.  Such a miraculous fiber.  Isn
t it great when we find something that works for us, most of the time 
It's just amazing!  It's definately a game of trial and error, that's for
sure.  Life is so much fun when you have TM. 

The majority of my sensitivity is in the evening and during the night. 
There are times when I cannot even stand skin to skin contact.  That's why I
sleep on my back with my knees bent many nights. 

Take care everyone!

Hugs, Barbara A








-Original Message-
From: Janice jan...@centurytel.net
To: tmic-list@eskimo.com; balmat...@aol.com
Sent: Wed, 15 Apr 2009 8:30 pm
Subject: Re: [TMIC] leg and foot comfort in bed
I have the sensitivity of cloth rubbing (or barely touching) my legs too.  
But, I have no problem with sheets and blankets on
me at nite.   I sleep with a pillow between my knees and that takes care of
any problems I guess.  I have slept with a summer
gown all winter, otherwise I get too hot. Janice
- Original Message - 
From: balmat...@aol.com 
To: tmic-list@eskimo.com 
Sent: Wednesday, April 15, 2009 12:23 AM
Subject: [TMIC] leg and foot comfort in bed
 
I think that this is something that most of us suffer from at some point
during our TM lives, skin sensitivity against fabric, and it's the worst
when we are trying to get some much needed sleep.

I have purchased so many sets of sheets and blankets over my TM years (T
8-10, 6/1/99), and I have had this sensitivity for most of that time.  It
started as sensitivity and is so often PAIN.  I've gone from egyptian cotton
 very good quality flannel, jersey (like T-shirt material) and all sorts of
thread counts of cotton.  In sheets, I think that most of the time, my most
comfortable sheet happens to be the jersey.  I'm not saying that I can
always have my legs against them, because I cannot, I lay on my back many
nights with my knees bent so nothing touches my legs.  Blankets are much
worse, so you need to get the most comfortable sheet you can near your skin.
 If you have any old pajama bottoms, those are also some of the most
comfortable, or I wear the short ones.  

I've bought some microfiber plush pants this year from OldNavy.com and they
have been warm on my legs and haven't irritated them.  I am very much
looking forward to warmer weather when I can wear short pants all the time
and not being uncomfortable.

Hugs to all, Barbara A in CA 
 



Great deals on 

Re: [TMIC] transverse myelitis

2009-04-19 Thread jrushton
 Welcome, Betty and you have come to a wonderful group of people who will
soon become friends!  Just keep reading and you will soon learn all sorts of
different things about TM from physical to emotional and everything in
between.  The banding you talk about is a real issue to some of us. Mine is
right at the exact same area where my bra is and is really painful a good
part of the time but meds truly do help. Everyone has to find their own med 
solution' and that's a whole new area to talk about!!!  Again, welcome, and
you are blessed for having found this good group!  Jeanne in Dayton, WA
 
---Original Message---
 
From: Betty Shaffer
Date: 4/19/2009 11:07:03 AM
To: tmic-list@eskimo.com
Subject: [TMIC] transverse myelitis
 
I'm a new subscriber to the TM internet club and find the messages
interesting.
I was diagnosed with T.M. ( Cl and C 2 level) in 2004 at the age of 77.
Numb from my toes up to and inclucing my neck, I rar3ly feel pain but have
much discomfort from the banding, especially in my torso and neck.  I walk
well with a walker, but need my eyes to tell me where my feet ( and seat)
are.  Without the walker , balance is a problem.
 
Anybody have problems similiar to those ?  I live in a retirement home where
I'm able to walk and to exercise 5 days a week, and I know this helps.
There is no support group in the area
 
Betty in Oregon
 SuperStock_1196-107.jpg

FW: [TMIC] leg and foot comfort in bed

2009-04-19 Thread Patricia Cooley
 

 

From: heyjude48...@aol.com [mailto:heyjude48...@aol.com] 
Sent: Sunday, April 19, 2009 12:09 PM
To: patticoo...@wi.rr.com
Subject: Fwd: [TMIC] leg and foot comfort in bed

 


Pattie,  Please forward this string to the List as I must have a wrong addy for 
it and I keep getting my mail back.  Thanks, Jude

 


  _  


From: Heyjude48458
To: patticoo...@wi.rr.com, www.tmic-l...@eskimo.com
Sent: 4/19/2009 12:19:43 P.M. Eastern Daylight Time
Subj: Re: [TMIC] leg and foot comfort in bed

 


I too, believe that much of the power of this

group is in the fact that there are such a 

diverse type of symptoms and problems 

endured by the people who make up this site.

 

It makes my own aches and pains seem less

important than they really are and gives me

something to focus on besides myself.  I don't 

have a lot of the symptoms that others do, for

example, the problem of fabric touching skin

that has been the latest topic of conversation

on the List.  

 

It doesn't take long for TM to make one humble, especially when exposed to 
others with it and reading how they suffer with different symptoms than I. 
There is no way I would want to suffer with some of the difficulties that 
others describe and without a doubt, it is this fabulously giving group of 
people, who, in their suffering, take the time to give support, knowledge and 
love to people seeking help for the terrors of the initial fears of TM.

 

God help us all...

Jude 

 

 

 

In a message dated 4/19/2009 11:48:35 A.M. Eastern Daylight Time, 
patticoo...@wi.rr.com writes:

I, TOO, AM FORTUNATE THAT I DON’T HAVE ANY SKIN SENSITIVITY.  I ALSO DON’T HAVE 
THE PAIN SO MANY OF US HAVE.  I DO HAVE A SPASMS IN MY LEFT LEG ONCE IN A 
WHILE.  IN FACT, I CAN CAUSE A SPASM BY TURNING MY LEFT FOOT TO THE LEFT AND 
ALL OF A SUDDEN I CAN FEEL A SPASM.   WHEN I GOT TM AND WAS IN THE HOSPITAL I 
WAS UNABLE TO TURN OVER AND HAD TO SLEEP ON MY BACK WHICH WAS ALSO SO 
UNCOMFORTABLE BEFORE.  I FOUND THE HOSPITAL BED PROVIDED SOME RELIEF AS I COULD 
RAISE THE HEAD OF THE BED SO I WASN’T SO FLAT ON MY BACK.  I WAS EVEN NOT ABLE 
TO LIFT MY LEGS UP IF THEY SLID OFF THE SIDE OF THE BAD AND HAD TO RING FOR A 
NURSE.   I HAVE A STRONG RAILING ON THE SIDE OF MY BED WHICH MADE IT POSSIBLE 
FOR ME TO FINALLY TURN OVER.  I HAVE IMPROVED TREMDOUSLY AND AM ABLE TO TURN 
OVER WITHOUT MUCH ASSISTANCE.  ONE OF MY PROBLEMS THIS PAST WINTER WAS I WAS 
ALWAYS SO COLD???  I SLEPT IN FLANNEL NIGHTGOWNS AND AT LEAST 3-4 BLANKETS.  IT 
WAS THE ONLY PLACE I COULD GET WARM.  WITH WARMER TEMPS I AM NOW ABLE TO SWITCH 
TO SUMMER SLEEPWEAR.  AS MUCH AS I FEEL SORRY FOR MYSELF AT TIMES, I KNOW HOW 
VERY LUCKY I AM THAT I DON’T SUFFER MANY OF THE PROBLEMS A LOT OF TM’ERS DO.  
MY MENTAL OUTLOOK HAS IMPROVED TREMDOUSLY, WHICH I THINK IS BECAUSE OF ALL THE 
SUPPORT FROM ALL OF YOU ON THIS WEB SITE.

 

PATTI IN WISCONSIN

 

From: Janice [mailto:jan...@centurytel.net] 
Sent: Saturday, April 18, 2009 11:34 PM
To: tmic-list@eskimo.com; balmat...@aol.com
Subject: Re: [TMIC] leg and foot comfort in bed

 

I am s fortunate that I don't have the skin sensitivity that so many of you 
talk about.If I pull up something really soft, like my gown or robe, I will 
spasm for a minute, but I don't really have pain, just discomfort and only for 
a minute.   I would think that

the cotton knit would be a blessing.   I like 100% cotton to sleep in for 
summer - it helps keep me cool.

Janice

- Original Message - 

From: balmat...@aol.com 

To: tmic-list@eskimo.com 

Sent: Thursday, April 16, 2009 12:20 AM

Subject: Re: [TMIC] leg and foot comfort in bed

 

I am such a happy camper with my cotton knit.  Such a miraculous fiber.  Isn't 
it great when we find something that works for us, most of the time  It's 
just amazing!  It's definately a game of trial and error, that's for sure.  
Life is so much fun when you have TM. 

The majority of my sensitivity is in the evening and during the night.  There 
are times when I cannot even stand skin to skin contact.  That's why I sleep on 
my back with my knees bent many nights. 

Take care everyone!

Hugs, Barbara A








-Original Message-
From: Janice jan...@centurytel.net
To: tmic-list@eskimo.com; balmat...@aol.com
Sent: Wed, 15 Apr 2009 8:30 pm
Subject: Re: [TMIC] leg and foot comfort in bed

I have the sensitivity of cloth rubbing (or barely touching) my legs too.   
But, I have no problem with sheets and blankets on

me at nite.   I sleep with a pillow between my knees and that takes care of any 
problems I guess.  I have slept with a summer

gown all winter, otherwise I get too hot. Janice

- Original Message - 

From: balmat...@aol.com 

To: tmic-list@eskimo.com 

Sent: Wednesday, April 15, 2009 12:23 AM

Subject: [TMIC] leg and foot comfort in bed

 

I think that this is something that most of us suffer from at some point during 
our TM lives, skin sensitivity against fabric, and it's the worst 

[TMIC] quadraplegia

2009-04-19 Thread Amanda Diskey
  I was wondering if anyone else on here is a c6 quad that is in a wheelchair and not much use of their hands who
 lives independently. I am sooo frustrated that i have to depend so much on my family and friends, although I am blessed to have them, I want to be my independent self again. I want to be able to at least be able to handle my own self at home. I need someone to talk to for some advice if anyone has any.   



  

[TMIC] quadraplegia

2009-04-19 Thread Amanda Diskey


I was wondering if there is anyone here who is a c6 quad with very little use 
of their hands and no use of their legs that lives independently. I am needing 
to talk to someone who can offer some advice on how I can do some things.



From: tmic-digest-requ...@eskimo.com tmic-digest-requ...@eskimo.com
To: tmic-dig...@eskimo.com
Sent: Sunday, April 19, 2009 10:48:07 AM
Subject: tmic-digest Digest V2009 #291



-Inline Message Follows-

tmic-digest Digest                Volume 2009 : Issue 291

Today's Topics:
  Re: [TMIC] leg and foot comfort in b  [ Janice jan...@centurytel.net ]
  Re: [TMIC] leg and foot comfort in b  [ Janice jan...@centurytel.net ]


-Inline Message Follows-


I am s fortunate that I don't have the skin sensitivity that so many of you 
talk about.    If I pull up something really soft, like my gown or robe, I will 
spasm for a minute, but I don't really have pain, just discomfort and only for 
a minute.   I would think that
the cotton knit would be a blessing.   I like 100% cotton to sleep in for 
summer - it helps keep me cool.
Janice
- Original Message - 
From: balmat...@aol.com 
To: tmic-list@eskimo.com 
Sent: Thursday, April 16, 2009 12:20 AM
Subject: Re: [TMIC] leg and foot comfort in bed
I am such a happy camper with my cotton knit.  Such a miraculous fiber.  Isn't 
it great when we find something that works for us, most of the time  It's 
just amazing!  It's definately a game of trial and error, that's for 
sure.  Life is so much fun when you have TM. 

The majority of my sensitivity is in the evening and during the night.  There 
are times when I cannot even stand skin to skin contact.  That's why I sleep on 
my back with my knees bent many nights. 

Take care everyone!

Hugs, Barbara A








-Original Message-
From: Janice jan...@centurytel.net
To: tmic-list@eskimo.com; balmat...@aol.com
Sent: Wed, 15 Apr 2009 8:30 pm
Subject: Re: [TMIC] leg and foot comfort in bed


I have the sensitivity of cloth rubbing (or barely touching) my legs too.   
But, I have no problem with sheets and blankets on
me at nite.   I sleep with a pillow between my knees and that takes care of any 
problems I guess.  I have slept with a summer
gown all winter, otherwise I get too hot. Janice
- Original Message - 
From: balmat...@aol.com 
To: tmic-list@eskimo.com 
Sent: Wednesday, April 15, 2009 12:23 AM
Subject: [TMIC] leg and foot comfort in bed
I think that this is something that most of us suffer from at some point during 
our TM lives, skin sensitivity against fabric, and it's the worst when we are 
trying to get some much needed sleep.

I have purchased so many sets of sheets and blankets over my TM years (T 8-10, 
6/1/99), and I have had this sensitivity for most of that time.  It started as 
sensitivity and is so often PAIN.  I've gone from egyptian cotton, very good 
quality flannel, jersey (like T-shirt material) and all sorts of thread counts 
of cotton.  In sheets, I think that most of the time, my most comfortable sheet 
happens to be the jersey.  I'm not saying that I can always have my legs 
against them, because I cannot, I lay on my back many nights with my knees bent 
so nothing touches my legs.  Blankets are much worse, so you need to get the 
most comfortable sheet you can near your skin.  If you have any old pajama 
bottoms, those are also some of the most comfortable, or I wear the short 
ones.  

I've bought some microfiber plush pants this year from OldNavy.com and they 
have been warm on my legs and haven't irritated them.  I am very much looking 
forward to warmer weather when I can wear short pants all the time and not 
being uncomfortable.

Hugs to all, Barbara A in CA 



Great deals on Dell s most popular laptops Starting at $479 



Why pay full price? Check out this month's deals on the new AOL Shopping. 

-Inline Message Follows-


Just thought I'd let you know that I am completely opposite.   I can not sleep 
on my back.   I really spasm around my middle 
section trying to get in that position and trying to get back up is a 
nitemare.   I stick to sleeping on my side with a pillow between
my legs to lessen spasms.   Also take baclofen for spasms - helps a 
lot.  I also have developed a thing of needing to have
air movement when I go to bed.   I have the ceiling fan going on no matter what 
the room temperature is.   I just need air movement. 
This has really been an adventure/nitemare.   Love the support of family and 
friends - and other TM'ers!
- Original Message - 
From: Gillian Clark 
To: TM list 
Sent: Thursday, April 16, 2009 10:04 PM
Subject: Re: [TMIC] leg and foot comfort in bed

It has only just occurred to me that sleeping on my back is the only way I have 
slept now for years. Since the day of the attack I haven't been able to sleep 
any other way, in the beginning, I 

Re: [TMIC] transverse myelitis

2009-04-19 Thread gbthomas8374
Betty,
Welcome to the group.
My lesion was C-5-7 and my symptoms seem very much the same as yours as far as 
numbness and banding.

I like how you put that you need your eyes to see where your feet (and seat) 
are.  How true!
It is always a bit amusing to lose a slipper while walking through the house 
and not even know it!  Putting shoes on in the dark is a bad idea--I've put 
them on the wrong feet a couple of times and got out in public before I noticed.

It was nice to hear from you.

Gary in Michigan
  - Original Message - 
  From: Betty Shaffer 
  To: tmic-list@eskimo.com 
  Sent: Sunday, April 19, 2009 12:03 PM
  Subject: [TMIC] transverse myelitis


  I'm a new subscriber to the TM internet club and find the messages 
interesting.
  I was diagnosed with T.M. ( Cl and C 2 level) in 2004 at the age of 77.
  Numb from my toes up to and inclucing my neck, I rar3ly feel pain but have 
much discomfort from the banding, especially in my torso and neck.  I walk well 
with a walker, but need my eyes to tell me where my feet ( and seat) are.  
Without the walker , balance is a problem.

  Anybody have problems similiar to those ?  I live in a retirement home where 
I'm able to walk and to exercise 5 days a week, and I know this helps.
  There is no support group in the area

  Betty in Oregon

[TMIC] List

2009-04-19 Thread Jan Hargrove
 
Jude,
 
Here's the address    tmic-list@eskimo.com
 
or try resuscribing as you may have been kicked off,
it happen! for what reason, only the goblins know!!
 
The info is on TMA website.sorry I don't remember 
how to subscribeBarbara Harper knows how..
 
jharper33#aol.com
 
Hope that helps, jan

Re: [TMIC] transverse myelitis

2009-04-19 Thread Jan Hargrove
Jeanne,
 
My banding was at my bra line, too..I always said 
it was the bra God paying me back for hating bras!!
The banding is rare now, after 13 years the 29th of 
this month.but it does raise its head once in a 
while just to prove 'he' can still wreak havoc
 
jan
p.s.  Welcome, Betty..please know that laughter
is a must in the world of tm!!


--- On Sun, 4/19/09, jrushton jrush...@columbiaenergyllc.com wrote:




#yiv1956273918 v\:* {
}


#yiv1956273918 v\:* {
}






 Welcome, Betty and you have come to a wonderful group of people who will soon 
become friends!  Just keep reading and you will soon learn all sorts of 
different things about TM from physical to emotional and everything in 
between.  The banding you talk about is a real issue to some of us. Mine is 
right at the exact same area where my bra is and is really painful a good part 
of the time but meds truly do help. Everyone has to find their own med 
'solution' and that's a whole new area to talk about!!!  Again, welcome, and 
you are blessed for having found this good group!  Jeanne in Dayton, WA
 

---Original Message---
 

From: Betty Shaffer
Date: 4/19/2009 11:07:03 AM
To: tmic-list@eskimo.com
Subject: [TMIC] transverse myelitis
 
I'm a new subscriber to the TM internet club and find the messages interesting.
I was diagnosed with T.M. ( Cl and C 2 level) in 2004 at the age of 77.
Numb from my toes up to and inclucing my neck, I rar3ly feel pain but have much 
discomfort from the banding, especially in my torso and neck.  I walk well with 
a walker, but need my eyes to tell me where my feet ( and seat) are.  Without 
the walker , balance is a problem.
 
Anybody have problems similiar to those ?  I live in a retirement home where 
I'm able to walk and to exercise 5 days a week, and I know this helps.
There is no support group in the area
 
Betty in Oregon
 









Re: [TMIC] transverse myelitis

2009-04-19 Thread Alle111
Welcome Betty,
One symptom I'd say we all have is  definitely the banding yet other 
symptoms do vary. I'm a paraplegic since  9/2000, lesion T6-10. I don't have 
the 
numbness but a buzzing feeling that is  uncomfortable without meds. Ask us 
anything you wish and you will get an  answer. Have you talked with anyone 
since 2004 with TM? You have a group of  friends here.
 
Ella in  Ohio
**A Good Credit Score is 700 or Above. See yours in just 2 easy 
steps! 
(http://pr.atwola.com/promoclk/100126575x1220814852x1201410738/aol?redir=http:%2F%2Fwww.freecreditreport.com%2Fpm%2Fdefault.aspx%3Fsc%3D668072%26
hmpgID%3D62%26bcd%3DAprilfooter419NO62)


RE: [TMIC] transverse myelitis

2009-04-19 Thread Margaret Monson
I don't have the banding.  I did at the onset of TM but not any longer.

 

From: alle...@aol.com [mailto:alle...@aol.com] 
Sent: April-19-09 1:58 PM
To: tmic-list@eskimo.com
Subject: Re: [TMIC] transverse myelitis

 

Welcome Betty,

One symptom I'd say we all have is definitely the banding yet other symptoms
do vary. I'm a paraplegic since 9/2000, lesion T6-10. I don't have the
numbness but a buzzing feeling that is uncomfortable without meds. Ask us
anything you wish and you will get an answer. Have you talked with anyone
since 2004 with TM? You have a group of friends here.

 

Ella in Ohio

 

  _  

A Good Credit Score is 700 or Above. See
http://pr.atwola.com/promoclk/100126575x1220814852x1201410738/aol?redir=htt
p:%2F%2Fwww.freecreditreport.com%2Fpm%2Fdefault.aspx%3Fsc%3D668072%26hmpgID%
3D62%26bcd%3DAprilfooter419NO62  yours in just 2 easy steps!



Re: [TMIC] transverse myelitis

2009-04-19 Thread pjv1234
Hi Betty
Welcome to our on-line TM family.  I was diagnosed in 2003 at age 53 at C4-C6.  
I also have balance problems and just gave in to using a walker during a short 
vacation.  I was surprised that I was able to walk and enjoy looking at 
something besides my feet.  I hadn't thought about the seat problem, however, 
your right - I look and touch before I sit.  I think we TMers have trust 
issues.  We just don't trust much of anything that has to do with where we are 
or where we're going to be in the next few seconds!  

Patti - Michigan 
 Betty Shaffer vasso...@gmail.com wrote: 
 I'm a new subscriber to the TM internet club and find the messages
 interesting.
 I was diagnosed with T.M. ( Cl and C 2 level) in 2004 at the age of 77.
 Numb from my toes up to and inclucing my neck, I rar3ly feel pain but have
 much discomfort from the banding, especially in my torso and neck.  I walk
 well with a walker, but need my eyes to tell me where my feet ( and seat)
 are.  Without the walker , balance is a problem.
 
 Anybody have problems similiar to those ?  I live in a retirement home where
 I'm able to walk and to exercise 5 days a week, and I know this helps.
 There is no support group in the area
 
 Betty in Oregon



Re: [TMIC] transverse myelitis

2009-04-19 Thread Pieter and Heather

Well, talking about feet.
I guess I should say that I don't always watch my feet.

Tonight would have been a good time to watch my feet but don't think it 
would have helped my situation.


We drove into our driveway after being at the grandsons first birthday 
party.

Husband lets me out on the driveway as we park two cars in the garage.

I got out.
My right foot (which is my weak foot) goes out first, followed by me turning 
my body,

putting my left foot out and hoisting myself with my cane etc.

I stood up (or tried to,  like I usually do).
Howevermy right foot remained firmly (and I mean firmly) 
planted.


I moved.
My right foot didn't.
I was enough out of the car that I shut the car door.

Then BAM...down I went.
Onto my right hip, side etc.

Hubby (thank goodness) couldn't figure out where I moved to so fast. (do any 
TMer's move fast?)


Fortunately he realized that I 'moved too fast'.
He got out of the car and there I was.

Flat on my side.

On the driveway. with my cane and purse with me.

Glad he didn't try and drive into the garage.
Not sure how much of me was near the car.

So..not too sure if looking at my feet would have helped.
Haven't had that happen for a while, that my right foot doesn't want to go 
when I want to.


It used to happen quite often.
So Pieter had to help me stand up.

That is my story and I'm sticking to it.
Now I just have to wait and see if I end up with a big bruise on my right 
hip and see if my

right foot will be swollen tomorrow.

Hope everyone else had a good weekend.
The wee grandson had a good birthday and ate his first taste of chocolate 
cake.  Too cute.


Heather in Calgary

- Original Message - 
From: pjv1...@chartermi.net

To: tmic-list@eskimo.com; Betty Shaffer vasso...@gmail.com
Sent: Sunday, April 19, 2009 6:33 PM
Subject: Re: [TMIC] transverse myelitis



Hi Betty
Welcome to our on-line TM family.  I was diagnosed in 2003 at age 53 at 
C4-C6.  I also have balance problems and just gave in to using a walker 
during a short vacation.  I was surprised that I was able to walk and 
enjoy looking at something besides my feet.  I hadn't thought about the 
seat problem, however, your right - I look and touch before I sit.  I 
think we TMers have trust issues.  We just don't trust much of anything 
that has to do with where we are or where we're going to be in the next 
few seconds!


Patti - Michigan
 Betty Shaffer vasso...@gmail.com wrote:

I'm a new subscriber to the TM internet club and find the messages
interesting.
I was diagnosed with T.M. ( Cl and C 2 level) in 2004 at the age of 77.
Numb from my toes up to and inclucing my neck, I rar3ly feel pain but 
have
much discomfort from the banding, especially in my torso and neck.  I 
walk

well with a walker, but need my eyes to tell me where my feet ( and seat)
are.  Without the walker , balance is a problem.

Anybody have problems similiar to those ?  I live in a retirement home 
where

I'm able to walk and to exercise 5 days a week, and I know this helps.
There is no support group in the area

Betty in Oregon








Re: [TMIC] leg and foot comfort in bed

2009-04-19 Thread Janice
You reminded me of my old hospital days where I could not turn over without 
help, or slide up in the bed.   When you can
look back and see where your body has actually gotten stronger - even with the 
problems TM has left us - you realize how
fortunate we are.   I am comparing us to 2 people I know that are dying of 
cancer.   Parts of our lives are the pits, but we
know we have our lives to live and in most cases, improvement to look forward 
to.  Jance

  - Original Message - 
  From: Patricia Cooley 
  To: 'Janice' ; tmic-list@eskimo.com ; balmat...@aol.com 
  Sent: Sunday, April 19, 2009 10:47 AM
  Subject: RE: [TMIC] leg and foot comfort in bed


  I, TOO, AM FORTUNATE THAT I DON'T HAVE ANY SKIN SENSITIVITY.  I ALSO DON'T 
HAVE THE PAIN SO MANY OF US HAVE.  I DO HAVE A SPASMS IN MY LEFT LEG ONCE IN A 
WHILE.  IN FACT, I CAN CAUSE A SPASM BY TURNING MY LEFT FOOT TO THE LEFT AND 
ALL OF A SUDDEN I CAN FEEL A SPASM.   WHEN I GOT TM AND WAS IN THE HOSPITAL I 
WAS UNABLE TO TURN OVER AND HAD TO SLEEP ON MY BACK WHICH WAS ALSO SO 
UNCOMFORTABLE BEFORE.  I FOUND THE HOSPITAL BED PROVIDED SOME RELIEF AS I COULD 
RAISE THE HEAD OF THE BED SO I WASN'T SO FLAT ON MY BACK.  I WAS EVEN NOT ABLE 
TO LIFT MY LEGS UP IF THEY SLID OFF THE SIDE OF THE BAD AND HAD TO RING FOR A 
NURSE.   I HAVE A STRONG RAILING ON THE SIDE OF MY BED WHICH MADE IT POSSIBLE 
FOR ME TO FINALLY TURN OVER.  I HAVE IMPROVED TREMDOUSLY AND AM ABLE TO TURN 
OVER WITHOUT MUCH ASSISTANCE.  ONE OF MY PROBLEMS THIS PAST WINTER WAS I WAS 
ALWAYS SO COLD???  I SLEPT IN FLANNEL NIGHTGOWNS AND AT LEAST 3-4 BLANKETS.  IT 
WAS THE ONLY PLACE I COULD GET WARM.  WITH WARMER TEMPS I AM NOW ABLE TO SWITCH 
TO SUMMER SLEEPWEAR.  AS MUCH AS I FEEL SORRY FOR MYSELF AT TIMES, I KNOW HOW 
VERY LUCKY I AM THAT I DON'T SUFFER MANY OF THE PROBLEMS A LOT OF TM'ERS DO.  
MY MENTAL OUTLOOK HAS IMPROVED TREMDOUSLY, WHICH I THINK IS BECAUSE OF ALL THE 
SUPPORT FROM ALL OF YOU ON THIS WEB SITE.

   

  PATTI IN WISCONSIN

   

  From: Janice [mailto:jan...@centurytel.net] 
  Sent: Saturday, April 18, 2009 11:34 PM
  To: tmic-list@eskimo.com; balmat...@aol.com
  Subject: Re: [TMIC] leg and foot comfort in bed

   

  I am s fortunate that I don't have the skin sensitivity that so many of 
you talk about.If I pull up something really soft, like my gown or robe, I 
will spasm for a minute, but I don't really have pain, just discomfort and only 
for a minute.   I would think that

  the cotton knit would be a blessing.   I like 100% cotton to sleep in for 
summer - it helps keep me cool.

  Janice

- Original Message - 

From: balmat...@aol.com 

To: tmic-list@eskimo.com 

Sent: Thursday, April 16, 2009 12:20 AM

Subject: Re: [TMIC] leg and foot comfort in bed

 

I am such a happy camper with my cotton knit.  Such a miraculous fiber.  
Isn't it great when we find something that works for us, most of the time  
It's just amazing!  It's definately a game of trial and error, that's for sure. 
 Life is so much fun when you have TM. 

The majority of my sensitivity is in the evening and during the night.  
There are times when I cannot even stand skin to skin contact.  That's why I 
sleep on my back with my knees bent many nights. 

Take care everyone!

Hugs, Barbara A








-Original Message-
From: Janice jan...@centurytel.net
To: tmic-list@eskimo.com; balmat...@aol.com
Sent: Wed, 15 Apr 2009 8:30 pm
Subject: Re: [TMIC] leg and foot comfort in bed

I have the sensitivity of cloth rubbing (or barely touching) my legs too.   
But, I have no problem with sheets and blankets on

me at nite.   I sleep with a pillow between my knees and that takes care of 
any problems I guess.  I have slept with a summer

gown all winter, otherwise I get too hot. Janice

  - Original Message - 

  From: balmat...@aol.com 

  To: tmic-list@eskimo.com 

  Sent: Wednesday, April 15, 2009 12:23 AM

  Subject: [TMIC] leg and foot comfort in bed

   

  I think that this is something that most of us suffer from at some point 
during our TM lives, skin sensitivity against fabric, and it's the worst when 
we are trying to get some much needed sleep.

  I have purchased so many sets of sheets and blankets over my TM years (T 
8-10, 6/1/99), and I have had this sensitivity for most of that time.  It 
started as sensitivity and is so often PAIN.  I've gone from egyptian cotton, 
very good quality flannel, jersey (like T-shirt material) and all sorts of 
thread counts of cotton.  In sheets, I think that most of the time, my most 
comfortable sheet happens to be the jersey.  I'm not saying that I can always 
have my legs against them, because I cannot, I lay on my back many nights with 
my knees bent so nothing touches my legs.  Blankets are much worse, so you need 
to get the most comfortable sheet you can near your skin.  If you have any 

[TMIC] New Member

2009-04-19 Thread PWi1991449

I was diagnosed in 2002 C 4-C 6 I am having problems with balance . My  
hands and feet have started back to being extremely cold and sometimes hot.  
Any suggestions from anyone. I had surgery in 2007 to remove the disc. They 
were  pressing on the spine. It was very successful,however it seems as if I 
am going  backward with a lot of muscle weakness, bladder and bowel problems. 
What  Can I do? for 7 years I have been doing very well. I have never 
really had pain  except when I would pull a muscle in my back. Almost pain free 
from the time I  contracted the disease. I stayed in rehab and hospitals 
where I lost all muscle  strength. With therapy  on a daily basis I overcame  
until this sudden  backward spiral. I was taken off neurontin for a couple of 
month to try  something different  have to take an EMG on next month. I am 
trusting God  to touch, heal, and deliver me from this terrible disease
There is none so amazing as God
Peggy  Wilson
**Access 350+ FREE radio stations anytime from anywhere on the 
web. Get the Radio Toolbar! 
(http://toolbar.aol.com/aolradio/download.html?ncid=emlcntusdown0003)


Re: [TMIC] New Member

2009-04-19 Thread jrushton
 Hi, Peggy!  Welcome to this wonderful group of people who will be here for
you through everything!  

I constantly have the ice cold then hot feet.  I have just learned to live
with it.  When I wake each morning, my feet are always warm???  Don't know
why.

Just keep reading what all of the TMer's say and you will learn so much and
realize how you are not alone at all with this.  We are all so blessed to
have found this site..Jeanne in Dayton
 
---Original Message---
 
From: pwi1991...@aol.com
Date: 4/19/2009 10:43:23 PM
To: tmic-list@eskimo.com
Subject: [TMIC] New Member
 
 
I was diagnosed in 2002 C 4-C 6 I am having problems with balance . My hands
and feet have started back to being extremely cold and sometimes hot. Any
suggestions from anyone. I had surgery in 2007 to remove the disc. They were
pressing on the spine. It was very successful,however it seems as if I am
going backward with a lot of muscle weakness, bladder and bowel problems.
What Can I do? for 7 years I have been doing very well. I have never really
had pain except when I would pull a muscle in my back. Almost pain free from
the time I contracted the disease. I stayed in rehab and hospitals where I
lost all muscle strength. With therapy  on a daily basis I overcame  until
this sudden backward spiral. I was taken off neurontin for a couple of month
to try something different  have to take an EMG on next month. I am trusting
God to touch, heal, and deliver me from this terrible disease
There is none so amazing as God
Peggy Wilson



Access 350+ FREE radio stations anytime from anywhere on the web. Get the
Radio Toolbar!
 SuperStock_1196-107.jpg

Re: [TMIC] transverse myelitis

2009-04-19 Thread JHarper33
Ouch, Heather!! I'm glad it wasn't any worse, but I imagine  you'll feel 
pretty sore. It's strange how parts of our bodies don't turn or move  how 
we're expecting them to sometimes.
 
Barbara H.
_http://barbarah.wordpress.com/_ (http://barbarah.wordpress.com/) 
 
 
In a message dated 4/19/2009 11:21:18 P.M. Eastern Daylight Time,  
pieterheat...@shaw.ca writes:

Well,  talking about feet.
I guess I should say that I don't always watch my  feet.

Tonight would have been a good time to watch my feet but don't  think it 
would have helped my situation.

We drove into our driveway  after being at the grandsons first birthday 
party.
Husband lets me out  on the driveway as we park two cars in the garage.

I got out.
My  right foot (which is my weak foot) goes out first, followed by me 
turning  
my body,
putting my left foot out and hoisting myself with my cane  etc.

I stood up (or tried to,  like I usually  do).
Howevermy right foot remained firmly (and I mean firmly)  
planted.

I moved.
My right foot didn't.
I was enough out of  the car that I shut the car door.

Then BAM...down I  went.
Onto my right hip, side etc.

Hubby (thank goodness) couldn't  figure out where I moved to so fast. (do 
any 
TMer's move  fast?)

Fortunately he realized that I 'moved too fast'.
He got out  of the car and there I was.

Flat on my side.

On the driveway.  with my cane and purse with me.

Glad he didn't try and drive into the  garage.
Not sure how much of me was near the car.

So..not  too sure if looking at my feet would have helped.
Haven't had that happen  for a while, that my right foot doesn't want to go 
when I want  to.

It used to happen quite often.
So Pieter had to help me stand  up.

That is my story and I'm sticking to it.
Now I just have to wait  and see if I end up with a big bruise on my right 
hip and see if  my
right foot will be swollen tomorrow.

Hope everyone else had a  good weekend.
The wee grandson had a good birthday and ate his first taste  of chocolate 
cake.  Too cute.

Heather in Calgary

-  Original Message - 
From: pjv1...@chartermi.net
To:  tmic-list@eskimo.com; Betty Shaffer  vasso...@gmail.com
Sent: Sunday, April 19, 2009 6:33 PM
Subject:  Re: [TMIC] transverse myelitis


 Hi Betty
 Welcome to our  on-line TM family.  I was diagnosed in 2003 at age 53 at 
  C4-C6.  I also have balance problems and just gave in to using a walker  
 during a short vacation.  I was surprised that I was able to  walk and 
 enjoy looking at something besides my feet.  I hadn't  thought about the 
 seat problem, however, your right - I look and  touch before I sit.  I 
 think we TMers have trust issues.   We just don't trust much of anything 
 that has to do with where we are  or where we're going to be in the next 
 few seconds!

  Patti - Michigan
  Betty Shaffer vasso...@gmail.com  wrote:
 I'm a new subscriber to the TM internet club and find the  messages
 interesting.
 I was diagnosed with T.M. ( Cl  and C 2 level) in 2004 at the age of 77.
 Numb from my toes up to  and inclucing my neck, I rar3ly feel pain but 
 have
  much discomfort from the banding, especially in my torso and neck.  I  
 walk
 well with a walker, but need my eyes to tell me  where my feet ( and 
seat)
 are.  Without the walker , balance  is a problem.

 Anybody have problems similiar to those  ?  I live in a retirement home 
 where
 I'm able to  walk and to exercise 5 days a week, and I know this helps.
 There  is no support group in the area

 Betty in  Oregon

  




**Access 350+ FREE radio stations anytime from anywhere on the 
web. Get the Radio Toolbar! 
(http://toolbar.aol.com/aolradio/download.html?ncid=emlcntusdown0003)


Re: [TMIC] transverse myelitis

2009-04-19 Thread Janice
It is great to have a new member to the best support group around!   Actually, 
you sound as though you are doing
quite well.   I think balance is a problem for most of us.  The more exercise 
in building strength, the better the
balance issue will be.   Keep in touch with us and our conversations and I am 
sure you will see your problems
written out by someone else - many times with solutions.Glad you have 
joined us.Janice
  - Original Message - 
  From: jrushton 
  To: Betty Shaffer ; tmic 
  Sent: Sunday, April 19, 2009 9:15 AM
  Subject: Re: [TMIC] transverse myelitis


 Welcome, Betty and you have come to a wonderful group of people who 
will soon become friends!  Just keep reading and you will soon learn all sorts 
of different things about TM from physical to emotional and everything in 
between.  The banding you talk about is a real issue to some of us. Mine is 
right at the exact same area where my bra is and is really painful a good part 
of the time but meds truly do help. Everyone has to find their own med 
'solution' and that's a whole new area to talk about!!!  Again, welcome, and 
you are blessed for having found this good group!  Jeanne in Dayton, WA

---Original Message---

From: Betty Shaffer
Date: 4/19/2009 11:07:03 AM
To: tmic-list@eskimo.com
Subject: [TMIC] transverse myelitis

I'm a new subscriber to the TM internet club and find the messages 
interesting.
I was diagnosed with T.M. ( Cl and C 2 level) in 2004 at the age of 77.
Numb from my toes up to and inclucing my neck, I rar3ly feel pain but 
have much discomfort from the banding, especially in my torso and neck.  I walk 
well with a walker, but need my eyes to tell me where my feet ( and seat) are.  
Without the walker , balance is a problem.

Anybody have problems similiar to those ?  I live in a retirement home 
where I'm able to walk and to exercise 5 days a week, and I know this helps.
There is no support group in the area

Betty in Oregon
   
   
   
SuperStock_1196-107.jpg

Re: [TMIC] New Member

2009-04-19 Thread jrushton
Yes, it certainly is!!  ::))

---Original Message---
 
From: pwi1991...@aol.com
Date: 4/19/2009 11:13:32 PM
To: jrush...@columbiaenergyllc.com
Subject: Re: [TMIC] New Member
 
Thank you,  just to talk with someone is a blessing straight from God.
 
There is none so amazing as God
Peggy Wilson 
 
In a message dated 4/19/2009 8:49:56 P.M. US Mountain Standard Time,
jrush...@columbiaenergyllc.com writes:
 Hi, Peggy!  Welcome to this wonderful group of people who will be here for
you through everything!  
 
I constantly have the ice cold then hot feet.  I have just learned to live
with it.  When I wake each morning, my feet are always warm???  Don't know
why.
 
Just keep reading what all of the TMer's say and you will learn so much and
realize how you are not alone at all with this.  We are all so blessed to
have found this site..Jeanne in Dayton
 
---Original Message---
 
From: pwi1991...@aol.com
Date: 4/19/2009 10:43:23 PM
To: tmic-list@eskimo.com
Subject: [TMIC] New Member
 
 
I was diagnosed in 2002 C 4-C 6 I am having problems with balance . My hands
and feet have started back to being extremely cold and sometimes hot. Any
suggestions from anyone. I had surgery in 2007 to remove the disc. They were
pressing on the spine. It was very successful,however it seems as if I am
going backward with a lot of muscle weakness, bladder and bowel problems.
What Can I do? for 7 years I have been doing very well. I have never really
had pain except when I would pull a muscle in my back. Almost pain free from
the time I contracted the disease. I stayed in rehab and hospitals where I
lost all muscle strength. With therapy  on a daily basis I overcame  until
this sudden backward spiral. I was taken off neurontin for a couple of month
to try something different  have to take an EMG on next month. I am trusting
God to touch, heal, and deliver me from this terrible disease
There is none so amazing as God
Peggy Wilson



Access 350+ FREE radio stations anytime from anywhere on the web. Get the
Radio Toolbar!
 






Access 350+ FREE radio stations anytime from anywhere on the web. Get the Radio 
Toolbar!tile12.jpg

Re: [TMIC] leg and foot comfort in bed

2009-04-19 Thread Gillian Clark
Any you know what Barb?  It took me so damn long to learn about the 
wrinkles!!
  - Original Message - 
  From: balmat...@aol.com 
  To: mingalett...@activ8.net.au ; tmic-list@eskimo.com 
  Sent: Friday, April 17, 2009 1:41 PM
  Subject: Re: [TMIC] leg and foot comfort in bed


  Gilly, I know what you mean about the wrinkles in the bed.  It actually 
causes pain with the wrinkles, like something is stabbing you.  Using the knit 
sheets makes them warmer, and it's so hard for me to imagine you with the 
pillow on your feet.  I cannot stand much weight on me at all, especially my 
feet.  I love my down blanket, nice and lightweight, yet warm.

  The warmer weather brings less clothes, no blankets, and a happier me!  Come 
on summer!

  Warm hugs you Gilly, and all, Barbara A  




  -Original Message-
  From: Gillian Clark mingalett...@activ8.net.au
  To: TM list tmic-list@eskimo.com
  Sent: Thu, 16 Apr 2009 8:04 pm
  Subject: Re: [TMIC] leg and foot comfort in bed


  It has only just occurred to me that sleeping on my back is the only way I 
have slept now for years. Since the day of the attack I haven't been able to 
sleep any other way, in the beginning, I couldn't move at all from that 
position, I can now at least move my legs into a more comfy position.  I can't 
sleep with them bent up though Barb, that causes huge spasms.

  Everything hurts, no matter what but it's trying to minimize the pain is the 
answer isn't it?  I know that when you are new to this crap it's so hard to 
realise the things that you suddenly have to pay attention to.  Not only what 
you wear but where you are walking, avoiding anything that will brush on you.  
Shopping is a nightmare when someone brushes past etc.

  Since I was born being unconventional a lot of things came easily for me.  If 
you were not  born that way, it's time to change and not give an obese rodent's 
derriere what anyone else thinks. Find what works for you and don't worry about 
what the normal people are doing.

  I think I've just about got my life into a reasonable degree of comfort but 
sometimes it just changes again.

  hugs all
  Gilly

- Original Message - 
From: balmat...@aol.com 
To: tmic-list@eskimo.com 
Sent: Thursday, April 16, 2009 2:50 PM
Subject: Re: [TMIC] leg and foot comfort in bed


I am such a happy camper with my cotton knit.  Such a miraculous fiber.  
Isn't it great when we find something that works for us, most of the time  
It's just amazing!  It's definately a game of trial and error, that's for sure. 
 Life is so much fun when you have TM. 

The majority of my sensitivity is in the evening and during the night.  
There are times when I cannot even stand skin to skin contact.  That's why I 
sleep on my back with my knees bent many nights. 

Take care everyone!

Hugs, Barbara A








-Original Message-
From: Janice jan...@centurytel.net
To: tmic-list@eskimo.com; balmat...@aol.com
Sent: Wed, 15 Apr 2009 8:30 pm
Subject: Re: [TMIC] leg and foot comfort in bed


I have the sensitivity of cloth rubbing (or barely touching) my legs too.   
But, I have no problem with sheets and blankets on
me at nite.   I sleep with a pillow between my knees and that takes care of 
any problems I guess.  I have slept with a summer
gown all winter, otherwise I get too hot. Janice
  - Original Message - 
  From: balmat...@aol.com 
  To: tmic-list@eskimo.com 
  Sent: Wednesday, April 15, 2009 12:23 AM
  Subject: [TMIC] leg and foot comfort in bed


  I think that this is something that most of us suffer from at some point 
during our TM lives, skin sensitivity against fabric, and it's the worst when 
we are trying to get some much needed sleep.

  I have purchased so many sets of sheets and blankets over my TM years (T 
8-10, 6/1/99), and I have had this sensitivity for most of that time.  It 
started as sensitivity and is so often PAIN.  I've gone from egyptian cotton, 
very good quality flannel, jersey (like T-shirt material) and all sorts of 
thread counts of cotton.  In sheets, I think that most of the time, my most 
comfortable sheet happens to be the jersey.  I'm not saying that I can always 
have my legs against them, because I cannot, I lay on my back many nights with 
my knees bent so nothing touches my legs.  Blankets are much worse, so you need 
to get the most comfortable sheet you can near your skin.  If you have any 
old pajama bottoms, those are also some of the most comfortable, or I wear 
the short ones.  

  I've bought some microfiber plush pants this year from OldNavy.com and 
they have been warm on my legs and haven't irritated them.  I am very much 
looking forward to warmer weather when I can wear short pants all the time and 
not being uncomfortable.

  Hugs to all, Barbara A in CA 


--
 

Re: [TMIC] leg and foot comfort in bed

2009-04-19 Thread Gillian Clark
Janice, I am now able to move enough to get on my side but the pain is 
intolerable in that position and I can't do the pillow between the legs thing.  
I think it might be because they are too short and far too fat!
hugs
Gilly
  - Original Message - 
  From: Janice 
  To: Gillian Clark ; TM list 
  Sent: Sunday, April 19, 2009 2:27 PM
  Subject: Re: [TMIC] leg and foot comfort in bed


  Just thought I'd let you know that I am completely opposite.   I can not 
sleep on my back.   I really spasm around my middle 
  section trying to get in that position and trying to get back up is a 
nitemare.   I stick to sleeping on my side with a pillow between
  my legs to lessen spasms.   Also take baclofen for spasms - helps a lot.  
I also have developed a thing of needing to have
  air movement when I go to bed.   I have the ceiling fan going on no matter 
what the room temperature is.   I just need air movement. 
  This has really been an adventure/nitemare.   Love the support of family and 
friends - and other TM'ers!
- Original Message - 
From: Gillian Clark 
To: TM list 
Sent: Thursday, April 16, 2009 10:04 PM
Subject: Re: [TMIC] leg and foot comfort in bed


It has only just occurred to me that sleeping on my back is the only way I 
have slept now for years. Since the day of the attack I haven't been able to 
sleep any other way, in the beginning, I couldn't move at all from that 
position, I can now at least move my legs into a more comfy position.  I can't 
sleep with them bent up though Barb, that causes huge spasms.

Everything hurts, no matter what but it's trying to minimize the pain is 
the answer isn't it?  I know that when you are new to this crap it's so hard to 
realise the things that you suddenly have to pay attention to.  Not only what 
you wear but where you are walking, avoiding anything that will brush on you.  
Shopping is a nightmare when someone brushes past etc.

Since I was born being unconventional a lot of things came easily for me.  
If you were not  born that way, it's time to change and not give an obese 
rodent's derriere what anyone else thinks. Find what works for you and don't 
worry about what the normal people are doing.

I think I've just about got my life into a reasonable degree of comfort but 
sometimes it just changes again.

hugs all
Gilly

  - Original Message - 
  From: balmat...@aol.com 
  To: tmic-list@eskimo.com 
  Sent: Thursday, April 16, 2009 2:50 PM
  Subject: Re: [TMIC] leg and foot comfort in bed


  I am such a happy camper with my cotton knit.  Such a miraculous fiber.  
Isn't it great when we find something that works for us, most of the time  
It's just amazing!  It's definately a game of trial and error, that's for sure. 
 Life is so much fun when you have TM. 

  The majority of my sensitivity is in the evening and during the night.  
There are times when I cannot even stand skin to skin contact.  That's why I 
sleep on my back with my knees bent many nights. 

  Take care everyone!

  Hugs, Barbara A








  -Original Message-
  From: Janice jan...@centurytel.net
  To: tmic-list@eskimo.com; balmat...@aol.com
  Sent: Wed, 15 Apr 2009 8:30 pm
  Subject: Re: [TMIC] leg and foot comfort in bed


  I have the sensitivity of cloth rubbing (or barely touching) my legs too. 
  But, I have no problem with sheets and blankets on
  me at nite.   I sleep with a pillow between my knees and that takes care 
of any problems I guess.  I have slept with a summer
  gown all winter, otherwise I get too hot. Janice
- Original Message - 
From: balmat...@aol.com 
To: tmic-list@eskimo.com 
Sent: Wednesday, April 15, 2009 12:23 AM
Subject: [TMIC] leg and foot comfort in bed


I think that this is something that most of us suffer from at some 
point during our TM lives, skin sensitivity against fabric, and it's the worst 
when we are trying to get some much needed sleep.

I have purchased so many sets of sheets and blankets over my TM years 
(T 8-10, 6/1/99), and I have had this sensitivity for most of that time.  It 
started as sensitivity and is so often PAIN.  I've gone from egyptian cotton, 
very good quality flannel, jersey (like T-shirt material) and all sorts of 
thread counts of cotton.  In sheets, I think that most of the time, my most 
comfortable sheet happens to be the jersey.  I'm not saying that I can always 
have my legs against them, because I cannot, I lay on my back many nights with 
my knees bent so nothing touches my legs.  Blankets are much worse, so you need 
to get the most comfortable sheet you can near your skin.  If you have any 
old pajama bottoms, those are also some of the most comfortable, or I wear 
the short ones.  

I've bought some microfiber plush pants this year from OldNavy.com and 
they have been