Hi, everyone!  I've been reading all of the notes on body temps and could
not agree more that since the onset of TM, we no longer have a normal 
thermostat'!  We do have to be careful with our circulation and neuropathy
so it is so important to watch our limbs (as you learned from my last
mishap!) not only for hot and cold water but injuries.

Since day one, I have hypersensitivity on my right side and no sensation on
the left even tho it is by far the strongest. They both feel very heavy and
both have constant excruciating pain so Lyrica and Ultracet do help take the
edge off.  The temperature outside has really played havoc with the pain.
The cold and rain really increases the pain and I have added prescription
Ibuprofen.  It's tough but we just have to take care of it as it occurs. I
feel blessed that I can walk 
and am alive.  What more can I ask than that after
what I had when it first happened??  Jeanne

-------Original Message-------
 
From: Todd Tarno
Date: 3/22/2009 12:13:18 PM
To: Janice
Cc: TMIC
Subject: Re: [TMIC] Water Temp & Pin & Needle Pain
 
Hi Janice,
Water temperature are very hard to tell all the time.  I always but my
shower at it's hottest to warm up my shower chair, then lower the temp with
my hands telling me the temperature of the water.  I'm able to run very warm
water over both legs when they are cold.  But please be very careful.
Pin & Needles Pain are full time too.   They can start out really bad in the
beginning, then get better, and as you get NEW feeling, they can get worst
again.  You could ask your doctor to up & lower the dosage of your Pain Meds
 Neurontine/Lyrica.  I'm on 300 mg Lyrica a day.
Hope this helps,
Todd in Corpus Christi, TX
TM since April 1, 2002 @ T-4 to T-8

--- On Sat, 3/21/09, Janice <[email protected]> wrote:

From: Janice <[email protected]>
Subject: [TMIC]
To: "transverse myelitis" <[email protected]>
Date: Saturday, March 21, 2009, 4:15 PM


This is Janice - yet again with another question.   
 
It has been 2 years since the onset of TM.   From the top of my ribs to my
toes I can not tell water temperature on my skin.  I have to be very careful
with taking my showers.    Do any of you have that?   I am wondering if it
is something that will eventually go away or if it is something I will live
with.
 
Also, one improvement I have just noticed lately is the constant "buzzing"
that I had in my legs as soon as feeling started coming back.   Did you all
have that and have any of you also lost it?
 
Thanks again, Janice

 

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