Linda, where are you at in Texas?  I am in Splendora Tx.  You  need to call 
your doctor and see if you may need a round of steriods to reverse  the 
numbness and weakness.  I have taken prenisone several times and it has  helped.
 
Jane Splendora Tx  TM since April 26, 1998 - 12 years
 
 
In a message dated 10/6/2010 5:08:14 P.M. Central Daylight Time,  
[email protected] writes:

 
It was 6 years for me in April.  I do pretty well most of the time  but 
when my symptoms get worse, it can be hard to be positive.  I have  had 
increased numbness & weakness in my hands  that now sometimes  goes into my 
arms & 
the body fatigue is back with a vengence, but  I  try to live with it.  
There is no use calling the nuerologist -he just  says I am worse, orders 
another MRI & then calls saying the MRI is  improving (???).  I miss most being 
able to using my hands easily -  I used to do all kinds of crafts -  
crossstitch, scraping booking , &  sewing - it is almost impossible now.  I had 
to 
retire from a  wonderful job.  I hate having to ask for help with things.  So 
much  for the pitty party - I try to remember NOT why God did this to me , 
but  why he did this FOR me - there has to be a purpose. 
Linda E. - Texas  


 
____________________________________
 From: "[email protected]"  <[email protected]>
To:  [email protected]
Cc: [email protected]
Sent: Wed, October 6, 2010 9:49:10  AM
Subject: [TMIC] 6th  anniversary


    
Hi,
   It's been 15 yrs  for me,and I still mourn for the losses. Not all the 
time,but it  is especially sad for me around this time of year. Good old  
seasonal affective disorder;It gets dark earlier. Plus,this week  has been 
rainy and gloomy,so that has me down.
   The hardest part  for me is that unless you have tm,you don't "get it". 
The  unrelenting tiredness,burning  pain,numbness,tingling,tightness,etc. My 
sister once said she  "couldn't stand to have the numbness all the time." I 
said there  isn't a choice,it's reality,and you learn to accept  it.
   I thank God for the  TMIC;I'd be adrift in a sea of loneliness without 
all of  you.
 
   Cheryl in rainy  (again) Easthampton,MA
 
 
 

--- On Wed, 10/6/10, [email protected]  
<[email protected]> wrote:



From:  [email protected]  <[email protected]>
Subject: [TMIC]  10-06-04, the 6th anniversary TM came into my life.
To:  "TMIC" <[email protected]>
Date: Wednesday,  October 6, 2010, 3:10 AM

  

10-06-04, today is the  6th anniversary TM (Transverse Myelits) came into  
my life. I live in Atlanta and was on a business trip to  Dallas .  I would 
have never thought that  waking up; putting my feet on the ground one 
Wednesday morning  would have changed my life so much.  I would  like to say is 
thank you to my husband Brian, my rock that  keeps me grounded. I could not 
have made it thru this without  him by my side and support. To God for 
bringing Brian into my  life 24 years ago, and to friends and family and my 
extended  TM family that have stuck by me regardless of what this spinal  cord 
disease has thrown at me. 


There are days that it  seems like it’s been forever and I can not remember 
walking,  running, riding a bike, ect and days that it seems like I just  
woke up and realized life as I knew it would never be the  same. I still have 
days I mourn for the loss of the life style  I had but at the same time 
blessed at how much appreciation  for life has been given me. I know I am 
blessed that this  disease did leave me one good leg that I can use a walker 
for  
short distances around the house, but need a wheel chair for  
distance/public use. By reading so many TM stories on this  site I do not feel 
as alone 
with the pain, frustration, and  just plain old bad days as I read other 
stories and puts my  issues back in perspective.  
Thanks again to my TM  family for always being there and sometimes that 
extra kick in  the rear when the pity party starts!  
So a journey in life  began, but the adventure continues  
Love and bless you  all  
Kim/Atlanta  
TM  T-10







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