I agree.    When you start getting worse, there is usually help you can get to 
reverse or at least settle down the problem.   Sure doesn't hurt to
get checked out.
Janice


From: [email protected] 
Sent: Wednesday, October 06, 2010 10:33 PM
To: [email protected] ; [email protected] 
Subject: Re: [TMIC] 6th anniversary


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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