Jeanne,

It is okay to have a 'Pity Party for One' at times.  Sort of clears the air.  I 
do that every once in a while myself and I'm sure that more of us do it as well.

Heather in Calgary 
  ----- Original Message ----- 
  From: jrushton 
  To: Gerry Surette ; [email protected] 
  Sent: Monday, March 24, 2008 10:14 AM
  Subject: [TMIC] It's okay...


        You can be as emotional as you want, any time you want!!  I think most 
of us try to be 'up' and 'positive' as often as we can but there comes a time 
when our old bodies just plain get bone tired and then it's time to take the 
time for ourselves to rest, both physically and emotionally.

        When I first came down with TM, I decided I was going to be old Mary 
Poppins and choose the positive over the negative which is the way I've always 
liked to live my life as often as I could...the 'cup is half full' not 'half 
empty', and laugh so I don't cry?  Well, that can still work a good part of the 
time but by gosh, you just can't always make it!  AND it's okay!!!

        Not too long ago I decided I was taking way too much Lyrica (approved 
by my provider) because I didn't like the side effects.  Well, the first week 
was one of the worst and there were definite withdrawals both horribly painful 
and emotional.  One day I was on the front porch swing just sobbing from my 
toes and who shows up but one of my daughters right out of the blue.  (God's 
doing, for sure) and I just couldn't stop crying.  It scared her to death 
because both my girls don't see me cry very often.  I usually laugh just to 
hear myself laugh (true!).  Well, this was a cleansing of the soul and a good 
way to get some of that 'stuff' out of my body, I would swear.  After that, I 
felt better, got lots of good hugs from my daughter and Jack and I was back on 
my way.  Sometimes we are so hard on ourselves.  God wants us to be good to 
ourselves so we can also be good to others.

        Jeanne 

        -------Original Message-------

        From: Gerry Surette
        Date: 3/24/2008 11:58:01 AM
        To: [EMAIL PROTECTED]
        Cc: [email protected]
        Subject: RE: [TMIC] So strange

        many thanks; The procedure itself is not painful; the bone marrow 
retival
        for biopsy is uncomfortable. the side effects though of three days for 
five
        hours each day is to say the least" NEVER AGAIN" I had a high fever 
chills
        etc; on top of my leg and feet spasms. It was certainly a memerable week
        Thank God jesus was by my side as well as my wife who when I had my 
spams I
        tend to hypervenilate; the pain is so great. She is there to calm me 
down
        and help me breathe normally until my spasm ends. You all know what 
these
        are. it is T<M<: life is never preditable. you have to roll with the
        punches. You just have to be thankful that the day you have no pain is a
        blessing. You have to make the best of it. Sorry if I am being 
emotional but
        the is the way I feel I have to take each day as it comes and be 
thankful
        for any blessing I receive. gerry

        >From: "jrushton" <[EMAIL PROTECTED]>
        >To: "Gerry Surette" <[EMAIL PROTECTED]>, <[email protected]>
        >Subject: RE: [TMIC] So strange
        >Date: Mon, 24 Mar 2008 09:04:10 -0500 (Central Daylight Time)
        >
        >Gerry!  I was just getting ready to ask if anyone had heard from you!  
You
        >have really gone thru some rough times and now they are going to remove
        >your
        >spleen?  Your advise is good...thank you!  You are in my 
prayers..Jeanne in
        >Dayton, WA
        >
        >-------Original Message-------
        >
        >From: Gerry Surette
        >Date: 3/24/2008 10:15:02 AM
        >To: [EMAIL PROTECTED]
        >Cc: [email protected]
        >Subject: RE: [TMIC] So strange
        >
        >I know exactly how you feel. I 've had tm since the age 0f 21 have been
        >able
        >to function until 2001 when I had a relapse. I too am 60 years young. 
My
        >plete count has gone way down a side effect of TM after numerous
        >treatments
        >i now have itp. I have gone through three treatments of immunoglobiulin
        >which have not worked. Now I have another treatment to go through to 
raise
        >my plete count at which time they will remove my speen. I urge 
everyone to
        >have there white blood cells plete count examined on a regular bases. 
Life
        >with TM is always a daily challenge. like they say it is like a box of
        >choclate you never know what will happen day to day. yes you have to 
have a
        >positive attidude. It is your life and you only have control of it. It 
is
        >up
        >to you to decide if you will fight it or let it get to you. for me I 
would
        >rather fight . It is hard but life is worth it
        >
        >
        > >From: "Robert Pall" <[EMAIL PROTECTED]>
        > >To: <[email protected]>
        > >Subject: [TMIC] So strange
        > >Date: Mon, 24 Mar 2008 10:56:52 -0400
        > >
        > >        Just a fast topic for discussion. In my case TM is like a 
box of
        > >chocolates...you never know what you are going to get!
        > >        It seems to me that how I feel from day to day is never the 
same!
        > >Some days are just terrible and some days are not so bad. I cannot 
point
        > >to the weather because that does not always have an effect on me. I 
do
        > >know if I get sick, even with a cold, my symptoms are always worse.
        > >Today is a beautiful day in sunny New Jersey and yet I feel
        > >terrible...why?
        > >       For me the biggest problem is the "banding" on my right leg 
just
        > >above the knee. When it gets very bad (like today) it makes walking 
much
        > >more difficult and I walk with an even stiffer leg than usual. Is it
        > >possible that as our spine regenerates (even though it is a very long
        > >process...decades) we still experience changes all the time, because 
the
        > >feelings are somewhat different, and for TM'rs change is never good. 
It
        > >seems that when I start to get used to the feelings I have, and try 
to
        > >accept them, they suddenly change.
        > >      I try to live with TM as best as I can. I try to keep a 
positive
        > >attitude and give thanks that I am able to work, walk and drive 
which so
        > >many of my fellow TM'rs cannot do....but some days are harder than
        > >others!
        > >     Last week I heard from one of our group who after 11 years had a
        > >relapse. For me this is truly scary. I don't know what I would do if
        > >this happened to me. I have had TM for more than 10 years and I am 
now
        > >60, which means that on top of TM I am starting to experience the
        > >problems that come with aging such as arthritis. Sometimes I feel 
that
        > >the only place we can go is down!
        > >     Sorry for the depressing attitude...I just need to talk to the 
group
        > >when I feel this way and then forget about it, get back my positive
        > >attitude, and move on.
        > >     Thank you for letting me vent!
        > >
        > >Rob in New Jersey
        >
        >
        >


       
              
       



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