I just got off the phone talking with Cyndy in Indiana.

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Veteran Member

Date Joined Jul 2003
Total Posts : 2921
   Posted 2/7/2007 2:32 PM (GMT -7)   
It has been a long time since we have heard from her.  For all she has been through and is still going through she sounded wonderful and we talked a good while.  She said to tell you all she sends hugs and kisses.  She also said that it is hard to post because she doesn't want to share her struggles which may seem negative to newbies.  I told her she is one of our success stories staying here on this earth for much longer than the doctors predicted.  She asked about many of you that she met in Cincy and knew through the board.  Keep her in your prayers as she continues her battle and goes through a hip replacement in the next month or so.  Hugs,  MK

Veteran Member

Date Joined Jul 2003
Total Posts : 1564
   Posted 2/8/2007 4:20 PM (GMT -7)   
My goodness, MK, I just don't understand why people with mets are afraid of scaring the newbies. We all know, even the newbies, what the odds are with this disease, and to me, it is always an inspiration to hear from our friends who are keeping up their fight through recurrence after recurrence, or hang in there for years after the doctors had dared let them hope for.

I remember Cyndy saying once that her doctor told her to look at mets as you would look at diabetes...as a chronic disease. And while her disease has been chronic, she has done a lot of living in the years she's been with us!

Cyndy, if you're out there reading this, I hope you'll come and post occasionally. Girl, you don't have to talk about the cancer...tell us about the grandbabies or the trips or the stopped up toilet! This board isn't all about cancer...it's about our lives, too.

If all I had to talk about was my cancer, well, I wouldn't have much to say. And we all know that I make it a policy to always have something to say! LOL

Love and hugs to all...
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