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Re: Need to be able to...EAT!
and JML..thanks for posting. Its nice to hear someone who has the same results after WBR. I too said..they must have damaged the part of my brain that tells me to eat..or I must have a tumor in the part of the brain that controls my appetite. I think Denise is right, I need to quit obsessing about it, and if I am getting in enough calories with the Boost and making sure to take supplements and eating what I can here and there...well, then maybe its enough for now. I hope so. 
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Diagnosed in October 2011 Stage IV with metastasis to liver.
January 2012 after double mastectomy, started taxotere, carboplatin and herceptin.
Clear.
December 2012 was diagnosed with five brain mets, and had whole brain radiation.
Around July 2014 two mets in brain, one a residual spot and one new one growing in size. Received Cyberknife on both areas
Clear/NED
April 2015 remain NED
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