<?xml version="1.0" encoding="UTF-8" ?>
<?xml-stylesheet type="text/xsl" href="https://community.macmillan.org.uk/cfs-file/__key/system/syndication/atom.xsl" media="screen"?><feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en-US"><title type="html">yulia&amp;#39;s blog </title><subtitle type="html">yulia&amp;#39;s blog </subtitle><id>https://community.macmillan.org.uk/cancer-blogs/b/yulia/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/yulia" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/yulia/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2009-01-26T19:22:42Z</updated><entry><title>Unknown Neuroendocrine Primary with Mets to Liver -- Feeling Helpless</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/yulia/posts/unknown-neuroendocrine-primary-with-mets-to-liver-feeling-helpless" /><id>https://community.macmillan.org.uk/cancer-blogs/b/yulia/posts/unknown-neuroendocrine-primary-with-mets-to-liver-feeling-helpless</id><published>2009-01-26T18:22:42Z</published><updated>2009-01-26T18:22:42Z</updated><content type="html">Hi All,

My mom was diagnosed with Neuroendocrine Cancer with mets to her liver (Stage IV) in August 2007. She&amp;#39;s unoperable as there are too many mets in her liver. We are in New York, US. She was seen by Dr. Warner and was offer SIR Radiation Treatment at the time she was first seen by him. My father, her primary caretaker opted out from the Conventional Treatment and decided to use &amp;quot;Watch and See&amp;quot; approach with regular monitoring and tests/scans. She was also doing a Gerson Protocol and Budwig Protocol (both Alternative Nutruition Diets) and up until recently (about a month ago) has been feeling ok, her liver function was normal and she was generally feeling ok. About a few weeks ago my mom&amp;#39;s condition took a turn for the worse. Her Chromogranin A marker got very high and her general condition got worsen. My father seems to be in denial and is still reluctant to do SIR or the Sandostatin injections. I don&amp;#39;t know what to do and feel pretty helpless! Has anyone had a succes with either SIR or Sandostatin? I&amp;#39;d appreciate your feedback.

Yulia
&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=223998&amp;AppID=19107&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="Protocol" scheme="https://community.macmillan.org.uk/cancer-blogs/b/yulia/archive/tags/Protocol" /><category term="radiation" scheme="https://community.macmillan.org.uk/cancer-blogs/b/yulia/archive/tags/radiation" /></entry></feed>