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    <title>CancerCompass Message Board: more info</title>
    <description>CancerCompass message board discussion started by Smitty on 6/21/2007</description>
    <link>http://www.cancercompass.com/message-board/message/all,13651,0.htm</link>
    <pubDate>Sun, 23 Nov 2008 00:00:00 GMT</pubDate>
    <lastBuildDate>Sun, 23 Nov 2008 00:00:00 GMT</lastBuildDate>
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      <title>more info</title>
      <description>Hello,&amp;nbsp;&amp;nbsp;&amp;nbsp; I have been seeing oncologists for about 4-5 years now because I had pains in my legs and didn&amp;#39;t know why. One of the many doctors I was referred to told me I had too much protein in my blood and I should see an oncologist. I did and all I was told was to come in every 3 months so we could keep an eye on my protein levels and that &amp;quot;one day&amp;quot; I could have a problem. So I did as I was told pretty much thinking that I &amp;quot;might&amp;quot; be a canditate&amp;nbsp; for some type of&amp;nbsp; bone cancer&amp;nbsp; down the road.&amp;nbsp; Three years ago my husband and I moved&amp;nbsp; to another&amp;nbsp; city and I changed&amp;nbsp; doctors to be closer to my home&amp;nbsp; and&amp;nbsp; just&amp;nbsp; 2 months ago&amp;nbsp; he mentions how&amp;nbsp; great it is that I have multiple myeloma and that when it&amp;#39;s time for treatment there is a good hospital in Arkansas or I could consider M D Anderson. Well, I have to tell you it was like a slap in the face.......he said that I do have the disease but that it is smoldering right now. That&amp;#39;s why it&amp;#39;s important that I get checked every 3 months. He also told me they usually don&amp;#39;t see this disease in someone as young as I am. I am 53. I have another appt in July which my husband is coming with me so we can get much more info on this. I am also wondering if I should look into an appt with one of these other cancer treatment centers to get a second opinion and possibly some kind of nutritional treatment or vitamins. I have been told to just do what I have been doing. I&amp;#39;m pretty confused right now and more than a little afraid. Any info would be appreciated. Also is mutiple myeloma also called lymphoma? And what is CLL? Thanks for any info. Paula :) &amp;nbsp; </description>
      <author>Smitty</author>
      <pubDate>Thu, 21 Jun 2007 00:00:00 GMT</pubDate>
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      <title>RE: more info</title>
      <description>Your physician is doing the right thing.&amp;nbsp; Aggressive treatment of Myeloma has had no effect on the natural course of the disease.&amp;nbsp; It could go along for years with no treatment.&amp;nbsp; Treatment is symptom based and designed to prolong the symptom free interval.&amp;nbsp; Sometimes the smoldering phase never converts.&amp;nbsp; Another reason not the treat aggressively since it may do more harm.&amp;nbsp; Since you are in Arkansas, then you should know Sam Walton had Myeloma as well.&amp;nbsp; Have you had a bone survey??&amp;nbsp; Myeloma can cause erosion of bone.&amp;nbsp; You should be taking Calcium and vitamn D an treatd at least moderately like you have osteoporosis.</description>
      <author>Witchdoctor</author>
      <pubDate>Sun, 24 Jun 2007 00:00:00 GMT</pubDate>
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