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    <title>CancerCompass Message Board: side effects of xeloda</title>
    <description>CancerCompass message board discussion started by annamaria1 on 4/8/2008</description>
    <link>http://www.cancercompass.com/message-board/message/all,22803,0.htm</link>
    <pubDate>Thu, 04 Dec 2008 00:00:00 GMT</pubDate>
    <lastBuildDate>Thu, 04 Dec 2008 00:00:00 GMT</lastBuildDate>
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      <title>side effects of xeloda</title>
      <description>Hi, This is my&amp;nbsp; first time trying this but I have some concerns and worries about the side effect of xeloda.&amp;nbsp; In 2006 I had a mastectomy, and 1 out of 23 lymph nodes with ca.&amp;nbsp; I had chemo and did well, and was on Arminidex.&amp;nbsp; &amp;nbsp;I now has mets&amp;nbsp; to my spine and shoulder.&amp;nbsp;I am on my second round to xeloda 2000mg a day two weeks on one week off.&amp;nbsp; I have also started once a month IV of Zometa.&amp;nbsp; I feel good, but am so worried about the side effects expecially the hands and feet.&amp;nbsp; I cream them 3 times a day, but can&amp;#39;t walk for a long time.&amp;nbsp; I am starting to get some buring in my feet, is this the start.&amp;nbsp; I just need someone to write me back and reasure me of what I can expect with this treatment.&amp;nbsp;</description>
      <author>annamaria1</author>
      <pubDate>Tue, 08 Apr 2008 00:00:00 GMT</pubDate>
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      <title>RE: side effects of xeloda</title>
      <description>&amp;nbsp;On 4/8/2008 annamaria1 wrote:Hi, This is my&amp;nbsp; first time trying this but I have some concerns and worries about the side effect of xeloda.&amp;nbsp; In 2006 I had a mastectomy, and 1 out of 23 lymph nodes with ca.&amp;nbsp; I had chemo and did well, and was on Arminidex.&amp;nbsp; &amp;nbsp;I now has mets&amp;nbsp; to my spine and shoulder.&amp;nbsp;I am on my second round to xeloda 2000mg a day two weeks on one week off.&amp;nbsp; I have also started once a month IV of Zometa.&amp;nbsp; I feel good, but am so worried about the side effects expecially the hands and feet.&amp;nbsp; I cream them 3 times a day, but can&amp;#39;t walk for a long time.&amp;nbsp; I am starting to get some buring in my feet, is this the start.&amp;nbsp; I just need someone to write me back and reasure me of what I can expect with this treatment.&amp;nbsp;&amp;nbsp;</description>
      <author>annamaria1</author>
      <pubDate>Wed, 09 Apr 2008 00:00:00 GMT</pubDate>
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      <title>RE: side effects of xeloda</title>
      <description>&amp;nbsp;On 4/8/2008 annamaria1 wrote:Hi, This is my&amp;nbsp; first time trying this but I have some concerns and worries about the side effect of xeloda.&amp;nbsp; In 2006 I had a mastectomy, and 1 out of 23 lymph nodes with ca.&amp;nbsp; I had chemo and did well, and was on Arminidex.&amp;nbsp; &amp;nbsp;I now has mets&amp;nbsp; to my spine and shoulder.&amp;nbsp;I am on my second round to xeloda 2000mg a day two weeks on one week off.&amp;nbsp; I have also started once a month IV of Zometa.&amp;nbsp; I feel good, but am so worried about the side effects expecially the hands and feet.&amp;nbsp; I cream them 3 times a day, but can&amp;#39;t walk for a long time.&amp;nbsp; I am starting to get some buring in my feet, is this the start.&amp;nbsp; I just need someone to write me back and reasure me of what I can expect with this treatment.&amp;nbsp;This is my first time on this link serve.&amp;nbsp; I&amp;#39;m on 2500 mg of Xeloda for pancreatic cancer.&amp;nbsp; The burning of the hands and feet is called hand and foot syndrome and a typical side effect of the Xeloda.&amp;nbsp; My oncologist has instructed me to put Ban Roll-on antiperspirant on my feet and hands 15 minutes before taking the Xeloda.&amp;nbsp; His helps cut down somewhat on the side effects to the hands and feet.&amp;nbsp; Then I also keep them moisturized, feet with Bag Balm and hands with a good moisturizing lotion.&amp;nbsp; I&amp;#39;ve been using Cetaphil cream and also Triple Lanolin Aloe Vera Hand and Body Lotion.&amp;nbsp;&amp;nbsp; I still get the burning, more on my feet, which makes walking painful, but it does subside during the &amp;quot;off&amp;quot; week into the first week of the next 2-week cycle of Xeloda.&amp;nbsp; From my understanding the effect of the Xeloda is cumulative, so the hand and foot syndrome may get a little worse.&amp;nbsp; If it gets intolerable, tell your oncologist, who may then reduce the dosage or give you an extra &amp;quot;off&amp;quot; week.&amp;nbsp; Hope this helps.&amp;nbsp;</description>
      <author>asdfgklj</author>
      <pubDate>Wed, 23 Apr 2008 00:00:00 GMT</pubDate>
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      <title>RE: side effects of xeloda</title>
      <description>My message was also the first time to this site.&amp;nbsp; So far I have only had a little burning of my feet when I stand to long or walk for about a half an hour.&amp;nbsp; I am only on my third round of xeloda.&amp;nbsp; I am going away this summer for 3 months&amp;nbsp; and wondering what to expect.&amp;nbsp; When the syndrom occurs about how long does it take to clear up once your off the xeloda, and are you really immoblizie, as far as normal routine?&amp;nbsp; Sorry I took so long to reply I was away for 2 weeks no computer available.&amp;nbsp; Think positive, and all the best to you.&amp;nbsp;&amp;nbsp;&amp;nbsp; AMD Long Island, New York</description>
      <author>annamaria1</author>
      <pubDate>Wed, 30 Apr 2008 00:00:00 GMT</pubDate>
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