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    <title>Back for the 3rd time</title>
    <description>Latest messages for CancerCompass discussion</description>
    <link>http://www.cancercompass.com/message-board/message/all,37413,0.htm</link>
    <pubDate>Mon, 23 Nov 2009 00:00:00 GMT</pubDate>
    <lastBuildDate>Mon, 23 Nov 2009 00:00:00 GMT</lastBuildDate>
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      <title>RE: Back for the 3rd time</title>
      <description>I have had Stage IV Colon Cancer for three years now. My treatment was acombination of Folfox and Avastin.....I was given 12-18 months and have outlived that!!!!! I stopped treatment in February because the over toxicity ( I had constant treatment without interruption) was damaging to the rest of my body. My Oncologists believe that Avastin has prolonged my life. There is always the issue of quality/quantity. But, I am grateful for my situation.We are all praying as there is no other known case with these same results, therefore, we don&amp;#39;t know what to expect.My advice to you and your family is constant prayer, love and appreciation. I had to learn to stop WAITING to die, and focus on still being alive.My thoughts and prayers to you,Lori&amp;nbsp;&amp;nbsp;</description>
      <author>lori1</author>
      <pubDate>Thu, 25 Jun 2009 00:00:00 GMT</pubDate>
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      <title>RE: Back for the 3rd time</title>
      <description>William,I have&amp;nbsp;mets to the liver and celiac &amp;nbsp;lymph nodes.&amp;nbsp; You are right that this can limit treatment options.&amp;nbsp; Systemic chemo is pretty much a must I think.&amp;nbsp; Has anyone discussed the possibilty of radiation to the nodes?&amp;nbsp; Sometimes it can wipe out the ones that light up.&amp;nbsp; Just know it can turn into a game of centipede!&amp;nbsp; The chemo regimens get easier to handle&amp;nbsp;as the canzer becomes more&amp;nbsp;under control.&amp;nbsp; &amp;nbsp;Lifetime chemo seems scarier than the reality of it all.&amp;nbsp; I&amp;#39;m waiting for the new treatments that will come in the future.&amp;nbsp; I intend to be here to utilize them, so chemo it is.&amp;nbsp; Help&amp;nbsp;her to find joy in&amp;nbsp;the small moments.&amp;nbsp; My only rule is to have fun every.single.day.&amp;nbsp; No exceptions.&amp;nbsp; So far this philosophy is working for me.&amp;nbsp;Kimby&amp;nbsp;&amp;nbsp;</description>
      <author>kimby2</author>
      <pubDate>Tue, 23 Jun 2009 00:00:00 GMT</pubDate>
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      <title>RE: Back for the 3rd time</title>
      <description>I wanted to correct something I put on my 1st post...Folfiri is 5FU along with CPT-11 (CPT-11 is also called Irinotecan).&amp;nbsp; My Dad is only on the CPT-11 (Irinotecan) with Avastin&amp;nbsp;and NOT on the 5FU.&amp;nbsp; Sorry...just wanted to clarify.&amp;nbsp;</description>
      <author>HIGH_STRUNG_DAUGHTER</author>
      <pubDate>Tue, 23 Jun 2009 00:00:00 GMT</pubDate>
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      <title>RE: Back for the 3rd time</title>
      <description>Hi, I&amp;#39;m sorry to hear about her going back into a new treatment.&amp;nbsp; My Dad did 13 rounds of FOLFOX with Avastin (oops, sorry...Dad is 54 yrs old) and then it wasn&amp;#39;t working anymore (although it did work very well for awhile).&amp;nbsp; He then went to CPT-11 with Avastin which I think is the same one you&amp;#39;re talking about (Folfori and CPT-11 are the same thing if my memory is right).&amp;nbsp; He does it every Monday for three weeks and a week off.&amp;nbsp; The side effects have only been somewhat tired and every once and awhile some slight nausea and a mouth sore here and there.&amp;nbsp; It has been so much easier for him to handle compared to the FOLFOX and Avastin.&amp;nbsp; He just finished his 9th treatment of the CPT-11 and Avastin and his scans came back clear again.&amp;nbsp; We know it&amp;#39;s still there but it&amp;#39;s much much better than it was before.&amp;nbsp; His CEA is down to a 3.89 and he feels more like himself than he has in a long time.&amp;nbsp; I hope that things go the same for your wife, I will pray that you do indeed have her for many many many more years.&amp;nbsp; Please keep us updated.&amp;nbsp; God Bless and tell your wife to keep her chin up.&amp;nbsp; Remember to take care of yourself too....sometimes I think this whole thing has been harder for my Mom than anyone so take time for yourself to relax too.&amp;nbsp;</description>
      <author>HIGH_STRUNG_DAUGHTER</author>
      <pubDate>Tue, 23 Jun 2009 00:00:00 GMT</pubDate>
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      <title>Back for the 3rd time</title>
      <description>My wife 37 now has cancer in 4 different lymph nodes.&amp;nbsp; The highest one being under her collarbone.&amp;nbsp; She will start chemo July 13th for the 3rd time.&amp;nbsp; Folfiri is the chemo this time with avastin.&amp;nbsp; She will continue chemo pretty much for the rest of her life.&amp;nbsp; She will do chemo every 2 weeks for 3 months at a time with a scan in between.Does anyone know about this regiment of chemo?&amp;nbsp; Any advice you can give would be appreciative.&amp;nbsp; We have 3 children and need her to be with us for a very long time.&amp;nbsp;&amp;nbsp;</description>
      <author>William8</author>
      <pubDate>Tue, 23 Jun 2009 00:00:00 GMT</pubDate>
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