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    <title>CancerCompass Message Board: Does anyone else have CMML?</title>
    <description>CancerCompass message board discussion started by wendyv on 3/5/2008</description>
    <link>http://www.cancercompass.com/message-board/message/all,21658,0.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>Does anyone else have CMML?</title>
      <description>Recently diagnosed with CMML. I live in Australia, and have been told there is no treatment, and just to &amp;quot;watch and wait&amp;quot; Has anyone else been in this situation? I am also told it is aggressive, and terminal!... but that I may have 4-6 years symptom free... doesn&amp;#39;t really sound agressive, does it?</description>
      <author>wendyv</author>
      <pubDate>Wed, 05 Mar 2008 00:00:00 GMT</pubDate>
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      <title>RE: Does anyone else have CMML?</title>
      <description>&amp;nbsp;On 3/5/2008 wendyv wrote:Recently diagnosed with CMML. I live in Australia, and have been told there is no treatment, and just to &amp;quot;watch and wait&amp;quot; Has anyone else been in this situation? I am also told it is aggressive, and terminal!... but that I may have 4-6 years symptom free... doesn&amp;#39;t really sound agressive, does it?Hi,How are you doing these days .. 4 months after your original post?&amp;nbsp; I have just been told (have refused biopsy thus far, but will get one soon, once I&amp;#39;m more educated) that my blood over the last 5 years are showing the Pattern of CMML.&amp;nbsp; Definitely NOT a pretty thing from what I&amp;#39;ve been able to learn the last couple of days.&amp;nbsp; I&amp;#39;m Only 38!CMML is classified among MyeloDysplastic AND MyeloProliferative Diseases because it shares features of BOTH.&amp;nbsp; As far as &amp;quot;treatment&amp;quot; from your doctors, UNTIL they see (my understanding) WHICH WAY your disease will progreess, there is really nothing They can do except watch and wait.&amp;nbsp; This is not a very understood disease and there are no specific treatment protocols.IF your blood shows that you have PDGF-R Fusion Genes (it&amp;#39;s a long arm of chromosome 5(5q33) ) then Roferon-A .. GLEEVEC.... Imatinib...WILL HELP.&amp;nbsp; MD Anderson.org has seen rapid hemotologic improvement and sometimes molecular remissions in CMML patients.IF you do NOT Have Fusion genes, in 2002 Hydroxyurea (Droxia, Hydrea) was the medicine of choice &amp;lt;different study&amp;gt; for CMML, but with modest success.&amp;nbsp; Personally, am doing MEGA Supplementation and research on my own.&amp;nbsp; Layman&amp;#39;s terms are best understood on LEF.org on their various Cancer Treatments and Protocols (from all over World).&amp;nbsp; There are also various Scientific Studies you can find on the net.&amp;nbsp; Just takes Lots of Time, Energy, Patience ... and FAITH, and Dedication! DEFINITELY suggest Turmeric(Curcumin) 2400mg up to 3x day... GREEN TEA 2-3 750mg caps/day&amp;nbsp;.. and up to&amp;nbsp;10mg Melatonin to start as you do your own research.&amp;nbsp; Then again, I am NOT a doctor.&amp;nbsp; I just know that I WANT TO LIVE and the Prognosis that I&amp;#39;ve read on various pharmaceutical studies is not that promising.&amp;nbsp; YOU must become Very Involved and Educated in your care.&amp;nbsp; I hope that you are doing well.&amp;nbsp; This is Certainly a LONELY route to be on.&amp;nbsp;God Bless You and Big Hugs Your Way,M.</description>
      <author>Best Isnt Easy</author>
      <pubDate>Sat, 05 Jul 2008 00:00:00 GMT</pubDate>
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      <title>RE: Does anyone else have CMML?</title>
      <description>Hi, &amp;nbsp;I am from India and my father has been diagnosed to CMML-2.&amp;nbsp; Doctors has put him on VIADAZA , but he says that it will not be 100% cure. &amp;nbsp;Have you heard on the BML sucess for patient with age 60 years. &amp;nbsp;Nimesh&amp;nbsp;</description>
      <author>nimesh</author>
      <pubDate>Wed, 05 Nov 2008 00:00:00 GMT</pubDate>
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