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 <title>Cancer Survivors Network - MM in the spinal fluid - Comments</title>
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 <title>MM in spinal fluid</title>
 <link>http://csn.cancer.org/node/168150#comment-926485</link>
 <description>&lt;p&gt;My wife was recently diag. with MM in spinal fluid.   Also told a very small percentage of patients experience this.   She has had transplants and on Chemo for 3 years.  We were going to participate in trial program since normal treatments are not working for her.  Due to MM in spinal fluid, we can not participate in trials.  Any advice, I am all ears.  We (wife &amp; myself) have elected not to do the lumbar infusion since it has not worked with bone marrow.  Not sure of next step.&lt;/p&gt;
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 <pubDate>Sat, 23 Oct 2010 11:16:12 -0400</pubDate>
 <dc:creator>tj44</dc:creator>
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 <title>MM in the spinal fluid</title>
 <link>http://csn.cancer.org/node/168150</link>
 <description>&lt;p&gt;I was diagnosed w/mm in Sept 08. Stage 3. I&#039;ve undergone several sessions of chemo with positive results and a transplant in march this year. I&#039;ve been experiencing problems with my shoulds/arms. The nerves that drive the muscles in my shoulders have stopped working. My Dr. says that in about 1% of mm cases the disease finds it way into the spinal fluid. Has anyone else ever heard of this or experienced it. I&#039;m going in tomorrow for a spinal tap to confirm/deny presence of mm. tks.  &lt;/p&gt;
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 <comments>http://csn.cancer.org/node/168150#comment</comments>
 <category domain="http://csn.cancer.org/taxonomy/term/168">Multiple Myeloma</category>
 <pubDate>Sun, 03 May 2009 18:14:15 -0400</pubDate>
 <dc:creator>kkra</dc:creator>
 <guid isPermaLink="false">168150 at http://csn.cancer.org</guid>
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