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    <title>CancerCompass Message Board: confused????</title>
    <description>CancerCompass message board discussion started by rnojax on 3/31/2008</description>
    <link>http://www.cancercompass.com/message-board/message/all,22554,0.htm</link>
    <pubDate>Fri, 05 Sep 2008 00:00:00 GMT</pubDate>
    <lastBuildDate>Fri, 05 Sep 2008 00:00:00 GMT</lastBuildDate>
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      <title>confused????</title>
      <description>my&amp;nbsp; dad was diagnosed with MM 2 yrs ago this May, has gone through radiation, thalydamide (sp) and radiation....recently (November) he started having high spiking fevers that would caused him to get delirious, 103-105 range, at the hospital they said it wasn&amp;#39;t the MM but can find nothing else---after several days of crying and heated discussions with his insurance and oncologist, we got a second opinion,,,his numbers aren&amp;#39;t high they even did a 2nd bone scan and said the MM is in partial remission----one Dr said that 1% of MM patients do get high fevers, the 2nd opinion was helpful and made some recommendations, but then in his error he did not read my dad&amp;#39;s entire history and my dad can&amp;#39;t have the radiation again, several Dr&amp;#39;s are telling us that he is in the final phase of stage 3 but it just doesn&amp;#39;t nake sense...his numbers aren&amp;#39;t bad, he&amp;#39;s in partial remission and he doesn&amp;#39;t have any severe bone breakage (like some I have read about)---he is diabetic and is currently getting his 16th unit of blood in 10 weeks but his oncologist keeps saying it&amp;#39;s not the MM that there is a secondary problem with his blood----HELLO I want to yell, they can&amp;#39;t find anything and she keeps saying &amp;quot;it&amp;#39;s not the MM&amp;quot; but when I ask what it is she says &amp;quot;not my specialty&amp;quot;---now they are saying that they want to start Velcade--I have read wonderful things about it, but I am also afraid that the trial or begining stage will be the final straw for his body-----the fever gets so high that he won&amp;#39;t eat and then his sugars go out of whack and he&amp;#39;s semi-cohesive and the dr&amp;#39;s say this is it and we all rush to him and then they get blood in him and some tylenol for the fever and he looks and feels better---I guess I&amp;#39;m just feeling like they are missing something and I not sure if there are others that have similiar symptoms????? advice, experience are welcome thanks for reading&amp;nbsp;rnojax&amp;nbsp;</description>
      <author>rnojax</author>
      <pubDate>Mon, 31 Mar 2008 00:00:00 GMT</pubDate>
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      <title>RE: confused????</title>
      <description>I&amp;#39;ve been fighting fevers, infection, and hot flushes since Jan 08.&amp;nbsp; My doctor assumes each time I get a fever it&amp;#39;s the staph infection I picked up during stem cell collection.&amp;nbsp; However, cultures come back negative.&amp;nbsp; I&amp;#39;ve been on Vancomycine for what seems like forever, but the fevers kept coming back.&amp;nbsp; I had the port removed from my chest about 10 days ago and I haven&amp;#39;t spiked a fever since.&amp;nbsp; I&amp;#39;m on doxycycline as a preventive measure, but that&amp;#39;s it.&amp;nbsp; Though I haven&amp;#39;t had a fever lately, I have continued to have night sweats and hot flashes.........if any one&amp;nbsp;has insight in to those two happenings, I&amp;#39;d love to hear it.&amp;nbsp; Some times they just don&amp;#39;t know what&amp;#39;s causing the fever.&amp;nbsp; However, they should be eleminating possibilities.A good indicator of possible infection or inflamation is his C-Reactive Protien.&amp;nbsp; Have them print you a graph/chart so you can see if he&amp;#39;s trending high from HIS normal range...not THE normal range, but HIS.&amp;nbsp; Also, an increase in White blood cells could be indicating something.&amp;nbsp; C-Reactive Protien however can tell a hemo/blood guy alot about what&amp;#39;s going on.I believe your doctors should have done cultures testing for molds, virus, bacteria, everythingThis link is pretty interesting http://209.85.173.104/search?q=cache:Qf6Ggr3o92MJ:www.siteman.wustl.edu/PDQ.aspx%3Fid%3D842%26xml%3DCDR62827.xml+myeloma%2Bhot+flashes&amp;amp;hl=en&amp;amp;ct=clnk&amp;amp;cd=33&amp;amp;gl=us</description>
      <author>UTboy</author>
      <pubDate>Mon, 31 Mar 2008 00:00:00 GMT</pubDate>
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      <title>RE: confused????</title>
      <description>I&amp;#39;m with both of you UTboy -- especially with the hot flushes!!&amp;nbsp; I am seeing this more and more often with people with MM as well as with other cancers.&amp;nbsp; I never had this problem with menopause, but recently I&amp;#39;ve been watching Whoppie Goldberg on The View and she has been experiencing hot flushes -- exactly the same as what I&amp;#39;ve been going through with big dropplets of water falling from my head like rain drops!&amp;nbsp; Her face becomes very shiny - as does my own - and she can&amp;#39;t cool down but must just ride it through until it stops.&amp;nbsp; Well, I have found the exact same problem.So, I carry a dry washcloth to mop up my head and neck - it doesn&amp;#39;t seem to happen to the rest of my body.&amp;nbsp; I have posted this problem on the net in the past but have never recieved a response that actually works for me, except that the sweats have eased quite a bit now that the weather has become cooler (I live in Australia)!&amp;nbsp; I&amp;#39;m hoping that the flushes will go away during winter -- and won&amp;#39;t come back again next summer!!&amp;nbsp; If you hear of anything that does work please post it in BIG letters on this site!!&amp;nbsp; Many thanks, Cath</description>
      <author>poppy/cath</author>
      <pubDate>Fri, 04 Apr 2008 00:00:00 GMT</pubDate>
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