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    <title>Metastes in brain anyone else have them</title>
    <description>Latest messages for CancerCompass discussion</description>
    <link>http://www.cancercompass.com/message-board/message/all,30856,0.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: Metastes in brain anyone else have them</title>
      <description>Hi,First of all I would like to tell you to stay strong!&amp;nbsp; My dad was diagnosed with kidney cancer in 2003.&amp;nbsp; His kidney was removed. In April of 2006 we were infomed that it has spread to his lungs.&amp;nbsp; The drugs tried were nexavar sutent.&amp;nbsp; My dad suffered from terrible side effects on both of these drugs with minimal or no response from them.&amp;nbsp; In August of 2008 he was diagnosed with tumors now on his brain.&amp;nbsp; This was so scary for all of us.&amp;nbsp; He took 3 weeks of radiation and now is taking weekly iv treatments of torisel.&amp;nbsp;&amp;nbsp; Now for the good news.....as of last week he had a chest xray and the doc is thinking about a 30% reduction of the tumors in his lungs.&amp;nbsp; I was thrilled.&amp;nbsp; The side effects of the torisel are minimal compared to the others.&amp;nbsp; They are going to do a CT scan shortly to get a better picture.&amp;nbsp; They have also looked at his brain and see no progression and he has not experienced any more seizures from them so we are hopeful that there as been a reduction there as well.&amp;nbsp;&amp;nbsp; My dad is 58 years old and I will tell you the same thing I tell him.................Fight Fight Fight&amp;nbsp;&amp;nbsp; More drugs and treatments are constantly coming out and we will find the one that works. Ten years ago this may not have been an option. And PRAY.&amp;nbsp; Shelly</description>
      <author>Shellyb</author>
      <pubDate>Fri, 05 Dec 2008 00:00:00 GMT</pubDate>
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      <title>RE: Metastes in brain anyone else have them</title>
      <description>My father was just diagnosed in June with Stage 4 RCC with mets to his brain and lungs.&amp;nbsp; He went though 14 brain radiation treatments, and his current CT and MRI brain scans appear stable at this time.&amp;nbsp; We are very grateful!&amp;nbsp; He is also back on Sutent after a month off (he had blood clots in his lungs and was found to be severely hypothyroid).&amp;nbsp; I would encourage you to make sure your wife&amp;#39;s blood counts to be monitored, as well as keeping an eye out for her thyroid levels. As far as side effects, he experienced&amp;nbsp;extreme fatigue, slurred speech, loss of appetite, feeling cold, and weakness, but we think a lot of those symptoms might have been due to his low thyroid function in addition to the Sutent.&amp;nbsp;I wish you both the best,Julie D.</description>
      <author>LadyJulie</author>
      <pubDate>Wed, 03 Dec 2008 00:00:00 GMT</pubDate>
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      <title>RE: Metastes in brain anyone else have them</title>
      <description>It took me eight days to feel the SE&amp;#39;s of Sutent.&amp;nbsp; By day nine my blood pressure went up a lot and I felt terrible.&amp;nbsp; I do not have any first hand knowledge for the brain mets but have read of others who did well after they were treated.&amp;nbsp; I am sorry you are having trouble obtaining this drug, hopefully Phyzer will step up to the plate.&amp;nbsp; God Bless you and your wife.&amp;nbsp;</description>
      <author>Robbie2</author>
      <pubDate>Wed, 03 Dec 2008 00:00:00 GMT</pubDate>
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      <title>Metastes in brain anyone else have them</title>
      <description>The doctor has stated wife has some small spots in brain.&amp;nbsp; They are not big may 1-3mm.&amp;nbsp; They are being treated right now with radiation.&amp;nbsp; Has any one else have that diagnosis and how long has it been?&amp;nbsp; My wife is on her 2nd dosage of Sutent and still not having any bad side affects.&amp;nbsp; How long before she feels any?&amp;nbsp; I hope she doesn&amp;#39;t get any but trying to let her know that some might show up.&amp;nbsp; Have been trying to get a hold of pfizer to get the meds for free currently have paid for 14 days and hoping they will step in and help me pay for the rest.&amp;nbsp; Aslo see that they could reimburse me for what I have paid for already.&amp;nbsp; Anyone going through this??&amp;nbsp; Any feed back on the brain metastes is appreciated.&amp;nbsp; Fight, stay strong and think postive is all I have right now.&amp;nbsp; My prayers to all, and remember you can win!!!&amp;nbsp;</description>
      <author>Jimmy69</author>
      <pubDate>Tue, 02 Dec 2008 00:00:00 GMT</pubDate>
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