<?xml version="1.0" encoding="iso-8859-1"?>
<rss version="2.0">
  <channel>
    <title>CancerCompass Message Board: Ringing in the ears</title>
    <description>CancerCompass message board discussion started by Mediator on 2/27/2008</description>
    <link>http://www.cancercompass.com/message-board/message/all,21383,0.htm</link>
    <pubDate>Thu, 20 Nov 2008 00:00:00 GMT</pubDate>
    <lastBuildDate>Thu, 20 Nov 2008 00:00:00 GMT</lastBuildDate>
    <docs>http://backend.userland.com/rss</docs>
    <generator>RSS.NET: http://www.rssdotnet.com/</generator>
    <item>
      <title>Ringing in the ears</title>
      <description>Hello Friends:Time to start another one.&amp;nbsp; Who has had the ear ringing?&amp;nbsp; Is this from residual damage to the temporal lobe or ear canal?&amp;nbsp; What did any of you do?&amp;nbsp; Does it go away?&amp;nbsp; My husband was up all night going crazy.Thanks,&amp;nbsp;Kara</description>
      <author>Mediator</author>
      <pubDate>Wed, 27 Feb 2008 00:00:00 GMT</pubDate>
    </item>
    <item>
      <title>RE: Ringing in the ears</title>
      <description>I&amp;#39;ve got ringing and high frequency hearing loss. My docs say it&amp;#39;s from the Chemo. I think Cisplatin, but it might have been theErbitux? They told me it was a 50/50 shot that things would go back tonormal. Toward the end of treatment I was almost deaf as a post :) If I wasn&amp;#39;t looking right at whoever was talking to me, all I heard was blah-blah-blah.The good news is that the hearing loss got better. I waseven fitted for hearing aids that I ended up not getting. The bad newsis the ringing is still there. Sometimes it&amp;#39;s bad, other times I don&amp;#39;tnotice it. It&amp;#39;s just one more thing he&amp;#39;ll get used to. Mine seems tocome and go depending on how much fluid build up I have. Looking at thebig picture, I think it will become a non-issue. I wish him luck.</description>
      <author>ThreePutt</author>
      <pubDate>Wed, 27 Feb 2008 00:00:00 GMT</pubDate>
    </item>
    <item>
      <title>RE: Ringing in the ears</title>
      <description>Hi Kara&amp;nbsp;Have had this tinntinitus before chemo but it can be caused by the chemo.&amp;nbsp; I have heard -- and you shoulld check with the doc before trying anything -- that lipoflavinoids MAY give temporary or permanent aid.&amp;nbsp; Might be worth checking into.&amp;nbsp;Good luck&amp;nbsp;&amp;nbsp; gj</description>
      <author>Gregj</author>
      <pubDate>Wed, 27 Feb 2008 00:00:00 GMT</pubDate>
    </item>
    <item>
      <title>RE: Ringing in the ears</title>
      <description>Thanks again for the responses.He did have some ear wax build up too.&amp;nbsp; Ear wax removal liquid seemed to provide some relief.&amp;nbsp; I just think it is worse at night from laying down.Kara&amp;nbsp;&amp;nbsp;</description>
      <author>Mediator</author>
      <pubDate>Wed, 27 Feb 2008 00:00:00 GMT</pubDate>
    </item>
    <item>
      <title>RE: Ringing in the ears</title>
      <description>I have exactly the same as ThreePutt. It IS from the cisplatin-a published side effect. I was told it&amp;#39;s permanent-and it has not abated at all for me. ENT told me permanent because it&amp;#39;s nerve damage that cannot repair itself.&amp;nbsp;I get use to the ringing, but sometimes when I&amp;#39;m quiet &amp;amp; contemplative, I focus on it and it nearly drives me batty. I have to have people looking at me while talking, or cannot make out all the words.&amp;nbsp;Lots of&amp;nbsp;phone conversations are hard. When I watch a movie or TV-seldom--if they whisper, I cannot make it out at all. Lots of DVD&amp;#39;s seem muffled, talking not clear. I&amp;#39;m always asking my husband: WHAT did they just&amp;nbsp;say?&amp;nbsp;&amp;nbsp;&amp;nbsp;We miss alot this way! :)&amp;nbsp; Gayle</description>
      <author>gayleann</author>
      <pubDate>Wed, 27 Feb 2008 00:00:00 GMT</pubDate>
    </item>
    <item>
      <title>RE: Ringing in the ears</title>
      <description>I&amp;#39;ve got it too, I had Cisplatin for my chemo and the oncologist told me it might happen. I&amp;#39;d like to know if anyone has had success with the lipoflavinoid route or not.</description>
      <author>micromisterphone</author>
      <pubDate>Wed, 27 Feb 2008 00:00:00 GMT</pubDate>
    </item>
  </channel>
</rss>