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	<title>Myeloma Forum | Derek Debuse | Activity</title>
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				<title>Derek Debuse replied to the topic Side Effects in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/side-effects#post-103666</link>
				<pubDate>Thu, 24 Feb 2011 08:03:47 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi, ChrisB<br />
Yes, I have had profuse sweats. Not for a while though and I wasn&#039;t able to identify what was causing it. It just comes on&#8230;.unexpected and uninvited.<br />
The PN is significant and I have it quite badly now. Not painful, but means that a stick is helpful to stop me overbalancing! It also causes those cold feet. Sometimes my feet and&hellip;<span class="activity-read-more" id="activity-read-more-19203"><a href="http://www.myeloma.org.uk/forums/topic/side-effects#post-103666" rel="nofollow">[Read more]</a></span></p>
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				<title>Derek Debuse replied to the topic Side Effects in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/side-effects#post-103662</link>
				<pubDate>Fri, 21 Jan 2011 08:54:37 +0000</pubDate>

									<content:encoded><![CDATA[<p>Peripheral neuropathy is generally in feet and hands. I haven&#039;t heard of it in the the spine or back. Mine is still mainly on feet, but at least I have not got the &quot;restless legs&quot; aby more. I have changed from Amitryptilline to Gabapentin. That may have had a good effect.<br />
the neuropathy does not trouble me during the day, but gets worse during&hellip;<span class="activity-read-more" id="activity-read-more-19200"><a href="http://www.myeloma.org.uk/forums/topic/side-effects#post-103662" rel="nofollow">[Read more]</a></span></p>
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				<title>Derek Debuse started the topic Side Effects. in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/side-effects</link>
				<pubDate>Fri, 17 Dec 2010 10:02:14 +0000</pubDate>

									<content:encoded><![CDATA[<p>I have had Thalidomide and am now on Revlimid. I have neurophy on both feet which is manageable. Recently I have been getting &quot;restless leg syndrome&quot; accompanied by similar symptoms covering the whole body. It doesn&#039;t trouble me during the day but makes it very difficult to get off to sleep. Has anyone had any similar symptons@ I am assuming that&hellip;<span class="activity-read-more" id="activity-read-more-19197"><a href="http://www.myeloma.org.uk/forums/topic/side-effects" rel="nofollow">[Read more]</a></span></p>
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