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	<title>Myeloma Forum | Judy2 | Activity</title>
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				<title>Judy2 replied to the topic Lambda light chain MM in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/lambda-light-chain-mm/#post-117430</link>
				<pubDate>Tue, 05 Aug 2014 09:41:46 +0100</pubDate>

									<content:encoded><![CDATA[<p>Dear Carol</p>
<p>Sorry for delay in replying to you and it&#8217;s good to know I&#8217;m not the only one with light chain myeloma.  When I first told I had it (5 months ago) I was looking for pretty little lights in my urine!  Doh.</p>
<p>I&#8217;ve responded well so far and after my bone marrow biopsy reply will be on the list for a stem cell transplant so things are m&hellip;<span class="activity-read-more" id="activity-read-more-27310"><a href="http://www.myeloma.org.uk/forums/topic/lambda-light-chain-mm/#post-117430" rel="nofollow">[Read more]</a></span></p>
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				<title>Judy2 replied to the topic Lambda light chain MM in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/lambda-light-chain-mm/#post-117429</link>
				<pubDate>Tue, 05 Aug 2014 09:37:38 +0100</pubDate>

									<content:encoded><![CDATA[<p>Dear Eve</p>
<p>It&#8217;s taken me a while to get back on this site but just to let you know that I&#8217;m not at all possessive about my posts!  Everyone seems to be so positive about the &#8216;roller coaster ride&#8217; that we&#8217;re all on.  I&#8217;m a very positive person and just biting the bullet and getting on with it all.  I&#8217;ve had good news and have responded well to the&hellip;<span class="activity-read-more" id="activity-read-more-27308"><a href="http://www.myeloma.org.uk/forums/topic/lambda-light-chain-mm/#post-117429" rel="nofollow">[Read more]</a></span></p>
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				<title>Judy2 replied to the topic Lambda light chain MM in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/lambda-light-chain-mm/#post-117047</link>
				<pubDate>Thu, 24 Jul 2014 21:05:32 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello Wendy</p>
<p>CCRD involves IV chemo twice a week for  3 weeks in each monthly cycle with a drug called carfilzomib.  Together with Lenalidomide and steroids.  Quite a cocktail but sadly not the sort I would rather have!  After 4 cycles I have responded well and, like you, will have a stem cell transplant in due course.  Good luck with your treatment Wendy.</p>
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				<title>Judy2 started the topic Lambda light chain MM in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/lambda-light-chain-mm/</link>
				<pubDate>Wed, 16 Jul 2014 13:41:46 +0100</pubDate>

									<content:encoded><![CDATA[<p>I have recently been diagnosed with lambda light chain MM.  I am on a clinical trial CCRD &#8211; anyone else on this trial?</p>
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				<title>judy2 posted an update: Hello.  I was diagnosed with lambda light chain myeloma in [&#133;]</title>
				<link>https://forum.myeloma.org.uk/activity/p/2491/</link>
				<pubDate>Fri, 23 May 2014 21:13:53 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello.  I was diagnosed with lambda light chain myeloma in February  and elected to go on clinical trial XI.  I was randomly chosen to trial Carfilzomib, lenalidomide, cyclophosphamide and dexamethasone.  I have only  had two cycles both of which had to be halted as blood tests showed that my liver was not happy!  Has anyone else had the same&hellip;<span class="activity-read-more" id="activity-read-more-2491"><a href="https://forum.myeloma.org.uk/activity/p/2491/" rel="nofollow">[Read more]</a></span></p>
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