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	<title>Myeloma Forum | Nick Carrington | Activity</title>
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				<title>Nick Carrington replied to the topic How confusing is this journey? in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/how-confusing-is-this-journey/page/3/#post-116084</link>
				<pubDate>Wed, 18 Jun 2014 21:35:31 +0100</pubDate>

									<content:encoded><![CDATA[<p>To put the other side of the coin, I think I had exactly 2 months in a smouldering status, then my PP level went over 30, which, combined with some lytic lesions in my skull, led to treatment starting. 8 1/2 months and 2 different chemo regimes later I&#8217;m almost back down low enough to consider stem cell harvest. As someone said higher up, every&hellip;<span class="activity-read-more" id="activity-read-more-25599"><a href="http://www.myeloma.org.uk/forums/topic/how-confusing-is-this-journey/page/3/#post-116084" rel="nofollow">[Read more]</a></span></p>
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				<title>Nick Carrington replied to the topic Friendly reminder in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/friendly-reminder/#post-115853</link>
				<pubDate>Sun, 08 Jun 2014 22:45:07 +0100</pubDate>

									<content:encoded><![CDATA[<p>There&#8217;s a community here which is obviously long-established. Unfortunately it doesn&#8217;t seem to welcome newcomers, which is the reason I gave up posting. I hope it will prove useful to some. You need a thick skin to persevere, though.</p>
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				<title>Nick Carrington replied to the topic New member in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/new-member-2/page/2/#post-112069</link>
				<pubDate>Fri, 17 Jan 2014 17:17:07 +0000</pubDate>

									<content:encoded><![CDATA[<p>Have a great weekend together!</p>
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				<title>Nick Carrington replied to the topic New member in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/new-member-2/page/2/#post-111902</link>
				<pubDate>Sun, 12 Jan 2014 11:58:29 +0000</pubDate>

									<content:encoded><![CDATA[<p>The infosheet is here: <a href="http://www.myeloma.org.uk/information/myeloma-uk-publications-list/living-well-with-myeloma/diet-and-nutrition-infosheet/" rel="nofollow">http://www.myeloma.org.uk/information/myeloma-uk-publications-list/living-well-with-myeloma/diet-and-nutrition-infosheet/</a></p>
<p>Nick</p>
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				<title>Nick Carrington replied to the topic New member in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/new-member-2/page/2/#post-111899</link>
				<pubDate>Sun, 12 Jan 2014 11:31:35 +0000</pubDate>

									<content:encoded><![CDATA[<p>Andy,</p>
<p>I don&#8217;t think I&#8217;m playing Russsian roulette with my health, and I&#8217;m not sure that kind of emotive language is helpful. I don&#8217;t tend to eat much in the way of seafood etc. that carries high risk anyway. I just wanted to put the other side of the coin for Sarah who had been warned about a great long list of foods, and wanted to know if others&hellip;<span class="activity-read-more" id="activity-read-more-560"><a href="http://www.myeloma.org.uk/forums/topic/new-member-2/page/2/#post-111899" rel="nofollow">[Read more]</a></span></p>
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				<title>Nick Carrington replied to the topic New member in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/new-member-2/#post-111892</link>
				<pubDate>Sat, 11 Jan 2014 22:52:01 +0000</pubDate>

									<content:encoded><![CDATA[<p>Sarah,</p>
<p>We got all the scary food advice as well. I&#8217;ve mostly ignored it and carried on eating what I normally eat. I&#8217;ve found my skin is a little bit more sensitive than normal, and my digestion has been put out of whack by the drugs, but I don&#8217;t think I&#8217;ve suffered from eating any particular foods or from any infections acquired during cooking&hellip;<span class="activity-read-more" id="activity-read-more-542"><a href="http://www.myeloma.org.uk/forums/topic/new-member-2/#post-111892" rel="nofollow">[Read more]</a></span></p>
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				<title>Nick Carrington replied to the topic New member in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/new-member-2/#post-111752</link>
				<pubDate>Tue, 07 Jan 2014 14:21:31 +0000</pubDate>

									<content:encoded><![CDATA[<p>From my point of view going through chemo at present I would say psychological support is as important as or more important than physical. Physical help is easily measured &#8211; if he can&#8217;t do something, you may have to help. I personally can do most things albeit a bit more slowly and with attendant fatigue so I try to get on and do so. Encourage M&hellip;<span class="activity-read-more" id="activity-read-more-472"><a href="http://www.myeloma.org.uk/forums/topic/new-member-2/#post-111752" rel="nofollow">[Read more]</a></span></p>
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				<title>Nick Carrington replied to the topic Hi in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hi-3/#post-111495</link>
				<pubDate>Tue, 17 Dec 2013 15:57:54 +0000</pubDate>

									<content:encoded><![CDATA[<p>Ah, thanks Ted. You&#8217;ll notice I didn&#8217;t say I don&#8217;t know what Light Chains are, just that I don&#8217;t know what my figures are &#8211; not quite the same thing. In fact I&#8217;m not sure if they&#8217;re being measured or not (Edit: from reading the leaflet on the test available here, I&#8217;m pretty sure they&#8217;re not, but also that it&#8217;s not so relevant for me anyway with my&hellip;<span class="activity-read-more" id="activity-read-more-283"><a href="http://www.myeloma.org.uk/forums/topic/hi-3/#post-111495" rel="nofollow">[Read more]</a></span></p>
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				<title>Nick Carrington replied to the topic Hi in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hi-3/#post-111419</link>
				<pubDate>Sun, 15 Dec 2013 20:25:51 +0000</pubDate>

									<content:encoded><![CDATA[<p>Good luck to Colin, sounds like he has had a tough time but is in a good place now. Unfortunately I&#8217;m still learning the terminology, no idea what my light chains value is or even what pps is, but hopefully not something I need to worry about or they would have told me? What do I need to ask&#8230;.?</p>
<p>SCT has been presented to me not exactly as a fait&hellip;<span class="activity-read-more" id="activity-read-more-258"><a href="http://www.myeloma.org.uk/forums/topic/hi-3/#post-111419" rel="nofollow">[Read more]</a></span></p>
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				<title>Nick Carrington replied to the topic Hi in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hi-3/#post-111400</link>
				<pubDate>Sat, 14 Dec 2013 22:08:29 +0000</pubDate>

									<content:encoded><![CDATA[<p>I&#8217;m hoping so too, Harmony. Stinks, doesn&#8217;t it! 🙁</p>
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				<title>Nick Carrington replied to the topic Hi in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hi-3/#post-111377</link>
				<pubDate>Thu, 12 Dec 2013 21:13:07 +0000</pubDate>

									<content:encoded><![CDATA[<p>Thanks for the welcome, Mavis. What made you decide against SCT &#8211; was it the high intensity chemo?</p>
<p>I&#8217;m not sure how long I could expect to stay stable after just the CDT &#8211; my paraprotein levels were shooting up before I started on the chemo &#8211; around 3 per month. When it got to 31 the decision was taken out of my hands, more or less.</p>
<p>I was&hellip;<span class="activity-read-more" id="activity-read-more-215"><a href="http://www.myeloma.org.uk/forums/topic/hi-3/#post-111377" rel="nofollow">[Read more]</a></span></p>
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				<title>Nick Carrington replied to the topic A &#039;get rid of these peasents&#039; rant in the forum Off topic</title>
				<link>http://www.myeloma.org.uk/forums/topic/a-get-rid-of-these-peasents-rant/#post-111359</link>
				<pubDate>Thu, 12 Dec 2013 11:39:01 +0000</pubDate>

									<content:encoded><![CDATA[<p>A captcha on the signup form will trap a good proportion of them as they are signed up by bots (automated programs), or by humans from other cultures who don&#8217;t necessarily understand the content of the site they&#8217;re joining up on. So a question like &#8220;What does the first M in MM stand for?&#8221; or something along those lines would probably filter most&hellip;<span class="activity-read-more" id="activity-read-more-199"><a href="http://www.myeloma.org.uk/forums/topic/a-get-rid-of-these-peasents-rant/#post-111359" rel="nofollow">[Read more]</a></span></p>
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				<title>Nick Carrington started the topic Hi in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hi-3/</link>
				<pubDate>Thu, 12 Dec 2013 11:33:28 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi, Nick here.</p>
<p>Diagnosed in June &#8211; initially hoped it would just be MGUS, but that soon escalated &#8211; smouldering between then and October, started CDT on 25th October, so on my 3rd cycle at the moment. Guess I&#8217;ll be in for SCT some time between Feb and April if I respond well (I&#8217;m 56).</p>
<p>Not much else to say really, look forward to reading more of&hellip;<span class="activity-read-more" id="activity-read-more-198"><a href="http://www.myeloma.org.uk/forums/topic/hi-3/" rel="nofollow">[Read more]</a></span></p>
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