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	<title>Myeloma Forum | MicheleWaters | Activity</title>
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				<title>MicheleWaters replied to the topic Newcomer in the forum Carers</title>
				<link>http://www.myeloma.org.uk/forums/topic/newcomer1326746159#post-106244</link>
				<pubDate>Tue, 17 Jan 2012 20:13:27 +0000</pubDate>

									<content:encoded><![CDATA[<p>Thanks, Eve. The differences in each Myeloma patient make decision making and planning very difficult.  My husband has just reached his second bout of remission, the first lasted just over a year. Sadly he was never well enough to go through SCT at the first remission. I don&#039;t think he will choose to go through it this time either. We still have a&hellip;<span class="activity-read-more" id="activity-read-more-21473"><a href="http://www.myeloma.org.uk/forums/topic/newcomer1326746159#post-106244" rel="nofollow">[Read more]</a></span></p>
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				<title>MicheleWaters replied to the topic Newcomer in the forum Carers</title>
				<link>http://www.myeloma.org.uk/forums/topic/newcomer1326746159#post-106242</link>
				<pubDate>Tue, 17 Jan 2012 09:58:42 +0000</pubDate>

									<content:encoded><![CDATA[<p>Thank you so much, Mari, for your reply. We do have a MacMillan nurse assigned to us. My husband is very self-contained, if you know what I mean 🙂 and finds it difficult to express his feelings. But this &quot;thing&quot; is bigger than both of us and I could happily hang onto any comfort! I will certainly make an extra (above the monthly visit)&hellip;<span class="activity-read-more" id="activity-read-more-21471"><a href="http://www.myeloma.org.uk/forums/topic/newcomer1326746159#post-106242" rel="nofollow">[Read more]</a></span></p>
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				<title>MicheleWaters started the topic Newcomer. in the forum Carers</title>
				<link>http://www.myeloma.org.uk/forums/topic/newcomer1326746159</link>
				<pubDate>Mon, 16 Jan 2012 20:35:59 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hello everyone,<br />
I am new to all this and am quite overwhelmed at how courageous knowledgeable and patient every one seems to be. 🙂  I care for my husband who has had a relapse.  After only two months of chemo, he is in remission.  I should be celebrating &#8211; and desperately want to,and know that I should take joy in each day as it comes.  He has&hellip;<span class="activity-read-more" id="activity-read-more-21469"><a href="http://www.myeloma.org.uk/forums/topic/newcomer1326746159" rel="nofollow">[Read more]</a></span></p>
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