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	<title>Myeloma Forum | jimbob | Activity</title>
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				<title>JimBob replied to the topic Bone Pain in the forum Related conditions</title>
				<link>http://www.myeloma.org.uk/forums/topic/bone-pain-2/#post-111647</link>
				<pubDate>Sat, 28 Dec 2013 23:01:13 +0000</pubDate>

									<content:encoded><![CDATA[<p>Mandy,</p>
<p>How do I accept you as a friend or invite others to friendship?</p>
<p>Going to drink some seriously expensive Macallan Single malt that my son got me for Christmas and bugger the consequences! No Oxy&#8217;s tonight and maybe, just maybe, I will get at least a quarter of a nights sleep!!! LOL!!</p>
<p>Cheers</p>
<p>Jim (JimBob)</p>
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				<title>JimBob replied to the topic Bone Pain in the forum Related conditions</title>
				<link>http://www.myeloma.org.uk/forums/topic/bone-pain-2/#post-111646</link>
				<pubDate>Sat, 28 Dec 2013 22:44:11 +0000</pubDate>

									<content:encoded><![CDATA[<p>Thanks Mandy!</p>
<p>Got your mail/response. I am new to this forum. Despite spending my working life in acute care / tertiary hospitals, I am struggling. I AM, though, still positive and trust ALL the cancer charities and research units to continue their invaluable and dedicated work to finding cures for ALL cancers, if not for us, but for all who f&hellip;<span class="activity-read-more" id="activity-read-more-358"><a href="http://www.myeloma.org.uk/forums/topic/bone-pain-2/#post-111646" rel="nofollow">[Read more]</a></span></p>
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				<title>JimBob posted a new activity comment</title>
				<link>https://forum.myeloma.org.uk/activity/p/350/#acomment-356</link>
				<pubDate>Sat, 28 Dec 2013 22:23:29 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Carol,<br />
Just GFI&#8230;&#8230;..Go For It&#8230;..All of it!!!!! I have had a very rough time with my MM, but ALL has been worth it! Will I do it again? Sure as hell will, if God spares me. Memories of Pain,puking and sickness all fade when you start feeling a bit better. Most things about MM are negative except US! We think and live positively. Just GO FOR&hellip;<span class="activity-read-more" id="activity-read-more-356"><a href="https://forum.myeloma.org.uk/activity/p/350/#acomment-356" rel="nofollow">[Read more]</a></span></p>
				<strong>In reply to</strong> -
				<a href="http://www.myeloma.org.uk/members/CarolSymons/" rel="nofollow">Carolsymons</a> started the topic <a href="http://www.myeloma.org.uk/forums/topic/hair-loss/" rel="nofollow">Hair loss</a> in the forum <a href="http://www.myeloma.org.uk/forums/forum/sideeffects/" rel="nofollow">Side-effects</a> It is 2 weeks now since I had the high dose chemo etoposide, as preparation for stem cell collection and every day now I have an ever increasing [&hellip;]			]]></content:encoded>
				
				
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				<title>JimBob posted a new activity comment</title>
				<link>https://forum.myeloma.org.uk/activity/p/72/#acomment-355</link>
				<pubDate>Sat, 28 Dec 2013 22:02:23 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Mandy!<br />
Likewise I have a lot of pain post transplant (April 2012) and getting worse. Skull, shoulder, ribs. left hip, both knees and left ankle and foot. Fingers and neuropathy do not help either! However, do not despair, Oxycontin and Oxynorm help with pain management, as does radiotherapy when required. A simple walking stick helps with&hellip;<span class="activity-read-more" id="activity-read-more-355"><a href="https://forum.myeloma.org.uk/activity/p/72/#acomment-355" rel="nofollow">[Read more]</a></span></p>
				<strong>In reply to</strong> -
				<a href="http://www.myeloma.org.uk/members/MANDYPHILLIPS/" rel="nofollow">mandyphillips41</a> started the topic <a href="http://www.myeloma.org.uk/forums/topic/bone-pain-2/" rel="nofollow">Bone Pain</a> in the forum <a href="http://www.myeloma.org.uk/forums/forum/related-conditions/" rel="nofollow">Related conditions</a> Hi

I was diagnosed on 12th October 2012 with Multiple Myeloma and I am now 6 months post stem cell transplant and I am feeling terrible [&hellip;]			]]></content:encoded>
				
				
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				<title>JimBob posted a new activity comment</title>
				<link>https://forum.myeloma.org.uk/activity/p/299/#acomment-354</link>
				<pubDate>Sat, 28 Dec 2013 21:14:44 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Gilaine.<br />
I don&#8217;t have smouldering MM. I have had my first transplant (April 2012) and now have Zometa every 30 days to 6 weeks. I live in Belfast and the Zometa is funded without problem. I worked in Healthcare (Senior Management) all my life (I am now 59) and know the cost of the drugs we need / use. Although Zometa is pricey, it is not&hellip;<span class="activity-read-more" id="activity-read-more-354"><a href="https://forum.myeloma.org.uk/activity/p/299/#acomment-354" rel="nofollow">[Read more]</a></span></p>
				<strong>In reply to</strong> -
				<a href="https://forum.myeloma.org.uk/members/Gilaine/" rel="nofollow">Gilaine</a> posted an update Hi still lookijng for anyone else with smoldering Myeloma who is being treated with Zometa ?I can&#8217;t be the only one ?			]]></content:encoded>
				
				
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