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	<title>Myeloma Forum | jollyjosh | Activity</title>
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				<title>jollyjosh replied to the topic Start of treatment  VTD. in the forum Newcomers</title>
				<link>https://www.myeloma.org.uk/forums/topic/start-of-treatment-vtd/page/2/#post-133395</link>
				<pubDate>Mon, 15 May 2017 18:24:52 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello Dawn,</p>
<p>I am replying on my wife behalf. Sue was diagnosed in Sep 2016 with non secretory myeloma. The treatment was 4 cycles of VTD with weekly injections. The visual side effects were minimal with no hair loss, just hunger pains after the injection. Sue was also given Zometa on a monthly basis again no real problems.</p>
<p>Sue returned home a&hellip;<span class="activity-read-more" id="activity-read-more-49678"><a href="https://www.myeloma.org.uk/forums/topic/start-of-treatment-vtd/page/2/#post-133395" rel="nofollow">[Read more]</a></span></p>
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				<title>jollyjosh replied to the topic Just been informed my dad has Myeloma in the forum Newcomers</title>
				<link>https://www.myeloma.org.uk/forums/topic/just-been-informed-my-dad-has-myeloma/#post-132047</link>
				<pubDate>Tue, 28 Feb 2017 15:17:36 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hello, i am writing on behalf of my wife who was diagnosed in sep last year. She had four breaks in her back, pelvis and sternum breaks also.</p>
<p>What i would advise is take the information in slowly or you may feel bombarded, if you are able to attend clinic appointments with your dad then do so. In our experience the whole set up of the medical&hellip;<span class="activity-read-more" id="activity-read-more-48705"><a href="https://www.myeloma.org.uk/forums/topic/just-been-informed-my-dad-has-myeloma/#post-132047" rel="nofollow">[Read more]</a></span></p>
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				<title>jollyjosh became a registered member</title>
				<link>https://forum.myeloma.org.uk/activity/p/48704/</link>
				<pubDate>Tue, 28 Feb 2017 14:31:36 +0000</pubDate>

				
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