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	<title>Myeloma Forum | GrahamLane | Activity</title>
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				<title>GrahamLane replied to the topic Revlamid and Neutropenia in the forum Treatment</title>
				<link>https://www.myeloma.org.uk/forums/topic/revlamid-and-neutropenia/#post-129355</link>
				<pubDate>Mon, 05 Sep 2016 17:42:02 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thanks Chris. Sounds familiar. I too was reduced to 5mg after about 3 years or so.</p>
<p>&nbsp;</p>
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				<title>GrahamLane started the topic Revlamid and Neutropenia in the forum Treatment</title>
				<link>https://www.myeloma.org.uk/forums/topic/revlamid-and-neutropenia/</link>
				<pubDate>Mon, 05 Sep 2016 16:41:35 +0100</pubDate>

									<content:encoded><![CDATA[<p>&nbsp;</p>
<p>Is anyone else suffering from neutropenia after long term Revlamid use?</p>
<p>I have been on Revlamid maintenance therapy since my SCT 4 years ago. It&#8217;s been great, no sign of the myeloma returning but it&#8217;s beginning to take its toll. A few weeks ago I had to stop treatment due to a very low neutrophil blood count. And it&#8217;s showing no sign of&hellip;<span class="activity-read-more" id="activity-read-more-46718"><a href="https://www.myeloma.org.uk/forums/topic/revlamid-and-neutropenia/" rel="nofollow">[Read more]</a></span></p>
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				<title>GrahamLane replied to the topic Facebook pages for Support Groups in the forum Miscellaneous</title>
				<link>https://leaders.myeloma.org.uk/forums/topic/facebook-pages-for-support-groups-2/#post-49</link>
				<pubDate>Thu, 01 Sep 2016 09:25:04 +0100</pubDate>

									<content:encoded><![CDATA[<p>No, we don&#8217;t have one for North Yorkshire. I produce a monthly e-newsletter and reminder of up-coming meeting but most of the group don&#8217;t use email let alone Facebook.</p>
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				<title>GrahamLane replied to the topic Remission in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/remission1360843170#post-94381</link>
				<pubDate>Thu, 14 Feb 2013 13:39:29 +0000</pubDate>

									<content:encoded><![CDATA[<p>Tina<br />
Yes I am a fellow MyelomaXI trial it&#039;s now in remission. I was randomised onto a different maintenance treatment to yourself though. As well as 10mg dose of Revlimid I also get vorinostat too. 3 cycles so far and my only side effect is itchy skin but I have had this since the SCT last year so not sure what specifically causes it. The medics&hellip;<span class="activity-read-more" id="activity-read-more-12221"><a href="http://www.myeloma.org.uk/forums/topic/remission1360843170#post-94381" rel="nofollow">[Read more]</a></span></p>
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				<title>GrahamLane replied to the topic About to begin treatment - but which one ? in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/about-to-begin-treatment-but-which-one-/page/2/#post-87156</link>
				<pubDate>Thu, 24 Jan 2013 20:18:56 +0000</pubDate>

									<content:encoded><![CDATA[<p>Lesley,<br />
I can&#039;t speak for everyone but the Myeloma XI trial is certainly working for me. I was diagnosed just over a year ago, had 6 cycles of RCD by which time there was virtually no sign of myeloma any more, had my SCT in July 2012 and am now in complete remission but taking maintenance treatment, again as part of the trial, with the view to&hellip;<span class="activity-read-more" id="activity-read-more-5913"><a href="http://www.myeloma.org.uk/forums/topic/about-to-begin-treatment-but-which-one-/page/2/#post-87156" rel="nofollow">[Read more]</a></span></p>
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				<title>GrahamLane replied to the topic Second anniversary visit to haematology in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/second-anniversary-visit-to-haematology/page/2/#post-94002</link>
				<pubDate>Thu, 20 Dec 2012 07:59:45 +0000</pubDate>

									<content:encoded><![CDATA[<p>Great news Helen, I too had Professor Jackson for my SCT at the Freeman this summer so it looks like he knows what he&#039;s doing!  We&#039;ve got all the family arriving for Christmas tomorrow. Slightly different mood from last year&#039;s gathering. I was diagnosed a few weeks before last Christmas but now I&#039;m in full remission. I&#039;ve even got more hair now&hellip;<span class="activity-read-more" id="activity-read-more-11886"><a href="http://www.myeloma.org.uk/forums/topic/second-anniversary-visit-to-haematology/page/2/#post-94002" rel="nofollow">[Read more]</a></span></p>
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				<title>GrahamLane replied to the topic revlimid and vorinostat in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/revlimid-and-vorinostat#post-104977</link>
				<pubDate>Mon, 17 Dec 2012 19:11:49 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Babs<br />
Day 19 and no adverse side-effects yet. Perhaps you were just unlucky and your next cycle will be better.<br />
Graham</p>
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				<title>GrahamLane replied to the topic Peripheral Neuropathy in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/peripheral-neuropathy1355696409#post-105020</link>
				<pubDate>Mon, 17 Dec 2012 19:03:09 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Christine and Chris<br />
I too suffer from PN at times but not as severe as in your case. Apart from keeping myself hydrated (as if we don&#039;t have to drink enough!) my hospital also offer Complementary Therapeutic Services such as massages and acupuncture into my feet, legs and hands. It works for me!<br />
Graham</p>
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				<title>GrahamLane replied to the topic revlimid and vorinostat in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/revlimid-and-vorinostat#post-104973</link>
				<pubDate>Mon, 03 Dec 2012 21:19:44 +0000</pubDate>

									<content:encoded><![CDATA[<p>Babs<br />
Sorry to hear you are suffering side-effects. I too am on Revlimid and Vorinostat, everything okay at the moment but I am only on day 5 of my maintenance regime so just a couple of weeks behind you.  Handy to know someone on the same treatment plan and at a similar stage though, I&#039;ll let you know if and when owt goes wrong with me.<br />
Graham</p>
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				<title>GrahamLane started the topic Newcomer on trial. in the forum Under 50s</title>
				<link>http://www.myeloma.org.uk/forums/topic/newcomer-on-trial</link>
				<pubDate>Tue, 17 Jan 2012 04:32:00 +0000</pubDate>

									<content:encoded><![CDATA[<p>Now Then everyone,<br />
I&#039;ve been reading this discussion board a while and have learnt some invaluable insights but been too busy to contribute until now. But I am back on the steroids so have all night &#8211; I haven&#039;t been this wide awake at 4am since I was 18!</p>
<p>I am 48 and was diagnosed last December after breaking some ribs moving a garden shed&hellip;<span class="activity-read-more" id="activity-read-more-22068"><a href="http://www.myeloma.org.uk/forums/topic/newcomer-on-trial" rel="nofollow">[Read more]</a></span></p>
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