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	<title>Myeloma Forum | Myeloma2016 | Activity</title>
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				<title>myeloma2016 posted a new activity comment</title>
				<link>https://forum.myeloma.org.uk/activity/p/138554/#acomment-140134</link>
				<pubDate>Sat, 27 Nov 2021 16:08:41 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Jane,<br />
I really appreciate you for taking time to write me and explain the reason for not having BMB after SCT. I&#8217;m fine and I hope you are also continuing to do well.<br />
I think I told you earlier that I&#8217;m from Iran and I used to compare the general treatment protocol I received here, to the treatment that other myeloma patients from other&hellip;<span class="activity-read-more" id="activity-read-more-140134"><a href="https://forum.myeloma.org.uk/activity/p/138554/#acomment-140134" rel="nofollow">[Read more]</a></span></p>
				<strong>In reply to</strong> -
				<a href="https://forum.myeloma.org.uk/members/myeloma2016/" rel="nofollow">myeloma2016</a> posted an update <a class='bp-suggestions-mention' href='https://forum.myeloma.org.uk/members/mulberry/' rel="nofollow">@mulberry</a> hi Jane. hope you are doing fine. I’m now 9 months post (SCT). I have been on lenalidomide 10 mg. So far everything seems ok except my WBC is slightly bellow 3000.
I was t [&hellip;]			]]></content:encoded>
				
				
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				<title>myeloma2016 posted a new activity comment</title>
				<link>https://forum.myeloma.org.uk/activity/p/138554/#acomment-138564</link>
				<pubDate>Sat, 19 Jun 2021 09:23:20 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thank you Jane,  your response was very helpful and informative as usual. I have another question if you don&#8217;t mind.<br />
Before having first SCT, my plasma cell was 5% due to induction therapy. However, my oncologist didn&#8217;t prescribe bone marrow aspiration 3 months post SCT for me. When I requested separately from two oncologists, they said no need&hellip;<span class="activity-read-more" id="activity-read-more-138564"><a href="https://forum.myeloma.org.uk/activity/p/138554/#acomment-138564" rel="nofollow">[Read more]</a></span></p>
				<strong>In reply to</strong> -
				<a href="https://forum.myeloma.org.uk/members/myeloma2016/" rel="nofollow">myeloma2016</a> posted an update <a class='bp-suggestions-mention' href='https://forum.myeloma.org.uk/members/mulberry/' rel="nofollow">@mulberry</a> hi Jane. hope you are doing fine. I’m now 9 months post (SCT). I have been on lenalidomide 10 mg. So far everything seems ok except my WBC is slightly bellow 3000.
I was t [&hellip;]			]]></content:encoded>
				
				
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				<title>myeloma2016 posted a new activity comment</title>
				<link>https://forum.myeloma.org.uk/activity/p/138553/#acomment-138557</link>
				<pubDate>Sat, 19 Jun 2021 08:45:38 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello Kevin,<br />
Thanks indeed for clarification.<br />
I’m now 9 months post (ASCT). This is my first SCT. I was diagnosed when I was 42 years old, now 46. I have been on lenalidomide 10 mg( maintenance medication). So far everything seems ok except my WBC is slightly bellow 3000 (2600) due to lenalidomide.<br />
I know very well that every myeloma patient is d&hellip;<span class="activity-read-more" id="activity-read-more-138557"><a href="https://forum.myeloma.org.uk/activity/p/138553/#acomment-138557" rel="nofollow">[Read more]</a></span></p>
				<strong>In reply to</strong> -
				<a href="https://forum.myeloma.org.uk/members/myeloma2016/" rel="nofollow">myeloma2016</a> posted an update <a class='bp-suggestions-mention' href='https://forum.myeloma.org.uk/members/kevin/' rel="nofollow">@kevin</a> hi Kevin. hope you are doing great. May I know how may years you are in remission after your 3rd ASCT?  			]]></content:encoded>
				
				
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				<title>myeloma2016 posted an update: @mulberry hi Jane. hope you are doing fine. I’m now 9 m [&#133;]</title>
				<link>https://forum.myeloma.org.uk/activity/p/138554/</link>
				<pubDate>Fri, 18 Jun 2021 15:23:51 +0100</pubDate>

									<content:encoded><![CDATA[<p><a class='bp-suggestions-mention' href='https://forum.myeloma.org.uk/members/mulberry/' rel="nofollow">@mulberry</a> hi Jane. hope you are doing fine. I’m now 9 months post (SCT). I have been on lenalidomide 10 mg. So far everything seems ok except my WBC is slightly bellow 3000.<br />
I was told that ill be on lenalidomide as maintenance therapy for only one year, and second year they will change it to thalidomide. I have not ask further clarification yet a&hellip;<span class="activity-read-more" id="activity-read-more-138554"><a href="https://forum.myeloma.org.uk/activity/p/138554/" rel="nofollow">[Read more]</a></span></p>
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									<slash:comments>4</slash:comments>
				
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				<title>myeloma2016 posted an update: @kevin hi Kevin. hope you are doing great. May I know how [&#133;]</title>
				<link>https://forum.myeloma.org.uk/activity/p/138553/</link>
				<pubDate>Fri, 18 Jun 2021 13:23:22 +0100</pubDate>

									<content:encoded><![CDATA[<p><a class='bp-suggestions-mention' href='https://forum.myeloma.org.uk/members/kevin/' rel="nofollow">@kevin</a> hi Kevin. hope you are doing great. May I know how may years you are in remission after your 3rd ASCT?  </p>
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									<slash:comments>2</slash:comments>
				
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				<title>myeloma2016 and mulberry are now friends</title>
				<link>https://forum.myeloma.org.uk/activity/p/137646/</link>
				<pubDate>Sat, 30 Jan 2021 11:33:24 +0000</pubDate>

				
									<slash:comments>0</slash:comments>
				
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				<title>myeloma2016 posted an update: @mulberry Hi Jane
I have been taking lenalidomide 10 mg [&#133;]</title>
				<link>https://forum.myeloma.org.uk/activity/p/137643/</link>
				<pubDate>Sat, 30 Jan 2021 10:26:04 +0000</pubDate>

									<content:encoded><![CDATA[<p><a class='bp-suggestions-mention' href='https://forum.myeloma.org.uk/members/mulberry/' rel="nofollow">@mulberry</a> Hi Jane<br />
I have been taking lenalidomide 10 mg starting from 11 November 2020 just two months and half after my CST. My WBC are decreasing every two moths I check my blood. Now its 2.6<br />
One of my oncologist advised me to stopped Lenalidomide temporarily for one month. The other one advised me just to continue with the lenalidomide but&hellip;<span class="activity-read-more" id="activity-read-more-137643"><a href="https://forum.myeloma.org.uk/activity/p/137643/" rel="nofollow">[Read more]</a></span></p>
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									<slash:comments>1</slash:comments>
				
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				<title>myeloma2016 posted an update: Diagnosed with carpal tunnel syndrome on both hands 3 months after SCT</title>
				<link>https://forum.myeloma.org.uk/activity/p/137466/</link>
				<pubDate>Fri, 11 Dec 2020 13:53:26 +0000</pubDate>

									<content:encoded><![CDATA[<p>Diagnosed with carpal tunnel syndrome on both hands 3 months after SCT</p>
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									<slash:comments>0</slash:comments>
				
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				<title>myeloma2016 became a registered member</title>
				<link>https://forum.myeloma.org.uk/activity/p/137248/</link>
				<pubDate>Fri, 09 Oct 2020 08:54:45 +0100</pubDate>

				
									<slash:comments>0</slash:comments>
				
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