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	<title>Myeloma Forum | cartdaw | Activity</title>
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				<title>cartdaw replied to the topic I&#039;m still here! in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/im-still-here/#post-131967</link>
				<pubDate>Tue, 21 Feb 2017 00:21:04 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hy all it&#8217;s good to see familiar names I have not posted either for a while. Had a stem cell in sept 2015  and still in remission all bloods are normal. Occasional chest infections but nothing major touchwood. I am on revlimid 5mg have got occasional neuropathy in my feet and dry skin . As Andy says every day is a gift and I am very grateful. Xxx Dawn</p>
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				<title>cartdaw posted an update: Hi Andrea ,Peter, Andy , Mike and all have not been on here [&#133;]</title>
				<link>https://forum.myeloma.org.uk/activity/p/47824/</link>
				<pubDate>Thu, 08 Dec 2016 22:18:22 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Andrea ,Peter, Andy , Mike and all have not been on here for a while so not sure where everyone is at. Andy g have just read your post glad you are ok . You are an inspiration. I am doing well so far bloods still normal after 15 moths after SCT.,taking lenolidomide 5mg on the myeloma trial. Get aching joints and legs but cope ok with that. Xxx</p>
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				<title>cartdaw replied to the topic Maintenance after SCT in the forum Treatment</title>
				<link>https://www.myeloma.org.uk/forums/topic/maintenance-after-sct/#post-127966</link>
				<pubDate>Mon, 16 May 2016 19:54:41 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi I commenced maintenance treatment around March time after my SCT.  I am on the myeloma IV trial and was randomised to Revlimid.  I started on 10mg but had mild neuropathy in my feet and fingers going numb so it was dropped down to 5mg and seem ok on this.  I&#8217;m giving it a go and my pps are stable at 2 at the moment.  I am back at work now alt&hellip;<span class="activity-read-more" id="activity-read-more-45439"><a href="https://www.myeloma.org.uk/forums/topic/maintenance-after-sct/#post-127966" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic A short post. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/a-short-post/page/3/#post-127087</link>
				<pubDate>Thu, 03 Mar 2016 16:45:35 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi buzz i too was diagnosed in june 2014 .no treatment for the first year as asymptomatic .In may 2015 started cdt and my pp had jumped to 29. And my light chains 7000.  Had melphalen and sct in sept 2015. My pp now 2 and light chains 12 so very happy at the moment. I too have been randomised to revlimid 4 weeks ago so i am also waiting with&hellip;<span class="activity-read-more" id="activity-read-more-43791"><a href="http://www.myeloma.org.uk/forums/topic/a-short-post/page/3/#post-127087" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic A short post. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/a-short-post/page/2/#post-125595</link>
				<pubDate>Fri, 08 Jan 2016 00:32:49 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hy jan my name is dawn x</p>
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				<title>cartdaw replied to the topic A short post. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/a-short-post/page/2/#post-125594</link>
				<pubDate>Fri, 08 Jan 2016 00:31:45 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi jan Iv just had excellent results 3mths post SCT. Pp 2 and normal bone marrow result.  I will be monitored every 8/12 weeks or so. My light chains have always been on the high side 700 prior to SCT and 2400 prior CDT in March so much lower.  Did you have any treatment when they rose or is it a watch and wait. My cons not concerned about light c&hellip;<span class="activity-read-more" id="activity-read-more-42490"><a href="http://www.myeloma.org.uk/forums/topic/a-short-post/page/2/#post-125594" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic No remission! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/no-remission/page/4/#post-125593</link>
				<pubDate>Fri, 08 Jan 2016 00:17:06 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hya Andrea, Ian, Peter and all   Just an update I have had my results 3 months after SCT and feeling very happy, pp 2 and bone marrow normal,  hope it lasts, feeling well now probably able to return to work albeit reluctantly, thinking of retiring,  I know nothing is guaranteed with mm but for now I&#8217;m happy,.  Hope you are all well and happy new year xx</p>
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				<title>cartdaw replied to the topic A short post. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/a-short-post/#post-125364</link>
				<pubDate>Fri, 11 Dec 2015 23:08:36 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hya andy glad you seem to be doing ok. I&#8217;m 3 months after SCT my bloods due after Xmas so fingers x. Feel well though I must say. X.  Dawn</p>
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				<title>cartdaw posted an update: @AndyG   Hi andy have just read your recent post hope you [&#133;]</title>
				<link>https://forum.myeloma.org.uk/activity/p/41543/</link>
				<pubDate>Mon, 26 Oct 2015 11:30:29 +0000</pubDate>

									<content:encoded><![CDATA[<p><a href='http://www.myeloma.org.uk/members/AndyG/' rel="nofollow">@AndyG</a>   Hi andy have just read your recent post hope you are doing ok.    I had pneumonia and sepsis 3 yrs ago was in hospital a month not ITU tho so not as ill as you were but I do feel for you it&#8217;s horrible.  Looking back I think that&#8217;s when my myloma started.   Have just had my SCT and doing ok.  Hope you continue to do well fingers x for you.&hellip;<span class="activity-read-more" id="activity-read-more-41543"><a href="https://forum.myeloma.org.uk/activity/p/41543/" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic No remission! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/no-remission/page/4/#post-124726</link>
				<pubDate>Mon, 26 Oct 2015 11:22:28 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Ian, Peter and Andrea   Hope you are all doing ok.  I have been home now for nearly 4 weeks after my SCT at the HAllamshire Hospital in Sheffield.   I am doing OK now and starting to feel more human.  I had a problem with sickness all the way through it really and mucositis mainly in my throat and Gastro. Intestinal tract.  Very painful.  The&hellip;<span class="activity-read-more" id="activity-read-more-41542"><a href="http://www.myeloma.org.uk/forums/topic/no-remission/page/4/#post-124726" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic Heading for treatment  in the forum Smouldering myeloma / MGUS</title>
				<link>http://www.myeloma.org.uk/forums/topic/heading-for-treatment/page/4/#post-124725</link>
				<pubDate>Mon, 26 Oct 2015 11:10:22 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi mike I have been at home now for 3 weeks after my SCT.  Feeling quite well now only occasional nausea . The energy levels are still low but improving.  On the whole the downside for me was the sickness and the mucositis which not everyone has but it doesn&#8217;t last . The staff at the HAllamshire were amazing.  Hope you are doing ok.  Good luck wit&hellip;<span class="activity-read-more" id="activity-read-more-41541"><a href="http://www.myeloma.org.uk/forums/topic/heading-for-treatment/page/4/#post-124725" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic No remission! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/no-remission/page/3/#post-123994</link>
				<pubDate>Tue, 08 Sep 2015 08:48:14 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Ian , Peter and Andrea   I am going into Sheffield Hallamshire tomorrow for my stem cell transplant.  I am a little anxious now but I am sure I will cope.  Everybody has a different story to tell but everyone says it is doable.    Fingers x I will cope with all the side effects.   Dawn  x</p>
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				<title>cartdaw replied to the topic Starting Stem Cell Therapy in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/starting-stem-cell-therapy/#post-123992</link>
				<pubDate>Tue, 08 Sep 2015 08:44:17 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi dino I am going into hospital for my stem cell transplant tomorrow.  not looking forward to it as there are many different reviews on it and everyone has a different story to tell but it is part of the recommended treatment and I feel I have to see it through.  I was diagnosed with myeloma last year and commenced 6 cycles of CDT in March this y&hellip;<span class="activity-read-more" id="activity-read-more-40803"><a href="http://www.myeloma.org.uk/forums/topic/starting-stem-cell-therapy/#post-123992" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic No remission! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/no-remission/page/3/#post-123528</link>
				<pubDate>Mon, 10 Aug 2015 18:09:55 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi dave sounds like you have had an excellent response. I finished my 6th cycle last week and have a stem cell harvest bookd for 24th aug the stem cell transplnt might be 3 or 4 weeks after that.  We wanted a holiday and they said said they could work around us. Is there a possibility they could  wait to do the actual transplant after your sons w&hellip;<span class="activity-read-more" id="activity-read-more-40284"><a href="http://www.myeloma.org.uk/forums/topic/no-remission/page/3/#post-123528" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic My latest Consult in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-latest-consult/#post-123519</link>
				<pubDate>Sat, 08 Aug 2015 10:07:28 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Andy glad you are doing well.  I have just completed my 6th cycle of CDT have to say tho the last cycle was rough.   and my stemcell harvest is booked for 24th August so finger x.  My proteins are now 2 and im hoping they stay there and not creep up. xx</p>
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				<title>cartdaw replied to the topic Heading for treatment  in the forum Smouldering myeloma / MGUS</title>
				<link>http://www.myeloma.org.uk/forums/topic/heading-for-treatment/page/4/#post-123518</link>
				<pubDate>Sat, 08 Aug 2015 10:00:25 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Mike hope you are well.  I have just completed my 6th cycle of CDT that last cycle was rough and struggling with muscle cramps in my legs presumable from the Thalidomide.  No meds at the moment and I feel relatively normal but still have muscle cramps in my legs. My paraproteins are now 2 , light chains 900 but were 7000.  I think they wou&hellip;<span class="activity-read-more" id="activity-read-more-40264"><a href="http://www.myeloma.org.uk/forums/topic/heading-for-treatment/page/4/#post-123518" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic No remission! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/no-remission/page/3/#post-123517</link>
				<pubDate>Sat, 08 Aug 2015 09:46:00 +0100</pubDate>

									<content:encoded><![CDATA[<p>hi Andrea, Ian and Peter</p>
<p>Sorry you havn&#8217;t been so well Andrea , Ian and Peter you both seem to be doing well apart from the odd side effects.  I have just completed 6 cycles of CDT , the last last cycle was rough with constant diorrhea and muscle cramps in my legs from the Thalidomide I presume.  I feel relatively normal at the moment with no m&hellip;<span class="activity-read-more" id="activity-read-more-40263"><a href="http://www.myeloma.org.uk/forums/topic/no-remission/page/3/#post-123517" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic Heading for treatment  in the forum Smouldering myeloma / MGUS</title>
				<link>http://www.myeloma.org.uk/forums/topic/heading-for-treatment/page/3/#post-122594</link>
				<pubDate>Sat, 13 Jun 2015 22:20:19 +0100</pubDate>

									<content:encoded><![CDATA[<p>That&#8217;s good news mike. I&#8217;m hopefully going to have the SCT early sept at sheffield if all goes to plan. Para proteins now 4 after 4 cycles but not taking anything for granted hope they stay down. Hating the days when I&#8217;m on the dex. But otherwise coping reasonably ok.  Have already been in hospital with a chest infection.  Good luck with your j&hellip;<span class="activity-read-more" id="activity-read-more-39399"><a href="http://www.myeloma.org.uk/forums/topic/heading-for-treatment/page/3/#post-122594" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic Ian home after SCT in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/ian-home-after-sct/page/2/#post-122593</link>
				<pubDate>Sat, 13 Jun 2015 22:06:18 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hope you soon on the mend Ian . My SCT  pencilled in for early sept all being well. Not looking forward to it. Two more cycles of CDT making it 6 then harvest early August.</p>
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				<title>cartdaw replied to the topic No remission! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/no-remission/page/2/#post-122590</link>
				<pubDate>Sat, 13 Jun 2015 18:14:31 +0100</pubDate>

									<content:encoded><![CDATA[<p>The info days sound informative peter I really must get myself booked onto one of these.  Dawn</p>
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				<title>cartdaw replied to the topic No remission! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/no-remission/page/2/#post-122589</link>
				<pubDate>Sat, 13 Jun 2015 18:12:12 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hya Andrea Ian and Peter  Iv just completed my 4th cycle of the CDT . My para proteins are down to 4 . Have had an appt at sheffield hallamhire to discuss stem cell transplant. The harvest is pencilled in for around early August and the transplant around early sept. All being well. Not looking forward to it as you can imagine but now on this&hellip;<span class="activity-read-more" id="activity-read-more-39392"><a href="http://www.myeloma.org.uk/forums/topic/no-remission/page/2/#post-122589" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic 4th Anniversary - where to next? in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/4th-anniversary-where-to-next/page/2/#post-122064</link>
				<pubDate>Tue, 05 May 2015 15:47:30 +0100</pubDate>

									<content:encoded><![CDATA[<p>hi Helen, jan and andy have been reading your posts it all sounds very daunting. I have just started cdt treatment into my second cycle. my paraproteins have gone down to 8 from 29 already but I am not taking anything for granted as they will probably go up and down over the next few months.  I have been diagnosed for a year now.  first s&hellip;<span class="activity-read-more" id="activity-read-more-38883"><a href="http://www.myeloma.org.uk/forums/topic/4th-anniversary-where-to-next/page/2/#post-122064" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic No remission! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/no-remission/page/2/#post-122063</link>
				<pubDate>Tue, 05 May 2015 15:26:17 +0100</pubDate>

									<content:encoded><![CDATA[<p>hi andrea,  ian and peter.  hope you are all well and coping I have just completed my 2nd cycle of cdt and my paraproteins have gone down from 29 to 8 already.  hope they stay down fingers x.  but im not taking anything for granted.  havnt got the light chain results back yet so im hoping they have gone down as well.  I can cope with the thali&hellip;<span class="activity-read-more" id="activity-read-more-38882"><a href="http://www.myeloma.org.uk/forums/topic/no-remission/page/2/#post-122063" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic Heading for treatment  in the forum Smouldering myeloma / MGUS</title>
				<link>http://www.myeloma.org.uk/forums/topic/heading-for-treatment/page/2/#post-122062</link>
				<pubDate>Tue, 05 May 2015 15:16:26 +0100</pubDate>

									<content:encoded><![CDATA[<p>hi mike how are you doing have you started your treatment yet.  I am just completing my second cycle and my paraproteins have gone down from 29 to 8 already.  fingers x they stay down . havnt got the latest light chain results but they had fallen before I started treatment from 7000 to 5000.  good luck.</p>
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				<title>cartdaw replied to the topic No remission! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/no-remission/page/2/#post-121508</link>
				<pubDate>Tue, 31 Mar 2015 18:41:03 +0100</pubDate>

									<content:encoded><![CDATA[<p>hi peter glad things are improving for you, feeling fine except I feel really shaky and dizzy mainly until lunchtime not sure if its the thalidomide which I take at night or the days off when I don&#8217;t have the dex.  Its just my first week so im not sure what to expect.</p>
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				<title>cartdaw replied to the topic No remission! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/no-remission/#post-121470</link>
				<pubDate>Sat, 28 Mar 2015 10:45:46 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Ian and Andrea hope you are both doing ok have been watching your posts as I have just started treatment as have gone from asymptomatic myeloma to active myloma my paraprotein in 26 and my free light chains have jumped to 7,000 which is high risk for kidney damage.  everything else is stable.  I have just gone into the myeloma x1 trial and r&hellip;<span class="activity-read-more" id="activity-read-more-38334"><a href="http://www.myeloma.org.uk/forums/topic/no-remission/#post-121470" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic Day 5 of treatment chemo and stem cell replacement done  in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/day-5-of-treatment-chemo-and-stem-cell-replacement-done/#post-121326</link>
				<pubDate>Wed, 18 Mar 2015 23:19:15 +0000</pubDate>

									<content:encoded><![CDATA[<p>It&#8217;s good to hear positive comments . I&#8217;m just about to embark on my first treatment after being. Asymptomatic for a year. Stem cell transplant in about 6 mths if all goes well with the initial treatment. Good luck guys  dawn x</p>
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				<title>cartdaw posted an update: @docmike    Hi mike heading for treatment next week. Got the [&#133;]</title>
				<link>https://forum.myeloma.org.uk/activity/p/38203/</link>
				<pubDate>Wed, 18 Mar 2015 23:11:14 +0000</pubDate>

									<content:encoded><![CDATA[<p><a href='http://www.myeloma.org.uk/members/docmike/' rel="nofollow">@docmike</a>    Hi mike heading for treatment next week. Got the info for the myeloma x1 trial. Light chains have jumped to 7,000. From October when they were 2,000. Everything else stable. Para proteins at 26.  Good news for you tho . </p>
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				<title>cartdaw started the topic Progression to myeloma in the forum Smouldering myeloma / MGUS</title>
				<link>http://www.myeloma.org.uk/forums/topic/progression-to-myeloma/</link>
				<pubDate>Sat, 14 Mar 2015 22:29:34 +0000</pubDate>

									<content:encoded><![CDATA[<p>I have been smouldering for a year now but looks looks like I&#8217;m heading for treatment . Para proteins have jumped from 21 to 26 since dec.  my creatinine has increased slowly although have had a uti recently. Just waiting for my light chains to come back if these have increased  &#8211; well not looking too good. Quite anxious but positive. They t&hellip;<span class="activity-read-more" id="activity-read-more-38142"><a href="http://www.myeloma.org.uk/forums/topic/progression-to-myeloma/" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic Heading for treatment  in the forum Smouldering myeloma / MGUS</title>
				<link>http://www.myeloma.org.uk/forums/topic/heading-for-treatment/#post-121278</link>
				<pubDate>Sat, 14 Mar 2015 22:15:15 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi mike good luck I don&#8217;t think il be far behind u x</p>
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				<title>cartdaw replied to the topic Stem cell transplant booked for Sunday 15 February 2015 in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/stem-cell-transplant-booked-for-sunday-15-february-2015/#post-120773</link>
				<pubDate>Wed, 11 Feb 2015 15:34:36 +0000</pubDate>

									<content:encoded><![CDATA[<p>My name is dawn Cartlidge  god knows y I put my username as cart daw lol</p>
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				<title>cartdaw replied to the topic Stem cell transplant booked for Sunday 15 February 2015 in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/stem-cell-transplant-booked-for-sunday-15-february-2015/#post-120771</link>
				<pubDate>Wed, 11 Feb 2015 15:32:19 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Andrea hope all goes well for u. I may be going down the same route so please let me know how u get on. My para proteins are up to 24 so bloods to be rptd in 1 month.  If light chains r high May start treatment due to new guidelines although I&#8217;m well with no bone damage</p>
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				<title>cartdaw replied to the topic Heading for treatment  in the forum Smouldering myeloma / MGUS</title>
				<link>http://www.myeloma.org.uk/forums/topic/heading-for-treatment/#post-120770</link>
				<pubDate>Wed, 11 Feb 2015 15:16:12 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Michael I wish u well. Iv been to see cons today and para proteins have gone up to 24 . So all bloods have to be rptd in 3 weeks. If anything else raised then ie light chains may have to start treatment also   due to new guidelines. Otherwise I&#8217;m well . MRI ok</p>
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				<title>cartdaw posted an update: Hi all have been diagnosed with smouldering myloma in June [&#133;]</title>
				<link>https://forum.myeloma.org.uk/activity/p/37542/</link>
				<pubDate>Wed, 11 Feb 2015 15:03:10 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi all have been diagnosed with smouldering myloma in June 14 with para proteins of 21 and abnormal bone marrow cells of 70%. I feel weel no bone damage all bloods normal. But today my paraprotein is 24. So if my light chains are high in 1 month and para proteins still raised I may have to start treatment due to a change in guidelines . So feel&hellip;<span class="activity-read-more" id="activity-read-more-37542"><a href="https://forum.myeloma.org.uk/activity/p/37542/" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic Smouldering myeloma in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/smouldering-myeloma-2/page/3/#post-119512</link>
				<pubDate>Mon, 17 Nov 2014 09:19:01 +0000</pubDate>

									<content:encoded><![CDATA[<p>hi all my friend has a friend who has had myloma for 20 yrs and is now in her 70s.  started with smouldering myloma but now myloma.  She apparently hasn&#8217;t always been well but has treatments and remission etc. and is still here. so I try to keep as positive as possible.  Most of the time myloma is at the back of my mind ( I was diagnosed as a sm&hellip;<span class="activity-read-more" id="activity-read-more-36465"><a href="http://www.myeloma.org.uk/forums/topic/smouldering-myeloma-2/page/3/#post-119512" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic smouldering myeloma;IMWG update criteria to predict CRAB  features . in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/smouldering-myelomaimwg-update-criteria-to-predict-crab-features/#post-119140</link>
				<pubDate>Tue, 28 Oct 2014 20:24:07 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Michael it&#8217;s dawn I received ur message thank u .   Ur  post is interesting my plasma cells from the biopsy were 70% so  does this mean I may be offered treatment in light of this  new criteria .</p>
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				<title>cartdaw replied to the topic Smouldering myeloma in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/smouldering-myeloma-2/page/2/#post-118998</link>
				<pubDate>Wed, 22 Oct 2014 08:32:40 +0100</pubDate>

									<content:encoded><![CDATA[<p>hi its dawn. does anyone else feel tired with smouldering myloma although my iron  blood count is normal i feel extremely tired.  I work two twelve hour shifts per week as a midwife so busy but more tired than usual.</p>
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				<title>cartdaw replied to the topic Smouldering myeloma in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/smouldering-myeloma-2/page/2/#post-118997</link>
				<pubDate>Wed, 22 Oct 2014 08:19:34 +0100</pubDate>

									<content:encoded><![CDATA[<p>hi chrissie, im dawn. I too become anxious around hospital visits and I have to be seen every 8 weeks as although im smouldering my abnormal cell count from my bone biopsy was high. 70%.  although im well with no effects so far.  I would be interested how you get on with the aloe vera etc.  will try anything.  i feel im living my life in 8 wee&hellip;<span class="activity-read-more" id="activity-read-more-29956"><a href="http://www.myeloma.org.uk/forums/topic/smouldering-myeloma-2/page/2/#post-118997" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic Smouldering myeloma in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/smouldering-myeloma-2/page/2/#post-118996</link>
				<pubDate>Wed, 22 Oct 2014 08:15:28 +0100</pubDate>

									<content:encoded><![CDATA[<p>hi brian  my name is dawn I think iv mentioned earlier that I was diagnosed with smouldering myloma in april im 57. I am with what appears to be a very good team of haematologists at chesterfield royal. and appear to be quite knowledgeable re myloma.   I asked multi-vits and they said it wouldn&#8217;t hurt re iron count and well=being etc. but water is&hellip;<span class="activity-read-more" id="activity-read-more-29951"><a href="http://www.myeloma.org.uk/forums/topic/smouldering-myeloma-2/page/2/#post-118996" rel="nofollow">[Read more]</a></span></p>
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				<title>cartdaw replied to the topic Smouldering myeloma in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/smouldering-myeloma-2/#post-118866</link>
				<pubDate>Fri, 17 Oct 2014 11:00:56 +0100</pubDate>

									<content:encoded><![CDATA[<p>hi brian  I have also been diagnosed with smouldering myloma i am 57 yrs and feel healthy at the moment.  I have blood tests every 8 weeks and so far all still stable.  my paraproteins are 21,   Iv had the bone marrow biopsy which was quite high apparantley but the skeletal survey was normal thank goodness.   I hope to have a few years yet just smouldering</p>
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				<title>cartdaw replied to the topic smouldering myloma in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/smouldering-myloma/#post-116458</link>
				<pubDate>Mon, 07 Jul 2014 20:09:33 +0100</pubDate>

									<content:encoded><![CDATA[<p>thank you for your messages of support all of you , I am just getting my head around it.  Im 57yrs old and work part-time as a midwife so Im happy to smoulder  for a few years yet but hopefully will be better prepared if I have to have treatment.  I have to have my bloods taken every 2 &#8211; 3 months at the moment.</p>
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				<title>cartdaw started the topic smouldering myloma in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/smouldering-myloma/</link>
				<pubDate>Thu, 03 Jul 2014 12:34:03 +0100</pubDate>

									<content:encoded><![CDATA[<p>hi my name is Dawn and after having been through hell for the past 3 weeks have been diagnosed with smouldering myloma.  Its is a very scary time and although no treatment at the moment , I am assurred it will turn into myloma at some time.  My family have been very supportive but its difficult to talk to them sometimes as I feel as if i am w&hellip;<span class="activity-read-more" id="activity-read-more-25792"><a href="http://www.myeloma.org.uk/forums/topic/smouldering-myloma/" rel="nofollow">[Read more]</a></span></p>
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