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	<title>Myeloma Forum | Chris Taylor | Activity</title>
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				<title>Chris Taylor replied to the topic Zometa in the forum Treatment</title>
				<link>https://www.myeloma.org.uk/forums/topic/zometa-2/page/2/#post-131839</link>
				<pubDate>Thu, 09 Feb 2017 21:20:25 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Ian, Thank you for your post, and the kind thoughtful ways of trying to make our minds up on which path to take. I really understand where your coming from, it&#8217;s like when I go to day care at my local hospice I find solace with another chap who is in the same situation and we both enjoy each other&#8217;s company. He understands what I am going&hellip;<span class="activity-read-more" id="activity-read-more-48499"><a href="https://www.myeloma.org.uk/forums/topic/zometa-2/page/2/#post-131839" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Zometa in the forum Treatment</title>
				<link>https://www.myeloma.org.uk/forums/topic/zometa-2/page/2/#post-131769</link>
				<pubDate>Fri, 03 Feb 2017 22:04:35 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Jan, Thank you for your post, and especially the point about continuing the Zometa at a time when further bone damage has been shown by the latest scans. I will mention it to the Consultant in April so that I can get the best outcome when considering all the factors.  The second SCT option I just cannot see the overall benefit of going through&hellip;<span class="activity-read-more" id="activity-read-more-48431"><a href="https://www.myeloma.org.uk/forums/topic/zometa-2/page/2/#post-131769" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Zometa in the forum Treatment</title>
				<link>https://www.myeloma.org.uk/forums/topic/zometa-2/page/2/#post-131761</link>
				<pubDate>Fri, 03 Feb 2017 00:28:35 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hello Sand, I found your post so interesting and positive about your SCT, yes like you my first dozen or or so Zometa infusions gave me plenty of bone pain but I had really bad bone damage to start with. And after my SCT in March 2015 I was in partial remission until January this year, although the MM was rising all the time and by December last&hellip;<span class="activity-read-more" id="activity-read-more-48421"><a href="https://www.myeloma.org.uk/forums/topic/zometa-2/page/2/#post-131761" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor 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-131750</link>
				<pubDate>Thu, 02 Feb 2017 00:34:04 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hello, I didn&#8217;t reply at first because being a little under the weather due to Chemo, but I would just like to say a little late, yes it must very daunting when someone you love is given this type of news so I do really feel for you and your family. Just a little about me first, I was diagnosed with MM in 2014 having severe bone damage, so much so&hellip;<span class="activity-read-more" id="activity-read-more-48405"><a href="https://www.myeloma.org.uk/forums/topic/just-been-informed-my-dad-has-myeloma/#post-131750" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Velcade and what to expect. in the forum Side-effects</title>
				<link>https://www.myeloma.org.uk/forums/topic/velcade-and-what-to-expect/#post-131385</link>
				<pubDate>Fri, 23 Dec 2016 23:43:57 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi all, thank you so much for all the replies in regards to the Velcade, I think now I ve read the Velcade info guide I will see if my Consultant is to recommend VCD , if not I will ask. Seems the better combination .</p>
<p>At the moment I feel I need to get onto some sort of treatment straight away because my bone pain has taken off, both my shoulders&hellip;<span class="activity-read-more" id="activity-read-more-47960"><a href="https://www.myeloma.org.uk/forums/topic/velcade-and-what-to-expect/#post-131385" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Velcade and what to expect. in the forum Side-effects</title>
				<link>https://www.myeloma.org.uk/forums/topic/velcade-and-what-to-expect/#post-131339</link>
				<pubDate>Sun, 18 Dec 2016 23:29:29 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi David, thank you for the quick reply and info, I will certainly check it out. All the very best. CT.</p>
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				<title>Chris Taylor started the topic Velcade and what to expect. in the forum Side-effects</title>
				<link>https://www.myeloma.org.uk/forums/topic/velcade-and-what-to-expect/</link>
				<pubDate>Sun, 18 Dec 2016 00:08:17 +0000</pubDate>

									<content:encoded><![CDATA[<p>Dear all, having been in remission for the last 18 months following a SCT my blood test results show a marked rise in my light chains. Therefore my Consultant has sent me for a Pet scan, MRI scan and a BMB. If these tests conclude that the MM is coming he told me I will be going onto Velcade for my treatment, even without the test result I think&hellip;<span class="activity-read-more" id="activity-read-more-47903"><a href="https://www.myeloma.org.uk/forums/topic/velcade-and-what-to-expect/" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Verterbroplasty in the forum Treatment</title>
				<link>https://www.myeloma.org.uk/forums/topic/verterbroplasty/#post-131112</link>
				<pubDate>Tue, 29 Nov 2016 22:17:47 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Molly, I hope your Mum operation really goes well and is fully successful, I had 3 fractured vertibaes repaired and another damaged 1 repaired last October. It was carried out in Medway hospital, they called it Kyphoplasty so a little bit unsure if it&#8217;s the same thing, it basically was key hole surgery and the Surgeon filled the fractured&hellip;<span class="activity-read-more" id="activity-read-more-47714"><a href="https://www.myeloma.org.uk/forums/topic/verterbroplasty/#post-131112" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Myeloma bone lesions in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/myeloma-bone-lesions/page/2/#post-129345</link>
				<pubDate>Thu, 01 Sep 2016 21:16:22 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello Cheryl,  seems like you were diagnosed the same year as me and went the CDT which again is the same. I was offered to do trials but back then in my shocked confused mind I decided just to take the standard treatment, however it worked in that it managed to knock it back in order to have a SCT.</p>
<p>Your right in thinking about further scans to&hellip;<span class="activity-read-more" id="activity-read-more-46696"><a href="https://www.myeloma.org.uk/forums/topic/myeloma-bone-lesions/page/2/#post-129345" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Myeloma bone lesions in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/myeloma-bone-lesions/#post-129177</link>
				<pubDate>Sun, 14 Aug 2016 23:02:13 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Peter, sorry for not replying to you for the message you have written before now, but I have been in hospital with a severe upper respiratory infection. I felt so ill and I suppose I was lucky in that I had an appointment with my Consultant and my wife and I only sat down, and when I said I felt so unwell they examined me and said I was going&hellip;<span class="activity-read-more" id="activity-read-more-46544"><a href="https://www.myeloma.org.uk/forums/topic/myeloma-bone-lesions/#post-129177" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Myeloma bone lesions in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/myeloma-bone-lesions/#post-129099</link>
				<pubDate>Fri, 05 Aug 2016 11:47:13 +0100</pubDate>

									<content:encoded><![CDATA[<p>Peter, thanks for letting us share your funny situation in the MRI scanner I can imagine the state you must have been in. It would have been an awful type of torture when all you want is to get it all over and done with. It reminded me of a incident of mine in the MRI scanner, I too was waiting to go into the tunnel and the technician asked if I&hellip;<span class="activity-read-more" id="activity-read-more-46491"><a href="https://www.myeloma.org.uk/forums/topic/myeloma-bone-lesions/#post-129099" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Myeloma bone lesions in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/myeloma-bone-lesions/#post-129070</link>
				<pubDate>Thu, 04 Aug 2016 09:49:37 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Peter, yes sorry I cannot help with how they anylis the various types of MM but also would be interested to know. All I know was what was written up on my hospital discharge letter, having spent 3 weeks with so many test every day they would say still looking. I had so so many bloods, Bence jones urine, MRI, CT scans, bone marrow and even bone&hellip;<span class="activity-read-more" id="activity-read-more-46474"><a href="https://www.myeloma.org.uk/forums/topic/myeloma-bone-lesions/#post-129070" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Dad just diagnosed with MM in the forum Newcomers</title>
				<link>https://www.myeloma.org.uk/forums/topic/dad-just-diagnosed-with-mm-2/#post-129059</link>
				<pubDate>Wed, 03 Aug 2016 21:05:54 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Karen, good to hear some of the issues your Dad was having have improved a little, the fatigue is a big issue with me even now after being drug free for some time. It&#8217;s the drugs the pain relief and MM itself, the other thing you may want to tell your Dad is that when taking Thelidomide it can give you tingling dumbness in the toes and fingers&hellip;<span class="activity-read-more" id="activity-read-more-46471"><a href="https://www.myeloma.org.uk/forums/topic/dad-just-diagnosed-with-mm-2/#post-129059" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Myeloma bone lesions in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/myeloma-bone-lesions/#post-129053</link>
				<pubDate>Wed, 03 Aug 2016 08:13:38 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Tom, firstly thanks for the very quick reply I thought that maybe you were off line at the present so was happily surprised.</p>
<p>Again that&#8217;s really interesting about the scans because the only MRI , CT scans I have had was during the 3 weeks I was in hospital getting the MM diagnosed back in 2014 . So I have really no idea the latest situation&hellip;<span class="activity-read-more" id="activity-read-more-46464"><a href="https://www.myeloma.org.uk/forums/topic/myeloma-bone-lesions/#post-129053" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Myeloma bone lesions in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/myeloma-bone-lesions/#post-129051</link>
				<pubDate>Tue, 02 Aug 2016 22:54:21 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Tom, I know it&#8217;s been a number of months since you posted your situation, I haven&#8217;t been on the web site for a while so been playing catch up. But if you read this I would be very much interested how you progressed . I also have non secretary MM with no PP indications which meant not getting diagnosed through the normal blood test, until I had&hellip;<span class="activity-read-more" id="activity-read-more-46460"><a href="https://www.myeloma.org.uk/forums/topic/myeloma-bone-lesions/#post-129051" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic SCT question in the forum Treatment</title>
				<link>https://www.myeloma.org.uk/forums/topic/sct-question-2/#post-129034</link>
				<pubDate>Sun, 31 Jul 2016 21:10:33 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Emsie, Firstly sorry to hear about your husband and I can truly understand the anxiety your feeling, the replies that have been posted are so positive and that is what you need for both you and your husband along side the treatment. I was diagnosed with MM but mine is the kappa light chain one but still amounts to the same treatment. I had my&hellip;<span class="activity-read-more" id="activity-read-more-46439"><a href="https://www.myeloma.org.uk/forums/topic/sct-question-2/#post-129034" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Dad just diagnosed with MM in the forum Newcomers</title>
				<link>https://www.myeloma.org.uk/forums/topic/dad-just-diagnosed-with-mm-2/#post-129033</link>
				<pubDate>Sun, 31 Jul 2016 20:33:33 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Karen, I am Chris and was diagnosed in June 2014 at the age of 61, I can understand that you are worried about your Dad and hope that messages like these will help to reassure you.</p>
<p>After I came out of hospital I undertook CDT treatment and after about a year I was able to have a stem cell transplant. However it was pretty tough along the way&hellip;<span class="activity-read-more" id="activity-read-more-46438"><a href="https://www.myeloma.org.uk/forums/topic/dad-just-diagnosed-with-mm-2/#post-129033" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Starting Stem Cell Therapy in the forum Treatment</title>
				<link>https://www.myeloma.org.uk/forums/topic/starting-stem-cell-therapy-2/#post-124605</link>
				<pubDate>Wed, 14 Oct 2015 09:01:32 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Dino,  I read your post with fascination and admiration, it brought back memories of Feb/Mar this year. The pain you describe while doing the cell boosting injections is something that I found underestimated wow it was so painful, my friend who was injecting the same time as me ended up in A&amp;E with chest pain it was that bad. Your positive&hellip;<span class="activity-read-more" id="activity-read-more-41361"><a href="https://www.myeloma.org.uk/forums/topic/starting-stem-cell-therapy-2/#post-124605" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Starting Stem Cell Therapy in the forum Newcomers</title>
				<link>https://www.myeloma.org.uk/forums/topic/starting-stem-cell-therapy/page/2/#post-124462</link>
				<pubDate>Thu, 01 Oct 2015 10:15:25 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello, I had my SCT in March this year, and yes had a tough time. I think most of us don&#8217;t like to be too graffic for fear of putting off, and also adding to their anxiety. From what you describe is about right although you will find everyone reacts different. I had a pretty torrid time for about 10 days, with infections and all sorts the worst&hellip;<span class="activity-read-more" id="activity-read-more-41179"><a href="https://www.myeloma.org.uk/forums/topic/starting-stem-cell-therapy/page/2/#post-124462" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Thalidomide side effects - how long do they last? in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/thalidomide-side-effects-how-long-do-they-last/#post-124310</link>
				<pubDate>Tue, 22 Sep 2015 09:26:36 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello, Sorry to read about your Dad and that he has come off Thelidomide, due to the side effects.  The CDT treatment has proven to work very well, and yes you get the nasty side effects with these toxic drugs. When I was on CDT the Thelidomide dose was 100mg which I took late at night with Horlicks and a biscuit. I did get neuropathy in the&hellip;<span class="activity-read-more" id="activity-read-more-41044"><a href="http://www.myeloma.org.uk/forums/topic/thalidomide-side-effects-how-long-do-they-last/#post-124310" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Thalidomide side effects - how long do they last? in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/thalidomide-side-effects-how-long-do-they-last/#post-124310</link>
				<pubDate>Tue, 22 Sep 2015 09:26:36 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello, Sorry to read about your Dad and that he has come off Thelidomide, due to the side effects.  The CDT treatment has proven to work very well, and yes you get the nasty side effects with these toxic drugs. When I was on CDT the Thelidomide dose was 100mg which I took late at night with Horlicks and a biscuit. I did get neuropathy in the&hellip;<span class="activity-read-more" id="activity-read-more-41043"><a href="http://www.myeloma.org.uk/forums/topic/thalidomide-side-effects-how-long-do-they-last/#post-124310" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Starting Stem Cell Therapy in the forum Newcomers</title>
				<link>https://www.myeloma.org.uk/forums/topic/starting-stem-cell-therapy/#post-123912</link>
				<pubDate>Fri, 04 Sep 2015 22:05:03 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Graeme,   I had my SCT in March this year in Kings College Hospital London, for me it was tough however managed to get through it, Like the posts say ice lollies and yogurts for the throat and sleep don&#8217;t worry about how much. There were a number of blood transfusions and Platlets transfusions even after being discharged from hospital. I think&hellip;<span class="activity-read-more" id="activity-read-more-40686"><a href="https://www.myeloma.org.uk/forums/topic/starting-stem-cell-therapy/#post-123912" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic The awful truth... in the forum Newcomers</title>
				<link>https://www.myeloma.org.uk/forums/topic/the-awful-truth/#post-123824</link>
				<pubDate>Mon, 31 Aug 2015 11:03:19 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello, my name is Chris also and was diagnosed with MM June 2014, by that time it had servealy damage lots of bones. My legs and spine in particular,  I decided to go for the standard treatment which was CDT tablet form, so that was the chemo, steroids, and Thelidomide, my kappa light chain reduced to 64 from 1250. I then had a stem cell&hellip;<span class="activity-read-more" id="activity-read-more-40585"><a href="https://www.myeloma.org.uk/forums/topic/the-awful-truth/#post-123824" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic medication after transplant in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/medication-after-transplant/#post-122848</link>
				<pubDate>Tue, 30 Jun 2015 12:09:15 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Brian, first good luck with the SCT, I hope it all goes through soon and with no complications. I had my SCT in March and slowly reducing the various Meds that I was on once my blood levels stablelised the last tablets I am on is Aciclovir which the Consultant said would be on it for 6 months. I get my post 100 days result next week so at this&hellip;<span class="activity-read-more" id="activity-read-more-39632"><a href="http://www.myeloma.org.uk/forums/topic/medication-after-transplant/#post-122848" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Zometa side effect ? in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/zometa-side-effect/#post-122714</link>
				<pubDate>Mon, 22 Jun 2015 11:43:23 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello Susie, I do have bone pain after a Zometa infusion especially my femur leg bones and back I do suffer this pain as a matter of course but it certainly seems worse after the infusion. I normally have to take extra pain relief for this period of 3 to 4 days then it settles. I have mentioned it to the nurses who give it to me and they say the&hellip;<span class="activity-read-more" id="activity-read-more-39484"><a href="http://www.myeloma.org.uk/forums/topic/zometa-side-effect/#post-122714" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Bone pain in the forum Related conditions</title>
				<link>http://www.myeloma.org.uk/forums/topic/bone-pain-4/#post-122524</link>
				<pubDate>Sat, 06 Jun 2015 23:01:59 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Mavis, sorry for not getting back sooner, Re: OxyContin I am not too sure about the sleepy  but probably yes. I am only 3 month post SCT and have been sleeping so much, prior to the transplant the tablet is a 12 hour slow release. I take it at 8am &amp; 8pm so with the evening one I am already in bed due to pain &amp; fatigue therefore if I sleep is&hellip;<span class="activity-read-more" id="activity-read-more-39337"><a href="http://www.myeloma.org.uk/forums/topic/bone-pain-4/#post-122524" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic bone pain after sct in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/bone-pain-after-sct/#post-122519</link>
				<pubDate>Sat, 06 Jun 2015 11:23:06 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello,</p>
<p>Thats strange because I also had SCT in March and although I already had lots of bone damage therefore have painful legs &amp; back. I have noticed that my shoulder is really painful, and my lower legs painful when I first get out of bed in the morning. The other strange thing that happens is when I have a wee my lower legs feel like they are&hellip;<span class="activity-read-more" id="activity-read-more-39328"><a href="http://www.myeloma.org.uk/forums/topic/bone-pain-after-sct/#post-122519" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Bone pain in the forum Related conditions</title>
				<link>http://www.myeloma.org.uk/forums/topic/bone-pain-4/#post-122326</link>
				<pubDate>Sat, 30 May 2015 10:33:18 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Mavis,</p>
<p>Sorry to read about your bone pain and fully understand what is like having bad bone damage myself. Before I was diagnosed I was eventually put on Tramadol which I was taking in large amounts however once diagnosed because I was on the maximum amount of Tramadol they put me on OxyContin which I am still on. I think it is Morphine based&hellip;<span class="activity-read-more" id="activity-read-more-39179"><a href="http://www.myeloma.org.uk/forums/topic/bone-pain-4/#post-122326" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic SCT Recovery. in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/sct-recovery/#post-121850</link>
				<pubDate>Mon, 20 Apr 2015 13:08:02 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello Michele,  Thank you for the information ,  yes have been keeping myself very much in isolation, my appetite is slowly getting back along with the taste buds.  I just hope that my Neutraphil level start to rise, they have given me some more injections to promote this, but I really wanted them to come back on their own accord. The diet su&hellip;<span class="activity-read-more" id="activity-read-more-38662"><a href="http://www.myeloma.org.uk/forums/topic/sct-recovery/#post-121850" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor started the topic SCT Recovery. in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/sct-recovery/</link>
				<pubDate>Sat, 18 Apr 2015 22:49:43 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi everyone ,  After a number of issues I was finally able  to have a Stem Cell Transplant in Kings College Hospital on 12 March.  I was discharged from hospital on the 2nd April, since then I have had 1 bag of Platlets and 2 bags of Blood as levels are still settling down. However my worry is my Neutraphil has dropped right back to less than 1.&hellip;<span class="activity-read-more" id="activity-read-more-38636"><a href="http://www.myeloma.org.uk/forums/topic/sct-recovery/" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Very ill, IgG kappa elevated, could it be myeloma? in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/very-ill-igg-kappa-elevated-could-it-be-myeloma/#post-120727</link>
				<pubDate>Tue, 10 Feb 2015 22:13:52 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi  Eva</p>
<p>i fully understand the worry and frustration you must be going through, and I am sorry I cannot allay those for you. I can give just a personal account of the very little I know regarding blood test and diagnosis of Myeloma.</p>
<p>After hospitalization,</p>
<p>I had no Paraprotien level indicated, but my Serum free kappa light chain reading was&hellip;<span class="activity-read-more" id="activity-read-more-37519"><a href="http://www.myeloma.org.uk/forums/topic/very-ill-igg-kappa-elevated-could-it-be-myeloma/#post-120727" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Very ill, IgG kappa elevated, could it be myeloma? in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/very-ill-igg-kappa-elevated-could-it-be-myeloma/#post-120727</link>
				<pubDate>Tue, 10 Feb 2015 22:13:52 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi  Eva</p>
<p>i fully understand the worry and frustration you must be going through, and I am sorry I cannot allay those for you. I can give just a personal account of the very little I know regarding blood test and diagnosis of Myeloma.</p>
<p>After hospitalization,</p>
<p>I had no Paraprotien level indicated, but my Serum free kappa light chain reading was&hellip;<span class="activity-read-more" id="activity-read-more-37518"><a href="http://www.myeloma.org.uk/forums/topic/very-ill-igg-kappa-elevated-could-it-be-myeloma/#post-120727" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic Very ill, IgG kappa elevated, could it be myeloma? in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/very-ill-igg-kappa-elevated-could-it-be-myeloma/#post-120727</link>
				<pubDate>Tue, 10 Feb 2015 22:13:52 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi  Ava,</p>
<p>i fully understand the worry and frustration you must be going through, and I am sorry I cannot allay those for you. I can give just a personal account of the very little I know regarding blood test and diagnosis of Myeloma.</p>
<p>After hospitalization,</p>
<p>I had no Paraprotien level indicated, but my Serum free kappa light chain reading was&hellip;<span class="activity-read-more" id="activity-read-more-37509"><a href="http://www.myeloma.org.uk/forums/topic/very-ill-igg-kappa-elevated-could-it-be-myeloma/#post-120727" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic My husband has been diagnosed with Myeloma in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-husband-has-been-diagnosed-with-myeloma/#post-120500</link>
				<pubDate>Fri, 23 Jan 2015 14:50:01 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi, Sorry to read about your husband and fully understand how you both must feel also how life can change so quickly.</p>
<p>I did not have that reading of kappa light chain figure mine was approx 1200,  the reason why I thought to reply is that most people quote Para protein levels and rarely kappa light. I am no expert in any respect of this but my&hellip;<span class="activity-read-more" id="activity-read-more-37266"><a href="http://www.myeloma.org.uk/forums/topic/my-husband-has-been-diagnosed-with-myeloma/#post-120500" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic advice please in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/advice-please-2/#post-119485</link>
				<pubDate>Sat, 15 Nov 2014 19:50:18 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Julie, read your post and wish you all the best with the SCT,  I hope to do the same in the near future,  when i was diagnosed with MM back in June I chose the standard treatment not sure why I think I was still in shock at that time and had little time to make my mind up. Anyway I am on my 7th cycle of CDT and my kappa light chain has reduce f&hellip;<span class="activity-read-more" id="activity-read-more-36433"><a href="http://www.myeloma.org.uk/forums/topic/advice-please-2/#post-119485" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic advice please in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/advice-please-2/#post-119485</link>
				<pubDate>Sat, 15 Nov 2014 19:50:18 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Julie, read your post and wish you all the with the SCT,  I hope to do the same in the near future,  when i was diagnosed with MM back in June I chose the standard treatment not sure why I think I was still in shock at that time and had little time to make my mind up. Anyway I am on my 7th cycle of CDT and my kappa light chain has reduce from 1&hellip;<span class="activity-read-more" id="activity-read-more-36432"><a href="http://www.myeloma.org.uk/forums/topic/advice-please-2/#post-119485" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic My story to Date in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-story-to-date-by-christaylor/page/2/#post-118879</link>
				<pubDate>Fri, 17 Oct 2014 20:17:23 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello John,</p>
<p>Glad to read you had the infusion all ok I hope that it works well, I had my zometa the other week the day after CDT and after 2 days had terrible shakes but it wore off.  And yes I also hope that it will help repair the bone damage, once a month for 2 years.  I took my CDT this morning 09:00 with breakfast, plus a glass of milk to h&hellip;<span class="activity-read-more" id="activity-read-more-28717"><a href="http://www.myeloma.org.uk/forums/topic/my-story-to-date-by-christaylor/page/2/#post-118879" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic My story to Date in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-story-to-date-by-christaylor/#post-118840</link>
				<pubDate>Thu, 16 Oct 2014 18:23:25 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Mavis,  Thanks for the message.</p>
<p>I agree with what you have written albeit I have not got one yet but I  certainly will do so, it can be parked in the garage ready to use at anytime.</p>
<p>Regards Chris.</p>
<p>&nbsp;</p>
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				<title>Chris Taylor replied to the topic My story to Date in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-story-to-date-by-christaylor/#post-118795</link>
				<pubDate>Wed, 15 Oct 2014 20:33:08 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello Stanley , Many thanks for your message, I really appreciate the encouragement from everyone and the tell tale signs of the side effects. A nice cup of Horlicks just before I take the Thalidomide tablets seem to help, well what I mean is that&#8217;s my little treat with a biscuit then it&#8217;s sleep time ha ha. I don&#8217;t have any blood test results&hellip;<span class="activity-read-more" id="activity-read-more-28670"><a href="http://www.myeloma.org.uk/forums/topic/my-story-to-date-by-christaylor/#post-118795" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic My story to Date in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-story-to-date-by-christaylor/#post-118794</link>
				<pubDate>Wed, 15 Oct 2014 20:13:14 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi John,  Good luck with the treatment I hope that the infusion indeed helps with walking, my legs are really painful at the moment not sure if it&#8217;s the CDT or what. Thinking about buying a mobility scooter just to get down the shops and around. Crying I do a lot of that, not too ashamed to say, for all sorts of things. I think the Dex sometimes&hellip;<span class="activity-read-more" id="activity-read-more-28669"><a href="http://www.myeloma.org.uk/forums/topic/my-story-to-date-by-christaylor/#post-118794" rel="nofollow">[Read more]</a></span></p>
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				<title>Chris Taylor replied to the topic My story to Date in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-story-to-date-by-christaylor/#post-118762</link>
				<pubDate>Mon, 13 Oct 2014 15:11:36 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Rebecca &amp; Tony,  just like to say thank you for your encouragement and knowledge about MM and the treatment. As you will both know it&#8217;s pretty tough at the moment and dare I say scary but reading everyone&#8217;s stories gives me strength knowing Iam not alone in this situation. My lovely wife has been a tremendous help in both looking after me and&hellip;<span class="activity-read-more" id="activity-read-more-28614"><a href="http://www.myeloma.org.uk/forums/topic/my-story-to-date-by-christaylor/#post-118762" rel="nofollow">[Read more]</a></span></p>
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				<title>christaylor changed their profile picture</title>
				<link>https://forum.myeloma.org.uk/activity/p/28592/</link>
				<pubDate>Sun, 12 Oct 2014 09:38:10 +0100</pubDate>

				
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				<title>Chris Taylor replied to the topic My story to Date in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-story-to-date-by-christaylor/#post-118746</link>
				<pubDate>Sun, 12 Oct 2014 09:32:53 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Mavis,  thank you for writing on my first posting,  I have been learning quite a lot from everyone&#8217;s comments and replies. Hopefully soon I will change the photo from a flower to one of me at least your see who I am. Once again thanks.</p>
<p>Take Care,</p>
<p>Chris.</p>
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				<title>christaylor replied to the topic Hi just starting chemo in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hi-just-starting-chemo/#post-118644</link>
				<pubDate>Mon, 06 Oct 2014 18:44:21 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Botope,  I am Chris diagnosed this June, me too have multiple lytic lesions, some fractured ribs, bad lower back and both legs. Anyway  the big bag of CDT chemo drug were indeed daunting when I first got them home from the hospital, my first 2 cycles were not good in that I developed an infection that they never really got to the bottom of , i&hellip;<span class="activity-read-more" id="activity-read-more-28457"><a href="http://www.myeloma.org.uk/forums/topic/hi-just-starting-chemo/#post-118644" rel="nofollow">[Read more]</a></span></p>
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				<title>christaylor started the topic My story to Date in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-story-to-date-by-christaylor/</link>
				<pubDate>Fri, 03 Oct 2014 18:16:43 +0100</pubDate>

									<content:encoded><![CDATA[<p><strong>Hello everybody, my name is Chris &amp; I am 61, married with 2 grandsons. My story begins early this year with painful ribs to which the GPs were prescribing pain killers. Eventually my lower back and both legs started to give me a lot of pain to the point I was struggling to walk. I hobbled into Dartford A&amp;E on the 29th May a quick X-ray suggested&hellip;</strong><span class="activity-read-more" id="activity-read-more-28390"><a href="http://www.myeloma.org.uk/forums/topic/my-story-to-date-by-christaylor/" rel="nofollow">[Read more]</a></span></p>
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