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	<title>Myeloma Forum | JefferyCrawford | Activity</title>
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				<title>JefferyCrawford replied to the topic The best hospital to treat Myeloma??? in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/the-best-hospital-to-treat-myeloma/#post-135233</link>
				<pubDate>Wed, 27 Sep 2017 15:30:38 +0100</pubDate>

									<content:encoded><![CDATA[<p>Difficult to find information on hospital rankings I found. I attend the Leicester Royal Infirmary, and have found the oncology team there fine. There are a number of consultants and you don&#8217;t always see the same one ( I believe you can ask to see the same one, but  I have just seen whichever one I am asigned to) They have always treated me with&hellip;<span class="activity-read-more" id="activity-read-more-51157"><a href="https://www.myeloma.org.uk/forums/topic/the-best-hospital-to-treat-myeloma/#post-135233" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford started the topic Desensitisation of painful feet in the forum Side-effects</title>
				<link>https://www.myeloma.org.uk/forums/topic/desensitisation-of-painful-feet/</link>
				<pubDate>Mon, 14 Aug 2017 13:16:39 +0100</pubDate>

									<content:encoded><![CDATA[<blockquote><p>Hi, part of the effects of the neuropathy I have in my legsand feet is extreme sensitivity in my feet, especially the left. It is so sensitive that the slightest brush against anything is painful ( although strange to say, I can trap it under my wheelchair and not know that I have done so and wonder why the chair doesn&#8217;t want to move!!)  Has a&hellip;</p></blockquote>
<p><span class="activity-read-more" id="activity-read-more-50777"><a href="https://www.myeloma.org.uk/forums/topic/desensitisation-of-painful-feet/" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Peripheral neuropathy and the DVLA in the forum Side-effects</title>
				<link>https://www.myeloma.org.uk/forums/topic/peripheral-neuropathy-and-the-dvla/#post-132018</link>
				<pubDate>Sun, 26 Feb 2017 23:38:34 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi, nice to hear from you.  Sofar I have had acknowledgment of my letter, and no decision yet. Bit irrelevant atm as I can’t drive,  as I&#8217;m not mobile enough to get to the car let alone drive it! Glad you have kept your licence,  it really is a trial not being able to drive, makes every thing difficult.  Regards, Jeff</p>
<p>&nbsp;</p>
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				<title>JefferyCrawford replied to the topic Sct not an option in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/sct-not-an-option/#post-131621</link>
				<pubDate>Sat, 21 Jan 2017 04:37:02 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Millie12. Yes I know what you mean.  I have just reached remission after some 3 years of treatment without SCT,  how long it will last who knows!  Fingers crossed.  I did post that I almost felt under a death sentence the way the posts seemed to read. Perhaps others who have not had sct could comment or post of their stories to encourage oth&hellip;<span class="activity-read-more" id="activity-read-more-48250"><a href="https://www.myeloma.org.uk/forums/topic/sct-not-an-option/#post-131621" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Peripheral neuropathy and the DVLA in the forum Side-effects</title>
				<link>https://www.myeloma.org.uk/forums/topic/peripheral-neuropathy-and-the-dvla/#post-130478</link>
				<pubDate>Wed, 16 Nov 2016 09:29:06 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi, Andy, thanks for the information,  I will download the form and send it off, I have booked the car in to have hand controls fitted later this month, and bought a scooter lift to make things easier.  I certainly wouldn&#8217;t consider continuing to drive the car as I am and it is, the risk of hitting something or someone is far to likely to h&hellip;<span class="activity-read-more" id="activity-read-more-47573"><a href="https://www.myeloma.org.uk/forums/topic/peripheral-neuropathy-and-the-dvla/#post-130478" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Peripheral neuropathy and the DVLA in the forum Side-effects</title>
				<link>https://www.myeloma.org.uk/forums/topic/peripheral-neuropathy-and-the-dvla/#post-130448</link>
				<pubDate>Sat, 12 Nov 2016 17:36:23 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi, haven&#8217;t posted for a while, decided to wait and see what would happen after I highlighted my Neuropathy to my consultant group after giving it low rating in importance until I came across this post when having a catch up session. I was concerned about the DVLA aspect. Since then it is having a much more negative effect on my abilities to drive&hellip;<span class="activity-read-more" id="activity-read-more-47531"><a href="https://www.myeloma.org.uk/forums/topic/peripheral-neuropathy-and-the-dvla/#post-130448" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Travel insurance in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/travel-insurance-6/#post-129694</link>
				<pubDate>Thu, 22 Sep 2016 21:16:41 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi, I have just got insured through HSBC, £62 For 8 days Malta excluding anything connected with Myeloma,  after a lot of searching.  Jeff</p>
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				<title>JefferyCrawford replied to the topic Lenalidomide/dexamethasone in the forum Side-effects</title>
				<link>https://www.myeloma.org.uk/forums/topic/lenalidomidedexamethasone/#post-128940</link>
				<pubDate>Mon, 25 Jul 2016 15:17:19 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Lennie, I recognise these symptoms only too well.I have been on Revlimid for some 2 years, and the lack of taste is a real downer, together with as you describe a burnt feel to the tongue.  I think about what I would like to eat, sit down to it and don&#8217;t want it, usually steuggle through most of it. Thank goodness puddings aren&#8217;t affected so&hellip;<span class="activity-read-more" id="activity-read-more-46297"><a href="https://www.myeloma.org.uk/forums/topic/lenalidomidedexamethasone/#post-128940" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Holidays in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/holidays-2/#post-128617</link>
				<pubDate>Tue, 28 Jun 2016 13:18:57 +0100</pubDate>

									<content:encoded><![CDATA[<p>Susie, I am in the same situation, cant get insurance while taking meds,  talked to the consultant about it, if I am well enough will be able to have a drugs holiday for a month or so and should then be able to get insured. but won&#8217;t know until close to holiday so have taken a chance and paid!! Might lose it, I did try several insurers but always&hellip;<span class="activity-read-more" id="activity-read-more-46011"><a href="https://www.myeloma.org.uk/forums/topic/holidays-2/#post-128617" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Blue Badge in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/blue-badge-2/#post-127809</link>
				<pubDate>Sun, 01 May 2016 20:51:07 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Susie Afraid that feeling comes to us all, I hate having to use a walking stick, but needs must!! I think we have enough to deal with,anything that makes it easier is welcome Take care Jeff xx </p>
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				<title>JefferyCrawford replied to the topic Blue Badge in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/blue-badge-2/#post-127803</link>
				<pubDate>Sun, 01 May 2016 08:51:55 +0100</pubDate>

									<content:encoded><![CDATA[<p>Contact MacMillan, they sorted mine out initially, there is I think some arrangements for terminal cancer patients Good luck Jeff </p>
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				<title>JefferyCrawford replied to the topic Lenalidomide/dexamethasone in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/lenalidomidedexamethasone/#post-127476</link>
				<pubDate>Thu, 31 Mar 2016 09:30:39 +0100</pubDate>

									<content:encoded><![CDATA[<p>Wow Pennie,  what a breath of fresh air at just the right time for me.  Andie&#8217;s story is so similar to mine, except I am only 5 years down the line as against Andie&#8217;s 16, even to an emergency op resulting in an ileostomy! On the same treatment too. I am in a bit of a down just now mainly due to a painful back problem, and this post has cheered me&hellip;<span class="activity-read-more" id="activity-read-more-44536"><a href="http://www.myeloma.org.uk/forums/topic/lenalidomidedexamethasone/#post-127476" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic one week (and a bit) in in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/one-week-and-a-bit-in/#post-127457</link>
				<pubDate>Wed, 30 Mar 2016 07:47:55 +0100</pubDate>

									<content:encoded><![CDATA[<p>Quick update :- back now a lot better,after a very difficult MRI scan no evidence of cancer or new damage which was a big relief. I decided to live with a bit of pain and reduced my morphine dosage as the heavy dose the GP recommended wiped  me out,  sleepy and dreamy all day, so am now seeing how it settles down, if possible will reduce it&hellip;<span class="activity-read-more" id="activity-read-more-44505"><a href="http://www.myeloma.org.uk/forums/topic/one-week-and-a-bit-in/#post-127457" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford started the topic Mirtazapine in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/mirtazapine/</link>
				<pubDate>Thu, 24 Mar 2016 19:10:41 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi all, I am going through quite a down spell at present, caused by a series of not nice events that have caused me to struggle to maintain my usual positive attitude.  My GP,a good family doctor ( he spotted my Myeloma early on)  wants me to start a course of Mirtazapine tablets.  I am concerned about side effects ( we all have enough of those&hellip;<span class="activity-read-more" id="activity-read-more-44383"><a href="http://www.myeloma.org.uk/forums/topic/mirtazapine/" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Sis back in hospital in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/sis-back-in-hospital/#post-127373</link>
				<pubDate>Mon, 21 Mar 2016 20:30:41 +0000</pubDate>

									<content:encoded><![CDATA[<p>Ahh, Nippy, sorry to hear about the latest news, hope it gets sorted ok. Best wishes xx</p>
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				<title>JefferyCrawford replied to the topic Sis back in hospital in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/sis-back-in-hospital/#post-127257</link>
				<pubDate>Sun, 20 Mar 2016 19:24:00 +0000</pubDate>

									<content:encoded><![CDATA[<p>Nippy, chest infections seem to be the bane of chemo drugs, I&#8217;ve had several, and have even been given antibiotics to keep at home in case I start developing one! Hope sis recovers quickly, they do drag you down </p>
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				<title>JefferyCrawford replied to the topic GP letters in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/gp-letters-2/#post-127253</link>
				<pubDate>Sat, 19 Mar 2016 17:07:04 +0000</pubDate>

									<content:encoded><![CDATA[<p>I know a while ago someone on the forum was having great difficulty with the Leicester Royal Infirmary oncology unit getting letters passed on to him and had to demand them through &#8211; I think it was &#8211; the pals network, and had to pay a fee. It was a long time ago so not sure of the details, but you are evidently entitled to this information. Since&hellip;<span class="activity-read-more" id="activity-read-more-44281"><a href="http://www.myeloma.org.uk/forums/topic/gp-letters-2/#post-127253" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic GP letters in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/gp-letters-2/#post-127250</link>
				<pubDate>Fri, 18 Mar 2016 22:35:55 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Susie the Leicester Royal Infirmary oncology unit now always sends copies of the Doctor&#8217;s letters, weren&#8217;t so good in the past,  usually about 2 weeks after the event.  As you say, a useful reference to check back on events and dates, and the consultant&#8217;s remarks.<br />
All the best xx </p>
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				<title>JefferyCrawford replied to the topic Bone pain in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/bone-pain-5/#post-127175</link>
				<pubDate>Sun, 13 Mar 2016 16:22:28 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Peter, I would be inclined to take action tomorrow rather than wait for the consultant meeting as it is a fair while away, and things can change quickly.  Also you may be able to find help with the pain, even if it&#8217;s only to lessen it to a degree, as happened to me with my back problem. Don&#8217;t worry about being a nuisance, that&#8217;s what the system&hellip;<span class="activity-read-more" id="activity-read-more-44156"><a href="http://www.myeloma.org.uk/forums/topic/bone-pain-5/#post-127175" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic one week (and a bit) in in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/one-week-and-a-bit-in/#post-127017</link>
				<pubDate>Sun, 28 Feb 2016 11:59:27 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hallo Nick, done it again came off this page lost a long script! Try again!<br />
Nick, sorry to hear things haven&#8217;t improved much for you. The lack of mobility is so limiting,and constant pain drags you down mentally as well as physically as we both know. I have many of the problems that you have, tiredness and fatigue in particular. I hope things&hellip;<span class="activity-read-more" id="activity-read-more-43663"><a href="http://www.myeloma.org.uk/forums/topic/one-week-and-a-bit-in/#post-127017" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic one week (and a bit) in in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/one-week-and-a-bit-in/#post-127017</link>
				<pubDate>Sun, 28 Feb 2016 11:59:27 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hallo Nick, done it again came off this page lost a long script! Try again!<br />
Nick, sorry to hear things haven&#8217;t improved much for you. The lack of mobility is so limiting,and constant pain drags you down mentally as well as physically as we both know. I have many of the problems that you have, tiredness and fatigue in particular. I hope things&hellip;<span class="activity-read-more" id="activity-read-more-43662"><a href="http://www.myeloma.org.uk/forums/topic/one-week-and-a-bit-in/#post-127017" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Hello All in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-all-2/#post-126889</link>
				<pubDate>Sat, 13 Feb 2016 11:28:33 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi, Vicki. Just a quick one regarding the       ball, where will it be held? Need to know   how far away from me it will be before thinking about it.<br />
Thanks, Jeff     </p>
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				<title>JefferyCrawford replied to the topic Lenalidomide/dexamethasone in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/lenalidomidedexamethasone/#post-126887</link>
				<pubDate>Sat, 13 Feb 2016 10:12:25 +0000</pubDate>

									<content:encoded><![CDATA[<p>Margaret,  I have been &#8211; cycle 23 &#8211; of Dex and Revlimid for nearly two years.  The symptoms you have described about sums up mine! Get all of those to varying degrees.  This morning I can just about support myself standing up and walking, this will last for an hour or two. Breathless is getting worse,  any activity causes it now.Interesting that&hellip;<span class="activity-read-more" id="activity-read-more-43209"><a href="http://www.myeloma.org.uk/forums/topic/lenalidomidedexamethasone/#post-126887" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic 5 Years Ago Today in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/5-years-ago-today/#post-125898</link>
				<pubDate>Wed, 20 Jan 2016 10:17:52 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi,  Phil, good to hear your good news,long may it last,  gives all of us struggling on hope.  Best wishes for a long future, Jeff</p>
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				<title>JefferyCrawford replied to the topic Loose bowels &#38; occassional dizzy spells in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/loose-bowels-occassional-dizzy-spells/#post-125859</link>
				<pubDate>Mon, 18 Jan 2016 17:49:59 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Eric, I am just coming up to my Revlimid free week, I shall monitor it carefully and see how I feel day by day, and get back to you Jeff </p>
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				<title>JefferyCrawford replied to the topic Tiredness in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/tiredness-2/#post-125852</link>
				<pubDate>Mon, 18 Jan 2016 14:43:41 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Mavis, thanks so much for your kind thoughts, it means more than you realise for me to know that there are people out there who care. I am fortunate in that I have a close family near to me who are supportive, but I don&#8217;t like to put too much on them, they have their own lives to live and way to make. My way of dealing with things is to get up&hellip;<span class="activity-read-more" id="activity-read-more-42637"><a href="http://www.myeloma.org.uk/forums/topic/tiredness-2/#post-125852" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Loose bowels &#38; occassional dizzy spells in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/loose-bowels-occassional-dizzy-spells/#post-125683</link>
				<pubDate>Tue, 12 Jan 2016 00:56:47 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hallo Eric, I was drifting through the posts on a steroid night and found yours. I am in about the same position as yourself with results, haven&#8217;t had a SCT, and am on the 21 cycle of Revlimid ( same dose and frequency ) and Dex.<br />
I was interested in you saying about your fatigue, I have hit a real high level of this, really tired out, falling&hellip;<span class="activity-read-more" id="activity-read-more-42566"><a href="http://www.myeloma.org.uk/forums/topic/loose-bowels-occassional-dizzy-spells/#post-125683" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Thank you.. in the forum Off topic</title>
				<link>http://www.myeloma.org.uk/forums/topic/thank-you-2/#post-125570</link>
				<pubDate>Sun, 03 Jan 2016 18:19:03 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Tony,happy new year to you and all our readers,let&#8217;s hope for many more years of them. Well said in your post, it&#8217;s easy to forget all that&#8217;s done for us when we are sitting in the waiting room at LRI with appointments running 2 hours late!!  It really is an interesting time, there is such a lot of research in so many directions, several sound&hellip;<span class="activity-read-more" id="activity-read-more-42439"><a href="http://www.myeloma.org.uk/forums/topic/thank-you-2/#post-125570" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Tiredness in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/tiredness-2/#post-125567</link>
				<pubDate>Sat, 02 Jan 2016 21:36:32 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hallo, all, I haven&#8217;t posted for a while, my middle daughter who I have mentioned before (she suffered a brain bleed a while ago unfortunately was finally overcome by the long term effects of her ongoing problems and passed away at the end of November,  which although not a complete surprise wasn&#8217;t expected and needless to say was a big shock.&hellip;<span class="activity-read-more" id="activity-read-more-42428"><a href="http://www.myeloma.org.uk/forums/topic/tiredness-2/#post-125567" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Tiredness in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/tiredness-2/#post-125567</link>
				<pubDate>Sat, 02 Jan 2016 21:36:32 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hallo, all, I haven&#8217;t posted for a while, mypmiddle daughter who I have mentioned before (she suffered a brain bleed a while agounfortunately was finally overcome by the long term effects of her ongoing problems and passed away at the end of November,  which although not a complete surprise wasn&#8217;t expected and needless to say was a big shock. Life&hellip;<span class="activity-read-more" id="activity-read-more-42427"><a href="http://www.myeloma.org.uk/forums/topic/tiredness-2/#post-125567" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic CURCUMIN in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/curcumin1379683671/page/3/#post-125004</link>
				<pubDate>Mon, 16 Nov 2015 11:10:56 +0000</pubDate>

									<content:encoded><![CDATA[<p>I took curcumin for many months while smouldering. When my wife died I sort of went to pieces and stopped several things, such as buying newspapers, watching Tv, and also taking curcumin. Within 2 months my Myeloma became active and I started chemotherapy. Coincidence? Who knows. Jeff</p>
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				<title>JefferyCrawford replied to the topic Criteria for Remission in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/criteria-for-remission/page/2/#post-124894</link>
				<pubDate>Tue, 10 Nov 2015 01:08:29 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi, an interesting Post. I am in the situation of hopefully being offered a reversal of a stoma I ended up with after an emergency operation last year. My myeloma is in partial remission, and stable at the moment. To have this operation I shall need to come off Dex for a month or so, the surgeon flatly refuses to carry out the operation while I am&hellip;<span class="activity-read-more" id="activity-read-more-41825"><a href="http://www.myeloma.org.uk/forums/topic/criteria-for-remission/page/2/#post-124894" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Just a little update on my progress. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/just-a-little-update-on-my-progress/#post-124766</link>
				<pubDate>Thu, 29 Oct 2015 10:52:13 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi, Andy, so pleased to hear of your progress, and your recovery from your hospitalisation. I had a similar &#8221; out of it &#8221; session while in I.T.U. following an emergency admission. On recovery, I was about to put pen to paper to write to the newspapers asking why our hospital was being run by a private concern, when I had to revisit the I.T.U.  and&hellip;<span class="activity-read-more" id="activity-read-more-41618"><a href="http://www.myeloma.org.uk/forums/topic/just-a-little-update-on-my-progress/#post-124766" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic What a fourth myeloma anniversary in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/what-a-fourth-myeloma-anniversary/#post-124554</link>
				<pubDate>Thu, 08 Oct 2015 12:42:14 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hallo Andy, sorry to hear about your experiences,  no doubt you met them with your usual resilience. Very pleased to hear of your recovery, I hope it&#8217;s not too slow, I know only too well the frustration continued tiredness brings with it.<br />
Just keep taking it one day at a time,  and as you say, each one we get through is a gift   Best wishes,Jeff</p>
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				<title>JefferyCrawford replied to the topic Vaccination in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/vaccination/#post-124517</link>
				<pubDate>Mon, 05 Oct 2015 16:06:09 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Susie, had a slight reaction to the first years jab, bit feverish and felt rough for a day or two, but since then have had no significant reaction at all Had this year&#8217;s last week. So maybe it&#8217;s one of these things that seems so common with Myeloma where we are all different, but I would go with the consultant&#8217;s wishes, mine was the same,&hellip;<span class="activity-read-more" id="activity-read-more-41246"><a href="http://www.myeloma.org.uk/forums/topic/vaccination/#post-124517" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic CANCER DRUG FUND CAMPAIGN - 38 DEGREES - PLEASE SIGN... in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/cancer-drug-fund-campaign-38-degrees-please-sign/#post-124307</link>
				<pubDate>Tue, 22 Sep 2015 08:53:18 +0100</pubDate>

									<content:encoded><![CDATA[<p>Rebecca,found the 38degrees petitions on the drugs and signed them all!!!  Best wishes Jef</p>
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				<title>JefferyCrawford replied to the topic one week (and a bit) in in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/one-week-and-a-bit-in/#post-124306</link>
				<pubDate>Tue, 22 Sep 2015 08:50:51 +0100</pubDate>

									<content:encoded><![CDATA[<p>Nick, what a struggle you have had!  I sympathise as I have endured back problems with two vertebrae more or less disappeared together with 5 1/2&#8243; in height Have you lost any height?  I had a vertobroplasty over a year ago which has lessened the pain and I can now walk a few hundred yards &#8211; big improvement so hang on in there!  I have been very&hellip;<span class="activity-read-more" id="activity-read-more-41041"><a href="http://www.myeloma.org.uk/forums/topic/one-week-and-a-bit-in/#post-124306" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Removal of Revlimid and pomalidomide from Cancer Drugs Fund in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/page/4/#post-124148</link>
				<pubDate>Tue, 15 Sep 2015 08:54:45 +0100</pubDate>

									<content:encoded><![CDATA[<p>Dusk, I think you are right about a campaign across all the<br />
Cancer groups , it would be that more a powerful representation. I would suggest a petition similar to those set up by 38 Degrees, which have wide veiwing on the internet.( Ive signed several). These attract attention from those not directly involved too. Unfortunately due to family&hellip;<span class="activity-read-more" id="activity-read-more-40933"><a href="http://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/page/4/#post-124148" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Removal of Revlimid and pomalidomide from Cancer Drugs Fund in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/page/3/#post-124144</link>
				<pubDate>Tue, 15 Sep 2015 00:17:02 +0100</pubDate>

									<content:encoded><![CDATA[<p>Point taken, letter to Sir Allan Duncan to be composed and sent forthwith!! I shall wait until steroids wear off though. </p>
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				<title>JefferyCrawford replied to the topic Removal of Revlimid and pomalidomide from Cancer Drugs Fund in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/page/3/#post-124142</link>
				<pubDate>Mon, 14 Sep 2015 22:11:11 +0100</pubDate>

									<content:encoded><![CDATA[<p>Alex, please don&#8217;t think that I unaware of the political aspect of these problems. However I do feel that blaming/accusing individual politicians is a waste of effort, which hopefully can be better applied. What political party has ever carried out what they promised when seeking power. I would add that I am actively supporting the campaign&hellip;<span class="activity-read-more" id="activity-read-more-40925"><a href="http://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/page/3/#post-124142" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Removal of Revlimid and pomalidomide from Cancer Drugs Fund in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/page/3/#post-124136</link>
				<pubDate>Mon, 14 Sep 2015 18:08:18 +0100</pubDate>

									<content:encoded><![CDATA[<p>Can I suggest that we don&#8217;t get involved in political personal slurs however well intentioned, I can&#8217;t see the value to the campaign against the actions being taken concerning the withdrawal of the drugs Jeff </p>
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				<title>JefferyCrawford replied to the topic Removal of Revlimid and pomalidomide from Cancer Drugs Fund in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/page/3/#post-124135</link>
				<pubDate>Mon, 14 Sep 2015 18:01:40 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi, talked about this with my consultant last Thursday -good news was p/ps down another point  now at 1.7!- saying how concerned we all are.  She was &#8211; and she is one I trust &#8211; not to be worried, they were confident that they could deal with remissions and saw no real cause for concern. She is not one to mince her words, she tells you as it is.&hellip;<span class="activity-read-more" id="activity-read-more-40912"><a href="http://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/page/3/#post-124135" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Removal of Revlimid and pomalidomide from Cancer Drugs Fund in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/page/3/#post-124005</link>
				<pubDate>Tue, 08 Sep 2015 18:18:04 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Ellen thanks for the information, looks like we just have to hang on and  hope for the best. If there is anything we can do to help influence the decision making please let us forum users know. Jeff</p>
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				<title>JefferyCrawford replied to the topic Removal of Revlimid and pomalidomide from Cancer Drugs Fund in the forum General</title>
				<link>https://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/page/2/#post-123946</link>
				<pubDate>Sat, 05 Sep 2015 20:57:34 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi All, well this has really stirred things up hasn&#8217;t it? I&#8217;ve contacted Myeloma UK and asked them if they can explain exactly where we stand in the light of these decisions, as I for one am not fully conversant with whats been decided &#8211; I just know it&#8217;s not good news. I will feedback any answer and information I get. Try not to get too down over&hellip;<span class="activity-read-more" id="activity-read-more-40730"><a href="https://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/page/2/#post-123946" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Removal of Revlimid and pomalidomide from Cancer Drugs Fund in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/#post-123924</link>
				<pubDate>Sat, 05 Sep 2015 10:35:34 +0100</pubDate>

									<content:encoded><![CDATA[<p>I don&#8217;t know if Myeloma UK could give us some guidance on how these decisions will affect our future treatment, it is certainly very disturbing information with huge implications on our future treatment and survival. I will look at contacting Myeloma UK to request further details. Jeff  </p>
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				<title>JefferyCrawford replied to the topic Removal of Revlimid and pomalidomide from Cancer Drugs Fund in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/#post-123919</link>
				<pubDate>Sat, 05 Sep 2015 08:11:05 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Tom, I am in the same position as as yourself, on Revlimid and Dex, which is working well at present. As you say, devastating that what is probably the last fall &#8211; back drug has been put out of reach to us. It has kept a friend of mine going for several months although it has now ceased to work for him. It&#8217;s even more annoying that this  is a&hellip;<span class="activity-read-more" id="activity-read-more-40694"><a href="http://www.myeloma.org.uk/forums/topic/removal-of-revlimid-and-pomalidomide-from-cancer-drugs-fund/#post-123919" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Colin in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/colin/#post-123569</link>
				<pubDate>Sat, 15 Aug 2015 08:28:50 +0100</pubDate>

									<content:encoded><![CDATA[<p>So sorry to hear of Colin&#8217;s passing, as I know even when you expect it it&#8217;s still. so hard. Jeff</p>
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				<title>JefferyCrawford replied to the topic Do you deal with a single consultant or a rotating team? in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/do-you-deal-with-a-single-consultant-or-a-rotating-team/#post-123338</link>
				<pubDate>Sun, 26 Jul 2015 09:10:12 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi, Ben.When I was diagnosed the S.C.T.cut off point was just past my age although I was told I could still have one ( this age has since changed I believe). I had researched the procedure, realised how arduous and lenghty it would be, talked it over with the consultant and family,and decided it wasn&#8217;t for me. History has proved it to be probably&hellip;<span class="activity-read-more" id="activity-read-more-40038"><a href="http://www.myeloma.org.uk/forums/topic/do-you-deal-with-a-single-consultant-or-a-rotating-team/#post-123338" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Do you deal with a single consultant or a rotating team? in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/do-you-deal-with-a-single-consultant-or-a-rotating-team/#post-123330</link>
				<pubDate>Sat, 25 Jul 2015 02:17:41 +0100</pubDate>

									<content:encoded><![CDATA[<p>Interesting subject and one I have wondered about. At Leicester I see one of 5 consultants, and occasionally a registrar, these vary, this so far hasn&#8217;t been a problem. The consultants are all pretty good &#8211; although I do have favourites &#8211; and seem to have a good knowledge of my case and my problems. I believe they have a case conference the day&hellip;<span class="activity-read-more" id="activity-read-more-40023"><a href="http://www.myeloma.org.uk/forums/topic/do-you-deal-with-a-single-consultant-or-a-rotating-team/#post-123330" rel="nofollow">[Read more]</a></span></p>
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				<title>JefferyCrawford replied to the topic Whacked out days in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/whacked-out-days/#post-122809</link>
				<pubDate>Sat, 27 Jun 2015 09:00:41 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Capeltor, thank you for taking the trouble to reply, I am so sorry to hear of the loss of your husband. What you say is very interesting,I have noticed of late that I seem to be drinking more than previously, which is another sign of possible diabetes I have been told.I shall call in at Lloyds Chemists and get myself checked. Steroid induced&hellip;<span class="activity-read-more" id="activity-read-more-39557"><a href="http://www.myeloma.org.uk/forums/topic/whacked-out-days/#post-122809" rel="nofollow">[Read more]</a></span></p>
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