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	<title>Myeloma Forum | JacquiReeks | Activity</title>
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				<title>JacquiReeks replied to the topic velcade in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/velcade#post-86814</link>
				<pubDate>Fri, 19 Oct 2012 23:47:54 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello Michael, my name is Jacqui.</p>
<p>Like Josephine I had initial treatment with oral CDT and I was very fortunate to achieve a complete response in 3 months. I went on to have STC and I am now on a clinical trial with weekly treatment with velcade.</p>
<p>It was explained to me that it is usually used for patients who have already had at least one&hellip;<span class="activity-read-more" id="activity-read-more-5571"><a href="http://www.myeloma.org.uk/forums/topic/velcade#post-86814" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic Colin SCT plan b! in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/colin-sct-plan-b/page/6/#post-100248</link>
				<pubDate>Sat, 22 Sep 2012 00:30:46 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Ali &amp; Vicki. I am now 4 months post SCT and no one has mentioned immunisations. My next appointment is next week so I will ask then. My holiday aspirations are a little closer to home and I am really hoping to have a holiday to the Greek island with extended family next summer. Missed out last year so fingers crossed all will be well for next&hellip;<span class="activity-read-more" id="activity-read-more-16805"><a href="http://www.myeloma.org.uk/forums/topic/colin-sct-plan-b/page/6/#post-100248" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic My dad... in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-dad1346884470/page/2/#post-100465</link>
				<pubDate>Sat, 22 Sep 2012 00:18:03 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Joanne. I am sorry that your dad is going through a tough time and I can imagine it is very difficult for you. </p>
<p>I started on Velcade 3 weeks ago so I am no expert but just wanted to let you know that so far I am feeling very good. I am working 3 days a week and also running around like a headless chicken with my daughters.</p>
<p>I have it once&hellip;<span class="activity-read-more" id="activity-read-more-17021"><a href="http://www.myeloma.org.uk/forums/topic/my-dad1346884470/page/2/#post-100465" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic ASPARTAME??? in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/aspartame#post-93482</link>
				<pubDate>Sun, 09 Sep 2012 23:54:11 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thank you Dai &amp; Helen<br />
I don&#039;t really know why I went onto that thinking. Probably because I am curious as to why MM was not historically common in women and especially not young women yet it seems to be quite increasingly evident lately.<br />
Anyway, I think I need to stop quizzing and just accept it, but I&#039;ve always have an enquiring mind, even as a&hellip;<span class="activity-read-more" id="activity-read-more-11366"><a href="http://www.myeloma.org.uk/forums/topic/aspartame#post-93482" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic ASPARTAME??? in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/aspartame#post-93478</link>
				<pubDate>Fri, 07 Sep 2012 09:00:46 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Michele</p>
<p>Thank you for your reply.</p>
<p>Yes, same here. I will not let my children drink diet drinks and avoid anything that says &quot;no added sugar&quot; as I have found this usually means aspartame is present. Before you became aware of it&#039;s toxicity did you buy products with aspartame?</p>
<p>Looking at your profile you seem to be very similar to me. I&hellip;<span class="activity-read-more" id="activity-read-more-11362"><a href="http://www.myeloma.org.uk/forums/topic/aspartame#post-93478" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks started the topic ASPARTAME???. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/aspartame</link>
				<pubDate>Thu, 06 Sep 2012 23:28:53 +0100</pubDate>

									<content:encoded><![CDATA[<p>In my puzzling as to why so many younger women are developing MM, I was questioning my somewhat excessive use of the artificial sweetner Aspartame in my quest to lose weight (for many years). </p>
<p>This lead me to think that dieting is generally more of an issue for women (plse dont think i am being sexist) and got to thinking how many would be&hellip;<span class="activity-read-more" id="activity-read-more-11360"><a href="http://www.myeloma.org.uk/forums/topic/aspartame" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic My dad... in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-dad1346884470#post-100451</link>
				<pubDate>Thu, 06 Sep 2012 23:16:52 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello Joanne<br />
I had my stem cell transplant in May of this year, just under 4 months ago. Like your dad I had previously been treated with chemo, steroid and Thalidomide. The worst part of that for me was the steroids but apart from that it wasnt too troublesome, although looking back I realise I was far from the person that I was prior to the&hellip;<span class="activity-read-more" id="activity-read-more-17007"><a href="http://www.myeloma.org.uk/forums/topic/my-dad1346884470#post-100451" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic Hello again to all in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-again-to-all#post-100374</link>
				<pubDate>Tue, 04 Sep 2012 20:11:56 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thanks Tom</p>
<p>Aim is to see if weekly Velcade given within 4 mnths of SCT extends remission.  Thing is I can&#039;t really see how they will know but hey ho I&#039;ll give it a try.</p>
<p>Jacqui</p>
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				<title>JacquiReeks replied to the topic Hello again to all in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-again-to-all#post-100372</link>
				<pubDate>Tue, 04 Sep 2012 19:32:14 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Paul</p>
<p>Good Luck with the Allo.  When you say you have been offered clinical trial for that &#8211; do you mean the same one as me or for your allo?</p>
<p>Getting my first dose on Thursday.  Will keep the updates on &quot;TREATMENT&quot; part of the forum.</p>
<p>Jacqui</p>
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				<title>JacquiReeks replied to the topic Hello again to all in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-again-to-all#post-100368</link>
				<pubDate>Tue, 04 Sep 2012 18:46:42 +0100</pubDate>

									<content:encoded><![CDATA[<p>04-09-2012 at 6:44 PM<br />
Hi Tracey</p>
<p>I have posted a general reply to my original post but just wanted to say that I am also being treated at The Royal Free.</p>
<p>Like you, I tend to look on here according to my moods. Not because I don&#039;t care about others, but because for me I find it easier to keep my spirits high if I do not focus too much on my&hellip;<span class="activity-read-more" id="activity-read-more-16924"><a href="http://www.myeloma.org.uk/forums/topic/hello-again-to-all#post-100368" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic Hello again to all in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-again-to-all#post-100370</link>
				<pubDate>Tue, 04 Sep 2012 18:39:55 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thank you all so much for replying.  I finally got to the bottom of my questions and basically it is something to do with a chromosome abnormality known as 4:14 trans-location ????</p>
<p>I don&#039;t really understand what that means but just understand that is the &quot;aggressive&quot; bit that my consultant is talking about.</p>
<p>After over 2 weeks of swinging&hellip;<span class="activity-read-more" id="activity-read-more-16926"><a href="http://www.myeloma.org.uk/forums/topic/hello-again-to-all#post-100370" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic Another joining the Stem Cell Transplant Brigade! in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/another-joining-the-stem-cell-transplant-brigade#post-100419</link>
				<pubDate>Tue, 04 Sep 2012 18:19:53 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello Catlyn</p>
<p>My name is Jacqui and I am almost 4 months post SCT. </p>
<p>A bit of history :- I was diagnosed in November 2011 aged 51. </p>
<p>Following surgery to fix a lesion in my right femur which was picked up on diagnosis of MM, I started on CTD. 3 cycles of treatment resulted in 0 detectable paraprotein. I then had one more cycle until end of&hellip;<span class="activity-read-more" id="activity-read-more-16975"><a href="http://www.myeloma.org.uk/forums/topic/another-joining-the-stem-cell-transplant-brigade#post-100419" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic Feeling Useless in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/feeling-useless#post-86614</link>
				<pubDate>Sun, 02 Sep 2012 21:54:04 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello Maxine. My name is Jacqui. I am 52 and was diagnosed with MM in Nov 2011. I live in London and I am under the Royal Free Hospital. I don&#039;t post on here as often as I would like to because I always seem to be so busy with my 2 daughters (aged 19 &amp; 12),  but whenever I do people are always kind enough to reply so I am sure you will get plenty&hellip;<span class="activity-read-more" id="activity-read-more-5371"><a href="http://www.myeloma.org.uk/forums/topic/feeling-useless#post-86614" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks started the topic Hello again to all. in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-again-to-all</link>
				<pubDate>Fri, 24 Aug 2012 21:14:39 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi everyone. I haven&#039;t posted for a while as been quite busy getting on with life with the children before they go back to school and university. I am sorry to seem to be only posting now that I need something and I hope you all don&#039;t mind. </p>
<p>As you know from my previous posts I had my SCT on 18th May.  Now recovered and getting ready to return&hellip;<span class="activity-read-more" id="activity-read-more-16919"><a href="http://www.myeloma.org.uk/forums/topic/hello-again-to-all" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic getting ready for stem cell tranceplant in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/getting-ready-for-stem-cell-tranceplant#post-86495</link>
				<pubDate>Fri, 24 Aug 2012 20:59:17 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello Angela</p>
<p>I am Jacqui, aged 52 and diagnosed with MM in November 2011. We are very similar in our situation as on diagnosis I presented with a fractured hip.  I immediately had an operation where a pin was put in my right leg to support the hip. All quite straight forward but I appreciate is was not a hip replacement so not quite the same as&hellip;<span class="activity-read-more" id="activity-read-more-5258"><a href="http://www.myeloma.org.uk/forums/topic/getting-ready-for-stem-cell-tranceplant#post-86495" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic Hello to All in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-to-all/page/2/#post-85678</link>
				<pubDate>Tue, 05 Jun 2012 08:21:35 +0100</pubDate>

									<content:encoded><![CDATA[<p>Good Morning All. Just a quick update to let u all know that I came home.on Saturday following my SCT. So how was it for me?  Well the results.show that I am in complete remisssion with no trace of paraprotein 🙂<br />
 I have to be honest and say it was certainly not plain sailing but i dont want to dwell on that because it is behind be now and&hellip;<span class="activity-read-more" id="activity-read-more-4447"><a href="http://www.myeloma.org.uk/forums/topic/hello-to-all/page/2/#post-85678" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic Newly diagnosed Monday at only 39. in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/newly-diagnosed-monday-at-only-39/page/2/#post-86094</link>
				<pubDate>Sun, 20 May 2012 20:03:46 +0100</pubDate>

									<content:encoded><![CDATA[<p>Dear Antionette. My heartfelt thoughts to you especially in relation to you having such young children. Although i am older than you and my children are older than yours, i truly understand how you must be feeling right now. You know it does sometimes seem so unfair but the raw fact is that we cant change what we have. The only way I can deal with&hellip;<span class="activity-read-more" id="activity-read-more-4863"><a href="http://www.myeloma.org.uk/forums/topic/newly-diagnosed-monday-at-only-39/page/2/#post-86094" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic Hello to All in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-to-all/page/2/#post-85669</link>
				<pubDate>Wed, 16 May 2012 22:04:44 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Vicki &amp; Colin<br />
My treatment so far has been ok.  My main problems came from Dexamethasone with tremors and general weakness being at the worst 2 days after stopping each cycle. I have tried to be positive about this as there is nothing I can do to change my affair with Myeloma. On just a few occasions it has been hard and I have sobbed but i&hellip;<span class="activity-read-more" id="activity-read-more-4438"><a href="http://www.myeloma.org.uk/forums/topic/hello-to-all/page/2/#post-85669" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic Hello to All in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-to-all/page/2/#post-85665</link>
				<pubDate>Wed, 16 May 2012 07:53:57 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thanyou Dai for your positive and understanding message. I have just posted a brief update below. Jacqui</p>
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				<title>JacquiReeks replied to the topic Hello to All in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-to-all/page/2/#post-85667</link>
				<pubDate>Wed, 16 May 2012 07:52:21 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hello again. Just a quick update. Now in hospital waiting to have my hickman line put in and then high dose melphalan. Mixed emotions as children left in tears yesterday but doing my best to keep thinking positive thoughts. Jacqui x</p>
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				<title>JacquiReeks replied to the topic Hello to All in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-to-all#post-85663</link>
				<pubDate>Thu, 03 May 2012 21:53:28 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Ali<br />
My harvesting was a breeze.  No problems at all and they got everything they needed and more 🙂</p>
<p>My Children are just 18 and 12. They both started their own new journeys in September last year, just before my diagnosis in November.  The eldest started university and the youngest started secondary school. </p>
<p>I was immediately admitted&hellip;<span class="activity-read-more" id="activity-read-more-4432"><a href="http://www.myeloma.org.uk/forums/topic/hello-to-all#post-85663" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks replied to the topic Hello to All in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-to-all#post-85660</link>
				<pubDate>Tue, 01 May 2012 22:11:03 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi again. I can see i will have to get used to understanding how the threads work.  I have now managed to find your original post and i see that your mum has been on treatment so I apologise for my question about it.<br />
Jacqui x</p>
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				<title>JacquiReeks replied to the topic Hello to All in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-to-all#post-85659</link>
				<pubDate>Tue, 01 May 2012 22:03:03 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Alison. Not entirely sure how the replying system works but hopefully you can see my updated news which gives my treatment regimen.  Please ask if you want more details such as dosage etc. Has your mum started treatment yet?</p>
<p>Jacqui</p>
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				<title>JacquiReeks replied to the topic Hello to All in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-to-all#post-85653</link>
				<pubDate>Tue, 01 May 2012 21:56:20 +0100</pubDate>

									<content:encoded><![CDATA[<p>Many thanks to all of you for the warm welcome. I am afraid all the terminology is still quite new to me but I will attempt to tell you where I am with my journey.<br />
I was diagnosed with stage 2 IgA MM and multiple lytic lesions.  I had been limping around all summer having been told I had mild osteo-arthritis.  In fact, I had a fractured hip which&hellip;<span class="activity-read-more" id="activity-read-more-4422"><a href="http://www.myeloma.org.uk/forums/topic/hello-to-all#post-85653" rel="nofollow">[Read more]</a></span></p>
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				<title>JacquiReeks started the topic Hello to All. in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-to-all</link>
				<pubDate>Mon, 30 Apr 2012 18:51:39 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Everyone 🙂 I am new to the forum and i am afraid I don&#039;t really have anything specific to say at the moment but just wanted to introduce myself. I am a 52 year old mother of 2 beautiful girls and was diagnosed with MM in November 2011.</p>
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