<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>Myeloma Forum | KAYNEVILL | Activity</title>
	<link>https://forum.myeloma.org.uk/members/kaychappers/activity/</link>
	<atom:link href="https://forum.myeloma.org.uk/members/kaychappers/activity/feed/" rel="self" type="application/rss+xml" />
	<description>Activity feed for KAYNEVILL.</description>
	<lastBuildDate>Sun, 05 Apr 2026 15:01:06 +0100</lastBuildDate>
	<generator>https://buddypress.org/?v=2.9.4</generator>
	<language>en-GB</language>
	<ttl>30</ttl>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>2</sy:updateFrequency>
	
						<item>
				<guid isPermaLink="false">48eb81e49086faebf39bcd30eed8f415</guid>
				<title>kaychappers changed their profile picture</title>
				<link>https://forum.myeloma.org.uk/activity/p/39120/</link>
				<pubDate>Sun, 24 May 2015 07:39:50 +0100</pubDate>

				
									<slash:comments>0</slash:comments>
				
							</item>
					<item>
				<guid isPermaLink="false">80eb8f98d9b6e70a47c1d889cb4e8048</guid>
				<title>kaychappers changed their profile picture</title>
				<link>https://forum.myeloma.org.uk/activity/p/39119/</link>
				<pubDate>Sun, 24 May 2015 07:34:01 +0100</pubDate>

				
									<slash:comments>0</slash:comments>
				
							</item>
					<item>
				<guid isPermaLink="false">2480da1518978313e2c30266bb18deae</guid>
				<title>KAYNEVILL started the topic Low Blood Counts after SCT in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/low-blood-counts-after-sct/</link>
				<pubDate>Sun, 24 May 2015 07:31:37 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi everyone<br />
I have not been on this site for a long time but keep up with what is going on. I had my second SCT in October 2014 after relapsing after 18 months. My problem is low blood counts still. My platelets now seem to be stabalising around 26 my neutrophils are at 1 so I have one injection a week and my Hb goes down to just below 9. I had&hellip;<span class="activity-read-more" id="activity-read-more-39118"><a href="http://www.myeloma.org.uk/forums/topic/low-blood-counts-after-sct/" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">71a06658d7bcd560dd52cbce912306e1</guid>
				<title>KAYNEVILL replied to the topic Getting to the scary bit now!! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/getting-to-the-scary-bit-now/page/2/#post-122246</link>
				<pubDate>Sun, 24 May 2015 07:24:16 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Mandy<br />
I&#8217;m really sorry I don&#8217;t think my post posted last week. Yes I am local in Brentwood.. Please feel free to email me. I&#8217;m not sure how privacy works. It would be nice to chat. It&#8217;s not an illness that you hear about much so at times you can feel lonely with your own thoughts.</p>
<p>Kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">c16b0fe380f2688a49da5b2a24fe187c</guid>
				<title>KAYNEVILL replied to the topic Getting to the scary bit now!! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/getting-to-the-scary-bit-now/page/2/#post-122175</link>
				<pubDate>Mon, 18 May 2015 21:47:11 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi cupcake<br />
I have not been on this forum for a few years and I believe I was meant to come on here tonight and read your posts. I was diagnosed with smouldering myeloma in 2009 at the age of 44 at Queens. I had treatment in 2011 followed by SCT then more treatment in 2014 and my 2nd SCT in 2014 both in Barts. I was at Barts today and my PP is 11&hellip;<span class="activity-read-more" id="activity-read-more-39033"><a href="http://www.myeloma.org.uk/forums/topic/getting-to-the-scary-bit-now/page/2/#post-122175" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">d7f9eaf18526fee7243c65f45b8669f3</guid>
				<title>KAYNEVILL replied to the topic Phil&#039;s SCT Journey in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/phils-sct-journey/page/4/#post-101295</link>
				<pubDate>Sun, 30 Dec 2012 10:39:27 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Megan and Phil. I was on Bodley Scott Ward but started on A4 absolutely no difference so Phil is not missing out on anything. Infact the ward in A4 is nicer as on BS ward you are lined up in cubicles but the isolation rooms are the same. So pleased he no longer has the IV once they put the stem cells back in me they came in 11 days later and&hellip;<span class="activity-read-more" id="activity-read-more-17847"><a href="http://www.myeloma.org.uk/forums/topic/phils-sct-journey/page/4/#post-101295" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">803ddaac5f861589a6d304f149dc0d5d</guid>
				<title>KAYNEVILL replied to the topic Phil&#039;s SCT Journey in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/phils-sct-journey/page/4/#post-101288</link>
				<pubDate>Fri, 28 Dec 2012 23:29:33 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Megan. I have not posted on this site for a while (which I feel bad about as it is so supportive). I have been reading your daily diary regarding Phil&#039;s SCT. I had mine in Barts in sept 2011. I was put in an isolation room after a few days, only because there were so many men that they could not have men and women together on the transplant&hellip;<span class="activity-read-more" id="activity-read-more-17840"><a href="http://www.myeloma.org.uk/forums/topic/phils-sct-journey/page/4/#post-101288" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">679af69992d65f974149b9c5dcb577b8</guid>
				<title>KAYNEVILL replied to the topic The Under 50s Group in the forum Under 50s</title>
				<link>http://www.myeloma.org.uk/forums/topic/the-under-50s-group/page/2/#post-106767</link>
				<pubDate>Sun, 18 Nov 2012 20:37:56 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Karen<br />
Just got your email that came straight through to my personal email which I was pleased about or I would not have seen it. I had CDT 5 cycles then Revlimid for 4 cycles. I then had my stem cell transplant in September 2011 so I am now post one year. I am now stable although my PPs like to have little blips every now and then which&hellip;<span class="activity-read-more" id="activity-read-more-21902"><a href="http://www.myeloma.org.uk/forums/topic/the-under-50s-group/page/2/#post-106767" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">f998aebff1c7188d8a9ba3f918c53ce9</guid>
				<title>KAYNEVILL replied to the topic FAILED SCT I THINK!!!! in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/failed-sct-i-think/page/2/#post-98629</link>
				<pubDate>Sun, 14 Oct 2012 09:18:45 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Dawn<br />
Not been on site for a long time, so thank you for bringing me back. Life goes on Im pleased to say. My PP fluctuate between 18 and 22. I went back to Barts on Monday and had what I hope now is my yearly visit. I have blood tests once a month at my local hospital and hope that it will go to two months now. My consultant said she will not&hellip;<span class="activity-read-more" id="activity-read-more-15191"><a href="http://www.myeloma.org.uk/forums/topic/failed-sct-i-think/page/2/#post-98629" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">1adf09c4bffad3f90e08dda36a6e9198</guid>
				<title>KAYNEVILL 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-86097</link>
				<pubDate>Tue, 29 May 2012 17:39:43 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Antoinette<br />
Like the others say there is life beyond MM but there is a journey to go through. I was diagnosed in 2009 when I was 45. I was smouldering for 18 months then became anemic too, but with no other symptoms. I have gone through the chemo and stem cell transplant in Barts (who were amazing) and am now on the other side. Everyone is&hellip;<span class="activity-read-more" id="activity-read-more-4866"><a href="http://www.myeloma.org.uk/forums/topic/newly-diagnosed-monday-at-only-39/page/2/#post-86097" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">18691fefe861fe1388690ba511bbde95</guid>
				<title>KAYNEVILL replied to the topic The Under 50s Group in the forum Under 50s</title>
				<link>http://www.myeloma.org.uk/forums/topic/the-under-50s-group#post-106764</link>
				<pubDate>Mon, 28 May 2012 22:38:06 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Karen<br />
Your posting got mixed up in the dates.  So sorry you have to join us but this is a wonderful site for help, support, understanding and encouragement. I&#039;m on the other side of treatment now. It was not a walk in the park but it&#039;s certainly manageable. It sounds like they have caught yours early as they did with me. It is a complete&hellip;<span class="activity-read-more" id="activity-read-more-21899"><a href="http://www.myeloma.org.uk/forums/topic/the-under-50s-group#post-106764" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">6ca114fca5277b42bf40f4a69d9f2721</guid>
				<title>KAYNEVILL replied to the topic Joint pain in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/joint-pain#post-104426</link>
				<pubDate>Sat, 21 Apr 2012 20:33:38 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Mavis. Feeling much better after slowing down. Getting plenty of rest. My body kicks me when I&#039;m over doing it.  Good for you with your positive attitude. I need small goals to keep me going. Rushed them first of all but getting balance now. Just had monthly blood test back and all stable. Love kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">b6f552e59a8f877beb82a052e3bf46e7</guid>
				<title>KAYNEVILL replied to the topic bereavment in the forum End of Life and Grief</title>
				<link>http://www.myeloma.org.uk/forums/topic/bereavment#post-107569</link>
				<pubDate>Thu, 19 Apr 2012 09:19:14 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Stephen. So sorry to hear your loss. Not as articulate as the others but wanted to say my thoughts and prayers are with you and your children. Day at a time stuff.  kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">f9bddc42d1716bea742966057216e198</guid>
				<title>KAYNEVILL replied to the topic coughs, colds and the like in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/coughs-colds-and-the-like#post-104459</link>
				<pubDate>Thu, 19 Apr 2012 09:12:30 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi David. My thing is sore throats. Get them regularly but clear up after couple of days. Scared me the first time but when it went, like everyone else said, it proved my body can fight infection or viruses sooooo grateful. Glad u got your plumbing sorted 🙂  kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">30ad88a6e1beb86f5c2f1f78fdfd5ed8</guid>
				<title>KAYNEVILL replied to the topic Joint pain in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/joint-pain#post-104424</link>
				<pubDate>Thu, 19 Apr 2012 09:07:25 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thanks to everyone. Have slowed down a lot and feeling much better. Joints still painful but I have acceptance now.  Wishing you all well kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">c06a6e2e7188e0b01cb99bd316c116e0</guid>
				<title>KAYNEVILL replied to the topic Newcomer... in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/newcomer1334519210/page/3/#post-85810</link>
				<pubDate>Thu, 19 Apr 2012 09:01:25 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi tony lovely to meet you. I too was on trial. SCT last September and doing well. Keep in touch with the people here. They will either have been through or going through similar stuff and are supportive and knowledgeable of this illness. Good luck  one day at a time kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">67779bdc5a8555488b2f57a2760fafd7</guid>
				<title>KAYNEVILL replied to the topic Joint pain in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/joint-pain#post-104418</link>
				<pubDate>Wed, 04 Apr 2012 17:35:35 +0100</pubDate>

									<content:encoded><![CDATA[<p>Ha ha 🙂  thanks Dai. I feel like I have been well told off. I needed it too. Think I am still in denial that I even had myeloma and the treatment. But as they say &quot;denial is not a river in Egypt&quot;. It&#039;s a powerful feeling. Will take note and slow down. Think I just needed reassurance that I was not imagining my tiredness. Thanks Tom for your&hellip;<span class="activity-read-more" id="activity-read-more-19955"><a href="http://www.myeloma.org.uk/forums/topic/joint-pain#post-104418" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">53c3eb0af0a0bd2dbef779c249ef15fb</guid>
				<title>KAYNEVILL started the topic Joint pain. in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/joint-pain</link>
				<pubDate>Wed, 04 Apr 2012 07:33:33 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi everyone. Has anyone suffered joint pain following SCT. First they thought it was peripheral neuropathy and put me on amyolotryptilin (can&#039;t spell it) then gabapentin then cocodamol but nothing stopped the pain. I was sent to rheumatologist had pet scan nothing (which I&#039;m grateful  for). Consultant then put me on 30mg peredisone steroids which&hellip;<span class="activity-read-more" id="activity-read-more-19951"><a href="http://www.myeloma.org.uk/forums/topic/joint-pain" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">f35e7190b6332f35717719d073b56431</guid>
				<title>KAYNEVILL replied to the topic SCT completed in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/sct-completed#post-99104</link>
				<pubDate>Wed, 04 Apr 2012 07:21:33 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Sarah so pleased Henry is home. Patience is the key. Rest when his body tells him too. Eat when he wants. I found little and often was better. Wish you and Henry best wishes. Love kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">988a9bb7b8157b620b0457dca1427ed8</guid>
				<title>KAYNEVILL replied to the topic Another 3 months in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/another-3-months1333128671#post-92409</link>
				<pubDate>Mon, 02 Apr 2012 21:11:05 +0100</pubDate>

									<content:encoded><![CDATA[<p>What fantastic news David. Keep up the good work. Best wishes kay</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">fae97314a3e11b4f7a4ef323ccae39af</guid>
				<title>KAYNEVILL replied to the topic Will anything work? in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/will-anything-work/page/2/#post-99085</link>
				<pubDate>Mon, 02 Apr 2012 21:09:21 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Andy. Can&#039;t help out on the alcohol as I don&#039;t drink. But on the pp level I went down from 38 to 20 on CDT then plateaued. I went in for harvest   After first day of harvest consultant came round to say pp had gone back to 34 in 3 weeks and sent me home to be put on velcade. Plateaued again at 18 but they put stem cells they had collected at 34&hellip;<span class="activity-read-more" id="activity-read-more-15644"><a href="http://www.myeloma.org.uk/forums/topic/will-anything-work/page/2/#post-99085" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">9fca57733ccdef17ae189a69267dd9d4</guid>
				<title>KAYNEVILL replied to the topic Another newcomer in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/another-newcomer1333394144#post-85732</link>
				<pubDate>Mon, 02 Apr 2012 20:49:39 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi suzie sorry u have to join the happy bunch here but that is what they are and very supportive. I went to my doctor with tiredness and was sent to a haematologist soon after as my para proteins were 37. But I had no calcium or anaemia. My bone marrow was 13% I was told anything above 10% without other symptoms was called asymptomatic or&hellip;<span class="activity-read-more" id="activity-read-more-4501"><a href="http://www.myeloma.org.uk/forums/topic/another-newcomer1333394144#post-85732" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">4e2f6d0ce14a50c513e11f487b980420</guid>
				<title>KAYNEVILL replied to the topic HERE WE GO AGAIN !! in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/here-we-go-again-/page/4/#post-98804</link>
				<pubDate>Tue, 06 Mar 2012 08:55:30 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Bridget just been reading all your posts. Like everyone I can&#039;t find the words but wanted to let u know I am thinking of you and will be praying that they find something that will help you. You are so positive and an inspiration to us all. You are always their with a kind word for others. Keep that positive attitude. Day at a time Love kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">36470a679e194f7d21fc044f57144a52</guid>
				<title>KAYNEVILL replied to the topic Starting CDT in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/starting-cdt#post-98923</link>
				<pubDate>Tue, 06 Mar 2012 08:44:04 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Mavis I was on CDT and thalidomide gave me lovely night sleeps. Dex kept me awake and made me irritable when I came off them each time. But all in all I still continued to work 4days a week. I injected myself each day and I found it was ok but I agree with others don&#039;t do it if u don&#039;t feel comfortable with it. All the best kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">0e16a5179d9c058f48a0b3d1b04366b2</guid>
				<title>KAYNEVILL replied to the topic What is stem cell transplant really like? in the forum Under 50s</title>
				<link>http://www.myeloma.org.uk/forums/topic/what-is-stem-cell-transplant-really-like#post-106960</link>
				<pubDate>Tue, 06 Mar 2012 08:32:54 +0000</pubDate>

									<content:encoded><![CDATA[<p>Everyone is different. It will be up to your consultant. But whatever they say they know what they are doing and it will be for the best. Have another chat with them and ask the question. I just wrote down questions as they popped into my head. There is light at the end of the tunnel now. Best wishes kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">487529c2bd089ff199e728fa9c6e190c</guid>
				<title>KAYNEVILL replied to the topic What is stem cell transplant really like? in the forum Under 50s</title>
				<link>http://www.myeloma.org.uk/forums/topic/what-is-stem-cell-transplant-really-like#post-106958</link>
				<pubDate>Wed, 29 Feb 2012 08:28:38 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi penny how did it go yesterday. Any date for SCT. I was also a lucky one. They kept telling me I was boring 🙂  no infection, one bout of diarrhoea, one bout of sickness and home in two weeks. I was also quite fit when I went in and 46 years old. I think it helps. Good luck and keep in touch  kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">a7d938a241620af5336611b00baee3a0</guid>
				<title>KAYNEVILL replied to the topic Joined the forum @ 1:00am. in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/joined-the-forum-100am#post-85591</link>
				<pubDate>Wed, 29 Feb 2012 08:03:01 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Andy good luck with your journey. It is an emotional roller coaster. But as It was said to me &quot;it&#039;s not a walk in the park but you will get through it&quot; and like others I did with the help and support of this site. People here have either been through it, are going through it or will be going to go through it. So stay close x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">502027311cf794d9dbceb340f7f1d23a</guid>
				<title>KAYNEVILL replied to the topic Treatment Free :-) in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/treatment-free-/page/2/#post-98896</link>
				<pubDate>Tue, 28 Feb 2012 16:54:49 +0000</pubDate>

									<content:encoded><![CDATA[<p>Such great news Tom.  It will keep me going, positive and strong. Kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">c1f3b66db4c167ad0c0a6d7aa6c65560</guid>
				<title>KAYNEVILL replied to the topic Starting stem cell harvest next Monday. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/starting-stem-cell-harvest-next-monday/page/2/#post-92192</link>
				<pubDate>Wed, 22 Feb 2012 08:57:47 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi terry. It is a shame they did not tell u about two day stint. Me and my friend stayed in the hostel over the road free of charge and it was really nice. They wanted 8 million from me for two transplants but got 4 which was enough for one transplant.  I am at barts for last time on 19th march. Would be happy to pop in and say hello if u wish.&hellip;<span class="activity-read-more" id="activity-read-more-10083"><a href="http://www.myeloma.org.uk/forums/topic/starting-stem-cell-harvest-next-monday/page/2/#post-92192" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">bedaf214d5c5b4a3eaaeb210ce60509c</guid>
				<title>KAYNEVILL replied to the topic Starting stem cell harvest next Monday. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/starting-stem-cell-harvest-next-monday#post-92190</link>
				<pubDate>Tue, 21 Feb 2012 11:52:58 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi terry I&#039;m assuming u had your harvest yesterday. Hope all went well. I was in barts too and they are fantastic. I was one of the lucky ones who breezed thru it. One bout of diarrhoea, one bout of sickness and no infection. They kept telling me I was boring:-)  but even if you do have any side affects they are constantly monitoring you and give&hellip;<span class="activity-read-more" id="activity-read-more-10081"><a href="http://www.myeloma.org.uk/forums/topic/starting-stem-cell-harvest-next-monday#post-92190" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">b695d159851a0fddb0c87cd610824946</guid>
				<title>KAYNEVILL replied to the topic My mum was diagnosed with MM in December 2011 in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-mum-was-diagnosed-with-mm-in-december-2011#post-85491</link>
				<pubDate>Sun, 22 Jan 2012 20:02:43 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Mandy so sorry to hear about your mums pain and also that she has this horrible illness.  Treatment affects people differently, but I can understand her frustration with the PN. I was extremely active before treatment and now I have finished the only thing that is still with me is PN. Gabepentin is what I am on. It takes time to build up in the&hellip;<span class="activity-read-more" id="activity-read-more-4260"><a href="http://www.myeloma.org.uk/forums/topic/my-mum-was-diagnosed-with-mm-in-december-2011#post-85491" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">9d52eaf2df66be260e9c619cf18db6b2</guid>
				<title>KAYNEVILL replied to the topic FAILED SCT I THINK!!!! in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/failed-sct-i-think/page/2/#post-98624</link>
				<pubDate>Sat, 14 Jan 2012 15:19:54 +0000</pubDate>

									<content:encoded><![CDATA[<p>Oh well saw Rheumatologist. He does not think it is arthritis. Did loads of blood tests. Maybe gout!!!!! oh great on top of MM I have pain in every joint of my body now. Prescribed co codomol for pain until blood tests back. Dont want me to have anti inflamatories because may cause kidney problems.  Saw that Bonefos can cause joint pain. Maybe&hellip;<span class="activity-read-more" id="activity-read-more-15186"><a href="http://www.myeloma.org.uk/forums/topic/failed-sct-i-think/page/2/#post-98624" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">35c06cc53672f988d0fb578e59f53431</guid>
				<title>KAYNEVILL replied to the topic Newly diagnosed and unable to swallow Thalidamide Capsules in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/newly-diagnosed-and-unable-to-swallow-thalidamide-capsules#post-98695</link>
				<pubDate>Sat, 14 Jan 2012 15:03:24 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Mandy.  Your poor friend. Firstly to find out she has Myeloma and then having difficulty in swallowing the medication which is ment to help her.  I think Anne&#039;s suggestion of contacting Ellen on the Myeloma infoline is a way forward. Your friend&#039;s problem must have come up before. Wishing you both all the best. Kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">72dc9373198c7285b5cb762de382ee72</guid>
				<title>KAYNEVILL replied to the topic Is it back? in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/is-it-back#post-92009</link>
				<pubDate>Fri, 13 Jan 2012 17:42:23 +0000</pubDate>

									<content:encoded><![CDATA[<p>It will be a tough few days, but for me the waiting is the worst. Once you know what is happening at least you can start to deal with it. HB is haemoglobin which makes the red blood cells which carry oxygen around the body.  It fell and I was exhausted. My consultant said &#039;it proves to me you cannot make healthy blood and we have to start&hellip;<span class="activity-read-more" id="activity-read-more-9900"><a href="http://www.myeloma.org.uk/forums/topic/is-it-back#post-92009" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">a83df02000799d8e73e4088a1196cc55</guid>
				<title>KAYNEVILL replied to the topic FAILED SCT I THINK!!!! in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/failed-sct-i-think/page/2/#post-98622</link>
				<pubDate>Thu, 12 Jan 2012 10:06:12 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi everyone.  Just wanted to let you know I saw my consultant Monday and it all looked grim. She said my SCT was a disappointment. My last 3 PP results were 16, 18 and 22.  Good news was she believed my bone/joint pain was rheumatoid arthritis and she wanted to get that under control as I am in so much pain, but she did not have the results of the&hellip;<span class="activity-read-more" id="activity-read-more-15184"><a href="http://www.myeloma.org.uk/forums/topic/failed-sct-i-think/page/2/#post-98622" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">cccc8d5589f26636fa9bb390746b59bc</guid>
				<title>KAYNEVILL replied to the topic Remission?  What remission? in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/remission-what-remission#post-98682</link>
				<pubDate>Thu, 12 Jan 2012 09:53:13 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Dai I do wish you all the very best.  When I was speaking to my consultant on Monday she was telling me about a new trial (did not take in the name) and she was so excited about it. It gave me hope that if I did need it I was more than happy to try it. Do let us know what you are randomised too. Kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">f5f32de7810255930370f922ba761982</guid>
				<title>KAYNEVILL replied to the topic Is it back? in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/is-it-back#post-92007</link>
				<pubDate>Thu, 12 Jan 2012 09:44:55 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Amelie I had my SCT in September and my PP has risen for the last 3 blood tests, but my consultant said she is not worried due to my HB rising consistently. When I had to have treatment it was because I became anaemic and that is what they will look for rather than rising PP. Myeloma is so so different for everybody. I do wish you both all the&hellip;<span class="activity-read-more" id="activity-read-more-9898"><a href="http://www.myeloma.org.uk/forums/topic/is-it-back#post-92007" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">9029bd52fd0eb1e7b9875c81dba8bd35</guid>
				<title>KAYNEVILL replied to the topic REMISSION. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/remission#post-91971</link>
				<pubDate>Sat, 07 Jan 2012 15:03:04 +0000</pubDate>

									<content:encoded><![CDATA[<p>What fantastic news for you both.  Enjoy hearing the positive side of this illness.  I had SCT in September and came through it really well. Out in two weeks and now I am back to work.  Love Kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">019a3b4a467551378caf7a88ef2ea0ff</guid>
				<title>KAYNEVILL replied to the topic FAILED SCT I THINK!!!! in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/failed-sct-i-think#post-98619</link>
				<pubDate>Fri, 06 Jan 2012 17:08:08 +0000</pubDate>

									<content:encoded><![CDATA[<p>Thank you all so much for your replies.  Lorraine you have given me a lot of hope. Scan went ok. I believe they are thinking about putting me on revlimid but we shall see on Monday love Kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">1481706f257844aea58981e57d9caf1c</guid>
				<title>KAYNEVILL replied to the topic FAILED SCT I THINK!!!! in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/failed-sct-i-think#post-98611</link>
				<pubDate>Wed, 04 Jan 2012 16:13:33 +0000</pubDate>

									<content:encoded><![CDATA[<p>Thank you all for your lovely replies and thoughts.  What a pain Myeloma is. So great to have the support to share with. Kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">d77757833942ce76eb474c45d3ffaf3b</guid>
				<title>KAYNEVILL replied to the topic How do you start to say good bye?? in the forum End of Life and Grief</title>
				<link>http://www.myeloma.org.uk/forums/topic/how-do-you-start-to-say-good-bye#post-107381</link>
				<pubDate>Tue, 03 Jan 2012 16:51:47 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Michelle I am so sorry that you and your husband are at the stage that you are especially the young age that he is as well (although whatever age this terrible disease does not care and is hard and awful for all concerned). I agree with the others, always make sure you say how much you love the person and try to keep positive.  There are other&hellip;<span class="activity-read-more" id="activity-read-more-22438"><a href="http://www.myeloma.org.uk/forums/topic/how-do-you-start-to-say-good-bye#post-107381" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">bdc4d95072b6925511242c9b13f53214</guid>
				<title>KAYNEVILL started the topic FAILED SCT I THINK!!!!. in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/failed-sct-i-think</link>
				<pubDate>Tue, 03 Jan 2012 14:59:33 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Everyone<br />
I hope you had a good Christmas and a Happy and healthy new year. I had my stem cell transplant in September. Unfortunately, my para proteins have gone from 16, 18 and 22.  I go back to hospital Friday for CT pet scan to see if there is any bone disease and then consultant on Monday to see where we go from here.  My bones ache and&hellip;<span class="activity-read-more" id="activity-read-more-15169"><a href="http://www.myeloma.org.uk/forums/topic/failed-sct-i-think" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">016568667c59d66e1e868f472fff43c6</guid>
				<title>KAYNEVILL replied to the topic Painful Bones in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/painful-bones#post-104280</link>
				<pubDate>Tue, 25 Oct 2011 19:19:15 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thank you all so much for your replies. I think the answer is BE PATIENT and just do as much as my body will allow.<br />
Best wishes Kay</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">a678e14df6b21eadbb2f0dd53c3b1ca8</guid>
				<title>KAYNEVILL replied to the topic Painful Bones in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/painful-bones#post-104277</link>
				<pubDate>Mon, 24 Oct 2011 20:11:36 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thanks Min and Wendy. Paracetemol seem to help. I also have been told my feet hurt due to the velcade, I only hope it does wear off. I think I just want to feel better yesterday, even though the consultant told me it will be 3-6 months. Patience has never been my strong point. Sorry to hear you are going through the same Wendy, but nice to know it&hellip;<span class="activity-read-more" id="activity-read-more-19814"><a href="http://www.myeloma.org.uk/forums/topic/painful-bones#post-104277" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">08fd287cb92c799046218555d7ec33d3</guid>
				<title>KAYNEVILL replied to the topic New and need advice on Myeloma XI in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/new-and-need-advice-on-myeloma-xi#post-85222</link>
				<pubDate>Mon, 24 Oct 2011 20:02:14 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Jim sorry you have to come here, but the people here offer lots of support.  I was 44 and extremely fit too.  I was completely shocked, but I think we are going to here more and more younger people being diagnosed as they can pick it up earlier and that I am so pleased about. I was on the XI trial. There are lots of pills to take, but you soon&hellip;<span class="activity-read-more" id="activity-read-more-3992"><a href="http://www.myeloma.org.uk/forums/topic/new-and-need-advice-on-myeloma-xi#post-85222" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">a6b0990ee85eca3a848df7218f16aa1c</guid>
				<title>KAYNEVILL started the topic Painful Bones. in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/painful-bones</link>
				<pubDate>Sun, 23 Oct 2011 14:36:17 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi everyone not been on the site for soooooo long, but been reading a lot on here and found it so useful as always.  Been in hospital having SCT.  Was very lucky with side effects. One bout of sickness, one bout of diarrhea and in and out of hospital in two weeks. I identify with the hot flushes and PN which has been posted. I have just been put&hellip;<span class="activity-read-more" id="activity-read-more-19811"><a href="http://www.myeloma.org.uk/forums/topic/painful-bones" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">6d3756bffe91f8556d103202ea48cd31</guid>
				<title>KAYNEVILL replied to the topic Allopurinol allergy in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/allopurinol-allergy#post-104271</link>
				<pubDate>Sun, 23 Oct 2011 14:21:29 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Peggy so sorry to hear about what has happened and I sincerely hope that you are on the mend.  I also had an allergy to allopurinol and ended up in hospital with the rash from neck to toes and shivery.  They pumped antibiotics into me and sent me home with lots of antibiotics which thankfully cleared it up.  My best wishes to you.<br />
Kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">c66eafc148fb4a508bf675a00e637fdd</guid>
				<title>KAYNEVILL replied to the topic I Told You I Was Ill... in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/i-told-you-i-was-ill#post-97797</link>
				<pubDate>Sat, 16 Jul 2011 12:37:23 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Dai<br />
In a positive way its good there was a reason for you being so down, but it must have been pretty rough for you with the needles. So glad they got you sorted.  Everything crossed for good news on Monday.<br />
Kay x</p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">930d7dc674f1b5d0c1ea6049d76d4b02</guid>
				<title>KAYNEVILL replied to the topic Weight Gain in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/weight-gain#post-104035</link>
				<pubDate>Sat, 16 Jul 2011 12:31:46 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Gill<br />
I have put on 2 and half stone in weight and gone from a size 8 to a size 14-16 (closer to the 16 :-)) I was on CDT now on Velcade. I found it hard putting on the weight in the beginning, now I am going with the flow. Its going to be the only time I can eat what I want so I am going to enjoy it. I know it will come off once I have my SCT&hellip;<span class="activity-read-more" id="activity-read-more-19572"><a href="http://www.myeloma.org.uk/forums/topic/weight-gain#post-104035" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">b040853c2023422dbe6b17e7fdeaf2e4</guid>
				<title>KAYNEVILL replied to the topic Confused in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/confused#post-84727</link>
				<pubDate>Sun, 10 Jul 2011 17:41:10 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Claire<br />
I was diagnosed in 2009 and only started treatment this year. It was a watch and wait for me too. I was monitored with blood checks and my consultant said that the treatment would make me more poorly than the disease at that stage. They can tell so much from blood tests and intervene before you get, as the others have said, the bone&hellip;<span class="activity-read-more" id="activity-read-more-3499"><a href="http://www.myeloma.org.uk/forums/topic/confused#post-84727" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
		
	</channel>
</rss>