<?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 | sueharley | Activity</title>
	<link>https://forum.myeloma.org.uk/members/sueharley/activity/</link>
	<atom:link href="https://forum.myeloma.org.uk/members/sueharley/activity/feed/" rel="self" type="application/rss+xml" />
	<description>Activity feed for sueharley.</description>
	<lastBuildDate>Sat, 11 Apr 2026 23:27:57 +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">66e5a57a3607fa428bf6c4bcca6ee220</guid>
				<title>sueharley posted an update: Hi, I have just returned from a clinic appointment where I [&#133;]</title>
				<link>https://forum.myeloma.org.uk/activity/p/53605/</link>
				<pubDate>Thu, 23 Aug 2018 14:19:12 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi, I have just returned from a clinic appointment where I have found out that I am no longer in remission (after only 5 months) as my light chains are going up. They are 200 at the moment. My consultant is now suggesting a double SCT as my Myeloma now counts as aggresive. I was wondering if anyone else has any experience of this and what the&hellip;<span class="activity-read-more" id="activity-read-more-53605"><a href="https://forum.myeloma.org.uk/activity/p/53605/" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
									<slash:comments>0</slash:comments>
				
							</item>
					<item>
				<guid isPermaLink="false">7f2a1770280aa3323b474f2f303f69e4</guid>
				<title>sueharley replied to the topic Lenalidomide from India in the forum Treatment</title>
				<link>https://www.myeloma.org.uk/forums/topic/lenalidomide-from-india/#post-137412</link>
				<pubDate>Sat, 17 Mar 2018 15:43:21 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Sara,</p>
<p>Revlimid (Lenalidomide) is not available on NHS as a maintenance chemo in England,  although I think it is possible to get it on relapse. Was your mum was part of the Myeloma XI trial? If patients received Revlimid as part of the trial I believe they are entitled to have it funded by the NHS for maintenance. Also the rules in Wales and&hellip;<span class="activity-read-more" id="activity-read-more-52720"><a href="https://www.myeloma.org.uk/forums/topic/lenalidomide-from-india/#post-137412" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">d52af0c4d300f46aabf583d835b7c091</guid>
				<title>sueharley started the topic Lenalidomide from India in the forum Treatment</title>
				<link>https://www.myeloma.org.uk/forums/topic/lenalidomide-from-india/</link>
				<pubDate>Thu, 15 Mar 2018 18:22:23 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Everyone,</p>
<p>I am planning to visit India to get Lenalidomide (Revlimid) as a maintenance chemo. I have already found a hospital and a haemotologist who is happy to see me and prescribe 6 months of Lenalidomide. My question is, has anyone else gone down this route and were there any problems bringing medication back into the UK? Also can I travel&hellip;<span class="activity-read-more" id="activity-read-more-52701"><a href="https://www.myeloma.org.uk/forums/topic/lenalidomide-from-india/" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">7f714a1b80c8c3fad3b8ecb2a66a53eb</guid>
				<title>sueharley became a registered member</title>
				<link>https://forum.myeloma.org.uk/activity/p/52461/</link>
				<pubDate>Tue, 20 Feb 2018 11:47:01 +0000</pubDate>

				
									<slash:comments>0</slash:comments>
				
							</item>
		
	</channel>
</rss>