<?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 | chrismac67 | Activity</title>
	<link>https://forum.myeloma.org.uk/members/chrismac67/activity/</link>
	<atom:link href="https://forum.myeloma.org.uk/members/chrismac67/activity/feed/" rel="self" type="application/rss+xml" />
	<description>Activity feed for chrismac67.</description>
	<lastBuildDate>Wed, 22 Apr 2026 01:10:54 +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">a862c8bbe63de0585521cda78295e555</guid>
				<title>chrismac67 replied to the topic life after the transplant  in the forum Under 50s</title>
				<link>http://www.myeloma.org.uk/forums/topic/life-after-the-transplant/page/2/#post-127099</link>
				<pubDate>Fri, 04 Mar 2016 14:35:53 +0000</pubDate>

									<content:encoded><![CDATA[<p>Wow I could have written this post myself.  I had my SCT Oct 2015 and am having weekly blood tests as Paraproteins still traceable. So far they remain stable but each month when I go to clinic for zometa and pentamidine, I dread the appointment with consultant in case I&#8217;m told the Paraproteins are rising, despite being on maintenance treatment.&hellip;<span class="activity-read-more" id="activity-read-more-43817"><a href="http://www.myeloma.org.uk/forums/topic/life-after-the-transplant/page/2/#post-127099" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">e68cbe1f2001132a0120ea955de9d600</guid>
				<title>chrismac67 replied to the topic Starting Stem Cell Therapy in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/starting-stem-cell-therapy/#post-124244</link>
				<pubDate>Fri, 18 Sep 2015 13:33:31 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi everyone. I was diagnosed in February this year following a surgical procedure after which I had kidney problems. PPs down to 14 from 87 and I&#8217;m due to start SCT 28th September.  I&#8217;m not looking forward to it, most anxious I&#8217;ve felt about anything since diagnosis. It is reassuring to read other people&#8217;s experiences. I am a 48 year old mother&hellip;<span class="activity-read-more" id="activity-read-more-41000"><a href="http://www.myeloma.org.uk/forums/topic/starting-stem-cell-therapy/#post-124244" rel="nofollow">[Read more]</a></span></p>
]]></content:encoded>
				
				
							</item>
					<item>
				<guid isPermaLink="false">2e0ceb507c11e09689f0f9f32e912384</guid>
				<title>chrismac67 became a registered member</title>
				<link>https://forum.myeloma.org.uk/activity/p/38926/</link>
				<pubDate>Sun, 10 May 2015 18:48:06 +0100</pubDate>

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