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	<title>Myeloma Forum | sandra | Activity</title>
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				<title>sandra replied to the topic TABLETOP SALE &#38; COFFEE MORNING FOR MMUK in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/tabletop-sale-coffee-morning-for-mmuk#post-91513</link>
				<pubDate>Mon, 12 Dec 2011 17:14:33 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Sarah I wish I had logged on earlier and read your post I would have come along as I am in Westham !! I had a coffee morning at my house on the 19th November raising £430 . I have had mm for 4 years , am 46 and have 2 teenage kids , I am still working and carrying on pretty normally after a stem cell transplant in 08 and one pending for 2012&hellip;<span class="activity-read-more" id="activity-read-more-9415"><a href="http://www.myeloma.org.uk/forums/topic/tabletop-sale-coffee-morning-for-mmuk#post-91513" rel="nofollow">[Read more]</a></span></p>
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				<title>sandra replied to the topic Just a query on Allo transplants in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/just-a-query-on-allo-transplants#post-90031</link>
				<pubDate>Tue, 29 Mar 2011 16:13:23 +0100</pubDate>

									<content:encoded><![CDATA[<p>As usual gang a very mixed bag with different areas , circumstances and results . We certainly didnt get ourselves a predictable disease did we ! Thanks everyone its interesting to see the different journeys . Good luck and best wishes<br />
Sandra xx</p>
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				<title>sandra replied to the topic Just a query on Allo transplants in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/just-a-query-on-allo-transplants#post-90027</link>
				<pubDate>Sat, 26 Mar 2011 08:43:48 +0000</pubDate>

									<content:encoded><![CDATA[<p>Thanks gang for all your replies , I know that 2 or 3 people on the under 50 site have had them and others have been spoken to about them but I was amazed when my Doc almost thought I was mistaken when I said this ! </p>
<p>When I was diagnosed in 2008 he automatically tested my sister who was not a match and that was the last time he mentioned it as&hellip;<span class="activity-read-more" id="activity-read-more-7935"><a href="http://www.myeloma.org.uk/forums/topic/just-a-query-on-allo-transplants#post-90027" rel="nofollow">[Read more]</a></span></p>
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				<title>sandra replied to the topic Hello everyone, I&#039;m new! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/hello-everyone-im-new#post-84385</link>
				<pubDate>Sat, 19 Mar 2011 18:44:15 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Tracey just to add a welcome to the gang , I am 3 years post diagnosis , was 43 when diagnosed and had a very successful CTD and stem cell transplant process 2008 . Loads of good advice and guidance on here<br />
Hope you are feeling ok on CTD Best wishes<br />
Sandra xx</p>
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				<title>sandra started the topic Just a query on Allo transplants. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/just-a-query-on-allo-transplants</link>
				<pubDate>Wed, 16 Mar 2011 13:59:10 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi all ,<br />
I just wanted to get an idea on how many of you have experienced allo ( donor )transplants during your time with mm .<br />
Have you been offered one by your consultant , what age are you , where are you along the mm journey and which hospital are you with .<br />
My interest is just general as I was told recently that they are so rarely carried&hellip;<span class="activity-read-more" id="activity-read-more-7926"><a href="http://www.myeloma.org.uk/forums/topic/just-a-query-on-allo-transplants" rel="nofollow">[Read more]</a></span></p>
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				<title>sandra replied to the topic Feeling Rough in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/feeling-rough#post-97112</link>
				<pubDate>Tue, 15 Mar 2011 09:59:12 +0000</pubDate>

									<content:encoded><![CDATA[<p>Thankyou guys ,<br />
I just seem to have hit a wall at the moment with the whole bloody lot . Like everyone else life is so busy and I just wish I had the energy to deal with it all . I much preferred CTD which didnt have me tied to the hosp 2 days a week and I didnt look like a pin cushion ! But I am determined to get on with this and enjoy another&hellip;<span class="activity-read-more" id="activity-read-more-13697"><a href="http://www.myeloma.org.uk/forums/topic/feeling-rough#post-97112" rel="nofollow">[Read more]</a></span></p>
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				<title>sandra replied to the topic Feeling Rough in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/feeling-rough#post-97109</link>
				<pubDate>Mon, 14 Mar 2011 16:32:43 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi all ,</p>
<p>Cycle 4 of Vel/Dex halfway under my belt and feeling pretty p****d off with it so far . Very tired and the taste is disgusting !! After a rapid drop from 20 to 11 the counts are static but my very enthusiastic Doc in Eastbourne still assures me he is not worried by this and its not just the pp,s he is interested in but the whole&hellip;<span class="activity-read-more" id="activity-read-more-13694"><a href="http://www.myeloma.org.uk/forums/topic/feeling-rough#post-97109" rel="nofollow">[Read more]</a></span></p>
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				<title>sandra replied to the topic Need a laugh? in the forum Off topic</title>
				<link>http://www.myeloma.org.uk/forums/topic/need-a-laugh#post-108902</link>
				<pubDate>Tue, 08 Mar 2011 16:29:29 +0000</pubDate>

									<content:encoded><![CDATA[<p>Thankyou Min I really lost it at the rectal examination of the thyroid !! priceless :)xx<br />
Sandra</p>
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				<title>sandra replied to the topic Who the heck are you. in the forum Off topic</title>
				<link>http://www.myeloma.org.uk/forums/topic/who-the-heck-are-you#post-108845</link>
				<pubDate>Thu, 03 Mar 2011 17:28:30 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi all,<br />
My name is Sandra I am 46 and I was diagnosed in Jan 08 after reporting in to the blood doner people and being refused and sent to my doc . Like the rest of you the rest is history I was given 3 months of iron tablets and then obviously alarm bells rang with my doc ( also your wonderful one at Eastbourne Sarah !)who ordered a bmb and&hellip;<span class="activity-read-more" id="activity-read-more-23639"><a href="http://www.myeloma.org.uk/forums/topic/who-the-heck-are-you#post-108845" rel="nofollow">[Read more]</a></span></p>
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				<title>sandra replied to the topic Velcade in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/velcade1298948366#post-103787</link>
				<pubDate>Thu, 03 Mar 2011 17:15:55 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hiya ,<br />
I dont post on here much but do a lot of reading , I am on my 3rd cycle of Velcade at the moment and luckily have had no p/n but for me the worst side affect is definately the moon face and very piggy eyes . I am sure that people double take me in supermarkets ! When I was on thal/dex first time round 3 years ago I suffered the same thing&hellip;<span class="activity-read-more" id="activity-read-more-19324"><a href="http://www.myeloma.org.uk/forums/topic/velcade1298948366#post-103787" rel="nofollow">[Read more]</a></span></p>
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