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	<title>Myeloma Forum | pauline22 | Activity</title>
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				<title>pauline22 replied to the topic CURCUMIN in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/curcumin1379683671/page/3/#post-125120</link>
				<pubDate>Wed, 25 Nov 2015 01:57:20 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi everyone not been on hear for a while and just looking through your very interesting posts on what we all take to try to prolong our remission I personally take Pomi-t each day which contains four super foods squeezed into a capsule to boost my daily polyphenols which has been a government backed and scientifically tested in a national UK&hellip;<span class="activity-read-more" id="activity-read-more-41991"><a href="http://www.myeloma.org.uk/forums/topic/curcumin1379683671/page/3/#post-125120" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 replied to the topic Vigilance - temperature and feeling unwell in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/vigilance-temperature-and-feeling-unwell/page/2/#post-124553</link>
				<pubDate>Thu, 08 Oct 2015 12:08:38 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Andy </p>
<p>so pleased you&#8217;re OK and on the mend been quiet concerned about you, take care and listen to your body.</p>
<p>Onwards and upwards as Tom would say xxx</p>
<p>Polly</p>
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				<title>pauline22 replied to the topic Colin in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/colin/#post-123583</link>
				<pubDate>Sat, 15 Aug 2015 21:49:07 +0100</pubDate>

									<content:encoded><![CDATA[<p>Dear Vicki</p>
<p>So very sorry to hear your news of Collins passing my heartfelt thoughts go out to you and your family at this very sad time.</p>
<p>Polly xxx</p>
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				<title>pauline22 replied to the topic Worried in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/worried/page/3/#post-123033</link>
				<pubDate>Sun, 12 Jul 2015 10:36:41 +0100</pubDate>

									<content:encoded><![CDATA[<p>What wonderful news congratulations to you both &#x1f490; xx</p>
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				<title>pauline22 replied to the topic Worried in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/worried/page/3/#post-123033</link>
				<pubDate>Sun, 12 Jul 2015 10:36:41 +0100</pubDate>

									<content:encoded><![CDATA[<p>What wonderful news congratulations to you both &#x1f490; xx</p>
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				<title>polly changed their profile picture</title>
				<link>https://forum.myeloma.org.uk/activity/p/39730/</link>
				<pubDate>Sun, 05 Jul 2015 21:14:29 +0100</pubDate>

				
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				<title>pauline22 replied to the topic No remission! in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/no-remission/page/3/#post-122596</link>
				<pubDate>Sun, 14 Jun 2015 12:17:11 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Andrea</p>
<p>It&#8217;s all about steps and as time goes on you will regain your strength and pull away from feeling weak and tired as for the grey hair I decided to keep it because I wanted to take some control of my wellbeing and decided against adding chemicals to the mix even though you can have it done without touching your scalp  nevertheless I&hellip;<span class="activity-read-more" id="activity-read-more-39406"><a href="http://www.myeloma.org.uk/forums/topic/no-remission/page/3/#post-122596" rel="nofollow">[Read more]</a></span></p>
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				<title>polly changed their profile picture</title>
				<link>https://forum.myeloma.org.uk/activity/p/39345/</link>
				<pubDate>Sun, 07 Jun 2015 23:15:20 +0100</pubDate>

				
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				<title>polly changed their profile picture</title>
				<link>https://forum.myeloma.org.uk/activity/p/39344/</link>
				<pubDate>Sun, 07 Jun 2015 23:13:53 +0100</pubDate>

				
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				<title>pauline22 replied to the topic Myeloma X1 maintenance in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/myeloma-x1-maintenance/#post-121528</link>
				<pubDate>Thu, 02 Apr 2015 10:34:34 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi</p>
<p>I have been a member of this forum for some time although I don&#8217;t post often I like to keep up to date with other members journey&#8217;s and overall I have shared the good the bad and the sad with you all.  I have done the Myeloma X1 the chemo the SCT and all that jazz with the fallout of the before and after side effects I have noted people on&hellip;<span class="activity-read-more" id="activity-read-more-38394"><a href="http://www.myeloma.org.uk/forums/topic/myeloma-x1-maintenance/#post-121528" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 replied to the topic Advice required - dilemma in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/advice-required-dilemma/#post-119979</link>
				<pubDate>Tue, 16 Dec 2014 00:26:06 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Chystal</p>
<p>Please don&#8217;t feel angry it&#8217;s just that this forum is for people who have multiple myeloma a cancer that at the moment is incurable and terminal therefore any fundraising by our family and friends goes towards research for this cruel disease in the hope of finding better treatments and a possible cure in the future, I truly hope you&hellip;<span class="activity-read-more" id="activity-read-more-36849"><a href="http://www.myeloma.org.uk/forums/topic/advice-required-dilemma/#post-119979" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 replied to the topic Advice required - dilemma in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/advice-required-dilemma/#post-119967</link>
				<pubDate>Sun, 14 Dec 2014 21:25:22 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi </p>
<p>Whilst I feel sad to hear what you have been through I have to agree with Tony this really isn&#8217;t the place to start a discussion on this subject and sincerely hope you find the right kind of forum of similar mindset to you to share your interest.</p>
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				<title>pauline22 replied to the topic Advice required - dilemma in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/advice-required-dilemma/#post-119967</link>
				<pubDate>Sun, 14 Dec 2014 21:25:22 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi </p>
<p>Whilst I feel sad to hear what you have been through I have to agree with Tony this really isn&#8217;t the place to start a discussion on this subject and sincerely hope you find the right kind of forum of similar mindset to share your interest.</p>
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				<title>pauline22 replied to the topic Help needed! in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/help-needed-2/#post-118254</link>
				<pubDate>Sun, 21 Sep 2014 09:43:05 +0100</pubDate>

									<content:encoded><![CDATA[<p>Done 🙂 </p>
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				<title>pauline22 replied to the topic The pain is back... in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/the-pain-is-back/#post-118237</link>
				<pubDate>Fri, 19 Sep 2014 13:41:40 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Tom</p>
<p>You mention the pain is in the left rib as before could it not be a weak spot that&#8217;s now susceptible to all kinds of everyday things that we do without thinking especially when we feel better, it&#8217;s normal to get the jitters when pain comes especially nerve pain that can be a bitch my advise would be get it checked out if its worrying you&hellip;<span class="activity-read-more" id="activity-read-more-28180"><a href="http://www.myeloma.org.uk/forums/topic/the-pain-is-back/#post-118237" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 replied to the topic SLIM  in the forum End of Life and Grief</title>
				<link>http://www.myeloma.org.uk/forums/topic/slim-my-soul/page/2/#post-117867</link>
				<pubDate>Sun, 31 Aug 2014 21:52:05 +0100</pubDate>

									<content:encoded><![CDATA[<p>Dear Eve </p>
<p>Deeply saddened to hear the news of Slims passing thinking of you at this sad time </p>
<p>Love Polly xx</p>
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				<title>pauline22 replied to the topic Curcumin in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/curcumin-2/#post-116198</link>
				<pubDate>Tue, 24 Jun 2014 12:33:10 +0100</pubDate>

									<content:encoded><![CDATA[<p>Yes there is a lot of nonsense out there regarding alternative shall we say trends however my own experience regarding complimentary medicine has been successful, firstly after the birth of my son in the 80s I came down with quite bad hayfever tried all the usual tablets and so forth whilst they where good the effects didn&#8217;t last and left me&hellip;<span class="activity-read-more" id="activity-read-more-25657"><a href="http://www.myeloma.org.uk/forums/topic/curcumin-2/#post-116198" rel="nofollow">[Read more]</a></span></p>
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				<title>polly changed their profile picture</title>
				<link>https://forum.myeloma.org.uk/activity/p/25566/</link>
				<pubDate>Sat, 14 Jun 2014 18:56:33 +0100</pubDate>

				
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				<title>polly changed their profile picture</title>
				<link>https://forum.myeloma.org.uk/activity/p/25563/</link>
				<pubDate>Sat, 14 Jun 2014 18:42:42 +0100</pubDate>

				
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				<title>pauline22 replied to the topic My Remission is over!!  in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-remission-is-over/page/2/#post-114391</link>
				<pubDate>Wed, 09 Apr 2014 21:28:35 +0100</pubDate>

									<content:encoded><![CDATA[<p>hi Mandy</p>
<p>Today I read another article from the Myeloma Beacon which again brought me back to you  and your dilema and like our friend Eve who claims to be  pleasantly plump lol said its a matter of attitude that will carry you a long way, and she is right , I consider this desease sly and deceitful and dos&#8217;nt care who you are, and so you&#8217; must&hellip;<span class="activity-read-more" id="activity-read-more-1989"><a href="http://www.myeloma.org.uk/forums/topic/my-remission-is-over/page/2/#post-114391" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 replied to the topic My Remission is over!!  in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/my-remission-is-over/page/2/#post-114311</link>
				<pubDate>Sun, 06 Apr 2014 19:42:18 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Mandy</p>
<p>The day you posted your sad news April 3rd I also got an email through from the Myeloma Beacon namely Pats Place a fellow sufferer stating( when the end isn&#8217;t the end ) it makes interesting reading and as far as I am conerned nothing is over until the curvey lady sings give it a read you may find it reasuring and hope you take some&hellip;<span class="activity-read-more" id="activity-read-more-1925"><a href="http://www.myeloma.org.uk/forums/topic/my-remission-is-over/page/2/#post-114311" rel="nofollow">[Read more]</a></span></p>
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				<title>polly changed their profile picture</title>
				<link>https://forum.myeloma.org.uk/activity/p/1494/</link>
				<pubDate>Sun, 09 Mar 2014 22:54:04 +0000</pubDate>

				
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				<title>polly changed their profile picture</title>
				<link>https://forum.myeloma.org.uk/activity/p/1488/</link>
				<pubDate>Sun, 09 Mar 2014 17:53:25 +0000</pubDate>

				
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				<title>polly changed their profile picture</title>
				<link>https://forum.myeloma.org.uk/activity/p/1487/</link>
				<pubDate>Sun, 09 Mar 2014 17:50:03 +0000</pubDate>

				
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				<title>pauline22 replied to the topic Zometa &#039;flu&#039; in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/zometa-flu/page/2/#post-105051</link>
				<pubDate>Wed, 20 Mar 2013 20:52:27 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Tom</p>
<p>Same here when first introduced to Zometa some 18 months ago had a bad night with the said symptons  very unpleasant  floored mentioned it to my consultant so second time and thereafter given one piriton<br />
 tablet and 2 paracetamol some 20 minutes before a 30 minute infusion and that cured it  never looked back hope this helps.</p>
<p>Polly</p>
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				<title>pauline22 replied to the topic Trials and maintenance therapies etc. in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/trials-and-maintenance-therapies-etc#post-101161</link>
				<pubDate>Sun, 09 Dec 2012 14:42:58 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Tom </p>
<p>Just to add my input on Zometa </p>
<p>I get daily emails from the  Myloma Beacon with the latest news from America and Europe I am also hooked up to Andrew Schorr Patient Power and on occasions he talks to Dr  James Berenson a leading myeloma expert<br />
some time ago I recall a conversation regarding Zometa and how long you should be on it&hellip;<span class="activity-read-more" id="activity-read-more-17715"><a href="http://www.myeloma.org.uk/forums/topic/trials-and-maintenance-therapies-etc#post-101161" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 replied to the topic starting treatment in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/starting-treatment/page/2/#post-86841</link>
				<pubDate>Wed, 31 Oct 2012 00:06:37 +0000</pubDate>

									<content:encoded><![CDATA[<p>Well hospital appointment today Tuesday at 9.15 for THE TREATMENT signed a few forms had a talk with consultant all done and dusted by 10.00 then directed to pharmacy for drugs which took them two and a half hours to prepare :-/ then back to nurse to go through the cocktail with me and what a cocktail it is apart from CDT you can add to the mix&hellip;<span class="activity-read-more" id="activity-read-more-5598"><a href="http://www.myeloma.org.uk/forums/topic/starting-treatment/page/2/#post-86841" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 replied to the topic starting treatment in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/starting-treatment/page/2/#post-86838</link>
				<pubDate>Mon, 29 Oct 2012 22:16:37 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Tom as you say its best not to have notice of BMB takes some of the worry away before hand, and when I go for treatment tomorrow I shall take a hand full of your onwards and upwards with me along with one day at a time and hopefully I wont feel to bad on treatment 🙂 </p>
<p>Hi Mavis I shall certainly keep a watch out for those shingles as for&hellip;<span class="activity-read-more" id="activity-read-more-5595"><a href="http://www.myeloma.org.uk/forums/topic/starting-treatment/page/2/#post-86838" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 replied to the topic starting treatment in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/starting-treatment#post-86835</link>
				<pubDate>Sun, 28 Oct 2012 13:35:49 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Vicki</p>
<p>Yes its a bit of a bummer to have to start treatment which I believe will be this Tuesday coming I have been randomised on the CDT arm which is a little disappointing due to the trials consultant realy selling to me how positive the RCD side of the trial has been with his other patients giving such good results but at the same time I&hellip;<span class="activity-read-more" id="activity-read-more-5592"><a href="http://www.myeloma.org.uk/forums/topic/starting-treatment#post-86835" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 replied to the topic starting treatment in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/starting-treatment#post-86833</link>
				<pubDate>Tue, 23 Oct 2012 13:32:42 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Andy</p>
<p>Thanks for your advise and experience which I appreciate, thinking I might bomb it and let my husband do the injections for me as he has done it for himself when he had a dvt </p>
<p>Went to the hospital today thinking I was just signing the concent forms prior to treatment only to find a bmb sprung on me, well did not see that one coming,&hellip;<span class="activity-read-more" id="activity-read-more-5590"><a href="http://www.myeloma.org.uk/forums/topic/starting-treatment#post-86833" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 replied to the topic starting treatment in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/starting-treatment#post-86831</link>
				<pubDate>Mon, 22 Oct 2012 23:19:18 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Ali as you say its the fear of the unknown that&#039;s scary  but hopefully like your mum I will get through it..</p>
<p>Eve I shall not rub the  site after the injection and thankyou for the  tip</p>
<p>Tom I shall take your advise and  take one day at a time.</p>
<p>Once again I would like to thank you all for the advise given today I feel a little more&hellip;<span class="activity-read-more" id="activity-read-more-5588"><a href="http://www.myeloma.org.uk/forums/topic/starting-treatment#post-86831" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 replied to the topic starting treatment in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/starting-treatment#post-86826</link>
				<pubDate>Mon, 22 Oct 2012 17:37:49 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Eve and Jean</p>
<p>Thankyou so much for your kind welcome and advise I feel a bit more  easy by the need to have the injections given the side affects of clots  which sound nasty.</p>
<p>Eve I am so sorry to hear of your husbands experiance with the clots but please be assured your advise has been a big help to me.</p>
<p>Jean I so look forward to that&hellip;<span class="activity-read-more" id="activity-read-more-5583"><a href="http://www.myeloma.org.uk/forums/topic/starting-treatment#post-86826" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 started the topic starting treatment. in the forum Newcomers</title>
				<link>http://www.myeloma.org.uk/forums/topic/starting-treatment</link>
				<pubDate>Mon, 22 Oct 2012 12:49:39 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi everybody I feel like I know you all as I have been a member of the site for over a year and have quietly shared all your trials and tribulations, I am 58 and was diagnosed with a solitary plasmacytoma on my T7 vertebra in 2011 which was dealt with radiotherapy at clatterbridge followed by stabilation of my spine at the walton centre in&hellip;<span class="activity-read-more" id="activity-read-more-5580"><a href="http://www.myeloma.org.uk/forums/topic/starting-treatment" rel="nofollow">[Read more]</a></span></p>
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				<title>pauline22 replied to the topic Kyphoplasty in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/kyphoplasty1341573880#post-93104</link>
				<pubDate>Sat, 07 Jul 2012 15:43:34 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Myra after my T7 vertebrae collapsed I was in a lot of pain with lack of mobility and life was grim I therefore decided to go for the op whereby they not only put in the cement but placed rods and screws in as well to stabilise the rest of my spine and prevent any further collapse all done through keyhole surgery, a year on and life and&hellip;<span class="activity-read-more" id="activity-read-more-10989"><a href="http://www.myeloma.org.uk/forums/topic/kyphoplasty1341573880#post-93104" rel="nofollow">[Read more]</a></span></p>
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