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	<title>Myeloma Forum | IanPiatczanyn | Activity</title>
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				<title>IanPiatczanyn started the topic Calcium levels in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/calcium-levels/</link>
				<pubDate>Wed, 03 Sep 2014 17:36:49 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi<br />
I&#8217;ve MM for6.5 years then all of a sudden I get told my calcium levels have gone up and showing slight increase in kidneys have been in hospital for 3 days having seline flushs and calcium levels dropped has anybody else had issues with this just a bit paranoid as this illness makes you.Yust started 2nd cycle of Pom and dex<br />
Thanks Ian</p>
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				<title>IanPiatczanyn replied to the topic cramps in fingers in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/cramps-in-fingers/#post-115844</link>
				<pubDate>Sun, 08 Jun 2014 12:30:58 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thanks for the reply&#8217;s I was given Quinine sulphate and take it on the first and second day&#8217;s of taking steroids and it is really helping with the cramps.<br />
Many thanks Ian</p>
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				<title>IanPiatczanyn started the topic cramps in fingers in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/cramps-in-fingers/</link>
				<pubDate>Wed, 14 May 2014 06:47:32 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi All</p>
<p>Just checking to see if anyone has the same symptons its when I take re,cyclo and dx within a day of taking these my fingers cramp and lock in together I have to force the fingers out and and stretch them with a few aches,It&#8217;s doesnt allow me to hold things with my fingers such as pen, knife and folk etc this only usually lasts for the&hellip;<span class="activity-read-more" id="activity-read-more-2394"><a href="http://www.myeloma.org.uk/forums/topic/cramps-in-fingers/" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic Decisions - To have a transplant or not!!  in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/decisions-to-have-a-transplant-or-not/#post-114273</link>
				<pubDate>Fri, 04 Apr 2014 13:59:49 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Mandy</p>
<p>I&#8217;ve had a tanderm transplant auto then a mini allo using my brothers cells in 2011 only got a year out of the allo but we are all different currently on rev and cyclo I was diagnosed in 2008 Jan and still here.I found the actual allo alot easier to get over as you dont have a high dose chemo.Like someone else mentioned there are a lot&hellip;<span class="activity-read-more" id="activity-read-more-1889"><a href="http://www.myeloma.org.uk/forums/topic/decisions-to-have-a-transplant-or-not/#post-114273" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn started the topic and a new relapse. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/and-a-new-relapse</link>
				<pubDate>Tue, 16 Apr 2013 23:00:49 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Been on velcade i just started my 8th cycle of velcade the light chain results were rising minimal but have risen now to 70,Got to nip to Birmingham tomorrow and discuss my next treatment,oh was looking for some time off treatment possibly going on revlimid what are the side effects of this and what is the procdure in taking it<br />
Thanks Ian</p>
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				<title>IanPiatczanyn replied to the topic Wow that Velcade must be good stuff! in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/wow-that-velcade-must-be-good-stuff#post-94710</link>
				<pubDate>Tue, 02 Apr 2013 22:14:52 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Pete<br />
Thanks for the reply i know its was a long time ago but what treatment and dates were your not on treatment and on treatment it&#039;s 9 years since you were diagnosed and to have had only one ASCT is amazing,let us know how the scan results are if you want you can e-mail me on <a href="mailto:piatkaz@aol.com" rel="nofollow">piatkaz@aol.com</a><br />
All the best Ian</p>
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				<title>IanPiatczanyn replied to the topic Wow that Velcade must be good stuff! in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/wow-that-velcade-must-be-good-stuff#post-94712</link>
				<pubDate>Tue, 02 Apr 2013 21:07:49 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Nicki<br />
When i was on Velcade it hammered my lightchains down from 2000 to 30 on one cycle and after auto Stem cell I only got 18 months remission but you look on this forum and many have had years everyone is different,I&#039;m even on velcade again for the next treatment and it&#039;s hammered it again I&#039;ve been diagnosed for 5 years and still going&hellip;<span class="activity-read-more" id="activity-read-more-12552"><a href="http://www.myeloma.org.uk/forums/topic/wow-that-velcade-must-be-good-stuff#post-94712" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic Wow that Velcade must be good stuff! in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/wow-that-velcade-must-be-good-stuff#post-94708</link>
				<pubDate>Tue, 02 Apr 2013 20:59:39 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Pete<br />
Wow 4yrs remission from velcade hope I get something like that I was diagnosed Jan 2008 had C-Vamp then stem cell transplant that only gave me 18 months remission,then had Velcade for 6 cycles then a mini allo using brothers cells but only got 12 months remission but similar to you my results lightchains were ok but ended up having&hellip;<span class="activity-read-more" id="activity-read-more-12548"><a href="http://www.myeloma.org.uk/forums/topic/wow-that-velcade-must-be-good-stuff#post-94708" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic leg muscle weakness in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/leg-muscle-weakness#post-102126</link>
				<pubDate>Tue, 19 Mar 2013 20:46:51 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Tom<br />
Had my next treatment this morning and had my dex reduced to 10mg so far no problems with my legs touch wood and had the velcade subcut also, that way really does reduce the side effects of the velcade.<br />
Onwards and upwards<br />
Ian</p>
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				<title>IanPiatczanyn replied to the topic leg muscle weakness in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/leg-muscle-weakness#post-102124</link>
				<pubDate>Fri, 15 Mar 2013 18:56:39 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi I spoke to my specialist and she seems to think it&#039;s because of the Dex so thinking of reducing it.</p>
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				<title>IanPiatczanyn started the topic leg muscle weakness. in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/leg-muscle-weakness</link>
				<pubDate>Wed, 13 Mar 2013 22:26:24 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi&#8230;Just checking in to see if anyone else has had te same symptons the last 2 evenings I&#039;ve found it hard to stand up from sitting down feels like my thigh muscles are very weak.<br />
I had my Zometa and velcade subcut and 20 mg of dex yesterday and just my dex today,I had these symptoms yesterday evening then all ok this morning just a little&hellip;<span class="activity-read-more" id="activity-read-more-18670"><a href="http://www.myeloma.org.uk/forums/topic/leg-muscle-weakness" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic Croaky/husky voice on Dex in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/croakyhusky-voice-on-dex#post-105105</link>
				<pubDate>Wed, 23 Jan 2013 19:34:33 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Ozzy</p>
<p>Yes i had the husky and high pitch voice whilst on Dex am still on it and still get it also suffer with hiccups for the days I&#039;m on dex.Hope all goes well for you.<br />
Ian</p>
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				<title>IanPiatczanyn replied to the topic hi from another newbie!!! in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/hi-from-another-newbie#post-94037</link>
				<pubDate>Thu, 20 Dec 2012 19:06:28 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Steve</p>
<p>Welcome to the site,Sorry cant help with the issue with kidney problems I just have issues with bone damage but after treatment,radiotherapy and surgery I&#039;m doing well.I see you mentioned eye trouble I am on Velcade also, This is the second time I&#039;ve had Velcade on the first lot of treatments (Nov 2010)I suffered with eye trouble&hellip;<span class="activity-read-more" id="activity-read-more-11920"><a href="http://www.myeloma.org.uk/forums/topic/hi-from-another-newbie#post-94037" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn started the topic Curcumin. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/curcumin</link>
				<pubDate>Wed, 18 Jul 2012 20:09:10 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi&#8230;Just checking to see if anyone is or have been using Curcumin as a supplement,if so where do you get it from,what dosage,when to take it,is it in a capsule etc.It seems to be taken a lot in America as a supplement and have seen they are doing trials with it in America at the moment.<br />
Thanks Ian</p>
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				<title>IanPiatczanyn replied to the topic radio therapy in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/radio-therapy#post-99864</link>
				<pubDate>Wed, 11 Jul 2012 21:33:33 +0100</pubDate>

									<content:encoded><![CDATA[<p>Cheers Tom (twinkle toes) I&#039;m lucky I&#039;ve only got 5 to have 25 would do my head in,I&#039;ve made the most of today been out fishing and got a nice red face from that thing in the sky I think it&#039;s called the sun made the most of it before the treatment started.<br />
onwards and upwards<br />
Ian</p>
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				<title>IanPiatczanyn started the topic radio therapy. in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/radio-therapy</link>
				<pubDate>Wed, 11 Jul 2012 20:31:34 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi<br />
Start my radiotherapy tomorrow only 5 days Thurs,Fri, Mon,Tues and Wed on my neck vertebrae and two small spots on my upper ribs.I am going to go on Velcade the Tuesday after (24th) I had this treatment about 18 mths ago and because it put me in CR they are going to use it again so leaves other options for a later date,Only having it once a&hellip;<span class="activity-read-more" id="activity-read-more-16419"><a href="http://www.myeloma.org.uk/forums/topic/radio-therapy" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic restless feet in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/restless-feet#post-104581</link>
				<pubDate>Sun, 01 Jul 2012 12:14:28 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thanks for all the replies,I had surgery on my neck putting a cage around my vertebrae (C6) due to the pesky mm destroying it and was taking gabapentine for the nerve pain,I stopped taking this a week ago due to pain in neck subsiding and found out through a friend (Deb) that this is used for PN so took it again last night and had best nights&hellip;<span class="activity-read-more" id="activity-read-more-20118"><a href="http://www.myeloma.org.uk/forums/topic/restless-feet#post-104581" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic restless feet in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/restless-feet#post-104577</link>
				<pubDate>Sat, 30 Jun 2012 21:49:18 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Gill<br />
I have got neuropathy from old treatments but not like this strange how it&#039;s just started up when I&#039;m not started any treatment yet<br />
Ian</p>
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				<title>IanPiatczanyn started the topic restless feet. in the forum Side-effects</title>
				<link>http://www.myeloma.org.uk/forums/topic/restless-feet</link>
				<pubDate>Sat, 30 Jun 2012 20:49:44 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi<br />
Just wanted to see if anyone suffers from restless feet it&#039;s hard to describe but your feet ache and you keep wanting to scrunch your toes up,while your active and walking it&#039;s ok but as soon as you sit down you get this odd feeling in your feet and and the more you think of it it makes it more uncomfortable not painful but weird.Bedtime seems&hellip;<span class="activity-read-more" id="activity-read-more-20112"><a href="http://www.myeloma.org.uk/forums/topic/restless-feet" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic failed allo in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/failed-allo/page/2/#post-99495</link>
				<pubDate>Mon, 18 Jun 2012 13:59:19 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thanks for all the replies,David you said you had similar procedure how long is it before the backache subsides due to the stretching of the spine in the operation,Not hurting just aches I know it&#039;s only been 12 days since the op but just woundering.<br />
Thanks Ian</p>
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				<title>IanPiatczanyn replied to the topic failed allo in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/failed-allo#post-99486</link>
				<pubDate>Thu, 14 Jun 2012 18:54:05 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Tom</p>
<p>good luck with the x-ray I&#039;m sure it&#039;s nothing you didnt look that old on fb with the skipping rope nimble feet you still have<br />
Ian</p>
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				<title>IanPiatczanyn replied to the topic failed allo in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/failed-allo#post-99482</link>
				<pubDate>Wed, 13 Jun 2012 22:44:09 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Tom<br />
I came out of hospital last week 48hrs after op and doing really well just got a few aches from where they stretched my spine for the op.The neck injury just started after falling a sleep in a transport car 3 months ago just shows what damage this pesky MM does to your bones without you knowing it.<br />
Onwards and upwards<br />
Ian</p>
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				<title>IanPiatczanyn started the topic failed allo. in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/failed-allo</link>
				<pubDate>Wed, 13 Jun 2012 21:45:11 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi all just to let  you know my mini allo has officially failed,found a fracture in my neck vertebrae C6 so had surgery last week removed 90% of the vertebrae and put a cage in and plated it to C5 &amp; C7,the biopsy showed active lession and also now lightchains in blood are increasing.When area to operation has healed i will have radio therapy on&hellip;<span class="activity-read-more" id="activity-read-more-16037"><a href="http://www.myeloma.org.uk/forums/topic/failed-allo" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic Penny Lane in the forum End of Life and Grief</title>
				<link>http://www.myeloma.org.uk/forums/topic/penny-lane#post-107492</link>
				<pubDate>Wed, 02 May 2012 16:44:17 +0100</pubDate>

									<content:encoded><![CDATA[<p>So sad to hear this such a wonderful bubbly women and friend RIP</p>
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				<title>IanPiatczanyn replied to the topic Swollen ankles in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/swollen-ankles#post-92459</link>
				<pubDate>Tue, 10 Apr 2012 13:56:04 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thanks for all the replies,Hi Bridget it seems the swollen ankles were due to being prescribed naproxen by my GP when my specialist heard I was on Naproxen (anti inflamatory drug) he made me stop taking it straight away and my ankles have returned to normal.I&#039;m on codiene now due to firstly falling a sleep in the transport car and having a very&hellip;<span class="activity-read-more" id="activity-read-more-10350"><a href="http://www.myeloma.org.uk/forums/topic/swollen-ankles#post-92459" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn started the topic Swollen ankles. in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/swollen-ankles</link>
				<pubDate>Sat, 07 Apr 2012 20:34:55 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi all<br />
Just wondering if anyone has had any issues with swollen ankles I&#039;m on revlamid as a maint drug at the moment and have slight neuropathy.</p>
<p>Thanks Ian</p>
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				<title>IanPiatczanyn replied to the topic Mini Allo Update in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/mini-allo-update#post-99051</link>
				<pubDate>Mon, 02 Apr 2012 18:48:44 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thanks Mavis</p>
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				<title>IanPiatczanyn replied to the topic Mini Allo Update in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/mini-allo-update#post-99049</link>
				<pubDate>Thu, 29 Mar 2012 18:35:00 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thanks Tom</p>
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				<title>IanPiatczanyn started the topic Mini Allo Update. in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/mini-allo-update</link>
				<pubDate>Wed, 28 Mar 2012 21:28:16 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi<br />
Just thought I would let people know how my mini allo is going,Had it in June 2011 and been to see specialist today (28/03/2012) and I seem to be one of the lucky ones I&#039;m still disease free had a few issues with GVHD mainly skin issues rashes skin peeling off the palms of my hands, itchy scalp but no hospital stays yet feel extremely lucky.<br />
Ian</p>
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				<title>IanPiatczanyn replied to the topic allogeneic SCT in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/allogeneic-sct#post-98986</link>
				<pubDate>Tue, 13 Mar 2012 12:21:06 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Shirley</p>
<p>I&#039;m feeling really well at the moment I had issues with gvhd but mainly skin issues itchy palms and all the skin peeling off,itchy eyes,skin all over coated in a red rash still a very slight red tinge on my chest had a skin biopsy to prove it was gvhd.I have been lucky that it hasnt got to my organs so far so have been lucky havent&hellip;<span class="activity-read-more" id="activity-read-more-15545"><a href="http://www.myeloma.org.uk/forums/topic/allogeneic-sct#post-98986" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic allogeneic SCT in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/allogeneic-sct#post-98984</link>
				<pubDate>Mon, 12 Mar 2012 19:05:28 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Penny</p>
<p>I had an auto in January 2011 then a mini allo in June (brothers cells)It&#039;s been 9 months since my allo and at the moment all is still going really well,but as Shirley says you&#039;ve got to watch out for the gvhd.The mini allo is designed to reduce the chances of the gvhd of which I&#039;ve had three bouts of but all minor.ask as many&hellip;<span class="activity-read-more" id="activity-read-more-15543"><a href="http://www.myeloma.org.uk/forums/topic/allogeneic-sct#post-98984" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic Is there anyone here from South Wales/poss link between prostate cancer &#38; MM? in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/is-there-anyone-here-from-south-walesposs-link-between-prostate-cancer-mm/page/2/#post-98660</link>
				<pubDate>Sun, 15 Jan 2012 20:41:18 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Helen<br />
I found from past experiences they never offered me a sedation but when I asked they were only to willing to give me one,I had bad experiences with the last 2 BMB&#039;s thats why the last one was done under sedation and what a difference didnt feel a thing it was all like a dream.<br />
I had an Auto in Jan 11 then my mini in June 11 using my&hellip;<span class="activity-read-more" id="activity-read-more-15222"><a href="http://www.myeloma.org.uk/forums/topic/is-there-anyone-here-from-south-walesposs-link-between-prostate-cancer-mm/page/2/#post-98660" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic Is there anyone here from South Wales/poss link between prostate cancer &#38; MM? in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/is-there-anyone-here-from-south-walesposs-link-between-prostate-cancer-mm#post-98656</link>
				<pubDate>Sun, 15 Jan 2012 17:08:08 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Helen and John<br />
I havent heard the connection between MM and prostate cancer the only thing I&#039;ve heard is using maintenance drugs for long periods may possibly cause secondary cancers.Them Bone Marrow Biopsies arent pleasant I had 5 without sedation but the last one I used sedation it was so better so it will be sedation from now on.<br />
The only&hellip;<span class="activity-read-more" id="activity-read-more-15218"><a href="http://www.myeloma.org.uk/forums/topic/is-there-anyone-here-from-south-walesposs-link-between-prostate-cancer-mm#post-98656" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic Mini Allo Transplant in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/mini-allo-transplant/page/2/#post-91434</link>
				<pubDate>Thu, 22 Dec 2011 16:14:04 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Wendy<br />
Portugal hopefully is a good omen also my brother has just gone over there to live so theres another coincidence all the best with that.<br />
When ever I&#039;ve discussed the outcome with my specialist he&#039;s always said there a 20% chance of a cure and a much better chance of a long remission with this treatment.If you ever decide to go ahead&hellip;<span class="activity-read-more" id="activity-read-more-9336"><a href="http://www.myeloma.org.uk/forums/topic/mini-allo-transplant/page/2/#post-91434" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic Mini Allo Transplant in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/mini-allo-transplant/page/2/#post-91432</link>
				<pubDate>Wed, 21 Dec 2011 19:06:07 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Wendy<br />
I was talking to my trial nurse today and she said they havent checked for chromosomal abnormalities but she would check it out with my specialist,on another note I was given my results from my 6 monthly bone marrow biopsy and was told I&#039;m disease free at the moment so all going to plan after the mini allo.<br />
Ian</p>
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				<title>IanPiatczanyn replied to the topic Mini Allo Transplant in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/mini-allo-transplant/page/2/#post-91430</link>
				<pubDate>Mon, 19 Dec 2011 21:21:09 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Wendy<br />
Welcome to the mini allo journey,the whole purpose of the mini allo is to reduce the chances of getting serious GVHD they remove the T cells from your donor cells and they dont give you the Melphalan they give a more gently chemo as the specialist said its just to punch a hole in your immune system.They have mirrored the treatment used&hellip;<span class="activity-read-more" id="activity-read-more-9332"><a href="http://www.myeloma.org.uk/forums/topic/mini-allo-transplant/page/2/#post-91430" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic Mini Allo Transplant in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/mini-allo-transplant#post-91426</link>
				<pubDate>Wed, 02 Nov 2011 19:14:43 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Shirley.</p>
<p>Its 90+ days post my mini allo using my brothers cells just got all my results back from the bone marrow biopsy I am still in complete remission my immune system is now 99% my brothers and my T cells are 95%,I&#039;ve had low forms of gvhd (even had a skin biopsy to prove it) red skin rashes itchy eyes and itchy scalp,hoping to be really&hellip;<span class="activity-read-more" id="activity-read-more-9328"><a href="http://www.myeloma.org.uk/forums/topic/mini-allo-transplant#post-91426" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic Mini Allo Transplant in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/mini-allo-transplant#post-91424</link>
				<pubDate>Tue, 04 Oct 2011 18:05:38 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Wendy<br />
I had an auto in Jan this year then had my mini allo in June At present I&#039;m doing very well had issues with Graft versus host which included red and itchy skin all over my body and itchy scalp.My allo was a sibling donor (my brother).I know this is a difficult decision to make but mine was very aggresive and my hospital doesnt normally&hellip;<span class="activity-read-more" id="activity-read-more-9326"><a href="http://www.myeloma.org.uk/forums/topic/mini-allo-transplant#post-91424" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic Radiotherapy Appointment Tomorrow!! Yippee!! in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/radiotherapy-appointment-tomorrow-yippee#post-98116</link>
				<pubDate>Wed, 07 Sep 2011 22:51:20 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Bridget</p>
<p>Hope all goes well and they sort that pain out<br />
Look after yourself<br />
Ian x</p>
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				<title>IanPiatczanyn replied to the topic Radiotherapy Appointment Tomorrow!! Yippee!! in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/radiotherapy-appointment-tomorrow-yippee#post-98115</link>
				<pubDate>Wed, 07 Sep 2011 22:50:55 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Bridget</p>
<p>Hope all goes well and they sort that pain out<br />
Look after yourself<br />
Ian x</p>
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				<title>IanPiatczanyn replied to the topic trial mini allo in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/trial-mini-allo#post-97495</link>
				<pubDate>Fri, 08 Jul 2011 10:45:05 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi All</p>
<p>Just to let you know I&#039;ve had my mini allo trial June 25th and am out of hospital after 15 days,feeling well just need to physically build my strength up,when having ATG (antibodies) got a reaction which the nurses seemed to expect and was quite poorly for 4 &#8211; 5 days.</p>
<p>Ian</p>
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				<title>IanPiatczanyn replied to the topic trial mini allo in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/trial-mini-allo#post-97493</link>
				<pubDate>Tue, 07 Jun 2011 19:50:37 +0100</pubDate>

									<content:encoded><![CDATA[<p>Thanks very much all<br />
Really nice to hear you doing well Shirley,and Dai I will have my laptop whilst in hospital so as long as I&#039;m feeling well I will keep in touch<br />
Ian</p>
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				<title>IanPiatczanyn started the topic trial mini allo. in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/trial-mini-allo</link>
				<pubDate>Tue, 07 Jun 2011 15:46:45 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi all</p>
<p>Just to let you know I go in for my trial mini allo 20th June,had hectic day at Birmingham hospital yesterday had all the checks lungs,heart,kidneys,bone marrow biopsy,meeting with radioligist,blood tests and meeting with specialist to sign consent forms<br />
Ian</p>
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				<title>IanPiatczanyn replied to the topic All going to Plan in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/all-going-to-plan#post-97259</link>
				<pubDate>Sat, 16 Apr 2011 23:27:10 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Kieth<br />
Sorry for the lack of response,I&#039;ve just been through what you are, went on velcade and dex and had my 2nd SCT middle of Jan (1st one was in May 08)I know we are all different but I found this one much easier than the 1st and was released after 14 days.<br />
All the best Ian</p>
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				<title>IanPiatczanyn replied to the topic Some good news at long last in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/some-good-news-at-long-last#post-90120</link>
				<pubDate>Sun, 03 Apr 2011 23:29:48 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi Shirley<br />
Fantastic news so good to hear positive news on the allo front I should be having mine around June all the best<br />
Ian</p>
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				<title>IanPiatczanyn started the topic 2nd Auto SCT. in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/2nd-auto-sct</link>
				<pubDate>Wed, 30 Mar 2011 15:28:12 +0100</pubDate>

									<content:encoded><![CDATA[<p>Hi<br />
I had my second auto in Jan this year my first auto was in 08 which I didnt get a complete remission only a plateau and got 18 months remission from this.The second one in Jan 2011 I got a complete remission with the use of velcade, I&#039;ve been told I will get only approx half the 18 months I got with the first one does anyone know of anyone who&hellip;<span class="activity-read-more" id="activity-read-more-13826"><a href="http://www.myeloma.org.uk/forums/topic/2nd-auto-sct" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic SCT What to Pack? in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/sct-what-to-pack#post-89963</link>
				<pubDate>Tue, 08 Mar 2011 23:22:19 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Sarah</p>
<p>If you can get some audiobooks because as stated before its hard to concentrate at times and with the audiobook you can chill and listen with the headphones on,I&#039;ve had 2 transplants now and on the first one I had terrible troubles with mouth ulcers but on the 2nd I used ice lollies to suck on durring the melphalan and my mouth was&hellip;<span class="activity-read-more" id="activity-read-more-7871"><a href="http://www.myeloma.org.uk/forums/topic/sct-what-to-pack#post-89963" rel="nofollow">[Read more]</a></span></p>
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				<title>IanPiatczanyn replied to the topic update on allo sct in the forum Treatment</title>
				<link>http://www.myeloma.org.uk/forums/topic/update-on-allo-sct#post-96880</link>
				<pubDate>Tue, 04 Jan 2011 13:07:49 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi Shirley</p>
<p>I&#039;m so happy for you that alls going well and no sore mouth did you use ice cubes or is it a bit different from an auto,I&#039;ve been waiting since 27th Dec for my auto but no beds at moment,I&#039;ll be having a allo 3 months after my auto mine will be a mini was yours a mini or full keep the updates going<br />
Ian xx</p>
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				<title>IanPiatczanyn replied to the topic I got here at last in the forum General</title>
				<link>http://www.myeloma.org.uk/forums/topic/i-got-here-at-last#post-88811</link>
				<pubDate>Tue, 09 Nov 2010 23:14:43 +0000</pubDate>

									<content:encoded><![CDATA[<p>Hi all<br />
Just trying out the new web site after eventually getting in so lets hope for the best<br />
Ian Piatczanyn</p>
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