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        <title>My Diary with Copaxone</title>
        <link>http://msrcsharing.yuku.com/topic/2056/t/My-Diary-with-Copaxone.html</link>
        <description>
        <![CDATA[ I am starting this Diary in the hope that it will help others new to MS that come on this board. First a bit about me I am 36 and was diagnosed with ms in April this year After losing my vision in one eye over night in January this year and then this spreading to the right eye soon after I was sent to London for tests, Was told that I had Optic Neuritis I had never heard of this I had large doses of steroids and this in time has led to the return of my vision all though left me Registered... ]]>
        </description>

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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/43114/t/My-Diary-with-Copaxone.html#reply-43114</link>
			<description><![CDATA[ Hi Sarah and welcome to the MSRC boards <img src="http://static.yuku.com//domainskins/bypass/img/smileys/happy.gif" alt="image">
<br>
<br>
You may also like to pose your questions on the main All About MS board as that gets a lot more &quot;traffic&quot;
<br>
<br>
kind regards
<br>
<br>
squiffs<img src="http://static.yuku.com//domainskins/bypass/img/smileys/happy.gif" alt="image"> ]]></description>

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			<pubDate>Sat, 29 Mar 2008 11:32:36 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/43113/t/My-Diary-with-Copaxone.html#reply-43113</link>
			<description><![CDATA[ Good morning everyone, I&#39;m a newie on this forum, and would like just to say hello, and thanks to Denise for her comments on starting on copaxone... very
useful as I&#39;m at the decision point at the moment. just got my 100% diagnosis, after 3 years of  waiting, and have been offered Copaxone... am really very
unsure about taking on this medication so will be following your progress avidly Denise!
<br>
Personally i like the idea of alternative therapies and would be grateful if anyone... ]]></description>

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			<author>feeds@yuku.com (sphere1965)</author>
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			<pubDate>Sat, 29 Mar 2008 11:23:48 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/42939/t/My-Diary-with-Copaxone.html#reply-42939</link>
			<description><![CDATA[ HI all
<br>
<br>
Well back into copaxone, well was not using auto injector and that seemed to be working well, until the welts came back<img src="http://msrcsharing.yuku.com/domain/bypass/images/thumbdown.gif" alt="image"> but it seems that if you cant take penecilian then copaxone is a no no , not sure
how true that is, so on the case will let you know.
<br>
<br>
Short but sweet bye four now
<br>
<br>
Denise
<br> ]]></description>

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			<author>feeds@yuku.com (vespula)</author>
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			<pubDate>Tue, 18 Mar 2008 22:50:39 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19082/t/My-Diary-with-Copaxone.html#reply-19082</link>
			<description><![CDATA[ Thanks Mac and Dave for your comments, and sorry stella you are not finding it so easy.<br><br>After my last my post back in April, I did carry on with copaxone, and still get the nasty site reactions but not as much and only in my legs.<br><br>On the positive no serious relapses since April<br><br>Anne hope you are now well over your nasty bug <br><br>Denise ]]></description>

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			<pubDate>Mon, 17 Dec 2007 13:48:10 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19081/t/My-Diary-with-Copaxone.html#reply-19081</link>
			<description><![CDATA[ Sorry you've had such a tough time, Stellarlife.  Over here you have to stop taking Copaxone once you get what you refer to as 'sinking skin'.  Also I was told from the first time I started looking into these drugs that this particular side effect of Copaxone is permanent.<br><br>Like you  I don't relish the thought of daily injections but I DO know thatI have had the best 16 months since I started on this and although I am quite poorly at the moment with a general virus type thing, it looks... ]]></description>

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			<author>feeds@yuku.com (Cecilia Duracell Bunny)</author>
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			<pubDate>Sat, 03 Nov 2007 14:32:05 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19080/t/My-Diary-with-Copaxone.html#reply-19080</link>
			<description><![CDATA[ I was dx 1990,ON-legally blind, foot drop,etc. One month later a football sized tumor was found in my uterus. Had hysterectomy. Off work for 8weeks, during that time my eyes started improving, in 8 months they were20/20, been so ever since. My Dr. kept pushing Copaxone (he was a researcher for it as well) but I refused until. 1999 when I became &quot;MS Numb&quot; neck to toes. Solumedral fixed the exacerbation.<br>Copaxone was ok, though I DESPISE the idea of a drug,&quot;we are not sure how... ]]></description>

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			<author>feeds@yuku.com (Stellarlife)</author>
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			<pubDate>Sat, 03 Nov 2007 04:26:20 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19079/t/My-Diary-with-Copaxone.html#reply-19079</link>
			<description><![CDATA[ It is indeed good news that NICE are being NICE and agreeing to the prescription of Tysabri<br><br>BUT please note that what (little) I have seen so far is that it is to be for SEVERE RRMS -and we have yet to see what severe means in their terms.  I was at a talk given by an eminent MS doctor last year and he felt that it would be prescribed for severe cases where other ABC type drugs had been tried and not been effective.<br><br>Don't want to rain on anyone's parade but feel folks shouldn't... ]]></description>

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			<author>feeds@yuku.com (Cecilia Duracell Bunny)</author>
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			<pubDate>Sat, 06 Oct 2007 09:16:32 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19078/t/My-Diary-with-Copaxone.html#reply-19078</link>
			<description><![CDATA[ Dear Vespula,<br><br>I had missed your diary before, and it is sad to read that it was unfortunately short. I do hope you are holding up well since your last entry. I remember Copaxone well for the injection ritual too, and because it made absolutely no difference to me, I am actually taking nothing now. I wonder when you say &quot;have stopped it, waiting to try something else&quot; - would that something else be Tysabri ? <br><br>I see you are in the UK and in July it passed muster by the... ]]></description>

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			<pubDate>Sat, 06 Oct 2007 01:50:41 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19083/t/My-Diary-with-Copaxone.html#reply-19083</link>
			<description><![CDATA[ Hi Denise,<br><br>Interesting reading your Diary.<br><br>I am a 35 year old male, I live in South Africa. I was diagnosed with MS about 10 years ago, I had blurry vision and my face was numb for about a month. I was completely free of any symptoms after that. I had a relapse in Dec this year, both my legs went numb. After a 2 week stint in the hospital, being given Cortisone intravenously, I started on Betaferon about 4 months ago. I inject every second day, I am used to the injections, but... ]]></description>

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			<pubDate>Tue, 24 Jul 2007 10:05:50 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19077/t/My-Diary-with-Copaxone.html#reply-19077</link>
			<description><![CDATA[ Very long time since I posted about copaxone have stopped it <!--EZCODE EMOTICON START :( --><img src=http://www.ezboard.com/images/emoticons/frown.gif ALT=":("><!--EZCODE EMOTICON END-->  waiting to try something else.<br><br>Copaxone is good for a lot of people so please do not let my experience put any one off trying it.<br><br>But so far no side effects from stopping it<br><br>Den<div class='signature'><!--EZCODE LINK START--><a... ]]></description>

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			<pubDate>Sat, 14 Apr 2007 21:54:41 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19076/t/My-Diary-with-Copaxone.html#reply-19076</link>
			<description><![CDATA[ Sorry you are feeling like packing it in. do let us know what neuro says.  I started mine in May and i am trying to go on as long as possible.  I also get the saucer size welts.  My ms nurse arranged an appointment with the nurse from teva, who was lovely, I actually took a photo of some of them with a 10p in the middle of them, the coin looked lost.  I had a biggie at the time and she said my legs were too badly bruised underneath to carry on, and to leave my legs for a couple of months or... ]]></description>

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			<pubDate>Tue, 31 Oct 2006 16:41:15 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19075/t/My-Diary-with-Copaxone.html#reply-19075</link>
			<description><![CDATA[ An update .... I have an appointment with my neuro in November to discuss copaxone.  My eyes are still a problem with ON and uveitis  Im having to put steriod drops in both eyes up to 12 times a day.<br><br>I have been on copaxone now for 13 months and I feel I have given it a good go.  A recent MRI I had to test for devics showed no more lesions so the question is..... is it doing its job or should I bin the copaxone and try something else LDN maybe if neuro agrees that is<br><br>Denise... ]]></description>

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			<pubDate>Tue, 24 Oct 2006 08:09:26 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19074/t/My-Diary-with-Copaxone.html#reply-19074</link>
			<description><![CDATA[ Thanks Cecilia, keep get nasty rash's and big saucer welts, maybe because I'm a little bit stressy at the moment, hope it's going ok with you and your injections.<br><br>Denise x<div class='signature'><!--EZCODE LINK START--><a href="http://beautiful-bungalow.blogspot.com/">beautiful-bungalow</a><!--EZCODE LINK END--></div> ]]></description>

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			<pubDate>Wed, 23 Aug 2006 16:39:30 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19073/t/My-Diary-with-Copaxone.html#reply-19073</link>
			<description><![CDATA[ Sorry to hear things aren't going well <!--EZCODE EMOTICON START :| --><img src=http://www.ezboard.com/images/emoticons/indifferent.gif ALT=":|"><!--EZCODE EMOTICON END--> <br><br>Take care of yourself<br><br>Cecilia ]]></description>

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			<author>feeds@yuku.com (Cecilia Duracell Bunny)</author>
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			<pubDate>Wed, 23 Aug 2006 16:26:18 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19072/t/My-Diary-with-Copaxone.html#reply-19072</link>
			<description><![CDATA[ Me thinks Im going to stop injections, have only 2 sites left to inject without welts coming up, and eyes so bad think they maybe not working so will give it a month if eyes no better best say<!--EZCODE EMOTICON START :( --><img src=http://www.ezboard.com/images/emoticons/frown.gif ALT=":("><!--EZCODE EMOTICON END--> <!--EZCODE EMOTICON START :( --><img src=http://www.ezboard.com/images/emoticons/frown.gif ALT=":("><!--EZCODE EMOTICON END--> <!--EZCODE EMOTICON START :\ --><img... ]]></description>

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			<author>feeds@yuku.com (vespula)</author>
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			<pubDate>Tue, 22 Aug 2006 21:27:20 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19071/t/My-Diary-with-Copaxone.html#reply-19071</link>
			<description><![CDATA[ Hi Suzie<br><br>Probably best to weigh things up for the next few weeks  - just try not to overload your brain with information.  I know I did when making my choice!!<br><br>Cant really offer any advice but I just feel that anything I can do to try and take some sort of control over this thing has to be a positive so when it came down to it, thats kind of how I decided.<br><br>Please keep in touch and let me know how you get on.  I'll be thinking about you.<br><br>Denise xx ]]></description>

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			<author>feeds@yuku.com (weedenise)</author>
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			<pubDate>Wed, 28 Jun 2006 20:47:03 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19070/t/My-Diary-with-Copaxone.html#reply-19070</link>
			<description><![CDATA[ hi Denise <br>the ms nurse came out and we both decided i needed a few weeks to decide that i was doing the right thing for me at the moment as i was only diagnosed 4 months ago.  Hope things are going ok with you, thanks for asking about me! Still think i will be starting but im going to wait a few weeks. <br><br>keep in touch, sue ]]></description>

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			<author>feeds@yuku.com (boozysuzy)</author>
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			<pubDate>Wed, 28 Jun 2006 20:32:00 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19069/t/My-Diary-with-Copaxone.html#reply-19069</link>
			<description><![CDATA[ Suzie<br><br>Was just wondering how you were doing with the injections?  <br><br>Hope you're well.<br><br>Denise xx ]]></description>

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			<pubDate>Fri, 23 Jun 2006 19:58:02 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19068/t/My-Diary-with-Copaxone.html#reply-19068</link>
			<description><![CDATA[ Vespula, good luck with house move.  It is not easy I did it a year ago, and also went to a different town and left everything I had known for over 15 years I thought it was going to be reasonably easy, but I have had a few probs settling and that left me totally stressed and lead to a couple of relapses. So I have joined the copaxone club, just done second jab today fine except for immediate wrist pain that has lasted hours. probably tense, nurse doesnt know.<br>Boozy susy, you are on your... ]]></description>

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			<pubDate>Tue, 16 May 2006 14:57:24 GMT</pubDate>
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			<title><![CDATA[ Re: My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/reply/19067/t/My-Diary-with-Copaxone.html#reply-19067</link>
			<description><![CDATA[ Hi Denise,<br><br>Sorry to hear you've had a rough time, hope the move goes OK.<br>Remember if you need to talk, just phone, text what ever.<br><br>I've had a call today. Copaxone to be delivered next Thursday, Waiting for the MS nurse to phone, i'll let you know how things go.<br><br>Take care<br><br>Sue XxX ]]></description>

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			<pubDate>Mon, 15 May 2006 21:37:17 GMT</pubDate>
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			<title><![CDATA[ My Diary with Copaxone ]]></title>
			<link>http://msrcsharing.yuku.com/topic/2056/t/My-Diary-with-Copaxone.html</link>
			<description><![CDATA[ I am starting this Diary in the hope that it will help others new to MS that come on this board. First a bit about me I am 36 and was diagnosed with ms in April this year <br>After losing my vision in one eye over night in January this year and then this spreading to the right eye soon after I was sent to London for tests, Was told that I had Optic Neuritis I had never heard of this I had large doses of steroids and this in time has led to the return of my vision all though left me Registered... ]]></description>

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			<author>feeds@yuku.com (vespula)</author>
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			<pubDate>Tue, 27 Sep 2005 10:40:12 GMT</pubDate>
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