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<?xml-stylesheet type="text/xsl" href="https://community.macmillan.org.uk/cfs-file/__key/system/syndication/atom.xsl" media="screen"?><feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en-US"><title type="html">TC&amp;#39;s blog </title><subtitle type="html">TC&amp;#39;s blog </subtitle><id>https://community.macmillan.org.uk/cancer-blogs/b/tc/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/tc" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/tc/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2009-07-02T07:52:19Z</updated><entry><title>Swine Flu Vaccinations</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/tc/posts/swine-flu-vaccinations" /><id>https://community.macmillan.org.uk/cancer-blogs/b/tc/posts/swine-flu-vaccinations</id><published>2009-10-08T09:54:26Z</published><updated>2009-10-08T09:54:26Z</updated><content type="html">&lt;p&gt;





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&lt;p class="MsoNormal"&gt;I&amp;#39;ve been to get my annual flu jab this morning.&amp;nbsp; I
asked about having a swine flu jab while I was there and the nurse told me that
the surgery had not received their allocation yet and when they did it would
only be for 250 shots, apparently each person needs two.&amp;nbsp; My G.P. surgery
has around 800 patients who have the annual flu&amp;nbsp;jab and have now got the
job of allocating&amp;nbsp;the swine flu vaccine to the people that they
consider&amp;nbsp;need it most. Yet another cock-up by the cretins that laughingly
call themselves a government.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=259098&amp;AppID=28396&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="vaccine" scheme="https://community.macmillan.org.uk/cancer-blogs/b/tc/archive/tags/vaccine" /></entry><entry><title>Do I belong here now?</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/tc/posts/do-i-belong-here-now" /><id>https://community.macmillan.org.uk/cancer-blogs/b/tc/posts/do-i-belong-here-now</id><published>2009-07-13T08:38:05Z</published><updated>2009-07-13T08:38:05Z</updated><content type="html">Hello my friends, I&amp;#39;ve been wondering, since I went into remission, whether it is appropriate for me to be in the chat rooms any more.  
The rooms are for patients and carers and although I have been both over the past few years, I am not any more.      
 I suppose I should &amp;quot;get on with life now&amp;quot; which is exactly what my doctors have been telling me.&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=245970&amp;AppID=28396&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="Prostate cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/tc/archive/tags/Prostate%2bcancer" /><category term="carers" scheme="https://community.macmillan.org.uk/cancer-blogs/b/tc/archive/tags/carers" /><category term="remission" scheme="https://community.macmillan.org.uk/cancer-blogs/b/tc/archive/tags/remission" /></entry><entry><title>In Remission</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/tc/posts/in-remission" /><id>https://community.macmillan.org.uk/cancer-blogs/b/tc/posts/in-remission</id><published>2009-07-02T06:52:19Z</published><updated>2009-07-02T06:52:19Z</updated><content type="html">For those of all my wonderful friends that I haven;t yet shouted the good news at in the chat room, &amp;quot;I AM IN REMISSION&amp;quot;  While I realise that I still have to wait untill October 2012 for the full 5 year effect of my treatments to take effect, I am really happy that I now have a PSA reading of 0.2.  I have learned to live with the cumulative side effects of my treatment and I&amp;#39;m really going to enoy this summer, especially now I know it&amp;#39;s not going to be my last.  &lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=245955&amp;AppID=28396&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="Prostate cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/tc/archive/tags/Prostate%2bcancer" /><category term="side effects" scheme="https://community.macmillan.org.uk/cancer-blogs/b/tc/archive/tags/side%2beffects" /><category term="remission" scheme="https://community.macmillan.org.uk/cancer-blogs/b/tc/archive/tags/remission" /></entry></feed>