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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">jeff</title><subtitle type="html" /><id>https://community.macmillan.org.uk/cancer-blogs/b/jeff/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/jeff" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/jeff/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2010-02-11T19:09:55Z</updated><entry><title>Third lot of chemo coming up</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/third-lot-of-chemo-coming-up" /><id>https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/third-lot-of-chemo-coming-up</id><published>2010-04-19T20:11:55Z</published><updated>2010-04-19T20:11:55Z</updated><content type="html">&lt;p&gt;I&amp;#39;m due my last (hopefully) dose of chemo,next port of call is scan time and then the results,which i will be sweating on.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=332460&amp;AppID=30467&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="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/jeff/archive/tags/chemotherapy" /></entry><entry><title>chemo this Thursday!!!!!</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/chemo-this-thursday" /><id>https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/chemo-this-thursday</id><published>2010-03-09T16:14:18Z</published><updated>2010-03-09T16:14:18Z</updated><content type="html">&lt;p&gt;Well,the time has come for my chemo to start.I should be going in this Thursday 11th,so i will soon find out how i will feel after this.The hardest part is the boredom at home,but i have rediscovered an old talent,thank god for Airfix models,it really does help pass the time &amp;amp; take your mind off things.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=322402&amp;AppID=30467&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="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/jeff/archive/tags/chemotherapy" /></entry><entry><title>The big easy(dealing with boredom}</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/the-big-easy-dealing-with-boredom" /><id>https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/the-big-easy-dealing-with-boredom</id><published>2010-02-27T10:19:04Z</published><updated>2010-02-27T10:19:04Z</updated><content type="html">&lt;p&gt;Yep,great film title but how on earth do you cure&amp;quot;stuck at home boredom&amp;quot;.Strewth,i&amp;#39;m trying to be real positive here,but i&amp;#39;m sooooo bored.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=319642&amp;AppID=30467&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></entry><entry><title>No sleep till Brooklyn</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/no-sleep-till-brooklyn" /><id>https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/no-sleep-till-brooklyn</id><published>2010-02-24T09:06:58Z</published><updated>2010-02-24T09:06:58Z</updated><content type="html">&lt;p&gt;Since my surgery,i cannot sleep.Is it just me,i manage about 3 hours per night!It&amp;#39;s doing the other arfs head in with me wandering around a 2 in the morning and going downstairs to watch TV.I have a meeting at the QE in Birmingham on March 2nd.So i will know when my treatment will start.Anyone else having the same problems?&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=318872&amp;AppID=30467&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></entry><entry><title>Thank you</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/thank-you" /><id>https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/thank-you</id><published>2010-02-20T18:00:59Z</published><updated>2010-02-20T18:00:59Z</updated><content type="html">&lt;p&gt;Wife reading all these messages,thank you.I am sure we will get through this,i&amp;#39;ve got holidays to go on,things to do etc etc etc,as the bald man said.So lets get on with it,and get it sorted.By the way,does anyone have a spare ball,i have lost one,do not know where.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=318020&amp;AppID=30467&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></entry><entry><title>After the Op!</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/after-the-op" /><id>https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/after-the-op</id><published>2010-02-19T07:40:55Z</published><updated>2010-02-19T07:40:55Z</updated><content type="html">&lt;p&gt;Well,the operation went fine,now lopsided(sic),will shortly commence chemo so i will hopefully get the all clear some months from now.I have accepted i have cancer,and can now talk about it without getting upset.Now for the future,ABOVE AND BEYOND!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=317652&amp;AppID=30467&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="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/jeff/archive/tags/chemotherapy" /><category term="operation" scheme="https://community.macmillan.org.uk/cancer-blogs/b/jeff/archive/tags/operation" /></entry><entry><title>can't sleep</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/can-t-sleep" /><id>https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/can-t-sleep</id><published>2010-02-13T06:18:14Z</published><updated>2010-02-13T06:18:14Z</updated><content type="html">&lt;p&gt;Yet another restless night worrying about my op on Monday morning.I will be glad when this is finished with one way or the other.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=316018&amp;AppID=30467&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></entry><entry><title>It's hospital time</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/it-s-hospital-time" /><id>https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/it-s-hospital-time</id><published>2010-02-12T18:43:54Z</published><updated>2010-02-12T18:43:54Z</updated><content type="html">&lt;p&gt;Phone call to-day,the 12th,I&amp;#39;m into Hospital on Sunday for operation on Monday morning,i&amp;#39;ve got to have&amp;quot;one of the lads removed&amp;quot;,which is a bit worrying.So i&amp;#39;ll have to wait to see if it&amp;#39;s spreadi&amp;#39;m also somewhat scared,i wont look the same afterwards.The wife says she is not worried,but i am.I&amp;#39;m hoping i can do this without getting too depressed,time will tell.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=315921&amp;AppID=30467&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="Hospital" scheme="https://community.macmillan.org.uk/cancer-blogs/b/jeff/archive/tags/Hospital" /><category term="operation" scheme="https://community.macmillan.org.uk/cancer-blogs/b/jeff/archive/tags/operation" /></entry><entry><title>Still waiting</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/still-waiting" /><id>https://community.macmillan.org.uk/cancer-blogs/b/jeff/posts/still-waiting</id><published>2010-02-11T18:09:55Z</published><updated>2010-02-11T18:09:55Z</updated><content type="html">&lt;p&gt;Been nearly a week,still waiting to see the dude at the QE Birmingham wheteher or not it has spread,or even if i have TC.The wait is killing us,every time the phone rings i jump 6 foot in the air.Just wish they would hurry up.On another note,now i don&amp;#39;t get upset when i tell people i may have cancer,i have accepted that i may have,i just need it confirming.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=315655&amp;AppID=30467&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></entry></feed>